Table 4 Autosomal common fragile sites, whose locations on the human genome sequence have been demarcated by flanking markers, and their overlap with evolutionary breakpoint intervals.
Fragile site [reference] | Location in the human genome | Overlap with evo breakpoint | |||
|---|---|---|---|---|---|
| Â | 5' Boundary | 3' Boundary | Â | ||
| Â | Marker designation | Position (Mb) | Marker designation | Position (Mb) | Â |
FRA2G [38] | LASSG | 169 | PPJG | 170.2 | -- |
FRA3B [39] | SHGC86352 | 59.7 | RH41625 | 60.5 | -- |
FRA4F [40] | SNCA | 90.8 | MNC5C | 96.7 | 95.62–95.73 |
FRA6E [41] | D6S1581 | 160.2 | D6S1719 | 165.9 | -- |
FRA6F [42] | SHGC144121 | 111.7 | SHGC82095 | 112.7 | -- |
FRA7E [43] | D7S1934 | 80.3 | SHGC104456 | 84.7 | 84.40–85.92 |
FRA7G [44] | SHGC143971 | 115.6 | RH44861 | 116.2 | -- |
FRA7H [45] | D7S614 | 130.2 | STSG33535FS | 130.4 | -- |
FRA7I [46] | SHGC153624 | 144.3 | SWSS2627 | 145.7 | -- |
FRA7K [47] | IMMP22L | 109.9 | IMMP22L | 110.7 | -- |
FRA9E [48] | D9S1866 | 106.9 | D9S154 | 118.4 | -- |
FRA16D [49] | SHGC150973 | 76.7 | WJ2755 | 77.8 | -- |