Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:141423539-141423767 | Common:6; Rare:86 | ||||
chr5:141431587-141431847 | Rare:69 | ||||
chr5:141431930-141432047 | Rare:39 | ||||
chr5:141477464-141478081 | Rare:176 | ||||
chr5:141532089-141532161 | Rare:12 | ||||
chr5:141635706-141635758 | Rare:7 | ||||
chr5:141644858-141645090 | Rare:68 | ||||
chr5:141648337-141648478 | Common:1; Rare:15 | ||||
chr5:141649773-141650178 | Common:2; Rare:75 | ||||
chr5:141659411-141659580 | Rare:48 | ||||
chr5:142316989-142317134 | Rare:21 | ||||
chr5:144169840-144170089 | Rare:66 | ||||
chr5:146122337-146122561 | Rare:41; Clinvar (benign):1 | ||||
chr5:148828086-148828199 | Common:7; Rare:43 | ||||
chr5:149186902-149187138 | Common:1; Rare:39 |