| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144291357-144291663 | Common:1; Rare:100 | ||||
| chr8:144308783-144309096 | Rare:85 | ||||
| chr8:144317632-144317996 | Common:2; Rare:127; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr8:144373756-144374080 | Common:3; Rare:103 | ||||
| chr8:144395514-144395712 | Common:1; Rare:52 | ||||
| chr8:144413542-144413773 | Common:1; Rare:81; Clinvar:1 | ||||
| chr8:144416499-144416684 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):2 | ||||
| chr8:144416826-144417045 | Common:1; Rare:50 | ||||
| chr8:144427721-144427975 | Common:1; Rare:70 | ||||
| chr8:144428492-144428708 | Common:2; Rare:83 | ||||
| chr8:144465329-144465449 | Common:1; Rare:46 | ||||
| chr8:144466871-144466979 | Common:2; Rare:59 | ||||
| chr8:144477902-144478154 | Common:6; Rare:82 | ||||
| chr8:144478261-144478490 | Rare:57 | ||||
| chr8:144500691-144500850 | Rare:69 |