| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:103452262-103452453 | Rare:56 | ||||
| chr10:103917743-103917872 | Rare:25 | ||||
| chr10:103918117-103918551 | Common:5; Rare:115 | ||||
| chr10:104121884-104122171 | Common:2; Rare:90 | ||||
| chr10:104254790-104254955 | Rare:46 | ||||
| chr10:104268906-104269193 | Common:3; Rare:69 | ||||
| chr10:104338381-104338539 | Rare:42 | ||||
| chr10:109923423-109923682 | Common:2; Rare:100 | ||||
| chr10:110007690-110008125 | Common:1; Rare:120 | ||||
| chr10:110076966-110077075 | Rare:21 | ||||
| chr10:110225838-110226204 | Common:2; Rare:96 | ||||
| chr10:110871728-110871970 | Rare:78 | ||||
| chr10:110919326-110919654 | Common:7; Rare:91; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:111076790-111077039 | Common:1; Rare:67 | ||||
| chr10:112183676-112183851 | Common:3; Rare:61 |