| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:113627041-113627314 | Common:4; Rare:80 | ||||
| chr2:113756532-113756804 | Common:3; Rare:95 | ||||
| chr2:113889705-113890165 | Common:8; Rare:153 | ||||
| chr2:118013991-118014216 | Common:2; Rare:120 | ||||
| chr2:118088344-118088509 | Common:1; Rare:50 | ||||
| chr2:119366795-119367059 | Common:1; Rare:77 | ||||
| chr2:119679090-119679219 | Common:3; Rare:41 | ||||
| chr2:120252665-120252964 | Common:2; Rare:92 | ||||
| chr2:121530596-121530884 | Common:7; Rare:119 | ||||
| chr2:121649418-121649701 | Common:2; Rare:80 | ||||
| chr2:121649918-121650138 | Common:1; Rare:59 | ||||
| chr2:121736760-121737086 | Common:4; Rare:129 | ||||
| chr2:121755402-121755716 | Common:3; Rare:101 | ||||
| chr2:127294077-127294188 | Common:2; Rare:43; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387941-127388227 | Common:6; Rare:124 |