| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:112481923-112482236 | Common:2; Rare:200 | ||||
| chr2:112541770-112542518 | Common:7; Rare:372 | ||||
| chr2:112584346-112584656 | Common:2; Rare:175 | ||||
| chr2:112584772-112584930 | Rare:36 | ||||
| chr2:112645688-112645972 | Common:2; Rare:211 | ||||
| chr2:112764582-112764871 | Common:4; Rare:171; Clinvar (pathogenic):2 | ||||
| chr2:113127193-113127598 | Rare:135 | ||||
| chr2:113157292-113157495 | Common:4; Rare:102 | ||||
| chr2:113173725-113174036 | Common:4; Rare:92 | ||||
| chr2:113219980-113220380 | Common:3; Rare:138; Clinvar:4 | ||||
| chr2:113627078-113627304 | Common:5; Rare:124 | ||||
| chr2:113756460-113756823 | Common:7; Rare:189 | ||||
| chr2:113889697-113890185 | Common:16; Rare:287 | ||||
| chr2:113890959-113891312 | Rare:83 | ||||
| chr2:118013967-118014268 | Common:6; Rare:277 |