Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:111139731-111139889 | Rare:27 | ||||
chr1:111140033-111140506 | Common:2; Rare:145 | ||||
chr1:111739341-111740050 | Common:7; Rare:176 | ||||
chr1:111754978-111755186 | Common:6; Rare:79 | ||||
chr1:111755474-111755579 | Common:2; Rare:32 | ||||
chr1:112395981-112396272 | Common:1; Rare:91 | ||||
chr1:112396360-112396562 | Rare:46 | ||||
chr1:112619090-112619253 | Rare:62 | ||||
chr1:112619634-112619875 | Common:2; Rare:86 | ||||
chr1:112956145-112956626 | Common:6; Rare:165; Clinvar:10; Clinvar (benign):3 | ||||
chr1:113073052-113073255 | Common:1; Rare:83 | ||||
chr1:113390424-113390556 | Common:1; Rare:39 | ||||
chr1:113758891-113759066 | Common:1; Rare:44 | ||||
chr1:113759073-113759343 | Rare:67 | ||||
chr1:113812163-113812598 | Common:2; Rare:173 |