Tag | Content |
---|
EnhancerAtlas ID | HS145-05662 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr12:52548750-52550090 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Esrra | MA0592.2 | chr12:52548818-52548829 | TTGACCTTGAA | - | 6.14 | Foxo1 | MA0480.1 | chr12:52549447-52549458 | TGTAAACAGCA | - | 6.14 |
|
| Number of super-enhancer constituents: 12 | ID | Coordinate | Tissue/cell |
SE_03090 | chr12:52548731-52549373 | Bladder | SE_23126 | chr12:52548724-52550474 | Colon_Crypt_1 | SE_23778 | chr12:52548742-52549422 | Colon_Crypt_2 | SE_23778 | chr12:52549428-52550433 | Colon_Crypt_2 | SE_24790 | chr12:52548867-52549456 | Colon_Crypt_3 | SE_26568 | chr12:52536245-52551492 | Esophagus | SE_32153 | chr12:52548699-52549742 | Gastric | SE_33678 | chr12:52548650-52550036 | H2171 | SE_34302 | chr12:52548711-52549721 | HCT-116 | SE_34629 | chr12:52536709-52551617 | HeLa | SE_35885 | chr12:52537041-52552074 | HMEC | SE_64292 | chr12:52537455-52551439 | NHEK |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH12I052143 | chr12 | 52536922 | 52551852 |
|
Enhancer Sequence | GCCTCCCAAG GTGCTAGGAT TACAGGCATG AGCCACTGCA CCCAGCCAGA AAGCTACACT 60 TTCGAGGGTT GACCTTGAAA CTACGTGGGG CCATGTGGCT ATCCCTGATC CCCTGGAAGG 120 TCTTCAGAGT TAGCTTATCA GCTCAAGTTA TTCTCCACTC TGAGTACACG ACAGGGAACT 180 CCTCTCCCTC AGTGCTTAGG CACTGGGGTG GCCATGGGGG TTGGGGCAGC AGTGGCCTGT 240 CAGGGCAGGG TTTTGCAAGG GGACTTAGCA TCCTCGGGAG AGGAGGACAC TGGCCATCTT 300 CCTTTTTCCA GGAGGTCATG GGGAGAGTAT GTGGTGGGAC ACCGTGGGCC TCCCTCCACC 360 AGAAACATGG TCTTAGCAGC CACGGGCTTG TAGGGGGATG GAGCTGAGGA GAGGACTGTC 420 AGGCAGGCTG GAGAGCCTCC AGGGGGACCC TAGTCTCCCC CAATCTCAGG GAGCTCCTTA 480 AAGCAGCCAC AATCCACTGC AAAAGGGCAA AGCCTATGGG GGGGCCTGGG GGAAGTAGGA 540 CTCCAAGGCC TCCATTTTGT ACCCCTAAAG GCTGTAGCCA AGAGGAGGAG GAATGCAGGA 600 TTCCCCGCTA GGCCCTGTTC TGACAGGCTG GGGAGGAAGG GTGGGGCTCC CAAGTGAGCC 660 CACATGCTCC TGATCTCAGG TCGTAGCTAG GCAGCTTTGT AAACAGCAGA AACACAGAGC 720 AGCCTCTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGCA TGTGTATGTG TGTGCCTGTG 780 CTGGGGGACT CACGCCCCAG AGGGGACCCT TCTCATTACT TTATAGTCAC AGTTATATAC 840 AGGTCTGAGG CTGGGGTTCT GCCAGCTAAT GCTTGCTGGC ATTAGCTGTG TTGCAGGTCT 900 GTGTTGCAGG TCTGCTCCAT GTATTGTCTC CTTTAATCTT CCCAACCCTA TAGGCAGGCA 960 TCCTTATTAC CCAGTTTTAC AGGTGGGGAA ACTGAGGCTC TGAAAGTTGC AGATGCTCAG 1020 GGTCACAGAG CAACTGAGTG ATAAAGCCAG GTCAGGGTTC AAATTGAGGT CTGTCTGACT 1080 TCAGTCCAGT TATACTCCTG GCACCTGTGG ACGTGTGTGC ATGTGAGCAC TGATCAAGGG 1140 CTATGTGTAT GCACATGTGC GGATGTGTGC TTTGATGGTG GGCCTCAGTC TGCCTGCGCC 1200 TGTTGAGGAC ACCTGCATGT AGGCGTGGAT GTCTCCGCCC AGGGATGGAG GTGTGCACAC 1260 AGATGTCCAT TTGCACTTAT GTTTGCACAA TGCACGTATG TTGGGTACAC ATGTATGTGT 1320 TGTATGTGTG CACATGTGAA 1340
|