Tag | Content |
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EnhancerAtlas ID | HS145-13175 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr2:121954810-121955600 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Ar | MA0007.3 | chr2:121955217-121955234 | AAGTACATTCTGTTCTT | - | 6.1 | NR3C1 | MA0113.3 | chr2:121955217-121955234 | AAGTACATTCTGTTCTT | - | 6.15 | NR3C1 | MA0113.3 | chr2:121955217-121955234 | AAGTACATTCTGTTCTT | + | 6 | NR3C2 | MA0727.1 | chr2:121955217-121955234 | AAGTACATTCTGTTCTT | - | 6 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_27526 | chr2:121952973-121956095 | Esophagus | SE_36212 | chr2:121952713-121956652 | HMEC |
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| 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 |
GH02I121196 | chr2 | 121953673 | 121956580 |
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Enhancer Sequence | TGAACCCTGG AGGCGGAGGT TGCAGTGAGC CAAGCTCGTG CCACTGCACT CCAGCCTGGG 60 CGACAGGGTG AGATTCGGTC ACCTAAAAAA AAAAAAAAAA GACAGGAGGC TCAGAGAGGA 120 CCGCATCTTG CCTGAGCTCA CAAGCCAGCC ACGGCTGAAT TCAAACCGAG CTGTGAATAA 180 CTCCGAGTCC ACGTGCCCCG GGAACACCAA GCTGAGAGGA GAACAGTGCT GGAACAAGAG 240 ACCAGCTCGG GGGTGACACG GAAGGAGCAG GCCTTGGAGA AGAGTGGTGA CTCACTGGGA 300 CACTTCGTGG TTACAAAACA GGCCAGGCTC CTGCCAGACA CTCACACTCG GTTACTTTTC 360 TTTTAATTCC TTCCCTGCCC TTCCACTCCC TGTTCCCTGG GCACAGTAAG TACATTCTGT 420 TCTTCCTGAA CTTCTCACTG AACAGGGCAA CTCGATTCTT CTCCCATGGA CTGAGGGCCC 480 TTGGCCGACT GGAATCACGG GTGCCAGGCC AGGGCATCAG GAAGGACACA AGAGGGACCA 540 GCCTGTTCTG GCCAGCCTGC CAATCTGCCG GCTCCCCAGT GCTTTGGGGT CAAGTTCAAC 600 CCTCAACTAA GTCCCAGGCC TTTGAGATGA GCTTACTCTG CAATCTCGTG TCCCCTACCC 660 CTCTCGGGTA CCAGCACGGA AGTGCTGACC AACCCTGCAT ACTCACTGGC CACCCCACAC 720 CCCCGGCCTG CCCACGCCAC ACCTCACCAG TGTTGACCAG AGGAGTTCCT CAAAATAAAA 780 TCCAAATTAG 790
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