Tag | Content |
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EnhancerAtlas ID | HS012-06610 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr11:117963370-117964540 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr11:117964142-117964157 | AGGGTTCAGAGGGCA | + | 6.03 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_23705 | chr11:117963534-117964316 | Colon_Crypt_1 | SE_29489 | chr11:117961401-117964585 | Fetal_Intestine_Large |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I118092 | chr11 | 117961986 | 117964343 |
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Enhancer Sequence | CCCAGACAAG AAGGCAGTCT GCTCTGGGAA AGAGCTGTTA CCAACTTTGT TTAAACTATA 60 AACTAAGTTT CTCCCAAAGT TAGTTCTGCC TACCCCTAGG AATGAACAAG GACAGTTTGG 120 AGGTTAGAAG CAAGATGGAG TCGCTAAGTT AGATCTCTTT CACTGTCTCA GTCATCATTT 180 TGCCAAGGCA GTTTCAATGG GAGGGCAGAG GAAAGAGAGT TCCCATGTGA GAGCCCAGCA 240 TTTCCCACCA GACAACTCAT GTAAACCTCA CAGTAGTCTT TTGAAGCAGG TTTTATTGTC 300 CCCACTCTAC AGAGGGTAAG CCTGGAGCTC AGAGAGGTGA AGGATCTTTC CTGAAAGCAC 360 ACAGTTAATA GGAGGCCGGT CTTGTATTCT GACTCGACCC CTGCAGACTG CAGAACCAGG 420 CTGTGTGCTA CATCACAAGG CCACCCATGG CCTAGTGTTA CCCAAGGGCA AGGCCAGGCA 480 TGTCCCTCCA TCAGACTACA GGCTCGTTTG GGAGGGAACG AAAGAGCTCC TTCCTATTGC 540 TGTGTCCACC GTGCTTAGCC GTGGAGCAAG CAACACCCAG GGACCCTCCC TCCATATCTA 600 ATCTGGGTCA CCCACTCAGG GATTAAAAGA GGCCCTCTCA CTCCCAAGAG GAACAGAAAA 660 AATTTCCAGC CAGAAATGTA CAAGGTCCTG TGACTCCTTC AACCACCACC AAGGTGGGTC 720 ATGACCTCAG CACAATAGGG CAGGCGAGTC CCTGGGTGGA GACCTAGACC ACAGGGTTCA 780 GAGGGCATAA ACCCAGACAG CATGCTCCTT TTAACCTTTG CCTGGCAGAA AGGGCCTGCA 840 TTTTTTTGTA TGTGAGCCTT TGTGTCAGTG GCTCCTCCAT GTGACTCTGT GGCTGTGTGC 900 GTGCTGAGTG CACACATGAA GTGGTGTAAA TAGAAATGCC TTTGCGTGTA TTTGTGCACA 960 TGCGTCGACG GCAGCCTAAG ACCACTCTCT CAGAAATATC ATAATGTTGA TAGCACATAT 1020 GTAGTAAAGT ACTCAAGTCT AAAGTCTACC ACCCAGTGAA TTTTTGCACA TATAAACACC 1080 TATGTAACCA ATGTTGAAAA CAAGATCCAG AAGTTTTCCT ATGTTCCAGA AGACTCCACT 1140 GTGTTCCTTC CAATAACTAA CTGCCCCCCC 1170
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