Tag | Content |
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EnhancerAtlas ID | HS012-19188 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr4:78067060-78068340 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CEBPA | MA0102.3 | chr4:78067682-78067693 | ATTGCACAACA | + | 6.14 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_11624 | chr4:78066185-78069422 | CD20 | SE_29270 | chr4:78062699-78070153 | Fetal_Intestine_Large | SE_58508 | chr4:78041768-78081592 | Ly1 | SE_60297 | chr4:78046313-78080209 | Ly4 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr4 | 78067816 | 78068100 | chr4 | 78067536 | 78068168 | chr4 | 78067600 | 78068235 |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I077144 | chr4 | 78065414 | 78069919 |
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Enhancer Sequence | AAAGTATAAC TTGAAGTAGT TTTAGTTAGG ATAATGGGTT TCACAAATAT ACCGGAAGCA 60 CCAGTGTCAA AAGGACATCC TGAAGGTGGA AGTTCTACCC ACATGTACTC TTGAGTTGCT 120 TAGATGCTGT TAATCTGTTC TTGTGCAGAG CTGCTCATTC TTAAAAATGT ATGTAACATT 180 CTGAGTTGAA AGGAGAAGAC AGTCACACAG TGAAATCTCT CCCTCCTGAG ATAACTATTC 240 TCTCCCTGTT TTGCTGCTAT CCTTTCTACA CACTGCTATT GTTGCAAAAC TTGCATAACA 300 GTATTGTGAT TTGTCAATTC TGTTCTCTCC CATTAGGCTC TGAGCTCTCT GAGGGTAGGG 360 TTTAAACCAT AGCCATTTTG CGTCTACTGT TTCCTCCACT GTGCCTGGAA TAGATTAGCT 420 GCCCAGACAA CTTTTATTAA ACTGAACAAA AGAAGCAATG AAGATTTTAA AATGCTGCAT 480 TTGTAAGACA CATGGCTACA GAAACCTGAA TATTCTTGGA AGCTAATCTT CACGCAGGAT 540 GAGTCAATAT GTTTCTGTCC TGTTTAAATA CAAGATCTCG AGATAGCATA TTATTTATGT 600 GCATCATAAA AACTTAACAA ACATTGCACA ACACAATAAG CACAATACAT TGGTAACTTC 660 TGGCACATTT CTAAAAAAGT TTATTTTCTA TGTACTCTTT TTGTCCACCC CTTACCATCT 720 CTACCTCCTA GAATCCAGCA CAGGCTGTAA ACCTCAAACC TGCTGTTTTA GCAGTGAGTT 780 ATCAGAGGGC CTTGACTTCC TCTTAGAATG ATGGTATGCA GCTGAGCTAA CAATAGTAGA 840 GTCATCAGAG TATTTGCTGA TTGCCATCTT CTGTTTTAAA GACTTTAAAA ACACTTCCTT 900 GTCATAAGGT AGAAAAGAAC CCACATGTCT GCAAAATAGT CCTTATCAGG AGAAATAGGA 960 ACATAGCACA ATTTCTTTCT GGCCCCTAAA CATTTGCAAA CTACTGACAT GACACACTCA 1020 CATGATGTCT CAAATCTTTA GACATCTCCC CCCAGGCAGA AAAGAAGGAG CCTCATTTTT 1080 CTTCCCCTGC TGGCTTTCCT GAGATTTGAG TGGTGGGACT GTGTTGAAAC AACTGGCTGG 1140 CTTTTTTTAA GAAACATGTT AATTCAAAAC TCTAGGGTAA GGGTAGCTGA TCCTGGCAGG 1200 CCTGATCTGT CTGGACAGTT TCTTTTCAGA TTAGTTTGAC AGAGATAAGT CTAAGATTTC 1260 TCAAAAGCAT ATTTGCTTTC 1280
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