Tag | Content |
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EnhancerAtlas ID | HS101-09583 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr12:6197680-6199210 |
Target genes | Number: 29 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYA | MA0060.3 | chr12:6198441-6198452 | TCTGATTGGCT | - | 6.32 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_27167 | chr12:6197847-6198954 | Esophagus | SE_37940 | chr12:6196664-6208010 | HUVEC |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 6197889 | 6198887 | chr12 | 6197800 | 6198800 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I006088 | chr12 | 6197275 | 6199142 |
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Enhancer Sequence | GGTGCCTTTT TCTAATTAGC AAAAGCATGC TATGAGCTGG ATGCAGCCCA AGCCCAGCCC 60 CCCGGAGCCT TGGGCTTCCT GTTGCAGACA GGACTACAGG ACAAAGCCAA GATCCCTTTG 120 TAAGGTTCAG TCCTTGCTGG CCTTCCCCAG TCTGATCGAA TTTTTTTAAA GTGATCTAAG 180 GGTCTTTCTT TCTCAAAGGT ACACTTTGTG ATAGTTACCT GCAGATGAAC ATCAATTATC 240 TGAATGTTCA TAGCTTGGGG CTCCAAACTC CAACCATCTT GCCTTCAGTT TGAAAAGCTG 300 AAAAAACTGC AAATTTGCAT GCAATCAAAC AAGGCCATTA TCAGTCCCAG TGGAGACAGG 360 CATTGGGTTT TGTTGGCATA ACAAGGAAAC ATTCATTCCC TAGGTATAAC TAACAAGTAA 420 TATGACCTGG CTCTCAGAAT GAGCTGACTC CTTGCTATGC CCTAGAAAGA CAGAAAGCAC 480 CAGAGGGTTG GGGAAGTAGA TTCTGGAGGC TGTCAAGGAA AGTTTCAAGG TCAGTGTGAA 540 CTCCCACACA AAACACTCTG CCACCCCGAA CGGCCCTTGG AGCCACAACA GCAGACACTC 600 ATAAATGATG CGGCATTTAC CAGACCGGAC TTCTGAACCT GGGGGCCCTG CGGGACTACA 660 CAGGCTGTGA ACAATTCAAA AGGCCATATT AATCACCTCT TGGGAGACGA GTCATTGTGC 720 TTCCGAGCCA GTGAAAAAAC CTCGGTTGTG GGCAAACACT ATCTGATTGG CTGAGGACAA 780 AGCAGTCTTC TCTTCTCAGG TAAACAACCT GAAACCGGGA GTTCTGAGCT GGGAGGAGCT 840 TGTGCCTCTG GGAGGTCTCA CGTGTTTGTG GCCTCAGCCC AACACGAAGA ACCTGGTACC 900 CAGTTTTTTC AGCTGTTCCC AGGACACTGG TTAGTAAGGA CTTTAATGCA CCCAGGAGAC 960 AAAGCGAGTA GCTAGGGTAC AGCTGGAGCC TCAGAAAGGT GCCCCGGGAG GCAAACAAGG 1020 CTTCTCTTGC ATTCTCCCTC CCCTTTGTCT CCAGGAGACA AACCTCCCAG TCTCCCTCCT 1080 CAACCCGACC TCAGGATCAG GTTCTCCACT TGAGAATCCT GTCTTTACCT CCCACTCAGT 1140 ATGGATAAAT GAGATCATTC CTTTGTATTC CGAGGGTAGG GAACATTTGT CAAGTACTTA 1200 CTCTGCACTG GGCTATGTTT GCAAAATAAA ATGAGACCAA AAATAATAAA TCTTTGAAGC 1260 CATGTTTCAG TATTAGAGGT ACCTCCACAG CCACCCTGAC CCCACCTCAC CCACTGAAGC 1320 ACCCACCACC TCCCCTTCAT CTGCCTGGAG AACACTGAAG GGCAGCCGAG GGTGACCCAC 1380 CTGCCAACAG CACAACTGTA TGTTTGGGAA AAAAAGAAAG AAATTATGAA AATCTGTCCT 1440 CTTTTTTCTT TTTTTTTGTT TGAGATGGAG TCTCGCTGTG TCACCCAGGC TGGAGTGCAG 1500 TAGTGCAATC TCGGCTCACT GCAAGCTCTG 1530
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