Tag | Content |
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EnhancerAtlas ID | HS101-06159 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr10:114278470-114279760 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr10:114279252-114279264 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr10:114279256-114279268 | GTTTGTTTGTTT | + | 6.32 | HOXA13 | MA0650.2 | chr10:114278769-114278780 | GTTTTATTGGC | - | 6.14 | JUN(var.2) | MA0489.1 | chr10:114279130-114279144 | ATGACTCACCCTCT | - | 6.23 | LHX6 | MA0658.1 | chr10:114279301-114279311 | ACTAATTAGC | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_34260 | chr10:114273642-114301126 | HCT-116 |
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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 |
GH10I112519 | chr10 | 114278921 | 114279150 |
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Enhancer Sequence | TACACTTAAA AGTGTTGATA TACCTACCAT AAAGGAAAGA ACCAGTAGAG GGTGAAACAT 60 TGAAGATACT CAAGAAAACA TTTAATTGAT GAAGCGAAAC ATCTGAGTAG GCAAGATTTT 120 ATTTTATTCA ACTGAAAATG GAGAATCTTT CAGGAAGAAT ATGTTATTTA TGAATGAGGT 180 ATGAAGTTTC ATATTCATTA TATTTTGTTT TGGGTCACCC TAGTATAGAA GTAACCGTCA 240 AAATGTTTTC ATAGAAAATT TGGACTAAAT TAATTTTCTT ATATTGCCTA AACATCATAG 300 TTTTATTGGC TATATCCATA AAACATTAAA AGACATTGTA TATCTCTGAA TTATGAACCC 360 TATAACCTCA CTATAACACA GCATAGTCTA TAATAAAGAA ACTGTCGCAA CATGGGTCCA 420 AAAGTAAGTA CCAGGAAAAT AGGTTATAAA AATTGTTTGC CTATGAGATG GCTGATTCCA 480 ATCTAGAATT TTGAAGTAAC CAGGAGTTAC CAGATTTTCT GAGTAAGCAA GCAGTTCTGA 540 ACACATCTTA ATAGCTGGTG CGGCTCCTCT CTGAGCCATA GGTAGGCTAT TGTTGCTTTA 600 TGGTACAGCC TTTGAAGATT AATCTTGAAA CTTGTCTAAA TAACACCCAT AGGTGTGGTT 660 ATGACTCACC CTCTGAGATC AGATGCTTTA TTCTATCAAA TAAAACAGTT TACCTTAAGC 720 ATTTATCACC CTCGATCTTG ATTGGTGTCC AATATTCTAG CTATTGATAG CAAAGAATAA 780 AGGTTTGTTT GTTTGTTTTT AGAGAAGGGT GACCAGAAAC AAAACCTTTA GACTAATTAG 840 CTGATGATAA GTTGATAGAA CTAGGTGAAT CGTTCATCCA ACCATGGCTT TGGAGAATGA 900 AGGTAGGGGG ACTCCAGCCT GTTGTGGCGG TGTAATAAAG TGAAAAGAAC ACTGGCATTG 960 AGGAATGGGG TTCTGTCCTT GTTCTGCCTC ATCTTTCCTA GCTCCGTGGC CTTGGATAGA 1020 TCATTCATCT GGCTTAGAAC CCCTTGTTTT TAAATTTGCA GCCTGATCTA GATGAAACCT 1080 CATGCGATAA CTTAGGGTCA GTTACGGAGA ATCCTCAGGA TAACTTGTTC TTGGATGTTT 1140 AGATCACTTG AAACTGTGAC TATGGACAGA TTTTCAATGA ATGACCCCTT TTCCTTCCCA 1200 ATGCTAGGCA GATGATATAG AGAAACTAGC ATTATAGGAA TTAATTGTAT ACACTTATAT 1260 ACTTTGTTGC AGTAGTTTAT TTTAAAATAC 1290
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