Tag | Content |
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EnhancerAtlas ID | HS089-00246 |
Organism | Homo sapiens |
Tissue/cell | Hela |
Coordinate | chr1:27489880-27490870 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr1:27490589-27490604 | TGAACTTCTGACCTC | - | 6.38 | ONECUT1 | MA0679.1 | chr1:27490137-27490151 | GGAAAATCAATAAT | + | 6.42 | ONECUT2 | MA0756.1 | chr1:27490137-27490151 | GGAAAATCAATAAT | + | 6.49 | ONECUT3 | MA0757.1 | chr1:27490137-27490151 | GGAAAATCAATAAT | + | 6.84 | RARA | MA0729.1 | chr1:27490586-27490604 | TCTTGAACTTCTGACCTC | - | 6.88 |
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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 |
GH01I027163 | chr1 | 27489681 | 27489890 |
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Enhancer Sequence | CCATAGAGCT GGGAAGAAGA GGAGCCAGGT TTGGATGCAG GTCTGCCTAA CTCTGAAGTC 60 CAGGCTTTTC CCAGTTCTCC AGGCTGATAG CTACCATGAA AAAGCATGTA CATGTTGGGT 120 AACTAGAAGA GAGTTCGGAG GTTGGTAAGG AGTTGGAATT TAGGATCCAG CGAATTGCCT 180 TTAAGCTAAG TTCATAATTT TACAATAAAC ATTTAGTGAG TTCCTACTAT GTGCAACTCC 240 CTGTGCTTTC TGCTGGAGGA AAATCAATAA TGGATTTGAT AAACACCTAT CGGCAACCTT 300 GACACCCTAA TGTTCACTGA CTGGATGTCC CACAGGCACC TCCATCAACT TCACCCACCA 360 TCTTCCACTA AACTTGCCCC CATTCTACAC TGTCAGAATC CTGTGTGTGT GTGTGTGTGT 420 GTGTGTGTGT GTACTGGAAA AGTTAGGATT TAGCAGATCT GAGGGAACGG GTCCGGGATT 480 GACTTTTTTT TTTTTTTTTT TGAGACGGAG TTTTGCTCTT GTCTCCCAGC TGCAGTGGCA 540 CAATCTCGGC TCACTGCTCA CTGCAACTTC CGCCTCTTGG GTTCAAGGGC TTCTCCTGTC 600 TCAGCCTCCC GCGTAGCTGG GATTACAACA AGCACCTGCC ACCACGCTCA GCTAATTTTT 660 TTGTATTTTT AGTAGAGATG GGGTTTCACC ATGTTGATCA GGCTGGTCTT GAACTTCTGA 720 CCTCAGGTGA TCTGCCCATC TCGGCCTCCC AAAGTGCTGG GATTACAGGC GTGAGCCACC 780 ACCCTCAGCC TACACAGCTT TCAGGAAGAG CTGTCTGAGC CATGTTCATC CCCTGTTTAG 840 ACAGGCACAT ACCCCATCCC AGCATGGCAC TCAAAGTCCT GCACACGATT TGGCCCACAA 900 ACCTTTTTTT CCCCTAATTA TTTGTAAGAA AATTTAAAAG TATAAAGGTA ATATAGCAAA 960 CATCCAAATT CAGAATTATC AGCTGTAACA 990
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