Tag | Content |
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EnhancerAtlas ID | HS095-05689 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr11:71050250-71051620 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gfi1b | MA0483.1 | chr11:71050908-71050919 | AGCTGTGATTT | - | 6.14 | ZNF263 | MA0528.1 | chr11:71051334-71051355 | GAAGGAGGATGAGATAGGGAG | + | 6.43 |
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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 |
GH11I071338 | chr11 | 71049248 | 71051377 |
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Enhancer Sequence | CTGTTTTTGC AGCGTGACTC TGAAAGCCTG CATTTGCTCC AGAGCTTATT AAGACAAGCC 60 ATTTCCACCA CGATGAAGAG CACGCACGCA CAGCCGTATC CCAGAATCAA CGGTGTCTCA 120 ACGACAAAAT TGAAAGCATT CTCACGTATT CCACCACTGG GAGTCCAATA TGAAGCAGCA 180 ACACCCTTCT GGGTCATTAT GGCTCATTTT CACTTTCAAA AGCACATGCT TCTGGGTGGT 240 CTGGCCCCCG CGCCTGCCTC CGGCCCTCCT GTTCCTCACA CCCACGCATA GTTAAGGTCC 300 ATTATGCACC CGACTCTGTC CAGGCAGGGA GCTGCCAGGG ACAGTCATTT TCCAAAGAGG 360 AAACACATTT GCTTAGCAAG TCTAGGCCTG CTGGTCTCCC CATCCAGACA GACAGGGAAG 420 CTTCTCGTTA CTTCTAATGC ATCGCCCTGG GAGGCCGAAG GAGACCATTT CGGGAACTGT 480 GCTTCCCAGC ACAGGCTCTA CCTCCAAAAC ACAGCAGGCA GGGGACAGAG CCTGGTGGCT 540 GCCGCATGGT TACCTGTAAC CAAGAGGTCA CCCAGGGCTG AGGTGTAGGT GAGTCAGCGG 600 CTACCCGTGT GTGGTCTCTC TGGAGCCCGC AGAGCTGGCA ACTCAACTAG GAGTTCAAAG 660 CTGTGATTTT ACACGTCCGT GGAGCAGATA TCAGGAGCTT AAAGAAATCA TCTTCATCCC 720 TTACAGTCCC TGGGGATGCA TCTCCTGTGC TTCTCTGGTC TTTAAAGAGA AGGGCGATTT 780 GGGTTAATTA CCATAGTTAC TGTCATTGCC TATTGGGCTC TGTGATGCTG GTTTCTCAGG 840 ATTAGTCATA AAATACGTGG ATGGCCATTC CAAAGATGAG TTCTTACTGT AGTTGATTTT 900 AAAGGCACTT CAGGGGAAGC CAAGGAACCA AGCTGCCAAA GGGCTACTGA TGTTCTTTTT 960 GGACCGAGCG CAACGGTCCT TTCATGTCTG CGTTCCTCCA TCCGTCACTG ATTCGCTCCA 1020 ACGACACTGG CGGCACATTC ACTGTGCGCT GAGGCTTCTG GGTGGGGTGT GGGGCCTCTG 1080 TGGTGAAGGA GGATGAGATA GGGAGGCCCA TGTCCTGCAG GTCACAGTCC AGTGAGGAGT 1140 GCTCCTGAGA CAGAGTTCAG CCTACATGCC GTGGAAATGG GCAGCTCCAC GGTGAGCAAG 1200 CCTCAGGGGG CTGCACAGCA GGCAGTGGGT GTCAGGGGTG CAGTGGGGGC AGCTCCAACT 1260 CCACCTGGCC ACAGACTCAT ACTCCGTCTT TCTCAGCTTC TGCCCTAATC CTGGTCCTCC 1320 TCCCTGTGCC CCCCACCCCT GCATGATGAC ACCTAGCATT GGTGCAGGCT 1370
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