Tag | Content |
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EnhancerAtlas ID | HS187-07789 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr14:91668330-91669220 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LHX6 | MA0658.1 | chr14:91668560-91668570 | GCTAATTAGT | - | 6.02 | STAT3 | MA0144.2 | chr14:91668851-91668862 | TTTCCCAGAAG | - | 6.62 |
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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 |
GH14I091201 | chr14 | 91668021 | 91669313 |
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Enhancer Sequence | GGAAGTTACA GTGAGCCAAG ATCGCGCCAC TGCACTCCAG CCTGGGCGAC AAGAGCAAGA 60 CTCTGTCTCA AAAATAATAA TAATAATAAT AATAATAATG TGATAATTTG TGTTTGCACA 120 AAACTTTGTA CTTTTCCAAG AGGCTTCACA TTCATTGTAG TGTTTAAGCT TCTGTGAAAA 180 CCCTGTGAGG CAGGTAAGGT GAGTCCCAGG AGGTTTTCCC AGATGGCGCA GCTAATTAGT 240 GTTGCTGGTA GCATTAGGAG TAGACTGCAG ACTCCTGGGG CCCCAGCCCT TTATCAGGGA 300 ATCATGCCTT TATGAATTGC GGAAAGGCTT AGTGTAAGCC CCAAGGAGAA CCTTTCTTCC 360 CTCTGGGTGG GTCTCAGGCC CTGGGGTAAT GAAGACTTGT TTGTCATTGC ATGTTTCCAA 420 GTGTTTCCCA GACTCATTAG TCTCCTTTGG CTTTTGAGGT TTTGATGAGA CAGTGAGAGC 480 CTTCTGCGCT GATTAGAACG TTTCTGCAAA TCGCCCTGGC TTTTCCCAGA AGAGGCTGTG 540 GGTGTGGTGC ACACAGTGCG GTTGGCTTCC AGCTTCCTGT TGGCTTCCAG CTTCCTGTTG 600 GCTTCCAGCT TCCTGTCCCT CCGGCTGGGC AGGCAGAGGA CCTCAGCCTG TGGGGGAGGG 660 GTTCTCAGAG TGGAGAAAAA AGAGATCTCT GTGGCTACAG GGGCAAACAG GGTCTGAGGG 720 AGCTGCTAGA GCAATCCCGT CCTCCCACAC CCGCAATGGG ACCCCCATCT GTGCTGTGAC 780 GACCCTGAGA TCCCAGAGGA GGCAGGTGGA GCTGGCCGTT CATGGCTTCG AACCGCCCCC 840 TTTGTAGACC CTTGGGCCCT TCTCACGGCC TCAGGAGCCC AGTCTCCTCC 890
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