Tag | Content |
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EnhancerAtlas ID | HS175-09294 |
Organism | Homo sapiens |
Tissue/cell | SK-N-MC |
Coordinate | chr14:91668410-91669880 |
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 | ZNF263 | MA0528.1 | chr14:91669277-91669298 | TTTTTCTCTTCTTCTTCCTCA | - | 6.12 |
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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 | TAATAATAAT AATAATAATG TGATAATTTG TGTTTGCACA AAACTTTGTA CTTTTCCAAG 60 AGGCTTCACA TTCATTGTAG TGTTTAAGCT TCTGTGAAAA CCCTGTGAGG CAGGTAAGGT 120 GAGTCCCAGG AGGTTTTCCC AGATGGCGCA GCTAATTAGT GTTGCTGGTA GCATTAGGAG 180 TAGACTGCAG ACTCCTGGGG CCCCAGCCCT TTATCAGGGA ATCATGCCTT TATGAATTGC 240 GGAAAGGCTT AGTGTAAGCC CCAAGGAGAA CCTTTCTTCC CTCTGGGTGG GTCTCAGGCC 300 CTGGGGTAAT GAAGACTTGT TTGTCATTGC ATGTTTCCAA GTGTTTCCCA GACTCATTAG 360 TCTCCTTTGG CTTTTGAGGT TTTGATGAGA CAGTGAGAGC CTTCTGCGCT GATTAGAACG 420 TTTCTGCAAA TCGCCCTGGC TTTTCCCAGA AGAGGCTGTG GGTGTGGTGC ACACAGTGCG 480 GTTGGCTTCC AGCTTCCTGT TGGCTTCCAG CTTCCTGTTG GCTTCCAGCT TCCTGTCCCT 540 CCGGCTGGGC AGGCAGAGGA CCTCAGCCTG TGGGGGAGGG GTTCTCAGAG TGGAGAAAAA 600 AGAGATCTCT GTGGCTACAG GGGCAAACAG GGTCTGAGGG AGCTGCTAGA GCAATCCCGT 660 CCTCCCACAC CCGCAATGGG ACCCCCATCT GTGCTGTGAC GACCCTGAGA TCCCAGAGGA 720 GGCAGGTGGA GCTGGCCGTT CATGGCTTCG AACCGCCCCC TTTGTAGACC CTTGGGCCCT 780 TCTCACGGCC TCAGGAGCCC AGTCTCCTCC TGTGGCCCCC GCCGCCCCAG ACCCTCCTGC 840 CCAGCAAGGC TACCTCCTGA ATTTTCCTTT TTCTCTTCTT CTTCCTCAAA ACCCCTGTTC 900 CTCAGGTTCC ATGGGCAACT GCCATGTCAT GGGCATAGTG CTCAATTGAG AATCAAGTCA 960 CCTGGGTTTA AGTCTCCACC TTCCACTGAC TGCCCAGGTA CTGCCCCCAT CAGGGACTGC 1020 CAGCTCTATA CAGTGAGGAT CATGATACCC ATGACAGGAT GGATGTGAAG CCCAAAAGAG 1080 ATGGAATTCA TAAGATGCTA AAAAGAGACA GCTATAGACC AGATACCAGT GTTACATGTT 1140 GGGTGTTATT CTCCTCATTC AGTGGGCTGT CATAGATCTA GAGAAGTGTT CTGAGAAAAA 1200 CCATCAGGAT ATAAATCTAA GGTGTTTGGT CCTTCACAAT TGTGTCATTC TTTTGGCCAA 1260 ATTCACTCCC TGATGTTTGA GATGGATCAG CTCTAGATCC CACAAAGAAC ACTAGCCTCT 1320 GACAGAATTC TTCCGCATCT TCCAAGCCTT TATAGAAGCA GACACAAAAA CAATGATGTA 1380 CCTGTTCCAT AGGCTTGGAG AGTCCAGCCC TCTGGCCTTG AGAGACTCAG ACAGGTGCAT 1440 TGCATGAAAG GTTATTGAGA CAGCTGTAAC 1470
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