| Tag | Content |
|---|
EnhancerAtlas ID | HS133-00636 | Organism | Homo sapiens | Tissue/cell | melanoma | Coordinate | chr1:23780930-23782370 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXH1 | MA0479.1 | chr1:23781947-23781958 | TGTGGATTGGG | - | 6.14 | | ZNF263 | MA0528.1 | chr1:23782151-23782172 | GAAGGAGGAGAACAGAGAGAA | + | 6.13 | | ZNF263 | MA0528.1 | chr1:23782154-23782175 | GGAGGAGAACAGAGAGAAGAG | + | 6.14 | | ZNF263 | MA0528.1 | chr1:23781973-23781994 | GAGGGAGTGAGGAGAGGAGGA | + | 6.84 | | ZNF263 | MA0528.1 | chr1:23782142-23782163 | GGGTGAAGAGAAGGAGGAGAA | + | 6 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGCCTCCCAA AGTGCTGGGA TTACAGGCGT GAGCCACCGC ACCCGGCAAT TTTCATACTT 60
TTGTAGAGTC AGGGTCTCAC TACATTGCCC AGGCTGGTCT AGAGCTTCTG GGCTCAAGCG 120
ATCCACACAC CTCAGGCTCC TAAACCACTG GGATTAAGGT TTGAAATGTT GCACCCAGCC 180
TCAAACACTG TTAAAGGCTT TTTACATGCA GGACAGTGTA CGAGGCACAG CTATGCCAAG 240
AGCTATAACA ATGATAGATT TTATTAGGTT GGTGCAAAAG TAATTGCTGT TTTGCCATTA 300
ATATAATATT AGCCAACATT TACTGAGCGC TTACCATAAA GTAGGCACTA ACTTGCTTAA 360
TCCTCATTAC CGCTCTGTGA GGTAGGCAGC ATTATTATCC CAGTTTCACA GATGAGAGAC 420
CTGGGGCTTG GGCAGACTGA GTGACTTGAC CTAGTAAGCA GCAGAGTGAA GATTCCAAGC 480
TGGAGTCTAG GTCCAAGGTT GGGTGCTTAA CCACTGAGCA CACTGCCTCT CAAGGATGAT 540
GTGGCCCCTG CCAACCAGGG AGGATGCTGG GTAGGACTGG AGCCACAAGA GCTGGTCCAG 600
TGCCATGGAG CCTGGAGGGA GATGAGAGGC TTTCCTGGGA GGCAGTGTAG CCAGGCTTAT 660
GCTTGGACTC TGGAGCCAGA CAACCTGGGT TCAAACCGAA CCGTGTGACC TCGGGCAAGC 720
TGCTTAACCT TGAGGTCCTA GTTTCCTAGC CTGTAAGGTG GAGACAACAG TCACACCAGC 780
CCCACAGAGC TGTGCATCCG GATCGAATGA GTGAACACAT GAACTAGTGA GAACTGTGCC 840
TGCACATGGG AAGAGCTGCT GTCACAGGGT GGCCTTGAGG AAAGGACTTG AAGGACCAGA 900
GAGGAGGCAG TCACCAAGGA GGCCATCGGG AAGCAACCCG AGGCCACTGG GCCATGTACA 960
GGGGCTGAGA CGCTTGTGGA GGCAGGGACA GGTCCTGGGA TTTAAGTACG AAGCAGATGT 1020
GGATTGGGAA AGCAGAGGAC AAAGAGGGAG TGAGGAGAGG AGGAGGCGGT GGCAGCGGTG 1080
GTGGTGGCAG TGGCAGCAGT AGTGGTATAA AGGTAGGAAC CCCCGAGCCT GTCTCTCCTT 1140
TATCCCAAAG CTCCTCCAGG GAACCCTCCC TTGCACGGGG CTCTTCCCTG CTGTGAGACC 1200
CCCTCTGCTC CTGGGTGAAG AGAAGGAGGA GAACAGAGAG AAGAGTTAGT TGGGTAAGAA 1260
GCCAGAGAGA AAGGAGGATT ATCCAAAAGA AGGGTCAGGG CTGGAAAGGG ACCTCAGGTC 1320
TGAACTCAGG TCAGAGATCA AGGGCAAATT GGGAGAAGGA AGGAAACGGA CCCTTTCCCA 1380
GTCAGGTTCT TAAGACCACT AGATTTACCC TGAGTCTGGG CAAGGAAGAG ACAGGGGCCT 1440
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