| Tag | Content |
|---|
EnhancerAtlas ID | HS133-29609 | Organism | Homo sapiens | Tissue/cell | melanoma | Coordinate | chr7:127711720-127713560 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZEB1 | MA0103.3 | chr7:127712893-127712904 | CCCACCTGCCC | + | 6.14 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr7 | 127712094 | 127712176 | | chr7 | 127712211 | 127712266 |
| Enhancer Sequence | CCACAGCCTC GTCCAGGCTG AGGTTTGTGG AGAAGGAGAG ACACCGCATG GGGTTTGGCT 60
AGAGAGGAGC CAGCCCACCT TCCCCGAGTG CCTTTGTTTG ATTGAGAAAT TACTGTGGCT 120
GTGGCAGCTG TAATAAAAGG GAACAGAGCC CCATGGGCGA CAGCTTTATC GCCATCTACA 180
ACCCAGGATG GATTCGGTGG CAGCACTGTG CCCAAGGCCA GAGATTTCTT TCATCTGCGG 240
CTGGCTGGGC CCAGGGACTT GTCAAGCCCA AGTTAGCATA TCGATTGCAG GCGACAGGCT 300
GGTTAAGTGT GAAGCTGGTG CTCACCTGCG CAGGAGAGCC CGGCTGCACC CTGCAGTGTT 360
GGCCCCAGGT GTGGCTGCTC ATTGCTGGGT TCCTTCTCAT GTAAGCCCTG GAGAAAGGCG 420
AGCATGTGGA TTGCAGCCTC AGAGAGCGAG GTGTGAATGT GGGGTTTGCC ATGTGGGTTG 480
GGGTCTGAGC ATTGGCACCT CACAGGATAG ACAGCAACTG TGCGTGCCTG GTTGGTTGCC 540
TCTGCAGCGT ATCTCTGACA TTCTTGCACC AACCCCAGCA ACCCAGTGCT AAGAGCCACA 600
CTGGCCCACC ACAAGCTGTC TAGTGGCCTG CCAGGCCTGG AGAGAGGCCT TGTGTCCAAG 660
CAGGGCAGAC ATCCTTGGTT TTAGGGAAAG GACACTTGGC TACTAAAATT GTGGAAGACG 720
AGAGGTCAGG GAATGCGGAA ACTGATGTGG GCCTGGGCTC AGTGTTGGCT GGGAACTGTA 780
CCAGCCTCAT TTGCTTTTGC CCAGACATGT GTCCAGGAAC CCCTAAACAC AAGGCAAGCA 840
ACCTCTCTGT TCTTCCTTCA GCTTCCCCAG AATTCCTCTA GGACCTGCTG CTTCTTGAGC 900
TTAGCATGTT TGATAAAGCT TGGCAAGTTA AGATGAGCAA GAGACAGTCT TCTCATGTAT 960
CATTTTGCCC CTCACAGGTC TTGTCCACCC CTACCACACT ACCCCCGCCA CCTCCCCCAG 1020
CCCCTGCAGG CATGACAGTC TGTTCCCCAT TCCTGGCCTC CCACTGGAGG AGGCGCTCAG 1080
TCTTCCAGTG GCCAAGCTTC TCCTTTGTTC CAGCGCCCTG GGCATTTGCA AGGTGGATCC 1140
AAGGTGTTGA AACCTGAGCA ACCTCAGATT TTGCCCACCT GCCCTTCTCT CCTACAAGAG 1200
TAGGTCCTTC AGCAGGTTAG TTGCCAAAAT TAGAGATAGG AGAAACTGGT TTTAACACCC 1260
ACAGACACTG GACTCTGTCG TGAATTCAGG CACTGGGTCA GCCCAGCCCA GAATTGGGGC 1320
CAGCACTTAC GCCCAGACTC TACTAGTGAG CTGCAGGGTC CCACGGTCCT GGATGGTGGA 1380
GGGGGCAGAG GTATGGCAGT GGAAGGAAGG GCTGCTCCTG AAACAGAAGG CTGTGGAAAG 1440
GGGGTATTAG GGAGGGGCAG GGTCTTTTCT GCCAGGAGGC AGTGTAGAGA AGGCATTGGG 1500
GAAACCTGGA TTCTGCTCTC AGCTCTGTCC CTTAATAGCT ACACTTCTCC AGTGCCACCT 1560
ACAGAATCAA CATGGACTGG ACCTATATGT TCTCCATTAT CTCTTTTTCG TTAATAACTC 1620
TAATAGACTC CACATATCCC CTTCTATACC ACACTCCAAC TTCAGTTGTC ATTGAACCTG 1680
CATTTCCTCT TGAAGGATCA AATGTGGGCC TCAAGGACGC AGAGGGTATT CAAGGATGGG 1740
AGGAAGCGAG GGTCCTGCCT CTCGGGCCCT GCCTGTTTTC CTCCCCGCTA CCTTCTCTCT 1800
GCACACCCAG ACCACCTCCT TGTCCTTCTG GGGAGGCATG 1840
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