Tag | Content |
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EnhancerAtlas ID | HS133-08919 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr13:114267760-114269110 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REST | MA0138.2 | chr13:114268927-114268948 | GCCCCTGGCCCTGGTCCTGGT | - | 6.37 | ZNF143 | MA0088.2 | chr13:114268097-114268113 | CAGTGCATTGTGCGTG | - | 6.22 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_68913 | chr13:114267638-114272122 | H9 |
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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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Enhancer Sequence | CCGGTGTTCG TTCCAGAGAA TTCTGTTTAA CAAATAGAAT GGTTTGTTGG TGTTTGCATG 60 TGTCTGTGTC AATATGTGTG CATGAGTGTG TGTGAGGAAT GTGTGTGTCA CTGAGTGTGC 120 ATACGAGTGT GTGTGTGCAT GAGTGTGTGT GTGTATGCGT GAATGCGTGG GTATGTGAGG 180 AGTGTGTGTG CATGTGTGTC TGCGTGAATG CGTGGGTATG AGTGTGTGTG TGCATGAGTG 240 TGTGTGTGTA TGCGTGAATG CGTGGGTATG TGAGGAGTGT GTGCATGAGT GTGTCTGTGT 300 GTATGCGTGA ATGCGTGGGT GTGTGAGGAG TGCTTATCAG TGCATTGTGC GTGTGGAGTG 360 TCTGTGCGTG TCTGTTCATG GGTTGCATAT GTGTTGAGTG TGCATGTGTG TTGAGTGTGC 420 ATGAGTTGTG TGAGTGGATG TGAGTGTACC TGTGAGTTTG CGTGTGTGTG CATGCGTGTG 480 AGTTGTGTGC GTGTGTGTGC ATGTGAATTG TGAGGAGTGC ATATGGAGTG CATGTGTTGT 540 GAGTGTGCAT GAGTTCACGT GAGTTGTGTC AGTTGTGTGC GTGCGTTTGT GAGTTGTGTG 600 TGAGATGTGT GTTGTGTGCA TGAGTTGTGT GCATGAGATG TATGTGAGTT GTGTGCATAT 660 GCACGTGTGA GTTGAGTTGT GTGCATGGAG TGTTATGTGC GTGTGCATGT GTGTGTGTTG 720 TGTGCATGAG TTGAATGAGT TGTATGTGTG TGTTGTGTGC GAGTTGAGTA TGATGTGTGT 780 GCGTGTGTGA GTTGAGTGTG AGTTCTGATT GTGCGTGTGT GTGAGTTGTG TGTGTGTAAG 840 CGTGCAGTCC TCGCCTCCCC AACAGACACC TGTCTTCACT AGTGGGCCCC CCTTGCCTCT 900 AGTTGGGAGT GGGGTGGTCC AGGCAGGGTC CTCGGCGCCC TTAGATGGAG CCGTTGCAGC 960 TGCTTTTTGA GTTGCCCTCG GCGGTGCCAG TGAGCAAGGC TCTGCCTTCC TCCGTTTGTG 1020 CCCTGGGAGC CCAGGGCATG GTCGGTAGCA CTTTGAGGGC TGTAGAGGCC TCCCTTGAGT 1080 CAGACCTTGA GGAAGGACAG GAGCTGTCCA GGTGAGAGTG GATCAGGGGA AGGTAGAGGG 1140 GACCAGCCCA GCCGAGGCTC CTCATGGGCC CCTGGCCCTG GTCCTGGTCC TCCCAGCTCC 1200 ACTCCACGTC ACAGCCTCCC GGGGCCACTG TGTCTCTTCC TGCTGCTGCT GTGGGGGGCC 1260 TGTGTCCAGT TCCCCACTGT GTCAGCGTTC TCTAAAGTAG CAGCCAGTGA GCGACGGGAA 1320 CCTGGGTGGG GACTCACTAC AGGACCCACC 1350
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