Tag | Content |
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EnhancerAtlas ID | HS133-17233 | Organism | Homo sapiens | Tissue/cell | melanoma | Coordinate | chr2:88539110-88540030 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESRRB | MA0141.3 | chr2:88539348-88539359 | TCAAGGTCAAA | + | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 88539332 | 88539520 | chr2 | 88539305 | 88539552 |
| | Number: 1 | ID | Chromosome | Start | End |
GH02I088239 | chr2 | 88539332 | 88539550 |
| Enhancer Sequence | CCCTACTTCC AAGTAAAATG ACAGTCACAG GTCCTGGGGG TTAGGGCTTC AATGTATCAT 60 TTTTGGGGAT GCAATTCAAC CTATAACCTT AATCATACTT AACCTTTAAA CAAAAGATTT 120 TCCTGGATGC CAGGCTCTTT TGCATGGGTA ATCTCATTTA ACAGGTACGT GAAGTGAGCT 180 CTATTATTAT CTTCCTTTTA TATGGGAAGA GGCTGAAGAG AGCAGCTGGG TAACTTGCTC 240 AAGGTCAAAC AGACGCTAAC ACCACCTCAG CTGACTGCTG AGGCTGCACC CTTAGCCAAC 300 CGGCAGCGCT GCCTCTGCTG TGGCCCCTGA GCCTGCGGTT TCACGTGGGG GTGGCTGTGA 360 AGAAGGCTGT GTCTGTGTGG TGAGGAGGAC CAAGCACGGC TGGTCTGGTA GTGTTGTTTT 420 GTCAGCTGAA ACGCCAACAC ACAGTGAGTA GATATTGAGT CTGGCGTCCT CCCTGCAACT 480 CTCCAAGTGG CTGTGGTTTC CCACAGCAGC CCGCGGCCCA GGGTGAAGTC ATGGGGAGAA 540 AGTGGGCACG ATGAGAGTCC CAGGGAGACA GGAACACTGG GAATTTCACC TCGACATTGA 600 GCTTGGGTGG AGAAGGAGTG CAAAAGGCAG GGACCAGCTC ACAAGAAGGG CCCAGTGTGG 660 GTGGTTAGAG GCAATGTGGG TATAAGCAGG GCCTGTGGAT TCAGGCAGCC CTAGGATGGG 720 GTCCCTGATC CATTGTCTAT TATCTGTGTG ACCTCAGAGA AGTTGCCTAA ATTCTCTGAG 780 CCTCAGTTTC CCTCAGCTAT CCTCACTTCA CGGTGCTGTT GTGAAGACTC AGAAAAAACC 840 TAAGGCCAGT GTTTCACCCA GAGGAAGGGC AGCCAACACC CACAAATGGC TGGTGTGGCT 900 GACTTGAGGA GGGCCAAGGA 920
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