Tag | Content |
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EnhancerAtlas ID | HS133-27953 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr7:6357230-6358450 |
Target genes | Number: 23 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Ar | MA0007.3 | chr7:6357745-6357762 | CGGTACAGGATGTTCTC | - | 6.01 | GATA2 | MA0036.3 | chr7:6358095-6358106 | TTCTTATCTTT | + | 6.62 | NR3C1 | MA0113.3 | chr7:6357745-6357762 | CGGTACAGGATGTTCTC | + | 6.11 | NR3C2 | MA0727.1 | chr7:6357745-6357762 | CGGTACAGGATGTTCTC | + | 6.1 |
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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 |
GH07I006317 | chr7 | 6356929 | 6358400 |
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Enhancer Sequence | GGAGACGGGA TCTCGCCATG TTGGAGGGCA TCATTATTAA TATTCAAGCA TGCTTTGTTT 60 ATGAAGCAGA AACACCCAAG AGCGTCCAAA TCCAGCCAAT CTAACCTCTT TCGCTGCATA 120 GTGTGGAAAA GCACGCTGCG CTTCCAAATG GAAGAAAATC GCCTTAAAAT GAAGGCGTTG 180 AAGTTCTATT GTGAAGCAGG ACGAGGAGTA CCCTTCCCAG CTCATCTCCA GGGGACCTCA 240 CAGGCCTGGC AGGAAAACAG CCACTTCCTG CCCATGACTG TAAGATGTAT TATGTCACTT 300 GGGGAATAAG TTCCAAATCC TATTTTTGGG AAAAGAGGTA ACGTTGGAGG CAGTAAGGGG 360 GAGGCCAAGT CCAGCCTGGA GCTGGAAGGA GCCCAGAGAC TCCTCAGTAA GCCTGCCGTT 420 CCAGGGAGAC AGACGCTTGC AAAACCTGCC TCCATTCCTC GAGCGGTTCC GCTCTCACGT 480 TTTGAGGCCC CCAGTGGCTC TAGAGGGAGA GGGGGCGGTA CAGGATGTTC TCATGAATCA 540 CCCCTTGTTC GATGAACTGT CCCGTTACCA GAGCCAAGGT CAAGCTTTAA ACCTGAGTAT 600 GTATTTCCTC TGGAGTGTGC TAAAGGGTAA GTGCACTCTT CTACAAGTCA CACGCTCAGG 660 CTGCAGTGTA AGAGAAATTG AAGTTTTTCT TTGTTCTGTT TTTTTGAGAC AGGGACTTAC 720 TCTGTCACCC AAGCTGGAGT GTAGTGACAC GAACGCGGCT CACTACAGCA TCAGCTTCGC 780 TGGTTCATGC AGTCCTCCCA CCTCAGCTTC CCAAAGTGCT GGGATTACAG GCATGAGCCA 840 CCGCGCCCAG CCAAAAGTGA AGTTTTTCTT ATCTTTCCTT TTTCTCTTTT TTTGAAACAG 900 TTTCCCTCTT GTTGCCCAGG CTGGAGTGCA ATGGAGCGAT CTCGGCTCAT TGCAACCTCC 960 GCCTCCCGGG TTCAAGCGAT TCTCCTGCCT CAGCCTCCCA AGCAGCTGGG ATTACAGGCG 1020 CCTGCCACCA CGCCAGGCTA ATTTTTGTAT TTTTAGTAGA AAGAGAGTTT CACCATGTTG 1080 GCAAGGTTGG TTTCGAACTC CTGACCTCAG GTGATCCACC TGCCTCGGCC TCCCAAAGTG 1140 TTGGGACTAC AGGCGTGAAC CACTGGGCCC AGCCGAAAAA GAAGTTTTTC AAAAGGTTCG 1200 AGACAATGAG ACATTGAAAT 1220
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