Tag | Content |
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EnhancerAtlas ID | HS133-04809 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr10:99640900-99642540 |
Target genes | Number: 13 | Name | Ensembl ID |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_65707 | chr10:99640359-99643432 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr10 | 99641370 | 99641434 | chr10 | 99641794 | 99641800 |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I097881 | chr10 | 99641556 | 99643198 |
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Enhancer Sequence | TGAATCACAT CATGTCACTC CCCAGTTTAG CTTCTAAGGC TCCTAAGAGC AAAATTCAGA 60 CTCCCTACAG GGGCCTCATG GACTCTCCAT CATCTCCAGG CCATACTGGC ATCCCTCCTG 120 CTCCTTCAAC ACACAAAGCC TTTGTCCTGT CTCCCGCTTT TCACTCCTGC CCTTCCCTCA 180 ACTCTTTCTG GGCCTAGATC CTTCTCATCC TTCAGGTCTC AGCTCAGAGT CTTCCCCCCG 240 AGGCCCTCCC TGACCACTCT CTCTGGAACA GTCTCCAGGG AGCACCTTGC TCAGAGGGTT 300 CTGAAATCAT CTTGTCCAGG TGTGTGGTCA TGCGTTCAGG GTCTGTCTCC CTCCACTAGA 360 ATGGATGCCC CTCTTGTGGA GGCGCGGGGG TGGCACTTGG CCTACATCCC CAGCTCCCAG 420 CATGACACTT GCTGTGTACG AGGCACATAA CTGCCTGTTG GGCGATGAAA AGGAAGAGGA 480 GGCTGATCTC AAAGGGTCCT TCCTGCAGGC AGAGAAGACT CTGGAATTTC TATGCACCTG 540 CACTATGTGT TTGGAGTGGG GCTGGGTGGG CATGTGGAGA GTGTAGGGGA GTCATTTCCT 600 CCTCCAGCCA CCCTTGGCAC CACTGCTCCT CCACCTCCCC ACCTGTGCTC CTTTGTTCAG 660 ACAGTGCCCC CCACCAGAAC CATGTCTCCC CTCTCTGTGA CTGCCGAACT GCTCCTCATT 720 CCTCAGGGCC CAGCTTGGAC CTCACTTTCT CTAGGGCACC TTCTAGGACC CTCCCTAGGC 780 TGGTTTAGGG CCCCTGCTTT GTCATCTCCA AGCCCCTGCC CTCCCCCATC TGGGCCCTGA 840 TCACACTGTG TGGTCGACAG CTGTTTACTT TTGTGGCTCT CCATTGGTTT TCAGCTCCTG 900 AGAGTGGTAT CTGTCTTGTT TACTCCTGTA TCTCAGTAGC AAAGGGTTAA TGAGCAGCTG 960 CAGAGTAGAC TTGGGAAGAA TGCTGGATGA GGGTTCAAGG AAGGAGGGAT CCTTGGCCTG 1020 ACCCCTCCTT GCTGGTCACT GGGATGGAAA GTGTTGGGGG TGAAGGTCTC CTGGACACTG 1080 AACTTCTAGG CTGCCCCTTC CCATTCCAGG CTCTTGGGGA CTTTCAGAAG GTTCTTGGAC 1140 CGTCAAGGAG CTGCCATCCT GGTAGTGCTG CAGCTACCTG CCTGCCCCAG TACTGCACCA 1200 GGCTGCAGTC TCCGTTCCAC ACTGTGACCA CACTCCATAC ACTATTTTGC CCCAATGCCC 1260 TTGGCAATGC ACACCCTTGC CTGCCAGCCC CCTTGCTTGC TGCTCCACAT GGACTTGCTG 1320 GCCATGGCAT GTGGCTATTC CCCCTGTGCC AGGTTGGTGG TGTGTCTCCT TCCCATCTGC 1380 AGTTTCTCGG TACTCATGGC AGGAAAACAC TGCCAGTTTC CAGAACCGCA GTGATTCAGC 1440 CTGTGGGTCA CTAATATCAC TCCCACCCTG GTGAGTCATG TGGTGGTTGT CTTGGCATCT 1500 GGAGTCCCAG GACAAACAAC ACCCTCCCCT GTCCTCCTTT CTGCCCCTTG CTTGCACCCT 1560 GGACCTTGGC ATGAGTCAGG CGGGCATTCC CCAGGGAGAT TCCGGCCTCT ACCCCATGCC 1620 CTGGTGACTG AAGGCAACTC 1640
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