Tag | Content |
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EnhancerAtlas ID | HS133-32260 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr9:127620350-127621710 |
Target genes | Number: 10 | Name | Ensembl ID |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_13820 | chr9:127620826-127625336 | CD34_Primary_RO01536 | SE_19001 | chr9:127621181-127625185 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19375 | chr9:127620922-127625243 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_21355 | chr9:127621486-127625305 | CD8_Memory_7pool | SE_22873 | chr9:127621312-127625207 | CD8_primiary | SE_34989 | chr9:127621203-127626991 | HeLa |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 127621610 | 127621665 | chr9 | 127620391 | 127621152 |
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Enhancer Sequence | GAGACAGACG GCAGGGTGAA TCCAAGGACC CAGGGCTGAG GAGCTACTGC AGCAGCTAAG 60 GGGGCTGGGG AGGGCCATCC AGAGCCACTC AGGAGGAGGC TGCCACCATG GGACTGCCAG 120 CAGGCCACAC ATGTCACTAA CTCAATTAAT CCCCCCAAAT CTAAGGCTGG TGGGACCATC 180 CTCATTTCAT GTAAGTCTGC TGACCTACTG GGCTGAGTGT CCAAGTCTTG GCAAAGCTGT 240 GGAAGAGCCG GGGCTTGCAT CTCAGTCAAG TGACTCCCAA CTCAGTGCTC CTTCCACTGC 300 CCGATTCCCA GTCACGAGGA CAGTCACATG ACAACCTAGT ACAGGGCACG CAGCACCCAC 360 CAAGCCCCGG GGGTAGTTAC CATTACCTCG GCTCTGGTTA GCAAGAGCAT GCTGGGGGCT 420 GAGGCAGTAC TCTGTCCATC TGTATGCAGG GCCCACCAGC TGCTGCCTGT ATGAACGTCC 480 AGCCTCAGAG GCCTGGCTGG CCAAGGCCAC TTGCCCCACC TGCTTCCGGC TTTGGGGCCC 540 CTGCCCACAG CTGTCACAGA GCCATCATCT GTCTTTCCAT CCTTGGCTCC CACTCCTGCC 600 CCACTTGTTC TCCAGCAGGG GGTTCTAGAC CATGGCAGCT CTCACTGGTC TCTCCTGTGT 660 TCTGCAAAGG TCCCCTGGGC CCCCTTCAGG ACTGGGCCCT GTGCTGGGAG CTGGCTTGGC 720 AAAGGATCTG ACCCAGTCCC TGCTCAGGGG TCCCAGCCTA GTGGGGGAAG ACTGAACAGG 780 TAACAAGTGG CCCATGGTAT GGGGGATTCT GAGGTCACAG GGCCCCAGGC CCCTGCAGGT 840 GGGCAGAGGA CTGCAGAAAG ATCCTGGACA ATGAGGGCCA GCCCTGGAGG GTACTTGGAA 900 GCAGGAAAGT CTTTGTCCTC CCACATCCCT CACTCCTGCT GGCATCGGCT GGGCATTCGT 960 CCTTTTCACA TTGGCTAACC CCCTAGAGTT CTGCTGTCCA ACAGAGCAGC CACTAGCCAC 1020 ACACGTAGCT GCTGACATTA AAGGTTTACT TTTGCCACAC ACGTGCTAGT GTCCCCTGAA 1080 CAGCTAACAT AGCCACACTA TGGCCCTTCT CATTTTTTTG AGATGAGGCC TCACTATGTT 1140 GCCCAGGCTA CACTTTAACT CCTGGGCTCA AGCCATCCTC CTGCCTCGGC CTCCCAGTAG 1200 CTGGGGTTAT AGGCCTGTGG CACTTCATCA GCCATGGCTG CTTTTCCCTT GTGTCAAATC 1260 TTCAAGTTAT TCAAACACAA TTTGGGTAGT GATGTGGAAC CATTTTGCAG ATGAAATTAA 1320 AGACCCTCAT CAGGTAACTT TAGGGGAGAT TATCCTGGGT 1360
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