Tag | Content |
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EnhancerAtlas ID | HS133-03339 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:205461870-205463180 |
Target genes | Number: 11 | Name | Ensembl ID |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_04118 | chr1:205462099-205463595 | Brain_Anterior_Caudate | SE_04919 | chr1:205461718-205465613 | Brain_Cingulate_Gyrus | SE_05883 | chr1:205461024-205465738 | Brain_Hippocampus_Middle | SE_06802 | chr1:205461993-205463608 | Brain_Hippocampus_Middle_150 | SE_08023 | chr1:205461954-205463781 | Brain_Inferior_Temporal_Lobe | SE_37621 | chr1:205461168-205463237 | HSMMtube | SE_41325 | chr1:205461801-205463545 | Left_Ventricle | SE_49110 | chr1:205461619-205463446 | Right_Atrium |
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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 |
GH01I205492 | chr1 | 205461421 | 205463130 |
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Enhancer Sequence | AGGTAAACTT GCCAGGTACC ACTGCCTGGC CACTCAGATA GTGGCACCTG GTAGTAACTG 60 ACACACTCAG GTGCATTTTG GTTGGATATA CCTGTTCATG TGGGTGTGGG CCCCTGAGTC 120 TCGCTGATCA TTCAGGGGTG TCTGAGCTGA ACAGGCCTGA TAACTGCCCT ATCACTCAGC 180 TTGCATTCCC GGGAGGCCCT GGTAACTGGA ACCATTCTGG TCCCGGGGCT CAGCCGAGAG 240 GAAAAGGAAG TGCGAGTCTA AACCCCAGGC TCTTCCTCAC TGGTCCCGAT GTGGTTCCCA 300 CCTTACGCCT GTCCAGACTG TTCCCAGGTC CTGACCCCTC CCTGTTCTGC CAGGCCCCAC 360 TCTTATCCCT GGGGCCACAC CTGGCTGCTC TGTGGGTCCC AGCCCCTCCC AGGCTTCAGG 420 GAAAGGGGAA GCTGGTCTGG GAGGAAATTA GGGAAATTAG CTGCAACTCC AGGAAACAAC 480 ATCCCCAGGA CTGGGCTAAG GACTCCGTGC TGGTCCCGCA GGCAAGGGAA CTTGGTGCCT 540 CCAGGCTGAG GTTGGGGCAT GACAGCTGTC TCTCCTCAGT CTTGGGCACA GGTCCCAAGC 600 CTGGCCAAGG GCTGCTTCTC AAACTGAGCT TCTGAGTGAG GAGTGGGAGG AACACAGCCT 660 GCCCGGGCAT TTCTCTGGGC TGTGCTAACC TCAGAGGACA ACACTCTGAG TCACCACCAC 720 AAGTCTGTCC TCACCCCTGC CCCTAGGATG GAGGGAGGCA AAGAGTGAGC GGTGGAGGCA 780 AGATCTGGGG CCAAAAAATC ACAGTGTTGG CCTGGGGCCA ATTGGAGCCA GAAGAACCAC 840 CAGGGGAGAA GGGCAGGGGC TGGGGGAATT TCTATGCACT TTTCTGATGC TGTCAGCAGA 900 GTTAGTTCCC TGGGCTCTAG CTGAATGCTG GCACCAATGC AGTGGCTCAG TTTTAACATA 960 AAATGCCATG CAAATGTCTG CCAAATAGCA TCCACATCTT CTACCCATGC CCTGGTTTCA 1020 GAGGCTCTGG CCTCTGGGTC CCCTGTCTCT GTCTCCAGTA AACTCGCCTG CTTGCACGAT 1080 TTTCTCTCAG GCTCTGTCCT TCCCTATCAA GATCCAGCGG CTGGAGCTGG AGCCTGGCGT 1140 CATCCTGGCC CAAGCTGCCC AGGCGGGACG ACCAGAGAAC TCAGAGGTGG GGATGCAGGT 1200 GGGGATGCTC CCCTCCCCAG GCGCCAGGCA GCTGCCCTCT CTCCTCTGCT TCTGCTCCCA 1260 TCCTGGCTGT CCCTGGACAG CAGCAGTTGG GTGGGATTCA GAAGCCTGGA 1310
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