Tag | Content |
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EnhancerAtlas ID | HS133-22231 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr3:46130400-46131780 |
| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_09171 | chr3:46128819-46144854 | CD14 | SE_26406 | chr3:46130079-46133313 | Duodenum_Smooth_Muscle | SE_43735 | chr3:46130136-46137236 | MM1S | SE_53728 | chr3:46130174-46133265 | Spleen | SE_55804 | chr3:46130199-46133588 | u87 | SE_59476 | chr3:46098871-46141336 | Ly3 | SE_67332 | chr3:46130136-46137236 | MM1S | SE_67604 | chr3:46130199-46133588 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr3 | 46130545 | 46131548 | chr3 | 46130670 | 46131183 | chr3 | 46131249 | 46131612 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I046088 | chr3 | 46130094 | 46143491 |
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Enhancer Sequence | TCTGAAGAAC CCTAAGGCTC CAAGGAACCC AGGCTGAAAA CCATTAGGTT GATTTGACTC 60 ATGAGGAAAC TGAGGCTGGA ATTGGCCAAC AACTTGTTCA TGGCTATCGA AGTGGTAGAA 120 TGTTGAATTT ACATGAAAAC CCAGATGTTC TATGCCCTGT TTGTTTTTTT CTCTCCTATC 180 CTGGAGGTGC TTGGATACCA TGTGAGGATG TAGGCACAAG CCACTCTGCT GGGCCTTTGA 240 GGTCCTTCAT CAGAAAGCTT CACCATCTCA AGTCTGTCTT GGCTGGAGAC CCTGGAGACA 300 AGCAGTGACT GCTCCGCCCT TCTTGCCCTC TTGTCTTAAA CTACCCTTTT GACTTGCCCA 360 ATCCCAGTCC TGCTCCCAGG ACCATAGTAA CTCTTGCTGG AATAAGTCCA ATCTAGTTGG 420 AAGGATGAGA AAACAGAGAC AGCTTGGCTT TGTCACTCGC TGACCCCATG ACCACAACAC 480 TCAGCTCACT GCTGAGCACT CACATAGCCC AGGCCTCTCT TGTGCATGGG TGACTGGTAT 540 CCACATGGCC AGTGACTCAC ATGGGAACTG AAAGCTCCCT TTGGTGGGGC AACTTCTCTA 600 AAGTAGCCCC ATGAATCAGC AGTGTGGGGT GCTGGAAAGC AAGGGCTGAC CCTGACTTGC 660 AGTCAGTCAG GGACCCTGAG CAGAAGCCCC TGCATCACAG GCTTCCACCA CAGCCCGGAA 720 GAGTTGCAGC ACTGTGGGCC AGTGGTAGTT CCATGTATAG CACGAGTGGA GGCCCAAGAT 780 GCATGTGCAT GTATGGGCCT AAGAGGTCTC CATGAATTGT TTCTCTGGGT GGTAGAGAAC 840 CCAAGCAAGT GGGAGCCAAG AGTATCTACC CCCGTCCCTG ACTCTGTTTC CTGTGAGAGG 900 GGCTGTGTTG GCCCAGGCCT GAGTGTGCCA GGGTTGCTTG GGCAACCACT GCCCCATGCC 960 TGCAGTCTCA TCTCTCCTTC TGAAGCCAAA TCAGAGAAGT GCAGACTCAT GGGGCTATGA 1020 GGAAACCCAT GTTGTGTGGA TCAGCAGTCA CAAGGTGAAG GCTCTCTTCC CACTTCTTCC 1080 GCAGCTCTAG CTGTGTGGCT TTGAGCTAGT TGCTATATGT CTCTGAGACT TCATTTCTAA 1140 TTTATGTAAT AGGTATATTA ATGTTAGTTA TACTTTGCTA TATAAACAAA TCAAGACTTC 1200 GTGGCTTAAA CAATAAACAT TTCTTATACA GTTTCTGTGG GTCAGGAATT TGGGAGTGAC 1260 TACACAGGGT GGTTTCAGCT TAGGGTCTTT CAGGTATGGA GTTCCTTTGA CAAGGTACCT 1320 GGCTTCCTCC AGAGTGAGCG ATCTAAGACA GCAAGACAGA ATTCACACTG TCTTTTATGA 1380
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