Tag | Content |
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EnhancerAtlas ID | HS133-20993 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr22:20927950-20929390 |
Target genes | Number: 28 | Name | Ensembl ID |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_43192 | chr22:20927443-20928956 | Lung | SE_44919 | chr22:20928051-20928961 | NHLF |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr22 | 20929017 | 20929098 | chr22 | 20928644 | 20928976 |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I020574 | chr22 | 20928336 | 20929100 |
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Enhancer Sequence | TTATAAGAAC ATCAGTCAGC AGTACATTAG ACTTAAGCTT TGCATTCCTT GCGTTTTTTT 60 GTTTGTTTTT CTCTTCCTGG AAAAAAGTTT GCTTCTCTCA TACCATCTGA CTTACTTCCA 120 GGCTTTTCTC CCTTGTGGAA CGAGTGCCGT TGAGCCCTGC TGCACTCTCA GACGGGCTCC 180 TCCGAAGTGC CGCAGGTGGT GGTAAATCGA CTCTCACCCA CTGGGGTCGC TCCTTCGTGT 240 CTCCCCCCGG TCGGTTCATC TGTTGCTCTG GCTGCAGGAG GAACGAGTGA GCTTCTGGTC 300 GGCGTCTGCC ATGCCGTGTC ACCCCGGCTT CTGGCACCTC CTGTGCGTGC CCAGGATTGT 360 GAATGTGGGC CGTGTGTGTG AGGCCACGGG TCTCCCTGCA GCCACTCTCC TGCTGGAGCT 420 CTGTTACTGG CACCTGTCGC TGCCTGCACC GAAGGCTGGC AGCACCTCCT GGAGCTTGGG 480 ACCCAGAGCA CAGCCTCCCA CCATGAGATG TGTTGTTTTT CTGTGGATCA GTCCTCCTTT 540 CTTTCTGAGC CTGGCGTGTT TTGTTCTAGT TTGTTACCGT CCTAAGTGCC TGTAGGCCCT 600 GCTCTCCAGG GACGAGACTC GGGCTCTACC CCCAACTCAG AACCCAGAGC AAGAGTGGTC 660 GGGCCCGGGC CCACAACAGT GCTCAGCTGT CCTGCTGCCT TTGTAGTTCA AGAAGTGTCC 720 ATTGATGAGG GGAATGGTCC TGGCTCATGC TGGAGTTCCT GACTCGCATC CCTGTGGAGA 780 TGAACTTCCT CGTCAGGGCG GAGGCCTGCC AAGCAGTCCC CCCAGGCTTC TCTTGCTCAC 840 CTTTGCCCAT TTTTATTACG AAAGAAAACC AGTTCCTTGA TAGATACCAG GACCATCAGC 900 CTCAGGCCTG GAGGAGGAGA GGAGGATGAT TTGGGTTCGG GCTGTAAGAG GTGTGCCACT 960 GAGAAGGAGG GATGCTGTGA GCAGGCTTAA CTGAGCTCAT GGTTCAGTGG GAGTTGAGTG 1020 TTCTCATCAC AGGCTTTGGT GGAATGTACT CTTGACATCT GTCCCCAGGA GCCTGGTCTC 1080 CAGAAACACC AGCTCAGGCC CTCAAGGTCT GGCTCTGATG GTTCTGTGGG CTATAGGATT 1140 CTGATCTGTT AGCGAGGTGT GTTCAGAAGT GTGTTGAGGA CACCAGTGCA GGAGAGCAAC 1200 CAGTAGAACA GAAAGGTCTG GAAGCAGCAT TCTTGGCAAA TCTTCTAGAT TCCCAATGCC 1260 CAGACAGACC TGGAGGTGCT GTGGGCTTGA ACATGTGGGT GGCCTCCCCT CCCAGGCTGC 1320 CCCGAGCTGC CCAAGCTTTC CTTGCCCTGG TGCTCCTTCT TGCAGAGGCT ACACGTGCCC 1380 TCTCCACCTG CCCAGGCACT GAGTTTCTTT GTTGCGATCA CCTTGTCTGT TGTCCCTCTG 1440
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