Tag | Content |
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EnhancerAtlas ID | HS133-00714 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:25327160-25328260 |
Target genes | Number: 21 | Name | Ensembl ID |
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SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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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 |
GH01I025000 | chr1 | 25327370 | 25328214 |
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Enhancer Sequence | ACTTTGGCTC TCGAGGGCAG AGGGGACAGC CTGTCATTGT CCTCTACCAC TTCCTTGCTG 60 TGTAATGTTG AGCAAGTTTC TTAATTTCTC TGGGCCTCAG TTTCCATGTA AATGGCAGTA 120 TAACCATACC TCCTTCCCAG GGCTTTCGGG GAGGATCTGG TGAAAAGATG CTGCAGGGAG 180 ACTACGTGGT CAGTGGTCAG CGGGTGTCAG CCACTCCAGT CATGAACACT CCAGGAGACG 240 CTCAGTCCGC GTGAATTCCT CTCCCTTTCC TTTTTCATCC TGCCTCTTGT TCCTCCCTCC 300 AGGTCCCTCA TCCCAGGCCC TCCCCAGTGA TAGAGAGCCT CCAGAGACCC AGCTTGGAGC 360 ACTTGTGGTC CCTGGAACAG GCCAGGGCCT GTGGGCTTGT CCTTGGGCAC CTGGAAGACA 420 TCACACCATG GCCTCACTAC CATCTGCCTG GGCTCCCCCA AGCCGCCCCT CCTGTGCCCT 480 CTGCTCTGGC TACTGCCAGC CATGCCCCCA GGAGACAAGC TTGGGCTGGG CAGGGCTGGA 540 TGTATTTACT CTTTGCCGAG GCTGGTTTCT CTGTTGCTGA CGTGAAGGCC TGCTGGGTGC 600 CCATGTTTCC TGCCTGGGTT TTCCCTGGCC GGTGCTGGGT TGCCATGTCT TCCAGCCACC 660 CAACCCGGGG CCCCTCCACC TTGGCCACAA GCTCTCCCGC TACGTACCCT CCCTGGCCAC 720 CGGAAATCAG ACTCAGAAGC CTCCAGGGGC CCTCGGGTTC TCCCTCAGCA GGAAGTTGGC 780 ACCCAAGGGC AACTGGCCTG GGCCAGGTCG TTCTTTGGTC CAACTAGGAA GGCCGCAGAC 840 TACACACTGG TCAGCTGTTC CGGAACACAG GGAGCCACTG CCTTGCAGCC CCGGGTCTAC 900 AAAGAGGTGC TTTCTGCCTC AGGCGCTTCT GACCATTGTT AGAGACCAGC ATCCTGGATT 960 GGGCTGGGGA GTTGGGGCTG GGGGCGGTGA CCCATCTTAA AGACCCGTTT TAAACTCCTG 1020 CCTGTTGGCT TGATGACTCA GGAAGAAACA GCCACACCCC ACAACCTTGG GCTCTGGGGC 1080 CACTCTGTGG TGAACTGTCT 1100
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