| Tag | Content |
|---|
EnhancerAtlas ID | HS132-00833 | Organism | Homo sapiens | Tissue/cell | Melanocyte | Coordinate | chr2:102843960-102845050 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH02I102226 | chr2 | 102842670 | 102846324 |
| Enhancer Sequence | TCTGAACCTT AAGTGTCCAG TGCAACCTGA AGTGCTGCTA GTACTGTGGA TAGTCCGACT 60
GGGCATGGGG AGGGGGTCTC TGGTTTTGGC TCTGGCATCT GCAGAGGCCG CCCCGTCTAA 120
GCACACCCAT GACTGCTCTC TCCTGCTTGC GTCTTTGAGA AGAAGACAGT TCAGTCCCCC 180
ACCACTGATT GTTTTCTGAC ACAGAGTTGA GTGGTTCAGT TGCTTTCTAC TTTTTGACTA 240
ACAGAAGCCT GCGTCACTTT ACGTATTCTT CCTGGAAGCT CAGGCCCCAT GGTGTGTCTC 300
TCTCACTGTC TCTCTCTCTC ACTGACTCTG TCAGTGACTC TCTCACTGAG TCATTGCGAC 360
TCCCAGGAGC GTGACTATAG CTGTGACTTA TGGGTGTTGT GCAGTGTGTG GGGAAGCTGC 420
TAGTGAGGTC GAGTTTAGCA GGAAGAGAAA ACAGGAATAG TGACTCACAC GGAGTAGTGG 480
GGGCTGGGCA GATGAGAGAG TTAGGCAGCC CCGCCCTCTG CTGAGACTGG GACGCAGCCC 540
AGATTCTGCA ACAGTGGGCA GAGGATTTGG CGATGGAGGC TAACAGGCAG CCAGGGGTCC 600
TTTTTTTCTT TATTTTTATT TTGCTTAATT CAGAAAAGTA TGTGTGCATT TTGTGATGAA 660
ATTCTCTACA GCTCTGTCTA CGAGAACTGC CCTGTAATAT CTCTGTGTGT TGGCTTTAAC 720
AGTGAGCTAC TGATGAGATT CTGAGATTAG TCCCAGATCT TGTTTATGTC CTTGTTCCCC 780
TTGAGGATAT TTTCTGAGTT AAATCAGGAA ATACCGATTA ATGGATGAAA ATGAGAAAGA 840
GAGAAATAAT GTCCTTCGTA GGATAAGTCA TTTACCCTGA CTAGGTTAGC TAAGCTGTAT 900
CACTCAATTA ATAATTAGGT GTGCATGACT CACCATTTTA GAAGGAGCCA TTGACAGCCC 960
TAGCTGAAGT CAGCAAGTTC TGTATCTTCT CTAGCAAGCC ACTGGAGCTT TACAAATTCT 1020
CCTGGCAGGG GTGCATGTGT GTACGAGGAT GGAAGGGTCT GTGCACGGAT CTCCTAGAGA 1080
GATTTGAAAA 1090
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