Tag | Content |
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EnhancerAtlas ID | HS138-04187 | Organism | Homo sapiens | Tissue/cell | MSC_BM | Coordinate | chr10:3862110-3863340 | 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 |
GH10I003820 | chr10 | 3862626 | 3863206 |
| Enhancer Sequence | ATGGAAGGGT TCAAAAAAAG ATTTCAATCA GACTTAAGGC AAACACTTCA ATTCACTCCA 60 TACTGGTGAA CACTCTGCCC TCACGCTCAT TGGAAGGCTG CTTGGATCTA TCACTATTAC 120 TTCCTAATTG ACTGGAATCT ATTGAACTTG CAGCTTTGTT GACAGTGCAC TAAGAAGTAC 180 TATTAATCAC AACTACCTCC ATTGGTGAAC GCCATTTATC TCTGTCATCG TGCGTGCTTA 240 AGAAACATCT TTGCACTGAG ATGATCCCAG GTCCAATCAC AATGATCATT ATCTGATGTC 300 ACCTTCAAAA CGTGGCTCAG CCAGAGCAAA ATCTGTAAGG ACAACACCAT GGTGACCAGT 360 GGTCCAACCC ACTATGGGGG AAGTAGAGAG TTGGACAAAA ATGGTTTTGA GCTTTCAGAG 420 GTGACAGGAG TCAAGTAAGT GAGTTTATGA TGTAAGCACA CTTGAATGCT CCTTTAATCT 480 TTAGAGCGGG GGCCACTGAT CTTTGTTAAT TTCCACAAAA TCTCTGCAAA GCCGCGTTCT 540 TCCTGGATTA CTCAGAAAAG CCTTCCAGAT GGTGACGGCC GGGCATCAGA GGCCACACCT 600 TCAACTGGAG CTCCAACCCC ACAGCGTCAG CACCTTTCTG TCGGGGAGAG AGTGTGACCG 660 TGATGAGAAC AACAGTGCTT CCACACGGTC TTCCCTTGCA GAAGGAGAAC GTCAGACAGA 720 GTTCTAGTTA TACCTCGACA TAGCTTTTCA GCTGAAAAAT TCCATTTTAC CAGCTGAGCA 780 TGTGGCTTGG TCTGGGATAT TTGGTCGCAA AACAAAACAA AACAAAACCT GCTCAAATCG 840 TGTTAAAACA AGCAAACAAA CTCGCTGAGA AGTTTATATT GGAAGATGCT GAATGTAAGG 900 GCAGAAAGCA ATGCTATCCC CAGAAGAGAT CAGCGCCTGA GCCTGAGAAG TCATCCAGAG 960 GGAGGCAGGG CCCTTCCTCA GATCCCACGG GGTCTGGGAT CCTGCTGTCC TCTGCCTCCA 1020 TGGGCAAAGA CCACGATTTC TGTGACATGC CCCATCCAGG ATCCCAGCTA GTGCTGATGA 1080 GGAAGGTCCC CTCGTGGAAT AGTTACTAGT AAATTCATTG AGAGGAGCCC TGGCTTTATT 1140 CCATCCAGGT GTGTGCATGT GTGTACACGC ATGCCTATGT GTATGTGTAC ATAAACACAC 1200 ATATGCGTAC ACTGGGCTTC CAGATTAGAA 1230
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