| Tag | Content |
|---|
EnhancerAtlas ID | HS050-01931 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr1:41780200-41781800 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 41780949 | 41781152 | | chr1 | 41781359 | 41781793 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH01I041314 | chr1 | 41780190 | 41781230 |
| Enhancer Sequence | ATAGGTCTGC TCTCACACGA CAGGAATGCT AAAGGGAGGT GGTGGTTAGA CTAGATGACT 60
CTTGCTTTTT GCCAGTTCTG AGATGTTGGA GACGCCATAG CTTCAGCCAT TTCTTCCTCA 120
GGATTCCAGG TTGATGGAGC TAAACCTGAT CATTGTGATT CAAGCACCTG CTGGGACCAG 180
AACTGAGAAC TCTGGAGCTG GCTTTTTAGA TCATCGAATT CAGACTCTTG TGTTGCAGTT 240
AAGCTATGGG AACAAAGGTC ATCCAGCAAC TCAGCTGCAG AACTGGGGTT GGAACATGGG 300
CCCCCGGACT CCTGATCCCA TGATCTTCCC TGCATCTTGC TCCAGTTTGC ACTTCTGAGC 360
ACCCCTTAGA GAAGCCCAGG GTCTTACTTC TTGAGTGGGA TCAGGCTGTG TCTCCACCCC 420
AGGATACTCA GGGTTGAAGG ACTTGAGGCT AGAATTGCCC CCAATGAGAC AGATGTCTGT 480
CTGGCCCCTC CTCCCAAAAG GCGATTATTT GAGCTAGAGA CGCCAGCCGC GTTTGAATCC 540
TAGATTCTCT TTCTCCCTCC AGCGCCCTCT CTCTCCCACT CGGTTATCTA TTTACCTATC 600
TATTTACGTG AGCTACCCCC CACCCCAAAT GAATTACGTC TGCAAGGCAG TAAAATGTTA 660
TGTATTTGCA AGGCCCATAA TCTTTAAAAG CCCAGTGATG CCAGCTCCAG ACAGCAGCGA 720
GCTCCCTCCA GTATGTTAAT AGATAGTATT AGGGCAATAA TGAAAACACT TGAGACAAGT 780
AAGCTCCTAT CAAAAGCTGA GTAATAGGGC TTTGCCGAGT GAATCACAAT GCAGAAGAGA 840
TTAAGACGTC TGCCGTTGTG CAGTGTCTAT TCAGACTAAC AGCTGCTCTG TTTCTGATTA 900
AAATGGGGTT GGGGAGACCT TTTCGAGCGA GTCCCCTTTT TATCCTGCAC TGTCCTCACC 960
CTTCCCACCT CCACCTCCAA GCACAGGCAC CTTTATTTGC ACTTAACTAC TGCCATTCAT 1020
AAACACACAC ACACACACAC ACACACACAC ACTGGAGTCT CAATCATGCA TTGCATCATC 1080
ACACACACGG AGCCTCAGAA GCACACACAG CCATTAGCCG ACACACAGCT ACACCGATAT 1140
ATCCAAGCAC GTACACACAG TCACATCCTC ACACACCGGT GCACAGTCAC GCATGCAACC 1200
AGTCTCTCAC ACACTCATGG CCTCAGCCAG TCTCACACGC GCATTAAATT ACAATCTGTC 1260
ACAAACACAG TCTCACATAT GCATTAAATT GCAATCTGTC ACACATATAC TCTTCACACA 1320
CAGTCACAAC CAGACACTCA GAGACAATCT AATCAGTGTC AAAAACGCAC ACATACCTGG 1380
CTGGTCATAT CCACGTATGG CAAGTCCTTC ATGTGCAAAA TCACACTTGC ACACTCACAC 1440
TTGTGATGAC TGTTTGTCAT ATACACACAG CCCTTCACTC ACAGACTGTC ATGTGCTCTC 1500
TTACCCACAC ACAGTCACCT TCATAAATAA TCACACATGG CCATGTGCTC ACTCACACAT 1560
GGCCACAGCC CAGGCTCATA TGAAGTCATG CTTTTCCTGC 1600
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