| Tag | Content |
|---|
EnhancerAtlas ID | HS050-14771 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr12:4070810-4072420 | 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 |
| GH12I003961 | chr12 | 4071012 | 4072749 |
| Enhancer Sequence | ATAAGTGTCA TCAAAACTCA GTTGGCAATG TGTTTCTTGT GATCACGAAG CAGTCTGGGA 60
TCTGACACGC CTTTGGACTG TGAGTCTCAT GATCCGCCAT CCTTGGATAC ATCCTCAGAT 120
TCATCAAGTT GAGACGGTCA GAAAAGCATG CAGGGGCACT TCTCTGTTTG GCACACGGCC 180
AGTGTTGGAG CACGGACTTT ACAAGGAAAT AGTTTTCTCA AACTTTATCC CGGTACCATT 240
TTCCTCGCTT TCATTCCCAG CTATGTACAA AATTCTTGCT ATTCCTAGAG AGAGAACAAA 300
AAGCCACAGT GGGAAATGAA AGATTTGGCA TTGACGTCTC AGTCTGTGAC TTCTAGGCCT 360
CCAAATAAGG CTTTCTCTCC TCTCTTCTCG TTCTTTAACA GCCCTCAGTC ACAAAATTCA 420
GCTAAATGTA CCACATCAAT CTCTGCAGTT TGTCTTCATG GTCAGCATGC CGTCAAGGTC 480
GTTGTACACC ACGTCACCTT CTCTGTGACC TTGAGCAGGT CACTCTGCTT CCCCCTCTCG 540
GCCTTACTTT CTTCATCCTT AAATGGAGTG CAAAGGACTA GATGGTTTCA GATTTCCCCT 600
CCAGTTTGGA GTGTGTTTGT TCATGACAGG ATTCCCGGTT CCTAGCACAG TCCCTGGCAC 660
AGAGGGAGAG CTTAGTAAAT GTCTGTTAAC TCTGTGAATA AATCCGGTGA TTTAACGAAT 720
CCATCCATTC CATGGTGCCG GAGAAAGGAG CAGGGGCTGA GCTTTAAGTG CTACTGTGTC 780
ATAGCTTGCT GGGTGAACTT AGTAAGTCGC TTCCCCTCTC TAAGTCCAGA GAGGGAATGA 840
GCTTAACCCA AGGTCATACA GCCAGTAAGA GCAGAGCTAG GACTAAAACA CGGACCTTCT 900
GATTCTCTTT TACCAAGATG CCGTGCTTCA AAGGTCTTTT TTAAACTGGG AGAGGGCGCT 960
GAGGACCTGT TGATATCATT TTTCTGTCTA GACTCTGGAT TTAGAGCAAC CACCACAAAC 1020
TTGAGAACAA ACACATGCTT GCAAAAAAGA AAGCCTCCCA GGGGCCCCTA ACCAACAATT 1080
TCTCCTTCAC TGCCAGTTTG AGATAAGCAG CCACCAAGGA GGCTGAGTGA CGTGGACTCA 1140
GCCCACAGCC CTGCCCAGCA AGGGCTTGCT GCTTCCTCCT AGAGGCGGCT CATGTCTGGG 1200
CTGGTGGCAC ACACTTCTGC TTCTATTGCC TCCTAGGTGT GGGTGCCAGA CACTAGAAAG 1260
AAAGCTGAGA GTAAAAGCTT AAATCACGAC GGTTTCCTTT GACCTACACC TTCTGCAAGG 1320
CAGAGGTGGC TCTGGCTCTG GTGATTAGCT ATGTGCTTGA GGTGGCCTGA GCTGGGCCAG 1380
GGTTGCCCCA GTGGGTCCTG GTACCAGCTG TAAGCTTACC TCTACTCAGC TTCCCCCACT 1440
CCCAGCAGGA GGGATCATCT TCACCTTCTC CTTCCCTGGC ACTGTGACTG AGGAGTATGC 1500
TTGGAACCAG ACTCCAATAT ACTGATTTCC AGCACAGTTC TTGCTGTCAG AGGGGCTGTG 1560
AAAAGGTCCG GCCTTCGCGT TCCAGCTTTG CTGCTTGCTA GCTCTGTGAC 1610
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