| Tag | Content |
|---|
EnhancerAtlas ID | HS048-01097 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr1:41779610-41781900 | 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: 2 | ID | Chromosome | Start | End |
| GH01I041313 | chr1 | 41779272 | 41779672 | | GH01I041314 | chr1 | 41780190 | 41781230 |
| Enhancer Sequence | TGCATTATGC TTGCTAAGGG CCCGTTGACC AAAGCAAGTG AAATTGCCCA TTACAAGGTC 60
AATGTGTAGG GGACTCCACA AGGCTGTGAA TACTAAGAGA TTTGGTTCAT TGCCACCAGT 120
GTAACCATTT ACTACACTTC CTAAGGTGAT CTTCCATTTT GCTCAGAACG CAGTTCACCA 180
GGCTTCAAGA TCAGAGACAA AAGCCACAGC CAGGCATTGC ATGTATGTTG GGAGAGGAAG 240
AGGCTAGCTG GCCCATTGGC TTATTCAATA GTCCTTACCT GATGGTCGTG CTGTGGCCTG 300
CTCCTTCTCC CCTGTACTTG GAGTTTCTCC AAGGTTCTGT TGAAAAGAAC AGTTTACATC 360
TCCTTAGCCA ATTTCTTCTG TGCTGATTTA ACCATTCTGG TTTCCTCTGT AGATTTGATT 420
CTCTCTGCTT TTTATCTTCT AGAAAGTCCT TAAAATTTTC TGATTGACAG ATGCTGCAAT 480
TTCTAGTTTG GGATGGAGGG CTTATATGAA TGTATTCATT TTATGTCTCT GTTATTTCAA 540
GGAAATATGT CTTGTAAAAA GGAAAAGAAA GCAGTGAGAT TCCTGTCACT ATAGGTCTGC 600
TCTCACACGA CAGGAATGCT AAAGGGAGGT GGTGGTTAGA CTAGATGACT CTTGCTTTTT 660
GCCAGTTCTG AGATGTTGGA GACGCCATAG CTTCAGCCAT TTCTTCCTCA GGATTCCAGG 720
TTGATGGAGC TAAACCTGAT CATTGTGATT CAAGCACCTG CTGGGACCAG AACTGAGAAC 780
TCTGGAGCTG GCTTTTTAGA TCATCGAATT CAGACTCTTG TGTTGCAGTT AAGCTATGGG 840
AACAAAGGTC ATCCAGCAAC TCAGCTGCAG AACTGGGGTT GGAACATGGG CCCCCGGACT 900
CCTGATCCCA TGATCTTCCC TGCATCTTGC TCCAGTTTGC ACTTCTGAGC ACCCCTTAGA 960
GAAGCCCAGG GTCTTACTTC TTGAGTGGGA TCAGGCTGTG TCTCCACCCC AGGATACTCA 1020
GGGTTGAAGG ACTTGAGGCT AGAATTGCCC CCAATGAGAC AGATGTCTGT CTGGCCCCTC 1080
CTCCCAAAAG GCGATTATTT GAGCTAGAGA CGCCAGCCGC GTTTGAATCC TAGATTCTCT 1140
TTCTCCCTCC AGCGCCCTCT CTCTCCCACT CGGTTATCTA TTTACCTATC TATTTACGTG 1200
AGCTACCCCC CACCCCAAAT GAATTACGTC TGCAAGGCAG TAAAATGTTA TGTATTTGCA 1260
AGGCCCATAA TCTTTAAAAG CCCAGTGATG CCAGCTCCAG ACAGCAGCGA GCTCCCTCCA 1320
GTATGTTAAT AGATAGTATT AGGGCAATAA TGAAAACACT TGAGACAAGT AAGCTCCTAT 1380
CAAAAGCTGA GTAATAGGGC TTTGCCGAGT GAATCACAAT GCAGAAGAGA TTAAGACGTC 1440
TGCCGTTGTG CAGTGTCTAT TCAGACTAAC AGCTGCTCTG TTTCTGATTA AAATGGGGTT 1500
GGGGAGACCT TTTCGAGCGA GTCCCCTTTT TATCCTGCAC TGTCCTCACC CTTCCCACCT 1560
CCACCTCCAA GCACAGGCAC CTTTATTTGC ACTTAACTAC TGCCATTCAT AAACACACAC 1620
ACACACACAC ACACACACAC ACTGGAGTCT CAATCATGCA TTGCATCATC ACACACACGG 1680
AGCCTCAGAA GCACACACAG CCATTAGCCG ACACACAGCT ACACCGATAT ATCCAAGCAC 1740
GTACACACAG TCACATCCTC ACACACCGGT GCACAGTCAC GCATGCAACC AGTCTCTCAC 1800
ACACTCATGG CCTCAGCCAG TCTCACACGC GCATTAAATT ACAATCTGTC ACAAACACAG 1860
TCTCACATAT GCATTAAATT GCAATCTGTC ACACATATAC TCTTCACACA CAGTCACAAC 1920
CAGACACTCA GAGACAATCT AATCAGTGTC AAAAACGCAC ACATACCTGG CTGGTCATAT 1980
CCACGTATGG CAAGTCCTTC ATGTGCAAAA TCACACTTGC ACACTCACAC TTGTGATGAC 2040
TGTTTGTCAT ATACACACAG CCCTTCACTC ACAGACTGTC ATGTGCTCTC TTACCCACAC 2100
ACAGTCACCT TCATAAATAA TCACACATGG CCATGTGCTC ACTCACACAT GGCCACAGCC 2160
CAGGCTCATA TGAAGTCATG CTTTTCCTGC ACCAAGATAC AGAGCTAGTC TGCACACCTG 2220
CAACTCCCCA GCCACAAGTG TGCATGGAGT GCAAGGCACA AATACATATA GGCACACAGG 2280
CACAGACACC 2290
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