Tag | Content |
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EnhancerAtlas ID | HS159-01192 | Organism | Homo sapiens | Tissue/cell | Pancreatic_islet | Coordinate | chr11:64735850-64737600 | 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 |
chr11 | 64737402 | 64737561 | chr11 | 64736663 | 64737138 |
| | Number: 1 | ID | Chromosome | Start | End |
GH11I064968 | chr11 | 64736225 | 64737614 |
| Enhancer Sequence | TCCCACCTCA GCCTCCCAAG TAGCTGGGAC TACAGGTGCC CACCACTATA CCCAGCTAAT 60 TTTTGCAGAG ATGGGGTTTC ACTATGTTGC CCATGCTGGT CTCGAACTCC GGAGCTCAAG 120 TGATCTGCCC ACCTCGGCTT CCCTAAATGC TGGGATTACA AGCATGAGCC ATCAGGCCAG 180 GCATGGTGGC TCACGCCTGT AATCCCAGCA CTTTGGGAGG CTGAGGCGGG CGGATCATGA 240 GGTCAGGAGA TCGAGACCAT CCTGTGAATG GTGAAACCCC ATCTCTACTA AAAATAAAAA 300 AAAATTAGCT GGGCGTGGTG GCGGGTGCCT GTAGTCCCAG CTACTCAGGA GGCTGAGGTG 360 GGAGAATGGC ACGAACCCAG GAGGTGGAGC TCGCAGTGAG CCGAGATCGC ACCACTACAC 420 TCCAGCCTGG GCCACAGAGC GAGACTCTGT CTCAAAAAAA AAAAAAACAA GAATGAGCCA 480 CCAAGCTTGG TCCAAAATAT CTAAATATCT GGTGACTGAA AGGAAGATGA ACTGTAAGGG 540 GACAGGAGGA GAAATAGGGA GACCAGTTAA GAAGCTTCTG TAGTCGTCCA GGAGAAAGAT 600 GCTGCTGATT TGGACTTGGG ATTTTAGAAA TTAATAAATA GTTAGATTTG AGATATACTT 660 TAGACTAACT AACGGACTAG ATGTGGGAAT CAAGGATGGC TCTCAGATTT TTTTGCCTTT 720 GCAATTAGGT AGACAATGGT ACATACTCTA CTGAGATGGG GAATAATTCT AGGGAAAGAG 780 ATTTGGGGTG GGAGGGAGCA GTGAAAATTA GTAGTTGTGT TTTAAGTCTA AGAGGCCTAT 840 GAGACATCCA AGTGGATATA CCGAGGAGGC AGTCTCCTAG TGTGTAAGGG ACAGAAATCA 900 GAACGGAAAT ATACATTTGA GTCACCAGTG TTTAGATGGT ATGTGAAACT ACTGGAATAG 960 ATGATGAGAT CATCCAGGAA GAAATTATAG AGAAGGGATG AGGGCCTTCC TTATAAGCCA 1020 GGTTACAGAT TGTGGAATCT GTTGTCAGAG CAATCAGAAG GCACTGAAGG GTATAATAAA 1080 AAAAAAAAAC GACATGACCA GATGGCTGTG ACTTAAAAAA AAAAAAAAAT CCCTCCTGGC 1140 TGCAATGTGG GAAACAACCC GGAACAAGAA CAGATGAAAG GAGACCAGCT AGGAGCCTCC 1200 TGCGGCTCAA GGCAGAAGCT GACAGTAGCC AGGTCTACAG TGATAAAAGT GAAGATGACA 1260 AAAGGTGAAC TGATTTGGAA GATGGTACTC AGGAAGCTGA GGCAGGCAAG ACTCTGTCTT 1320 TTTTTTTTTT GAGACGGAGT CTTACTCTGT TGCCCAGGCT GGAGTGCAGT GGTGCGATCT 1380 TGGCTCACTG CAACCTCTGC CTCCCGGGTT CAAGCGATTC TCCTCCCTCA GTAATGACCT 1440 GGTGACTTGA TAAGGTGAGG GAGAGCGATG ACTCCTGGTT GCTTGAGCAA CTAACTGAAG 1500 AGGTAAAAGC ACCATTTTCT GAAAACAGGA GCCTTGGAAA GTAAATTTTT GAAGGCAAGA 1560 TGTTGAGTCT GTATCTGGAG ATGCTGAAGT TTGAGATGCC AATGAGATAG CCAAAGAGAG 1620 ATTCTAGATA AGACTGCTGG AAACTGGCTT CCTACCTGCA GATACATACA TGAAGGAACT 1680 AGAGTTCAAA AAAGTGAAGG ATGGGCCAGG CGCAGTGACA CTTGCCTGTA ATCCCAGCAC 1740 TTTGGGAGGC 1750
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