| Tag | Content |
|---|
EnhancerAtlas ID | HS052-00177 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr1:8657110-8659370 | 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 |
| GH01I008597 | chr1 | 8657861 | 8660319 |
| Enhancer Sequence | ACAGCAAATG CTTAATCATT TAATTTGTAC TGATGCTGAT TTTTTTTTTT TTTTGAGACA 60
GGGACTTCCT TTGTCACCCA GGCCAGAGCG CAGTGGCGTG ATCGTGGCTC ACTGCAGCCT 120
CAGCATCCCA GGTTCAACTG ATCCCTCTGG CCTCAGCCTC CTAAGCAGCT GGGACTAGAG 180
GTGTGTGCCA CCATGCCCAG CTAATTTTTA TATTATTTAT AGTGACGGGG TTTTGCCATG 240
TTGCCCAGGC TGGTCTCGAA CTCCTGAACT CAAGCAATCC ACCCGCTGCC TCAGCCTCCC 300
AAAGTGCCAG GATTACAGGT GTGAGCCACT GTGCCCAGCC CCTGATGCTA ATTTTTAAAT 360
GGACATTTGA ATTCTCAAAG AAATTTGTGT TGCCTCTTGT CAAACCAGGT CACTGAAATG 420
ATAACCCACA CAATAAGCCA ATGAGAAGGA AAAAATATAT GGGATTGGAA AACAGAATGA 480
AAATCAACAT TAAAATTCCA TAATTAAAAC ACGCAGATAG AAAAGAATTT ATCTGACAAC 540
GTGCTAAGAA CCCCCTGTCC TGTGTTTGCT GTCATGGGGA GGGAAGAATG TCTGCAGCAC 600
AGGCTTTCCC AGTCTGATTC ACAGCCCTGT TATATATGAA TGTGCACACT CGAAACAAGA 660
TCTGATCTGG ACAATAGTCA AGTCTCTAAA AGCAAGGGAG TTCAATTAAT TTTTTAAATA 720
AACATTTCAC TGGATTTTTT TTTTTTAATG ATCAATCCTG TTGACAGTTT TCCCGTCCAT 780
CTTCCAGAAG AACTCACTAC TCAACCAACT GCCTGGTATT CAGCTGTGAC TGTGAGGATG 840
GATAACTATA TTTCCTTAAG AAATAGCAGG AAGGTATCTC ATCCAAGCAG AAAATAAGAC 900
CAACAGTTGT CCAGGTCTCA GTGGTTCTGC ATTTCTTCCT AAAAGAGAAA TATGTCTCTA 960
AACATCTCTT TCCCGCCTCA TGGGGTTGGG GGAAGCAATA TGCTCAGAAA AATTTTAACT 1020
ACTCCAGGCA GCTGAATAAA ACAAGCTGAA AACCCTAGAT GTGTTCTCCA CATTACTGTG 1080
ACAGAATGCA AGTGTGTATT CGAAAGATTT CCTCGCTGGA ATTATAAAGC GTACAGCAAG 1140
CCAGCCTGCT GTACTGCCAC CTCGCTCTTG CTCCCAGACT CCCTCCCATG GACTAAGCAG 1200
GAACGAACAT ACGAGCTGTG AATCTGGTAG GGGAAACAGG AAACATCCAA CCAGGAACAC 1260
ACTGGAGAGA AGAGAAAACA GTTAACCACC TATGAGAAGA TGGCGCTGAT TCCAGCAGGT 1320
GACAGGTGGG ACGTGAAGGG CATTCCCGGC CCTCCAGCAG AAGCAACGTC ACGGAGCTGG 1380
GTGCTGGGTG GGTTGCACCG TTCTGAGGCA GCACGGTTCT CTCCAATGAC TCTCACACAG 1440
GAACCAGACC TGACTCTGTT TCTTCCAGGA CGGTCCTCCC TCACTCCACA GCCTCTCATG 1500
GCAGCTGGAC ACCCACCAGG GCTGGATTCC ACACACAGAA ACCACATCCA ATGCTCTGTT 1560
ACTAGAAGTC GACCATCTGG ATTTCAAAGA CCTCTGTCTC TTTCTGTCCT TTGTTAATCA 1620
GTCTCCCTTC CCACTCAACC CTCTCCCCTC CATGCCAGAG AAAAGGATTT TTAAATCTGA 1680
TGAGTTTTTC AGGGAAGCAG AAATGTGAGA TTACACTGTT CTTTAGCCTC ACCTCATGGT 1740
TTTGCTACAG AGATCAACGT CTTCTAACAC AGCTTTGCCC ATACTCTTCC TGAGGCTGAA 1800
CCAAAAAATC TTTCATGAAC AGTACTGTCT CCACCAGCAG AATGTAAATA TACCACAGCA 1860
CTGACTTCAA AACACTGAAG TAGAGAGTCT TAACTCTCCT TAGACAGAAG GCAGAAGGCT 1920
GCAAACATCC CCCAGCAGAC TGCAATTGTG CTGTTCCAAC TGACAAGCCC AGTAAGCACT 1980
GCCCATGACA GGACCTCCTG CAGAACTTCT CCCAGCCTGG CGGACAGCGG GGCAGGGGTC 2040
ACCCTCAGAG GCTCGCCTTC TCTTTGCTCC CTAGCCATCA CACTACACTG GGATGAGACA 2100
CAACAAGCAC CCAAATGACA CAGTGACCAT TTCTTTTGGT CACTGAGGTT CACGAGATGG 2160
GCTGTTTTTC TTTTTCAATC GAGGAGCTGA AATCCTACCA GCCACCTAAC AATTAACAAC 2220
CCCAACCCTG TCCACGGTTA AAATCAACGA AAAAAGCAAG 2260
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