| Tag | Content |
|---|
EnhancerAtlas ID | HS091-12133 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr13:99000880-99003080 | 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: 2 | ID | Chromosome | Start | End |
| GH13I098349 | chr13 | 99002063 | 99002142 | | GH13I098350 | chr13 | 99002281 | 99002470 |
| Enhancer Sequence | CATCCGTAGA CGATGTGAAA TGAATGGATG TGGCTGTGTT CCAATACAGC TTTATTTATG 60
GGCACAGAGA TTTGGCTTTT ATATAGTTTT CACATATCAC GAAATGTGAT TCTTTTGATT 120
TTTTTTTTAA CCACTGAAAA ATGTAAAAGC CAATCTCTGC TTCGGACCTG TGCCAGAACA 180
GGGAGTAGCC TGGCCGTATT TGGCCCATGT GCCGTAGTTT GCCAATCTCT GTGGTAGGTA 240
TTCTATAACC CAAATTTTAC AGTGAGCAAA TCCAGAGAAG TAACGTGCCC AGTCCTTAAC 300
AATGAAATGT GTAACCAGGA TCCACACAGA GCCTCTCTTA GCTAAAGCTC ATGTTCTGTA 360
TGTCGCATGT GGCTGCCTGT CCTTGGATCT CCCGTCGGAA AGAGCTGCAC AAACCGTAAC 420
AGCAGAGATA GTTGTATACG GAAAATTTAT CTCATTGGCC TATTGAGGCT AGCTGGAAAA 480
GCTCTGCATT GTGGCTTGCA TATCTGTTTA AACATTCGCT TTGTCATTTA GCTGCTAGGT 540
TGATTCTTAA CTTCCTTGAT TTTGCACTTC ATCTGAGAAA TGAGAGGAAT AAATGACCAT 600
TTTACAAGGT TATTATGAGG GCTAATCAGA TACTTTACAA TGATGAGCCC AGCAGGTCTC 660
ATGGCACATA GTAGGCACTC AGATATCTGT TGTATTTCAT TTTTGCAATC TAACTCAGAA 720
ACCAGTGAAG CCAGCCCACC ACTGTTTTAT TAAAATGACA TTGTGGCTGG GTGGGTGGCT 780
CATGCCTGTA ATCCCAGCAC TTTGGGAGGC CGAGGCAGGC AGATCACTTG AGGTCAGGTG 840
ATTGACACCA GCCTGGCCAA CATGGTGAAA CCCCATCTCT ACTAAAAATA CAAAAATTAG 900
CCCGTTTGGT GGCACGCGTC TATATTCGCA GTTACTTGAG AGGCTGTGGC AGGAGAATCA 960
CTTGAACCCA GGAGGCGGAG GATGCAGTGA GCCGAGATCG CACCACTGCA CTCAAGCTTG 1020
GCGACAGAGC AAGACCCATC TCAGGGAAAA AAAAAAAAAA AAAAAAAAAA AAAAAAGACA 1080
ATGCTTACTG GCCTGATAAA ATCAATTCTG GTTTCTTATA AATAAATACT GTCGAAGCTC 1140
CAGGAAGAAG ATTGGCACCT TGTCATTCAT TTTCTGTCCT CCATGCTAGG AGAAAAGCTT 1200
TGTCAATAGT GGGACTGCTT TTGAGGGGCA GGAGGTCATG GAAACTGCAG TTCCCGGGGA 1260
TGACGGGCAT CCCTTGCTGG AGGTTTCTAG ACCCTGCTGG AGTCAGACAC ACCTCCTTCA 1320
TCTGTGCTTA GCCGCAGCGT CTGCCCTCGC TTCTTCCTAG GGGTCTGAGG ACCTCTGAGG 1380
TGAGGAGGAG CTTTTTGAGG AACATGGGAG GTGTAAAGGA TGGAGAATGT CACAGGATCG 1440
AGGACAGCCT GCAGCTGTGG GAAGCCAGCA GAGGTGAGGT TGTACAGCGG CTCGGTCACC 1500
TCGCGGGGCA GCACCATCTA ATGGTGACTG TGTTGACAGG CAGGTCCCCA GAGGAGGCAA 1560
AGCTCCCCTC AAGCAGAGAG TCTGGGAGGA CAGGCCCTTT GGAAAATACA GCTGTGGGAG 1620
ATGCTCCAGC TCTCAAGTGG GAAGGAGAAT AACTGATTTT GGGGCTTTTA GTGTTTTGTT 1680
TGTTTAATTA ATAGATTTAA TATTTGTATT GCAGTTTTAA GTTGACAACA AAATTGAGCC 1740
AGAAGTACAG AGGTTCCTAT ATACTGTTCC CGCTCTGTCC GTACTTACAG TGTCCCCCGT 1800
TACTGACACT GTGCCTTCGT GTGGCATGTG TGTCCTCGCT GATGGGCCAG TGTCAATCCA 1860
TTATCATTCA TTCACTGCGG TCCAAACTTG ACATTAGGCT TCACTCTTGC TGTTGAACAT 1920
TCTGTGGGTT TTGACACATG TTTCTGGACT TGCATCTACC ACAACAGTAT TACACAGAGT 1980
TGTGTTACCG CCCTGATCCT TCCCTGTGCT CCTCCAGTTC CTCCCTCTCT CCTCGTGAGC 2040
ACCTGGCAAC CCCTGATCTT TTCCCTCTGT ACTTTTTAAT TTTCTGTACT CTCTGACACC 2100
TGAGGCCTTG TTGACTGGGG AGCTACTTCC CCTCCCCGGG CTAGCCAATT CTTAGAGATG 2160
GCAAATGGCT CCCTGTGAGT GTACCCTTTA TTTGCCAATT 2200
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