| Tag | Content |
|---|
EnhancerAtlas ID | HS043-02856 | Organism | Homo sapiens | Tissue/cell | Fetal_heart | Coordinate | chr1:161980380-161982920 | 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 |
| GH01I162010 | chr1 | 161980455 | 161982114 |
| Enhancer Sequence | TGTCCAGCTC TTAGACACGT GTGCGTGTGC CCGGGTGAGA CCGTGTAGTA TCTTAAGCCA 60
AAACCTTGGG ACCAGGGGAA AGATGACCAT GGGGCAGAAT TCTGGCAGTT CTCTGTGGTC 120
TCGTTTTTAC AAATAGAACC AGGGACAGGG GTGTGGTCGG GGGAGGGTGC TGGCTCTGGA 180
GATCAGGTGT AAACCCACAC CACAGTCATG GCCTACTTAT ATAACCACAT AGGGCAAGGG 240
ATGAAACCTC TCTAGGCCCC AGGCAGGAAA AGAAGGAATG ATGACACCTA CCTCACCCAA 300
GCTTGGCACA GAGATGGATA AGGGGCTGCA TGTGGTACAG TGCTGGGCAA GGAAATCAGG 360
CTTGAGGCAT GTGGGTGAAG CTGGAGTGGG AGGGACCCTT GGGGTCTCCA TAGCAGACAT 420
GCAGGTGGAA AAGGAAAGGG AAGCCAGGGT TTGGTATGGC TGGCATGGGG AGGAAGGTAA 480
GAACCCAAGG CTGGTGTGCT GTAGAGAGAC ACACTAGACA CCTGTGGGAG TAGACAAAGC 540
CAGACTGCAG GTGAGGCAAA CCCTGGCCCC AAGTCACACA GCAGGTGCAC ACAGCCATAT 600
CTAAGGAGGC TGCCTGGGAG GCTGCCTGGT AGGTCCTGTG GGCATCAGGA TTCCCTGGCA 660
GATAGCTGGA TGCGCACAGG GCTAAGATAC AGATGGCAAG CCCAAGGGCA GATGGGACAT 720
AGTTTCTCAT GGGAGTGACC TGAGCAAGTG TGAGGGTAAC TGGACCCAAG GGGGGAGGGC 780
TCGTAGTTCC CATCAGCTCA CCGTGCTCAA CCTTTGCACC CTCCAGGAGA CAGCTACGAC 840
CAGATGGCCT GGGACAGCAA CCCCAGCTGA CAGCTGTCTC CTAGCCCCTG GTAAGAGAGC 900
TGGGGAAGAG AACAGCTGGA AACAGCCGGT GCTCCTGATG GCAGGACAGG CAGGCCATGG 960
CCTAATCCCT CCGACCACAG CTGATGGGAG AGACAGGCAG GCCTGGGTTC AGGGAGCCAC 1020
CAGCTGCCCC ATTGAACATT CATCCAACCA AACAGCTGTG GAGCATCTGT CCCACATCAG 1080
GTGCTGGACC AGGGCCTGGG AAACAAAGAT GACTTGACCC AGCTTGCCCT TAAGAAGTCC 1140
AGGGCCTGGC AGGAAAGTCA AACAAGGCAA CAGCAAGAAG ACCCAGGCCT CTGGTGATGA 1200
ATTTCTATAT TAGGGTAATC TTACCCCTTA AAATAGAGCC ACTCGAGCCA TGCACACTTG 1260
CACATCCTGG CAGCTCTAAA CTGTTCCTAG GCCGACGGAT GGAGGGCTGA CACTCGCACT 1320
GTAAGTCTCT TCAGCCAAGA AGAAAACTTT ATATCCCACA ATTGCAAATT AGATTTGAAG 1380
TATATACAAC CCTGGGAGAG GTAATATATT GGCTTTAACT CATATTAAGA TGTAAATTGA 1440
ATTAAATAGT GTTAGGCTGA AATATATTTT AGAAACACTA ACTTCGACCC TCTGCCTTTT 1500
CACGTATAAG GACACTGAAG TCAGGCCGGG TAAGCAGTGC CCCTCTCCAA GCCTTCACTT 1560
GAGGAAGAAG AGTGAAATGA CTTACAGCAA ACCCCTCGGA AAGAGCAGAT TTGATCAGGA 1620
GAGTGAGCCC TGGGGGTGTC TCGACAGGGG TGGAGGGTGG AAGGAAAGGT AGGGCTTGGA 1680
AAGAGACAGC TCCCCCAACT CACAGCCAAG TCTGCACAGA TGAAAATTAC GTTTTCCTAT 1740
TAGCTGGTGA AACGATATAT CCCCCAGGGT CAGGAATGCT TCTTTGATCA TGCCTTTCAG 1800
TCCAGAAACA CAAAAGCCAC CAAAGCTTTA GGTGTGGGGG AGAAGCCCTC AGCAATGCCT 1860
GTGCCAGTAC ATTCTGGGGA GCGGACCAGT TCTGGGTCTG GTAAATCCAT CGTGGACTTA 1920
AATCTTCCTC GGAGGCAACA TTATCAGGAG AAAAGTCTTC AGCTGGGACA CAAGGTTCCC 1980
TCGTGCCATC TATGCTCATG GGTGTGGTTT GCAAATTCCA GCAGGTAGAT TCGTGAAAAA 2040
GGAAAGAGAT ACACACACCA GAAGGGACAA AGCAGAAACC ACGCTATGGA AAGCTTGCAG 2100
GCATGCATCT ATTTTAAGAG CATGGGCTAT GCACCCACAC ATATACAAAG GCACATGTGT 2160
ACATAAGCAT TTCAAGCACT TATAAACACT TACAGGTATC CTGCAGCAAG GTGGGGGTGG 2220
GACATTTCTT CATAAAATTT GCAAATTTTA CAGAAATGAC TGAAACCAAC TAAAGCCTTG 2280
ATGCTAGAAG ATTATTATAA TGATCTGTCC CTCTGTTTGT CTTTTTCTCC ACTTTAGTAA 2340
TAAATCTGCC CCTGGAAGCA GTATGTGCTG CTAGGGGTTG AACACCATGC CTCTAGTCCT 2400
GCTGCCTTCA GAATCCACCT TTAGGCCTGG CAGCCTACAA GTCTATGGGT CTCTGAGTGC 2460
ACTCAGAGCC CGGATGAAGT CTTTTCTTGA GCTGAGTGAG TGCCACTGCC AGCTCTGTAT 2520
GCAATGAACA GGGCTTGCCT 2540
|
| |
|
|
|
