Tag | Content |
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EnhancerAtlas ID | HS191-24327 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr22:18286630-18288160 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_58864 | chr22:18253071-18294709 | Ly3 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 2 | ID | Chromosome | Start | End |
GH22I017803 | chr22 | 18286741 | 18286890 | GH22I017804 | chr22 | 18287015 | 18287944 |
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Enhancer Sequence | CAACAAGGAA TCGGTGAAGA GAGAGTTATT CCATCAGGTA GTCCTCCTGT CCCCCCATAC 60 CCAATCAATG ATATGATATG GAGCAATCAA TGATATGGAG CGCAAGAAAC ACAGACACAG 120 CGAGGCGGCA GAGGAACGGC TGGAAGGCAT GCGTGCCTAA GTGCATCACA TACTGCATGT 180 CCACACATGC CGTATCTGCA TACTGCGTGG CTGCGGGAGG AGGGCGGTAA CTAAAACTCA 240 CTGTGGGGAG TCAATGGTCA CTATCAACAT GATCCCACGT ACACCAGGGA TCAGCCAGGA 300 CAGAGGCTTT GGCTTTGCTG GGAACTCCTG CCCCTGGGAC TGAACCTTCT CTAACTAAGA 360 GTTAATAGAG CGGGGCTGCC TGCGTGTCAG TTGCTGATAC TGGAAGCCCC AGGCTGAGGG 420 CCTGGAGGCA GGAGGCAAAC GTCCTACAGA AGCTCTGAAA TCCTTAGGTT TCGTGCAGTC 480 AGTGCTCTCC CAGGAATTCC CACGACCCCA CTGCTGACTC TATCAAATGC CTTGCAGACC 540 CACTTTTGCC GAATGGGTTT GAGAGAAAGG GGATCCTGTT TCGAGGCTTA GGCCTCCAAA 600 TTCAGTCGGC CTTCTTAACA ACAGGAAACG AGCAGAGACT CATGCAGAGT TCTTCCCCCA 660 GGCACTCGGC CGAAGGCTCC TGGAGGTGTG CTGGCCTGGG GCACTCCTAG CCTGGTAGTT 720 CCACAGCTGT CTGGCCAAGA GCGCTATGTA ATTTCCACGC CTGAGATGCA GACTGGGCAC 780 TGCCGAGAGG CTGGGCTTGA GCAGGCGGTC CTCATCTCCC CAGAATCATA AAGACACACA 840 GAGCACAGCA CTCGGCCGCC ATGGTGTTGC CCTCTCTCCA AACCCCGCAT TCTGAATGCA 900 GATCCTCACA GCCTCCGGTC CCACCTGAGG GCCTCCCCTT GAGAGTGACA CAGCAGACAC 960 AGTGGTAGAA TGCGGTCCTG CCCCAGTTTT TCAATGCATG CTCAAGGCTG AGTCAGTGTT 1020 TTTGTAACAA AAAGGCTTCC CAGGTGCCCC AGGACTGGAA ATTACCTAAG TTGTGGCCTG 1080 GCCCTAGGAT CAAAGGTGCT GAAGCTAATC CTTGCAGCCT GGCCATACGT CGTCATACCT 1140 TAGACAAACG GAGAACGGGA TGGCAGGTCC ATGCTAGAGC GCTTCTCTGG AAAGGCAGCT 1200 TGGCTAACAA AGTCTGACGC CCTCAGACGG TGATGGAAGC TGGAGACCCC CAAGTGAGAT 1260 GATGGCAGGT TCCAGCCAGT TTACTACAGT CCCCAGGGAA GGGCAGACTG CCATGATGAG 1320 AAGACTCCAG ATTATTATCA TGCCCAGCTG CCACTGCCTT CTTCAGGGCT CAGCCAGGTG 1380 CCACAAGACT AAGAAGAGGA ACGGGACGCA GAAGCAGGAG AGAAAGCAGC AGCAGCACGC 1440 ACACCTGGGC TTCAGAGACG GCATCGGCCA AGGAGGGGCA GGGCCACGGG GAACTGTGAT 1500 GGGAGACCAG CTTGGAAGGG ATGTATTCAC 1530
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