Tag | Content |
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EnhancerAtlas ID | HS108-14620 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr16:11248880-11249980 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_56497 | chr16:11248748-11249699 | u87 |
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| 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 |
GH16I011155 | chr16 | 11249025 | 11249946 |
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Enhancer Sequence | GAGGTGGGAG GATCAGCTGA GCCTGGCGAG GTCAAGAGGC TGCAGTGAGC CGGGATCATG 60 CCACTGCACT CCAGGCTTGG TGACAGAGTG AGACCCTGTC TCCAAAAAAA GAGAAGAAAA 120 TCCCAGTTAT TGCCTCATTG GGCCCAAGTT CCAGGCACCG TAAATTCCAG CCGAGGAATC 180 AAAACAGCGA GTGCTACCTG AACATTTAGA TTGCGTTAAT GCTTTCATCC TCACGAACCC 240 TGTAAGGTGT GGTGGTGTCA CTCTGCTTTA GAGTGACAAC AGTGCTTTAG AGGACACAGG 300 CTCGTGGGGT GAACAGGTCC CCTGCTGTCA CATGCCCAGA GCCACGGCAC TCTCCTCACC 360 ACCGTATCCT GTAGCCAGAG TAAAAGTGAC AAGCCTAAAG CCAAGTTGCT GCTCTTCAGG 420 TTTCTCCCCT GCAGATAGCA GAAGGCTCGT GTCCAGCCGT CCGGTTAGCC ATGTCCCACA 480 GGTCTGCCAG GGCAGACGTC AACAGAGCCC TGTCCACTTA ACAACCTCAG CTGTGGGTTT 540 TTGAAGCTTG TTCTGTGCTG TTATCCATCA CGGCCTTTCT GTGGCTCCGC ACATACTCCC 600 TGATTCTATC TGACTCACAT AGTTCCAGAT AGTATCTTCA GTTCTTGTTG TAGATGATGT 660 GTCATAGAAC GTCATCAGCC ATCGGTCTGG CCTAGCCCCA ATCTGTTAAA ACACACGGTA 720 GGAGAGACTT TGGTGAGGTG ACCCAGCTGC AGAAGTTAAC TACCCCACCC TGCAAAGTCG 780 GAGTCCTGGC GAACACAAGC AAATGGAATG GGTCCACAGG CATGGTGCTC TCTGCCTTGG 840 GTGCATACTA AGTATGTGTC AACGGCAGGT GCCTTTTGCA GAGAATCAAG ACTAATTCCC 900 TGGCCCCTTT GTACAGTGCC ACCTCCTAGA ACACACGGAG CAGGCCAAAC ATGTCAGTGT 960 AGGATACACA CTGTACGGCC TCCCTGCTTC TGGCCAAAAA GGTCAAAATG GGGCTGATGG 1020 GATAAGAGAC TTGCTGGGGA AGAATCTGGC GCTCCTGGCC GGGCATGGTG GCTCATGCCT 1080 GTAATCCCAG CACTTTGGGA 1100
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