Tag | Content |
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EnhancerAtlas ID | HS108-01827 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr1:54276840-54277900 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr1:54277442-54277461 | AAGCGCCACCTCCTGGCAG | - | 6.05 | NFE2L1 | MA0089.2 | chr1:54277191-54277206 | GCATGACTCAGCAGA | + | 7.23 | Nfe2l2 | MA0150.2 | chr1:54277189-54277204 | CTGCATGACTCAGCA | + | 7.41 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 54277031 | 54277480 | chr1 | 54277510 | 54277783 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I053811 | chr1 | 54276906 | 54277746 |
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Enhancer Sequence | GATCCATCAG AAGGTTGACC AGAGGAGCAG GGAGTAAAAC TCCACAGGGA AAAGGAAATC 60 TCCAGCTGAA CTTTGTAACA ATTTAAATGG GGCAAGAAGC CTCCTGGCCA GAACTTGGGG 120 GAGAGGGCAA ATCTAATGTG TAGACTCCAC AGGTGGGGCA AGAACCAAGC TCTTTTCTCT 180 CCCAGCTGGG AGGCGGGTAG CCCAGGGCAA GTTTTCAAGC CCATCTGGCC TTCCACCTGG 240 AAACAGACTC AGGGCTGTTG CAGGGCGGTG GGAGTGAGAC TGGCCCTTTG GTTTGCATGG 300 GACCTGGGTG AGGCCTGTGA CTGCCACTTT CCCCCACTTC CCTGACAGCC TGCATGACTC 360 AGCAGAGGCA GCCATAATCC TCCTAGGCAC ACAACTCCAG TGACCTAGGA ATCTAACTCC 420 CATTCCCCAC AGCAGCTGCA GCAAAAACTG ACCCAGGAGA GTCTGAGCTC AGACTCGCCT 480 ATCCCCACCC CCACCTGATG GTCCTTCCCT ACCTCAATAC AAAGGACATA TAATCTTGGG 540 AGTTCTAGGG CCCCACCCAC TGCCAGTCCC TCTCCACACT ACTACAGCTG AGGTTTTCCG 600 GAAAGCGCCA CCTCCTGGCA GGAGGCCCAA TCAGCACAAA AGTAGAGCAT TAAACCACCA 660 AAGCTAAGAA CCCTCATGGA GTCCACTGCA CCCCCTCACC ACCTCCACTG GAACACGCAC 720 TGGTATCCAT GCCTGAGAGA CCCAGAAACA GTTCACATCA CAGGACTCTG TGCAGACAAC 780 CCCCAGTATC AGCCCAGAGA CAGGCAGACT CGCTGGGTGG CTAGACCCAG AAGAGAAACA 840 ACAATCACTG CAGTTCGGCT CACAGGAAGC CACATCCATA GGAAAAGGCG GAGAGTACTG 900 CATCAAAGGA ACACCTCGTG GGACAAAAGA ATGTGAACAA CAGCCTTCAG CCCTAGACCT 960 TCCCTCTGAC AGAGCCTACC CAAATGAGAA GGAACCAGAA AACCAACCCT GGTAATATGA 1020 CTATACAAGG CTCTTCAACA CCCCCAAAAA AAATCACACT 1060
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