Tag | Content |
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EnhancerAtlas ID | HS141-01698 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr1:212856170-212857330 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:212856887-212856905 | CCTTCCTTCCTTCAGCCC | - | 6.57 | EWSR1-FLI1 | MA0149.1 | chr1:212856883-212856901 | GCTGCCTTCCTTCCTTCA | - | 7.33 | ZNF263 | MA0528.1 | chr1:212856401-212856422 | CCTCTTTCCTTCTCTTCCTCC | - | 6.82 | ZNF263 | MA0528.1 | chr1:212856404-212856425 | CTTTCCTTCTCTTCCTCCTCT | - | 8.06 |
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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: 1 | ID | Chromosome | Start | End |
GH01I212683 | chr1 | 212855710 | 212857342 |
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Enhancer Sequence | ATTTCCAAAT GGGCACTCCA GAAAAGTTCC CTTGACTCCA AGCATACAAC AGTTTCGAGA 60 TTTGGGCCTT GGTTGGCCAC ACCCCCAAAC CTCAAATTAT GCAGCATTAT GGGGGTGTGA 120 GGGAACTTCC CCCAGCACAC CCTCCTGTGG ATTCAGCAAA ACCGTCCCAG GAGAAGGGAT 180 GATTTAGATT CAGAGAACAA GGATCCCCAT TCCCTCCTTC CCTTTTCCAA CCCTCTTTCC 240 TTCTCTTCCT CCTCTCCATT CTTGCTTTCT TTTTGCTCCC TGGCTCTCTT CTACAGGCCT 300 CCTTCATGCA GCACGGATGA CCCTGCCAGG ACTTCCTGGA CCTCAAGGGA GGGAAGGTGT 360 GTCACTGAGA GCTGGGGCCT CCCTTTTTTT TTTTTTTTTC TAGTTCTTGC TGGGGCAAAG 420 CCCACAGCCC TGTGTCAGTA AATACCTCCC GGGTGGCGGA GACCCCAGCA TTGGTGGGAA 480 AGAAGAGAGG GGCTTTTGGG ACTGTCGCTT TCCTGTCTGT TAAGAGTCAT CATTCTTTAC 540 CAAGATTTGG GGTCAAAATT GGGTCCTGAT TACTGAATGG AAACCCCAAG GTTCAAGGCT 600 GGCTGGTGCA ATACAGGGCG AGATTGCGGA CAGGAAGTGG TGTGGCTGTG TGGGTGTGAA 660 GGAAGGACTT CCTCCCTCTC TGACACTTTC TATGCCGAGG GGGCCTTTCT CAGGCTGCCT 720 TCCTTCCTTC AGCCCAGCAG GCAGCCGCTC TGAGACTTGA GATGCAGATG CCCAGCACAA 780 GTCCTGGTGC CCAGCGGCAG TACGAATAGA ACCACGCAAA TCCAGTCCTC AGCACCTTGT 840 GTACTACCCT AGTCCCTCCT GGAAGAATAC AGCACCTTCT CAGGCTTATA CTCTGCAGAA 900 CTTTTACTTT TTCAGGTAGG AGTAGCCCAG GGGACATTTG TTTTTCAGGA CTCTGGTCCC 960 ATCTCCAGTT ATCTCAGAGG GGACATGACC CTCAGCACCA TGGGCTGCCT TAGTTTTGCT 1020 TCCCTGCTTC CAAATATATT GCTTTCACAT TGAAAGTGGA GGCAGTCTTG ATCCTCCCAA 1080 AATTCAAGCT CAACCTCAAG CTCAACACAG CAGCTAGGGA GGAGGACGCC TGATTCAGTG 1140 GCTAATTTGA ATAAAGTTCT 1160
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