Tag | Content |
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EnhancerAtlas ID | HS108-28988 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr3:149886160-149887980 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr3:149887586-149887601 | AAGTGACTCAGCACT | + | 6.51 | Nfe2l2 | MA0150.2 | chr3:149887584-149887599 | GAAAGTGACTCAGCA | + | 6.43 | TFAP2A | MA0003.3 | chr3:149887606-149887617 | TGCCTGAGGCA | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr3 | 149886569 | 149886600 | chr3 | 149886600 | 149886808 |
| Enhancer Sequence | TCAGGTAGGA ACAGACAGAT CCAATCACAT GAAACCTCAA TGAGTTGACA TCCTCTTAAG 60 AAAACCAAGT ACTCTAACGT GAGCACCTTG GGTCAGCATA AGCGTGAACC AAAAAGAGTA 120 TCTCAGGCAG TGCCTGGCAT CAGGACCACT CTAACATACC CACATGTAGG TAACTGAGGC 180 TCCATATAAA TAAAAAGTGC TGTGTAAGTG ACTGCCAGGA TATTGCTAGT CTAGTGAGCT 240 AATCTTTTTT CTTTTTTTCA ACTATTTCTC TCCTAAAAAT AAAAAAAGAA AAAAAGAAAA 300 AAGAAAACAA AAACCTTAAG ATCCAGACAA CTGGGTCAAA AGATGTGTTC TCTTTTACCT 360 AATAGGGAAA CTTGCCTTTG CTTTCTTAGC TTAAATCATC TGAGAACGTT GGGAGTGACA 420 GGGACCTTGG AGATCATCTA GGTTATTCTC CACATGTCAC CAAGCCAGAA AGCTCTGGAA 480 ATTGGCTGCC TCCATGGGAC AGTCATCGCA GACTTTGCCA AAGCAAAAGT GCTGATGTCA 540 CTCATCATAC TAGCAGTTGG CTGCTAAGTG ATTAAGATAA AAGGGGCCAA GCTAGTGAAA 600 GCTTGTGGGG GTAAGGAAGG AGGGCACAAT GTGACTTACA TGCAAGAAGA GTTTGTATAA 660 TGGAAAGAGT ACTGGGCTTT TATTGACTAT GTGACCTTGG GCATTAATCT CCTTGGATTT 720 TCCTCACCTA CAATAAATAA TCTAAGCAGT TAACACTTAC TGTGTTCTTA GTACTTCATA 780 TGAACTGTTC ATGTTGAAAC TTCACAATAA TCTATCAGCC AGGGCCTACT ATTTTCTCCA 840 TTTACAGATG AGAAAACTGA GGCACAACGA GGTTAAGTTA CTTGCCCAAG GCCACTCAAT 900 CAAATTCAGG CAGTCCAACT TCAGAGTCTG AGCTTTGTCA ACTGAGAGGG TCAAAGAGAT 960 GAATGCTAAA GACCCTTTGC ACCTGTGCTA TTAATTTTTC CCTCCTGTTA AATTGGGATA 1020 ATAATAAAGT TGTTGCCAAG ATTATGAGAT AATGCAGGTT AAGTCCTTAG CGCAGTGCCT 1080 GAAGCATAAG TGCTCAGTAA ATGTCAGCTA TTACTATTGT TCATACTTGT ACTCTTGCCA 1140 TTAACATTTT ATGGAACAAA TCACTTCTGT CATCTCAACA GCTGCCTGAG TGCACAGTTA 1200 TTCCAACTAA ACTGATTAAT AAATTCAAAC AACGAGTCAA TTTAATCATA AAATCAAGCA 1260 AGCCTGAATT GATGCTGGAG TGAATTGCCT AGTTAGTCTT AAGCGGTGCT GTCTGATAGA 1320 ACTTTCTGTG ATAATGAAAA TGCTCTATAT GTGTGCTGTC TGATACAGTA GCCAGTAGCT 1380 GCACGCGCCT CCTGAGCACT TGAAATGTGA CTTGAATGTG ACTTGAAAGT GACTCAGCAC 1440 TTTCAGTGCC TGAGGCACTG AAAATTTAAT ATATTTAATT TTACTTAATT TACATTTTTA 1500 TTTTAGTCAC CTCATGTGGC TAGTGGCTGC CATGTTGGTC AGTTCAGGCA AAGCCTAGAT 1560 GGCAGCCAGA AACCCTTGGT GAGGGGACGC CAAGGTGTCA GGCACAAGAA GGAAATCCAG 1620 GAACTCTCTG GCCACAACTG TTTTGTTAAC AGATGTCTTA AAGAATCACA AATATTCTAA 1680 TGCTGGGGGT TCCCTCCCCC TGGTATGTGG GAATGTATAT TTTGGGGGAG AGGGCAGGAA 1740 AGAAGACAAT TCCACTTTCC TCACCAGGAT GCCCCCAGTG AATTCTCAGT AGATTTTAAT 1800 TCCTTATTGT TGTTAAAAAT 1820
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