Tag | Content |
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EnhancerAtlas ID | HS108-11371 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr13:53275850-53277350 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr13:53276288-53276300 | TTTATTTTTAGA | - | 6.07 | TBX20 | MA0689.1 | chr13:53276064-53276075 | CTTCACACCTC | - | 6.02 | TBX20 | MA0689.1 | chr13:53277048-53277059 | AAGGTGTGAAG | + | 6.32 | TBX21 | MA0690.1 | chr13:53277048-53277058 | AAGGTGTGAA | + | 6.02 |
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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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Enhancer Sequence | ACCAAGGGGG ATTCATCTAA GGTGAAAACT TAACCAGCTC CCTCCTTGCC TGCAACTTTT 60 CATTTCCTAT TTCCTACACA CACACAGACA CACACACACA CACACACACA CTCCCCAGAT 120 TAACATGCCA CTTAAAGCTT CTGCCTACAT TTTCATCTTG ATATTTCCTA CCCCGACCTG 180 AATGCTGTTT TCCTGCTTGT ACCATGCAGC TTCACTTCAC ACCTCTGGTC TTACTCAAAC 240 TCCCTCTGCC TGGAATGCAA ATCTTCTGTC ACCTTCACTT GGCTAATTCC TGCTCATCCT 300 TGAAAATCTA GAGAGTAGAC ATTCTCCAAG AAGCCCATTG CTTCCATCTT TATCAAGGCT 360 TTGTCTGGTG TGCCTTGATT ATCTGTATCT CTCATAAGAC CATATGCTCT TCTGGGCTGG 420 GATCACTAAA TCATTCTCTT TATTTTTAGA ACCCAGTACA GGTTGCTGAG CCATGGGGGT 480 GGGAGATGAT ATGCAGAACC ATTGACGCAT ATTTCTTTCG TTAATAGAGT AACAGCAGTT 540 TTAAAGACTA AACGTGGAAT TCATAACTGC AGGAAGTAGC TGCTTCCTGA GAACAGTGTG 600 ACCATTACAT GTCATTACGG TGCCTTTCCT TCGTCTCTTT TCTCCAGAGA CCTAGGCTTG 660 CTGTGTATTT CATTAAATGG AGGGATCTGA GTGTTCACCT GAAAACCAGG TTTTTAAAAT 720 TCTGTATCAT TTTTATAGAC TTTAATTGGA AAACACCAGT ATTAGGGATT TACTGTGGAA 780 TACACAATAA TAAGGTATAT TCTGAATATG AGAGTGTAGT GAGATCATGG CATCAAGACC 840 TTTCTGTCGT CTCAGAATCT GTGTTTTGGA AAACTTCTAT TTTCCTTAGG AAAGTTGTTT 900 ATCTATCAAA CGGTGGGATG CAAAACTGAA ATGTCAAAAA TATAAAATAC CTGCTCATCC 960 TCTTGATCTA ATATTTCAAT TTCTAAAGAC AGTCCTTGTT CCTGAGAGAC TTTATGTCAT 1020 TATACATAAA TAAGCTATTC CTCCTCAGCT GTATCTGCCA AGCAACACTG TCAGCCCTGT 1080 AACTAGGAGA GTAACTTATT GGTAATTGGA CTACAGCCGC AGCCTGATTT GTACTACAAA 1140 GGTAAAAATC ATTATGCTTC TTCATGCCCA GTGACCACTT ACTGAAAACA GATTGAGAAA 1200 GGTGTGAAGA CCTGCTTTTC AGAATGTCAA TAAAGTCCTT CCTCCCCACA AGTCTGATTT 1260 ATCTTCGACT GCATTTTTCT TTATCCTAGT GCTGTTTCCC TGGAGGTGAC TCTTAACACA 1320 GGTCACATGC CAGTGCACTC AAATAATTCC CCATGAGCTT CCAGATTGAG GCTAAAAATG 1380 TTCACTTTTA GGTAGATTCC ATTATATATC CTTTCCTTTT TCTGTGTGTT TTTATCTGGG 1440 AATTCTGGGG ACAAAAAAGA TTAAGAACAG TTGAGGAATT CTGTACAAAT AACAATGACT 1500
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