Tag | Content |
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EnhancerAtlas ID | HS108-02734 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr1:144593160-144594770 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Rhox11 | MA0629.1 | chr1:144593901-144593918 | ACGGTTTACAGCGAAGT | - | 6.29 | ZNF263 | MA0528.1 | chr1:144593535-144593556 | AGAGGCGGAGGGGAGAGAGGG | + | 6.42 |
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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 |
GH01I120414 | chr1 | 144592862 | 144595660 |
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Enhancer Sequence | TCTTGTTGAA AAAGTTTTTC TTTTTCTCAA AGGCTTATTT CAGTGGAAGC CCATCTGCAA 60 AATCTGTTAT TAATTTAAAT TAGAAAATCA TTACAAGTCC CACTGACATG TGGGTTATTG 120 TTTTTGCGAG TGACCTAAGG CCACTTCTCG GGGGAGCTGG GGGTTGCCTT CCCACGTCTG 180 CGCGTCTGCA CCCCATGCCC GGGCCTGGAA GTCAGACTCG GGGGCGGTGC TGCAGCACCA 240 GGCCTGCAGT CCTAAGCGCG GGGTCGCTCC GGGCCCCCGA GGGGGTGTGT CTTCTGCCCC 300 TTTAACCTGG CAGGGGCGGT TCAAGTGGCC CTGGAAATCA GCGATTTGTA GGGTCAAGGG 360 CTGGTGCTTT AAAAGAGAGG CGGAGGGGAG AGAGGGATTT CCCGGTCTCT GCTGCACTCT 420 GTCTATCCGC TCGGTTACTC CTTTTCCTGG CCCGCGCGAA CCCGCTGTGC TGCAGAGGCG 480 GCCATGTACC TTTAAGGCCC CGCTGCGCCT GCGCCTTGGG CTCTCCTGAC GCGCTGAGCG 540 GGACCCTGAG GAGCCAGCTG GCGCAGGCTA TGGGCTGGGC GGCGGTTGAG ACAGCGGCGG 600 TATTGGGAGG GGTAGGTGAG GGTCGCGAGG CTGCGTGAGC ATCTGAGTGA ACGCGGTGCT 660 TTTGGGAACG CGGGACGGGC GACCTGTGGC GCCAGGAGCG GGCCGAGGCG CGGCGCACGG 720 ATGCCGTCTG GATGGGAAGT TACGGTTTAC AGCGAAGTCC ACCCAGCGTT TCCGAGGTGA 780 AGGCGCCGCG CCAGGCCGGG GGGCGGTGAG TCCGGGACCC GCGGGTACAC AGCTGGGTCG 840 AGCTGCGGCT GTCGCAAGTT TTGTTGCGAG CGACGGAGGG CGAGGCGGGG TGGGGGGTTG 900 GGAGGGCATG TGTTCCGGCC CCGCCGAGGC TTAAGTTCCA TGCGTTCGAT TCCTCGCTTG 960 CCGCTGCCGC CCGCAGCCCT CATCTCTTGG GCGCTGGGGA AGAAACTCGC TGGCGGGTGT 1020 TCTGTGGCAT CCCAGGGGGT GGAGGGACGA GCAGCTTCGG GGGCACGTCC TCGTGTATCC 1080 TGTGGAGGAC CCTGACCCCG CACCCCACCC TCGAGGCCAG AAATCAGTTG CCTCTGGGGA 1140 CCTGAGAGGC GAGACCACTC GCGCCCCTGA CTTGCAAAGT TGGGGTCTTT ATTGGCCTCC 1200 GGGATTCTGC TCCTGGCGGT TTCTCCAGGC TGGTGATGGG CAACACATGA GGCGCGTTTG 1260 TAGCCATCAC TGAATCACCT CATGACTAGC GGGGCAGGCC TCTAATTCAC CGCAGGATTT 1320 CCAGTAGGTT GGATTGTGGG GTTGGTGTTT GCACTCCAAA GAGTTGGCGT GATTTCCCTG 1380 TATCTGTCTT TCTGGCTTGT TAGATCTTCT CATTTGGCGT CCTTTCTCCG AAGAGTTAAC 1440 CAAGACGTTT GGCGTGGTTT TCTTGCTTTC CTCCTATCTT TTGCTGCTAG AGCTGCTTTC 1500 AAAAAGAAGT CTTTTCTTGC AGTGATACCT TTTCTTTGGG TTACAGTGTT GTTCATCCTT 1560 TCTTTGCCGA AAGAATGAAT CCCAGTGCTT CACGAAGTTA AAGGAAAGAT 1610
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