Tag | Content |
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EnhancerAtlas ID | HS018-10964 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr19:10483430-10484860 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2F1 | MA0017.2 | chr19:10484428-10484441 | CCCTTGACCCTTG | - | 6.48 | Six3 | MA0631.1 | chr19:10484515-10484532 | AAAATTGATACCCCAGT | - | 6.09 |
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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 |
GH19I010372 | chr19 | 10483277 | 10484826 |
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Enhancer Sequence | TGCTGGGATT GCAGGCGTGA GCCACTGCAT CCAGCTTTGA CTGTGTTATC AAATCACTCT 60 CCAAAGTCAC ACCATGGAAT TATACTGCCC CTCTGTGAAG GGAGGATACC TCCCTGTGAA 120 ACAATATATA TTTTTTTTAG ATGGAGTCAC CCAGACTGGA GTGCAATGTT GCAATCTTGG 180 TTCACCGCAA CTTCTGCCTT TCAGGTTCAA GTCATTCTCC TGTCTCAGCC TCCTGAGTAG 240 CTGGGACTAC AGGCATGTGC CACCATGCCC AGCTAATTTT TTGTATTTTT TTTTTTTTTG 300 GATAGAGTTT TTGCTCTTGT TGCCCAGGCT GGAGTGCAGT GGCGTGATCT CGGCTCACTG 360 TAACCTCCAC CCCCTGGGTT CAAGCGATTC TCCTGCCTCA GCCTCCTGAG TAGCTGGGAT 420 TACAGGCGCC CGCCACCACG CCCGGCTAAT TTTTTGTATT TTCAGTAGAG ATGGGGTTTC 480 ATCATGTTGA CCAGACTGGT CTCCAACTCC TGACCTCAAG TGATCCACCC GCCTTGGCCT 540 CCCTAAGCGC AAGGATTACA AGTGTGAGCT ACGGCACCTG GCCAATGTTT CATATTTTTG 600 TTTTTTGAGA CCGAGTCTCT GTCACCCAGG CTGGAGTGCA GTGGTGCGAT CTCGGCTCAC 660 TGCAACTCCG CCTCCCAGGT TTAAGTGATT CTCCTGCCTC AGCCTCCCAA GTAGCTGGGA 720 TGTGCGTCAC CACGCCCAGC TAATTTTTAT ATTTTTAGTA GAGACGGGGT TTCACCATGT 780 TGGCCATGCT GGTCTCAAAC TCCTAACCTC AAGTGATCTG CCCGCCTCAG CCTCCCAAAG 840 TGCTGGGATT ACAGGCGTGA CCCACTGTGC CTGGCTTGAG ACAACTTCTT AAAGAACCAG 900 TCAAAAATAA AAAATAAAAA TAAAAGAACT AGTCAGACTG CTTCACTCTC TGGCTTAAAC 960 CTTCCATGGC TCCCCATTGC TCCCGGAGAA TGCCCAACCC CTTGACCCTT GATTCTGAGT 1020 ACCCCCACCC TGGCTTTTGC CTGCTATGCC CCAATTTCAA TTGTTACTTC CCCTTCCAAA 1080 CTCTCAAAAT TGATACCCCA GTCACCCTGA AGGTCTTTCG CTTCCTCAAA CAGATCAAGC 1140 TCTCCGGGCC TCCATGCATG CTGTTCCCTC TGCTGAGCGT GTTTCACATC ACCCGCACAC 1200 CTGTCTGAAT CCTTTAATAA TCAGTCATGG GGGCGGGCAC AGTGGCTCAC ACCTGTAATC 1260 CCAGCACTTT GGGAGGCTGA GGTGGGCGGA TCACGAGGTC AGGAGATCGA GACCATCCTG 1320 GCTAGCACAG TGAAACCCTG TCTCTACTAA AAATACAAAA AATTAGCCAG GCGTGGTGGT 1380 GGGTGCCTAT AGTCCCAGCT CCTCGGGAGG CTGAGGCAGG AGAATGGCGT 1430
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