Tag | Content |
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EnhancerAtlas ID | HS010-00446 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr1:212015920-212016870 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CUX1 | MA0754.1 | chr1:212016809-212016819 | TTATCGATTA | - | 6.02 | CUX2 | MA0755.1 | chr1:212016809-212016819 | TTATCGATTA | - | 6.02 | IRF1 | MA0050.2 | chr1:212016667-212016688 | TCTTCCTTTCACTTTCACTTA | + | 7.86 | PRDM1 | MA0508.2 | chr1:212016675-212016685 | TCACTTTCAC | + | 6.02 | RAX | MA0718.1 | chr1:212016701-212016711 | GTTAATTGGC | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 212016062 | 212016200 | chr1 | 212016200 | 212016763 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I211843 | chr1 | 212016343 | 212016742 |
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Enhancer Sequence | GTCATCCACG CTTTGTTGTC CCATTGATAG AGCACAGAAA GAGTCAATTT AGTGTAATTC 60 TTAAGGGCTA GAATTTTCAG AATGGTAAAT GAGCATTGGC TTCTGCCCAG TCATCAGTTA 120 CATTAGTCCC TAACAAGAGC CTTAGTCATC CTTTGAAGCT TTGAAGTCAG GCATTGACTT 180 CTCTCTAGCT GTGAAAGTTC TAGATGGCAT CTCCTCCCAA TATAAATCTA TTCTGTCGAC 240 ATTGAAAATC TAGGGTGTAG TGTAGCCCCC TTCATCAATC ATCTTAGCTA GATCTTCTGG 300 ATAACTTGCT ACAGTTTCTA CATCAGCACT TGCTGCTTCA CTTTGCACTT TATGTTATGG 360 AAATGGCTTC TTTCCTTAAA CCTCATGAAC CAACCTCTGC TAGCTTTCAA CTTTTCTTTT 420 GCAGCTTCCT CACCTGTCTC AGCCTTCATC AAATTAAAGA GTTAGGGCCT TGCTCTGGAT 480 TAGACTTTAG CTTAAGTAAA TGTTGTGGCT GATTTGATCT ATCTAGACCA CAAACTTTCT 540 CCCTATCTGC AGTAAGCCTG TTTTGCTTTC TTATTCATGT GTTTACTACA GTAGCACTTT 600 TAATTTCCTT CAATAACTTT TTCTTTGCAG TCACAACCTG GGTAACTGGT GAAAAAGGCC 660 TAGTTTTTGG CCTGTCTTGG CTTTCAACCT GCCTTCCTCA CTAAGCTTCA TTATGTCCAG 720 CTTTTGATTT AAAGTGAAAA ATGCAACTCT TCCTTTCACT TTCACTTAGA GGCCATTGTA 780 GGTTAATTGG CCTAATTTCA ATTTTGTTGT GCCTCAAGGA ATAGGGAGGC TCAAGGAGAG 840 GAAGAAAGAT GGGAATGGCC AGTTGGTGGA AAGAACAGAA CACACACATT TATCGATTAA 900 GTTCACCCAC CTTCTATGAG CAAGGTTCTT GGAACTCCAA AACAATTACA 950
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