Tag | Content |
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EnhancerAtlas ID | HS010-00134 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr1:53832950-53834090 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SPI1 | MA0080.4 | chr1:53833921-53833935 | TGCTTCCTCTTTTC | - | 6 | SPIC | MA0687.1 | chr1:53833921-53833935 | TGCTTCCTCTTTTC | - | 6.1 |
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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 |
GH01I053367 | chr1 | 53832884 | 53834793 |
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Enhancer Sequence | TGGGGAAGAG ATAGGGAGGA AGCAGGATTT GGTAGAGAGA AGGTGAACAG TGACGCAGCT 60 CCAACGGAGT TTCAGCCATC CCTGGAGCCC ATGTGGCCCA TCTAAATTAT CCCATGGGAG 120 GTCAAAATGT CTGCACCTTT ACATCGTAGC CATGATCAGT CGCTGGTCAG CCCTTCACGA 180 AACGAGGGCG ATGATAGCTC CTAACTCCTA GGTCAGAAGG GTTAAGTGAA ATGTCCTGAG 240 CGCTGACAGC TGCCATACAC AGCCACCCCT GGAGGGAGTT CTATGGTTAT CTTCCCCTTA 300 CAGAGGGGAA AAGCCAGCCT CAGAGATGAC AAGCAACTTC CCAAGGCCAC CCAGCTAGTA 360 ATGGCAGAGC CAGGACTTAA ACTGAGGTGT GCCTGATGCA GAGCTTGAGT CCCTGAGAGC 420 TGCTGGGGGA ACCCAGAAGC CCGGCAGGTG CCTGGCTCCA CACCCAGCTC CCTGGCACTC 480 ACTTCCCCAC ACCCCATGCC CTGTGCAGCG TCCTCCCAGT CACTTCCCAT CCCCATGCTC 540 CAAGCCCCAG GGCTATCTCC CCAGGGGACC CCATCAGGGG TTGCCTGGCC TCCCTCCCTT 600 CCCCACAACC AGTGATCCAG CCTCCCAGGA CCCCTCACAA TTCTCCAAGC ACGGCCCTCA 660 CCTGCCTGCC CCCATGCCCT CTGTCCCCAA GTCCTTTTTC CCCATGCCCT CTTTCCCCTT 720 GTCTTACCTT TTAAAGTGGT ACACAGAGGC CTAACTGTCC CAGTCAGATG CAACCTTCTT 780 CACGAAACCC TTTTGACTGG CACTCTCCCT CCCTTCTGTC TCCCAAAAGA CTCAATGTCT 840 ATCTCAATCA CAGCTGAGTT GCCTTGGGTC TGATATGAAT CTGCTTCCCC CAACAAACCA 900 AAGCTTCCGG GGAGGGGAGA AAGTACAAGT TAGGAGCTCT CACTCAGCCA GCTGCATGGC 960 CCGAGGCTGG CTGCTTCCTC TTTTCTGAAC CTTAGATTGC TTATCTGTAA AATGGAGCTA 1020 ACAGAGCACA TTGCCAGGCA CAAAAAAGGT GCTCAGTAAA TGCTGTCTCT CAGGCTTTAG 1080 CCCGGGTGCA ACTTTGTATC TGCCTCCAGG GCTGCAAACA CTCCCTGCCC AGCTGTCTCT 1140
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