Tag | Content |
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EnhancerAtlas ID | HS010-02742 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr20:5058570-5059600 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxq1 | MA0040.1 | chr20:5058985-5058996 | AATAAACAATG | - | 6.02 | IRF1 | MA0050.2 | chr20:5059274-5059295 | AGAGGGAAAGTGAAACTGGCG | - | 7.29 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr20 | 5058710 | 5058848 | chr20 | 5059148 | 5059500 |
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| Number: 1 | ID | Chromosome | Start | End |
GH20I005077 | chr20 | 5057957 | 5063045 |
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Enhancer Sequence | AGTGAGTATT AAGGAGAAAA ATGAATCAGG ATCAGAGATA AGTAGCATGG GGCCTGGGGG 60 CTTAGCTTCA CTGAGGTGAT ATTTGTATCA ACACTTCATG AATGACACAC AGACATCAAC 120 CTCACTGCCC CATGGAAGTA TAATCTGAGG CAGAGCAGTA GAAACTGGCT CAGGAGAAAA 180 GGGAGGATGC AGACATGTCA ATTAGACACA GCCAAAGATG CTTCATGATT TCCTGGGTGT 240 GTGACCTGTG TAGACGCCCA GGGACCCATG CTTAGAGGGA CTCTGTGCTT GATTTAATGC 300 TCTGCTGTCA CCCTCTTGAA GTTTTTAATC AGTTTTTAAA CAAGGGACTG CGCATTTTCA 360 TTTGGCACTG GGCCCCACAA GTTACAAGTT ATGTAGCCGG TCCTTCACTC TGTTGAATAA 420 ACAATGGCTT CTCCCTATCA CCCTCTTTGG AAGCACAGAT ACTCCCAGCA AATGCTAATC 480 ATTCATGTTT CTAATTTCCT GGGGTGACTT GTTTTTCCTC TAACAGGTGT GAAGTATGAG 540 ATAGAGACTG TATCATCCAG GGTAGGCTGG GATATGCTGC ATGACAGAAA CCCCCAAATC 600 TAGTGGCTTA ACACAACAAA GGTGTACTTC ACTCTCGCAC TTTGTGTTCA TTATGGGTCA 660 ACGCGGGGCT CTGTTGTGCA TCACGATCAC TCTAGGACCG TGGCAGAGGG AAAGTGAAAC 720 TGGCGGTTAG AGCCGCTACT CAGAAATGAC ACATATTGCT TGAACTCACA TTTCCTCGCC 780 AAGGCAAGTC ATGTGGCGAC GCCCTCCTTT AAGAGATGAG GAAGTTCAAT CCAAACATGA 840 GCCCACAGAA CTGGGCCACT TGTCTTTTGG TGTGTTTTTT TGAGACACAG ACTCTTGCTC 900 TGTTGCCCAG GCTGGACTGC AGTGGTGTGA TCATGGTTCC CTGCAGCCTC AACCTCCTGG 960 CCTCGAGCAA TCCTCCTGCC TCAGCCTTCC AAGTAGCTGG GACTACAAGC ATGCACCAAT 1020 GGGCCCAGCC 1030
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