Tag | Content |
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EnhancerAtlas ID | HS018-23850 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr9:99160710-99162160 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr9:99162110-99162122 | AAACAAACAAAC | - | 6.32 | Foxo1 | MA0480.1 | chr9:99161520-99161531 | TGTAAACAGCA | - | 6.14 | Nr2f6(var.2) | MA0728.1 | chr9:99161883-99161898 | GAGGTCAGGAGTTCA | + | 6.22 | SOX10 | MA0442.2 | chr9:99160808-99160819 | AAAACAAAGCA | + | 6.02 |
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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 |
GH09I096398 | chr9 | 99160521 | 99162420 |
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Enhancer Sequence | ACTTATAGTC CCAGCTATTT AGGAGGCTGA GGTAGGAGGA TCACTTGAGG CCAGGAGTTC 60 GAAGCAACAT AGCACAAAAC ATTTTTGTTT TGTCTCTAAA AACAAAGCAA AAGCCTTTCT 120 TAAGGGACAT CAGTAAAAAT GGTGAGGCAG GTAACTCCAA TGGCCCATCC CTCCACAGAT 180 GACTAAAAAA TCAAGCAAAA ACTGTCAGAT CAGCTTTGTC ACAACTCCAG AAAATACATT 240 TATAGCAACT CAGCAAACTG AATAAAAAAG CAACTTGAAA CAGTAGAAAA GCTTTGCAGC 300 ATTTTGACTT GCCCTCTCTC TTTCCCTTCC CCAGTGGCAG TCTTGAAGAC AGCAGCCTGC 360 ATTCTCAGTC TGGGAACCTA CTCCTTTAGT CCCTGCTTCC AGAGGAAGAA ATTCTGAAAG 420 AATTGCGTTT GCCTGTTTTG AGCCTGCGGG TTACCTAAAG GACTGACACA AGACATTGGT 480 CTTTGCTTTC CCTAACTTGG AACAGGGCAG AGAGGTGTCT CTTCAGAGGG TATTGCTCAA 540 AAAACTTGTA AGGCAAATAA TCTGCAGCCA CCTGGGGCAA AAGATTTCAG TTGAAGCAAA 600 CAGACACACC AACAGCCTGA GAGGAAAAGC TGGGAGAAAG TTTCTTTTGG AAATTTGGGC 660 ATTCAACAAT GTCCACTTAT ACTAAGGTTA GGAATTTAGA AAGTCATGCA TATATGCCCA 720 GGGCAGGAAG CATGCTCAGA AAAGATCTGA AAAGACCCTT TAGCTGAACT TTCGGCTCAG 780 CACAAGCAGG AAATGAGGCT ACAGTAGAGT TGTAAACAGC AGGGCTAAGC AACCACAGTG 840 TCCCCCAACA CAGCCATTCT GCAAAGACTG GGAGAAGGTG GTTGTCCTCC TTTCTGTCTA 900 CTCTTTTTTG GGGGATGGTG GAGGGAAGCT CTAGGTATTC AAAAAAGTCT GTCAAAACAC 960 TAGTGGTGGC TCAGCCTATA ATCCCAGTGA CTCAGGTGGG AGGATCACTT GAGCAAAGGA 1020 GTTCAAGGCT ACAGTGAGTT ATGATGCCCC TGCACTGTAG CCTGAGTGAC AGAGTGAGAC 1080 CCCATCTCTA AAAAACAAAA AACAAAGTGT CGGGCGTGGT AGCTTACGCC TATAATCCCA 1140 GCACTTTGAG AGGCTGAGGC CAGTGGATCA CCTGAGGTCA GGAGTTCAAG ACCAGCCTGG 1200 CCAACATGGC GAAACCCCAT CTCTACTAAA AATACAAAAA TTAGCCAGGC ATAGTGGCAC 1260 ACACCACTAG TCCCAGCTAC TCAGGAGGCT GACGCAGGAG AATTGCTTGA ACCCGAGAGG 1320 TGGAGGTTGC AGTGAGCTGA GATCGCGCCA CTGCATCCTG GCCTGGGTGA CAGAGCAAGA 1380 CTCCATCTCA AAAAAACAAA AAACAAACAA ACAAAGCATC AGCTGAACAC AGGCTAAGAA 1440 AGAGACTTTA 1450
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