Tag | Content |
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EnhancerAtlas ID | HS018-02260 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr1:236588060-236589140 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:236588254-236588275 | TGTGGCTTTCAGTTTTTGTCT | + | 6.05 | Lhx3 | MA0135.1 | chr1:236588168-236588181 | TAATTAATTAACT | + | 6.64 |
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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 |
GH01I236425 | chr1 | 236588721 | 236588850 |
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Enhancer Sequence | GGGCATAAGC TGCAGCGTGG TCCAGCCCAA TGGAAGAGTG CTGGCCTATA ACCCAGAGGT 60 GGAGGGACTC TGCTACAACT TTGTCTTTTC TGCCATGAGG GTTTTCCTTA ATTAATTAAC 120 TAATTTGTTT ATGGATTTTT TCCTGTCTTG TACAAATGCC CTCAGAATAT TTTGGATTTC 180 TAGCCACATA AAGTTGTGGC TTTCAGTTTT TGTCTCCATA TGTCCCAAGG GACCTTCTGG 240 GAGGTTACGA GCAAAGTGTT GGGAGCCAGG TGGCCCCCGT CGCAGGCAGC CACCTCTTCC 300 TCCAGGGAAT ACCAGTCGGT CTCCCTGGGG ATGGGGTCCT CATCCAGCCA GGTGGTTTTG 360 TCTGTGGCCC AAGTGGGGAC ATTAAACCCA CTATGGCAAG ATGAGCTCTT TGGCGTGTTG 420 GAAGCAGCAG CGCTAAGCAC AGCTGGGTGC GCTCGCCAGG GGCTCTGTGC CGAGAGAGCA 480 GTTGAGTACC AAATGCTTTT TCCCGTTTTC TTTCTTCATT AGCACCTGGG CCACAGACTG 540 CCATGGCTGT GTACCTCGAT GCCCCTGGGG GTCAGGAGAA CACATGGGCA GCAGCAAGGG 600 AAGCAGCAGC TGAGGGGATG GGCAGGGTCA CTGCCTTTGC CTTAGCAGCA ACCAGGGCAC 660 CAGGGAAACT CCCCTGGGGA ACTCCCTGGT CTCTCTCCTT CCTTTCTGCA AACCTCTGTC 720 TGCAAAGGAC CGCCCCCGTG GCTGACCTGG GGATGCACTT CACAAACAGT GCCTGTACAG 780 CTGCCCCAAG TGGCCAGTGA TGGTCACCAA GCTAGTTGTA TTGCTAAGAG AGCTTGCACC 840 TGTCCCTTGA TAAGTGGGAC TTAAGCAGCA ACCGGTTAGG GGGATGTGCT ACCACCGTCT 900 TTACAGATGG GAGCCTCAAG AGACCACCTG CCAAACACAG GCCCAAACTG ACAGCTCTGG 960 GGTCCAGTCA GTTCACAACA GTTTTCATCT TGGGATGAGA TACCAAACAA TCAACAAAGA 1020 CAACACAGCA TTGCATAGGC CAGAGTGCAA ATCTTCCAGT AATTGTCAAT TCTATCCCAG 1080
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