Tag | Content |
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EnhancerAtlas ID | HS018-23015 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr8:123921500-123922930 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr8:123921768-123921780 | CCTAAAAATAGA | + | 6.14 | ZNF263 | MA0528.1 | chr8:123921829-123921850 | CCCCTCCTCCTCCTCTCCCCC | - | 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: 2 | ID | Chromosome | Start | End |
GH08I122909 | chr8 | 123921761 | 123921910 | GH08I122910 | chr8 | 123922641 | 123923684 |
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Enhancer Sequence | GTCTCTACTA AAAATACAAA AAATTAGCCA GGCATGGTGG TGCATGCCTG TAGTCCCAGC 60 TACTAAGGAG GCTGAGGCAG GAGAATGGCT TGAACCCAGG AGGTGGAGGT TGCAGTGAAT 120 AAAGATCGTG CCACTGCACT CCAGCCTGGG TGACAGAGCA AGAATCTGTC TCAAAAAGAA 180 AAAAAAAAAA AAGTGGGGCA GGCGTTAGGG GACAACTTTG TGAATACTCG TTGCTCTTTA 240 ATTTTTAGAG TTTGCATCCC TGGAGGTTCC TAAAAATAGA CAAAACACCC AACACTCTTA 300 TTCACTCGCC TTGGGGCTGG ACAGATAATC CCCTCCTCCT CCTCTCCCCC CCACAACCTG 360 TTCCTCCTGA TTCTCTCTCA CTCAAGCAGA AACCTGGGAG GTGCCAGGGC GTGGTATTCA 420 CACTGGCTTC CACATTCACT CCAGCCTCCG GAGTGATCCT GATCTTCTGC ACTCCATCCC 480 CACTGCTGCT GTCCTGTGGG CTGCATCTCA CACCTGGCCT CTTCCGGAAG TCTTGGGCTT 540 CACTCCCTCC CATCCATCTT GCAGCCTGCA GCCAGGGCAA TCCTGGAAGG CAGGGGTCTC 600 CCCATGCTTC TTGCCCGCCT AAAACCCTGC CTTCATTGGC TGCCCCAGGA GCCCAGGTTG 660 CCCAGTTGCC CCTCCCACCA GCTTACCTCT CACTGGAAGG GCAGCCTCTC AGAAAAGATT 720 TGCTCTCACT TCCCTTAAAC ACACCATGCC CCTGAGCCTC TGCTGTTCTG TCTACTCAGA 780 CATCCTCCTT CCCTCTCTTG TCCACCCAGT AAACCTCTGC TTGCTTCTCA GAGCCCAGCT 840 CAGGAATCTC TTCCTCCGAG AAATCAAAGT AGGGAAAAAA AAAAAATCAG AGCTGGACAA 900 AAGACTAGAG GGACCTAGTA ATAATCATAA TGACTTTCTT AGATTCAGGG CACTGCCCCG 960 GGCACATCGC ATTACCTTAT TCAGTCCCCA CTATGACTCT AAAAGTAGGT CTCGGCATTA 1020 TCTTGGTTTT GCAGATGAGG ACACAGGACT TGAGAGTTCA GTGACATGCC CCAAAACACA 1080 GCCAATTCAT TGTAGAATTG TGATGGAAGC TTAAGTTCAC CTGATGGAGG TTTGCATTTT 1140 TGTCAGCTGC AACATCCTGC TGGCTAATGC AGTGTTTCTC AAACTGCCAG TCATGATGTA 1200 TCCGTGAGTT GTGAAATCGG TTTAGCAGGC AGGGCTGGCT GCATGATGTG TGGGGCTCAG 1260 TGCAAAATGA AGATGCAGGA CCCCTGTTCA AAAGGCAGGC AAAAGGCTTC TTCCTTTCTT 1320 TGGCAGTCTC TCAGCTTGTT GTGGCATTTT TTATGCGTAC TTTAATGTCA TACTCCCTCA 1380 GGCACGGGGT TACTGGTGGG GCAGTACGGA CCAACCCTCA CCCTGGAGGC 1430
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