Tag | Content |
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EnhancerAtlas ID | HS019-01809 |
Organism | Homo sapiens |
Tissue/cell | CD20+ |
Coordinate | chr10:3811130-3812400 |
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) |
NKX2-3 | MA0672.1 | chr10:3811288-3811298 | TTCAAGTGGT | - | 6.02 | POU2F2 | MA0507.1 | chr10:3812060-3812073 | AAATGCAAATGAA | - | 6.59 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_09469 | chr10:3809960-3813591 | CD14 | SE_53372 | chr10:3811179-3812762 | Spleen | SE_62321 | chr10:3783568-3829344 | Tonsil |
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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 |
GH10I003769 | chr10 | 3811668 | 3812392 |
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Enhancer Sequence | TGAAAATAAT CAACCAAAAA TAACAAAATT CAATTAATCA AAACAGAACA AAATAAAATG 60 AGCCAAACAG CATATCTGAA TATAAGCATA ATAATTGTCG TTGGACAAAC CTTTGTCAAA 120 TCAAATTGGC TTCTAGCACA CGGGCTGATA CTTTGTGATT CAAGTGGTGT TCTACCCACA 180 TAATTCATTT AGTTGCAAAG AATGTAACAA ATAATGCAAT TATTCCAGAG GATCACGGTG 240 AGACATCTAT TTGGTGGTGC CTTAAGCAGA GTGCCCTGAT TCAGAAGAAT TAGACCAATC 300 TCTGGATTCA CAGCCACTCA TGAAAACTGT AGGCCGGGCA CGGTGGCTCA TGCCTGTAAT 360 CCCAGCACTT TGGGAGGCCA AGGCGGGTGG ATCACGAGGT CAGGTGATCG AGACCATCCT 420 GGCTAACATG GTGAAACCCC GTCTCTACCA AAAATACAAA AAGAAATTAG CTGGGAGTGG 480 TGGCGGGCAC CTGTAGTCCC AGCTACTCGG GAGGCTGAGG CAGGAGAATC GCTTGAACCC 540 AGGAGGTGGA GGTTGCCGTG AGCCGAGATC ACGCTACTGC ACTCCAATCT GGGTGACCGA 600 GCAATACTCC GTCTAAAAAA AAAAAGTAAT AATAATAATA AAATAGGAAA CTGCAGTAAC 660 TCGGGACATC TGGGTTCCTT GTCTTTTGTC AAAATCACAG GGAATTCAAC TCACTGAATC 720 TATTGGTCAA TTCAATTCCG CCATTGGTCA GTATGACTCG GCTTTTGACA GAGAGTTTTA 780 CCCAAAGACT TGCAGAACTT CCTTCCTGCA AGATTTCAGA AGCACAGCAA GCATTGCAAG 840 AGGAAACTAC CTTATAAATC ATACAAACCC AGCATCGTGT TCTTTGCTTG TCCTTGCCTG 900 AATTTACTGG AAAATCATGT TGTGAAACCT AAATGCAAAT GAACCTTTCT TATTGCAAAT 960 TAAAAACTAA ATCCATTTTC AACTGAATTC AATGGGAAAA ACAAGAATTA TTTTCCTAAA 1020 AAGTAAATAT CCACCACTCC GTAATAATTG TGATCCGCTG TGGCTTATGT GTCGTGTCTC 1080 AGGACATGGA CTCGGTCCTC TGCATACCTT ACCTCTCATC CTGCAATAAT CCTGAACAGG 1140 TTCCCATTAT CCCCATTTTA GAGGTAAGAA AAACACAGCT CTAAGGGTCT AAGTAACAAT 1200 CCCAAAGCCA GAAATCAGTG CAATCTTTCC TTGTAGGTTC CATAAAGGAA GACTCCTCAT 1260 TGCTCGCTCA 1270
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