Tag | Content |
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EnhancerAtlas ID | HS019-00265 |
Organism | Homo sapiens |
Tissue/cell | CD20+ |
Coordinate | chr1:24321500-24322880 |
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) |
IRF9 | MA0653.1 | chr1:24322412-24322427 | AACAAAAGCGAAACT | + | 6.52 | ZBTB18 | MA0698.1 | chr1:24322512-24322525 | AAACATCTGTATG | - | 6.01 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_02205 | chr1:24321450-24322858 | Aorta |
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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 |
GH01I023994 | chr1 | 24321451 | 24322858 |
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Enhancer Sequence | TCCCGGGCGG CGCTCGCCGG CGCGGCGGCA AAGACTGATT GTGGGTCTTA AGACCCTCCC 60 ATAAGAGGGT CCCATCCTAT ACCCTGAGGT AAGGAATGCT GATGTCATGA AGCCTCCGTG 120 AAAATCCACG AGGACAGGGT TCAGGAGCTT CTGGATACTT GAAAAAGTGG AGCCTCCTGA 180 AGGGTGGCAC AACCAGGGAG GCCATGGAAG CTCTGAGCCC CTTCCCCCAT ACCTTGCCTT 240 ACATGTCCCT TCTTCTGTAT CCCTGGCAAT ATCCTATATA ATAAACCAGT AAATGTAAGT 300 GTTTCTCTGA ATTCTGTGAG CCGCTCCAGC AAATTAATTG AACTCAAAGA GGGGGTCATG 360 GGAACCTCAA CTTGAAGCTG GTTGGTCAGA AGTTCTGGAG GCCTGGACTT ATGACTGATG 420 TTTGTATGTA TTGTTGGGGG TAGGGGCAGT CTTGGGGACT GAGCCCTCAA CCTGTGGGAT 480 CTGGCACTGT CTTAGGGTAC ATAGTGTTAG AGCCGAATTG GAGAACACCC AGCTGGTGTC 540 TGCTGCTTGG TGTGTGTGGG AAAAAACCGA CTCATTTGGT CACAGAAATC TTTTGTGTTG 600 ACGTGGTTGT TGTGGTATGA GAGTAGGGGA AAAACACAGA GTTCTCGGGG CGCGGGGGCG 660 GGGGGGCTCA CGGCTGTAAT CCCACCACTT TGGGAGGCCG AGATGGGTGG ATTACCTGAG 720 TTCAGGAGTT AGTGACCACC CTGGCCAACG TGGTGAAACC CCATCTCTAC TAAAAATACA 780 AACATTAGCC GGGCGTGGTG GCGGGTGCCT GTAATCCCAG CTACTCAGGA GGCTGAGGCA 840 GGAGAATCGC TTGAACCCAG GAGGCAGAGG TTGCAGTAAG CTGAGATTGC ACCACCGCAC 900 TCCAGCCTGG GCAACAAAAG CGAAACTCCA TCTCAAAAAA CAAAAAACAA AAGCCACAGA 960 GTTTTTCCTA CACAGGGTCT TTATTTTCAA ATGGGGGCTC CTATGTAGAT GTAAACATCT 1020 GTATGCTTTC CTCCTGTTAA TTTGCATTAT GTCAATTTAA TTTGCAGACC CAGTTGGAGA 1080 CCCTAAGAGG GCAGAGAAAA GTCGTGCCCC CCTATTCCCT TCTCAGGCCA GGTTGCAGTA 1140 CTTGTCCATT CACTTTACAA TTGGCAAAGA AAATCACAAG GCACCCACAT AGATCACCTG 1200 GGTTCCACGT ATATTCATCC CAACCCCCAT TCTATTATTT AATGATTTAT TTATTTATTT 1260 ATTTTGAGAG TCTCACTCTG TCACCCAGGC TGGAGTGCAG TGGTGGGATC TTGGCTCACT 1320 GCAACCTCCT CCTGCCGGGT TCAAGCGACT CTCCTGCCTT AGCCTCCTGA GTAGCTGGGA 1380
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