Tag | Content |
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EnhancerAtlas ID | HS019-16020 |
Organism | Homo sapiens |
Tissue/cell | CD20+ |
Coordinate | chr9:96383040-96384220 |
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) |
NFAT5 | MA0606.1 | chr9:96383049-96383059 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr9:96383049-96383059 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr9:96383049-96383059 | ATTTTCCATT | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_65512 | chr9:96383148-96384654 | Pancreatic_islets |
|
| Number: 1 | ID | Chromosome | Start | End |
GH09I093621 | chr9 | 96383149 | 96384654 |
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Enhancer Sequence | GAGGAAAATA TTTTCCATTT TTCTGTAGTT ATTATTCTCC TCTTATTTTT CGTTTTGCCA 60 ATTTTCTGAA TAATTTCTTA GGGGGCATTT AGAAAGCCCT AATTCTGGTA CAATAAAATA 120 AATGCCCAGT GTCGGCAAAC AGTCTCTTCT GTGAGAACAG GATGGCCCCT AATGGAGCTC 180 ACTGTGCTGG AGCTTGCACA ATCGAAGCCC TGGATCCTCG TTAGGTGCTG TCTCCTTGGC 240 ATATAGCCAC AGCTAGTGGC AGAGCCAGGC TGAATGCCCT GAGACTTAGT TTCACCTGCC 300 AAGTGGCCAC TGTCGGGGTT GGTGGCACAG GCAGCAGGGG TTGGAGCAGC AATGCAGATG 360 TAGGGTCGGT GCTAGCAGGG GATCTGGCCT GGATCCCTGT GGAGGGTCTA CTTCCTTCAG 420 CCTTGGAGGG GCAGGAGGGG CAGCCCAGTG GTCACCCCCC ACAACCCTGG TGGGCGGGCC 480 CTGGATGCAG CCCCTGCCTC TGGCCCAGGC ACCTAGGTGG TGAGGGGGTG CTGAGGCCTT 540 TGGTTCTCTG AGCTTCTTTT GGGCGGCAGA AGGACCCTTC CACCATGACC ACCTCTCTTT 600 TCTCTCAGTC TCTTGGGGTC TCCTGCACAA AGCAGTAAAT GACTGACCAA GGCAGCTGTC 660 CTGGCCAAGG TGAGGCCTTT CACCTGTGCC ACCCAGTTCA TCCTCCCAGC AGATGGCCCA 720 GGGGTGGGTG GTGCTGGAAG GAGGAAGCCC ACAAGGGGCC CCTCCTTGTG CAAGTGGATT 780 GGCTGTGCCA GGGCAGAGCG TCCTAAAGTG GACACTGGCC CAGAGCCTGG AGCCACACAG 840 GTGGGCACGT TATGGAGGGC GGGGCCAGGT GTGAGGACTG GATCCCCACC TGACCTTTGT 900 GCCTCTGAGT CCTTGTGCTG GCCGTGCACG TTCTTGTGAC CCCTGAGCCT CGGCCTTCCC 960 CCCTGTAAAG TAGGCTTGTG CTGTCTGCCC CCAGGATCCA GGACCCCGTG CCAATATCCA 1020 GAGCTGAGGA GCCTGATTCT TGGTGGGGAG GTGTATTTTA AGGACATGTT GATTTCCATC 1080 CTTGTTGACT GACTGCAGCT CTAACTCCCA TGTGGCCTTT GGACAGGGCA GTTCCCTCTG 1140 CACCCTTAGA GCCGAGGTCT GGAGAGCCCT TCAGCTCCTG 1180
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