Tag | Content |
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EnhancerAtlas ID | HS007-06418 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr16:57566660-57568350 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr16:57568063-57568083 | CCCCAACCCCACCCCCACCT | + | 6.43 | ZNF263 | MA0528.1 | chr16:57566733-57566754 | GGGGGAGGGGAGGAGGAGGAG | + | 6.56 | ZNF263 | MA0528.1 | chr16:57566741-57566762 | GGAGGAGGAGGAGGAGGCAGG | + | 6.82 | ZNF263 | MA0528.1 | chr16:57566738-57566759 | AGGGGAGGAGGAGGAGGAGGC | + | 7.6 | ZNF263 | MA0528.1 | chr16:57566744-57566765 | GGAGGAGGAGGAGGCAGGAAA | + | 7.71 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_12431 | chr16:57566643-57567219 | CD3 | SE_12431 | chr16:57567666-57573363 | CD3 | SE_19883 | chr16:57566325-57573897 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20447 | chr16:57563106-57573716 | CD56 |
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Enhancer Sequence | ACACTCCTCC TTTTCCTGGC CTAGCTCCAC ATAGAGAAGC TCTTGGAAAA GAAAAACAAT 60 GTGAGAGCCT GTGGGGGGAG GGGAGGAGGA GGAGGAGGCA GGAAACCCGA ATGCCAGCCG 120 GCAGCTGTGC TGGGTATGGG GGCCCGGGCC CTGTCTGCTG GGCCCTTCTT GCAGCCGCTG 180 AACTAGGAGC CTGGCAGGGA GGGGGCCACT GCCACATCCT CCCTGCCTCT GGGAGCTGCC 240 AGGCCTGGCA CAGGGCTTGG CCCAGAGAGG GCCACCGGCT TCTTCCAGGA ATCCAAGCCT 300 GTTGGGCAGG GCCAGGGCAG GCACCACCCA GGTCTCTAAT GGCTTCCAGG CACCCATGCT 360 AAAGGCAGAG ATGGGGGCTC CAGACTCACC TCATTCTCCT TCCCAGCGGC CTGGCCAGGC 420 CCCTCCTAGG GGCTGGGGGA GAAGGAAAGG GCACAGCAGG AGCACGGAAG TTTTGGAACA 480 GCACTCCCAC CTTTGCACTT CAGGCCCAGG GTCCCCTGGA GCGGGTGTGT GGGAAGGGGT 540 GGGGGTCGGG GTCCTCAGGG GAGTTTTCTG GAGAAGCCCA CCCCGCCCCC AGCACACCAG 600 GAATCCTGCA CTCCCACATA GACCCAAGGG CAGCCAGACC CTGCCTTGCA ACGCCTCCCC 660 CTACCCTGCC CCACTCATAC AGCACAGCCC TGGGGACACA CACTCACATA CAGCCCCAGT 720 AATGCACACA TTCACACACA CACCCCCAGG GACCCGCACT CACACACAGC CCCAGTAATG 780 CACACACTCA CACACACACC CCCAGGGACC TGCACTCACA CACAGCCCCA GTAACGCGCA 840 CACTCACACA TGGCCCCAGG GACCCGCACT CACACACAGC CCCAGTAACA CTCACACTCA 900 CACATGGCCC GAGGGACCTG CACTCACACA CAGCCCCAGT AACGTGCACA CACACACATA 960 CAGCCCCGGT AATGCACAGA CTCACACGCA GCCCCAGTAA CGTGCACACT CACACACAGC 1020 CCTGGTAACG CACACACTCA CTGAGGGGCA GCAGCAGCGC AGAGCATGGC TTACAGTCGT 1080 GGAGATGCCC CAGCTGCCCT GCCCGCCCCT TCCACCAGGC TCAATGCCCT CTTGCCATGG 1140 GGTGTCTATG TGCGTGGGGC GTGGCCTCCT GTTCCCTTGG CATACTGCCC CACCAAGGGG 1200 CAGGTCACGG TGGGACCGGC CACCACAGGC CCCGGGGAGC CTTTCCTACC CCACCCTTCG 1260 TTGTCCTGCC TCCCAACAGC CAGACAGGTC TATTACTGCT TTAAGTCTCT GGGTTTGTAT 1320 TCCAAATGCC CATGTCCCAG ACTCCAAAAC CCCCACCCAT CTTCAAGTTC AGCTGCCACC 1380 AACTCCAGGA AATGCCTTGA TCTCCCCAAC CCCACCCCCA CCTGGGGACC ACAGCCCTAC 1440 AACCTCCCAC AGCCAAGCCT GGCAAGCTGC CATCTCTCTT CTGGCAGTAC AGGCTTCCCT 1500 CATCCAGATG GGACACTTGT GCCACTTAGA GCTTCCATCA GGGCTCCTGA ACCCCAGCCC 1560 CACAGCTGTG CTCACTGGTA GCTCACTCCA GGACAGAAAC AAGAATATTT TGAGCTGACA 1620 CTTGCTGCAG GCTAGGCCCT CATCAGCCCT GCCCACAGAA AGTGACCCAG TGGTTCCTGT 1680 TGCTTGTGGA 1690
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