Tag | Content |
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EnhancerAtlas ID | HS182-08597 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr16:81532570-81533860 |
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) |
EWSR1-FLI1 | MA0149.1 | chr16:81533842-81533860 | ATTTCCTTCCTTCCTTCC | - | 9.03 | Esrra | MA0592.2 | chr16:81532865-81532876 | CTCAAGGTCAT | + | 6.02 | Esrrg | MA0643.1 | chr16:81532866-81532876 | TCAAGGTCAT | + | 6.02 | HEY2 | MA0649.1 | chr16:81533198-81533208 | GACACGTGCC | + | 6.02 | Npas2 | MA0626.1 | chr16:81533198-81533208 | GACACGTGCC | - | 6.02 | Stat6 | MA0520.1 | chr16:81533298-81533313 | GGCTTCCTGAGAAGT | + | 6.33 | ZNF263 | MA0528.1 | chr16:81533692-81533713 | TCCTCTTTCCCTCCCTCACTC | - | 6.34 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_09239 | chr16:81529931-81532741 | CD14 | SE_09239 | chr16:81532844-81537999 | CD14 | SE_11291 | chr16:81532822-81542648 | CD20 | SE_26527 | chr16:81532504-81534038 | Esophagus | SE_35877 | chr16:81530694-81535589 | HMEC |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I081499 | chr16 | 81532685 | 81540040 |
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Enhancer Sequence | CAAGCATCTG AGTGCTTTAC AAATTCAAAT GTATTTAATC CCCCTATCAA CACTAGGAGG 60 TAGTTTCTGT TATTAGCGCC ATTTTACAAA TGAGGAAACT GAGGTGTAGA GCAGTTAGAT 120 CGGTGTAGAG AAGCTAGATC GTGTGCTCAA GGCTTCAGTC CAGGCTCTTG GCCCTGACAC 180 GATGCTGTTT GCCTGTTGAA GATGTGTGTG CATGCATGCA CCATTCACAC TGTGAACGTG 240 TCCCAGCATG GCCACACCCC CTCACCGTAT ACACATATGG CCATGAGCAC TCAATCTCAA 300 GGTCATGGAT GCACATGCCT CACACCTATG CATGGAAGGA CACTCGGCAC ACATACTTGT 360 CTCTGCACAC ACACACCACT TGCACACCCA TGTACACATG TGCCCCAAGC CTCGCCCCAA 420 TCTCCAGCTC CCTTTCAGAG TCCCTTCTAG GATATTCTCT GATTTCTCCC AAGTGCCCAG 480 TTCGGGAGGG AAGTGACTGC ACAGATCTGG ACCTGGCGAT GACCTCTGAG TGGGAGGCAG 540 CCCTGGCTGA GCTGTCTCCT CACCTTAGCA TCCGCCTGTC CCGGCGCCCA TGTAGCTTCC 600 TTGTCATCCA TCTTCTGGGC TGGCCCAGGA CACGTGCCCC CATCCCAGCC TCCAAGAATC 660 TGGGAATGTC CTTAGCAGAC TGGGCTGGCA TGTGGCCTCT GCCCGGGGAG CAGAGGTGGC 720 TCCCCAAAGG CTTCCTGAGA AGTGGTGGAG GAGACTCAGC TTCCCCGTCC AGTCCTTTAC 780 CCCTCCTTTA CCCAGCAGCG CCCTCTGAAT CTGAAACAGT TTTGGGGGCG GCAGCTCCGG 840 TCCTGCCCAG CAACTCGCAG TTGTTGCCTG TGGCATTCAG ATTCAAGTCT GGGCTTGTCA 900 GCCCGGGCGA GACTCTCCTA TTTTGGCCCT ATGGGAGGCA TCCAAACTCC TCTGCCCTTG 960 CCTTCCGGGG CGCCCCACGC ACTCTGGGCT TCACCTGGCT CCTCTGCTTT GCTTGGGCTG 1020 CTGACTTCTG GAGGAGCCCT TTCTTCCTTC TCTCTCCTGA TGCAGAACAT ACCCAGTCTC 1080 CCTGGGGCAA TCGGCCTTCT TCAGCCACTC CTTGGTCTCT GCTCCTCTTT CCCTCCCTCA 1140 CTCTGTGTCC TGCCAGCCCC AGCCTCTGGC GACTTTTAGA GCTGGTGCGC AGTCCTGCCT 1200 GAGCATCGGT GAACATGACG CCATGGGCTG TGGCTTAACG ATTCTTTTGG TGAATTTTGA 1260 TTCTTTATCA AAATTTCCTT CCTTCCTTCC 1290
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