Tag | Content |
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EnhancerAtlas ID | HS193-17866 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr2:61686850-61687720 |
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) |
Foxq1 | MA0040.1 | chr2:61687370-61687381 | AATAAACAATT | - | 6.02 | HSF1 | MA0486.2 | chr2:61687358-61687371 | GAAAATTCCAGAA | - | 6.17 | IRF2 | MA0051.1 | chr2:61687300-61687318 | TCTTTGGTTTTGCTTTCC | - | 6 | NFAT5 | MA0606.1 | chr2:61687354-61687364 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr2:61687354-61687364 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr2:61687354-61687364 | AATGGAAAAT | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_60516 | chr2:61645792-61699770 | DHL6 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH02I061459 | chr2 | 61686736 | 61688385 |
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Enhancer Sequence | GCAGTGAGCT GATATTAAGC CACTGCACTC CAGCCTGGGC TACAGAGCCA AAAAAAAAAA 60 AAGGCCAGGC ACAGTGACTC ACACCTGTAA TCGTAGCACT TTGGGAGGCC AAGGTGGGCA 120 GATCACCTGA GGTCAGGAGA TCAAGACCAT CCTGATTAAC ACGGTAAAAC CCCATCTCTA 180 CTAAAAATAC AAAAAAATTA GCTGGACATG GTGGCGGACG CCTGTAGTCC CAGCCACTCG 240 GGTGGCTGAG GGAGGAGAAT GGCGTCAACC CAGGAAGCAG AACTTGCAGT GAGCCGAGAT 300 CGCACCACTG CACTCCAGCC TGAGCGACAG AGCAAGACTC CATCTCAGAA AAAAGATACT 360 TGAAAACAGT TTTATGTTGG CTTTTTTTGA GCACCCACAT ATTACTTAGT TTCCAAGCTT 420 ATTAAGAAAT TACAATAGTC TCCCTTATTA TCTTTGGTTT TGCTTTCCAT AGTTAACCAC 480 AGTCACTATG GTCCAAAAAT ATTAAATGGA AAATTCCAGA AATAAACAAT TCATAAGTTT 540 TAAATTGCCA TTCCGAGTGG CATGATGAAA TCTTGTGCCG TCCCGTCTAG GATGTGAATC 600 ATCCTTTTGT CCAGCATATC CAGGCTGCAC ATGCAACCTA CCCATTAAGT CACTAAGTAG 660 CTGTCCTGGT TATCAGATCC ACTGTGGCAC TACACAATGC TTGTATTCAA GTAACCCTTA 720 CTTTACCCAA TAATGGCCCC AAAGTGCAAG AGCAGCGATA CTAGTAATTC AGATATGCCA 780 AAGAAAAGCT TATTTGAAGT GAAAAGGTGA AAGTTCTTAA AATAATGAGA AAAAAAACAG 840 TATATAGGGT ACAGCACTAT CTGTGGTTTG 870
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