Tag | Content |
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EnhancerAtlas ID | HS060-13865 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr17:1529680-1531000 |
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) |
TBX20 | MA0689.1 | chr17:1530250-1530261 | AAGGTGTGAAG | + | 6.32 | TBX21 | MA0690.1 | chr17:1530250-1530260 | AAGGTGTGAA | + | 6.02 | ZNF263 | MA0528.1 | chr17:1530383-1530404 | TTCTTCTCTTCCCCTTCATCC | - | 6.03 | ZNF263 | MA0528.1 | chr17:1530386-1530407 | TTCTCTTCCCCTTCATCCCCA | - | 6.26 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_50860 | chr17:1529439-1533868 | Sigmoid_Colon | SE_53184 | chr17:1528732-1533569 | Small_Intestine | SE_60874 | chr17:1528522-1534018 | DHL6 |
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Enhancer Sequence | TCCCAAGATT TCTTGCTGAT GTGGGGAAAG ACCTGCCAAG AACCCTTAGG CTATTAGGAA 60 ATATTTTTGA GTGGCTAAAG GCTAAAGGTT AGTTATAAAT GATATACTTT CTGTCCTCTC 120 CCCGCGGCCT CTGCATTCTC CTGCTTTCTC CTGCCCTGAA CCTCTCCAGC TAAGCCTCCC 180 TCCCTAGAGA CTGGGACACA CAGGAATCTC CGGGGCAGAT CAGAGAAGGG AAACAGGGAG 240 GCTTCCACAA AGGATTACAC CCAGCATGAG CTGGTCCAAA GCTTTCTCTT CCTGCAAAGA 300 GCTCTAGAAA GAAAAGGCCT GCTGCTGGGG ATTCAGGAAG TCAAACCTGG GCTACCTCCA 360 TCTAAGGGCA CTCTAGCACT GGCGACAGGG ATTATGTGAG CTCAGCTATT ATGCAGCTAC 420 CGTTGGGATC AAGGAGAAGG CAGAGGGAAA ATTTCCTGTC AAGGTTGCCT AAGAAGGAGG 480 GTAGGAGGCT AGAGGCTGGG GGCTGCTGTG GCCCTCCTGT GGGGCTGAAT TTACTGCCCT 540 GTAGTCATCA GGACCCTCCA ACAGGGTATG AAGGTGTGAA GGTAAGTGTG TGTTGGGTGG 600 TGCAGATGTC ATGTAGAGAA GCATCCTCAG CCTGCCTTCA GCAATTCCAG TGACAAGGCA 660 AAGAGGAGAG AACAACCCTA GCATCATTTC CATAAACGTT CCTTTCTTCT CTTCCCCTTC 720 ATCCCCATGG GGTTGGAAAG CCACGGAGAT GTCCTCAGAG CCCGTGGGGG AAATGTCCTT 780 TGGAGAATCA TAAGGCAGCA AAAATAGACA AGAAATTGTG TCCAGCAAGC ACTTAGGAGA 840 CTCCACAATG GCCTGAGGAA CGTCTAGATT CTAGATGAGC CCTCCCTGGG GTGGAGGCAA 900 GGCCACTTCC TCTCCTGCTG CACCCCAGCC CCTTAATCTG GAGTTCCTCT TTCTCACAAG 960 CAGACAGCAA CATGTTTACT ACCAGCCAAG CTATGTTCCA GGGCTGGGAG GAGAGGAGAG 1020 CAGTCCAGCA CTGTTCGTAG CGGGTGGAAG GAACACCCTG GACAGCAGGT GGGGTTCTGG 1080 GTGGATGGCA GGCCCAGGCT CTGCGGCCTT GCGCAAGACA GATCGCTCTG AGCCTCGATG 1140 TCTTCGTCCA CAAAACAGGG GCAATGACAA GTACCCGGCA GGGCTGGGTG AGGATCAGAT 1200 GGGCCTTCTG ATACCCTAGA GGCACTGGGC AATGCGGTGC TGTGGCTCGC TAGGTCTTCG 1260 CCCCCATCCC GCCCCCTCCC AAAGCCCCAG CTCCAGGAGC CCCCCGCAAC CCCAGGCGCT 1320
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