Tag | Content |
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EnhancerAtlas ID | HS085-01161 |
Organism | Homo sapiens |
Tissue/cell | Heart |
Coordinate | chr17:1529610-1531000 |
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 | ATTAATCTCC TAACAACTCT TGGCCAAAGC AGAAAGCTTG TTCAGGGAAC AAGGTCTGAC 60 TCTTCCCAAC TCCCAAGATT TCTTGCTGAT GTGGGGAAAG ACCTGCCAAG AACCCTTAGG 120 CTATTAGGAA ATATTTTTGA GTGGCTAAAG GCTAAAGGTT AGTTATAAAT GATATACTTT 180 CTGTCCTCTC CCCGCGGCCT CTGCATTCTC CTGCTTTCTC CTGCCCTGAA CCTCTCCAGC 240 TAAGCCTCCC TCCCTAGAGA CTGGGACACA CAGGAATCTC CGGGGCAGAT CAGAGAAGGG 300 AAACAGGGAG GCTTCCACAA AGGATTACAC CCAGCATGAG CTGGTCCAAA GCTTTCTCTT 360 CCTGCAAAGA GCTCTAGAAA GAAAAGGCCT GCTGCTGGGG ATTCAGGAAG TCAAACCTGG 420 GCTACCTCCA TCTAAGGGCA CTCTAGCACT GGCGACAGGG ATTATGTGAG CTCAGCTATT 480 ATGCAGCTAC CGTTGGGATC AAGGAGAAGG CAGAGGGAAA ATTTCCTGTC AAGGTTGCCT 540 AAGAAGGAGG GTAGGAGGCT AGAGGCTGGG GGCTGCTGTG GCCCTCCTGT GGGGCTGAAT 600 TTACTGCCCT GTAGTCATCA GGACCCTCCA ACAGGGTATG AAGGTGTGAA GGTAAGTGTG 660 TGTTGGGTGG TGCAGATGTC ATGTAGAGAA GCATCCTCAG CCTGCCTTCA GCAATTCCAG 720 TGACAAGGCA AAGAGGAGAG AACAACCCTA GCATCATTTC CATAAACGTT CCTTTCTTCT 780 CTTCCCCTTC ATCCCCATGG GGTTGGAAAG CCACGGAGAT GTCCTCAGAG CCCGTGGGGG 840 AAATGTCCTT TGGAGAATCA TAAGGCAGCA AAAATAGACA AGAAATTGTG TCCAGCAAGC 900 ACTTAGGAGA CTCCACAATG GCCTGAGGAA CGTCTAGATT CTAGATGAGC CCTCCCTGGG 960 GTGGAGGCAA GGCCACTTCC TCTCCTGCTG CACCCCAGCC CCTTAATCTG GAGTTCCTCT 1020 TTCTCACAAG CAGACAGCAA CATGTTTACT ACCAGCCAAG CTATGTTCCA GGGCTGGGAG 1080 GAGAGGAGAG CAGTCCAGCA CTGTTCGTAG CGGGTGGAAG GAACACCCTG GACAGCAGGT 1140 GGGGTTCTGG GTGGATGGCA GGCCCAGGCT CTGCGGCCTT GCGCAAGACA GATCGCTCTG 1200 AGCCTCGATG TCTTCGTCCA CAAAACAGGG GCAATGACAA GTACCCGGCA GGGCTGGGTG 1260 AGGATCAGAT GGGCCTTCTG ATACCCTAGA GGCACTGGGC AATGCGGTGC TGTGGCTCGC 1320 TAGGTCTTCG CCCCCATCCC GCCCCCTCCC AAAGCCCCAG CTCCAGGAGC CCCCCGCAAC 1380 CCCAGGCGCT 1390
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