Tag | Content |
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EnhancerAtlas ID | HS073-05768 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr17:1529380-1531000 |
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 | ZNF263 | MA0528.1 | chr17:1529548-1529569 | GGGGGAGAGAGGAAAGGAGAG | + | 6.65 |
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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 | ACACAAAAAA ACACCTGCCC ACAACAGTTC TCTGGTCTGG GTGAGACACT AAAAGCTTTC 60 TCTGGGGACG ATGACTTTTT TTCTGCTTTT TTTTTTTTTT TTTAAACCCT GTGTCCAGCC 120 TGAAAGAGCC CACCAGGGAG GCAAGCAGGA AGGGTCACGA TCTCTAAGGG GGGAGAGAGG 180 AAAGGAGAGG AAGAAGTAAA CACTCCAACC TGTGCCTTTC GGGGACAGGC ATTAATCTCC 240 TAACAACTCT TGGCCAAAGC AGAAAGCTTG TTCAGGGAAC AAGGTCTGAC TCTTCCCAAC 300 TCCCAAGATT TCTTGCTGAT GTGGGGAAAG ACCTGCCAAG AACCCTTAGG CTATTAGGAA 360 ATATTTTTGA GTGGCTAAAG GCTAAAGGTT AGTTATAAAT GATATACTTT CTGTCCTCTC 420 CCCGCGGCCT CTGCATTCTC CTGCTTTCTC CTGCCCTGAA CCTCTCCAGC TAAGCCTCCC 480 TCCCTAGAGA CTGGGACACA CAGGAATCTC CGGGGCAGAT CAGAGAAGGG AAACAGGGAG 540 GCTTCCACAA AGGATTACAC CCAGCATGAG CTGGTCCAAA GCTTTCTCTT CCTGCAAAGA 600 GCTCTAGAAA GAAAAGGCCT GCTGCTGGGG ATTCAGGAAG TCAAACCTGG GCTACCTCCA 660 TCTAAGGGCA CTCTAGCACT GGCGACAGGG ATTATGTGAG CTCAGCTATT ATGCAGCTAC 720 CGTTGGGATC AAGGAGAAGG CAGAGGGAAA ATTTCCTGTC AAGGTTGCCT AAGAAGGAGG 780 GTAGGAGGCT AGAGGCTGGG GGCTGCTGTG GCCCTCCTGT GGGGCTGAAT TTACTGCCCT 840 GTAGTCATCA GGACCCTCCA ACAGGGTATG AAGGTGTGAA GGTAAGTGTG TGTTGGGTGG 900 TGCAGATGTC ATGTAGAGAA GCATCCTCAG CCTGCCTTCA GCAATTCCAG TGACAAGGCA 960 AAGAGGAGAG AACAACCCTA GCATCATTTC CATAAACGTT CCTTTCTTCT CTTCCCCTTC 1020 ATCCCCATGG GGTTGGAAAG CCACGGAGAT GTCCTCAGAG CCCGTGGGGG AAATGTCCTT 1080 TGGAGAATCA TAAGGCAGCA AAAATAGACA AGAAATTGTG TCCAGCAAGC ACTTAGGAGA 1140 CTCCACAATG GCCTGAGGAA CGTCTAGATT CTAGATGAGC CCTCCCTGGG GTGGAGGCAA 1200 GGCCACTTCC TCTCCTGCTG CACCCCAGCC CCTTAATCTG GAGTTCCTCT TTCTCACAAG 1260 CAGACAGCAA CATGTTTACT ACCAGCCAAG CTATGTTCCA GGGCTGGGAG GAGAGGAGAG 1320 CAGTCCAGCA CTGTTCGTAG CGGGTGGAAG GAACACCCTG GACAGCAGGT GGGGTTCTGG 1380 GTGGATGGCA GGCCCAGGCT CTGCGGCCTT GCGCAAGACA GATCGCTCTG AGCCTCGATG 1440 TCTTCGTCCA CAAAACAGGG GCAATGACAA GTACCCGGCA GGGCTGGGTG AGGATCAGAT 1500 GGGCCTTCTG ATACCCTAGA GGCACTGGGC AATGCGGTGC TGTGGCTCGC TAGGTCTTCG 1560 CCCCCATCCC GCCCCCTCCC AAAGCCCCAG CTCCAGGAGC CCCCCGCAAC CCCAGGCGCT 1620
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