Tag | Content |
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EnhancerAtlas ID | HS101-03768 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:206694020-206695370 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr1:206694981-206694996 | TGCCCTTTGCCCCTT | - | 6.06 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_27159 | chr1:206693253-206696232 | Esophagus | SE_32205 | chr1:206693876-206695796 | Gastric |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I206521 | chr1 | 206694396 | 206695154 |
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Enhancer Sequence | GCTGTGGCTC CTCCTACAGA TTAACCTCTC TGAGCCTCAT TTTTCCAAGT ATAGGATAGG 60 GCAGAATATC TCAACCTCAG ACTGGTGTGG GGTAAATTAA ATGTCAAACA GTTGAAACCA 120 TGTTTGGTGC ATAGAAAGCC CTGCACTGGG AGCTGCTGTT GCTGAGTGCT CCCAGGAAGA 180 CTTTTCATAA CTGCTCCCCG TGGGTCATTG GGACAAGCCT GCAGCACGGC TGTCTGCCCC 240 TCCATTGTAC CTGGACCAGG GTGGACTGCC TGCATCTCAG TGGGAGACAT AGGACTTGAA 300 GGTTGCCCAG GTAAAAGTAG AGGAGAGACA TAAACTCACA AACACATTCC CTGGAAAAAT 360 TCCTATCATT GAGTTTACCA CATCACATAA TTAACAGGCA GAGCTAGATT AGCCCACCGG 420 GTATCTTTAG GAGCTAAGCA AGCATGTCGC CAAGGAGCAA GTCATATGTC ATTTTAAAAG 480 GCTGCTAGGG GGGTCTGTGG GAAATAGGCC TAGGTCTCTC CAGAAGTCTC TGGTGGTCCT 540 GGCTGCAGCG ATGCAGCTGT AAAGAAACCT TTGTGTGTCT CCAGCAGAGA GGTCCTCTGA 600 CATAATCTAT TTACTTTCCT TCCCACTGCA AAAAAGCCTG CTTTCGCCCG GTTGATGATT 660 GGCACTTTGA ATAGCTGCAA GTGACATCAA AGCAGGTGTG GAAAAACCAG TTGGATGTAG 720 TAGCCTGGTT GTCCCATGAT AGACTGAACC TGCCTGCTCC TGGCCTCCTG TGACCTCCTG 780 GCACTAGAAC TGGGCATACC TGCGGTGCAT TCATATCTGT ATTTCTGCAT GAACTTCATC 840 TGCCATCTTG CAGTTTGCAT ATGCCCAGCC AGGTCTCCTT GCAATCCTAT TTGGCTGTCC 900 TTATCTTTGG GGTCTGTGGC ATACTACCAC AAATATACTC TAGGCTAACA AGAGGCTAGG 960 CTGCCCTTTG CCCCTTCTCA GAGATGATTG TCTGCCTTAA AAACAGAAAC ACAAGCAAAC 1020 AAAAACAACC CTCCCCTTCT CTTTCCGTAT GTGCCCCTCA CTTCTAGAGC CCAAATCCTT 1080 TGTCAGCTAC CCAGGGTCCT CCGTCTGTCT TCTCAGGGGC CCAGGGATGG GTGAGAGGGC 1140 CCAGAGCCCA GGGCTGGGAG ACCTCTGCTG CTTTGTCTCT CTTACACCCA GAGCAAAGTG 1200 ACACATGCCT AGACGAGGGG CCCCTCCTGA GCAGGCCTGG GGCCGAGAGG GTATCTGGCA 1260 GCTCCACACT GGCTTTGGAT ATCATGGGCT TGTTGCTATT TGTTGAGTTC CCTTAAACCC 1320 AACTGCCTAC AGTGTTTTAA ATTATTTTTT 1350
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