Tag | Content |
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EnhancerAtlas ID | HS105-79596 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr8:128808280-128809780 |
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) |
Nkx3-2 | MA0122.3 | chr8:128808366-128808379 | GTTAAGTGGTTGT | - | 6.02 | ZNF740 | MA0753.2 | chr8:128809631-128809644 | CCACACCCCCCAC | + | 6.03 |
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| Number of super-enhancer constituents: 13 | ID | Coordinate | Tissue/cell |
SE_34061 | chr8:128806748-128809244 | HCC1954 | SE_38517 | chr8:128805989-128809578 | HUVEC | SE_43463 | chr8:128805802-128809222 | MCF-7 | SE_44406 | chr8:128805831-128809154 | NHDF-Ad | SE_45281 | chr8:128805907-128809125 | NHLF | SE_45549 | chr8:128805875-128809411 | Osteoblasts | SE_47113 | chr8:128805716-128846840 | Panc1 | SE_60911 | chr8:128800542-128824452 | DHL6 | SE_63266 | chr8:128805887-128813518 | GLC16 | SE_63286 | chr8:128800421-128841375 | NCI-H82 | SE_68169 | chr8:128805731-128832871 | TC32 | SE_68395 | chr8:128805788-128948274 | TC71 | SE_68675 | chr8:128805860-128809938 | H9 |
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Enhancer Sequence | CTTCGGCACA AGGGCCCAAC TGGAATTCCA CTTACGGGTA TGACTGTGGG GTATATGCTG 60 TACCCATTGA ATTCCCAGAG GGATTTGTTA AGTGGTTGTG TTGCTGTTTT GCCTGGTTAA 120 GAGTGGCTTA TTCTTGTTGC CTCATCTATC TTGAGTGCAG AATTTTTGCA TAAACGGCTT 180 CTCTTGAAAA ATAGAAGTCC GTTTTTGTTT TGTTTTGTTT TTTTTCTGAT TAACTTTCCT 240 TTTCCTCTGT CTTAAACACC TTCCCCCGCC CCTCGCCACC TCCATGCTGT GTTTCTGTGG 300 CTGGAGCTTT TCTGCACTGG AAAGGAGGAG TTCTCCCCTC TGTTCTGACA TATCTGATCC 360 CCACTAGTTT ATATGATTGC TGGTCTGAAA ACCTGGTGAA TTCTCACTGC CCACATCAAA 420 TCAATTCCCT GTTCTTTAGT TGTTTTTTTT TTCCGCCTCC TGAGCGGTAG GCAGGCACTC 480 TGGCTGGATT CTGGAGCCTG TGTTTGCCAT GCCTGGGCCT TCTGCCTGCC CAAGATGGAC 540 ACGTTTCTCT GGCAGCTTTG TCAAGAGATC TCCTGGACTA TAAGACACCC TGTTCTTTCC 600 TCCTGTTTGT GTGAGTGGCC CTGCATTTGG GCAGAGTATT GGCAGAATAT CTGGGGGAAG 660 TGGAAGACTT TGGATAGTTG CCGGTCCAGG TCGTCTGGAG AGGCAGTGGC AGGCCTGCTG 720 ATGGCTGCCC CTTTGCTATT TGTTTTATAT CAGGTGGCCC TTCTGGATGT GTGGCCTTTT 780 TATTTTGCAT TTCCTTTCAT AGTTGGCTGC AGACATAAGA TTCTTCTTTT TCTCTTGTTT 840 TGCTTTTTTT TTTTTTTTTT TGAGACAGAG TTTCACTCTT GTTGCCCAGG CTGGAGTAAA 900 ATGGCTGGAT TTCAGCTCAC TGCAACTTCC GCCTCCCAGG TTCAAGCGAT TCTCCTGCCT 960 CAGCCTCCCA AGTAGCTAGG ATTACAGGCA TGCATCACCA CACCCAGCTA ATTTTGTATT 1020 TTTAGTAGAG ACGGAGTTTC TCCAGATTGG TCAGGCTGGT CTTGAACTCC CAGCCTCAGG 1080 TGATCCGCCC GCCTTGGCCT CCCAAAATGC TGGGAGGCCT CCCAAGTTGC TGGGATTACA 1140 GGCATGGACC ACCATGCCTG GCTAATTTTG TATTTTTAGT AGAGACGGAG TTTCTCCAGA 1200 TTGGTCAAGC TGGTCTCGAA CATCTGACCT CAGGTGATCT GCCCTCCTCG GCCTCCCAAA 1260 GTACTGGGAT TACAGGTGCC ACAGTACCCG GCCTTGTTTT GCTTTTTATT GTTTCCTGAT 1320 GCAGGTTTGT GATCTCTTTG AGGGATCAGG ACCACACCCC CCACCCCAAT TTATATTCCC 1380 AGTGTCCATG GTGGGACCCT GACTGAGGAT GGGAACAGAG CAACAATCTG GAATCATTTG 1440 GACCATTGAG TCCTGTGGAC AGTCACTTCA ATATCATCCC TAGAGAGTCT CAGAAATTCA 1500
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