Tag | Content |
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EnhancerAtlas ID | HS105-73538 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr7:47708790-47710000 |
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) |
STAT3 | MA0144.2 | chr7:47708847-47708858 | TTTCCCAGAAG | - | 6.62 | Stat6 | MA0520.1 | chr7:47709929-47709944 | AGTTCTCAGGAAAGA | - | 6.7 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_36990 | chr7:47708071-47710661 | HSMMtube | SE_43771 | chr7:47707639-47713135 | MM1S | SE_46013 | chr7:47708357-47710362 | Osteoblasts |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr7 | 47709189 | 47709374 | chr7 | 47709618 | 47709974 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I047668 | chr7 | 47708317 | 47712973 |
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Enhancer Sequence | GAATTTTGGG TAACACAATT CAGCTGGTGA CATTGACACA GCCTGGGGCT GCCCAGTTTT 60 CCCAGAAGGG GCAGCAGGAA TGGGTCAAAA ACCCATCACT CATCAAGAAA AACCAGTTCA 120 TGTGTTGAGG AACCGTCTTG TCTGCCGTCC TTCAGAATGA GTGCGCAGTT GTTTTGCTGT 180 TTTCTTGGGA ACCAGCTGTG GAACACTGCG CTTCCCTTTC CTTTCTTTTC AAGAACCTTG 240 GTGCCCACCT GGCCTCCTGG AGGACACCTT TGTGCAGAGG CTGCCAGAGA TGGAACATAG 300 AGATGGGGGA GGGGAGCAGG TGATGCTGGC CCCTGTTGAA AGAAAGTGGG CAAGAGCAGG 360 GGTAGTTATT TCTCCTCTTA CAGAAAGGGC TTGCTGAGTT AGGCTTCATG TGGCATTGTG 420 TTCTTTTGAA CGTCACTTAA GGCATACATG AAGCGTGTGC ACATGACACA GCCCAGTGGA 480 GCCAGGGAGT GACTCAGCCT GCTGCCCAAC ACCCACTGCA AGTTGTTCCT GTGGCTGCCT 540 CTAGCTGTTC CCCAATCTGA AATTTGTTTT TCGTTTTCCT TCACTTAAAA AAACTTGTTG 600 GCCGGGCTCG GTGGCTCACA CCTGTCATCT CAGCACTTTG AAAGGCCAAC GAGGGAGGAC 660 TGCTTGAGCC CAGGAGTTTG AGACCAGCCT GGGCAACATA GAGAGACCCT GTCTCTACTA 720 AAAGATAAAA ATAAAACAAT TAGCCGGCCA CGGTGGTGCA TGCCTGTGGT CTCAGCTACT 780 GGGGAAGCTG AGGTGGGAGG ACGGCTCAAG TCCGGGAGGT TGCGATTACA GTGAGCCATG 840 ATCTCGCCAC TGTACTCCAG CCTGGGCAAC AAAGTGAGAT CTTTTCTCAA AAAAAAAAAA 900 AAGTTGTAAC ATGCGTGTAT CCCCAAACAA TAAATTGCTT AGTCAGGCTT ATGTGGGACT 960 TTCTAGAAAT GCTATCACAC TTTGTGTTGA CTTCTGAGCC TTGCTTTTTT CCCTTCAAGT 1020 TTATGTTCCT TTCCCAAGGC TCTCCCAGGC CCAAGGGTCT CTCACGCTCT GTAAAACCTG 1080 TGCTCAAAGC TTCTCCCCTG AGGCTGTGGG CAGAGACTGG GTGATACTGA AGTAATACAA 1140 GTTCTCAGGA AAGATCCTTT TTTTTTTTTT TTTTTTTTTT TTACACCAGG CCAGGCCCAG 1200 ATTGGGTATT 1210
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