Tag | Content |
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EnhancerAtlas ID | HS037-26743 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr3:185444950-185446300 |
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) |
IRF1 | MA0050.2 | chr3:185445007-185445028 | AAAAAAAAAAAAAAAGTAAAA | - | 6.16 | IRF1 | MA0050.2 | chr3:185445019-185445040 | AAAGTAAAAGAAAAAGAAAAA | - | 6.35 | IRF1 | MA0050.2 | chr3:185445013-185445034 | AAAAAAAAAGTAAAAGAAAAA | - | 6.89 | PHOX2A | MA0713.1 | chr3:185445244-185445255 | TAATTGGATTA | - | 6.02 | Phox2b | MA0681.1 | chr3:185445244-185445255 | TAATTGGATTA | - | 6.02 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_35919 | chr3:185442482-185452977 | HMEC | SE_38159 | chr3:185445068-185457627 | HUVEC | SE_64468 | chr3:185444024-185448358 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I185723 | chr3 | 185441446 | 185456662 |
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Enhancer Sequence | AGCTGAGATC ATGCCACTGA ACTCCAGCCT GGGCGACAGA GAGAGACTCC GTCTCAAAAA 60 AAAAAAAAAA AAGTAAAAGA AAAAGAAAAA GAAATCACAG GAGCAATGGA GATCGTTAAG 120 AACAGCAAGG GAGACGCAGA GCCCTCCGGA AGGTTAGTCT GGGCAGATCC AGAGGCTGTG 180 GGGAGGGGCC TCACAGAGCG GGCTATGCAC CAGCCTTAGC CTCCTCACTT GGGGCAGACA 240 CAGCATGAAC ATGGCTGGCT TGGACTGAGG CTCTTGGCCT CAAAGACAGA ACAGTAATTG 300 GATTACTCAC AGGTTGAACA GGTGAACAAA AAGGTAGTGC TGTGGATGAG AACACCTCAG 360 GGGGCCCCAG AAACAGTGAA GAGGAAGAGT AATGGTTTTG TGAAAAAGAC TTTACTTGAA 420 ATCCCTGGAG AAGCAGTAGC ATCATAATCC TTCCTCTTCC TATATTTACT TTTTTCCTAA 480 AAATTCAATT TCTTAATAAA ACTAAAAATG CAATCATGAC ACTGTTTGAA TATTATAAAT 540 TAGATGGAGT GGAGGATAAA CAAAGTTGGC ACAGGGAAGG CAAGAGGCAT TTACTGAATG 600 TCTATCATAT GCCCTCTCAA TATTTAGAAT CCCCTCATGA GATACTGGCA GCCCATTTTA 660 CACAGACTAA ACAGAGACTT AGAAAGGATA AATCTTTTAC CCAAGGCCAT GCAGCTAGTC 720 TATGATGGAG CCAGGATTCC AGCCCTGACA TGCCTCATTC CAGAGCTCTT GTTCTTTTCT 780 GTATACTGCA CTACCTACAT CTCAACAGTC GTGAGTTCAA CATTAATCAG GTCTGAACTA 840 ATGAGATTTA CTATAATGCC CCGGAGATGA CTGTACCCTA CAGCTGGAGA ATGCATAGGG 900 AGGGGCACTT CCGTTACGTA TACCTGAACT ATGTTTGCGA TTCACACAAA ATAAAGAATT 960 GACCAGGACC AACCCCAGCC TATGAGAGGC AAAGTTACTG CTGCCCGCTT TACCCCACCC 1020 TAGAGCGCCC TCTGATCCAC ACTCTCACAC TGCCTTCCAG CTTTCCCACG GCGCCAGACC 1080 CTTGCTGCTC CTGGGCCCCT TCCCCTTGCT CCCTTCATCA GGCGCTCTCC GCTCCTCCAG 1140 CCCATCAGCG CCTTGACTCG GGTGGCAAGA GTTGGTAGGT TAACCAGATT CACCAATCCC 1200 TGTTAAGTCG CTCACTCACA TGTTACCCTT CTAGGATATG GGCTTTTTGT GTTTTTGTTT 1260 TTTAACTCAG TTAACATGTA CTTTACCACC ATAAAGGTAA AATGACAATG GTGGACGTCT 1320 CATTCATCCT GGAAGACTGA CAGAGGAGAC 1350
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