Tag | Content |
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EnhancerAtlas ID | HS094-13191 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr14:95686630-95688020 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr14:95686732-95686747 | TGAACTCCTGACCTC | - | 6.22 | ZNF263 | MA0528.1 | chr14:95687631-95687652 | CCCCTCTTCCCCTTCTTCTCC | - | 6.45 | Zfx | MA0146.2 | chr14:95686757-95686771 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_65498 | chr14:95686570-95687388 | Pancreatic_islets |
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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 |
GH14I095220 | chr14 | 95686481 | 95689489 |
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Enhancer Sequence | AGCCTCCCTC GTAGCTAGGA TTATAGCTCC CCACGACCGT GCCCAGCTAA TTTTTGCATT 60 TTTAGTAGAG ATGGCGTTTC ATCATGTTGG CCAGGCTAGT CTTGAACTCC TGACCTCAGG 120 TGATCCACCC GCCTCGGCCT CCCAAAGTGC TGGGATTACA GGCGTGAGCC ACCGCGCCCA 180 GCCATCTAAG TCACATTTTG AGAATCCACT TGTCCGTGGG TGGACAGGCG GGTTGTTCCC 240 ACCTTTTGGC TGTTGTGAAT TGTGCTGCCA TGAACTGTAA TGCGCTTGCT GGCCGCCACC 300 ATCTGAACCT CCCCTCTGTG CCTGGGACTT TCTCCTAGAA CTACTGGGAG GGGACTATTG 360 GGAAGCAGAG CCTACCCCTG TTCAGACAGT GAAAGTGCTT TCCCATCCTC CTTTGCCCCT 420 GGAATGTGGG CTGAGGCCCA GGCTGTGCAG CCACACATCC TGTCCGGGCC TTTGAATCTG 480 GACCTGTGAT GCTGAGACGA CCACAAAGCA GAGAGAGCTC CTTCTGCAGG CTGTGGTGGG 540 GCTGCCCAGA GGTTGCAGGG GCAGGGCGGT GAGGGCATGT CCTGCCGTCT CTTCAGGGGG 600 CTCTGCGGTA GTCCTGGTGC CTGGCATGGG TTCTGTCCCT GATTCGCTGG TCTTTCAAGT 660 CATTCTGTGG CTACTCGGCA TATTTCAACA AATTCCTTTA CTGCTTAAAT CAGCTGAGTT 720 CAGCTTCTGT TACTATGAAG AACCCCAGAT GAATCCTACT TTATGATAAA ATCTCACTGT 780 ATGTGCCAAT GTGTCAGGCA AGCTGGGTTT TGTTTTAACC CGGATTGATT GGTGAAACCT 840 AATGAGAGGC GTGATGAAAC GTCCTCCCTG CTGAGCCACC CCCTCCCCTC TGTGAAGAAT 900 GTGGAGCAGG GTTCCAGGCA CAGAAAAAGA TCATCGGAGT CTAGAAAGTT ACATCAAGAA 960 TGGGAGAATT TTGTAACTTT TTTCCCCTGG CTCATTTGGC CCCCCTCTTC CCCTTCTTCT 1020 CCCATATTCT AAGTTCCAAG AGAAAGTTCT ACACTCGGAC ATGCTCGCCA TACTCTTATT 1080 CAAGGGAATG AAGGAGAAAA CGTGAACTGA ATTCTAAATA TCTGAGAGCC AGTTAGCTGC 1140 TCTGCCTTTC TACGACTGAA CGTACATCAG AGTTTTAATC CTGATGGCTG CAAAGTGGGT 1200 GGGCACGGAG TCAGGGACTA TGTTCCCAAC GGAGGGGTCA TCTGAGTGAT TTCTGTGAAA 1260 TTTAAGCTTA GTTTAATTTG ACCATTTTAG CTCAGTCCCC GTCTCACGCT TCTCTTGCGA 1320 CCAGCACTGA ACTTCAAATG ACGTCCTTTT CCTAACAGGA CAAGCTTGTG TTAGCAGGAT 1380 GAGCTTCAAA 1390
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