Tag | Content |
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EnhancerAtlas ID | HS094-15749 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr16:74597270-74598220 |
Target genes | Number: 13 | Name | Ensembl ID |
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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 | chr16:74597627-74597648 | AAAAAAAAAAAGAAAGAAAAA | - | 6.59 | IRF1 | MA0050.2 | chr16:74597633-74597654 | AAAAAGAAAGAAAAAGAAAAA | - | 6.68 | Nr2f6(var.2) | MA0728.1 | chr16:74597410-74597425 | GAGGTCAGGAGTTCA | + | 6.22 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr16 | 74597691 | 74598012 | chr16 | 74598024 | 74598138 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I074562 | chr16 | 74596780 | 74598563 |
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Enhancer Sequence | TGGCCTTCAT TGTTAGGTCA CTTTTTCCAG AGTTTGGAGT AAACGATACA GTGTCTAGAA 60 ATTTGTCCCT CATGGGCTGG ACGCAGTGGC TCATGCCTGT AATCCAAGCA CTTTGGGAGG 120 CTGAGGTGGG CAGATCACTT GAGGTCAGGA GTTCAAGACC AGCCTGGTCA AAATGGGAAC 180 TCTGTCTCTA GCAGAAACAC AAAAATTAGC GGGGCGTGGT GGCGTGTGCC TGTAGTCCCA 240 GCTATTTGCG AGGCTGAGGT GGGAGAACTG CTTGAACCCA GGAGGCAGAG GTTGCAGGGA 300 GCCGAGATCA CGCCACTATT CTCCAGCCTG CGCAACAGAG TGAGACCCTG TCTCAAAAAA 360 AAAAAAAAGA AAGAAAAAGA AAAAAAAAAG AAATTTGTTC CTCATGATAT GCTCCATAGC 420 AGATTCTACT GCAAAGGCTA TGGTTACAAA ACAGACTTCT TTAAATTATC TTGCTAAAGG 480 TCTACTGGAT AACAGAATTG CTCAAGGTTG CCTACTGGCT AATCAGGGAA GTATCTGTGA 540 AGTTGCTGAC ACTTTTATTT TTATTCTTTG AGACAGGTTT TTGCTCTGTC ACCCAGGCCG 600 GACTGCAGTG GCTCAATCAT GACTCATTTA GCCTCAACCT TCTGGGCTCA AGTGATCCTC 660 CCACCCAGCC TCCTGAGTAG TGGAACTACC AGCATGTGCC ACGAGGCCCG GCTAATTTTT 720 GTATTTTCTG TAGAGACAGG GTCTTGCTAT GTTGCCTACG CTGTCTTGAA CTCCTGGCCT 780 CAGGGATCCT CCCGCTTCGG CCTTCCAAAA TGCTGGGATT AACAGGTGTG AGCCATCATA 840 CCAGGCCTTG CTGACACCTC TTGTTGCACG TGGATGAATA TACTGGATAT TACAGAGATT 900 CAGTTGTAGG GGATTAATGA ACTGGCTGCT TGGTTGAAAT GAGTAGATTG 950
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