Tag | Content |
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EnhancerAtlas ID | HS044-11790 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr6:160675470-160676520 |
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) |
MYC | MA0147.3 | chr6:160676287-160676299 | GTGCACGTGGCC | - | 6.22 | ZNF263 | MA0528.1 | chr6:160676033-160676054 | GGAGGAGGGAGTGCAGAGAGA | + | 6.9 |
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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 |
GH06I160254 | chr6 | 160675199 | 160676599 |
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Enhancer Sequence | TACAATCTTT TCATAATGCC TTACTGTTTT TTTAAAAAAT TATTCATGGA AGACAATGTG 60 TTTTATTTAA AGTTGGCTTA ATCTGTGAAT ACAATGGGGA TCCATGACAT TCTTGTCCTA 120 TTGTATAAAA TCTGGAAATT GTAGGCATTA ACTATACAAA AAACAAATTG CTTTCTCATT 180 TCTTTAGGCT AGGCTTCTCA CTCCTGCATG CAGGCACAGA ACAGAAGAAG GGCAATGACC 240 GGCCAAGCTT CAGATGGTGT AAGAAAAAGA AGTCGAGGCA TGGAGACAGC CTTTGGGGGA 300 AGAATAATGA GTACTTACCT TGACAGAGGG GATTTCAACA ATAGGAACAA AATAATGAGA 360 TCATCTAAGA AGGTGGATAA TTGACCAGGG CTTATAACAC AGGAATGCAC TGTCAGTAGG 420 GATTTATGAC CAATCTCCTA CTTGTTGAGT GGGATGTGAA TAATTAACTA ATTTCTTAAC 480 CCACTGAGCA AGGGTTAAAG ATTGAGTCAC CTGTTTACTC ACAGCCTGTC AGGGAGTGAG 540 TGTTAGCACC TCTACCTGGT GGCGGAGGAG GGAGTGCAGA GAGAGTGAAT GCCTGCAGGG 600 CCAGAGCTGC CCAGGGGTGC AAGGTGGACT CCGGACCTCC CCTTGTTAAT GTGTCTCTCC 660 TGATTTAATG CGTCATCTTT AAAGAATCAT CCTCAATTCT GCAGCAATAA AAATAAAAAC 720 CTTCCCTTTC ACCTTGCAAG CCTCCCGCAG AAAGCCCCAG GAAGAGCCTT GTCAGGGCAG 780 CTGAGGAGAC AATTAATAAC CATGGGTGAT GGATGAGGTG CACGTGGCCT GTGCCTCCAC 840 TTTTATCCCT CTTCCCTTCT GCTGCCAGTT GGGCCCCAGG CCCCTGTGAA GTGCATATGC 900 CTTGGGGGTG TGATATATTA AGCCATCATT ATTCATCCTT AACACATTTG CAAGTTTTAA 960 TTCAGCCTAA AATAATATAA TCAGAGAAAA TGTTCTACTT GCATTTAACA TTATACTCAC 1020 AGGTTTGGAT TATATCATAG ATGTAGTTGG 1050
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