Tag | Content |
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EnhancerAtlas ID | HS044-10981 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr6:5132600-5133710 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr6:5132655-5132676 | AAACAAAAACAGAAACTACAA | - | 6.64 | MIXL1 | MA0662.1 | chr6:5132709-5132719 | TCTAATTAAC | + | 6.02 |
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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 |
GH06I005131 | chr6 | 5132210 | 5133833 |
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Enhancer Sequence | GAGATACTCC TTTCTAGGTC TTCTGACTTC AAAATCTAGC ACTTAAAAAA AACAAAAACA 60 AAAACAGAAA CTACAACACA CCTCCTCTGA AAGAATGTCT TCTATTCTTT CTAATTAACA 120 TTTTAAACGA AAATCCCATG CTTTCAAAGA GAAGAGTACC CAGCCTGTGC TACAAAAGGC 180 TGAGAGTGAA AGTGGGAGGT TTGATTTCCA AGTTTAATTT GTAGTTCTGC TCCAGGAGCA 240 CATCTCAGCT ACAGTTGTTT TCAGAAATGT GAGTTCAGGA TATTAACGAG TAATGCTGAG 300 CAAAGAAAAT CACAAGCCAA CCACCTCTTG GATCACATAA GTGGAACTTA CCTTTGTGAA 360 GCACCATGGG GAGCCGTAAA CCCCTTGCCC AGTTTCTTTT GAGTTTACTC AGATTTAGCC 420 AGAAAAGGAA GCTGGCTGAA GCAAAAGAGA ACTAGAACTC CCATCTCCGT TTAACCTATT 480 TGCAACTCTG CCAAGGCTGC AGAGCCAGCA GCAGCTGTGG CCTATCAGTG CTCATGAGAA 540 GTGAGTCTTG CAAGGAAATG ACATTTCCTT CCCAGGGTAG GGAAGCACGC ACTGCTGAGA 600 TTCTACGGGT ATGACGGCAG CACCAGCCAC TGCAGGACAA AGATGACTAG AGAAGGTTCG 660 CCCGCCTCCC CAAGGAATCA GGACTGGTTA CTTTGTCTCT TTTTGTTACT GTTGTTGTGT 720 TGGGCAGGGT GTGTGTGCTG GGCAGCCTGA GGGCCACTTG TCCCCGTGCT GCCATCTCAC 780 GGGTGAGGCT ATGGGTGGCA CTGTTTTACA CATCTATATG GTAGCTAGAA ACAGAGGGCT 840 CTTTCCTCTC ACATAAAAGC AAAATCAAGA TGATCGATCG TTTTCTTCTT AGGTTTTCCT 900 AAATTTTATT TTCTAAAAAA GGAGAGAACA TTTTTTGTGA CTGTAGGCAG CAGATTCCTG 960 ACAGCGTCTG CTGTCTGACA GGAGTGCAAA AGACATAGTT ATCCTTTAGA ATACAGAAGC 1020 AAACTTGCAC GGGCTTAAAT CTAGCACGCC ACCACCACCT GTGAGGAAGG CTCCAAAGAC 1080 ACGATCCTGA CCCGTCCAGC CTCTGTCAAT 1110
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