Tag | Content |
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EnhancerAtlas ID | HS059-44634 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr8:9320480-9322130 |
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) |
Foxq1 | MA0040.1 | chr8:9320780-9320791 | TATTGTTTATT | + | 6.62 | IRF1 | MA0050.2 | chr8:9321135-9321156 | AAAGAGTAAGTGAAAGAAATA | - | 6.26 | NR2C2 | MA0504.1 | chr8:9320582-9320597 | GGAGGTCAGAGGTTA | + | 6.66 | Nr2f6 | MA0677.1 | chr8:9320583-9320597 | GAGGTCAGAGGTTA | + | 6.04 | POU4F2 | MA0683.1 | chr8:9321825-9321841 | CTGCATTTTTAATGAG | + | 7 |
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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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Enhancer Sequence | GTCTGTACAA AAAAGAAAAA GGAAAAATTA GCCAGGCGTG GTAGTGCACA CCTGTAGTCC 60 CAGCTACTTG GAAGCCTGAG GCAAAAGGAT CACTTGGGCC CAGGAGGTCA GAGGTTACAG 120 TGAGCTGTGG TCACGCCATC ACACTCCAGC CTGAATGACA GAGGAAGACC CTGTCTCAAT 180 TTTTTTTAAA GGACAATGTA AAGATGCCAA GTGATGAAAA CAGAATTCAA AAAACATTGT 240 TTTAAAAAGA ATGAATAGCA ATACAATAAT GACAGAAGTG ATTGTTTTGG TGAATAGGAT 300 TATTGTTTAT TGTTTTCCTC AAATTTTCTA AATTTTCTCT AATTATTTGT GTAACTGAAA 360 AATTTTTAAA TAACAAACAA AAGATTAAAT AACAATAACA GCTGTATCTA TTGGACTTCA 420 CTGCCAACAT AGCAAACACT TTGGACTACT CTTTGTATAT GTTATCTAAT TTAATCTGCA 480 CATTAACTCC ATAAGTCACT ACCAATATAG TCCCAATTTT GCAATAGAGG AACCGAAGCC 540 ACAAGAAATG TTAAGTTCTT CACCCAGGGA CACAGCCAGG ACCATGGCAG AGAGCGTTTC 600 AATCCATATA TGTCTGACTA TAGAATCCAA CATTTCAAAC ACTGGGCTAA AGAGCAAAGA 660 GTAAGTGAAA GAAATACAAA TAGCAAGTAA CATTTCATGA GAGAAATGAG TGGGTAAGGC 720 AATTGCCCAG GAAATCACAT TGAGGGGAGA AATGAATACA GCTCATAAAT TCAAAACCAA 780 AAGTCCACAG CCTTCTGGAT GTCACAGGGC TTTTGGTATC GTATTTTAAT GTTTAGACAT 840 TCAACATTTT AAGAGCTCAC TCCTTTGTGG TCAAGCCCTT TGAAACAATG AGCTTTATGC 900 ATGGCTTGTT TTTGTGCCTA ATGATCCGTG GTAGAAGAAC TTACTGTCTC GGTGACCTCT 960 GTCTCCTGGC GACAGTGAGG CCCACCTGGT CTTCCCAGCA TCCCTGTGGT TATGTGGCAG 1020 TTTATCAAAT GGCCACAAGC ACAATAGTGA ATCAGTATTG AATGACAATA ATTTCAAAGG 1080 TAAGTTCAAA AATAAGCTCT TTCTAAAATT CTTTTCATGA GTCATACCAC AAGAGTAAAA 1140 AACAGATTTT GTGAGCAAGG AGGTACTTCT CTCACACAAA TGACAAGTTT TTATATATAA 1200 TAATAACTTA GAGTTGCTAA CCTCCATATG CAGGAATGAA ACTATTCTGC ATTAGGTCAT 1260 CAGCAATTCA GCTCTGATCT TTCTATCTGT TTTGAAGAAC CTTTCCTTCA TCTGAGGTCA 1320 ATGTTTGTAG GATCAGAATA ACATCCTGCA TTTTTAATGA GCTTTTCAAA TCACATATTT 1380 TGCAAAAGGT CATGCCTCCT GTGTTATTTT TATTTCATTT TGGAAGGAAA GTTAAATGTT 1440 TATAGCTCAA TGGGCAATTT TAAGTTCTTC TACAAGATCC TGTTCAAAGG AAATACATTA 1500 GAGTTTGTGT GTATTCTGTA AACTTGCATT TGGGAGAGAA TATGATGTGC ATATGTGTCC 1560 ACATGGTGAT CATAATTCCT CTAATATGAT ACCCTTGGGT TTAATCATAC CATGTTAATT 1620 CAACTGGACT TAGAGTTCTA ATTAATTTAA 1650
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