Tag | Content |
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EnhancerAtlas ID | HS106-02343 |
Organism | Homo sapiens |
Tissue/cell | iPSC |
Coordinate | chrX:10008540-10010080 |
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) |
EBF1 | MA0154.3 | chrX:10008842-10008856 | AATCCCAAGGGATT | - | 6.04 | EBF1 | MA0154.3 | chrX:10008842-10008856 | AATCCCAAGGGATT | + | 6.34 |
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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 |
GH0XI010040 | chrX | 10008040 | 10009967 |
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Enhancer Sequence | CGAACAGCCA GATGAAGAAA CACACAGAGG CCTGGAAGGC TCCTGAGCAC AGGAGCTTCT 60 GTCCCTATGG AGTTGGGATG CACACGGATG CGTCTGCCAA CCCGGGAGCT CTCTGAACCC 120 GGCACTTTAA AGGGATTTTT GTGGAGGTTT CATCACGTAG GCATGATTGA TTATTAACTC 180 AGTCTCCGCC TTTCTCCCTC TCTCCAAGCC TCCAATCATG GCTTGGTCTT TCTGGTGCCC 240 AGCCCCCATC CAGGAGCCCA CCAAGAATCA CCTAATTAAA AAAGACCTCC CATCACTCAG 300 GAAATCCCAA GGGATTAGGA GCTCTGTGTC AGGATTCCAG GGTCAAAGAC GAAATATCAG 360 AACAAAAGAT GTACCTAGCA CCCCTATTGC TCAGGAAATT CCAAGGGTTT TAGGAGCTGT 420 GTGCCAGGAC CCTGGAGCAG AAGCAAATAT ATTTCTTCAT TTGCCACAAT ATCACACTTC 480 TGACCCTGCT CACCTGGAAT CTTCCTTGTC CATTTAGATG CCAGGCACGT GGGGGACAGA 540 TGAATATTTA CCTGTGAGCA TCAGTCATAC AAGTGGTTCT AAACCTGGGC TTCCAGTTCG 600 AATGTAGCAT TTCAGAAATA CTGCTGCCTG TGTTCCACCA CAGACCAGTT AAGTCCCCAT 660 CGAAATGGCC CCTGGCCAGG GTGGAGATTC ACTGGCTATG GGACTCCATC TTGCTCACAA 720 TAACCAGTGA ATGTTTGTTG ATCATTTCAA CCCCTTAATG ACCTTGGAAA CTAGAAATGG 780 GGTTTGTAAA GGGGAAAGAG GTGGAATAGC TATAAATGCC ACGGTATTAT TTTTATGGAA 840 TGGGAGTGGG AGTGGGGCGT GGGTAGTGAG GCTGGGGCTA AGGTTTGATG TTCTGCTGAC 900 CATAAAATAA TTTGTATTTG TGTCGAGTAG CTTTCTCCTC TCAGCTCCCA TGGCTGTGTC 960 CCTGCCTTTG AGTGAATCTG TTGTGTAGTG GTAATTTGTT ATGTATTTGG TCCCCCGGTG 1020 AGCTGAATTC CTTGAGGTTA ACTCCTGGCA CTGAGCATCT CAAATAGCTT TCCTGCAGTG 1080 AATATTTAAA CAAATGAATA GCACTTTGCA GTTTTTTCAC AGTGCTTTTC CTAGGGTGCG 1140 GTCCCCAAGC CCTCTCATCC TTAGCCAAGA TTACATGCCC GAGGCTTGTG AGCATCATTT 1200 AGACCAAGCT TCATGCATGC CTTGCCTAGC AGGAGCTCTC TGTACATACC ATCTGTTTGC 1260 CAGGAAGACT GCCCACCTCT GTGCCTTGGC ATGGTCATTA CAGACAAATG CCCACTGGGG 1320 TTGGGCCTAC AACCAGATGG CAAGCTGTCA GAGGGGTAAC AGGGAGTGGT GGGGACTGTG 1380 GTGAACTAGC GAGCAGCCCC TTCTAAAGGG ATGGCTCTAG TCAGCTTTAG CCAGTTACCG 1440 TCTTTGGGCA CTGTAATCCC TATGTGCCAA CCCTTCTGAT TTTCTTTTTT TAATTTAAAA 1500 CAATTTAAGG AAGATGGGGT CTCCCTATGT TGCCCAGACT 1540
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