Tag | Content |
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EnhancerAtlas ID | HS060-04751 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr10:112668110-112669690 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr10:112668871-112668881 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr10:112668871-112668881 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr10:112668871-112668881 | ATTTTCCATT | + | 6.02 | ZNF263 | MA0528.1 | chr10:112668311-112668332 | GAAGGATGGGGGTGGAGGGAG | + | 6.11 |
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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 |
GH10I110909 | chr10 | 112668861 | 112669237 |
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Enhancer Sequence | GACGCAAGTA CAATATTTTG TGCCAAAATG TTAACTAATG ATTACTTATG GGCCTTATTT 60 CTACTTTCTA TTACATGAAC ATCCATTACT AAGAAAGGGT TAAGAACAAA ACTGAAGTAT 120 TCAAATAGCA AGTCATCTTA TATTGAAATT TTAATTCAGC ATCAAACTTA CTAAGGCATA 180 GTCTCTAGGC TTGAGGATCC TGAAGGATGG GGGTGGAGGG AGAAGAAACA GGCACATAAG 240 CGAAGAAGCA TAATGCAATA TAAGTTCTAT ACTTAGAAGT ATTTGTAAAA ATGCCATGGG 300 AACACAGAAT AGGGAGCAAT TGTGTCAGGT ACAGATGATG GGGGAGGAAC TTTAGGTGCA 360 GGTAACAACA GTTTGTGCAG AGGCATGAAG ATAGGCAACA CAAAGCACAT GGTGCATTAT 420 GGGGGAGGCA AGGAATGCTT AAAAAAAAAA AAAAAGAGTT ACGAGCAATC TGTCTGGAAA 480 CAAACCCTAA CCAAACTGCA ATCAAATTGA TTTTGAAGGA AATAAGGAGA ACCACTGAAA 540 TATTTTAAGA ATGAGAATGA CCTGAACAGA TCTAAAATGT ATTCAGGAGG ACAATTACAG 600 GGCTATTTCA AATAGTTTAG GTGCAGGTGA AAAATGGGTG CTTCAACTGA GCACCTAGCT 660 ACACTGTGAA ATCATAAAGC TAGGGAAAGA CAAGATTTAA GTAAAAGCTG TGATGGGGTG 720 GTGATTAACT CAGGCCAGCA AAACAATGAT ACCCTCAACA GATTTTCCAT TAATCAGGCA 780 AGCATCTTCA CAGAAACAAC TTCAAACTGT AAAGACTAAG ATTTATATAA TTTTGTTATG 840 AAAAAGTTGG CCTTTTTTTT TTTTGAGACG GAGTCTTGCT CTGGCACCAG GCTGGAGTGC 900 AGTGGCGCGA TCTCGGCTCA CTGCAACCCC CACCTCCTGG GTTCAAGCGA TTCCCCAGCC 960 TCAGCCTCCT GAGTTGGGAT TACAGGCATG TGCCACCACA CCCAGCTAAT TTTTTGTATT 1020 TTTAGTAGAG ATGGGGTTTC ATCATGTTGG CCAGGATGGT CTCGATCTCC TGACCTCGTG 1080 ATCCACCCGC CTTGGCCTCC CAAAGTGCTG GGATTACAGG CATGAGCCAC CGTGCCCGGC 1140 CAGAAAAGGT TGGCTCTTAT GTCATCTTTT GAACTTAAAT GTTGTGGACT TGCAGGAGAC 1200 CTACAAGTGA AAGTCTTAGA AAAAGACAGA ATCCTTCGCT AAGATCTTCC CTGCACACCT 1260 ATTACATATT TGGGAAAAGA GCCTAGCTCC TAGTTCTCTG TTCAAGAAAG TATAAATCTT 1320 TACAGTGGAC AGAAATTGTG AGTTAATAGG CCAAATTAAT GCTGTACCTT GTATTCTATT 1380 TGGAAATAAG CACTGGACAG TAAAGACTAG AGTGATAAAC ATGAGAATGA TGTTGTTTTA 1440 GGTGACAACA AAAGCATTAC TCTTTCAGAG TAGAAAACTA ACAAATGTAA CATAAAAATA 1500 ATTTGGAATG ATAAAGTACC TATACGAACA GATTTTTTCT TTCAACAAAC ATACTAAATG 1560 TCTATAATGT ACCAGCCGTA 1580
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