Tag | Content |
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EnhancerAtlas ID | HS059-12902 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr13:53495090-53496280 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GFI1 | MA0038.2 | chr13:53495687-53495699 | TGCTGTGATTTC | - | 6.22 | Gfi1b | MA0483.1 | chr13:53495687-53495698 | TGCTGTGATTT | - | 6.62 |
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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 |
GH13I052920 | chr13 | 53494906 | 53496073 |
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Enhancer Sequence | CAGGATGGTC TTGATCTCTC GACCTCGTGA TTCGCCCACC TGGGCCTCCC AAAGGGCTGG 60 GATTACAGAT GTGAGCCACC GTGCCCGGCC CACACTACTG TTTTGATGGA GTGGAAGCAA 120 GTCCAAAGTT GTGAGGAGTA AATAAATGAT GGATTGAGAA ATTCTCTGTG AACCCTCAAT 180 GGAGTTATTG TGCAGAGCTT CTATAGAAGG GGACCTGTCT CTTTGTGCTA CGTGTTTATC 240 TGCTTGTCTA GGGGAAGCCA AAGCAGATTC TTGTCACCTT CATTCTCAGT GTTGGGGAAG 300 TATGCTGCTG GAGCGTGGCC TTCACCTTTT CTATGGCCCC TCTCAGCATC CGAAGCACAG 360 CAAGGTATCA CATGATGTGA CTGTCACTAG TAAGCTCATG TGACATGACA CAGGGAGGAC 420 TTATCCAAAA CAATAAAGGG AACTGAAAGT CAGAAAGCAG AAGTGGCCAC ATATTAGATT 480 TTGTATGCAT TCATGGGTAA GCTGAGATTA AACCACTCAG CATTTGTTCC TAAGTGCGAA 540 GCCAGAGAGG GCTCTGAGGC AGAAATGCTC AGTGTTCACC CACAACTAGA GTGACCCTGC 600 TGTGATTTCT GCCTTCACAA CCATGTGGAT TTAGTGCCTT CCCCAAAACT TGTTTCTCGT 660 TGAAAGAAGG AGGGTCCAAA TGCCCACAGT CACAGGATGA TAGATTCAGT ACAAAGTTAT 720 GGAGACAGTA TGGGCAGGCA TGGCCATGGT CAACCATTGG CCAAAATTCA AGGCTGTGGA 780 ACACATAGAG CCTCTATTGA GGAGGGAGCT TGTTCAGACT TTGCTATTAG GAGACTCTTT 840 TTACTCAGAA GACAAAGCAA CATATTCTTT GTGCTCCTTT CTGCATTTCT TCTCCAGCTA 900 AGTGCTGGTG GCTCTTACTG TGAGCTTCGT GGGTTTCACT AGAGCACTGT GGGCAACTCA 960 GACTGCTGGT CTCTCACAGG ACTCCTCTGA GTGATAATTA GATGGTATAC TTTATGAGCT 1020 CATGGTAGAC AGTCTAAATG TAATTGTAAT AAAGTTTTCT TCATGGCAGC TTAACATACT 1080 AAGGATAGGA ACATCACTTC TCAGCTAAGG AGCTAAGTGC AGAGAAGGCC AGTGACTAAA 1140 ATGAGTTCAA CCAGTCAGTG GCTTGGACTG GCTCTGAAGT TGCAGTTGTT 1190
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