Tag | Content |
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EnhancerAtlas ID | HS182-05643 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr12:132662650-132663950 |
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 | chr12:132663148-132663162 | TGTCCCTTGGGATT | - | 6.24 | KLF16 | MA0741.1 | chr12:132663670-132663681 | GCCCCGCCCCC | + | 6.02 | KLF5 | MA0599.1 | chr12:132663670-132663680 | GCCCCGCCCC | + | 6.02 | Myod1 | MA0499.1 | chr12:132663005-132663018 | TCCAGCTGTCCCT | + | 6.16 | SP4 | MA0685.1 | chr12:132663667-132663684 | CGAGCCCCGCCCCCTCC | + | 6.16 | ZNF740 | MA0753.2 | chr12:132662876-132662889 | CCGCCCCCCCCAC | + | 7.82 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr12 | 132662941 | 132663228 | chr12 | 132663524 | 132663727 | chr12 | 132662936 | 132663290 | chr12 | 132663332 | 132663875 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I132178 | chr12 | 132662746 | 132663750 |
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Enhancer Sequence | TCTGCCGGGC ACAGTGGCTC GCGCCTGTAA TCCCAGCTCT TTGGGAGGCC AAAGTGGGAG 60 GAGTGTTTGA GGCTGGGAGC TCGAGACCAG GCTGGGCAAC ATGGCAACAA AAAAAATTAA 120 AAACTTAGCT GGGTATGGCG GTGTGCACCT GTAGTCCCAG TGACCGGGGA GGGTGTGACG 180 GGAGGGTGGG GAGCCCGGGA GTTTGAGGCT GTACTGAGCT CAGAACCCGC CCCCCCCACC 240 CCCTGCACTC CAGCCTGGGC GACAGAATGA GACCCCTGAA AAGTGTTGGT TTCTGACTTT 300 TTTCGTTTTT GAAATCGTTT CCGGCTGGCC CAAGTCGAAA AATAATGCAG ATGTCTCCAG 360 CTGTCCCTGA GAACACTTCC TGTTCCTTGA TCTGTGGCTT GTGATTCTCC CCCCGCCCCC 420 ACTCCCCTTA CATGGGGCTG TGGCTGCCCC CAGCCTTTCC CTTTCGTGAC CTCAGGATTG 480 TATGACTGCA GGTTGGGCTG TCCCTTGGGA TTCAGGGCCT CAAATGTACC TGCTGACCAG 540 TTGAAGAGTG CTGACCAGCT GTCCTGCTGA ACACCTCTCA ATCTGGATTT TTGACATTTC 600 CCTGTGATTA AATTCAGGGA ATCCAGCTTT GGTGACAGAG CCACTGAAGC AAGGCTGTTC 660 CCTGCTTGGA GACGCACCCA CTTTACACGT GTAGGGTGGC GAGTCTGACA AACGCAGCCA 720 CAGGCAGCCC CCACCGGGGG AGCCGGACGT TTCCATCCAC CCAGACAGCA GCGTTCACGC 780 CCAGGACCAT GTGGGCCTGC GCCCCGGGCC GCACCTGCCT CTCCTGCATT CCGTGTCTGG 840 CATCTTGTGT CGTTGCCACC CTGCGTGCCA TGTCTGGCTT CTCTCTCTCA GCGAGTGTCC 900 TCCGTGTCTC CGAGTCGCGC CCGTTCTGTT GTGCGTAAAT GCCGTTCTCA GAGCTGTTGT 960 TTGTTTAGGG ATGTATCATG TTTTCAGCTT AACATTTGTG CCATTCGTGT GCCCTGGCGA 1020 GCCCCGCCCC CTCCAAGTTA CTGGCGTGCT GTGGGCGTTC TCGGGTTTCT ACTCTTCCTG 1080 CTGTCGCCAG CGCAGCCGAA GCACCAAGCA GGAAGCTCTG CCGAGTTCTT GGCTTCAGGT 1140 AACGTGTCAG ACCCAGGGCA TGAGCTCCAG TCCCTCTTGC CTCCACAAAG GACAGCACAT 1200 TTCCAGTTCA GGGTGCTGTG GCCGACACCG TGCGTGTGGC TGGGGCCAGT GTCACCGCGA 1260 ATCTCGGCTG CTCCACGCCC TTGCTGTGGG CTTGGGGCCA 1300
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