Tag | Content |
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EnhancerAtlas ID | HS105-20024 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chr12:97271980-97273610 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr12:97272768-97272779 | TGTGACTCATT | + | 6.62 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH12I096878 | chr12 | 97272061 | 97273551 |
| Enhancer Sequence | AAGGAACAGT GCACTTCCAG CTGACCTCCT GCAATCCCTG CTCAGCTTCT ACATCCCTGC 60 CCTGTGATAC ACCCACAGCC TTTTACTGTG GGGTCCCCTA GTTCCAGAAG GCTGCCCTCT 120 TGAGTGGGAT TCCTTCAAGA TGCTCAGAGC TGGTGTCCCT TCTGTGGCAT CCTATCCCAC 180 CAAACACCGA GTGTGCAGGT TGCCCACACC ACTGCCTTCT ATCCTTGCCT TGGGCAGCCT 240 TCCACCTTCA GAATTCTGCA GGCAGGAAGC ACACACTCCA TGTTCACATA CAGCCCCAAC 300 CTCAAGAGAT AAAAAATCCT TCTTCCCAAC ATCTCTGCCC ACACCTGATG GCCCCAGATG 360 AAGCTGACAA GTGATTACAG TCTTTCCCTG TTGCCAGCAC TCTGGTCTCT ACTGTGCTAC 420 CCTCTAGAGC CCTCAGTTTT GCAAAGAGAA CACTCTTCTC CATCACCCCC AACCCAAGGA 480 GAGAGAAGAG AAGAACAAAA AGCCATAGCA CTCCACTCCC AACAAATTCC CTTGTTAAAT 540 GAGCTCTCAT TTGCTTGCAT AGGATGTGTG GGGTGGCAGG AATGAGTGAG GTGGGAGAGC 600 AAGTATGCCA TTTTTTGGCA AGTCTTGGAA GGGGGTGATG GGAAGCTCTT TTTCTGCATT 660 CTTTAGAGTG GGAATGGAAT AGAATGTGAT TAACCACTAG TCTTATCTTT GGGGCTTAGC 720 AAAAATTCTG AGAATACAGA AATTCCATTG CACATGTTTT TGTAATCTTA TACCTCATAG 780 CCTCTAAATG TGACTCATTT TAAAGACAGT GAATGTTAGG TATAAAACAG TTTGCAGATC 840 ATTGCACAGC CTTTAAAGTG TGAGCGGCAG AGACCAGAGA TTCTGCCTCT TATCTGTTCA 900 ACTCTGTTTG ATGTACCCCT TCTGAGGACC AAGAACAAGA TAGATATGGC CCTTGCCCCC 960 TTAGAGCTTA TACTACCGGG AATGACTGCT AATAAATACA CAATTACAAT AAAGTATAAT 1020 AATGCTTTGA TAGAAGAATC ACAGCACAAA CCAGGAGCCC CTAACTTAGG ATGAAAGATT 1080 AGTATGCATG AGGGCAGGCT TCCTAGAGGA GTCGCCTTGA CTCTTGTGTC AAATACAGAT 1140 CCTGGTTTGT CACCTCAGGT TCTCTCAGTC TTTACCCTGG ACTGTGCTGC CAATGCGAGG 1200 GACCCACCAC TCAGTGGCCC TGAGAGTGCC AGGCCCTCCC TCTTGGCCTC TGCCACTCAC 1260 CTAGAGATTG CAGCTGTTTG TGGTGACCAG GAAATGCACC ACTCAGATCT CAGGCTGAGC 1320 GGAATGGAAG TGACATGACT CCAGCTTCTG CATTCTGAAA CCCCACTGTG TTAGTGCTGA 1380 TGCCTGCCTC CCCAGTCTGT GCCCAGCCAG GGACTAAGTG GTTCAGGGAT AGCAAAGCAG 1440 GCCCATATCT GTGAGATGTG GGACCCTTCT GCGGGGTGAC TTGGGCACTG TGCTTCCCCA 1500 TCAGCCTAGT GCCCCAGGGA ACTTCCTTCC CTGTCTCTAT CATGGTTTGA CATTCCCTGC 1560 TTTCTCAAGT TCCTTCCCCT TTCTCCCGTG CAGTTGTTTC ACCAAGTAAA TCTCTCGGAT 1620 ATCTAATCCA 1630
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