Tag | Content |
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EnhancerAtlas ID | HS193-08655 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr12:122205280-122206720 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr12:122206416-122206437 | GAAAAAAAAGAGAAAGCACGT | - | 6.18 | Zfx | MA0146.2 | chr12:122205309-122205323 | CCCGCCTCGGCCTC | + | 6.01 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 122206350 | 122206670 | chr12 | 122205366 | 122206325 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I121765 | chr12 | 122203081 | 122206677 |
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Enhancer Sequence | TGGTCTCGAT CTCCTGACCT GGTGATCTGC CCGCCTCGGC CTCCCAAAGT GCTGGGATTA 60 CAGGCGTGAG CCACCGCGCC CAGCTGCCCC TGCAAGCTTT AACTTCTGTG GTGAAATGAG 120 CCCAGAGAGT GACTGCAAAT GGGTGTAGGT TTCTTTCTGC AATGATAAAA AGGTTTTAAA 180 ACAGATTCTG GTGACAGTTG CACAACTCTG TGAATATACT AAAAGCCACT CAGTTGTGCA 240 CTTTCAGTGA GTGAATTGTA CGGTATCTGA ATCACATCAC AGTAAAATGG CTACATAAAC 300 ACATGTGCAC ACAACCAGCC CAGAGCCCCG GGGTGTGCAG ATGGACGCCT GGGCTTGTGA 360 ATGCCGGGCC AGGGAAGGAG CGATTTCTAG CCTCACCCGA TGTCACTGAG CTGTGTTTAT 420 TGGTGGCATC TGTCAGAGCT GGGCTCTGGG CACGGCGAGC TGTGAAATGA AAAGCTGCTG 480 CTCAGTCAGG CTTGTTGCCT GGAGTCTGTG TCTGCCTCAG GCTGCTCCTA GACAGAGGGC 540 ATTTCTCAGG GGAGCTTTGG GAGCAGGACA AAGGAGTGTG GCGCCTGCCA AGTGCTGAGG 600 GCTGACGTGG CTCTGCAGAG CTCTGGGAAG TTGCAGAGAG ACCTCCTGGT TGCTCTTCAA 660 GCTGGAAGTT GGGGGATCTG GCCAACTGCC TTTGCTGTCA GAAATTTGGA GCCCAGGGGC 720 TTCTTAGACT CTGACAGGCG AGACTAGGAT ACATGAGTGG AGGTGGGAGT TTTCTGGGGA 780 CAAAGAAGTA GATGGACATC TCACCCTGTC CCCATGACCG CACGTGGCAC CTGCAACAAT 840 CTCCTGTCAC CTCTGCGCTG GTGGCATCCA GATTAGCTGC TGCTTTCACC AGCCACACCT 900 CCCAGGCATC ATTCATGTCA ACATTTATTG AGTGCCTGTT GTTTACCTGG TGCTGTTAGT 960 GCTGTGAACA CAGAGCTGCA TAAAACCTTG CCCCTCAGCA TAACTCCTGG GGAACACACA 1020 GGCTGTTGCT TGAAAAGCCA ATTTATGCCC AGAACTGTTG CATGGGCCGT CAAGGGAAGA 1080 GTGATGGTTT AGATCCAGTC TCGTTCTTAC GATGTGCGTA TGCGAGACCC TGCCTGGAAA 1140 AAAAAGAGAA AGCACGTGGG CGTGTGTGTG GACCCATTTC CCTGCCCAGT CCCAAGAGAG 1200 TTCTGGAGGG ATGAAGGTTA ATGACTGTTC CCACGAGCAT CCCCAGCCTC CACCTCCCAG 1260 TCCTGGGGAG GAGGGAGTTG GCTGCTCCTG GGTGCATTTG GCAAGTTGCT GCCATGTGTT 1320 TGGACTAGAG GAGCCTGGGG AGGCCAGCCA AGGCCTGAGA CACACTCTGG GATGTTGAAG 1380 GTTACAGGGT TGAGGGGTCC AACTCCTTTT TTCCTAGGCT GCCCCTGATG CTGGGGGTGG 1440
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