Tag | Content |
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EnhancerAtlas ID | HS046-09346 |
Organism | Homo sapiens |
Tissue/cell | Fetal_muscle_leg |
Coordinate | chr12:121179310-121180680 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr12:121180475-121180490 | TGAACTCCTGACCTC | - | 6.22 | RREB1 | MA0073.1 | chr12:121179374-121179394 | GGGGAGGGGGTGTTTGGAGG | - | 7.24 | Zfx | MA0146.2 | chr12:121180500-121180514 | CCCGCCTCGGCCTC | + | 6.01 |
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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 |
GH12I120741 | chr12 | 121179620 | 121180698 |
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Enhancer Sequence | AGCCCTTCCA CCTGGGGGCA GATGAAGGCC TGTCATTCCC TGTCCCCATG AGCCCGGGGA 60 CAGTGGGGAG GGGGTGTTTG GAGGCGCTGT GCCCCCGCCC GGCGAGGCAG CGCTGCTCCT 120 GACGCAGATG CGGCGTGGGG TTGAGGTTGT CTTTGGGCCC TTCCTCCAGG TGATGGGGGA 180 GAGGAACCCA AACAGCATTC ATCCCAGGCT GGGGACCTGG CTGTCTTGGC TGGAGTTCAG 240 GCCCCTCAGC TCCCCTGCCC TACCCGCTGA GAAGGGTCTG GGCCCTGGAG GGTCAAAGGT 300 AGCCGACTTG AGCCACACCG CTCCCAGCAG GGCAGAGGGC TGGAGTCAGC ACAGGCCGAG 360 TGGCAGCCCT GGAGGGGTTT CTGCTTCTCA GACCTGCCCA GGGCTCGTTC AGGTGGCCAC 420 GAAGAGCCTT TCCAGGAAGT GCAGCCTCGG AGGCCTGGGG TCCTCCATTT CAGATGAAGC 480 AACCCAGGCT CCGACCCAAG AGCCAGTCTG TGCACTCGGG GGCTTTGAGG TGCCGTCGTG 540 GGTCCGGGGT CTGTCCTTCG GTGAGGGAGA GTCGGCACAA ACCCTTGGCT TTGACGGGGT 600 GCTGCCCGTT AGTGGAAGCT CCTCCTAACT TAGAACTGAA TGTGGACTCT GCCCCCGGGC 660 CACTGGAGCC CGAACTGTCC TAGAGCCCAT GCCCCTCTGG ATACAGTTTC CTCAGTGTAG 720 ATTTCCTAAG GACAAGGACG TTCACTTACA GAACAACAGG ACCGTTTCCC ACCCTGGTCA 780 ACTTTCACAT CTGCACACTC CACTCGGATT GTGCCAGCTG GCACGGTGTC TGCGAAGTCA 840 GCTCTTCTCA AGGTCCAGGG GCCTGCATTG CATGTAGCTG AGAGGCCACC TGTTTCCTTC 900 CCTCTAGCCC TCTGGGACAA GTTCTCCATG CTTTGGTTCT TTTTTTTTTT TTTTTTGGAG 960 ATGGAGTCTC GCTCTGTTGC CAGGCTGGAG TACAGTGGCG CAATCTCGGC TCACCGCAGC 1020 CTCCACATCC CGGTTTCAAG CGATAAAGCG ATTCTCCTGC CTCAGCCTCC CGAGTAGCTG 1080 GGGTTACAGG CATGCGCCAC CACGCCTGGC TAATTTTTGT ATTTTTAGTA GAGACGGGCT 1140 TTCATCATGT TGGCCAGGCT GGTCTTGAAC TCCTGACCTC AGGTGATCCG CCCGCCTCGG 1200 CCTCCCAAAG TTCTGGGATT ACAGGCGTGG GCCACCATGC CTGGCCTGAA TTCATACATT 1260 TCTAAGTGTG GCTTTTGCTT CATCTCATAC ATTTTAGTGT CATATTTTCC TTATTACTCA 1320 GTTTTCTGAG GCCCATTGTG CTTTCTATTT TGATTTATCA GTTATTTAGG 1370
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