Tag | Content |
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EnhancerAtlas ID | HS034-06870 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr12:52256810-52259020 |
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) |
E2F6 | MA0471.1 | chr12:52257715-52257726 | GGGCGGGAAAG | + | 6.32 | EWSR1-FLI1 | MA0149.1 | chr12:52257040-52257058 | CCTTCCCTCCCTCCCTTC | - | 6.02 | EWSR1-FLI1 | MA0149.1 | chr12:52257041-52257059 | CTTCCCTCCCTCCCTTCC | - | 6.36 |
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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 |
GH12I051863 | chr12 | 52256796 | 52260450 |
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Enhancer Sequence | CCTGGCACAT AGCAGGTACT CCTTAAACGG TGATAATAAG GTCATCATCC CTTCATCCCT 60 TCACAGCCTG CGTCTTCGGG TTAGGCCTAG GAGGGCAGCC TCCTGCTGAG CCTCTGCACT 120 AGAATACCAA ACTCAGCGTG AGGCTCTTTG GGCTTTCAGC TTACTCTCTC TTGCCTCAAA 180 CAGGATGATC CCCTGTGGAA GATTTCTTCT CCTTTCCTTT TTCCTTGACC CCTTCCCTCC 240 CTCCCTTCCA GTCTCTACTC TGCCCTGCCT CTAACAGGAA GCCTTCCTTG ACTAATGTCT 300 CTCCATTCTC TGCCAACCTC CCCACTGCCT CCGTGTAGGT TCTGGCCTTC CAGCCCAGAG 360 CTCTATCCAC CCTACTCCAT TGCCCATGCC CCCAGTACAA ACCGTGGGCT TTCTCCGTGC 420 CAGCTCAAGG GAGGTCTGAC CCCATGGGGA CGCCTGACTG CAAAGGGAAG GATGCCGCCT 480 TCCACCGCAG CACCACCACA GCTCCGTGGA CCCGCTGGGA AAGGGGTGGG GCTGGCGAGG 540 AGGAGGCCAC CTGCCAGAGT GGCAGCAGAC AGGCCAGCTA AATCCTTGAC CTATGATTTA 600 AGAGGTCGGG CATAGTTCAA TAGAGCCCTC CAGGCTGAGT CCCAGCTCAT TCACACAGGT 660 CAGAGGGATG AGGGGCAAGG CGGAGAGGAG GGCCGTCTCC TCCGAGGGCC CTTGGCTTCC 720 TCCCTAGCCT TCTGGGGCAT AATCCAGCCT GAAAACCACA AAAACCCTGA AAACCACCAG 780 CTCCATTCCC ATCAGCGTAG ATGCCCCCTC TGAGAGGCCG GGGGAGGAGG GCGGGGCCGG 840 GAGGGGGTGG GCAGCAGGGC AGGAAAGTGG AGATTTAGGC AGGCACAGCG CCTGGCACAC 900 AGCAAGGGCG GGAAAGGCTC CTCCCTCTGC TAACCGCGGC GCCCTTTGTT AGGTCCCGAG 960 ACGCAGCGGA GCTGCCTGGC TTCCAGGTCG GCCCTGGTCT CTGCTCCCCT CCGTTGCCTT 1020 TGGAATTTGC CCTCAGACCT GGACCCTACC AGGGAACAGC GGGATTGTCT GATGGAATTC 1080 CACGTGCAAA CCGAGAGAGG TTTTGCCATA AATTCTAGTC CGGCCCCGGG AGGAGGGCCA 1140 CGCCTGGGCC CCACTCCCCA TCACCCTCCC GCCTCCCAGA CCCCCGGCAC AGGGCCTCCC 1200 CAGGCCGTGC CCCGGGCTGC CCCTGGGAGC GCTATGCAAA TGAGATGCAA AGTAGGCCGA 1260 GGCAGCCGCA AAGATTGGCT GCCGCAGAGG CTCAGTCCGC CCAATCCCCG GCCGCCCGCC 1320 ATCCTGGGCG CCCCCGGCCC GGGGCCCGGT CCCGCCCGTA AATCAGCTCC GTCAGCGTTA 1380 ATGGCTCCTG ACTAATTGCC TGGACTTGGG CTCCGGGCTC GGGTCGCCAG CATTAAAATT 1440 CAATCAGGCC TAGCGCTATG CTATTAAATA TTCATTGGGA GAGCTTCCCG AAATCGGGCT 1500 GGGGGATGGG GACGGACTGG GTTGGAGGGA CTACCCGAAT CCTCAGCTCC AGAGGAGGTG 1560 CCGCTCCTCC CCAGCGTGCT GTCAGCTTCT GCAGCGGCTG CCGGGCTTCC ATTCGGCTGG 1620 GTCTGATTTC TCTCTGGAGG TCCCTGCGCC CTCTCTAGAG ACTTTTGGGA GACTGAGCTG 1680 CCCTGCAGAA GGAATGTTAA GTTATGCCAA GGGGGCTGTG TCTGCTCAAC GCCTGGTCAC 1740 CTCGCCGCAC GACCCTTTAC CCAGTGCCCA CCATGAGCTC CTATTCATGC TGGAACCTTA 1800 GGTCCCACCG GGAGTGGAAG AGCTCCAGGG CACAGAAGGC TTAATCTTTA GAAGAGCCCC 1860 TACTTCCCTG GCCCTACTGC CGGGTTTTTA TGGAGCTACA CTGGCCATCC TCAGCGTGGC 1920 TAGAGAGAGC ATCAGTCTGG GCAGCTCCGG GTGTGTGCTG GAAGGGAGTA GTGGGCTTTG 1980 TACAGTCCTC CCCTCCTCTT CCCTGCCCTC AGGAATGCAG CCTGTCCGAG CTCCTGGGCC 2040 CCTGGCCTGA TGCTGAGCAG GCTGCCTGGA AGTTCTCAAA GAGGGTACCA AGGGGGAGGG 2100 GGCTGGGCCT GAGGGGGCCC TTGGGAGTGT CAGGGACTTA AGCAGAAACT GCATCCTCCA 2160 CCCACACACA CACACAATAG TCAGAGGGTT ATGAAGAGGG CTTAGCAGAT 2210
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