Tag | Content |
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EnhancerAtlas ID | HS062-08035 | Organism | Homo sapiens | Tissue/cell | GM18486 | Coordinate | chr19:8082080-8083500 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TFAP2C | MA0524.2 | chr19:8082369-8082381 | TGCCCTGAGGCA | - | 6.18 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 8082513 | 8082563 | chr19 | 8082606 | 8082713 |
| | Number: 1 | ID | Chromosome | Start | End |
GH19I008017 | chr19 | 8082821 | 8082970 |
| Enhancer Sequence | GGCTAGTCTC GAACTCCTGA CCTCAAGTGA TCCACCCGCC TTGGCCTCCC AAAGTGCTGG 60 GATTACAGGC ATGAGCCACC ACATCTGGCT CTGTTTTGCT TTTTTTTTTT TTTTAAATGA 120 GAAGCATAGT CTTGATCCTG GGGAGTAGGA ATCGGCCACG GTAGTTCGGG GTACTCTTGC 180 TGTCCCTCTC AGTCCCTGTC TGTTCCTTCA GCACAAGCTA TTGTGAGTCC AGGAGGTCAG 240 GAGACAGAGA AGCTGACTGA GCCCAAGTCC CTGTTCTAGA GGACATCACT GCCCTGAGGC 300 AACGATGGAC ACGTGGACAC ATAAATCCAC CCAACGTGAC AAGGGACGGG CACAGATCGG 360 CCTCCCATGG AGGGCAGTGT TGGGGCCACA TTAATCCATG AGGAAGGGTC GGCTAGGCAG 420 AGAAGAGAGG TGGGGAGTTC CAGACAGAGG GACCGACAGG AGTAACGGCA CAAATTTGTC 480 AGGGAGGATC ATTCAGGGAG CAGGGGTGCC GGTTCGGAGG GGAGATCACA GTGAGGTGGC 540 ACTGGCCTTG AGGAGCCCTG GAAAGTCGGG CAGAGAAGAT CTGATGTGAT CCCATAGCCC 600 ACGTAGTCAG CCCACAACAG CCCGATTCAG CCCATGCCTG TTTTCCGGCG GCCCGTGAGC 660 CAAGAATGAT TTTTCCACAG TTGGAAAAAT AACAGTAGCG TTTTGTGACA TGTGAAAATT 720 ACATGAAATG CAAGTTTCAG CGTCCATAAA GTTTGACAGT AACACAGCCA CGCCTCTCCT 780 TTGTGTGTGG CCAGGGGACG CTCTTGAGCT GTCATAGAGG CGGAAGTGGT GCACAGGACG 840 CGCTTCATGG ATGTGCACAC TGCCTCACAC GGGGCCCTGC CCTTCCACTG TCCCTGTTCT 900 GAAGTTCTTT ATGATTGAAG GGCCCCAGGT TTTTATTTTG CATCAGACCA TGCACATTAT 960 GTCATGTAGG GTACACAGCA ACAGAGACCG TGTGCCCTAG AAAGCCCCGA GTATTTGCTG 1020 TGAAGCCCTT TTCAGAAAAC ACTGGTGGAT CCCCCGCAGA GACTTCCATG TCCTGATACC 1080 CTGGAACCCA TGAATATGGT ACCTCACACG GCAGGCTTAA GGGTCTTTTT TTTTTTCTTT 1140 AAGAGATAGG GTCTTGCTCT GTCACCCAGG CTGGAGTGCA GTGGCACGAT CACAGTTCAC 1200 TACAGCCTCA AAACTTTTAG TCTCAAGTGA TCCGCCTGGC TTAGCCTCCT GAGTAGCTGG 1260 GGCTACAGAC ATAATGCCCA GCTAATTAAA AAAAAAAAAA AATAGAGATG GGGTCTCACT 1320 ATGTTGCCCA AGCTGGTTTT ATTGAACTCC TGGCCTCAAG TGATACTCCC AACTCAGCCT 1380 CCCAGTGTTG GGATTACAGG CATGAGCCAC CGTGCCCAAC 1420
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