Tag | Content |
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EnhancerAtlas ID | HS175-03897 |
Organism | Homo sapiens |
Tissue/cell | SK-N-MC |
Coordinate | chr11:1356550-1358290 |
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) |
KLF16 | MA0741.1 | chr11:1357943-1357954 | GGGGGCGGGGC | - | 6.02 | KLF16 | MA0741.1 | chr11:1357965-1357976 | GGGGGCGGGGC | - | 6.02 | KLF16 | MA0741.1 | chr11:1357986-1357997 | GGGGGCGGGGC | - | 6.02 | KLF16 | MA0741.1 | chr11:1358006-1358017 | GGGGGCGGGGC | - | 6.02 | KLF16 | MA0741.1 | chr11:1358025-1358036 | GGGGGCGGGGC | - | 6.02 | KLF16 | MA0741.1 | chr11:1358038-1358049 | GGGGGCGGGGC | - | 6.02 | KLF16 | MA0741.1 | chr11:1358060-1358071 | GGGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr11:1357922-1357932 | GGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr11:1357927-1357937 | GGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr11:1357944-1357954 | GGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr11:1357966-1357976 | GGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr11:1357987-1357997 | GGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr11:1358007-1358017 | GGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr11:1358026-1358036 | GGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr11:1358039-1358049 | GGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr11:1358061-1358071 | GGGGCGGGGC | - | 6.02 | SP2 | MA0516.2 | chr11:1357984-1358001 | CGGGGGGCGGGGCGTGG | - | 6.27 | SP2 | MA0516.2 | chr11:1358036-1358053 | GTGGGGGCGGGGCGTGG | - | 6.32 | SP2 | MA0516.2 | chr11:1357941-1357958 | GGGGGGGCGGGGCGTGG | - | 6.63 | SP2 | MA0516.2 | chr11:1357963-1357980 | GGGGGGGCGGGGCGTGG | - | 6.63 | SP2 | MA0516.2 | chr11:1358058-1358075 | GGGGGGGCGGGGCGTGG | - | 6.63 | SP3 | MA0746.2 | chr11:1357942-1357955 | GGGGGGCGGGGCG | - | 6.11 | SP3 | MA0746.2 | chr11:1357964-1357977 | GGGGGGCGGGGCG | - | 6.11 | SP3 | MA0746.2 | chr11:1357985-1357998 | GGGGGGCGGGGCG | - | 6.11 | SP3 | MA0746.2 | chr11:1358059-1358072 | GGGGGGCGGGGCG | - | 6.11 | ZNF263 | MA0528.1 | chr11:1357320-1357341 | AAAGGAGTGGGGTGGGGAGGG | + | 6.08 | ZNF263 | MA0528.1 | chr11:1357590-1357611 | CTCCTCCCTCCTCCCACCTCC | - | 6.19 | ZNF263 | MA0528.1 | chr11:1357560-1357581 | CCTCCCCCCTCCCCCGCCCTC | - | 6.3 | ZNF263 | MA0528.1 | chr11:1357547-1357568 | CCTCCCCCGCCGTCCTCCCCC | - | 6.45 | ZNF263 | MA0528.1 | chr11:1357579-1357600 | TCTCTCCCACCCTCCTCCCTC | - | 6.67 | ZNF263 | MA0528.1 | chr11:1357583-1357604 | TCCCACCCTCCTCCCTCCTCC | - | 7.51 | ZNF263 | MA0528.1 | chr11:1357576-1357597 | CCCTCTCTCCCACCCTCCTCC | - | 8.03 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 1356600 | 1357964 | chr11 | 1357863 | 1358286 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I001335 | chr11 | 1356472 | 1359269 |
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Enhancer Sequence | ACTGCACTCC ACCTGTCCCT GAGAATGACT CCTGACTCCA CTGCATACGA GTCCCTCTCC 60 CCCACCTTCT ACCTGGAAAA CTCCTATTCA TCCCATCAAG ACCCAGCCCT GGGTTGCTCC 120 TGGGTGGCTT TTTTCACTCT CCTTGGCAGC TTTAACTGCT GCCTGGGATG TGGGCTCAGG 180 GCCAGTGCCC TGGAGGGCCC CTGTCATAGC CCTTCTCACC AGCACTGAGA TTGGTCACCT 240 CCGAGTCTGG TGGGCCCGGG GCCCCCATGC AGGTGCACAC AAGTGCTGCT GAGTGACTGG 300 TGATCATACA GCCAACATTC GCGGTGACAT TCATGCACCG GGGACTTCAC AATTCCCCGG 360 ACTCGTCATA AGGGCTGCTC GGCCCCATCT TACAAATGGG GAAACTGAGC CTGGGGGGTT 420 CAGTAACTTG CTGAGTTCAC ACAAACAGTG AGTGGATGGC TGGATGAGTT TGTAAAAGGA 480 AGGTCGATTC TGCATGATGA AGCTAAATTG GAGCCCAAAA TTCTCTCTTC CGGCCCCCAG 540 TAGAATATTA TGGGTGCACC CAAAGGAATG TAAAAAGACC AGATGCCCAG GACACGGGGC 600 GGTGCCTGAT GAAACAGCTG CATTAGAGAG TGACTTTGCA ACTCTGGAGA GAAGCCACTG 660 AAACCCAGCG CTCCTATAAA TAGCAGCTCT TGCAAAGCAT CGGGTGTGAA TTTTCGTGGT 720 GTTGGCAAAT TCAGAGATTG AGAAATCCAG AGACGTTCAT GTTCCCGGAG AAAGGAGTGG 780 GGTGGGGAGG GAGGTCGCAA GCAATGCCAT CTTCAGGAAC AAAACTCCTG CATAACGAAG 840 CCCAGGTTTC TGTGTTTTCG TGGGTGTTCC CGGGCACCTT CGGGCAGGTG GCCCCAGGCG 900 ATGTTGTGTG TCTCTCCTGG CTGTGGACGA ATGGACGCCT GGGGTGAGGC TGGGCCAGGG 960 ACCTGGGGCT TGTGGGTGTC GGCTCCCATC CCGGGGTCCT CCCCCGCCGT CCTCCCCCCT 1020 CCCCCGCCCT CTCTCCCACC CTCCTCCCTC CTCCCACCTC CCCTGCCCTC TCCCACCGGC 1080 GTGCACCCCC CCGCCCCGCT GCTCACCGCC CACCACTCCC CAGAGGCCGC TTGCTTCCCC 1140 GTCTTTGGCC CTGGGCCCCC AGTACCGCCC CGTGCCCCCC TCACTTCTCC CCCGGAAGCG 1200 CATCCGTCAG GGAAACCGTC CTAAGACCGT CCGCACTCGC TTCAGAGCCG CTGCAAACGG 1260 CCGTCAATCC GTCATTCAGA CGCGAAGACA AAGCGTCCCT GGCTCAGCCC TGAGAAGCAG 1320 CGGGACGGCG GCGCGTTCCT GAGTTCCCGC CACGCGGGCG CCCGGCGAGG GCGGGGCGGG 1380 GCGGGGCGGG CGGGGGGGCG GGGCGTGGAG GGCGGGGGGG CGGGGCGTGG AGGGCGGGGG 1440 GCGGGGCGTG GAGGGCGGGG GCGGGGCGTG GGGGCGGGGG CGGGGCGTGG GGGCGGGGCG 1500 TGGAGGGCGG GGGGGCGGGG CGTGGAGGGC GGGGGGCGGG GGGATGGGGA CAAGGTAGGG 1560 GTCGTGGGGC GCTGGGCTCA CCCCAGGCCC TCAGGTGTCT CGAGATGGCC CGGGCTCCGA 1620 GCGCTCCCGG CGCTTACGCT AGAGCCTCCT CCTGTGCGAA ACGCGTCCGT GCCCAGGCGC 1680 GGGGACCCTG CAGGGCTGTG GGTTCGCGCT GCCGCTGATC CTGCGTCTTC CCCCCTCCCA 1740
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