Tag | Content |
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EnhancerAtlas ID | HS127-04954 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr11:1356040-1358020 |
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) |
BCL6B | MA0731.1 | chr11:1356350-1356367 | TGATTTTGAGGAATTCA | + | 6.1 | 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 | 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 | SP2 | MA0516.2 | chr11:1357984-1358001 | CGGGGGGCGGGGCGTGG | - | 6.27 | SP2 | MA0516.2 | chr11:1357941-1357958 | GGGGGGGCGGGGCGTGG | - | 6.63 | SP2 | MA0516.2 | chr11:1357963-1357980 | 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 | 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: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I001335 | chr11 | 1356472 | 1359269 |
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Enhancer Sequence | TAGTAGAGAC AGGGTTTCAC CGTGTTAGCC AGGATGGTCT CGATCTCCTG ACCTCATGAT 60 TCGCCCGCCT CAGCCTCCCA AAGTGCTGGG ATTGCAGGCG TGAGCCGCTG CGCCTGGCCC 120 CTTTGCCATT TTTTAATTGA GCTGCTTGTC TTTTCGTTGT CAAGTTGCAA TTGTTCTTTG 180 TGTAATATAA CCCCCTTTAT ATATGCCAGA TACAAGTCTC TTATAGACAA GTGATTTGCA 240 AATATGTTCT CCCATTTTGC AGATTGTTTT TTGGTTTTCT TGATGGTGTC CTTTGAAGCA 300 CAAAATTTGT TGATTTTGAG GAATTCAGTT TATCTATCTT TTTCTTTTGT TTCTGTGCTT 360 TTTGGGTCAT ATCTAAGTAA ACCAAGCTCA AAAAGATTCA CCCCATGTCT TCTCAGTGAT 420 TTATAGTTTG AATTTCTACA TCTAGGTCTT TAACCCACTT TAAACTAATT GTTCTATGTG 480 GTATGAGGCA CCTGTCTCTT CCTAGAGACC ACTGCACTCC ACCTGTCCCT GAGAATGACT 540 CCTGACTCCA CTGCATACGA GTCCCTCTCC CCCACCTTCT ACCTGGAAAA CTCCTATTCA 600 TCCCATCAAG ACCCAGCCCT GGGTTGCTCC TGGGTGGCTT TTTTCACTCT CCTTGGCAGC 660 TTTAACTGCT GCCTGGGATG TGGGCTCAGG GCCAGTGCCC TGGAGGGCCC CTGTCATAGC 720 CCTTCTCACC AGCACTGAGA TTGGTCACCT CCGAGTCTGG TGGGCCCGGG GCCCCCATGC 780 AGGTGCACAC AAGTGCTGCT GAGTGACTGG TGATCATACA GCCAACATTC GCGGTGACAT 840 TCATGCACCG GGGACTTCAC AATTCCCCGG ACTCGTCATA AGGGCTGCTC GGCCCCATCT 900 TACAAATGGG GAAACTGAGC CTGGGGGGTT CAGTAACTTG CTGAGTTCAC ACAAACAGTG 960 AGTGGATGGC TGGATGAGTT TGTAAAAGGA AGGTCGATTC TGCATGATGA AGCTAAATTG 1020 GAGCCCAAAA TTCTCTCTTC CGGCCCCCAG TAGAATATTA TGGGTGCACC CAAAGGAATG 1080 TAAAAAGACC AGATGCCCAG GACACGGGGC GGTGCCTGAT GAAACAGCTG CATTAGAGAG 1140 TGACTTTGCA ACTCTGGAGA GAAGCCACTG AAACCCAGCG CTCCTATAAA TAGCAGCTCT 1200 TGCAAAGCAT CGGGTGTGAA TTTTCGTGGT GTTGGCAAAT TCAGAGATTG AGAAATCCAG 1260 AGACGTTCAT GTTCCCGGAG AAAGGAGTGG GGTGGGGAGG GAGGTCGCAA GCAATGCCAT 1320 CTTCAGGAAC AAAACTCCTG CATAACGAAG CCCAGGTTTC TGTGTTTTCG TGGGTGTTCC 1380 CGGGCACCTT CGGGCAGGTG GCCCCAGGCG ATGTTGTGTG TCTCTCCTGG CTGTGGACGA 1440 ATGGACGCCT GGGGTGAGGC TGGGCCAGGG ACCTGGGGCT TGTGGGTGTC GGCTCCCATC 1500 CCGGGGTCCT CCCCCGCCGT CCTCCCCCCT CCCCCGCCCT CTCTCCCACC CTCCTCCCTC 1560 CTCCCACCTC CCCTGCCCTC TCCCACCGGC GTGCACCCCC CCGCCCCGCT GCTCACCGCC 1620 CACCACTCCC CAGAGGCCGC TTGCTTCCCC GTCTTTGGCC CTGGGCCCCC AGTACCGCCC 1680 CGTGCCCCCC TCACTTCTCC CCCGGAAGCG CATCCGTCAG GGAAACCGTC CTAAGACCGT 1740 CCGCACTCGC TTCAGAGCCG CTGCAAACGG CCGTCAATCC GTCATTCAGA CGCGAAGACA 1800 AAGCGTCCCT GGCTCAGCCC TGAGAAGCAG CGGGACGGCG GCGCGTTCCT GAGTTCCCGC 1860 CACGCGGGCG CCCGGCGAGG GCGGGGCGGG GCGGGGCGGG CGGGGGGGCG GGGCGTGGAG 1920 GGCGGGGGGG CGGGGCGTGG AGGGCGGGGG GCGGGGCGTG GAGGGCGGGG GCGGGGCGTG 1980
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