Tag | Content |
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EnhancerAtlas ID | HS017-00222 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr1:10999940-11001460 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:11000046-11000064 | GGGAGGCAGGAAGGCAGA | + | 6.18 | ZNF263 | MA0528.1 | chr1:11000406-11000427 | TATGGAGGAGTGGGAGGGAGG | + | 6.11 | ZNF263 | MA0528.1 | chr1:11001246-11001267 | AGAGGATGAAAAGGAAGGAGG | + | 6.52 | ZNF263 | MA0528.1 | chr1:11000409-11000430 | GGAGGAGTGGGAGGGAGGAGG | + | 7.28 | ZNF263 | MA0528.1 | chr1:11000419-11000440 | GAGGGAGGAGGAGGGAGGAGG | + | 7.77 | ZNF263 | MA0528.1 | chr1:11000422-11000443 | GGAGGAGGAGGGAGGAGGAAG | + | 8.16 |
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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 |
GH01I010939 | chr1 | 10999858 | 11000657 |
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Enhancer Sequence | AAACCAGCAA GAAGACCTGC ATTGACCAGA TCAGAGCTCA GGTGGGAAGG GGCTGGAAAG 60 GAGTGCCCTG GCCCCCCTGG CCACATGGAC AGGAGAGAGG GACTCAGGGA GGCAGGAAGG 120 CAGAGCCCAG GAGAGGAAAG GGAGAAAGCC GAGTAGATGC ATCTACCCAA GGACCCCGCG 180 TGGAGCCTGG AAGCCACATT GCTGCCTCCC GCCCTGGGCC ACCCTGTCCG CAGCTGGCTG 240 ATGTAAAACA CACATGTTTT GACTGAAGCC GCTCTCCCCC CACCTCCTGA AAAACGCCAA 300 CATTAAAGGG AGCGTAGCTT TGTAAAACTG AAACTGTAAA ATGCTTCTGA AACCCAGCCT 360 GGGGGATTAA AGAAACCACA TGAAAAGGGA CTCGGGACGA CCTGGATGCT GACTTCCTGT 420 TCAGAAGTTC GTTCAACATG TGCCTCCCAC CCGGGCCCGT AGCGTGTATG GAGGAGTGGG 480 AGGGAGGAGG AGGGAGGAGG AAGGCCAGGG CCAGTGGAGG CTGGCGGGTG CCTCAGGGGC 540 CTCCAGAAAC CCAGAGCATG GCTAAGTCTG AGGCCTGCAA CCCTAGGCCA CCGCCTTCCC 600 AGGCCTCTGA CCTCCAGGGG CTCTGGGGAA AAGGGTTGAT GTTGATCTTG GCCTTGGGAC 660 CCTGCCCTGT AGTAACAGAG GGGTCAGGAG AAAAAGACCG TAGGCACCCG ATGCCCTACC 720 TCCCTGCCTC TGCCAGTCTC CCCTGCTGTT CCCAGCATGG TCCTCCCTGG CCCTGGGCAT 780 TCGGAGATGT AGAATGTGCT TGGATCCCAG CTCAGCCTCC CATCCAATGG TAGTTAAGAA 840 CCTTCCCCAG CCAGGCACAG GAGCGACTGT GGGTTCAAAT CCCAGCTCTG CCATTTCTTA 900 GCTGTGGGTC CACCCAGGAA TCCTAAAATA CTCAACCCAT ATGGCTGTTC AGGGGAATGT 960 GCTCAGCAGG GTGCCTGGCA TGTAGTAAGG GCTCCAGGAA TGGCAGCCAC CACCAGCAAC 1020 CACCCACCTT CTCCCCACGG GGAGGTCAGA GCATGCAGTG TGTGTGCAAG GATGCTAGGG 1080 CCGGATGGTG CAGCCAGCGC CCTGTGCTGC GACTAGAGGG ACGAGGCAGT TCCTCCTCTG 1140 CCCCTCTCAA GACTGGGTCC AACTTTCCCC CCGGTCCCCT TCTTACTACG TGGCCTTGGC 1200 CAAGTCACCT GCCCTCTCTG GGCTCAGGGC CTGCATCCTG GGGAAAAGAG GAGAAGAGGA 1260 ACTGGGTCAA AGGTCCCCTC CAGTTCAGAT GTTCTAGTTT GGGGCCAGAG GATGAAAAGG 1320 AAGGAGGAAG CCTGTCTGTC CCCTATGGCT GAGGGACCCC AGCAGGTGTA ATAAGTGATT 1380 TCTGGCACTA CGGCTGAAGA CGGGGCCCAC TGTCCAGGGC TGTGTCTGGG AGAAGCCCTC 1440 TCTATGGACA CTCACACCCC CCGGATCTTG CACAGGTCAC ACAGACACAG ACAGCCATCC 1500 ATCACCCACA CACACCACAG 1520
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