| Tag | Content |
|---|
EnhancerAtlas ID | HS136-07960 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr17:16170230-16172450 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2F1 | MA0017.2 | chr17:16170327-16170340 | CAGTTGACCTTTG | - | 6.41 | | ZNF263 | MA0528.1 | chr17:16170695-16170716 | GGTGGAGGAAGTGGATGGGAA | + | 6.49 | | ZNF263 | MA0528.1 | chr17:16170653-16170674 | AGAGGCGGAAGAGGTGGAGGA | + | 6.64 | | ZNF263 | MA0528.1 | chr17:16170665-16170686 | GGTGGAGGAAGTGGATGGGGA | + | 6.96 | | ZNF263 | MA0528.1 | chr17:16170683-16170704 | GGAGGCGGAAGAGGTGGAGGA | + | 7.5 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr17 | 16171181 | 16171830 | | chr17 | 16170735 | 16170820 | | chr17 | 16170732 | 16172264 | | chr17 | 16170837 | 16170924 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I016267 | chr17 | 16170516 | 16172323 |
|
Enhancer Sequence | GGGTTGTCGT GGAAATTAAG TTTATGAATC TCCTTGATCT CTGAATTATT CCAAACAGCA 60
CCATCCCAGC AATTCCTTTT AATTGTTTTT AGAACTACAG TTGACCTTTG AACAATGAGA 120
GGGTTAGGGT GCCAACTCCC ACCAATGCAG CTGAAAATCT ACATAAAAGA TTAGATTCCC 180
CAAACCACTA GTAGCCTATT GACCAGAAGC CTTCTTGATA ACCTAAACAA TTAACACATA 240
TTTTGTATCT TTATCATATA CTGTATTTTT ACAATAAAGT AAGCTAGAGA AAAGAAATGT 300
TATTAAGAAA ATCATAAGGA AGAGTAAGTG TATTTACTAT TCATGAAGTG GAAATGGATC 360
ATCATGAAGG TCTTCATCCC TGTCTTCACA TTGAGTAGGC TATCTTGCTG TCTCAGGGGT 420
GGCAGAGGCG GAAGAGGTGG AGGAAGTGGA TGGGGAGGCG GAAGAGGTGG AGGAAGTGGA 480
TGGGAAGGCG GGAGAGGCAG GCACACTTGG TGTAACTTTT GTTGAAAAAA TATCTTTGTA 540
TAAGTGGACC CACGCAGTTC AAACGTGTTG TTCAAGGGTC AACTGTGGTC ATATTGTCGG 600
GGTTCTTTAG CCATTAGGTC TCAGAAATTA GCCTGAATTT AGCCAGACAT AGTAGCACAC 660
GCCTATAGTT CCAGCTGCTT GAGAGGCTGA GGCGGGAAGA TCACTTGAAC CCAGACTGCA 720
GTGGGCTATG ATGGTGTCAC TGCACTCCAG CCTGGGTAAC ACAGTGAGAC TCCATATCAA 780
AAAAAAGAAA AAAAGAAAAA AAAAAGAAAA GGAAAGAAAT TAACCCGAAT TTGTGGTTTC 840
TAACTTGGCA ATTAGTCTTT CTTTGACCCC AAGTTTAGAC TCAATATCTT CACTAAGAGC 900
CAGCCCAGGG GGTGCAACTT GGAGCACCAG AATGTTTGTG TAATACTAGC CATGGTAAAG 960
AAGGTGTCCC AGGCTCTCCT GGTGGAGGCA GGCTCTGCTC TACTTAACTC TACTCCAGGC 1020
AAGAGCAGAC AAAGAGCAGA CTCTTTAGAC TGGTAAGCAG AACAGACTCG TCCCTCAAGG 1080
AGCTCCCAGA CCAGGGAGGG GAGGAGACTG TAAATATTCA CCATGCCGTG GTAACAGCAG 1140
AGATGGAGCA CAAGGGGAAG TTCAGAGAAA GATCTCAGAA GAGAGGTACT TTGTCTAACC 1200
TGAGATTTAG GGAAAGTTCT CCTGAAGATG ATGACTGGTC TACATGACCT GAGCCGAGAT 1260
GGGAATGAGT TGAAAGGTAG GCTTGTGAAG AAGCAGGAGA AGAGCATTAT AGATAGAAAA 1320
CTCAAAGGCA TCAGAGGCCC CAAGCTGCAT GCTATGATAT TGGGATAATA GTAGTACAAA 1380
CATAGTGCAA GACAGTGGTG TAAAGTGAGA TATTTGCTTC TGAGCCATTT CCCTTCTGTT 1440
GCCACTTCCT CTTCCTCTTT TAAGTGAAAC ATTACTAGCA GCCTAATAAT TATCATAGCT 1500
GACATATATT AGGTGTTTTT TGTTTTGTTT TGTTTGTTTT GTTTTTCTTG AGATGAAGTC 1560
TCGCTCTTGT TGCCCAGACT GGACTGCAAT GGTGCCATCT TGGTTCACTG CAACCTCTGC 1620
CCCCTGGGTT CAAGCGATTC TCCTACCTTA GCCTCCTGAG TAGCTGGGAT TACAGGCGCC 1680
TGCCACCATG CCTGACTAGT TTTTTGTATT TTTAGTAGAG ATGGGGTTTC ACCATGTTGG 1740
CCAGGCTGGT CTCGAACTCC TGACCTCAAG TGATCCACCC ACCTCAGCCT CCCAAAGTGC 1800
TGAAATTACA GGCATGAGCC ACTGCGCCTG GCGTTTTTTT GTTGTTCTTG TTATTTGTTT 1860
TTTTAGATGG GAGTCTTGTT CTGTCGCCCA GGCTGGAGTG CAGTGGCGCA ATTTCGGCTC 1920
ACTGTAGCCT CTGCCTCCAG GATTCAAGCA ATTCTCCTGC CTCAGCCTCC TGAGTAGCTG 1980
GGACTACAGG CGCGTGCCAC CACGCCTGGC TATTTTTTTG TATTTTTAGT AGAGACAGGG 2040
TTTTACCATG TTGGCCAAGA TGGTCTTGAT CTCCTGACCT AATGATCTGC CCGCCTCAGC 2100
CTCCCAAAGT GCTGGGATTA CATGCGTAAG CAACCATGCC CAGCCAGGTT TTTACTCTGT 2160
CCAACTCTAT TCTACATCCC TTAAATTTAT TAACTTGTTA AATTCTCTAG GAGTAAATGC 2220
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