| Tag | Content |
|---|
EnhancerAtlas ID | HS052-16199 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr17:44819300-44821520 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr17:44819363-44819377 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I046741 | chr17 | 44818771 | 44821397 |
|
Enhancer Sequence | TAGTAGAGAC AGCATTTCAC CGTGTTGGTC AGGCTAGTCT CCAACTCCTG ACCTCGTGAT 60
CCACCCGCCT CGGCCTCCCA AAGTGTTGAG ATTATAGGTG TGAGCCACTG CACTGGCCAA 120
TAGTACTTGT TATCTCACTA GCTTAGGTTA ATGACAGCTA ATGAATCTTA TCTTTCCTCT 180
GCTAGAGAAG TCTGTGTTAT CCAGTCAATA GCTAATCAAT TGATTAAAAG AGATAAGCCA 240
GACTTTGGCA CGAAGCATAC ATGCCGTTCA TTCTAGATTA TTTTCTTTAA AATTTGTTGC 300
TATCAACACT TGGGGCTCAG AGGTGTAGAC TCTGAAATGA TAGTTACTTT CCTTTTGGAC 360
ACTTAATATA ATGTGCATTT TTCTAGGACC AGAAAGTAAT AATGAAGGAG TGATCTGCTA 420
CCCTTGAAAG CTATACTGGG ATTATCATTC ATTCAGTGCA TATTTATTAA CTTTGTACTT 480
TGTACAAGGC AGTATGCTAG CCCTGGAAAC ATCAGTAAAG CCAAACCGAC TTAAGTCCTG 540
TCCTGATGAA GGAGAACTAG CAAGAAATAC AGTAAATATA GTAAGTATAT AGTATGTAAA 600
AGGCGATCCA AACTGGAGGA GGGAAAGGGC AGGATAAGGG TTGGGGAGTT GCAGTTTTAA 660
ATGGAGGTAT GTGGGGATTG AGTTGGCCTG TGGAAAAGCT GACATTCAGG CAGGTCCTTG 720
ACTTGGAGGG AAAGGCCTGT GTGGCTATGG AAGGGAAGAG CATTCCAGGC AGAGGAATCC 780
TCTCTGTGTG CCAGGCATGC CATGCTGAGT ACTGCAAGGG CGCAGATGGA TGATACGTGG 840
TTTCTACCAT CGGGGAGTTG ACAGGCTAGA AACAAGATTC AGGCTTGAAG ATAAATGCAG 900
AGAAGCACTA TGGCAAGGTA GAATTTTTCT AAGGGTCTCT GTTGAATAAT ACAAGCTAAG 960
AAAATATGAA AAATTATTCC TATTTCAAGA ATGAAGCCAG GTTAAGTGAT AGACCAAAGG 1020
ACCTCTACCA GGAAAGCTTC TTACTCTTGG CTCTGAGCCA ATTTCCTCCT CAGAAGTTGC 1080
TGCCTCTCCC TGAGGCCCCA CGCTGCCATG AGTCCTTCTG ACTCTCTGTG AGTCACCCCA 1140
CTGCCATGAC TCCTTCGGAG GGGGTGTCTG ACCTCTTGCT TCAGGCCTCT TCTGGGCCTC 1200
ACAGTAACCC TTGTGAAGCT GAAGATGGGA GCTCTCATCT TCCCTAACCC AGAGCCAACC 1260
TTGGCCTCTC TGCGTCATTT GCTGCCAGTG CCCTGTGTTT GTTTTTGGGA AGAGAGGGAT 1320
TTTCAGGCAT CCCGTCCCTC ACCCACCTGA CCTAACCGTA TGGATTCCTG ACACCACAGG 1380
CAGAGGACTA TTCTTCAGGT TCCTCTGAAG CCCACCTGTT CAGATGCTTG CTTCTTTTCC 1440
TTCTTGCCTG TTCTGACTGT GATGACAGAG ACCCCGCCTC AGGAATCTCC ACCTCACACT 1500
CTATTCTCAT AAGTAGGTAG AATTTTCTCA TCGCATATTT ATGGTTGAGG AGGAGATAGA 1560
TGCTGAGAAG TTAAATAATC TACCCCAAAT CACACAGCTG TGAGTGATGG GGCCTCTACT 1620
TCTGTTGCAC CAAGCTACCT GTCCATCAGG GGACTTGCCT CACCATTGCT TTCTGCCAGC 1680
CCTGGGCTTG CCTTAAAAAG GACATCATAT GCATAAGACA CTGGTTAAAA GGTGCAGCAT 1740
GGTCCCTGGA GATGCTCACT CTTACAACTG GCCTGTCCTT GGGGCAGCAG CTCCTCACAG 1800
GCCCCTAAGA GGTAGACCTC CTGCCTGTGG CTGCCAGAAC CCTCTTCTCC ATCACAGGTC 1860
TTCCTCCTCA AGAGCCTTCT CTGGTTTCCT GTTGCTTTTT ATATTAAATA TTTCCCTTAG 1920
TTTAGCATCC CGAGTCTGCC TTTTGCTGAT TGTTCCCTCC CTGTGTCTGC AGACAACTTC 1980
GTTTTCAGCC TTGGTGCTCT GTCTCAGCTG CTTCTACCAC ACACATAGGA TTTAGGCGCA 2040
TTCAGGACCT GTCCCTTCTT TTCAAGGGCC TTGCCAGTGC CTACTTGTTG TCATTGTCTT 2100
TGCAGTACTA CGGATAACCT TCCTAGATAA CCCCCCTCCA GGAAACTGTC CCCATAAACC 2160
GGGTGCCCTC CGCCATGATT AGTTTGTATT TGCGAGTGTG TTACTTGGTT GTGTTCCCTG 2220
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