| Tag | Content |
|---|
EnhancerAtlas ID | HS053-36493 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr7:44263680-44265940 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr7:44263698-44263710 | AAGTAAACAGAA | + | 7.22 | | FOXP2 | MA0593.1 | chr7:44263698-44263709 | AAGTAAACAGA | + | 6.32 | | ZNF263 | MA0528.1 | chr7:44263949-44263970 | GATGGAGGGAAAGGAGGGGGG | + | 7.4 | | Znf423 | MA0116.1 | chr7:44265179-44265194 | GGCACCCAGGGTGGA | + | 6.7 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr7 | 44265119 | 44265222 | | chr7 | 44265366 | 44265766 |
|
Enhancer Sequence | ATGGGAAGAG AAAGCGTGAA GTAAACAGAA GAGGAGATGC ATGGTCAGAG TTCCAATCAA 60
GAGTGGTAAC CGTGCTGAAG TACGGGAAGC AGGTCCGTTG TGAGACCCAC CCACCCATTC 120
CACAGATGGG AAGCCTAGGC TGCCCCTGCC CTGCGGAATG GCGCTGCCCA GACCCCAGCT 180
CAACCCAGCC CCCACTCTGC CTCCCCACAT AGCACATGGG AGCTTTTGTG TCCTTGATAT 240
CCAGGCCCCT GAAGAAGGGC ATGATCCCTG ATGGAGGGAA AGGAGGGGGG CCCAACATGA 300
AGAGGTGCCC GGGTCGGGAA ACCTGCTGGC TGAGGACAAG CTGTCCTGGC AGTTCCAGAG 360
ACAAAGGGGA GGTGGTGGGC AGGGCCTGGG CTTGGAGGGG TCTGCACGAG CCAAGAGCCT 420
CTGCAAGTCA GGCCTTCCAG GTGCCCTGAC ATGAACAGGA GCCTTTGCAT TGCCTGTGGC 480
TCTCTTGGGG TGAGGCAACA GGTCCAGGCA GGCCTAATGC GTCCAGGTGG GGTCAGAGCA 540
GGTTCTCATC CTGGCCTGGA CTCCTGGGAC CCCAGGCTGG CCCCAAGCCC ATCTCTCAGA 600
GCCAGAGGTG GCTGCGGGAG GGAGGGCAGC TGCCCAGGGA TCAGGCTGGA TTGTGTATAA 660
TCCGCGATTA GAGAGCGTGG GTGGGGAGGA GACGGGGCCT GAGGCGGGCC GTGGGCACCT 720
GCCCTATTTA CACAGCTGGT GGGTGCCTTC TGGAGAAAGG AGGTGGAAAG GAGGCAGAAA 780
GCTGGCCACC TGCCACCTGG GCCCAGGTGC CCCCAGGGCA GTACCCAGAC TCTTCCTTTC 840
CCTGAGTTCC GGAACATCTC ACCCACCCCT TTCCCAGCCC TGCCCAGCCC CTCCCAGGAG 900
GGCCACACGA ATCTCCATCC TGCCCTGCTC ACAGCTCCTT CCTGCAGCCC CCTCCTCCCC 960
AGCCAAGCTC AGGGAAGACT CTGGAAGGGC AGGTCTGTGC TGTGGCCCCT GAAGGTGAGC 1020
CTGGACACCG AGCCCCGAGC TGGCCACTCC ACACCCACCC TGGGCCCTGT CCTCAGAGGA 1080
CTCACCCCAG ATACTGCACA GACCTTGAGG GCAGGCTGCA GTCCTGGGCT GGGGTCATGC 1140
CAACCTGATG GGGTGACCTT CCAGGCAGGC TCCTTTGGGC ACACCCCTCC ACTTCTGCAA 1200
GGGCAGCAAG CCCCTTAAAA TCAGATGAGC TGCTGTAGAA GTGGCAGGTG TCGGGGGTTC 1260
TGACCACTCC CAGAGGCTCT GCGGTGCACC CACCCCAGCT GCACGGCGGC CCCTCCCCAT 1320
GCCTCCCTCC TTGAGTTCTG GTCGCCCAGG CACCCCGACC CTATCAGCAT CAAGAACCTG 1380
GCCTCTCCCC TCAGCTGCTT GCCTCTGATC CCCTCAGTCA ACCCCTGCTG GGGGTCCTCA 1440
GCCGACCACA GAAGCTCTGG GGGTGAGTAC CCCTCCAGGG GCTGCCCCCT GCTCTCTCGG 1500
GCACCCAGGG TGGATCCAGT GCCCCTTTGA GCCTGCAGCC TGCATCCCCC TCCTCGAGCC 1560
GCTGCTCCTG TGGGTTCACT CTCCCCACAC CCTTCTGCCC TGGCCGCCTG CAGCAGCCCC 1620
CAGGCCCAGC CTGCAGAGGG GACGGTGGCA AGCAGACCCC ACCTGTCCCT CAAGTACTTA 1680
CCTAGCCACT GCCCTGCCAT GCCGAGCCCG TGGCCCAGCA GCCTCTTCTC TAAGAGTATC 1740
TCCACACCAC CCCCAGTCTG GTGTCTCCCC ACAGGTGGGG GTGGCAGCAG CCCTGGGATG 1800
TCATCCATCC CTGTAAGTGA TACTGCGGGT AGTCGGCAGA CAGACCGGGA GGTGGCCCAG 1860
CCTGGCTCCT CCCTGGCCGG GGAGGCTGCC CAGCCTGTGC TTCCTGTCCC GCCCGCTCTG 1920
TTTCAGCCTG GCCCCAGCTG CCCCCCAGAT CCGCGCCTCC CGATCCCCAC CTGCTCCCTG 1980
CTGTCTGGAC TTGGACAGCT CTAATGCTAG AGCGTCTCAG GCCGGGACTG ACACTTTTCT 2040
GTCCCGGCCC AGCAGGTCCA CCTTGACCCA AGCCAGCAGC TCCTGGCGTG CTAGCCCTTG 2100
CCACACGCGC AGACCCTTTG CCACCCATTC CCCTCCCATC AGGAGAAAGC TGTGGACCTC 2160
AGGGTTGCGA ATGCTGGGGT CGGCAACAAA CCTGCTCTTT CGGACGCTCT TCCTATACAC 2220
ATATGTCATA CACACTTCAT AACCATAACC TCCATTTTCT 2260
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