| Tag | Content |
|---|
EnhancerAtlas ID | HS002-02141 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr11:125070350-125072610 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr11:125072013-125072034 | AGGGGAAGGAGAGGGGGAAAG | + | 6.14 |
|
| | 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 |
| GH11I125201 | chr11 | 125070981 | 125072437 |
|
Enhancer Sequence | GTGATAGGTT CTGTGAATTC CACCTGTCAT GTAAGGTGTG ACTCTTGGCC CAACCATGGC 60
TCTCCATGCA CCATGCCGCC CCCTGAGCCC AAGTCTCTGC CACCGCTTGC CTGGCTCATT 120
GCAGTGCCTC CCGCCGGTTC CCAACCTCCC CCTGGCCCTC CGTCTGTTCT CTACACTGAA 180
GCCACAGCCG TCACCCATGC CCATGTTTCT CCTGCACCAA GGCCACCACA GTCTGCAGTC 240
ACGTATGTAT TTATGTGATG TGGAGTTTAT TGTCTGACTT GCCCATGAGA CGTGCTCCAG 300
GAGGTCAAGG GCAGGGCCTG GGTTGACCGT CACTGCATCC CCAGTGCCCT TGATGAGGAA 360
CGGTTAAGCA ACTGAGTGAA TGACCCAGGC AGGGCCCTTG TTTCCTTGCT GTCTCTTGCT 420
TCTTTTCCAA AGGGACTCCC CCTCTAGACC GTGTGATCCT CATGGGCAGG GGGTCTCTGC 480
CTTTTGTACA CTGCACATCG AGGGACTTGG TAAAGCTTTG GTGAATGAAT CGTGAGTCTC 540
TGAAGTAGAG AACTTGATGG GGATCCCTTA ATGCAGACCA CTGTCCTCAG ATTCAGCCTG 600
GGGCCACCTT CTCTGTGCCA TCATTGCTCA TTTTAGCTCC TTCTCACTGG TCTCCCAGGA 660
CCTTGGTTTC CATGAACCCT TTCTGACCTG AGAGCTTAGG CTGGGGCTGA ACCCAGATTG 720
CTGCTTGGTT ATGGCCATTC TACCCCCAAG AGGAAGCGGG GTCTTCCTTT CCACTTTCCA 780
GTGGGGTTTG GAAGCTAGAG GAGACATGCG GGAGCTCTGA GTGAAGCCCC CTCACTGCTG 840
ATGCCTAGAG CCTTTGGCCT GATGAGCTCT TCAGAACCTC TGTGACCTCT GGAACTGCAT 900
CCTTCCCAGA TATTGCTTTC TTCCTTGGTA GAAAAAAAAA AAGCAGCCTC CCTCCAAAGT 960
TCTGGGGACT TCCAGATGAT ATGGAAAATG TCCACAAGGA ATGGCCACAG AAGAGCAGGT 1020
AAAGCCCTGG AGAGAGAGTC AAGGCTGGCT GGAGAAGGTG CCTGGTGCTG TGTGATTTGC 1080
TGCCTGTGTC CCTCTCCGAG CTGGAGTTTC CACCTGTGAA AGGAAGATTG CGCCACCTGT 1140
GCGGCTGCCA AGCTAAGGAG TATCTGACAG ATTCACTGGA AGCAGGAAGT GTGCCAGCTG 1200
GAAAATGGTG ATTTTTCATC CGACACCATC AGGAAAGCCC CAGACTTCAC CCCCTCCCTC 1260
TCTCCTGTTA TTAATGGCCA TGTGGATCAA ATTCCTCAGC CTTACTTCCT TCAAGGTTTT 1320
CTTCCAGAGC CTTATCTCAG GCACTCCTGG CTCCTTTTAG TTTCTTTCCT GCTGGGTAGG 1380
CATTTCCCCC AAGAGCCCAG TGAGTTTAGC ATCAGCCTAG GTTGGGGAAG AATGTGGGCT 1440
CGGCTGGGAG GCTGGGGGTC ACGAGCTGCC TTGTGGCTGC TCCTTGGGGT CTGGTGGAGC 1500
CCCAGCCTCT GGCTGTGACA TACAGCCCCC TTCATGAAGC CAGACAGAAT TAAGCCTTTT 1560
GTTTCCTGTT TGCTAGGCCG GCTTAAAGAA AACACAGAGG GTCCGTGCGG CTGGGACTCC 1620
CAACAAGACG GCCTTTGTAT TCATTTAATT AATCAGTTAG CTGAGGGGAA GGAGAGGGGG 1680
AAAGTTCATG TTATAAATAC ATGTTTTTCT TTGGCTTCCC CTCCTGCAAA AGACACAGCC 1740
TGAATGGCAT CCCCAAGACA GCCCCCCATC TCGCTGCAGA CATGCTGAGG GCCAGGGGCC 1800
AGCCAGGCTG CAGCTGGGAC CCTCCTTGCC CCTTTGCTTG CCCTGCCCCC TGCACCCCTC 1860
ACCAAGGGGC CTTATCCCTG ATGGCTGTGT GTCCTGGGGG AATGTTAATG CTGATGGGGT 1920
GGGCAAGGAG TGGTGACCAC TGGCTTCTAG AGCCCATCCT TCCTCTTTAC CTCTCCCCTC 1980
AGACCCCATA CCCTCCAGGG ATGAGGTGGC TGCACTGCCA TGTGGGTGAA GTGTCTGTCC 2040
CCAAAGAGGT CTGGGCAGTT GGCAGGTGCA CCGTGGAGAA GAAGTCCAGG CACACAGAAG 2100
GGCTGAAACT GGCACCAAGG TGTCCAGGCC GACAGAGTGC TGAGCACTGG CAGGGGACAC 2160
CGAGGGATGT CTGGCATCCT CCATCCCACC TTCCATTGGA GCCTTCTGGA GTGCAGGGGG 2220
AGGAGCCGTG GAATGTGCTC TTAGGGCTCT GGGGAGGCTG 2260
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