| Tag | Content |
|---|
EnhancerAtlas ID | HS047-05313 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr11:2129560-2131350 |
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 | chr11:2129815-2129836 | CCTCCAGCCCCCTCCTCCTTC | - | 7.19 |
|
| | 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 |
| GH11I002108 | chr11 | 2129954 | 2131415 |
|
Enhancer Sequence | GGCCTCAGAA GTCACCCGCC GTCATTCCCA CTGTTGGTTA CACAAATCCA TCCTGTTAAT 60
GTGAGGGGGG CCGCACAGTG GCCGAATTCC TGGAAGTGCA GATCTAGGCC CATGGCTACC 120
ATGACCTGCA GCTGACATGC TCTTCTTTCT TCCACAAATG ACATGAAGTG AGAGAAGCAG 180
TGGGCAAGGT AGCCCCAGAC TGACCATCTT CTTGTGGTTC CATTGCCGAC ACCTGGTGAC 240
CTGGCCCAGC CAACACCTCC AGCCCCCTCC TCCTTCCCCA CAATAGGCTC AGCTCAGGCC 300
ACCCTGAGCG CCAGGGGCAA GGTGTGCCTG GAGCTCTTCA GTGAGACAGT GACTGTTTCT 360
GGGGTAGCCC TGGACCCTGA ACCCCTCCAG TGCTGAGATA GACGAGGGGT CCCTCCTTAC 420
TGTCCCCTTC CCTGGCCCCA TGACTCTGCA GATTCCCCAG CCACAGGGCA GGAAGGGTAG 480
AGCCAGCGTT TTGGGTGGGA TAGGGAAGGG CCCGGCTGGG AGGCAGAACA GCTGGTGGAG 540
GGTGGGGGAG GCATCCTGAG GCCCTGGGGG ACACCAGGGC ACCGACTGTA CGTTGTTCTC 600
CATCCCCAGC CTGGGCCAAG AGGGCAACCC AGGGAGCCCA GGACCTTGTC CAGCAGCTGA 660
GGCCTCTGAG GGGAGAGTGC CAGAAAGAGT GGGGGTGCCA GGGCTCTGTC CCCCATCTTT 720
CCTGGCTTGG GTTTCTGGGA GAGGGGGCGG GTGTTGACTC CCGGAGGGGC TGCCCTGGAA 780
GTCAGGTGGC CTGGCGGTTC CCAGACCTGC CAGCCCTTGC TGAGGGAGCC TGCAGGCTCT 840
TCTCCTTCCC AGGCCTCCCC GGCATCTGAG AACCTTCTCC CCAGCACTGA CCCATGGCTG 900
GGAGAGGGTC AGGGCCCTCA GGGAGCCCGG CTGAGCCAGC ACGGGACGCA GGGGTCGGCT 960
CCTTCAGACC CCCCCACTTT CGGGCAGCGG TGCCCACGCC CAGCTGGGCA GGGCCGAGTC 1020
CATGAGACCC ACTGCCCTCC CCGGGAGCTC CCGGCCAGCC GCCCACTGCA GCAGCCCGTG 1080
TAAAAGTAAC GCCTGTTATG CCAGGAACGT CACAGGGCCC TGGGGCTGCA GACAAGCTGG 1140
GTCTTTTTTT TTTTTTATTA TTAAAAAGCA AAACCTAAAC CAAGAAAACA AAGTGATTAA 1200
GTTTCTCCTC AGAACAGCAG GCCCCACAGA AACGAGGAGC GACCGTCCCA CTGGGTGCTT 1260
GGACCCTCAC CCACCACTCG GGAAAACAGC CGAATTCTTC ACACAAACAG GAAGCAGCTG 1320
GTCTTCCCTG AACATGAGGG GAGGGCTGGG GCCTCAGCAT GCGGGCTGCC TAGAAGGTGG 1380
CGCTGCAGCC AGGCCCTCGG CTGGGCTGGG CAGTCCCAGC CCTCCAGGAA ACGGCCAGGC 1440
TGCAACTCCC CCGCCAGGAA CCCCTGGGCT TCGCGCTTGA CCAGTGGAGC CGTGCAGGTC 1500
AGAGGAGGGT GGGCTCCCAG CACACACCCT TCTCTGCCAC GGTGGGCTCA GCTGCTCCAC 1560
CCAGGCTGCC AAGACCCAGC CCAGAGCACA CAAACTAGCT GGGCTTCTCA TGGGGTACAA 1620
TGGGAGTGGG CAGGAGCTGG CAGCCATGCT GGGCAGGTCA AGGGCCTTCA AAGGGCTGCC 1680
ACAGCCCAGC TGGGGCGCTG AGGCCTGCAG AAGCTCACTC TGGTGGCATT GAGTTGGGGA 1740
AGGGGTCTCT GTGAGCCAGG TTCAGAAAGG AAGATGTGAG GCAAGTTTTA 1790
|
