| Tag | Content |
|---|
EnhancerAtlas ID | HS052-11754 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr14:71672950-71674280 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PPARG | MA0066.1 | chr14:71673735-71673755 | AGTGAGTCACAGCCACCTAC | - | 6.13 |
|
| | 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 |
| GH14I071206 | chr14 | 71673160 | 71674270 |
|
Enhancer Sequence | GAGTTGAGTT TCTCATCTCT TCTCCCCAAC CCAACAGTAA GCACAAATAT CACAGATTTT 60
CAGAGAGGGA TCTGTGTGAA CTCATCAGCC TAGTGACTAA GGCTTAGCAT GGGTGCTGCA 120
GCTGTGCATG GGCACCCATC ATCAGACACA GCCTTCTGAT CACTTGATAT GGTTTGGCTG 180
TGTCCCCACC CAAATCTCAT CGTTAGCTCC CATAATTCCC ACATTTTGTA GGAGGGACCC 240
AGTGGGAGAT AAATGAATCA TGGGCATGGT TTCCCCCATA CTGTTCTCTT GGTAGTGAAT 300
AAGTATCACG AGATCTGATG GTTTTATAAG GGGAAACCCC TTTCACTTGG TTCTCGTTCT 360
CACTTTGCCT GCCACCATGT AAGACCTGCC TTTGTTCTTC CCTTGCCTTC CGCCATGATT 420
GTGAGGCCTC CCCAGCCATG TGGAACTGTG AGTCCATTAA ACCTCTTTTT CTTTATAAAT 480
TACCCAGTCT CGAGGACGTC TTATCAGCAG CATGAAAACG GACTAATACA TCACCTCTCG 540
TCACATGCTC CAGCCTCTGC ACAAGGCTCT GTTGTTTCTG TTCTCAATCC CAGTCCCCAG 600
TTAGTCCCGA AGCTGAGAGC TGGACACAGG CTGTTGCAGT GGCTGAACCT GAACAGAACC 660
AGAGCTGCTG GCTCACTGGC TGCAGGCAGC TTGTTCTCTG CCCTCTACAA GGATCTGGGA 720
TTTATTTAGC CTGTTTCCCT GGCAGCGCTG GTTACAGTGG CAGCATCTGC TTCCCCAGGA 780
GGCTGAGTGA GTCACAGCCA CCTACGCTAA CCCTTGGCAC AGCACAACTC TGTTCTGCTG 840
GGGACCACTG ATAATAAGCC AGCAGGAAGA TGCTGGAACA CAGGCTCGAT GCAGACAGTG 900
CACTGGGCAT GGGGTCCTGG GAAAGGCTTA CCTACCTCCT CGTGCAAAAG AGGTTAAGGC 960
TGGAGGCTGA GTTAACCCTG GCACGCTCTC CCTACAAGAG CTGTTAAGTC TGCTTAACAA 1020
CTTAACAAAG TGGCTCACCT CAGCTGCTGC CAGCAGCTAC AAGGTCTCAT GGGAAAGGCC 1080
TGCAGGATTT TGGACTCCAA GTCCAGGCCC TCTTTTCACT ATGCAAGGAT AAGCCCTCAA 1140
ATTTGTCTTT CCACGGCCAC CTCTGCACCC ATATTGGCCC CTGGTTCCTT CTGGCTCTCA 1200
ACCCCAGGAC CTTCTTTTAA GACATCGTCA GTCCCTCCTC TGGGCAGCAG TCCTCAAAAC 1260
TGTATTCTTT CCCAGGCCCA CCCCTTCCTG AAACTTTTAT TTCCTCCATC TTGTCTCCCC 1320
TTATCATCTG 1330
|
