| Tag | Content |
|---|
EnhancerAtlas ID | HS052-25201 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr22:43027460-43028900 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr5a2 | MA0505.1 | chr22:43028690-43028705 | AGGGTCAAGGTCAGA | + | 6.16 | | ZNF263 | MA0528.1 | chr22:43027529-43027550 | CCCCCATCCCATTCCTCCTTT | - | 6.65 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AGAGAGGCCC AAAGCTGCTG AACGGTCCCC AGGGCAGAGG CCTCCCAGGG CGGCTCCCAG 60
GCCTCGGAGC CCCCATCCCA TTCCTCCTTT GTGTCCCCAC CCTTCCCCAG TGCCTGCTTG 120
TCCTTGTAAG ACGTGACGCC GACGCCAAGC ACAGATGCAC ACACATGCAC GCTGCGTGTG 180
AGGTGCTGAG GCCAGGCGCA CGCTGGGTGT GTCTGTCCTG CTGGCCTAGA GGGGCCACAA 240
ACAAGGTGGC CAGAACAGGG AATGAACCCA GGGTCCCAAA GGGAGGATGC CAGACAGGAC 300
GGGGAGGGAG GAATCCATCT CTGCCATCAG CTCAAGCAGT GGCCTGAAGG GGCAGGAAGA 360
ACTTGAGGGC TGGATGGGCA AACTGGGGCA GAGCTAGACA AGGCTGCACG TGCCCAGGCC 420
TGCATCCCAA GAGAGGGGCT GCAGAAGCCA CTGCACCTGA GAGCCCCTTG GGAAATGGGG 480
CAGCCAGGAC TGAGGTGGGC TTCACAGGGC AGAAAGTGGG AGCCTTCCCT GCCCAGGAAC 540
TCCAAGAGCC CAAAGCCAGG CTTCCACCCT GCACAGGGTG GGCACCCAGG GCATGGTCAG 600
TGGCTGGGAC AGTGGCAGAG GAGGAGGGGG GCTGGCTAAG AGCCAGATTG GGCCAGGGAA 660
GGAGCTGAGA CTAAAACCCC TGAGGTCTTG TTAAGTGGGT CTTACGCTCA GGCCAGGGAC 720
GATCACATAA TCAGTTCCAG TCGGAGCTGG AACCAAACCC AGCGTCCTGA GGGTGCACTC 780
CCTGTGGGGT CCCCAGTACC CAGCATGGCC AGGAGAGGGA GTGTGAAGAA GCCATGCGGA 840
AGGTCGGCGC TGCAGAGGCG CTTACATCCA AACGTGGCAA AGTCCACATG TGGATGGTGT 900
CATCACTTAG AGGGGGACAA CAGACCTCTC CAACAGGGCA GGACATCACA GATGCCCATC 960
TCGGCTCAGT ACGAGAACTC TCCGACCTGA GCAGTGTTCC AGCACAGAGC AGCTGCCTCA 1020
AGGAGAGACC CGTCCCTACA CGTGTGAGCA GAGGCAAATC GCAGGAAAGA CGGTGCAAAC 1080
GCCACTCAGG ATCAGGTGTG CAGGGGGCCC ACCAACCTCT CCCAGGCAGC CCAGGCCTCA 1140
AAGCTGCCTC TACCAGAAGC TTCTGCATTA GGGGCAAACA GAGCCCCAAG GCCTTCTGGA 1200
AGTGGATTCC AGGACTATCA ACTGGTCCTA AGGGTCAAGG TCAGACACCC ATGTACCAGA 1260
AAATATTTGG AGGAAGAATA GAAATGAGAT GGCCAGGCGT GGTGGCTCAT GCCTGTAATC 1320
CCAGCACTTT GGGAGGCCGA GGTGGGCGAA TCATCTGAGG TCGGAAGTTC GAGACCAGTC 1380
TGAACAACAT GGAGAAATCC CGTCTCTACT AAAACTACAA TGTTAGCCAG GCGTGGTGGC 1440
|
