| Tag | Content |
|---|
EnhancerAtlas ID | HS089-07041 |
Organism | Homo sapiens |
Tissue/cell | Hela |
Coordinate | chr19:52269260-52270470 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PLAG1 | MA0163.1 | chr19:52269417-52269431 | CCCCCCTTGGCCTC | - | 6.06 | | ZNF263 | MA0528.1 | chr19:52270327-52270348 | CTCCCCTCACCCTCCACCTTC | - | 6.53 | | ZNF263 | MA0528.1 | chr19:52270324-52270345 | TCCCTCCCCTCACCCTCCACC | - | 6.91 |
|
| | 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 |
| GH19I051766 | chr19 | 52269692 | 52270063 |
|
Enhancer Sequence | CTCCCGGGTT CAAGCGATTC TCCTGCCTCA GCCTCCCGAG TAGCTGGGAC TGCAAGTGCA 60
TGCCACCAGG CCCGGCTAAT TTTTTGTATT TTCGGTAGAG ACGGGGCTTC ACCGTATTGC 120
CCAGGGTGGT CTGGAACTCC TGACCTCAGG CAATCCACCC CCCTTGGCCT CCCAAAGTGT 180
TGGGATTACA GGCGTGAGCC ACCGTATCTG GCTGAGCCCA GTATTCTTTG TAACAGTGAC 240
TCTCAATTGG GGGTGACTTT GCCTCCGAGG GGACCTTTGA CAATGTTTAT GGAACCTGTT 300
GATTGTCATT TCTGGAGAAG GAGTTGCTAC TGGTGTCTGT GGATAGAGGC CAGGGGGGCT 360
GCTCAACATC CTACTGTGTC CAGAACAGTC TGCCACAACG AAGAATTACC CAGACCCAGA 420
TGTCAAAGGT GCCAAGGTTG AGAAACCCTG AGCTACATTA AATAACGTCC CATGGAATAC 480
CTCAGTGAAA CTCACTGGTA ATAGCAGGAA GAAAAGGAGG AAATAAGGAA AAGGAAGAAG 540
GCTAAAAATC ACCAGACTGA GGCATAGCCC TATCCTAGTA ATCTTGGGGG AATCCCTTTC 600
AAAGGCAGGA CTTCCGTATG CAAAGGCAGT GGCTCTGGAG TTGTTCATCT CGGTTTCCGT 660
ATCTTGCTGC CTCCACTGAC TGGCTGGGCA TGATGTTGAA AAAAACTACA GAAGTCCCCG 720
GGCCATGAAT TCCCCCAGAT GTGATGGCTG TTTCCCAATG TTATTATGAG CATTAGATGT 780
GAACAAGTGC TATGGAATTG CTATTTCTCT TAAAGATGCT GAATAGCCCA GTCTGAGATG 840
ATTCTCAAAT TCTCATGGCC ATAGCAAATC ATCCTGGCTT TTACACATAC AGATTCTAGA 900
ATGAGATTTA TGGATATAAT TGTTTTTCAT TTTTATTATA AGTTCAGGGG TATATGTGCA 960
GGTTTGTTAT ACAGGTAAAC TTGTATCCTG GTGTTTTCTT GTACAGATTA TTTCATCACT 1020
GAGATATTAA GCCTAATACC CACTACTTAT TTTTCCTGAT CCTGTCCCTC CCCTCACCCT 1080
CCACCTTCCG GTAGGCCCCA GTGTTCCCCT CTTTGTGTCC ATGTGTTCTC ATCATTTACC 1140
TCCCATTTGT AAATGAGAAC ATGTGGTATT TGGTTTTCTG TTCCTGCATT AGTTTGCTAA 1200
GGATAATGAA 1210
|
