| Tag | Content |
|---|
EnhancerAtlas ID | HS197-10115 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr19:984560-985860 |
Target genes | | Number: 29 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NRF1 | MA0506.1 | chr19:984698-984709 | GCGCATGCGCG | + | 6.02 | | NRF1 | MA0506.1 | chr19:984697-984708 | TGCGCATGCGC | - | 6.32 | | ZNF263 | MA0528.1 | chr19:985786-985807 | CCCCTCCCCTCGCCCTCCACT | - | 6.05 |
|
| | 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 |
| GH19I000985 | chr19 | 985721 | 985870 |
|
Enhancer Sequence | AAGGTGCGGC GGTGCGGTCT CGCTGCTGGG GTCATGGGGC GCCCGAGGCT GAAGTCGGGG 60
GATGGGTTGG TGGGGGCCGC GTGCACCCTT AGTCGGAATT GGCGTGGGGA GGGGAGGTGG 120
TCTCCGTTCG GGCGCTCTGC GCATGCGCGG GTCTGGGGGC TTTGGGGAGA TACGTGCGAC 180
CTGTTAGGCC GCTCTGCGCA CGCGCGGGGC TCAGGCCTGA GCTGCTATGG GGGCAGTGGG 240
GGAAAATGGG AGACGCTCCG GGGGGTCCCT TGGGGCAATT GCGCATGCAC GAGTTCTTGG 300
AGCGCGAAAT TTGATTAAAA GGGGCCTATG AGCTCTGTGG ATGTTGTGGT TCTGGAGGAA 360
AAGGGAGAAG GACCAAGGTC TGGGGGAGTC TCCCATGAAG GGGTGGCGCA GGAAACTCAT 420
GTTTATTCCT CCAATAAAGC AACAGATACT CACCGTCGCC CACAGTTTCC CCTCTACTCC 480
CAAGCCCAAA TGCAGCCAGT CCCTGAAGCT ACTCGCTTCC CCCGTGTGCC CGCTGAGATC 540
TCTTGGGACT GGCTCTGTGC TCCAGCATTG CCTGATGGAG TCTACACACA ACTCATAAAT 600
TTCTCCCATT TTATTTTAGT TTTGAGACAG GGTCTCACTC TGTCGCTGAG GCTGGAGTGC 660
AGTGGTGCGA TCTCGGCTCA CTGCAGCCTC TGCCTCTAGG GTTCAAGCGA TTCTCGGGCC 720
TCAGCCTCCT GAGTAGCTGC AACTACAGGC CCGCACCAAC CACCACACCC GGCCCACATT 780
TGTATTTTTT GTAGAGGCAG GGTTTCACCA TGTTGGCCAG GCTGGTCTCG AACTCCTGAC 840
CTCAAGTGAT CTGCCCACCT CAGCCTCCCA AAGTGCTGGG ATTACAGCCG TGAGCCACCA 900
CGCCCGGCTG AGTTTTCCCA TTTTAGAGAG GAGGAAGCTG AGGCTTGGGG TCTTAGGTTG 960
GACATTATGG ATAGAAGGAT TGGGGCACAA GCCTACTGGG CTCTTGGGCC CCAGTGTCCT 1020
TCTGGATCCT CTTTGTTCTG TTCCTGTACT CCTCCCACCC AGGGCCCCTC TGACCCTCAG 1080
AGGAAGCACC AACCTCACAT CTACCACCTC CAGCCTCGAA GCCTCTTGCA GGGGCGAACA 1140
CTTCCTTGCT GGACCATGCA TTTGCTCAAA CCACCCTGCT CCCGACTCCT CTTCCTGGTT 1200
CTCTGACTTA GCCATTGCCC AGGCGTCCCC TCCCCTCGCC CTCCACTGCT GTAGTAGCTC 1260
CCGTGTCCTG CATGGGGCTC ACGAGGCTGA CTGTGCATCC 1300
|
