| Tag | Content |
|---|
EnhancerAtlas ID | HS041-10034 |
Organism | Homo sapiens |
Tissue/cell | EWS502 |
Coordinate | chr19:5889580-5890900 |
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 | chr19:5890122-5890143 | AGGAGAGGGAGGGGAGGGAGA | + | 6.06 | | ZNF263 | MA0528.1 | chr19:5890100-5890121 | GGAGCAGTGAAGAGGGGAGGG | + | 6.07 | | ZNF263 | MA0528.1 | chr19:5890126-5890147 | GAGGGAGGGGAGGGAGAGGAG | + | 6.8 | | ZNF263 | MA0528.1 | chr19:5890117-5890138 | AGGGGAGGAGAGGGAGGGGAG | + | 7.35 | | ZNF263 | MA0528.1 | chr19:5890120-5890141 | GGAGGAGAGGGAGGGGAGGGA | + | 7.88 | | Zfx | MA0146.2 | chr19:5890827-5890841 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr19 | 5889633 | 5889941 | | chr19 | 5889952 | 5890095 | | chr19 | 5890231 | 5890592 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I005889 | chr19 | 5889394 | 5890118 |
|
Enhancer Sequence | CCCCCTCCGA GAGCCTATAC CACCCAGGCA GCAAAGCAGG GCCAGGCAGG GTGCACAGCC 60
ACCCCCAAGT GGTTCTCAGG CCCCACCTCT GGACCTCCTA CCCTTTGCAG ACCTGGAGAT 120
TCATTCATTT GTTTATCCAT TCATTCATTC CACACATAGT TCTGGAGCCC TGCTGCGTTC 180
CTCGGCTGGG TGCCGGGGTG TAGGCAGAGG ATATAACAGC CAGGATACGT CCCAGTCCTC 240
AAGGAGGTGC ACATAAATAA CACACGTGAT GGTGACGTGG GACTTAGAAA CTGGCAGGGG 300
CTACGGGCAA AACTAGAAGG CAAATGAGTG TGGAGTGCTG GTGGCCTGGG GACGGGGGAT 360
GAGGAGGTGG CTTGTGAGCT GAGAATTGAA GGAGGTGAGG GGTGAGCTTG GGGACATCTA 420
GGGGACAGGC ATTGCAGGCA GAGGGTATGG ACTATGCAAA GGCCCTAGGG CAGGACTGTG 480
CCAGGGGTTT TGGAGGAAGA GTGAGGAGGC TGGTGGGGCT GGAGCAGTGA AGAGGGGAGG 540
GGAGGAGAGG GAGGGGAGGG AGAGGAGGGG TCGGGACACA CAGGGCATAG TGGGCTGTAG 600
AGAGGATTTG GGCTTTTCCC CCAAGTGGGG TGGGAGCCAT GGAGGACTGT GGGCAGGGGA 660
GGGGCGGGAC CTGACTTAGG GGCTCACAGG CGCCTTCTGG CTCAGGGGGT AGCCGGGTGA 720
CCAGGGCAGA GGGGACTACG CTTGTCGTGA TGATGGAATC AGACTAGAGG CAGATCTGGG 780
ACAGATTCTG AAGGCAAAGG GGCTCGAGAT GCGGGGAGGG CGGGAGCAGC TCTTCAGTCC 840
CAGGAGGGGC ACACATCAGC CCCGTGGGGT CTTCTCAGCT GTGTCCCACC CCAATCATGT 900
CAAACACATT TATAGGAGCC CACAGCCCAC ACTCAACACA AGTTTAAAGG AGTACAGTTG 960
TGCTCAAGTT GGCAGCGAAA ACACCTTCCT TTCTCAGTGA GGTATTTTCT TTTTTTTTTT 1020
TTTTGAGACG GAGTCTCACT CTGTCGCCCA AGCTGGAGTG CAGTGGCGTG ATCTTGGCTC 1080
ACTGCAAGCT CCGCCTCCCG GGTTCACGCC ATTCTCGTGC CTCAGCCTCC CGAGTAGCTG 1140
GGACTACAGA CGCCCGCCAC CATGCCAGAC TGTTTTTGTA TTCTTAGTAG AGACAGGGTT 1200
TCACCGTGTT AGTCAGGATG GTCTCAATCT CCTGACCTTG TGATCCGCCC GCCTCGGCCT 1260
CCCAAAGTGC TGGGATTACA GGCGTGAGCC ACCGCGCCCA GCCCTTAGTG GGGTGTTTTC 1320
|
