| Tag | Content |
|---|
EnhancerAtlas ID | HS060-16813 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr19:5889340-5890630 |
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 |
|
| | 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 | TCGCTTGAAC CCCTAGGCGG CAGAGACTCA GTGTCAAAAA AAAAAAAAAA AAAAAAGTCT 60
CATGGGACTC CCTTCACATA TGTGGTCCGT CAGTGACCGA AATGCTGTTA TACTGCACAT 120
GACTGTTTGC TGAATGAACT CTGAGTCTTG CCCCCGGGTC TGGAGGGCTT CTCTTCCCGT 180
GCCTTCCCGC ACTCCACTGC AGCCATCATC TCATGTGGGG AGAGTGAGAA GGACCCTGAT 240
CCCCCTCCGA GAGCCTATAC CACCCAGGCA GCAAAGCAGG GCCAGGCAGG GTGCACAGCC 300
ACCCCCAAGT GGTTCTCAGG CCCCACCTCT GGACCTCCTA CCCTTTGCAG ACCTGGAGAT 360
TCATTCATTT GTTTATCCAT TCATTCATTC CACACATAGT TCTGGAGCCC TGCTGCGTTC 420
CTCGGCTGGG TGCCGGGGTG TAGGCAGAGG ATATAACAGC CAGGATACGT CCCAGTCCTC 480
AAGGAGGTGC ACATAAATAA CACACGTGAT GGTGACGTGG GACTTAGAAA CTGGCAGGGG 540
CTACGGGCAA AACTAGAAGG CAAATGAGTG TGGAGTGCTG GTGGCCTGGG GACGGGGGAT 600
GAGGAGGTGG CTTGTGAGCT GAGAATTGAA GGAGGTGAGG GGTGAGCTTG GGGACATCTA 660
GGGGACAGGC ATTGCAGGCA GAGGGTATGG ACTATGCAAA GGCCCTAGGG CAGGACTGTG 720
CCAGGGGTTT TGGAGGAAGA GTGAGGAGGC TGGTGGGGCT GGAGCAGTGA AGAGGGGAGG 780
GGAGGAGAGG GAGGGGAGGG AGAGGAGGGG TCGGGACACA CAGGGCATAG TGGGCTGTAG 840
AGAGGATTTG GGCTTTTCCC CCAAGTGGGG TGGGAGCCAT GGAGGACTGT GGGCAGGGGA 900
GGGGCGGGAC CTGACTTAGG GGCTCACAGG CGCCTTCTGG CTCAGGGGGT AGCCGGGTGA 960
CCAGGGCAGA GGGGACTACG CTTGTCGTGA TGATGGAATC AGACTAGAGG CAGATCTGGG 1020
ACAGATTCTG AAGGCAAAGG GGCTCGAGAT GCGGGGAGGG CGGGAGCAGC TCTTCAGTCC 1080
CAGGAGGGGC ACACATCAGC CCCGTGGGGT CTTCTCAGCT GTGTCCCACC CCAATCATGT 1140
CAAACACATT TATAGGAGCC CACAGCCCAC ACTCAACACA AGTTTAAAGG AGTACAGTTG 1200
TGCTCAAGTT GGCAGCGAAA ACACCTTCCT TTCTCAGTGA GGTATTTTCT TTTTTTTTTT 1260
TTTTGAGACG GAGTCTCACT CTGTCGCCCA 1290
|
