| Tag | Content |
|---|
EnhancerAtlas ID | HS034-14468 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr19:5889310-5890580 |
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: 2 | Chromosome | Start | End |
| chr19 | 5889633 | 5889941 | | chr19 | 5889952 | 5890095 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I005889 | chr19 | 5889394 | 5890118 |
|
Enhancer Sequence | CCAGATACTC GGGAGGCTGA GGCTGGAGAA TCGCTTGAAC CCCTAGGCGG CAGAGACTCA 60
GTGTCAAAAA AAAAAAAAAA AAAAAAGTCT CATGGGACTC CCTTCACATA TGTGGTCCGT 120
CAGTGACCGA AATGCTGTTA TACTGCACAT GACTGTTTGC TGAATGAACT CTGAGTCTTG 180
CCCCCGGGTC TGGAGGGCTT CTCTTCCCGT GCCTTCCCGC ACTCCACTGC AGCCATCATC 240
TCATGTGGGG AGAGTGAGAA GGACCCTGAT CCCCCTCCGA GAGCCTATAC CACCCAGGCA 300
GCAAAGCAGG GCCAGGCAGG GTGCACAGCC ACCCCCAAGT GGTTCTCAGG CCCCACCTCT 360
GGACCTCCTA CCCTTTGCAG ACCTGGAGAT TCATTCATTT GTTTATCCAT TCATTCATTC 420
CACACATAGT TCTGGAGCCC TGCTGCGTTC CTCGGCTGGG TGCCGGGGTG TAGGCAGAGG 480
ATATAACAGC CAGGATACGT CCCAGTCCTC AAGGAGGTGC ACATAAATAA CACACGTGAT 540
GGTGACGTGG GACTTAGAAA CTGGCAGGGG CTACGGGCAA AACTAGAAGG CAAATGAGTG 600
TGGAGTGCTG GTGGCCTGGG GACGGGGGAT GAGGAGGTGG CTTGTGAGCT GAGAATTGAA 660
GGAGGTGAGG GGTGAGCTTG GGGACATCTA GGGGACAGGC ATTGCAGGCA GAGGGTATGG 720
ACTATGCAAA GGCCCTAGGG CAGGACTGTG CCAGGGGTTT TGGAGGAAGA GTGAGGAGGC 780
TGGTGGGGCT GGAGCAGTGA AGAGGGGAGG GGAGGAGAGG GAGGGGAGGG AGAGGAGGGG 840
TCGGGACACA CAGGGCATAG TGGGCTGTAG AGAGGATTTG GGCTTTTCCC CCAAGTGGGG 900
TGGGAGCCAT GGAGGACTGT GGGCAGGGGA GGGGCGGGAC CTGACTTAGG GGCTCACAGG 960
CGCCTTCTGG CTCAGGGGGT AGCCGGGTGA CCAGGGCAGA GGGGACTACG CTTGTCGTGA 1020
TGATGGAATC AGACTAGAGG CAGATCTGGG ACAGATTCTG AAGGCAAAGG GGCTCGAGAT 1080
GCGGGGAGGG CGGGAGCAGC TCTTCAGTCC CAGGAGGGGC ACACATCAGC CCCGTGGGGT 1140
CTTCTCAGCT GTGTCCCACC CCAATCATGT CAAACACATT TATAGGAGCC CACAGCCCAC 1200
ACTCAACACA AGTTTAAAGG AGTACAGTTG TGCTCAAGTT GGCAGCGAAA ACACCTTCCT 1260
TTCTCAGTGA 1270
|
