Variant report

Variant	rs11084818
Chromosome Location	chr19:35999251-35999252
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2)
CpG islands
(count:0)
Chromatin interactive
region (count:3)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr19:35996502-35999278	H1-hESC	embryonic stem cell:	n/a	n/a
2	POLR2A	chr19:35999217-35999355	MCF10A-Er-Src	breast:	n/a	n/a

No data

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:35996698..35999600-chr19:36003100..36006051,2	MCF-7	breast:
2	chr19:35991475..35994230-chr19:35996710..35999292,3	MCF-7	breast:
3	chr19:35991484..35996459-chr19:35997926..36003071,7	MCF-7	breast:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DMKN-1	chr19:35996841-35999459	NONHSAT065857

No data

Variant related genes	Relation type
DMKN	TF binding region
ENSG00000161249	Chromatin interaction

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs4254439	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4358061	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6510492	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6510494	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7245699	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432045	chr19:35556260-36520760	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
2	nsv1060100	chr19:35658505-36170042	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
3	nsv543993	chr19:35658505-36170042	Enhancers Strong transcription Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
4	nsv833811	chr19:35850257-36029535	Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:35986400-35999600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr19:35986400-36000000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr19:35986400-36000600	Weak transcription	Right Atrium	heart
4	chr19:35986800-36000200	Weak transcription	Gastric	stomach
5	chr19:35986800-36000400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr19:35990200-36000400	Weak transcription	Lung	lung
7	chr19:35991000-36000200	Weak transcription	Ovary	ovary
8	chr19:35991200-36000200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr19:35992200-36000400	Weak transcription	Aorta	Aorta
10	chr19:35993200-35999400	Strong transcription	HUES6 Cell Line	embryonic stem cell
11	chr19:35993200-35999600	Weak transcription	Brain Anterior Caudate	brain
12	chr19:35993400-36000000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr19:35993400-36000200	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr19:35996400-35999800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr19:35997200-35999400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr19:35997200-36000000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr19:35997600-35999600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr19:35997600-36000200	Weak transcription	Pancreas	Pancrea
19	chr19:35997800-36000000	Weak transcription	Fetal Intestine Small	intestine
20	chr19:35998200-35999600	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr19:35998200-35999800	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr19:35998400-35999400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr19:35998800-35999400	Transcr. at gene 5' and 3'	HUES64 Cell Line	embryonic stem cell
24	chr19:35998800-35999400	Genic enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr19:35999000-35999400	Genic enhancers	H1 Cell Line	embryonic stem cell
26	chr19:35999000-35999400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr19:35999000-35999400	Enhancers	Hela-S3	cervix
28	chr19:35999000-35999600	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr19:35999000-36000600	Active TSS	GM12878-XiMat	blood
30	chr19:35999200-35999400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr19:35999200-35999400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr19:35999200-35999400	Genic enhancers	HMEC	breast
33	chr19:35999200-35999400	Weak transcription	NHEK	skin
34	chr19:35999200-35999600	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr19:35999200-35999600	Transcr. at gene 5' and 3'	HUES48 Cell Line	embryonic stem cell
36	chr19:35999200-35999600	Transcr. at gene 5' and 3'	iPS-20b Cell Line	embryonic stem cell
37	chr19:35999200-36000000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr19:35999200-36000200	Enhancers	HepG2	liver
39	chr19:35999200-36000800	Weak transcription	Esophagus	oesophagus

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