Variant report

Variant	rs919785
Chromosome Location	chr19:19925470-19925471
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:43164363..43165895-chr19:19923263..19926242,2	K562	blood:

Extended variants
information (count: 40 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10407920	0.85[EUR][1000 genomes]
rs10412409	0.84[EUR][1000 genomes]
rs10419635	0.93[CEU][hapmap];0.89[EUR][1000 genomes]
rs11878280	0.88[EUR][1000 genomes]
rs12461018	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12973032	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs12975121	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12983372	0.88[AFR][1000 genomes]
rs2304171	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs2335360	0.80[EUR][1000 genomes]
rs23654	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs248939	1.00[CEU][hapmap]
rs248940	1.00[CEU][hapmap]
rs248941	1.00[CEU][hapmap]
rs248955	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2878398	0.85[EUR][1000 genomes]
rs34277739	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs34366671	0.87[AFR][1000 genomes]
rs35018071	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs35280091	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4808989	0.93[CEU][hapmap]
rs4990741	0.86[EUR][1000 genomes]
rs60041535	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7246983	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs7252985	0.93[CEU][hapmap];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs8104136	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs8108416	0.84[EUR][1000 genomes]
rs8111421	0.93[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1063273	chr19:19591146-20061367	ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv458375	chr19:19863014-19949209	Weak transcription Active TSS Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv578798	chr19:19863014-19949209	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv911313	chr19:19866371-19936078	Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
5	nsv911314	chr19:19866371-20021046	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
6	nsv519535	chr19:19871250-20595412	Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
7	nsv911315	chr19:19872093-20021046	Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
8	nsv911316	chr19:19890450-20021046	Flanking Active TSS ZNF genes & repeats Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
9	nsv578799	chr19:19901136-19967970	ZNF genes & repeats Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
10	nsv961192	chr19:19906394-20083740	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
11	esv3319016	chr19:19917475-20819154	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
12	esv3319017	chr19:19917475-20819154	ZNF genes & repeats Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs919785	ZNF506	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:19888400-19927800	Weak transcription	Psoas Muscle	Psoas
2	chr19:19888600-19931800	Weak transcription	Fetal Heart	heart
3	chr19:19895000-19931200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr19:19902600-19931600	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr19:19905000-19930000	Weak transcription	Colon Smooth Muscle	Colon
6	chr19:19907000-19931400	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr19:19907000-19931600	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr19:19907600-19929600	Weak transcription	Small Intestine	intestine
9	chr19:19907800-19931600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr19:19908000-19931600	Weak transcription	Stomach Mucosa	stomach
11	chr19:19909200-19931600	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr19:19914200-19926200	Weak transcription	Rectal Smooth Muscle	rectum
13	chr19:19914400-19926000	Weak transcription	Brain Substantia Nigra	brain
14	chr19:19914400-19926000	Weak transcription	Spleen	Spleen
15	chr19:19914400-19927600	Weak transcription	Gastric	stomach
16	chr19:19914400-19927800	Weak transcription	Aorta	Aorta
17	chr19:19914400-19929600	Weak transcription	HSMMtube	muscle
18	chr19:19914400-19931400	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr19:19914400-19931600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr19:19914600-19925600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr19:19915200-19929600	Weak transcription	NHLF	lung
22	chr19:19915800-19926800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
23	chr19:19915800-19930400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr19:19916200-19931200	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
25	chr19:19916800-19931600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr19:19917000-19929400	Weak transcription	Fetal Brain Male	brain
27	chr19:19917000-19931400	Weak transcription	Stomach Smooth Muscle	stomach
28	chr19:19917000-19931600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr19:19917600-19926200	Weak transcription	Placenta	Placenta
30	chr19:19919200-19931200	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
31	chr19:19920000-19926400	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
32	chr19:19920000-19926400	Strong transcription	Fetal Lung	lung
33	chr19:19920200-19926800	ZNF genes & repeats	Liver	Liver
34	chr19:19920200-19931200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
35	chr19:19920600-19931200	Weak transcription	Right Atrium	heart
36	chr19:19921200-19929600	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr19:19921400-19926800	Genic enhancers	Primary T helper cells PMA-I stimulated	--
38	chr19:19922000-19931200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr19:19922200-19926600	Enhancers	Brain Inferior Temporal Lobe	brain
40	chr19:19922200-19927000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr19:19922200-19931600	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr19:19922400-19926600	Strong transcription	Fetal Muscle Leg	muscle
43	chr19:19922400-19927000	Genic enhancers	Primary T helper cells fromperipheralblood	blood
44	chr19:19922600-19929400	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr19:19922600-19931600	Weak transcription	Ovary	ovary
46	chr19:19923200-19926200	Weak transcription	Left Ventricle	heart
47	chr19:19923200-19931600	Weak transcription	Pancreas	Pancrea
48	chr19:19923400-19926200	Weak transcription	Right Ventricle	heart
49	chr19:19923400-19927000	Strong transcription	Primary B cells from peripheral blood	blood
50	chr19:19923600-19927600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood

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