Variant report

Variant	rs2967534
Chromosome Location	chr19:36942777-36942778
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:36940091..36943076-chr19:37061156..37065481,3	K562	blood:

Variant related genes	Relation type
ENSG00000233527	Chromatin interaction
ENSG00000186020	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs11665865	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11670917	0.84[AMR][1000 genomes]
rs11672024	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11673325	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12971760	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12985198	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17206393	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2385797	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2912415	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2912423	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2912435	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2912439	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2912441	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2945953	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2945976	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2967443	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2967444	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2967445	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2967446	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2967453	0.92[AMR][1000 genomes]
rs2967528	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2967530	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2967531	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2967535	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2967537	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2967539	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2967540	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3107235	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3107236	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3111553	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs34550124	0.84[AMR][1000 genomes]
rs34664029	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs34830781	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs35408779	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62113910	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62113945	0.85[AMR][1000 genomes]
rs67276862	0.83[EUR][1000 genomes]
rs8104181	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833816	chr19:36824257-37034287	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
2	nsv1066026	chr19:36878441-36947928	ZNF genes & repeats Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
3	nsv1067101	chr19:36901010-36956251	ZNF genes & repeats Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
4	nsv1064851	chr19:36910259-37689721	Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
5	nsv911648	chr19:36914171-37047472	Weak transcription Active TSS Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
6	nsv1065698	chr19:36916796-37690124	Active TSS ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
7	nsv543999	chr19:36916796-37690124	Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
8	nsv1067364	chr19:36921204-36985874	ZNF genes & repeats Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
9	nsv529817	chr19:36930549-37654062	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2967534	ZNF567	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:93 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:36931800-36946800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
2	chr19:36934200-36950000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr19:36934400-36944000	ZNF genes & repeats	Adipose Nuclei	Adipose
4	chr19:36934400-36946600	ZNF genes & repeats	Liver	Liver
5	chr19:36936000-36950000	ZNF genes & repeats	Fetal Brain Female	brain
6	chr19:36936200-36943600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
7	chr19:36936200-36949600	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr19:36936400-36943600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
9	chr19:36936400-36943600	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
10	chr19:36936400-36946600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
11	chr19:36936400-36978400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr19:36936800-36943800	ZNF genes & repeats	A549	lung
13	chr19:36936800-36944200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr19:36937200-36943600	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
15	chr19:36937600-36943000	ZNF genes & repeats	Psoas Muscle	Psoas
16	chr19:36937800-36943400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr19:36937800-36943600	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
18	chr19:36937800-36944200	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr19:36938000-36943600	ZNF genes & repeats	Stomach Smooth Muscle	stomach
20	chr19:36938000-36943800	ZNF genes & repeats	Primary B cells from cord blood	blood
21	chr19:36938000-36946600	ZNF genes & repeats	Brain Germinal Matrix	brain
22	chr19:36938200-36943600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
23	chr19:36938200-36943800	ZNF genes & repeats	Dnd41	blood
24	chr19:36938200-36944000	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr19:36938200-36944200	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr19:36938200-36946000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
27	chr19:36938200-36947200	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
28	chr19:36938200-36952200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr19:36938400-36942800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
30	chr19:36938400-36943600	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
31	chr19:36938400-36946000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr19:36938400-36946400	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
33	chr19:36938400-36946600	ZNF genes & repeats	Fetal Lung	lung
34	chr19:36938400-36951200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr19:36938600-36943400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
36	chr19:36938600-36943600	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
37	chr19:36938600-36943600	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
38	chr19:36938600-36944200	ZNF genes & repeats	Primary T killer naive cells fromperipheralblood	blood
39	chr19:36938600-36946400	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr19:36938600-36946600	ZNF genes & repeats	Duodenum Mucosa	Duodenum
41	chr19:36938800-36943800	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
42	chr19:36939000-36943600	ZNF genes & repeats	Brain Hippocampus Middle	brain
43	chr19:36939000-36944200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr19:36939200-36948600	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
45	chr19:36939200-36949000	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
46	chr19:36939600-36943600	ZNF genes & repeats	Primary B cells from peripheral blood	blood
47	chr19:36939600-36943600	Strong transcription	Placenta Amnion	Placenta Amnion
48	chr19:36939600-36943800	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
49	chr19:36939800-36942800	ZNF genes & repeats	NHEK	skin
50	chr19:36939800-36943000	ZNF genes & repeats	Ovary	ovary

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links