Variant report

Variant	rs34101156
Chromosome Location	chr6:167341698-167341699
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs11159	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13201493	0.89[EUR][1000 genomes]
rs13201941	0.89[EUR][1000 genomes]
rs13202098	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13213544	0.87[EUR][1000 genomes]
rs13216122	0.85[EUR][1000 genomes]
rs13220568	0.89[EUR][1000 genomes]
rs13437363	0.88[ASN][1000 genomes]
rs34078068	0.85[EUR][1000 genomes]
rs34116393	0.89[EUR][1000 genomes]
rs34159386	0.89[EUR][1000 genomes]
rs34431091	0.89[EUR][1000 genomes]
rs35147976	0.80[EUR][1000 genomes]
rs35206089	0.87[EUR][1000 genomes]
rs35614625	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35615089	0.89[EUR][1000 genomes]
rs35731380	0.94[EUR][1000 genomes]
rs36032379	0.89[EUR][1000 genomes]
rs58251236	0.89[EUR][1000 genomes]
rs59988493	0.89[EUR][1000 genomes]
rs60908348	0.89[EUR][1000 genomes]
rs6913013	0.85[ASN][1000 genomes]
rs6916542	0.89[EUR][1000 genomes]
rs6930995	0.82[ASN][1000 genomes]
rs71571463	0.89[EUR][1000 genomes]
rs71571464	0.89[EUR][1000 genomes]
rs71571465	0.89[EUR][1000 genomes]
rs71571466	0.87[EUR][1000 genomes]
rs7740833	0.94[EUR][1000 genomes]
rs7755545	0.89[EUR][1000 genomes]
rs9295378	0.85[EUR][1000 genomes]
rs9295379	0.87[EUR][1000 genomes]
rs9295380	0.94[EUR][1000 genomes]
rs9295382	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9457239	0.91[EUR][1000 genomes]
rs9457243	0.89[EUR][1000 genomes]
rs9457244	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9457245	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9459799	0.87[EUR][1000 genomes]
rs9459800	0.94[EUR][1000 genomes]
rs9459802	0.94[EUR][1000 genomes]
rs9459803	0.94[EUR][1000 genomes]
rs9459804	0.96[EUR][1000 genomes]
rs9459806	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv605260	chr6:166984094-167455139	Enhancers Strong transcription Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1019381	chr6:167090236-167558598	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
3	nsv538541	chr6:167090236-167558598	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
4	nsv1022866	chr6:167108740-167345629	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv605327	chr6:167185674-167360389	Enhancers Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv1027314	chr6:167194653-167355961	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	nsv538542	chr6:167194653-167355961	Strong transcription Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
8	nsv605332	chr6:167198027-167353701	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv948634	chr6:167200671-167838993	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
10	nsv482507	chr6:167282376-167474915	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
11	nsv532074	chr6:167320656-167781977	Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats 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	23 gene(s)	inside rSNPs	diseases
12	nsv1031039	chr6:167324021-167741439	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	21 gene(s)	inside rSNPs	diseases
13	nsv538543	chr6:167324021-167741439	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	21 gene(s)	inside rSNPs	diseases
14	nsv1026972	chr6:167335031-167671042	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:87 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167318400-167343800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:167318600-167342400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr6:167321800-167342200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr6:167332800-167342400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr6:167334000-167343600	Weak transcription	Fetal Brain Male	brain
6	chr6:167335400-167343800	Weak transcription	Right Atrium	heart
7	chr6:167335600-167346200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr6:167336600-167342200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr6:167337200-167342400	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr6:167337400-167343000	Weak transcription	Brain Cingulate Gyrus	brain
11	chr6:167337600-167342200	Weak transcription	Colonic Mucosa	Colon
12	chr6:167337600-167350000	Weak transcription	Ovary	ovary
13	chr6:167337600-167363400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr6:167338200-167356000	Strong transcription	Primary neutrophils fromperipheralblood	blood
15	chr6:167338400-167342000	Weak transcription	Brain Anterior Caudate	brain
16	chr6:167338800-167342400	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr6:167339000-167342000	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr6:167339000-167343800	Strong transcription	GM12878-XiMat	blood
19	chr6:167339200-167342200	Weak transcription	Fetal Intestine Large	intestine
20	chr6:167339200-167342400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
21	chr6:167339200-167344000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr6:167339200-167348400	Strong transcription	Primary T cells from cord blood	blood
23	chr6:167339400-167343800	Weak transcription	Brain Angular Gyrus	brain
24	chr6:167339800-167342000	Weak transcription	Placenta Amnion	Placenta Amnion
25	chr6:167340000-167358800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr6:167340000-167363000	Strong transcription	Primary monocytes fromperipheralblood	blood
27	chr6:167340000-167363000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr6:167340200-167341800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr6:167340200-167342400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr6:167340200-167342400	Strong transcription	Fetal Stomach	stomach
31	chr6:167340200-167342600	Strong transcription	Primary B cells from peripheral blood	blood
32	chr6:167340200-167342800	Strong transcription	Fetal Thymus	thymus
33	chr6:167340200-167343800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr6:167340200-167344200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr6:167340200-167344800	Strong transcription	Primary T cells fromperipheralblood	blood
36	chr6:167340200-167349800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr6:167340200-167354600	Strong transcription	Fetal Intestine Small	intestine
38	chr6:167340200-167362800	Strong transcription	Monocytes-CD14+_RO01746	blood
39	chr6:167340400-167342200	Enhancers	Fetal Muscle Trunk	muscle
40	chr6:167340400-167342400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr6:167340400-167342600	Strong transcription	Primary B cells from cord blood	blood
42	chr6:167340400-167343400	Strong transcription	Duodenum Mucosa	Duodenum
43	chr6:167340400-167343800	Strong transcription	Primary T helper cells fromperipheralblood	blood
44	chr6:167340400-167344600	Strong transcription	Stomach Smooth Muscle	stomach
45	chr6:167340400-167357200	Strong transcription	Sigmoid Colon	Sigmoid Colon
46	chr6:167340400-167363000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
47	chr6:167340600-167342200	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr6:167340600-167342200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr6:167340600-167342400	Weak transcription	Esophagus	oesophagus
50	chr6:167340600-167342800	Weak transcription	Brain Germinal Matrix	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links