Variant report

Variant	rs6911272
Chromosome Location	chr6:34296962-34296963
allele	A/C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:34218417..34220144-chr6:34295375..34297652,2	K562	blood:
2	chr6:34295706..34297302-chr6:34301411..34303154,2	K562	blood:
3	chr6:34216785..34218325-chr6:34295929..34298863,2	K562	blood:
4	chr6:34295957..34297774-chr6:34297858..34299653,2	K562	blood:
5	chr6:34264509..34267143-chr6:34295354..34298132,2	K562	blood:

Variant related genes	Relation type
ENSG00000186577	Chromatin interaction

Extended variants
information (count: 59 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10484267	0.88[CEU][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10484268	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1057691	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1060308	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10648	0.88[CEU][hapmap];1.00[CHB][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1127084	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1265	0.88[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.96[TSI][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12654	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13466	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16883137	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16883475	0.88[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16883896	0.88[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16888452	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17628798	0.88[CEU][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs17628946	0.88[CEU][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17629180	0.85[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17629270	0.88[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17696583	0.88[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17696774	0.88[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17696829	0.88[CEU][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1994923	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs206922	0.88[CEU][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.96[TSI][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs3798554	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3798557	0.88[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs41269032	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs41269034	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs41269036	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41269038	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4713771	0.87[EUR][1000 genomes]
rs55674397	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55684754	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55694290	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs55763242	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55779010	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55798596	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs55812200	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55833185	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55863933	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55864834	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs56033036	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56039915	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56107559	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56188036	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56274913	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56309550	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56323997	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56330729	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59832183	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs62399870	0.85[EUR][1000 genomes]
rs7738665	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7760373	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7770443	0.85[TSI][hapmap];0.84[EUR][1000 genomes]
rs875274	0.88[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9368811	0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1798756	chr6:34203406-34319041	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	esv1798835	chr6:34204183-34319041	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
3	esv1792088	chr6:34204285-34318837	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
4	esv1793127	chr6:34204285-34319041	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
5	esv1794528	chr6:34267024-34308816	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs6911272	NUDT3	cis	lymphoblastoid	seeQTL
rs6911272	NUDT3	cis	parietal	SCAN
rs6911272	NUDT3	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:100 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34261800-34330800	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr6:34262200-34301200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr6:34264000-34299000	Weak transcription	Dnd41	blood
4	chr6:34274400-34306400	Weak transcription	Brain Germinal Matrix	brain
5	chr6:34274400-34309000	Weak transcription	NHDF-Ad	bronchial
6	chr6:34275200-34298000	Weak transcription	Fetal Muscle Trunk	muscle
7	chr6:34275800-34299600	Weak transcription	Lung	lung
8	chr6:34284000-34301600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr6:34284000-34308200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr6:34284600-34300400	Weak transcription	Primary T cells from cord blood	blood
11	chr6:34284800-34299000	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr6:34284800-34310800	Weak transcription	Primary T cells fromperipheralblood	blood
13	chr6:34285000-34305600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr6:34285200-34330600	Weak transcription	Thymus	Thymus
15	chr6:34285400-34299200	Weak transcription	HSMM	muscle
16	chr6:34285400-34305200	Weak transcription	Primary T helper cells fromperipheralblood	blood
17	chr6:34285400-34305400	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr6:34285400-34307800	Weak transcription	Liver	Liver
19	chr6:34285800-34308800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr6:34285800-34326600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr6:34286000-34308200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr6:34286600-34302800	Weak transcription	Osteobl	bone
23	chr6:34287000-34298000	Weak transcription	Primary monocytes fromperipheralblood	blood
24	chr6:34287000-34299400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr6:34287000-34301200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr6:34287000-34305000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr6:34287200-34299000	Weak transcription	Primary B cells from cord blood	blood
28	chr6:34287200-34299400	Weak transcription	Primary hematopoietic stem cells	blood
29	chr6:34287400-34297800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr6:34287400-34299200	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr6:34287400-34299400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr6:34287400-34300400	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr6:34287400-34300800	Weak transcription	Brain Angular Gyrus	brain
34	chr6:34287400-34300800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr6:34287400-34301600	Weak transcription	Spleen	Spleen
36	chr6:34287400-34304000	Weak transcription	Colonic Mucosa	Colon
37	chr6:34287600-34299200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr6:34287600-34299400	Weak transcription	GM12878-XiMat	blood
39	chr6:34287600-34305400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
40	chr6:34287600-34305400	Weak transcription	Right Atrium	heart
41	chr6:34287600-34306400	Weak transcription	Fetal Lung	lung
42	chr6:34287600-34309200	Weak transcription	Pancreas	Pancrea
43	chr6:34287800-34299600	Weak transcription	Primary B cells from peripheral blood	blood
44	chr6:34288000-34299200	Weak transcription	HepG2	liver
45	chr6:34288600-34298800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr6:34289000-34325200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr6:34289400-34308200	Weak transcription	Fetal Intestine Large	intestine
48	chr6:34290800-34299200	Weak transcription	HUVEC	blood vessel
49	chr6:34290800-34299400	Weak transcription	Small Intestine	intestine
50	chr6:34291400-34298200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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