Variant report

Variant	rs9469843
Chromosome Location	chr6:34649893-34649894
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	chr6:34639252..34641704-chr6:34648806..34650396,2	K562	blood:
2	chr6:34649586..34652220-chr6:34663564..34665833,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000196821	Chromatin interaction
ENSG00000272288	Chromatin interaction

Extended variants
information (count: 68 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs1201872	0.83[ASN][1000 genomes]
rs13196983	0.80[ASN][1000 genomes]
rs13209544	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs16892384	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16892386	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs205261	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs205263	0.86[ASN][1000 genomes]
rs205264	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs205265	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs205266	0.85[ASN][1000 genomes]
rs205267	0.86[ASN][1000 genomes]
rs205284	0.83[ASN][1000 genomes]
rs34374374	0.86[ASN][1000 genomes]
rs35286877	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35987776	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs36032186	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs451263	0.86[ASN][1000 genomes]
rs451603	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6457784	0.85[ASN][1000 genomes]
rs66948142	0.84[EUR][1000 genomes]
rs6900426	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6908462	0.80[ASN][1000 genomes]
rs6909393	0.80[ASN][1000 genomes]
rs6909637	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6937428	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72910111	0.83[ASN][1000 genomes]
rs7738377	0.88[ASN][1000 genomes]
rs7748836	0.81[AFR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7749750	0.80[ASN][1000 genomes]
rs7759412	0.80[ASN][1000 genomes]
rs7759985	0.80[ASN][1000 genomes]
rs7763989	0.80[ASN][1000 genomes]
rs7764921	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7765969	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9461992	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9461993	0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9461994	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9461997	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9462001	0.86[ASN][1000 genomes]
rs9462002	0.86[ASN][1000 genomes]
rs9462003	0.86[ASN][1000 genomes]
rs9469812	0.83[ASN][1000 genomes]
rs9469813	0.86[ASN][1000 genomes]
rs9469814	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9469820	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9469822	0.88[ASN][1000 genomes]
rs9469827	0.90[EUR][1000 genomes]
rs9469832	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9469836	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9469837	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9469838	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9469840	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9469842	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9469847	0.85[ASN][1000 genomes]
rs9469852	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022844	chr6:34317219-35060519	Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv538195	chr6:34317219-35060519	Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
3	esv2758046	chr6:34382492-34714677	Genic enhancers Enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
4	esv2759418	chr6:34382492-34714677	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
5	nsv885785	chr6:34404636-34874002	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
6	nsv1033583	chr6:34471572-34828372	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats 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	38 gene(s)	inside rSNPs	diseases
7	nsv885793	chr6:34520267-34886436	Active TSS Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer 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 target site	47 gene(s)	inside rSNPs	diseases
8	nsv830640	chr6:34542489-34714677	Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Weak transcription Genic enhancers 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 target site	24 gene(s)	inside rSNPs	diseases
9	nsv885794	chr6:34561585-34673149	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
10	nsv1032557	chr6:34565802-34802008	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
11	nsv538196	chr6:34565802-34802008	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
12	esv2763967	chr6:34566255-34925463	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
13	nsv1020710	chr6:34607214-34890143	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs9469843	UHRF1BP1	cis	Muscle Skeletal	GTEx
rs9469843	SNRPC	cis	Nerve Tibial	GTEx
rs9469843	SNRPC	cis	lung	GTEx

Chromatin state (count:90 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34626000-34662000	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr6:34626800-34662400	Weak transcription	Fetal Muscle Trunk	muscle
3	chr6:34632800-34655200	Weak transcription	Fetal Stomach	stomach
4	chr6:34633000-34662800	Weak transcription	Aorta	Aorta
5	chr6:34634800-34663200	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr6:34636400-34662200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr6:34639800-34662800	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr6:34639800-34662800	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr6:34640200-34656600	Weak transcription	Spleen	Spleen
10	chr6:34640800-34655800	Weak transcription	Fetal Muscle Leg	muscle
11	chr6:34641400-34662800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr6:34641600-34654800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr6:34641600-34654800	Weak transcription	Dnd41	blood
14	chr6:34641600-34655400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr6:34641800-34656400	Weak transcription	Left Ventricle	heart
16	chr6:34641800-34661200	Weak transcription	Brain Hippocampus Middle	brain
17	chr6:34641800-34663200	Weak transcription	Gastric	stomach
18	chr6:34642200-34656000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr6:34642200-34663000	Weak transcription	Thymus	Thymus
20	chr6:34643000-34655400	Weak transcription	Fetal Thymus	thymus
21	chr6:34643000-34655800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr6:34643000-34655800	Weak transcription	Lung	lung
23	chr6:34643000-34656400	Weak transcription	Pancreas	Pancrea
24	chr6:34643000-34661200	Weak transcription	Right Atrium	heart
25	chr6:34643000-34662800	Weak transcription	Stomach Mucosa	stomach
26	chr6:34643200-34650600	Enhancers	Liver	Liver
27	chr6:34647400-34650800	Enhancers	Primary B cells from peripheral blood	blood
28	chr6:34647600-34650600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
29	chr6:34647800-34652200	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr6:34647800-34652600	Weak transcription	Psoas Muscle	Psoas
31	chr6:34647800-34660800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr6:34647800-34661000	Weak transcription	Duodenum Smooth Muscle	Duodenum
33	chr6:34647800-34662000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr6:34647800-34662200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr6:34647800-34662400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr6:34647800-34662600	Weak transcription	Ovary	ovary
37	chr6:34647800-34662800	Weak transcription	Brain Substantia Nigra	brain
38	chr6:34647800-34662800	Weak transcription	HSMMtube	muscle
39	chr6:34648000-34651600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr6:34648000-34662600	Weak transcription	Right Ventricle	heart
41	chr6:34648000-34662800	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr6:34648200-34650000	Enhancers	Primary T cells fromperipheralblood	blood
43	chr6:34648400-34655800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr6:34648400-34662000	Weak transcription	Brain Anterior Caudate	brain
45	chr6:34648600-34650200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr6:34649200-34651400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
47	chr6:34649200-34652800	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr6:34649200-34660200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
49	chr6:34649200-34660400	Weak transcription	Primary T cells from cord blood	blood
50	chr6:34649200-34662200	Weak transcription	Rectal Mucosa Donor 31	rectum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links