Variant report

Variant	rs6907192
Chromosome Location	chr6:5502627-5502628
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PPP1R3G-7	chr6:5502505-5504640	NONHSAT107521

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10080503	0.85[EUR][1000 genomes]
rs11243015	1.00[EUR][1000 genomes]
rs55637366	1.00[EUR][1000 genomes]
rs55776619	1.00[EUR][1000 genomes]
rs6920599	0.85[EUR][1000 genomes]
rs6934984	1.00[EUR][1000 genomes]
rs73356383	0.85[EUR][1000 genomes]
rs73719627	1.00[EUR][1000 genomes]
rs73719628	0.85[EUR][1000 genomes]
rs7738121	0.98[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7742495	1.00[EUR][1000 genomes]
rs9502315	0.85[EUR][1000 genomes]
rs9504425	0.85[EUR][1000 genomes]
rs9504428	0.85[EUR][1000 genomes]
rs9504429	0.85[EUR][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	nsv1019428	chr6:5216835-5627839	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv538118	chr6:5216835-5627839	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1034607	chr6:5311590-5573514	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv538120	chr6:5311590-5573514	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv916361	chr6:5315853-5695486	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1023027	chr6:5377308-5556749	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv538121	chr6:5377308-5556749	Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv600886	chr6:5426265-5511614	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv1017506	chr6:5443538-5551125	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:5461600-5507200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr6:5466400-5518200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr6:5466600-5506400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr6:5471800-5505800	Weak transcription	Primary B cells from peripheral blood	blood
5	chr6:5472400-5511600	Weak transcription	Fetal Stomach	stomach
6	chr6:5472600-5506200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr6:5482200-5506600	Weak transcription	Primary hematopoietic stem cells	blood
8	chr6:5485200-5506400	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr6:5486000-5505400	Weak transcription	Primary T helper cells fromperipheralblood	blood
10	chr6:5486200-5506800	Weak transcription	Thymus	Thymus
11	chr6:5486400-5502800	Weak transcription	HepG2	liver
12	chr6:5488000-5510600	Weak transcription	Aorta	Aorta
13	chr6:5488200-5506200	Weak transcription	Primary T cells fromperipheralblood	blood
14	chr6:5488200-5506400	Weak transcription	Fetal Intestine Small	intestine
15	chr6:5488600-5506000	Weak transcription	Primary B cells from cord blood	blood
16	chr6:5488600-5521600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr6:5495400-5505400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr6:5498400-5506200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr6:5498800-5513000	Weak transcription	Fetal Muscle Leg	muscle
20	chr6:5500000-5510600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr6:5500200-5511000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr6:5500400-5507600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr6:5500400-5510600	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr6:5500400-5511800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr6:5500400-5525000	Weak transcription	Spleen	Spleen
26	chr6:5500600-5508200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
27	chr6:5500600-5510600	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr6:5500800-5511600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr6:5501000-5511800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr6:5501000-5550600	Weak transcription	Pancreas	Pancrea
31	chr6:5501200-5505800	Weak transcription	Primary T cells from cord blood	blood
32	chr6:5501200-5511800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr6:5501400-5502800	Enhancers	Fetal Heart	heart
34	chr6:5501400-5506600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr6:5501400-5506800	Weak transcription	Brain Cingulate Gyrus	brain
36	chr6:5501400-5513400	Weak transcription	Brain Anterior Caudate	brain
37	chr6:5501600-5506400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr6:5501600-5506800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr6:5501600-5506800	Weak transcription	Osteobl	bone
40	chr6:5501600-5509000	Weak transcription	Right Ventricle	heart
41	chr6:5502200-5503000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr6:5502200-5505800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr6:5502200-5506600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr6:5502400-5503200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr6:5502400-5506200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr6:5502400-5508600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr6:5502400-5511200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr6:5502400-5511200	Weak transcription	Gastric	stomach
49	chr6:5502600-5508600	Weak transcription	Left Ventricle	heart

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