Variant report

Variant	rs6674933
Chromosome Location	chr1:213048638-213048639
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	chr1:213045207..213049301-chr1:213053372..213057994,4	K562	blood:

Variant related genes	Relation type
ENSG00000162769	Chromatin interaction

Extended variants
information (count: 58 )
Associated
traits (count: 12 )

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10127459	1.00[ASN][1000 genomes]
rs10746436	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10779594	0.81[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];0.87[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10864003	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10864013	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10864017	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10864019	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11120033	1.00[ASN][1000 genomes]
rs11804466	1.00[CHB][hapmap]
rs11808834	1.00[CHB][hapmap]
rs11810592	1.00[CHB][hapmap]
rs12036735	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12408694	0.89[GIH][hapmap]
rs1284800	1.00[ASN][1000 genomes]
rs1284864	1.00[ASN][1000 genomes]
rs1390501	0.89[GIH][hapmap]
rs1615680	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs1692178	1.00[ASN][1000 genomes]
rs1692179	1.00[ASN][1000 genomes]
rs1692180	1.00[ASN][1000 genomes]
rs17020044	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17020046	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs1770777	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs1770778	1.00[ASN][1000 genomes]
rs1874419	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2047289	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2047292	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2047293	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2359321	1.00[CHB][hapmap]
rs2359324	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2456815	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs2644545	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs2792558	1.00[ASN][1000 genomes]
rs2792560	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs2792561	1.00[CHB][hapmap];0.81[GIH][hapmap];0.86[MEX][hapmap];1.00[ASN][1000 genomes]
rs35976699	1.00[ASN][1000 genomes]
rs41315581	1.00[ASN][1000 genomes]
rs4418676	0.90[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs4951468	0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4951649	0.81[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59252582	1.00[ASN][1000 genomes]
rs6540768	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6666362	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6667161	1.00[ASN][1000 genomes]
rs6688865	1.00[CEU][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6689134	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6703612	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7518378	1.00[CHB][hapmap]
rs7528119	0.81[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7533932	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7542906	1.00[ASN][1000 genomes]
rs963327	1.00[CEU][hapmap];0.82[YRI][hapmap];0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1011186	chr1:213005165-213069563	Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv1013705	chr1:213005344-213064209	Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv1008383	chr1:213025546-213114894	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
4	nsv998261	chr1:213029814-213064209	Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv998979	chr1:213029814-213073013	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS 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	16 gene(s)	inside rSNPs	diseases
6	nsv1007129	chr1:213037244-213083261	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:12)

SNP	Gene	Cis/trans	Tissue	Source
rs6674933	FLVCR1	cis	lymphoblastoid	seeQTL
rs6674933	LQK1	Cis_1M	lymphoblastoid	RTeQTL
rs6674933	FLVCR1-AS1	cis	Heart Left Ventricle	GTEx
rs6674933	FLVCR1	Cis_1M	lymphoblastoid	RTeQTL
rs6674933	FLVCR1-AS1	cis	Skin Sun Exposed Lower leg	GTEx
rs6674933	NSL1	cis	parietal	SCAN
rs6674933	FLVCR1-AS1	cis	Nerve Tibial	GTEx
rs6674933	FLVCR1-AS1	cis	Artery Tibial	GTEx
rs6674933	LOC642946	cis	multi-tissue	Pritchard
rs6674933	NCRNA00292	cis	lymphoblastoid	seeQTL
rs6674933	FLVCR1	cis	multi-tissue	Pritchard
rs6674933	FLVCR1-AS1	cis	Whole Blood	GTEx

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:213032600-213049200	Weak transcription	Right Atrium	heart
2	chr1:213032600-213073000	Weak transcription	Colonic Mucosa	Colon
3	chr1:213032600-213073000	Weak transcription	Esophagus	oesophagus
4	chr1:213032800-213056800	Weak transcription	Fetal Thymus	thymus
5	chr1:213032800-213057800	Weak transcription	Placenta	Placenta
6	chr1:213032800-213061800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr1:213032800-213062000	Weak transcription	Psoas Muscle	Psoas
8	chr1:213033600-213062000	Weak transcription	Thymus	Thymus
9	chr1:213034400-213058000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
10	chr1:213034400-213068000	Weak transcription	Colon Smooth Muscle	Colon
11	chr1:213034600-213049200	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr1:213034600-213049200	Weak transcription	Lung	lung
13	chr1:213034600-213049400	Weak transcription	Gastric	stomach
14	chr1:213034600-213056200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr1:213034600-213057000	Weak transcription	Brain Substantia Nigra	brain
16	chr1:213034600-213057000	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr1:213034600-213057200	Weak transcription	Right Ventricle	heart
18	chr1:213034600-213061800	Weak transcription	Fetal Heart	heart
19	chr1:213034600-213067800	Weak transcription	NHLF	lung
20	chr1:213034600-213070600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr1:213035800-213049400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr1:213035800-213073000	Weak transcription	Small Intestine	intestine
23	chr1:213036000-213070800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr1:213036200-213062000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
25	chr1:213036400-213062000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
26	chr1:213036600-213051400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
27	chr1:213036600-213053200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
28	chr1:213037600-213073200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr1:213037800-213052000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr1:213037800-213052400	Strong transcription	HUES48 Cell Line	embryonic stem cell
31	chr1:213037800-213052600	Strong transcription	HUES6 Cell Line	embryonic stem cell
32	chr1:213038200-213052400	Strong transcription	HUES64 Cell Line	embryonic stem cell
33	chr1:213038400-213072000	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr1:213039400-213054000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
35	chr1:213039600-213073000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr1:213040400-213073000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr1:213040800-213055200	Weak transcription	Primary T helper cells PMA-I stimulated	--
38	chr1:213041400-213055000	Strong transcription	Fetal Intestine Small	intestine
39	chr1:213041800-213050400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr1:213043200-213062000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr1:213043200-213073400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr1:213044000-213053800	Strong transcription	Fetal Intestine Large	intestine
43	chr1:213044200-213049800	Strong transcription	Aorta	Aorta
44	chr1:213044200-213050600	Strong transcription	H9 Cell Line	embryonic stem cell
45	chr1:213044400-213049600	Strong transcription	ES-I3 Cell Line	embryonic stem cell
46	chr1:213044400-213049600	Strong transcription	Hela-S3	cervix
47	chr1:213044400-213050000	Strong transcription	Primary hematopoietic stem cells	blood
48	chr1:213044400-213063200	Weak transcription	Placenta Amnion	Placenta Amnion
49	chr1:213044600-213050400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr1:213044600-213052600	Strong transcription	H1 Cell Line	embryonic stem cell

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