Variant report

Variant	rs7214335
Chromosome Location	chr17:57158840-57158841
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:57095356..57201201-chr17:57905452..57953516,1644	MCF-7	breast:
2	chr17:57113105..57201250-chr17:57905452..57952793,1492	MCF-7	breast:
3	chr17:57157616..57160054-chr17:57231097..57232959,2	MCF-7	breast:
4	chr17:56707649..56710360-chr17:57157403..57160114,2	MCF-7	breast:
5	chr17:57153600..57155674-chr17:57158694..57160249,2	K562	blood:
6	chr17:56734970..56736527-chr17:57158639..57161306,2	MCF-7	breast:
7	chr17:56735002..56737726-chr17:57157606..57159322,2	K562	blood:
8	chr17:57158398..57161721-chr17:57968843..57973327,4	MCF-7	breast:
9	chr17:57157697..57159270-chr17:57970364..57972127,2	MCF-7	breast:
10	chr17:56735612..56737890-chr17:57158805..57161929,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000199004	Chromatin interaction
ENSG00000108443	Chromatin interaction
ENSG00000212195	Chromatin interaction
ENSG00000182628	Chromatin interaction
ENSG00000202077	Chromatin interaction
ENSG00000201524	Chromatin interaction
ENSG00000062716	Chromatin interaction
ENSG00000108423	Chromatin interaction
ENSG00000068489	Chromatin interaction

Extended variants
information (count: 67 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs11079368	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11654986	0.87[CEU][hapmap];0.86[YRI][hapmap]
rs11656413	0.91[CEU][hapmap];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11868348	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12603238	0.86[CEU][hapmap];0.86[YRI][hapmap];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12936058	0.87[CEU][hapmap]
rs12947785	0.86[CEU][hapmap]
rs12948039	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12948746	0.87[CEU][hapmap];0.88[ASN][1000 genomes]
rs1588322	0.91[CEU][hapmap]
rs1967415	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2055779	0.91[CEU][hapmap]
rs2158966	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2333410	0.91[CEU][hapmap];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34523895	0.81[EUR][1000 genomes]
rs3826353	0.91[CEU][hapmap];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4372750	0.91[CEU][hapmap]
rs4398153	0.91[CEU][hapmap]
rs4598970	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4636974	0.92[CEU][hapmap]
rs4932693	0.91[CEU][hapmap];0.86[YRI][hapmap];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs56297715	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs57869245	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs58092632	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6416932	0.91[CEU][hapmap];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6416933	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6503887	0.92[CEU][hapmap]
rs6503890	0.87[CEU][hapmap];0.81[ASN][1000 genomes]
rs6503893	0.91[CEU][hapmap];0.86[YRI][hapmap];0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6503894	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7207693	0.91[CEU][hapmap]
rs7208505	0.87[CEU][hapmap];0.86[YRI][hapmap]
rs7214098	0.87[CEU][hapmap];0.86[YRI][hapmap]
rs7214892	0.82[ASN][1000 genomes]
rs7218105	0.91[CEU][hapmap]
rs72628394	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7503190	0.91[CEU][hapmap];0.86[YRI][hapmap];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8067264	0.91[CEU][hapmap];0.81[YRI][hapmap];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8069033	0.91[CEU][hapmap];0.81[YRI][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8071280	0.91[CEU][hapmap]
rs8072712	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8076121	0.92[CEU][hapmap]
rs8081297	0.88[ASN][1000 genomes]
rs8081967	0.87[CEU][hapmap];0.86[YRI][hapmap];0.88[ASN][1000 genomes]
rs8082544	0.91[CEU][hapmap];0.86[YRI][hapmap];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8182277	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9892062	0.91[CEU][hapmap]
rs9893351	0.82[EUR][1000 genomes]
rs9894274	0.91[CEU][hapmap]
rs9898916	0.81[CEU][hapmap]
rs9901181	0.92[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv908643	chr17:56803028-57249010	Bivalent/Poised TSS Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	227 gene(s)	inside rSNPs	diseases
2	nsv908644	chr17:56803028-57371432	Strong transcription Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	238 gene(s)	inside rSNPs	diseases
3	esv3335958	chr17:56849544-57385398	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	233 gene(s)	inside rSNPs	diseases
4	nsv908645	chr17:56857281-57208752	Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	150 gene(s)	inside rSNPs	diseases
5	nsv1065063	chr17:56954121-57346694	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	227 gene(s)	inside rSNPs	diseases
6	nsv1064384	chr17:57049519-57346694	Active TSS ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	219 gene(s)	inside rSNPs	diseases
7	nsv908646	chr17:57061238-57255810	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	206 gene(s)	inside rSNPs	diseases
8	nsv833499	chr17:57070693-57288410	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	208 gene(s)	inside rSNPs	diseases
9	nsv1066388	chr17:57082013-57339981	Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	209 gene(s)	inside rSNPs	diseases
10	esv2758462	chr17:57082579-57425634	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	213 gene(s)	inside rSNPs	diseases
11	esv2758699	chr17:57082579-57425634	Weak transcription Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	213 gene(s)	inside rSNPs	diseases
12	nsv1066467	chr17:57117682-57338731	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	200 gene(s)	inside rSNPs	diseases
13	nsv1057209	chr17:57117682-57742240	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	240 gene(s)	inside rSNPs	diseases
14	nsv543396	chr17:57117682-57742240	Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	240 gene(s)	inside rSNPs	diseases
15	nsv1066788	chr17:57126446-57344129	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS 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	193 gene(s)	inside rSNPs	diseases
16	nsv482858	chr17:57136446-57288615	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	184 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs7214335	RAD51C	Cis_1M	lymphoblastoid	RTeQTL
rs7214335	TRIM37	cis	Adipose Subcutaneous	GTEx
rs7214335	TRIM37	cis	Muscle Skeletal	GTEx
rs7214335	FAM33A	Cis_1M	lymphoblastoid	RTeQTL
rs7214335	TRIM37	cis	Whole Blood	GTEx

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:57079800-57167000	Weak transcription	Small Intestine	intestine
2	chr17:57104200-57159600	Weak transcription	Psoas Muscle	Psoas
3	chr17:57106200-57170400	Weak transcription	NHLF	lung
4	chr17:57115000-57159000	Strong transcription	HUES48 Cell Line	embryonic stem cell
5	chr17:57121400-57183400	Weak transcription	Gastric	stomach
6	chr17:57121600-57166200	Weak transcription	Esophagus	oesophagus
7	chr17:57121800-57166400	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr17:57121800-57181800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr17:57124800-57167600	Strong transcription	Dnd41	blood
10	chr17:57127000-57166400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr17:57127000-57181800	Weak transcription	Brain Cingulate Gyrus	brain
12	chr17:57127200-57167000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr17:57130600-57159200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr17:57135400-57183400	Weak transcription	Pancreas	Pancrea
15	chr17:57137000-57167000	Weak transcription	Spleen	Spleen
16	chr17:57137400-57166400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr17:57137600-57166400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr17:57137600-57175800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr17:57137600-57183000	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr17:57137800-57166400	Weak transcription	Right Ventricle	heart
21	chr17:57140200-57172000	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr17:57140400-57165600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr17:57141600-57165000	Weak transcription	Colon Smooth Muscle	Colon
24	chr17:57143200-57167400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
25	chr17:57144400-57163600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr17:57145000-57159200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr17:57145200-57159200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr17:57147400-57165800	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr17:57147600-57162000	Weak transcription	Fetal Brain Female	brain
30	chr17:57147800-57165000	Weak transcription	HSMMtube	muscle
31	chr17:57148000-57164400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
32	chr17:57148000-57165200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr17:57148200-57166400	Weak transcription	Ovary	ovary
34	chr17:57148200-57170800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr17:57148400-57164800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
36	chr17:57148400-57165600	Weak transcription	Left Ventricle	heart
37	chr17:57149800-57164400	Weak transcription	Fetal Muscle Leg	muscle
38	chr17:57150400-57160200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr17:57150600-57163200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr17:57151000-57163200	Strong transcription	Primary T helper cells fromperipheralblood	blood
41	chr17:57151000-57172200	Weak transcription	Lung	lung
42	chr17:57151200-57182600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr17:57152200-57168200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
44	chr17:57152600-57165000	Weak transcription	NHEK	skin
45	chr17:57154000-57165800	Weak transcription	Thymus	Thymus
46	chr17:57154000-57170600	Weak transcription	Aorta	Aorta
47	chr17:57154400-57166000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr17:57155400-57165800	Weak transcription	Fetal Intestine Small	intestine
49	chr17:57155600-57159200	Strong transcription	HepG2	liver
50	chr17:57155600-57163600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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