Variant report

Variant	rs3829956
Chromosome Location	chr17:18219835-18219836
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2)
CpG islands
(count:0)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	WRNIP1	chr17:18219620-18219868	GM12878	blood:	n/a	n/a
2	POLR2A	chr17:18219478-18219908	MCF10A-Er-Src	breast:	n/a	n/a

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:18138823..18141039-chr17:18218928..18220976,2	MCF-7	breast:
2	chr17:18209725..18212720-chr17:18219456..18221596,2	MCF-7	breast:
3	chr17:18086084..18087983-chr17:18217517..18220819,3	MCF-7	breast:
4	chr17:18150730..18153746-chr17:18217976..18219850,3	MCF-7	breast:
5	chr17:18217609..18225680-chr17:18226125..18232187,14	K562	blood:
6	chr17:18159194..18166260-chr17:18215929..18222740,16	MCF-7	breast:
7	chr17:18218839..18221214-chr17:18276166..18278374,2	MCF-7	breast:
8	chr17:18217812..18219938-chr17:18264805..18267202,2	MCF-7	breast:
9	chr17:18160366..18162830-chr17:18217207..18220188,2	K562	blood:
10	chr17:18156705..18166530-chr17:18215131..18220177,19	MCF-7	breast:
11	chr17:18127269..18131326-chr17:18216439..18220320,6	MCF-7	breast:

No data

Variant related genes	Relation type
TOP3A	TF binding region
ENSG00000266677	Chromatin interaction
ENSG00000176974	Chromatin interaction
ENSG00000177731	Chromatin interaction
ENSG00000091542	Chromatin interaction
ENSG00000177302	Chromatin interaction
ENSG00000267350	Chromatin interaction
ENSG00000177427	Chromatin interaction
ENSG00000131899	Chromatin interaction

Extended variants
information (count: 96 )
Associated
traits (count: 10 )

rSNPs within LD-proxies of this variant (count:83)

rs_ID	r²[population]
rs11078411	0.94[GIH][hapmap]
rs11078412	0.94[GIH][hapmap]
rs11078415	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11655588	0.94[GIH][hapmap]
rs11658477	0.93[GIH][hapmap];0.82[TSI][hapmap]
rs11867855	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11867895	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11868708	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11869515	0.93[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11869582	0.94[CEU][hapmap]
rs11869952	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11871761	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11872031	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12449313	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12450760	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12451555	0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12451698	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12451807	0.93[AFR][1000 genomes];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12600694	0.91[GIH][hapmap]
rs12939851	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13284	0.94[GIH][hapmap]
rs1563371	0.94[GIH][hapmap]
rs16960980	0.94[GIH][hapmap]
rs16960983	0.94[GIH][hapmap]
rs16960986	0.94[GIH][hapmap]
rs16960990	0.94[GIH][hapmap]
rs16961114	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16961133	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16961153	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1925	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1962949	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1962950	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2015336	0.94[GIH][hapmap]
rs2071242	0.92[ASW][hapmap];1.00[CEU][hapmap];0.87[CHB][hapmap];0.97[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2273029	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2290502	0.94[CEU][hapmap];0.89[CHD][hapmap];0.97[GIH][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];0.91[TSI][hapmap];0.93[YRI][hapmap];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2290503	0.94[CEU][hapmap];0.94[CHD][hapmap];0.97[GIH][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];0.91[TSI][hapmap];1.00[YRI][hapmap];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2290504	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2290505	0.94[JPT][hapmap];0.82[TSI][hapmap];1.00[YRI][hapmap];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2294913	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28364628	1.00[ASW][hapmap];0.94[CEU][hapmap];0.88[CHB][hapmap];0.94[CHD][hapmap];0.97[GIH][hapmap];0.94[JPT][hapmap];0.96[LWK][hapmap];0.94[MEX][hapmap];0.98[MKK][hapmap];0.94[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3088233	0.94[GIH][hapmap]
rs35738574	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3817992	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.88[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3862147	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs3889544	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4386179	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4450455	1.00[CEU][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4500798	0.83[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4556848	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4925151	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4925177	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4925178	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs57490980	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs57697650	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59366579	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62072507	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62072509	0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62072511	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62072515	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62072537	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62072540	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62072541	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62072544	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62072545	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6502640	0.94[GIH][hapmap]
rs6502641	0.86[EUR][1000 genomes]
rs7211573	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7215678	1.00[CEU][hapmap];0.94[CHD][hapmap];0.97[GIH][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];0.94[TSI][hapmap];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7405677	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7498	0.89[CEU][hapmap];0.91[CHD][hapmap];0.97[GIH][hapmap];0.94[JPT][hapmap];0.89[MEX][hapmap];0.91[TSI][hapmap];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs8065026	0.93[GIH][hapmap]
rs8077577	0.94[GIH][hapmap]
rs8081042	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8081155	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8081343	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8082494	0.83[CHB][hapmap]
rs9901160	1.00[CHB][hapmap];0.82[CHD][hapmap];0.81[JPT][hapmap]
rs9901707	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9909104	0.89[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.86[TSI][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9910090	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9913139	0.94[CEU][hapmap];0.87[CHB][hapmap];0.97[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9913266	0.82[JPT][hapmap]

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	nsv916653	chr17:17651916-18454952	Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
2	nsv533142	chr17:17691726-18236686	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	116 gene(s)	inside rSNPs	diseases
3	nsv1061162	chr17:17978838-18259234	Flanking Active TSS Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
4	nsv492305	chr17:17980441-18424702	Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers 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	68 gene(s)	inside rSNPs	diseases
5	nsv833386	chr17:18170261-18332726	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer 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	30 gene(s)	inside rSNPs	diseases
6	nsv1057081	chr17:18171516-18256347	Active TSS Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers 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 miRNA target site	15 gene(s)	inside rSNPs	diseases
7	nsv543247	chr17:18171516-18256347	Weak transcription Active TSS Genic enhancers Strong transcription Enhancers Flanking Active TSS 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 miRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
8	nsv1062368	chr17:18180747-18259234	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
9	nsv833387	chr17:18200081-18378155	Active TSS Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
10	esv1806346	chr17:18200081-18446384	Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
11	esv1812661	chr17:18200081-18446384	Genic enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
12	nsv428333	chr17:18200081-18446384	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS 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	39 gene(s)	inside rSNPs	diseases
13	nsv427992	chr17:18200081-19192047	Strong transcription Genic enhancers Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	100 gene(s)	inside rSNPs	diseases

mRNA abundance (count:10)

SNP	Gene	Cis/trans	Tissue	Source
rs3829956	FLII	cis	cerebellum	SCAN
rs3829956	LOC162632	cis	cerebellum	SCAN
rs3829956	LOC162632	cis	parietal	SCAN
rs3829956	FLJ36492	cis	multi-tissue	Pritchard
rs3829956	SHMT1	cis	lymphoblastoid	seeQTL
rs3829956	PIGL	cis	parietal	SCAN
rs3829956	SHMT1	cis	cerebellum	SCAN
rs3829956	PLD6	cis	cerebellum	SCAN
rs3829956	TRPV2	cis	cerebellum	SCAN
rs3829956	FLII	cis	parietal	SCAN

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:18217400-18220400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr17:18218600-18221200	ZNF genes & repeats	Fetal Intestine Large	intestine
3	chr17:18218600-18221600	Transcr. at gene 5' and 3'	Dnd41	blood
4	chr17:18218800-18222200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
5	chr17:18219000-18220000	Flanking Active TSS	Duodenum Mucosa	Duodenum
6	chr17:18219000-18220000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
7	chr17:18219000-18220200	Flanking Active TSS	Primary T cells from cord blood	blood
8	chr17:18219000-18220400	Flanking Active TSS	Hela-S3	cervix
9	chr17:18219000-18221800	ZNF genes & repeats	Fetal Intestine Small	intestine
10	chr17:18219200-18220000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
11	chr17:18219200-18220000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
12	chr17:18219200-18220000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
13	chr17:18219400-18220000	Transcr. at gene 5' and 3'	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr17:18219400-18220000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
15	chr17:18219400-18220000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr17:18219400-18220000	Enhancers	Sigmoid Colon	Sigmoid Colon
17	chr17:18219400-18220000	Transcr. at gene 5' and 3'	NHDF-Ad	bronchial
18	chr17:18219400-18220200	Flanking Active TSS	K562	blood
19	chr17:18219400-18220800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
20	chr17:18219400-18220800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
21	chr17:18219400-18221800	Enhancers	Small Intestine	intestine
22	chr17:18219400-18224200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr17:18219400-18224200	Enhancers	Fetal Brain Male	brain
24	chr17:18219400-18224400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr17:18219400-18224800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr17:18219400-18227200	Genic enhancers	Primary T cells fromperipheralblood	blood
27	chr17:18219400-18266000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
28	chr17:18219600-18220000	Enhancers	H1 Cell Line	embryonic stem cell
29	chr17:18219600-18220000	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
30	chr17:18219600-18220000	Transcr. at gene 5' and 3'	Colon Smooth Muscle	Colon
31	chr17:18219600-18220000	Transcr. at gene 5' and 3'	Duodenum Smooth Muscle	Duodenum
32	chr17:18219600-18220000	Transcr. at gene 5' and 3'	A549	lung
33	chr17:18219600-18220200	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr17:18219600-18220200	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr17:18219600-18220200	Genic enhancers	Fetal Kidney	kidney
36	chr17:18219600-18220200	Enhancers	Gastric	stomach
37	chr17:18219600-18220400	Weak transcription	Ovary	ovary
38	chr17:18219600-18220600	Genic enhancers	Brain Cingulate Gyrus	brain
39	chr17:18219600-18220600	Enhancers	Right Ventricle	heart
40	chr17:18219600-18220800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr17:18219600-18220800	Enhancers	Primary T helper cells fromperipheralblood	blood
42	chr17:18219600-18220800	Genic enhancers	Adipose Nuclei	Adipose
43	chr17:18219600-18220800	Weak transcription	Aorta	Aorta
44	chr17:18219600-18220800	Enhancers	Pancreas	Pancrea
45	chr17:18219600-18221000	Genic enhancers	Brain Inferior Temporal Lobe	brain
46	chr17:18219600-18221600	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr17:18219600-18221800	Genic enhancers	Thymus	Thymus
48	chr17:18219600-18222200	Enhancers	Placenta Amnion	Placenta Amnion
49	chr17:18219600-18222400	Genic enhancers	Fetal Thymus	thymus
50	chr17:18219600-18222400	Genic enhancers	HMEC	breast

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