Variant report

Variant	rs16961153
Chromosome Location	chr17:18227101-18227102
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:21)
CpG islands
(count:0)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:21 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr17:18227090-18227643	GM12878	blood:	n/a	n/a
2	POLR2A	chr17:18226492-18227689	HepG2	liver:	n/a	n/a
3	POLR2A	chr17:18227087-18227376	A549	lung:	n/a	n/a
4	POLR2A	chr17:18227100-18227341	GM12878	blood:	n/a	n/a
5	POLR2A	chr17:18226950-18227467	GM12892	blood:	n/a	n/a
6	POLR2A	chr17:18226473-18227705	HepG2	liver:	n/a	n/a
7	CTCF	chr17:18227000-18227150	GM12871	blood:	n/a	n/a
8	POLR2A	chr17:18226948-18227529	GM12878	blood:	n/a	n/a
9	POLR2A	chr17:18227045-18227468	HepG2	liver:	n/a	n/a
10	POLR2A	chr17:18226937-18227135	GM12878	blood:	n/a	n/a
11	POLR2A	chr17:18225710-18229090	A549	lung:	n/a	n/a
12	POLR2A	chr17:18227068-18227516	A549	lung:	n/a	n/a
13	POLR2A	chr17:18226793-18228183	PFSK-1	brain:	n/a	n/a
14	POLR2A	chr17:18226942-18227649	PFSK-1	brain:	n/a	n/a
15	POLR2A	chr17:18225638-18227595	Hela-S3	cervix:	n/a	n/a
16	POLR2A	chr17:18226464-18228976	K562	blood:	n/a	n/a
17	POLR2A	chr17:18227084-18227327	H1-hESC	embryonic stem cell:	n/a	n/a
18	POLR2A	chr17:18227093-18227361	MCF-7	breast:	n/a	n/a
19	POLR2A	chr17:18226530-18229024	H1-hESC	embryonic stem cell:	n/a	n/a
20	MXI1	chr17:18226115-18227123	IMR90	lung:	n/a	n/a
21	POLR2A	chr17:18226872-18227122	H1-hESC	embryonic stem cell:	n/a	n/a

No data

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:18217609..18225680-chr17:18226125..18232187,14	K562	blood:
2	chr17:18042115..18044970-chr17:18226720..18228381,2	MCF-7	breast:
3	chr17:18158849..18161472-chr17:18226331..18228845,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000267350	TF binding region
ENSG00000091536	Chromatin interaction
ENSG00000176994	Chromatin interaction
ENSG00000177731	Chromatin interaction
ENSG00000177302	Chromatin interaction

Extended variants
information (count: 97 )
Associated
traits (count: 10 )

rSNPs within LD-proxies of this variant (count:84)

rs_ID	r²[population]
rs11078411	0.94[GIH][hapmap]
rs11078412	0.94[GIH][hapmap]
rs11078415	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[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];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11867895	0.87[AMR][1000 genomes];0.88[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];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11869515	0.93[AFR][1000 genomes];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11869582	0.94[CEU][hapmap]
rs11869952	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11871761	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11872031	0.87[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];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12450760	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12451555	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12451698	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12451807	0.93[AFR][1000 genomes];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12600694	0.91[GIH][hapmap]
rs12939851	0.80[AMR][1000 genomes];0.85[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];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16961133	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[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];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1962949	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1962950	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[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];0.84[AMR][1000 genomes];0.91[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];0.95[AMR][1000 genomes];0.96[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];0.85[AMR][1000 genomes];0.86[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];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2290504	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2290505	0.94[JPT][hapmap];0.82[TSI][hapmap];1.00[YRI][hapmap];0.85[AMR][1000 genomes];0.88[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];0.90[AMR][1000 genomes];0.99[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];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3088233	0.94[GIH][hapmap]
rs35738574	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[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];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3829956	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]
rs3862147	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs3889544	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4386179	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4450455	1.00[CEU][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4500798	0.83[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4556848	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4925151	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4925177	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4925178	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs57490980	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs57697650	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59366579	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62072507	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62072509	0.97[AFR][1000 genomes];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62072511	0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62072515	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62072537	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62072540	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62072541	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62072544	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62072545	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62072546	0.80[EUR][1000 genomes]
rs6502640	0.94[GIH][hapmap]
rs6502641	0.85[EUR][1000 genomes]
rs7211573	0.81[AMR][1000 genomes];0.87[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];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7405677	0.85[AMR][1000 genomes];0.87[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];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs8065026	0.93[GIH][hapmap]
rs8077577	0.94[GIH][hapmap]
rs8081042	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8081155	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8081343	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[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	0.80[AMR][1000 genomes];0.87[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];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9910090	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.87[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];0.82[AMR][1000 genomes];0.89[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
rs16961153	LOC162632	cis	cerebellum	SCAN
rs16961153	FLII	cis	cerebellum	SCAN
rs16961153	PLD6	cis	cerebellum	SCAN
rs16961153	FLJ36492	cis	multi-tissue	Pritchard
rs16961153	LOC162632	cis	parietal	SCAN
rs16961153	SHMT1	cis	lymphoblastoid	seeQTL
rs16961153	TRPV2	cis	cerebellum	SCAN
rs16961153	SHMT1	cis	cerebellum	SCAN
rs16961153	PIGL	cis	parietal	SCAN
rs16961153	FLII	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:18219400-18227200	Genic enhancers	Primary T cells fromperipheralblood	blood
2	chr17:18219400-18266000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr17:18220200-18228000	Weak transcription	Fetal Kidney	kidney
4	chr17:18220400-18228000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr17:18222400-18227200	Weak transcription	HUVEC	blood vessel
6	chr17:18222400-18266200	Weak transcription	Small Intestine	intestine
7	chr17:18222600-18227200	Weak transcription	Psoas Muscle	Psoas
8	chr17:18222600-18240800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
9	chr17:18222600-18243200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr17:18222800-18236800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr17:18223000-18228200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr17:18223400-18228400	Strong transcription	Primary B cells from cord blood	blood
13	chr17:18223400-18235400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr17:18223600-18240800	Strong transcription	Fetal Muscle Leg	muscle
15	chr17:18223600-18265400	Strong transcription	Fetal Stomach	stomach
16	chr17:18223800-18227400	Weak transcription	NH-A	brain
17	chr17:18223800-18229200	Strong transcription	NHEK	skin
18	chr17:18223800-18236800	Strong transcription	Primary T cells from cord blood	blood
19	chr17:18223800-18236800	Strong transcription	Lung	lung
20	chr17:18223800-18240800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr17:18223800-18253600	Strong transcription	Thymus	Thymus
22	chr17:18224000-18231000	Strong transcription	Primary T helper naive cells from peripheral blood	blood
23	chr17:18224000-18236600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr17:18224000-18236600	Strong transcription	Fetal Intestine Large	intestine
25	chr17:18224000-18236800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr17:18224000-18240800	Strong transcription	Dnd41	blood
27	chr17:18224200-18227400	Weak transcription	Fetal Brain Male	brain
28	chr17:18224200-18227600	Strong transcription	Primary monocytes fromperipheralblood	blood
29	chr17:18224200-18228000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr17:18224200-18228200	Strong transcription	Fetal Intestine Small	intestine
31	chr17:18224200-18229400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr17:18224200-18230200	Strong transcription	Brain Anterior Caudate	brain
33	chr17:18224200-18234600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr17:18224200-18235600	Strong transcription	Esophagus	oesophagus
35	chr17:18224200-18236200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr17:18224200-18236400	Strong transcription	Rectal Mucosa Donor 31	rectum
37	chr17:18224200-18236600	Strong transcription	Rectal Smooth Muscle	rectum
38	chr17:18224200-18236600	Strong transcription	Sigmoid Colon	Sigmoid Colon
39	chr17:18224200-18240800	Strong transcription	Fetal Muscle Trunk	muscle
40	chr17:18224200-18253000	Weak transcription	Fetal Heart	heart
41	chr17:18224400-18227800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr17:18224400-18249400	Weak transcription	K562	blood
43	chr17:18224600-18227200	Weak transcription	Right Atrium	heart
44	chr17:18224600-18228000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
45	chr17:18224600-18236400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr17:18224800-18228400	Strong transcription	Primary B cells from peripheral blood	blood
47	chr17:18224800-18229000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr17:18224800-18229600	Strong transcription	Primary T helper cells fromperipheralblood	blood
49	chr17:18224800-18236600	Strong transcription	Primary neutrophils fromperipheralblood	blood
50	chr17:18224800-18236800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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