Variant report

Variant	rs14235
Chromosome Location	chr16:31121793-31121794
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5)
CpG islands
(count:0)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:5 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr16:31120913-31121958	K562	blood:	n/a	n/a
2	POLR2A	chr16:31121507-31122035	MCF-7	breast:	n/a	n/a
3	POLR2A	chr16:31119694-31122744	K562	blood:	n/a	n/a
4	POLR2A	chr16:31121788-31121813	K562	blood:	n/a	n/a
5	POLR2A	chr16:31121189-31129707	HepG2	liver:	n/a	n/a

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:31104992..31108435-chr16:31119873..31122866,3	K562	blood:
2	chr16:31117975..31125175-chr16:31188698..31192934,10	MCF-7	breast:
3	chr16:31043673..31046674-chr16:31119786..31122161,3	MCF-7	breast:
4	chr16:31043215..31044919-chr16:31118800..31122188,4	K562	blood:
5	chr16:31115598..31118169-chr16:31120150..31122491,2	K562	blood:
6	chr16:31043294..31046227-chr16:31119706..31121913,2	MCF-7	breast:
7	chr16:31120937..31123085-chr16:31137751..31141720,3	MCF-7	breast:
8	chr16:31118165..31121962-chr16:31151611..31155077,5	K562	blood:
9	chr16:31118494..31122515-chr16:31143591..31148259,6	MCF-7	breast:
10	chr16:31119811..31122617-chr16:31200745..31202517,2	K562	blood:
11	chr16:31083571..31086239-chr16:31118530..31123064,5	MCF-7	breast:
12	chr16:31099505..31101378-chr16:31121565..31123348,2	K562	blood:

No data

Variant related genes	Relation type
BCKDK	TF binding region
ENSG00000167394	Chromatin interaction
ENSG00000103496	Chromatin interaction
ENSG00000089280	Chromatin interaction
ENSG00000167395	Chromatin interaction
ENSG00000052344	Chromatin interaction
ENSG00000255439	Chromatin interaction
ENSG00000151006	Chromatin interaction
ENSG00000178226	Chromatin interaction
ENSG00000167397	Chromatin interaction
ENSG00000103507	Chromatin interaction
ENSG00000103510	Chromatin interaction

Extended variants
information (count: 137 )
Associated
traits (count: 12 )

rSNPs within LD-proxies of this variant (count:123)

rs_ID	r²[population]
rs1060506	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10782001	0.89[JPT][hapmap]
rs10782002	0.89[JPT][hapmap]
rs10871454	1.00[CEU][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.81[MKK][hapmap];0.85[TSI][hapmap];0.80[ASN][1000 genomes]
rs11076	0.88[JPT][hapmap]
rs1108431	0.84[ASN][1000 genomes]
rs11150600	0.89[JPT][hapmap]
rs11150601	0.89[JPT][hapmap]
rs11150604	1.00[CEU][hapmap];1.00[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.83[MKK][hapmap];0.85[TSI][hapmap];0.84[ASN][1000 genomes]
rs11640534	0.89[JPT][hapmap]
rs11640767	0.82[ASN][1000 genomes]
rs11640957	0.82[ASN][1000 genomes]
rs11640961	0.87[CEU][hapmap];0.81[GIH][hapmap];0.89[JPT][hapmap]
rs11642192	0.93[ASN][1000 genomes]
rs11647284	0.95[ASN][1000 genomes]
rs11647442	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11862744	1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs11864806	0.95[ASN][1000 genomes]
rs11864839	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs11865038	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs11865499	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12102776	0.82[CHB][hapmap];0.92[CHD][hapmap]
rs12445650	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs12448321	0.84[ASN][1000 genomes]
rs12597511	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];0.96[MEX][hapmap];1.00[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12716981	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12716982	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12924903	1.00[JPT][hapmap]
rs12928852	0.89[JPT][hapmap]
rs12931046	0.89[JPT][hapmap]
rs12934418	0.84[ASN][1000 genomes]
rs13708	0.89[JPT][hapmap]
rs1458202	0.89[JPT][hapmap]
rs1549293	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];0.91[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17839567	0.84[ASN][1000 genomes]
rs17839568	0.95[ASN][1000 genomes]
rs1870293	0.89[JPT][hapmap]
rs1978485	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1978487	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.91[TSI][hapmap];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2032915	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2054213	0.89[JPT][hapmap]
rs2288004	0.84[ASN][1000 genomes]
rs2303222	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.95[ASN][1000 genomes]
rs2303223	1.00[CEU][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs2305880	0.89[JPT][hapmap]
rs2305884	0.89[JPT][hapmap]
rs2359612	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.87[TSI][hapmap];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2855475	0.87[CEU][hapmap];1.00[CHB][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.98[TSI][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28725459	0.96[ASN][1000 genomes]
rs28814987	0.95[ASN][1000 genomes]
rs2884738	1.00[ASN][1000 genomes]
rs34649473	0.81[ASN][1000 genomes]
rs35351013	0.89[ASN][1000 genomes]
rs35468353	1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs35675346	1.00[JPT][hapmap]
rs35713203	0.95[ASN][1000 genomes]
rs3751855	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs4468641	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs4527034	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4889525	0.89[JPT][hapmap]
rs4889530	0.82[ASN][1000 genomes]
rs4889599	0.89[JPT][hapmap]
rs4889603	0.84[CEU][hapmap];0.81[GIH][hapmap];0.89[JPT][hapmap]
rs4889604	0.89[JPT][hapmap]
rs4889606	0.96[CEU][hapmap];0.81[GIH][hapmap];0.89[JPT][hapmap];0.91[MEX][hapmap];0.87[TSI][hapmap]
rs4889609	1.00[JPT][hapmap]
rs4889619	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4889620	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4889623	0.82[CHB][hapmap]
rs55766044	1.00[ASN][1000 genomes]
rs55979739	0.84[ASN][1000 genomes]
rs56284083	0.84[ASN][1000 genomes]
rs56314408	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56813533	0.89[ASN][1000 genomes]
rs57434408	0.86[ASN][1000 genomes]
rs58726213	0.82[ASN][1000 genomes]
rs59061704	0.82[ASN][1000 genomes]
rs59735493	1.00[ASN][1000 genomes]
rs60996860	0.96[ASN][1000 genomes]
rs61162043	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs61320757	1.00[ASN][1000 genomes]
rs6565217	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs6950	0.89[JPT][hapmap]
rs7187995	0.89[ASN][1000 genomes]
rs7190802	0.82[CHB][hapmap]
rs7196161	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7196726	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs7197717	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs7199949	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs7200879	1.00[JPT][hapmap]
rs7203999	0.82[CHD][hapmap];0.89[JPT][hapmap]
rs7204459	0.89[JPT][hapmap]
rs7206511	0.89[JPT][hapmap]
rs7294	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs729482	1.00[JPT][hapmap]
rs732172	1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs732173	0.84[ASN][1000 genomes]
rs73530203	0.93[ASN][1000 genomes]
rs749670	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs749671	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.86[TSI][hapmap];0.80[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs749767	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.91[TSI][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7500176	0.84[ASN][1000 genomes]
rs750952	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs8047803	0.95[ASN][1000 genomes]
rs8050588	0.89[JPT][hapmap]
rs8050894	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs8056842	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs8060857	0.89[JPT][hapmap]
rs8061047	0.89[ASN][1000 genomes]
rs8062719	0.89[JPT][hapmap]
rs881929	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.87[TSI][hapmap];0.95[ASN][1000 genomes]
rs889548	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs889555	1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs897986	0.89[JPT][hapmap]
rs9923231	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.91[MKK][hapmap];0.87[TSI][hapmap];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9925964	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9926533	0.96[CEU][hapmap];0.82[CHD][hapmap];0.81[GIH][hapmap];0.89[JPT][hapmap];0.91[MEX][hapmap];0.82[TSI][hapmap]
rs9929899	0.82[ASN][1000 genomes]
rs9934438	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.91[MKK][hapmap];0.87[TSI][hapmap];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9936329	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];0.89[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9939417	1.00[CEU][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.83[MKK][hapmap];0.87[TSI][hapmap];0.84[ASN][1000 genomes]
rs9939558	0.84[ASN][1000 genomes]
rs9972727	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1062456	chr16:30442166-31253997	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	437 gene(s)	inside rSNPs	diseases
2	nsv542898	chr16:30442166-31253997	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	437 gene(s)	inside rSNPs	diseases
3	nsv905729	chr16:30642867-31247924	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	387 gene(s)	inside rSNPs	diseases
4	nsv431451	chr16:30682399-31340999	Transcr. at gene 5' and 3' Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	350 gene(s)	inside rSNPs	diseases
5	nsv905734	chr16:30877544-31191482	Active TSS Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases
6	nsv905735	chr16:30890538-31247924	Strong transcription Genic enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	264 gene(s)	inside rSNPs	diseases
7	nsv457483	chr16:30903679-31191482	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	253 gene(s)	inside rSNPs	diseases
8	nsv571820	chr16:30903679-31191482	Enhancers Genic enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	253 gene(s)	inside rSNPs	diseases
9	esv1797877	chr16:30948643-31188432	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
10	nsv833193	chr16:30960796-31133604	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
11	nsv905740	chr16:31066249-31232437	Flanking Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	202 gene(s)	inside rSNPs	diseases
12	nsv905741	chr16:31066249-31247924	Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	202 gene(s)	inside rSNPs	diseases
13	nsv905742	chr16:31102321-31247924	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	188 gene(s)	inside rSNPs	diseases
14	nsv905743	chr16:31111064-31129942	Genic enhancers Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases

Variant related diseases (count:1)

Disease	PMID	Source
Parkinson's disease	25064009	GWAS catalog

mRNA abundance (count:11)

SNP	Gene	Cis/trans	Tissue	Source
rs14235	NCRNA00095	cis	cerebellum	SCAN
rs14235	KAT8	cis	Artery Tibial	GTEx
rs14235	STX1B	cis	cerebellum	SCAN
rs14235	ZNF668	cis	cerebellum	SCAN
rs14235	MYST1	cis	parietal	SCAN
rs14235	YPEL3	cis	cerebellum	SCAN
rs14235	RP11-196G11.2	cis	Muscle Skeletal	GTEx
rs14235	KAT8	cis	Nerve Tibial	GTEx
rs14235	HSD3B7	cis	Whole Blood	GTEx
rs14235	KAT8	cis	Skin Sun Exposed Lower leg	GTEx
rs14235	MYST1	cis	cerebellum	SCAN

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31120000-31128400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr16:31120400-31121800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr16:31120400-31121800	Transcr. at gene 5' and 3'	Skeletal Muscle Male	skeletal muscle
4	chr16:31120400-31122000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr16:31120400-31122400	Weak transcription	Aorta	Aorta
6	chr16:31120400-31124200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr16:31120400-31128400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr16:31120600-31121800	Transcr. at gene 5' and 3'	Muscle Satellite Cultured Cells	--
9	chr16:31120600-31122000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr16:31120600-31122000	Genic enhancers	Fetal Muscle Trunk	muscle
11	chr16:31120600-31122000	Flanking Active TSS	HSMMtube	muscle
12	chr16:31120600-31122200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr16:31120600-31122200	Transcr. at gene 5' and 3'	HSMM	muscle
14	chr16:31120600-31127800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr16:31120600-31128200	Weak transcription	Fetal Kidney	kidney
16	chr16:31120600-31128400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr16:31120800-31121800	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr16:31120800-31121800	Genic enhancers	Gastric	stomach
19	chr16:31120800-31122000	Genic enhancers	Fetal Muscle Leg	muscle
20	chr16:31120800-31122400	Weak transcription	Primary B cells from cord blood	blood
21	chr16:31120800-31122800	Strong transcription	Primary neutrophils fromperipheralblood	blood
22	chr16:31120800-31123400	Strong transcription	K562	blood
23	chr16:31120800-31123600	Weak transcription	Psoas Muscle	Psoas
24	chr16:31120800-31123800	Strong transcription	Fetal Lung	lung
25	chr16:31120800-31124000	Strong transcription	Placenta Amnion	Placenta Amnion
26	chr16:31120800-31124200	Genic enhancers	Esophagus	oesophagus
27	chr16:31120800-31124400	Strong transcription	Fetal Intestine Large	intestine
28	chr16:31120800-31124400	Weak transcription	Right Atrium	heart
29	chr16:31120800-31124600	Strong transcription	H9 Cell Line	embryonic stem cell
30	chr16:31120800-31124600	Strong transcription	HUES6 Cell Line	embryonic stem cell
31	chr16:31120800-31124800	Strong transcription	NHEK	skin
32	chr16:31120800-31125200	Strong transcription	Thymus	Thymus
33	chr16:31120800-31128200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr16:31120800-31128200	Weak transcription	Fetal Heart	heart
35	chr16:31120800-31128200	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr16:31120800-31129000	Weak transcription	Small Intestine	intestine
37	chr16:31121000-31121800	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr16:31121000-31121800	Weak transcription	Primary T helper cells fromperipheralblood	blood
39	chr16:31121000-31121800	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr16:31121000-31121800	Genic enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr16:31121000-31122600	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr16:31121000-31123400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr16:31121000-31123800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr16:31121000-31123800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr16:31121000-31123800	Strong transcription	A549	lung
46	chr16:31121000-31124000	Strong transcription	Primary T helper cells PMA-I stimulated	--
47	chr16:31121000-31124000	Strong transcription	Brain Angular Gyrus	brain
48	chr16:31121000-31124000	Strong transcription	Brain Substantia Nigra	brain
49	chr16:31121000-31124000	Strong transcription	Colonic Mucosa	Colon
50	chr16:31121000-31124000	Strong transcription	Fetal Thymus	thymus

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