Variant report

Variant	rs749671
Chromosome Location	chr16:31088347-31088348
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:9)
CpG islands
(count:0)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:9 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	USF2	chr16:31088311-31088480	Hela-S3	cervix:	n/a	n/a
2	POLR2A	chr16:31088261-31090192	PBDE	blood:	n/a	n/a
3	POLR2A	chr16:31088254-31090781	K562	blood:	n/a	n/a
4	POLR2A	chr16:31088168-31088692	U87	brain:	n/a	n/a
5	POLR2A	chr16:31088303-31088906	HepG2	liver:	n/a	n/a
6	POLR2A	chr16:31088203-31088396	HepG2	liver:	n/a	n/a
7	POLR2A	chr16:31088162-31088698	U87	brain:	n/a	n/a
8	POLR2A	chr16:31087448-31088769	Hela-S3	cervix:	n/a	n/a
9	POLR2A	chr16:31087379-31088367	K562	blood:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr16:31087818..31090792-chr16:31123412..31125216,2	MCF-7	breast:
2	chr16:31082772..31088721-chr16:31466605..31471958,8	MCF-7	breast:
3	chr16:30967179..30972282-chr16:31082507..31088894,13	MCF-7	breast:
4	chr16:31082869..31088846-chr16:31189629..31192848,9	MCF-7	breast:
5	chr16:31087688..31090399-chr16:31119019..31121318,2	MCF-7	breast:
6	chr16:31083873..31090665-chr16:31187351..31192875,15	MCF-7	breast:
7	chr16:30991043..31010547-chr16:31082350..31088728,42	MCF-7	breast:
8	chr16:31086708..31088428-chr16:31122064..31123983,2	MCF-7	breast:
9	chr16:30967393..30971949-chr16:31083830..31088417,7	K562	blood:
10	chr16:31083576..31088702-chr16:31125774..31130494,10	K562	blood:
11	chr16:31007019..31009950-chr16:31086954..31088883,2	MCF-7	breast:

No data

Variant related genes	Relation type
ZNF668	TF binding region
ENSG00000268863	Chromatin interaction
ENSG00000103510	Chromatin interaction
ENSG00000252809	Chromatin interaction
ENSG00000103507	Chromatin interaction
ENSG00000089280	Chromatin interaction
ENSG00000099377	Chromatin interaction
ENSG00000262766	Chromatin interaction
ENSG00000099365	Chromatin interaction
ENSG00000099381	Chromatin interaction
ENSG00000140691	Chromatin interaction
ENSG00000260267	Chromatin interaction

Extended variants
information (count: 147 )
Associated
traits (count: 11 )

rSNPs within LD-proxies of this variant (count:135)

rs_ID	r²[population]
rs1046276	1.00[JPT][hapmap]
rs1060506	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs10782001	0.89[JPT][hapmap]
rs10782002	0.89[JPT][hapmap]
rs10871454	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.89[TSI][hapmap];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11076	0.88[JPT][hapmap]
rs1108431	0.89[ASN][1000 genomes]
rs11150599	0.88[JPT][hapmap]
rs11150600	0.89[JPT][hapmap]
rs11150601	0.89[JPT][hapmap]
rs11150604	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.89[TSI][hapmap];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11640534	0.89[JPT][hapmap]
rs11640767	0.86[ASN][1000 genomes]
rs11640957	0.86[ASN][1000 genomes]
rs11640961	0.91[CEU][hapmap];0.84[GIH][hapmap];0.89[JPT][hapmap];0.84[TSI][hapmap]
rs11642003	0.82[ASN][1000 genomes]
rs11642192	0.98[ASN][1000 genomes]
rs11647284	1.00[ASN][1000 genomes]
rs11647442	0.95[ASN][1000 genomes]
rs11649653	0.81[GIH][hapmap];1.00[JPT][hapmap]
rs11862744	1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs11864806	1.00[ASN][1000 genomes]
rs11864839	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11865038	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11865499	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs12102776	0.82[CHB][hapmap];0.92[CHD][hapmap]
rs12445650	1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs12448321	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12597511	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.82[TSI][hapmap];0.93[ASN][1000 genomes]
rs12716981	0.95[ASN][1000 genomes]
rs12716982	0.95[ASN][1000 genomes]
rs12924903	1.00[JPT][hapmap]
rs12926295	0.88[JPT][hapmap]
rs12928852	0.89[JPT][hapmap]
rs12931046	0.89[JPT][hapmap]
rs12934418	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13708	0.89[JPT][hapmap]
rs14235	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]
rs1458201	0.89[JPT][hapmap]
rs1458202	0.89[JPT][hapmap]
rs1549293	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]
rs17839567	0.89[ASN][1000 genomes]
rs17839568	1.00[ASN][1000 genomes]
rs17882368	0.81[LWK][hapmap]
rs1870293	0.89[JPT][hapmap]
rs1978485	0.95[ASN][1000 genomes]
rs1978487	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2032915	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];0.95[ASN][1000 genomes]
rs2054213	0.89[JPT][hapmap]
rs2288004	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2303222	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.83[TSI][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2303223	0.96[CEU][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2305880	0.89[JPT][hapmap]
rs2305884	0.89[JPT][hapmap]
rs2359612	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.91[TSI][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2855475	0.83[CEU][hapmap];1.00[CHB][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.84[TSI][hapmap];0.80[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28725459	0.91[ASN][1000 genomes]
rs28814987	1.00[ASN][1000 genomes]
rs2884738	0.95[ASN][1000 genomes]
rs34649473	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs34898535	0.89[EUR][1000 genomes]
rs35351013	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35468353	1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs35675346	1.00[JPT][hapmap]
rs35713203	1.00[ASN][1000 genomes]
rs3751855	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4468641	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4527034	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.86[TSI][hapmap];0.80[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4889525	0.89[JPT][hapmap]
rs4889530	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4889599	0.89[JPT][hapmap]
rs4889603	0.81[CEU][hapmap];0.84[GIH][hapmap];0.89[JPT][hapmap]
rs4889604	0.89[JPT][hapmap]
rs4889606	0.92[CEU][hapmap];0.84[GIH][hapmap];0.89[JPT][hapmap];0.87[MEX][hapmap];0.87[TSI][hapmap]
rs4889609	1.00[JPT][hapmap]
rs4889619	0.84[ASN][1000 genomes]
rs4889620	0.80[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4889623	0.82[CHB][hapmap]
rs4889651	0.88[JPT][hapmap]
rs4889653	0.88[JPT][hapmap]
rs55766044	0.95[ASN][1000 genomes]
rs55979739	0.89[ASN][1000 genomes]
rs56284083	0.89[ASN][1000 genomes]
rs56314408	0.95[ASN][1000 genomes]
rs56813533	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57434408	0.91[ASN][1000 genomes]
rs58726213	0.87[ASN][1000 genomes]
rs59061704	0.86[ASN][1000 genomes]
rs59735493	0.95[ASN][1000 genomes]
rs60996860	0.91[ASN][1000 genomes]
rs61162043	1.00[ASN][1000 genomes]
rs61320757	0.95[ASN][1000 genomes]
rs6565217	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6950	0.89[JPT][hapmap]
rs7187995	0.93[ASN][1000 genomes]
rs7190802	0.82[CHB][hapmap]
rs7196161	1.00[ASN][1000 genomes]
rs7196726	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7197717	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7199949	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[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];1.00[ASN][1000 genomes]
rs729482	1.00[JPT][hapmap]
rs732172	1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs732173	0.89[ASN][1000 genomes]
rs73530203	0.98[ASN][1000 genomes]
rs749670	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs749767	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs7500176	0.89[ASN][1000 genomes]
rs750952	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs8046707	0.84[GIH][hapmap];0.89[JPT][hapmap]
rs8047803	1.00[ASN][1000 genomes]
rs8050588	0.89[JPT][hapmap]
rs8050894	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8056842	1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs8060857	0.89[JPT][hapmap]
rs8061047	0.93[ASN][1000 genomes]
rs8062719	0.89[JPT][hapmap]
rs881929	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.91[TSI][hapmap];0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs889548	0.96[CEU][hapmap];1.00[CHB][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]
rs889555	1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs897986	0.89[JPT][hapmap]
rs9923231	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];0.91[MEX][hapmap];0.87[MKK][hapmap];0.91[TSI][hapmap];0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9925964	0.95[CEU][hapmap];0.80[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9926533	0.92[CEU][hapmap];0.82[CHD][hapmap];0.84[GIH][hapmap];0.89[JPT][hapmap];0.87[MEX][hapmap];0.82[TSI][hapmap]
rs9929899	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9933843	0.88[JPT][hapmap]
rs9934438	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];0.91[MEX][hapmap];0.87[MKK][hapmap];0.91[TSI][hapmap];0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9936329	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]
rs9939417	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.81[MKK][hapmap];0.91[TSI][hapmap];0.97[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9939558	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9972727	0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 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

mRNA abundance (count:11)

SNP	Gene	Cis/trans	Tissue	Source
rs749671	MYST1	cis	cerebellum	SCAN
rs749671	HSD3B7	cis	Whole Blood	GTEx
rs749671	MYST1	cis	parietal	SCAN
rs749671	STX1B	cis	cerebellum	SCAN
rs749671	KAT8	cis	Skin Sun Exposed Lower leg	GTEx
rs749671	NCRNA00095	cis	cerebellum	SCAN
rs749671	C16orf93	cis	parietal	SCAN
rs749671	ZNF668	cis	cerebellum	SCAN
rs749671	YPEL3	cis	cerebellum	SCAN
rs749671	RP11-196G11.2	cis	Muscle Skeletal	GTEx
rs749671	ITGAX	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31086400-31092400	Weak transcription	Small Intestine	intestine
2	chr16:31086400-31104400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr16:31086600-31089400	Weak transcription	NH-A	brain
4	chr16:31086600-31091000	Weak transcription	Psoas Muscle	Psoas
5	chr16:31086600-31104200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr16:31086600-31105200	Weak transcription	Right Atrium	heart
7	chr16:31086800-31093000	Weak transcription	Fetal Heart	heart
8	chr16:31087000-31089400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr16:31087200-31088400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
10	chr16:31087200-31088400	Genic enhancers	Dnd41	blood
11	chr16:31087200-31090800	Strong transcription	Primary B cells from cord blood	blood
12	chr16:31087200-31092800	Strong transcription	Brain Substantia Nigra	brain
13	chr16:31087200-31093000	Strong transcription	Cortex derived primary cultured neurospheres	brain
14	chr16:31087200-31093200	Strong transcription	Stomach Smooth Muscle	stomach
15	chr16:31087200-31093400	Strong transcription	HUES48 Cell Line	embryonic stem cell
16	chr16:31087200-31095800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr16:31087200-31097000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr16:31087200-31102000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr16:31087200-31103800	Strong transcription	NHLF	lung
20	chr16:31087200-31104200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr16:31087400-31088400	Strong transcription	Fetal Stomach	stomach
22	chr16:31087400-31089000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
23	chr16:31087400-31089200	Strong transcription	Esophagus	oesophagus
24	chr16:31087400-31089200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr16:31087400-31089400	Weak transcription	Fetal Brain Male	brain
26	chr16:31087400-31089600	Strong transcription	Brain Germinal Matrix	brain
27	chr16:31087400-31090000	Strong transcription	Monocytes-CD14+_RO01746	blood
28	chr16:31087400-31090600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr16:31087400-31090600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr16:31087400-31091200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
31	chr16:31087400-31091200	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
32	chr16:31087400-31092400	Strong transcription	Fetal Brain Female	brain
33	chr16:31087400-31092600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr16:31087400-31093000	Strong transcription	Brain Anterior Caudate	brain
35	chr16:31087400-31093000	Strong transcription	Brain Cingulate Gyrus	brain
36	chr16:31087400-31093000	Strong transcription	Brain Hippocampus Middle	brain
37	chr16:31087400-31093200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr16:31087400-31093200	Weak transcription	Stomach Mucosa	stomach
39	chr16:31087400-31093400	Strong transcription	Duodenum Mucosa	Duodenum
40	chr16:31087400-31095400	Strong transcription	Rectal Mucosa Donor 29	rectum
41	chr16:31087400-31095600	Strong transcription	Osteobl	bone
42	chr16:31087400-31096000	Strong transcription	HUES64 Cell Line	embryonic stem cell
43	chr16:31087400-31099200	Strong transcription	HepG2	liver
44	chr16:31087400-31101800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr16:31087400-31102800	Strong transcription	Thymus	Thymus
46	chr16:31087400-31103000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr16:31087400-31104400	Strong transcription	Primary T cells from cord blood	blood
48	chr16:31087400-31104400	Strong transcription	Fetal Intestine Small	intestine
49	chr16:31087600-31088400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
50	chr16:31087600-31088400	Strong transcription	HUVEC	blood vessel

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