Variant report

Variant	rs11865038
Chromosome Location	chr16:31095171-31095172
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr16:30994078..30998079-chr16:31091714..31095478,6	K562	blood:
2	chr16:30994729..30997345-chr16:31091777..31095535,3	K562	blood:
3	chr16:30995968..30997772-chr16:31092336..31095227,3	MCF-7	breast:
4	chr16:30968009..30970213-chr16:31093511..31095824,2	MCF-7	breast:
5	chr16:31091808..31095643-chr16:31127671..31129489,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000099381	Chromatin interaction
ENSG00000262766	Chromatin interaction
ENSG00000103510	Chromatin interaction
ENSG00000099377	Chromatin interaction
ENSG00000268863	Chromatin interaction

Extended variants
information (count: 155 )
Associated
traits (count: 11 )

rSNPs within LD-proxies of this variant (count:142)

rs_ID	r²[population]
rs1046276	0.87[GIH][hapmap];1.00[JPT][hapmap]
rs1060506	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.95[ASN][1000 genomes]
rs10782001	0.89[JPT][hapmap]
rs10782002	0.88[GIH][hapmap];0.89[JPT][hapmap]
rs10871454	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs11076	0.88[JPT][hapmap]
rs1108431	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11150599	0.88[JPT][hapmap]
rs11150600	0.88[GIH][hapmap];0.89[JPT][hapmap]
rs11150601	0.83[CEU][hapmap];0.88[GIH][hapmap];0.89[JPT][hapmap]
rs11150604	1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs11640534	0.88[GIH][hapmap];0.89[JPT][hapmap]
rs11640767	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11640957	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11640961	0.89[JPT][hapmap]
rs11642003	0.82[ASN][1000 genomes]
rs11642192	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11647284	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11647442	0.95[ASN][1000 genomes]
rs11649653	1.00[JPT][hapmap]
rs11862744	0.93[ASW][hapmap];0.92[CEU][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.94[MKK][hapmap];0.83[YRI][hapmap];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11864806	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11864839	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11865499	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.95[ASN][1000 genomes]
rs12102776	0.82[CHB][hapmap]
rs12445568	0.83[CEU][hapmap];0.88[GIH][hapmap];0.87[MEX][hapmap]
rs12445650	0.91[CEU][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12448321	0.89[ASN][1000 genomes]
rs12597511	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs12716981	0.95[ASN][1000 genomes]
rs12716982	0.95[ASN][1000 genomes]
rs12924903	0.88[GIH][hapmap];1.00[JPT][hapmap]
rs12928852	0.88[GIH][hapmap];0.89[JPT][hapmap]
rs12930545	0.88[GIH][hapmap]
rs12931046	0.88[GIH][hapmap];0.89[JPT][hapmap]
rs12934418	0.89[ASN][1000 genomes]
rs13708	0.83[CEU][hapmap];0.89[JPT][hapmap]
rs14235	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs1458201	0.89[JPT][hapmap]
rs1458202	0.88[GIH][hapmap];0.89[JPT][hapmap]
rs1549293	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs17839567	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17839568	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1870293	0.83[CEU][hapmap];0.88[GIH][hapmap];0.89[JPT][hapmap]
rs1978485	0.95[ASN][1000 genomes]
rs1978487	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2032915	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2054213	0.83[CEU][hapmap];0.88[GIH][hapmap];0.89[JPT][hapmap]
rs2288004	0.89[ASN][1000 genomes]
rs2303222	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2303223	1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2305880	0.83[CEU][hapmap];0.88[GIH][hapmap];0.89[JPT][hapmap]
rs2305884	0.83[CEU][hapmap];0.85[GIH][hapmap];0.89[JPT][hapmap]
rs2359612	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2855475	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs28725459	0.91[ASN][1000 genomes]
rs28814987	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2884738	0.95[ASN][1000 genomes]
rs34649473	0.85[ASN][1000 genomes]
rs35351013	0.93[ASN][1000 genomes]
rs35468353	0.93[ASW][hapmap];0.92[CEU][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];0.91[MEX][hapmap];0.94[MKK][hapmap];0.83[YRI][hapmap];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs35675346	1.00[JPT][hapmap]
rs35713203	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35961830	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs3751855	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3813020	0.87[GIH][hapmap]
rs4468641	0.81[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];0.82[YRI][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4527034	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs4889525	0.88[GIH][hapmap];0.89[JPT][hapmap]
rs4889526	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4889530	0.87[ASN][1000 genomes]
rs4889599	0.83[CEU][hapmap];0.88[GIH][hapmap];0.89[JPT][hapmap]
rs4889603	0.89[JPT][hapmap]
rs4889604	0.88[GIH][hapmap];0.89[JPT][hapmap]
rs4889606	0.89[JPT][hapmap]
rs4889609	0.93[ASW][hapmap];0.92[CEU][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.84[MKK][hapmap];0.83[YRI][hapmap];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4889619	0.84[ASN][1000 genomes]
rs4889620	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	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs56284083	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs56314408	0.95[ASN][1000 genomes]
rs56813533	0.93[ASN][1000 genomes]
rs57434408	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs57576577	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs58726213	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs59061704	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];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	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];0.95[MEX][hapmap];0.97[MKK][hapmap];0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6950	0.82[CEU][hapmap];0.89[JPT][hapmap]
rs7184567	0.92[CEU][hapmap]
rs7187995	0.93[ASN][1000 genomes]
rs7190802	0.82[CHB][hapmap]
rs7196161	1.00[ASN][1000 genomes]
rs7196726	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7197717	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];1.00[MKK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7199949	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][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]
rs7200879	1.00[JPT][hapmap]
rs7203999	0.83[CEU][hapmap];0.88[GIH][hapmap];0.89[JPT][hapmap];0.91[MEX][hapmap]
rs7204459	0.88[GIH][hapmap];0.89[JPT][hapmap]
rs7206511	0.88[GIH][hapmap];0.89[JPT][hapmap]
rs7294	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs729482	0.83[CEU][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap]
rs732172	0.92[CEU][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs732173	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73530203	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs749670	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs749671	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs749767	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs7500176	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs750952	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8046707	0.89[JPT][hapmap]
rs8047803	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8050588	0.88[GIH][hapmap];0.89[JPT][hapmap]
rs8050894	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs8056842	0.92[CEU][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8060857	0.88[GIH][hapmap];0.89[JPT][hapmap]
rs8061047	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8062719	0.83[CEU][hapmap];0.88[GIH][hapmap];0.89[JPT][hapmap]
rs881929	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs889548	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs889555	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs897986	0.83[CEU][hapmap];0.88[GIH][hapmap];0.89[JPT][hapmap]
rs9673641	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9923231	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9925964	0.95[ASN][1000 genomes]
rs9926533	0.89[JPT][hapmap]
rs9927295	0.82[YRI][hapmap]
rs9929899	0.86[ASN][1000 genomes]
rs9933843	0.88[JPT][hapmap]
rs9934438	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9936329	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs9938550	0.83[CEU][hapmap];0.88[GIH][hapmap]
rs9939417	1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs9939558	0.89[ASN][1000 genomes]
rs9972727	0.95[ASN][1000 genomes]

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	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	esv993244	chr16:31091981-31101565	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	13 gene(s)	inside rSNPs	diseases

Variant related diseases (count:1)

Disease	PMID	Source
Parkinson's disease	22451204	GWAS catalog

mRNA abundance (count:10)

SNP	Gene	Cis/trans	Tissue	Source
rs11865038	HSD3B7	cis	Skin Sun Exposed Lower leg	GTEx
rs11865038	STX4	Cis_1M	lymphoblastoid	RTeQTL
rs11865038	STX1B	cis	Thyroid	GTEx
rs11865038	KAT8	cis	Skin Sun Exposed Lower leg	GTEx
rs11865038	RP11-196G11.2	cis	Esophagus Muscularis	GTEx
rs11865038	HSD3B7	cis	Muscle Skeletal	GTEx
rs11865038	HSD3B7	cis	Esophagus Mucosa	GTEx
rs11865038	KAT8	cis	Artery Tibial	GTEx
rs11865038	RP11-196G11.2	cis	Muscle Skeletal	GTEx
rs11865038	MYST1	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31086400-31104400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr16:31086600-31104200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr16:31086600-31105200	Weak transcription	Right Atrium	heart
4	chr16:31087200-31095800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr16:31087200-31097000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr16:31087200-31102000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr16:31087200-31103800	Strong transcription	NHLF	lung
8	chr16:31087200-31104200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr16:31087400-31095400	Strong transcription	Rectal Mucosa Donor 29	rectum
10	chr16:31087400-31095600	Strong transcription	Osteobl	bone
11	chr16:31087400-31096000	Strong transcription	HUES64 Cell Line	embryonic stem cell
12	chr16:31087400-31099200	Strong transcription	HepG2	liver
13	chr16:31087400-31101800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr16:31087400-31102800	Strong transcription	Thymus	Thymus
15	chr16:31087400-31103000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr16:31087400-31104400	Strong transcription	Primary T cells from cord blood	blood
17	chr16:31087400-31104400	Strong transcription	Fetal Intestine Small	intestine
18	chr16:31087600-31096800	Strong transcription	Ovary	ovary
19	chr16:31087600-31097000	Strong transcription	Sigmoid Colon	Sigmoid Colon
20	chr16:31087600-31098400	Strong transcription	Fetal Thymus	thymus
21	chr16:31087600-31100200	Weak transcription	Hela-S3	cervix
22	chr16:31087600-31103000	Strong transcription	HUES6 Cell Line	embryonic stem cell
23	chr16:31087600-31103000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr16:31087800-31096000	Strong transcription	Colon Smooth Muscle	Colon
25	chr16:31087800-31096400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr16:31087800-31101800	Strong transcription	Liver	Liver
27	chr16:31087800-31101800	Strong transcription	Placenta Amnion	Placenta Amnion
28	chr16:31087800-31102200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr16:31087800-31102800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr16:31087800-31103000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
31	chr16:31087800-31104000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
32	chr16:31088000-31096200	Strong transcription	Muscle Satellite Cultured Cells	--
33	chr16:31088000-31096200	Strong transcription	Duodenum Smooth Muscle	Duodenum
34	chr16:31088000-31099400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr16:31090000-31105200	Weak transcription	Fetal Kidney	kidney
36	chr16:31090400-31104200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
37	chr16:31090600-31096600	Weak transcription	NH-A	brain
38	chr16:31090600-31099000	Strong transcription	Esophagus	oesophagus
39	chr16:31090800-31101200	Weak transcription	HMEC	breast
40	chr16:31090800-31101800	Weak transcription	A549	lung
41	chr16:31090800-31102000	Weak transcription	HUVEC	blood vessel
42	chr16:31090800-31102200	Weak transcription	Primary B cells from cord blood	blood
43	chr16:31091000-31104000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
44	chr16:31091200-31097000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr16:31091200-31099200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr16:31091400-31096400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr16:31091400-31099000	Strong transcription	Primary monocytes fromperipheralblood	blood
48	chr16:31091400-31102800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
49	chr16:31091800-31100800	Strong transcription	Fetal Intestine Large	intestine
50	chr16:31092000-31095800	Genic enhancers	Fetal Muscle Leg	muscle

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