Variant report

Variant	rs6850199
Chromosome Location	chr4:49000850-49000851
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:48993956..48996256-chr4:49000276..49001827,2	K562	blood:

Extended variants
information (count: 84 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:70)

rs_ID	r²[population]
rs10024211	0.90[CEU][hapmap];0.83[CHB][hapmap];0.87[EUR][1000 genomes]
rs10222924	0.85[ASW][hapmap];1.00[CEU][hapmap];0.93[GIH][hapmap];0.80[JPT][hapmap];0.93[MEX][hapmap];0.88[TSI][hapmap];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1051447	0.84[ASW][hapmap];1.00[CEU][hapmap];0.81[CHB][hapmap];0.93[GIH][hapmap];0.80[JPT][hapmap];0.93[MEX][hapmap];0.91[MKK][hapmap];0.88[TSI][hapmap];0.87[EUR][1000 genomes]
rs11410065	0.93[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs11725397	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11730515	0.91[CEU][hapmap];0.93[GIH][hapmap];0.80[JPT][hapmap];0.87[TSI][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12499992	0.85[ASW][hapmap];0.83[CEU][hapmap];0.95[GIH][hapmap];0.88[TSI][hapmap];0.80[AMR][1000 genomes]
rs12502614	1.00[ASW][hapmap];0.83[CEU][hapmap];0.95[GIH][hapmap];0.93[LWK][hapmap];0.80[MEX][hapmap];0.94[MKK][hapmap];0.88[TSI][hapmap];0.93[YRI][hapmap];0.94[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs12505576	0.91[CEU][hapmap];0.93[GIH][hapmap];0.80[JPT][hapmap];0.87[TSI][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13132977	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13135263	0.91[CEU][hapmap];0.91[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];0.91[TSI][hapmap];0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1350121	0.91[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1350122	1.00[CEU][hapmap];0.85[CHB][hapmap];0.94[JPT][hapmap];0.86[YRI][hapmap];0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1350123	0.91[CEU][hapmap];0.91[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[TSI][hapmap];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1350125	0.91[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1455937	0.94[AFR][1000 genomes]
rs16861606	0.94[AFR][1000 genomes]
rs17611143	0.85[ASW][hapmap];1.00[CEU][hapmap];0.93[GIH][hapmap];0.80[JPT][hapmap];0.93[MEX][hapmap];0.91[TSI][hapmap];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17657136	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1840629	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1840630	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2260962	0.87[EUR][1000 genomes]
rs2572344	1.00[ASW][hapmap];0.83[CEU][hapmap];0.96[GIH][hapmap];0.93[LWK][hapmap];0.80[MEX][hapmap];0.94[MKK][hapmap];0.88[TSI][hapmap];0.93[YRI][hapmap];0.94[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs2605231	0.91[CEU][hapmap];0.80[JPT][hapmap];0.87[EUR][1000 genomes]
rs2605233	0.85[ASW][hapmap];1.00[CEU][hapmap];0.93[GIH][hapmap];0.80[JPT][hapmap];0.93[MEX][hapmap];0.93[MKK][hapmap];0.88[TSI][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2605235	0.87[EUR][1000 genomes]
rs2605236	0.86[CEU][hapmap];0.93[GIH][hapmap];0.87[EUR][1000 genomes]
rs2605237	0.87[EUR][1000 genomes]
rs2605238	0.91[CEU][hapmap];0.93[GIH][hapmap];0.80[JPT][hapmap];0.83[TSI][hapmap];0.88[EUR][1000 genomes]
rs2605239	0.91[CEU][hapmap];0.93[GIH][hapmap];0.80[JPT][hapmap];0.87[TSI][hapmap];0.90[EUR][1000 genomes]
rs2605243	0.94[AFR][1000 genomes]
rs2768951	0.87[EUR][1000 genomes]
rs2768952	0.87[EUR][1000 genomes]
rs2768957	0.85[ASW][hapmap];1.00[CEU][hapmap];0.93[GIH][hapmap];0.80[JPT][hapmap];0.93[MEX][hapmap];0.93[MKK][hapmap];0.88[TSI][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2768958	0.91[CEU][hapmap];0.93[GIH][hapmap];0.80[JPT][hapmap];0.83[TSI][hapmap];0.87[EUR][1000 genomes]
rs2768959	0.87[EUR][1000 genomes]
rs2768965	0.85[ASW][hapmap];1.00[CEU][hapmap];0.93[GIH][hapmap];0.80[JPT][hapmap];0.93[MEX][hapmap];0.93[MKK][hapmap];0.88[TSI][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2768966	1.00[CEU][hapmap];0.81[CHB][hapmap];0.83[JPT][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2768968	0.91[CEU][hapmap];0.93[GIH][hapmap];0.80[JPT][hapmap];0.83[TSI][hapmap];0.87[EUR][1000 genomes]
rs2768969	0.91[CEU][hapmap];0.93[GIH][hapmap];0.80[JPT][hapmap];0.83[TSI][hapmap];0.87[EUR][1000 genomes]
rs2768970	0.84[EUR][1000 genomes]
rs2768971	0.90[CEU][hapmap];0.93[GIH][hapmap];0.80[JPT][hapmap];0.87[TSI][hapmap];0.90[EUR][1000 genomes]
rs2768973	0.85[ASW][hapmap];1.00[CEU][hapmap];0.93[GIH][hapmap];0.80[JPT][hapmap];0.93[MEX][hapmap];0.93[MKK][hapmap];0.91[TSI][hapmap];0.90[EUR][1000 genomes]
rs2768974	0.89[EUR][1000 genomes]
rs2768975	0.91[CEU][hapmap];0.89[EUR][1000 genomes]
rs2768976	0.91[CEU][hapmap];0.80[JPT][hapmap];0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2768977	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2768978	0.91[CEU][hapmap];0.80[JPT][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs28590759	0.80[AMR][1000 genomes]
rs4273436	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4552435	0.94[AFR][1000 genomes]
rs4694908	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4695413	0.94[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs4695414	1.00[ASW][hapmap];0.83[CEU][hapmap];0.96[GIH][hapmap];0.93[LWK][hapmap];0.80[MEX][hapmap];0.94[MKK][hapmap];0.88[TSI][hapmap];0.93[YRI][hapmap];0.94[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs4695415	0.94[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs4695416	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4695417	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4695418	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4695419	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.91[TSI][hapmap];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs55688634	0.87[EUR][1000 genomes]
rs6822902	0.91[CEU][hapmap];0.80[CHB][hapmap];0.93[GIH][hapmap];0.87[TSI][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7655341	0.93[GIH][hapmap];0.80[JPT][hapmap]
rs7674086	0.81[EUR][1000 genomes]
rs7674928	0.94[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs7694122	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs936134	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs936135	1.00[ASW][hapmap];0.83[CEU][hapmap];0.96[GIH][hapmap];0.89[LWK][hapmap];0.80[MEX][hapmap];0.93[MKK][hapmap];0.88[TSI][hapmap];0.93[YRI][hapmap];0.94[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs9683541	0.85[ASW][hapmap];0.83[CEU][hapmap];0.96[GIH][hapmap];0.80[MEX][hapmap];0.88[TSI][hapmap];0.80[AMR][1000 genomes]
rs9683610	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9992335	0.81[EUR][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	nsv1002674	chr4:48507608-49032909	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv537087	chr4:48507608-49032909	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv1010923	chr4:48575156-49083089	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv537088	chr4:48575156-49083089	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
5	nsv1013762	chr4:48580484-49032909	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv537089	chr4:48580484-49032909	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
7	nsv1010381	chr4:48701525-49309842	Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
8	nsv1003718	chr4:48771947-49083089	Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
9	nsv916809	chr4:48784318-49083302	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
10	nsv1011910	chr4:48784332-49154757	ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
11	nsv879010	chr4:48794403-49061141	Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
12	nsv427680	chr4:48829607-49660117	ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
13	nsv1004364	chr4:48961611-49083089	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
14	nsv998769	chr4:48989185-49083089	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs6850199	TEC	cis	parietal	SCAN
rs6850199	SGCB	cis	multi-tissue	Pritchard

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:48991400-49018400	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr4:48993600-49017400	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr4:48997200-49018200	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr4:49000400-49001400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr4:49000800-49001800	Weak transcription	Gastric	stomach
6	chr4:49000800-49002200	Weak transcription	Liver	Liver

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