Variant report

Variant	rs10951155
Chromosome Location	chr7:3359684-3359685
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	chr7:3351745..3355702-chr7:3356161..3359964,4	K562	blood:

Extended variants
information (count: 127 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:111)

rs_ID	r²[population]
rs10215256	0.87[JPT][hapmap]
rs10224769	0.82[ASN][1000 genomes]
rs10228151	0.91[CHB][hapmap];0.89[CHD][hapmap];0.95[JPT][hapmap]
rs10228723	0.85[ASN][1000 genomes]
rs10232431	0.91[JPT][hapmap]
rs10233166	0.91[CHB][hapmap];0.85[ASN][1000 genomes]
rs10243467	0.86[JPT][hapmap]
rs10250421	0.95[CHB][hapmap];0.88[CHD][hapmap];0.85[JPT][hapmap]
rs10250444	1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs10254665	0.91[JPT][hapmap]
rs10258501	0.95[CHB][hapmap];0.83[CHD][hapmap];0.91[JPT][hapmap]
rs10260145	0.85[ASN][1000 genomes]
rs10266047	0.95[CHB][hapmap];0.95[JPT][hapmap]
rs10268249	0.82[ASN][1000 genomes]
rs10268837	1.00[CHB][hapmap];0.81[JPT][hapmap]
rs10271803	0.82[CHB][hapmap];0.83[JPT][hapmap]
rs10276190	0.85[ASN][1000 genomes]
rs10276933	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10807838	0.91[CHB][hapmap];0.93[CHD][hapmap];0.84[ASN][1000 genomes]
rs1112428	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs11974620	0.82[ASN][1000 genomes]
rs11979128	0.82[CEU][hapmap]
rs12056172	0.91[CHB][hapmap]
rs12537113	0.84[ASN][1000 genomes]
rs12537528	0.91[CHB][hapmap];0.93[CHD][hapmap];0.81[ASN][1000 genomes]
rs12537549	0.84[ASN][1000 genomes]
rs12540305	0.81[ASN][1000 genomes]
rs12673513	0.83[CHB][hapmap];0.84[CHD][hapmap]
rs12700789	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs12700808	0.88[TSI][hapmap]
rs13221852	0.82[CHB][hapmap];0.87[JPT][hapmap]
rs13224926	0.93[ASN][1000 genomes]
rs13230698	0.84[ASN][1000 genomes]
rs1357311	0.91[JPT][hapmap]
rs1403158	0.95[CHB][hapmap];0.84[CHD][hapmap];0.87[JPT][hapmap]
rs1525556	0.91[CHB][hapmap];0.85[ASN][1000 genomes]
rs1525557	0.84[ASN][1000 genomes]
rs17133257	0.84[CHD][hapmap]
rs17133334	0.87[CHB][hapmap]
rs2340848	0.87[JPT][hapmap]
rs34608458	0.85[ASN][1000 genomes]
rs34735349	0.85[ASN][1000 genomes]
rs4131987	0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs4255031	0.90[CHB][hapmap];0.82[ASN][1000 genomes]
rs4295560	0.85[ASN][1000 genomes]
rs4298408	0.98[ASN][1000 genomes]
rs4316064	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs4320450	0.91[CHB][hapmap];0.84[ASN][1000 genomes]
rs4327753	0.86[CHB][hapmap];0.84[ASN][1000 genomes]
rs4336505	0.84[ASN][1000 genomes]
rs4349886	0.84[ASN][1000 genomes]
rs4358698	0.91[CHB][hapmap]
rs4385365	0.99[ASN][1000 genomes]
rs4416733	0.88[TSI][hapmap]
rs4443553	0.91[CHB][hapmap];0.82[ASN][1000 genomes]
rs4495320	0.91[CHB][hapmap];0.84[ASN][1000 genomes]
rs4499989	0.91[CHB][hapmap];0.82[ASN][1000 genomes]
rs4506106	0.91[CHB][hapmap];0.91[CHD][hapmap];0.84[ASN][1000 genomes]
rs4521670	0.91[CHB][hapmap];0.93[CHD][hapmap];0.82[ASN][1000 genomes]
rs4544975	0.95[CHB][hapmap];0.95[CHD][hapmap];0.95[JPT][hapmap];0.95[ASN][1000 genomes]
rs4588749	0.83[ASN][1000 genomes]
rs4607498	0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs4719883	0.84[ASN][1000 genomes]
rs4719894	0.95[CHB][hapmap];0.98[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs4719944	0.83[JPT][hapmap]
rs4722655	0.85[ASN][1000 genomes]
rs4722663	1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4722673	0.85[ASN][1000 genomes]
rs4722674	0.85[ASN][1000 genomes]
rs4722693	0.91[CHB][hapmap];0.83[ASN][1000 genomes]
rs4722696	0.91[CHB][hapmap];0.82[ASN][1000 genomes]
rs4722708	0.91[CHB][hapmap];0.81[ASN][1000 genomes]
rs4722709	0.94[ASN][1000 genomes]
rs4722710	0.95[ASN][1000 genomes]
rs4722712	0.93[ASN][1000 genomes]
rs4722850	0.84[CEU][hapmap]
rs6461983	0.81[ASN][1000 genomes]
rs6461993	0.85[ASN][1000 genomes]
rs6461994	0.91[CHB][hapmap];0.93[CHD][hapmap];0.85[ASN][1000 genomes]
rs6462030	0.95[CHB][hapmap];0.91[JPT][hapmap];0.92[ASN][1000 genomes]
rs6651070	1.00[JPT][hapmap]
rs67586312	0.98[ASN][1000 genomes]
rs6949513	0.87[JPT][hapmap]
rs6958390	0.84[ASN][1000 genomes]
rs6959232	0.91[CHB][hapmap]
rs6959702	0.85[ASN][1000 genomes]
rs6962796	0.82[CHB][hapmap];0.87[JPT][hapmap]
rs6964838	0.86[JPT][hapmap]
rs6965684	0.84[ASN][1000 genomes]
rs6966619	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6974075	0.94[ASN][1000 genomes]
rs6980323	0.85[ASN][1000 genomes]
rs7776559	0.88[TSI][hapmap]
rs7780027	0.95[ASN][1000 genomes]
rs7780498	0.86[TSI][hapmap]
rs7785994	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7789887	0.91[CHB][hapmap];0.84[ASN][1000 genomes]
rs7791617	0.91[JPT][hapmap]
rs7791820	0.85[ASN][1000 genomes]
rs7794279	0.85[ASN][1000 genomes]
rs7797018	1.00[CHB][hapmap];0.94[JPT][hapmap];0.93[ASN][1000 genomes]
rs7798418	0.94[ASN][1000 genomes]
rs7798672	0.83[ASN][1000 genomes]
rs7802250	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs7803004	0.91[CHB][hapmap];0.89[CHD][hapmap];1.00[JPT][hapmap]
rs7803993	0.91[CHB][hapmap];0.85[ASN][1000 genomes]
rs7811244	0.91[CHB][hapmap];0.91[CHD][hapmap];0.85[ASN][1000 genomes]
rs7811286	1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs885011	0.83[CHB][hapmap];0.87[JPT][hapmap]
rs9648354	0.86[JPT][hapmap]
rs9969270	1.00[CHB][hapmap];1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023127	chr7:3216344-3466223	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1018173	chr7:3258989-3879848	Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv538660	chr7:3258989-3879848	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	esv2758100	chr7:3286625-3560229	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	esv2759500	chr7:3286625-3560229	Genic enhancers Flanking Bivalent TSS/Enh Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1016555	chr7:3298478-3872512	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv538661	chr7:3298478-3872512	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv1019515	chr7:3300048-3479972	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv887324	chr7:3308195-3400105	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv605892	chr7:3341589-3424878	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv1020764	chr7:3348458-3554820	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv538662	chr7:3348458-3554820	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
13	nsv981785	chr7:3353184-3367204	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
14	nsv1019492	chr7:3359294-3479972	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
15	nsv538663	chr7:3359294-3479972	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
16	esv2757204	chr7:3359491-3460355	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10951155	C7orf50	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3344600-3366600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr7:3346200-3362400	Weak transcription	Aorta	Aorta
3	chr7:3350200-3366800	Weak transcription	Fetal Brain Male	brain
4	chr7:3357800-3361000	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr7:3358800-3360600	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr7:3358800-3360800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr7:3358800-3366800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr7:3359000-3359800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr7:3359000-3360600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr7:3359000-3385800	Weak transcription	Pancreas	Pancrea
11	chr7:3359200-3362400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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