Variant report

Variant	rs6948685
Chromosome Location	chr7:99970188-99970189
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr7:99968973-99971363	HL-60	blood:	n/a	n/a
2	POLR2A	chr7:99968932-99970631	HL-60	blood:	n/a	n/a
3	MYC	chr7:99969307-99971224	NB4	blood:	n/a	chr7:99970444-99970453 chr7:99970442-99970455 chr7:99970442-99970455 chr7:99969549-99969558 chr7:99969550-99969557 chr7:99970444-99970453 chr7:99970443-99970454 chr7:99970442-99970450 chr7:99970442-99970455
4	POLR2A	chr7:99969969-99970291	IMR90	lung:	n/a	n/a
5	POLR2A	chr7:99967723-99970407	MCF10A-Er-Src	breast:	n/a	n/a
6	POLR2A	chr7:99969925-99970357	ECC-1	luminal epithelium:	n/a	n/a
7	POLR2A	chr7:99969846-99970306	SK-N-MC	brain:	n/a	n/a
8	ELF1	chr7:99969879-99970754	GM12878	blood:	n/a	n/a
9	POLR2A	chr7:99970038-99970432	HepG2	liver:	n/a	n/a
10	POLR2A	chr7:99969557-99971251	NB4	blood:	n/a	n/a
11	POLR2A	chr7:99963980-99970675	Hela-S3	cervix:	n/a	n/a
12	POLR2A	chr7:99967786-99971318	A549	lung:	n/a	n/a
13	POLR2A	chr7:99959279-99970406	K562	blood:	n/a	n/a
14	POLR2A	chr7:99970183-99970725	GM12878	blood:	n/a	n/a
15	POLR2A	chr7:99969588-99970217	HUVEC	blood vessel:	n/a	n/a
16	POLR2A	chr7:99968525-99971068	H1-hESC	embryonic stem cell:	n/a	n/a
17	POLR2A	chr7:99969049-99970670	Hela-S3	cervix:	n/a	n/a
18	POLR2A	chr7:99969922-99971920	K562	blood:	n/a	n/a
19	POLR2A	chr7:99968372-99971597	K562	blood:	n/a	n/a
20	POLR2A	chr7:99969931-99971258	Hela-S3	cervix:	n/a	n/a
21	POLR2A	chr7:99969938-99970331	MCF-7	breast:	n/a	n/a
22	POLR2A	chr7:99968507-99971027	HepG2	liver:	n/a	n/a
23	CEBPB	chr7:99969883-99970238	IMR90	lung:	n/a	n/a
24	POLR2A	chr7:99970023-99970288	K562	blood:	n/a	n/a
25	POLR2A	chr7:99969905-99970268	ECC-1	luminal epithelium:	n/a	n/a
26	POLR2A	chr7:99970060-99970329	A549	lung:	n/a	n/a
27	CEBPB	chr7:99969890-99970232	Hela-S3	cervix:	n/a	n/a
28	POLR2A	chr7:99969888-99970422	U87	brain:	n/a	n/a
29	POLR2A	chr7:99968988-99971291	Hela-S3	cervix:	n/a	n/a
30	POLR2A	chr7:99970087-99970485	GM12878	blood:	n/a	n/a
31	USF1	chr7:99970171-99970649	K562	blood:	n/a	n/a
32	POLR2A	chr7:99969897-99970404	GM12878	blood:	n/a	n/a
33	CHD2	chr7:99970157-99970242	Hela-S3	cervix:	n/a	n/a
34	MAZ	chr7:99969278-99970675	IMR90	lung:	n/a	chr7:99970444-99970453 chr7:99970442-99970455 chr7:99970442-99970455 chr7:99969549-99969558 chr7:99969550-99969557 chr7:99970444-99970453 chr7:99970443-99970454 chr7:99970442-99970450 chr7:99970442-99970455
35	POLR2A	chr7:99967810-99971498	Hela-S3	cervix:	n/a	n/a
36	MAX	chr7:99969322-99971176	NB4	blood:	n/a	chr7:99970444-99970453 chr7:99970442-99970455 chr7:99970442-99970455 chr7:99969549-99969558 chr7:99969550-99969557 chr7:99970444-99970453 chr7:99970443-99970454 chr7:99970442-99970450 chr7:99970442-99970455
37	POLR2A	chr7:99968420-99970512	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:99967799..99970553-chr7:100006640..100009998,3	K562	blood:
2	chr16:2254016..2256891-chr7:99969269..99971399,2	MCF-7	breast:
3	chr7:99968617..99970756-chr7:99989605..99991411,2	K562	blood:
4	chr7:99965641..99971124-chr7:100025245..100028820,5	MCF-7	breast:
5	chr7:99954589..99956463-chr7:99967936..99970860,2	K562	blood:
6	chr7:99752659..99755597-chr7:99969374..99971671,2	K562	blood:

Variant related genes	Relation type
PILRA	TF binding region
ENSG00000146834	Chromatin interaction
ENSG00000121716	Chromatin interaction
ENSG00000266154	Chromatin interaction
ENSG00000252958	Chromatin interaction
ENSG00000146826	Chromatin interaction
ENSG00000078487	Chromatin interaction
ENSG00000167965	Chromatin interaction

Extended variants
information (count: 96 )
Associated
traits (count: 61 )

rSNPs within LD-proxies of this variant (count:93)

rs_ID	r²[population]
rs1000215	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs10085549	1.00[CEU][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];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10241492	0.85[CEU][hapmap];1.00[JPT][hapmap]
rs1059129	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1063945	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1073	0.87[ASW][hapmap];0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.93[MKK][hapmap]
rs11559117	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap]
rs11760536	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap]
rs11761253	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.84[LWK][hapmap];1.00[MEX][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];0.85[YRI][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11761306	1.00[ASN][1000 genomes]
rs11761426	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11761725	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap]
rs11761784	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap]
rs11763414	0.85[CEU][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs11763511	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap]
rs11765869	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11766752	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap]
rs11766917	0.83[ASN][1000 genomes]
rs11768933	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11768967	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11769057	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11769700	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap]
rs11769886	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs11771241	0.85[CEU][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs11771419	0.84[CEU][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11771799	1.00[ASN][1000 genomes]
rs11771936	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11773661	0.85[CEU][hapmap]
rs1636980	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1962269	0.91[CEU][hapmap]
rs1964242	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2003507	0.84[ASN][1000 genomes]
rs2108269	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2406253	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap]
rs2406255	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap]
rs28401739	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28490152	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs28495773	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28578163	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap]
rs28660238	0.84[ASN][1000 genomes]
rs28680963	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3087502	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34989573	1.00[CHD][hapmap];1.00[GIH][hapmap];0.86[MEX][hapmap]
rs35111986	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs35986051	1.00[ASN][1000 genomes]
rs3900792	0.87[ASW][hapmap];0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[MKK][hapmap];0.84[ASN][1000 genomes]
rs3991498	0.83[EUR][1000 genomes]
rs3991564	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4074838	0.87[ASW][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];0.93[MKK][hapmap]
rs41280971	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4472444	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap]
rs61735533	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66632384	0.84[ASN][1000 genomes]
rs67163493	0.84[ASN][1000 genomes]
rs67315960	0.84[ASN][1000 genomes]
rs67471932	0.84[ASN][1000 genomes]
rs68116612	0.84[ASN][1000 genomes]
rs6945952	0.87[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6946768	1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6953749	0.84[ASN][1000 genomes]
rs6955362	0.85[CEU][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];0.89[MKK][hapmap]
rs6955367	1.00[CEU][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];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6957928	0.84[ASN][1000 genomes]
rs6965207	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6965458	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6970806	0.84[ASN][1000 genomes]
rs6975514	0.85[CEU][hapmap]
rs6975563	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6975660	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6975729	0.87[ASW][hapmap];0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.93[MKK][hapmap]
rs6979910	1.00[CEU][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs705866	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73161745	0.85[ASN][1000 genomes]
rs73161759	0.84[ASN][1000 genomes]
rs73161762	0.84[ASN][1000 genomes]
rs73401443	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73401450	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73401451	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7341507	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7783159	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs7783550	0.87[ASW][hapmap];0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[MKK][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7786844	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7787620	0.92[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap]
rs7792525	1.00[CEU][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7792959	1.00[CEU][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7794485	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap]
rs7795656	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7795805	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7799894	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7799901	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7799932	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7803454	0.84[ASN][1000 genomes]
rs7809801	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3350965	chr7:99747460-100146105	Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	304 gene(s)	inside rSNPs	diseases
2	esv1829095	chr7:99814675-100494084	Bivalent Enhancer Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	393 gene(s)	inside rSNPs	diseases
3	nsv831071	chr7:99918025-100113413	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers 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 miRNA target site	287 gene(s)	inside rSNPs	diseases

mRNA abundance (count:61)

SNP	Gene	Cis/trans	Tissue	Source
rs6948685	PILRB	cis	Skin Sun Exposed Lower leg	GTEx
rs6948685	PVRIG2P	cis	Esophagus Mucosa	GTEx
rs6948685	STAG3L5P	cis	Muscle Skeletal	GTEx
rs6948685	PILRA	cis	Thyroid	GTEx
rs6948685	PILRA	cis	Nerve Tibial	GTEx
rs6948685	GNB2	cis	parietal	SCAN
rs6948685	ZCWPW1	cis	cerebellum	SCAN
rs6948685	PVRIG2P	cis	lung	GTEx
rs6948685	PILRB	cis	lung	GTEx
rs6948685	PILRB	cis	Adipose Subcutaneous	GTEx
rs6948685	PILRB	cis	Stomach	GTEx
rs6948685	PILRB	cis	Nerve Tibial	GTEx
rs6948685	PILRA	cis	cerebellum	SCAN
rs6948685	PILRB	cis	Esophagus Muscularis	GTEx
rs6948685	PILRB	cis	multi-tissue	Pritchard
rs6948685	STAG3L5P	cis	Thyroid	GTEx
rs6948685	PVRIG	cis	cerebellum	SCAN
rs6948685	ZCWPW1	cis	parietal	SCAN
rs6948685	PVRIG2P	cis	Thyroid	GTEx
rs6948685	PILRA	cis	Esophagus Muscularis	GTEx
rs6948685	CNPY4	cis	cerebellum	SCAN
rs6948685	STAG3L5P	cis	Heart Left Ventricle	GTEx
rs6948685	PILRA	cis	Artery Tibial	GTEx
rs6948685	STAG3L5P	cis	Esophagus Mucosa	GTEx
rs6948685	PMS2P1	cis	Esophagus Mucosa	GTEx
rs6948685	PILRB	cis	Whole Blood	GTEx
rs6948685	PVRIG2P	cis	Nerve Tibial	GTEx
rs6948685	STAG3L5P	cis	Nerve Tibial	GTEx
rs6948685	PILRB	cis	Esophagus Mucosa	GTEx
rs6948685	MEPCE	cis	lymphoblastoid	seeQTL
rs6948685	STAG3L5P	cis	Adipose Subcutaneous	GTEx
rs6948685	STAG3L5P	cis	Stomach	GTEx
rs6948685	PILRB	cis	parietal	SCAN
rs6948685	PILRB	cis	lymphoblastoid	seeQTL
rs6948685	PVRIG2P	cis	Adipose Subcutaneous	GTEx
rs6948685	ORAI2	cis	cerebellum	SCAN
rs6948685	PILRB	cis	cerebellum	SCAN
rs6948685	PILRA	cis	Artery Aorta	GTEx
rs6948685	GATS	cis	parietal	SCAN
rs6948685	PVRIG2P	cis	Artery Tibial	GTEx
rs6948685	PILRB	cis	Artery Tibial	GTEx
rs6948685	PILRA	cis	Adipose Subcutaneous	GTEx
rs6948685	PVRIG2P	cis	Heart Left Ventricle	GTEx
rs6948685	STAG3L5P	cis	Esophagus Muscularis	GTEx
rs6948685	PILRA	cis	Esophagus Mucosa	GTEx
rs6948685	PILRB	cis	Artery Aorta	GTEx
rs6948685	PVRIG	Cis_1M	lymphoblastoid	RTeQTL
rs6948685	PILRB	cis	Thyroid	GTEx
rs6948685	STAG3L5P	cis	Skin Sun Exposed Lower leg	GTEx
rs6948685	PILRA	cis	Skin Sun Exposed Lower leg	GTEx
rs6948685	PILRB	cis	Muscle Skeletal	GTEx
rs6948685	STAG3L5P	cis	Artery Aorta	GTEx
rs6948685	STAG3L5P	cis	Artery Tibial	GTEx
rs6948685	PILRA	cis	Heart Left Ventricle	GTEx
rs6948685	PILRA	cis	parietal	SCAN
rs6948685	PILRA	cis	Stomach	GTEx
rs6948685	PILRA	cis	Muscle Skeletal	GTEx
rs6948685	PILRB	cis	Heart Left Ventricle	GTEx
rs6948685	PILRB	Cis_1M	lymphoblastoid	RTeQTL
rs6948685	STAG3L5P	cis	lung	GTEx
rs6948685	PVRIG2P	cis	Esophagus Muscularis	GTEx

Chromatin state (count:96 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99934000-99977600	Weak transcription	Fetal Brain Male	brain
2	chr7:99940800-100014600	Weak transcription	Right Atrium	heart
3	chr7:99959600-99970200	Weak transcription	HSMM	muscle
4	chr7:99960200-99975400	Weak transcription	Rectal Smooth Muscle	rectum
5	chr7:99960400-99984800	Weak transcription	Pancreas	Pancrea
6	chr7:99960600-99975600	Weak transcription	Brain Angular Gyrus	brain
7	chr7:99960600-99977600	Weak transcription	Colon Smooth Muscle	Colon
8	chr7:99960600-99985200	Weak transcription	Aorta	Aorta
9	chr7:99960800-99971800	Weak transcription	HSMMtube	muscle
10	chr7:99960800-99976600	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr7:99961400-99977400	Weak transcription	Brain Substantia Nigra	brain
12	chr7:99961600-99970400	Weak transcription	Fetal Lung	lung
13	chr7:99961600-99970600	Weak transcription	HepG2	liver
14	chr7:99962000-99970200	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr7:99962200-99970800	Weak transcription	NH-A	brain
16	chr7:99962400-100020600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr7:99962800-99972800	Enhancers	Primary B cells from peripheral blood	blood
18	chr7:99963000-99971400	Enhancers	Primary B cells from cord blood	blood
19	chr7:99964800-99977600	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr7:99965000-99970200	Weak transcription	Primary T helper cells fromperipheralblood	blood
21	chr7:99965200-99976800	Weak transcription	Duodenum Mucosa	Duodenum
22	chr7:99965200-99979200	Weak transcription	Right Ventricle	heart
23	chr7:99966000-99971400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr7:99966000-99974000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
25	chr7:99966400-99998000	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr7:99966600-99972000	Weak transcription	Liver	Liver
27	chr7:99966600-99972800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr7:99966600-99973600	Weak transcription	Ovary	ovary
29	chr7:99966800-99972600	Enhancers	H1 Cell Line	embryonic stem cell
30	chr7:99967000-99970200	Weak transcription	Primary T cells from cord blood	blood
31	chr7:99967000-99971400	Enhancers	Placenta	Placenta
32	chr7:99967000-99972200	Weak transcription	Thymus	Thymus
33	chr7:99967200-99970200	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr7:99967200-99971400	Weak transcription	Brain Cingulate Gyrus	brain
35	chr7:99967200-99971800	Weak transcription	K562	blood
36	chr7:99967400-99970800	Weak transcription	Fetal Intestine Small	intestine
37	chr7:99967400-99974600	Weak transcription	Fetal Brain Female	brain
38	chr7:99967800-99970400	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr7:99967800-99971400	Enhancers	Adipose Nuclei	Adipose
40	chr7:99968000-99970200	Enhancers	Skeletal Muscle Male	skeletal muscle
41	chr7:99968200-99970200	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr7:99968200-99970400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr7:99968400-99970400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
44	chr7:99968400-99971600	Enhancers	Fetal Muscle Trunk	muscle
45	chr7:99968600-99971000	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr7:99969000-99970200	Enhancers	Brain Anterior Caudate	brain
47	chr7:99969000-99970400	Enhancers	Hela-S3	cervix
48	chr7:99969200-99970200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr7:99969200-99970200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr7:99969200-99970400	Enhancers	Dnd41	blood

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