Variant report

Variant	rs1736921
Chromosome Location	chr6:29696209-29696210
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:35)
CpG islands
(count:0)
Chromatin interactive
region (count:2)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:35 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	NFATC1	chr6:29695785-29699667	GM12878	blood:	n/a	n/a
2	POLR2A	chr6:29695736-29696450	GM12878	blood:	n/a	n/a
3	POLR2A	chr6:29690658-29699867	GM12891	blood:	n/a	n/a
4	POLR2A	chr6:29695149-29697426	GM12891	blood:	n/a	n/a
5	POLR2A	chr6:29695427-29697285	GM15510	blood:	n/a	n/a
6	RUNX3	chr6:29695939-29696399	GM12878	blood:	n/a	n/a
7	PML	chr6:29695415-29699000	GM12878	blood:	n/a	n/a
8	POLR2A	chr6:29695188-29697002	GM12891	blood:	n/a	n/a
9	POLR2A	chr6:29695131-29697353	GM12891	blood:	n/a	n/a
10	POLR2A	chr6:29695163-29699574	GM19099	blood:	n/a	n/a
11	POLR2A	chr6:29694623-29699123	GM12892	blood:	n/a	n/a
12	MTA3	chr6:29695276-29699589	GM12878	blood:	n/a	n/a
13	POLR2A	chr6:29695304-29697234	GM12878	blood:	n/a	n/a
14	POLR2A	chr6:29690785-29699707	GM12878	blood:	n/a	n/a
15	POLR2A	chr6:29695342-29697252	GM19193	blood:	n/a	n/a
16	POLR2A	chr6:29690681-29699847	GM12878	blood:	n/a	n/a
17	POLR2A	chr6:29690708-29699614	GM18505	blood:	n/a	n/a
18	STAT5A	chr6:29695345-29696882	GM12878	blood:	n/a	n/a
19	POLR2A	chr6:29690566-29699452	GM12892	blood:	n/a	n/a
20	NFATC1	chr6:29695654-29699504	GM12878	blood:	n/a	n/a
21	POLR2A	chr6:29696196-29699754	MCF10A-Er-Src	breast:	n/a	n/a
22	POLR2A	chr6:29690657-29697457	GM12892	blood:	n/a	n/a
23	POU2F2	chr6:29695816-29696339	GM12878	blood:	n/a	n/a
24	POLR2A	chr6:29695365-29699302	GM18526	blood:	n/a	n/a
25	POLR2A	chr6:29690618-29699456	GM12892	blood:	n/a	n/a
26	POLR2A	chr6:29690594-29697494	GM12878	blood:	n/a	n/a
27	STAT5A	chr6:29696137-29696873	GM12878	blood:	n/a	n/a
28	POLR2A	chr6:29695198-29698947	GM12891	blood:	n/a	n/a
29	POLR2A	chr6:29695079-29697466	GM12892	blood:	n/a	n/a
30	POLR2A	chr6:29695038-29699514	GM12878	blood:	n/a	n/a
31	POLR2A	chr6:29695318-29696429	GM12878	blood:	n/a	n/a
32	BCLAF1	chr6:29695785-29696868	GM12878	blood:	n/a	n/a
33	POLR2A	chr6:29695270-29699448	GM18951	blood:	n/a	n/a
34	MTA3	chr6:29696073-29696518	GM12878	blood:	n/a	n/a
35	POLR2A	chr6:29695318-29697307	GM12878	blood:	n/a	n/a

No data

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:29691971..29693668-chr6:29693958..29696725,2	K562	blood:
2	chr6:29689319..29693460-chr6:29694038..29698697,5	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MOG-2	chr6:29695734-29697128	NONHSAT108542

No data

Variant related genes	Relation type
HCG4P11	TF binding region
RPL23AP1	TF binding region
ENSG00000225864	Chromatin interaction
ENSG00000204642	Chromatin interaction

Extended variants
information (count: 116 )
Associated
traits (count: 26 )

rSNPs within LD-proxies of this variant (count:105)

rs_ID	r²[population]
rs1059174	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1474610	0.86[EUR][1000 genomes]
rs1610600	0.80[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1610603	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1610604	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1610605	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1610607	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1610613	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1610623	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1610626	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1610627	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1610630	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1610632	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1610727	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1610728	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1610737	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1610738	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1610740	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1611278	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1611279	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1611294	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1611297	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1611300	0.83[EUR][1000 genomes]
rs1611352	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1625607	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1625636	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1626636	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1632447	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1632956	0.95[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1632958	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1632959	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1633025	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1633026	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1633036	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1633038	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1633042	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1633043	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1633045	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1633046	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1633048	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1633049	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1633050	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1633051	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1633052	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1633055	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1633056	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1633057	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1633058	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1633060	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1633061	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1633062	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1633064	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1633069	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1633070	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1633071	0.98[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1633074	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1633076	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1633091	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1736910	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1736911	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1736914	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1736916	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1737022	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1737039	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1737058	0.85[EUR][1000 genomes]
rs1737060	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1737065	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1737066	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1737067	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1737068	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1737070	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1737071	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1737073	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1737074	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1737075	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1737079	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1737081	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1737084	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1737087	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17875375	0.82[AFR][1000 genomes]
rs17875384	0.82[AFR][1000 genomes]
rs17875387	0.82[AFR][1000 genomes]
rs2248693	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2735050	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3117297	0.93[ASN][1000 genomes]
rs3117303	0.93[ASN][1000 genomes]
rs3129081	0.93[ASN][1000 genomes]
rs3130252	0.93[ASN][1000 genomes]
rs3131858	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3131862	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3135050	0.93[ASN][1000 genomes]
rs6933762	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs733840	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs733841	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs909717	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs909723	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs909724	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs909725	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs909726	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs909727	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs909732	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs909735	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9258243	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs932338	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs932341	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv20940	chr6:29653954-29923410	Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
2	nsv428475	chr6:29659525-29763392	Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv428139	chr6:29659525-29892317	Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
4	nsv427749	chr6:29659525-29975144	Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
5	nsv508397	chr6:29663132-29761448	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
6	esv1821077	chr6:29670915-29726207	Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
7	esv1794141	chr6:29670915-29765814	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
8	nsv462673	chr6:29689590-29700183	Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
9	nsv601230	chr6:29689590-29700183	Flanking Active TSS Active TSS Genic enhancers Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
10	nsv883531	chr6:29692562-29705402	Genic enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
11	nsv10809	chr6:29692573-29794119	Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases

mRNA abundance (count:26)

SNP	Gene	Cis/trans	Tissue	Source
rs1736921	HLA-A	cis	Adipose Subcutaneous	GTEx
rs1736921	HCG4P5	cis	Esophagus Mucosa	GTEx
rs1736921	FKSG83	cis	parietal	SCAN
rs1736921	KIT	trans	multi-tissue	Pritchard
rs1736921	HLA-A	cis	Muscle Skeletal	GTEx
rs1736921	ZFP57	cis	lymphoblastoid	seeQTL
rs1736921	HCG4P5	cis	lung	GTEx
rs1736921	HLA-F	cis	multi-tissue	Pritchard
rs1736921	HCG4P5	cis	Muscle Skeletal	GTEx
rs1736921	ZKSCAN4	cis	cerebellum	SCAN
rs1736921	FLJ35429	cis	multi-tissue	Pritchard
rs1736921	HCG4P5	cis	Esophagus Muscularis	GTEx
rs1736921	NDUFS1	trans	multi-tissue	Pritchard
rs1736921	HLA-A	cis	Heart Left Ventricle	GTEx
rs1736921	HCG4P5	cis	Adipose Subcutaneous	GTEx
rs1736921	HLA-A	cis	multi-tissue	Pritchard
rs1736921	HCG4P5	cis	Whole Blood	GTEx
rs1736921	HLA-A	cis	Skin Sun Exposed Lower leg	GTEx
rs1736921	HLA-J	cis	Whole Blood	GTEx
rs1736921	HLA-H	cis	multi-tissue	Pritchard
rs1736921	HLA-A	cis	Whole Blood	GTEx
rs1736921	HCG4P5	cis	Artery Tibial	GTEx
rs1736921	HCG4P5	cis	Heart Left Ventricle	GTEx
rs1736921	HCG4P5	cis	Skin Sun Exposed Lower leg	GTEx
rs1736921	HLA-A	cis	Artery Tibial	GTEx
rs1736921	HCG4P5	cis	Thyroid	GTEx

Chromatin state (count:72 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:29692200-29701800	Weak transcription	HMEC	breast
2	chr6:29692200-29715800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr6:29692400-29715800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr6:29692600-29696400	Genic enhancers	Spleen	Spleen
5	chr6:29692600-29697400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr6:29692800-29712000	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr6:29693200-29711400	Weak transcription	Pancreas	Pancrea
8	chr6:29693400-29697000	Weak transcription	Fetal Thymus	thymus
9	chr6:29693400-29700000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr6:29693400-29715600	Weak transcription	Esophagus	oesophagus
11	chr6:29693600-29696800	Weak transcription	Fetal Intestine Large	intestine
12	chr6:29693600-29697600	Weak transcription	Brain Substantia Nigra	brain
13	chr6:29693600-29715600	Weak transcription	NHLF	lung
14	chr6:29693800-29696400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr6:29693800-29705400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr6:29693800-29715400	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr6:29693800-29716000	Weak transcription	Small Intestine	intestine
18	chr6:29694000-29696400	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
19	chr6:29694000-29696400	Strong transcription	Lung	lung
20	chr6:29694000-29696400	Strong transcription	Sigmoid Colon	Sigmoid Colon
21	chr6:29694000-29696400	Strong transcription	Stomach Smooth Muscle	stomach
22	chr6:29694000-29696600	Genic enhancers	Primary B cells from peripheral blood	blood
23	chr6:29694000-29696600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr6:29694000-29696600	Strong transcription	Brain Anterior Caudate	brain
25	chr6:29694000-29696600	Strong transcription	Rectal Mucosa Donor 29	rectum
26	chr6:29694000-29696800	Strong transcription	Colonic Mucosa	Colon
27	chr6:29694000-29707000	Weak transcription	Rectal Smooth Muscle	rectum
28	chr6:29694000-29711200	Weak transcription	Skeletal Muscle Male	skeletal muscle
29	chr6:29694000-29711400	Weak transcription	Gastric	stomach
30	chr6:29694000-29712200	Weak transcription	Aorta	Aorta
31	chr6:29694000-29715600	Weak transcription	Colon Smooth Muscle	Colon
32	chr6:29694200-29696400	Strong transcription	Primary neutrophils fromperipheralblood	blood
33	chr6:29694200-29696400	Genic enhancers	Primary T helper naive cells from peripheral blood	blood
34	chr6:29694200-29696400	Strong transcription	Duodenum Mucosa	Duodenum
35	chr6:29694200-29696800	Genic enhancers	Primary T cells fromperipheralblood	blood
36	chr6:29694200-29696800	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
37	chr6:29694200-29697000	Weak transcription	Brain Cingulate Gyrus	brain
38	chr6:29694200-29701800	Weak transcription	NHEK	skin
39	chr6:29694200-29705600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr6:29694600-29696800	Strong transcription	Monocytes-CD14+_RO01746	blood
41	chr6:29694600-29697800	Weak transcription	Brain Hippocampus Middle	brain
42	chr6:29694800-29696800	Strong transcription	GM12878-XiMat	blood
43	chr6:29695000-29696400	Strong transcription	Primary T cells from cord blood	blood
44	chr6:29695000-29696400	Genic enhancers	Primary T helper cells fromperipheralblood	blood
45	chr6:29695000-29696600	Strong transcription	Primary B cells from cord blood	blood
46	chr6:29695000-29696800	Genic enhancers	Primary T helper cells PMA-I stimulated	--
47	chr6:29695400-29696800	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
48	chr6:29695600-29696400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr6:29695600-29696400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr6:29695800-29697600	Weak transcription	Fetal Intestine Small	intestine

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