Variant report

Variant	nsv884014
Chromosome Location	chr6:29926082-29939240
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:980)
CpG islands
(count:610)
Chromatin interactive
region (count:22)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:980 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:29931139-29931164	K562	blood:	n/a	n/a
2	ARID3A	chr6:29933748-29934309	K562	blood:	n/a	n/a
3	ARID3A	chr6:29935249-29935871	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:29933775-29934240	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:29934522-29934914	K562	blood:	n/a	n/a
6	ARID3A	chr6:29932290-29932954	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:29937042-29937091	K562	blood:	n/a	n/a
8	ARID3A	chr6:29932477-29933236	K562	blood:	n/a	n/a
9	ARID3A	chr6:29935252-29935904	K562	blood:	n/a	n/a
10	ATF1	chr6:29935286-29935585	K562	blood:	n/a	n/a
11	ATF1	chr6:29932584-29933076	K562	blood:	n/a	n/a
12	ATF2	chr6:29932433-29933091	GM12878	blood:	n/a	n/a
13	ATF2	chr6:29932488-29932978	GM12878	blood:	n/a	n/a
14	ATF3	chr6:29932615-29932943	K562	blood:	n/a	n/a
15	ATF3	chr6:29932539-29933023	K562	blood:	n/a	n/a
16	BACH1	chr6:29932453-29933278	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr6:29932608-29933062	K562	blood:	n/a	n/a
18	BATF	chr6:29932589-29933017	GM12878	blood:	n/a	chr6:29932797-29932808 chr6:29932798-29932808
19	BATF	chr6:29932612-29932987	GM12878	blood:	n/a	chr6:29932797-29932808 chr6:29932798-29932808
20	BCL11A	chr6:29932639-29932881	GM12878	blood:	n/a	chr6:29932797-29932806
21	BCL11A	chr6:29932602-29932969	GM12878	blood:	n/a	chr6:29932797-29932806
22	BCL3	chr6:29932533-29932943	GM12878	blood:	n/a	chr6:29932797-29932806
23	BCLAF1	chr6:29932428-29933119	GM12878	blood:	n/a	chr6:29932797-29932806
24	BCLAF1	chr6:29932494-29933203	GM12878	blood:	n/a	chr6:29932797-29932806
25	BHLHE40	chr6:29932548-29933279	GM12878	blood:	n/a	n/a
26	BHLHE40	chr6:29932569-29933159	K562	blood:	n/a	n/a
27	BHLHE40	chr6:29933714-29934091	HepG2	liver:	n/a	n/a
28	BHLHE40	chr6:29934607-29934610	GM12878	blood:	n/a	n/a
29	BHLHE40	chr6:29933866-29934118	GM12878	blood:	n/a	n/a
30	BHLHE40	chr6:29933686-29934301	K562	blood:	n/a	n/a
31	BHLHE40	chr6:29935166-29935758	K562	blood:	n/a	n/a
32	CBX3	chr6:29935860-29936460	HCT-116	colon:	n/a	n/a
33	CBX3	chr6:29932504-29933475	K562	blood:	n/a	n/a
34	CBX3	chr6:29933685-29934511	HCT-116	colon:	n/a	n/a
35	CBX3	chr6:29935109-29935665	K562	blood:	n/a	n/a
36	CBX3	chr6:29932608-29932997	K562	blood:	n/a	n/a
37	CBX3	chr6:29932403-29933273	HCT-116	colon:	n/a	n/a
38	CBX3	chr6:29935905-29936437	HCT-116	colon:	n/a	n/a
39	CCNT2	chr6:29932623-29932970	K562	blood:	n/a	n/a
40	CCNT2	chr6:29935317-29935569	K562	blood:	n/a	n/a
41	CEBPB	chr6:29932409-29933285	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr6:29932451-29933116	GM12878	blood:	n/a	n/a
43	CEBPB	chr6:29929562-29929884	HepG2	liver:	n/a	n/a
44	CEBPB	chr6:29935138-29935549	K562	blood:	n/a	chr6:29935249-29935260 chr6:29935210-29935221
45	CEBPB	chr6:29934230-29934543	IMR90	lung:	n/a	n/a
46	CEBPB	chr6:29929504-29929848	K562	blood:	n/a	n/a
47	CEBPB	chr6:29932577-29933269	K562	blood:	n/a	n/a
48	CEBPB	chr6:29936002-29936359	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr6:29932426-29933189	K562	blood:	n/a	n/a
50	CEBPB	chr6:29935064-29935418	HepG2	liver:	n/a	chr6:29935249-29935260 chr6:29935210-29935221

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:29932621-29932671	NHBE	bronchial:	n/a
2	chr6:29933697-29933747	HUVEC	blood vessel:	n/a
3	chr6:29928362-29928412	CMK	blood:	n/a
4	chr6:29933915-29933965	NB4	blood:	n/a
5	chr6:29928362-29928412	GM12891	blood:	n/a
6	chr6:29933411-29933461	HL-60	blood:	n/a
7	chr6:29932864-29932914	PFSK-1	brain:	n/a
8	chr6:29933697-29933747	NHDF-neo	bronchial:	n/a
9	chr6:29933411-29933461	HAEpiC	amniotic membrane:	n/a
10	chr6:29933915-29933965	A549	lung:	n/a
11	chr6:29933925-29933975	HRPEpiC	eye:	n/a
12	chr6:29933971-29934021	HRCEpiC	kidney:	n/a
13	chr6:29933697-29933747	HMEC	breast:	n/a
14	chr6:29933411-29933461	HUVEC	blood vessel:	n/a
15	chr6:29932621-29932671	SK-N-MC	brain:	n/a
16	chr6:29933411-29933461	Hepatocyte	liver:	n/a
17	chr6:29933915-29933965	SK-N-SH	brain:	n/a
18	chr6:29933971-29934021	ECC-1	luminal epithelium:	n/a
19	chr6:29933511-29933561	K562	blood:	n/a
20	chr6:29932621-29932671	K562	blood:	n/a
21	chr6:29928362-29928412	HUVEC	blood vessel:	n/a
22	chr6:29933971-29934021	HCT-116	colon:	n/a
23	chr6:29933511-29933561	HRPEpiC	eye:	n/a
24	chr6:29932743-29932793	NHDF-neo	bronchial:	n/a
25	chr6:29933915-29933965	HNPCEpiC	eye:	n/a
26	chr6:29932621-29932671	HCPEpiC	choroid plexus:	n/a
27	chr6:29928362-29928412	ovcar-3	ovarian:	n/a
28	chr6:29933697-29933747	RPTEC	kidney:	n/a
29	chr6:29928362-29928412	AG04449	skin:	fetal
30	chr6:29932864-29932914	T-47D	breast:	n/a
31	chr6:29928362-29928412	AG09319	gingival:	n/a
32	chr6:29933697-29933747	HIPEpiC	eye:	n/a
33	chr6:29933411-29933461	AG04450	lung:	fetal
34	chr6:29933925-29933975	A549	lung:	n/a
35	chr6:29933925-29933975	HRE	kidney:	n/a
36	chr6:29933925-29933975	T-47D	breast:	n/a
37	chr6:29933697-29933747	AG04449	skin:	fetal
38	chr6:29932621-29932671	PANC-1	pancreas:	n/a
39	chr6:29933511-29933561	SKMC	muscle:	n/a
40	chr6:29928362-29928412	HEK293	kidney:	embryo
41	chr6:29933971-29934021	MCF10A-Er-Src	breast:	n/a
42	chr6:29933971-29934021	IMR90	lung:	fetal
43	chr6:29932864-29932914	U87	brain:	n/a
44	chr6:29932621-29932671	ProgFib	skin:	n/a
45	chr6:29933511-29933561	CMK	blood:	n/a
46	chr6:29932621-29932671	AG04449	skin:	fetal
47	chr6:29933915-29933965	HUVEC	blood vessel:	n/a
48	chr6:29933697-29933747	PrEC	prostate:	n/a
49	chr6:29932864-29932914	HL-60	blood:	n/a
50	chr6:29933971-29934021	AG04450	lung:	fetal

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:29937339..29939716-chr6:29942275..29944965,3	MCF-7	breast:
2	chr6:29937696..29939359-chr6:30032545..30034517,2	K562	blood:
3	chr6:29921960..29924230-chr6:29934596..29936833,2	K562	blood:
4	chr6:29815528..29816550-chr6:29935117..29936165,4	MCF-7	breast:
5	chr14:77247003..77248532-chr6:29931290..29933642,2	K562	blood:
6	chr6:29820786..29821478-chr6:29935191..29935715,2	MCF-7	breast:
7	chr6:29931492..29933251-chr6:30034694..30036479,2	K562	blood:
8	chr6:29926306..29930004-chr6:29943804..29947247,3	K562	blood:
9	chr6:29931972..29934794-chr6:30027595..30029471,2	K562	blood:
10	chr6:29920527..29922060-chr6:29926055..29928693,2	K562	blood:
11	chr6:29820931..29821695-chr6:29935492..29936150,2	MCF-7	breast:
12	chr6:29927397..29931336-chr6:29932208..29936273,8	K562	blood:
13	chr6:29932263..29935141-chr6:29936079..29939709,3	K562	blood:
14	chr6:29917413..29919975-chr6:29932108..29934788,2	K562	blood:
15	chr6:29927397..29931336-chr6:29932208..29936273,8	K562	blood:
16	chr6:29931653..29934276-chr6:29943760..29946372,5	K562	blood:
17	chr6:29937399..29939324-chr6:29949163..29951713,2	K562	blood:
18	chr6:29929604..29934270-chr6:29942846..29948120,6	K562	blood:
19	chr6:29933916..29936718-chr6:29943405..29945040,3	MCF-7	breast:
20	chr6:29920547..29922811-chr6:29925895..29928597,2	MCF-7	breast:
21	chr6:29932263..29935141-chr6:29936079..29939709,3	K562	blood:
22	chr6:29892582..29894711-chr6:29932418..29935205,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNF39-8	chr6:29938578-29938853	NONHSAT108570

No data

Variant related genes	Relation type
HCG9	TF binding region
HCG9	CpG island
ENSG00000259081	chromatin interactions
ENSG00000204619	chromatin interactions
ENSG00000230795	chromatin interactions
ENSG00000204625	chromatin interactions
ENSG00000066379	chromatin interactions
ENSG00000204623	chromatin interactions

Extended variants
information (count: 726 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:726 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370067006	chr6:29926091-29926092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs373072087	chr6:29926098-29926099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs376310256	chr6:29926101-29926102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs2571397	chr6:29926128-29926129	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs541426250	chr6:29926135-29926136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs9260676	chr6:29926139-29926140	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs191203180	chr6:29926142-29926143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs575021985	chr6:29926172-29926173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs6918953	chr6:29926182-29926183	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs2735086	chr6:29926192-29926193	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs199654139	chr6:29926193-29926194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs117421600	chr6:29926216-29926217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs72848163	chr6:29926222-29926223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs201184985	chr6:29926227-29926228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs77156021	chr6:29926234-29926235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs111557534	chr6:29926257-29926258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs386698627	chr6:29926267-29926268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs182530920	chr6:29926272-29926273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs149058366	chr6:29926284-29926285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs551067274	chr6:29926285-29926286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs2975040	chr6:29926295-29926296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs11267511	chr6:29926301-29926302	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs35102653	chr6:29926302-29926303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs375927576	chr6:29926303-29926304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs187925905	chr6:29926366-29926367	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs9260679	chr6:29926377-29926378	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs2975039	chr6:29926379-29926380	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs115200927	chr6:29926389-29926390	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
29	rs556134818	chr6:29926402-29926403	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs142127475	chr6:29926404-29926405	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs151190807	chr6:29926409-29926410	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs115280716	chr6:29926415-29926416	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
33	rs140259909	chr6:29926439-29926440	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs2905760	chr6:29926461-29926462	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs190843316	chr6:29926473-29926474	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs9260682	chr6:29926476-29926477	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs9260683	chr6:29926487-29926488	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs183108659	chr6:29926493-29926494	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs570034721	chr6:29926547-29926548	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs114600011	chr6:29926549-29926550	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs113741702	chr6:29926573-29926574	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs564735932	chr6:29926594-29926595	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs1632994	chr6:29926597-29926598	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs187401847	chr6:29926613-29926614	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs533976254	chr6:29926618-29926619	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs9260684	chr6:29926654-29926655	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs9260685	chr6:29926668-29926669	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs192872777	chr6:29926684-29926685	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs9260686	chr6:29926696-29926697	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs552014129	chr6:29926750-29926751	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:112)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571809	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Breast cancer	21509527	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:700 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:29913400-29932200	Weak transcription	Brain Anterior Caudate	brain
2	chr6:29913400-29932600	Weak transcription	Brain Substantia Nigra	brain
3	chr6:29913800-29932200	Weak transcription	Small Intestine	intestine
4	chr6:29914000-29932200	Weak transcription	Colon Smooth Muscle	Colon
5	chr6:29914600-29932200	Weak transcription	Colonic Mucosa	Colon
6	chr6:29914800-29932200	Weak transcription	Right Ventricle	heart
7	chr6:29915400-29931800	Weak transcription	Fetal Thymus	thymus
8	chr6:29915600-29932000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr6:29916400-29926400	Weak transcription	GM12878-XiMat	blood
10	chr6:29916800-29928200	Weak transcription	HepG2	liver
11	chr6:29916800-29930000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr6:29916800-29932200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr6:29916800-29932200	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr6:29916800-29932200	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr6:29916800-29933000	Weak transcription	Esophagus	oesophagus
16	chr6:29916800-29933000	Weak transcription	Pancreas	Pancrea
17	chr6:29916800-29933200	Weak transcription	Lung	lung
18	chr6:29916800-29940200	Weak transcription	Gastric	stomach
19	chr6:29917000-29926800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr6:29917000-29931800	Weak transcription	Primary T helper cells fromperipheralblood	blood
21	chr6:29917200-29932000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr6:29917200-29932200	Weak transcription	Liver	Liver
23	chr6:29917200-29932200	Weak transcription	Brain Hippocampus Middle	brain
24	chr6:29917400-29927400	Weak transcription	Fetal Muscle Leg	muscle
25	chr6:29917800-29926400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr6:29917800-29932200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr6:29918000-29926600	Weak transcription	Primary B cells from peripheral blood	blood
28	chr6:29918000-29926600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr6:29918000-29932000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
30	chr6:29918000-29932200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr6:29918000-29932200	Weak transcription	Fetal Intestine Small	intestine
32	chr6:29918200-29926600	Weak transcription	Primary monocytes fromperipheralblood	blood
33	chr6:29918200-29931800	Weak transcription	Primary T cells from cord blood	blood
34	chr6:29918400-29927400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr6:29919000-29926800	Weak transcription	Primary B cells from cord blood	blood
36	chr6:29920400-29932200	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr6:29921800-29929400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr6:29921800-29929600	Weak transcription	Psoas Muscle	Psoas
39	chr6:29921800-29932200	Weak transcription	Skeletal Muscle Male	skeletal muscle
40	chr6:29922000-29929600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr6:29922400-29927600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr6:29924600-29932200	Weak transcription	Left Ventricle	heart
43	chr6:29924600-29932200	Weak transcription	Right Atrium	heart
44	chr6:29924800-29932200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr6:29924800-29933000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr6:29925600-29926400	Enhancers	Primary neutrophils fromperipheralblood	blood
47	chr6:29926000-29926200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr6:29926000-29926200	Enhancers	Skeletal Muscle Female	skeletal muscle
49	chr6:29926000-29926200	Enhancers	K562	blood
50	chr6:29926000-29926400	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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