Variant report

Variant	nsv886740
Chromosome Location	chr6:145105354-145199259
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:412)
CpG islands
(count:183)
Chromatin interactive
region (count:27)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

(count:412 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr6:145132292-145132711	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr6:145119111-145119684	A549	lung:	n/a	chr6:145119400-145119409
3	BHLHE40	chr6:145175732-145175742	K562	blood:	n/a	n/a
4	CBX3	chr6:145194870-145195222	K562	blood:	n/a	n/a
5	CBX3	chr6:145141368-145141753	HCT-116	colon:	n/a	n/a
6	CBX3	chr6:145185043-145185284	K562	blood:	n/a	n/a
7	CBX3	chr6:145130120-145131824	HCT-116	colon:	n/a	n/a
8	CBX3	chr6:145118807-145119850	HCT-116	colon:	n/a	n/a
9	CBX3	chr6:145130124-145130868	HCT-116	colon:	n/a	n/a
10	CBX3	chr6:145194787-145195276	HCT-116	colon:	n/a	n/a
11	CCNT2	chr6:145151492-145151607	K562	blood:	n/a	n/a
12	CCNT2	chr6:145118767-145118899	K562	blood:	n/a	n/a
13	CEBPB	chr6:145134355-145134543	HepG2	liver:	n/a	chr6:145134380-145134391
14	CEBPB	chr6:145130319-145130516	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr6:145118734-145120030	HCT-116	colon:	n/a	chr6:145119453-145119464
16	CEBPB	chr6:145129926-145130996	HCT-116	colon:	n/a	n/a
17	CEBPB	chr6:145118851-145119688	Hela-S3	cervix:	n/a	chr6:145119453-145119464
18	CEBPB	chr6:145154751-145154967	HepG2	liver:	n/a	chr6:145154879-145154888
19	CEBPB	chr6:145130118-145130846	HCT-116	colon:	n/a	n/a
20	CEBPB	chr6:145141358-145141857	HCT-116	colon:	n/a	n/a
21	CEBPB	chr6:145107971-145107990	K562	blood:	n/a	n/a
22	CHD1	chr6:145187998-145188049	GM12878	blood:	n/a	n/a
23	CTCF	chr6:145130340-145130490	HMEC	breast:	n/a	chr6:145130427-145130445
24	CTCF	chr6:145130360-145130510	WERI-Rb-1	eye:	n/a	chr6:145130427-145130445
25	CTCF	chr6:145142950-145142967	K562	blood:	n/a	n/a
26	CTCF	chr6:145193513-145193539	LNCaP	prostate:	n/a	n/a
27	CTCF	chr6:145149977-145150028	GM20000	blood:	n/a	n/a
28	CTCF	chr6:145130320-145130470	AG04449	skin:	n/a	chr6:145130427-145130445
29	CTCF	chr6:145108140-145108290	GM12875	blood:	n/a	n/a
30	CTCF	chr6:145130331-145130522	Hela-S3	cervix:	n/a	chr6:145130427-145130445
31	CTCF	chr6:145130360-145130510	HRE	kidney:	n/a	chr6:145130427-145130445
32	CTCF	chr6:145130360-145130510	HEEpiC	esophagus:	n/a	chr6:145130427-145130445
33	CTCF	chr6:145130440-145130590	RPTEC	kidney:	n/a	n/a
34	CTCF	chr6:145130440-145130590	NHEK	skin:	n/a	n/a
35	CTCF	chr6:145130340-145130490	HMF	breast:	n/a	chr6:145130427-145130445
36	CTCF	chr6:145130360-145130510	HRPEpiC	eye:	n/a	chr6:145130427-145130445
37	CTCF	chr6:145130300-145130450	AG10803	skin:	n/a	chr6:145130427-145130445
38	CTCF	chr6:145136581-145136672	Kidney_OC	kidney:	n/a	n/a
39	CTCF	chr6:145130365-145130493	Gliobla	brain:	n/a	chr6:145130427-145130445
40	CTCF	chr6:145130320-145130470	HMEC	breast:	n/a	chr6:145130427-145130445
41	CTCF	chr6:145130320-145130470	SAEC	small airway:	n/a	chr6:145130427-145130445
42	CTCF	chr6:145130300-145130450	RPTEC	kidney:	n/a	chr6:145130427-145130445
43	CUX1	chr6:145194835-145194839	K562	blood:	n/a	n/a
44	CUX1	chr6:145123107-145123114	GM12878	blood:	n/a	n/a
45	CUX1	chr6:145196149-145196225	K562	blood:	n/a	n/a
46	E2F4	chr6:145149491-145149552	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr6:145195309-145195402	MCF10A-Er-Src	breast:	n/a	n/a
48	EBF1	chr6:145138337-145138398	GM12878	blood:	n/a	n/a
49	EBF1	chr6:145178316-145178378	GM12878	blood:	n/a	chr6:145178333-145178344
50	EGR1	chr6:145140894-145141139	K562	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:145165986-145166036	SK-N-MC	brain:	n/a
2	chr6:145168602-145168652	SK-N-SH_RA	brain:	n/a
3	chr6:145165986-145166036	GM12891	blood:	n/a
4	chr6:145168602-145168652	HCM	heart:	n/a
5	chr6:145172144-145172194	K562	blood:	n/a
6	chr6:145168602-145168652	PANC-1	pancreas:	n/a
7	chr6:145172144-145172194	HNPCEpiC	eye:	n/a
8	chr6:145168602-145168652	GM12878	blood:	n/a
9	chr6:145165986-145166036	HRE	kidney:	n/a
10	chr6:145168602-145168652	HIPEpiC	eye:	n/a
11	chr6:145168602-145168652	HRE	kidney:	n/a
12	chr6:145165986-145166036	CMK	blood:	n/a
13	chr6:145165986-145166036	NB4	blood:	n/a
14	chr6:145172144-145172194	HUVEC	blood vessel:	n/a
15	chr6:145165986-145166036	NHDF-neo	bronchial:	n/a
16	chr6:145168602-145168652	BE2_C	brain:	n/a
17	chr6:145168602-145168652	SK-N-SH	brain:	n/a
18	chr6:145165986-145166036	LNCaP	prostate:	n/a
19	chr6:145172144-145172194	HMEC	breast:	n/a
20	chr6:145165986-145166036	HCPEpiC	choroid plexus:	n/a
21	chr6:145165986-145166036	BJ	skin:	n/a
22	chr6:145165986-145166036	NT2-D1	testis:	n/a
23	chr6:145168602-145168652	Hela-S3	cervix:	n/a
24	chr6:145168602-145168652	GM06990	blood:	n/a
25	chr6:145168602-145168652	AG09309	skin:	n/a
26	chr6:145172144-145172194	AG10803	skin:	n/a
27	chr6:145165986-145166036	HRPEpiC	eye:	n/a
28	chr6:145172144-145172194	HAEpiC	amniotic membrane:	n/a
29	chr6:145165986-145166036	RPTEC	kidney:	n/a
30	chr6:145165986-145166036	HRCEpiC	kidney:	n/a
31	chr6:145168602-145168652	LNCaP	prostate:	n/a
32	chr6:145172144-145172194	CMK	blood:	n/a
33	chr6:145172144-145172194	AG09309	skin:	n/a
34	chr6:145172144-145172194	HL-60	blood:	n/a
35	chr6:145172144-145172194	HPAEpiC	pulmonary alveolar:	n/a
36	chr6:145165986-145166036	HIPEpiC	eye:	n/a
37	chr6:145168602-145168652	ProgFib	skin:	n/a
38	chr6:145168602-145168652	HepG2	liver:	n/a
39	chr6:145165986-145166036	SK-N-SH	brain:	n/a
40	chr6:145165986-145166036	NH-A	brain:	n/a
41	chr6:145172144-145172194	AG09319	gingival:	n/a
42	chr6:145172144-145172194	NHDF-neo	bronchial:	n/a
43	chr6:145168602-145168652	IMR90	lung:	fetal
44	chr6:145168602-145168652	PrEC	prostate:	n/a
45	chr6:145168602-145168652	HMEC	breast:	n/a
46	chr6:145165986-145166036	GM19239	blood:	n/a
47	chr6:145168602-145168652	NB4	blood:	n/a
48	chr6:145168602-145168652	HAEpiC	amniotic membrane:	n/a
49	chr6:145168602-145168652	SKMC	muscle:	n/a
50	chr6:145172144-145172194	GM12891	blood:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:145101856..145103538-chr6:145103795..145105406,2	K562	blood:
2	chr6:145177565..145179136-chr6:145179298..145181387,2	MCF-7	breast:
3	chr6:145101184..145102780-chr6:145106740..145108278,2	K562	blood:
4	chr6:145154339..145157220-chr6:145158653..145160590,2	MCF-7	breast:
5	chr6:145131225..145133895-chr6:145136272..145138554,2	K562	blood:
6	chr6:145168696..145171336-chr6:145172610..145175556,2	K562	blood:
7	chr6:145092621..145095309-chr6:145101462..145105366,3	K562	blood:
8	chr6:145120568..145122991-chr6:145140332..145141910,2	K562	blood:
9	chr6:145150089..145150807-chr6:145166846..145167435,2	K562	blood:
10	chr6:145177565..145179136-chr6:145179298..145181387,2	MCF-7	breast:
11	chr6:145164758..145167653-chr6:145170294..145172652,2	K562	blood:
12	chr6:145120568..145122991-chr6:145140332..145141910,2	K562	blood:
13	chr6:145150972..145152508-chr6:145156968..145158659,2	K562	blood:
14	chr6:145166979..145168602-chr6:145169324..145170941,2	MCF-7	breast:
15	chr6:145166979..145168602-chr6:145169324..145170941,2	MCF-7	breast:
16	chr6:145164758..145167653-chr6:145170294..145172652,2	K562	blood:
17	chr6:145141754..145144576-chr6:145155600..145157131,2	K562	blood:
18	chr6:145150089..145150807-chr6:145166846..145167435,2	K562	blood:
19	chr6:145131225..145133895-chr6:145136272..145138554,2	K562	blood:
20	chr6:145195775..145198771-chr6:145199592..145202837,3	K562	blood:
21	chr6:145169081..145170847-chr6:145177041..145178659,2	MCF-7	breast:
22	chr6:145137078..145138640-chr6:145140565..145142974,2	K562	blood:
23	chr3:110022159..110024501-chr6:145141877..145144734,2	MCF-7	breast:
24	chr6:145169081..145170847-chr6:145177041..145178659,2	MCF-7	breast:
25	chr6:145141754..145144576-chr6:145155600..145157131,2	K562	blood:
26	chr6:145137078..145138640-chr6:145140565..145142974,2	K562	blood:
27	chr6:145168696..145171336-chr6:145172610..145175556,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	UTRN	hsa-miR-1	chr6:145172533-145172539
2	UTRN	hsa-miR-206	chr6:145172519-145172540
3	UTRN	hsa-let-7b-5p	chr6:145173717-145173740
4	UTRN	hsa-miR-1	chr6:145172519-145172540
5	UTRN	hsa-let-7b-5p	chr6:145173733-145173740
6	UTRN	hsa-miR-206	chr6:145172533-145172539

Variant related genes	Relation type
UTRN	TF binding region
UTRN	CpG island
ENSG00000152818	chromatin interactions

Extended variants
information (count: 3579 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:3579 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6926377	chr6:145105354-145105355	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs570773382	chr6:145105358-145105359	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs185171083	chr6:145105403-145105404	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs188833701	chr6:145105404-145105405	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs567969752	chr6:145105433-145105434	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs192879981	chr6:145105445-145105446	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs556655512	chr6:145105454-145105455	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs184288632	chr6:145105480-145105481	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs4896745	chr6:145105537-145105538	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs188573029	chr6:145105540-145105541	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs373619017	chr6:145105611-145105612	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs530497997	chr6:145105649-145105650	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs572363508	chr6:145105759-145105760	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs550930439	chr6:145105805-145105806	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs541362705	chr6:145105806-145105807	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs79165904	chr6:145105827-145105828	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs76607868	chr6:145105831-145105832	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs139408104	chr6:145105841-145105842	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs370757618	chr6:145105842-145105843	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs180935562	chr6:145105866-145105867	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs535011400	chr6:145105868-145105869	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs570697756	chr6:145105956-145105957	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs531025923	chr6:145105963-145105964	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs55994018	chr6:145105990-145105991	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs118133898	chr6:145105991-145105992	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs528246504	chr6:145106040-145106041	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs546599920	chr6:145106042-145106043	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs568311199	chr6:145106044-145106045	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs535115922	chr6:145106081-145106082	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs550139722	chr6:145106136-145106137	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs75376047	chr6:145106148-145106149	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs111564013	chr6:145106153-145106154	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs142251769	chr6:145106222-145106223	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs557786623	chr6:145106223-145106224	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs73007419	chr6:145106243-145106244	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs190409097	chr6:145106246-145106247	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs561550956	chr6:145106353-145106354	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs182592477	chr6:145106425-145106426	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs566862481	chr6:145106535-145106536	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs376475528	chr6:145106621-145106622	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs543836584	chr6:145106633-145106634	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs563664378	chr6:145106640-145106641	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs565538503	chr6:145106690-145106691	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs575671499	chr6:145106739-145106740	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs141965394	chr6:145106741-145106742	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs149994031	chr6:145106764-145106765	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs375686066	chr6:145106778-145106779	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs6905730	chr6:145106814-145106815	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs6905731	chr6:145106817-145106818	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs368619423	chr6:145106968-145106969	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1592 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:145040000-145114600	Weak transcription	NHLF	lung
2	chr6:145046000-145122200	Weak transcription	Colonic Mucosa	Colon
3	chr6:145047600-145115000	Weak transcription	Esophagus	oesophagus
4	chr6:145047600-145115000	Weak transcription	Rectal Smooth Muscle	rectum
5	chr6:145066200-145126200	Weak transcription	Stomach Mucosa	stomach
6	chr6:145067800-145115800	Strong transcription	Monocytes-CD14+_RO01746	blood
7	chr6:145068800-145115000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr6:145073200-145105400	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr6:145075000-145108800	Strong transcription	Primary B cells from cord blood	blood
10	chr6:145080000-145115000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr6:145084000-145155800	Weak transcription	Right Ventricle	heart
12	chr6:145085400-145119000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr6:145085800-145134800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr6:145086800-145115000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr6:145087400-145115000	Weak transcription	Gastric	stomach
16	chr6:145089600-145138400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr6:145090000-145136800	Weak transcription	Fetal Heart	heart
18	chr6:145090400-145115000	Weak transcription	Brain Anterior Caudate	brain
19	chr6:145090800-145115400	Weak transcription	Fetal Brain Male	brain
20	chr6:145091000-145107800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr6:145091000-145107800	Weak transcription	Ovary	ovary
22	chr6:145091000-145114400	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr6:145091000-145114400	Weak transcription	NHDF-Ad	bronchial
24	chr6:145091000-145115000	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr6:145091000-145115000	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr6:145091000-145145000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr6:145091200-145117200	Weak transcription	Psoas Muscle	Psoas
28	chr6:145093400-145119800	Weak transcription	Fetal Intestine Small	intestine
29	chr6:145093800-145114800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
30	chr6:145094400-145136800	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr6:145095000-145114800	Weak transcription	Placenta	Placenta
32	chr6:145095000-145119000	Weak transcription	NH-A	brain
33	chr6:145095200-145115400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr6:145095200-145118800	Weak transcription	GM12878-XiMat	blood
35	chr6:145096000-145118600	Weak transcription	Muscle Satellite Cultured Cells	--
36	chr6:145096600-145105400	Weak transcription	Fetal Lung	lung
37	chr6:145096800-145114600	Weak transcription	Stomach Smooth Muscle	stomach
38	chr6:145096800-145114800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
39	chr6:145096800-145118600	Weak transcription	HUVEC	blood vessel
40	chr6:145097200-145114600	Weak transcription	Duodenum Mucosa	Duodenum
41	chr6:145097400-145115000	Weak transcription	Skeletal Muscle Female	skeletal muscle
42	chr6:145097600-145108000	Weak transcription	Fetal Kidney	kidney
43	chr6:145097600-145114800	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr6:145097800-145107600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr6:145097800-145114400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr6:145097800-145114400	Weak transcription	Fetal Muscle Trunk	muscle
47	chr6:145097800-145114600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr6:145097800-145114800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
49	chr6:145097800-145115000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr6:145097800-145115000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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