Variant report

Variant	nsv885819
Chromosome Location	chr6:38148770-38190439
allele	n/a
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	ATF2	chr6:38187181-38187476	GM12878	blood:	n/a	n/a
2	ATF2	chr6:38187191-38187584	GM12878	blood:	n/a	n/a
3	BCL3	chr6:38182843-38183146	GM12878	blood:	n/a	n/a
4	BCL3	chr6:38183148-38183468	GM12878	blood:	n/a	n/a
5	BHLHE40	chr6:38185658-38185991	K562	blood:	n/a	chr6:38185822-38185835 chr6:38185818-38185839 chr6:38185824-38185833 chr6:38185825-38185834 chr6:38185823-38185832 chr6:38185824-38185833
6	BHLHE40	chr6:38183744-38184107	GM12878	blood:	n/a	chr6:38183964-38183973 chr6:38183964-38183973
7	BHLHE40	chr6:38155175-38155515	K562	blood:	n/a	n/a
8	CBX3	chr6:38165961-38166281	K562	blood:	n/a	n/a
9	CEBPB	chr6:38188342-38188650	HepG2	liver:	n/a	chr6:38188484-38188493 chr6:38188482-38188495 chr6:38188483-38188494
10	CEBPB	chr6:38181652-38181828	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr6:38187213-38187510	HepG2	liver:	n/a	chr6:38187371-38187382
12	CEBPB	chr6:38188350-38188588	H1-hESC	embryonic stem cell:	n/a	chr6:38188484-38188493 chr6:38188482-38188495 chr6:38188483-38188494
13	CEBPB	chr6:38181657-38181842	K562	blood:	n/a	n/a
14	CEBPB	chr6:38187234-38187503	IMR90	lung:	n/a	chr6:38187371-38187382
15	CEBPB	chr6:38181640-38181846	HepG2	liver:	n/a	n/a
16	CEBPB	chr6:38188354-38188606	K562	blood:	n/a	chr6:38188484-38188493 chr6:38188482-38188495 chr6:38188483-38188494
17	CEBPB	chr6:38181639-38181839	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr6:38187222-38187487	A549	lung:	n/a	chr6:38187371-38187382
19	CREB1	chr6:38180253-38180773	HepG2	liver:	n/a	chr6:38180506-38180519
20	CREB1	chr6:38187202-38187628	GM12878	blood:	n/a	n/a
21	CREB1	chr6:38187183-38187573	GM12878	blood:	n/a	n/a
22	CREB1	chr6:38180347-38180647	H1-hESC	embryonic stem cell:	n/a	chr6:38180506-38180519
23	CTCF	chr6:38155214-38155310	MCF-7	breast:	n/a	chr6:38155257-38155265 chr6:38155252-38155270
24	CTCF	chr6:38165921-38166400	K562	blood:	n/a	chr6:38166094-38166107
25	CTCF	chr6:38175247-38175310	ProgFib	skin:	n/a	n/a
26	CTCF	chr6:38167825-38168110	GM12878	blood:	n/a	n/a
27	CTCF	chr6:38155180-38155330	HA-sp	spinal cord:	n/a	chr6:38155257-38155265 chr6:38155252-38155270
28	CTCF	chr6:38155160-38155310	WERI-Rb-1	eye:	n/a	chr6:38155257-38155265 chr6:38155252-38155270
29	CTCF	chr6:38155113-38155431	K562	blood:	n/a	chr6:38155257-38155265 chr6:38155252-38155270
30	CTCF	chr6:38166040-38166190	WERI-Rb-1	eye:	n/a	chr6:38166094-38166107
31	CTCF	chr6:38166040-38166181	MCF-7	breast:	n/a	chr6:38166094-38166107
32	CTCF	chr6:38167877-38168048	MCF-7	breast:	n/a	n/a
33	CTCF	chr6:38166020-38166170	SK-N-SH_RA	brain:	n/a	chr6:38166094-38166107
34	CTCF	chr6:38165966-38166261	K562	blood:	n/a	chr6:38166094-38166107
35	CTCF	chr6:38165922-38166251	K562	blood:	n/a	chr6:38166094-38166107
36	CTCF	chr6:38167924-38168034	HepG2	liver:	n/a	n/a
37	CTCF	chr6:38167871-38168026	MCF-7	breast:	n/a	n/a
38	CTCF	chr6:38155213-38155263	A549	lung:	n/a	n/a
39	CTCF	chr6:38155200-38155350	AG04449	skin:	n/a	chr6:38155257-38155265 chr6:38155252-38155270
40	CTCF	chr6:38166052-38166167	H1-hESC	embryonic stem cell:	n/a	chr6:38166094-38166107
41	CTCF	chr6:38155213-38155338	HepG2	liver:	n/a	chr6:38155257-38155265 chr6:38155252-38155270
42	CTCF	chr6:38166080-38166230	BE2_C	brain:	n/a	chr6:38166094-38166107
43	CTCF	chr6:38167851-38167991	MCF-7	breast:	n/a	n/a
44	CTCF	chr6:38155220-38155370	BE2_C	brain:	n/a	chr6:38155257-38155265 chr6:38155252-38155270
45	CTCF	chr6:38165960-38166110	HMEC	breast:	n/a	chr6:38166094-38166107
46	CTCF	chr6:38167877-38167996	MCF-7	breast:	n/a	n/a
47	CTCF	chr6:38155100-38155250	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr6:38167864-38167958	GM19239	blood:	n/a	n/a
49	CTCF	chr6:38155140-38155290	K562	blood:	n/a	chr6:38155257-38155265 chr6:38155252-38155270
50	CTCF	chr6:38165980-38166130	Caco-2	colon:	n/a	chr6:38166094-38166107

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:38160321-38160371	MCF-7	breast:	n/a
2	chr6:38180047-38180097	T-47D	breast:	n/a
3	chr6:38180047-38180097	K562	blood:	n/a
4	chr6:38180047-38180097	RPTEC	kidney:	n/a
5	chr6:38180047-38180097	NT2-D1	testis:	n/a
6	chr6:38180047-38180097	GM12891	blood:	n/a
7	chr6:38160321-38160371	ECC-1	luminal epithelium:	n/a
8	chr6:38160321-38160371	AG04450	lung:	fetal
9	chr6:38180047-38180097	HMEC	breast:	n/a
10	chr6:38160321-38160371	HCF	heart:	n/a
11	chr6:38160321-38160371	HUVEC	blood vessel:	n/a
12	chr6:38180047-38180097	A549	lung:	n/a
13	chr6:38160321-38160371	BE2_C	brain:	n/a
14	chr6:38160321-38160371	K562	blood:	n/a
15	chr6:38160321-38160371	HEEpiC	esophagus:	n/a
16	chr6:38180047-38180097	SK-N-SH	brain:	n/a
17	chr6:38180047-38180097	HepG2	liver:	n/a
18	chr6:38180047-38180097	ovcar-3	ovarian:	n/a
19	chr6:38180047-38180097	MCF10A-Er-Src	breast:	n/a
20	chr6:38180047-38180097	GM12878	blood:	n/a
21	chr6:38160321-38160371	Hepatocyte	liver:	n/a
22	chr6:38160321-38160371	NT2-D1	testis:	n/a
23	chr6:38180047-38180097	Hepatocyte	liver:	n/a
24	chr6:38180047-38180097	GM19239	blood:	n/a
25	chr6:38160321-38160371	GM12891	blood:	n/a
26	chr6:38160321-38160371	HCM	heart:	n/a
27	chr6:38180047-38180097	ECC-1	luminal epithelium:	n/a
28	chr6:38160321-38160371	HL-60	blood:	n/a
29	chr6:38180047-38180097	NH-A	brain:	n/a
30	chr6:38160321-38160371	AoSMC	blood vessel:	n/a
31	chr6:38180047-38180097	HRE	kidney:	n/a
32	chr6:38160321-38160371	HRE	kidney:	n/a
33	chr6:38180047-38180097	Jurkat	blood:	n/a
34	chr6:38180047-38180097	Hela-S3	cervix:	n/a
35	chr6:38160321-38160371	ovcar-3	ovarian:	n/a
36	chr6:38160321-38160371	CMK	blood:	n/a
37	chr6:38180047-38180097	HCF	heart:	n/a
38	chr6:38160321-38160371	NHBE	bronchial:	n/a
39	chr6:38160321-38160371	HPAEpiC	pulmonary alveolar:	n/a
40	chr6:38180047-38180097	HCPEpiC	choroid plexus:	n/a
41	chr6:38160321-38160371	HEK293	kidney:	embryo
42	chr6:38180047-38180097	HPAEpiC	pulmonary alveolar:	n/a
43	chr6:38180047-38180097	HNPCEpiC	eye:	n/a
44	chr6:38160321-38160371	BJ	skin:	n/a
45	chr6:38160321-38160371	Jurkat	blood:	n/a
46	chr6:38160321-38160371	ProgFib	skin:	n/a
47	chr6:38180047-38180097	BE2_C	brain:	n/a
48	chr6:38160321-38160371	MCF10A-Er-Src	breast:	n/a
49	chr6:38180047-38180097	AG04450	lung:	fetal
50	chr6:38180047-38180097	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:38138513..38140843-chr6:38152378..38154915,2	K562	blood:
2	chr6:38116607..38119118-chr6:38160290..38163067,2	K562	blood:
3	chr6:38163651..38165832-chr6:38213347..38216236,2	K562	blood:
4	chr6:38143259..38145952-chr6:38146356..38150615,4	K562	blood:
5	chr6:38178185..38180709-chr6:38183811..38185746,2	K562	blood:
6	chr6:38178185..38180709-chr6:38183811..38185746,2	K562	blood:
7	chr6:38143298..38146088-chr6:38153690..38155707,2	K562	blood:
8	chr6:38158880..38161557-chr6:38164282..38166120,2	K562	blood:
9	chr6:38148276..38150715-chr6:38151734..38153951,2	K562	blood:
10	chr6:38184010..38186134-chr6:38187890..38189397,2	K562	blood:
11	chr17:18793387..18794889-chr6:38147135..38149735,2	MCF-7	breast:
12	chr6:38185221..38187351-chr6:38192774..38196279,3	K562	blood:
13	chr6:38149475..38152864-chr6:38153550..38156647,3	K562	blood:
14	chr6:38149475..38152864-chr6:38153550..38156647,3	K562	blood:
15	chr6:38144288..38145943-chr6:38150370..38152832,2	MCF-7	breast:
16	chr6:38147181..38149521-chr6:38161439..38163786,2	K562	blood:
17	chr6:38150165..38152745-chr6:38153295..38155930,2	MCF-7	breast:
18	chr6:38188305..38192389-chr6:38192840..38195857,4	K562	blood:
19	chr6:38147181..38149521-chr6:38161439..38163786,2	K562	blood:
20	chr6:38148276..38150715-chr6:38151734..38153951,2	K562	blood:
21	chr6:38158880..38161557-chr6:38164282..38166120,2	K562	blood:
22	chr6:38150165..38152745-chr6:38153295..38155930,2	MCF-7	breast:
23	chr6:38184010..38186134-chr6:38187890..38189397,2	K562	blood:
24	chr6:38165196..38166057-chr6:38246936..38247494,2	MCF-7	breast:
25	chr6:38189033..38190926-chr6:38201361..38202956,2	K562	blood:

Variant related genes	Relation type
ENSG00000200706	TF binding region
ENSG00000200706	CpG island

Extended variants
information (count: 1530 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1530 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2235711	chr6:38148770-38148771	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs145880431	chr6:38148773-38148774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs555239925	chr6:38148784-38148785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs569387204	chr6:38148895-38148896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs567678431	chr6:38148908-38148909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs538299587	chr6:38148909-38148910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs190369834	chr6:38148939-38148940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs578104488	chr6:38148983-38148984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs533930920	chr6:38148999-38149000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs570174238	chr6:38149031-38149032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs143080487	chr6:38149081-38149082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574229460	chr6:38149107-38149108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs2235710	chr6:38149238-38149239	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs577202520	chr6:38149247-38149248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs575000431	chr6:38149465-38149466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs543952053	chr6:38149538-38149539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs4314486	chr6:38149539-38149540	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs182785521	chr6:38149579-38149580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs560422201	chr6:38149642-38149643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs80293182	chr6:38149687-38149688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs529138890	chr6:38149712-38149713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs371131086	chr6:38149718-38149719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs549168072	chr6:38149747-38149748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs144948064	chr6:38149750-38149751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs71835036	chr6:38149767-38149768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs56722679	chr6:38149770-38149771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs187763990	chr6:38149835-38149836	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs374314898	chr6:38149837-38149838	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs551943936	chr6:38149853-38149854	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs547147988	chr6:38149892-38149893	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs571753261	chr6:38149975-38149976	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs148299794	chr6:38149984-38149985	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs553852866	chr6:38150079-38150080	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs574286029	chr6:38150142-38150143	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs141467000	chr6:38150155-38150156	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs73734342	chr6:38150162-38150163	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs546298914	chr6:38150183-38150184	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs199854541	chr6:38150204-38150205	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs115562400	chr6:38150228-38150229	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs117411729	chr6:38150257-38150258	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs10947716	chr6:38150323-38150324	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs577638690	chr6:38150375-38150376	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs62397003	chr6:38150378-38150379	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs559850695	chr6:38150385-38150386	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs150862282	chr6:38150407-38150408	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549342507	chr6:38150425-38150426	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs12664507	chr6:38150437-38150438	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs568167902	chr6:38150443-38150444	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs562760725	chr6:38150445-38150446	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs531570580	chr6:38150448-38150449	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
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
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	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
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Osteosarcoma	16790693	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Lung cancer	19153074	CNVD
Ovarian cancer	21720365	CNVD
Melanoma	21693616	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Breast cancer	16397240	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
abnormal development	18461090	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:701 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:38121000-38159600	Weak transcription	Primary T cells fromperipheralblood	blood
2	chr6:38121800-38153600	Weak transcription	Primary B cells from peripheral blood	blood
3	chr6:38123200-38153200	Weak transcription	Primary T helper cells fromperipheralblood	blood
4	chr6:38123400-38155400	Weak transcription	Aorta	Aorta
5	chr6:38123400-38157000	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr6:38123400-38176800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr6:38123600-38153000	Weak transcription	Primary B cells from cord blood	blood
8	chr6:38123800-38151200	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr6:38124000-38152200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr6:38124200-38151800	Weak transcription	Brain Anterior Caudate	brain
11	chr6:38131800-38167800	Weak transcription	Right Atrium	heart
12	chr6:38133600-38160400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr6:38133600-38164000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr6:38136000-38159800	Weak transcription	Primary T helper cells PMA-I stimulated	--
15	chr6:38136800-38156000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr6:38138600-38169400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr6:38141200-38152400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr6:38141600-38166200	Weak transcription	Left Ventricle	heart
19	chr6:38141800-38168000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr6:38142000-38150200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr6:38142200-38155400	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr6:38142400-38153000	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr6:38142800-38162000	Weak transcription	Adipose Nuclei	Adipose
24	chr6:38143200-38159200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr6:38143200-38161200	Weak transcription	Placenta	Placenta
26	chr6:38143600-38162400	Weak transcription	Right Ventricle	heart
27	chr6:38143600-38177200	Weak transcription	Ovary	ovary
28	chr6:38143800-38149800	Weak transcription	Primary T cells from cord blood	blood
29	chr6:38144000-38151600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr6:38144000-38159200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr6:38144000-38161400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr6:38144000-38161400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
33	chr6:38144000-38161600	Weak transcription	Thymus	Thymus
34	chr6:38144200-38155600	Weak transcription	Spleen	Spleen
35	chr6:38144600-38151800	Weak transcription	Stomach Smooth Muscle	stomach
36	chr6:38145000-38151800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr6:38145200-38155600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr6:38145200-38156400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr6:38145200-38163400	Weak transcription	Colonic Mucosa	Colon
40	chr6:38145600-38155000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
41	chr6:38145600-38155200	Weak transcription	Fetal Muscle Leg	muscle
42	chr6:38145800-38152000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr6:38145800-38154600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr6:38145800-38159600	Weak transcription	Fetal Intestine Large	intestine
45	chr6:38145800-38159800	Weak transcription	Liver	Liver
46	chr6:38146000-38150200	Weak transcription	Fetal Intestine Small	intestine
47	chr6:38146000-38151400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr6:38146000-38162400	Weak transcription	Pancreas	Pancrea
49	chr6:38146200-38155000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr6:38146400-38151400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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