Variant report

Variant	nsv981205
Chromosome Location	chr6:166748596-166751156
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:154)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:154 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:166749131-166749929	GM12878	blood:	n/a	n/a
2	ATF2	chr6:166749059-166750047	GM12878	blood:	n/a	n/a
3	BATF	chr6:166749111-166749557	GM12878	blood:	n/a	n/a
4	BATF	chr6:166748460-166748786	GM12878	blood:	n/a	n/a
5	BCL11A	chr6:166749243-166749802	GM12878	blood:	n/a	n/a
6	BCL3	chr6:166749131-166749642	GM12878	blood:	n/a	n/a
7	BCLAF1	chr6:166749009-166749797	GM12878	blood:	n/a	n/a
8	BCLAF1	chr6:166749004-166749819	GM12878	blood:	n/a	n/a
9	BHLHE40	chr6:166750489-166750668	GM12878	blood:	n/a	n/a
10	BHLHE40	chr6:166749021-166749933	GM12878	blood:	n/a	n/a
11	BRCA1	chr6:166750699-166750766	GM12878	blood:	n/a	n/a
12	CEBPB	chr6:166748984-166750300	GM12878	blood:	n/a	n/a
13	CHD2	chr6:166748632-166748757	K562	blood:	n/a	n/a
14	CHD2	chr6:166750528-166750890	GM12878	blood:	n/a	n/a
15	CUX1	chr6:166750535-166750553	GM12878	blood:	n/a	n/a
16	EBF1	chr6:166750353-166750904	GM12878	blood:	n/a	chr6:166750607-166750618
17	EBF1	chr6:166748924-166749860	GM12878	blood:	n/a	n/a
18	EBF1	chr6:166750388-166750689	GM12878	blood:	n/a	chr6:166750607-166750618
19	EBF1	chr6:166749080-166749477	GM12878	blood:	n/a	n/a
20	EBF1	chr6:166749162-166749459	GM12878	blood:	n/a	n/a
21	EBF1	chr6:166751145-166751331	GM12878	blood:	n/a	n/a
22	EBF1	chr6:166750384-166750736	GM12878	blood:	n/a	chr6:166750607-166750618
23	EP300	chr6:166750748-166750766	GM12878	blood:	n/a	n/a
24	EP300	chr6:166749196-166749973	GM12878	blood:	n/a	n/a
25	EP300	chr6:166750076-166750088	GM12878	blood:	n/a	n/a
26	EP300	chr6:166750717-166750780	GM12878	blood:	n/a	n/a
27	EP300	chr6:166749284-166749848	GM12878	blood:	n/a	n/a
28	FOXM1	chr6:166749055-166750253	GM12878	blood:	n/a	n/a
29	FOXM1	chr6:166748789-166749960	GM12878	blood:	n/a	n/a
30	IRF1	chr6:166751132-166751236	K562	blood:	n/a	n/a
31	MAFF	chr6:166748923-166749234	HepG2	liver:	n/a	n/a
32	MAFK	chr6:166748944-166749192	IMR90	lung:	n/a	n/a
33	MAFK	chr6:166751067-166751255	HepG2	liver:	n/a	n/a
34	MAFK	chr6:166751065-166751303	HepG2	liver:	n/a	n/a
35	MAFK	chr6:166748957-166749219	HepG2	liver:	n/a	n/a
36	MAFK	chr6:166748918-166749216	HepG2	liver:	n/a	n/a
37	MAX	chr6:166749047-166749674	GM12878	blood:	n/a	chr6:166749213-166749222
38	MEF2A	chr6:166749133-166749656	GM12878	blood:	n/a	chr6:166749427-166749444
39	MEF2C	chr6:166749141-166749728	GM12878	blood:	n/a	chr6:166749427-166749444
40	MTA3	chr6:166746591-166750124	GM12878	blood:	n/a	n/a
41	MXI1	chr6:166749318-166749794	GM12878	blood:	n/a	n/a
42	NFATC1	chr6:166749027-166749948	GM12878	blood:	n/a	n/a
43	NFATC1	chr6:166748961-166749951	GM12878	blood:	n/a	n/a
44	NFATC1	chr6:166750881-166751602	GM12878	blood:	n/a	n/a
45	NFATC1	chr6:166746279-166748938	GM12878	blood:	n/a	n/a
46	NFATC1	chr6:166748037-166748947	GM12878	blood:	n/a	n/a
47	NFIC	chr6:166749103-166749862	GM12878	blood:	n/a	n/a
48	NFIC	chr6:166748979-166750359	GM12878	blood:	n/a	n/a
49	PAX5	chr6:166749153-166749432	GM12878	blood:	n/a	n/a
50	PBX3	chr6:166748378-166748600	GM12878	blood:	n/a	n/a

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:166748322..166751240-chr6:166751244..166753150,2	MCF-7	breast:
2	chr6:166743072..166748840-chr6:166793771..166798653,8	K562	blood:
3	chr6:166748234..166750279-chr6:166754280..166756518,2	MCF-7	breast:
4	chr6:166751051..166752685-chr6:166755340..166756896,2	MCF-7	breast:
5	chr6:166750967..166754365-chr6:166755785..166758738,3	MCF-7	breast:
6	chr6:166750705..166753304-chr6:166793796..166795469,2	K562	blood:
7	chr6:166698710..166701539-chr6:166750702..166753192,3	K562	blood:

No data

Variant related genes	Relation type
SFT2D1	TF binding region
ENSG00000198818	chromatin interactions
ENSG00000261420	chromatin interactions
ENSG00000060762	chromatin interactions

Extended variants
information (count: 102 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:102 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10455976	chr6:166748622-166748623	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs552681597	chr6:166748684-166748685	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs114719390	chr6:166748708-166748709	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs557688253	chr6:166748716-166748717	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs572664952	chr6:166748749-166748750	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs146174189	chr6:166748763-166748764	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs555417730	chr6:166748770-166748771	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs377436372	chr6:166748823-166748824	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs562916965	chr6:166748840-166748841	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs145591756	chr6:166748914-166748915	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs545345908	chr6:166748943-166748944	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs115721809	chr6:166748983-166748984	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs148901697	chr6:166749016-166749017	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs527873724	chr6:166749030-166749031	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs546747933	chr6:166749108-166749109	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs190058423	chr6:166749139-166749140	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs528926262	chr6:166749169-166749170	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs181009166	chr6:166749182-166749183	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs114264023	chr6:166749204-166749205	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs538112839	chr6:166749222-166749223	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs117678306	chr6:166749247-166749248	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs566355774	chr6:166749260-166749261	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs533733511	chr6:166749267-166749268	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs555481369	chr6:166749268-166749269	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs184987593	chr6:166749270-166749271	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs544648065	chr6:166749288-166749289	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs192430288	chr6:166749289-166749290	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs577936312	chr6:166749321-166749322	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs545414065	chr6:166749344-166749345	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs560747762	chr6:166749363-166749364	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs183699350	chr6:166749376-166749377	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs543236865	chr6:166749390-166749391	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs561429676	chr6:166749391-166749392	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs528998795	chr6:166749410-166749411	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs188740294	chr6:166749430-166749431	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs562377220	chr6:166749567-166749568	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs532917891	chr6:166749572-166749573	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs551307742	chr6:166749610-166749611	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs566419024	chr6:166749627-166749628	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs143571228	chr6:166749669-166749670	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs548768724	chr6:166749675-166749676	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs75914195	chr6:166749692-166749693	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs191393504	chr6:166749705-166749706	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs556606979	chr6:166749709-166749710	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs145226904	chr6:166749724-166749725	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs577982307	chr6:166749755-166749756	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs9348120	chr6:166749766-166749767	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs142481828	chr6:166749773-166749774	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs144641295	chr6:166749810-166749811	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs182709590	chr6:166749859-166749860	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
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
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
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	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
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ependymoma	20639864	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:219 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:166732400-166751600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr6:166733200-166753600	Weak transcription	Fetal Heart	heart
3	chr6:166733800-166749600	Weak transcription	Psoas Muscle	Psoas
4	chr6:166733800-166753800	Weak transcription	Hela-S3	cervix
5	chr6:166734600-166754800	Weak transcription	HUVEC	blood vessel
6	chr6:166738200-166754200	Weak transcription	NH-A	brain
7	chr6:166739400-166755400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr6:166740000-166750800	Weak transcription	HSMMtube	muscle
9	chr6:166740400-166748600	Weak transcription	Brain Germinal Matrix	brain
10	chr6:166741400-166750000	Weak transcription	HMEC	breast
11	chr6:166741400-166752400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr6:166742200-166751200	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr6:166742600-166754000	Weak transcription	Fetal Kidney	kidney
14	chr6:166742800-166749200	Weak transcription	NHEK	skin
15	chr6:166742800-166750000	Weak transcription	Colonic Mucosa	Colon
16	chr6:166742800-166751000	Weak transcription	HSMM	muscle
17	chr6:166743000-166749200	Weak transcription	Fetal Lung	lung
18	chr6:166743000-166749600	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr6:166743400-166749600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr6:166744400-166750600	Weak transcription	NHLF	lung
21	chr6:166744400-166752000	Weak transcription	Right Atrium	heart
22	chr6:166744400-166754800	Weak transcription	NHDF-Ad	bronchial
23	chr6:166744600-166750400	Weak transcription	Ovary	ovary
24	chr6:166744800-166749400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
25	chr6:166745200-166749400	Enhancers	Primary T helper cells PMA-I stimulated	--
26	chr6:166745200-166750400	Weak transcription	Stomach Mucosa	stomach
27	chr6:166745400-166754400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr6:166745400-166755000	Weak transcription	A549	lung
29	chr6:166745600-166749000	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr6:166745600-166749200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
31	chr6:166745800-166748800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr6:166745800-166749200	Enhancers	Primary T helper cells fromperipheralblood	blood
33	chr6:166745800-166749800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr6:166745800-166752200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr6:166746000-166752000	Strong transcription	Fetal Intestine Large	intestine
36	chr6:166746200-166752800	Strong transcription	Fetal Intestine Small	intestine
37	chr6:166746200-166753800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr6:166746200-166754800	Genic enhancers	Primary B cells from peripheral blood	blood
39	chr6:166746400-166749800	Genic enhancers	Thymus	Thymus
40	chr6:166746400-166752600	Genic enhancers	Spleen	Spleen
41	chr6:166746600-166749200	Weak transcription	Brain Angular Gyrus	brain
42	chr6:166746600-166750400	Weak transcription	Brain Anterior Caudate	brain
43	chr6:166746600-166751800	Weak transcription	Colon Smooth Muscle	Colon
44	chr6:166746600-166752400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr6:166746800-166748600	Genic enhancers	Fetal Thymus	thymus
46	chr6:166746800-166749000	Weak transcription	Fetal Brain Female	brain
47	chr6:166747000-166750000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr6:166747000-166750000	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr6:166747000-166750400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr6:166747000-166753400	Weak transcription	Fetal Brain Male	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links