Variant report

Variant	nsv818645
Chromosome Location	chr8:95967838-95974373
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	ARID3A	chr8:95972103-95973068	K562	blood:	n/a	n/a
2	ARID3A	chr8:95971463-95973357	HepG2	liver:	n/a	n/a
3	ATF1	chr8:95972045-95972773	K562	blood:	n/a	n/a
4	ATF2	chr8:95972310-95973305	GM12878	blood:	n/a	n/a
5	ATF3	chr8:95974144-95974403	K562	blood:	n/a	n/a
6	BATF	chr8:95972409-95972774	GM12878	blood:	n/a	n/a
7	BCLAF1	chr8:95972388-95973267	GM12878	blood:	n/a	n/a
8	BHLHE40	chr8:95971925-95972337	HepG2	liver:	n/a	n/a
9	BHLHE40	chr8:95971947-95972498	HepG2	liver:	n/a	n/a
10	BHLHE40	chr8:95972012-95972713	K562	blood:	n/a	n/a
11	BHLHE40	chr8:95973046-95973119	K562	blood:	n/a	n/a
12	CBX3	chr8:95974039-95974431	K562	blood:	n/a	n/a
13	CCNT2	chr8:95972081-95972763	K562	blood:	n/a	n/a
14	CEBPB	chr8:95972862-95973314	HepG2	liver:	n/a	n/a
15	CEBPB	chr8:95968480-95968722	K562	blood:	n/a	n/a
16	CEBPB	chr8:95971937-95972391	HepG2	liver:	n/a	n/a
17	CEBPB	chr8:95973006-95973226	HepG2	liver:	n/a	n/a
18	CEBPB	chr8:95971861-95972406	HepG2	liver:	n/a	n/a
19	CEBPB	chr8:95971946-95973361	HepG2	liver:	n/a	n/a
20	CEBPB	chr8:95972003-95972243	HepG2	liver:	n/a	n/a
21	CEBPB	chr8:95972850-95973274	HepG2	liver:	n/a	n/a
22	CEBPB	chr8:95972995-95973206	K562	blood:	n/a	n/a
23	CEBPB	chr8:95973017-95973326	IMR90	lung:	n/a	n/a
24	CEBPD	chr8:95971918-95972325	HepG2	liver:	n/a	n/a
25	CHD2	chr8:95974262-95974268	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr8:95972285-95973273	GM12878	blood:	n/a	n/a
27	CREB1	chr8:95972922-95973361	HepG2	liver:	n/a	n/a
28	CREB1	chr8:95971864-95973400	HepG2	liver:	n/a	n/a
29	CREB1	chr8:95972384-95973321	GM12878	blood:	n/a	n/a
30	CREB1	chr8:95972377-95973455	GM12878	blood:	n/a	n/a
31	CUX1	chr8:95972225-95973188	GM12878	blood:	n/a	n/a
32	CUX1	chr8:95972069-95972651	K562	blood:	n/a	n/a
33	EBF1	chr8:95972328-95973190	GM12878	blood:	n/a	n/a
34	EGR1	chr8:95974078-95974343	K562	blood:	n/a	n/a
35	EGR1	chr8:95974055-95974370	K562	blood:	n/a	n/a
36	ELF1	chr8:95971945-95972689	HepG2	liver:	n/a	n/a
37	ELF1	chr8:95972060-95972460	HepG2	liver:	n/a	n/a
38	ELK1	chr8:95972459-95973172	GM12878	blood:	n/a	n/a
39	EP300	chr8:95968393-95968768	K562	blood:	n/a	n/a
40	EP300	chr8:95972240-95973249	GM12878	blood:	n/a	chr8:95972905-95972915 chr8:95972378-95972387 chr8:95972848-95972862
41	EP300	chr8:95972134-95973353	GM12878	blood:	n/a	chr8:95972905-95972915 chr8:95972378-95972387 chr8:95972848-95972862
42	EP300	chr8:95972065-95973208	K562	blood:	n/a	chr8:95972125-95972139 chr8:95972905-95972915 chr8:95972119-95972129 chr8:95972378-95972387 chr8:95972848-95972862
43	EP300	chr8:95971512-95971734	K562	blood:	n/a	n/a
44	EP300	chr8:95971807-95973340	HepG2	liver:	n/a	chr8:95972125-95972139 chr8:95972905-95972915 chr8:95972119-95972129 chr8:95972378-95972387 chr8:95972848-95972862
45	EP300	chr8:95971964-95973252	HepG2	liver:	n/a	chr8:95972125-95972139 chr8:95972905-95972915 chr8:95972119-95972129 chr8:95972378-95972387 chr8:95972848-95972862
46	EP300	chr8:95972448-95973208	GM12878	blood:	n/a	chr8:95972905-95972915 chr8:95972848-95972862
47	EP300	chr8:95971906-95973314	HepG2	liver:	n/a	chr8:95972125-95972139 chr8:95972905-95972915 chr8:95972119-95972129 chr8:95972378-95972387 chr8:95972848-95972862
48	FOS	chr8:95974044-95974335	MCF10A-Er-Src	breast:	n/a	chr8:95974044-95974058
49	FOS	chr8:95974060-95974288	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr8:95974150-95974250	MCF10A-Er-Src	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:95972771..95975327-chr8:95979134..95982751,4	MCF-7	breast:
2	chr8:95966010..95969504-chr8:96000231..96003334,3	MCF-7	breast:
3	chr8:95970122..95973774-chr8:95974138..95977559,4	MCF-7	breast:
4	chr8:95972569..95974816-chr8:95983655..95986247,2	MCF-7	breast:
5	chr8:95961511..95965084-chr8:95968441..95972141,5	K562	blood:
6	chr8:95960008..95964622-chr8:95970124..95974538,6	MCF-7	breast:
7	chr8:95960036..95962900-chr8:95966783..95969994,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-INTS8-4	chr8:95970223-95970407	NONHSAT127811
2	lnc-INTS8-4	chr8:95972378-95972781	NONHSAT127811

Variant related genes	Relation type
NDUFAF6	TF binding region
ENSG00000164938	chromatin interactions
ENSG00000253878	chromatin interactions
ENSG00000156170	chromatin interactions

Extended variants
information (count: 263 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:263 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs481887	chr8:95967838-95967839	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs575626130	chr8:95967868-95967869	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs193268888	chr8:95967937-95967938	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs551725284	chr8:95967941-95967942	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs544293801	chr8:95967955-95967956	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs564475552	chr8:95968107-95968108	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs112638010	chr8:95968163-95968164	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs184547966	chr8:95968164-95968165	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs148060721	chr8:95968254-95968255	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs188940903	chr8:95968333-95968334	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs113360308	chr8:95968335-95968336	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs4442107	chr8:95968355-95968356	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs112519572	chr8:95968362-95968363	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs141657948	chr8:95968374-95968375	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs528136772	chr8:95968383-95968384	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs4336579	chr8:95968389-95968390	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs568080956	chr8:95968391-95968392	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs726816	chr8:95968413-95968414	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs550311964	chr8:95968458-95968459	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs568293179	chr8:95968515-95968516	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs570387605	chr8:95968524-95968525	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs140866936	chr8:95968537-95968538	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs192278737	chr8:95968587-95968588	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs573100604	chr8:95968604-95968605	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs376961339	chr8:95968649-95968650	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs145000222	chr8:95968679-95968680	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs550887189	chr8:95968692-95968693	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs4338072	chr8:95968698-95968699	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs956344	chr8:95968710-95968711	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs74745770	chr8:95968728-95968729	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs368259338	chr8:95968768-95968769	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs530010110	chr8:95968824-95968825	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs138802993	chr8:95968833-95968834	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs184290410	chr8:95968850-95968851	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs188669201	chr8:95968859-95968860	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs142091427	chr8:95968928-95968929	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs529511238	chr8:95968968-95968969	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs549335082	chr8:95969010-95969011	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs76388970	chr8:95969042-95969043	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs552606542	chr8:95969064-95969065	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs375996863	chr8:95969067-95969068	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs530531623	chr8:95969118-95969119	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs146330789	chr8:95969124-95969125	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs570403022	chr8:95969138-95969139	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs181187333	chr8:95969153-95969154	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs546948183	chr8:95969160-95969161	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs569797787	chr8:95969185-95969186	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs186158160	chr8:95969193-95969194	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs549866232	chr8:95969197-95969198	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs535717577	chr8:95969245-95969246	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:111)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	17847001	CNVD
Neuropsychiatric disorder	20069037	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Colorectal cancer	21645411	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Breast cancer	17142309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:338 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:95962200-95977800	Weak transcription	Hela-S3	cervix
2	chr8:95962400-95971400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr8:95962600-95970600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr8:95962800-95969400	Weak transcription	Dnd41	blood
5	chr8:95962800-95972400	Weak transcription	Aorta	Aorta
6	chr8:95962800-95974200	Weak transcription	Gastric	stomach
7	chr8:95962800-95975800	Weak transcription	Right Ventricle	heart
8	chr8:95962800-95977000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr8:95962800-95979800	Weak transcription	Fetal Muscle Trunk	muscle
10	chr8:95962800-95980200	Weak transcription	Ovary	ovary
11	chr8:95962800-95980600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr8:95963000-95970000	Weak transcription	Primary hematopoietic stem cells	blood
13	chr8:95963000-95971200	Weak transcription	Fetal Intestine Small	intestine
14	chr8:95963000-95971400	Weak transcription	Primary B cells from cord blood	blood
15	chr8:95963000-95975800	Weak transcription	Fetal Stomach	stomach
16	chr8:95963000-95980400	Weak transcription	HSMM	muscle
17	chr8:95963400-95970200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr8:95963400-95974200	Weak transcription	Psoas Muscle	Psoas
19	chr8:95963600-95968400	Weak transcription	Spleen	Spleen
20	chr8:95963600-95970000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr8:95963600-95970000	Weak transcription	Left Ventricle	heart
22	chr8:95963600-95971400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
23	chr8:95963600-95972400	Weak transcription	NHLF	lung
24	chr8:95963600-95973800	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr8:95963600-95974000	Weak transcription	Esophagus	oesophagus
26	chr8:95963600-95977800	Weak transcription	HUVEC	blood vessel
27	chr8:95963600-95979600	Weak transcription	A549	lung
28	chr8:95963800-95970800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr8:95963800-95973800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr8:95963800-95979400	Weak transcription	Colon Smooth Muscle	Colon
31	chr8:95964000-95970200	Weak transcription	Fetal Muscle Leg	muscle
32	chr8:95964000-95971000	Weak transcription	Primary B cells from peripheral blood	blood
33	chr8:95964200-95968200	Weak transcription	K562	blood
34	chr8:95964200-95969400	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr8:95964200-95970000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr8:95964200-95970200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr8:95964200-95970400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr8:95964200-95971400	Weak transcription	Fetal Intestine Large	intestine
39	chr8:95964400-95969200	Weak transcription	Fetal Heart	heart
40	chr8:95964400-95969600	Weak transcription	Right Atrium	heart
41	chr8:95964400-95971000	Weak transcription	HMEC	breast
42	chr8:95964400-95972000	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr8:95964400-95973600	Weak transcription	Skeletal Muscle Male	skeletal muscle
44	chr8:95964400-95973800	Weak transcription	Osteobl	bone
45	chr8:95964400-95976000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr8:95964400-95980000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr8:95964400-96002200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr8:95964600-95970200	Weak transcription	Stomach Smooth Muscle	stomach
49	chr8:95964600-95970200	Weak transcription	Thymus	Thymus
50	chr8:95964600-95970400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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