Variant report

Variant	nsv934182
Chromosome Location	chr8:100533461-100548588
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	CEBPB	chr8:100540115-100540381	IMR90	lung:	n/a	chr8:100540222-100540235 chr8:100540223-100540234 chr8:100540224-100540233 chr8:100540222-100540233 chr8:100540222-100540235
2	CEBPB	chr8:100540080-100540378	K562	blood:	n/a	chr8:100540222-100540235 chr8:100540223-100540234 chr8:100540224-100540233 chr8:100540222-100540233 chr8:100540222-100540235
3	CEBPB	chr8:100540042-100540347	HepG2	liver:	n/a	chr8:100540222-100540235 chr8:100540223-100540234 chr8:100540224-100540233 chr8:100540222-100540233 chr8:100540222-100540235
4	CTCF	chr8:100548257-100548328	Medullo	brain:	n/a	n/a
5	CTCF	chr8:100535622-100535709	MCF-7	breast:	n/a	n/a
6	CTCF	chr8:100536318-100536378	GM20000	blood:	n/a	n/a
7	CTCF	chr8:100541459-100541466	MCF-7	breast:	n/a	n/a
8	CTCF	chr8:100539600-100539750	HMEC	breast:	n/a	chr8:100539701-100539714
9	E2F4	chr8:100533617-100533969	MCF10A-Er-Src	breast:	n/a	n/a
10	FOS	chr8:100533679-100534025	MCF10A-Er-Src	breast:	n/a	n/a
11	FOS	chr8:100533679-100534014	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr8:100533648-100534001	MCF10A-Er-Src	breast:	n/a	n/a
13	FOS	chr8:100533679-100534000	MCF10A-Er-Src	breast:	n/a	n/a
14	GATA3	chr8:100547537-100547620	SH-SY5Y	brain:	n/a	n/a
15	GATA3	chr8:100543236-100543882	MCF-7	breast:	n/a	n/a
16	GATA3	chr8:100543269-100543824	MCF-7	breast:	n/a	n/a
17	HEY1	chr8:100545214-100545347	HepG2	liver:	n/a	n/a
18	JUN	chr8:100538878-100538999	H1-hESC	embryonic stem cell:	n/a	n/a
19	JUND	chr8:100545217-100545312	HepG2	liver:	n/a	n/a
20	MAFF	chr8:100534969-100535255	HepG2	liver:	n/a	chr8:100535079-100535093
21	MAFF	chr8:100534986-100535164	K562	blood:	n/a	chr8:100535079-100535093
22	MAFK	chr8:100533639-100533734	HepG2	liver:	n/a	n/a
23	MAFK	chr8:100542083-100542323	HepG2	liver:	n/a	chr8:100542198-100542212
24	MAFK	chr8:100534930-100535243	HepG2	liver:	n/a	chr8:100535076-100535096 chr8:100535079-100535093 chr8:100535078-100535094
25	MAFK	chr8:100542081-100542282	HepG2	liver:	n/a	chr8:100542198-100542212
26	MAFK	chr8:100534952-100535171	Hela-S3	cervix:	n/a	chr8:100535076-100535096 chr8:100535079-100535093 chr8:100535078-100535094
27	MAFK	chr8:100534969-100535218	IMR90	lung:	n/a	chr8:100535076-100535096 chr8:100535079-100535093 chr8:100535078-100535094
28	MAFK	chr8:100547624-100547841	HepG2	liver:	n/a	n/a
29	MAFK	chr8:100542844-100543050	HepG2	liver:	n/a	n/a
30	MAFK	chr8:100534922-100535260	HepG2	liver:	n/a	chr8:100535076-100535096 chr8:100535079-100535093 chr8:100535078-100535094
31	MAZ	chr8:100546307-100546366	HepG2	liver:	n/a	n/a
32	MYC	chr8:100535645-100535687	MCF-7	breast:	n/a	n/a
33	MYC	chr8:100535699-100535724	MCF-7	breast:	n/a	n/a
34	MYC	chr8:100535643-100535767	MCF-7	breast:	n/a	n/a
35	MYC	chr8:100536917-100536932	MCF-7	breast:	n/a	n/a
36	MYC	chr8:100535569-100535743	MCF-7	breast:	n/a	n/a
37	MYC	chr8:100535606-100535771	MCF-7	breast:	n/a	n/a
38	MYC	chr8:100545195-100545323	MCF-7	breast:	n/a	n/a
39	MYC	chr8:100535628-100535637	MCF-7	breast:	n/a	n/a
40	MYC	chr8:100536899-100536907	MCF-7	breast:	n/a	n/a
41	POLR2A	chr8:100542553-100542680	MCF-7	breast:	n/a	n/a
42	POLR2A	chr8:100545200-100545316	MCF-7	breast:	n/a	n/a
43	POLR2A	chr8:100541575-100541659	MCF10A-Er-Src	breast:	n/a	n/a
44	POLR2A	chr8:100545182-100545326	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr8:100548572-100548772	MCF10A-Er-Src	breast:	n/a	n/a
46	POLR2A	chr8:100535579-100535740	MCF-7	breast:	n/a	n/a
47	POLR2A	chr8:100535618-100535619	Hela-S3	cervix:	n/a	n/a
48	POLR2A	chr8:100545192-100545436	ProgFib	skin:	n/a	n/a
49	POLR2A	chr8:100545372-100545416	K562	blood:	n/a	n/a
50	POLR2A	chr8:100535531-100535545	MCF-7	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:100539051..100543758-chr8:100545879..100549609,5	K562	blood:
2	chr8:100534887..100536607-chr8:100537446..100539997,2	K562	blood:
3	chr8:100534887..100536607-chr8:100537446..100539997,2	K562	blood:
4	chr8:100532719..100535105-chr8:100539628..100541847,3	MCF-7	breast:
5	chr8:100544046..100548556-chr8:100548656..100552103,4	K562	blood:
6	chr8:100532719..100535105-chr8:100539628..100541847,3	MCF-7	breast:
7	chr8:100539051..100543758-chr8:100545879..100549609,5	K562	blood:

Variant related genes	Relation type
ENSG00000206699	TF binding region
ENSG00000132549	chromatin interactions
ENSG00000216069	chromatin interactions
ENSG00000206699	chromatin interactions
ENSG00000207804	chromatin interactions

Extended variants
information (count: 484 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:484 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528116264	chr8:100533534-100533535	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs547886057	chr8:100533544-100533545	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs542959050	chr8:100533548-100533549	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs562538273	chr8:100533555-100533556	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs182621388	chr8:100533563-100533564	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs551246334	chr8:100533649-100533650	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs564863907	chr8:100533732-100533733	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs527452234	chr8:100533755-100533756	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs56174158	chr8:100533777-100533778	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs115898277	chr8:100533813-100533814	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs112053382	chr8:100533818-100533819	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs549943270	chr8:100533869-100533870	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs569653947	chr8:100533913-100533914	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs538668938	chr8:100533933-100533934	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs558463758	chr8:100533961-100533962	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs578200356	chr8:100533963-100533964	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs539624471	chr8:100534014-100534015	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs7832916	chr8:100534044-100534045	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs148298084	chr8:100534052-100534053	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs574219562	chr8:100534065-100534066	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs79938246	chr8:100534084-100534085	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs555496825	chr8:100534089-100534090	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs13249351	chr8:100534093-100534094	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs17325741	chr8:100534130-100534131	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs545022760	chr8:100534185-100534186	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs7833256	chr8:100534292-100534293	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs187281541	chr8:100534309-100534310	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs76406675	chr8:100534321-100534322	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs547718225	chr8:100534382-100534383	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs141596221	chr8:100534458-100534459	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs76851021	chr8:100534484-100534485	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs549883833	chr8:100534523-100534524	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs569792343	chr8:100534548-100534549	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs368131620	chr8:100534581-100534582	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs78863931	chr8:100534584-100534585	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs552213524	chr8:100534615-100534616	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs539428796	chr8:100534630-100534631	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs6468690	chr8:100534666-100534667	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs554487065	chr8:100534669-100534670	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs6468691	chr8:100534705-100534706	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs369020945	chr8:100534715-100534716	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs34792259	chr8:100534723-100534724	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs201932891	chr8:100534803-100534804	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs77292104	chr8:100534812-100534813	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs576143197	chr8:100534834-100534835	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs541882157	chr8:100534890-100534891	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs544959605	chr8:100534939-100534940	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs192148604	chr8:100535035-100535036	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs561547445	chr8:100535041-100535042	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs184695860	chr8:100535091-100535092	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:110)

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
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	17260012	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Colorectal cancer	19455253	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Cohen syndrome	20461111	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:210 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:100491200-100537000	Weak transcription	Placenta	Placenta
2	chr8:100496400-100537200	Weak transcription	Brain Hippocampus Middle	brain
3	chr8:100499400-100535200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr8:100503800-100536600	Weak transcription	Fetal Muscle Leg	muscle
5	chr8:100505000-100534800	Weak transcription	Fetal Intestine Large	intestine
6	chr8:100506000-100535400	Weak transcription	Fetal Stomach	stomach
7	chr8:100508400-100535400	Weak transcription	Aorta	Aorta
8	chr8:100508400-100535400	Weak transcription	Right Ventricle	heart
9	chr8:100508400-100535600	Weak transcription	Pancreas	Pancrea
10	chr8:100508400-100538400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr8:100508400-100574000	Weak transcription	Gastric	stomach
12	chr8:100511200-100538400	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr8:100511600-100535400	Weak transcription	Ovary	ovary
14	chr8:100511600-100559400	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr8:100511800-100539000	Weak transcription	Liver	Liver
16	chr8:100512000-100535400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr8:100512200-100534200	Weak transcription	NH-A	brain
18	chr8:100512200-100534800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
19	chr8:100512200-100538400	Weak transcription	Fetal Intestine Small	intestine
20	chr8:100512200-100545800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr8:100512200-100549800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr8:100512200-100557400	Weak transcription	Duodenum Mucosa	Duodenum
23	chr8:100512200-100559400	Weak transcription	Small Intestine	intestine
24	chr8:100512400-100535400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr8:100512400-100545800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr8:100512600-100537400	Weak transcription	Brain Substantia Nigra	brain
27	chr8:100513200-100535400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr8:100514400-100535400	Weak transcription	Lung	lung
29	chr8:100516400-100589000	Weak transcription	Primary T cells fromperipheralblood	blood
30	chr8:100517000-100539000	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr8:100517200-100533800	Weak transcription	Primary B cells from peripheral blood	blood
32	chr8:100517200-100535400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr8:100517600-100542600	Weak transcription	Left Ventricle	heart
34	chr8:100520200-100535400	Weak transcription	Esophagus	oesophagus
35	chr8:100524600-100535200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr8:100524600-100536800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr8:100525000-100545600	Weak transcription	Primary T helper cells PMA-I stimulated	--
38	chr8:100527400-100545600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr8:100527800-100538600	Weak transcription	Thymus	Thymus
40	chr8:100528200-100537800	Weak transcription	Brain Anterior Caudate	brain
41	chr8:100529800-100535200	Weak transcription	Fetal Lung	lung
42	chr8:100530600-100548400	Weak transcription	HUVEC	blood vessel
43	chr8:100531400-100535600	Weak transcription	Primary T cells from cord blood	blood
44	chr8:100531600-100535200	Weak transcription	Fetal Thymus	thymus
45	chr8:100531600-100559200	Weak transcription	Fetal Kidney	kidney
46	chr8:100531800-100537600	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr8:100532400-100534000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr8:100532400-100534800	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr8:100532400-100534800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
50	chr8:100532400-100554200	Weak transcription	Rectal Mucosa Donor 29	rectum

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