Variant report

Variant	nsv395879
Chromosome Location	chr8:66631732-66635776
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:24)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:24 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr8:66634300-66634450	BE2_C	brain:	n/a	n/a
2	FOXA1	chr8:66635386-66635631	HepG2	liver:	n/a	n/a
3	FOXA2	chr8:66635313-66635709	A549	lung:	n/a	n/a
4	GTF2F1	chr8:66633191-66633203	K562	blood:	n/a	n/a
5	MAFK	chr8:66633634-66633856	HepG2	liver:	n/a	n/a
6	MAFK	chr8:66633731-66633794	HepG2	liver:	n/a	n/a
7	POLR2A	chr8:66634748-66635196	GM12878	blood:	n/a	n/a
8	POLR2A	chr8:66634748-66635388	H1-hESC	embryonic stem cell:	n/a	n/a
9	POLR2A	chr8:66634266-66635721	K562	blood:	n/a	n/a
10	POLR2A	chr8:66634886-66635376	PFSK-1	brain:	n/a	n/a
11	POLR2A	chr8:66632237-66632563	GM12878	blood:	n/a	n/a
12	POLR2A	chr8:66634397-66634431	ProgFib	skin:	n/a	n/a
13	POLR2A	chr8:66632889-66633102	MCF-7	breast:	n/a	n/a
14	POLR2A	chr8:66635116-66635301	H1-hESC	embryonic stem cell:	n/a	n/a
15	POLR2A	chr8:66633963-66634000	MCF-7	breast:	n/a	n/a
16	POLR2A	chr8:66632533-66633268	K562	blood:	n/a	n/a
17	POLR2A	chr8:66635042-66635279	Hela-S3	cervix:	n/a	n/a
18	POLR2A	chr8:66634383-66634623	MCF-7	breast:	n/a	n/a
19	POLR2A	chr8:66634312-66634373	ProgFib	skin:	n/a	n/a
20	POLR2A	chr8:66634008-66634040	MCF-7	breast:	n/a	n/a
21	POLR2A	chr8:66632813-66633484	SK-N-MC	brain:	n/a	n/a
22	POLR2A	chr8:66634923-66635298	Hela-S3	cervix:	n/a	n/a
23	POLR2A	chr8:66628232-66632311	K562	blood:	n/a	n/a
24	STAT3	chr8:66632544-66632566	MCF10A-Er-Src	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:66635187-66635237	HNPCEpiC	eye:	n/a
2	chr8:66635187-66635237	HCF	heart:	n/a
3	chr8:66635187-66635237	HMEC	breast:	n/a
4	chr8:66635187-66635237	HCPEpiC	choroid plexus:	n/a
5	chr8:66635187-66635237	Jurkat	blood:	n/a
6	chr8:66635187-66635237	ECC-1	luminal epithelium:	n/a
7	chr8:66635187-66635237	AG09309	skin:	n/a
8	chr8:66635187-66635237	K562	blood:	n/a
9	chr8:66635187-66635237	HCT-116	colon:	n/a
10	chr8:66635187-66635237	AG04449	skin:	fetal
11	chr8:66635187-66635237	PrEC	prostate:	n/a
12	chr8:66635187-66635237	RPTEC	kidney:	n/a
13	chr8:66635187-66635237	HUVEC	blood vessel:	n/a
14	chr8:66635187-66635237	NH-A	brain:	n/a
15	chr8:66635187-66635237	LNCaP	prostate:	n/a
16	chr8:66635187-66635237	GM12891	blood:	n/a
17	chr8:66635187-66635237	NHDF-neo	bronchial:	n/a
18	chr8:66635187-66635237	PFSK-1	brain:	n/a
19	chr8:66635187-66635237	SKMC	muscle:	n/a
20	chr8:66635187-66635237	SAEC	small airway:	n/a
21	chr8:66635187-66635237	HRE	kidney:	n/a
22	chr8:66635187-66635237	ProgFib	skin:	n/a
23	chr8:66635187-66635237	GM19239	blood:	n/a
24	chr8:66635187-66635237	AoSMC	blood vessel:	n/a
25	chr8:66635187-66635237	HPAEpiC	pulmonary alveolar:	n/a
26	chr8:66635187-66635237	Caco-2	colon:	n/a
27	chr8:66635187-66635237	HEEpiC	esophagus:	n/a
28	chr8:66635187-66635237	AG10803	skin:	n/a
29	chr8:66635187-66635237	A549	lung:	n/a
30	chr8:66635187-66635237	SK-N-SH	brain:	n/a
31	chr8:66635187-66635237	Hela-S3	cervix:	n/a
32	chr8:66635187-66635237	AG09319	gingival:	n/a
33	chr8:66635187-66635237	BE2_C	brain:	n/a
34	chr8:66635187-66635237	HRCEpiC	kidney:	n/a
35	chr8:66635187-66635237	AG04450	lung:	fetal
36	chr8:66635187-66635237	HCM	heart:	n/a
37	chr8:66635187-66635237	IMR90	lung:	fetal
38	chr8:66635187-66635237	MCF10A-Er-Src	breast:	n/a
39	chr8:66635187-66635237	PANC-1	pancreas:	n/a
40	chr8:66635187-66635237	BJ	skin:	n/a
41	chr8:66635187-66635237	HEK293	kidney:	embryo
42	chr8:66635187-66635237	MCF-7	breast:	n/a
43	chr8:66635187-66635237	SK-N-MC	brain:	n/a
44	chr8:66635187-66635237	SK-N-SH_RA	brain:	n/a
45	chr8:66635187-66635237	NT2-D1	testis:	n/a
46	chr8:66635187-66635237	HL-60	blood:	n/a
47	chr8:66635187-66635237	HRPEpiC	eye:	n/a
48	chr8:66635187-66635237	T-47D	breast:	n/a
49	chr8:66635187-66635237	CMK	blood:	n/a
50	chr8:66635187-66635237	H1-hESC	embryonic stem cell:	embryo

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:66634454..66636927-chr8:66637677..66640769,3	K562	blood:
2	chr8:66634318..66636259-chr8:66648468..66650206,2	K562	blood:
3	chr8:66629168..66631194-chr8:66635372..66637144,2	MCF-7	breast:
4	chr8:66630735..66632714-chr8:66718636..66720891,2	K562	blood:
5	chr8:66629100..66631894-chr8:66634676..66636367,2	K562	blood:
6	chr8:66629100..66631894-chr8:66634676..66636367,2	K562	blood:
7	chr8:66634454..66636931-chr8:66637677..66639411,3	K562	blood:
8	chr8:66628174..66631200-chr8:66633706..66636943,3	K562	blood:
9	chr8:66631641..66633524-chr8:66633808..66636306,2	K562	blood:
10	chr8:66632066..66634128-chr8:66637203..66640616,3	K562	blood:
11	chr8:66631641..66633524-chr8:66633808..66636306,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DNAJC5B-1	chr8:66632639-66632831	NONHSAT126994

No data

Variant related genes	Relation type
MTFR1	TF binding region
ENSG00000272155	TF binding region
MTFR1	CpG island
ENSG00000272155	CpG island
ENSG00000066855	chromatin interactions
ENSG00000205268	chromatin interactions

Extended variants
information (count: 129 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:129 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191262062	chr8:66631756-66631757	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs200359177	chr8:66631769-66631770	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs553377921	chr8:66631773-66631774	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs370634214	chr8:66631776-66631777	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs199548673	chr8:66631777-66631778	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs536035418	chr8:66631809-66631810	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs557524238	chr8:66631867-66631868	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs575772849	chr8:66631895-66631896	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs115218934	chr8:66631898-66631899	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs953593	chr8:66631972-66631973	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs573065258	chr8:66631980-66631981	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs540561360	chr8:66632030-66632031	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs182041078	chr8:66632039-66632040	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs529116112	chr8:66632058-66632059	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs77950482	chr8:66632164-66632165	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs79892102	chr8:66632190-66632191	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs532815902	chr8:66632209-66632210	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs17304488	chr8:66632217-66632218	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs17304516	chr8:66632266-66632267	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs375083621	chr8:66632394-66632395	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs527283416	chr8:66632517-66632518	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs547299817	chr8:66632539-66632540	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs186679862	chr8:66632555-66632556	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs559418178	chr8:66632564-66632565	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs116327382	chr8:66632613-66632614	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs192359051	chr8:66632718-66632719	Strong transcription Weak transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
27	rs185774547	chr8:66632727-66632728	Strong transcription Weak transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
28	rs189897405	chr8:66632788-66632789	Strong transcription Weak transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
29	rs369734511	chr8:66632850-66632851	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs193188027	chr8:66632875-66632876	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs78080459	chr8:66632920-66632921	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs76311439	chr8:66632922-66632923	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs555670989	chr8:66632940-66632941	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs184713476	chr8:66633015-66633016	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs544026718	chr8:66633024-66633025	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs17304551	chr8:66633039-66633040	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs550492994	chr8:66633052-66633053	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs150588739	chr8:66633073-66633074	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs10504391	chr8:66633109-66633110	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs16932314	chr8:66633143-66633144	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs527315898	chr8:66633165-66633166	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs548666381	chr8:66633187-66633188	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs568756614	chr8:66633317-66633318	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs139682764	chr8:66633346-66633347	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs150607693	chr8:66633368-66633369	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs140550332	chr8:66633393-66633394	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs144368102	chr8:66633394-66633395	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs147798970	chr8:66633427-66633428	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs540036261	chr8:66633435-66633436	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs558262018	chr8:66633503-66633504	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	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
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	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
Salivary gland tumor	18059337	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
Acute myeloid leukemia	21251322	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
Colorectal cancer	16272173	CNVD
Melanoma	22183965	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	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
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Sezary syndrome	18413736	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Adenoid cystic carcinoma	18332873	CNVD
early-passage human iPS cells	21368824	CNVD
Prostate cancer	22341455	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:224 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:66599200-66633000	Weak transcription	Fetal Kidney	kidney
2	chr8:66602800-66641800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr8:66602800-66650600	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr8:66606600-66639400	Weak transcription	Fetal Heart	heart
5	chr8:66611600-66634600	Weak transcription	Fetal Brain Male	brain
6	chr8:66613400-66634600	Weak transcription	Colonic Mucosa	Colon
7	chr8:66617600-66646200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr8:66620200-66632000	Weak transcription	Brain Anterior Caudate	brain
9	chr8:66620200-66632800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr8:66620800-66632600	Weak transcription	Lung	lung
11	chr8:66620800-66633000	Weak transcription	Brain Angular Gyrus	brain
12	chr8:66620800-66648800	Weak transcription	Psoas Muscle	Psoas
13	chr8:66621000-66632600	Weak transcription	Brain Substantia Nigra	brain
14	chr8:66621000-66634800	Weak transcription	Ovary	ovary
15	chr8:66621400-66673000	Weak transcription	Colon Smooth Muscle	Colon
16	chr8:66624600-66661200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr8:66625600-66661400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
18	chr8:66626200-66633800	Strong transcription	Cortex derived primary cultured neurospheres	brain
19	chr8:66626200-66652000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr8:66626200-66664600	Strong transcription	Fetal Thymus	thymus
21	chr8:66626400-66656600	Strong transcription	Primary T cells from cord blood	blood
22	chr8:66626600-66640400	Strong transcription	Primary T helper cells PMA-I stimulated	--
23	chr8:66626600-66653600	Strong transcription	Primary B cells from peripheral blood	blood
24	chr8:66626600-66655600	Strong transcription	Primary T cells fromperipheralblood	blood
25	chr8:66627200-66640400	Strong transcription	Left Ventricle	heart
26	chr8:66627200-66655000	Strong transcription	Primary T helper cells fromperipheralblood	blood
27	chr8:66627400-66637600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr8:66627400-66640400	Strong transcription	Thymus	Thymus
29	chr8:66628000-66652000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr8:66628200-66636400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr8:66628200-66640800	Strong transcription	Primary hematopoietic stem cells	blood
32	chr8:66628200-66660000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr8:66628200-66660200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr8:66628400-66632200	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr8:66628400-66635400	Strong transcription	Adipose Nuclei	Adipose
36	chr8:66628400-66635400	Strong transcription	Skeletal Muscle Male	skeletal muscle
37	chr8:66628400-66635600	Strong transcription	Brain Germinal Matrix	brain
38	chr8:66628400-66636600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
39	chr8:66628400-66636600	Strong transcription	Fetal Brain Female	brain
40	chr8:66628400-66637200	Strong transcription	GM12878-XiMat	blood
41	chr8:66628400-66637800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr8:66628400-66638000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr8:66628400-66638000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr8:66628400-66638000	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
45	chr8:66628400-66640000	Strong transcription	Primary T killer memory cells from peripheral blood	blood
46	chr8:66628400-66650200	Strong transcription	Primary neutrophils fromperipheralblood	blood
47	chr8:66628400-66651600	Strong transcription	Primary monocytes fromperipheralblood	blood
48	chr8:66628400-66652400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr8:66628400-66652800	Strong transcription	Primary B cells from cord blood	blood
50	chr8:66628400-66663800	Strong transcription	Monocytes-CD14+_RO01746	blood

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