Variant report

Variant	esv3438938
Chromosome Location	chr8:10888542-10893040
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:44)
CpG islands
(count:122)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:44 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr8:10889516-10889660	H1-hESC	embryonic stem cell:	n/a	n/a
2	CTCF	chr8:10889537-10889622	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTCF	chr8:10889480-10889630	GM12873	blood:	n/a	n/a
4	CTCF	chr8:10890858-10890861	GM19239	blood:	n/a	n/a
5	CTCF	chr8:10889540-10889690	GM12875	blood:	n/a	chr8:10889655-10889663
6	CTCF	chr8:10889533-10889645	MCF-7	breast:	n/a	n/a
7	CTCF	chr8:10889480-10889630	GM12871	blood:	n/a	n/a
8	CTCF	chr8:10889540-10889690	GM12872	blood:	n/a	chr8:10889655-10889663
9	CTCF	chr8:10889530-10889606	MCF-7	breast:	n/a	n/a
10	CTCF	chr8:10889516-10889613	MCF-7	breast:	n/a	n/a
11	CTCF	chr8:10889400-10889745	K562	blood:	n/a	chr8:10889655-10889663
12	CTCF	chr8:10888500-10888650	GM12866	blood:	n/a	n/a
13	CTCF	chr8:10889480-10889630	GM12865	blood:	n/a	n/a
14	CTCF	chr8:10889460-10889610	MCF-7	breast:	n/a	n/a
15	CTCF	chr8:10889343-10889791	K562	blood:	n/a	chr8:10889655-10889663
16	CTCF	chr8:10889448-10889736	H1-hESC	embryonic stem cell:	n/a	chr8:10889655-10889663
17	CTCF	chr8:10889544-10889598	GM12878	blood:	n/a	n/a
18	CTCF	chr8:10889500-10889650	GM06990	blood:	n/a	n/a
19	CTCF	chr8:10889400-10889550	GM12869	blood:	n/a	n/a
20	CTCF	chr8:10890670-10890856	GM19239	blood:	n/a	n/a
21	CTCF	chr8:10889519-10889703	GM12878	blood:	n/a	chr8:10889655-10889663
22	CTCF	chr8:10889480-10889630	GM12864	blood:	n/a	n/a
23	CTCF	chr8:10889440-10889590	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr8:10889506-10889623	MCF-7	breast:	n/a	n/a
25	CTCF	chr8:10889460-10889610	GM12873	blood:	n/a	n/a
26	CTCF	chr8:10889437-10889773	K562	blood:	n/a	chr8:10889655-10889663
27	CTCF	chr8:10889480-10889630	SK-N-SH_RA	brain:	n/a	n/a
28	CTCF	chr8:10889490-10889588	GM12891	blood:	n/a	n/a
29	CTCF	chr8:10889518-10889678	K562	blood:	n/a	chr8:10889655-10889663
30	CTCF	chr8:10889602-10889610	MCF-7	breast:	n/a	n/a
31	CTCF	chr8:10889411-10889756	K562	blood:	n/a	chr8:10889655-10889663
32	CTCF	chr8:10889444-10889797	MCF-7	breast:	n/a	chr8:10889655-10889663
33	JUND	chr8:10890837-10890977	HepG2	liver:	n/a	n/a
34	MYC	chr8:10890811-10890844	HUVEC	blood vessel:	n/a	n/a
35	MYC	chr8:10890850-10890937	HUVEC	blood vessel:	n/a	n/a
36	POLR2A	chr8:10892734-10892750	MCF-7	breast:	n/a	n/a
37	POLR2A	chr8:10890693-10890940	H1-hESC	embryonic stem cell:	n/a	n/a
38	POLR2A	chr8:10892003-10892075	GM12878	blood:	n/a	n/a
39	POLR2A	chr8:10890770-10890788	Gliobla	brain:	n/a	n/a
40	RAD21	chr8:10889539-10889650	K562	blood:	n/a	n/a
41	RAD21	chr8:10889487-10889751	H1-hESC	embryonic stem cell:	n/a	n/a
42	RAD21	chr8:10889320-10889741	H1-hESC	embryonic stem cell:	n/a	n/a
43	SUZ12	chr8:10890625-10890934	H1-hESC	embryonic stem cell:	n/a	n/a
44	TCF12	chr8:10889359-10889650	H1-hESC	embryonic stem cell:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:10892823-10892873	GM12878	blood:	n/a
2	chr8:10892734-10892784	HepG2	liver:	n/a
3	chr8:10892823-10892873	K562	blood:	n/a
4	chr8:10892734-10892784	Hepatocyte	liver:	n/a
5	chr8:10892823-10892873	SK-N-SH	brain:	n/a
6	chr8:10892823-10892873	AG04449	skin:	fetal
7	chr8:10892734-10892784	CMK	blood:	n/a
8	chr8:10892734-10892784	HRE	kidney:	n/a
9	chr8:10892823-10892873	HRE	kidney:	n/a
10	chr8:10892823-10892873	CMK	blood:	n/a
11	chr8:10892823-10892873	MCF-7	breast:	n/a
12	chr8:10892734-10892784	AoSMC	blood vessel:	n/a
13	chr8:10892734-10892784	BJ	skin:	n/a
14	chr8:10892823-10892873	SK-N-MC	brain:	n/a
15	chr8:10892734-10892784	SAEC	small airway:	n/a
16	chr8:10892823-10892873	HEK293	kidney:	embryo
17	chr8:10892734-10892784	HCF	heart:	n/a
18	chr8:10892734-10892784	HRPEpiC	eye:	n/a
19	chr8:10892823-10892873	HAEpiC	amniotic membrane:	n/a
20	chr8:10892734-10892784	PANC-1	pancreas:	n/a
21	chr8:10892823-10892873	PrEC	prostate:	n/a
22	chr8:10892734-10892784	T-47D	breast:	n/a
23	chr8:10892734-10892784	NT2-D1	testis:	n/a
24	chr8:10892823-10892873	RPTEC	kidney:	n/a
25	chr8:10892734-10892784	AG09319	gingival:	n/a
26	chr8:10892734-10892784	AG04449	skin:	fetal
27	chr8:10892734-10892784	HEK293	kidney:	embryo
28	chr8:10892734-10892784	HEEpiC	esophagus:	n/a
29	chr8:10892823-10892873	HL-60	blood:	n/a
30	chr8:10892734-10892784	HNPCEpiC	eye:	n/a
31	chr8:10892823-10892873	AoSMC	blood vessel:	n/a
32	chr8:10892823-10892873	AG09319	gingival:	n/a
33	chr8:10892734-10892784	HCM	heart:	n/a
34	chr8:10892734-10892784	HIPEpiC	eye:	n/a
35	chr8:10892734-10892784	NH-A	brain:	n/a
36	chr8:10892823-10892873	AG09309	skin:	n/a
37	chr8:10892823-10892873	AG04450	lung:	fetal
38	chr8:10892734-10892784	AG09309	skin:	n/a
39	chr8:10892823-10892873	GM06990	blood:	n/a
40	chr8:10892734-10892784	Jurkat	blood:	n/a
41	chr8:10892823-10892873	HIPEpiC	eye:	n/a
42	chr8:10892734-10892784	AG10803	skin:	n/a
43	chr8:10892734-10892784	Caco-2	colon:	n/a
44	chr8:10892734-10892784	PFSK-1	brain:	n/a
45	chr8:10892823-10892873	PFSK-1	brain:	n/a
46	chr8:10892734-10892784	AG04450	lung:	fetal
47	chr8:10892823-10892873	SKMC	muscle:	n/a
48	chr8:10892734-10892784	HUVEC	blood vessel:	n/a
49	chr8:10892823-10892873	HCF	heart:	n/a
50	chr8:10892823-10892873	Hela-S3	cervix:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:10887222..10889685-chr8:10905766..10908616,2	K562	blood:
2	chr8:10883944..10886637-chr8:10888412..10890996,2	K562	blood:
3	chr8:10886694..10889685-chr8:10905766..10907458,2	K562	blood:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-598-5p	chr8:10892767-10892789	MIMAT0026620
hsa-miR-598-3p	chr8:10892731-10892752	MIMAT0003266

No data

Variant related genes	Relation type
MIR598	TF binding region
MIR598	CpG island
PTMA	Mature miRNA region
GTF3C1	Mature miRNA region
CASP8AP2	Mature miRNA region
FAM21A	Mature miRNA region
HIST4H4	Mature miRNA region
C1orf174	Mature miRNA region
BCOR	Mature miRNA region
CCT7	Mature miRNA region
TNPO2	Mature miRNA region
SPIN1	Mature miRNA region
CALM1	Mature miRNA region
NCL	Mature miRNA region
HIVEP2	Mature miRNA region
URI1	Mature miRNA region
NPM1	Mature miRNA region

Extended variants
information (count: 233 )
Associated
traits (count: 138 )

Variant overlapped rSNPs/rCNVs (count:233 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17779063	chr8:10888602-10888603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs7826139	chr8:10888617-10888618	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs544864127	chr8:10888624-10888625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs76851050	chr8:10888649-10888650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs554001444	chr8:10888682-10888683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs572280622	chr8:10888692-10888693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs542527741	chr8:10888693-10888694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs554863232	chr8:10888705-10888706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs576291699	chr8:10888750-10888751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs543778425	chr8:10888814-10888815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs564982810	chr8:10888827-10888828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs183688732	chr8:10888867-10888868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs541134592	chr8:10888886-10888887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs559471923	chr8:10888917-10888918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs530340339	chr8:10888930-10888931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs36000781	chr8:10889019-10889020	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs548568932	chr8:10889034-10889035	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs563995580	chr8:10889074-10889075	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs11997616	chr8:10889075-10889076	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs186641106	chr8:10889077-10889078	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs571305486	chr8:10889121-10889122	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs574265441	chr8:10889142-10889143	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs191487983	chr8:10889149-10889150	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs547520397	chr8:10889199-10889200	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140307803	chr8:10889201-10889202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs146015495	chr8:10889219-10889220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs115323244	chr8:10889225-10889226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs554494487	chr8:10889239-10889240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs576283563	chr8:10889243-10889244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs372768429	chr8:10889271-10889272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs139981047	chr8:10889312-10889313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs558480961	chr8:10889313-10889314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs11998417	chr8:10889315-10889316	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs34614241	chr8:10889339-10889340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs541100010	chr8:10889359-10889360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs143572895	chr8:10889372-10889373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs574873740	chr8:10889379-10889380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs563202452	chr8:10889383-10889384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs529371152	chr8:10889404-10889405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs563776168	chr8:10889456-10889457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs372797963	chr8:10889462-10889463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs549521066	chr8:10889487-10889488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs531227791	chr8:10889488-10889489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs552913948	chr8:10889501-10889502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs367742548	chr8:10889519-10889520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs569226726	chr8:10889557-10889558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs564823181	chr8:10889560-10889561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs532159417	chr8:10889609-10889610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs547449544	chr8:10889621-10889622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs10110123	chr8:10889623-10889624	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:138)

Disease	PMID	Source
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:74 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10874400-10892800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr8:10875000-10890000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr8:10879600-10890000	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr8:10879600-10890400	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr8:10879800-10890600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr8:10880000-10890200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr8:10880000-10896800	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr8:10880200-10890400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr8:10880200-10890400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr8:10880200-10890600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr8:10881400-10893200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr8:10883400-10899600	Weak transcription	Brain Anterior Caudate	brain
13	chr8:10884400-10892800	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr8:10887200-10890200	Weak transcription	Pancreas	Pancrea
15	chr8:10887800-10894800	Weak transcription	Fetal Stomach	stomach
16	chr8:10888200-10890200	Weak transcription	Gastric	stomach
17	chr8:10888200-10890600	Enhancers	Fetal Brain Male	brain
18	chr8:10888400-10889800	Enhancers	HSMMtube	muscle
19	chr8:10888400-10890200	Weak transcription	Stomach Smooth Muscle	stomach
20	chr8:10888400-10892600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr8:10888800-10890600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr8:10889000-10889200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr8:10889000-10890600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
24	chr8:10889000-10891800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr8:10889200-10890200	Weak transcription	Spleen	Spleen
26	chr8:10889200-10890600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr8:10889200-10890600	Enhancers	Ovary	ovary
28	chr8:10889400-10890200	Weak transcription	Brain Angular Gyrus	brain
29	chr8:10889400-10890600	Enhancers	Fetal Brain Female	brain
30	chr8:10889600-10890400	Enhancers	Brain Cingulate Gyrus	brain
31	chr8:10889800-10890200	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr8:10889800-10892200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr8:10889800-10894000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr8:10889800-10910800	Weak transcription	HSMMtube	muscle
35	chr8:10890000-10890200	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr8:10890000-10890800	Strong transcription	HUES48 Cell Line	embryonic stem cell
37	chr8:10890200-10890400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr8:10890200-10890400	Genic enhancers	Brain Angular Gyrus	brain
39	chr8:10890200-10890400	Enhancers	Brain Inferior Temporal Lobe	brain
40	chr8:10890200-10890400	Enhancers	Esophagus	oesophagus
41	chr8:10890200-10890400	Bivalent Enhancer	Right Ventricle	heart
42	chr8:10890200-10890400	ZNF genes & repeats	Spleen	Spleen
43	chr8:10890200-10890800	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr8:10890200-10891200	Strong transcription	Gastric	stomach
45	chr8:10890200-10891800	Strong transcription	Pancreas	Pancrea
46	chr8:10890200-10891800	Strong transcription	Stomach Smooth Muscle	stomach
47	chr8:10890400-10890800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr8:10890400-10891000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
49	chr8:10890400-10891000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr8:10890400-10891000	Strong transcription	HUES6 Cell Line	embryonic stem cell

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