Variant report

Variant	nsv610675
Chromosome Location	chr8:17137687-17155432
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:136)
CpG islands
(count:61)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:136 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:17142585-17142622	K562	blood:	n/a	n/a
2	CEBPB	chr8:17141447-17141810	IMR90	lung:	n/a	n/a
3	CEBPB	chr8:17142470-17142562	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr8:17141545-17141764	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr8:17143949-17143999	HepG2	liver:	n/a	chr8:17143968-17143979
6	CTCF	chr8:17142440-17142590	HA-sp	spinal cord:	n/a	n/a
7	CTCF	chr8:17142360-17142510	HRPEpiC	eye:	n/a	n/a
8	CTCF	chr8:17142500-17142650	HFF	foreskin:	n/a	n/a
9	CTCF	chr8:17142420-17142570	BJ	skin:	n/a	n/a
10	CTCF	chr8:17142440-17142590	Caco-2	colon:	n/a	n/a
11	CTCF	chr8:17142420-17142570	HMF	breast:	n/a	n/a
12	CTCF	chr8:17148479-17148594	GM10248	blood:	n/a	n/a
13	CTCF	chr8:17142420-17142573	SK-N-SH_RA	brain:	n/a	n/a
14	CTCF	chr8:17142500-17142650	AG09319	gingival:	n/a	n/a
15	CTCF	chr8:17142420-17142570	HPAF	blood vessel:	n/a	n/a
16	CTCF	chr8:17142405-17142571	HepG2	liver:	n/a	n/a
17	CTCF	chr8:17142420-17142570	AG04449	skin:	n/a	n/a
18	CTCF	chr8:17142454-17142522	Pancreas_OC	pancreas:	n/a	n/a
19	CTCF	chr8:17142480-17142630	HMF	breast:	n/a	n/a
20	CTCF	chr8:17142380-17142530	GM12871	blood:	n/a	n/a
21	CTCF	chr8:17142418-17142552	MCF-7	breast:	n/a	n/a
22	CTCF	chr8:17142420-17142570	HAc	cerebellar:	n/a	n/a
23	CTCF	chr8:17142420-17142570	AG04450	lung:	n/a	n/a
24	CTCF	chr8:17142391-17142592	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr8:17142380-17142530	RPTEC	kidney:	n/a	n/a
26	CTCF	chr8:17142460-17142610	BJ	skin:	n/a	n/a
27	CTCF	chr8:17142420-17142570	HRPEpiC	eye:	n/a	n/a
28	CTCF	chr8:17142360-17142510	HUVEC	blood vessel:	n/a	n/a
29	CTCF	chr8:17142414-17142534	Gliobla	brain:	n/a	n/a
30	CTCF	chr8:17142400-17142550	AG09319	gingival:	n/a	n/a
31	CTCF	chr8:17142400-17142550	AG04449	skin:	n/a	n/a
32	CTCF	chr8:17142340-17142490	HCFaa	heart:	n/a	n/a
33	CTCF	chr8:17142360-17142645	IMR90	lung:	n/a	n/a
34	CTCF	chr8:17142420-17142570	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr8:17142500-17142650	HAc	cerebellar:	n/a	n/a
36	CTCF	chr8:17142420-17142570	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr8:17142400-17142550	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr8:17142390-17142581	K562	blood:	n/a	n/a
39	CTCF	chr8:17142420-17142570	Caco-2	colon:	n/a	n/a
40	CTCF	chr8:17142445-17142534	K562	blood:	n/a	n/a
41	CTCF	chr8:17142440-17142590	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr8:17142380-17142530	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr8:17142420-17142570	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr8:17142500-17142650	HVMF	connective:	n/a	n/a
45	CTCF	chr8:17142340-17142490	HVMF	connective:	n/a	n/a
46	CTCF	chr8:17142340-17142490	HA-sp	spinal cord:	n/a	n/a
47	CTCF	chr8:17142440-17142590	HFF-Myc	foreskin:	n/a	n/a
48	CTCF	chr8:17142620-17142770	Caco-2	colon:	n/a	n/a
49	CTCF	chr8:17142440-17142590	HVMF	connective:	n/a	n/a
50	CTCF	chr8:17142441-17142541	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:17146201-17146251	HRCEpiC	kidney:	n/a
2	chr8:17146201-17146251	T-47D	breast:	n/a
3	chr8:17146201-17146251	H1-hESC	embryonic stem cell:	embryo
4	chr8:17146201-17146251	PFSK-1	brain:	n/a
5	chr8:17146201-17146251	AG09309	skin:	n/a
6	chr8:17146201-17146251	HCPEpiC	choroid plexus:	n/a
7	chr8:17146201-17146251	AG04450	lung:	fetal
8	chr8:17146201-17146251	ProgFib	skin:	n/a
9	chr8:17146201-17146251	RPTEC	kidney:	n/a
10	chr8:17146201-17146251	GM12892	blood:	n/a
11	chr8:17146201-17146251	U87	brain:	n/a
12	chr8:17146201-17146251	HAEpiC	amniotic membrane:	n/a
13	chr8:17146201-17146251	BE2_C	brain:	n/a
14	chr8:17146201-17146251	SK-N-SH	brain:	n/a
15	chr8:17146201-17146251	HNPCEpiC	eye:	n/a
16	chr8:17146201-17146251	Jurkat	blood:	n/a
17	chr8:17146201-17146251	Hepatocyte	liver:	n/a
18	chr8:17146201-17146251	NHDF-neo	bronchial:	n/a
19	chr8:17146201-17146251	HCF	heart:	n/a
20	chr8:17146201-17146251	HIPEpiC	eye:	n/a
21	chr8:17146201-17146251	PANC-1	pancreas:	n/a
22	chr8:17146201-17146251	NT2-D1	testis:	n/a
23	chr8:17146201-17146251	Hela-S3	cervix:	n/a
24	chr8:17146201-17146251	HCM	heart:	n/a
25	chr8:17146201-17146251	HEEpiC	esophagus:	n/a
26	chr8:17146201-17146251	HMEC	breast:	n/a
27	chr8:17146201-17146251	HepG2	liver:	n/a
28	chr8:17146201-17146251	CMK	blood:	n/a
29	chr8:17146201-17146251	SAEC	small airway:	n/a
30	chr8:17146201-17146251	IMR90	lung:	fetal
31	chr8:17146201-17146251	BJ	skin:	n/a
32	chr8:17146201-17146251	HEK293	kidney:	embryo
33	chr8:17146201-17146251	GM06990	blood:	n/a
34	chr8:17146201-17146251	GM19239	blood:	n/a
35	chr8:17146201-17146251	NH-A	brain:	n/a
36	chr8:17146201-17146251	SK-N-SH_RA	brain:	n/a
37	chr8:17146201-17146251	GM12878	blood:	n/a
38	chr8:17146201-17146251	HRE	kidney:	n/a
39	chr8:17146201-17146251	AoSMC	blood vessel:	n/a
40	chr8:17146201-17146251	HUVEC	blood vessel:	n/a
41	chr8:17146201-17146251	SKMC	muscle:	n/a
42	chr8:17146201-17146251	AG04449	skin:	fetal
43	chr8:17146201-17146251	ECC-1	luminal epithelium:	n/a
44	chr8:17146201-17146251	HPAEpiC	pulmonary alveolar:	n/a
45	chr8:17146201-17146251	HRPEpiC	eye:	n/a
46	chr8:17146201-17146251	K562	blood:	n/a
47	chr8:17146201-17146251	A549	lung:	n/a
48	chr8:17146201-17146251	AG09319	gingival:	n/a
49	chr8:17146201-17146251	ovcar-3	ovarian:	n/a
50	chr8:17146201-17146251	MCF10A-Er-Src	breast:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:17150961..17152900-chr8:17155018..17157841,2	K562	blood:
2	chr8:17140191..17142110-chr8:17143983..17147187,3	K562	blood:
3	chr8:17140191..17142110-chr8:17143983..17147187,3	K562	blood:
4	chr8:17135210..17137746-chr8:17141581..17143958,2	MCF-7	breast:
5	chr8:17129178..17133989-chr8:17134678..17139635,6	K562	blood:
6	chr8:17103075..17105052-chr8:17136390..17138704,2	K562	blood:
7	chr8:17138059..17140841-chr8:17141112..17143535,3	K562	blood:
8	chr8:17135210..17137746-chr8:17141581..17143958,2	MCF-7	breast:
9	chr8:17131674..17134373-chr8:17137994..17139635,2	K562	blood:
10	chr8:17138059..17140841-chr8:17141112..17143535,3	K562	blood:
11	chr8:17135640..17137186-chr8:17138924..17140760,2	K562	blood:
12	chr8:17136101..17138499-chr8:17144330..17145871,2	K562	blood:
13	chr8:17012171..17015039-chr8:17137782..17140431,2	K562	blood:
14	chr8:17136101..17138499-chr8:17144330..17145871,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	VPS37A	hsa-miR-148b-3p	chr8:17152675-17152702

Variant related genes	Relation type
VPS37A	TF binding region
VPS37A	CpG island
ENSG00000104219	chromatin interactions
ENSG00000155975	chromatin interactions
ENSG00000198791	chromatin interactions

Extended variants
information (count: 863 )
Associated
traits (count: 126 )

Variant overlapped rSNPs/rCNVs (count:863 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3213601	chr8:17137687-17137688	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs560249010	chr8:17137691-17137692	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs375487182	chr8:17137707-17137708	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs368525670	chr8:17137712-17137713	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs201026976	chr8:17137715-17137716	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs571908373	chr8:17137716-17137717	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs376210724	chr8:17137772-17137773	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs369901222	chr8:17137852-17137853	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs368005823	chr8:17137875-17137876	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs370931373	chr8:17137901-17137902	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs146110170	chr8:17137912-17137913	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs375086724	chr8:17137916-17137917	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs199613484	chr8:17137918-17137919	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs200458295	chr8:17137933-17137934	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs542266150	chr8:17137936-17137937	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs545635309	chr8:17137941-17137942	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs201073603	chr8:17137944-17137945	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs200114657	chr8:17137965-17137966	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs202036712	chr8:17137968-17137969	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs200298605	chr8:17137975-17137976	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs371282134	chr8:17137987-17137988	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs79817412	chr8:17137996-17137997	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs3216864	chr8:17137998-17137999	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs149520550	chr8:17138007-17138008	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs200160687	chr8:17138045-17138046	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs144099578	chr8:17138059-17138060	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs192584902	chr8:17138068-17138069	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs184437509	chr8:17138070-17138071	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs187621481	chr8:17138089-17138090	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs556603512	chr8:17138093-17138094	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs569147500	chr8:17138101-17138102	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs538174437	chr8:17138110-17138111	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs191739262	chr8:17138119-17138120	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs7007753	chr8:17138139-17138140	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs533639302	chr8:17138163-17138164	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs577968304	chr8:17138185-17138186	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs17502646	chr8:17138188-17138189	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs573656910	chr8:17138299-17138300	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs542579710	chr8:17138340-17138341	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs184331239	chr8:17138342-17138343	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs532379560	chr8:17138349-17138350	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs148273637	chr8:17138371-17138372	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs141135402	chr8:17138373-17138374	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs34249980	chr8:17138515-17138516	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs10503590	chr8:17138539-17138540	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs150714830	chr8:17138545-17138546	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs2188015	chr8:17138567-17138568	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs561389652	chr8:17138569-17138570	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs559749499	chr8:17138571-17138572	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs547570453	chr8:17138582-17138583	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:126)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	17603634	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	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
Prostate cancer	21965145	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
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Colorectal cancer	17229543	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	20606397	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
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Colorectal cancer	16774939	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Epilepsy	22083797	CNVD
Cancer	18840272	CNVD
Epithelial cancer	20478067	CNVD
Non-small cell lung cancer	19010865	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Intracranial arachnoid cysts	17641416	CNVD
Breast cancer	19287154	CNVD
Breast cancer	21956041	CNVD
Gastric adenocarcinoma	19115996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Colorectal cancer	19455253	CNVD
Prostate cancer	17217626	CNVD
Cervical cancer	16585170	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	21811587	CNVD
Schizophrenia	19197363	CNVD
Breast cancer	21364760	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:635 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:17114400-17157200	Weak transcription	Stomach Mucosa	stomach
2	chr8:17117600-17145200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr8:17121800-17170600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr8:17122000-17152000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr8:17123000-17141800	Weak transcription	Small Intestine	intestine
6	chr8:17124000-17149400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr8:17124000-17162400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr8:17124400-17147600	Strong transcription	Monocytes-CD14+_RO01746	blood
9	chr8:17124600-17145600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr8:17124800-17145400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr8:17125000-17164200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr8:17125200-17161000	Strong transcription	Primary T helper cells fromperipheralblood	blood
13	chr8:17125400-17146800	Strong transcription	Dnd41	blood
14	chr8:17125600-17145200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr8:17125600-17145200	Weak transcription	Colonic Mucosa	Colon
16	chr8:17125600-17163600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr8:17125800-17145200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr8:17125800-17162000	Strong transcription	Primary T helper cells PMA-I stimulated	--
19	chr8:17126000-17145200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr8:17126000-17145800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr8:17126000-17148600	Strong transcription	Liver	Liver
22	chr8:17126600-17148200	Strong transcription	Primary neutrophils fromperipheralblood	blood
23	chr8:17126600-17148400	Strong transcription	Placenta	Placenta
24	chr8:17126600-17160200	Strong transcription	Duodenum Mucosa	Duodenum
25	chr8:17126800-17146600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
26	chr8:17128200-17142600	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr8:17128400-17145200	Weak transcription	Right Ventricle	heart
28	chr8:17128600-17144600	Weak transcription	Spleen	Spleen
29	chr8:17129800-17142200	Weak transcription	Fetal Intestine Small	intestine
30	chr8:17129800-17145200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr8:17130600-17148200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
32	chr8:17130600-17160600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr8:17131200-17145800	Strong transcription	HUES64 Cell Line	embryonic stem cell
34	chr8:17131200-17149800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr8:17131400-17148400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr8:17131400-17148800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr8:17131400-17150200	Strong transcription	Muscle Satellite Cultured Cells	--
38	chr8:17131400-17174600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
39	chr8:17131600-17141000	Strong transcription	Primary hematopoietic stem cells	blood
40	chr8:17131600-17145200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr8:17131600-17147200	Strong transcription	Adipose Nuclei	Adipose
42	chr8:17131600-17154000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
43	chr8:17131800-17137800	Strong transcription	Primary T cells from cord blood	blood
44	chr8:17131800-17138200	Strong transcription	Fetal Muscle Trunk	muscle
45	chr8:17131800-17140200	Strong transcription	HepG2	liver
46	chr8:17131800-17140800	Strong transcription	NH-A	brain
47	chr8:17131800-17144800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
48	chr8:17131800-17145200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
49	chr8:17131800-17145400	Strong transcription	HUES6 Cell Line	embryonic stem cell
50	chr8:17131800-17145600	Strong transcription	GM12878-XiMat	blood

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