Variant report

Variant	nsv886727
Chromosome Location	chr6:141610933-141793547
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:964)
CpG islands
(count:184)
Chromatin interactive
region (count:20)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:964 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:141702263-141702688	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:141647618-141647926	HepG2	liver:	n/a	n/a
3	ATF1	chr6:141612636-141612753	K562	blood:	n/a	n/a
4	ATF2	chr6:141709759-141710160	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr6:141702222-141702676	GM12878	blood:	n/a	n/a
6	ATF2	chr6:141702298-141702702	GM12878	blood:	n/a	n/a
7	ATF3	chr6:141647541-141647917	A549	lung:	n/a	n/a
8	BATF	chr6:141625060-141625335	GM12878	blood:	n/a	n/a
9	BATF	chr6:141784851-141785027	GM12878	blood:	n/a	n/a
10	BATF	chr6:141702264-141702585	GM12878	blood:	n/a	chr6:141702436-141702447
11	BATF	chr6:141647651-141647932	GM12878	blood:	n/a	chr6:141647803-141647814
12	BATF	chr6:141702232-141702646	GM12878	blood:	n/a	chr6:141702436-141702447
13	BCL11A	chr6:141702335-141702575	GM12878	blood:	n/a	chr6:141702430-141702439 chr6:141702440-141702449 chr6:141702439-141702448
14	BCL11A	chr6:141702248-141702564	GM12878	blood:	n/a	chr6:141702430-141702439 chr6:141702440-141702449 chr6:141702439-141702448
15	BCL11A	chr6:141709759-141710112	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL3	chr6:141702321-141702647	GM12878	blood:	n/a	chr6:141702430-141702439 chr6:141702440-141702449 chr6:141702439-141702448
17	BCL3	chr6:141647588-141647832	GM12878	blood:	n/a	n/a
18	BCL3	chr6:141647553-141647910	GM12878	blood:	n/a	n/a
19	BCLAF1	chr6:141702322-141702563	GM12878	blood:	n/a	chr6:141702430-141702439 chr6:141702440-141702449 chr6:141702439-141702448
20	BHLHE40	chr6:141702358-141702623	GM12878	blood:	n/a	n/a
21	BHLHE40	chr6:141785736-141785898	GM12878	blood:	n/a	n/a
22	BRCA1	chr6:141647463-141648010	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr6:141630527-141630762	H1-hESC	embryonic stem cell:	n/a	n/a
24	CBX3	chr6:141647435-141648087	HCT-116	colon:	n/a	n/a
25	CBX3	chr6:141742585-141742940	HCT-116	colon:	n/a	n/a
26	CBX3	chr6:141647419-141648088	HCT-116	colon:	n/a	n/a
27	CEBPB	chr6:141722290-141722536	HepG2	liver:	n/a	chr6:141722379-141722390
28	CEBPB	chr6:141711106-141711414	IMR90	lung:	n/a	chr6:141711246-141711257 chr6:141711244-141711255 chr6:141711244-141711257 chr6:141711244-141711257 chr6:141711244-141711257
29	CEBPB	chr6:141632391-141632610	HepG2	liver:	n/a	n/a
30	CEBPB	chr6:141742530-141742887	IMR90	lung:	n/a	n/a
31	CEBPB	chr6:141622931-141623296	Hela-S3	cervix:	n/a	chr6:141622957-141622968
32	CEBPB	chr6:141711132-141711395	K562	blood:	n/a	chr6:141711246-141711257 chr6:141711244-141711255 chr6:141711244-141711257 chr6:141711244-141711257 chr6:141711244-141711257
33	CEBPB	chr6:141711121-141711389	Hela-S3	cervix:	n/a	chr6:141711246-141711257 chr6:141711244-141711255 chr6:141711244-141711257 chr6:141711244-141711257 chr6:141711244-141711257
34	CEBPB	chr6:141724820-141725300	MCF-7	breast:	n/a	n/a
35	CEBPB	chr6:141696297-141696635	HepG2	liver:	n/a	chr6:141696471-141696482
36	CEBPB	chr6:141647486-141648087	A549	lung:	n/a	n/a
37	CEBPB	chr6:141711069-141711425	HepG2	liver:	n/a	chr6:141711246-141711257 chr6:141711244-141711255 chr6:141711244-141711257 chr6:141711244-141711257 chr6:141711244-141711257
38	CEBPB	chr6:141622933-141623251	HepG2	liver:	n/a	chr6:141622957-141622968
39	CEBPB	chr6:141746002-141746317	IMR90	lung:	n/a	chr6:141746166-141746177
40	CEBPB	chr6:141742602-141742871	A549	lung:	n/a	n/a
41	CEBPB	chr6:141717070-141717316	HepG2	liver:	n/a	n/a
42	CEBPB	chr6:141696314-141696617	IMR90	lung:	n/a	chr6:141696471-141696482
43	CEBPB	chr6:141742530-141742888	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr6:141647469-141647992	A549	lung:	n/a	n/a
45	CEBPB	chr6:141760039-141760303	HepG2	liver:	n/a	chr6:141760191-141760202
46	CEBPB	chr6:141746032-141746219	K562	blood:	n/a	chr6:141746166-141746177
47	CEBPB	chr6:141622937-141623281	IMR90	lung:	n/a	chr6:141622957-141622968
48	CEBPB	chr6:141647417-141648140	IMR90	lung:	n/a	n/a
49	CEBPB	chr6:141746014-141746310	HepG2	liver:	n/a	chr6:141746166-141746177
50	CEBPB	chr6:141622940-141623257	A549	lung:	n/a	chr6:141622957-141622968

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:141793045-141793095	NH-A	brain:	n/a
2	chr6:141793045-141793095	NH-A	brain:	n/a
3	chr6:141643325-141643375	MCF-7	breast:	n/a
4	chr6:141793045-141793095	GM12891	blood:	n/a
5	chr6:141782625-141782675	GM12891	blood:	n/a
6	chr6:141782625-141782675	PrEC	prostate:	n/a
7	chr6:141782625-141782675	HAEpiC	amniotic membrane:	n/a
8	chr6:141782625-141782675	HRPEpiC	eye:	n/a
9	chr6:141793045-141793095	HCPEpiC	choroid plexus:	n/a
10	chr6:141782625-141782675	NHDF-neo	bronchial:	n/a
11	chr6:141793045-141793095	NHBE	bronchial:	n/a
12	chr6:141643325-141643375	Hepatocyte	liver:	n/a
13	chr6:141793045-141793095	HCF	heart:	n/a
14	chr6:141643325-141643375	K562	blood:	n/a
15	chr6:141793045-141793095	NB4	blood:	n/a
16	chr6:141782625-141782675	AG04449	skin:	fetal
17	chr6:141643325-141643375	U87	brain:	n/a
18	chr6:141793045-141793095	BJ	skin:	n/a
19	chr6:141782625-141782675	MCF10A-Er-Src	breast:	n/a
20	chr6:141782625-141782675	H1-hESC	embryonic stem cell:	embryo
21	chr6:141643325-141643375	LNCaP	prostate:	n/a
22	chr6:141782625-141782675	HIPEpiC	eye:	n/a
23	chr6:141782625-141782675	SK-N-MC	brain:	n/a
24	chr6:141643325-141643375	HMEC	breast:	n/a
25	chr6:141643325-141643375	AoSMC	blood vessel:	n/a
26	chr6:141643325-141643375	HUVEC	blood vessel:	n/a
27	chr6:141643325-141643375	AG09319	gingival:	n/a
28	chr6:141643325-141643375	SK-N-SH	brain:	n/a
29	chr6:141643325-141643375	HEK293	kidney:	embryo
30	chr6:141782625-141782675	HUVEC	blood vessel:	n/a
31	chr6:141793045-141793095	HEK293	kidney:	embryo
32	chr6:141643325-141643375	A549	lung:	n/a
33	chr6:141782625-141782675	NHBE	bronchial:	n/a
34	chr6:141793045-141793095	ECC-1	luminal epithelium:	n/a
35	chr6:141782625-141782675	AG09309	skin:	n/a
36	chr6:141643325-141643375	ovcar-3	ovarian:	n/a
37	chr6:141793045-141793095	HepG2	liver:	n/a
38	chr6:141793045-141793095	ProgFib	skin:	n/a
39	chr6:141782625-141782675	PANC-1	pancreas:	n/a
40	chr6:141782625-141782675	BJ	skin:	n/a
41	chr6:141793045-141793095	MCF10A-Er-Src	breast:	n/a
42	chr6:141793045-141793095	A549	lung:	n/a
43	chr6:141643325-141643375	AG04449	skin:	fetal
44	chr6:141643325-141643375	BJ	skin:	n/a
45	chr6:141793045-141793095	RPTEC	kidney:	n/a
46	chr6:141793045-141793095	LNCaP	prostate:	n/a
47	chr6:141643325-141643375	NH-A	brain:	n/a
48	chr6:141643325-141643375	HNPCEpiC	eye:	n/a
49	chr6:141782625-141782675	MCF-7	breast:	n/a
50	chr6:141643325-141643375	AG09309	skin:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:141630271..141631033-chr6:141883682..141884206,2	MCF-7	breast:
2	chr6:141607703..141609358-chr6:141615352..141617178,2	K562	blood:
3	chr6:141723648..141725230-chr6:141726285..141728524,2	K562	blood:
4	chr6:141737292..141738838-chr6:141741938..141743477,2	MCF-7	breast:
5	chr6:141606885..141609429-chr6:141611912..141614017,2	MCF-7	breast:
6	chr6:141630179..141631093-chr6:141883723..141884605,3	MCF-7	breast:
7	chr6:141630409..141632111-chr6:141635351..141637298,2	MCF-7	breast:
8	chr6:141670532..141672796-chr6:141769039..141771621,2	K562	blood:
9	chr16:29985064..29985849-chr6:141782106..141782678,2	MCF-7	breast:
10	chr6:141783152..141786051-chr6:141790020..141792885,2	MCF-7	breast:
11	chr6:141781801..141783387-chr6:141785165..141786989,2	K562	blood:
12	chr6:141737292..141738838-chr6:141741938..141743477,2	MCF-7	breast:
13	chr6:141724021..141726766-chr6:141733635..141735399,2	K562	blood:
14	chr6:141723648..141725230-chr6:141726285..141728524,2	K562	blood:
15	chr6:141630409..141632111-chr6:141635351..141637298,2	MCF-7	breast:
16	chr6:141670532..141672796-chr6:141769039..141771621,2	K562	blood:
17	chr6:141781801..141783387-chr6:141785165..141786989,2	K562	blood:
18	chr6:141783152..141786051-chr6:141790020..141792885,2	MCF-7	breast:
19	chr6:141602459..141604737-chr6:141622065..141624728,2	K562	blood:
20	chr6:141724021..141726766-chr6:141733635..141735399,2	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GJE1-3	chr6:141724684-141725047	NONHSAT115293
2	lnc-GJE1-3	chr6:141724593-141724626	NONHSAT115293
3	lnc-GJE1-3	chr6:141767146-141767709	NONHSAT115291
4	lnc-GJE1-2	chr6:141768148-141771097	NONHSAT115296
5	lnc-GJE1-3	chr6:141724525-141724626	NONHSAT115292
6	lnc-GJE1-2	chr6:141771117-141772143	NONHSAT115296
7	lnc-GJE1-3	chr6:141724707-141725411	NONHSAT115291
8	lnc-GJE1-3	chr6:141724594-141724626	XLOC_005486
9	lnc-GJE1-2	chr6:141768148-141772143	ENSG00000259828.1
10	lnc-GJE1-3	chr6:141767470-141767655	NONHSAT115294
11	lnc-GJE1-2	chr6:141768147-141772155	NONHSAT115295
12	lnc-GJE1-3	chr6:141724707-141725475	NONHSAT115292
13	lnc-GJE1-3	chr6:141724525-141724626	NONHSAT115291
14	lnc-GJE1-3	chr6:141724707-141724930	XLOC_005486
15	lnc-GJE1-3	chr6:141742782-141743070	NONHSAT115294

No data

Variant related genes	Relation type
ENSG00000259828	TF binding region
ENSG00000259828	CpG island
ENSG00000149930	chromatin interactions
WIPF1	miRNA target sites
FBLIM1	miRNA target sites

Extended variants
information (count: 4581 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:4581 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9403283	chr6:141610933-141610934	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs534239755	chr6:141610938-141610939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs9403284	chr6:141610967-141610968	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs551749543	chr6:141611005-141611006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs563888732	chr6:141611006-141611007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs9376601	chr6:141611024-141611025	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs9376602	chr6:141611039-141611040	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs77399852	chr6:141611073-141611074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs184357533	chr6:141611083-141611084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs535626843	chr6:141611088-141611089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs551264013	chr6:141611096-141611097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs565428322	chr6:141611120-141611121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs569437925	chr6:141611154-141611155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs189501038	chr6:141611191-141611192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558162010	chr6:141611201-141611202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs534367352	chr6:141611226-141611227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs61142151	chr6:141611254-141611255	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs555552101	chr6:141611270-141611271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs374085514	chr6:141611321-141611322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs114264500	chr6:141611350-141611351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs541620194	chr6:141611421-141611422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs557687183	chr6:141611434-141611435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575180883	chr6:141611437-141611438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs546057335	chr6:141611458-141611459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs915261	chr6:141611492-141611493	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs67552051	chr6:141611532-141611533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs200284951	chr6:141611546-141611547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs181890760	chr6:141611604-141611605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs117138880	chr6:141611616-141611617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs573492459	chr6:141611628-141611629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs118085781	chr6:141611667-141611668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs561586170	chr6:141611676-141611677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs142626302	chr6:141611738-141611739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs17070752	chr6:141611739-141611740	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs569598082	chr6:141611743-141611744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs17070754	chr6:141611748-141611749	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs375076334	chr6:141611789-141611790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs57714624	chr6:141611798-141611799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs552068389	chr6:141611806-141611807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs144968399	chr6:141611864-141611865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs534137463	chr6:141611892-141611893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs185484652	chr6:141611897-141611898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188193186	chr6:141611916-141611917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs9321808	chr6:141611920-141611921	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs115364367	chr6:141611943-141611944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs181402330	chr6:141611995-141611996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545709367	chr6:141612053-141612054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs186626435	chr6:141612084-141612085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs572513081	chr6:141612096-141612097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs111568788	chr6:141612099-141612100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Gastric cancer	17908304	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Breast cancer	21364760	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute monocytic leukemia	16498392	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
craniofacial dysmorphism	21918468	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:698 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:141610000-141613400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr6:141610200-141612200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr6:141610400-141612200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr6:141612000-141612400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr6:141612200-141612400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr6:141612200-141613400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr6:141617000-141617200	ZNF genes & repeats	Left Ventricle	heart
8	chr6:141622400-141623600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr6:141622600-141623400	Enhancers	Muscle Satellite Cultured Cells	--
10	chr6:141628000-141630000	Weak transcription	Aorta	Aorta
11	chr6:141628800-141629200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
12	chr6:141629000-141629200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
13	chr6:141629200-141630200	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr6:141630000-141630200	ZNF genes & repeats	Aorta	Aorta
15	chr6:141630200-141630400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
16	chr6:141630400-141630600	Enhancers	H9 Cell Line	embryonic stem cell
17	chr6:141630800-141631000	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr6:141630800-141631800	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr6:141631400-141631800	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr6:141631400-141631800	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr6:141631600-141631800	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr6:141633200-141637600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr6:141633800-141634400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr6:141634000-141635000	Enhancers	NHDF-Ad	bronchial
25	chr6:141634000-141636000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr6:141635000-141635800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr6:141635000-141635800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr6:141635200-141635400	Enhancers	Psoas Muscle	Psoas
29	chr6:141635200-141635600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr6:141635200-141635600	Enhancers	Brain Hippocampus Middle	brain
31	chr6:141635200-141635600	Enhancers	Brain Inferior Temporal Lobe	brain
32	chr6:141635200-141635600	Enhancers	HMEC	breast
33	chr6:141635200-141635800	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr6:141635200-141635800	Enhancers	Brain Cingulate Gyrus	brain
35	chr6:141635400-141635800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr6:141635400-141648200	Weak transcription	Psoas Muscle	Psoas
37	chr6:141635600-141647600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr6:141637600-141638600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr6:141638200-141638600	Weak transcription	Ovary	ovary
40	chr6:141638600-141639000	ZNF genes & repeats	Ovary	ovary
41	chr6:141638600-141639200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr6:141638600-141639400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr6:141639000-141643000	Weak transcription	Ovary	ovary
44	chr6:141639400-141642600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr6:141642400-141642600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr6:141642400-141642800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr6:141642400-141642800	Enhancers	NHLF	lung
48	chr6:141642400-141643400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr6:141642400-141643600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr6:141642600-141643000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links