Variant report

Variant	nsv1022911
Chromosome Location	chr6:5286297-5322133
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:617)
CpG islands
(count:244)
Chromatin interactive
region (count:39)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:617 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:5302507-5302854	K562	blood:	n/a	n/a
2	ARID3A	chr6:5299473-5299621	K562	blood:	n/a	n/a
3	ATF1	chr6:5300478-5300736	K562	blood:	n/a	n/a
4	ATF1	chr6:5302305-5302992	K562	blood:	n/a	n/a
5	ATF1	chr6:5294668-5294952	K562	blood:	n/a	n/a
6	ATF2	chr6:5302657-5303223	GM12878	blood:	n/a	n/a
7	ATF2	chr6:5303469-5303900	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr6:5302721-5303188	GM12878	blood:	n/a	n/a
9	ATF3	chr6:5287879-5288150	K562	blood:	n/a	n/a
10	BACH1	chr6:5309454-5309486	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr6:5303473-5303784	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr6:5302740-5303111	GM12878	blood:	n/a	n/a
13	BATF	chr6:5287873-5288218	GM12878	blood:	n/a	chr6:5288074-5288085 chr6:5288075-5288085
14	BATF	chr6:5302751-5303177	GM12878	blood:	n/a	n/a
15	BCL11A	chr6:5302695-5303166	GM12878	blood:	n/a	n/a
16	BCL11A	chr6:5302827-5303127	GM12878	blood:	n/a	n/a
17	BCLAF1	chr6:5302694-5303208	GM12878	blood:	n/a	n/a
18	BHLHE40	chr6:5302700-5303149	GM12878	blood:	n/a	n/a
19	BHLHE40	chr6:5302378-5303223	K562	blood:	n/a	chr6:5303157-5303173
20	BHLHE40	chr6:5294781-5294796	GM12878	blood:	n/a	n/a
21	BHLHE40	chr6:5303415-5303850	GM12878	blood:	n/a	n/a
22	BHLHE40	chr6:5294594-5295481	K562	blood:	n/a	n/a
23	BHLHE40	chr6:5303460-5303853	HepG2	liver:	n/a	n/a
24	BHLHE40	chr6:5303479-5303817	K562	blood:	n/a	n/a
25	CCNT2	chr6:5302407-5303003	K562	blood:	n/a	n/a
26	CCNT2	chr6:5301725-5302022	K562	blood:	n/a	n/a
27	CEBPB	chr6:5293505-5293747	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr6:5303331-5303567	HepG2	liver:	n/a	chr6:5303385-5303396
29	CEBPB	chr6:5294370-5294450	HepG2	liver:	n/a	n/a
30	CEBPB	chr6:5287939-5288260	IMR90	lung:	n/a	n/a
31	CEBPB	chr6:5306244-5306591	HepG2	liver:	n/a	n/a
32	CEBPB	chr6:5301729-5301974	IMR90	lung:	n/a	chr6:5301839-5301850
33	CEBPB	chr6:5301611-5302033	K562	blood:	n/a	chr6:5301839-5301850
34	CEBPB	chr6:5293477-5293659	K562	blood:	n/a	n/a
35	CEBPB	chr6:5319561-5319680	HepG2	liver:	n/a	chr6:5319626-5319637
36	CEBPB	chr6:5294248-5294468	K562	blood:	n/a	n/a
37	CEBPB	chr6:5302467-5302775	K562	blood:	n/a	n/a
38	CEBPB	chr6:5301726-5301934	Hela-S3	cervix:	n/a	chr6:5301839-5301850
39	CEBPB	chr6:5301695-5301973	K562	blood:	n/a	chr6:5301839-5301850
40	CEBPB	chr6:5310974-5311291	HepG2	liver:	n/a	chr6:5311162-5311173 chr6:5311133-5311144
41	CEBPB	chr6:5301726-5302015	HepG2	liver:	n/a	chr6:5301839-5301850
42	CEBPB	chr6:5301651-5302017	K562	blood:	n/a	chr6:5301839-5301850
43	CEBPB	chr6:5306298-5306468	HepG2	liver:	n/a	n/a
44	CEBPD	chr6:5302360-5302888	K562	blood:	n/a	n/a
45	CHD1	chr6:5314239-5314269	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr6:5302698-5303863	GM12878	blood:	n/a	n/a
47	CHD2	chr6:5303538-5303761	HepG2	liver:	n/a	n/a
48	CTCF	chr6:5303620-5303770	GM12869	blood:	n/a	chr6:5303671-5303689 chr6:5303666-5303687
49	CTCF	chr6:5303580-5303730	Caco-2	colon:	n/a	chr6:5303671-5303689 chr6:5303666-5303687
50	CTCF	chr6:5303589-5303787	HepG2	liver:	n/a	chr6:5303671-5303689 chr6:5303666-5303687

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:5313645-5313695	GM12891	blood:	n/a
2	chr6:5316922-5316972	CMK	blood:	n/a
3	chr6:5296249-5296299	SK-N-SH	brain:	n/a
4	chr6:5313645-5313695	HRPEpiC	eye:	n/a
5	chr6:5313645-5313695	PFSK-1	brain:	n/a
6	chr6:5313645-5313695	AG10803	skin:	n/a
7	chr6:5296249-5296299	HAEpiC	amniotic membrane:	n/a
8	chr6:5316922-5316972	LNCaP	prostate:	n/a
9	chr6:5296249-5296299	NB4	blood:	n/a
10	chr6:5296249-5296299	HEEpiC	esophagus:	n/a
11	chr6:5287843-5287893	AG09309	skin:	n/a
12	chr6:5316922-5316972	IMR90	lung:	fetal
13	chr6:5287843-5287893	H1-hESC	embryonic stem cell:	embryo
14	chr6:5316922-5316972	MCF10A-Er-Src	breast:	n/a
15	chr6:5287843-5287893	CMK	blood:	n/a
16	chr6:5313645-5313695	HIPEpiC	eye:	n/a
17	chr6:5313645-5313695	HEK293	kidney:	embryo
18	chr6:5287843-5287893	K562	blood:	n/a
19	chr6:5287843-5287893	AG09319	gingival:	n/a
20	chr6:5313645-5313695	SK-N-SH	brain:	n/a
21	chr6:5313645-5313695	AG04450	lung:	fetal
22	chr6:5316922-5316972	PrEC	prostate:	n/a
23	chr6:5316922-5316972	GM12892	blood:	n/a
24	chr6:5316922-5316972	HEEpiC	esophagus:	n/a
25	chr6:5287843-5287893	NHBE	bronchial:	n/a
26	chr6:5313645-5313695	HNPCEpiC	eye:	n/a
27	chr6:5313645-5313695	RPTEC	kidney:	n/a
28	chr6:5287843-5287893	SKMC	muscle:	n/a
29	chr6:5313645-5313695	HepG2	liver:	n/a
30	chr6:5296249-5296299	AG04450	lung:	fetal
31	chr6:5313645-5313695	ECC-1	luminal epithelium:	n/a
32	chr6:5296249-5296299	RPTEC	kidney:	n/a
33	chr6:5313645-5313695	AG09309	skin:	n/a
34	chr6:5287843-5287893	AoSMC	blood vessel:	n/a
35	chr6:5287843-5287893	AG04449	skin:	fetal
36	chr6:5316922-5316972	AG10803	skin:	n/a
37	chr6:5296249-5296299	AoSMC	blood vessel:	n/a
38	chr6:5296249-5296299	AG04449	skin:	fetal
39	chr6:5296249-5296299	GM06990	blood:	n/a
40	chr6:5316922-5316972	Hela-S3	cervix:	n/a
41	chr6:5313645-5313695	AoSMC	blood vessel:	n/a
42	chr6:5313645-5313695	AG04449	skin:	fetal
43	chr6:5313645-5313695	HPAEpiC	pulmonary alveolar:	n/a
44	chr6:5313645-5313695	SK-N-MC	brain:	n/a
45	chr6:5316922-5316972	ovcar-3	ovarian:	n/a
46	chr6:5316922-5316972	SK-N-SH	brain:	n/a
47	chr6:5313645-5313695	NHBE	bronchial:	n/a
48	chr6:5287843-5287893	T-47D	breast:	n/a
49	chr6:5287843-5287893	HCPEpiC	choroid plexus:	n/a
50	chr6:5287843-5287893	GM12891	blood:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:5259367..5263928-chr6:5312372..5314632,4	K562	blood:
2	chr6:5260357..5262137-chr6:5285896..5288338,2	MCF-7	breast:
3	chr6:5285992..5290262-chr6:5291687..5294091,5	K562	blood:
4	chr6:5279637..5281330-chr6:5284508..5287117,2	K562	blood:
5	chr6:5287945..5289983-chr6:5297023..5298876,2	K562	blood:
6	chr6:5259190..5262495-chr6:5294603..5298881,4	K562	blood:
7	chr6:5262260..5264033-chr6:5288601..5290275,2	K562	blood:
8	chr6:5287945..5289983-chr6:5297023..5298876,2	K562	blood:
9	chr6:5261565..5263835-chr6:5284540..5287301,3	MCF-7	breast:
10	chr6:5259995..5261574-chr6:5300847..5302570,2	K562	blood:
11	chr6:5308485..5310755-chr6:5312679..5315010,2	K562	blood:
12	chr6:5280760..5282906-chr6:5284734..5288197,3	K562	blood:
13	chr6:5316219..5318124-chr6:5321436..5323216,2	K562	blood:
14	chr6:5308485..5310755-chr6:5312679..5315010,2	K562	blood:
15	chr6:5316201..5319010-chr6:5321352..5323470,3	K562	blood:
16	chr6:5285992..5290262-chr6:5291687..5294091,5	K562	blood:
17	chr6:5316201..5319010-chr6:5321352..5323470,3	K562	blood:
18	chr6:5259190..5262242-chr6:5295930..5298881,3	K562	blood:
19	chr6:5285977..5287695-chr6:5316657..5318764,2	MCF-7	breast:
20	chr6:5295190..5297508-chr6:5331125..5333153,2	K562	blood:
21	chr6:5308101..5310755-chr6:5313510..5315565,2	K562	blood:
22	chr6:5285714..5287859-chr6:5301778..5303462,2	K562	blood:
23	chr6:5295225..5299115-chr6:5300154..5305822,5	K562	blood:
24	chr6:5295225..5299115-chr6:5300154..5305822,5	K562	blood:
25	chr6:5259520..5261609-chr6:5287252..5289754,2	K562	blood:
26	chr6:5290716..5292630-chr6:5296814..5299702,2	K562	blood:
27	chr6:5285714..5287859-chr6:5301778..5303462,2	K562	blood:
28	chr6:5299459..5300981-chr6:5301727..5303514,2	MCF-7	breast:
29	chr6:5299459..5300981-chr6:5301727..5303514,2	MCF-7	breast:
30	chr6:5284244..5290564-chr6:5292142..5296092,7	K562	blood:
31	chr6:5302902..5305704-chr6:5324020..5325616,2	K562	blood:
32	chr6:5284244..5290564-chr6:5292142..5296092,7	K562	blood:
33	chr6:5314865..5316963-chr6:5319263..5320833,2	K562	blood:
34	chr6:5269061..5270683-chr6:5285353..5286881,2	K562	blood:
35	chr6:5285977..5287695-chr6:5316657..5318764,2	MCF-7	breast:
36	chr6:5316219..5318124-chr6:5321436..5323216,2	K562	blood:
37	chr6:5259574..5262375-chr6:5317058..5319115,2	K562	blood:
38	chr6:5308101..5310755-chr6:5313510..5315565,2	K562	blood:
39	chr6:5314865..5316963-chr6:5319263..5320833,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LYRM4-1	chr6:5291263-5291621	NONHSAT107517

No data

Variant related genes	Relation type
ENSG00000220446	TF binding region
ENSG00000220446	CpG island
ENSG00000220446	chromatin interactions
ENSG00000145982	chromatin interactions
ENSG00000214113	chromatin interactions

Extended variants
information (count: 1411 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1411 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562006454	chr6:5286298-5286299	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs17140092	chr6:5286306-5286307	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs547876012	chr6:5286333-5286334	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs376530654	chr6:5286355-5286356	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs76487949	chr6:5286371-5286372	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs552264798	chr6:5286416-5286417	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs185956696	chr6:5286418-5286419	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs533926957	chr6:5286504-5286505	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs370860124	chr6:5286528-5286529	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs534761585	chr6:5286531-5286532	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs553212273	chr6:5286629-5286630	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs574635219	chr6:5286643-5286644	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs190403498	chr6:5286656-5286657	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs375729467	chr6:5286694-5286695	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs369884368	chr6:5286706-5286707	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs545900779	chr6:5286710-5286711	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs147234235	chr6:5286718-5286719	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs376698740	chr6:5286732-5286733	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs544080451	chr6:5286742-5286743	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs139699402	chr6:5286744-5286745	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs149949618	chr6:5286745-5286746	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs116579221	chr6:5286770-5286771	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs377716755	chr6:5286774-5286775	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs371414965	chr6:5286795-5286796	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs145068193	chr6:5286797-5286798	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs530495709	chr6:5286821-5286822	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs373686523	chr6:5286824-5286825	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs367557080	chr6:5286828-5286829	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs542855287	chr6:5286842-5286843	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs371435638	chr6:5286852-5286853	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs116681043	chr6:5286868-5286869	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs546813383	chr6:5286893-5286894	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs568274665	chr6:5286905-5286906	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs148699023	chr6:5286906-5286907	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs183396648	chr6:5286916-5286917	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs569060868	chr6:5286940-5286941	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs539409349	chr6:5286971-5286972	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs186210930	chr6:5286984-5286985	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs556754902	chr6:5286989-5286990	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs572999303	chr6:5286996-5286997	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs540358021	chr6:5287002-5287003	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs368181403	chr6:5287003-5287004	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs112852546	chr6:5287004-5287005	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs555668671	chr6:5287040-5287041	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs374603606	chr6:5287059-5287060	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs368130163	chr6:5287086-5287087	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs191201505	chr6:5287087-5287088	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs563148873	chr6:5287101-5287102	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs371863264	chr6:5287110-5287111	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs12205949	chr6:5287116-5287117	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Developmental delay	19490664	CNVD
Cancer	21183584	CNVD
Multiple Epiphyseal Dysplasia	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Glaucoma	18694899	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
small cell lung cancer	20016488	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
dysmorphism	22105932	CNVD
psychomotor delay	22105932	CNVD
Ovarian cancer	19193619	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:701 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:5262400-5287200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr6:5262400-5302400	Weak transcription	Aorta	Aorta
3	chr6:5262600-5287200	Weak transcription	Esophagus	oesophagus
4	chr6:5262600-5287600	Weak transcription	Ovary	ovary
5	chr6:5262800-5287200	Weak transcription	Spleen	Spleen
6	chr6:5262800-5287400	Weak transcription	Fetal Muscle Leg	muscle
7	chr6:5263000-5287200	Weak transcription	Stomach Smooth Muscle	stomach
8	chr6:5263000-5287400	Weak transcription	Fetal Stomach	stomach
9	chr6:5263000-5287800	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr6:5263000-5301000	Weak transcription	Fetal Brain Male	brain
11	chr6:5263200-5287800	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr6:5263400-5287400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr6:5263400-5287600	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr6:5263800-5291800	Weak transcription	Fetal Intestine Small	intestine
15	chr6:5267000-5290400	Weak transcription	HepG2	liver
16	chr6:5268000-5294400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr6:5274600-5287200	Weak transcription	Left Ventricle	heart
18	chr6:5274800-5287800	Weak transcription	NHEK	skin
19	chr6:5275000-5290400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr6:5275200-5287400	Weak transcription	Psoas Muscle	Psoas
21	chr6:5276600-5287400	Weak transcription	Fetal Muscle Trunk	muscle
22	chr6:5276600-5294000	Weak transcription	Fetal Intestine Large	intestine
23	chr6:5277400-5287200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr6:5278600-5287200	Weak transcription	Right Ventricle	heart
25	chr6:5279200-5287400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr6:5279200-5289800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr6:5279400-5288200	Weak transcription	Rectal Mucosa Donor 29	rectum
28	chr6:5279400-5298200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr6:5280400-5294000	Weak transcription	Primary T cells fromperipheralblood	blood
30	chr6:5280600-5287200	Weak transcription	HMEC	breast
31	chr6:5280600-5289800	Weak transcription	Primary B cells from cord blood	blood
32	chr6:5280800-5289400	Weak transcription	Primary B cells from peripheral blood	blood
33	chr6:5280800-5293200	Weak transcription	Primary T helper cells fromperipheralblood	blood
34	chr6:5280800-5308200	Weak transcription	Primary T cells from cord blood	blood
35	chr6:5281000-5294400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr6:5281400-5287600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr6:5281400-5293400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
38	chr6:5282600-5287400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr6:5282600-5287800	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr6:5282600-5292200	Weak transcription	Fetal Heart	heart
41	chr6:5282800-5287400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr6:5282800-5287400	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr6:5282800-5287600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr6:5284400-5287400	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr6:5284800-5287400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr6:5285200-5286400	Enhancers	K562	blood
47	chr6:5285200-5287200	Weak transcription	Lung	lung
48	chr6:5285400-5294600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr6:5285600-5287200	Weak transcription	Gastric	stomach
50	chr6:5286000-5287400	Weak transcription	Pancreas	Pancrea

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