Variant report

Variant	nsv966675
Chromosome Location	chr6:4819733-4855009
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:641)
CpG islands
(count:244)
Chromatin interactive
region (count:34)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:641 , 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	chr6:4848908-4849295	K562	blood:	n/a	n/a
2	ARID3A	chr6:4848932-4849319	HepG2	liver:	n/a	n/a
3	ATF1	chr6:4854209-4854597	K562	blood:	n/a	n/a
4	ATF1	chr6:4840513-4840713	K562	blood:	n/a	n/a
5	ATF2	chr6:4820164-4820520	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr6:4854171-4854468	K562	blood:	n/a	n/a
7	BATF	chr6:4820952-4821324	GM12878	blood:	n/a	chr6:4821144-4821154
8	BATF	chr6:4839392-4839615	GM12878	blood:	n/a	chr6:4839525-4839536
9	BCL3	chr6:4820922-4821294	GM12878	blood:	n/a	n/a
10	BCLAF1	chr6:4844288-4844783	K562	blood:	n/a	n/a
11	BHLHE40	chr6:4854089-4854680	HepG2	liver:	n/a	n/a
12	BHLHE40	chr6:4854153-4854564	K562	blood:	n/a	n/a
13	CBX3	chr6:4854146-4854549	K562	blood:	n/a	n/a
14	CBX3	chr6:4828502-4828968	K562	blood:	n/a	n/a
15	CBX3	chr6:4829338-4829689	K562	blood:	n/a	n/a
16	CBX3	chr6:4828562-4828850	K562	blood:	n/a	n/a
17	CBX3	chr6:4844332-4844744	K562	blood:	n/a	n/a
18	CBX3	chr6:4844306-4844685	K562	blood:	n/a	n/a
19	CEBPB	chr6:4826994-4827150	HepG2	liver:	n/a	chr6:4827080-4827091
20	CEBPB	chr6:4826977-4827199	K562	blood:	n/a	chr6:4827080-4827091
21	CEBPB	chr6:4826944-4827230	MCF-7	breast:	n/a	chr6:4827080-4827091
22	CEBPB	chr6:4849000-4849344	Hela-S3	cervix:	n/a	n/a
23	CHD2	chr6:4829582-4829640	GM12878	blood:	n/a	n/a
24	CTCF	chr6:4848936-4849167	GM19238	blood:	n/a	chr6:4849057-4849075 chr6:4849064-4849072
25	CTCF	chr6:4848949-4849183	K562	blood:	n/a	chr6:4849057-4849075 chr6:4849064-4849072
26	CTCF	chr6:4849000-4849150	HAc	cerebellar:	n/a	chr6:4849057-4849075 chr6:4849064-4849072
27	CTCF	chr6:4844448-4844550	Medullo	brain:	n/a	n/a
28	CTCF	chr6:4848969-4849103	SK-N-SH_RA	brain:	n/a	chr6:4849057-4849075 chr6:4849064-4849072
29	CTCF	chr6:4848980-4849130	AG04449	skin:	n/a	chr6:4849057-4849075 chr6:4849064-4849072
30	CTCF	chr6:4844441-4844638	MCF-7	breast:	n/a	n/a
31	CTCF	chr6:4844420-4844570	NB4	blood:	n/a	n/a
32	CTCF	chr6:4844380-4844530	WI-38	lung:	n/a	n/a
33	CTCF	chr6:4844370-4844780	K562	blood:	n/a	n/a
34	CTCF	chr6:4844300-4844450	GM12868	blood:	n/a	n/a
35	CTCF	chr6:4844380-4844530	HL-60	blood:	n/a	n/a
36	CTCF	chr6:4848967-4849198	Spleen_OC	spleen:	n/a	chr6:4849057-4849075 chr6:4849064-4849072
37	CTCF	chr6:4848880-4849030	HFF	foreskin:	n/a	n/a
38	CTCF	chr6:4848960-4849110	WERI-Rb-1	eye:	n/a	chr6:4849057-4849075 chr6:4849064-4849072
39	CTCF	chr6:4849000-4849150	A549	lung:	n/a	chr6:4849057-4849075 chr6:4849064-4849072
40	CTCF	chr6:4844460-4844610	AG10803	skin:	n/a	n/a
41	CTCF	chr6:4848940-4849090	AG04449	skin:	n/a	chr6:4849057-4849075 chr6:4849064-4849072
42	CTCF	chr6:4848980-4849130	HUVEC	blood vessel:	n/a	chr6:4849057-4849075 chr6:4849064-4849072
43	CTCF	chr6:4849000-4849150	SK-N-SH_RA	brain:	n/a	chr6:4849057-4849075 chr6:4849064-4849072
44	CTCF	chr6:4844380-4844530	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr6:4848660-4848810	HEK293	kidney:	n/a	n/a
46	CTCF	chr6:4849100-4849250	BE2_C	brain:	n/a	n/a
47	CTCF	chr6:4848940-4849090	HA-sp	spinal cord:	n/a	chr6:4849057-4849075 chr6:4849064-4849072
48	CTCF	chr6:4844460-4844610	HCT-116	colon:	n/a	n/a
49	CTCF	chr6:4848980-4849130	GM12864	blood:	n/a	chr6:4849057-4849075 chr6:4849064-4849072
50	CTCF	chr6:4849020-4849170	GM12865	blood:	n/a	chr6:4849057-4849075 chr6:4849064-4849072

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:4848062-4848112	HNPCEpiC	eye:	n/a
2	chr6:4820670-4820720	H1-hESC	embryonic stem cell:	embryo
3	chr6:4848062-4848112	AG09309	skin:	n/a
4	chr6:4836018-4836068	HEK293	kidney:	embryo
5	chr6:4848062-4848112	MCF-7	breast:	n/a
6	chr6:4820670-4820720	GM12878	blood:	n/a
7	chr6:4836018-4836068	Jurkat	blood:	n/a
8	chr6:4820670-4820720	HRCEpiC	kidney:	n/a
9	chr6:4848062-4848112	HCM	heart:	n/a
10	chr6:4836018-4836068	SK-N-MC	brain:	n/a
11	chr6:4820670-4820720	AG09309	skin:	n/a
12	chr6:4848062-4848112	HRCEpiC	kidney:	n/a
13	chr6:4836018-4836068	ovcar-3	ovarian:	n/a
14	chr6:4848062-4848112	HEK293	kidney:	embryo
15	chr6:4854374-4854424	ovcar-3	ovarian:	n/a
16	chr6:4854374-4854424	SK-N-MC	brain:	n/a
17	chr6:4854374-4854424	ECC-1	luminal epithelium:	n/a
18	chr6:4836018-4836068	K562	blood:	n/a
19	chr6:4854374-4854424	AG09309	skin:	n/a
20	chr6:4848062-4848112	PFSK-1	brain:	n/a
21	chr6:4854374-4854424	PrEC	prostate:	n/a
22	chr6:4854374-4854424	HRPEpiC	eye:	n/a
23	chr6:4854374-4854424	HIPEpiC	eye:	n/a
24	chr6:4848062-4848112	GM12891	blood:	n/a
25	chr6:4836018-4836068	PrEC	prostate:	n/a
26	chr6:4836018-4836068	HCT-116	colon:	n/a
27	chr6:4836018-4836068	HIPEpiC	eye:	n/a
28	chr6:4836018-4836068	AoSMC	blood vessel:	n/a
29	chr6:4836018-4836068	HL-60	blood:	n/a
30	chr6:4854374-4854424	U87	brain:	n/a
31	chr6:4848062-4848112	Hela-S3	cervix:	n/a
32	chr6:4854374-4854424	HL-60	blood:	n/a
33	chr6:4854374-4854424	T-47D	breast:	n/a
34	chr6:4854374-4854424	HCPEpiC	choroid plexus:	n/a
35	chr6:4854374-4854424	HCT-116	colon:	n/a
36	chr6:4820670-4820720	HCM	heart:	n/a
37	chr6:4854374-4854424	MCF-7	breast:	n/a
38	chr6:4820670-4820720	AoSMC	blood vessel:	n/a
39	chr6:4854374-4854424	PANC-1	pancreas:	n/a
40	chr6:4820670-4820720	U87	brain:	n/a
41	chr6:4836018-4836068	RPTEC	kidney:	n/a
42	chr6:4854374-4854424	HRE	kidney:	n/a
43	chr6:4836018-4836068	HAEpiC	amniotic membrane:	n/a
44	chr6:4854374-4854424	HMEC	breast:	n/a
45	chr6:4854374-4854424	HAEpiC	amniotic membrane:	n/a
46	chr6:4836018-4836068	Caco-2	colon:	n/a
47	chr6:4820670-4820720	A549	lung:	n/a
48	chr6:4854374-4854424	K562	blood:	n/a
49	chr6:4848062-4848112	GM19239	blood:	n/a
50	chr6:4848062-4848112	HCT-116	colon:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:4823551..4825869-chr6:4828345..4830418,3	MCF-7	breast:
2	chr6:4818061..4820249-chr6:4821057..4823900,2	MCF-7	breast:
3	chr6:4812864..4816772-chr6:4818234..4821083,3	MCF-7	breast:
4	chr6:4776573..4778136-chr6:4847031..4849578,2	K562	blood:
5	chr6:4806891..4809234-chr6:4853712..4855967,2	K562	blood:
6	chr6:4848197..4852151-chr6:4852565..4855208,4	MCF-7	breast:
7	chr6:4754621..4757244-chr6:4826945..4828835,2	K562	blood:
8	chr6:4818944..4820656-chr6:4826722..4829112,2	K562	blood:
9	chr6:4848197..4852151-chr6:4852565..4855208,4	MCF-7	breast:
10	chr6:4847558..4849642-chr6:4852103..4854411,2	K562	blood:
11	chr6:4845889..4847519-chr6:4848149..4850482,2	MCF-7	breast:
12	chr6:4823551..4825869-chr6:4828345..4830418,3	MCF-7	breast:
13	chr6:4853835..4856430-chr6:4856609..4858869,2	MCF-7	breast:
14	chr6:4775417..4779410-chr6:4834974..4837006,3	MCF-7	breast:
15	chr6:4840303..4841822-chr6:4847282..4849004,2	MCF-7	breast:
16	chr6:4772950..4775571-chr6:4849691..4852683,2	K562	blood:
17	chr6:4818061..4820249-chr6:4821057..4823900,2	MCF-7	breast:
18	chr6:4818944..4820656-chr6:4826722..4829112,2	K562	blood:
19	chr6:4849119..4850755-chr6:4898473..4900044,2	MCF-7	breast:
20	chr6:4815291..4819346-chr6:4820857..4822798,4	K562	blood:
21	chr6:4840303..4841822-chr6:4847282..4849004,2	MCF-7	breast:
22	chr6:4807875..4808462-chr6:4848723..4849408,2	MCF-7	breast:
23	chr6:4816460..4818196-chr6:4821244..4822798,2	K562	blood:
24	chr6:4853455..4855875-chr6:4862739..4864405,2	K562	blood:
25	chr6:4795026..4796942-chr6:4836958..4839141,2	K562	blood:
26	chr6:4847745..4850576-chr6:4852287..4854812,4	K562	blood:
27	chr6:4820521..4822637-chr6:4825444..4827766,3	MCF-7	breast:
28	chr6:4850106..4852238-chr6:4856143..4858051,2	K562	blood:
29	chr6:4845889..4847519-chr6:4848149..4850482,2	MCF-7	breast:
30	chr6:4820521..4822637-chr6:4825444..4827766,3	MCF-7	breast:
31	chr6:4847745..4850576-chr6:4852287..4854812,4	K562	blood:
32	chr6:4775945..4778797-chr6:4852829..4854855,2	MCF-7	breast:
33	chr6:4813316..4814921-chr6:4820948..4822599,2	MCF-7	breast:
34	chr6:4847558..4849642-chr6:4852103..4854411,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PPP1R3G-4	chr6:4847760-4848591	NONHSAT107490

No data

Variant related genes	Relation type
CDYL	TF binding region
CDYL	CpG island
ENSG00000153046	chromatin interactions
ENSG00000236336	chromatin interactions

Extended variants
information (count: 1454 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:1454 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532815276	chr6:4819750-4819751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs546437995	chr6:4819787-4819788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs375493811	chr6:4819790-4819791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs576014349	chr6:4819792-4819793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs369889110	chr6:4819835-4819836	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs542249264	chr6:4819915-4819916	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs542306675	chr6:4819935-4819936	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531919351	chr6:4819966-4819967	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs146905963	chr6:4819967-4819968	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs1016878	chr6:4819976-4819977	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs6936040	chr6:4819981-4819982	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs1016877	chr6:4820005-4820006	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs376664601	chr6:4820025-4820026	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs570429163	chr6:4820065-4820066	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs144923005	chr6:4820072-4820073	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs369912130	chr6:4820076-4820077	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs367893581	chr6:4820077-4820078	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs116344216	chr6:4820089-4820090	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs139206316	chr6:4820117-4820118	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs569545472	chr6:4820135-4820136	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs535281095	chr6:4820145-4820146	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs143202377	chr6:4820168-4820169	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs377460766	chr6:4820256-4820257	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs12527481	chr6:4820273-4820274	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs572001582	chr6:4820275-4820276	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs11966448	chr6:4820277-4820278	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs369186350	chr6:4820313-4820314	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs572562425	chr6:4820316-4820317	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs182226101	chr6:4820342-4820343	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs148107316	chr6:4820345-4820346	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs563160715	chr6:4820362-4820363	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs531974377	chr6:4820372-4820373	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs76769363	chr6:4820377-4820378	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs562219131	chr6:4820411-4820412	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs527748141	chr6:4820459-4820460	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs113875817	chr6:4820537-4820538	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs570539235	chr6:4820578-4820579	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs373900318	chr6:4820581-4820582	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs549702147	chr6:4820582-4820583	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs112761643	chr6:4820588-4820589	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs369688985	chr6:4820604-4820605	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs113490831	chr6:4820605-4820606	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs141908404	chr6:4820634-4820635	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs75755651	chr6:4820663-4820664	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs534663292	chr6:4820669-4820670	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs557867390	chr6:4820686-4820687	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs577749098	chr6:4820700-4820701	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs544718879	chr6:4820714-4820715	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs141782191	chr6:4820715-4820716	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs150605377	chr6:4820737-4820738	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
Breast cancer	21364760	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
Pancreatic cancer	17952125	CNVD

Chromatin state (count:604 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:4806800-4819800	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr6:4806800-4820200	Weak transcription	NHLF	lung
3	chr6:4806800-4820400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr6:4806800-4829400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr6:4807000-4821200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr6:4807200-4819800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr6:4807200-4827800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr6:4811200-4820000	Weak transcription	Colonic Mucosa	Colon
9	chr6:4811200-4820000	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr6:4811200-4820000	Weak transcription	Spleen	Spleen
11	chr6:4811800-4820000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr6:4812400-4820000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr6:4812400-4820000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr6:4812400-4820000	Weak transcription	Placenta	Placenta
15	chr6:4812400-4820000	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr6:4812400-4829600	Weak transcription	Left Ventricle	heart
17	chr6:4812600-4820200	Weak transcription	Right Ventricle	heart
18	chr6:4812600-4820800	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr6:4812600-4826800	Weak transcription	HepG2	liver
20	chr6:4812800-4819800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr6:4812800-4822800	Weak transcription	Adipose Nuclei	Adipose
22	chr6:4812800-4823000	Weak transcription	Primary T cells from cord blood	blood
23	chr6:4812800-4828800	Weak transcription	Hela-S3	cervix
24	chr6:4813200-4820200	Weak transcription	Primary hematopoietic stem cells	blood
25	chr6:4813400-4820200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr6:4814200-4829600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr6:4815000-4821000	Weak transcription	Fetal Intestine Small	intestine
28	chr6:4815000-4826000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr6:4815000-4827400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr6:4815200-4823000	Weak transcription	Ovary	ovary
31	chr6:4815200-4824200	Weak transcription	Primary B cells from cord blood	blood
32	chr6:4815200-4829600	Weak transcription	Lung	lung
33	chr6:4815400-4820000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr6:4815600-4820400	Weak transcription	Colon Smooth Muscle	Colon
35	chr6:4816200-4820800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
36	chr6:4817000-4819800	Weak transcription	Skeletal Muscle Female	skeletal muscle
37	chr6:4817200-4820000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr6:4817600-4820000	Weak transcription	NHEK	skin
39	chr6:4817800-4820000	Weak transcription	NHDF-Ad	bronchial
40	chr6:4817800-4820400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr6:4817800-4821000	Enhancers	Primary T helper cells PMA-I stimulated	--
42	chr6:4817800-4827000	Weak transcription	K562	blood
43	chr6:4818000-4820000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr6:4818200-4819800	Weak transcription	A549	lung
45	chr6:4818200-4820400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
46	chr6:4818200-4821200	Enhancers	Primary T cells fromperipheralblood	blood
47	chr6:4818400-4820000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr6:4818400-4820400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
49	chr6:4818600-4820200	Enhancers	Primary T helper naive cells from peripheral blood	blood
50	chr6:4818600-4820800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood

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