Variant report

Variant	nsv883530
Chromosome Location	chr6:29645038-29677641
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:29673475-29673798	HepG2	liver:	n/a	n/a
2	BACH1	chr6:29653483-29653888	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr6:29657216-29657411	K562	blood:	n/a	n/a
4	BHLHE40	chr6:29653749-29653814	K562	blood:	n/a	n/a
5	BHLHE40	chr6:29676624-29677113	GM12878	blood:	n/a	n/a
6	BHLHE40	chr6:29670295-29670532	K562	blood:	n/a	chr6:29670470-29670486
7	BRCA1	chr6:29670292-29670616	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr6:29661417-29661685	K562	blood:	n/a	n/a
9	CBX3	chr6:29661393-29661720	K562	blood:	n/a	n/a
10	CEBPB	chr6:29670342-29670806	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr6:29654995-29655093	HepG2	liver:	n/a	chr6:29655058-29655069 chr6:29655058-29655071 chr6:29655059-29655070
12	CEBPB	chr6:29645936-29646243	Hela-S3	cervix:	n/a	chr6:29646040-29646051
13	CEBPB	chr6:29658970-29659247	IMR90	lung:	n/a	chr6:29659097-29659108
14	CEBPB	chr6:29677057-29677429	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr6:29670010-29670014	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr6:29664383-29664634	K562	blood:	n/a	n/a
17	CEBPB	chr6:29664269-29664602	MCF-7	breast:	n/a	n/a
18	CEBPB	chr6:29664336-29664568	K562	blood:	n/a	n/a
19	CEBPB	chr6:29658955-29659256	HepG2	liver:	n/a	chr6:29659097-29659108
20	CEBPB	chr6:29659074-29659159	K562	blood:	n/a	chr6:29659097-29659108
21	CEBPB	chr6:29645998-29646158	HepG2	liver:	n/a	chr6:29646040-29646051
22	CEBPB	chr6:29645826-29646413	HCT-116	colon:	n/a	chr6:29646040-29646051
23	CEBPB	chr6:29670518-29670744	HepG2	liver:	n/a	n/a
24	CHD2	chr6:29670456-29670488	K562	blood:	n/a	n/a
25	CHD2	chr6:29673478-29673778	Hela-S3	cervix:	n/a	n/a
26	CHD2	chr6:29673503-29673796	HepG2	liver:	n/a	n/a
27	CTCF	chr6:29653646-29653788	GM12892	blood:	n/a	n/a
28	CTCF	chr6:29664381-29664633	NHEK	skin:	n/a	n/a
29	CTCF	chr6:29670420-29670570	NHDF-neo	bronchial:	n/a	chr6:29670463-29670479 chr6:29670465-29670478 chr6:29670462-29670480
30	CTCF	chr6:29670352-29670543	SK-N-SH_RA	brain:	n/a	chr6:29670463-29670479 chr6:29670465-29670478 chr6:29670462-29670480
31	CTCF	chr6:29653604-29653828	Hela-S3	cervix:	n/a	chr6:29653634-29653641
32	CTCF	chr6:29670400-29670550	HEEpiC	esophagus:	n/a	chr6:29670463-29670479 chr6:29670465-29670478 chr6:29670462-29670480
33	CTCF	chr6:29673560-29673710	HRPEpiC	eye:	n/a	chr6:29673595-29673608 chr6:29673592-29673610 chr6:29673594-29673615
34	CTCF	chr6:29670321-29670626	IMR90	lung:	n/a	chr6:29670463-29670479 chr6:29670465-29670478 chr6:29670462-29670480
35	CTCF	chr6:29653621-29653813	GM19239	blood:	n/a	chr6:29653634-29653641
36	CTCF	chr6:29673464-29673723	K562	blood:	n/a	chr6:29673595-29673608 chr6:29673592-29673610 chr6:29673594-29673615
37	CTCF	chr6:29673520-29673670	GM12870	blood:	n/a	chr6:29673595-29673608 chr6:29673592-29673610 chr6:29673594-29673615
38	CTCF	chr6:29670360-29670510	HPF	lung:	n/a	chr6:29670463-29670479 chr6:29670465-29670478 chr6:29670462-29670480
39	CTCF	chr6:29664420-29664570	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr6:29648320-29648470	HepG2	liver:	n/a	chr6:29648349-29648358
41	CTCF	chr6:29653646-29653794	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr6:29664460-29664610	HCM	heart:	n/a	n/a
43	CTCF	chr6:29664383-29664629	LNCaP	prostate:	n/a	n/a
44	CTCF	chr6:29669959-29670772	SK-N-SH	brain:	n/a	chr6:29670107-29670115 chr6:29670463-29670479 chr6:29670465-29670478 chr6:29670462-29670480
45	CTCF	chr6:29669960-29670110	GM12866	blood:	n/a	n/a
46	CTCF	chr6:29653521-29653887	HepG2	liver:	n/a	chr6:29653634-29653641
47	CTCF	chr6:29670380-29670530	GM12870	blood:	n/a	chr6:29670463-29670479 chr6:29670465-29670478 chr6:29670462-29670480
48	CTCF	chr6:29648237-29648432	GM12891	blood:	n/a	chr6:29648349-29648358
49	CTCF	chr6:29673500-29673650	HA-sp	spinal cord:	n/a	chr6:29673595-29673608 chr6:29673592-29673610 chr6:29673594-29673615
50	CTCF	chr6:29653640-29653790	GM12864	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:29648345-29648395	HCF	heart:	n/a
2	chr6:29648345-29648395	HCF	heart:	n/a
3	chr6:29663039-29663089	GM12878	blood:	n/a
4	chr6:29648628-29648678	HRPEpiC	eye:	n/a
5	chr6:29649084-29649134	GM06990	blood:	n/a
6	chr6:29648275-29648325	ProgFib	skin:	n/a
7	chr6:29648736-29648786	HAEpiC	amniotic membrane:	n/a
8	chr6:29648348-29648398	HCF	heart:	n/a
9	chr6:29649092-29649142	ovcar-3	ovarian:	n/a
10	chr6:29645937-29645987	A549	lung:	n/a
11	chr6:29648271-29648321	K562	blood:	n/a
12	chr6:29648271-29648321	AG04450	lung:	fetal
13	chr6:29648590-29648640	RPTEC	kidney:	n/a
14	chr6:29649024-29649074	IMR90	lung:	fetal
15	chr6:29649092-29649142	BE2_C	brain:	n/a
16	chr6:29663039-29663089	HMEC	breast:	n/a
17	chr6:29648381-29648431	NHBE	bronchial:	n/a
18	chr6:29648360-29648410	A549	lung:	n/a
19	chr6:29648271-29648321	HepG2	liver:	n/a
20	chr6:29648360-29648410	ovcar-3	ovarian:	n/a
21	chr6:29648381-29648431	AG04449	skin:	fetal
22	chr6:29648623-29648673	Caco-2	colon:	n/a
23	chr6:29648161-29648211	NH-A	brain:	n/a
24	chr6:29648225-29648275	HCT-116	colon:	n/a
25	chr6:29648379-29648429	AoSMC	blood vessel:	n/a
26	chr6:29648525-29648575	ovcar-3	ovarian:	n/a
27	chr6:29648525-29648575	SKMC	muscle:	n/a
28	chr6:29649024-29649074	HCT-116	colon:	n/a
29	chr6:29648275-29648325	HRCEpiC	kidney:	n/a
30	chr6:29648271-29648321	HEK293	kidney:	embryo
31	chr6:29648901-29648951	HCT-116	colon:	n/a
32	chr6:29648161-29648211	PANC-1	pancreas:	n/a
33	chr6:29648623-29648673	HPAEpiC	pulmonary alveolar:	n/a
34	chr6:29648525-29648575	HEK293	kidney:	embryo
35	chr6:29648736-29648786	ovcar-3	ovarian:	n/a
36	chr6:29648275-29648325	ovcar-3	ovarian:	n/a
37	chr6:29648590-29648640	HRCEpiC	kidney:	n/a
38	chr6:29649807-29649857	T-47D	breast:	n/a
39	chr6:29648275-29648325	SK-N-SH_RA	brain:	n/a
40	chr6:29648736-29648786	NHDF-neo	bronchial:	n/a
41	chr6:29648901-29648951	Jurkat	blood:	n/a
42	chr6:29648379-29648429	AG04449	skin:	fetal
43	chr6:29663039-29663089	SKMC	muscle:	n/a
44	chr6:29663039-29663089	SAEC	small airway:	n/a
45	chr6:29649084-29649134	HRCEpiC	kidney:	n/a
46	chr6:29648590-29648640	AG04449	skin:	fetal
47	chr6:29648525-29648575	NHDF-neo	bronchial:	n/a
48	chr6:29648225-29648275	HCPEpiC	choroid plexus:	n/a
49	chr6:29648381-29648431	LNCaP	prostate:	n/a
50	chr6:29648400-29648450	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:29673901..29676614-chr6:29690934..29692528,2	MCF-7	breast:
2	chr6:29673331..29674077-chr6:29980846..29981765,3	K562	blood:
3	chr10:38965666..38966167-chr6:29670107..29670640,2	MCF-7	breast:
4	chr6:29670114..29670993-chr6:29802276..29803394,5	K562	blood:
5	chr6:29609140..29610048-chr6:29673773..29674677,2	MCF-7	breast:
6	chr6:29617916..29618459-chr6:29653660..29654518,2	MCF-7	breast:
7	chr6:29673244..29674572-chr6:29802335..29803091,3	MCF-7	breast:
8	chr6:29343821..29344378-chr6:29664074..29664947,2	MCF-7	breast:
9	chr6:29617940..29618834-chr6:29653305..29654103,4	MCF-7	breast:
10	chr6:29664440..29666391-chr6:29667385..29669684,2	K562	blood:
11	chr6:29618832..29619613-chr6:29653205..29653756,2	MCF-7	breast:
12	chr6:29673438..29674041-chr6:30098583..30099284,2	MCF-7	breast:
13	chr6:29615212..29617400-chr6:29662195..29664604,2	MCF-7	breast:
14	chr6:29673586..29674252-chr6:29706679..29707289,2	MCF-7	breast:
15	chr6:29637497..29639601-chr6:29651008..29653048,2	K562	blood:
16	chr6:29619566..29622372-chr6:29653366..29655066,2	MCF-7	breast:
17	chr6:29673185..29674019-chr6:29806166..29806939,2	MCF-7	breast:
18	chr6:29664440..29666391-chr6:29667385..29669684,2	K562	blood:
19	chr6:29673528..29674438-chr6:29802360..29803231,5	K562	blood:
20	chr6:29619162..29620164-chr6:29653167..29654163,5	MCF-7	breast:
21	chr6:29617501..29618041-chr6:29673112..29673633,2	K562	blood:
22	chr6:29620955..29621482-chr6:29664090..29665046,2	MCF-7	breast:
23	chr6:29615478..29616411-chr6:29663958..29664983,4	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZFP57-8	chr6:29675902-29676324	NONHSAT108537
2	lnc-ZFP57-9	chr6:29677357-29677787	NONHSAT108538

Variant related genes	Relation type
ZFP57	TF binding region
ZDHHC20P1	TF binding region
ZFP57	CpG island
ZDHHC20P1	CpG island
ENSG00000225864	chromatin interactions
ENSG00000204655	chromatin interactions
ENSG00000204642	chromatin interactions

Extended variants
information (count: 1437 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:1437 , 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	rs2535238	chr6:29645038-29645039	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs563829445	chr6:29645039-29645040	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
3	rs371727322	chr6:29645073-29645074	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs552472247	chr6:29645075-29645076	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs2747421	chr6:29645118-29645119	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs550545958	chr6:29645148-29645149	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
7	rs552950660	chr6:29645167-29645168	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs3823312	chr6:29645236-29645237	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs369920154	chr6:29645244-29645245	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs548820083	chr6:29645275-29645276	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs571009774	chr6:29645281-29645282	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs191728813	chr6:29645299-29645300	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs207466840	chr6:29645315-29645316	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs373875556	chr6:29645372-29645373	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs554252275	chr6:29645452-29645453	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs570944653	chr6:29645453-29645454	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs182403617	chr6:29645507-29645508	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs116211033	chr6:29645532-29645533	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
19	rs71550149	chr6:29645545-29645546	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs374649115	chr6:29645546-29645547	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs75834742	chr6:29645549-29645550	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs61380265	chr6:29645567-29645568	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs576153454	chr6:29645568-29645569	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs35798759	chr6:29645574-29645575	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs387603	chr6:29645578-29645579	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs3129063	chr6:29645613-29645614	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs572047826	chr6:29645630-29645631	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs387642	chr6:29645634-29645635	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs116414636	chr6:29645663-29645664	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs151101933	chr6:29645676-29645677	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs372259171	chr6:29645692-29645693	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs4391284	chr6:29645726-29645727	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs387640	chr6:29645770-29645771	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs4085264	chr6:29645885-29645886	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs3129062	chr6:29645937-29645938	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs568762529	chr6:29645938-29645939	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs141981685	chr6:29645944-29645945	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
38	rs3117288	chr6:29645958-29645959	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs570833161	chr6:29645968-29645969	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
40	rs4085262	chr6:29645989-29645990	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs145798158	chr6:29646015-29646016	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs573473774	chr6:29646124-29646125	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs570056640	chr6:29646136-29646137	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs396660	chr6:29646165-29646166	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs3906306	chr6:29646201-29646202	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs571986180	chr6:29646204-29646205	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs540899358	chr6:29646253-29646254	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs557645152	chr6:29646265-29646266	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs577522961	chr6:29646303-29646304	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs544313073	chr6:29646426-29646427	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	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
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
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	19571809	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Breast cancer	21509527	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:343 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:29625000-29663600	Weak transcription	Right Atrium	heart
2	chr6:29639600-29647400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr6:29643000-29646400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr6:29643000-29648800	Enhancers	HMEC	breast
5	chr6:29643200-29648400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr6:29643400-29648400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr6:29643800-29647600	Enhancers	Fetal Heart	heart
8	chr6:29644400-29645200	Enhancers	Primary hematopoietic stem cells	blood
9	chr6:29644400-29645400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr6:29644400-29645600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr6:29644400-29646200	Enhancers	H9 Cell Line	embryonic stem cell
12	chr6:29644600-29645200	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr6:29644600-29645200	Enhancers	Primary T helper cells fromperipheralblood	blood
14	chr6:29644600-29645400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr6:29644600-29645400	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr6:29644600-29645800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr6:29644600-29646000	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr6:29644600-29647800	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr6:29644800-29645200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr6:29644800-29645200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
21	chr6:29644800-29645200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr6:29644800-29645200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr6:29644800-29645400	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr6:29644800-29645400	Enhancers	Primary T helper naive cells from peripheral blood	blood
25	chr6:29644800-29645400	Enhancers	GM12878-XiMat	blood
26	chr6:29644800-29645400	Flanking Active TSS	NHEK	skin
27	chr6:29644800-29645600	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr6:29644800-29646200	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr6:29644800-29647400	Enhancers	Hela-S3	cervix
30	chr6:29644800-29647600	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr6:29644800-29648000	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr6:29644800-29648000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr6:29645000-29645200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr6:29645000-29645400	Enhancers	Primary T helper cells PMA-I stimulated	--
35	chr6:29645000-29646800	Enhancers	H1 Cell Line	embryonic stem cell
36	chr6:29645000-29648000	Weak transcription	Primary monocytes fromperipheralblood	blood
37	chr6:29645200-29645400	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr6:29645200-29646200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr6:29645200-29648200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr6:29645200-29648400	Weak transcription	Primary hematopoietic stem cells	blood
41	chr6:29645400-29645800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr6:29645400-29646000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr6:29645400-29646000	Enhancers	NHEK	skin
44	chr6:29645400-29646600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr6:29645600-29647000	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr6:29645800-29646000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr6:29645800-29648200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr6:29646000-29646200	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr6:29646000-29648400	Flanking Active TSS	NHEK	skin
50	chr6:29646000-29648800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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