Variant report

Variant	nsv527037
Chromosome Location	chr6:29615822-29624112
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	chr6:29619396-29619782	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:29617682-29618095	K562	blood:	n/a	n/a
3	ARID3A	chr6:29615844-29616035	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:29617599-29618201	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:29621247-29621552	K562	blood:	n/a	chr6:29621519-29621535
6	ATF1	chr6:29617449-29618222	K562	blood:	n/a	n/a
7	ATF2	chr6:29617484-29618084	H1-hESC	embryonic stem cell:	n/a	chr6:29617956-29617967
8	ATF2	chr6:29617503-29618190	H1-hESC	embryonic stem cell:	n/a	chr6:29617956-29617967
9	ATF2	chr6:29617560-29618105	GM12878	blood:	n/a	chr6:29617956-29617967
10	ATF3	chr6:29617505-29617881	K562	blood:	n/a	n/a
11	BACH1	chr6:29617773-29618042	K562	blood:	n/a	n/a
12	BACH1	chr6:29617698-29617977	H1-hESC	embryonic stem cell:	n/a	n/a
13	BHLHE40	chr6:29617585-29618189	HepG2	liver:	n/a	n/a
14	BHLHE40	chr6:29624080-29624088	GM12878	blood:	n/a	n/a
15	BHLHE40	chr6:29617434-29618448	GM12878	blood:	n/a	n/a
16	BHLHE40	chr6:29621364-29621479	K562	blood:	n/a	n/a
17	BHLHE40	chr6:29617431-29618296	K562	blood:	n/a	n/a
18	BRCA1	chr6:29617749-29618195	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr6:29617708-29618204	GM12878	blood:	n/a	n/a
20	BRCA1	chr6:29617753-29618323	H1-hESC	embryonic stem cell:	n/a	n/a
21	BRCA1	chr6:29617788-29618102	HepG2	liver:	n/a	n/a
22	CBX3	chr6:29617454-29618215	K562	blood:	n/a	n/a
23	CCNT2	chr6:29617616-29618101	K562	blood:	n/a	n/a
24	CEBPB	chr6:29617691-29618207	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr6:29617587-29618098	H1-hESC	embryonic stem cell:	n/a	chr6:29617664-29617675
26	CEBPZ	chr6:29619445-29619793	HepG2	liver:	n/a	n/a
27	CHD2	chr6:29617569-29618367	K562	blood:	n/a	n/a
28	CHD2	chr6:29617668-29618371	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr6:29617467-29618517	GM12878	blood:	n/a	chr6:29618406-29618416
30	CHD2	chr6:29617414-29618101	H1-hESC	embryonic stem cell:	n/a	n/a
31	CREB1	chr6:29617383-29618224	A549	lung:	n/a	chr6:29617955-29617968
32	CREB1	chr6:29617726-29618067	A549	lung:	n/a	chr6:29617955-29617968
33	CREB1	chr6:29617433-29618206	H1-hESC	embryonic stem cell:	n/a	chr6:29617955-29617968
34	CREB1	chr6:29617454-29618278	HepG2	liver:	n/a	chr6:29617955-29617968
35	CREB1	chr6:29617333-29618274	GM12878	blood:	n/a	chr6:29617955-29617968
36	CREB1	chr6:29617349-29618290	H1-hESC	embryonic stem cell:	n/a	chr6:29617955-29617968
37	CREB1	chr6:29617421-29618238	HepG2	liver:	n/a	chr6:29617955-29617968
38	CREB1	chr6:29617321-29618247	GM12878	blood:	n/a	chr6:29617955-29617968
39	CREB1	chr6:29617405-29618321	K562	blood:	n/a	chr6:29617955-29617968
40	CREB1	chr6:29617348-29618301	K562	blood:	n/a	chr6:29617955-29617968
41	CREB1	chr6:29617697-29618240	ECC-1	luminal epithelium:	n/a	chr6:29617955-29617968
42	CREB1	chr6:29617683-29618243	ECC-1	luminal epithelium:	n/a	chr6:29617955-29617968
43	CTCF	chr6:29617940-29618090	AoAF	blood vessel:	n/a	chr6:29618018-29618034 chr6:29618017-29618035
44	CTCF	chr6:29615840-29615990	GM12866	blood:	n/a	chr6:29615915-29615933 chr6:29615917-29615938
45	CTCF	chr6:29619520-29619670	AG09319	gingival:	n/a	chr6:29619582-29619600 chr6:29619587-29619595 chr6:29619584-29619605 chr6:29619583-29619599
46	CTCF	chr6:29619480-29619630	GM12874	blood:	n/a	chr6:29619582-29619600 chr6:29619587-29619595 chr6:29619584-29619605 chr6:29619583-29619599
47	CTCF	chr6:29615880-29616030	GM12871	blood:	n/a	chr6:29615915-29615933 chr6:29615917-29615938
48	CTCF	chr6:29621320-29621470	AG04449	skin:	n/a	chr6:29621412-29621428 chr6:29621406-29621427 chr6:29621416-29621424 chr6:29621413-29621426 chr6:29621413-29621426 chr6:29621411-29621429
49	CTCF	chr6:29622020-29622170	HCM	heart:	n/a	n/a
50	CTCF	chr6:29621143-29621649	HCT-116	colon:	n/a	chr6:29621412-29621428 chr6:29621406-29621427 chr6:29621416-29621424 chr6:29621413-29621426 chr6:29621413-29621426 chr6:29621411-29621429

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:29621375-29621425	HepG2	liver:	n/a
2	chr6:29623721-29623771	ovcar-3	ovarian:	n/a
3	chr6:29617602-29617652	A549	lung:	n/a
4	chr6:29621375-29621425	HepG2	liver:	n/a
5	chr6:29623721-29623771	ovcar-3	ovarian:	n/a
6	chr6:29617602-29617652	A549	lung:	n/a
7	chr6:29617868-29617918	ProgFib	skin:	n/a
8	chr6:29618347-29618397	Hela-S3	cervix:	n/a
9	chr6:29617766-29617816	HepG2	liver:	n/a
10	chr6:29623821-29623871	HUVEC	blood vessel:	n/a
11	chr6:29623721-29623771	Caco-2	colon:	n/a
12	chr6:29623992-29624042	HUVEC	blood vessel:	n/a
13	chr6:29617848-29617898	HPAEpiC	pulmonary alveolar:	n/a
14	chr6:29621467-29621517	PFSK-1	brain:	n/a
15	chr6:29617599-29617649	HRCEpiC	kidney:	n/a
16	chr6:29617902-29617952	SKMC	muscle:	n/a
17	chr6:29617973-29618023	PANC-1	pancreas:	n/a
18	chr6:29618315-29618365	CMK	blood:	n/a
19	chr6:29618347-29618397	Hepatocyte	liver:	n/a
20	chr6:29617586-29617636	NHBE	bronchial:	n/a
21	chr6:29617766-29617816	MCF10A-Er-Src	breast:	n/a
22	chr6:29618347-29618397	MCF10A-Er-Src	breast:	n/a
23	chr6:29623721-29623771	AoSMC	blood vessel:	n/a
24	chr6:29617973-29618023	HEK293	kidney:	embryo
25	chr6:29617549-29617599	ovcar-3	ovarian:	n/a
26	chr6:29617613-29617663	AG09309	skin:	n/a
27	chr6:29623821-29623871	U87	brain:	n/a
28	chr6:29623721-29623771	HAEpiC	amniotic membrane:	n/a
29	chr6:29617902-29617952	ECC-1	luminal epithelium:	n/a
30	chr6:29617817-29617867	GM19239	blood:	n/a
31	chr6:29617868-29617918	NH-A	brain:	n/a
32	chr6:29621375-29621425	RPTEC	kidney:	n/a
33	chr6:29618315-29618365	LNCaP	prostate:	n/a
34	chr6:29617817-29617867	HIPEpiC	eye:	n/a
35	chr6:29621441-29621491	HepG2	liver:	n/a
36	chr6:29617973-29618023	GM12892	blood:	n/a
37	chr6:29617961-29618011	GM12891	blood:	n/a
38	chr6:29617613-29617663	AG04449	skin:	fetal
39	chr6:29617613-29617663	HCT-116	colon:	n/a
40	chr6:29617791-29617841	SAEC	small airway:	n/a
41	chr6:29618382-29618432	HCM	heart:	n/a
42	chr6:29617817-29617867	Caco-2	colon:	n/a
43	chr6:29617771-29617821	PrEC	prostate:	n/a
44	chr6:29618205-29618255	AG09309	skin:	n/a
45	chr6:29618315-29618365	HPAEpiC	pulmonary alveolar:	n/a
46	chr6:29623821-29623871	HepG2	liver:	n/a
47	chr6:29617956-29618006	AoSMC	blood vessel:	n/a
48	chr6:29621375-29621425	HRPEpiC	eye:	n/a
49	chr6:29618382-29618432	PFSK-1	brain:	n/a
50	chr6:29617973-29618023	HCPEpiC	choroid plexus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:29593421..29596019-chr6:29617479..29619432,2	K562	blood:
2	chr6:29608179..29610477-chr6:29617988..29619609,2	K562	blood:
3	chr6:29617940..29618834-chr6:29653305..29654103,4	MCF-7	breast:
4	chr6:29618832..29619613-chr6:29653205..29653756,2	MCF-7	breast:
5	chr6:29619657..29623284-chr6:29624891..29627355,4	K562	blood:
6	chr6:29619566..29622372-chr6:29653366..29655066,2	MCF-7	breast:
7	chr6:29615912..29617460-chr6:29617899..29619662,2	MCF-7	breast:
8	chr6:29585702..29586556-chr6:29620907..29621418,2	K562	blood:
9	chr6:29615912..29617460-chr6:29617899..29619662,2	MCF-7	breast:
10	chr6:29616642..29621245-chr6:29621568..29627231,6	K562	blood:
11	chr6:29615478..29616411-chr6:29663958..29664983,4	MCF-7	breast:
12	chr6:29619372..29622160-chr6:29632758..29634460,2	K562	blood:
13	chr6:29594126..29596213-chr6:29619646..29621373,2	K562	blood:
14	chr6:29598640..29604637-chr6:29614654..29620933,9	K562	blood:
15	chr6:29617501..29618041-chr6:29673112..29673633,2	K562	blood:
16	chr6:29608179..29609839-chr6:29617502..29619488,2	K562	blood:
17	chr6:29615212..29617400-chr6:29662195..29664604,2	MCF-7	breast:
18	chr6:29620955..29621482-chr6:29664090..29665046,2	MCF-7	breast:
19	chr6:29617916..29618459-chr6:29653660..29654518,2	MCF-7	breast:
20	chr6:29593197..29596046-chr6:29616000..29618979,4	K562	blood:
21	chr6:29598560..29601918-chr6:29614006..29619393,6	K562	blood:
22	chr6:29619162..29620164-chr6:29653167..29654163,5	MCF-7	breast:
23	chr6:29600937..29601437-chr6:29617570..29618328,2	MCF-7	breast:

Variant related genes	Relation type
MOG	TF binding region
MOG	CpG island
ENSG00000235238	chromatin interactions
ENSG00000204655	chromatin interactions
ENSG00000204681	chromatin interactions

Extended variants
information (count: 229 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:229 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3129073	chr6:29615822-29615823	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs567257972	chr6:29615847-29615848	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs142741016	chr6:29615864-29615865	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs563167254	chr6:29615873-29615874	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs531924059	chr6:29615879-29615880	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs542164155	chr6:29615931-29615932	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs562113753	chr6:29615949-29615950	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs527780073	chr6:29615954-29615955	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs369306051	chr6:29615983-29615984	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs188121919	chr6:29615993-29615994	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs533132946	chr6:29616003-29616004	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs376707158	chr6:29616019-29616020	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs114273413	chr6:29616035-29616036	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs569892105	chr6:29616119-29616120	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs425997	chr6:29616125-29616126	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs548959285	chr6:29616137-29616138	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs192649778	chr6:29616143-29616144	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs183892815	chr6:29616176-29616177	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs571184523	chr6:29616201-29616202	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs56191234	chr6:29616216-29616217	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs538426949	chr6:29616220-29616221	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs577338422	chr6:29616267-29616268	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs539986705	chr6:29616315-29616316	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs553574874	chr6:29616343-29616344	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs556488062	chr6:29616350-29616351	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs576627313	chr6:29616352-29616353	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs199635035	chr6:29616353-29616354	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs542200799	chr6:29616396-29616397	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs145573658	chr6:29616507-29616508	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs142271717	chr6:29616508-29616509	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs9280628	chr6:29616522-29616523	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs562050654	chr6:29616565-29616566	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs374991281	chr6:29616595-29616596	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs572969653	chr6:29616606-29616607	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs188272775	chr6:29616616-29616617	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs564537579	chr6:29616654-29616655	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs200504112	chr6:29616665-29616666	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs145789607	chr6:29616721-29616722	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs549902060	chr6:29616746-29616747	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs140094840	chr6:29616785-29616786	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs529177693	chr6:29616830-29616831	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs182043106	chr6:29616841-29616842	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs565315039	chr6:29616849-29616850	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs184742666	chr6:29616850-29616851	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs544318823	chr6:29616887-29616888	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs145627033	chr6:29616893-29616894	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs12660997	chr6:29616912-29616913	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs570965963	chr6:29616955-29616956	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs12663925	chr6:29616961-29616962	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs189993062	chr6:29617019-29617020	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:513 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:29608400-29616400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr6:29609600-29617200	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr6:29610000-29617200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr6:29610600-29617200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr6:29610600-29617400	Weak transcription	K562	blood
6	chr6:29610800-29617200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr6:29611400-29616800	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr6:29612000-29616800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr6:29615400-29616000	Enhancers	NHEK	skin
10	chr6:29615800-29616200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr6:29615800-29616600	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr6:29615800-29616600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr6:29615800-29617200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr6:29615800-29617200	Weak transcription	HMEC	breast
15	chr6:29615800-29617400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr6:29616000-29617200	Weak transcription	NHEK	skin
17	chr6:29616200-29616400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr6:29616200-29617400	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr6:29616400-29617200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
20	chr6:29616400-29618600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr6:29616600-29616800	Enhancers	Primary neutrophils fromperipheralblood	blood
22	chr6:29616600-29616800	Enhancers	Primary hematopoietic stem cells	blood
23	chr6:29616600-29616800	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr6:29616600-29617000	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr6:29616600-29617200	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr6:29616600-29617200	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr6:29616600-29617200	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr6:29616600-29617200	Enhancers	Primary B cells from cord blood	blood
29	chr6:29616600-29617200	Enhancers	Primary B cells from peripheral blood	blood
30	chr6:29616600-29617200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
31	chr6:29616600-29617400	Enhancers	H1 Cell Line	embryonic stem cell
32	chr6:29616600-29617400	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr6:29616600-29617400	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr6:29616600-29617400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr6:29616800-29617000	Flanking Active TSS	Primary hematopoietic stem cells	blood
36	chr6:29616800-29617000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr6:29616800-29617200	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr6:29616800-29617200	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr6:29616800-29617200	Enhancers	Primary T cells from cord blood	blood
40	chr6:29616800-29617200	Enhancers	Primary T cells fromperipheralblood	blood
41	chr6:29616800-29617200	Enhancers	Primary T helper cells PMA-I stimulated	--
42	chr6:29616800-29617200	Enhancers	Primary T helper cells fromperipheralblood	blood
43	chr6:29616800-29617200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
44	chr6:29616800-29617200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
45	chr6:29616800-29617200	Enhancers	Primary T killer memory cells from peripheral blood	blood
46	chr6:29616800-29617200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr6:29616800-29617400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
48	chr6:29616800-29618200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
49	chr6:29617000-29617200	Enhancers	Primary hematopoietic stem cells	blood
50	chr6:29617000-29617200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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