Variant report

Variant	nsv884023
Chromosome Location	chr6:29927095-29937924
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:971)
CpG islands
(count:610)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:971 , 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	chr6:29935249-29935871	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:29937042-29937091	K562	blood:	n/a	n/a
3	ARID3A	chr6:29935252-29935904	K562	blood:	n/a	n/a
4	ARID3A	chr6:29932290-29932954	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:29934522-29934914	K562	blood:	n/a	n/a
6	ARID3A	chr6:29933775-29934240	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:29932477-29933236	K562	blood:	n/a	n/a
8	ARID3A	chr6:29933748-29934309	K562	blood:	n/a	n/a
9	ARID3A	chr6:29931139-29931164	K562	blood:	n/a	n/a
10	ATF1	chr6:29935286-29935585	K562	blood:	n/a	n/a
11	ATF1	chr6:29932584-29933076	K562	blood:	n/a	n/a
12	ATF2	chr6:29932433-29933091	GM12878	blood:	n/a	n/a
13	ATF2	chr6:29932488-29932978	GM12878	blood:	n/a	n/a
14	ATF3	chr6:29932539-29933023	K562	blood:	n/a	n/a
15	ATF3	chr6:29932615-29932943	K562	blood:	n/a	n/a
16	BACH1	chr6:29932608-29933062	K562	blood:	n/a	n/a
17	BACH1	chr6:29932453-29933278	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr6:29932589-29933017	GM12878	blood:	n/a	chr6:29932797-29932808 chr6:29932798-29932808
19	BATF	chr6:29932612-29932987	GM12878	blood:	n/a	chr6:29932797-29932808 chr6:29932798-29932808
20	BCL11A	chr6:29932639-29932881	GM12878	blood:	n/a	chr6:29932797-29932806
21	BCL11A	chr6:29932602-29932969	GM12878	blood:	n/a	chr6:29932797-29932806
22	BCL3	chr6:29932533-29932943	GM12878	blood:	n/a	chr6:29932797-29932806
23	BCLAF1	chr6:29932494-29933203	GM12878	blood:	n/a	chr6:29932797-29932806
24	BCLAF1	chr6:29932428-29933119	GM12878	blood:	n/a	chr6:29932797-29932806
25	BHLHE40	chr6:29934607-29934610	GM12878	blood:	n/a	n/a
26	BHLHE40	chr6:29933686-29934301	K562	blood:	n/a	n/a
27	BHLHE40	chr6:29935166-29935758	K562	blood:	n/a	n/a
28	BHLHE40	chr6:29932548-29933279	GM12878	blood:	n/a	n/a
29	BHLHE40	chr6:29932569-29933159	K562	blood:	n/a	n/a
30	BHLHE40	chr6:29933866-29934118	GM12878	blood:	n/a	n/a
31	BHLHE40	chr6:29933714-29934091	HepG2	liver:	n/a	n/a
32	CBX3	chr6:29932403-29933273	HCT-116	colon:	n/a	n/a
33	CBX3	chr6:29932608-29932997	K562	blood:	n/a	n/a
34	CBX3	chr6:29933685-29934511	HCT-116	colon:	n/a	n/a
35	CBX3	chr6:29935109-29935665	K562	blood:	n/a	n/a
36	CBX3	chr6:29935860-29936460	HCT-116	colon:	n/a	n/a
37	CBX3	chr6:29935905-29936437	HCT-116	colon:	n/a	n/a
38	CBX3	chr6:29932504-29933475	K562	blood:	n/a	n/a
39	CCNT2	chr6:29935317-29935569	K562	blood:	n/a	n/a
40	CCNT2	chr6:29932623-29932970	K562	blood:	n/a	n/a
41	CEBPB	chr6:29935073-29935816	K562	blood:	n/a	chr6:29935249-29935260 chr6:29935210-29935221
42	CEBPB	chr6:29936002-29936359	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr6:29929504-29929848	K562	blood:	n/a	n/a
44	CEBPB	chr6:29934230-29934543	IMR90	lung:	n/a	n/a
45	CEBPB	chr6:29935064-29935418	HepG2	liver:	n/a	chr6:29935249-29935260 chr6:29935210-29935221
46	CEBPB	chr6:29932451-29933116	GM12878	blood:	n/a	n/a
47	CEBPB	chr6:29932426-29933189	K562	blood:	n/a	n/a
48	CEBPB	chr6:29932409-29933285	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr6:29932577-29933269	K562	blood:	n/a	n/a
50	CEBPB	chr6:29935138-29935549	K562	blood:	n/a	chr6:29935249-29935260 chr6:29935210-29935221

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:29932743-29932793	HCT-116	colon:	n/a
2	chr6:29933925-29933975	HCPEpiC	choroid plexus:	n/a
3	chr6:29928362-29928412	A549	lung:	n/a
4	chr6:29932621-29932671	A549	lung:	n/a
5	chr6:29933411-29933461	Hepatocyte	liver:	n/a
6	chr6:29933915-29933965	HL-60	blood:	n/a
7	chr6:29933511-29933561	MCF10A-Er-Src	breast:	n/a
8	chr6:29933971-29934021	RPTEC	kidney:	n/a
9	chr6:29933511-29933561	AG09319	gingival:	n/a
10	chr6:29933971-29934021	NHDF-neo	bronchial:	n/a
11	chr6:29932864-29932914	AG10803	skin:	n/a
12	chr6:29933511-29933561	ProgFib	skin:	n/a
13	chr6:29933511-29933561	Caco-2	colon:	n/a
14	chr6:29933915-29933965	ovcar-3	ovarian:	n/a
15	chr6:29933697-29933747	HUVEC	blood vessel:	n/a
16	chr6:29932621-29932671	HEK293	kidney:	embryo
17	chr6:29928362-29928412	PrEC	prostate:	n/a
18	chr6:29932743-29932793	HPAEpiC	pulmonary alveolar:	n/a
19	chr6:29933697-29933747	SK-N-MC	brain:	n/a
20	chr6:29933411-29933461	Caco-2	colon:	n/a
21	chr6:29928362-29928412	Hepatocyte	liver:	n/a
22	chr6:29932621-29932671	AG10803	skin:	n/a
23	chr6:29932621-29932671	NHDF-neo	bronchial:	n/a
24	chr6:29933411-29933461	HCT-116	colon:	n/a
25	chr6:29932621-29932671	NHBE	bronchial:	n/a
26	chr6:29928362-29928412	PANC-1	pancreas:	n/a
27	chr6:29928362-29928412	H1-hESC	embryonic stem cell:	embryo
28	chr6:29932864-29932914	HCT-116	colon:	n/a
29	chr6:29932621-29932671	PANC-1	pancreas:	n/a
30	chr6:29932864-29932914	BJ	skin:	n/a
31	chr6:29932743-29932793	HepG2	liver:	n/a
32	chr6:29928362-29928412	HPAEpiC	pulmonary alveolar:	n/a
33	chr6:29933971-29934021	Hepatocyte	liver:	n/a
34	chr6:29933511-29933561	GM12878	blood:	n/a
35	chr6:29933925-29933975	SAEC	small airway:	n/a
36	chr6:29933915-29933965	NB4	blood:	n/a
37	chr6:29932743-29932793	NB4	blood:	n/a
38	chr6:29933915-29933965	NHDF-neo	bronchial:	n/a
39	chr6:29933971-29934021	Caco-2	colon:	n/a
40	chr6:29933511-29933561	Hepatocyte	liver:	n/a
41	chr6:29933971-29934021	ProgFib	skin:	n/a
42	chr6:29933411-29933461	NB4	blood:	n/a
43	chr6:29933971-29934021	ovcar-3	ovarian:	n/a
44	chr6:29933971-29934021	H1-hESC	embryonic stem cell:	embryo
45	chr6:29932621-29932671	Caco-2	colon:	n/a
46	chr6:29932621-29932671	GM12892	blood:	n/a
47	chr6:29933925-29933975	U87	brain:	n/a
48	chr6:29933697-29933747	SK-N-SH	brain:	n/a
49	chr6:29928362-29928412	MCF10A-Er-Src	breast:	n/a
50	chr6:29932864-29932914	Hepatocyte	liver:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:29931653..29934276-chr6:29943760..29946372,5	K562	blood:
2	chr6:29920527..29922060-chr6:29926055..29928693,2	K562	blood:
3	chr6:29926306..29930004-chr6:29943804..29947247,3	K562	blood:
4	chr6:29931492..29933251-chr6:30034694..30036479,2	K562	blood:
5	chr6:29927397..29931336-chr6:29932208..29936273,8	K562	blood:
6	chr14:77247003..77248532-chr6:29931290..29933642,2	K562	blood:
7	chr6:29932263..29935141-chr6:29936079..29939709,3	K562	blood:
8	chr6:29931972..29934794-chr6:30027595..30029471,2	K562	blood:
9	chr6:29815528..29816550-chr6:29935117..29936165,4	MCF-7	breast:
10	chr6:29937399..29939324-chr6:29949163..29951713,2	K562	blood:
11	chr6:29921960..29924230-chr6:29934596..29936833,2	K562	blood:
12	chr6:29920547..29922811-chr6:29925895..29928597,2	MCF-7	breast:
13	chr6:29932263..29935141-chr6:29936079..29939709,3	K562	blood:
14	chr6:29892582..29894711-chr6:29932418..29935205,2	K562	blood:
15	chr6:29820786..29821478-chr6:29935191..29935715,2	MCF-7	breast:
16	chr6:29820931..29821695-chr6:29935492..29936150,2	MCF-7	breast:
17	chr6:29937339..29939716-chr6:29942275..29944965,3	MCF-7	breast:
18	chr6:29937696..29939359-chr6:30032545..30034517,2	K562	blood:
19	chr6:29929604..29934270-chr6:29942846..29948120,6	K562	blood:
20	chr6:29917413..29919975-chr6:29932108..29934788,2	K562	blood:
21	chr6:29927397..29931336-chr6:29932208..29936273,8	K562	blood:
22	chr6:29933916..29936718-chr6:29943405..29945040,3	MCF-7	breast:

No data

Variant related genes	Relation type
HCG9	TF binding region
HCG9	CpG island
ENSG00000230795	chromatin interactions
ENSG00000066379	chromatin interactions
ENSG00000204623	chromatin interactions
ENSG00000259081	chromatin interactions
ENSG00000204625	chromatin interactions
ENSG00000204619	chromatin interactions

Extended variants
information (count: 592 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:592 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2735085	chr6:29927095-29927096	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs571902795	chr6:29927139-29927140	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs2394246	chr6:29927168-29927169	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs2523937	chr6:29927221-29927222	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs567285816	chr6:29927274-29927275	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs114577328	chr6:29927282-29927283	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs2571398	chr6:29927303-29927304	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs544722407	chr6:29927307-29927308	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs12529094	chr6:29927331-29927332	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs200756775	chr6:29927393-29927394	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs572997912	chr6:29927406-29927407	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs201927050	chr6:29927417-29927418	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs112992829	chr6:29927420-29927421	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs201371481	chr6:29927422-29927423	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs2735083	chr6:29927463-29927464	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs187971242	chr6:29927491-29927492	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs377532318	chr6:29927523-29927524	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs9260693	chr6:29927534-29927535	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs560885079	chr6:29927599-29927600	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs386698628	chr6:29927610-29927611	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs2517696	chr6:29927611-29927612	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs2517695	chr6:29927629-29927630	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs375780843	chr6:29927712-29927713	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs2571400	chr6:29927722-29927723	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs192799031	chr6:29927730-29927731	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs138754415	chr6:29927740-29927741	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs531250267	chr6:29927757-29927758	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs183492408	chr6:29927807-29927808	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs567322488	chr6:29927866-29927867	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs377386189	chr6:29927879-29927880	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs574976325	chr6:29927888-29927889	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs202171205	chr6:29927896-29927897	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs377364045	chr6:29927902-29927903	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs2735082	chr6:29927936-29927937	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs144751566	chr6:29927944-29927945	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs148118074	chr6:29927951-29927952	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs189344283	chr6:29927997-29927998	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs73414567	chr6:29928019-29928020	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs141919361	chr6:29928025-29928026	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs200579835	chr6:29928077-29928078	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs558737177	chr6:29928081-29928082	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs568926339	chr6:29928113-29928114	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs369812645	chr6:29928119-29928120	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs441808	chr6:29928137-29928138	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs562229631	chr6:29928159-29928160	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs554858058	chr6:29928173-29928174	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs55897388	chr6:29928188-29928189	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs446787	chr6:29928196-29928197	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs553622769	chr6:29928214-29928215	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs559850339	chr6:29928216-29928217	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:112)

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
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
Ovarian cancer	21781307	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
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	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
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	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	21293372	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:662 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:29913400-29932200	Weak transcription	Brain Anterior Caudate	brain
2	chr6:29913400-29932600	Weak transcription	Brain Substantia Nigra	brain
3	chr6:29913800-29932200	Weak transcription	Small Intestine	intestine
4	chr6:29914000-29932200	Weak transcription	Colon Smooth Muscle	Colon
5	chr6:29914600-29932200	Weak transcription	Colonic Mucosa	Colon
6	chr6:29914800-29932200	Weak transcription	Right Ventricle	heart
7	chr6:29915400-29931800	Weak transcription	Fetal Thymus	thymus
8	chr6:29915600-29932000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr6:29916800-29928200	Weak transcription	HepG2	liver
10	chr6:29916800-29930000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr6:29916800-29932200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr6:29916800-29932200	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr6:29916800-29932200	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr6:29916800-29933000	Weak transcription	Esophagus	oesophagus
15	chr6:29916800-29933000	Weak transcription	Pancreas	Pancrea
16	chr6:29916800-29933200	Weak transcription	Lung	lung
17	chr6:29916800-29940200	Weak transcription	Gastric	stomach
18	chr6:29917000-29931800	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr6:29917200-29932000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
20	chr6:29917200-29932200	Weak transcription	Liver	Liver
21	chr6:29917200-29932200	Weak transcription	Brain Hippocampus Middle	brain
22	chr6:29917400-29927400	Weak transcription	Fetal Muscle Leg	muscle
23	chr6:29917800-29932200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr6:29918000-29932000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
25	chr6:29918000-29932200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr6:29918000-29932200	Weak transcription	Fetal Intestine Small	intestine
27	chr6:29918200-29931800	Weak transcription	Primary T cells from cord blood	blood
28	chr6:29918400-29927400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr6:29920400-29932200	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr6:29921800-29929400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr6:29921800-29929600	Weak transcription	Psoas Muscle	Psoas
32	chr6:29921800-29932200	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr6:29922000-29929600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr6:29922400-29927600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr6:29924600-29932200	Weak transcription	Left Ventricle	heart
36	chr6:29924600-29932200	Weak transcription	Right Atrium	heart
37	chr6:29924800-29932200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr6:29924800-29933000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr6:29926000-29927200	Enhancers	Spleen	Spleen
40	chr6:29926000-29930600	Enhancers	Adipose Nuclei	Adipose
41	chr6:29926200-29929400	Weak transcription	K562	blood
42	chr6:29926200-29932600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr6:29926400-29927800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr6:29926400-29927800	Enhancers	GM12878-XiMat	blood
45	chr6:29926400-29931800	Weak transcription	Primary neutrophils fromperipheralblood	blood
46	chr6:29926400-29931800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr6:29926600-29927600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr6:29926600-29927800	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr6:29926600-29927800	Enhancers	Primary B cells from peripheral blood	blood
50	chr6:29926600-29927800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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