Variant report

Variant	nsv886938
Chromosome Location	chr6:166859725-166904398
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:652)
CpG islands
(count:2321)
Chromatin interactive
region (count:21)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:652 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:166879275-166879413	HepG2	liver:	n/a	n/a
2	ATF1	chr6:166879162-166879476	K562	blood:	n/a	n/a
3	BCL3	chr6:166880029-166880872	GM12878	blood:	n/a	n/a
4	BCL3	chr6:166880160-166880825	GM12878	blood:	n/a	n/a
5	BCLAF1	chr6:166901584-166901942	GM12878	blood:	n/a	n/a
6	BHLHE40	chr6:166888791-166889071	K562	blood:	n/a	chr6:166888947-166888956
7	BHLHE40	chr6:166901672-166902025	GM12878	blood:	n/a	n/a
8	BHLHE40	chr6:166891641-166891785	K562	blood:	n/a	chr6:166891719-166891740
9	BRCA1	chr6:166879298-166879354	HepG2	liver:	n/a	n/a
10	CBX3	chr6:166901555-166901924	K562	blood:	n/a	n/a
11	CEBPB	chr6:166874189-166874844	MCF-7	breast:	n/a	n/a
12	CEBPB	chr6:166879642-166879983	ECC-1	luminal epithelium:	n/a	n/a
13	CHD1	chr6:166901584-166901762	GM12878	blood:	n/a	n/a
14	CHD2	chr6:166870168-166870184	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr6:166901721-166901895	GM12878	blood:	n/a	n/a
16	CREB1	chr6:166879200-166879489	A549	lung:	n/a	chr6:166879305-166879318
17	CTCF	chr6:166879235-166879414	A549	lung:	n/a	n/a
18	CTCF	chr6:166899860-166900010	GM12867	blood:	n/a	chr6:166899887-166899905
19	CTCF	chr6:166879280-166879430	HAc	cerebellar:	n/a	n/a
20	CTCF	chr6:166869920-166870098	Gliobla	brain:	n/a	n/a
21	CTCF	chr6:166872940-166873090	HMF	breast:	n/a	n/a
22	CTCF	chr6:166869910-166870120	LNCaP	prostate:	n/a	n/a
23	CTCF	chr6:166869960-166870110	HA-sp	spinal cord:	n/a	n/a
24	CTCF	chr6:166879280-166879430	AG09309	skin:	n/a	n/a
25	CTCF	chr6:166869780-166869930	NHLF	lung:	n/a	n/a
26	CTCF	chr6:166879228-166879427	ProgFib	skin:	n/a	n/a
27	CTCF	chr6:166899780-166899930	RPTEC	kidney:	n/a	chr6:166899887-166899905
28	CTCF	chr6:166899860-166900010	HEK293	kidney:	n/a	chr6:166899887-166899905
29	CTCF	chr6:166869880-166870030	AG09319	gingival:	n/a	n/a
30	CTCF	chr6:166879260-166879410	HUVEC	blood vessel:	n/a	n/a
31	CTCF	chr6:166869920-166870070	HAc	cerebellar:	n/a	n/a
32	CTCF	chr6:166869900-166870050	A549	lung:	n/a	n/a
33	CTCF	chr6:166879240-166879390	HCPEpiC	choroid plexus:	n/a	n/a
34	CTCF	chr6:166879220-166879370	HPAF	blood vessel:	n/a	n/a
35	CTCF	chr6:166869980-166870130	AG09309	skin:	n/a	n/a
36	CTCF	chr6:166869940-166870090	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr6:166869900-166870115	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr6:166876360-166876510	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr6:166869940-166870090	GM12874	blood:	n/a	n/a
40	CTCF	chr6:166879280-166879430	HMF	breast:	n/a	n/a
41	CTCF	chr6:166899820-166899970	HRPEpiC	eye:	n/a	chr6:166899887-166899905
42	CTCF	chr6:166879320-166879470	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr6:166899859-166899931	LNCaP	prostate:	n/a	chr6:166899887-166899905
44	CTCF	chr6:166879260-166879410	HEK293	kidney:	n/a	n/a
45	CTCF	chr6:166876400-166876550	HEK293	kidney:	n/a	n/a
46	CTCF	chr6:166876386-166876546	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr6:166869920-166870070	AG09309	skin:	n/a	n/a
48	CTCF	chr6:166869940-166870090	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr6:166870200-166870350	HAc	cerebellar:	n/a	n/a
50	CTCF	chr6:166879580-166879730	HPF	lung:	n/a	n/a

(count:2321 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:166876490-166876540	AoSMC	blood vessel:	n/a
2	chr6:166892216-166892266	HRCEpiC	kidney:	n/a
3	chr6:166892649-166892699	HRPEpiC	eye:	n/a
4	chr6:166876490-166876540	AoSMC	blood vessel:	n/a
5	chr6:166892216-166892266	HRCEpiC	kidney:	n/a
6	chr6:166892649-166892699	HRPEpiC	eye:	n/a
7	chr6:166891902-166891952	SK-N-SH_RA	brain:	n/a
8	chr6:166876736-166876786	Jurkat	blood:	n/a
9	chr6:166868193-166868243	PANC-1	pancreas:	n/a
10	chr6:166868953-166869003	BJ	skin:	n/a
11	chr6:166884430-166884480	NT2-D1	testis:	n/a
12	chr6:166876490-166876540	HCT-116	colon:	n/a
13	chr6:166859733-166859783	HRCEpiC	kidney:	n/a
14	chr6:166876890-166876940	HEK293	kidney:	embryo
15	chr6:166891729-166891779	GM06990	blood:	n/a
16	chr6:166868856-166868906	MCF10A-Er-Src	breast:	n/a
17	chr6:166876490-166876540	IMR90	lung:	fetal
18	chr6:166868856-166868906	HCPEpiC	choroid plexus:	n/a
19	chr6:166901831-166901881	K562	blood:	n/a
20	chr6:166859733-166859783	GM19239	blood:	n/a
21	chr6:166900456-166900506	SK-N-MC	brain:	n/a
22	chr6:166900456-166900506	HepG2	liver:	n/a
23	chr6:166892362-166892412	PrEC	prostate:	n/a
24	chr6:166892921-166892971	HIPEpiC	eye:	n/a
25	chr6:166892762-166892812	SK-N-MC	brain:	n/a
26	chr6:166868856-166868906	GM12878	blood:	n/a
27	chr6:166868856-166868906	HRE	kidney:	n/a
28	chr6:166891650-166891700	ovcar-3	ovarian:	n/a
29	chr6:166876535-166876585	HEEpiC	esophagus:	n/a
30	chr6:166900415-166900465	HL-60	blood:	n/a
31	chr6:166901854-166901904	SKMC	muscle:	n/a
32	chr6:166891729-166891779	T-47D	breast:	n/a
33	chr6:166892649-166892699	Hepatocyte	liver:	n/a
34	chr6:166876890-166876940	ProgFib	skin:	n/a
35	chr6:166891902-166891952	ovcar-3	ovarian:	n/a
36	chr6:166892216-166892266	ProgFib	skin:	n/a
37	chr6:166876490-166876540	AG04450	lung:	fetal
38	chr6:166891617-166891667	SAEC	small airway:	n/a
39	chr6:166868953-166869003	HL-60	blood:	n/a
40	chr6:166900456-166900506	HCPEpiC	choroid plexus:	n/a
41	chr6:166859733-166859783	HRPEpiC	eye:	n/a
42	chr6:166892362-166892412	HEK293	kidney:	embryo
43	chr6:166891959-166892009	ProgFib	skin:	n/a
44	chr6:166876490-166876540	GM12892	blood:	n/a
45	chr6:166859806-166859856	ovcar-3	ovarian:	n/a
46	chr6:166877002-166877052	RPTEC	kidney:	n/a
47	chr6:166877038-166877088	GM12891	blood:	n/a
48	chr6:166901854-166901904	SK-N-MC	brain:	n/a
49	chr6:166900442-166900492	GM19239	blood:	n/a
50	chr6:166901854-166901904	Hela-S3	cervix:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:166873172..166875809-chr6:166876336..166878720,2	K562	blood:
2	chr6:166869209..166870208-chr6:166925864..166926725,2	MCF-7	breast:
3	chr6:166858354..166860474-chr6:166862060..166863705,2	K562	blood:
4	chr6:166867376..166869497-chr6:166875533..166878478,2	K562	blood:
5	chr6:166893774..166896880-chr6:166897771..166899718,3	MCF-7	breast:
6	chr6:166867376..166869497-chr6:166875533..166878478,2	K562	blood:
7	chr6:166892327..166894616-chr6:166897228..166898880,2	K562	blood:
8	chr6:166873172..166875809-chr6:166876336..166878720,2	K562	blood:
9	chr6:166867400..166870305-chr6:166873619..166875332,2	K562	blood:
10	chr6:166869518..166870276-chr6:166927954..166928779,2	MCF-7	breast:
11	chr6:166877343..166879705-chr6:166880050..166881798,2	MCF-7	breast:
12	chr6:166858354..166860474-chr6:166862060..166863705,2	K562	blood:
13	chr6:166871889..166873613-chr6:166879410..166881105,2	K562	blood:
14	chr6:166870182..166872414-chr6:167234943..167236564,2	K562	blood:
15	chr6:166877740..166880123-chr6:166885130..166887516,2	K562	blood:
16	chr6:166867400..166870305-chr6:166873619..166875332,2	K562	blood:
17	chr6:166892327..166894616-chr6:166897228..166898880,2	K562	blood:
18	chr6:166881013..166882996-chr6:166884544..166886077,2	K562	blood:
19	chr6:166881013..166882996-chr6:166884544..166886077,2	K562	blood:
20	chr6:166754479..166756533-chr6:166881640..166884124,2	MCF-7	breast:
21	chr6:166893774..166896880-chr6:166897771..166899718,3	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BRP44L-1	chr6:166878813-166878871	ENSG00000232082.1
2	lnc-BRP44L-1	chr6:166874151-166874326	ENSG00000232082.1
3	lnc-BRP44L-1	chr6:166876474-166876629	ENSG00000232082.1
4	lnc-BRP44L-1	chr6:166876808-166876995	ENSG00000232082.1

No data

Variant related genes	Relation type
RPS6KA2	TF binding region
RPS6KA2-IT1	TF binding region
RPS6KA2	CpG island
RPS6KA2-IT1	CpG island
ENSG00000232082	chromatin interactions
ENSG00000071242	chromatin interactions
ENSG00000198818	chromatin interactions

Extended variants
information (count: 2212 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:2212 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2246553	chr6:166859725-166859726	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs139966924	chr6:166859734-166859735	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs7756092	chr6:166859772-166859773	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs568996855	chr6:166859808-166859809	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs73271205	chr6:166859828-166859829	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs573477730	chr6:166859829-166859830	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs557985223	chr6:166859834-166859835	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs372304878	chr6:166859860-166859861	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs184492448	chr6:166859863-166859864	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs533874109	chr6:166859897-166859898	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs189064911	chr6:166859916-166859917	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs573337691	chr6:166859931-166859932	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs540896375	chr6:166859962-166859963	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs370518581	chr6:166859971-166859972	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs2281061	chr6:166859991-166859992	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs2281060	chr6:166860024-166860025	Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs2281059	chr6:166860052-166860053	Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs545284475	chr6:166860070-166860071	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs528139472	chr6:166860081-166860082	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563372550	chr6:166860082-166860083	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs115204405	chr6:166860145-166860146	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs144220401	chr6:166860172-166860173	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs2281058	chr6:166860194-166860195	Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs560910513	chr6:166860215-166860216	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs561248735	chr6:166860222-166860223	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs531750249	chr6:166860249-166860250	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs2281057	chr6:166860270-166860271	Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs535437883	chr6:166860271-166860272	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565237108	chr6:166860288-166860289	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533108078	chr6:166860337-166860338	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs551276142	chr6:166860340-166860341	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs148486929	chr6:166860341-166860342	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs113570346	chr6:166860409-166860410	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs533822563	chr6:166860411-166860412	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs182455764	chr6:166860478-166860479	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs142658525	chr6:166860510-166860511	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs2281056	chr6:166860546-166860547	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs571198162	chr6:166860562-166860563	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs115479548	chr6:166860563-166860564	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs577658634	chr6:166860571-166860572	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs538775351	chr6:166860622-166860623	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs114515904	chr6:166860635-166860636	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs572709986	chr6:166860665-166860666	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs2281055	chr6:166860690-166860691	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs185684480	chr6:166860702-166860703	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs113810697	chr6:166860719-166860720	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs543462183	chr6:166860722-166860723	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs143375302	chr6:166860732-166860733	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs532495222	chr6:166860748-166860749	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs2281054	chr6:166860792-166860793	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ependymoma	20639864	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1430 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:166808200-166911800	Weak transcription	Psoas Muscle	Psoas
2	chr6:166824000-166901400	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr6:166825200-166875800	Weak transcription	Colonic Mucosa	Colon
4	chr6:166827000-166873400	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr6:166827600-166867200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr6:166830000-166866600	Weak transcription	Fetal Intestine Large	intestine
7	chr6:166833200-166864400	Weak transcription	Fetal Kidney	kidney
8	chr6:166833200-166879000	Weak transcription	NH-A	brain
9	chr6:166833400-166879000	Weak transcription	HSMM	muscle
10	chr6:166834000-166866400	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr6:166834200-166863800	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr6:166834200-166879400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr6:166834600-166862000	Weak transcription	NHDF-Ad	bronchial
14	chr6:166838200-166860400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr6:166843000-166865200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr6:166844200-166860400	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr6:166844200-166865200	Weak transcription	Rectal Smooth Muscle	rectum
18	chr6:166845800-166860000	Weak transcription	Colon Smooth Muscle	Colon
19	chr6:166845800-166860200	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr6:166845800-166862000	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr6:166845800-166863400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr6:166846000-166860600	Weak transcription	Liver	Liver
23	chr6:166846000-166861000	Weak transcription	HSMMtube	muscle
24	chr6:166846000-166861800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr6:166846000-166862200	Weak transcription	Fetal Intestine Small	intestine
26	chr6:166846000-166863200	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr6:166846000-166881000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr6:166846200-166860400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr6:166848800-166865200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr6:166849400-166861000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr6:166850200-166862000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr6:166850200-166863400	Weak transcription	Stomach Mucosa	stomach
33	chr6:166850200-166865200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr6:166850200-166870000	Weak transcription	Right Atrium	heart
35	chr6:166850400-166862000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr6:166851600-166860600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr6:166852000-166860000	Weak transcription	Brain Germinal Matrix	brain
38	chr6:166853400-166860200	Weak transcription	Spleen	Spleen
39	chr6:166853600-166861000	Weak transcription	Fetal Lung	lung
40	chr6:166853600-166862000	Weak transcription	Primary T cells from cord blood	blood
41	chr6:166854000-166859800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr6:166854000-166864200	Weak transcription	HUVEC	blood vessel
43	chr6:166854400-166862000	Strong transcription	Lung	lung
44	chr6:166854800-166860600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
45	chr6:166854800-166862800	Strong transcription	Left Ventricle	heart
46	chr6:166855200-166864800	Strong transcription	Pancreas	Pancrea
47	chr6:166855400-166863200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr6:166855400-166864600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr6:166855600-166864600	Strong transcription	Muscle Satellite Cultured Cells	--
50	chr6:166855800-166860400	Weak transcription	Primary B cells from cord blood	blood

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