Variant report

Variant	nsv5533
Chromosome Location	chr6:149748047-149793072
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1033)
CpG islands
(count:1281)
Chromatin interactive
region (count:64)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1033 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:149761833-149761881	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:149762478-149762931	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:149753093-149753436	HepG2	liver:	n/a	n/a
4	ATF2	chr6:149792810-149793813	GM12878	blood:	n/a	n/a
5	ATF2	chr6:149789927-149790416	GM12878	blood:	n/a	n/a
6	ATF2	chr6:149753036-149753475	GM12878	blood:	n/a	n/a
7	ATF2	chr6:149753021-149753565	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr6:149792855-149793395	GM12878	blood:	n/a	n/a
9	ATF2	chr6:149789899-149790409	GM12878	blood:	n/a	n/a
10	ATF3	chr6:149777942-149778134	K562	blood:	n/a	n/a
11	ATF3	chr6:149766740-149766941	K562	blood:	n/a	n/a
12	BACH1	chr6:149771870-149772280	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr6:149760096-149760455	GM12878	blood:	n/a	n/a
14	BATF	chr6:149792984-149793324	GM12878	blood:	n/a	n/a
15	BATF	chr6:149792884-149793330	GM12878	blood:	n/a	n/a
16	BATF	chr6:149789990-149790354	GM12878	blood:	n/a	n/a
17	BATF	chr6:149759878-149760455	GM12878	blood:	n/a	n/a
18	BCL11A	chr6:149760019-149760454	GM12878	blood:	n/a	n/a
19	BCL11A	chr6:149792911-149793305	GM12878	blood:	n/a	n/a
20	BCL11A	chr6:149765256-149765749	GM12878	blood:	n/a	n/a
21	BCL11A	chr6:149789963-149790382	GM12878	blood:	n/a	n/a
22	BCL11A	chr6:149792950-149793283	GM12878	blood:	n/a	n/a
23	BCL3	chr6:149762178-149762410	GM12878	blood:	n/a	n/a
24	BCL3	chr6:149778683-149778929	GM12878	blood:	n/a	n/a
25	BCL3	chr6:149789909-149790414	GM12878	blood:	n/a	n/a
26	BCL3	chr6:149792891-149793836	GM12878	blood:	n/a	n/a
27	BCL3	chr6:149765589-149766196	GM12878	blood:	n/a	n/a
28	BCL3	chr6:149764924-149765402	GM12878	blood:	n/a	n/a
29	BCL3	chr6:149761942-149762469	GM12878	blood:	n/a	n/a
30	BCL3	chr6:149765027-149765359	GM12878	blood:	n/a	n/a
31	BCL3	chr6:149765582-149766061	GM12878	blood:	n/a	n/a
32	BCLAF1	chr6:149789876-149790420	GM12878	blood:	n/a	n/a
33	BCLAF1	chr6:149753042-149753521	GM12878	blood:	n/a	n/a
34	BCLAF1	chr6:149792820-149793613	GM12878	blood:	n/a	n/a
35	BCLAF1	chr6:149759965-149760388	GM12878	blood:	n/a	n/a
36	BCLAF1	chr6:149789706-149790418	GM12878	blood:	n/a	n/a
37	BHLHE40	chr6:149760223-149760371	GM12878	blood:	n/a	n/a
38	BHLHE40	chr6:149766729-149766965	K562	blood:	n/a	n/a
39	BHLHE40	chr6:149777820-149778360	K562	blood:	n/a	n/a
40	BHLHE40	chr6:149753100-149753494	K562	blood:	n/a	n/a
41	BHLHE40	chr6:149789510-149790348	GM12878	blood:	n/a	n/a
42	BHLHE40	chr6:149787532-149787791	GM12878	blood:	n/a	n/a
43	BHLHE40	chr6:149753137-149753431	GM12878	blood:	n/a	n/a
44	BHLHE40	chr6:149781060-149781226	K562	blood:	n/a	n/a
45	BHLHE40	chr6:149792963-149793836	GM12878	blood:	n/a	n/a
46	BRCA1	chr6:149771895-149772095	H1-hESC	embryonic stem cell:	n/a	n/a
47	BRCA1	chr6:149753165-149753443	H1-hESC	embryonic stem cell:	n/a	n/a
48	BRCA1	chr6:149753154-149753362	HepG2	liver:	n/a	n/a
49	BRCA1	chr6:149775357-149776029	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr6:149753303-149753611	GM12878	blood:	n/a	n/a

(count:1281 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:149772854-149772904	SAEC	small airway:	n/a
2	chr6:149772716-149772766	HL-60	blood:	n/a
3	chr6:149771807-149771857	NHDF-neo	bronchial:	n/a
4	chr6:149777806-149777856	GM19239	blood:	n/a
5	chr6:149775853-149775903	NHDF-neo	bronchial:	n/a
6	chr6:149772892-149772942	HCT-116	colon:	n/a
7	chr6:149781248-149781298	MCF-7	breast:	n/a
8	chr6:149769803-149769853	K562	blood:	n/a
9	chr6:149769803-149769853	AoSMC	blood vessel:	n/a
10	chr6:149772892-149772942	Jurkat	blood:	n/a
11	chr6:149751329-149751379	Hepatocyte	liver:	n/a
12	chr6:149751329-149751379	MCF10A-Er-Src	breast:	n/a
13	chr6:149769803-149769853	HRPEpiC	eye:	n/a
14	chr6:149751415-149751465	HAEpiC	amniotic membrane:	n/a
15	chr6:149777984-149778034	SK-N-MC	brain:	n/a
16	chr6:149772150-149772200	ovcar-3	ovarian:	n/a
17	chr6:149772707-149772757	GM06990	blood:	n/a
18	chr6:149751329-149751379	SK-N-SH_RA	brain:	n/a
19	chr6:149772346-149772396	SAEC	small airway:	n/a
20	chr6:149772892-149772942	MCF10A-Er-Src	breast:	n/a
21	chr6:149781248-149781298	GM12878	blood:	n/a
22	chr6:149775853-149775903	SK-N-SH_RA	brain:	n/a
23	chr6:149770103-149770153	ProgFib	skin:	n/a
24	chr6:149778058-149778108	HEEpiC	esophagus:	n/a
25	chr6:149777984-149778034	SK-N-SH	brain:	n/a
26	chr6:149778058-149778108	SAEC	small airway:	n/a
27	chr6:149772707-149772757	GM12878	blood:	n/a
28	chr6:149785754-149785804	IMR90	lung:	fetal
29	chr6:149751225-149751275	PANC-1	pancreas:	n/a
30	chr6:149778775-149778825	RPTEC	kidney:	n/a
31	chr6:149777984-149778034	HAEpiC	amniotic membrane:	n/a
32	chr6:149772854-149772904	HRCEpiC	kidney:	n/a
33	chr6:149772854-149772904	IMR90	lung:	fetal
34	chr6:149778775-149778825	AoSMC	blood vessel:	n/a
35	chr6:149771807-149771857	NHBE	bronchial:	n/a
36	chr6:149771845-149771895	HRPEpiC	eye:	n/a
37	chr6:149751225-149751275	LNCaP	prostate:	n/a
38	chr6:149751329-149751379	HMEC	breast:	n/a
39	chr6:149785754-149785804	HCF	heart:	n/a
40	chr6:149777806-149777856	HCM	heart:	n/a
41	chr6:149751415-149751465	NB4	blood:	n/a
42	chr6:149751415-149751465	HRE	kidney:	n/a
43	chr6:149769803-149769853	T-47D	breast:	n/a
44	chr6:149777984-149778034	HIPEpiC	eye:	n/a
45	chr6:149775853-149775903	HRE	kidney:	n/a
46	chr6:149777806-149777856	IMR90	lung:	fetal
47	chr6:149775853-149775903	HNPCEpiC	eye:	n/a
48	chr6:149772150-149772200	T-47D	breast:	n/a
49	chr6:149777806-149777856	PANC-1	pancreas:	n/a
50	chr6:149772150-149772200	HAEpiC	amniotic membrane:	n/a

(count:64 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:149749032..149751401-chr6:149754918..149757804,2	K562	blood:
2	chr6:149763379..149766103-chr6:149776553..149779366,2	MCF-7	breast:
3	chr6:149750637..149752761-chr6:149774465..149776310,2	MCF-7	breast:
4	chr6:149403053..149404232-chr6:149752839..149753842,8	K562	blood:
5	chr6:149792520..149794344-chr6:149794518..149797030,2	K562	blood:
6	chr10:123366642..123368236-chr6:149751907..149753798,2	MCF-7	breast:
7	chr6:149748841..149750725-chr6:149751621..149753759,2	K562	blood:
8	chr6:149749225..149751406-chr6:149752259..149754784,2	K562	blood:
9	chr6:149381576..149384224-chr6:149749932..149753109,3	MCF-7	breast:
10	chr6:149352642..149354997-chr6:149758061..149760104,2	MCF-7	breast:
11	chr6:149398184..149404330-chr6:149748783..149757211,17	MCF-7	breast:
12	chr6:149748430..149751387-chr6:149751741..149754089,3	MCF-7	breast:
13	chr6:149749032..149751401-chr6:149754918..149757804,2	K562	blood:
14	chr6:149744819..149747181-chr6:149748180..149751163,2	MCF-7	breast:
15	chr6:149748430..149751387-chr6:149751741..149754089,3	MCF-7	breast:
16	chr6:149767445..149770252-chr6:149772541..149774258,2	MCF-7	breast:
17	chr6:149335068..149337695-chr6:149751708..149753851,2	MCF-7	breast:
18	chr6:149742080..149743974-chr6:149748766..149751309,2	MCF-7	breast:
19	chr6:149404330..149406131-chr6:149751650..149753242,2	MCF-7	breast:
20	chr6:149347837..149348431-chr6:149752868..149753657,2	MCF-7	breast:
21	chr6:149638351..149641682-chr6:149748296..149751639,3	MCF-7	breast:
22	chr6:149638278..149640828-chr6:149750311..149753449,4	MCF-7	breast:
23	chr6:149764839..149766396-chr6:149774052..149775951,2	MCF-7	breast:
24	chr6:149762143..149764363-chr6:149765543..149768268,2	K562	blood:
25	chr6:149757368..149759713-chr6:149765073..149766703,2	K562	blood:
26	chr6:149407753..149410844-chr6:149747576..149751159,3	MCF-7	breast:
27	chr6:149394698..149396657-chr6:149749436..149751094,2	MCF-7	breast:
28	chr6:149379587..149381868-chr6:149752319..149755254,2	MCF-7	breast:
29	chr6:149763441..149766003-chr6:149768583..149771236,2	K562	blood:
30	chr6:149352319..149353862-chr6:149749427..149751302,2	MCF-7	breast:
31	chr6:149511094..149511659-chr6:149753092..149753721,3	MCF-7	breast:
32	chr6:149401238..149401748-chr6:149748753..149749409,2	MCF-7	breast:
33	chr6:149763319..149765484-chr6:149839894..149842239,2	MCF-7	breast:
34	chr6:149703892..149707802-chr6:149748749..149751962,4	MCF-7	breast:
35	chr6:149380842..149383187-chr6:149749461..149751628,2	MCF-7	breast:
36	chr6:149757368..149759713-chr6:149765073..149766703,2	K562	blood:
37	chr6:149736139..149738247-chr6:149750968..149753957,2	K562	blood:
38	chr6:149785728..149788361-chr6:149790642..149793612,2	K562	blood:
39	chr6:149401238..149401990-chr6:149748324..149749629,5	MCF-7	breast:
40	chr6:149352390..149354385-chr6:149752598..149755216,2	MCF-7	breast:
41	chr6:149745176..149748304-chr6:149748732..149751749,4	MCF-7	breast:
42	chr6:149748841..149750725-chr6:149751621..149753759,2	K562	blood:
43	chr6:149403173..149404038-chr6:149750454..149751288,2	MCF-7	breast:
44	chr6:149349695..149350816-chr6:149752428..149753382,4	K562	blood:
45	chr6:149762143..149764363-chr6:149765543..149768268,2	K562	blood:
46	chr6:149767445..149770252-chr6:149772541..149774258,2	MCF-7	breast:
47	chr6:149769726..149773853-chr6:149775332..149778151,3	K562	blood:
48	chr6:149351119..149355583-chr6:149748923..149756337,13	MCF-7	breast:
49	chr6:149779659..149781916-chr6:149782862..149785427,2	K562	blood:
50	chr6:149378979..149381253-chr6:149751036..149753374,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZC3H12D-9	chr6:149768794-149769181	NONHSAT115500
2	lnc-ZC3H12D-9	chr6:149769570-149770516	NONHSAT115500

No data

Variant related genes	Relation type
ZC3H12D	TF binding region
ZC3H12D	CpG island
ENSG00000236591	chromatin interactions
ENSG00000055208	chromatin interactions
ENSG00000178199	chromatin interactions

Extended variants
information (count: 1813 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1813 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4895788	chr6:149748091-149748092	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs142128980	chr6:149748167-149748168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs12664492	chr6:149748185-149748186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs117187174	chr6:149748229-149748230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs189203565	chr6:149748230-149748231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs568808863	chr6:149748235-149748236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs377414629	chr6:149748279-149748280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs370442822	chr6:149748292-149748293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs557778768	chr6:149748388-149748389	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs544194817	chr6:149748389-149748390	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs76736361	chr6:149748403-149748404	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs674919	chr6:149748411-149748412	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs574913081	chr6:149748478-149748479	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs376371357	chr6:149748482-149748483	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs573403079	chr6:149748538-149748539	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs62426122	chr6:149748585-149748586	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs117354560	chr6:149748633-149748634	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs538461833	chr6:149748639-149748640	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs544841857	chr6:149748661-149748662	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs558301897	chr6:149748670-149748671	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs564648501	chr6:149748685-149748686	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs561078420	chr6:149748737-149748738	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs572048807	chr6:149748746-149748747	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs534674015	chr6:149748759-149748760	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs546226620	chr6:149748808-149748809	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs145903253	chr6:149748827-149748828	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs529002313	chr6:149748828-149748829	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs548758713	chr6:149748928-149748929	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs138720582	chr6:149748941-149748942	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs181286400	chr6:149749017-149749018	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs537648746	chr6:149749028-149749029	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs530019573	chr6:149749041-149749042	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs571484886	chr6:149749074-149749075	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs539799672	chr6:149749134-149749135	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs76130423	chr6:149749143-149749144	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs566958651	chr6:149749222-149749223	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs371125096	chr6:149749263-149749264	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs149252027	chr6:149749335-149749336	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs554308137	chr6:149749338-149749339	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs386706933	chr6:149749403-149749404	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs374292181	chr6:149749404-149749405	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs544496614	chr6:149749413-149749414	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs144432990	chr6:149749429-149749430	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs186525397	chr6:149749441-149749442	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs539841954	chr6:149749449-149749450	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs559758386	chr6:149749460-149749461	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs540131078	chr6:149749485-149749486	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs542269193	chr6:149749516-149749517	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs562457304	chr6:149749524-149749525	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs560324902	chr6:149749533-149749534	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
Autism	21448237	CNVD
Autism	22495311	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
Follicular lymphoma	20505157	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
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
Cancer	17160897	CNVD
Breast cancer	17417639	CNVD
Breast cancer	17850661	CNVD
Renal cell carcinoma	18765545	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20556506	CNVD
Hirschsprung''s Disease	21712996	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1234 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:149709600-149750200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:149745400-149748600	Weak transcription	HSMMtube	muscle
3	chr6:149745400-149750400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:149745600-149749000	Weak transcription	Stomach Smooth Muscle	stomach
5	chr6:149745600-149750200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr6:149745600-149752800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr6:149745600-149752800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr6:149745600-149752800	Weak transcription	HSMM	muscle
9	chr6:149745600-149753000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr6:149745600-149753000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr6:149745600-149753000	Weak transcription	Fetal Muscle Leg	muscle
12	chr6:149746800-149753000	Weak transcription	Placenta	Placenta
13	chr6:149746800-149762000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr6:149747800-149748800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr6:149748600-149749400	Enhancers	HSMMtube	muscle
16	chr6:149748800-149753200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr6:149749000-149749200	Enhancers	Stomach Smooth Muscle	stomach
18	chr6:149749200-149749400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr6:149749400-149753400	Weak transcription	HSMMtube	muscle
20	chr6:149749800-149764400	Weak transcription	Right Atrium	heart
21	chr6:149750200-149750600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr6:149750200-149750800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr6:149750400-149750800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr6:149751000-149751800	Bivalent Enhancer	HepG2	liver
25	chr6:149751600-149751800	Enhancers	Hela-S3	cervix
26	chr6:149752000-149753200	Weak transcription	Hela-S3	cervix
27	chr6:149752600-149753000	Enhancers	Primary T helper cells PMA-I stimulated	--
28	chr6:149752600-149753000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr6:149752600-149753000	Enhancers	Dnd41	blood
30	chr6:149752800-149753000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr6:149752800-149753000	Enhancers	Primary T cells fromperipheralblood	blood
32	chr6:149752800-149753000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
33	chr6:149752800-149753000	Enhancers	Primary T helper naive cells from peripheral blood	blood
34	chr6:149752800-149753000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
35	chr6:149752800-149753000	Enhancers	Primary T helper cells fromperipheralblood	blood
36	chr6:149752800-149753000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
37	chr6:149752800-149753000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr6:149752800-149753000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr6:149752800-149753000	Enhancers	Brain Anterior Caudate	brain
40	chr6:149752800-149753000	Enhancers	Brain Cingulate Gyrus	brain
41	chr6:149752800-149753000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
42	chr6:149752800-149753000	Enhancers	HSMM	muscle
43	chr6:149752800-149753200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
44	chr6:149752800-149753200	Enhancers	Duodenum Smooth Muscle	Duodenum
45	chr6:149752800-149753400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr6:149752800-149753600	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr6:149752800-149753600	Enhancers	Primary T killer memory cells from peripheral blood	blood
48	chr6:149752800-149753600	Enhancers	Liver	Liver
49	chr6:149752800-149754400	Enhancers	Fetal Thymus	thymus
50	chr6:149753000-149753200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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