Variant report

Variant	nsv3963
Chromosome Location	chr3:119301064-119345904
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:719)
CpG islands
(count:734)
Chromatin interactive
region (count:29)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:719 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:119314488-119314801	HepG2	liver:	n/a	n/a
2	ATF2	chr3:119300762-119301323	GM12878	blood:	n/a	n/a
3	ATF2	chr3:119316171-119318970	GM12878	blood:	n/a	n/a
4	ATF2	chr3:119306866-119307406	GM12878	blood:	n/a	n/a
5	ATF2	chr3:119318262-119320560	GM12878	blood:	n/a	n/a
6	ATF2	chr3:119342802-119343437	GM12878	blood:	n/a	n/a
7	ATF2	chr3:119319437-119320241	GM12878	blood:	n/a	n/a
8	ATF2	chr3:119342686-119343340	GM12878	blood:	n/a	n/a
9	ATF2	chr3:119306778-119307395	GM12878	blood:	n/a	n/a
10	ATF2	chr3:119300642-119301539	GM12878	blood:	n/a	n/a
11	ATF2	chr3:119315942-119318112	GM12878	blood:	n/a	n/a
12	BACH1	chr3:119319593-119319815	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr3:119332101-119332332	GM12878	blood:	n/a	n/a
14	BATF	chr3:119316856-119317125	GM12878	blood:	n/a	n/a
15	BATF	chr3:119319513-119319956	GM12878	blood:	n/a	n/a
16	BATF	chr3:119311802-119312040	GM12878	blood:	n/a	n/a
17	BATF	chr3:119323776-119323995	GM12878	blood:	n/a	chr3:119323902-119323913 chr3:119323903-119323913
18	BATF	chr3:119317199-119317631	GM12878	blood:	n/a	n/a
19	BATF	chr3:119316751-119317180	GM12878	blood:	n/a	n/a
20	BCL11A	chr3:119307066-119307296	GM12878	blood:	n/a	n/a
21	BCL11A	chr3:119316773-119317613	GM12878	blood:	n/a	n/a
22	BCL11A	chr3:119306989-119307402	GM12878	blood:	n/a	n/a
23	BCL3	chr3:119318231-119318854	GM12878	blood:	n/a	chr3:119318543-119318552
24	BCL3	chr3:119316624-119317763	GM12878	blood:	n/a	n/a
25	BCL3	chr3:119342739-119343363	GM12878	blood:	n/a	n/a
26	BCL3	chr3:119301044-119301463	GM12878	blood:	n/a	n/a
27	BCLAF1	chr3:119342774-119343237	GM12878	blood:	n/a	n/a
28	BCLAF1	chr3:119319438-119320103	GM12878	blood:	n/a	n/a
29	BCLAF1	chr3:119317146-119317826	GM12878	blood:	n/a	n/a
30	BCLAF1	chr3:119316211-119318576	GM12878	blood:	n/a	chr3:119318543-119318552
31	BCLAF1	chr3:119306889-119307401	GM12878	blood:	n/a	n/a
32	BCLAF1	chr3:119319433-119320288	GM12878	blood:	n/a	n/a
33	BCLAF1	chr3:119315811-119317043	GM12878	blood:	n/a	n/a
34	BHLHE40	chr3:119319671-119319988	K562	blood:	n/a	n/a
35	BHLHE40	chr3:119304140-119304340	K562	blood:	n/a	n/a
36	BHLHE40	chr3:119300502-119301334	GM12878	blood:	n/a	n/a
37	BHLHE40	chr3:119314934-119314942	K562	blood:	n/a	n/a
38	BHLHE40	chr3:119312816-119312970	K562	blood:	n/a	n/a
39	BHLHE40	chr3:119319425-119320133	GM12878	blood:	n/a	n/a
40	BHLHE40	chr3:119318204-119318696	GM12878	blood:	n/a	n/a
41	BHLHE40	chr3:119309741-119309804	K562	blood:	n/a	n/a
42	BHLHE40	chr3:119314957-119315629	GM12878	blood:	n/a	n/a
43	BHLHE40	chr3:119323736-119323916	GM12878	blood:	n/a	n/a
44	BHLHE40	chr3:119316293-119317958	GM12878	blood:	n/a	n/a
45	BRCA1	chr3:119315097-119315100	GM12878	blood:	n/a	n/a
46	BRCA1	chr3:119316831-119316913	GM12878	blood:	n/a	n/a
47	BRCA1	chr3:119319291-119319957	GM12878	blood:	n/a	n/a
48	BRCA1	chr3:119318556-119318687	GM12878	blood:	n/a	n/a
49	CCNT2	chr3:119315181-119315511	K562	blood:	n/a	n/a
50	CCNT2	chr3:119344653-119344853	K562	blood:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:119315354-119315404	HNPCEpiC	eye:	n/a
2	chr3:119315354-119315404	AG09319	gingival:	n/a
3	chr3:119315354-119315404	HNPCEpiC	eye:	n/a
4	chr3:119315354-119315404	AG09319	gingival:	n/a
5	chr3:119316759-119316809	AG09319	gingival:	n/a
6	chr3:119315354-119315404	SK-N-MC	brain:	n/a
7	chr3:119315532-119315582	U87	brain:	n/a
8	chr3:119308390-119308440	MCF-7	breast:	n/a
9	chr3:119315532-119315582	HL-60	blood:	n/a
10	chr3:119306022-119306072	PrEC	prostate:	n/a
11	chr3:119316820-119316870	Hepatocyte	liver:	n/a
12	chr3:119301873-119301923	SK-N-SH_RA	brain:	n/a
13	chr3:119305506-119305556	HCT-116	colon:	n/a
14	chr3:119315590-119315640	ECC-1	luminal epithelium:	n/a
15	chr3:119308390-119308440	Caco-2	colon:	n/a
16	chr3:119316820-119316870	HAEpiC	amniotic membrane:	n/a
17	chr3:119315354-119315404	GM12878	blood:	n/a
18	chr3:119301873-119301923	HNPCEpiC	eye:	n/a
19	chr3:119315532-119315582	H1-hESC	embryonic stem cell:	embryo
20	chr3:119316673-119316723	AG04449	skin:	fetal
21	chr3:119316820-119316870	NHBE	bronchial:	n/a
22	chr3:119316759-119316809	HRCEpiC	kidney:	n/a
23	chr3:119315532-119315582	K562	blood:	n/a
24	chr3:119345741-119345791	AG04449	skin:	fetal
25	chr3:119316820-119316870	AG04449	skin:	fetal
26	chr3:119306022-119306072	HCT-116	colon:	n/a
27	chr3:119315532-119315582	MCF10A-Er-Src	breast:	n/a
28	chr3:119316820-119316870	SK-N-SH_RA	brain:	n/a
29	chr3:119315590-119315640	HCM	heart:	n/a
30	chr3:119345741-119345791	T-47D	breast:	n/a
31	chr3:119315532-119315582	AG04449	skin:	fetal
32	chr3:119308390-119308440	AG04449	skin:	fetal
33	chr3:119316673-119316723	HPAEpiC	pulmonary alveolar:	n/a
34	chr3:119310381-119310431	NHDF-neo	bronchial:	n/a
35	chr3:119301873-119301923	HEEpiC	esophagus:	n/a
36	chr3:119316759-119316809	HCM	heart:	n/a
37	chr3:119308390-119308440	ovcar-3	ovarian:	n/a
38	chr3:119308390-119308440	PrEC	prostate:	n/a
39	chr3:119316759-119316809	U87	brain:	n/a
40	chr3:119308390-119308440	HIPEpiC	eye:	n/a
41	chr3:119316759-119316809	LNCaP	prostate:	n/a
42	chr3:119316759-119316809	HNPCEpiC	eye:	n/a
43	chr3:119316820-119316870	H1-hESC	embryonic stem cell:	embryo
44	chr3:119315590-119315640	MCF-7	breast:	n/a
45	chr3:119315532-119315582	SK-N-SH_RA	brain:	n/a
46	chr3:119308390-119308440	NH-A	brain:	n/a
47	chr3:119308390-119308440	HRE	kidney:	n/a
48	chr3:119315532-119315582	HRCEpiC	kidney:	n/a
49	chr3:119308390-119308440	SK-N-SH	brain:	n/a
50	chr3:119345741-119345791	Hepatocyte	liver:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:119324918..119326771-chr3:119333086..119335282,2	K562	blood:
2	chr3:119319313..119321262-chr3:119322045..119324226,2	MCF-7	breast:
3	chr3:119298998..119301745-chr3:119303862..119306440,2	K562	blood:
4	chr3:119310790..119313134-chr3:119314484..119316186,2	K562	blood:
5	chr3:119314543..119316146-chr3:119316320..119318446,2	K562	blood:
6	chr3:119305600..119307239-chr3:119310554..119312770,2	K562	blood:
7	chr3:119321566..119324392-chr3:119394487..119396945,2	MCF-7	breast:
8	chr3:119297675..119300178-chr3:119317651..119319596,4	MCF-7	breast:
9	chr11:93474164..93475004-chr3:119310794..119311294,2	NB4	blood:
10	chr3:119305600..119307239-chr3:119310554..119312770,2	K562	blood:
11	chr3:119324918..119326771-chr3:119333086..119335282,2	K562	blood:
12	chr3:119337629..119339642-chr3:119343042..119344832,3	K562	blood:
13	chr3:119309806..119311897-chr3:119315565..119318074,3	K562	blood:
14	chr3:119319313..119321262-chr3:119322045..119324226,2	MCF-7	breast:
15	chr3:119214370..119217266-chr3:119338238..119340202,2	MCF-7	breast:
16	chr3:119305600..119307838-chr3:119310497..119312054,2	K562	blood:
17	chr3:119337629..119339642-chr3:119343042..119344832,3	K562	blood:
18	chr3:119318615..119321815-chr3:119324739..119327300,3	K562	blood:
19	chr3:119309459..119312426-chr3:119393975..119396413,2	MCF-7	breast:
20	chr3:119298069..119302115-chr3:119304955..119308560,6	MCF-7	breast:
21	chr3:119326194..119327898-chr3:119353631..119355784,2	K562	blood:
22	chr3:119305600..119307838-chr3:119310497..119312054,2	K562	blood:
23	chr3:119310790..119313134-chr3:119314484..119316186,2	K562	blood:
24	chr3:119326064..119328703-chr3:119343379..119345422,2	MCF-7	breast:
25	chr3:119328437..119330333-chr3:119390205..119392685,2	K562	blood:
26	chr3:119344313..119346275-chr3:119356031..119358042,2	K562	blood:
27	chr3:119297063..119300617-chr3:119303800..119308221,4	MCF-7	breast:
28	chr3:119297101..119299038-chr3:119322847..119325406,2	MCF-7	breast:
29	chr3:119297885..119300271-chr3:119300327..119302628,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLA1A-1	chr3:119313574-119313816	NONHSAT091395
2	lnc-ADPRH-2	chr3:119317432-119317473	NONHSAT091396
3	lnc-ADPRH-2	chr3:119325621-119325944	NONHSAT091396
4	lnc-PLA1A-1	chr3:119315003-119315208	NONHSAT091395

No data

Variant related genes	Relation type
PLA1A	TF binding region
ENSG00000272967	TF binding region
PLA1A	CpG island
ENSG00000272967	CpG island
ENSG00000272967	chromatin interactions
ENSG00000182919	chromatin interactions
ENSG00000138495	chromatin interactions
ENSG00000242052	chromatin interactions
ENSG00000144837	chromatin interactions
ENSG00000272662	chromatin interactions
ENSG00000166012	chromatin interactions
ENSG00000144843	chromatin interactions

Extended variants
information (count: 1987 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1987 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147901245	chr3:119301072-119301073	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs377477506	chr3:119301100-119301101	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs201822828	chr3:119301113-119301114	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs368027725	chr3:119301118-119301119	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs368811348	chr3:119301123-119301124	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs20568	chr3:119301139-119301140	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs547308034	chr3:119301144-119301145	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs149799527	chr3:119301181-119301182	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs145782367	chr3:119301185-119301186	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs138015780	chr3:119301206-119301207	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs201028402	chr3:119301225-119301226	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs371003506	chr3:119301232-119301233	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs149117576	chr3:119301255-119301256	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs192856664	chr3:119301258-119301259	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs200634555	chr3:119301302-119301303	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs376074611	chr3:119301321-119301322	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs371701534	chr3:119301327-119301328	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs375353292	chr3:119301333-119301334	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs184688671	chr3:119301360-119301361	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs140608674	chr3:119301366-119301367	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs567076567	chr3:119301402-119301403	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs558016672	chr3:119301429-119301430	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs113991261	chr3:119301439-119301440	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs375526786	chr3:119301447-119301448	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs71619750	chr3:119301454-119301455	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs190401702	chr3:119301468-119301469	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs534375179	chr3:119301477-119301478	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs560735747	chr3:119301530-119301531	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs554715082	chr3:119301547-119301548	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs145652751	chr3:119301548-119301549	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs537096918	chr3:119301549-119301550	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs146542333	chr3:119301578-119301579	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs541028865	chr3:119301606-119301607	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs559359117	chr3:119301675-119301676	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs532943764	chr3:119301680-119301681	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs368880006	chr3:119301701-119301702	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs571121688	chr3:119301759-119301760	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs61689476	chr3:119301874-119301875	Weak transcription Strong transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs181594324	chr3:119301877-119301878	Weak transcription Strong transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs59807949	chr3:119301880-119301881	Weak transcription Strong transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs535526599	chr3:119301914-119301915	Weak transcription Strong transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs2629402	chr3:119301915-119301916	Weak transcription Strong transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs565770487	chr3:119301940-119301941	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs539798037	chr3:119301953-119301954	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs140419309	chr3:119302000-119302001	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs143587762	chr3:119302001-119302002	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs78274164	chr3:119302030-119302031	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs555551221	chr3:119302065-119302066	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs559252450	chr3:119302189-119302190	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs10212406	chr3:119302207-119302208	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Developmental delay	22180640	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
lymphocytic leukemia	21291569	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Glioblastoma multiforme	22286061	CNVD
Neurodevelopmental disorder	22521361	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:687 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:119299200-119303400	Weak transcription	Aorta	Aorta
2	chr3:119299200-119307800	Weak transcription	Esophagus	oesophagus
3	chr3:119299200-119308000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr3:119299200-119314600	Weak transcription	Ovary	ovary
5	chr3:119299200-119315000	Weak transcription	Gastric	stomach
6	chr3:119299400-119301200	Enhancers	Primary B cells from peripheral blood	blood
7	chr3:119299400-119304000	Weak transcription	HSMMtube	muscle
8	chr3:119299400-119306200	Weak transcription	Primary B cells from cord blood	blood
9	chr3:119299400-119306400	Weak transcription	Fetal Intestine Large	intestine
10	chr3:119299400-119307400	Weak transcription	Thymus	Thymus
11	chr3:119299400-119307800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr3:119299400-119314200	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr3:119299400-119314400	Weak transcription	Brain Angular Gyrus	brain
14	chr3:119299600-119303400	Weak transcription	Colon Smooth Muscle	Colon
15	chr3:119299600-119303400	Weak transcription	Placenta	Placenta
16	chr3:119299600-119303600	Weak transcription	Lung	lung
17	chr3:119299600-119304200	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr3:119299600-119304200	Weak transcription	Osteobl	bone
19	chr3:119299600-119304800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr3:119299600-119305000	Weak transcription	Fetal Stomach	stomach
21	chr3:119299600-119305000	Weak transcription	Right Ventricle	heart
22	chr3:119299600-119305000	Weak transcription	HSMM	muscle
23	chr3:119299600-119305200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr3:119299600-119305200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr3:119299600-119305200	Weak transcription	Pancreas	Pancrea
26	chr3:119299600-119306600	Weak transcription	Fetal Kidney	kidney
27	chr3:119299600-119307200	Weak transcription	Duodenum Mucosa	Duodenum
28	chr3:119299600-119307200	Weak transcription	Fetal Intestine Small	intestine
29	chr3:119299600-119307200	Weak transcription	Fetal Lung	lung
30	chr3:119299600-119307200	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr3:119299600-119307400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr3:119299600-119307800	Weak transcription	Brain Hippocampus Middle	brain
33	chr3:119299600-119308000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr3:119299600-119314200	Weak transcription	Brain Substantia Nigra	brain
35	chr3:119299600-119314200	Weak transcription	Psoas Muscle	Psoas
36	chr3:119299800-119301200	Weak transcription	Fetal Muscle Leg	muscle
37	chr3:119299800-119303600	Weak transcription	Monocytes-CD14+_RO01746	blood
38	chr3:119299800-119303800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr3:119299800-119304000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr3:119299800-119304800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr3:119299800-119305000	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr3:119299800-119305200	Weak transcription	Adipose Nuclei	Adipose
43	chr3:119299800-119305400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr3:119299800-119305400	Weak transcription	Stomach Smooth Muscle	stomach
45	chr3:119299800-119307200	Weak transcription	Primary hematopoietic stem cells	blood
46	chr3:119299800-119308000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr3:119299800-119308000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr3:119299800-119309200	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr3:119299800-119314600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr3:119299800-119314600	Weak transcription	Fetal Muscle Trunk	muscle

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