Variant report

Variant	nsv460861
Chromosome Location	chr3:136222954-136425600
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1271)
CpG islands
(count:305)
Chromatin interactive
region (count:101)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1271 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:136295376-136295960	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:136386046-136386366	K562	blood:	n/a	n/a
3	ARID3A	chr3:136343881-136344463	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:136391268-136391668	K562	blood:	n/a	n/a
5	ARID3A	chr3:136372591-136372893	K562	blood:	n/a	n/a
6	ARID3A	chr3:136264594-136264721	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:136351531-136352050	HepG2	liver:	n/a	n/a
8	ARID3A	chr3:136354525-136354555	K562	blood:	n/a	n/a
9	ARID3A	chr3:136408962-136409078	HepG2	liver:	n/a	n/a
10	ARID3A	chr3:136265535-136265813	K562	blood:	n/a	n/a
11	ARID3A	chr3:136335948-136336585	K562	blood:	n/a	n/a
12	ARID3A	chr3:136349715-136350621	K562	blood:	n/a	n/a
13	ATF1	chr3:136227712-136227915	K562	blood:	n/a	n/a
14	ATF1	chr3:136296681-136297004	K562	blood:	n/a	n/a
15	ATF3	chr3:136385891-136386248	K562	blood:	n/a	n/a
16	BACH1	chr3:136400016-136400200	K562	blood:	n/a	n/a
17	BACH1	chr3:136336100-136336183	K562	blood:	n/a	n/a
18	BACH1	chr3:136288309-136288380	K562	blood:	n/a	n/a
19	BACH1	chr3:136333619-136333697	K562	blood:	n/a	n/a
20	BACH1	chr3:136409514-136409718	K562	blood:	n/a	n/a
21	BATF	chr3:136336928-136337072	GM12878	blood:	n/a	chr3:136336989-136337000 chr3:136337017-136337028
22	BATF	chr3:136303620-136303859	GM12878	blood:	n/a	n/a
23	BCLAF1	chr3:136266136-136266529	GM12878	blood:	n/a	n/a
24	BHLHE40	chr3:136283473-136283478	GM12878	blood:	n/a	n/a
25	BHLHE40	chr3:136350291-136350660	K562	blood:	n/a	n/a
26	BHLHE40	chr3:136305498-136305790	HepG2	liver:	n/a	n/a
27	BHLHE40	chr3:136266318-136266353	GM12878	blood:	n/a	n/a
28	BRCA1	chr3:136390624-136390662	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr3:136271579-136271619	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr3:136413025-136413348	K562	blood:	n/a	n/a
31	CBX3	chr3:136411975-136412381	K562	blood:	n/a	n/a
32	CBX3	chr3:136414619-136415299	K562	blood:	n/a	n/a
33	CBX3	chr3:136251284-136251617	K562	blood:	n/a	n/a
34	CBX3	chr3:136404760-136405080	K562	blood:	n/a	n/a
35	CBX3	chr3:136369947-136370224	K562	blood:	n/a	n/a
36	CBX3	chr3:136296572-136297082	K562	blood:	n/a	n/a
37	CBX3	chr3:136346908-136347253	K562	blood:	n/a	n/a
38	CBX3	chr3:136372500-136372812	K562	blood:	n/a	n/a
39	CBX3	chr3:136404681-136405157	K562	blood:	n/a	n/a
40	CBX3	chr3:136372363-136372889	K562	blood:	n/a	n/a
41	CBX3	chr3:136373463-136373859	HCT-116	colon:	n/a	n/a
42	CCNT2	chr3:136422214-136422479	K562	blood:	n/a	n/a
43	CCNT2	chr3:136409566-136409775	K562	blood:	n/a	n/a
44	CCNT2	chr3:136386075-136386259	K562	blood:	n/a	n/a
45	CCNT2	chr3:136296609-136296909	K562	blood:	n/a	n/a
46	CEBPB	chr3:136238094-136238382	HepG2	liver:	n/a	chr3:136238219-136238232 chr3:136238219-136238230
47	CEBPB	chr3:136368883-136369208	K562	blood:	n/a	chr3:136369028-136369039
48	CEBPB	chr3:136410216-136410527	K562	blood:	n/a	n/a
49	CEBPB	chr3:136335038-136335346	K562	blood:	n/a	chr3:136335178-136335191
50	CEBPB	chr3:136368848-136369215	IMR90	lung:	n/a	chr3:136369028-136369039

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:136416224-136416274	HUVEC	blood vessel:	n/a
2	chr3:136340367-136340417	LNCaP	prostate:	n/a
3	chr3:136416224-136416274	GM12892	blood:	n/a
4	chr3:136350473-136350523	SK-N-SH_RA	brain:	n/a
5	chr3:136350473-136350523	A549	lung:	n/a
6	chr3:136350473-136350523	GM12878	blood:	n/a
7	chr3:136416224-136416274	HCM	heart:	n/a
8	chr3:136231858-136231908	RPTEC	kidney:	n/a
9	chr3:136340367-136340417	HEK293	kidney:	embryo
10	chr3:136416224-136416274	GM12878	blood:	n/a
11	chr3:136340367-136340417	ovcar-3	ovarian:	n/a
12	chr3:136350473-136350523	AG09319	gingival:	n/a
13	chr3:136231858-136231908	HRE	kidney:	n/a
14	chr3:136340367-136340417	BJ	skin:	n/a
15	chr3:136416224-136416274	AG10803	skin:	n/a
16	chr3:136377513-136377563	MCF10A-Er-Src	breast:	n/a
17	chr3:136416224-136416274	T-47D	breast:	n/a
18	chr3:136340367-136340417	AG09309	skin:	n/a
19	chr3:136340367-136340417	HCF	heart:	n/a
20	chr3:136350473-136350523	HL-60	blood:	n/a
21	chr3:136416224-136416274	HRCEpiC	kidney:	n/a
22	chr3:136377513-136377563	ovcar-3	ovarian:	n/a
23	chr3:136377513-136377563	HPAEpiC	pulmonary alveolar:	n/a
24	chr3:136350473-136350523	ovcar-3	ovarian:	n/a
25	chr3:136231858-136231908	CMK	blood:	n/a
26	chr3:136416224-136416274	GM19239	blood:	n/a
27	chr3:136350473-136350523	HCT-116	colon:	n/a
28	chr3:136231858-136231908	ECC-1	luminal epithelium:	n/a
29	chr3:136340367-136340417	HRE	kidney:	n/a
30	chr3:136231858-136231908	GM12891	blood:	n/a
31	chr3:136416224-136416274	AG09319	gingival:	n/a
32	chr3:136340367-136340417	H1-hESC	embryonic stem cell:	embryo
33	chr3:136340367-136340417	NT2-D1	testis:	n/a
34	chr3:136416224-136416274	PrEC	prostate:	n/a
35	chr3:136416224-136416274	HCF	heart:	n/a
36	chr3:136377513-136377563	Caco-2	colon:	n/a
37	chr3:136377513-136377563	AG09319	gingival:	n/a
38	chr3:136350473-136350523	HUVEC	blood vessel:	n/a
39	chr3:136340367-136340417	HMEC	breast:	n/a
40	chr3:136416224-136416274	HEK293	kidney:	embryo
41	chr3:136416224-136416274	MCF-7	breast:	n/a
42	chr3:136231858-136231908	HepG2	liver:	n/a
43	chr3:136377513-136377563	Hepatocyte	liver:	n/a
44	chr3:136350473-136350523	SK-N-MC	brain:	n/a
45	chr3:136350473-136350523	HPAEpiC	pulmonary alveolar:	n/a
46	chr3:136340367-136340417	HCT-116	colon:	n/a
47	chr3:136377513-136377563	U87	brain:	n/a
48	chr3:136231858-136231908	LNCaP	prostate:	n/a
49	chr3:136377513-136377563	HAEpiC	amniotic membrane:	n/a
50	chr3:136377513-136377563	PrEC	prostate:	n/a

(count:101 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr3:136347675..136350642-chr3:136351726..136354296,2	K562	blood:
2	chr3:136377566..136379306-chr3:136381547..136383907,2	K562	blood:
3	chr3:136226210..136226915-chr3:136470643..136471376,2	MCF-7	breast:
4	chr3:136336725..136341978-chr3:136470555..136473265,5	K562	blood:
5	chr3:136336725..136338284-chr3:136470870..136472665,2	K562	blood:
6	chr3:136405715..136407497-chr3:136411173..136412850,2	K562	blood:
7	chr3:136257749..136260401-chr3:136264258..136266069,2	MCF-7	breast:
8	chr3:136261604..136263396-chr3:136467886..136469461,2	K562	blood:
9	chr3:136388635..136392149-chr3:136467930..136472508,4	K562	blood:
10	chr3:136340612..136342191-chr3:136342513..136345195,2	MCF-7	breast:
11	chr3:136296430..136297424-chr3:136470742..136471664,7	MCF-7	breast:
12	chr3:136341644..136343243-chr3:136343703..136345406,2	K562	blood:
13	chr3:136334079..136336516-chr3:136469054..136471144,3	MCF-7	breast:
14	chr3:136365030..136366947-chr3:136367021..136371094,3	MCF-7	breast:
15	chr3:136371791..136373767-chr3:136377876..136379959,2	MCF-7	breast:
16	chr3:135914471..135916410-chr3:136223365..136225971,2	MCF-7	breast:
17	chr3:136282532..136284441-chr3:136285201..136287062,2	MCF-7	breast:
18	chr3:136392775..136395146-chr3:136470930..136472567,2	K562	blood:
19	chr3:136326023..136327530-chr3:136469307..136471684,2	K562	blood:
20	chr3:136344347..136346500-chr3:136421190..136423734,2	MCF-7	breast:
21	chr3:136346602..136349491-chr3:136356349..136359301,2	K562	blood:
22	chr3:136309554..136311362-chr3:136314085..136316749,2	K562	blood:
23	chr3:136317046..136319207-chr3:136469829..136472283,2	MCF-7	breast:
24	chr3:136257661..136259575-chr3:136470502..136472462,3	MCF-7	breast:
25	chr3:136223066..136225762-chr3:136237795..136239369,2	MCF-7	breast:
26	chr3:136364480..136366014-chr3:136376930..136379520,2	MCF-7	breast:
27	chr3:136344242..136347550-chr3:136468840..136471507,4	MCF-7	breast:
28	chr3:136343802..136345688-chr3:136349798..136351830,2	MCF-7	breast:
29	chr3:136265553..136266283-chr3:136470816..136471681,5	MCF-7	breast:
30	chr3:136389263..136391478-chr3:136467252..136469430,2	K562	blood:
31	chr3:136380655..136383814-chr3:136385853..136389244,3	MCF-7	breast:
32	chr3:136274473..136277671-chr3:136469304..136472148,3	K562	blood:
33	chr3:136405715..136407497-chr3:136411173..136412850,2	K562	blood:
34	chr3:136364480..136366014-chr3:136376930..136379520,2	MCF-7	breast:
35	chr3:136295071..136296962-chr3:136469759..136471295,2	K562	blood:
36	chr3:136389835..136392302-chr3:136408179..136409824,2	MCF-7	breast:
37	chr3:136280347..136282243-chr3:136470576..136472647,2	K562	blood:
38	chr3:136288919..136291137-chr3:136468719..136471296,3	MCF-7	breast:
39	chr3:136263091..136265454-chr3:136470690..136473476,4	K562	blood:
40	chr3:136371791..136373767-chr3:136377876..136379959,2	MCF-7	breast:
41	chr3:136377566..136379306-chr3:136381547..136383907,2	K562	blood:
42	chr3:136362757..136364544-chr3:136367826..136369357,2	MCF-7	breast:
43	chr19:58906309..58907021-chr3:136319840..136320595,2	HCT-116	colon:
44	chr3:136262930..136265454-chr3:136470250..136473086,3	K562	blood:
45	chr3:136340612..136342191-chr3:136342513..136345195,2	MCF-7	breast:
46	chr3:136257749..136260401-chr3:136264258..136266069,2	MCF-7	breast:
47	chr3:136339369..136341813-chr3:136469433..136472886,3	MCF-7	breast:
48	chr3:136344155..136348284-chr3:136354109..136358125,4	MCF-7	breast:
49	chr3:136360867..136363380-chr3:136456006..136458080,2	MCF-7	breast:
50	chr3:136341644..136343243-chr3:136343703..136345406,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM22-5	chr3:136327892-136328444	NONHSAT092278

No data

Variant related genes	Relation type
RNU7-198P	TF binding region
RNY4P4	TF binding region
HMGN1P10	TF binding region
STAG1	TF binding region
RNU7-198P	CpG island
RNY4P4	CpG island
HMGN1P10	CpG island
STAG1	CpG island
ENSG00000118007	chromatin interactions
ENSG00000261758	chromatin interactions
ENSG00000251708	chromatin interactions
ENSG00000240695	chromatin interactions
ENSG00000174579	chromatin interactions

Extended variants
information (count: 7917 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:7917 , 50 per page) page: 1 2 3 4 5 6 7 ... 159

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17298882	chr3:136222954-136222955	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs115057362	chr3:136222961-136222962	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs567383185	chr3:136222967-136222968	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs57494495	chr3:136222986-136222987	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs577535427	chr3:136222995-136222996	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs13072698	chr3:136222998-136222999	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs575893547	chr3:136223001-136223002	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs544908147	chr3:136223079-136223080	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs192993092	chr3:136223132-136223133	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs373338975	chr3:136223198-136223199	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs185098820	chr3:136223208-136223209	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs111557520	chr3:136223220-136223221	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370619397	chr3:136223262-136223263	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs560352488	chr3:136223312-136223313	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs529402941	chr3:136223352-136223353	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs67663578	chr3:136223354-136223355	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs371588264	chr3:136223361-136223362	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs531987352	chr3:136223394-136223395	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs189612320	chr3:136223426-136223427	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs572004140	chr3:136223454-136223455	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs117289761	chr3:136223517-136223518	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs547391874	chr3:136223522-136223523	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs144790038	chr3:136223531-136223532	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs368869737	chr3:136223536-136223537	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs146686387	chr3:136223557-136223558	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs140289593	chr3:136223584-136223585	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs569512776	chr3:136223621-136223622	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs538489648	chr3:136223640-136223641	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs113982549	chr3:136223658-136223659	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs550929588	chr3:136223660-136223661	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs112697474	chr3:136223729-136223730	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs572324573	chr3:136223752-136223753	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs373136090	chr3:136223781-136223782	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs181151047	chr3:136223788-136223789	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs554143770	chr3:136223807-136223808	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs111612402	chr3:136223827-136223828	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs183874758	chr3:136223845-136223846	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs563010484	chr3:136223881-136223882	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs576694443	chr3:136223889-136223890	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs545646055	chr3:136223891-136223892	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs143888450	chr3:136223896-136223897	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs565410930	chr3:136223926-136223927	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs150286213	chr3:136224029-136224030	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs555739449	chr3:136224067-136224068	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs562294282	chr3:136224148-136224149	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs547039291	chr3:136224149-136224150	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs560944925	chr3:136224184-136224185	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs529689924	chr3:136224197-136224198	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs34361206	chr3:136224204-136224205	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs569448887	chr3:136224213-136224214	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

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	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
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	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
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Intracranial aneurysm	16715129	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18511947	CNVD
Breast cancer	22522925	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2780 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:136176400-136314200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr3:136176600-136224200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr3:136176600-136224400	Weak transcription	Brain Hippocampus Middle	brain
4	chr3:136176600-136231800	Weak transcription	Psoas Muscle	Psoas
5	chr3:136176600-136240000	Weak transcription	HMEC	breast
6	chr3:136176600-136260800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr3:136176800-136228000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr3:136176800-136266200	Weak transcription	Hela-S3	cervix
9	chr3:136177200-136236400	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr3:136191400-136268000	Weak transcription	Stomach Smooth Muscle	stomach
11	chr3:136192200-136225600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr3:136192400-136252400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr3:136193800-136231400	Weak transcription	NHLF	lung
14	chr3:136193800-136239200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr3:136195000-136223000	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr3:136195200-136231000	Weak transcription	Osteobl	bone
17	chr3:136195400-136231400	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr3:136195400-136232000	Weak transcription	Right Ventricle	heart
19	chr3:136195400-136241800	Weak transcription	NH-A	brain
20	chr3:136195400-136250400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr3:136195400-136278800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr3:136195600-136224000	Weak transcription	Brain Angular Gyrus	brain
23	chr3:136203000-136224600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
24	chr3:136208400-136230400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
25	chr3:136210200-136225800	Weak transcription	NHDF-Ad	bronchial
26	chr3:136210800-136229600	Weak transcription	Primary T cells fromperipheralblood	blood
27	chr3:136211600-136232000	Weak transcription	Fetal Kidney	kidney
28	chr3:136212200-136229200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr3:136212200-136323400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr3:136212400-136223200	Weak transcription	Fetal Heart	heart
31	chr3:136212400-136231000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr3:136212400-136232000	Weak transcription	Aorta	Aorta
33	chr3:136212400-136241600	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr3:136212400-136249600	Weak transcription	Lung	lung
35	chr3:136212600-136248200	Weak transcription	Esophagus	oesophagus
36	chr3:136213000-136231000	Weak transcription	Ovary	ovary
37	chr3:136213000-136239000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr3:136213000-136251000	Weak transcription	Primary T helper cells PMA-I stimulated	--
39	chr3:136213000-136252200	Weak transcription	Left Ventricle	heart
40	chr3:136213000-136326600	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr3:136213200-136224600	Weak transcription	Pancreas	Pancrea
42	chr3:136213200-136246000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
43	chr3:136213200-136246600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr3:136213400-136231000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr3:136214000-136239600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr3:136214000-136246200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr3:136214400-136238400	Weak transcription	Duodenum Smooth Muscle	Duodenum
48	chr3:136214600-136223400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr3:136214600-136231000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr3:136215000-136230000	Weak transcription	Fetal Lung	lung

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