Variant report

Variant	nsv911263
Chromosome Location	chr19:18309365-18324329
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1117)
CpG islands
(count:1589)
Chromatin interactive
region (count:58)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1117 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:18316440-18316442	K562	blood:	n/a	n/a
2	ARID3A	chr19:18319310-18319477	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:18314829-18315119	HepG2	liver:	n/a	n/a
4	ARID3A	chr19:18314782-18315504	K562	blood:	n/a	n/a
5	ATF1	chr19:18314716-18315309	K562	blood:	n/a	n/a
6	ATF2	chr19:18314703-18315121	GM12878	blood:	n/a	n/a
7	ATF2	chr19:18315921-18316266	GM12878	blood:	n/a	n/a
8	ATF2	chr19:18315087-18315809	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr19:18313848-18314107	K562	blood:	n/a	chr19:18313905-18313913
10	BACH1	chr19:18313757-18314887	H1-hESC	embryonic stem cell:	n/a	n/a
11	BHLHE40	chr19:18319352-18319400	K562	blood:	n/a	n/a
12	BHLHE40	chr19:18313716-18316045	K562	blood:	n/a	chr19:18313961-18313977 chr19:18313862-18313878
13	BHLHE40	chr19:18313712-18314507	HepG2	liver:	n/a	chr19:18313961-18313977 chr19:18313862-18313878
14	BHLHE40	chr19:18313640-18316161	GM12878	blood:	n/a	chr19:18316105-18316121 chr19:18313961-18313977 chr19:18313862-18313878
15	BRCA1	chr19:18315048-18315379	HepG2	liver:	n/a	n/a
16	BRCA1	chr19:18314734-18315424	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr19:18313753-18314045	H1-hESC	embryonic stem cell:	n/a	n/a
18	BRCA1	chr19:18314965-18315309	GM12878	blood:	n/a	n/a
19	CBX3	chr19:18318897-18319592	K562	blood:	n/a	n/a
20	CBX3	chr19:18313682-18315634	K562	blood:	n/a	n/a
21	CCNT2	chr19:18313861-18315246	K562	blood:	n/a	chr19:18314481-18314490 chr19:18314507-18314516
22	CCNT2	chr19:18316039-18316239	K562	blood:	n/a	n/a
23	CEBPB	chr19:18314727-18314938	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr19:18314837-18315015	HepG2	liver:	n/a	n/a
25	CEBPB	chr19:18314792-18315039	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr19:18314801-18314991	K562	blood:	n/a	n/a
27	CEBPB	chr19:18314770-18315045	IMR90	lung:	n/a	n/a
28	CEBPD	chr19:18315889-18316226	HepG2	liver:	n/a	n/a
29	CEBPD	chr19:18314626-18314980	HepG2	liver:	n/a	n/a
30	CEBPZ	chr19:18314985-18315473	HepG2	liver:	n/a	n/a
31	CHD1	chr19:18315249-18315879	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD1	chr19:18316151-18316206	GM12878	blood:	n/a	n/a
33	CHD1	chr19:18316202-18316452	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD1	chr19:18315122-18315653	GM12878	blood:	n/a	n/a
35	CHD2	chr19:18314775-18315691	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr19:18314320-18315680	GM12878	blood:	n/a	n/a
37	CHD2	chr19:18314987-18315287	HepG2	liver:	n/a	n/a
38	CHD2	chr19:18315856-18316042	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr19:18314483-18315597	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr19:18314284-18315527	K562	blood:	n/a	n/a
41	CHD2	chr19:18316026-18316452	GM12878	blood:	n/a	n/a
42	CHD2	chr19:18314022-18314072	GM12878	blood:	n/a	n/a
43	CREB1	chr19:18314161-18315531	HepG2	liver:	n/a	chr19:18314887-18314900
44	CREB1	chr19:18314726-18315091	A549	lung:	n/a	chr19:18314887-18314900
45	CREB1	chr19:18314544-18315390	K562	blood:	n/a	chr19:18314887-18314900
46	CREB1	chr19:18313988-18315810	GM12878	blood:	n/a	chr19:18314887-18314900
47	CREB1	chr19:18313843-18315545	HepG2	liver:	n/a	chr19:18314887-18314900
48	CREB1	chr19:18315886-18316203	A549	lung:	n/a	n/a
49	CREB1	chr19:18314640-18315363	A549	lung:	n/a	chr19:18314887-18314900
50	CREB1	chr19:18314395-18315744	H1-hESC	embryonic stem cell:	n/a	chr19:18314887-18314900

(count:1589 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:18319564-18319614	AG09309	skin:	n/a
2	chr19:18314808-18314858	GM06990	blood:	n/a
3	chr19:18321168-18321218	Jurkat	blood:	n/a
4	chr19:18319564-18319614	AG09309	skin:	n/a
5	chr19:18314808-18314858	GM06990	blood:	n/a
6	chr19:18321168-18321218	Jurkat	blood:	n/a
7	chr19:18318950-18319000	PFSK-1	brain:	n/a
8	chr19:18320186-18320236	Hela-S3	cervix:	n/a
9	chr19:18314992-18315042	HMEC	breast:	n/a
10	chr19:18313954-18314004	AoSMC	blood vessel:	n/a
11	chr19:18313954-18314004	HRPEpiC	eye:	n/a
12	chr19:18320186-18320236	HAEpiC	amniotic membrane:	n/a
13	chr19:18313954-18314004	HRE	kidney:	n/a
14	chr19:18315256-18315306	HRPEpiC	eye:	n/a
15	chr19:18315067-18315117	GM06990	blood:	n/a
16	chr19:18319564-18319614	PANC-1	pancreas:	n/a
17	chr19:18314691-18314741	HAEpiC	amniotic membrane:	n/a
18	chr19:18314992-18315042	U87	brain:	n/a
19	chr19:18314992-18315042	GM06990	blood:	n/a
20	chr19:18314345-18314395	AG04450	lung:	fetal
21	chr19:18318950-18319000	GM06990	blood:	n/a
22	chr19:18319787-18319837	ECC-1	luminal epithelium:	n/a
23	chr19:18314808-18314858	HCPEpiC	choroid plexus:	n/a
24	chr19:18314776-18314826	HCPEpiC	choroid plexus:	n/a
25	chr19:18318950-18319000	K562	blood:	n/a
26	chr19:18319787-18319837	AG04450	lung:	fetal
27	chr19:18318950-18319000	RPTEC	kidney:	n/a
28	chr19:18315738-18315788	AG10803	skin:	n/a
29	chr19:18313388-18313438	GM12892	blood:	n/a
30	chr19:18313954-18314004	HepG2	liver:	n/a
31	chr19:18318950-18319000	HUVEC	blood vessel:	n/a
32	chr19:18321929-18321979	AG10803	skin:	n/a
33	chr19:18315067-18315117	HMEC	breast:	n/a
34	chr19:18319564-18319614	NB4	blood:	n/a
35	chr19:18320186-18320236	HIPEpiC	eye:	n/a
36	chr19:18316102-18316152	AG04449	skin:	fetal
37	chr19:18314808-18314858	HRCEpiC	kidney:	n/a
38	chr19:18316102-18316152	HRPEpiC	eye:	n/a
39	chr19:18314992-18315042	BE2_C	brain:	n/a
40	chr19:18313388-18313438	RPTEC	kidney:	n/a
41	chr19:18313561-18313611	HCF	heart:	n/a
42	chr19:18316102-18316152	SK-N-SH_RA	brain:	n/a
43	chr19:18319787-18319837	Jurkat	blood:	n/a
44	chr19:18314345-18314395	HRPEpiC	eye:	n/a
45	chr19:18314808-18314858	A549	lung:	n/a
46	chr19:18311216-18311266	HCM	heart:	n/a
47	chr19:18314776-18314826	H1-hESC	embryonic stem cell:	embryo
48	chr19:18314808-18314858	RPTEC	kidney:	n/a
49	chr19:18319564-18319614	MCF-7	breast:	n/a
50	chr19:18319564-18319614	AoSMC	blood vessel:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr19:18264824..18267615-chr19:18313161..18315862,2	MCF-7	breast:
2	chr19:18302239..18304970-chr19:18319302..18320810,2	K562	blood:
3	chr17:56707862..56710563-chr19:18319523..18322519,2	MCF-7	breast:
4	chr19:18323123..18325870-chr19:18329397..18331309,2	K562	blood:
5	chr19:18320465..18322447-chr19:18338955..18341903,2	K562	blood:
6	chr19:18308165..18311046-chr19:18390577..18392563,2	MCF-7	breast:
7	chr19:18314296..18317366-chr19:18383748..18385809,3	K562	blood:
8	chr19:18302057..18307216-chr19:18311605..18315914,14	MCF-7	breast:
9	chr19:18316952..18321677-chr19:18390588..18394858,6	K562	blood:
10	chr19:18270643..18273104-chr19:18313490..18316053,2	K562	blood:
11	chr19:18311642..18316628-chr19:18388957..18392513,10	K562	blood:
12	chr19:18318896..18319786-chr19:18521120..18522025,3	K562	blood:
13	chr19:18304348..18305156-chr19:18313206..18314123,2	K562	blood:
14	chr19:18319023..18319930-chr19:18362052..18363450,19	K562	blood:
15	chr19:18312530..18319182-chr19:18329520..18338113,19	K562	blood:
16	chr19:18318900..18319793-chr19:18365979..18366633,2	MCF-7	breast:
17	chr19:18265822..18267690-chr19:18314234..18316588,2	MCF-7	breast:
18	chr19:18318904..18320424-chr19:18383997..18386508,2	MCF-7	breast:
19	chr19:18315560..18317882-chr19:18321449..18323321,2	K562	blood:
20	chr19:18319161..18319750-chr19:18521098..18522038,2	MCF-7	breast:
21	chr19:18301872..18305883-chr19:18307026..18310830,7	K562	blood:
22	chr19:18311250..18312881-chr19:18314295..18315974,3	MCF-7	breast:
23	chr19:18313460..18314206-chr19:18362743..18363288,2	K562	blood:
24	chr19:18272069..18275031-chr19:18313759..18316428,2	K562	blood:
25	chr19:18307764..18309976-chr19:18313429..18315883,3	MCF-7	breast:
26	chr19:18302289..18309850-chr19:18311214..18320810,23	K562	blood:
27	chr19:18315856..18316660-chr19:18362767..18363282,2	K562	blood:
28	chr19:18276650..18279111-chr19:18312553..18314264,2	MCF-7	breast:
29	chr19:18319878..18322618-chr19:18403582..18405708,2	K562	blood:
30	chr19:18318310..18321246-chr19:18390961..18393521,2	K562	blood:
31	chr19:18321259..18323821-chr19:18388878..18390408,2	K562	blood:
32	chr19:18317340..18319670-chr19:18450737..18453714,2	K562	blood:
33	chr19:18320883..18322593-chr19:18524287..18527226,2	K562	blood:
34	chr19:18318722..18319754-chr19:18362345..18363296,6	MCF-7	breast:
35	chr19:18314629..18316965-chr19:18497132..18498761,2	K562	blood:
36	chr19:18314487..18317181-chr19:18321395..18324543,3	K562	blood:
37	chr19:18314746..18317215-chr19:18546753..18549806,3	K562	blood:
38	chr19:18322052..18324321-chr19:18391678..18393429,2	K562	blood:
39	chr19:18284538..18286189-chr19:18313497..18315527,2	K562	blood:
40	chr19:18301873..18308921-chr19:18309874..18315133,13	MCF-7	breast:
41	chr19:18311216..18316508-chr19:18389022..18394678,9	MCF-7	breast:
42	chr19:18312925..18315923-chr20:55967993..55969596,2	MCF-7	breast:
43	chr19:18313659..18316582-chr19:18386529..18393683,9	K562	blood:
44	chr19:18318859..18319901-chr19:18362087..18363625,12	MCF-7	breast:
45	chr19:18302289..18309850-chr19:18311214..18320810,23	K562	blood:
46	chr19:18323066..18325870-chr19:18329397..18331733,2	K562	blood:
47	chr19:18322572..18325155-chr19:18331832..18335033,4	K562	blood:
48	chr19:18313916..18318092-chr19:18528402..18531529,5	K562	blood:
49	chr19:18265635..18269832-chr19:18313306..18316630,4	K562	blood:
50	chr19:18313254..18314101-chr19:18520994..18521908,3	MCF-7	breast:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MPV17L2-1	chr19:18319100-18319239	ENSG00000268650.3
2	lnc-MPV17L2-1	chr19:18316266-18316371	XLOC_012991
3	lnc-MPV17L2-1	chr19:18315551-18315709	ENSG00000268650.3
4	lnc-MPV17L2-1	chr19:18318771-18319259	NONHSAT062945
5	lnc-MPV17L2-1	chr19:18322537-18322673	NONHSAT062942
6	lnc-MPV17L2-1	chr19:18319100-18319239	NONHSAT062944
7	lnc-MPV17L2-1	chr19:18315544-18315709	ENSG00000268650.3
8	lnc-MPV17L2-1	chr19:18315535-18315709	XLOC_012991
9	lnc-MPV17L2-1	chr19:18319748-18319856	ENSG00000268650.3
10	lnc-MPV17L2-1	chr19:18321895-18322038	NONHSAT062943
11	lnc-MPV17L2-1	chr19:18315540-18315709	NONHSAT062943
12	lnc-MPV17L2-1	chr19:18315540-18315709	ENSG00000268650.3
13	lnc-MPV17L2-1	chr19:18315546-18315709	NONHSAT062944
14	lnc-MPV17L2-1	chr19:18316266-18316373	ENSG00000268650.3
15	lnc-MPV17L2-1	chr19:18315540-18315709	NONHSAT062942
16	lnc-MPV17L2-1	chr19:18322537-18322673	ENSG00000268650.3
17	lnc-MPV17L2-1	chr19:18319748-18319859	NONHSAT062944
18	lnc-MPV17L2-1	chr19:18321895-18322035	ENSG00000268650.3
19	lnc-MPV17L2-1	chr19:18321895-18322035	NONHSAT062942

No data

Variant related genes	Relation type
ENSG00000268650	TF binding region
RAB3A	TF binding region
ENSG00000268650	CpG island
RAB3A	CpG island
ENSG00000267959	chromatin interactions
ENSG00000130513	chromatin interactions
ENSG00000096996	chromatin interactions
ENSG00000105650	chromatin interactions
ENSG00000216490	chromatin interactions
ENSG00000254858	chromatin interactions
ENSG00000105647	chromatin interactions
ENSG00000268650	chromatin interactions
ENSG00000105655	chromatin interactions
ENSG00000130522	chromatin interactions
ENSG00000130518	chromatin interactions
ENSG00000218018	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000130517	chromatin interactions
ENSG00000264175	chromatin interactions
ENSG00000099308	chromatin interactions
ENSG00000130511	chromatin interactions
ENSG00000105649	chromatin interactions
FPGT	miRNA target sites
FIGF	miRNA target sites

Extended variants
information (count: 554 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:554 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2271882	chr19:18309365-18309366	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs147978691	chr19:18309369-18309370	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs565776450	chr19:18309401-18309402	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs534695544	chr19:18309453-18309454	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs548132193	chr19:18309479-18309480	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs373549225	chr19:18309489-18309490	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs202229064	chr19:18309502-18309503	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs375156987	chr19:18309525-18309526	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs369617917	chr19:18309543-18309544	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs373161458	chr19:18309548-18309549	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs377115900	chr19:18309555-18309556	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs370570474	chr19:18309557-18309558	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs373134297	chr19:18309579-18309580	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs77889350	chr19:18309587-18309588	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs200156565	chr19:18309606-18309607	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs556347776	chr19:18309611-18309612	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs576136757	chr19:18309695-18309696	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs377450582	chr19:18309696-18309697	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs538763009	chr19:18309697-18309698	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs113704268	chr19:18309747-18309748	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs368111103	chr19:18309748-18309749	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs572122685	chr19:18309759-18309760	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs141699847	chr19:18309801-18309802	Weak transcription Strong transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs555568120	chr19:18309812-18309813	Weak transcription Strong transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs150530257	chr19:18309828-18309829	Weak transcription Strong transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs371937885	chr19:18309836-18309837	Weak transcription Strong transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs117464129	chr19:18309848-18309849	Weak transcription Strong transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs188645708	chr19:18309867-18309868	Weak transcription Strong transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs552687246	chr19:18309890-18309891	Weak transcription Strong transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs559425000	chr19:18309924-18309925	Weak transcription Strong transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs139500561	chr19:18309995-18309996	Weak transcription Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs548194466	chr19:18310005-18310006	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs12985673	chr19:18310006-18310007	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs111865479	chr19:18310020-18310021	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs146350629	chr19:18310029-18310030	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs575621876	chr19:18310030-18310031	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs139760676	chr19:18310116-18310117	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs372622570	chr19:18310197-18310198	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs114889959	chr19:18310280-18310281	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs191911793	chr19:18310333-18310334	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs371984150	chr19:18310342-18310343	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs184083382	chr19:18310395-18310396	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs112382185	chr19:18310399-18310400	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs534676395	chr19:18310408-18310409	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs564471316	chr19:18310426-18310427	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs188566501	chr19:18310432-18310433	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs191493728	chr19:18310437-18310438	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs548343469	chr19:18310467-18310468	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs145217701	chr19:18310482-18310483	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs377251396	chr19:18310483-18310484	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Follicular lymphoma	20505157	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	20179077	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Lung cancer	17297452	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Chordoma	18071362	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
ovarian endometriomas	16273235	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Cervical cancer	21063398	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Ovarian cancer	21720365	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Basal cell lymphoma	21115979	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21364760	CNVD
Mycobacterial infection	18421352	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute monocytic leukemia	16498392	CNVD
Lung cancer	18438408	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Liver carcinoma	19366792	CNVD
Colorectal cancer	19455253	CNVD
Lujan-Fryns syndrom	21521776	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Cancer	17440070	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1007 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18305200-18311000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr19:18305200-18314000	Weak transcription	HSMMtube	muscle
3	chr19:18305400-18312800	Weak transcription	Fetal Brain Male	brain
4	chr19:18305400-18313800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr19:18305400-18313800	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr19:18305400-18314000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr19:18305400-18314200	Weak transcription	Small Intestine	intestine
8	chr19:18305600-18311600	Strong transcription	Fetal Intestine Small	intestine
9	chr19:18305600-18313400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr19:18305600-18313400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr19:18305600-18313800	Weak transcription	Psoas Muscle	Psoas
12	chr19:18305600-18313800	Weak transcription	A549	lung
13	chr19:18305600-18313800	Weak transcription	NH-A	brain
14	chr19:18305600-18314000	Weak transcription	HSMM	muscle
15	chr19:18306000-18309400	Strong transcription	Muscle Satellite Cultured Cells	--
16	chr19:18306000-18309600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr19:18306000-18310000	Strong transcription	NHLF	lung
18	chr19:18306000-18310400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
19	chr19:18306000-18311400	Strong transcription	H1 Cell Line	embryonic stem cell
20	chr19:18306000-18311400	Strong transcription	HUES6 Cell Line	embryonic stem cell
21	chr19:18306000-18311400	Strong transcription	Skeletal Muscle Male	skeletal muscle
22	chr19:18306000-18311600	Strong transcription	HUES64 Cell Line	embryonic stem cell
23	chr19:18306000-18311600	Strong transcription	Cortex derived primary cultured neurospheres	brain
24	chr19:18306000-18311600	Strong transcription	Ovary	ovary
25	chr19:18306000-18312000	Strong transcription	Brain Hippocampus Middle	brain
26	chr19:18306000-18313000	Strong transcription	Brain Cingulate Gyrus	brain
27	chr19:18306000-18313400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr19:18306000-18313600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr19:18306000-18313600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
30	chr19:18306000-18313600	Strong transcription	Fetal Stomach	stomach
31	chr19:18306000-18313600	Weak transcription	Stomach Mucosa	stomach
32	chr19:18306000-18313800	Weak transcription	HMEC	breast
33	chr19:18306200-18311600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr19:18306200-18311800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr19:18306200-18313400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr19:18306200-18313400	Weak transcription	Primary hematopoietic stem cells	blood
37	chr19:18306200-18313400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
38	chr19:18306400-18309600	Strong transcription	Gastric	stomach
39	chr19:18306400-18309800	Strong transcription	Pancreas	Pancrea
40	chr19:18306400-18310200	Strong transcription	Spleen	Spleen
41	chr19:18306400-18311400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr19:18306400-18313000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr19:18306400-18313400	Strong transcription	H9 Cell Line	embryonic stem cell
44	chr19:18306400-18313400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr19:18306600-18309600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr19:18306600-18309600	Strong transcription	Primary T cells from cord blood	blood
47	chr19:18306600-18309600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr19:18306600-18309800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr19:18306600-18309800	Strong transcription	Primary monocytes fromperipheralblood	blood
50	chr19:18306600-18309800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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