Variant report

Variant	nsv543934
Chromosome Location	chr19:20061084-20574512
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2613)
CpG islands
(count:2992)
Chromatin interactive
region (count:23)
LncRNA
region (count:53)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:2613 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:20103566-20103765	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:20150099-20150414	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:20162795-20163547	HepG2	liver:	n/a	n/a
4	ARID3A	chr19:20277796-20277995	HepG2	liver:	n/a	n/a
5	ATF1	chr19:20349244-20349443	K562	blood:	n/a	n/a
6	ATF1	chr19:20162792-20163523	K562	blood:	n/a	n/a
7	ATF1	chr19:20344010-20344175	K562	blood:	n/a	n/a
8	ATF1	chr19:20153260-20153552	K562	blood:	n/a	n/a
9	ATF1	chr19:20289866-20289929	K562	blood:	n/a	n/a
10	ATF1	chr19:20357835-20358030	K562	blood:	n/a	n/a
11	ATF1	chr19:20277755-20278020	K562	blood:	n/a	n/a
12	ATF2	chr19:20348954-20349352	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr19:20278020-20278358	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr19:20067472-20067936	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr19:20162692-20163573	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr19:20213875-20214282	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr19:20193391-20193678	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF3	chr19:20188548-20188771	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr19:20213028-20213042	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr19:20349018-20349218	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr19:20149962-20150229	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr19:20111633-20111647	K562	blood:	n/a	n/a
23	BACH1	chr19:20478616-20479240	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr19:20272241-20272396	GM12878	blood:	n/a	n/a
25	BATF	chr19:20461481-20461636	GM12878	blood:	n/a	n/a
26	BATF	chr19:20290881-20291101	GM12878	blood:	n/a	chr19:20291013-20291024 chr19:20291014-20291024
27	BATF	chr19:20169491-20169839	GM12878	blood:	n/a	chr19:20169641-20169652 chr19:20169642-20169652
28	BATF	chr19:20172606-20172805	GM12878	blood:	n/a	n/a
29	BATF	chr19:20461475-20461637	GM12878	blood:	n/a	n/a
30	BATF	chr19:20460030-20460189	GM12878	blood:	n/a	chr19:20460120-20460131 chr19:20460121-20460131
31	BATF	chr19:20169489-20169738	GM12878	blood:	n/a	chr19:20169641-20169652 chr19:20169642-20169652
32	BATF	chr19:20071227-20071388	GM12878	blood:	n/a	n/a
33	BATF	chr19:20290857-20291100	GM12878	blood:	n/a	chr19:20291013-20291024 chr19:20291014-20291024
34	BHLHE40	chr19:20343872-20344192	K562	blood:	n/a	n/a
35	BHLHE40	chr19:20162803-20163166	K562	blood:	n/a	n/a
36	BHLHE40	chr19:20070163-20070165	K562	blood:	n/a	n/a
37	BHLHE40	chr19:20471668-20471688	K562	blood:	n/a	n/a
38	BHLHE40	chr19:20163508-20163708	GM12878	blood:	n/a	n/a
39	BRCA1	chr19:20328741-20328829	H1-hESC	embryonic stem cell:	n/a	n/a
40	BRCA1	chr19:20426599-20426652	GM12878	blood:	n/a	n/a
41	BRCA1	chr19:20162632-20162998	HepG2	liver:	n/a	n/a
42	BRCA1	chr19:20348754-20348954	H1-hESC	embryonic stem cell:	n/a	n/a
43	BRCA1	chr19:20149987-20150214	H1-hESC	embryonic stem cell:	n/a	n/a
44	BRCA1	chr19:20278082-20278233	H1-hESC	embryonic stem cell:	n/a	n/a
45	CBX3	chr19:20077683-20078014	K562	blood:	n/a	n/a
46	CBX3	chr19:20069962-20070297	K562	blood:	n/a	n/a
47	CBX3	chr19:20077721-20077986	K562	blood:	n/a	n/a
48	CEBPB	chr19:20163399-20163516	HepG2	liver:	n/a	chr19:20163461-20163472
49	CEBPB	chr19:20296988-20297354	HepG2	liver:	n/a	chr19:20297167-20297178
50	CEBPB	chr19:20150231-20150800	IMR90	lung:	n/a	chr19:20150648-20150661 chr19:20150648-20150659

(count:2992 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:20188738-20188788	ECC-1	luminal epithelium:	n/a
2	chr19:20276916-20276966	GM06990	blood:	n/a
3	chr19:20278059-20278109	GM19239	blood:	n/a
4	chr19:20188738-20188788	ECC-1	luminal epithelium:	n/a
5	chr19:20276916-20276966	GM06990	blood:	n/a
6	chr19:20278059-20278109	GM19239	blood:	n/a
7	chr19:20369061-20369111	IMR90	lung:	fetal
8	chr19:20278423-20278473	MCF-7	breast:	n/a
9	chr19:20150242-20150292	SK-N-MC	brain:	n/a
10	chr19:20187307-20187357	HCF	heart:	n/a
11	chr19:20149886-20149936	IMR90	lung:	fetal
12	chr19:20162905-20162955	K562	blood:	n/a
13	chr19:20150943-20150993	HRE	kidney:	n/a
14	chr19:20187745-20187795	PFSK-1	brain:	n/a
15	chr19:20162840-20162890	H1-hESC	embryonic stem cell:	embryo
16	chr19:20152700-20152750	AG09309	skin:	n/a
17	chr19:20349303-20349353	Hela-S3	cervix:	n/a
18	chr19:20277240-20277290	A549	lung:	n/a
19	chr19:20165122-20165172	SAEC	small airway:	n/a
20	chr19:20189702-20189752	HMEC	breast:	n/a
21	chr19:20160300-20160350	LNCaP	prostate:	n/a
22	chr19:20150943-20150993	NT2-D1	testis:	n/a
23	chr19:20188803-20188853	LNCaP	prostate:	n/a
24	chr19:20162840-20162890	NHBE	bronchial:	n/a
25	chr19:20163138-20163188	HL-60	blood:	n/a
26	chr19:20152700-20152750	HCF	heart:	n/a
27	chr19:20278015-20278065	SK-N-SH_RA	brain:	n/a
28	chr19:20162642-20162692	GM12878	blood:	n/a
29	chr19:20149684-20149734	HEK293	kidney:	embryo
30	chr19:20278059-20278109	ECC-1	luminal epithelium:	n/a
31	chr19:20150242-20150292	T-47D	breast:	n/a
32	chr19:20277963-20278013	AoSMC	blood vessel:	n/a
33	chr19:20163542-20163592	PFSK-1	brain:	n/a
34	chr19:20160300-20160350	HNPCEpiC	eye:	n/a
35	chr19:20349252-20349302	SAEC	small airway:	n/a
36	chr19:20349275-20349325	ECC-1	luminal epithelium:	n/a
37	chr19:20277919-20277969	GM12878	blood:	n/a
38	chr19:20152700-20152750	HCPEpiC	choroid plexus:	n/a
39	chr19:20277919-20277969	AG09319	gingival:	n/a
40	chr19:20278013-20278063	NHBE	bronchial:	n/a
41	chr19:20162840-20162890	NHDF-neo	bronchial:	n/a
42	chr19:20278051-20278101	HepG2	liver:	n/a
43	chr19:20188738-20188788	Hepatocyte	liver:	n/a
44	chr19:20278051-20278101	ECC-1	luminal epithelium:	n/a
45	chr19:20349252-20349302	MCF10A-Er-Src	breast:	n/a
46	chr19:20149886-20149936	ECC-1	luminal epithelium:	n/a
47	chr19:20150505-20150555	HCPEpiC	choroid plexus:	n/a
48	chr19:20149684-20149734	HEEpiC	esophagus:	n/a
49	chr19:20189112-20189162	HCT-116	colon:	n/a
50	chr19:20368371-20368421	BJ	skin:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:19887367..19888020-chr19:20162266..20162852,2	MCF-7	breast:
2	chr19:19886225..19889076-chr19:20160261..20164492,4	MCF-7	breast:
3	chr19:20107929..20110799-chr19:21687232..21688823,2	MCF-7	breast:
4	chr19:20150205..20157347-chr19:20159192..20163449,8	MCF-7	breast:
5	chr19:20142180..20144378-chr19:20148043..20150229,2	MCF-7	breast:
6	chr19:20160443..20163353-chr19:20178782..20180876,2	MCF-7	breast:
7	chr19:19976102..19978027-chr19:20081868..20083854,2	K562	blood:
8	chr19:20142180..20144378-chr19:20148043..20150229,2	MCF-7	breast:
9	chr19:20159294..20161641-chr19:20161675..20163278,2	MCF-7	breast:
10	chr19:20159294..20161641-chr19:20161675..20163278,2	MCF-7	breast:
11	chr19:20160443..20163353-chr19:20178782..20180876,2	MCF-7	breast:
12	chr19:20153292..20157209-chr19:20159968..20162896,6	MCF-7	breast:
13	chr19:19772761..19775083-chr19:20066186..20068546,2	MCF-7	breast:
14	chr19:20153292..20157209-chr19:20159968..20162896,6	MCF-7	breast:
15	chr19:20158142..20160017-chr19:20161211..20163624,2	MCF-7	breast:
16	chr19:20161148..20163684-chr19:20228612..20230172,2	MCF-7	breast:
17	chr19:20161148..20163684-chr19:20228612..20230172,2	MCF-7	breast:
18	chr19:19743070..19745753-chr19:20069128..20070689,2	MCF-7	breast:
19	chr19:20158142..20160017-chr19:20161211..20163624,2	MCF-7	breast:
20	chr19:20124182..20126498-chr19:20128063..20130239,2	MCF-7	breast:
21	chr19:19886850..19889020-chr19:20162387..20164184,2	MCF-7	breast:
22	chr19:20125599..20128590-chr19:20148799..20150667,2	MCF-7	breast:
23	chr19:20124182..20126498-chr19:20128063..20130239,2	MCF-7	breast:

(count:53 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF486-7	chr19:20190596-20191128	NONHSAT063624
2	lnc-ZNF682-3	chr19:20243270-20243396	NONHSAT063631
3	lnc-ZNF93-1	chr19:20067547-20067825	ENSG00000267268.1
4	lnc-ZNF682-3	chr19:20236228-20236318	ENSG00000267383.2
5	lnc-ZNF486-8	chr19:20462311-20462888	NONHSAT063650
6	lnc-ZNF737-3	chr19:20515776-20516941	NONHSAT063653
7	lnc-ZNF682-4	chr19:20285822-20286138	NONHSAT063634
8	lnc-ZNF682-5	chr19:20318001-20320598	NONHSAT063637
9	lnc-ZNF486-5	chr19:20361026-20361104	NONHSAT063644
10	lnc-ZNF93-1	chr19:20069298-20069363	ENSG00000267268.1
11	lnc-ZNF737-3	chr19:20519759-20519854	NONHSAT063649
12	lnc-ZNF486-1	chr19:20359548-20359682	XLOC_012999
13	lnc-ZNF737-3	chr19:20451078-20451910	NONHSAT063648
14	lnc-ZNF486-3	chr19:20332678-20333272	NONHSAT063642
15	lnc-ZNF737-3	chr19:20451177-20451910	NONHSAT063649
16	lnc-ZNF486-4	chr19:20231633-20232155	NONHSAT063627
17	lnc-ZNF737-3	chr19:20519759-20519854	NONHSAT063653
18	lnc-ZNF682-3	chr19:20236354-20236592	ENSG00000267383.2
19	lnc-ZNF486-5	chr19:20359861-20359993	NONHSAT063644
20	lnc-ZNF682-1	chr19:20326955-20328125	ENSG00000251268
21	lnc-ZNF682-3	chr19:20351309-20351446	ENSG00000267383.2
22	lnc-ZNF486-7	chr19:20188846-20188944	NONHSAT063624
23	lnc-ZNF682-3	chr19:20412118-20412196	ENSG00000267383.2
24	lnc-ZNF682-3	chr19:20431995-20432114	ENSG00000267383.2
25	lnc-ZNF90-3	chr19:20144253-20144356	NONHSAT063622
26	lnc-ZNF486-6	chr19:20378626-20379200	NONHSAT063645
27	lnc-ZNF682-3	chr19:20349097-20349240	ENSG00000267383.2
28	lnc-ZNF506-8	chr19:20141802-20141922	NONHSAT063621
29	lnc-ZNF737-3	chr19:20519759-20519854	NONHSAT063652
30	lnc-ZNF93-1	chr19:20073928-20074273	ENSG00000267268.1
31	lnc-ZNF737-3	chr19:20509467-20509847	NONHSAT063652
32	lnc-ZNF682-1	chr19:20331132-20331228	ENSG00000251268
33	lnc-ZNF486-1	chr19:20359091-20359256	XLOC_012999
34	lnc-ZNF682-3	chr19:20338819-20339292	ENSG00000267383.2
35	lnc-ZNF682-3	chr19:20349097-20349261	ENSG00000267383.2
36	lnc-ZNF682-3	chr19:20243270-20243396	ENSG00000267383.2
37	lnc-ZNF682-4	chr19:20287656-20287872	NONHSAT063634
38	lnc-ZNF682-3	chr19:20243270-20243396	ENSG00000267383.2
39	lnc-ZNF682-3	chr19:20262616-20262717	NONHSAT063631
40	lnc-ZNF682-3	chr19:20242703-20242756	NONHSAT063631
41	lnc-ZNF90-1	chr19:20247742-20248042	NONHSAT063632
42	lnc-ZNF506-8	chr19:20150152-20150259	NONHSAT063621
43	lnc-ZNF682-7	chr19:20434801-20435377	NONHSAT063647
44	lnc-ZNF737-3	chr19:20486769-20486818	NONHSAT063648
45	lnc-ZNF90-3	chr19:20144674-20145141	NONHSAT063622
46	lnc-ZNF486-1	chr19:20358336-20358508	XLOC_012999
47	lnc-ZNF737-3	chr19:20516818-20516941	NONHSAT063652
48	lnc-ZNF486-4	chr19:20235815-20235952	NONHSAT063627
49	lnc-ZNF682-2	chr19:20190979-20191348	NONHSAT063625
50	lnc-ZNF682-2	chr19:20190627-20190757	NONHSAT063625

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1270	chr19:20510129-20510151	MIMAT0005924

No data

Variant related genes	Relation type
ZNF486	TF binding region
ENSG00000268070	TF binding region
ENSG00000271524	TF binding region
ZNF682	TF binding region
ENSG00000270716	TF binding region
ENSG00000266609	TF binding region
ENSG00000224864	TF binding region
ENSG00000268620	TF binding region
ENSG00000269055	TF binding region
ENSG00000221181	TF binding region
ENSG00000267220	TF binding region
ENSG00000267771	TF binding region
ENSG00000271638	TF binding region
ENSG00000213985	TF binding region
ENSG00000240673	TF binding region
ENSG00000269154	TF binding region
ENSG00000267641	TF binding region
ZNF90	TF binding region
ENSG00000269274	TF binding region
ENSG00000271704	TF binding region
MIR1270-1	TF binding region
ENSG00000267383	TF binding region
ENSG00000264441	TF binding region
ZNF486	CpG island
ENSG00000268070	CpG island
ENSG00000271524	CpG island
ZNF682	CpG island
ENSG00000270716	CpG island
ENSG00000266609	CpG island
ENSG00000224864	CpG island
ENSG00000268620	CpG island
ENSG00000269055	CpG island
ENSG00000221181	CpG island
ENSG00000267220	CpG island
ENSG00000267771	CpG island
ENSG00000271638	CpG island
ENSG00000213985	CpG island
ENSG00000240673	CpG island
ENSG00000269154	CpG island
ENSG00000267641	CpG island
ZNF90	CpG island
ENSG00000269274	CpG island
ENSG00000271704	CpG island
MIR1270-1	CpG island
ENSG00000267383	CpG island
ENSG00000264441	CpG island
ENSG00000267419	chromatin interactions
ENSG00000256771	chromatin interactions
ENSG00000105726	chromatin interactions
ENSG00000266904	chromatin interactions
ENSG00000197013	chromatin interactions
ENSG00000197124	chromatin interactions
ENSG00000268070	chromatin interactions
FXN	Mature miRNA region
ARID3B	miRNA target sites
UBAP2L	miRNA target sites

Extended variants
information (count: 19033 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:19033 , 50 per page) page: 1 2 3 4 5 6 7 ... 381

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576721043	chr19:20064917-20064918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs62135332	chr19:20064923-20064924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs7254824	chr19:20065009-20065010	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs559308364	chr19:20065036-20065037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs142939837	chr19:20065057-20065058	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs76604098	chr19:20065126-20065127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs7255055	chr19:20065133-20065134	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs75520326	chr19:20065134-20065135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs561033105	chr19:20065155-20065156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs7254966	chr19:20065159-20065160	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs189486603	chr19:20065192-20065193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs368587502	chr19:20065195-20065196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs7258113	chr19:20065238-20065239	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs139669753	chr19:20065257-20065258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs552021196	chr19:20065270-20065271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs3220477	chr19:20065314-20065315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs200288682	chr19:20065315-20065316	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs143272372	chr19:20065319-20065320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs58914542	chr19:20065347-20065348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs55963356	chr19:20065353-20065354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs565822740	chr19:20065359-20065360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs528417209	chr19:20065365-20065366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs547875664	chr19:20065402-20065403	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs568090184	chr19:20065498-20065499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs537103773	chr19:20065514-20065515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs555233012	chr19:20065525-20065526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs200294983	chr19:20065554-20065555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs114395069	chr19:20065596-20065597	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs142648423	chr19:20065621-20065622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs368896622	chr19:20065632-20065633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs34639319	chr19:20065674-20065675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs374267027	chr19:20065675-20065676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs34099508	chr19:20065717-20065718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191277092	chr19:20065741-20065742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs4809016	chr19:20065742-20065743	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs371516160	chr19:20065762-20065763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs541749349	chr19:20065768-20065769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs554625049	chr19:20065821-20065822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs574777774	chr19:20065849-20065850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs562138881	chr19:20065867-20065868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs543481069	chr19:20065899-20065900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs563455047	chr19:20065910-20065911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs143495261	chr19:20065940-20065941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs545574318	chr19:20065982-20065983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs33921654	chr19:20065983-20065984	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs570540444	chr19:20066200-20066201	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs539587825	chr19:20066227-20066228	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs558873217	chr19:20066253-20066254	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs566271039	chr19:20066287-20066288	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs61699225	chr19:20066317-20066318	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:57)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	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
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Nasopharyngeal cancer	20548289	CNVD
Schizophrenia	20967226	CNVD
Colorectal cancer	20459617	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Type 2 diabetes	21526130	CNVD
Acute myeloid leukemia	20962326	CNVD
Glioma	20126413	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Obesity	21131291	CNVD
Bipolar disorder	19214233	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	20841430	CNVD
Autism	19492091	CNVD

Chromatin state (count:5747 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:20064800-20065800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr19:20064800-20066000	Enhancers	Ovary	ovary
3	chr19:20067200-20067400	Enhancers	H1 Cell Line	embryonic stem cell
4	chr19:20067200-20067400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr19:20067200-20067400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr19:20067200-20067400	Active TSS	Brain Germinal Matrix	brain
7	chr19:20067200-20067600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr19:20067200-20067600	Enhancers	Fetal Brain Male	brain
9	chr19:20067200-20067800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr19:20067200-20067800	Active TSS	iPS-15b Cell Line	embryonic stem cell
11	chr19:20067200-20067800	Active TSS	Fetal Brain Female	brain
12	chr19:20067400-20067600	Flanking Active TSS	H1 Cell Line	embryonic stem cell
13	chr19:20067400-20067600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr19:20067400-20067600	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr19:20067400-20067600	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
16	chr19:20067400-20067800	Active TSS	HUES64 Cell Line	embryonic stem cell
17	chr19:20067400-20067800	Active TSS	iPS-20b Cell Line	embryonic stem cell
18	chr19:20067400-20067800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr19:20067400-20067800	Flanking Active TSS	Brain Germinal Matrix	brain
20	chr19:20067400-20067800	Enhancers	Fetal Muscle Trunk	muscle
21	chr19:20067600-20067800	Active TSS	H1 Cell Line	embryonic stem cell
22	chr19:20067600-20067800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr19:20067800-20068000	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr19:20067800-20071400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr19:20069800-20070000	Enhancers	Primary T cells fromperipheralblood	blood
26	chr19:20069800-20070200	Enhancers	Primary B cells from peripheral blood	blood
27	chr19:20069800-20070200	Active TSS	Brain Anterior Caudate	brain
28	chr19:20070000-20070200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
29	chr19:20070000-20070200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
30	chr19:20070000-20070200	Enhancers	Primary T helper cells fromperipheralblood	blood
31	chr19:20070000-20070200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr19:20070000-20070200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr19:20070000-20070200	Enhancers	Adipose Nuclei	Adipose
34	chr19:20076800-20077800	ZNF genes & repeats	Spleen	Spleen
35	chr19:20076800-20078400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
36	chr19:20077400-20078000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
37	chr19:20103800-20106800	Weak transcription	Esophagus	oesophagus
38	chr19:20105000-20105200	Weak transcription	Pancreatic Islets	Pancreatic Islet
39	chr19:20105200-20105400	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
40	chr19:20105400-20112800	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr19:20106800-20107000	ZNF genes & repeats	Esophagus	oesophagus
42	chr19:20107400-20118600	Weak transcription	Right Atrium	heart
43	chr19:20108200-20109000	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr19:20108400-20109000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
45	chr19:20108600-20109000	Enhancers	Brain Substantia Nigra	brain
46	chr19:20109000-20115400	Weak transcription	H9 Cell Line	embryonic stem cell
47	chr19:20109800-20115400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr19:20110200-20115000	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr19:20111800-20113400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr19:20112000-20112200	ZNF genes & repeats	HSMM	muscle

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