Variant report

Variant	nsv911639
Chromosome Location	chr19:36342909-36365985
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:477)
CpG islands
(count:2810)
Chromatin interactive
region (count:36)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:477 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:36346631-36346781	K562	blood:	n/a	n/a
2	ARID3A	chr19:36360868-36361320	K562	blood:	n/a	n/a
3	ATF2	chr19:36360710-36361472	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr19:36359150-36359446	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr19:36346966-36347538	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr19:36351334-36352277	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr19:36359819-36361440	A549	lung:	n/a	chr19:36360912-36360921 chr19:36360553-36360562 chr19:36360410-36360418
8	BHLHE40	chr19:36360510-36360878	K562	blood:	n/a	n/a
9	BHLHE40	chr19:36347949-36347963	K562	blood:	n/a	n/a
10	BHLHE40	chr19:36349412-36349496	K562	blood:	n/a	n/a
11	BHLHE40	chr19:36352039-36352243	K562	blood:	n/a	n/a
12	BHLHE40	chr19:36346600-36346719	K562	blood:	n/a	n/a
13	BHLHE40	chr19:36353530-36353731	K562	blood:	n/a	n/a
14	BRCA1	chr19:36360143-36360299	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chr19:36347497-36347930	H1-hESC	embryonic stem cell:	n/a	n/a
16	CBX3	chr19:36353424-36353872	K562	blood:	n/a	n/a
17	CBX3	chr19:36360504-36360967	K562	blood:	n/a	n/a
18	CCNT2	chr19:36360552-36360822	K562	blood:	n/a	n/a
19	CCNT2	chr19:36359223-36359695	K562	blood:	n/a	chr19:36359297-36359306
20	CCNT2	chr19:36346508-36346708	K562	blood:	n/a	chr19:36346671-36346680
21	CEBPB	chr19:36346507-36346795	K562	blood:	n/a	n/a
22	CEBPB	chr19:36346492-36346752	K562	blood:	n/a	n/a
23	CEBPB	chr19:36363113-36363313	A549	lung:	n/a	chr19:36363188-36363201
24	CEBPB	chr19:36360297-36360450	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr19:36363154-36363326	K562	blood:	n/a	chr19:36363188-36363201
26	CEBPD	chr19:36346377-36346859	K562	blood:	n/a	n/a
27	CEBPD	chr19:36346414-36346910	K562	blood:	n/a	n/a
28	CEBPD	chr19:36352099-36352492	HepG2	liver:	n/a	n/a
29	CHD1	chr19:36361848-36361942	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr19:36360786-36360945	K562	blood:	n/a	n/a
31	CHD2	chr19:36353548-36353862	K562	blood:	n/a	n/a
32	CHD2	chr19:36353413-36353446	HepG2	liver:	n/a	n/a
33	CHD2	chr19:36347584-36348123	H1-hESC	embryonic stem cell:	n/a	chr19:36347778-36347788
34	CHD2	chr19:36346652-36346694	K562	blood:	n/a	n/a
35	CHD2	chr19:36353586-36353861	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr19:36360337-36361225	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr19:36360076-36361110	A549	lung:	n/a	n/a
38	CREB1	chr19:36359151-36359886	A549	lung:	n/a	n/a
39	CTCF	chr19:36351266-36351568	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr19:36361840-36361990	GM12878	blood:	n/a	n/a
41	CTCF	chr19:36361760-36361910	HEK293	kidney:	n/a	n/a
42	CTCF	chr19:36359560-36359710	GM12874	blood:	n/a	n/a
43	CTCF	chr19:36360360-36360510	GM12864	blood:	n/a	n/a
44	CTCF	chr19:36351260-36351410	HepG2	liver:	n/a	n/a
45	CTCF	chr19:36361723-36361973	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr19:36355500-36355650	HFF-Myc	foreskin:	n/a	n/a
47	CTCF	chr19:36361840-36361990	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr19:36361760-36361910	GM12866	blood:	n/a	n/a
49	CTCF	chr19:36361877-36361913	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr19:36361260-36361410	GM12875	blood:	n/a	n/a

(count:2810 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:36352376-36352426	HepG2	liver:	n/a
2	chr19:36359211-36359261	ECC-1	luminal epithelium:	n/a
3	chr19:36346314-36346364	ECC-1	luminal epithelium:	n/a
4	chr19:36359250-36359300	PANC-1	pancreas:	n/a
5	chr19:36352376-36352426	HepG2	liver:	n/a
6	chr19:36359211-36359261	ECC-1	luminal epithelium:	n/a
7	chr19:36346314-36346364	ECC-1	luminal epithelium:	n/a
8	chr19:36359250-36359300	PANC-1	pancreas:	n/a
9	chr19:36359772-36359822	SK-N-SH_RA	brain:	n/a
10	chr19:36347698-36347748	NHBE	bronchial:	n/a
11	chr19:36365307-36365357	LNCaP	prostate:	n/a
12	chr19:36342859-36342909	HPAEpiC	pulmonary alveolar:	n/a
13	chr19:36345675-36345725	HNPCEpiC	eye:	n/a
14	chr19:36347276-36347326	RPTEC	kidney:	n/a
15	chr19:36360834-36360884	K562	blood:	n/a
16	chr19:36362894-36362944	T-47D	breast:	n/a
17	chr19:36348034-36348084	HCPEpiC	choroid plexus:	n/a
18	chr19:36350479-36350529	K562	blood:	n/a
19	chr19:36360396-36360446	NB4	blood:	n/a
20	chr19:36365679-36365729	BJ	skin:	n/a
21	chr19:36347691-36347741	HCM	heart:	n/a
22	chr19:36359772-36359822	PFSK-1	brain:	n/a
23	chr19:36348415-36348465	HRCEpiC	kidney:	n/a
24	chr19:36359556-36359606	HRPEpiC	eye:	n/a
25	chr19:36359302-36359352	GM12891	blood:	n/a
26	chr19:36365679-36365729	SK-N-SH_RA	brain:	n/a
27	chr19:36347276-36347326	PrEC	prostate:	n/a
28	chr19:36347691-36347741	HRE	kidney:	n/a
29	chr19:36359302-36359352	GM12878	blood:	n/a
30	chr19:36360834-36360884	HMEC	breast:	n/a
31	chr19:36352376-36352426	HRPEpiC	eye:	n/a
32	chr19:36350479-36350529	PrEC	prostate:	n/a
33	chr19:36342859-36342909	SAEC	small airway:	n/a
34	chr19:36359283-36359333	SK-N-SH	brain:	n/a
35	chr19:36357700-36357750	HCF	heart:	n/a
36	chr19:36347698-36347748	SK-N-SH	brain:	n/a
37	chr19:36359516-36359566	NT2-D1	testis:	n/a
38	chr19:36347626-36347676	PFSK-1	brain:	n/a
39	chr19:36359295-36359345	BE2_C	brain:	n/a
40	chr19:36358613-36358663	NH-A	brain:	n/a
41	chr19:36361866-36361916	HRE	kidney:	n/a
42	chr19:36348415-36348465	Caco-2	colon:	n/a
43	chr19:36360605-36360655	MCF10A-Er-Src	breast:	n/a
44	chr19:36342859-36342909	T-47D	breast:	n/a
45	chr19:36359327-36359377	GM12878	blood:	n/a
46	chr19:36357700-36357750	BJ	skin:	n/a
47	chr19:36365800-36365850	A549	lung:	n/a
48	chr19:36344293-36344343	GM12891	blood:	n/a
49	chr19:36344293-36344343	Caco-2	colon:	n/a
50	chr19:36346314-36346364	HCT-116	colon:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:36301268..36304054-chr19:36346309..36349120,2	K562	blood:
2	chr19:36346452..36348477-chr19:36350234..36352680,3	K562	blood:
3	chr19:36339670..36341868-chr19:36344808..36347697,2	MCF-7	breast:
4	chr19:36352834..36354607-chr19:36359086..36361937,3	K562	blood:
5	chr19:36352085..36353689-chr19:36356633..36358980,2	K562	blood:
6	chr19:36359256..36363302-chr19:36368429..36371554,3	K562	blood:
7	chr19:36358705..36361314-chr19:36484649..36486725,2	K562	blood:
8	chr19:36348843..36352101-chr19:36356347..36359178,3	MCF-7	breast:
9	chr19:36358531..36360792-chr19:36503749..36506105,2	MCF-7	breast:
10	chr19:36338551..36341228-chr19:36359496..36361624,3	K562	blood:
11	chr19:36342113..36343944-chr19:36344326..36346095,2	MCF-7	breast:
12	chr19:36359233..36364587-chr19:36367940..36372688,7	K562	blood:
13	chr19:36336052..36339154-chr19:36344963..36347982,3	MCF-7	breast:
14	chr19:36208544..36210188-chr19:36360524..36362280,2	MCF-7	breast:
15	chr19:36339201..36341065-chr19:36345567..36348442,2	K562	blood:
16	chr19:36363822..36367543-chr19:36368056..36371316,4	K562	blood:
17	chr19:36336403..36338756-chr19:36340642..36343905,3	MCF-7	breast:
18	chr19:36348444..36350564-chr19:36358604..36360896,2	K562	blood:
19	chr19:36352834..36355328-chr19:36359086..36361256,3	K562	blood:
20	chr19:36341339..36343391-chr19:36346097..36348874,2	MCF-7	breast:
21	chr19:36208378..36210285-chr19:36358548..36361708,3	K562	blood:
22	chr19:36352085..36353647-chr19:36356633..36358816,2	K562	blood:
23	chr19:36341339..36343391-chr19:36346097..36348874,2	MCF-7	breast:
24	chr19:36359272..36362126-chr19:36389056..36392231,3	MCF-7	breast:
25	chr19:36208185..36209878-chr19:36358146..36361161,3	K562	blood:
26	chr19:36352312..36355033-chr19:36357971..36359905,3	MCF-7	breast:
27	chr19:36235922..36238148-chr19:36359346..36361404,2	MCF-7	breast:
28	chr19:36339201..36341036-chr19:36345575..36348442,2	K562	blood:
29	chr19:36335780..36337313-chr19:36359455..36361667,2	MCF-7	breast:
30	chr19:36247691..36250491-chr19:36351522..36354287,2	MCF-7	breast:
31	chr19:36335712..36337227-chr19:36349133..36352127,2	MCF-7	breast:
32	chr19:36208456..36210034-chr19:36345854..36347720,2	K562	blood:
33	chr19:36365053..36367604-chr19:36368904..36371843,2	MCF-7	breast:
34	chr19:36335744..36339702-chr19:36359166..36361673,6	MCF-7	breast:
35	chr19:36361275..36362791-chr19:36390518..36392697,2	K562	blood:
36	chr19:36359598..36361922-chr19:36393124..36395167,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NPHS1-3	chr19:36358777-36359032	NONHSAT065928
2	lnc-NPHS1-3	chr19:36359994-36360189	NONHSAT065928
3	lnc-NPHS1-3	chr19:36357389-36357495	NONHSAT065928

No data

Variant related genes	Relation type
NPHS1	TF binding region
KIRREL2	TF binding region
APLP1	TF binding region
NPHS1	CpG island
KIRREL2	CpG island
APLP1	CpG island
ENSG00000004776	chromatin interactions
ENSG00000272333	chromatin interactions
ENSG00000267698	chromatin interactions
ENSG00000250799	chromatin interactions
ENSG00000161270	chromatin interactions
ENSG00000205138	chromatin interactions
ENSG00000188223	chromatin interactions
ENSG00000267120	chromatin interactions
ENSG00000126264	chromatin interactions
ENSG00000161265	chromatin interactions
ENSG00000126259	chromatin interactions
ENSG00000205155	chromatin interactions
ENSG00000167604	chromatin interactions
ENSG00000105290	chromatin interactions
ENSG00000167595	chromatin interactions
ENSG00000239382	chromatin interactions

Extended variants
information (count: 1083 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1083 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs401824	chr19:36342909-36342910	Enhancers Weak transcription Bivalent/Poised TSS Active TSS	CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs184073252	chr19:36342980-36342981	Enhancers Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs370264974	chr19:36342999-36343000	Enhancers Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs202212644	chr19:36343000-36343001	Enhancers Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs202080765	chr19:36343002-36343003	Enhancers Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs550555999	chr19:36343055-36343056	Enhancers Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs1137844	chr19:36343079-36343080	Enhancers Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs539492326	chr19:36343111-36343112	Enhancers Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs551204205	chr19:36343118-36343119	Enhancers Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs75343898	chr19:36343126-36343127	Enhancers Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs372336333	chr19:36343147-36343148	Enhancers Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs187539929	chr19:36343166-36343167	Enhancers Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs386833860	chr19:36343207-36343208	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs555583031	chr19:36343300-36343301	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs189786245	chr19:36343341-36343342	Enhancers Weak transcription Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs537757562	chr19:36343357-36343358	Enhancers Weak transcription Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs202179767	chr19:36343388-36343389	Enhancers Weak transcription Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs182085838	chr19:36343440-36343441	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs79717911	chr19:36343441-36343442	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs545446995	chr19:36343466-36343467	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs560366485	chr19:36343467-36343468	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs565512860	chr19:36343472-36343473	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs73928332	chr19:36343500-36343501	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs566002111	chr19:36343520-36343521	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs542845159	chr19:36343521-36343522	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs369740601	chr19:36343522-36343523	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs561477578	chr19:36343524-36343525	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs566572727	chr19:36343530-36343531	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs531998056	chr19:36343548-36343549	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs57002105	chr19:36343549-36343550	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs562433331	chr19:36343573-36343574	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs532777568	chr19:36343637-36343638	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs73928333	chr19:36343679-36343680	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs566440036	chr19:36343692-36343693	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs78358415	chr19:36343696-36343697	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs548726783	chr19:36343700-36343701	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs576821830	chr19:36343711-36343712	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs567126676	chr19:36343713-36343714	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs144894017	chr19:36343766-36343767	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs370364967	chr19:36343782-36343783	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs577901568	chr19:36343810-36343811	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs79092619	chr19:36343833-36343834	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs554180650	chr19:36343837-36343838	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs113436268	chr19:36343907-36343908	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs186605240	chr19:36343911-36343912	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs139228791	chr19:36343952-36343953	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs576725517	chr19:36343967-36343968	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs544064633	chr19:36343977-36343978	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs541645727	chr19:36343995-36343996	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs370900692	chr19:36343998-36343999	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	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
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Ovarian cancer	21397856	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Ovarian cancer	20844748	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Neurodevelopmental disorder	22521361	CNVD
Endometrial cancer	23636398	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
Gastric cancer	21811585	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Glioma	17123091	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1151 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:36337000-36347000	Weak transcription	Right Atrium	heart
2	chr19:36342000-36343800	Active TSS	Pancreatic Islets	Pancreatic Islet
3	chr19:36342000-36344200	Active TSS	Pancreas	Pancrea
4	chr19:36342200-36343400	Active TSS	Fetal Kidney	kidney
5	chr19:36342200-36345600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr19:36342400-36343400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr19:36342600-36343000	Bivalent/Poised TSS	Fetal Intestine Small	intestine
8	chr19:36342600-36343400	Enhancers	H1 Cell Line	embryonic stem cell
9	chr19:36342800-36343600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr19:36343200-36343400	Bivalent Enhancer	Placenta	Placenta
11	chr19:36343200-36343600	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr19:36343200-36343800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr19:36343200-36344200	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr19:36343400-36343600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr19:36343400-36343600	Bivalent Enhancer	HepG2	liver
16	chr19:36343400-36343800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
17	chr19:36343400-36344200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr19:36343600-36344000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr19:36343600-36344000	Bivalent Enhancer	Fetal Muscle Leg	muscle
20	chr19:36343800-36346800	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr19:36344000-36344200	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
22	chr19:36344000-36344200	Bivalent Enhancer	Fetal Kidney	kidney
23	chr19:36344200-36344400	Enhancers	Pancreas	Pancrea
24	chr19:36344400-36345600	Weak transcription	Pancreas	Pancrea
25	chr19:36345400-36347000	Bivalent Enhancer	HepG2	liver
26	chr19:36345600-36345800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
27	chr19:36345600-36345800	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
28	chr19:36345600-36346200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr19:36345600-36346200	Enhancers	Pancreas	Pancrea
30	chr19:36345600-36346600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr19:36345600-36346600	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr19:36345600-36346600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
33	chr19:36345600-36346800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
34	chr19:36345600-36347200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr19:36345600-36347200	Enhancers	A549	lung
36	chr19:36345800-36346000	Bivalent/Poised TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr19:36345800-36346200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr19:36345800-36346800	Enhancers	Fetal Brain Female	brain
39	chr19:36345800-36347200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
40	chr19:36345800-36347200	Bivalent Enhancer	Fetal Muscle Leg	muscle
41	chr19:36346000-36346200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
42	chr19:36346000-36346200	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr19:36346000-36346400	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr19:36346000-36346800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
45	chr19:36346000-36346800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr19:36346000-36347400	Bivalent Enhancer	Fetal Intestine Small	intestine
47	chr19:36346200-36346400	Bivalent Enhancer	Esophagus	oesophagus
48	chr19:36346200-36346400	Bivalent Enhancer	Placenta	Placenta
49	chr19:36346200-36346400	Flanking Active TSS	Pancreas	Pancrea
50	chr19:36346200-36346600	Bivalent Enhancer	H9 Cell Line	embryonic stem cell

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