Variant report

Variant	nsv1063149
Chromosome Location	chr19:44059081-44087583
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1021)
CpG islands
(count:794)
Chromatin interactive
region (count:47)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1021 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:44079190-44079357	K562	blood:	n/a	n/a
2	ATF1	chr19:44079587-44080026	K562	blood:	n/a	n/a
3	ATF1	chr19:44085608-44086104	K562	blood:	n/a	n/a
4	ATF2	chr19:44066738-44067325	GM12878	blood:	n/a	n/a
5	ATF2	chr19:44066699-44067260	GM12878	blood:	n/a	n/a
6	ATF3	chr19:44079490-44079908	K562	blood:	n/a	chr19:44079885-44079905 chr19:44079684-44079693
7	ATF3	chr19:44079488-44079843	H1-hESC	embryonic stem cell:	n/a	chr19:44079684-44079693
8	ATF3	chr19:44079593-44079872	HepG2	liver:	n/a	chr19:44079684-44079693
9	ATF3	chr19:44079497-44080010	A549	lung:	n/a	chr19:44079885-44079905 chr19:44079684-44079693
10	BACH1	chr19:44059358-44059364	K562	blood:	n/a	n/a
11	BATF	chr19:44066704-44067029	GM12878	blood:	n/a	n/a
12	BCL3	chr19:44072419-44072697	GM12878	blood:	n/a	n/a
13	BCL3	chr19:44079091-44079798	A549	lung:	n/a	chr19:44079298-44079307
14	BCLAF1	chr19:44066657-44067132	GM12878	blood:	n/a	n/a
15	BCLAF1	chr19:44066652-44067305	GM12878	blood:	n/a	n/a
16	BHLHE40	chr19:44085658-44086026	K562	blood:	n/a	n/a
17	BHLHE40	chr19:44079517-44080045	GM12878	blood:	n/a	n/a
18	BHLHE40	chr19:44066770-44067323	GM12878	blood:	n/a	n/a
19	BHLHE40	chr19:44084585-44084785	GM12878	blood:	n/a	n/a
20	BHLHE40	chr19:44059354-44059660	K562	blood:	n/a	n/a
21	BHLHE40	chr19:44064791-44065037	K562	blood:	n/a	n/a
22	BHLHE40	chr19:44084521-44084860	K562	blood:	n/a	n/a
23	BHLHE40	chr19:44079507-44079895	K562	blood:	n/a	n/a
24	BHLHE40	chr19:44079029-44079274	K562	blood:	n/a	n/a
25	BRCA1	chr19:44079378-44080057	Hela-S3	cervix:	n/a	chr19:44079929-44079936
26	BRCA1	chr19:44079599-44079909	H1-hESC	embryonic stem cell:	n/a	n/a
27	BRCA1	chr19:44079595-44079904	HepG2	liver:	n/a	n/a
28	CBX3	chr19:44065446-44065784	K562	blood:	n/a	n/a
29	CBX3	chr19:44079508-44080025	K562	blood:	n/a	n/a
30	CBX3	chr19:44065437-44065781	K562	blood:	n/a	n/a
31	CBX3	chr19:44086649-44087033	K562	blood:	n/a	n/a
32	CCNT2	chr19:44079534-44079917	K562	blood:	n/a	chr19:44079684-44079693
33	CEBPB	chr19:44064967-44065061	K562	blood:	n/a	n/a
34	CEBPB	chr19:44079598-44079923	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr19:44079689-44080020	K562	blood:	n/a	n/a
36	CEBPB	chr19:44085282-44085359	K562	blood:	n/a	n/a
37	CEBPB	chr19:44079686-44080024	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr19:44074424-44074731	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr19:44079734-44079930	HepG2	liver:	n/a	n/a
40	CEBPB	chr19:44074436-44074715	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr19:44066858-44067270	IMR90	lung:	n/a	n/a
42	CEBPB	chr19:44085234-44085362	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr19:44079422-44079443	K562	blood:	n/a	n/a
44	CEBPB	chr19:44074446-44074667	K562	blood:	n/a	n/a
45	CEBPB	chr19:44074555-44074685	HepG2	liver:	n/a	n/a
46	CEBPD	chr19:44079440-44079770	HepG2	liver:	n/a	n/a
47	CHD1	chr19:44079199-44079893	GM12878	blood:	n/a	chr19:44079685-44079695
48	CHD1	chr19:44084299-44085020	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD1	chr19:44084497-44084782	GM12878	blood:	n/a	n/a
50	CHD2	chr19:44079504-44080055	GM12878	blood:	n/a	chr19:44079685-44079695

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:44079985-44080035	AoSMC	blood vessel:	n/a
2	chr19:44079985-44080035	AoSMC	blood vessel:	n/a
3	chr19:44079527-44079577	PFSK-1	brain:	n/a
4	chr19:44082535-44082585	PrEC	prostate:	n/a
5	chr19:44079876-44079926	HAEpiC	amniotic membrane:	n/a
6	chr19:44082535-44082585	AG10803	skin:	n/a
7	chr19:44079105-44079155	AG10803	skin:	n/a
8	chr19:44079285-44079335	T-47D	breast:	n/a
9	chr19:44079105-44079155	CMK	blood:	n/a
10	chr19:44079904-44079954	SAEC	small airway:	n/a
11	chr19:44079285-44079335	AG04450	lung:	fetal
12	chr19:44079876-44079926	HRCEpiC	kidney:	n/a
13	chr19:44079904-44079954	A549	lung:	n/a
14	chr19:44079778-44079828	ProgFib	skin:	n/a
15	chr19:44079285-44079335	SAEC	small airway:	n/a
16	chr19:44082535-44082585	BJ	skin:	n/a
17	chr19:44079945-44079995	AG09319	gingival:	n/a
18	chr19:44079778-44079828	HCT-116	colon:	n/a
19	chr19:44079985-44080035	MCF10A-Er-Src	breast:	n/a
20	chr19:44079945-44079995	NH-A	brain:	n/a
21	chr19:44079945-44079995	SAEC	small airway:	n/a
22	chr19:44079876-44079926	HCF	heart:	n/a
23	chr19:44079778-44079828	HL-60	blood:	n/a
24	chr19:44076586-44076636	U87	brain:	n/a
25	chr19:44079105-44079155	BJ	skin:	n/a
26	chr19:44076586-44076636	T-47D	breast:	n/a
27	chr19:44079876-44079926	SKMC	muscle:	n/a
28	chr19:44079876-44079926	AG09319	gingival:	n/a
29	chr19:44079904-44079954	HCM	heart:	n/a
30	chr19:44079876-44079926	Caco-2	colon:	n/a
31	chr19:44079876-44079926	CMK	blood:	n/a
32	chr19:44079945-44079995	AoSMC	blood vessel:	n/a
33	chr19:44079945-44079995	CMK	blood:	n/a
34	chr19:44079285-44079335	NHDF-neo	bronchial:	n/a
35	chr19:44079527-44079577	HCF	heart:	n/a
36	chr19:44079945-44079995	HRE	kidney:	n/a
37	chr19:44079628-44079678	HCT-116	colon:	n/a
38	chr19:44079792-44079842	HIPEpiC	eye:	n/a
39	chr19:44079985-44080035	BJ	skin:	n/a
40	chr19:44079792-44079842	IMR90	lung:	fetal
41	chr19:44079876-44079926	HNPCEpiC	eye:	n/a
42	chr19:44079105-44079155	A549	lung:	n/a
43	chr19:44082535-44082585	SK-N-SH_RA	brain:	n/a
44	chr19:44079628-44079678	ovcar-3	ovarian:	n/a
45	chr19:44079945-44079995	Caco-2	colon:	n/a
46	chr19:44079778-44079828	HEK293	kidney:	embryo
47	chr19:44082535-44082585	GM12878	blood:	n/a
48	chr19:44079285-44079335	AG04449	skin:	fetal
49	chr19:44079876-44079926	PFSK-1	brain:	n/a
50	chr19:44079778-44079828	LNCaP	prostate:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:44065444..44067870-chr19:44076256..44078138,2	MCF-7	breast:
2	chr19:44068557..44070681-chr19:44078939..44080938,2	K562	blood:
3	chr19:44077678..44083171-chr19:44093489..44103015,14	K562	blood:
4	chr19:44077687..44082496-chr19:44098234..44103069,7	MCF-7	breast:
5	chr19:44078643..44081382-chr19:44098876..44100782,4	K562	blood:
6	chr19:44058393..44061505-chr19:44095706..44100146,4	MCF-7	breast:
7	chr19:44078455..44080853-chr19:44098810..44102178,4	MCF-7	breast:
8	chr19:44036185..44038265-chr19:44078295..44081409,3	K562	blood:
9	chr19:44082516..44084852-chr19:44122314..44123953,3	K562	blood:
10	chr19:44078955..44081902-chr19:44082644..44085623,4	MCF-7	breast:
11	chr19:44079920..44081896-chr19:44082367..44084716,3	K562	blood:
12	chr19:44065179..44067890-chr19:44122794..44124973,2	K562	blood:
13	chr19:44059054..44060074-chr19:44156198..44156967,3	K562	blood:
14	chr19:44083278..44085752-chr19:44098903..44101247,2	MCF-7	breast:
15	chr19:44059273..44059814-chr19:44100326..44101062,2	MCF-7	breast:
16	chr19:44059108..44059674-chr19:44098601..44099306,2	MCF-7	breast:
17	chr19:44076409..44078057-chr19:44100171..44102190,2	MCF-7	breast:
18	chr19:44065444..44067870-chr19:44076256..44078138,2	MCF-7	breast:
19	chr19:43991164..43993354-chr19:44079151..44081521,2	K562	blood:
20	chr19:44067662..44069397-chr19:44123055..44125444,2	MCF-7	breast:
21	chr19:44080117..44083864-chr19:44085399..44088767,4	K562	blood:
22	chr19:44059581..44061634-chr19:44072814..44074549,2	MCF-7	breast:
23	chr19:44063536..44067996-chr19:44097389..44100718,5	MCF-7	breast:
24	chr19:44078138..44080459-chr19:44123311..44124978,2	MCF-7	breast:
25	chr19:44079733..44081896-chr19:44082367..44084669,4	K562	blood:
26	chr19:44079920..44081896-chr19:44082367..44084716,3	K562	blood:
27	chr19:44082767..44086072-chr19:44097414..44100193,3	MCF-7	breast:
28	chr19:44082536..44084852-chr19:44121728..44123814,2	K562	blood:
29	chr19:44082737..44084299-chr19:44149174..44151871,2	MCF-7	breast:
30	chr19:44082364..44084378-chr19:44084508..44086899,2	K562	blood:
31	chr19:44059035..44059991-chr19:44156189..44157100,4	MCF-7	breast:
32	chr19:43937158..43937719-chr19:44059063..44059904,2	K562	blood:
33	chr19:44076171..44077676-chr19:44133268..44135253,2	K562	blood:
34	chr19:44077932..44081099-chr19:44141868..44144910,3	MCF-7	breast:
35	chr19:44059185..44060976-chr19:44078373..44080974,2	K562	blood:
36	chr19:44079733..44081896-chr19:44082367..44084669,4	K562	blood:
37	chr19:44067153..44069901-chr19:44090568..44094410,3	MCF-7	breast:
38	chr19:44077515..44081647-chr19:44122454..44125105,4	K562	blood:
39	chr19:44064879..44067327-chr19:44069026..44071332,2	K562	blood:
40	chr19:44059581..44061634-chr19:44072814..44074549,2	MCF-7	breast:
41	chr19:44078733..44081444-chr19:44094635..44097229,2	MCF-7	breast:
42	chr19:44058980..44059977-chr19:44099035..44099807,2	MCF-7	breast:
43	chr19:44078955..44081902-chr19:44082644..44085623,4	MCF-7	breast:
44	chr19:44074412..44076868-chr19:44077789..44081867,6	K562	blood:
45	chr19:44074168..44077284-chr19:44077377..44081867,9	K562	blood:
46	chr19:44079594..44081331-chr19:44123672..44125242,2	MCF-7	breast:
47	chr19:44035923..44038107-chr19:44078243..44080720,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-L34079.1-2	chr19:44082742-44083238	NONHSAT066603
2	lnc-L34079.1-2	chr19:44080952-44081071	NONHSAT066603
3	lnc-L34079.1-3	chr19:44079551-44079770	ENSG00000269583.1
4	lnc-L34079.1-3	chr19:44078790-44079115	ENSG00000269583.1
5	lnc-XRCC1-1	chr19:44081697-44081907	expReg_chr19_5630_-
6	lnc-L34079.1-2	chr19:44081267-44081413	NONHSAT066603

No data

Variant related genes	Relation type
XRCC1	TF binding region
ENSG00000269583	TF binding region
PINLYP	TF binding region
XRCC1	CpG island
ENSG00000269583	CpG island
PINLYP	CpG island
ENSG00000269583	chromatin interactions
ENSG00000176531	chromatin interactions
ENSG00000073050	chromatin interactions
ENSG00000268361	chromatin interactions
ENSG00000105767	chromatin interactions
ENSG00000124444	chromatin interactions
ENSG00000176472	chromatin interactions
ENSG00000167378	chromatin interactions
ENSG00000131116	chromatin interactions
ENSG00000234465	chromatin interactions
ENSG00000226763	chromatin interactions

Extended variants
information (count: 1078 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1078 , 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	rs25494	chr19:44059082-44059083	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs1799778	chr19:44059141-44059142	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs552732045	chr19:44059153-44059154	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs201159298	chr19:44059187-44059188	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs566036857	chr19:44059191-44059192	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs7257978	chr19:44059230-44059231	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs116371014	chr19:44059232-44059233	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs555555982	chr19:44059254-44059255	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs3213354	chr19:44059258-44059259	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs3213353	chr19:44059278-44059279	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs3213352	chr19:44059322-44059323	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs3213351	chr19:44059325-44059326	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs537361716	chr19:44059381-44059382	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs573999000	chr19:44059424-44059425	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs557218093	chr19:44059480-44059481	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs3213350	chr19:44059514-44059515	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs3213349	chr19:44059517-44059518	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs558274868	chr19:44059519-44059520	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs373614606	chr19:44059525-44059526	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs572052780	chr19:44059540-44059541	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs562018200	chr19:44059552-44059553	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs372167305	chr19:44059554-44059555	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs534662835	chr19:44059578-44059579	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs560740437	chr19:44059581-44059582	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs574339486	chr19:44059585-44059586	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs543772876	chr19:44059593-44059594	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs563552626	chr19:44059610-44059611	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs3213348	chr19:44059637-44059638	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs571961956	chr19:44059657-44059658	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs142708123	chr19:44059684-44059685	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs559452838	chr19:44059713-44059714	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs528601253	chr19:44059727-44059728	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs548629671	chr19:44059738-44059739	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs568398632	chr19:44059741-44059742	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs3213347	chr19:44059789-44059790	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs190006585	chr19:44059853-44059854	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs138274010	chr19:44059855-44059856	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs539701672	chr19:44059937-44059938	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs34910672	chr19:44059948-44059949	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs2854501	chr19:44060001-44060002	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs3213346	chr19:44060019-44060020	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs10405049	chr19:44060046-44060047	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs554632195	chr19:44060050-44060051	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs35400658	chr19:44060073-44060074	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs576140579	chr19:44060107-44060108	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs574375868	chr19:44060189-44060190	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs538937476	chr19:44060246-44060247	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs543526833	chr19:44060307-44060308	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs543438673	chr19:44060318-44060319	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs185709236	chr19:44060378-44060379	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
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
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Astrocytoma	22246337	CNVD
Ovarian cancer	22174824	CNVD
Cancer	20164920	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	20800559	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Spondylocostal dysostosis	21085971	CNVD
Nicotine metabolism	21956041	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	20459617	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21240255	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:1996 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:44039200-44078600	Weak transcription	Hela-S3	cervix
2	chr19:44040800-44060800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr19:44041800-44065200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr19:44043200-44064600	Weak transcription	NHDF-Ad	bronchial
5	chr19:44043400-44059200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr19:44043600-44059200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr19:44043600-44065800	Strong transcription	Adipose Nuclei	Adipose
8	chr19:44043800-44065800	Weak transcription	Fetal Heart	heart
9	chr19:44043800-44074000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr19:44044600-44069000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr19:44045200-44062800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr19:44047400-44066600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr19:44048200-44062000	Weak transcription	NH-A	brain
14	chr19:44048200-44067000	Weak transcription	HUVEC	blood vessel
15	chr19:44048400-44078800	Weak transcription	Small Intestine	intestine
16	chr19:44050400-44063000	Strong transcription	Thymus	Thymus
17	chr19:44052600-44060600	Strong transcription	Osteobl	bone
18	chr19:44052800-44060400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr19:44052800-44068400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr19:44053000-44059200	Strong transcription	Primary monocytes fromperipheralblood	blood
21	chr19:44053000-44059200	Strong transcription	Placenta Amnion	Placenta Amnion
22	chr19:44053000-44059400	Strong transcription	HUES64 Cell Line	embryonic stem cell
23	chr19:44053000-44059400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
24	chr19:44053000-44059400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
25	chr19:44053000-44059400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr19:44053000-44059400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr19:44053000-44060000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr19:44053000-44064800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr19:44053000-44065600	Strong transcription	Primary neutrophils fromperipheralblood	blood
30	chr19:44053000-44066200	Strong transcription	Fetal Muscle Leg	muscle
31	chr19:44053200-44064600	Weak transcription	K562	blood
32	chr19:44053400-44059200	Strong transcription	Muscle Satellite Cultured Cells	--
33	chr19:44053400-44059400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr19:44053400-44061000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr19:44053400-44068800	Strong transcription	Fetal Intestine Small	intestine
36	chr19:44053400-44069400	Strong transcription	Fetal Stomach	stomach
37	chr19:44053600-44059200	Strong transcription	Spleen	Spleen
38	chr19:44053600-44062400	Strong transcription	Dnd41	blood
39	chr19:44053600-44068600	Strong transcription	Fetal Intestine Large	intestine
40	chr19:44053800-44060600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
41	chr19:44053800-44060600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr19:44053800-44062600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr19:44054000-44059200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr19:44054000-44059200	Strong transcription	Duodenum Smooth Muscle	Duodenum
45	chr19:44054000-44059200	Strong transcription	Fetal Thymus	thymus
46	chr19:44054000-44059200	Strong transcription	Lung	lung
47	chr19:44054000-44059600	Strong transcription	Right Ventricle	heart
48	chr19:44054000-44060000	Strong transcription	Brain Germinal Matrix	brain
49	chr19:44054000-44065600	Strong transcription	Placenta	Placenta
50	chr19:44054200-44060200	Strong transcription	Colon Smooth Muscle	Colon

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