Variant report

Variant	nsv912194
Chromosome Location	chr19:47540859-47562123
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:709)
CpG islands
(count:977)
Chromatin interactive
region (count:46)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:709 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:47551779-47552239	K562	blood:	n/a	n/a
2	ARID3A	chr19:47550927-47551350	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:47562104-47562304	HepG2	liver:	n/a	n/a
4	ARID3A	chr19:47551827-47552242	HepG2	liver:	n/a	n/a
5	ARID3A	chr19:47551276-47551371	K562	blood:	n/a	n/a
6	ATF1	chr19:47551781-47552235	K562	blood:	n/a	n/a
7	ATF2	chr19:47551645-47552188	GM12878	blood:	n/a	n/a
8	ATF2	chr19:47551183-47551487	GM12878	blood:	n/a	n/a
9	ATF3	chr19:47551979-47552202	K562	blood:	n/a	n/a
10	ATF3	chr19:47551135-47551445	A549	lung:	n/a	n/a
11	ATF3	chr19:47551656-47552044	A549	lung:	n/a	chr19:47551890-47551899
12	BACH1	chr19:47551249-47551351	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL3	chr19:47551155-47551650	A549	lung:	n/a	chr19:47551589-47551598
14	BCL3	chr19:47551089-47551475	A549	lung:	n/a	n/a
15	BCLAF1	chr19:47551982-47552338	GM12878	blood:	n/a	n/a
16	BHLHE40	chr19:47551200-47552115	K562	blood:	n/a	n/a
17	BHLHE40	chr19:47551629-47552225	GM12878	blood:	n/a	n/a
18	BRCA1	chr19:47562084-47562128	HepG2	liver:	n/a	n/a
19	BRCA1	chr19:47551821-47552222	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr19:47561887-47562317	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr19:47551191-47551321	HepG2	liver:	n/a	n/a
22	CBX3	chr19:47550850-47551475	K562	blood:	n/a	n/a
23	CCNT2	chr19:47551329-47551999	K562	blood:	n/a	chr19:47551645-47551654
24	CEBPB	chr19:47550898-47551173	A549	lung:	n/a	chr19:47551054-47551065
25	CEBPB	chr19:47541956-47542118	Hela-S3	cervix:	n/a	chr19:47542035-47542046
26	CEBPB	chr19:47550888-47551368	HepG2	liver:	n/a	chr19:47551054-47551065
27	CEBPB	chr19:47551882-47552056	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr19:47541959-47542104	A549	lung:	n/a	chr19:47542035-47542046
29	CEBPB	chr19:47550965-47551109	HepG2	liver:	n/a	chr19:47551054-47551065
30	CEBPB	chr19:47541977-47542062	HepG2	liver:	n/a	chr19:47542035-47542046
31	CEBPB	chr19:47550898-47551319	K562	blood:	n/a	chr19:47551054-47551065
32	CEBPB	chr19:47550996-47551167	H1-hESC	embryonic stem cell:	n/a	chr19:47551054-47551065
33	CEBPB	chr19:47550907-47551391	Hela-S3	cervix:	n/a	chr19:47551054-47551065
34	CEBPB	chr19:47561836-47562402	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr19:47550883-47551379	HepG2	liver:	n/a	chr19:47551054-47551065
36	CEBPB	chr19:47541928-47542145	K562	blood:	n/a	chr19:47542035-47542046
37	CEBPB	chr19:47541994-47542097	IMR90	lung:	n/a	chr19:47542035-47542046
38	CEBPB	chr19:47550882-47551367	IMR90	lung:	n/a	chr19:47551054-47551065
39	CEBPB	chr19:47556915-47557115	Hela-S3	cervix:	n/a	n/a
40	CEBPD	chr19:47551595-47551956	HepG2	liver:	n/a	n/a
41	CEBPD	chr19:47550867-47551515	HepG2	liver:	n/a	n/a
42	CEBPZ	chr19:47551785-47552217	HepG2	liver:	n/a	n/a
43	CHD1	chr19:47551317-47551851	GM12878	blood:	n/a	n/a
44	CHD2	chr19:47551698-47552269	GM12878	blood:	n/a	n/a
45	CHD2	chr19:47551070-47552261	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr19:47551110-47551431	K562	blood:	n/a	n/a
47	CHD2	chr19:47551735-47552210	K562	blood:	n/a	n/a
48	CHD2	chr19:47551760-47552181	HepG2	liver:	n/a	n/a
49	CHD2	chr19:47551061-47552260	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr19:47551126-47551489	GM12878	blood:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:47551847-47551897	HIPEpiC	eye:	n/a
2	chr19:47551847-47551897	HIPEpiC	eye:	n/a
3	chr19:47551847-47551897	GM19239	blood:	n/a
4	chr19:47548452-47548502	BE2_C	brain:	n/a
5	chr19:47551918-47551968	PrEC	prostate:	n/a
6	chr19:47551918-47551968	HIPEpiC	eye:	n/a
7	chr19:47551842-47551892	SAEC	small airway:	n/a
8	chr19:47551893-47551943	LNCaP	prostate:	n/a
9	chr19:47548982-47549032	NHDF-neo	bronchial:	n/a
10	chr19:47548982-47549032	HCT-116	colon:	n/a
11	chr19:47548452-47548502	HCF	heart:	n/a
12	chr19:47551842-47551892	MCF10A-Er-Src	breast:	n/a
13	chr19:47549865-47549915	GM06990	blood:	n/a
14	chr19:47549865-47549915	HRPEpiC	eye:	n/a
15	chr19:47551847-47551897	HCPEpiC	choroid plexus:	n/a
16	chr19:47551893-47551943	HEK293	kidney:	embryo
17	chr19:47548452-47548502	ovcar-3	ovarian:	n/a
18	chr19:47549464-47549514	HL-60	blood:	n/a
19	chr19:47552711-47552761	BE2_C	brain:	n/a
20	chr19:47551918-47551968	ovcar-3	ovarian:	n/a
21	chr19:47551918-47551968	Jurkat	blood:	n/a
22	chr19:47551509-47551559	HNPCEpiC	eye:	n/a
23	chr19:47549865-47549915	NT2-D1	testis:	n/a
24	chr19:47551642-47551692	SKMC	muscle:	n/a
25	chr19:47551898-47551948	GM19239	blood:	n/a
26	chr19:47551509-47551559	Jurkat	blood:	n/a
27	chr19:47551898-47551948	HepG2	liver:	n/a
28	chr19:47551509-47551559	IMR90	lung:	fetal
29	chr19:47545905-47545955	Caco-2	colon:	n/a
30	chr19:47549464-47549514	HRCEpiC	kidney:	n/a
31	chr19:47551991-47552041	GM06990	blood:	n/a
32	chr19:47549464-47549514	Caco-2	colon:	n/a
33	chr19:47549464-47549514	A549	lung:	n/a
34	chr19:47548452-47548502	AG09319	gingival:	n/a
35	chr19:47553215-47553265	HCF	heart:	n/a
36	chr19:47551991-47552041	AG04450	lung:	fetal
37	chr19:47549865-47549915	HEK293	kidney:	embryo
38	chr19:47548982-47549032	GM12892	blood:	n/a
39	chr19:47551847-47551897	AG04450	lung:	fetal
40	chr19:47551847-47551897	H1-hESC	embryonic stem cell:	embryo
41	chr19:47551971-47552021	AG10803	skin:	n/a
42	chr19:47552711-47552761	NH-A	brain:	n/a
43	chr19:47551842-47551892	AoSMC	blood vessel:	n/a
44	chr19:47553215-47553265	GM12891	blood:	n/a
45	chr19:47551509-47551559	SK-N-SH	brain:	n/a
46	chr19:47551847-47551897	HNPCEpiC	eye:	n/a
47	chr19:47548982-47549032	HL-60	blood:	n/a
48	chr19:47551642-47551692	CMK	blood:	n/a
49	chr19:47549865-47549915	NHBE	bronchial:	n/a
50	chr19:47551847-47551897	AoSMC	blood vessel:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:47551385..47554234-chr19:47614928..47616660,2	MCF-7	breast:
2	chr16:2204576..2205415-chr19:47551343..47551931,2	NB4	blood:
3	chr19:47539124..47541192-chr19:47549065..47553004,4	MCF-7	breast:
4	chr19:47550175..47552727-chr19:47729479..47731915,2	MCF-7	breast:
5	chr19:47537370..47542456-chr19:47608752..47618661,11	MCF-7	breast:
6	chr19:47541370..47542994-chr19:47549456..47551383,2	K562	blood:
7	chr19:47538787..47540867-chr19:47733145..47735937,2	MCF-7	breast:
8	chr19:47537595..47541132-chr19:47548303..47552925,5	K562	blood:
9	chr19:47561135..47563131-chr19:47615592..47617171,2	MCF-7	breast:
10	chr19:47541370..47542994-chr19:47549456..47551383,2	K562	blood:
11	chr19:47249454..47252042-chr19:47542996..47544758,2	MCF-7	breast:
12	chr19:47539124..47541192-chr19:47549065..47553004,4	MCF-7	breast:
13	chr17:56406854..56407520-chr19:47551176..47551676,2	NB4	blood:
14	chr19:47542487..47545191-chr19:47545795..47547768,2	K562	blood:
15	chr19:47561645..47562697-chr19:47584035..47585317,11	MCF-7	breast:
16	chr12:27167100..27167904-chr19:47551169..47552146,2	NB4	blood:
17	chr19:47551525..47552077-chr2:64067501..64068272,2	NB4	blood:
18	chr19:47549666..47554198-chr19:47613838..47618039,7	K562	blood:
19	chr19:47536875..47541608-chr19:47542231..47546350,8	K562	blood:
20	chr19:47542487..47545191-chr19:47545795..47547768,2	K562	blood:
21	chr19:47544284..47547116-chr19:47549771..47551356,2	K562	blood:
22	chr19:47539601..47541504-chr19:47542700..47544576,2	MCF-7	breast:
23	chr19:47547423..47549920-chr19:47617709..47619921,2	MCF-7	breast:
24	chr19:47546007..47548837-chr19:47551306..47553028,2	K562	blood:
25	chr19:47549317..47551372-chr19:47632654..47634516,2	MCF-7	breast:
26	chr19:47561990..47563746-chr19:47600717..47602737,2	K562	blood:
27	chr19:47561683..47562436-chr19:47599075..47599777,2	MCF-7	breast:
28	chr19:47551143..47553326-chr19:47633296..47636151,3	K562	blood:
29	chr19:47561724..47562616-chr19:47584136..47584703,3	MCF-7	breast:
30	chr19:47551339..47553570-chr19:47632652..47634525,2	MCF-7	breast:
31	chr19:47290385..47292241-chr19:47550652..47552913,2	K562	blood:
32	chr19:47544284..47547116-chr19:47549771..47551356,2	K562	blood:
33	chr19:47561704..47562574-chr19:47599070..47599896,7	MCF-7	breast:
34	chr19:47523048..47525181-chr19:47550453..47552080,2	K562	blood:
35	chr19:47538628..47541128-chr19:47545999..47547518,2	MCF-7	breast:
36	chr19:47539601..47541504-chr19:47542700..47544576,2	MCF-7	breast:
37	chr19:47537595..47541132-chr19:47548303..47552925,5	K562	blood:
38	chr19:47559138..47562031-chr19:47586588..47588278,2	K562	blood:
39	chr19:47561735..47562311-chr19:47584370..47585046,2	MCF-7	breast:
40	chr19:47521811..47526741-chr19:47550453..47554269,5	K562	blood:
41	chr19:47535802..47537501-chr19:47542760..47544792,2	MCF-7	breast:
42	chr19:47540296..47540838-chr19:47561822..47562413,2	MCF-7	breast:
43	chr19:47501784..47504160-chr19:47539723..47542156,2	K562	blood:
44	chr19:47540250..47540933-chr19:47584431..47584967,2	MCF-7	breast:
45	chr19:47550333..47554198-chr19:47612165..47616505,8	K562	blood:
46	chr19:47561843..47562574-chr19:47599081..47599874,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARHGAP35-1	chr19:47543702-47544016	NONHSAT066948

No data

Variant related genes	Relation type
TMEM160	TF binding region
TMEM160	CpG island
ENSG00000090372	chromatin interactions
ENSG00000181027	chromatin interactions
ENSG00000169764	chromatin interactions
ENSG00000130749	chromatin interactions
ENSG00000130748	chromatin interactions
ENSG00000142230	chromatin interactions
ENSG00000105281	chromatin interactions
ENSG00000105327	chromatin interactions
ENSG00000064115	chromatin interactions
ENSG00000160007	chromatin interactions
ENSG00000265148	chromatin interactions
ENSG00000130751	chromatin interactions
ENSG00000206630	chromatin interactions
ENSG00000260260	chromatin interactions
ENSG00000265134	chromatin interactions

Extended variants
information (count: 1114 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:1114 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12461916	chr19:47540859-47540860	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs540481193	chr19:47540870-47540871	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs554093998	chr19:47540873-47540874	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs573689810	chr19:47540875-47540876	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs542689844	chr19:47540877-47540878	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs562979505	chr19:47540896-47540897	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs531685521	chr19:47540897-47540898	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs191268855	chr19:47540910-47540911	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs529617720	chr19:47540929-47540930	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs143196547	chr19:47540937-47540938	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs527530573	chr19:47540997-47540998	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs184902568	chr19:47540999-47541000	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs17716389	chr19:47541001-47541002	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs141551562	chr19:47541012-47541013	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs377358253	chr19:47541055-47541056	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs377376586	chr19:47541070-47541071	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs569647363	chr19:47541093-47541094	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs189567166	chr19:47541096-47541097	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs538317063	chr19:47541148-47541149	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs114910109	chr19:47541176-47541177	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs182163250	chr19:47541205-47541206	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs540024349	chr19:47541262-47541263	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs558934026	chr19:47541267-47541268	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs534163329	chr19:47541286-47541287	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs532722410	chr19:47541374-47541375	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs554028676	chr19:47541454-47541455	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs551086358	chr19:47541496-47541497	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs574024060	chr19:47541499-47541500	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs536974774	chr19:47541503-47541504	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs556243681	chr19:47541514-47541515	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs569380605	chr19:47541519-47541520	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs545168095	chr19:47541531-47541532	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs565418465	chr19:47541534-47541535	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs572251852	chr19:47541536-47541537	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs147033160	chr19:47541543-47541544	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs186697666	chr19:47541547-47541548	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs529910878	chr19:47541548-47541549	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs553234106	chr19:47541559-47541560	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs550060397	chr19:47541572-47541573	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs141880230	chr19:47541580-47541581	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs368032961	chr19:47541587-47541588	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs189423576	chr19:47541595-47541596	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs181943958	chr19:47541598-47541599	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs534105336	chr19:47541604-47541605	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs10411622	chr19:47541643-47541644	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs138904465	chr19:47541644-47541645	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs186113561	chr19:47541646-47541647	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs189743400	chr19:47541662-47541663	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs149392096	chr19:47541678-47541679	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs539069967	chr19:47541706-47541707	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
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	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
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
Astrocytoma	22246337	CNVD
Ovarian cancer	22174824	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
Prostate cancer	19156837	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Muscular dystrophy	17160897	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Glioblastoma multiforme	21569311	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Wilms tumour	21544195	CNVD
Ewing''s sarcoma	17952124	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:747 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:47539000-47545800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr19:47539400-47545600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr19:47539600-47545600	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr19:47539600-47548200	Weak transcription	Lung	lung
5	chr19:47539600-47549200	Weak transcription	Ovary	ovary
6	chr19:47539600-47550400	Weak transcription	Left Ventricle	heart
7	chr19:47539800-47541400	Enhancers	A549	lung
8	chr19:47539800-47542200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr19:47539800-47543000	Weak transcription	Thymus	Thymus
10	chr19:47539800-47543800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr19:47539800-47544400	Weak transcription	Esophagus	oesophagus
12	chr19:47539800-47545400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr19:47539800-47545800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr19:47539800-47545800	Weak transcription	Brain Germinal Matrix	brain
15	chr19:47539800-47547000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr19:47539800-47547200	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr19:47539800-47548400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr19:47539800-47548400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr19:47539800-47548400	Weak transcription	Gastric	stomach
20	chr19:47539800-47548600	Weak transcription	Right Ventricle	heart
21	chr19:47539800-47549400	Weak transcription	Pancreas	Pancrea
22	chr19:47539800-47550200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
23	chr19:47539800-47550400	Weak transcription	Primary T cells from cord blood	blood
24	chr19:47539800-47550400	Weak transcription	Liver	Liver
25	chr19:47539800-47550400	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr19:47539800-47550400	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr19:47539800-47550600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr19:47539800-47550600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr19:47539800-47550600	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr19:47539800-47550600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr19:47539800-47550600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr19:47539800-47550600	Weak transcription	Brain Anterior Caudate	brain
33	chr19:47539800-47550600	Weak transcription	Colon Smooth Muscle	Colon
34	chr19:47539800-47550600	Weak transcription	Right Atrium	heart
35	chr19:47539800-47550600	Weak transcription	NHLF	lung
36	chr19:47539800-47550800	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr19:47539800-47551200	Weak transcription	Aorta	Aorta
38	chr19:47540000-47541400	Enhancers	HepG2	liver
39	chr19:47540000-47544400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr19:47540000-47545400	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr19:47540000-47545400	Weak transcription	Fetal Brain Female	brain
42	chr19:47540000-47545600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr19:47540000-47545600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr19:47540000-47545600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr19:47540000-47545600	Weak transcription	Fetal Intestine Small	intestine
46	chr19:47540000-47545600	Weak transcription	Monocytes-CD14+_RO01746	blood
47	chr19:47540000-47547400	Weak transcription	Fetal Stomach	stomach
48	chr19:47540000-47547600	Weak transcription	H1 Cell Line	embryonic stem cell
49	chr19:47540000-47548400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr19:47540000-47549200	Weak transcription	Spleen	Spleen

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