Variant report

Variant	nsv9740
Chromosome Location	chr19:52096231-52107021
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:508)
CpG islands
(count:916)
Chromatin interactive
region (count:16)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:508 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:52096972-52096983	K562	blood:	n/a	n/a
2	ATF1	chr19:52097534-52097994	K562	blood:	n/a	n/a
3	ATF2	chr19:52097431-52097950	GM12878	blood:	n/a	n/a
4	ATF2	chr19:52105602-52106196	GM12878	blood:	n/a	n/a
5	ATF3	chr19:52097389-52097919	GM12878	blood:	n/a	n/a
6	ATF3	chr19:52097523-52097947	K562	blood:	n/a	n/a
7	ATF3	chr19:52097310-52097803	A549	lung:	n/a	n/a
8	ATF3	chr19:52097438-52097902	A549	lung:	n/a	n/a
9	ATF3	chr19:52097564-52097900	HepG2	liver:	n/a	n/a
10	ATF3	chr19:52097603-52097818	GM12878	blood:	n/a	n/a
11	BACH1	chr19:52097272-52097342	K562	blood:	n/a	n/a
12	BACH1	chr19:52097209-52097438	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr19:52098147-52098159	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr19:52102436-52102722	GM12878	blood:	n/a	n/a
15	BATF	chr19:52105865-52106107	GM12878	blood:	n/a	n/a
16	BCL3	chr19:52097374-52098262	A549	lung:	n/a	chr19:52097706-52097719 chr19:52097907-52097920
17	BCLAF1	chr19:52105617-52106137	GM12878	blood:	n/a	n/a
18	BCLAF1	chr19:52097426-52097966	GM12878	blood:	n/a	chr19:52097706-52097719 chr19:52097907-52097920
19	BCLAF1	chr19:52097436-52098054	GM12878	blood:	n/a	chr19:52097706-52097719 chr19:52097907-52097920
20	BHLHE40	chr19:52096954-52097910	K562	blood:	n/a	n/a
21	BHLHE40	chr19:52097464-52097950	GM12878	blood:	n/a	n/a
22	BHLHE40	chr19:52098279-52098319	K562	blood:	n/a	n/a
23	BRCA1	chr19:52097478-52097932	GM12878	blood:	n/a	n/a
24	BRCA1	chr19:52097528-52097988	Hela-S3	cervix:	n/a	n/a
25	CBX3	chr19:52097436-52098009	K562	blood:	n/a	n/a
26	CCNT2	chr19:52097073-52098002	K562	blood:	n/a	n/a
27	CEBPB	chr19:52099102-52099364	HepG2	liver:	n/a	chr19:52099245-52099256
28	CEBPB	chr19:52097593-52097937	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr19:52099074-52099441	HepG2	liver:	n/a	chr19:52099245-52099256
30	CEBPB	chr19:52099030-52099494	K562	blood:	n/a	chr19:52099245-52099256
31	CEBPB	chr19:52098954-52099531	K562	blood:	n/a	chr19:52099245-52099256
32	CEBPB	chr19:52099145-52099402	Hela-S3	cervix:	n/a	chr19:52099245-52099256
33	CEBPB	chr19:52099181-52099271	HepG2	liver:	n/a	chr19:52099245-52099256
34	CEBPB	chr19:52099087-52099419	A549	lung:	n/a	chr19:52099245-52099256
35	CEBPB	chr19:52099019-52099403	MCF-7	breast:	n/a	chr19:52099245-52099256
36	CEBPB	chr19:52099076-52099402	K562	blood:	n/a	chr19:52099245-52099256
37	CEBPB	chr19:52097601-52098160	K562	blood:	n/a	n/a
38	CEBPB	chr19:52099075-52099432	IMR90	lung:	n/a	chr19:52099245-52099256
39	CEBPB	chr19:52097579-52097938	A549	lung:	n/a	n/a
40	CEBPD	chr19:52098975-52099435	K562	blood:	n/a	chr19:52099245-52099256
41	CHD2	chr19:52097118-52098214	K562	blood:	n/a	n/a
42	CHD2	chr19:52097212-52097989	Hela-S3	cervix:	n/a	n/a
43	CHD2	chr19:52097323-52098145	GM12878	blood:	n/a	n/a
44	CHD2	chr19:52097612-52097952	HepG2	liver:	n/a	n/a
45	CHD2	chr19:52097585-52098058	H1-hESC	embryonic stem cell:	n/a	n/a
46	CREB1	chr19:52097449-52098067	HepG2	liver:	n/a	chr19:52097943-52097956
47	CREB1	chr19:52097545-52098011	ECC-1	luminal epithelium:	n/a	chr19:52097943-52097956
48	CREB1	chr19:52097538-52097902	A549	lung:	n/a	n/a
49	CREB1	chr19:52097513-52098185	H1-hESC	embryonic stem cell:	n/a	chr19:52097943-52097956
50	CREB1	chr19:52097114-52098084	K562	blood:	n/a	chr19:52097943-52097956

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:52102010-52102060	AG04449	skin:	fetal
2	chr19:52102010-52102060	AG04449	skin:	fetal
3	chr19:52104997-52105047	NB4	blood:	n/a
4	chr19:52102010-52102060	HIPEpiC	eye:	n/a
5	chr19:52105721-52105771	GM12891	blood:	n/a
6	chr19:52101874-52101924	HCT-116	colon:	n/a
7	chr19:52104419-52104469	SK-N-SH	brain:	n/a
8	chr19:52097802-52097852	HCM	heart:	n/a
9	chr19:52097802-52097852	ProgFib	skin:	n/a
10	chr19:52099597-52099647	HUVEC	blood vessel:	n/a
11	chr19:52105721-52105771	GM06990	blood:	n/a
12	chr19:52103425-52103475	GM19239	blood:	n/a
13	chr19:52097905-52097955	HEK293	kidney:	embryo
14	chr19:52099597-52099647	HCF	heart:	n/a
15	chr19:52104997-52105047	T-47D	breast:	n/a
16	chr19:52102023-52102073	SAEC	small airway:	n/a
17	chr19:52104632-52104682	HNPCEpiC	eye:	n/a
18	chr19:52105721-52105771	NHBE	bronchial:	n/a
19	chr19:52104632-52104682	AG04449	skin:	fetal
20	chr19:52104419-52104469	Hela-S3	cervix:	n/a
21	chr19:52104419-52104469	ECC-1	luminal epithelium:	n/a
22	chr19:52097626-52097676	AG09309	skin:	n/a
23	chr19:52101661-52101711	SK-N-SH_RA	brain:	n/a
24	chr19:52104419-52104469	SAEC	small airway:	n/a
25	chr19:52097835-52097885	NB4	blood:	n/a
26	chr19:52099597-52099647	AG09319	gingival:	n/a
27	chr19:52102010-52102060	GM19239	blood:	n/a
28	chr19:52102010-52102060	ECC-1	luminal epithelium:	n/a
29	chr19:52104997-52105047	Hela-S3	cervix:	n/a
30	chr19:52104997-52105047	PrEC	prostate:	n/a
31	chr19:52097626-52097676	HL-60	blood:	n/a
32	chr19:52105721-52105771	MCF10A-Er-Src	breast:	n/a
33	chr19:52104632-52104682	AG10803	skin:	n/a
34	chr19:52105721-52105771	HepG2	liver:	n/a
35	chr19:52097276-52097326	SKMC	muscle:	n/a
36	chr19:52104632-52104682	H1-hESC	embryonic stem cell:	embryo
37	chr19:52097835-52097885	A549	lung:	n/a
38	chr19:52104632-52104682	HEEpiC	esophagus:	n/a
39	chr19:52097276-52097326	SK-N-SH	brain:	n/a
40	chr19:52101874-52101924	ECC-1	luminal epithelium:	n/a
41	chr19:52105721-52105771	PANC-1	pancreas:	n/a
42	chr19:52104997-52105047	SKMC	muscle:	n/a
43	chr19:52097835-52097885	HCM	heart:	n/a
44	chr19:52102010-52102060	HEK293	kidney:	embryo
45	chr19:52103425-52103475	MCF-7	breast:	n/a
46	chr19:52104997-52105047	HEEpiC	esophagus:	n/a
47	chr19:52101661-52101711	AG04449	skin:	fetal
48	chr19:52104632-52104682	BE2_C	brain:	n/a
49	chr19:52103425-52103475	HUVEC	blood vessel:	n/a
50	chr19:52101874-52101924	BE2_C	brain:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:52097772..52099435-chr19:52099519..52102447,4	K562	blood:
2	chr19:52096005..52097791-chr19:52103717..52105932,2	K562	blood:
3	chr19:52075666..52078013-chr19:52102124..52103680,2	K562	blood:
4	chr19:52096005..52097791-chr19:52103717..52105932,2	K562	blood:
5	chr19:52073066..52077206-chr19:52096074..52099799,4	K562	blood:
6	chr19:52095454..52097791-chr19:52104410..52105932,2	K562	blood:
7	chr19:52095454..52097791-chr19:52104410..52105932,2	K562	blood:
8	chr19:52101743..52103546-chr19:52105521..52108118,2	K562	blood:
9	chr19:52097772..52099435-chr19:52099519..52102447,4	K562	blood:
10	chr19:51915124..51917429-chr19:52094517..52096646,2	K562	blood:
11	chr19:51897297..51899400-chr19:52095029..52099296,3	K562	blood:
12	chr19:51869850..51871538-chr19:52096656..52099033,2	K562	blood:
13	chr19:52098792..52101789-chr19:52105276..52108057,2	K562	blood:
14	chr19:52097873..52100049-chr19:52100051..52101814,3	K562	blood:
15	chr19:51914893..51917429-chr19:52094517..52097128,3	K562	blood:
16	chr19:52098792..52101789-chr19:52105276..52108057,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF175-3	chr19:52104965-52104999	NONHSAT067455
2	lnc-AC018755.11.1-1	chr19:52095036-52096304	NR_034159
3	lnc-AC018755.11.1-1	chr19:52097202-52097633	NR_034159
4	lnc-ZNF175-2	chr19:52102542-52103723	ENSG00000267808.1
5	lnc-ZNF175-3	chr19:52105456-52105735	NONHSAT067455

No data

Variant related genes	Relation type
ENSG00000267808	TF binding region
ENSG00000269388	TF binding region
ENSG00000167765	TF binding region
ENSG00000267808	CpG island
ENSG00000269388	CpG island
ENSG00000167765	CpG island
ENSG00000167765	chromatin interactions
ENSG00000267808	chromatin interactions
ENSG00000269403	chromatin interactions
ENSG00000269388	chromatin interactions
ENSG00000268889	chromatin interactions
ENSG00000160318	chromatin interactions
ENSG00000105497	chromatin interactions

Extended variants
information (count: 537 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:537 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3794982	chr19:52096270-52096271	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs569671752	chr19:52096277-52096278	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
3	rs200135933	chr19:52096281-52096282	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
4	rs112034079	chr19:52096282-52096283	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
5	rs140853073	chr19:52096300-52096301	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
6	rs62113349	chr19:52096473-52096474	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs35478449	chr19:52096528-52096529	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs66517854	chr19:52096529-52096530	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs144743788	chr19:52096534-52096535	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs563054609	chr19:52096558-52096559	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs529682762	chr19:52096569-52096570	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs76165901	chr19:52096597-52096598	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs73934238	chr19:52096664-52096665	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs527422071	chr19:52096667-52096668	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs62113350	chr19:52096677-52096678	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs568282529	chr19:52096686-52096687	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs199924066	chr19:52096713-52096714	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs137936369	chr19:52096721-52096722	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs554374466	chr19:52096886-52096887	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs186539424	chr19:52096898-52096899	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs57351606	chr19:52096903-52096904	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs75095793	chr19:52096938-52096939	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs188591234	chr19:52097021-52097022	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs10412978	chr19:52097030-52097031	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs554586616	chr19:52097037-52097038	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs572999200	chr19:52097058-52097059	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs540747380	chr19:52097060-52097061	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs375518956	chr19:52097062-52097063	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs142784941	chr19:52097065-52097066	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs557864691	chr19:52097113-52097114	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs577331635	chr19:52097139-52097140	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs372994959	chr19:52097150-52097151	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs544498447	chr19:52097176-52097177	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs7253296	chr19:52097177-52097178	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs575219410	chr19:52097195-52097196	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs58301181	chr19:52097261-52097262	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs560236288	chr19:52097300-52097301	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
38	rs527367236	chr19:52097343-52097344	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
39	rs562177349	chr19:52097390-52097391	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
40	rs151333477	chr19:52097397-52097398	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
41	rs35740364	chr19:52097401-52097402	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs564048421	chr19:52097413-52097414	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
43	rs200953422	chr19:52097433-52097434	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
44	rs549721174	chr19:52097452-52097453	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
45	rs7252645	chr19:52097461-52097462	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs535407612	chr19:52097509-52097510	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
47	rs548154874	chr19:52097549-52097550	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
48	rs141848717	chr19:52097560-52097561	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
49	rs566559410	chr19:52097572-52097573	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
50	rs7252767	chr19:52097586-52097587	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:65)

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
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
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian cancer	22174824	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Wilms tumour	21544195	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	CNVD
Glioblastoma multiforme	17002787	CNVD
Cervical cancer	21062161	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	16573809	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Adrenocortical carcinoma	18281524	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Cancer	20164920	CNVD
Melanoma	17363583	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:621 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:52075800-52096800	Weak transcription	HepG2	liver
2	chr19:52077000-52097000	Weak transcription	Hela-S3	cervix
3	chr19:52091200-52096400	Weak transcription	Brain Substantia Nigra	brain
4	chr19:52091200-52096400	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr19:52091200-52096600	Weak transcription	Right Ventricle	heart
6	chr19:52091200-52096800	Weak transcription	Small Intestine	intestine
7	chr19:52091400-52096400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr19:52091400-52096400	Weak transcription	Brain Angular Gyrus	brain
9	chr19:52091400-52096400	Weak transcription	Brain Hippocampus Middle	brain
10	chr19:52091400-52096400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr19:52091400-52096400	Weak transcription	Fetal Intestine Large	intestine
12	chr19:52091400-52096400	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr19:52091400-52096400	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr19:52091400-52096600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr19:52091400-52096600	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr19:52091400-52096600	Weak transcription	Colonic Mucosa	Colon
17	chr19:52091400-52096600	Weak transcription	Colon Smooth Muscle	Colon
18	chr19:52091400-52096800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr19:52091400-52096800	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr19:52091400-52096800	Weak transcription	Rectal Smooth Muscle	rectum
21	chr19:52091600-52096400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr19:52091600-52096400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr19:52091600-52096400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr19:52091600-52096400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr19:52091600-52096400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr19:52091600-52096400	Weak transcription	Esophagus	oesophagus
27	chr19:52091600-52096400	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr19:52091600-52096400	Weak transcription	Stomach Smooth Muscle	stomach
29	chr19:52091600-52096400	Weak transcription	Thymus	Thymus
30	chr19:52091600-52096600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr19:52091600-52096600	Weak transcription	Adipose Nuclei	Adipose
32	chr19:52091600-52096600	Weak transcription	Fetal Muscle Leg	muscle
33	chr19:52091600-52096600	Weak transcription	Fetal Thymus	thymus
34	chr19:52091600-52096600	Weak transcription	Left Ventricle	heart
35	chr19:52091600-52096600	Weak transcription	Ovary	ovary
36	chr19:52091600-52096600	Weak transcription	NHEK	skin
37	chr19:52091600-52096800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr19:52091600-52097000	Weak transcription	Aorta	Aorta
39	chr19:52091800-52096400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr19:52091800-52096400	Weak transcription	Duodenum Mucosa	Duodenum
41	chr19:52091800-52096400	Weak transcription	GM12878-XiMat	blood
42	chr19:52091800-52096600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr19:52091800-52096600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr19:52091800-52096600	Weak transcription	Primary B cells from cord blood	blood
45	chr19:52091800-52096600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr19:52091800-52096600	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chr19:52091800-52096600	Weak transcription	Fetal Heart	heart
48	chr19:52091800-52096600	Weak transcription	Fetal Kidney	kidney
49	chr19:52091800-52096600	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr19:52091800-52096600	Weak transcription	Monocytes-CD14+_RO01746	blood

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