Variant report

Variant	nsv834457
Chromosome Location	chr2:172564939-172770901
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1731)
CpG islands
(count:977)
Chromatin interactive
region (count:173)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:1731 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:172663623-172663906	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:172667674-172668055	K562	blood:	n/a	n/a
3	ARID3A	chr2:172664221-172665139	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:172628651-172629610	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:172630180-172630274	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:172619372-172620031	HepG2	liver:	n/a	chr2:172619462-172619478
7	ARID3A	chr2:172667714-172668020	HepG2	liver:	n/a	n/a
8	ARID3A	chr2:172654707-172655146	HepG2	liver:	n/a	n/a
9	ARID3A	chr2:172585333-172586628	HepG2	liver:	n/a	n/a
10	ARID3A	chr2:172627314-172627323	K562	blood:	n/a	n/a
11	ARID3A	chr2:172750965-172751421	HepG2	liver:	n/a	n/a
12	ARID3A	chr2:172694396-172694624	HepG2	liver:	n/a	n/a
13	ARID3A	chr2:172735003-172735365	K562	blood:	n/a	n/a
14	ATF1	chr2:172667707-172668101	K562	blood:	n/a	n/a
15	ATF1	chr2:172655035-172655200	K562	blood:	n/a	n/a
16	ATF1	chr2:172663664-172663907	K562	blood:	n/a	n/a
17	ATF1	chr2:172734902-172735401	K562	blood:	n/a	n/a
18	ATF1	chr2:172766410-172766582	K562	blood:	n/a	n/a
19	ATF2	chr2:172750268-172750816	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr2:172766500-172766666	K562	blood:	n/a	n/a
21	BACH1	chr2:172751659-172751671	K562	blood:	n/a	n/a
22	BACH1	chr2:172750850-172751101	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr2:172580904-172581190	K562	blood:	n/a	chr2:172581133-172581147
24	BACH1	chr2:172632217-172632246	K562	blood:	n/a	n/a
25	BACH1	chr2:172580883-172581063	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr2:172571403-172571521	K562	blood:	n/a	n/a
27	BATF	chr2:172767114-172767279	GM12878	blood:	n/a	n/a
28	BATF	chr2:172734927-172735228	GM12878	blood:	n/a	n/a
29	BATF	chr2:172734980-172735230	GM12878	blood:	n/a	n/a
30	BATF	chr2:172663707-172663905	GM12878	blood:	n/a	chr2:172663803-172663813 chr2:172663802-172663813
31	BCL3	chr2:172750129-172750590	A549	lung:	n/a	chr2:172750443-172750452 chr2:172750574-172750587
32	BCLAF1	chr2:172750536-172751395	GM12878	blood:	n/a	chr2:172750574-172750587 chr2:172750918-172750931
33	BHLHE40	chr2:172735026-172735408	K562	blood:	n/a	n/a
34	BHLHE40	chr2:172750385-172751676	K562	blood:	n/a	chr2:172750859-172750875
35	BHLHE40	chr2:172654817-172654933	HepG2	liver:	n/a	n/a
36	BHLHE40	chr2:172580945-172581161	K562	blood:	n/a	n/a
37	BHLHE40	chr2:172585532-172586183	HepG2	liver:	n/a	n/a
38	BHLHE40	chr2:172750285-172751218	HepG2	liver:	n/a	chr2:172750859-172750875
39	BHLHE40	chr2:172750429-172751255	GM12878	blood:	n/a	chr2:172750859-172750875
40	BHLHE40	chr2:172628955-172629189	HepG2	liver:	n/a	n/a
41	BHLHE40	chr2:172654984-172655159	K562	blood:	n/a	n/a
42	CBX3	chr2:172734924-172735552	K562	blood:	n/a	chr2:172735491-172735502
43	CBX3	chr2:172687901-172688240	K562	blood:	n/a	n/a
44	CBX3	chr2:172750220-172751418	K562	blood:	n/a	n/a
45	CBX3	chr2:172687874-172688299	K562	blood:	n/a	n/a
46	CBX3	chr2:172687834-172688254	HCT-116	colon:	n/a	n/a
47	CBX3	chr2:172755013-172755358	K562	blood:	n/a	n/a
48	CBX3	chr2:172687974-172688322	HCT-116	colon:	n/a	n/a
49	CBX3	chr2:172754901-172755400	K562	blood:	n/a	n/a
50	CCNT2	chr2:172750542-172751128	K562	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	chr2:172747482-172747532	HUVEC	blood vessel:	n/a
2	chr2:172747482-172747532	HUVEC	blood vessel:	n/a
3	chr2:172750783-172750833	Hepatocyte	liver:	n/a
4	chr2:172751016-172751066	PrEC	prostate:	n/a
5	chr2:172751074-172751124	RPTEC	kidney:	n/a
6	chr2:172751074-172751124	MCF10A-Er-Src	breast:	n/a
7	chr2:172734703-172734753	SK-N-SH	brain:	n/a
8	chr2:172750719-172750769	AG09319	gingival:	n/a
9	chr2:172747482-172747532	Caco-2	colon:	n/a
10	chr2:172734703-172734753	ovcar-3	ovarian:	n/a
11	chr2:172750719-172750769	HCPEpiC	choroid plexus:	n/a
12	chr2:172750783-172750833	Caco-2	colon:	n/a
13	chr2:172645256-172645306	GM12878	blood:	n/a
14	chr2:172756307-172756357	PANC-1	pancreas:	n/a
15	chr2:172734703-172734753	SK-N-SH_RA	brain:	n/a
16	chr2:172734703-172734753	SKMC	muscle:	n/a
17	chr2:172645256-172645306	NHDF-neo	bronchial:	n/a
18	chr2:172650722-172650772	HRCEpiC	kidney:	n/a
19	chr2:172751088-172751138	MCF-7	breast:	n/a
20	chr2:172734703-172734753	NHDF-neo	bronchial:	n/a
21	chr2:172653274-172653324	HCF	heart:	n/a
22	chr2:172750994-172751044	PFSK-1	brain:	n/a
23	chr2:172751088-172751138	MCF10A-Er-Src	breast:	n/a
24	chr2:172641053-172641103	PrEC	prostate:	n/a
25	chr2:172750783-172750833	Hela-S3	cervix:	n/a
26	chr2:172750996-172751046	PFSK-1	brain:	n/a
27	chr2:172751016-172751066	RPTEC	kidney:	n/a
28	chr2:172734703-172734753	LNCaP	prostate:	n/a
29	chr2:172750719-172750769	HCF	heart:	n/a
30	chr2:172645256-172645306	BE2_C	brain:	n/a
31	chr2:172751016-172751066	GM19239	blood:	n/a
32	chr2:172750994-172751044	HepG2	liver:	n/a
33	chr2:172645256-172645306	MCF-7	breast:	n/a
34	chr2:172751088-172751138	HRPEpiC	eye:	n/a
35	chr2:172751074-172751124	ECC-1	luminal epithelium:	n/a
36	chr2:172650722-172650772	NH-A	brain:	n/a
37	chr2:172750661-172750711	BE2_C	brain:	n/a
38	chr2:172751016-172751066	HPAEpiC	pulmonary alveolar:	n/a
39	chr2:172750783-172750833	MCF10A-Er-Src	breast:	n/a
40	chr2:172751088-172751138	HepG2	liver:	n/a
41	chr2:172747482-172747532	K562	blood:	n/a
42	chr2:172750719-172750769	HUVEC	blood vessel:	n/a
43	chr2:172750996-172751046	Caco-2	colon:	n/a
44	chr2:172650722-172650772	AoSMC	blood vessel:	n/a
45	chr2:172645256-172645306	AG04450	lung:	fetal
46	chr2:172650722-172650772	HL-60	blood:	n/a
47	chr2:172751074-172751124	GM12892	blood:	n/a
48	chr2:172747482-172747532	AG04450	lung:	fetal
49	chr2:172750996-172751046	RPTEC	kidney:	n/a
50	chr2:172750661-172750711	GM19239	blood:	n/a

(count:173 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr2:172622700..172625512-chr2:172948357..172950530,2	K562	blood:
2	chr2:172720314..172722919-chr2:172744324..172746947,2	K562	blood:
3	chr2:172750354..172753126-chr2:172762746..172766983,5	MCF-7	breast:
4	chr2:172698622..172703344-chr2:172704675..172709046,4	K562	blood:
5	chr2:172750984..172752854-chr2:172776378..172780395,4	K562	blood:
6	chr2:172733666..172736692-chr2:172737293..172740256,4	K562	blood:
7	chr2:172578698..172580844-chr2:172604273..172606740,2	MCF-7	breast:
8	chr2:172656554..172659415-chr2:172948185..172950297,2	MCF-7	breast:
9	chr2:172690614..172693889-chr2:172702075..172704679,3	MCF-7	breast:
10	chr2:172289011..172290991-chr2:172749560..172752051,2	K562	blood:
11	chr2:172667461..172668379-chr2:172991701..172992562,2	K562	blood:
12	chr2:172733649..172740490-chr2:172749209..172752081,6	MCF-7	breast:
13	chr2:172767380..172770009-chr2:172775350..172777979,2	MCF-7	breast:
14	chr2:172666865..172669290-chr2:172948316..172950744,2	MCF-7	breast:
15	chr2:172585756..172589058-chr2:172589522..172592081,3	MCF-7	breast:
16	chr2:172746433..172748218-chr2:172754634..172756631,2	K562	blood:
17	chr2:172636565..172640348-chr2:172640968..172644401,3	MCF-7	breast:
18	chr2:172764720..172767665-chr2:172778015..172780432,2	K562	blood:
19	chr2:172738739..172740537-chr2:172778754..172780412,2	MCF-7	breast:
20	chr2:172599628..172601946-chr2:172603604..172606469,3	K562	blood:
21	chr2:172624804..172627383-chr2:172628518..172631199,2	K562	blood:
22	chr2:172577655..172579971-chr2:172783366..172785140,2	K562	blood:
23	chr2:172684640..172686879-chr2:172687489..172690776,3	K562	blood:
24	chr2:172570316..172572538-chr2:172576529..172578048,2	MCF-7	breast:
25	chr2:172669767..172671872-chr2:172676820..172679924,3	K562	blood:
26	chr2:172737251..172741632-chr2:172744127..172746151,4	K562	blood:
27	chr2:172722204..172724793-chr2:172734963..172736476,2	K562	blood:
28	chr2:172701236..172703599-chr2:172719950..172722171,2	K562	blood:
29	chr2:172578420..172580000-chr2:172586848..172589301,2	MCF-7	breast:
30	chr2:172568856..172572194-chr2:172572515..172575920,3	K562	blood:
31	chr2:172769627..172771187-chr2:172785586..172788506,2	K562	blood:
32	chr2:172642743..172644911-chr2:172668781..172670774,2	K562	blood:
33	chr2:172657341..172659183-chr2:172664680..172667470,2	K562	blood:
34	chr2:172758196..172762608-chr2:172762704..172765555,5	K562	blood:
35	chr2:172746433..172748218-chr2:172754634..172756631,2	K562	blood:
36	chr2:172673517..172675266-chr2:172684577..172687349,2	K562	blood:
37	chr2:172749328..172751742-chr2:172775594..172779310,3	MCF-7	breast:
38	chr2:172679219..172682051-chr2:172683706..172687568,3	K562	blood:
39	chr2:172737244..172739400-chr2:172984997..172987788,2	MCF-7	breast:
40	chr2:172669767..172671872-chr2:172676820..172679924,3	K562	blood:
41	chr2:172764440..172768356-chr2:172769175..172774540,8	K562	blood:
42	chr2:172734512..172737227-chr2:172778831..172780357,3	K562	blood:
43	chr2:172745241..172748938-chr2:172777169..172782251,7	K562	blood:
44	chr2:172764440..172768356-chr2:172769175..172774540,8	K562	blood:
45	chr2:172749780..172752389-chr2:172759130..172760701,2	K562	blood:
46	chr2:172542927..172544505-chr2:172566367..172569318,2	K562	blood:
47	chr2:172749510..172752866-chr2:172752874..172756053,4	K562	blood:
48	chr2:172665538..172668846-chr2:172671446..172673879,3	K562	blood:
49	chr2:172692494..172694148-chr2:172705814..172708790,3	K562	blood:
50	chr2:172696413..172698762-chr2:172699806..172701539,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DLX2-6	chr2:172664764-172665001	uc_98_-
2	lnc-DYNC1I2-3	chr2:172664764-172665001	uc_98_+
3	lnc-DYNC1I2-4	chr2:172666627-172667024	uc_99_+
4	lnc-DLX2-8	chr2:172666627-172667024	uc_99_-

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	SLC25A12	hsa-let-7f-5p	chr2:172640126-172640147
2	SLC25A12	hsa-miR-30c-5p	chr2:172641633-172641655
3	SLC25A12	hsa-let-7b-5p	chr2:172640126-172640146

Variant related genes	Relation type
ENSG00000228389	TF binding region
DYNC1I2	TF binding region
ENSG00000268821	TF binding region
RNU6-182P	TF binding region
SLC25A12	TF binding region
ENSG00000228389	CpG island
DYNC1I2	CpG island
ENSG00000268821	CpG island
RNU6-182P	CpG island
SLC25A12	CpG island
ENSG00000236651	chromatin interactions
ENSG00000136938	chromatin interactions
ENSG00000172878	chromatin interactions
ENSG00000115844	chromatin interactions
ENSG00000144355	chromatin interactions
ENSG00000115827	chromatin interactions
ENSG00000268821	chromatin interactions
ENSG00000170537	chromatin interactions
ENSG00000128708	chromatin interactions
ENSG00000228389	chromatin interactions
ENSG00000115840	chromatin interactions
ENSG00000252779	chromatin interactions
ENSG00000123600	chromatin interactions
ENSG00000077380	chromatin interactions

Extended variants
information (count: 7040 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:7040 , 50 per page) page: 1 2 3 4 5 6 7 ... 141

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146166632	chr2:172564973-172564974	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs370807374	chr2:172564991-172564992	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs576848675	chr2:172564998-172564999	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs543834196	chr2:172565022-172565023	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs375628167	chr2:172565106-172565107	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs182630803	chr2:172565140-172565141	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs186772799	chr2:172565151-172565152	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs201187028	chr2:172565152-172565153	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs80044521	chr2:172565160-172565161	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs191589108	chr2:172565259-172565260	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs560094480	chr2:172565263-172565264	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs527531588	chr2:172565303-172565304	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs552081083	chr2:172565329-172565330	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs57949060	chr2:172565352-172565353	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs564635962	chr2:172565401-172565402	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs184143103	chr2:172565422-172565423	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs534104561	chr2:172565445-172565446	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs187325530	chr2:172565481-172565482	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs192917691	chr2:172565509-172565510	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs185494232	chr2:172565521-172565522	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs528683322	chr2:172565534-172565535	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs140156566	chr2:172565546-172565547	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs312923	chr2:172565576-172565577	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs540059827	chr2:172565601-172565602	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs190458286	chr2:172565614-172565615	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs368365801	chr2:172565623-172565624	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs537515110	chr2:172565747-172565748	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs73976504	chr2:172565750-172565751	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs114887845	chr2:172565835-172565836	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs537907333	chr2:172565863-172565864	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs182542835	chr2:172565865-172565866	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs555992255	chr2:172565911-172565912	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs148960644	chr2:172565938-172565939	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs572234117	chr2:172565941-172565942	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs546010017	chr2:172565985-172565986	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs183713004	chr2:172566061-172566062	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs142885584	chr2:172566079-172566080	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs371033769	chr2:172566091-172566092	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs543897632	chr2:172566152-172566153	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs532117834	chr2:172566170-172566171	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs200418970	chr2:172566188-172566189	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs188480228	chr2:172566189-172566190	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs552544382	chr2:172566252-172566253	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs547465957	chr2:172566273-172566274	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs13432293	chr2:172566291-172566292	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs151058663	chr2:172566382-172566383	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs368867054	chr2:172566385-172566386	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs13406639	chr2:172566461-172566462	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs551965429	chr2:172566485-172566486	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs142208120	chr2:172566525-172566526	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Prostate cancer	16573809	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Donnai-Barrow syndrome	21085971	CNVD
Breast cancer	21045282	CNVD
Limb abnormalities	22140379	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	21364760	CNVD
Chronic myeloid leukemia	21384125	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD

Chromatin state (count:4659 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:172545000-172580200	Weak transcription	Pancreas	Pancrea
2	chr2:172545000-172580400	Weak transcription	Spleen	Spleen
3	chr2:172545000-172580800	Weak transcription	Gastric	stomach
4	chr2:172545200-172611200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr2:172545400-172588000	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr2:172545800-172573000	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr2:172545800-172575400	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr2:172545800-172588000	Weak transcription	Right Ventricle	heart
9	chr2:172546000-172567800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr2:172546000-172568600	Weak transcription	Hela-S3	cervix
11	chr2:172546400-172574600	Weak transcription	Right Atrium	heart
12	chr2:172546600-172602800	Weak transcription	Small Intestine	intestine
13	chr2:172547000-172578600	Weak transcription	Fetal Brain Male	brain
14	chr2:172548200-172571800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr2:172548400-172579600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr2:172550200-172567800	Weak transcription	Dnd41	blood
17	chr2:172551600-172584400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr2:172552200-172573400	Weak transcription	Fetal Brain Female	brain
19	chr2:172552200-172587600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr2:172554000-172580200	Weak transcription	Aorta	Aorta
21	chr2:172554400-172566200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr2:172554400-172588000	Weak transcription	Esophagus	oesophagus
23	chr2:172554600-172572000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr2:172554600-172572200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr2:172554800-172580400	Weak transcription	K562	blood
26	chr2:172555000-172566400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr2:172555000-172571800	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr2:172555000-172571800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
29	chr2:172555000-172580200	Weak transcription	Brain Anterior Caudate	brain
30	chr2:172555600-172566400	Weak transcription	Primary neutrophils fromperipheralblood	blood
31	chr2:172556800-172568600	Weak transcription	Fetal Kidney	kidney
32	chr2:172557000-172566200	Weak transcription	Left Ventricle	heart
33	chr2:172557000-172568600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
34	chr2:172557000-172571800	Weak transcription	Duodenum Mucosa	Duodenum
35	chr2:172557400-172584400	Weak transcription	Ovary	ovary
36	chr2:172557600-172572200	Weak transcription	Stomach Smooth Muscle	stomach
37	chr2:172558000-172565200	Weak transcription	Fetal Stomach	stomach
38	chr2:172558000-172574600	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr2:172558800-172571800	Weak transcription	Liver	Liver
40	chr2:172558800-172583400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr2:172559000-172568000	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr2:172559000-172585000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr2:172559600-172566200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr2:172559600-172567800	Weak transcription	NHLF	lung
45	chr2:172559600-172572000	Weak transcription	GM12878-XiMat	blood
46	chr2:172559600-172605200	Weak transcription	Colonic Mucosa	Colon
47	chr2:172559800-172566600	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr2:172559800-172571600	Weak transcription	Primary hematopoietic stem cells	blood
49	chr2:172559800-172571600	Weak transcription	Primary T helper cells PMA-I stimulated	--
50	chr2:172559800-172571800	Weak transcription	Adipose Nuclei	Adipose

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