Variant report

Variant	nsv897193
Chromosome Location	chr11:32838288-32903263
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:32851965-32852404	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:32850824-32851272	HepG2	liver:	n/a	n/a
3	ATF1	chr11:32888538-32888562	K562	blood:	n/a	n/a
4	ATF1	chr11:32878012-32878101	K562	blood:	n/a	n/a
5	ATF2	chr11:32850594-32851339	GM12878	blood:	n/a	n/a
6	ATF2	chr11:32850720-32851321	GM12878	blood:	n/a	n/a
7	BACH1	chr11:32862150-32862517	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr11:32902869-32903255	GM12878	blood:	n/a	n/a
9	BHLHE40	chr11:32846405-32846534	K562	blood:	n/a	n/a
10	BRCA1	chr11:32851524-32851531	GM12878	blood:	n/a	n/a
11	BRCA1	chr11:32897267-32897327	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr11:32851255-32851263	H1-hESC	embryonic stem cell:	n/a	n/a
13	BRCA1	chr11:32850715-32851268	Hela-S3	cervix:	n/a	n/a
14	CCNT2	chr11:32860829-32861008	K562	blood:	n/a	n/a
15	CEBPB	chr11:32852029-32852224	HepG2	liver:	n/a	chr11:32852133-32852144
16	CEBPB	chr11:32902896-32903471	IMR90	lung:	n/a	chr11:32903447-32903460
17	CEBPB	chr11:32865173-32865425	A549	lung:	n/a	chr11:32865248-32865259 chr11:32865290-32865301
18	CEBPB	chr11:32860171-32860840	ECC-1	luminal epithelium:	n/a	chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860560-32860573 chr11:32860560-32860571
19	CEBPB	chr11:32860199-32860800	MCF-7	breast:	n/a	chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860560-32860573 chr11:32860560-32860571
20	CEBPB	chr11:32899306-32899511	K562	blood:	n/a	n/a
21	CEBPB	chr11:32851813-32852506	MCF-7	breast:	n/a	chr11:32852309-32852320 chr11:32852133-32852144 chr11:32852309-32852322
22	CEBPB	chr11:32850788-32851520	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr11:32873897-32874252	K562	blood:	n/a	chr11:32874038-32874049
24	CEBPB	chr11:32873880-32874218	HepG2	liver:	n/a	chr11:32874038-32874049
25	CEBPB	chr11:32873949-32874191	IMR90	lung:	n/a	chr11:32874038-32874049
26	CEBPB	chr11:32851061-32851240	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr11:32851943-32852334	A549	lung:	n/a	chr11:32852309-32852320 chr11:32852133-32852144 chr11:32852309-32852322
28	CEBPB	chr11:32865136-32865413	K562	blood:	n/a	chr11:32865248-32865259 chr11:32865290-32865301
29	CEBPB	chr11:32892287-32892573	A549	lung:	n/a	n/a
30	CEBPB	chr11:32860376-32860759	IMR90	lung:	n/a	chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860560-32860573 chr11:32860560-32860571
31	CEBPB	chr11:32840508-32840570	A549	lung:	n/a	chr11:32840539-32840550
32	CEBPB	chr11:32860071-32860812	HCT-116	colon:	n/a	chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860560-32860573 chr11:32860560-32860571
33	CEBPB	chr11:32860368-32860760	H1-hESC	embryonic stem cell:	n/a	chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860560-32860573 chr11:32860560-32860571
34	CEBPB	chr11:32845218-32845505	HepG2	liver:	n/a	chr11:32845341-32845352
35	CEBPB	chr11:32843083-32843471	Hela-S3	cervix:	n/a	chr11:32843425-32843433
36	CEBPB	chr11:32860125-32861051	MCF-7	breast:	n/a	chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860560-32860573 chr11:32860560-32860571
37	CEBPB	chr11:32860453-32860674	K562	blood:	n/a	chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860560-32860573 chr11:32860560-32860571
38	CEBPB	chr11:32892285-32892603	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr11:32851942-32852327	K562	blood:	n/a	chr11:32852309-32852320 chr11:32852133-32852144 chr11:32852309-32852322
40	CEBPB	chr11:32860025-32860806	HCT-116	colon:	n/a	chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860560-32860573 chr11:32860560-32860571
41	CEBPB	chr11:32860134-32860823	ECC-1	luminal epithelium:	n/a	chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860560-32860573 chr11:32860560-32860571
42	CEBPB	chr11:32860503-32860617	HepG2	liver:	n/a	chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860562-32860571 chr11:32860560-32860573 chr11:32860560-32860571
43	CEBPB	chr11:32845224-32845500	A549	lung:	n/a	chr11:32845341-32845352
44	CEBPB	chr11:32851807-32852532	A549	lung:	n/a	chr11:32852309-32852320 chr11:32852133-32852144 chr11:32852309-32852322
45	CEBPB	chr11:32851870-32852240	HepG2	liver:	n/a	chr11:32852133-32852144
46	CEBPB	chr11:32873859-32874214	Hela-S3	cervix:	n/a	chr11:32874038-32874049
47	CEBPB	chr11:32883794-32884138	HepG2	liver:	n/a	n/a
48	CEBPB	chr11:32851940-32852322	HepG2	liver:	n/a	chr11:32852309-32852320 chr11:32852133-32852144 chr11:32852309-32852322
49	CEBPB	chr11:32851793-32852346	H1-hESC	embryonic stem cell:	n/a	chr11:32852309-32852320 chr11:32852133-32852144 chr11:32852309-32852322
50	CEBPB	chr11:32873881-32874288	A549	lung:	n/a	chr11:32874038-32874049

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:32851177-32851227	Hepatocyte	liver:	n/a
2	chr11:32854320-32854370	ECC-1	luminal epithelium:	n/a
3	chr11:32875930-32875980	Hela-S3	cervix:	n/a
4	chr11:32851260-32851310	HRE	kidney:	n/a
5	chr11:32851260-32851310	Hela-S3	cervix:	n/a
6	chr11:32851260-32851310	HUVEC	blood vessel:	n/a
7	chr11:32853267-32853317	BJ	skin:	n/a
8	chr11:32854320-32854370	HUVEC	blood vessel:	n/a
9	chr11:32847480-32847530	HepG2	liver:	n/a
10	chr11:32853267-32853317	HL-60	blood:	n/a
11	chr11:32847480-32847530	HCM	heart:	n/a
12	chr11:32851240-32851290	NHDF-neo	bronchial:	n/a
13	chr11:32854320-32854370	HRPEpiC	eye:	n/a
14	chr11:32851356-32851406	AG09319	gingival:	n/a
15	chr11:32851177-32851227	SK-N-SH	brain:	n/a
16	chr11:32851371-32851421	HUVEC	blood vessel:	n/a
17	chr11:32851260-32851310	GM19239	blood:	n/a
18	chr11:32847480-32847530	GM06990	blood:	n/a
19	chr11:32851371-32851421	NB4	blood:	n/a
20	chr11:32847480-32847530	AG04449	skin:	fetal
21	chr11:32851346-32851396	SAEC	small airway:	n/a
22	chr11:32847480-32847530	IMR90	lung:	fetal
23	chr11:32853267-32853317	HRE	kidney:	n/a
24	chr11:32875930-32875980	ovcar-3	ovarian:	n/a
25	chr11:32851356-32851406	HL-60	blood:	n/a
26	chr11:32851240-32851290	HMEC	breast:	n/a
27	chr11:32851531-32851581	HCF	heart:	n/a
28	chr11:32851177-32851227	HCM	heart:	n/a
29	chr11:32851378-32851428	NT2-D1	testis:	n/a
30	chr11:32851371-32851421	GM12878	blood:	n/a
31	chr11:32851177-32851227	HRE	kidney:	n/a
32	chr11:32851378-32851428	K562	blood:	n/a
33	chr11:32851361-32851411	ECC-1	luminal epithelium:	n/a
34	chr11:32847480-32847530	Caco-2	colon:	n/a
35	chr11:32851346-32851396	HEEpiC	esophagus:	n/a
36	chr11:32851087-32851137	SAEC	small airway:	n/a
37	chr11:32851361-32851411	K562	blood:	n/a
38	chr11:32847480-32847530	BE2_C	brain:	n/a
39	chr11:32851346-32851396	NHBE	bronchial:	n/a
40	chr11:32853267-32853317	SK-N-MC	brain:	n/a
41	chr11:32847480-32847530	NH-A	brain:	n/a
42	chr11:32851346-32851396	HCM	heart:	n/a
43	chr11:32851950-32852000	BJ	skin:	n/a
44	chr11:32851346-32851396	HRE	kidney:	n/a
45	chr11:32851950-32852000	RPTEC	kidney:	n/a
46	chr11:32851371-32851421	H1-hESC	embryonic stem cell:	embryo
47	chr11:32851371-32851421	HMEC	breast:	n/a
48	chr11:32851361-32851411	AG04449	skin:	fetal
49	chr11:32851361-32851411	HCPEpiC	choroid plexus:	n/a
50	chr11:32851950-32852000	GM06990	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:32851461..32852210-chr3:49058647..49059440,2	NB4	blood:
2	chr11:32900766..32903313-chr11:32912451..32914688,2	K562	blood:
3	chr11:32854588..32857057-chr11:32860540..32862429,2	K562	blood:
4	chr11:32845133..32847624-chr11:32847772..32849617,2	MCF-7	breast:
5	chr11:32851440..32852221-chr2:173420119..173420696,2	Hela-S3	cervix:
6	chr11:32861977..32862713-chr14:65386776..65387380,2	MCF-7	breast:
7	chr11:32854588..32857057-chr11:32860540..32862429,2	K562	blood:
8	chr11:32847589..32849311-chr11:32913725..32915620,2	K562	blood:
9	chr11:32873372..32875504-chr11:32882412..32884075,2	K562	blood:
10	chr11:32892015..32892872-chr11:32914554..32915403,2	MCF-7	breast:
11	chr11:32858756..32863139-chr11:32912593..32915314,4	MCF-7	breast:
12	chr11:32892094..32893817-chr11:32914118..32916253,2	K562	blood:
13	chr11:32873372..32875504-chr11:32882412..32884075,2	K562	blood:
14	chr11:32835440..32837233-chr11:32841490..32844292,2	K562	blood:
15	chr11:32851420..32852136-chr5:36606640..36607218,2	Hela-S3	cervix:
16	chr11:32851187..32853645-chr11:32854709..32858523,6	MCF-7	breast:
17	chr11:32850866..32853799-chr11:32862127..32863701,2	MCF-7	breast:
18	chr11:32850955..32851927-chr16:89752956..89753523,2	Hela-S3	cervix:
19	chr11:32862368..32865112-chr11:32868900..32870710,2	K562	blood:
20	chr11:32849868..32852880-chr11:32911360..32916794,6	MCF-7	breast:
21	chr11:32851076..32851981-chr12:123011655..123012268,2	Hela-S3	cervix:
22	chr11:32851501..32854370-chr11:32879596..32881538,2	MCF-7	breast:
23	chr11:32851501..32854370-chr11:32879596..32881538,2	MCF-7	breast:
24	chr11:32845133..32847624-chr11:32847772..32849617,2	MCF-7	breast:
25	chr11:32862368..32865112-chr11:32868900..32870710,2	K562	blood:
26	chr11:32850121..32852277-chr11:33088797..33091531,2	MCF-7	breast:
27	chr11:32843099..32845929-chr11:32851383..32853799,2	MCF-7	breast:
28	chr11:32850001..32854483-chr11:32912810..32915962,5	MCF-7	breast:
29	chr11:32862183..32864294-chr11:32914218..32916079,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCDC73-1	chr11:32875249-32875810	ENSG00000248689
2	lnc-PRRG4-2	chr11:32839176-32839252	NONHSAT018676
3	lnc-CCDC73-1	chr11:32878982-32879665	ENSG00000248689
4	lnc-PRRG4-1	chr11:32846016-32846832	NONHSAT018677
5	lnc-QSER1-1	chr11:32878980-32879666	NONHSAT018678
6	lnc-QSER1-1	chr11:32875249-32875808	NONHSAT018678
7	lnc-PRRG4-2	chr11:32839485-32839664	NONHSAT018676

Variant related genes	Relation type
PRRG4	TF binding region
PRRG4	CpG island
ENSG00000079215	chromatin interactions
ENSG00000178057	chromatin interactions
ENSG00000152256	chromatin interactions
ENSG00000260259	chromatin interactions
ENSG00000060749	chromatin interactions
ENSG00000185324	chromatin interactions
ENSG00000184445	chromatin interactions
ENSG00000178149	chromatin interactions
ENSG00000135378	chromatin interactions
ENSG00000176148	chromatin interactions
FBXW7	miRNA target sites
LMAN2L	miRNA target sites

Extended variants
information (count: 1959 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1959 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs197710	chr11:32838288-32838289	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs557814177	chr11:32838314-32838315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs189053485	chr11:32838322-32838323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs549776073	chr11:32838407-32838408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs141190184	chr11:32838430-32838431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs553862430	chr11:32838436-32838437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573780433	chr11:32838438-32838439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs542427352	chr11:32838442-32838443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs556435426	chr11:32838486-32838487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs373770075	chr11:32838502-32838503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs576291334	chr11:32838503-32838504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs569700023	chr11:32838519-32838520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs564987074	chr11:32838548-32838549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs197709	chr11:32838556-32838557	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs541138881	chr11:32838558-32838559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs555639484	chr11:32838573-32838574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs568778417	chr11:32838610-32838611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs35946642	chr11:32838620-32838621	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs200109223	chr11:32838724-32838725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs35052572	chr11:32838766-32838767	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs111894554	chr11:32838829-32838830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs377218928	chr11:32838873-32838874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs532901534	chr11:32838884-32838885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs552893328	chr11:32838887-32838888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs571272401	chr11:32838918-32838919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs529960172	chr11:32839022-32839023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs58961816	chr11:32839077-32839078	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs71479182	chr11:32839079-32839080	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs536328575	chr11:32839084-32839085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs556111081	chr11:32839111-32839112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs576184296	chr11:32839165-32839166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs115707183	chr11:32839205-32839206	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs563326978	chr11:32839222-32839223	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs572111950	chr11:32839223-32839224	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs540999674	chr11:32839231-32839232	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs536164798	chr11:32839256-32839257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs574871832	chr11:32839286-32839287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs575287930	chr11:32839393-32839394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs373867808	chr11:32839415-32839416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs181722709	chr11:32839432-32839433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs111668017	chr11:32839470-32839471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs375580532	chr11:32839479-32839480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs375823783	chr11:32839524-32839525	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs532712745	chr11:32839553-32839554	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs542990436	chr11:32839559-32839560	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs150863248	chr11:32839615-32839616	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs138265514	chr11:32839630-32839631	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs547110578	chr11:32839673-32839674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs184095912	chr11:32839694-32839695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs188775447	chr11:32839711-32839712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	22286061	CNVD
Aniridia syndrome	21572526	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Retinoblastoma	22278416	CNVD
Denys-drash syndrome	21085971	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
WAGR syndrome	16773131	CNVD
Disorders of sex development	22290220	CNVD
Aniridia syndrome	17204608	CNVD
Mental retardation	17204608	CNVD
WAGR syndrome	19617690	CNVD
genitourinary abnormalities	17204608	CNVD
Breast cancer	16397240	CNVD
Mental retardation	16773131	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Cancer	21183584	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
WAGR syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Denys-drash syndrome	19566914	CNVD
Familial wilms tumor	19566914	CNVD
Frasier syndrome	19566914	CNVD
Non-small cell lung cancer	21829676	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ependymoma	20639864	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:32837400-32850800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr11:32837600-32839800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr11:32838800-32839800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr11:32838800-32839800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr11:32838800-32839800	Enhancers	NHEK	skin
6	chr11:32839000-32839800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr11:32839200-32839800	Enhancers	Hela-S3	cervix
8	chr11:32839200-32840000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr11:32839400-32839600	Enhancers	HSMM	muscle
10	chr11:32839400-32839600	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr11:32839400-32839800	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr11:32839400-32840000	Enhancers	Liver	Liver
13	chr11:32839800-32841200	Weak transcription	HSMM	muscle
14	chr11:32839800-32841800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr11:32839800-32841800	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr11:32839800-32841800	Weak transcription	Hela-S3	cervix
17	chr11:32839800-32842000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr11:32839800-32842200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr11:32839800-32842200	Weak transcription	NHEK	skin
20	chr11:32839800-32843400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr11:32840000-32841800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr11:32840000-32850200	Weak transcription	Liver	Liver
23	chr11:32841600-32844000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr11:32841800-32843200	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr11:32841800-32843800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr11:32841800-32844000	Enhancers	Hela-S3	cervix
27	chr11:32841800-32844200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr11:32841800-32846400	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr11:32842000-32842400	Enhancers	HMEC	breast
30	chr11:32842000-32843200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr11:32842200-32843800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr11:32842200-32844000	Enhancers	NHEK	skin
33	chr11:32842400-32843400	Weak transcription	HMEC	breast
34	chr11:32843000-32843200	Enhancers	GM12878-XiMat	blood
35	chr11:32843200-32843600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr11:32843200-32844000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr11:32843200-32844000	Flanking Active TSS	GM12878-XiMat	blood
38	chr11:32843200-32844000	Enhancers	HSMM	muscle
39	chr11:32843200-32844600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
40	chr11:32843200-32846600	Enhancers	Primary neutrophils fromperipheralblood	blood
41	chr11:32843200-32850800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr11:32843400-32843600	Enhancers	Primary hematopoietic stem cells	blood
43	chr11:32843400-32843800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr11:32843400-32844000	Enhancers	HMEC	breast
45	chr11:32843600-32850200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr11:32843800-32850600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr11:32844000-32844200	Enhancers	GM12878-XiMat	blood
48	chr11:32844000-32848800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr11:32844000-32850000	Weak transcription	Hela-S3	cervix
50	chr11:32844000-32850400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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