Variant report

Variant	nsv1050935
Chromosome Location	chr11:120224544-120276373
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:544)
CpG islands
(count:428)
Chromatin interactive
region (count:44)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:544 , 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	chr11:120260874-120261520	HepG2	liver:	n/a	chr11:120261406-120261422
2	ARID3A	chr11:120252150-120252467	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:120271152-120271976	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:120262831-120263021	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:120225537-120225948	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:120242905-120243412	HepG2	liver:	n/a	n/a
7	ARID3A	chr11:120271520-120272009	K562	blood:	n/a	n/a
8	ARID3A	chr11:120270079-120270358	HepG2	liver:	n/a	n/a
9	ARID3A	chr11:120262017-120262419	HepG2	liver:	n/a	n/a
10	ARID3A	chr11:120248863-120248881	K562	blood:	n/a	n/a
11	ARID3A	chr11:120258977-120259426	HepG2	liver:	n/a	n/a
12	ARID3A	chr11:120255843-120256128	K562	blood:	n/a	n/a
13	ARID3A	chr11:120242410-120242754	K562	blood:	n/a	n/a
14	ARID3A	chr11:120257972-120257985	K562	blood:	n/a	n/a
15	ATF1	chr11:120271557-120271859	K562	blood:	n/a	n/a
16	ATF1	chr11:120257776-120257835	K562	blood:	n/a	n/a
17	ATF1	chr11:120255867-120256159	K562	blood:	n/a	n/a
18	ATF2	chr11:120271220-120271783	GM12878	blood:	n/a	n/a
19	BACH1	chr11:120248507-120248698	K562	blood:	n/a	n/a
20	BACH1	chr11:120276045-120276207	K562	blood:	n/a	n/a
21	BATF	chr11:120271214-120271809	GM12878	blood:	n/a	chr11:120271713-120271723
22	BATF	chr11:120271199-120271877	GM12878	blood:	n/a	chr11:120271713-120271723
23	BCL11A	chr11:120271229-120271761	GM12878	blood:	n/a	chr11:120271712-120271721 chr11:120271711-120271720 chr11:120271335-120271344
24	BCL11A	chr11:120271197-120271808	GM12878	blood:	n/a	chr11:120271712-120271721 chr11:120271711-120271720 chr11:120271335-120271344
25	CBX3	chr11:120271304-120272012	HCT-116	colon:	n/a	n/a
26	CBX3	chr11:120271425-120272041	HCT-116	colon:	n/a	n/a
27	CBX3	chr11:120249152-120249538	K562	blood:	n/a	n/a
28	CEBPB	chr11:120271426-120271869	ECC-1	luminal epithelium:	n/a	chr11:120271658-120271675
29	CEBPB	chr11:120271422-120271884	IMR90	lung:	n/a	chr11:120271658-120271675
30	CEBPB	chr11:120271379-120271919	ECC-1	luminal epithelium:	n/a	chr11:120271658-120271675
31	CEBPB	chr11:120268844-120268917	HepG2	liver:	n/a	n/a
32	CEBPB	chr11:120252160-120252441	A549	lung:	n/a	n/a
33	CEBPB	chr11:120271450-120271839	MCF-7	breast:	n/a	chr11:120271658-120271675
34	CEBPB	chr11:120268716-120269184	IMR90	lung:	n/a	chr11:120268747-120268760
35	CEBPB	chr11:120271483-120271853	A549	lung:	n/a	chr11:120271658-120271675
36	CEBPB	chr11:120271437-120271904	A549	lung:	n/a	chr11:120271658-120271675
37	CEBPB	chr11:120271442-120271850	K562	blood:	n/a	chr11:120271658-120271675
38	CEBPB	chr11:120271467-120271852	HepG2	liver:	n/a	chr11:120271658-120271675
39	CEBPB	chr11:120258456-120258649	HepG2	liver:	n/a	chr11:120258556-120258573
40	CEBPB	chr11:120271506-120271780	K562	blood:	n/a	chr11:120271658-120271675
41	CEBPB	chr11:120271104-120272242	HCT-116	colon:	n/a	chr11:120271658-120271675
42	CEBPB	chr11:120252037-120252474	HepG2	liver:	n/a	n/a
43	CEBPB	chr11:120274511-120274618	HepG2	liver:	n/a	chr11:120274583-120274600
44	CEBPB	chr11:120271433-120272534	Hela-S3	cervix:	n/a	chr11:120271658-120271675
45	CEBPB	chr11:120271481-120271851	HepG2	liver:	n/a	chr11:120271658-120271675
46	CEBPB	chr11:120271483-120271860	K562	blood:	n/a	chr11:120271658-120271675
47	CEBPB	chr11:120254530-120254817	IMR90	lung:	n/a	n/a
48	CEBPB	chr11:120271550-120271800	HepG2	liver:	n/a	chr11:120271658-120271675
49	CEBPB	chr11:120271540-120271738	HepG2	liver:	n/a	chr11:120271658-120271675
50	CEBPB	chr11:120254719-120254744	K562	blood:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:120275443-120275493	NHBE	bronchial:	n/a
2	chr11:120275443-120275493	NHBE	bronchial:	n/a
3	chr11:120256570-120256620	GM12891	blood:	n/a
4	chr11:120275443-120275493	RPTEC	kidney:	n/a
5	chr11:120262862-120262912	MCF10A-Er-Src	breast:	n/a
6	chr11:120251845-120251895	AoSMC	blood vessel:	n/a
7	chr11:120255253-120255303	BE2_C	brain:	n/a
8	chr11:120255253-120255303	HRCEpiC	kidney:	n/a
9	chr11:120233535-120233585	PFSK-1	brain:	n/a
10	chr11:120256570-120256620	BJ	skin:	n/a
11	chr11:120275443-120275493	HNPCEpiC	eye:	n/a
12	chr11:120275443-120275493	GM06990	blood:	n/a
13	chr11:120262862-120262912	ovcar-3	ovarian:	n/a
14	chr11:120262862-120262912	HepG2	liver:	n/a
15	chr11:120255253-120255303	T-47D	breast:	n/a
16	chr11:120275443-120275493	AG04450	lung:	fetal
17	chr11:120233535-120233585	GM19239	blood:	n/a
18	chr11:120255253-120255303	HCF	heart:	n/a
19	chr11:120262862-120262912	NH-A	brain:	n/a
20	chr11:120233535-120233585	CMK	blood:	n/a
21	chr11:120233535-120233585	AoSMC	blood vessel:	n/a
22	chr11:120255253-120255303	HL-60	blood:	n/a
23	chr11:120256570-120256620	HNPCEpiC	eye:	n/a
24	chr11:120233535-120233585	GM12892	blood:	n/a
25	chr11:120233535-120233585	HMEC	breast:	n/a
26	chr11:120255253-120255303	HCM	heart:	n/a
27	chr11:120255253-120255303	NT2-D1	testis:	n/a
28	chr11:120251845-120251895	K562	blood:	n/a
29	chr11:120262862-120262912	T-47D	breast:	n/a
30	chr11:120254723-120254773	GM12878	blood:	n/a
31	chr11:120256570-120256620	SK-N-MC	brain:	n/a
32	chr11:120275443-120275493	PFSK-1	brain:	n/a
33	chr11:120256570-120256620	LNCaP	prostate:	n/a
34	chr11:120255253-120255303	HMEC	breast:	n/a
35	chr11:120255253-120255303	SK-N-SH_RA	brain:	n/a
36	chr11:120254723-120254773	HCT-116	colon:	n/a
37	chr11:120262862-120262912	Hepatocyte	liver:	n/a
38	chr11:120254723-120254773	AG09319	gingival:	n/a
39	chr11:120233535-120233585	AG10803	skin:	n/a
40	chr11:120254723-120254773	HEK293	kidney:	embryo
41	chr11:120251845-120251895	GM12891	blood:	n/a
42	chr11:120262862-120262912	IMR90	lung:	fetal
43	chr11:120233535-120233585	HCPEpiC	choroid plexus:	n/a
44	chr11:120251845-120251895	NH-A	brain:	n/a
45	chr11:120255253-120255303	AG04449	skin:	fetal
46	chr11:120255253-120255303	AoSMC	blood vessel:	n/a
47	chr11:120256570-120256620	AG09319	gingival:	n/a
48	chr11:120233535-120233585	RPTEC	kidney:	n/a
49	chr11:120262862-120262912	NB4	blood:	n/a
50	chr11:120254723-120254773	ProgFib	skin:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:120243305..120247442-chr11:120248031..120252040,4	K562	blood:
2	chr11:120221307..120224053-chr11:120246585..120248517,2	K562	blood:
3	chr11:120227977..120230527-chr11:120258363..120260160,2	K562	blood:
4	chr11:120248045..120250205-chr11:120253387..120255694,2	K562	blood:
5	chr11:120223412..120225236-chr11:120267280..120269601,2	K562	blood:
6	chr11:120269290..120270957-chr11:120272815..120274780,2	K562	blood:
7	chr11:120248045..120250205-chr11:120253387..120255694,2	K562	blood:
8	chr11:120207370..120208927-chr11:120276135..120278811,2	K562	blood:
9	chr11:120221867..120224622-chr11:120232208..120234590,2	K562	blood:
10	chr11:120267548..120269343-chr11:120272156..120273879,2	K562	blood:
11	chr11:120243305..120247442-chr11:120248031..120252040,4	K562	blood:
12	chr11:120226152..120228748-chr11:120235115..120237770,2	K562	blood:
13	chr11:120206589..120208463-chr11:120241741..120244477,2	MCF-7	breast:
14	chr11:120252565..120254544-chr11:120265761..120267481,2	K562	blood:
15	chr11:120269290..120270957-chr11:120272815..120274780,2	K562	blood:
16	chr11:120265069..120267317-chr11:120306799..120308783,2	K562	blood:
17	chr11:120226152..120228748-chr11:120235115..120237770,2	K562	blood:
18	chr11:120227696..120230495-chr11:120243268..120245330,2	K562	blood:
19	chr11:120206159..120208664-chr11:120245042..120247050,2	MCF-7	breast:
20	chr11:120207083..120208772-chr11:120268301..120270438,2	MCF-7	breast:
21	chr11:120256139..120258853-chr11:120261413..120263735,2	K562	blood:
22	chr11:120221907..120224622-chr11:120232208..120233856,2	K562	blood:
23	chr11:120252565..120254544-chr11:120265761..120267481,2	K562	blood:
24	chr11:120234002..120236611-chr11:120244878..120247433,2	MCF-7	breast:
25	chr11:120234940..120237431-chr11:120239798..120241396,2	K562	blood:
26	chr11:120265286..120268187-chr11:120269932..120271605,2	K562	blood:
27	chr11:120223412..120225236-chr11:120267280..120269601,2	K562	blood:
28	chr11:120256139..120258853-chr11:120261413..120263735,2	K562	blood:
29	chr11:120240885..120243216-chr11:120268365..120270613,2	MCF-7	breast:
30	chr11:120240885..120243216-chr11:120268365..120270613,2	MCF-7	breast:
31	chr11:120207958..120210253-chr11:120247180..120249390,2	K562	blood:
32	chr11:120227696..120230495-chr11:120243268..120245330,2	K562	blood:
33	chr11:120227977..120230527-chr11:120258363..120260160,2	K562	blood:
34	chr11:120207062..120209255-chr11:120253882..120255463,2	MCF-7	breast:
35	chr11:120206632..120208724-chr11:120224150..120227495,4	MCF-7	breast:
36	chr11:120205280..120207973-chr11:120230843..120232754,2	K562	blood:
37	chr11:120265286..120268187-chr11:120269932..120271605,2	K562	blood:
38	chr11:120234002..120236611-chr11:120244878..120247433,2	MCF-7	breast:
39	chr11:120221867..120224622-chr11:120232208..120234590,2	K562	blood:
40	chr11:120234940..120237431-chr11:120239798..120241396,2	K562	blood:
41	chr11:120267548..120269343-chr11:120272156..120273879,2	K562	blood:
42	chr11:120221907..120224622-chr11:120232208..120233856,2	K562	blood:
43	chr11:120250268..120252452-chr11:120255237..120256890,2	K562	blood:
44	chr11:120205662..120208695-chr11:120270379..120272417,4	MCF-7	breast:

No data

Variant related genes	Relation type
ARHGEF12	TF binding region
ARHGEF12	CpG island
ENSG00000196914	chromatin interactions

Extended variants
information (count: 1695 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:1695 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10892563	chr11:120224544-120224545	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs189240267	chr11:120224574-120224575	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs570964357	chr11:120224585-120224586	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs12288721	chr11:120224591-120224592	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs556458545	chr11:120224615-120224616	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs10892564	chr11:120224650-120224651	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs193022748	chr11:120224715-120224716	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs183670982	chr11:120224742-120224743	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs553849164	chr11:120224748-120224749	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs572544938	chr11:120224765-120224766	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs11824032	chr11:120224789-120224790	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs565044571	chr11:120224847-120224848	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs532228659	chr11:120224876-120224877	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs79523289	chr11:120224889-120224890	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs551061164	chr11:120224919-120224920	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs569631531	chr11:120224925-120224926	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs562805124	chr11:120224967-120224968	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs529691023	chr11:120225015-120225016	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs369630699	chr11:120225038-120225039	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs115539383	chr11:120225073-120225074	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs566562777	chr11:120225082-120225083	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs201900980	chr11:120225123-120225124	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs367550823	chr11:120225124-120225125	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs527338077	chr11:120225141-120225142	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs555941840	chr11:120225218-120225219	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs551987223	chr11:120225228-120225229	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs188042528	chr11:120225239-120225240	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs538068558	chr11:120225254-120225255	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs149480252	chr11:120225285-120225286	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs556420789	chr11:120225300-120225301	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs368770213	chr11:120225302-120225303	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs535449799	chr11:120225313-120225314	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs553712312	chr11:120225326-120225327	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs572353978	chr11:120225350-120225351	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs11217835	chr11:120225383-120225384	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs574110016	chr11:120225404-120225405	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs373457757	chr11:120225433-120225434	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs180771237	chr11:120225436-120225437	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs536907240	chr11:120225535-120225536	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs184120810	chr11:120225544-120225545	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs144068904	chr11:120225551-120225552	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs188516981	chr11:120225567-120225568	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs574824435	chr11:120225582-120225583	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs542154381	chr11:120225586-120225587	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs567170978	chr11:120225597-120225598	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs35038927	chr11:120225606-120225607	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs560045654	chr11:120225609-120225610	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs527307733	chr11:120225646-120225647	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs140505683	chr11:120225651-120225652	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs182191419	chr11:120225714-120225715	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:111)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Renal cell carcinoma	21668985	CNVD
Developmental delay	21147756	CNVD
Emanuel syndrome	21549014	CNVD
Emanuel syndrome	18184694	CNVD
Non-syndromic sensorineural hearing loss	18184694	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Ovarian neoplasms	16753589	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cancer	21183584	CNVD
Retinoblastoma	22278416	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-syndromic sensorineural hearing loss	16829213	CNVD
Non-syndromic sensorineural hearing loss	16760666	CNVD
Squamous cell cancer	20885788	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Neurocytoma	17123091	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Central neurocytomas	17123091	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Hepatocellular carcinoma	16750200	CNVD
Multiple myeloma	17550852	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Acute myeloid leukemia	19651601	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	20409316	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Heart disease	20551144	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Autism	22543975	CNVD
Breast cancer	21509527	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Barrett''s syndrome	19417022	CNVD
Cancer	20164919	CNVD

Chromatin state (count:1340 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:120209600-120224600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr11:120213800-120224600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr11:120215400-120225600	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr11:120216000-120224800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr11:120216000-120239000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr11:120216200-120224600	Weak transcription	Spleen	Spleen
7	chr11:120216200-120224600	Weak transcription	NHEK	skin
8	chr11:120216400-120244800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr11:120217200-120228600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr11:120217200-120232000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr11:120217400-120225600	Weak transcription	Stomach Smooth Muscle	stomach
12	chr11:120217400-120234000	Weak transcription	Aorta	Aorta
13	chr11:120217600-120257000	Weak transcription	HSMM	muscle
14	chr11:120218000-120228400	Enhancers	Liver	Liver
15	chr11:120218200-120224600	Weak transcription	Fetal Muscle Leg	muscle
16	chr11:120218200-120224800	Weak transcription	NH-A	brain
17	chr11:120218200-120225600	Weak transcription	Psoas Muscle	Psoas
18	chr11:120218200-120229600	Weak transcription	GM12878-XiMat	blood
19	chr11:120218600-120224800	Weak transcription	Fetal Kidney	kidney
20	chr11:120218600-120231800	Weak transcription	Rectal Smooth Muscle	rectum
21	chr11:120218600-120232000	Weak transcription	Fetal Stomach	stomach
22	chr11:120218600-120232400	Weak transcription	HUVEC	blood vessel
23	chr11:120218800-120224800	Weak transcription	Osteobl	bone
24	chr11:120218800-120230600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr11:120220400-120232800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr11:120220600-120225000	Weak transcription	HSMMtube	muscle
27	chr11:120220600-120232000	Weak transcription	Colon Smooth Muscle	Colon
28	chr11:120220800-120225200	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr11:120221000-120224600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr11:120222600-120225000	Enhancers	K562	blood
31	chr11:120222800-120226000	Enhancers	HepG2	liver
32	chr11:120223200-120225600	Enhancers	Duodenum Mucosa	Duodenum
33	chr11:120223200-120225800	Enhancers	Fetal Intestine Small	intestine
34	chr11:120223200-120225800	Enhancers	Fetal Lung	lung
35	chr11:120223200-120225800	Enhancers	Left Ventricle	heart
36	chr11:120223400-120224800	Strong transcription	Cortex derived primary cultured neurospheres	brain
37	chr11:120223400-120225200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr11:120223400-120225200	Enhancers	Gastric	stomach
39	chr11:120223400-120225200	Enhancers	Pancreas	Pancrea
40	chr11:120223400-120225200	Enhancers	Right Atrium	heart
41	chr11:120223400-120225200	Enhancers	Stomach Mucosa	stomach
42	chr11:120223400-120226400	Enhancers	Fetal Intestine Large	intestine
43	chr11:120223400-120226400	Enhancers	Ovary	ovary
44	chr11:120223400-120226400	Enhancers	Right Ventricle	heart
45	chr11:120223600-120226400	Enhancers	Small Intestine	intestine
46	chr11:120223800-120224600	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr11:120223800-120225800	Enhancers	Skeletal Muscle Female	skeletal muscle
48	chr11:120224000-120224800	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr11:120224000-120224800	Enhancers	Sigmoid Colon	Sigmoid Colon
50	chr11:120224200-120224600	Enhancers	Placenta	Placenta

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