Variant report

Variant	nsv522706
Chromosome Location	chr11:120173845-120178632
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	ATF1	chr11:120177322-120177668	K562	blood:	n/a	n/a
2	BACH1	chr11:120177305-120177628	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr11:120177265-120177586	Hela-S3	cervix:	n/a	n/a
4	CBX3	chr11:120177099-120177963	HCT-116	colon:	n/a	n/a
5	CEBPB	chr11:120177172-120177603	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr11:120177117-120177602	IMR90	lung:	n/a	n/a
7	CHD2	chr11:120177272-120177683	Hela-S3	cervix:	n/a	n/a
8	CREB1	chr11:120173701-120174143	H1-hESC	embryonic stem cell:	n/a	n/a
9	CREB1	chr11:120173690-120174164	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr11:120177420-120177570	GM12875	blood:	n/a	chr11:120177508-120177526
11	CTCF	chr11:120177496-120177588	HepG2	liver:	n/a	chr11:120177508-120177526
12	CTCF	chr11:120177440-120177590	AG04449	skin:	n/a	chr11:120177508-120177526
13	CTCF	chr11:120173799-120174050	LNCaP	prostate:	n/a	chr11:120173903-120173924 chr11:120173909-120173925 chr11:120173952-120173973 chr11:120173959-120173972 chr11:120173908-120173926 chr11:120173913-120173921 chr11:120173957-120173975
14	CTCF	chr11:120173806-120174068	Kidney_OC	kidney:	n/a	chr11:120173903-120173924 chr11:120173909-120173925 chr11:120173952-120173973 chr11:120173959-120173972 chr11:120173908-120173926 chr11:120173913-120173921 chr11:120173957-120173975
15	CTCF	chr11:120173788-120174074	A549	lung:	n/a	chr11:120173903-120173924 chr11:120173909-120173925 chr11:120173952-120173973 chr11:120173959-120173972 chr11:120173908-120173926 chr11:120173913-120173921 chr11:120173957-120173975
16	CTCF	chr11:120177580-120177730	GM12873	blood:	n/a	n/a
17	CTCF	chr11:120177447-120177530	GM12878	blood:	n/a	chr11:120177508-120177526
18	CTCF	chr11:120173680-120174165	A549	lung:	n/a	chr11:120173903-120173924 chr11:120173909-120173925 chr11:120173952-120173973 chr11:120173959-120173972 chr11:120173908-120173926 chr11:120173913-120173921 chr11:120173957-120173975
19	CTCF	chr11:120173860-120174010	GM12872	blood:	n/a	chr11:120173903-120173924 chr11:120173909-120173925 chr11:120173952-120173973 chr11:120173959-120173972 chr11:120173908-120173926 chr11:120173913-120173921 chr11:120173957-120173975
20	CTCF	chr11:120177420-120177570	HRE	kidney:	n/a	chr11:120177508-120177526
21	CTCF	chr11:120177480-120177630	GM12871	blood:	n/a	chr11:120177508-120177526
22	CTCF	chr11:120173774-120174083	MCF-7	breast:	n/a	chr11:120173903-120173924 chr11:120173909-120173925 chr11:120173952-120173973 chr11:120173959-120173972 chr11:120173908-120173926 chr11:120173913-120173921 chr11:120173957-120173975
23	CTCF	chr11:120177480-120177630	MCF-7	breast:	n/a	chr11:120177508-120177526
24	CTCF	chr11:120177440-120177590	GM12874	blood:	n/a	chr11:120177508-120177526
25	CTCF	chr11:120174158-120174265	GM10266	blood:	n/a	n/a
26	CTCF	chr11:120173860-120174010	HCFaa	heart:	n/a	chr11:120173903-120173924 chr11:120173909-120173925 chr11:120173952-120173973 chr11:120173959-120173972 chr11:120173908-120173926 chr11:120173913-120173921 chr11:120173957-120173975
27	CTCF	chr11:120173840-120173990	GM12878	blood:	n/a	chr11:120173903-120173924 chr11:120173909-120173925 chr11:120173952-120173973 chr11:120173959-120173972 chr11:120173908-120173926 chr11:120173913-120173921 chr11:120173957-120173975
28	CTCF	chr11:120177780-120177930	HBMEC	blood vessel:	n/a	n/a
29	CTCF	chr11:120173860-120174010	GM12875	blood:	n/a	chr11:120173903-120173924 chr11:120173909-120173925 chr11:120173952-120173973 chr11:120173959-120173972 chr11:120173908-120173926 chr11:120173913-120173921 chr11:120173957-120173975
30	CTCF	chr11:120174040-120174190	A549	lung:	n/a	n/a
31	CTCF	chr11:120173716-120174102	HepG2	liver:	n/a	chr11:120173903-120173924 chr11:120173909-120173925 chr11:120173952-120173973 chr11:120173959-120173972 chr11:120173908-120173926 chr11:120173913-120173921 chr11:120173957-120173975
32	CTCF	chr11:120177440-120177590	HPF	lung:	n/a	chr11:120177508-120177526
33	CTCF	chr11:120173727-120174120	T-47D	breast:	n/a	chr11:120173903-120173924 chr11:120173909-120173925 chr11:120173952-120173973 chr11:120173959-120173972 chr11:120173908-120173926 chr11:120173913-120173921 chr11:120173957-120173975
34	CTCF	chr11:120173791-120174069	LNCaP	prostate:	n/a	chr11:120173903-120173924 chr11:120173909-120173925 chr11:120173952-120173973 chr11:120173959-120173972 chr11:120173908-120173926 chr11:120173913-120173921 chr11:120173957-120173975
35	CTCF	chr11:120177400-120177550	HUVEC	blood vessel:	n/a	chr11:120177508-120177526
36	CTCF	chr11:120177420-120177570	WERI-Rb-1	eye:	n/a	chr11:120177508-120177526
37	CTCF	chr11:120173860-120174010	AG04449	skin:	n/a	chr11:120173903-120173924 chr11:120173909-120173925 chr11:120173952-120173973 chr11:120173959-120173972 chr11:120173908-120173926 chr11:120173913-120173921 chr11:120173957-120173975
38	CTCF	chr11:120177820-120177970	HCFaa	heart:	n/a	n/a
39	CTCF	chr11:120177660-120177810	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr11:120177440-120177590	AG09309	skin:	n/a	chr11:120177508-120177526
41	CTCF	chr11:120173880-120174030	HL-60	blood:	n/a	chr11:120173903-120173924 chr11:120173909-120173925 chr11:120173952-120173973 chr11:120173959-120173972 chr11:120173908-120173926 chr11:120173913-120173921 chr11:120173957-120173975
42	CTCF	chr11:120177440-120177590	WI-38	lung:	n/a	chr11:120177508-120177526
43	CTCF	chr11:120173780-120174079	Gliobla	brain:	n/a	chr11:120173903-120173924 chr11:120173909-120173925 chr11:120173952-120173973 chr11:120173959-120173972 chr11:120173908-120173926 chr11:120173913-120173921 chr11:120173957-120173975
44	CTCF	chr11:120173860-120174010	BE2_C	brain:	n/a	chr11:120173903-120173924 chr11:120173909-120173925 chr11:120173952-120173973 chr11:120173959-120173972 chr11:120173908-120173926 chr11:120173913-120173921 chr11:120173957-120173975
45	CTCF	chr11:120177294-120177606	H1-hESC	embryonic stem cell:	n/a	chr11:120177508-120177526
46	CTCF	chr11:120177444-120177580	GM19238	blood:	n/a	chr11:120177508-120177526
47	CTCF	chr11:120174500-120174650	A549	lung:	n/a	n/a
48	CTCF	chr11:120177460-120177610	GM06990	blood:	n/a	chr11:120177508-120177526
49	CTCF	chr11:120177440-120177590	AG10803	skin:	n/a	chr11:120177508-120177526
50	CTCF	chr11:120177380-120177530	GM06990	blood:	n/a	chr11:120177508-120177526

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:120177486-120177536	Hela-S3	cervix:	n/a
2	chr11:120177486-120177536	HAEpiC	amniotic membrane:	n/a
3	chr11:120177486-120177536	AoSMC	blood vessel:	n/a
4	chr11:120177486-120177536	GM12891	blood:	n/a
5	chr11:120177486-120177536	HCM	heart:	n/a
6	chr11:120177486-120177536	ProgFib	skin:	n/a
7	chr11:120177486-120177536	NB4	blood:	n/a
8	chr11:120177486-120177536	HPAEpiC	pulmonary alveolar:	n/a
9	chr11:120177486-120177536	HRCEpiC	kidney:	n/a
10	chr11:120177486-120177536	U87	brain:	n/a
11	chr11:120177486-120177536	Caco-2	colon:	n/a
12	chr11:120177486-120177536	SAEC	small airway:	n/a
13	chr11:120177486-120177536	HMEC	breast:	n/a
14	chr11:120177486-120177536	SK-N-SH	brain:	n/a
15	chr11:120177486-120177536	MCF-7	breast:	n/a
16	chr11:120177486-120177536	HEK293	kidney:	embryo
17	chr11:120177486-120177536	HRPEpiC	eye:	n/a
18	chr11:120177486-120177536	BE2_C	brain:	n/a
19	chr11:120177486-120177536	PANC-1	pancreas:	n/a
20	chr11:120177486-120177536	AG09319	gingival:	n/a
21	chr11:120177486-120177536	HUVEC	blood vessel:	n/a
22	chr11:120177486-120177536	HNPCEpiC	eye:	n/a
23	chr11:120177486-120177536	RPTEC	kidney:	n/a
24	chr11:120177486-120177536	HCF	heart:	n/a
25	chr11:120177486-120177536	PFSK-1	brain:	n/a
26	chr11:120177486-120177536	LNCaP	prostate:	n/a
27	chr11:120177486-120177536	AG04449	skin:	fetal
28	chr11:120177486-120177536	HCPEpiC	choroid plexus:	n/a
29	chr11:120177486-120177536	GM12878	blood:	n/a
30	chr11:120177486-120177536	NHBE	bronchial:	n/a
31	chr11:120177486-120177536	K562	blood:	n/a
32	chr11:120177486-120177536	GM06990	blood:	n/a
33	chr11:120177486-120177536	HepG2	liver:	n/a
34	chr11:120177486-120177536	GM19239	blood:	n/a
35	chr11:120177486-120177536	GM12892	blood:	n/a
36	chr11:120177486-120177536	HCT-116	colon:	n/a
37	chr11:120177486-120177536	Hepatocyte	liver:	n/a
38	chr11:120177486-120177536	AG10803	skin:	n/a
39	chr11:120177486-120177536	H1-hESC	embryonic stem cell:	embryo
40	chr11:120177486-120177536	HEEpiC	esophagus:	n/a
41	chr11:120177486-120177536	ECC-1	luminal epithelium:	n/a
42	chr11:120177486-120177536	MCF10A-Er-Src	breast:	n/a
43	chr11:120177486-120177536	ovcar-3	ovarian:	n/a
44	chr11:120177486-120177536	NT2-D1	testis:	n/a
45	chr11:120177486-120177536	AG09309	skin:	n/a
46	chr11:120177486-120177536	IMR90	lung:	fetal
47	chr11:120177486-120177536	SKMC	muscle:	n/a
48	chr11:120177486-120177536	PrEC	prostate:	n/a
49	chr11:120177486-120177536	SK-N-SH_RA	brain:	n/a
50	chr11:120177486-120177536	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:120104420..120112680-chr11:120168705..120181524,41	K562	blood:
2	chr11:120173450..120174289-chr11:120195532..120196408,2	MCF-7	breast:
3	chr11:120171583..120174537-chr11:120174642..120177317,2	MCF-7	breast:
4	chr11:120105456..120106436-chr11:120173320..120174423,6	MCF-7	breast:
5	chr11:120126928..120129765-chr11:120172517..120174089,2	MCF-7	breast:
6	chr11:120104320..120113596-chr11:120167938..120177639,38	MCF-7	breast:
7	chr11:119983220..119983741-chr11:120173390..120173940,2	K562	blood:
8	chr11:120109877..120110557-chr11:120173590..120174191,2	K562	blood:
9	chr11:120105406..120106378-chr11:120172236..120174440,21	K562	blood:
10	chr11:120178572..120180297-chr11:120186032..120187655,2	K562	blood:
11	chr11:120174600..120176592-chr11:120196059..120198854,2	K562	blood:
12	chr11:120172975..120174511-chr11:120180188..120181790,2	MCF-7	breast:
13	chr11:119986921..119988576-chr11:120173602..120175252,2	MCF-7	breast:
14	chr11:120106492..120108262-chr11:120175100..120176692,2	MCF-7	breast:
15	chr11:120128846..120129977-chr11:120173377..120174320,3	K562	blood:
16	chr11:120172516..120174094-chr11:120193101..120194869,2	MCF-7	breast:
17	chr11:120177470..120179089-chr11:120179127..120181642,2	K562	blood:
18	chr11:120099468..120100385-chr11:120173694..120174331,2	MCF-7	breast:
19	chr11:120170944..120173449-chr11:120176604..120178687,2	K562	blood:
20	chr11:120104352..120110604-chr11:120164438..120175098,43	MCF-7	breast:
21	chr11:120042631..120043429-chr11:120173449..120174511,3	MCF-7	breast:
22	chr11:120105294..120106722-chr11:120173447..120174421,11	MCF-7	breast:
23	chr11:120110683..120111626-chr11:120173442..120174009,4	K562	blood:
24	chr11:120173019..120175401-chr11:120178309..120180098,2	MCF-7	breast:
25	chr11:120171583..120174537-chr11:120174642..120177317,2	MCF-7	breast:
26	chr11:120099434..120101938-chr11:120172403..120174898,2	K562	blood:
27	chr11:120110739..120111690-chr11:120173720..120174499,2	MCF-7	breast:
28	chr11:120177467..120179242-chr11:120206323..120208657,2	MCF-7	breast:
29	chr11:120101055..120116563-chr11:120160593..120179156,52	K562	blood:
30	chr11:120173019..120175401-chr11:120178309..120180098,2	MCF-7	breast:
31	chr11:120177200..120179089-chr11:120179127..120181932,2	K562	blood:
32	chr11:120106624..120107576-chr11:120173121..120174108,4	K562	blood:
33	chr11:120172949..120175534-chr2:55468115..55470994,2	MCF-7	breast:
34	chr11:120173473..120178843-chr11:120183667..120189130,9	MCF-7	breast:
35	chr11:120172447..120175021-chr11:120193864..120196695,3	MCF-7	breast:
36	chr11:120042598..120043820-chr11:120173442..120174406,6	K562	blood:

Variant related genes	Relation type
POU2F3	TF binding region
POU2F3	CpG island
ENSG00000137709	chromatin interactions
ENSG00000181264	chromatin interactions
ENSG00000137699	chromatin interactions
ENSG00000196914	chromatin interactions

Extended variants
information (count: 231 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:231 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12275681	chr11:120173845-120173846	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs376952532	chr11:120173862-120173863	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs558890999	chr11:120173887-120173888	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs577429701	chr11:120173911-120173912	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs386758124	chr11:120173912-120173913	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs200148467	chr11:120173917-120173918	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs114035566	chr11:120173919-120173920	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs116920110	chr11:120173961-120173962	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs551819580	chr11:120173975-120173976	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs542328062	chr11:120174019-120174020	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs560536582	chr11:120174073-120174074	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs527804025	chr11:120174172-120174173	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs540375474	chr11:120174181-120174182	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs184487310	chr11:120174220-120174221	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs532425483	chr11:120174236-120174237	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs550505740	chr11:120174257-120174258	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs17123835	chr11:120174261-120174262	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs529673421	chr11:120174263-120174264	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs11602280	chr11:120174301-120174302	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs566516943	chr11:120174319-120174320	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs533663209	chr11:120174322-120174323	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs559100333	chr11:120174350-120174351	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs189630288	chr11:120174366-120174367	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs371782237	chr11:120174369-120174370	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs372575229	chr11:120174371-120174372	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs144388497	chr11:120174381-120174382	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs73006674	chr11:120174414-120174415	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs566631234	chr11:120174417-120174418	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs534291864	chr11:120174428-120174429	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs139832753	chr11:120174429-120174430	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs186025631	chr11:120174455-120174456	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs553881575	chr11:120174464-120174465	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs189350777	chr11:120174534-120174535	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs180794689	chr11:120174587-120174588	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs528643854	chr11:120174595-120174596	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs376743941	chr11:120174596-120174597	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs546690798	chr11:120174601-120174602	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs57478850	chr11:120174615-120174616	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs146213383	chr11:120174655-120174656	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs544084061	chr11:120174670-120174671	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs10790375	chr11:120174671-120174672	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs185615513	chr11:120174699-120174700	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs190071057	chr11:120174720-120174721	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs566388585	chr11:120174756-120174757	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs139163561	chr11:120174780-120174781	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs79014721	chr11:120174782-120174783	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs563654783	chr11:120174791-120174792	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs538408032	chr11:120174802-120174803	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs556816422	chr11:120174821-120174822	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs568722037	chr11:120174849-120174850	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:110)

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

Chromatin state (count:143 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:120169600-120178200	Enhancers	Placenta	Placenta
2	chr11:120170800-120174600	Weak transcription	HMEC	breast
3	chr11:120170800-120174800	Weak transcription	Hela-S3	cervix
4	chr11:120170800-120175200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr11:120170800-120175200	Weak transcription	Small Intestine	intestine
6	chr11:120170800-120175800	Weak transcription	A549	lung
7	chr11:120170800-120176200	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr11:120170800-120176200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr11:120171000-120174000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr11:120171200-120175400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr11:120172000-120177600	Enhancers	Stomach Mucosa	stomach
12	chr11:120172200-120174000	Enhancers	Colonic Mucosa	Colon
13	chr11:120172200-120174000	Enhancers	Duodenum Mucosa	Duodenum
14	chr11:120172200-120174200	Enhancers	Esophagus	oesophagus
15	chr11:120172200-120177600	Enhancers	Rectal Mucosa Donor 31	rectum
16	chr11:120172400-120178200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr11:120172800-120174000	Enhancers	Rectal Mucosa Donor 29	rectum
18	chr11:120173000-120175400	Enhancers	NHEK	skin
19	chr11:120173200-120174400	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr11:120173200-120176800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr11:120173200-120181200	Weak transcription	Fetal Intestine Large	intestine
22	chr11:120173400-120175200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
23	chr11:120173400-120176200	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr11:120173400-120177000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr11:120173600-120174200	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr11:120173800-120174400	Weak transcription	GM12878-XiMat	blood
27	chr11:120173800-120175000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr11:120173800-120175800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr11:120173800-120175800	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr11:120173800-120175800	Weak transcription	Gastric	stomach
31	chr11:120173800-120175800	Weak transcription	Pancreas	Pancrea
32	chr11:120173800-120177800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr11:120173800-120177800	Weak transcription	Lung	lung
34	chr11:120173800-120181200	Weak transcription	Fetal Intestine Small	intestine
35	chr11:120174000-120174200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr11:120174000-120175800	Weak transcription	Colonic Mucosa	Colon
37	chr11:120174000-120175800	Weak transcription	Duodenum Mucosa	Duodenum
38	chr11:120174000-120175800	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr11:120174200-120174600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr11:120174200-120174600	Weak transcription	Esophagus	oesophagus
41	chr11:120174200-120177200	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr11:120174400-120174800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr11:120174400-120176400	Enhancers	GM12878-XiMat	blood
44	chr11:120174600-120174800	Enhancers	Esophagus	oesophagus
45	chr11:120174600-120174800	Enhancers	NHLF	lung
46	chr11:120174600-120178000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr11:120174600-120178000	Enhancers	HMEC	breast
48	chr11:120174800-120175400	Weak transcription	NHLF	lung
49	chr11:120174800-120175800	Weak transcription	Esophagus	oesophagus
50	chr11:120174800-120178000	Enhancers	Hela-S3	cervix

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