Variant report

Variant	nsv1066935
Chromosome Location	chr20:23123507-23146449
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1315)
CpG islands
(count:61)
Chromatin interactive
region (count:48)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1315 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:23126727-23127081	K562	blood:	n/a	chr20:23126763-23126779 chr20:23126762-23126778
2	ARID3A	chr20:23128078-23129295	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:23132989-23133541	K562	blood:	n/a	n/a
4	ARID3A	chr20:23123846-23124112	HepG2	liver:	n/a	n/a
5	ARID3A	chr20:23123649-23124122	K562	blood:	n/a	n/a
6	ARID3A	chr20:23136788-23137110	HepG2	liver:	n/a	n/a
7	ARID3A	chr20:23134572-23134923	K562	blood:	n/a	n/a
8	ARID3A	chr20:23127943-23128995	K562	blood:	n/a	n/a
9	ARID3A	chr20:23132967-23133286	HepG2	liver:	n/a	n/a
10	ARID3A	chr20:23136772-23137288	K562	blood:	n/a	n/a
11	ATF1	chr20:23132970-23133423	K562	blood:	n/a	n/a
12	ATF1	chr20:23134619-23134935	K562	blood:	n/a	n/a
13	ATF1	chr20:23136677-23137183	K562	blood:	n/a	n/a
14	ATF1	chr20:23135836-23136097	K562	blood:	n/a	n/a
15	ATF1	chr20:23123719-23124053	K562	blood:	n/a	n/a
16	ATF1	chr20:23128264-23128842	K562	blood:	n/a	n/a
17	ATF1	chr20:23139940-23140208	K562	blood:	n/a	n/a
18	ATF2	chr20:23128323-23129439	GM12878	blood:	n/a	n/a
19	ATF2	chr20:23128244-23129405	GM12878	blood:	n/a	n/a
20	ATF3	chr20:23133066-23133289	K562	blood:	n/a	n/a
21	ATF3	chr20:23128382-23128888	K562	blood:	n/a	n/a
22	ATF3	chr20:23123680-23123987	K562	blood:	n/a	n/a
23	ATF3	chr20:23128525-23128770	K562	blood:	n/a	n/a
24	ATF3	chr20:23132947-23133430	K562	blood:	n/a	n/a
25	ATF3	chr20:23136815-23137056	K562	blood:	n/a	n/a
26	ATF3	chr20:23136778-23137153	K562	blood:	n/a	n/a
27	BACH1	chr20:23132626-23132930	K562	blood:	n/a	n/a
28	BACH1	chr20:23133199-23133327	K562	blood:	n/a	n/a
29	BATF	chr20:23136792-23137082	GM12878	blood:	n/a	chr20:23136921-23136930 chr20:23136968-23136978 chr20:23136967-23136978
30	BATF	chr20:23123766-23123973	GM12878	blood:	n/a	chr20:23123881-23123891 chr20:23123880-23123891
31	BATF	chr20:23123769-23124030	GM12878	blood:	n/a	chr20:23123881-23123891 chr20:23123880-23123891
32	BATF	chr20:23128225-23128948	GM12878	blood:	n/a	n/a
33	BATF	chr20:23128485-23128779	GM12878	blood:	n/a	n/a
34	BCL11A	chr20:23136747-23137035	GM12878	blood:	n/a	n/a
35	BCL11A	chr20:23128510-23128805	GM12878	blood:	n/a	chr20:23128675-23128684 chr20:23128676-23128685
36	BCL11A	chr20:23128287-23128961	GM12878	blood:	n/a	chr20:23128675-23128684 chr20:23128676-23128685
37	BCL3	chr20:23136727-23137112	GM12878	blood:	n/a	n/a
38	BCL3	chr20:23136693-23137102	GM12878	blood:	n/a	n/a
39	BCL3	chr20:23128408-23128882	GM12878	blood:	n/a	chr20:23128675-23128684 chr20:23128676-23128685
40	BCL3	chr20:23128256-23129504	GM12878	blood:	n/a	chr20:23128675-23128684 chr20:23128676-23128685
41	BCL3	chr20:23142074-23142387	GM12878	blood:	n/a	n/a
42	BCLAF1	chr20:23128378-23128917	GM12878	blood:	n/a	chr20:23128675-23128684 chr20:23128676-23128685
43	BCLAF1	chr20:23128451-23128936	GM12878	blood:	n/a	chr20:23128675-23128684 chr20:23128676-23128685
44	BCLAF1	chr20:23132844-23133397	K562	blood:	n/a	n/a
45	BHLHE40	chr20:23136684-23137212	K562	blood:	n/a	n/a
46	BHLHE40	chr20:23129752-23130290	K562	blood:	n/a	n/a
47	BHLHE40	chr20:23127591-23127703	K562	blood:	n/a	n/a
48	BHLHE40	chr20:23139713-23139717	GM12878	blood:	n/a	n/a
49	BHLHE40	chr20:23143187-23143243	K562	blood:	n/a	n/a
50	BHLHE40	chr20:23133000-23133356	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:23123952-23124002	MCF10A-Er-Src	breast:	n/a
2	chr20:23123952-23124002	PrEC	prostate:	n/a
3	chr20:23123952-23124002	SK-N-SH	brain:	n/a
4	chr20:23123952-23124002	GM12892	blood:	n/a
5	chr20:23123952-23124002	CMK	blood:	n/a
6	chr20:23123952-23124002	HAEpiC	amniotic membrane:	n/a
7	chr20:23123952-23124002	NHDF-neo	bronchial:	n/a
8	chr20:23123952-23124002	HRE	kidney:	n/a
9	chr20:23123952-23124002	ECC-1	luminal epithelium:	n/a
10	chr20:23123952-23124002	HPAEpiC	pulmonary alveolar:	n/a
11	chr20:23123952-23124002	AG09319	gingival:	n/a
12	chr20:23123952-23124002	PFSK-1	brain:	n/a
13	chr20:23123952-23124002	HNPCEpiC	eye:	n/a
14	chr20:23123952-23124002	HIPEpiC	eye:	n/a
15	chr20:23123952-23124002	HCF	heart:	n/a
16	chr20:23123952-23124002	SK-N-SH_RA	brain:	n/a
17	chr20:23123952-23124002	H1-hESC	embryonic stem cell:	embryo
18	chr20:23123952-23124002	HEK293	kidney:	embryo
19	chr20:23123952-23124002	SAEC	small airway:	n/a
20	chr20:23123952-23124002	T-47D	breast:	n/a
21	chr20:23123952-23124002	GM19239	blood:	n/a
22	chr20:23123952-23124002	PANC-1	pancreas:	n/a
23	chr20:23123952-23124002	Jurkat	blood:	n/a
24	chr20:23123952-23124002	AG09309	skin:	n/a
25	chr20:23123952-23124002	AoSMC	blood vessel:	n/a
26	chr20:23123952-23124002	HEEpiC	esophagus:	n/a
27	chr20:23123952-23124002	HRPEpiC	eye:	n/a
28	chr20:23123952-23124002	HRCEpiC	kidney:	n/a
29	chr20:23123952-23124002	HL-60	blood:	n/a
30	chr20:23123952-23124002	LNCaP	prostate:	n/a
31	chr20:23123952-23124002	IMR90	lung:	fetal
32	chr20:23123952-23124002	HUVEC	blood vessel:	n/a
33	chr20:23123952-23124002	AG10803	skin:	n/a
34	chr20:23123952-23124002	GM12878	blood:	n/a
35	chr20:23123952-23124002	NT2-D1	testis:	n/a
36	chr20:23123952-23124002	GM06990	blood:	n/a
37	chr20:23123952-23124002	Hela-S3	cervix:	n/a
38	chr20:23123952-23124002	SKMC	muscle:	n/a
39	chr20:23123952-23124002	ProgFib	skin:	n/a
40	chr20:23123952-23124002	BE2_C	brain:	n/a
41	chr20:23123952-23124002	Hepatocyte	liver:	n/a
42	chr20:23123952-23124002	SK-N-MC	brain:	n/a
43	chr20:23123952-23124002	BJ	skin:	n/a
44	chr20:23123952-23124002	NHBE	bronchial:	n/a
45	chr20:23123952-23124002	NH-A	brain:	n/a
46	chr20:23123952-23124002	AG04449	skin:	fetal
47	chr20:23123952-23124002	Caco-2	colon:	n/a
48	chr20:23123952-23124002	ovcar-3	ovarian:	n/a
49	chr20:23123952-23124002	K562	blood:	n/a
50	chr20:23123952-23124002	NB4	blood:	n/a

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:23133916..23136553-chr20:23158776..23161352,2	K562	blood:
2	chr20:23128719..23130340-chr20:23179847..23182584,2	K562	blood:
3	chr20:23127644..23129779-chr20:23341695..23344048,2	K562	blood:
4	chr20:23145826..23148563-chr20:23157728..23159717,2	MCF-7	breast:
5	chr20:23125309..23128497-chr20:23131083..23133976,3	MCF-7	breast:
6	chr20:23030281..23032450-chr20:23128861..23131677,3	K562	blood:
7	chr20:23127669..23129280-chr20:23170551..23172653,2	K562	blood:
8	chr20:23094897..23098917-chr20:23130908..23134771,6	K562	blood:
9	chr20:23127608..23130209-chr20:23149080..23150975,2	K562	blood:
10	chr20:22391083..22392851-chr20:23127548..23129144,2	K562	blood:
11	chr20:23122593..23125054-chr20:23330206..23333059,2	MCF-7	breast:
12	chr20:23122546..23124571-chr20:23180527..23183160,2	MCF-7	breast:
13	chr20:23145677..23147489-chr20:23148679..23151441,2	MCF-7	breast:
14	chr20:23129251..23133596-chr20:23289860..23293957,6	K562	blood:
15	chr20:23128680..23132693-chr20:23173285..23175662,3	K562	blood:
16	chr20:23123944..23126735-chr20:23131086..23132834,2	MCF-7	breast:
17	chr20:23133379..23136064-chr20:23136582..23138082,2	MCF-7	breast:
18	chr20:23128655..23130225-chr20:23192779..23194718,2	K562	blood:
19	chr20:23106418..23109174-chr20:23126935..23129451,2	K562	blood:
20	chr20:23130043..23132232-chr20:23322579..23325341,2	K562	blood:
21	chr20:22387131..22389688-chr20:23128753..23131289,2	K562	blood:
22	chr20:23126510..23128987-chr20:23134466..23137305,2	MCF-7	breast:
23	chr20:22808161..22811157-chr20:23128815..23130470,2	K562	blood:
24	chr20:23073935..23077646-chr20:23127330..23130238,3	K562	blood:
25	chr20:23128094..23130694-chr20:23194983..23196835,2	K562	blood:
26	chr20:23094758..23097530-chr20:23123211..23126141,2	K562	blood:
27	chr20:23123944..23126735-chr20:23131086..23132834,2	MCF-7	breast:
28	chr20:23080110..23082822-chr20:23132025..23133564,2	K562	blood:
29	chr20:23131349..23133053-chr20:23183942..23185506,2	K562	blood:
30	chr20:23092388..23096498-chr20:23127168..23130418,4	K562	blood:
31	chr20:23131411..23133053-chr20:23183792..23185506,2	K562	blood:
32	chr20:23027375..23033068-chr20:23127953..23133190,8	K562	blood:
33	chr20:23068076..23069690-chr20:23128418..23130201,2	K562	blood:
34	chr20:23135912..23138297-chr20:23172308..23174497,2	K562	blood:
35	chr20:23038702..23039550-chr20:23145856..23146435,3	MCF-7	breast:
36	chr20:23068190..23071729-chr20:23127032..23130141,4	K562	blood:
37	chr20:23135433..23136976-chr20:23166923..23169516,2	K562	blood:
38	chr20:23129825..23131611-chr20:23330855..23333303,2	K562	blood:
39	chr20:23102523..23105175-chr20:23127807..23130561,3	K562	blood:
40	chr20:23130457..23132351-chr20:23132417..23135261,2	MCF-7	breast:
41	chr20:23133379..23136064-chr20:23136582..23138082,2	MCF-7	breast:
42	chr20:23092456..23098917-chr20:23127069..23136117,14	K562	blood:
43	chr20:23126510..23128987-chr20:23134466..23137305,2	MCF-7	breast:
44	chr20:23073207..23075435-chr20:23128612..23131372,2	K562	blood:
45	chr20:23130457..23132351-chr20:23132417..23135261,2	MCF-7	breast:
46	chr20:23064363..23066368-chr20:23127818..23130287,3	K562	blood:
47	chr20:22391351..22394320-chr20:23127644..23129795,2	K562	blood:
48	chr20:23125309..23128497-chr20:23131083..23133976,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SSTR4-13	chr20:23128723-23130576	NONHSAT079037

No data

Variant related genes	Relation type
RNA5SP478	TF binding region
RNA5SP478	CpG island
ENSG00000125812	chromatin interactions
ENSG00000178726	chromatin interactions
ENSG00000230387	chromatin interactions
ENSG00000234832	chromatin interactions
ENSG00000132661	chromatin interactions

Extended variants
information (count: 1097 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1097 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184646013	chr20:23123516-23123517	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs75168692	chr20:23123572-23123573	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs550211270	chr20:23123582-23123583	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs567566782	chr20:23123592-23123593	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs6048557	chr20:23123597-23123598	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs75444037	chr20:23123610-23123611	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs188665535	chr20:23123613-23123614	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs192992904	chr20:23123635-23123636	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs370738753	chr20:23123651-23123652	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs6048558	chr20:23123677-23123678	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs559008994	chr20:23123688-23123689	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs75464785	chr20:23123691-23123692	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs544722251	chr20:23123762-23123763	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs555099918	chr20:23123800-23123801	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs114916892	chr20:23123844-23123845	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs6036319	chr20:23123916-23123917	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs542793379	chr20:23123917-23123918	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs559419063	chr20:23123925-23123926	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs528400474	chr20:23123939-23123940	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs541997234	chr20:23123953-23123954	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs184827144	chr20:23123955-23123956	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs530419910	chr20:23123965-23123966	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs189281746	chr20:23123989-23123990	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs374151629	chr20:23124038-23124039	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs567006125	chr20:23124115-23124116	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs565289330	chr20:23124127-23124128	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs527727375	chr20:23124128-23124129	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs566917725	chr20:23124171-23124172	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs150594877	chr20:23124217-23124218	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs539328930	chr20:23124223-23124224	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs559247682	chr20:23124231-23124232	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs55980210	chr20:23124247-23124248	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs6137841	chr20:23124253-23124254	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs143012489	chr20:23124254-23124255	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs180962655	chr20:23124257-23124258	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs540343387	chr20:23124270-23124271	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs548106609	chr20:23124288-23124289	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs572903098	chr20:23124342-23124343	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs370997397	chr20:23124389-23124390	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs527622666	chr20:23124434-23124435	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs3220747	chr20:23124466-23124467	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs76119968	chr20:23124476-23124477	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs530457389	chr20:23124477-23124478	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs543781833	chr20:23124499-23124500	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs113211243	chr20:23124563-23124564	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs560693092	chr20:23124587-23124588	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs60484393	chr20:23124592-23124593	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs71183327	chr20:23124594-23124595	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs3067140	chr20:23124595-23124596	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs58331131	chr20:23124597-23124598	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Breast cancer	16608533	CNVD
Cancer	20164919	CNVD
Bladder cancer	21909424	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	17133270	CNVD
Thrombophilia	17576883	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Hepatocellular carcinoma	22174799	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
small cell lung cancer	17426248	CNVD

Chromatin state (count:929 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23118400-23131000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr20:23119800-23128600	Weak transcription	Gastric	stomach
3	chr20:23120200-23137600	Enhancers	HUVEC	blood vessel
4	chr20:23120400-23123600	Enhancers	K562	blood
5	chr20:23121000-23128000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr20:23121000-23144200	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr20:23121200-23128800	Enhancers	Muscle Satellite Cultured Cells	--
8	chr20:23121200-23128800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr20:23121200-23130800	Enhancers	HSMM	muscle
10	chr20:23121600-23123600	Enhancers	Fetal Muscle Trunk	muscle
11	chr20:23121600-23123600	Enhancers	Fetal Muscle Leg	muscle
12	chr20:23121600-23124000	Enhancers	HSMMtube	muscle
13	chr20:23121600-23127000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr20:23121600-23130800	Enhancers	NH-A	brain
15	chr20:23121600-23138200	Enhancers	Adipose Nuclei	Adipose
16	chr20:23121800-23123600	Enhancers	Esophagus	oesophagus
17	chr20:23121800-23123600	Enhancers	Left Ventricle	heart
18	chr20:23121800-23123600	Enhancers	Ovary	ovary
19	chr20:23121800-23123600	Enhancers	Psoas Muscle	Psoas
20	chr20:23121800-23124200	Enhancers	Primary T cells fromperipheralblood	blood
21	chr20:23121800-23124200	Enhancers	Spleen	Spleen
22	chr20:23121800-23125800	Enhancers	Skeletal Muscle Female	skeletal muscle
23	chr20:23121800-23137600	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr20:23121800-23143000	Enhancers	NHDF-Ad	bronchial
25	chr20:23122000-23124200	Enhancers	GM12878-XiMat	blood
26	chr20:23122000-23125800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr20:23122000-23126400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
28	chr20:23122200-23123800	Enhancers	Liver	Liver
29	chr20:23122200-23124000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
30	chr20:23122200-23124000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr20:23122200-23124200	Enhancers	Fetal Thymus	thymus
32	chr20:23122200-23124400	Enhancers	Primary B cells from cord blood	blood
33	chr20:23122200-23124400	Enhancers	Primary hematopoietic stem cells	blood
34	chr20:23122400-23123600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr20:23122400-23123600	Enhancers	Brain Anterior Caudate	brain
36	chr20:23122400-23123800	Enhancers	Primary T killer memory cells from peripheral blood	blood
37	chr20:23122400-23124000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
38	chr20:23122400-23124400	Enhancers	Primary T cells from cord blood	blood
39	chr20:23122400-23124600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
40	chr20:23122400-23124800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr20:23122400-23126400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr20:23122600-23123600	Enhancers	Brain Hippocampus Middle	brain
43	chr20:23122600-23123800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
44	chr20:23122600-23125000	Enhancers	HMEC	breast
45	chr20:23122600-23126400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr20:23122600-23138000	Enhancers	NHLF	lung
47	chr20:23122800-23123600	Enhancers	Duodenum Mucosa	Duodenum
48	chr20:23122800-23123600	Enhancers	Right Atrium	heart
49	chr20:23122800-23123800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr20:23122800-23124000	Enhancers	Primary T helper cells fromperipheralblood	blood

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