Variant report

Variant	nsv877534
Chromosome Location	chr3:136676303-136765859
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1463)
CpG islands
(count:854)
Chromatin interactive
region (count:50)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1463 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:136692316-136692728	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:136742236-136742541	HepG2	liver:	n/a	n/a
3	ATF1	chr3:136676561-136676934	K562	blood:	n/a	n/a
4	ATF3	chr3:136676491-136676984	K562	blood:	n/a	n/a
5	ATF3	chr3:136676420-136677089	HCT-116	colon:	n/a	n/a
6	BACH1	chr3:136732781-136733170	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr3:136754560-136754699	HepG2	liver:	n/a	n/a
8	BHLHE40	chr3:136754524-136754797	K562	blood:	n/a	n/a
9	BHLHE40	chr3:136676574-136676775	K562	blood:	n/a	n/a
10	BHLHE40	chr3:136676246-136676343	K562	blood:	n/a	n/a
11	BHLHE40	chr3:136751419-136751447	K562	blood:	n/a	n/a
12	BHLHE40	chr3:136732758-136733459	K562	blood:	n/a	n/a
13	BHLHE40	chr3:136732733-136733090	GM12878	blood:	n/a	n/a
14	BRCA1	chr3:136713733-136714089	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr3:136676499-136677086	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr3:136732724-136733045	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr3:136679520-136680278	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr3:136703429-136704107	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr3:136693566-136693864	K562	blood:	n/a	n/a
20	CBX3	chr3:136733221-136733563	K562	blood:	n/a	n/a
21	CCNT2	chr3:136676576-136676863	K562	blood:	n/a	chr3:136676595-136676615
22	CCNT2	chr3:136678179-136678333	K562	blood:	n/a	n/a
23	CEBPB	chr3:136679502-136680415	HCT-116	colon:	n/a	n/a
24	CEBPB	chr3:136703825-136704148	IMR90	lung:	n/a	n/a
25	CEBPB	chr3:136676415-136677146	HCT-116	colon:	n/a	chr3:136676622-136676630
26	CEBPB	chr3:136713443-136714186	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr3:136735097-136735820	HepG2	liver:	n/a	chr3:136735666-136735679
28	CEBPB	chr3:136711161-136711196	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr3:136713663-136714026	IMR90	lung:	n/a	n/a
30	CEBPB	chr3:136758453-136758744	IMR90	lung:	n/a	n/a
31	CEBPB	chr3:136742252-136742572	HepG2	liver:	n/a	n/a
32	CEBPB	chr3:136735160-136735823	IMR90	lung:	n/a	chr3:136735666-136735679
33	CEBPB	chr3:136676604-136676926	K562	blood:	n/a	chr3:136676622-136676630
34	CEBPB	chr3:136745464-136745649	IMR90	lung:	n/a	n/a
35	CEBPB	chr3:136679820-136680020	A549	lung:	n/a	n/a
36	CEBPB	chr3:136713575-136714116	ECC-1	luminal epithelium:	n/a	n/a
37	CEBPB	chr3:136758524-136758706	HepG2	liver:	n/a	n/a
38	CEBPB	chr3:136735164-136735811	A549	lung:	n/a	chr3:136735666-136735679
39	CEBPB	chr3:136679655-136680516	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr3:136698579-136698956	IMR90	lung:	n/a	n/a
41	CEBPB	chr3:136758425-136758775	HepG2	liver:	n/a	n/a
42	CEBPB	chr3:136742187-136742689	HepG2	liver:	n/a	n/a
43	CEBPB	chr3:136751339-136751605	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr3:136679516-136680475	HCT-116	colon:	n/a	n/a
45	CEBPB	chr3:136758513-136758821	MCF-7	breast:	n/a	n/a
46	CEBPB	chr3:136676572-136676939	H1-hESC	embryonic stem cell:	n/a	chr3:136676622-136676630
47	CEBPB	chr3:136751292-136751506	K562	blood:	n/a	n/a
48	CEBPB	chr3:136681710-136682318	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr3:136676576-136676906	IMR90	lung:	n/a	chr3:136676622-136676630
50	CEBPB	chr3:136676498-136677863	Hela-S3	cervix:	n/a	chr3:136676622-136676630

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:136751404-136751454	K562	blood:	n/a
2	chr3:136751342-136751392	HL-60	blood:	n/a
3	chr3:136751342-136751392	MCF-7	breast:	n/a
4	chr3:136751404-136751454	AG09319	gingival:	n/a
5	chr3:136753955-136754005	NB4	blood:	n/a
6	chr3:136751795-136751845	AG04450	lung:	fetal
7	chr3:136751404-136751454	NT2-D1	testis:	n/a
8	chr3:136753955-136754005	NH-A	brain:	n/a
9	chr3:136751342-136751392	HCF	heart:	n/a
10	chr3:136751342-136751392	HPAEpiC	pulmonary alveolar:	n/a
11	chr3:136751795-136751845	HAEpiC	amniotic membrane:	n/a
12	chr3:136751342-136751392	U87	brain:	n/a
13	chr3:136748211-136748261	PrEC	prostate:	n/a
14	chr3:136751404-136751454	HMEC	breast:	n/a
15	chr3:136751656-136751706	BJ	skin:	n/a
16	chr3:136750029-136750079	HRCEpiC	kidney:	n/a
17	chr3:136706417-136706467	GM12878	blood:	n/a
18	chr3:136732896-136732946	HEEpiC	esophagus:	n/a
19	chr3:136714183-136714233	GM12892	blood:	n/a
20	chr3:136748211-136748261	AG09319	gingival:	n/a
21	chr3:136706417-136706467	H1-hESC	embryonic stem cell:	embryo
22	chr3:136729091-136729141	PrEC	prostate:	n/a
23	chr3:136751795-136751845	HNPCEpiC	eye:	n/a
24	chr3:136706417-136706467	HNPCEpiC	eye:	n/a
25	chr3:136676672-136676722	NHDF-neo	bronchial:	n/a
26	chr3:136751404-136751454	Caco-2	colon:	n/a
27	chr3:136706417-136706467	K562	blood:	n/a
28	chr3:136706417-136706467	ECC-1	luminal epithelium:	n/a
29	chr3:136751342-136751392	Jurkat	blood:	n/a
30	chr3:136750029-136750079	AG04449	skin:	fetal
31	chr3:136676846-136676896	HCT-116	colon:	n/a
32	chr3:136751656-136751706	NT2-D1	testis:	n/a
33	chr3:136750029-136750079	HRE	kidney:	n/a
34	chr3:136750029-136750079	ProgFib	skin:	n/a
35	chr3:136706417-136706467	GM19239	blood:	n/a
36	chr3:136753955-136754005	HRCEpiC	kidney:	n/a
37	chr3:136751559-136751609	SK-N-SH	brain:	n/a
38	chr3:136751656-136751706	A549	lung:	n/a
39	chr3:136714183-136714233	NT2-D1	testis:	n/a
40	chr3:136753955-136754005	IMR90	lung:	fetal
41	chr3:136676846-136676896	RPTEC	kidney:	n/a
42	chr3:136676672-136676722	HL-60	blood:	n/a
43	chr3:136729091-136729141	HCT-116	colon:	n/a
44	chr3:136748211-136748261	NB4	blood:	n/a
45	chr3:136748211-136748261	NHBE	bronchial:	n/a
46	chr3:136706417-136706467	AG09319	gingival:	n/a
47	chr3:136750029-136750079	Hela-S3	cervix:	n/a
48	chr3:136748211-136748261	AG10803	skin:	n/a
49	chr3:136751342-136751392	Caco-2	colon:	n/a
50	chr3:136751559-136751609	MCF-7	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:136471576..136472305-chr3:136732784..136733377,2	MCF-7	breast:
2	chr3:136705210..136707039-chr3:136709265..136711240,2	K562	blood:
3	chr3:136751011..136751516-chr3:137665094..137665612,2	MCF-7	breast:
4	chr3:136486125..136487075-chr3:136732472..136733275,2	MCF-7	breast:
5	chr3:136675182..136678297-chr3:136678655..136683617,5	K562	blood:
6	chr3:136580222..136582633-chr3:136740948..136742731,2	MCF-7	breast:
7	chr3:136705210..136707039-chr3:136709265..136711240,2	K562	blood:
8	chr3:136739489..136740278-chr3:136753932..136754734,2	MCF-7	breast:
9	chr3:136469274..136471214-chr3:136728329..136730848,2	MCF-7	breast:
10	chr3:135794181..135794725-chr3:136732674..136733251,2	K562	blood:
11	chr3:136469703..136474003-chr3:136727974..136735265,9	MCF-7	breast:
12	chr3:136668269..136668963-chr3:136732444..136733289,2	MCF-7	breast:
13	chr3:136740086..136742353-chr3:136744519..136747302,3	K562	blood:
14	chr3:136750966..136751930-chr3:137690153..137690670,2	K562	blood:
15	chr3:136668150..136669138-chr3:136713935..136714623,2	MCF-7	breast:
16	chr3:136470992..136472753-chr3:136732141..136733640,9	MCF-7	breast:
17	chr3:136471274..136473260-chr3:136730800..136734438,3	MCF-7	breast:
18	chr3:136264451..136265000-chr3:136732487..136733381,2	MCF-7	breast:
19	chr3:136470779..136471460-chr3:136732509..136733338,3	MCF-7	breast:
20	chr3:136472151..136474742-chr3:136749777..136751390,2	K562	blood:
21	chr3:136470071..136471591-chr3:136741187..136743880,2	K562	blood:
22	chr3:136467223..136474007-chr3:136729764..136735930,11	K562	blood:
23	chr3:136470409..136473181-chr3:136674963..136676647,2	K562	blood:
24	chr3:136477054..136477907-chr3:136732416..136733197,2	K562	blood:
25	chr3:136693279..136695517-chr3:136697390..136699263,2	K562	blood:
26	chr3:136477479..136478033-chr3:136732451..136733138,2	MCF-7	breast:
27	chr3:136477071..136478229-chr3:136732340..136733343,4	MCF-7	breast:
28	chr3:136693279..136695517-chr3:136697390..136699263,2	K562	blood:
29	chr3:136739489..136740278-chr3:136753932..136754734,2	MCF-7	breast:
30	chr3:136751186..136751967-chr3:136828909..136829867,2	MCF-7	breast:
31	chr3:136110282..136111199-chr3:136732444..136733352,7	K562	blood:
32	chr3:136469800..136471530-chr3:136680331..136682096,2	K562	blood:
33	chr3:136734281..136736785-chr3:136737502..136739437,2	K562	blood:
34	chr3:136734281..136736785-chr3:136737502..136739437,2	K562	blood:
35	chr3:136697313..136700260-chr3:136703197..136704911,2	MCF-7	breast:
36	chr3:136752981..136754824-chr3:136759356..136761614,2	K562	blood:
37	chr3:136467223..136474337-chr3:136727110..136735930,17	K562	blood:
38	chr3:136754621..136755131-chr3:136815936..136816935,2	MCF-7	breast:
39	chr3:136579408..136582158-chr3:136706601..136709165,2	MCF-7	breast:
40	chr3:136750951..136751906-chr3:137664906..137665965,5	MCF-7	breast:
41	chr3:136740086..136742353-chr3:136744519..136746885,2	K562	blood:
42	chr3:136707042..136709272-chr3:136713786..136715462,2	K562	blood:
43	chr3:136707042..136709272-chr3:136713786..136715462,2	K562	blood:
44	chr3:136740086..136742353-chr3:136744519..136747302,3	K562	blood:
45	chr3:136751027..136751908-chr3:136823889..136824681,2	MCF-7	breast:
46	chr3:136670696..136673372-chr3:136678994..136680976,2	K562	blood:
47	chr3:135915033..135916905-chr3:136732149..136734847,2	MCF-7	breast:
48	chr3:136752981..136754824-chr3:136759356..136761614,2	K562	blood:
49	chr3:136264546..136265090-chr3:136732553..136733310,2	MCF-7	breast:
50	chr3:136740086..136742353-chr3:136744519..136746885,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IL20RB-2	chr3:136734713-136735851	NONHSAT092298
2	lnc-STAG1-2	chr3:136677967-136678394	ENSG00000249407.1
3	lnc-STAG1-2	chr3:136700905-136701038	ENSG00000249407.1
4	lnc-IL20RB-3	chr3:136744772-136745131	NONHSAT092299

No data

Variant related genes	Relation type
IL20RB-AS1	TF binding region
IL20RB	TF binding region
IL20RB-AS1	CpG island
IL20RB	CpG island
ENSG00000174564	chromatin interactions
ENSG00000158092	chromatin interactions
ENSG00000118007	chromatin interactions
ENSG00000239213	chromatin interactions
ENSG00000261758	chromatin interactions
ENSG00000174579	chromatin interactions

Extended variants
information (count: 3017 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:3017 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs835634	chr3:136676303-136676304	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs182873127	chr3:136676359-136676360	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs200129178	chr3:136676390-136676391	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs148967788	chr3:136676392-136676393	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs372127831	chr3:136676394-136676395	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs199763045	chr3:136676395-136676396	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs572005346	chr3:136676412-136676413	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs72978727	chr3:136676428-136676429	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs835633	chr3:136676496-136676497	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs537270757	chr3:136676499-136676500	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs543346103	chr3:136676522-136676523	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs835632	chr3:136676525-136676526	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs576405781	chr3:136676672-136676673	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs55871480	chr3:136676702-136676703	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs188303055	chr3:136676716-136676717	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs192679440	chr3:136676739-136676740	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs547907330	chr3:136676788-136676789	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs141518075	chr3:136676789-136676790	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs530284720	chr3:136676841-136676842	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs550474811	chr3:136676867-136676868	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs369164593	chr3:136676914-136676915	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs369355723	chr3:136676928-136676929	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs375715090	chr3:136676954-136676955	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs370891880	chr3:136677018-136677019	Weak transcription Genic enhancers Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs184674196	chr3:136677058-136677059	Weak transcription Genic enhancers Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs6773440	chr3:136677064-136677065	Weak transcription Genic enhancers Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs376726430	chr3:136677066-136677067	Weak transcription Genic enhancers Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs187532597	chr3:136677098-136677099	Weak transcription Genic enhancers Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565335460	chr3:136677127-136677128	Weak transcription Genic enhancers Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568339103	chr3:136677145-136677146	Weak transcription Genic enhancers Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs534440978	chr3:136677186-136677187	Weak transcription Genic enhancers Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs554227052	chr3:136677229-136677230	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
33	rs574305878	chr3:136677255-136677256	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
34	rs536821897	chr3:136677327-136677328	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
35	rs6762370	chr3:136677339-136677340	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs192637892	chr3:136677341-136677342	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
37	rs184757509	chr3:136677352-136677353	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
38	rs6762460	chr3:136677450-136677451	Weak transcription Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs114191581	chr3:136677460-136677461	Weak transcription Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
40	rs12054219	chr3:136677472-136677473	Weak transcription Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs189216280	chr3:136677486-136677487	Weak transcription Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
42	rs530324739	chr3:136677487-136677488	Weak transcription Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
43	rs181560578	chr3:136677488-136677489	Weak transcription Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
44	rs12054218	chr3:136677496-136677497	Weak transcription Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs561469915	chr3:136677578-136677579	Weak transcription Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
46	rs12054220	chr3:136677581-136677582	Weak transcription Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs552814765	chr3:136677610-136677611	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
48	rs543646135	chr3:136677616-136677617	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
49	rs12054408	chr3:136677645-136677646	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs184999366	chr3:136677677-136677678	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Intracranial aneurysm	16715129	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18511947	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1395 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:136656400-136681400	Weak transcription	Fetal Muscle Leg	muscle
2	chr3:136658600-136679400	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr3:136662000-136676600	Weak transcription	Psoas Muscle	Psoas
4	chr3:136662600-136676400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr3:136662800-136678800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr3:136665200-136676800	Weak transcription	Aorta	Aorta
7	chr3:136665200-136680200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr3:136665400-136679000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr3:136665400-136680200	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr3:136665400-136680200	Weak transcription	Fetal Muscle Trunk	muscle
11	chr3:136665600-136680000	Weak transcription	Dnd41	blood
12	chr3:136665600-136689400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr3:136666600-136680400	Weak transcription	Left Ventricle	heart
14	chr3:136669400-136680200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr3:136670000-136676600	Enhancers	Hela-S3	cervix
16	chr3:136670600-136676600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr3:136670600-136676800	Enhancers	HMEC	breast
18	chr3:136671600-136676600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr3:136671800-136676600	Enhancers	NHEK	skin
20	chr3:136673200-136676800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr3:136673400-136676600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr3:136673600-136676600	Enhancers	K562	blood
23	chr3:136673800-136676400	Enhancers	Muscle Satellite Cultured Cells	--
24	chr3:136673800-136680400	Weak transcription	Monocytes-CD14+_RO01746	blood
25	chr3:136674000-136680200	Weak transcription	Fetal Thymus	thymus
26	chr3:136674200-136679800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr3:136674200-136680200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr3:136674400-136676600	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr3:136674400-136677600	Weak transcription	Thymus	Thymus
30	chr3:136674600-136677000	Weak transcription	Primary T cells from cord blood	blood
31	chr3:136674600-136680000	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr3:136674800-136676800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr3:136674800-136677000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr3:136674800-136680200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr3:136675000-136676600	Weak transcription	Adipose Nuclei	Adipose
36	chr3:136675000-136679800	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr3:136675200-136677000	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr3:136675400-136676400	Weak transcription	HUVEC	blood vessel
39	chr3:136675400-136676800	Enhancers	NHDF-Ad	bronchial
40	chr3:136675400-136677000	Enhancers	NHLF	lung
41	chr3:136675400-136677800	Weak transcription	NH-A	brain
42	chr3:136675600-136676400	Weak transcription	Stomach Mucosa	stomach
43	chr3:136675600-136676600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr3:136675600-136676600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr3:136675600-136676600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr3:136675600-136677600	Weak transcription	Esophagus	oesophagus
47	chr3:136675600-136678200	Enhancers	A549	lung
48	chr3:136675600-136679400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr3:136675600-136679600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr3:136675600-136679800	Weak transcription	Osteobl	bone

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