Variant report

Variant	nsv901846
Chromosome Location	chr14:45702358-45783546
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1488)
CpG islands
(count:917)
Chromatin interactive
region (count:39)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1488 , 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	chr14:45721346-45721411	K562	blood:	n/a	n/a
2	ARID3A	chr14:45722356-45723128	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:45756958-45756994	K562	blood:	n/a	n/a
4	ARID3A	chr14:45722305-45722539	K562	blood:	n/a	n/a
5	ARID3A	chr14:45719321-45719834	K562	blood:	n/a	n/a
6	ATF1	chr14:45719315-45719720	K562	blood:	n/a	n/a
7	ATF2	chr14:45722078-45723054	GM12878	blood:	n/a	n/a
8	ATF2	chr14:45722322-45723116	GM12878	blood:	n/a	n/a
9	ATF2	chr14:45722269-45723075	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr14:45720949-45721641	GM12878	blood:	n/a	n/a
11	ATF2	chr14:45721046-45721503	GM12878	blood:	n/a	n/a
12	ATF2	chr14:45722376-45723046	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr14:45722329-45723000	A549	lung:	n/a	n/a
14	ATF3	chr14:45741418-45741630	K562	blood:	n/a	n/a
15	ATF3	chr14:45722372-45722682	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr14:45722453-45723019	A549	lung:	n/a	n/a
17	BACH1	chr14:45722065-45723061	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr14:45721069-45721411	GM12878	blood:	n/a	n/a
19	BATF	chr14:45721023-45721508	GM12878	blood:	n/a	n/a
20	BCL11A	chr14:45722473-45722840	GM12878	blood:	n/a	n/a
21	BCL11A	chr14:45721145-45721473	GM12878	blood:	n/a	n/a
22	BCL3	chr14:45722180-45723071	A549	lung:	n/a	n/a
23	BCL3	chr14:45722203-45723416	A549	lung:	n/a	n/a
24	BCLAF1	chr14:45722194-45723134	GM12878	blood:	n/a	n/a
25	BCLAF1	chr14:45721060-45721557	GM12878	blood:	n/a	n/a
26	BCLAF1	chr14:45737709-45738137	GM12878	blood:	n/a	n/a
27	BCLAF1	chr14:45722060-45723125	GM12878	blood:	n/a	n/a
28	BHLHE40	chr14:45722198-45723003	HepG2	liver:	n/a	n/a
29	BHLHE40	chr14:45722265-45722799	K562	blood:	n/a	n/a
30	BHLHE40	chr14:45722164-45723101	GM12878	blood:	n/a	n/a
31	BHLHE40	chr14:45721733-45721803	K562	blood:	n/a	n/a
32	BHLHE40	chr14:45737784-45738081	GM12878	blood:	n/a	n/a
33	BHLHE40	chr14:45721077-45721534	GM12878	blood:	n/a	n/a
34	BHLHE40	chr14:45718701-45719749	GM12878	blood:	n/a	n/a
35	BHLHE40	chr14:45723324-45723381	GM12878	blood:	n/a	n/a
36	BRCA1	chr14:45722007-45723004	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr14:45722387-45723098	HepG2	liver:	n/a	n/a
38	BRCA1	chr14:45722287-45722946	GM12878	blood:	n/a	n/a
39	CBX3	chr14:45751009-45751267	K562	blood:	n/a	n/a
40	CBX3	chr14:45722239-45722991	K562	blood:	n/a	n/a
41	CBX3	chr14:45721964-45723196	HCT-116	colon:	n/a	n/a
42	CBX3	chr14:45722300-45722833	K562	blood:	n/a	n/a
43	CBX3	chr14:45751010-45751209	K562	blood:	n/a	n/a
44	CBX3	chr14:45727350-45727582	K562	blood:	n/a	n/a
45	CBX3	chr14:45727253-45727633	K562	blood:	n/a	n/a
46	CCNT2	chr14:45722169-45722721	K562	blood:	n/a	n/a
47	CEBPB	chr14:45704412-45704703	A549	lung:	n/a	chr14:45704557-45704568
48	CEBPB	chr14:45716310-45716654	HepG2	liver:	n/a	chr14:45716476-45716487
49	CEBPB	chr14:45704395-45704721	IMR90	lung:	n/a	chr14:45704557-45704568
50	CEBPB	chr14:45704406-45704731	HepG2	liver:	n/a	chr14:45704557-45704568

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:45722622-45722672	LNCaP	prostate:	n/a
2	chr14:45725455-45725505	HCPEpiC	choroid plexus:	n/a
3	chr14:45722622-45722672	LNCaP	prostate:	n/a
4	chr14:45725455-45725505	HCPEpiC	choroid plexus:	n/a
5	chr14:45725455-45725505	HL-60	blood:	n/a
6	chr14:45722438-45722488	BE2_C	brain:	n/a
7	chr14:45722704-45722754	HMEC	breast:	n/a
8	chr14:45723353-45723403	GM12891	blood:	n/a
9	chr14:45722711-45722761	GM12891	blood:	n/a
10	chr14:45722043-45722093	H1-hESC	embryonic stem cell:	embryo
11	chr14:45722704-45722754	MCF10A-Er-Src	breast:	n/a
12	chr14:45759143-45759193	RPTEC	kidney:	n/a
13	chr14:45722987-45723037	Caco-2	colon:	n/a
14	chr14:45722745-45722795	K562	blood:	n/a
15	chr14:45722289-45722339	HCF	heart:	n/a
16	chr14:45722532-45722582	HAEpiC	amniotic membrane:	n/a
17	chr14:45722289-45722339	ovcar-3	ovarian:	n/a
18	chr14:45723353-45723403	MCF-7	breast:	n/a
19	chr14:45759143-45759193	GM12878	blood:	n/a
20	chr14:45722711-45722761	AG09309	skin:	n/a
21	chr14:45719962-45720012	NHDF-neo	bronchial:	n/a
22	chr14:45722532-45722582	AG04450	lung:	fetal
23	chr14:45759143-45759193	HRE	kidney:	n/a
24	chr14:45725455-45725505	HepG2	liver:	n/a
25	chr14:45759143-45759193	PANC-1	pancreas:	n/a
26	chr14:45722704-45722754	NHBE	bronchial:	n/a
27	chr14:45722438-45722488	NHDF-neo	bronchial:	n/a
28	chr14:45722532-45722582	SAEC	small airway:	n/a
29	chr14:45722721-45722771	HCM	heart:	n/a
30	chr14:45722043-45722093	K562	blood:	n/a
31	chr14:45722289-45722339	MCF10A-Er-Src	breast:	n/a
32	chr14:45722622-45722672	HEEpiC	esophagus:	n/a
33	chr14:45725455-45725505	HIPEpiC	eye:	n/a
34	chr14:45722438-45722488	NB4	blood:	n/a
35	chr14:45722043-45722093	SAEC	small airway:	n/a
36	chr14:45722987-45723037	BJ	skin:	n/a
37	chr14:45722289-45722339	PANC-1	pancreas:	n/a
38	chr14:45719962-45720012	HepG2	liver:	n/a
39	chr14:45722721-45722771	ovcar-3	ovarian:	n/a
40	chr14:45722987-45723037	Jurkat	blood:	n/a
41	chr14:45722721-45722771	MCF10A-Er-Src	breast:	n/a
42	chr14:45725455-45725505	BJ	skin:	n/a
43	chr14:45722043-45722093	NH-A	brain:	n/a
44	chr14:45719962-45720012	Hepatocyte	liver:	n/a
45	chr14:45719962-45720012	HCM	heart:	n/a
46	chr14:45725455-45725505	IMR90	lung:	fetal
47	chr14:45725455-45725505	HEK293	kidney:	embryo
48	chr14:45722289-45722339	GM12878	blood:	n/a
49	chr14:45722704-45722754	PANC-1	pancreas:	n/a
50	chr14:45725455-45725505	AG04450	lung:	fetal

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:45705828..45707853-chr14:45712067..45713833,2	MCF-7	breast:
2	chr14:45728008..45730307-chr14:45736451..45738128,2	MCF-7	breast:
3	chr14:45601339..45606570-chr14:45722040..45724234,5	MCF-7	breast:
4	chr14:45774667..45776638-chr14:45777456..45779936,2	MCF-7	breast:
5	chr14:45365477..45369212-chr14:45721451..45724440,3	MCF-7	breast:
6	chr14:45722471..45723281-chr15:75743983..75744975,2	Hela-S3	cervix:
7	chr14:45383078..45384611-chr14:45736865..45739302,2	MCF-7	breast:
8	chr12:57039223..57039923-chr14:45722606..45723303,3	Hela-S3	cervix:
9	chr14:45701019..45703145-chr14:45705910..45707479,2	MCF-7	breast:
10	chr14:45721810..45725859-chr14:45742099..45745950,4	MCF-7	breast:
11	chr14:45625132..45625884-chr14:45737446..45738063,2	MCF-7	breast:
12	chr14:45773220..45776127-chr14:45776332..45778274,2	K562	blood:
13	chr14:45427536..45430475-chr14:45702216..45704003,2	MCF-7	breast:
14	chr14:45588121..45589844-chr14:45722977..45725072,2	MCF-7	breast:
15	chr14:45705828..45707853-chr14:45712067..45713833,2	MCF-7	breast:
16	chr14:45553320..45554876-chr14:45714486..45717051,2	MCF-7	breast:
17	chr14:45721810..45725859-chr14:45742099..45745950,4	MCF-7	breast:
18	chr14:45717265..45719179-chr14:45721039..45722598,2	K562	blood:
19	chr14:45382903..45383965-chr14:45737675..45738717,4	MCF-7	breast:
20	chr14:45720720..45725312-chr14:45736349..45740437,5	MCF-7	breast:
21	chr14:45701019..45703145-chr14:45705910..45707479,2	MCF-7	breast:
22	chr14:45722237..45722750-chr18:3653037..3653537,2	HCT-116	colon:
23	chr14:45701847..45703730-chr14:45720111..45722706,2	MCF-7	breast:
24	chr14:45727473..45730434-chr14:45734970..45737678,2	MCF-7	breast:
25	chr14:45722872..45725627-chr6:151936857..151939807,2	MCF-7	breast:
26	chr14:45710936..45712506-chr14:45717032..45718785,2	K562	blood:
27	chr14:45773220..45776127-chr14:45776332..45778274,2	K562	blood:
28	chr14:45704719..45706830-chr14:45720747..45723150,2	MCF-7	breast:
29	chr14:45721734..45722708-chr16:28565152..28565667,2	Hela-S3	cervix:
30	chr14:45429725..45432587-chr14:45720437..45723992,3	MCF-7	breast:
31	chr14:45603451..45606015-chr14:45719614..45721854,2	K562	blood:
32	chr14:45710340..45712436-chr14:45717199..45718785,2	K562	blood:
33	chr14:45602054..45606945-chr14:45719959..45724414,9	MCF-7	breast:
34	chr14:45364937..45368444-chr14:45721075..45725396,9	MCF-7	breast:
35	chr14:45728008..45730307-chr14:45736451..45738128,2	MCF-7	breast:
36	chr14:45687729..45690041-chr14:45727283..45730126,2	MCF-7	breast:
37	chr14:45774667..45776638-chr14:45777456..45779936,2	MCF-7	breast:
38	chr14:45722854..45723434-chr16:58133168..58133726,2	Hela-S3	cervix:
39	chr14:45727473..45730434-chr14:45734970..45737678,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FKBP3-6	chr14:45711237-45711589	NONHSAT036649
2	lnc-FANCM-8	chr14:45759448-45759483	NONHSAT036653
3	lnc-FANCM-8	chr14:45759144-45759367	NONHSAT036652
4	lnc-FANCM-8	chr14:45759448-45759479	NONHSAT036652
5	lnc-FANCM-8	chr14:45759209-45759392	NONHSAT036653
6	lnc-FANCM-8	chr14:45759239-45759589	NONHSAT036654
7	lnc-FKBP3-6	chr14:45710671-45711073	NONHSAT036649

No data

Variant related genes	Relation type
DNAJC19P9	TF binding region
RNU6-552P	TF binding region
MIS18BP1	TF binding region
DNAJC19P9	CpG island
RNU6-552P	CpG island
MIS18BP1	CpG island
ENSG00000207422	chromatin interactions
ENSG00000258633	chromatin interactions
ENSG00000169375	chromatin interactions
ENSG00000179454	chromatin interactions
ENSG00000129534	chromatin interactions
ENSG00000100442	chromatin interactions
ENSG00000199739	chromatin interactions
ENSG00000187790	chromatin interactions
ENSG00000185246	chromatin interactions
ENSG00000110955	chromatin interactions
ENSG00000198718	chromatin interactions
ENSG00000266401	chromatin interactions
ENSG00000179476	chromatin interactions
ENSG00000176476	chromatin interactions

Extended variants
information (count: 1749 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:1749 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12433547	chr14:45702358-45702359	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs192614235	chr14:45702385-45702386	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs12433565	chr14:45702389-45702390	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs543838143	chr14:45702517-45702518	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs57607457	chr14:45702607-45702608	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs137900914	chr14:45702627-45702628	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs183328427	chr14:45702735-45702736	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs117354784	chr14:45702756-45702757	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs527540536	chr14:45702772-45702773	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs373513021	chr14:45702865-45702866	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs565414287	chr14:45702872-45702873	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs532630692	chr14:45702962-45702963	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs538421439	chr14:45703020-45703021	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs187536135	chr14:45703058-45703059	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs569175386	chr14:45703065-45703066	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs530066805	chr14:45703072-45703073	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs74853049	chr14:45703077-45703078	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs143037529	chr14:45703098-45703099	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs534346224	chr14:45703139-45703140	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs191957364	chr14:45703167-45703168	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs570239489	chr14:45703221-45703222	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs537569075	chr14:45703271-45703272	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs556187860	chr14:45703275-45703276	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs574359176	chr14:45703336-45703337	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs535380999	chr14:45703374-45703375	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs553822314	chr14:45703457-45703458	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs7160373	chr14:45703592-45703593	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs146166601	chr14:45703612-45703613	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs373028071	chr14:45703647-45703648	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs375378275	chr14:45703649-45703650	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs148347740	chr14:45703671-45703672	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs141498401	chr14:45703701-45703702	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs184963998	chr14:45703737-45703738	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs544728743	chr14:45703766-45703767	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs574472960	chr14:45703778-45703779	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs537387457	chr14:45703801-45703802	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs562956886	chr14:45703812-45703813	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs530088085	chr14:45703897-45703898	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs548551212	chr14:45703907-45703908	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs560653953	chr14:45703962-45703963	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs569300214	chr14:45703989-45703990	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs527954586	chr14:45703995-45703996	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs552424960	chr14:45703996-45703997	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs570725569	chr14:45703997-45703998	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs536256520	chr14:45703998-45703999	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs557269368	chr14:45704019-45704020	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs369432790	chr14:45704022-45704023	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538008914	chr14:45704032-45704033	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs549612864	chr14:45704033-45704034	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs568138928	chr14:45704077-45704078	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21364760	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:1122 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:45630800-45704400	Weak transcription	Fetal Brain Male	brain
2	chr14:45631800-45711400	Weak transcription	Brain Hippocampus Middle	brain
3	chr14:45632800-45707000	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr14:45633800-45721200	Weak transcription	Aorta	Aorta
5	chr14:45655600-45719200	Weak transcription	Stomach Smooth Muscle	stomach
6	chr14:45660600-45707000	Weak transcription	Gastric	stomach
7	chr14:45660800-45703400	Weak transcription	Psoas Muscle	Psoas
8	chr14:45662800-45711400	Weak transcription	Brain Anterior Caudate	brain
9	chr14:45669600-45712000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr14:45670000-45711400	Weak transcription	Brain Substantia Nigra	brain
11	chr14:45670000-45711600	Strong transcription	Monocytes-CD14+_RO01746	blood
12	chr14:45673200-45706400	Strong transcription	Fetal Thymus	thymus
13	chr14:45674600-45719200	Weak transcription	Colonic Mucosa	Colon
14	chr14:45675000-45711600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr14:45675200-45711600	Weak transcription	Colon Smooth Muscle	Colon
16	chr14:45676200-45711600	Weak transcription	NHLF	lung
17	chr14:45677200-45704800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr14:45678400-45711800	Strong transcription	Dnd41	blood
19	chr14:45680400-45714000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr14:45680800-45705600	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr14:45681800-45704200	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr14:45681800-45711000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr14:45682000-45703600	Weak transcription	Spleen	Spleen
24	chr14:45682000-45721200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr14:45682200-45711200	Weak transcription	Fetal Brain Female	brain
26	chr14:45682200-45714800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
27	chr14:45682200-45719200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr14:45682400-45720400	Weak transcription	Brain Germinal Matrix	brain
29	chr14:45682600-45705400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr14:45682600-45706200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr14:45683600-45703000	Weak transcription	Pancreatic Islets	Pancreatic Islet
32	chr14:45684200-45704200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr14:45684200-45705400	Weak transcription	Placenta Amnion	Placenta Amnion
34	chr14:45684800-45719400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr14:45685200-45710000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr14:45686400-45703800	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr14:45686600-45719200	Weak transcription	Fetal Heart	heart
38	chr14:45687200-45719200	Weak transcription	HSMMtube	muscle
39	chr14:45688800-45706400	Strong transcription	Primary neutrophils fromperipheralblood	blood
40	chr14:45690800-45709200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr14:45690800-45711600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr14:45691000-45702400	Strong transcription	Osteobl	bone
43	chr14:45691000-45704600	Strong transcription	HUVEC	blood vessel
44	chr14:45691000-45710200	Strong transcription	Primary B cells from cord blood	blood
45	chr14:45691000-45712200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
46	chr14:45691600-45709600	Strong transcription	Primary hematopoietic stem cells	blood
47	chr14:45691600-45712600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr14:45691600-45713800	Strong transcription	Primary B cells from peripheral blood	blood
49	chr14:45691800-45711400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr14:45691800-45711400	Strong transcription	Duodenum Mucosa	Duodenum

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