Variant report

Variant	esv2758357
Chromosome Location	chr14:45706082-45982410
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1919)
CpG islands
(count:1098)
Chromatin interactive
region (count:51)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1919 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

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	chr14:45722305-45722539	K562	blood:	n/a	n/a
3	ARID3A	chr14:45722356-45723128	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:45756958-45756994	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	chr14:45722269-45723075	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr14:45722322-45723116	GM12878	blood:	n/a	n/a
9	ATF2	chr14:45720949-45721641	GM12878	blood:	n/a	n/a
10	ATF2	chr14:45722078-45723054	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	chr14:45722372-45722682	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr14:45722329-45723000	A549	lung:	n/a	n/a
15	ATF3	chr14:45722453-45723019	A549	lung:	n/a	n/a
16	ATF3	chr14:45741418-45741630	K562	blood:	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	chr14:45721145-45721473	GM12878	blood:	n/a	n/a
21	BCL11A	chr14:45722473-45722840	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	chr14:45737709-45738137	GM12878	blood:	n/a	n/a
26	BCLAF1	chr14:45721060-45721557	GM12878	blood:	n/a	n/a
27	BCLAF1	chr14:45722060-45723125	GM12878	blood:	n/a	n/a
28	BHLHE40	chr14:45722164-45723101	GM12878	blood:	n/a	n/a
29	BHLHE40	chr14:45721077-45721534	GM12878	blood:	n/a	n/a
30	BHLHE40	chr14:45722265-45722799	K562	blood:	n/a	n/a
31	BHLHE40	chr14:45718701-45719749	GM12878	blood:	n/a	n/a
32	BHLHE40	chr14:45723324-45723381	GM12878	blood:	n/a	n/a
33	BHLHE40	chr14:45721733-45721803	K562	blood:	n/a	n/a
34	BHLHE40	chr14:45737784-45738081	GM12878	blood:	n/a	n/a
35	BHLHE40	chr14:45722198-45723003	HepG2	liver:	n/a	n/a
36	BRCA1	chr14:45722287-45722946	GM12878	blood:	n/a	n/a
37	BRCA1	chr14:45722387-45723098	HepG2	liver:	n/a	n/a
38	BRCA1	chr14:45722007-45723004	Hela-S3	cervix:	n/a	n/a
39	CBX3	chr14:45721964-45723196	HCT-116	colon:	n/a	n/a
40	CBX3	chr14:45722239-45722991	K562	blood:	n/a	n/a
41	CBX3	chr14:45751009-45751267	K562	blood:	n/a	n/a
42	CBX3	chr14:45727253-45727633	K562	blood:	n/a	n/a
43	CBX3	chr14:45727350-45727582	K562	blood:	n/a	n/a
44	CBX3	chr14:45751010-45751209	K562	blood:	n/a	n/a
45	CBX3	chr14:45722300-45722833	K562	blood:	n/a	n/a
46	CCNT2	chr14:45722169-45722721	K562	blood:	n/a	n/a
47	CEBPB	chr14:45716392-45716639	K562	blood:	n/a	chr14:45716476-45716487
48	CEBPB	chr14:45731939-45732247	HepG2	liver:	n/a	chr14:45732111-45732122
49	CEBPB	chr14:45719427-45719784	K562	blood:	n/a	n/a
50	CEBPB	chr14:45722240-45723410	HepG2	liver:	n/a	chr14:45722472-45722483

(count:1098 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:45840127-45840177	T-47D	breast:	n/a
2	chr14:45722532-45722582	HCPEpiC	choroid plexus:	n/a
3	chr14:45722438-45722488	NHDF-neo	bronchial:	n/a
4	chr14:45722711-45722761	GM19239	blood:	n/a
5	chr14:45722721-45722771	HRPEpiC	eye:	n/a
6	chr14:45759143-45759193	HRCEpiC	kidney:	n/a
7	chr14:45722617-45722667	NHBE	bronchial:	n/a
8	chr14:45870299-45870349	T-47D	breast:	n/a
9	chr14:45870299-45870349	AoSMC	blood vessel:	n/a
10	chr14:45722617-45722667	SAEC	small airway:	n/a
11	chr14:45722711-45722761	BJ	skin:	n/a
12	chr14:45722704-45722754	Hela-S3	cervix:	n/a
13	chr14:45722622-45722672	HEEpiC	esophagus:	n/a
14	chr14:45722532-45722582	GM12891	blood:	n/a
15	chr14:45722289-45722339	PANC-1	pancreas:	n/a
16	chr14:45759143-45759193	HNPCEpiC	eye:	n/a
17	chr14:45722043-45722093	MCF-7	breast:	n/a
18	chr14:45722721-45722771	Hela-S3	cervix:	n/a
19	chr14:45722745-45722795	HCF	heart:	n/a
20	chr14:45722043-45722093	CMK	blood:	n/a
21	chr14:45840127-45840177	SK-N-SH	brain:	n/a
22	chr14:45722721-45722771	K562	blood:	n/a
23	chr14:45759143-45759193	HCF	heart:	n/a
24	chr14:45722617-45722667	ovcar-3	ovarian:	n/a
25	chr14:45722987-45723037	MCF-7	breast:	n/a
26	chr14:45722745-45722795	HepG2	liver:	n/a
27	chr14:45722711-45722761	HCM	heart:	n/a
28	chr14:45870299-45870349	U87	brain:	n/a
29	chr14:45722711-45722761	MCF10A-Er-Src	breast:	n/a
30	chr14:45759143-45759193	HEK293	kidney:	embryo
31	chr14:45722532-45722582	HPAEpiC	pulmonary alveolar:	n/a
32	chr14:45722711-45722761	HMEC	breast:	n/a
33	chr14:45722704-45722754	HNPCEpiC	eye:	n/a
34	chr14:45722745-45722795	HEEpiC	esophagus:	n/a
35	chr14:45722704-45722754	MCF-7	breast:	n/a
36	chr14:45930824-45930874	Hela-S3	cervix:	n/a
37	chr14:45722532-45722582	BE2_C	brain:	n/a
38	chr14:45840127-45840177	BE2_C	brain:	n/a
39	chr14:45722532-45722582	IMR90	lung:	fetal
40	chr14:45870299-45870349	A549	lung:	n/a
41	chr14:45722745-45722795	PANC-1	pancreas:	n/a
42	chr14:45722745-45722795	HEK293	kidney:	embryo
43	chr14:45722711-45722761	HRCEpiC	kidney:	n/a
44	chr14:45722617-45722667	HL-60	blood:	n/a
45	chr14:45722704-45722754	PFSK-1	brain:	n/a
46	chr14:45722532-45722582	AG10803	skin:	n/a
47	chr14:45722622-45722672	Hela-S3	cervix:	n/a
48	chr14:45722532-45722582	ovcar-3	ovarian:	n/a
49	chr14:45722617-45722667	SK-N-MC	brain:	n/a
50	chr14:45722043-45722093	AG04450	lung:	fetal

(count:51 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:45727473..45730434-chr14:45734970..45737678,2	MCF-7	breast:
2	chr14:45720720..45725312-chr14:45736349..45740437,5	MCF-7	breast:
3	chr14:45721810..45725859-chr14:45742099..45745950,4	MCF-7	breast:
4	chr14:45728008..45730307-chr14:45736451..45738128,2	MCF-7	breast:
5	chr14:45973970..45976424-chr14:45980516..45983044,2	MCF-7	breast:
6	chr14:45365477..45369212-chr14:45721451..45724440,3	MCF-7	breast:
7	chr14:45705828..45707853-chr14:45712067..45713833,2	MCF-7	breast:
8	chr14:45705828..45707853-chr14:45712067..45713833,2	MCF-7	breast:
9	chr14:45603451..45606015-chr14:45719614..45721854,2	K562	blood:
10	chr14:45827598..45829425-chr14:45832240..45834984,2	MCF-7	breast:
11	chr14:45774667..45776638-chr14:45777456..45779936,2	MCF-7	breast:
12	chr14:45932172..45934812-chr14:45938386..45940699,2	K562	blood:
13	chr14:45364937..45368444-chr14:45721075..45725396,9	MCF-7	breast:
14	chr14:45721810..45725859-chr14:45742099..45745950,4	MCF-7	breast:
15	chr14:45833828..45835787-chr14:45839702..45842192,2	K562	blood:
16	chr14:45932172..45934812-chr14:45938386..45940699,2	K562	blood:
17	chr14:45588121..45589844-chr14:45722977..45725072,2	MCF-7	breast:
18	chr14:45833660..45834242-chr14:45996510..45997327,3	MCF-7	breast:
19	chr14:45773220..45776127-chr14:45776332..45778274,2	K562	blood:
20	chr14:45827598..45829425-chr14:45832240..45834984,2	MCF-7	breast:
21	chr14:45687729..45690041-chr14:45727283..45730126,2	MCF-7	breast:
22	chr14:45895702..45896616-chr14:45996086..45997189,11	MCF-7	breast:
23	chr14:45383078..45384611-chr14:45736865..45739302,2	MCF-7	breast:
24	chr14:45710936..45712506-chr14:45717032..45718785,2	K562	blood:
25	chr14:45722471..45723281-chr15:75743983..75744975,2	Hela-S3	cervix:
26	chr14:45710340..45712436-chr14:45717199..45718785,2	K562	blood:
27	chr14:45895709..45896868-chr14:45996158..45997180,10	MCF-7	breast:
28	chr14:45721734..45722708-chr16:28565152..28565667,2	Hela-S3	cervix:
29	chr14:45602740..45605100-chr14:45878381..45880365,2	MCF-7	breast:
30	chr14:45602054..45606945-chr14:45719959..45724414,9	MCF-7	breast:
31	chr14:45722872..45725627-chr6:151936857..151939807,2	MCF-7	breast:
32	chr14:45601339..45606570-chr14:45722040..45724234,5	MCF-7	breast:
33	chr14:45717265..45719179-chr14:45721039..45722598,2	K562	blood:
34	chr14:45722237..45722750-chr18:3653037..3653537,2	HCT-116	colon:
35	chr14:45980303..45983033-chr14:45994308..45996794,2	MCF-7	breast:
36	chr14:45835845..45838000-chr14:45843048..45845340,2	K562	blood:
37	chr14:45728008..45730307-chr14:45736451..45738128,2	MCF-7	breast:
38	chr14:45833828..45835787-chr14:45839702..45842192,2	K562	blood:
39	chr14:45973970..45976424-chr14:45980516..45983044,2	MCF-7	breast:
40	chr14:45835845..45838000-chr14:45843048..45845340,2	K562	blood:
41	chr14:45382903..45383965-chr14:45737675..45738717,4	MCF-7	breast:
42	chr14:45722854..45723434-chr16:58133168..58133726,2	Hela-S3	cervix:
43	chr14:45774667..45776638-chr14:45777456..45779936,2	MCF-7	breast:
44	chr14:45553320..45554876-chr14:45714486..45717051,2	MCF-7	breast:
45	chr12:57039223..57039923-chr14:45722606..45723303,3	Hela-S3	cervix:
46	chr14:45701019..45703145-chr14:45705910..45707479,2	MCF-7	breast:
47	chr14:45727473..45730434-chr14:45734970..45737678,2	MCF-7	breast:
48	chr14:45429725..45432587-chr14:45720437..45723992,3	MCF-7	breast:
49	chr14:45704719..45706830-chr14:45720747..45723150,2	MCF-7	breast:
50	chr14:45773220..45776127-chr14:45776332..45778274,2	K562	blood:

(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-FKBP3-6	chr14:45710671-45711073	NONHSAT036649
4	lnc-FANCM-8	chr14:45759239-45759589	NONHSAT036654
5	lnc-FANCM-8	chr14:45759209-45759392	NONHSAT036653
6	lnc-FANCM-8	chr14:45759144-45759367	NONHSAT036652
7	lnc-FANCM-8	chr14:45759448-45759479	NONHSAT036652

No data

Variant related genes	Relation type
ENSG00000260046	TF binding region
DNAJC19P9	TF binding region
RNU6-552P	TF binding region
MIS18BP1	TF binding region
ENSG00000257900	TF binding region
ENSG00000258746	TF binding region
ENSG00000260046	CpG island
DNAJC19P9	CpG island
RNU6-552P	CpG island
MIS18BP1	CpG island
ENSG00000257900	CpG island
ENSG00000258746	CpG island
ENSG00000179454	chromatin interactions
ENSG00000185246	chromatin interactions
ENSG00000187790	chromatin interactions
ENSG00000129534	chromatin interactions
ENSG00000169375	chromatin interactions
ENSG00000266401	chromatin interactions
ENSG00000207422	chromatin interactions
ENSG00000258633	chromatin interactions
ENSG00000110955	chromatin interactions
ENSG00000199739	chromatin interactions
ENSG00000179476	chromatin interactions
ENSG00000100442	chromatin interactions
ENSG00000198718	chromatin interactions
ENSG00000176476	chromatin interactions

Extended variants
information (count: 4431 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:4431 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568088945	chr14:45706102-45706103	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs564075822	chr14:45706199-45706200	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs200013792	chr14:45706204-45706205	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs546679433	chr14:45706216-45706217	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs145292555	chr14:45706271-45706272	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs568545160	chr14:45706277-45706278	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs386777041	chr14:45706315-45706316	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs79005360	chr14:45706316-45706317	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs562200085	chr14:45706343-45706344	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs188971050	chr14:45706345-45706346	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs147630678	chr14:45706353-45706354	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs181516688	chr14:45706376-45706377	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs533033932	chr14:45706387-45706388	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs551471062	chr14:45706459-45706460	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs577180968	chr14:45706462-45706463	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs149112610	chr14:45706497-45706498	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs537457083	chr14:45706558-45706559	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs549262129	chr14:45706596-45706597	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs567445803	chr14:45706611-45706612	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs539259821	chr14:45706618-45706619	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs534859389	chr14:45706629-45706630	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs546367864	chr14:45706700-45706701	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs186646025	chr14:45706721-45706722	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs539561936	chr14:45706763-45706764	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs142151153	chr14:45706786-45706787	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs74811036	chr14:45706798-45706799	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs537050061	chr14:45706855-45706856	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372902086	chr14:45706903-45706904	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554618008	chr14:45706907-45706908	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs377123303	chr14:45706936-45706937	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374485571	chr14:45706958-45706959	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs370382464	chr14:45706969-45706970	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs201889438	chr14:45706986-45706987	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs1252966	chr14:45707041-45707042	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs151199454	chr14:45707081-45707082	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs529395066	chr14:45707092-45707093	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs1252965	chr14:45707136-45707137	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs145374947	chr14:45707196-45707197	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs578190233	chr14:45707199-45707200	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs137880443	chr14:45707264-45707265	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs563188411	chr14:45707319-45707320	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs397708658	chr14:45707333-45707334	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs368682898	chr14:45707334-45707335	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs140839847	chr14:45707378-45707379	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs144608056	chr14:45707410-45707411	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191287575	chr14:45707439-45707440	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138930921	chr14:45707473-45707474	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561270098	chr14:45707493-45707494	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs149435835	chr14:45707556-45707557	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs8004730	chr14:45707573-45707574	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:58)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1192 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:45631800-45711400	Weak transcription	Brain Hippocampus Middle	brain
2	chr14:45632800-45707000	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr14:45633800-45721200	Weak transcription	Aorta	Aorta
4	chr14:45655600-45719200	Weak transcription	Stomach Smooth Muscle	stomach
5	chr14:45660600-45707000	Weak transcription	Gastric	stomach
6	chr14:45662800-45711400	Weak transcription	Brain Anterior Caudate	brain
7	chr14:45669600-45712000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr14:45670000-45711400	Weak transcription	Brain Substantia Nigra	brain
9	chr14:45670000-45711600	Strong transcription	Monocytes-CD14+_RO01746	blood
10	chr14:45673200-45706400	Strong transcription	Fetal Thymus	thymus
11	chr14:45674600-45719200	Weak transcription	Colonic Mucosa	Colon
12	chr14:45675000-45711600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr14:45675200-45711600	Weak transcription	Colon Smooth Muscle	Colon
14	chr14:45676200-45711600	Weak transcription	NHLF	lung
15	chr14:45678400-45711800	Strong transcription	Dnd41	blood
16	chr14:45680400-45714000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
17	chr14:45681800-45711000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr14:45682000-45721200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr14:45682200-45711200	Weak transcription	Fetal Brain Female	brain
20	chr14:45682200-45714800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chr14:45682200-45719200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr14:45682400-45720400	Weak transcription	Brain Germinal Matrix	brain
23	chr14:45682600-45706200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr14:45684800-45719400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr14:45685200-45710000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr14:45686600-45719200	Weak transcription	Fetal Heart	heart
27	chr14:45687200-45719200	Weak transcription	HSMMtube	muscle
28	chr14:45688800-45706400	Strong transcription	Primary neutrophils fromperipheralblood	blood
29	chr14:45690800-45709200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr14:45690800-45711600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr14:45691000-45710200	Strong transcription	Primary B cells from cord blood	blood
32	chr14:45691000-45712200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
33	chr14:45691600-45709600	Strong transcription	Primary hematopoietic stem cells	blood
34	chr14:45691600-45712600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr14:45691600-45713800	Strong transcription	Primary B cells from peripheral blood	blood
36	chr14:45691800-45711400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr14:45691800-45711400	Strong transcription	Duodenum Mucosa	Duodenum
38	chr14:45691800-45712000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr14:45692000-45707000	Strong transcription	Primary T helper cells fromperipheralblood	blood
40	chr14:45692200-45719000	Weak transcription	Small Intestine	intestine
41	chr14:45692200-45719800	Weak transcription	Esophagus	oesophagus
42	chr14:45692800-45718600	Weak transcription	Lung	lung
43	chr14:45693600-45719200	Weak transcription	K562	blood
44	chr14:45693600-45719200	Weak transcription	NHEK	skin
45	chr14:45695000-45721600	Weak transcription	Pancreas	Pancrea
46	chr14:45697200-45711200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr14:45698600-45706200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
48	chr14:45699000-45709200	Strong transcription	GM12878-XiMat	blood
49	chr14:45699400-45711400	Strong transcription	Primary monocytes fromperipheralblood	blood
50	chr14:45699600-45706600	Strong transcription	iPS-18 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links