Variant report

Variant	nsv1246
Chromosome Location	chr14:39656597-39701520
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:725)
CpG islands
(count:0)
Chromatin interactive
region (count:56)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:725 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:39700816-39701323	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:39687682-39688024	HepG2	liver:	n/a	n/a
3	ATF1	chr14:39692963-39693215	K562	blood:	n/a	n/a
4	ATF2	chr14:39698313-39698734	GM12878	blood:	n/a	n/a
5	ATF2	chr14:39698332-39698655	GM12878	blood:	n/a	n/a
6	ATF3	chr14:39700955-39701155	K562	blood:	n/a	n/a
7	BACH1	chr14:39673211-39673441	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr14:39698345-39698797	GM12878	blood:	n/a	n/a
9	BHLHE40	chr14:39701015-39701207	HepG2	liver:	n/a	n/a
10	BHLHE40	chr14:39657259-39657439	HepG2	liver:	n/a	n/a
11	BHLHE40	chr14:39688291-39688559	HepG2	liver:	n/a	n/a
12	BRCA1	chr14:39656901-39657298	H1-hESC	embryonic stem cell:	n/a	n/a
13	BRCA1	chr14:39673328-39673422	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr14:39672960-39673548	K562	blood:	n/a	n/a
15	CBX3	chr14:39686263-39687101	HCT-116	colon:	n/a	n/a
16	CBX3	chr14:39687213-39688053	HCT-116	colon:	n/a	n/a
17	CEBPB	chr14:39700646-39701636	HepG2	liver:	n/a	chr14:39701396-39701407
18	CEBPB	chr14:39679408-39679716	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr14:39701010-39701546	HepG2	liver:	n/a	chr14:39701396-39701407
20	CEBPB	chr14:39679419-39679747	HepG2	liver:	n/a	n/a
21	CEBPB	chr14:39692807-39693129	HepG2	liver:	n/a	chr14:39692949-39692960
22	CEBPB	chr14:39679437-39679623	HepG2	liver:	n/a	n/a
23	CEBPB	chr14:39687332-39688005	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr14:39692848-39693108	IMR90	lung:	n/a	chr14:39692949-39692960
25	CEBPB	chr14:39670879-39671145	MCF-7	breast:	n/a	chr14:39670976-39670987
26	CEBPB	chr14:39679495-39679634	K562	blood:	n/a	n/a
27	CEBPB	chr14:39679543-39679574	IMR90	lung:	n/a	n/a
28	CEBPB	chr14:39700933-39701540	HepG2	liver:	n/a	chr14:39701396-39701407
29	CEBPB	chr14:39686529-39686682	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr14:39692808-39693147	K562	blood:	n/a	chr14:39692949-39692960
31	CEBPB	chr14:39670920-39671055	HepG2	liver:	n/a	chr14:39670976-39670987
32	CEBPB	chr14:39670935-39670993	K562	blood:	n/a	chr14:39670976-39670987
33	CEBPB	chr14:39680427-39680572	HepG2	liver:	n/a	n/a
34	CEBPB	chr14:39700966-39701218	K562	blood:	n/a	n/a
35	CEBPB	chr14:39687180-39688059	HCT-116	colon:	n/a	n/a
36	CEBPB	chr14:39656772-39656882	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr14:39659722-39660054	HepG2	liver:	n/a	chr14:39659889-39659900
38	CEBPB	chr14:39659846-39659972	A549	lung:	n/a	chr14:39659889-39659900
39	CEBPB	chr14:39701301-39701487	HepG2	liver:	n/a	chr14:39701396-39701407
40	CEBPB	chr14:39679361-39679777	MCF-7	breast:	n/a	n/a
41	CEBPD	chr14:39701291-39701487	HepG2	liver:	n/a	n/a
42	CHD2	chr14:39686531-39686715	Hela-S3	cervix:	n/a	n/a
43	CHD2	chr14:39700964-39701179	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr14:39673295-39673516	K562	blood:	n/a	n/a
45	CHD2	chr14:39656917-39657213	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr14:39657042-39657987	HepG2	liver:	n/a	n/a
47	CHD2	chr14:39673185-39673601	Hela-S3	cervix:	n/a	n/a
48	CREB1	chr14:39700903-39701191	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr14:39700833-39701316	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chr14:39700798-39701372	HepG2	liver:	n/a	n/a

No data

(count:56 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:39582452..39584662-chr14:39670252..39672838,2	MCF-7	breast:
2	chr14:39666993..39668682-chr14:39671014..39673008,3	K562	blood:
3	chr14:39652084..39653603-chr14:39673208..39674961,2	K562	blood:
4	chr14:39654966..39657894-chr14:39668988..39671853,2	K562	blood:
5	chr14:39639912..39642266-chr14:39694401..39697374,2	K562	blood:
6	chr14:39687884..39690002-chr14:39715235..39717332,2	MCF-7	breast:
7	chr14:39659557..39662468-chr14:39664703..39667964,3	K562	blood:
8	chr14:39571020..39573430-chr14:39654386..39657374,3	K562	blood:
9	chr14:39687526..39690139-chr14:39695809..39697449,2	MCF-7	breast:
10	chr14:39581979..39584975-chr14:39691511..39693486,2	MCF-7	breast:
11	chr14:39669831..39673091-chr14:39734420..39737193,3	MCF-7	breast:
12	chr14:39659021..39661410-chr14:39671300..39673162,2	K562	blood:
13	chr14:39666993..39668682-chr14:39671014..39673008,3	K562	blood:
14	chr14:39680164..39682554-chr14:39734526..39737073,3	MCF-7	breast:
15	chr14:39655760..39659371-chr14:39734225..39738994,7	K562	blood:
16	chr14:39642610..39646092-chr14:39673338..39676993,4	MCF-7	breast:
17	chr14:39638891..39641141-chr14:39697742..39700523,2	MCF-7	breast:
18	chr14:39654749..39656779-chr14:39701075..39703630,2	K562	blood:
19	chr14:39700657..39701493-chr14:39938250..39938831,2	MCF-7	breast:
20	chr14:39654966..39657537-chr14:39669625..39671853,2	K562	blood:
21	chr14:39682657..39684941-chr14:39688892..39691527,2	MCF-7	breast:
22	chr14:39690148..39692016-chr14:39692891..39694587,2	MCF-7	breast:
23	chr14:39654966..39657894-chr14:39668988..39671853,2	K562	blood:
24	chr14:39655751..39657346-chr14:39681052..39683372,2	K562	blood:
25	chr14:39651767..39657982-chr14:39696424..39701629,5	MCF-7	breast:
26	chr14:39687526..39690139-chr14:39695809..39697449,2	MCF-7	breast:
27	chr14:39660811..39663578-chr14:39679373..39681871,2	MCF-7	breast:
28	chr14:39690148..39692016-chr14:39692891..39694587,2	MCF-7	breast:
29	chr14:39648211..39650713-chr14:39694377..39696720,2	MCF-7	breast:
30	chr14:39659557..39662468-chr14:39664703..39667964,3	K562	blood:
31	chr14:39653322..39655691-chr14:39686877..39688589,2	MCF-7	breast:
32	chr14:39637993..39640586-chr14:39685668..39689365,3	MCF-7	breast:
33	chr14:39642456..39648509-chr14:39688590..39693921,7	MCF-7	breast:
34	chr14:39654966..39657537-chr14:39669625..39671853,2	K562	blood:
35	chr14:39660968..39663251-chr14:39664703..39666593,2	K562	blood:
36	chr14:39571162..39573957-chr14:39700069..39703541,3	MCF-7	breast:
37	chr14:39652103..39654981-chr14:39673043..39674708,2	K562	blood:
38	chr14:39576686..39577197-chr14:39693179..39693779,2	MCF-7	breast:
39	chr14:39642562..39645375-chr14:39698449..39701112,2	MCF-7	breast:
40	chr14:39644203..39647101-chr14:39685504..39687288,2	MCF-7	breast:
41	chr14:39655421..39657718-chr14:39690495..39693068,2	K562	blood:
42	chr14:39655751..39657346-chr14:39681052..39683372,2	K562	blood:
43	chr14:39651862..39654641-chr14:39690512..39693459,3	K562	blood:
44	chr14:39660968..39663251-chr14:39664703..39666593,2	K562	blood:
45	chr14:39655012..39658223-chr14:39734448..39737542,3	MCF-7	breast:
46	chr14:39643409..39646477-chr14:39682252..39685201,4	MCF-7	breast:
47	chr14:39700567..39701347-chr14:39837621..39838221,3	MCF-7	breast:
48	chr14:39655214..39656857-chr14:39716747..39718592,2	K562	blood:
49	chr14:39686963..39689820-chr14:39735016..39736647,2	K562	blood:
50	chr14:39599049..39601642-chr14:39656945..39658704,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PNN-2	chr14:39664019-39664587	NONHSAT036525
2	lnc-MIA2-1	chr14:39680985-39681459	NONHSAT036526
3	lnc-PNN-1	chr14:39662567-39662912	NONHSAT036524

No data

Variant related genes	Relation type
ENSG00000258941	TF binding region
ENSG00000258671	TF binding region
MIA2	TF binding region
ENSG00000270503	TF binding region
ENSG00000150526	chromatin interactions
ENSG00000182400	chromatin interactions
ENSG00000259083	chromatin interactions
ENSG00000150527	chromatin interactions
ENSG00000100934	chromatin interactions
ENSG00000100941	chromatin interactions
ENSG00000258941	chromatin interactions
ENSG00000092208	chromatin interactions
ENSG00000258940	chromatin interactions
ENSG00000270503	chromatin interactions
ENSG00000258651	chromatin interactions
ENSG00000258671	chromatin interactions

Extended variants
information (count: 1716 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1716 , 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	rs144755964	chr14:39656638-39656639	Enhancers Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs551209821	chr14:39656649-39656650	Enhancers Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs571129914	chr14:39656692-39656693	Enhancers Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs148654384	chr14:39656709-39656710	Enhancers Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs553671937	chr14:39656718-39656719	Enhancers Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs142169392	chr14:39656772-39656773	Enhancers Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs71406503	chr14:39656818-39656819	Enhancers Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs79831097	chr14:39656826-39656827	Enhancers Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs55760039	chr14:39656846-39656847	Enhancers Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs199913021	chr14:39656847-39656848	Enhancers Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs200986444	chr14:39656848-39656849	Enhancers Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs140423287	chr14:39656860-39656861	Enhancers Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs11157048	chr14:39656863-39656864	Enhancers Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs372847166	chr14:39656875-39656876	Enhancers Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs543974911	chr14:39656876-39656877	Enhancers Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs183967839	chr14:39656878-39656879	Enhancers Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs28501673	chr14:39656896-39656897	Enhancers Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs576797174	chr14:39656931-39656932	Enhancers Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs540145369	chr14:39656973-39656974	Enhancers Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs531962473	chr14:39656988-39656989	Enhancers Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs550069166	chr14:39657032-39657033	Enhancers Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs187768725	chr14:39657115-39657116	Enhancers Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs560444615	chr14:39657170-39657171	Enhancers Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs528835509	chr14:39657180-39657181	Enhancers Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs191551546	chr14:39657297-39657298	Enhancers Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs78362689	chr14:39657372-39657373	Enhancers Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs371776832	chr14:39657387-39657388	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs184132722	chr14:39657417-39657418	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs9788627	chr14:39657427-39657428	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs571049310	chr14:39657430-39657431	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs78861409	chr14:39657448-39657449	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs546933193	chr14:39657468-39657469	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs567165920	chr14:39657508-39657509	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs141025252	chr14:39657516-39657517	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs376361977	chr14:39657517-39657518	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs535449039	chr14:39657566-39657567	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs58306156	chr14:39657618-39657619	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs72673357	chr14:39657637-39657638	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs34065215	chr14:39657664-39657665	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs537934244	chr14:39657709-39657710	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs565772455	chr14:39657756-39657757	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs557869979	chr14:39657781-39657782	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs577411564	chr14:39657810-39657811	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs188853085	chr14:39657872-39657873	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs553742540	chr14:39657881-39657882	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs376359335	chr14:39657904-39657905	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs73291596	chr14:39657909-39657910	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs144168426	chr14:39657917-39657918	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs536225000	chr14:39657926-39657927	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs545124316	chr14:39657937-39657938	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Thyroid cancer	19470727	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:341 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:39645800-39657200	Strong transcription	HSMM	muscle
2	chr14:39647800-39658800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr14:39651000-39656600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr14:39651000-39657000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr14:39651000-39661600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr14:39651000-39662000	Weak transcription	Pancreas	Pancrea
7	chr14:39651200-39657000	Weak transcription	Small Intestine	intestine
8	chr14:39652400-39657200	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr14:39653000-39658000	Weak transcription	Fetal Lung	lung
10	chr14:39653000-39662000	Weak transcription	Primary hematopoietic stem cells	blood
11	chr14:39653200-39656800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr14:39653200-39661600	Weak transcription	Right Ventricle	heart
13	chr14:39653400-39657000	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr14:39653400-39662000	Weak transcription	NHDF-Ad	bronchial
15	chr14:39653600-39658800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr14:39654000-39657200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr14:39654200-39657000	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr14:39654400-39656800	Weak transcription	Spleen	Spleen
19	chr14:39654400-39657000	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr14:39654400-39657400	Weak transcription	Primary B cells from cord blood	blood
21	chr14:39654400-39657800	Weak transcription	Primary T helper cells PMA-I stimulated	--
22	chr14:39654400-39658400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr14:39654400-39658800	Weak transcription	Thymus	Thymus
24	chr14:39654400-39661600	Weak transcription	Left Ventricle	heart
25	chr14:39654400-39661800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr14:39654400-39661800	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chr14:39654400-39672000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr14:39654600-39656800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr14:39654600-39657000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr14:39654600-39657400	Weak transcription	Osteobl	bone
31	chr14:39654600-39657800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr14:39654600-39661600	Weak transcription	Psoas Muscle	Psoas
33	chr14:39654800-39656600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr14:39654800-39656600	Weak transcription	Primary monocytes fromperipheralblood	blood
35	chr14:39654800-39656800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr14:39654800-39656800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr14:39654800-39657000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr14:39654800-39658000	Weak transcription	Fetal Brain Female	brain
39	chr14:39654800-39658200	Weak transcription	Adipose Nuclei	Adipose
40	chr14:39654800-39659400	Weak transcription	Primary neutrophils fromperipheralblood	blood
41	chr14:39654800-39662000	Weak transcription	Liver	Liver
42	chr14:39655000-39656600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr14:39655000-39656600	Weak transcription	Rectal Mucosa Donor 29	rectum
44	chr14:39655000-39656600	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr14:39655000-39656600	Weak transcription	HUVEC	blood vessel
46	chr14:39655000-39657000	Weak transcription	HMEC	breast
47	chr14:39655000-39657200	Weak transcription	NH-A	brain
48	chr14:39655000-39657600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr14:39655000-39658400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr14:39655000-39658800	Weak transcription	Stomach Smooth Muscle	stomach

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