Variant report

Variant	nsv84529
Chromosome Location	chr14:55512778-55517728
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr14:55516446-55517250	A549	lung:	n/a	n/a
2	BCL3	chr14:55517634-55518735	A549	lung:	n/a	chr14:55518583-55518596 chr14:55518579-55518592 chr14:55518585-55518598 chr14:55518297-55518310
3	CBX3	chr14:55517619-55518875	K562	blood:	n/a	n/a
4	CEBPB	chr14:55514590-55514790	K562	blood:	n/a	n/a
5	CEBPB	chr14:55514573-55514744	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD1	chr14:55517480-55520955	IMR90	lung:	n/a	n/a
7	CHD2	chr14:55517704-55519218	GM12878	blood:	n/a	n/a
8	CTCF	chr14:55517647-55519185	SK-N-SH	brain:	n/a	chr14:55519090-55519098 chr14:55518214-55518232 chr14:55518381-55518394 chr14:55518288-55518301 chr14:55518288-55518297 chr14:55518241-55518254 chr14:55518298-55518311 chr14:55518217-55518226 chr14:55518391-55518404 chr14:55518378-55518391
9	CTCF	chr14:55517680-55517830	GM12864	blood:	n/a	n/a
10	E2F6	chr14:55517604-55518856	K562	blood:	n/a	chr14:55518375-55518385 chr14:55518241-55518251 chr14:55518791-55518800 chr14:55518608-55518617 chr14:55518587-55518596 chr14:55518793-55518802
11	E2F6	chr14:55517588-55519087	H1-hESC	embryonic stem cell:	n/a	chr14:55518375-55518385 chr14:55518241-55518251 chr14:55518791-55518800 chr14:55518608-55518617 chr14:55518587-55518596 chr14:55518793-55518802
12	E2F6	chr14:55517655-55517813	K562	blood:	n/a	n/a
13	ELF1	chr14:55517548-55519032	MCF-7	breast:	n/a	chr14:55518344-55518353 chr14:55518578-55518590
14	EP300	chr14:55516888-55516889	K562	blood:	n/a	n/a
15	FOXM1	chr14:55517712-55518750	GM12878	blood:	n/a	n/a
16	FOXP2	chr14:55515677-55515911	SK-N-MC	brain:	n/a	n/a
17	GABPA	chr14:55517334-55519075	MCF-7	breast:	n/a	chr14:55518608-55518617 chr14:55518587-55518596 chr14:55518441-55518455
18	GABPA	chr14:55517424-55519353	MCF-7	breast:	n/a	chr14:55518608-55518617 chr14:55518587-55518596 chr14:55518441-55518455
19	HCFC1	chr14:55517640-55519220	Hela-S3	cervix:	n/a	n/a
20	HEY1	chr14:55517599-55520167	K562	blood:	n/a	chr14:55518793-55518802 chr14:55518933-55518948 chr14:55518791-55518800
21	JUN	chr14:55517373-55519468	K562	blood:	n/a	chr14:55518792-55518801
22	KAP1	chr14:55517647-55519251	HEK293	kidney:	n/a	n/a
23	MAFF	chr14:55515766-55516137	HepG2	liver:	n/a	chr14:55515940-55515958
24	MAFF	chr14:55515764-55516140	K562	blood:	n/a	chr14:55515940-55515958
25	MAFK	chr14:55515766-55516140	K562	blood:	n/a	chr14:55515942-55515957
26	MAFK	chr14:55515766-55516142	Hela-S3	cervix:	n/a	chr14:55515942-55515957
27	MAFK	chr14:55515552-55516187	GM12878	blood:	n/a	chr14:55515942-55515957
28	MAFK	chr14:55515767-55516158	IMR90	lung:	n/a	chr14:55515942-55515957
29	MAFK	chr14:55515780-55516337	H1-hESC	embryonic stem cell:	n/a	chr14:55515942-55515957
30	MAFK	chr14:55515765-55516137	HepG2	liver:	n/a	chr14:55515942-55515957
31	MAFK	chr14:55513884-55513950	Hela-S3	cervix:	n/a	n/a
32	MAFK	chr14:55515776-55516132	HepG2	liver:	n/a	chr14:55515942-55515957
33	MAX	chr14:55517665-55519045	HepG2	liver:	n/a	chr14:55518309-55518318
34	MAX	chr14:55517496-55519029	A549	lung:	n/a	chr14:55518309-55518318
35	MAX	chr14:55517425-55519263	MCF-7	breast:	n/a	chr14:55518309-55518318
36	MAX	chr14:55517491-55519101	MCF-7	breast:	n/a	chr14:55518309-55518318
37	MAX	chr14:55517653-55519156	ECC-1	luminal epithelium:	n/a	chr14:55518309-55518318
38	MAX	chr14:55517632-55519299	HepG2	liver:	n/a	chr14:55518309-55518318
39	MAX	chr14:55517507-55517917	K562	blood:	n/a	n/a
40	MAX	chr14:55517646-55519394	Hela-S3	cervix:	n/a	chr14:55518309-55518318
41	MAX	chr14:55517440-55519135	A549	lung:	n/a	chr14:55518309-55518318
42	MAZ	chr14:55517705-55519797	IMR90	lung:	n/a	chr14:55518309-55518318
43	MTA3	chr14:55517718-55518603	GM12878	blood:	n/a	n/a
44	MTA3	chr14:55516459-55516822	GM12878	blood:	n/a	n/a
45	MTA3	chr14:55517426-55519356	GM12878	blood:	n/a	n/a
46	MTA3	chr14:55516330-55517227	GM12878	blood:	n/a	n/a
47	MYC	chr14:55516811-55516843	H1-hESC	embryonic stem cell:	n/a	n/a
48	MYC	chr14:55517607-55517858	MCF-7	breast:	n/a	n/a
49	MYC	chr14:55517721-55517724	MCF-7	breast:	n/a	n/a
50	MYC	chr14:55517692-55517832	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:55514980-55515030	AoSMC	blood vessel:	n/a
2	chr14:55517313-55517363	MCF-7	breast:	n/a
3	chr14:55514980-55515030	NHDF-neo	bronchial:	n/a
4	chr14:55514980-55515030	SK-N-SH	brain:	n/a
5	chr14:55517313-55517363	HUVEC	blood vessel:	n/a
6	chr14:55514980-55515030	NT2-D1	testis:	n/a
7	chr14:55514980-55515030	SKMC	muscle:	n/a
8	chr14:55517313-55517363	MCF10A-Er-Src	breast:	n/a
9	chr14:55517313-55517363	HRPEpiC	eye:	n/a
10	chr14:55514980-55515030	LNCaP	prostate:	n/a
11	chr14:55514980-55515030	MCF10A-Er-Src	breast:	n/a
12	chr14:55517313-55517363	BJ	skin:	n/a
13	chr14:55514980-55515030	HEEpiC	esophagus:	n/a
14	chr14:55514980-55515030	Hela-S3	cervix:	n/a
15	chr14:55514980-55515030	NH-A	brain:	n/a
16	chr14:55514980-55515030	HRPEpiC	eye:	n/a
17	chr14:55517313-55517363	NHBE	bronchial:	n/a
18	chr14:55514980-55515030	NB4	blood:	n/a
19	chr14:55514980-55515030	HEK293	kidney:	embryo
20	chr14:55517313-55517363	BE2_C	brain:	n/a
21	chr14:55514980-55515030	GM06990	blood:	n/a
22	chr14:55517313-55517363	PFSK-1	brain:	n/a
23	chr14:55517313-55517363	GM12891	blood:	n/a
24	chr14:55514980-55515030	U87	brain:	n/a
25	chr14:55517313-55517363	GM12878	blood:	n/a
26	chr14:55514980-55515030	PrEC	prostate:	n/a
27	chr14:55514980-55515030	A549	lung:	n/a
28	chr14:55514980-55515030	Hepatocyte	liver:	n/a
29	chr14:55514980-55515030	Jurkat	blood:	n/a
30	chr14:55514980-55515030	HUVEC	blood vessel:	n/a
31	chr14:55517313-55517363	PrEC	prostate:	n/a
32	chr14:55517313-55517363	RPTEC	kidney:	n/a
33	chr14:55517313-55517363	A549	lung:	n/a
34	chr14:55514980-55515030	GM19239	blood:	n/a
35	chr14:55514980-55515030	GM12892	blood:	n/a
36	chr14:55514980-55515030	HMEC	breast:	n/a
37	chr14:55514980-55515030	AG04450	lung:	fetal
38	chr14:55517313-55517363	Caco-2	colon:	n/a
39	chr14:55514980-55515030	AG04449	skin:	fetal
40	chr14:55517313-55517363	ECC-1	luminal epithelium:	n/a
41	chr14:55514980-55515030	BJ	skin:	n/a
42	chr14:55517313-55517363	AG04449	skin:	fetal
43	chr14:55517313-55517363	HNPCEpiC	eye:	n/a
44	chr14:55517313-55517363	AG10803	skin:	n/a
45	chr14:55514980-55515030	SK-N-SH_RA	brain:	n/a
46	chr14:55514980-55515030	ovcar-3	ovarian:	n/a
47	chr14:55514980-55515030	ProgFib	skin:	n/a
48	chr14:55517313-55517363	AoSMC	blood vessel:	n/a
49	chr14:55514980-55515030	ECC-1	luminal epithelium:	n/a
50	chr14:55514980-55515030	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:55497119..55499887-chr14:55511946..55513977,2	MCF-7	breast:
2	chr14:55490790..55495805-chr14:55515486..55522658,19	MCF-7	breast:
3	chr12:120314625..120315526-chr14:55517585..55518582,2	Hela-S3	cervix:
4	chr14:55493972..55498765-chr14:55510765..55514879,5	K562	blood:
5	chr14:55492371..55495011-chr14:55512361..55514260,2	K562	blood:
6	chr14:55516892..55519791-chr14:55737278..55740152,4	K562	blood:
7	chr14:55491992..55498342-chr14:55515529..55520367,21	K562	blood:
8	chr14:55495289..55498964-chr14:55511770..55513714,3	K562	blood:
9	chr14:55509588..55512063-chr14:55512122..55515108,3	K562	blood:
10	chr14:55517347..55519818-chr14:55736283..55739378,3	MCF-7	breast:
11	chr14:55509907..55511424-chr14:55511623..55513423,2	MCF-7	breast:
12	chr14:55517345..55520488-chr14:55656247..55658381,3	K562	blood:
13	chr14:55367425..55371142-chr14:55516489..55521777,7	MCF-7	breast:
14	chr14:55492422..55495780-chr14:55511028..55514664,4	MCF-7	breast:
15	chr14:55516981..55523073-chr14:55594365..55600344,10	MCF-7	breast:
16	chr14:55517047..55520032-chr14:55601675..55604188,2	MCF-7	breast:
17	chr14:55500393..55503713-chr14:55510224..55513637,3	K562	blood:
18	chr14:55517037..55520851-chr14:55594266..55601656,13	MCF-7	breast:
19	chr14:55513055..55515662-chr3:156536623..156538871,2	MCF-7	breast:
20	chr14:55464474..55467382-chr14:55512370..55514260,2	K562	blood:
21	chr14:55504558..55506513-chr14:55512059..55513763,2	K562	blood:
22	chr14:55368105..55371463-chr14:55516987..55520396,7	MCF-7	breast:
23	chr1:24069447..24070358-chr14:55517586..55518557,2	Hela-S3	cervix:
24	chr14:54906668..54909344-chr14:55516272..55518741,3	K562	blood:
25	chr14:55491083..55496744-chr14:55514437..55523536,23	MCF-7	breast:
26	chr14:55336799..55338659-chr14:55514913..55516718,2	MCF-7	breast:
27	chr14:55516908..55519746-chr14:55654326..55658338,3	K562	blood:
28	chr14:55491921..55500295-chr14:55515389..55520812,24	K562	blood:

No.	miRNA target gene	miRNA name	Chromosome Location
1	SOCS4	hsa-miR-130b-3p	chr14:55513670-55513692
2	SOCS4	hsa-miR-98-5p	chr14:55512925-55512932
3	SOCS4	hsa-miR-98-5p	chr14:55512911-55512932
4	SOCS4	hsa-miR-34a-5p	chr14:55513373-55513379
5	SOCS4	hsa-miR-19b-3p	chr14:55513452-55513477

Variant related genes	Relation type
MAPK1IP1L	TF binding region
MAPK1IP1L	CpG island
ENSG00000198554	chromatin interactions
ENSG00000178974	chromatin interactions
ENSG00000258413	chromatin interactions
ENSG00000131981	chromatin interactions
ENSG00000122966	chromatin interactions
ENSG00000126787	chromatin interactions
ENSG00000131979	chromatin interactions
ENSG00000011007	chromatin interactions
ENSG00000180008	chromatin interactions
ENSG00000100528	chromatin interactions

Extended variants
information (count: 152 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:152 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541740394	chr14:55512812-55512813	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs190454735	chr14:55512843-55512844	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs146621006	chr14:55512847-55512848	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs368201830	chr14:55512902-55512903	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs541742955	chr14:55512907-55512908	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs111256781	chr14:55512942-55512943	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs528544061	chr14:55513127-55513128	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs540645892	chr14:55513132-55513133	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs561913675	chr14:55513160-55513161	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs529628326	chr14:55513163-55513164	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs551287936	chr14:55513179-55513180	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs535318893	chr14:55513207-55513208	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs145521728	chr14:55513320-55513321	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs533572689	chr14:55513356-55513357	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs10144957	chr14:55513454-55513455	Weak transcription Strong transcription	Chromatin interactive region miRNA target site	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs565670938	chr14:55513533-55513534	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs140056483	chr14:55513553-55513554	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs182747073	chr14:55513562-55513563	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs537519129	chr14:55513568-55513569	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs570545865	chr14:55513587-55513588	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs551176640	chr14:55513646-55513647	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs570767494	chr14:55513770-55513771	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs539717823	chr14:55513771-55513772	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs544247177	chr14:55513826-55513827	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs567951655	chr14:55513838-55513839	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs11849878	chr14:55513848-55513849	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs556839737	chr14:55513851-55513852	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs187038398	chr14:55513915-55513916	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs553777129	chr14:55514012-55514013	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs552539517	chr14:55514067-55514068	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs148816701	chr14:55514120-55514121	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs556212768	chr14:55514143-55514144	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs557641253	chr14:55514254-55514255	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs77080290	chr14:55514316-55514317	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs540356509	chr14:55514330-55514331	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs369026330	chr14:55514360-55514361	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs562155489	chr14:55514385-55514386	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs192877409	chr14:55514387-55514388	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs573227756	chr14:55514410-55514411	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs544573149	chr14:55514434-55514435	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs563187435	chr14:55514445-55514446	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs533635926	chr14:55514460-55514461	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs552029524	chr14:55514461-55514462	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs560502594	chr14:55514473-55514474	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs111527936	chr14:55514493-55514494	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs371203740	chr14:55514503-55514504	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs528227939	chr14:55514610-55514611	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs75593358	chr14:55514616-55514617	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs568100458	chr14:55514654-55514655	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs111857057	chr14:55514669-55514670	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

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
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
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	16397240	CNVD
Breast cancer	21633010	CNVD
Breast cancer	22032731	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
Breast cancer	21364760	CNVD
Medulloblastoma	19270706	CNVD

Chromatin state (count:260 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:55494400-55517600	Weak transcription	Lung	lung
2	chr14:55495000-55517600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr14:55495000-55517600	Weak transcription	Esophagus	oesophagus
4	chr14:55495200-55517600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr14:55495200-55517600	Weak transcription	Colonic Mucosa	Colon
6	chr14:55495200-55517800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr14:55495200-55517800	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr14:55495400-55517600	Weak transcription	Right Ventricle	heart
9	chr14:55495600-55517600	Weak transcription	Brain Substantia Nigra	brain
10	chr14:55495600-55517600	Weak transcription	Fetal Kidney	kidney
11	chr14:55495600-55517600	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr14:55496200-55517600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr14:55496200-55517600	Weak transcription	Fetal Heart	heart
14	chr14:55498400-55517600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr14:55501400-55517400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr14:55505600-55513000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr14:55506400-55517000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr14:55507800-55517600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr14:55508000-55516400	Weak transcription	Fetal Stomach	stomach
20	chr14:55508200-55513600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr14:55508400-55517600	Weak transcription	Fetal Intestine Small	intestine
22	chr14:55509200-55512800	Strong transcription	Primary monocytes fromperipheralblood	blood
23	chr14:55509200-55513000	Strong transcription	HSMM	muscle
24	chr14:55509400-55513000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr14:55509600-55512800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr14:55510200-55517600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
27	chr14:55510200-55517800	Weak transcription	Aorta	Aorta
28	chr14:55510600-55517600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr14:55510600-55517600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr14:55510800-55516400	Weak transcription	K562	blood
31	chr14:55510800-55517400	Weak transcription	Fetal Lung	lung
32	chr14:55510800-55517600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr14:55510800-55517600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr14:55510800-55517600	Weak transcription	Colon Smooth Muscle	Colon
35	chr14:55510800-55517600	Weak transcription	Left Ventricle	heart
36	chr14:55510800-55517600	Weak transcription	Stomach Mucosa	stomach
37	chr14:55510800-55517600	Weak transcription	Spleen	Spleen
38	chr14:55510800-55517600	Weak transcription	Hela-S3	cervix
39	chr14:55510800-55517800	Weak transcription	Thymus	Thymus
40	chr14:55511000-55516600	Weak transcription	NHEK	skin
41	chr14:55511000-55516800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr14:55511000-55517000	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr14:55511000-55517200	Weak transcription	Brain Germinal Matrix	brain
44	chr14:55511000-55517200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr14:55511000-55517400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr14:55511000-55517600	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr14:55511000-55517600	Weak transcription	H9 Cell Line	embryonic stem cell
48	chr14:55511000-55517600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr14:55511000-55517600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr14:55511000-55517600	Weak transcription	Primary neutrophils fromperipheralblood	blood

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