Variant report

Variant	nsv977468
Chromosome Location	chr14:55529336-55531777
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:63)
CpG islands
(count:122)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:63 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr14:55529921-55529993	Kidney_OC	kidney:	n/a	n/a
2	MYC	chr14:55529255-55529478	MCF10A-Er-Src	breast:	n/a	n/a
3	POLR2A	chr14:55529204-55530095	GM12892	blood:	n/a	n/a
4	POLR2A	chr14:55530408-55530453	MCF-7	breast:	n/a	n/a
5	POLR2A	chr14:55529653-55529846	GM12891	blood:	n/a	n/a
6	POLR2A	chr14:55530379-55530670	GM12891	blood:	n/a	n/a
7	POLR2A	chr14:55529369-55529374	MCF-7	breast:	n/a	n/a
8	POLR2A	chr14:55529185-55530225	GM12892	blood:	n/a	n/a
9	POLR2A	chr14:55529259-55530099	GM12892	blood:	n/a	n/a
10	POLR2A	chr14:55528959-55530084	A549	lung:	n/a	n/a
11	POLR2A	chr14:55530106-55530114	MCF-7	breast:	n/a	n/a
12	POLR2A	chr14:55529783-55529797	Gliobla	brain:	n/a	n/a
13	POLR2A	chr14:55528980-55530061	Hela-S3	cervix:	n/a	n/a
14	POLR2A	chr14:55529592-55530129	GM12891	blood:	n/a	n/a
15	POLR2A	chr14:55529751-55529770	MCF-7	breast:	n/a	n/a
16	POLR2A	chr14:55530418-55530610	Hela-S3	cervix:	n/a	n/a
17	POLR2A	chr14:55529218-55530222	GM12878	blood:	n/a	n/a
18	POLR2A	chr14:55529385-55529655	MCF-7	breast:	n/a	n/a
19	POLR2A	chr14:55529258-55529450	MCF10A-Er-Src	breast:	n/a	n/a
20	POLR2A	chr14:55529754-55529942	A549	lung:	n/a	n/a
21	POLR2A	chr14:55529869-55529966	Gliobla	brain:	n/a	n/a
22	POLR2A	chr14:55529387-55529416	MCF-7	breast:	n/a	n/a
23	POLR2A	chr14:55529458-55530101	GM12891	blood:	n/a	n/a
24	POLR2A	chr14:55529719-55529720	MCF-7	breast:	n/a	n/a
25	POLR2A	chr14:55529395-55529593	H1-hESC	embryonic stem cell:	n/a	n/a
26	POLR2A	chr14:55529618-55529983	GM12878	blood:	n/a	n/a
27	POLR2A	chr14:55529897-55529899	MCF-7	breast:	n/a	n/a
28	POLR2A	chr14:55530632-55530654	Hela-S3	cervix:	n/a	n/a
29	POLR2A	chr14:55529946-55530090	MCF-7	breast:	n/a	n/a
30	POLR2A	chr14:55529196-55530165	GM12892	blood:	n/a	n/a
31	POLR2A	chr14:55529635-55529918	K562	blood:	n/a	n/a
32	POLR2A	chr14:55531728-55532003	GM12892	blood:	n/a	n/a
33	POLR2A	chr14:55529452-55529575	A549	lung:	n/a	n/a
34	POLR2A	chr14:55529831-55529853	MCF-7	breast:	n/a	n/a
35	POLR2A	chr14:55529598-55530069	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr14:55529624-55529957	GM12878	blood:	n/a	n/a
37	POLR2A	chr14:55530368-55530727	GM12878	blood:	n/a	n/a
38	POLR2A	chr14:55529180-55530130	GM12891	blood:	n/a	n/a
39	POLR2A	chr14:55529523-55529905	ProgFib	skin:	n/a	n/a
40	POLR2A	chr14:55529421-55529782	MCF-7	breast:	n/a	n/a
41	POLR2A	chr14:55529805-55530155	HepG2	liver:	n/a	n/a
42	POLR2A	chr14:55529228-55529633	K562	blood:	n/a	n/a
43	POLR2A	chr14:55530328-55530733	GM12892	blood:	n/a	n/a
44	POLR2A	chr14:55529925-55529934	MCF-7	breast:	n/a	n/a
45	POLR2A	chr14:55529277-55529895	GM12878	blood:	n/a	n/a
46	POLR2A	chr14:55529645-55530021	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr14:55529856-55529895	MCF-7	breast:	n/a	n/a
48	POLR2A	chr14:55530795-55531025	HepG2	liver:	n/a	n/a
49	POLR2A	chr14:55529746-55529761	Gliobla	brain:	n/a	n/a
50	POLR2A	chr14:55529576-55530023	Hela-S3	cervix:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:55529590-55529640	NB4	blood:	n/a
2	chr14:55529590-55529640	HPAEpiC	pulmonary alveolar:	n/a
3	chr14:55529590-55529640	GM19239	blood:	n/a
4	chr14:55529590-55529640	HEK293	kidney:	embryo
5	chr14:55531556-55531606	HCT-116	colon:	n/a
6	chr14:55531556-55531606	HepG2	liver:	n/a
7	chr14:55531556-55531606	HCM	heart:	n/a
8	chr14:55529590-55529640	GM12878	blood:	n/a
9	chr14:55531556-55531606	PrEC	prostate:	n/a
10	chr14:55529590-55529640	SK-N-SH	brain:	n/a
11	chr14:55529590-55529640	U87	brain:	n/a
12	chr14:55531556-55531606	HMEC	breast:	n/a
13	chr14:55529590-55529640	LNCaP	prostate:	n/a
14	chr14:55529590-55529640	AG09309	skin:	n/a
15	chr14:55529590-55529640	A549	lung:	n/a
16	chr14:55529590-55529640	PFSK-1	brain:	n/a
17	chr14:55531556-55531606	MCF-7	breast:	n/a
18	chr14:55531556-55531606	K562	blood:	n/a
19	chr14:55531556-55531606	GM12891	blood:	n/a
20	chr14:55531556-55531606	HEK293	kidney:	embryo
21	chr14:55529590-55529640	GM12891	blood:	n/a
22	chr14:55531556-55531606	LNCaP	prostate:	n/a
23	chr14:55531556-55531606	HRE	kidney:	n/a
24	chr14:55531556-55531606	AG09319	gingival:	n/a
25	chr14:55531556-55531606	BE2_C	brain:	n/a
26	chr14:55531556-55531606	Hepatocyte	liver:	n/a
27	chr14:55531556-55531606	HRPEpiC	eye:	n/a
28	chr14:55529590-55529640	MCF-7	breast:	n/a
29	chr14:55531556-55531606	NHBE	bronchial:	n/a
30	chr14:55529590-55529640	HRPEpiC	eye:	n/a
31	chr14:55531556-55531606	HPAEpiC	pulmonary alveolar:	n/a
32	chr14:55531556-55531606	HEEpiC	esophagus:	n/a
33	chr14:55531556-55531606	HL-60	blood:	n/a
34	chr14:55529590-55529640	ovcar-3	ovarian:	n/a
35	chr14:55531556-55531606	AoSMC	blood vessel:	n/a
36	chr14:55531556-55531606	ovcar-3	ovarian:	n/a
37	chr14:55529590-55529640	ProgFib	skin:	n/a
38	chr14:55531556-55531606	SK-N-SH	brain:	n/a
39	chr14:55531556-55531606	H1-hESC	embryonic stem cell:	embryo
40	chr14:55531556-55531606	HIPEpiC	eye:	n/a
41	chr14:55529590-55529640	HL-60	blood:	n/a
42	chr14:55531556-55531606	GM06990	blood:	n/a
43	chr14:55531556-55531606	IMR90	lung:	fetal
44	chr14:55529590-55529640	Hela-S3	cervix:	n/a
45	chr14:55531556-55531606	SK-N-MC	brain:	n/a
46	chr14:55531556-55531606	PANC-1	pancreas:	n/a
47	chr14:55531556-55531606	AG09309	skin:	n/a
48	chr14:55529590-55529640	Hepatocyte	liver:	n/a
49	chr14:55529590-55529640	SK-N-SH_RA	brain:	n/a
50	chr14:55529590-55529640	AoSMC	blood vessel:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr14:55531311..55532985-chr14:55657049..55659558,2	K562	blood:
2	chr14:55527921..55530538-chr14:55530867..55533120,2	MCF-7	breast:
3	chr14:54907732..54909904-chr14:55529224..55531676,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	MAPK1IP1L	hsa-miR-374b-5p	chr14:55531503-55531525

Variant related genes	Relation type
MAPK1IP1L	TF binding region
MAPK1IP1L	CpG island
ENSG00000100528	chromatin interactions
ENSG00000126787	chromatin interactions
ENSG00000168175	chromatin interactions

Extended variants
information (count: 105 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:105 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573868631	chr14:55529366-55529367	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs145319180	chr14:55529379-55529380	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs544211530	chr14:55529396-55529397	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs201472281	chr14:55529419-55529420	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs376804721	chr14:55529465-55529466	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs375296592	chr14:55529481-55529482	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs147614556	chr14:55529484-55529485	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs568012336	chr14:55529487-55529488	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs532978787	chr14:55529512-55529513	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs146473581	chr14:55529514-55529515	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs151279209	chr14:55529539-55529540	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs560298537	chr14:55529540-55529541	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs140511390	chr14:55529572-55529573	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs150397932	chr14:55529590-55529591	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs527838670	chr14:55529603-55529604	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs201897422	chr14:55529607-55529608	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs567798198	chr14:55529641-55529642	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs138173342	chr14:55529712-55529713	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs143054292	chr14:55529750-55529751	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs145163223	chr14:55529767-55529768	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs550229007	chr14:55529778-55529779	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs571586087	chr14:55529779-55529780	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs138562462	chr14:55529842-55529843	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs138959248	chr14:55529857-55529858	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs17851309	chr14:55529860-55529861	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs145963007	chr14:55529896-55529897	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs148212738	chr14:55529907-55529908	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs141212085	chr14:55529910-55529911	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs114757196	chr14:55529911-55529912	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs199678260	chr14:55529976-55529977	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs139038695	chr14:55529980-55529981	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs536386053	chr14:55529987-55529988	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs374309422	chr14:55530019-55530020	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs368794840	chr14:55530030-55530031	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs555521608	chr14:55530064-55530065	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs143966958	chr14:55530090-55530091	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs544464354	chr14:55530096-55530097	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs556199146	chr14:55530098-55530099	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs557081381	chr14:55530111-55530112	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs3742564	chr14:55530120-55530121	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs376010686	chr14:55530127-55530128	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs370114545	chr14:55530169-55530170	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs191902020	chr14:55530176-55530177	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs545954659	chr14:55530223-55530224	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs568499736	chr14:55530242-55530243	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs545024254	chr14:55530244-55530245	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs200258902	chr14:55530247-55530248	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs375735501	chr14:55530252-55530253	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs560236325	chr14:55530262-55530263	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs3742565	chr14:55530296-55530297	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 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:243 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:55519200-55529400	Weak transcription	Spleen	Spleen
2	chr14:55519600-55529400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr14:55519600-55529400	Weak transcription	Esophagus	oesophagus
4	chr14:55519600-55534400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr14:55519600-55538000	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr14:55520000-55529400	Weak transcription	Aorta	Aorta
7	chr14:55520000-55529400	Weak transcription	Fetal Brain Female	brain
8	chr14:55520200-55529600	Weak transcription	Brain Cingulate Gyrus	brain
9	chr14:55520200-55538400	Weak transcription	Fetal Kidney	kidney
10	chr14:55520400-55538200	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr14:55520600-55533600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
12	chr14:55520600-55535000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr14:55520600-55538000	Weak transcription	Psoas Muscle	Psoas
14	chr14:55520600-55538600	Weak transcription	Fetal Brain Male	brain
15	chr14:55520800-55529400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr14:55520800-55529400	Weak transcription	Brain Angular Gyrus	brain
17	chr14:55520800-55534800	Strong transcription	HUES64 Cell Line	embryonic stem cell
18	chr14:55520800-55535200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr14:55521000-55529600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr14:55521200-55529400	Weak transcription	Right Ventricle	heart
21	chr14:55521600-55529400	Weak transcription	Primary B cells from cord blood	blood
22	chr14:55521600-55529400	Weak transcription	HSMMtube	muscle
23	chr14:55521600-55535400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr14:55521600-55535400	Strong transcription	NHEK	skin
25	chr14:55522000-55535600	Strong transcription	Fetal Thymus	thymus
26	chr14:55522600-55529600	Weak transcription	Right Atrium	heart
27	chr14:55522600-55532200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr14:55522600-55536600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr14:55523200-55533200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr14:55523600-55533600	Strong transcription	HUES6 Cell Line	embryonic stem cell
31	chr14:55523600-55535200	Strong transcription	Monocytes-CD14+_RO01746	blood
32	chr14:55524200-55535400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
33	chr14:55524400-55533400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr14:55524400-55536600	Strong transcription	Osteobl	bone
35	chr14:55524600-55533600	Strong transcription	Primary monocytes fromperipheralblood	blood
36	chr14:55524600-55533600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr14:55524600-55534800	Strong transcription	Muscle Satellite Cultured Cells	--
38	chr14:55524800-55529600	Strong transcription	Fetal Muscle Trunk	muscle
39	chr14:55524800-55531800	Strong transcription	HMEC	breast
40	chr14:55524800-55535600	Strong transcription	A549	lung
41	chr14:55524800-55535800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr14:55525000-55529400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr14:55525000-55529400	Weak transcription	Gastric	stomach
44	chr14:55525000-55529400	Weak transcription	Thymus	Thymus
45	chr14:55525200-55529400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
46	chr14:55525200-55529400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr14:55526000-55534800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr14:55526200-55536000	Strong transcription	Primary hematopoietic stem cells	blood
49	chr14:55526400-55529400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr14:55526400-55529400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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