Variant report

Variant	nsv977484
Chromosome Location	chr14:69352925-69355267
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:56)
CpG islands
(count:122)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr14:69355180-69355330	Caco-2	colon:	n/a	n/a
2	CTCF	chr14:69354920-69355070	HMEC	breast:	n/a	chr14:69355033-69355042 chr14:69355032-69355045 chr14:69355035-69355048
3	CTCF	chr14:69355260-69355410	HPAF	blood vessel:	n/a	n/a
4	CTCF	chr14:69355020-69355170	RPTEC	kidney:	n/a	chr14:69355033-69355042 chr14:69355032-69355045 chr14:69355035-69355048
5	CTCF	chr14:69355049-69355116	NHEK	skin:	n/a	n/a
6	CTCF	chr14:69355080-69355230	BJ	skin:	n/a	n/a
7	CTCF	chr14:69355040-69355058	ProgFib	skin:	n/a	n/a
8	CTCF	chr14:69355006-69355058	H1-hESC	embryonic stem cell:	n/a	chr14:69355033-69355042 chr14:69355032-69355045 chr14:69355035-69355048
9	CTCF	chr14:69352780-69352930	HBMEC	blood vessel:	n/a	n/a
10	CTCF	chr14:69355160-69355310	HAc	cerebellar:	n/a	n/a
11	CTCF	chr14:69354960-69355110	RPTEC	kidney:	n/a	chr14:69355033-69355042 chr14:69355032-69355045 chr14:69355035-69355048
12	CTCF	chr14:69355013-69355036	Lung_OC	lung:	n/a	n/a
13	CTCF	chr14:69354940-69355090	HRPEpiC	eye:	n/a	chr14:69355033-69355042 chr14:69355032-69355045 chr14:69355035-69355048
14	CTCF	chr14:69354940-69355090	A549	lung:	n/a	chr14:69355033-69355042 chr14:69355032-69355045 chr14:69355035-69355048
15	CTCF	chr14:69355180-69355330	AG04449	skin:	n/a	n/a
16	CTCF	chr14:69355180-69355330	HRE	kidney:	n/a	n/a
17	CTCF	chr14:69352780-69352930	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr14:69354880-69355030	MCF-7	breast:	n/a	n/a
19	CTCF	chr14:69355011-69355044	Kidney_OC	kidney:	n/a	chr14:69355033-69355042
20	NFIC	chr14:69352681-69353333	ECC-1	luminal epithelium:	n/a	chr14:69353017-69353033 chr14:69353016-69353033
21	NFIC	chr14:69352731-69353258	ECC-1	luminal epithelium:	n/a	chr14:69353017-69353033 chr14:69353016-69353033
22	POLR2A	chr14:69354795-69354824	H1-hESC	embryonic stem cell:	n/a	n/a
23	POLR2A	chr14:69354890-69354976	HUVEC	blood vessel:	n/a	n/a
24	POLR2A	chr14:69355127-69355133	ProgFib	skin:	n/a	n/a
25	POLR2A	chr14:69355236-69355282	ProgFib	skin:	n/a	n/a
26	POLR2A	chr14:69352094-69353087	Hela-S3	cervix:	n/a	n/a
27	POLR2A	chr14:69352791-69353037	H1-hESC	embryonic stem cell:	n/a	n/a
28	POLR2A	chr14:69352003-69353085	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr14:69352886-69353102	HCT-116	colon:	n/a	n/a
30	POLR2A	chr14:69355096-69355258	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr14:69352048-69353054	H1-hESC	embryonic stem cell:	n/a	n/a
32	POLR2A	chr14:69352983-69353041	Hela-S3	cervix:	n/a	n/a
33	POLR2A	chr14:69354812-69355214	HepG2	liver:	n/a	n/a
34	POLR2A	chr14:69353755-69354019	HUVEC	blood vessel:	n/a	n/a
35	POLR2A	chr14:69355203-69355316	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr14:69352312-69353050	ECC-1	luminal epithelium:	n/a	n/a
37	POLR2A	chr14:69354857-69354936	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr14:69350845-69353100	A549	lung:	n/a	n/a
39	POLR2A	chr14:69351911-69353285	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr14:69354942-69355457	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr14:69351056-69353154	HepG2	liver:	n/a	n/a
42	POLR2A	chr14:69355185-69355235	ProgFib	skin:	n/a	n/a
43	POLR2A	chr14:69352143-69352933	Hela-S3	cervix:	n/a	n/a
44	POLR2A	chr14:69352879-69352930	Hela-S3	cervix:	n/a	n/a
45	POLR2A	chr14:69355007-69356068	A549	lung:	n/a	n/a
46	POLR2A	chr14:69350926-69353152	IMR90	lung:	n/a	n/a
47	POLR2A	chr14:69354982-69355427	HUVEC	blood vessel:	n/a	n/a
48	POLR2A	chr14:69355050-69355079	HepG2	liver:	n/a	n/a
49	POLR2A	chr14:69352804-69353038	HepG2	liver:	n/a	n/a
50	POLR2A	chr14:69354431-69355252	H1-hESC	embryonic stem cell:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:69354734-69354784	ovcar-3	ovarian:	n/a
2	chr14:69354734-69354784	HUVEC	blood vessel:	n/a
3	chr14:69354819-69354869	PrEC	prostate:	n/a
4	chr14:69354819-69354869	A549	lung:	n/a
5	chr14:69354819-69354869	Jurkat	blood:	n/a
6	chr14:69354819-69354869	HAEpiC	amniotic membrane:	n/a
7	chr14:69354734-69354784	K562	blood:	n/a
8	chr14:69354819-69354869	HEK293	kidney:	embryo
9	chr14:69354734-69354784	LNCaP	prostate:	n/a
10	chr14:69354819-69354869	U87	brain:	n/a
11	chr14:69354819-69354869	SK-N-MC	brain:	n/a
12	chr14:69354819-69354869	GM12891	blood:	n/a
13	chr14:69354734-69354784	AG10803	skin:	n/a
14	chr14:69354734-69354784	MCF-7	breast:	n/a
15	chr14:69354819-69354869	HCT-116	colon:	n/a
16	chr14:69354734-69354784	T-47D	breast:	n/a
17	chr14:69354819-69354869	HRCEpiC	kidney:	n/a
18	chr14:69354819-69354869	MCF10A-Er-Src	breast:	n/a
19	chr14:69354819-69354869	LNCaP	prostate:	n/a
20	chr14:69354819-69354869	T-47D	breast:	n/a
21	chr14:69354734-69354784	NT2-D1	testis:	n/a
22	chr14:69354734-69354784	CMK	blood:	n/a
23	chr14:69354819-69354869	CMK	blood:	n/a
24	chr14:69354819-69354869	HCPEpiC	choroid plexus:	n/a
25	chr14:69354819-69354869	ECC-1	luminal epithelium:	n/a
26	chr14:69354734-69354784	IMR90	lung:	fetal
27	chr14:69354819-69354869	HUVEC	blood vessel:	n/a
28	chr14:69354734-69354784	HMEC	breast:	n/a
29	chr14:69354734-69354784	HRPEpiC	eye:	n/a
30	chr14:69354734-69354784	PANC-1	pancreas:	n/a
31	chr14:69354734-69354784	GM06990	blood:	n/a
32	chr14:69354734-69354784	HIPEpiC	eye:	n/a
33	chr14:69354819-69354869	HEEpiC	esophagus:	n/a
34	chr14:69354819-69354869	NHBE	bronchial:	n/a
35	chr14:69354734-69354784	NB4	blood:	n/a
36	chr14:69354734-69354784	Caco-2	colon:	n/a
37	chr14:69354734-69354784	PrEC	prostate:	n/a
38	chr14:69354819-69354869	HMEC	breast:	n/a
39	chr14:69354734-69354784	BE2_C	brain:	n/a
40	chr14:69354734-69354784	Jurkat	blood:	n/a
41	chr14:69354819-69354869	NHDF-neo	bronchial:	n/a
42	chr14:69354819-69354869	Hela-S3	cervix:	n/a
43	chr14:69354819-69354869	HRE	kidney:	n/a
44	chr14:69354734-69354784	HEK293	kidney:	embryo
45	chr14:69354819-69354869	PANC-1	pancreas:	n/a
46	chr14:69354819-69354869	NB4	blood:	n/a
47	chr14:69354819-69354869	H1-hESC	embryonic stem cell:	embryo
48	chr14:69354819-69354869	HCM	heart:	n/a
49	chr14:69354819-69354869	ovcar-3	ovarian:	n/a
50	chr14:69354734-69354784	PFSK-1	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:69347920..69352793-chr14:69354599..69357859,5	MCF-7	breast:
2	chr14:69351207..69353545-chr14:69360069..69361747,2	MCF-7	breast:

No data

Variant related genes	Relation type
ACTN1	TF binding region
HMGN1P3	TF binding region
ACTN1	CpG island
HMGN1P3	CpG island
ENSG00000072110	chromatin interactions

Extended variants
information (count: 109 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:109 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537785156	chr14:69352929-69352930	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs555775520	chr14:69352941-69352942	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs560334450	chr14:69352967-69352968	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs189140676	chr14:69352976-69352977	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs192191283	chr14:69352993-69352994	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs578035963	chr14:69352994-69352995	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs545943107	chr14:69352995-69352996	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs181470	chr14:69353025-69353026	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs147383815	chr14:69353032-69353033	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs148607159	chr14:69353050-69353051	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs375780828	chr14:69353106-69353107	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs743126	chr14:69353113-69353114	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs181471	chr14:69353164-69353165	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs547102471	chr14:69353237-69353238	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs373483021	chr14:69353247-69353248	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs565726017	chr14:69353248-69353249	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs532922842	chr14:69353257-69353258	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs551999072	chr14:69353291-69353292	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs150743580	chr14:69353328-69353329	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs537723760	chr14:69353372-69353373	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs556061225	chr14:69353393-69353394	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs567886779	chr14:69353413-69353414	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs534970385	chr14:69353441-69353442	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs553103044	chr14:69353456-69353457	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs2093009	chr14:69353504-69353505	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs377762909	chr14:69353510-69353511	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs545146372	chr14:69353525-69353526	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs531971517	chr14:69353529-69353530	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs144080576	chr14:69353530-69353531	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs541602218	chr14:69353580-69353581	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs186748142	chr14:69353584-69353585	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs191670327	chr14:69353595-69353596	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs184133934	chr14:69353596-69353597	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs541009087	chr14:69353606-69353607	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs371064353	chr14:69353615-69353616	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs561341730	chr14:69353622-69353623	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs116146726	chr14:69353679-69353680	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571916404	chr14:69353686-69353687	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs2093010	chr14:69353727-69353728	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs188784364	chr14:69353736-69353737	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs569782264	chr14:69353777-69353778	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs35045469	chr14:69353786-69353787	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs146493427	chr14:69353836-69353837	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs549601027	chr14:69353846-69353847	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs368584417	chr14:69353847-69353848	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs543767965	chr14:69353867-69353868	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs529968663	chr14:69353904-69353905	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs181472	chr14:69353909-69353910	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs546971291	chr14:69353915-69353916	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs371370924	chr14:69353980-69353981	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
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
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
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD

Chromatin state (count:228 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:69336400-69358800	Strong transcription	HSMMtube	muscle
2	chr14:69336400-69364200	Strong transcription	Primary neutrophils fromperipheralblood	blood
3	chr14:69336400-69378200	Strong transcription	Primary T cells from cord blood	blood
4	chr14:69336600-69358600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr14:69336800-69360400	Weak transcription	Right Atrium	heart
6	chr14:69337400-69353000	Strong transcription	HUES6 Cell Line	embryonic stem cell
7	chr14:69337400-69404400	Weak transcription	Fetal Brain Male	brain
8	chr14:69337600-69353000	Strong transcription	Aorta	Aorta
9	chr14:69337600-69361200	Strong transcription	Rectal Mucosa Donor 31	rectum
10	chr14:69337800-69353000	Strong transcription	HUES48 Cell Line	embryonic stem cell
11	chr14:69337800-69353000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
12	chr14:69337800-69379200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr14:69337800-69380600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
14	chr14:69338000-69353000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr14:69338000-69353000	Strong transcription	Gastric	stomach
16	chr14:69338000-69353200	Strong transcription	Rectal Mucosa Donor 29	rectum
17	chr14:69338000-69355800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
18	chr14:69338000-69365400	Strong transcription	Primary T cells fromperipheralblood	blood
19	chr14:69338000-69366200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
20	chr14:69338000-69378800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr14:69338200-69353000	Strong transcription	Spleen	Spleen
22	chr14:69338200-69354000	Strong transcription	Primary T helper cells PMA-I stimulated	--
23	chr14:69338200-69361400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr14:69338200-69361600	Strong transcription	Ovary	ovary
25	chr14:69338200-69361800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
26	chr14:69338200-69362200	Strong transcription	Fetal Muscle Leg	muscle
27	chr14:69338200-69362800	Strong transcription	Placenta	Placenta
28	chr14:69338200-69365000	Strong transcription	Pancreas	Pancrea
29	chr14:69338200-69365600	Strong transcription	H9 Cell Line	embryonic stem cell
30	chr14:69338200-69375000	Strong transcription	Placenta Amnion	Placenta Amnion
31	chr14:69338200-69378200	Strong transcription	HUES64 Cell Line	embryonic stem cell
32	chr14:69338400-69353000	Strong transcription	Sigmoid Colon	Sigmoid Colon
33	chr14:69338400-69353200	Strong transcription	H1 Cell Line	embryonic stem cell
34	chr14:69338400-69360600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr14:69338400-69377800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr14:69338600-69353000	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
37	chr14:69338600-69370600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
38	chr14:69339200-69394600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr14:69339600-69360800	Strong transcription	Fetal Stomach	stomach
40	chr14:69340800-69366800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
41	chr14:69341400-69353000	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr14:69341400-69353000	Strong transcription	Colonic Mucosa	Colon
43	chr14:69341800-69353200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr14:69341800-69360200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
45	chr14:69341800-69364800	Strong transcription	Monocytes-CD14+_RO01746	blood
46	chr14:69341800-69366400	Strong transcription	Primary monocytes fromperipheralblood	blood
47	chr14:69341800-69378400	Strong transcription	Fetal Intestine Small	intestine
48	chr14:69341800-69380400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr14:69342000-69378200	Strong transcription	Primary T helper cells fromperipheralblood	blood
50	chr14:69342200-69378200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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