Variant report

Variant	nsv974313
Chromosome Location	chr14:21678548-21679868
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:48)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:9)

(count:48 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	HEY1	chr14:21679036-21679974	HepG2	liver:	n/a	n/a
2	HEY1	chr14:21678115-21678599	HepG2	liver:	n/a	n/a
3	POLR2A	chr14:21679107-21679197	HUVEC	blood vessel:	n/a	n/a
4	POLR2A	chr14:21679457-21679566	H1-hESC	embryonic stem cell:	n/a	n/a
5	POLR2A	chr14:21679216-21679653	K562	blood:	n/a	n/a
6	POLR2A	chr14:21679245-21679416	MCF-7	breast:	n/a	n/a
7	POLR2A	chr14:21678753-21679004	MCF-7	breast:	n/a	n/a
8	POLR2A	chr14:21679682-21680983	MCF-7	breast:	n/a	n/a
9	POLR2A	chr14:21679684-21679970	GM12878	blood:	n/a	n/a
10	POLR2A	chr14:21677254-21678757	HepG2	liver:	n/a	n/a
11	POLR2A	chr14:21679526-21680128	PANC-1	pancreas:	n/a	n/a
12	POLR2A	chr14:21679127-21681526	SK-N-MC	brain:	n/a	n/a
13	POLR2A	chr14:21667116-21678581	HepG2	liver:	n/a	n/a
14	POLR2A	chr14:21678179-21678601	MCF-7	breast:	n/a	n/a
15	POLR2A	chr14:21678257-21678650	SK-N-MC	brain:	n/a	n/a
16	POLR2A	chr14:21679381-21679832	K562	blood:	n/a	n/a
17	POLR2A	chr14:21679476-21679654	MCF-7	breast:	n/a	n/a
18	POLR2A	chr14:21679580-21679594	H1-hESC	embryonic stem cell:	n/a	n/a
19	POLR2A	chr14:21678624-21680390	H1-hESC	embryonic stem cell:	n/a	n/a
20	POLR2A	chr14:21679833-21679835	HepG2	liver:	n/a	n/a
21	POLR2A	chr14:21679384-21679528	ProgFib	skin:	n/a	n/a
22	POLR2A	chr14:21679237-21681560	HepG2	liver:	n/a	n/a
23	POLR2A	chr14:21679738-21679769	ProgFib	skin:	n/a	n/a
24	POLR2A	chr14:21679284-21679479	H1-hESC	embryonic stem cell:	n/a	n/a
25	POLR2A	chr14:21679142-21680576	HepG2	liver:	n/a	n/a
26	POLR2A	chr14:21679366-21679838	K562	blood:	n/a	n/a
27	POLR2A	chr14:21679563-21680698	K562	blood:	n/a	n/a
28	POLR2A	chr14:21679548-21679578	ProgFib	skin:	n/a	n/a
29	POLR2A	chr14:21679377-21679622	K562	blood:	n/a	n/a
30	POLR2A	chr14:21678141-21678656	HepG2	liver:	n/a	n/a
31	POLR2A	chr14:21668653-21678640	GM12891	blood:	n/a	n/a
32	POLR2A	chr14:21678861-21679022	HepG2	liver:	n/a	n/a
33	POLR2A	chr14:21677351-21678647	HepG2	liver:	n/a	n/a
34	POLR2A	chr14:21679244-21679813	HepG2	liver:	n/a	n/a
35	POLR2A	chr14:21679539-21679752	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr14:21679323-21679694	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr14:21679327-21679787	H1-hESC	embryonic stem cell:	n/a	n/a
38	POLR2A	chr14:21667205-21678686	K562	blood:	n/a	n/a
39	POLR2A	chr14:21679320-21679803	Hela-S3	cervix:	n/a	n/a
40	POLR2A	chr14:21678928-21679008	K562	blood:	n/a	n/a
41	POLR2A	chr14:21678243-21678588	K562	blood:	n/a	n/a
42	POLR2A	chr14:21679297-21679821	HepG2	liver:	n/a	n/a
43	POLR2A	chr14:21679381-21679916	HL-60	blood:	n/a	n/a
44	POLR2A	chr14:21679605-21679935	SK-N-SH	brain:	n/a	n/a
45	POLR2A	chr14:21679663-21679802	Hela-S3	cervix:	n/a	n/a
46	POLR2A	chr14:21679200-21679228	HUVEC	blood vessel:	n/a	n/a
47	STAT3	chr14:21678545-21678704	MCF10A-Er-Src	breast:	n/a	n/a
48	ZBTB33	chr14:21679046-21679766	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:21679191-21679241	HUVEC	blood vessel:	n/a
2	chr14:21679191-21679241	PFSK-1	brain:	n/a
3	chr14:21679191-21679241	ECC-1	luminal epithelium:	n/a
4	chr14:21679191-21679241	Hela-S3	cervix:	n/a
5	chr14:21679191-21679241	SK-N-SH	brain:	n/a
6	chr14:21679191-21679241	GM12891	blood:	n/a
7	chr14:21679191-21679241	MCF-7	breast:	n/a
8	chr14:21679191-21679241	HRPEpiC	eye:	n/a
9	chr14:21679191-21679241	AG04449	skin:	fetal
10	chr14:21679191-21679241	NHDF-neo	bronchial:	n/a
11	chr14:21679191-21679241	ovcar-3	ovarian:	n/a
12	chr14:21679191-21679241	HCT-116	colon:	n/a
13	chr14:21679191-21679241	SAEC	small airway:	n/a
14	chr14:21679191-21679241	Caco-2	colon:	n/a
15	chr14:21679191-21679241	U87	brain:	n/a
16	chr14:21679191-21679241	NHBE	bronchial:	n/a
17	chr14:21679191-21679241	SK-N-MC	brain:	n/a
18	chr14:21679191-21679241	SKMC	muscle:	n/a
19	chr14:21679191-21679241	HPAEpiC	pulmonary alveolar:	n/a
20	chr14:21679191-21679241	MCF10A-Er-Src	breast:	n/a
21	chr14:21679191-21679241	HepG2	liver:	n/a
22	chr14:21679191-21679241	Hepatocyte	liver:	n/a
23	chr14:21679191-21679241	K562	blood:	n/a
24	chr14:21679191-21679241	GM06990	blood:	n/a
25	chr14:21679191-21679241	HEEpiC	esophagus:	n/a
26	chr14:21679191-21679241	AoSMC	blood vessel:	n/a
27	chr14:21679191-21679241	NH-A	brain:	n/a
28	chr14:21679191-21679241	T-47D	breast:	n/a
29	chr14:21679191-21679241	AG09309	skin:	n/a
30	chr14:21679191-21679241	IMR90	lung:	fetal
31	chr14:21679191-21679241	NB4	blood:	n/a
32	chr14:21679191-21679241	RPTEC	kidney:	n/a
33	chr14:21679191-21679241	HCPEpiC	choroid plexus:	n/a
34	chr14:21679191-21679241	HRE	kidney:	n/a
35	chr14:21679191-21679241	PrEC	prostate:	n/a
36	chr14:21679191-21679241	HMEC	breast:	n/a
37	chr14:21679191-21679241	SK-N-SH_RA	brain:	n/a
38	chr14:21679191-21679241	CMK	blood:	n/a
39	chr14:21679191-21679241	A549	lung:	n/a
40	chr14:21679191-21679241	HNPCEpiC	eye:	n/a
41	chr14:21679191-21679241	HEK293	kidney:	embryo
42	chr14:21679191-21679241	GM19239	blood:	n/a
43	chr14:21679191-21679241	LNCaP	prostate:	n/a
44	chr14:21679191-21679241	BE2_C	brain:	n/a
45	chr14:21679191-21679241	NT2-D1	testis:	n/a
46	chr14:21679191-21679241	Jurkat	blood:	n/a
47	chr14:21679191-21679241	AG09319	gingival:	n/a
48	chr14:21679191-21679241	HCF	heart:	n/a
49	chr14:21679191-21679241	AG04450	lung:	fetal
50	chr14:21679191-21679241	ProgFib	skin:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:21678499..21681454-chr14:21736107..21737906,2	MCF-7	breast:
2	chr14:21676404..21679681-chr14:21680227..21682594,3	K562	blood:
3	chr14:21678068..21679716-chr14:21682875..21685617,2	K562	blood:
4	chr14:21671465..21674942-chr14:21676988..21681110,7	MCF-7	breast:

No data

(count:9 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	HNRNPC	hsa-miR-186-5p	chr14:21679345-21679339
2	HNRNPC	hsa-miR-142-3p	chr14:21678567-21678589
3	HNRNPC	hsa-miR-186-5p	chr14:21679046-21679067
4	HNRNPC	hsa-miR-335-5p	chr14:21679069-21679091
5	HNRNPC	hsa-miR-30c-5p	chr14:21678673-21678667
6	HNRNPC	hsa-miR-30c-5p	chr14:21678667-21678690
7	HNRNPC	hsa-miR-335-5p	chr14:21678975-21678999
8	HNRNPC	hsa-miR-186-5p	chr14:21679340-21679361
9	HNRNPC	hsa-let-7e-5p	chr14:21679132-21679153

Variant related genes	Relation type
LINC00641	TF binding region
LINC00641	CpG island
ENSG00000258441	chromatin interactions
ENSG00000092199	chromatin interactions

Extended variants
information (count: 92 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:92 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573210629	chr14:21678585-21678586	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region miRNA target site	4 gene(s)	Overlapped CNVs	n/a
2	rs556485356	chr14:21678598-21678599	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs570008614	chr14:21678628-21678629	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs535848957	chr14:21678639-21678640	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs555756766	chr14:21678647-21678648	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs370214305	chr14:21678648-21678649	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs541484640	chr14:21678704-21678705	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs557994808	chr14:21678705-21678706	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs192348593	chr14:21678714-21678715	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs143591494	chr14:21678717-21678718	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs150756293	chr14:21678718-21678719	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs543648404	chr14:21678725-21678726	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs200290202	chr14:21678774-21678775	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs201584649	chr14:21678775-21678776	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs199533911	chr14:21678776-21678777	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs183757816	chr14:21678790-21678791	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs374204045	chr14:21678819-21678820	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs542923894	chr14:21678881-21678882	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs376992152	chr14:21678900-21678901	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs371373033	chr14:21678905-21678906	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs11559122	chr14:21678921-21678922	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs534340320	chr14:21678943-21678944	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs561691728	chr14:21678944-21678945	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs376022710	chr14:21678965-21678966	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs368387560	chr14:21678992-21678993	Strong transcription Weak transcription	TF binding region Chromatin interactive region miRNA target site	4 gene(s)	Overlapped CNVs	n/a
26	rs377326643	chr14:21679027-21679028	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs370953463	chr14:21679041-21679042	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs527310949	chr14:21679049-21679050	Strong transcription Weak transcription	TF binding region Chromatin interactive region miRNA target site	4 gene(s)	Overlapped CNVs	n/a
29	rs547446756	chr14:21679055-21679056	Strong transcription Weak transcription	TF binding region Chromatin interactive region miRNA target site	4 gene(s)	Overlapped CNVs	n/a
30	rs373650545	chr14:21679058-21679059	Strong transcription Weak transcription	TF binding region Chromatin interactive region miRNA target site	4 gene(s)	Overlapped CNVs	n/a
31	rs575929065	chr14:21679070-21679071	Strong transcription Weak transcription	TF binding region Chromatin interactive region miRNA target site	4 gene(s)	Overlapped CNVs	n/a
32	rs3203452	chr14:21679094-21679095	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs3208564	chr14:21679095-21679096	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs1064879	chr14:21679097-21679098	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs200418652	chr14:21679118-21679119	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs201687342	chr14:21679132-21679133	Strong transcription Weak transcription	TF binding region Chromatin interactive region miRNA target site	4 gene(s)	Overlapped CNVs	n/a
37	rs199683587	chr14:21679141-21679142	Strong transcription Weak transcription	TF binding region Chromatin interactive region miRNA target site	4 gene(s)	Overlapped CNVs	n/a
38	rs570490265	chr14:21679163-21679164	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs533144936	chr14:21679174-21679175	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs550049128	chr14:21679176-21679177	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs569870789	chr14:21679194-21679195	Strong transcription Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs371131630	chr14:21679214-21679215	Strong transcription Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs113941786	chr14:21679226-21679227	Strong transcription Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs535711889	chr14:21679244-21679245	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs549317790	chr14:21679264-21679265	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs28559592	chr14:21679266-21679267	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs566039910	chr14:21679274-21679275	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs112267670	chr14:21679275-21679276	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs1064971	chr14:21679287-21679288	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs534742193	chr14:21679329-21679330	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Cancer	20164919	CNVD
Breast cancer	21364760	CNVD
Mortal	21835882	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	21858162	CNVD
Schizophrenia	20967226	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22102821	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Neuroblastoma	19536264	CNVD
Schizophrenia	23813976	CNVD
Ovarian clear cell carcinoma	21343371	CNVD

Chromatin state (count:159 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21660600-21686200	Weak transcription	Right Atrium	heart
2	chr14:21660800-21679400	Weak transcription	Gastric	stomach
3	chr14:21661000-21679400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr14:21669000-21679400	Weak transcription	Aorta	Aorta
5	chr14:21669000-21685800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr14:21669400-21679800	Weak transcription	Small Intestine	intestine
7	chr14:21669400-21681600	Strong transcription	Left Ventricle	heart
8	chr14:21669400-21685600	Strong transcription	Muscle Satellite Cultured Cells	--
9	chr14:21670000-21679600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
10	chr14:21670000-21681600	Strong transcription	Fetal Muscle Leg	muscle
11	chr14:21670200-21683600	Strong transcription	Fetal Thymus	thymus
12	chr14:21670200-21684200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr14:21670200-21684600	Strong transcription	NHLF	lung
14	chr14:21670200-21685000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr14:21670200-21685400	Strong transcription	HSMM	muscle
16	chr14:21670200-21685400	Strong transcription	NH-A	brain
17	chr14:21670200-21685400	Strong transcription	Osteobl	bone
18	chr14:21670400-21679400	Weak transcription	Fetal Intestine Small	intestine
19	chr14:21670400-21697600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr14:21670600-21683400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr14:21670800-21682400	Strong transcription	A549	lung
22	chr14:21670800-21684800	Strong transcription	HSMMtube	muscle
23	chr14:21670800-21685000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr14:21670800-21687400	Strong transcription	Fetal Brain Female	brain
25	chr14:21670800-21702400	Strong transcription	Fetal Muscle Trunk	muscle
26	chr14:21671200-21732000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr14:21671400-21681000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
28	chr14:21671400-21684600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr14:21671400-21684800	Strong transcription	Stomach Smooth Muscle	stomach
30	chr14:21671600-21681600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr14:21671600-21682800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr14:21671600-21686000	Strong transcription	HUVEC	blood vessel
33	chr14:21671600-21688200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr14:21671800-21679600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr14:21671800-21683600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr14:21672200-21680000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
37	chr14:21672200-21684200	Strong transcription	HMEC	breast
38	chr14:21672200-21696600	Strong transcription	Primary B cells from cord blood	blood
39	chr14:21672400-21680000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr14:21672400-21680800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
41	chr14:21672400-21684800	Strong transcription	ES-I3 Cell Line	embryonic stem cell
42	chr14:21672400-21696000	Strong transcription	Adipose Nuclei	Adipose
43	chr14:21672400-21709000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr14:21672600-21683600	Strong transcription	NHEK	skin
45	chr14:21672600-21685400	Strong transcription	NHDF-Ad	bronchial
46	chr14:21672600-21703000	Strong transcription	Primary neutrophils fromperipheralblood	blood
47	chr14:21672800-21681400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
48	chr14:21672800-21682400	Strong transcription	Primary T cells from cord blood	blood
49	chr14:21672800-21682400	Strong transcription	Brain Anterior Caudate	brain
50	chr14:21672800-21682600	Weak transcription	Pancreatic Islets	Pancreatic Islet

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