Variant report

Variant	nsv565233
Chromosome Location	chr14:78366967-78390880
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:229)
CpG islands
(count:245)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:229 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:78384908-78385258	K562	blood:	n/a	n/a
2	ARID3A	chr14:78388472-78388487	K562	blood:	n/a	n/a
3	ARID3A	chr14:78389927-78390312	K562	blood:	n/a	n/a
4	ATF1	chr14:78389966-78390359	K562	blood:	n/a	n/a
5	ATF1	chr14:78384742-78385161	K562	blood:	n/a	n/a
6	ATF3	chr14:78380398-78380683	K562	blood:	n/a	n/a
7	BACH1	chr14:78389655-78390258	K562	blood:	n/a	n/a
8	BACH1	chr14:78380360-78380732	K562	blood:	n/a	n/a
9	BHLHE40	chr14:78384611-78385134	K562	blood:	n/a	n/a
10	BHLHE40	chr14:78389440-78389462	K562	blood:	n/a	n/a
11	BHLHE40	chr14:78380444-78380917	K562	blood:	n/a	n/a
12	BHLHE40	chr14:78390684-78391026	K562	blood:	n/a	n/a
13	BHLHE40	chr14:78375347-78375374	K562	blood:	n/a	n/a
14	BHLHE40	chr14:78389737-78390326	K562	blood:	n/a	n/a
15	CBX3	chr14:78389425-78390411	K562	blood:	n/a	n/a
16	CBX3	chr14:78380372-78380995	K562	blood:	n/a	n/a
17	CBX3	chr14:78386661-78386986	K562	blood:	n/a	n/a
18	CCNT2	chr14:78384890-78385149	K562	blood:	n/a	n/a
19	CCNT2	chr14:78389919-78390490	K562	blood:	n/a	n/a
20	CEBPB	chr14:78383038-78383271	K562	blood:	n/a	chr14:78383161-78383174
21	CEBPB	chr14:78383844-78384121	HepG2	liver:	n/a	chr14:78383983-78383996 chr14:78383983-78383994 chr14:78383980-78383997 chr14:78383985-78383996
22	CEBPB	chr14:78384762-78385175	K562	blood:	n/a	n/a
23	CEBPB	chr14:78389975-78390291	K562	blood:	n/a	n/a
24	CEBPB	chr14:78383807-78384162	K562	blood:	n/a	chr14:78383983-78383996 chr14:78383983-78383994 chr14:78383980-78383997 chr14:78383985-78383996
25	CEBPB	chr14:78375224-78375648	K562	blood:	n/a	n/a
26	CEBPB	chr14:78383800-78384186	K562	blood:	n/a	chr14:78383983-78383996 chr14:78383983-78383994 chr14:78383980-78383997 chr14:78383985-78383996
27	CHD2	chr14:78380339-78380906	K562	blood:	n/a	n/a
28	CTCF	chr14:78375880-78376030	WERI-Rb-1	eye:	n/a	chr14:78375941-78375950
29	CTCF	chr14:78369300-78369450	AG10803	skin:	n/a	n/a
30	CTCF	chr14:78369220-78369370	AG04449	skin:	n/a	n/a
31	CTCF	chr14:78375900-78376050	GM12871	blood:	n/a	chr14:78375941-78375950
32	CTCF	chr14:78375880-78376030	GM12873	blood:	n/a	chr14:78375941-78375950
33	CTCF	chr14:78375259-78375459	K562	blood:	n/a	n/a
34	CTCF	chr14:78373493-78373572	GM20000	blood:	n/a	n/a
35	CTCF	chr14:78377090-78377141	MCF-7	breast:	n/a	chr14:78377108-78377121
36	CTCF	chr14:78380020-78380170	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr14:78387214-78387247	GM10248	blood:	n/a	n/a
38	CTCF	chr14:78379200-78379350	MCF-7	breast:	n/a	n/a
39	CUX1	chr14:78379767-78380101	K562	blood:	n/a	n/a
40	CUX1	chr14:78384664-78385204	K562	blood:	n/a	n/a
41	CUX1	chr14:78380335-78380962	K562	blood:	n/a	n/a
42	CUX1	chr14:78389571-78390176	K562	blood:	n/a	n/a
43	E2F4	chr14:78369012-78369072	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F6	chr14:78380627-78380976	K562	blood:	n/a	n/a
45	E2F6	chr14:78383012-78383196	K562	blood:	n/a	n/a
46	EGR1	chr14:78373814-78373987	K562	blood:	n/a	chr14:78373927-78373941 chr14:78373926-78373941 chr14:78373928-78373939 chr14:78373927-78373940
47	EGR1	chr14:78373804-78374000	K562	blood:	n/a	chr14:78373927-78373941 chr14:78373926-78373941 chr14:78373928-78373939 chr14:78373927-78373940
48	EGR1	chr14:78390288-78390727	K562	blood:	n/a	n/a
49	EGR1	chr14:78390400-78390630	K562	blood:	n/a	n/a
50	EP300	chr14:78380321-78381004	K562	blood:	n/a	chr14:78380768-78380775

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:78388728-78388778	SKMC	muscle:	n/a
2	chr14:78388728-78388778	SKMC	muscle:	n/a
3	chr14:78388736-78388786	BJ	skin:	n/a
4	chr14:78388728-78388778	AG09309	skin:	n/a
5	chr14:78378994-78379044	HCPEpiC	choroid plexus:	n/a
6	chr14:78378994-78379044	HEK293	kidney:	embryo
7	chr14:78388728-78388778	GM12878	blood:	n/a
8	chr14:78388736-78388786	Hepatocyte	liver:	n/a
9	chr14:78389529-78389579	NB4	blood:	n/a
10	chr14:78389529-78389579	NHBE	bronchial:	n/a
11	chr14:78388728-78388778	K562	blood:	n/a
12	chr14:78389529-78389579	HEEpiC	esophagus:	n/a
13	chr14:78378994-78379044	RPTEC	kidney:	n/a
14	chr14:78388728-78388778	AG10803	skin:	n/a
15	chr14:78388736-78388786	PrEC	prostate:	n/a
16	chr14:78388728-78388778	SAEC	small airway:	n/a
17	chr14:78389529-78389579	AG09309	skin:	n/a
18	chr14:78389529-78389579	SK-N-MC	brain:	n/a
19	chr14:78388736-78388786	NHDF-neo	bronchial:	n/a
20	chr14:78388728-78388778	NHBE	bronchial:	n/a
21	chr14:78388728-78388778	U87	brain:	n/a
22	chr14:78388728-78388778	LNCaP	prostate:	n/a
23	chr14:78389529-78389579	HRE	kidney:	n/a
24	chr14:78388728-78388778	SK-N-SH	brain:	n/a
25	chr14:78388736-78388786	T-47D	breast:	n/a
26	chr14:78378994-78379044	Hela-S3	cervix:	n/a
27	chr14:78388728-78388778	GM12891	blood:	n/a
28	chr14:78378994-78379044	HRE	kidney:	n/a
29	chr14:78388736-78388786	GM12892	blood:	n/a
30	chr14:78389529-78389579	HIPEpiC	eye:	n/a
31	chr14:78378994-78379044	ECC-1	luminal epithelium:	n/a
32	chr14:78388736-78388786	ECC-1	luminal epithelium:	n/a
33	chr14:78388728-78388778	NHDF-neo	bronchial:	n/a
34	chr14:78378994-78379044	A549	lung:	n/a
35	chr14:78388728-78388778	AoSMC	blood vessel:	n/a
36	chr14:78388728-78388778	ECC-1	luminal epithelium:	n/a
37	chr14:78388728-78388778	SK-N-MC	brain:	n/a
38	chr14:78389529-78389579	NT2-D1	testis:	n/a
39	chr14:78388728-78388778	HIPEpiC	eye:	n/a
40	chr14:78388728-78388778	HL-60	blood:	n/a
41	chr14:78388728-78388778	AG04450	lung:	fetal
42	chr14:78378994-78379044	HCT-116	colon:	n/a
43	chr14:78389529-78389579	Jurkat	blood:	n/a
44	chr14:78388736-78388786	SKMC	muscle:	n/a
45	chr14:78388736-78388786	Caco-2	colon:	n/a
46	chr14:78388728-78388778	HEK293	kidney:	embryo
47	chr14:78378994-78379044	BE2_C	brain:	n/a
48	chr14:78378994-78379044	CMK	blood:	n/a
49	chr14:78388728-78388778	T-47D	breast:	n/a
50	chr14:78388736-78388786	HNPCEpiC	eye:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:78375925..78378556-chr14:78379735..78381780,2	MCF-7	breast:
2	chr14:78380542..78382156-chr14:78382539..78385215,4	K562	blood:
3	chr14:78364972..78368454-chr14:78368532..78373080,4	K562	blood:
4	chr14:78380542..78382156-chr14:78382539..78385215,4	K562	blood:
5	chr14:78367280..78368846-chr14:78373706..78376424,2	K562	blood:
6	chr14:78380586..78382152-chr14:78382643..78384269,2	K562	blood:
7	chr14:78383178..78385641-chr14:78388639..78391453,2	K562	blood:
8	chr14:78375925..78378556-chr14:78379735..78381780,2	MCF-7	breast:
9	chr14:78382649..78385767-chr14:78387779..78390139,4	K562	blood:
10	chr14:78367280..78368846-chr14:78373706..78376424,2	K562	blood:
11	chr14:78367251..78369822-chr3:38040138..38042954,2	MCF-7	breast:
12	chr14:78380586..78382152-chr14:78382643..78384269,2	K562	blood:
13	chr14:78374932..78377581-chr14:78382548..78385109,2	K562	blood:
14	chr14:78379164..78381775-chr14:78388793..78390991,2	K562	blood:
15	chr14:78367031..78369779-chr14:78376845..78379644,2	K562	blood:
16	chr14:78372395..78375467-chr14:78376028..78378909,3	K562	blood:
17	chr14:78344966..78346676-chr14:78382145..78384614,2	K562	blood:
18	chr14:78372404..78376597-chr14:78376677..78380306,3	K562	blood:
19	chr14:78374932..78377581-chr14:78382548..78385109,2	K562	blood:

No data

Variant related genes	Relation type
ADCK1	TF binding region
ADCK1	CpG island
ENSG00000063761	chromatin interactions
ENSG00000136059	chromatin interactions

Extended variants
information (count: 887 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:887 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs734654	chr14:78366967-78366968	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs547592268	chr14:78366984-78366985	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs570163662	chr14:78366996-78366997	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs139496998	chr14:78367003-78367004	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs183523986	chr14:78367004-78367005	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs569616973	chr14:78367008-78367009	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs535152248	chr14:78367059-78367060	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs189384515	chr14:78367073-78367074	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs113929495	chr14:78367090-78367091	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs145115253	chr14:78367091-78367092	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs17753249	chr14:78367092-78367093	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs577380324	chr14:78367147-78367148	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs147173876	chr14:78367197-78367198	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs118003737	chr14:78367211-78367212	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs576379667	chr14:78367246-78367247	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs541895774	chr14:78367263-78367264	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs192332723	chr14:78367288-78367289	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs527980419	chr14:78367292-78367293	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs546907535	chr14:78367299-78367300	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs10132606	chr14:78367301-78367302	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs113549927	chr14:78367318-78367319	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs140888046	chr14:78367329-78367330	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs570017917	chr14:78367349-78367350	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs386779085	chr14:78367380-78367381	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs369844509	chr14:78367386-78367387	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs370987527	chr14:78367388-78367389	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs35517904	chr14:78367399-78367400	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs185179916	chr14:78367419-78367420	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs190220419	chr14:78367420-78367421	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs548706499	chr14:78367443-78367444	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs565938869	chr14:78367474-78367475	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs150679587	chr14:78367546-78367547	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs534934198	chr14:78367560-78367561	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs530686193	chr14:78367574-78367575	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs149828570	chr14:78367620-78367621	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs577892559	chr14:78367651-78367652	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs537286743	chr14:78367658-78367659	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs568332897	chr14:78367706-78367707	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs556609137	chr14:78367720-78367721	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs145843378	chr14:78367785-78367786	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs149007341	chr14:78367787-78367788	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs75841105	chr14:78367795-78367796	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs561961676	chr14:78367825-78367826	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs181427693	chr14:78367903-78367904	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs78582784	chr14:78367975-78367976	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs186435587	chr14:78367984-78367985	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs578216647	chr14:78367985-78367986	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs146544794	chr14:78367992-78367993	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs543663603	chr14:78368027-78368028	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs35294185	chr14:78368042-78368043	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Hepatocellular carcinoma	16750200	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Myelofibrosis	22110671	CNVD
Biliary cancer	19435499	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	16608533	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Intracranial aneurysm	16715129	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21364760	CNVD
Bladder cancer	21909424	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Autism	22209245	CNVD
Prostate cancer	22553170	CNVD
Cancer	20164919	CNVD
Breast cancer	21509527	CNVD
Autism	22543975	CNVD

Chromatin state (count:278 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:78327800-78400600	Weak transcription	Colonic Mucosa	Colon
2	chr14:78346600-78375600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr14:78349200-78397200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr14:78349200-78407200	Weak transcription	Colon Smooth Muscle	Colon
5	chr14:78349400-78378000	Weak transcription	Fetal Brain Female	brain
6	chr14:78350800-78375800	Weak transcription	Brain Cingulate Gyrus	brain
7	chr14:78350800-78376200	Weak transcription	Brain Angular Gyrus	brain
8	chr14:78352600-78398800	Weak transcription	Primary T cells fromperipheralblood	blood
9	chr14:78354000-78375800	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr14:78354000-78375800	Weak transcription	Gastric	stomach
11	chr14:78354400-78374400	Weak transcription	Fetal Muscle Leg	muscle
12	chr14:78354600-78367400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr14:78354600-78368400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr14:78354600-78368600	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr14:78354600-78375800	Weak transcription	Brain Substantia Nigra	brain
16	chr14:78354800-78379200	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr14:78354800-78391600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
18	chr14:78355000-78374000	Weak transcription	Ovary	ovary
19	chr14:78355000-78375400	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr14:78355000-78390800	Weak transcription	Spleen	Spleen
21	chr14:78355000-78391600	Weak transcription	Esophagus	oesophagus
22	chr14:78355200-78375000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr14:78355400-78368400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr14:78355400-78370600	Weak transcription	Dnd41	blood
25	chr14:78355600-78398000	Weak transcription	Rectal Smooth Muscle	rectum
26	chr14:78356000-78368800	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr14:78356000-78393600	Weak transcription	Duodenum Mucosa	Duodenum
28	chr14:78356000-78398600	Weak transcription	Fetal Intestine Large	intestine
29	chr14:78356200-78390800	Weak transcription	Primary T helper cells fromperipheralblood	blood
30	chr14:78356800-78368000	Weak transcription	Brain Hippocampus Middle	brain
31	chr14:78356800-78369000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr14:78356800-78373800	Weak transcription	Fetal Intestine Small	intestine
33	chr14:78356800-78373800	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr14:78356800-78399600	Weak transcription	Thymus	Thymus
35	chr14:78357000-78398600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr14:78358200-78373800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr14:78358600-78368200	Weak transcription	Left Ventricle	heart
38	chr14:78359200-78399600	Weak transcription	HSMMtube	muscle
39	chr14:78359200-78399800	Weak transcription	Primary B cells from cord blood	blood
40	chr14:78359400-78384200	Weak transcription	Right Ventricle	heart
41	chr14:78359600-78369200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr14:78359800-78390800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr14:78360000-78373800	Weak transcription	Lung	lung
44	chr14:78360600-78378800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr14:78360600-78379200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr14:78363600-78369200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
47	chr14:78363800-78369200	Weak transcription	Fetal Muscle Trunk	muscle
48	chr14:78364000-78369800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr14:78364000-78398800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr14:78364200-78375400	Weak transcription	Osteobl	bone

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