Variant report

Variant	nsv84871
Chromosome Location	chr14:39698400-39707997
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:331)
CpG islands
(count:244)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:331 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:39700816-39701323	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:39701927-39703977	HepG2	liver:	n/a	n/a
3	ATF2	chr14:39698313-39698734	GM12878	blood:	n/a	n/a
4	ATF2	chr14:39698332-39698655	GM12878	blood:	n/a	n/a
5	ATF3	chr14:39700955-39701155	K562	blood:	n/a	n/a
6	BATF	chr14:39698345-39698797	GM12878	blood:	n/a	n/a
7	BHLHE40	chr14:39701015-39701207	HepG2	liver:	n/a	n/a
8	CEBPB	chr14:39701995-39702379	IMR90	lung:	n/a	n/a
9	CEBPB	chr14:39702013-39702366	HepG2	liver:	n/a	n/a
10	CEBPB	chr14:39700646-39701636	HepG2	liver:	n/a	chr14:39701396-39701407
11	CEBPB	chr14:39701991-39702375	HepG2	liver:	n/a	n/a
12	CEBPB	chr14:39702022-39702249	HepG2	liver:	n/a	n/a
13	CEBPB	chr14:39700933-39701540	HepG2	liver:	n/a	chr14:39701396-39701407
14	CEBPB	chr14:39701969-39702428	HepG2	liver:	n/a	n/a
15	CEBPB	chr14:39700966-39701218	K562	blood:	n/a	n/a
16	CEBPB	chr14:39701301-39701487	HepG2	liver:	n/a	chr14:39701396-39701407
17	CEBPB	chr14:39701010-39701546	HepG2	liver:	n/a	chr14:39701396-39701407
18	CEBPD	chr14:39701291-39701487	HepG2	liver:	n/a	n/a
19	CEBPD	chr14:39701948-39702258	HepG2	liver:	n/a	n/a
20	CEBPD	chr14:39702046-39702302	HepG2	liver:	n/a	n/a
21	CHD2	chr14:39700964-39701179	Hela-S3	cervix:	n/a	n/a
22	CREB1	chr14:39700798-39701372	HepG2	liver:	n/a	n/a
23	CREB1	chr14:39700833-39701316	H1-hESC	embryonic stem cell:	n/a	n/a
24	CREB1	chr14:39700903-39701191	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr14:39700960-39701110	HEK293	kidney:	n/a	chr14:39701048-39701056
26	CTCF	chr14:39701040-39701190	BJ	skin:	n/a	chr14:39701048-39701056
27	CTCF	chr14:39700960-39701110	HEEpiC	esophagus:	n/a	chr14:39701048-39701056
28	CTCF	chr14:39702300-39702450	GM12871	blood:	n/a	n/a
29	CTCF	chr14:39700880-39701030	HCM	heart:	n/a	n/a
30	CTCF	chr14:39700880-39701030	GM12867	blood:	n/a	n/a
31	CTCF	chr14:39700888-39701143	H1-hESC	embryonic stem cell:	n/a	chr14:39701048-39701056
32	CTCF	chr14:39700829-39701212	A549	lung:	n/a	chr14:39701048-39701056
33	CTCF	chr14:39700960-39701110	HepG2	liver:	n/a	chr14:39701048-39701056
34	CTCF	chr14:39700980-39701130	HCPEpiC	choroid plexus:	n/a	chr14:39701048-39701056
35	CTCF	chr14:39700940-39701090	GM06990	blood:	n/a	chr14:39701048-39701056
36	CTCF	chr14:39702240-39702390	GM06990	blood:	n/a	n/a
37	CTCF	chr14:39700817-39701348	HCT-116	colon:	n/a	chr14:39701048-39701056
38	CTCF	chr14:39700940-39701090	HA-sp	spinal cord:	n/a	chr14:39701048-39701056
39	CTCF	chr14:39700969-39701148	NHEK	skin:	n/a	chr14:39701048-39701056
40	CTCF	chr14:39701000-39701150	SK-N-SH_RA	brain:	n/a	chr14:39701048-39701056
41	CTCF	chr14:39700991-39701112	MCF-7	breast:	n/a	chr14:39701048-39701056
42	CTCF	chr14:39700960-39701145	Fibrobl	skin:	n/a	chr14:39701048-39701056
43	CTCF	chr14:39700980-39701130	GM12878	blood:	n/a	chr14:39701048-39701056
44	CTCF	chr14:39700923-39701180	GM12878	blood:	n/a	chr14:39701048-39701056
45	CTCF	chr14:39700960-39701110	GM12866	blood:	n/a	chr14:39701048-39701056
46	CTCF	chr14:39701000-39701150	NHLF	lung:	n/a	chr14:39701048-39701056
47	CTCF	chr14:39700960-39701110	HMEC	breast:	n/a	chr14:39701048-39701056
48	CTCF	chr14:39700937-39701111	A549	lung:	n/a	chr14:39701048-39701056
49	CTCF	chr14:39700920-39701070	Caco-2	colon:	n/a	chr14:39701048-39701056
50	CTCF	chr14:39701000-39701150	GM12868	blood:	n/a	chr14:39701048-39701056

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:39702965-39703015	AG10803	skin:	n/a
2	chr14:39703302-39703352	SK-N-SH	brain:	n/a
3	chr14:39703302-39703352	HEEpiC	esophagus:	n/a
4	chr14:39702922-39702972	LNCaP	prostate:	n/a
5	chr14:39703302-39703352	U87	brain:	n/a
6	chr14:39702922-39702972	SK-N-SH_RA	brain:	n/a
7	chr14:39703302-39703352	HAEpiC	amniotic membrane:	n/a
8	chr14:39706681-39706731	NT2-D1	testis:	n/a
9	chr14:39702965-39703015	CMK	blood:	n/a
10	chr14:39703302-39703352	SK-N-MC	brain:	n/a
11	chr14:39706681-39706731	GM19239	blood:	n/a
12	chr14:39702965-39703015	SK-N-MC	brain:	n/a
13	chr14:39706681-39706731	LNCaP	prostate:	n/a
14	chr14:39702965-39703015	LNCaP	prostate:	n/a
15	chr14:39706681-39706731	NHBE	bronchial:	n/a
16	chr14:39702922-39702972	Hela-S3	cervix:	n/a
17	chr14:39702965-39703015	SKMC	muscle:	n/a
18	chr14:39702922-39702972	HepG2	liver:	n/a
19	chr14:39703302-39703352	HUVEC	blood vessel:	n/a
20	chr14:39702965-39703015	HPAEpiC	pulmonary alveolar:	n/a
21	chr14:39702965-39703015	PrEC	prostate:	n/a
22	chr14:39702965-39703015	HepG2	liver:	n/a
23	chr14:39706681-39706731	GM12892	blood:	n/a
24	chr14:39706681-39706731	AG04449	skin:	fetal
25	chr14:39706681-39706731	HAEpiC	amniotic membrane:	n/a
26	chr14:39702922-39702972	HCT-116	colon:	n/a
27	chr14:39706681-39706731	NHDF-neo	bronchial:	n/a
28	chr14:39702922-39702972	MCF-7	breast:	n/a
29	chr14:39702922-39702972	RPTEC	kidney:	n/a
30	chr14:39703302-39703352	SK-N-SH_RA	brain:	n/a
31	chr14:39706681-39706731	HPAEpiC	pulmonary alveolar:	n/a
32	chr14:39703302-39703352	GM06990	blood:	n/a
33	chr14:39702922-39702972	GM12878	blood:	n/a
34	chr14:39702922-39702972	HIPEpiC	eye:	n/a
35	chr14:39702965-39703015	HEEpiC	esophagus:	n/a
36	chr14:39702965-39703015	HNPCEpiC	eye:	n/a
37	chr14:39706681-39706731	SK-N-SH_RA	brain:	n/a
38	chr14:39702922-39702972	GM12892	blood:	n/a
39	chr14:39706681-39706731	SAEC	small airway:	n/a
40	chr14:39703302-39703352	Hepatocyte	liver:	n/a
41	chr14:39703302-39703352	ovcar-3	ovarian:	n/a
42	chr14:39702922-39702972	T-47D	breast:	n/a
43	chr14:39703302-39703352	HL-60	blood:	n/a
44	chr14:39702922-39702972	HRE	kidney:	n/a
45	chr14:39703302-39703352	NT2-D1	testis:	n/a
46	chr14:39706681-39706731	AoSMC	blood vessel:	n/a
47	chr14:39703302-39703352	HRE	kidney:	n/a
48	chr14:39706681-39706731	HCPEpiC	choroid plexus:	n/a
49	chr14:39702965-39703015	HL-60	blood:	n/a
50	chr14:39702965-39703015	AG04450	lung:	fetal

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:39642562..39645375-chr14:39698449..39701112,2	MCF-7	breast:
2	chr14:39703653..39705206-chr14:39735472..39737859,2	MCF-7	breast:
3	chr14:39700657..39701493-chr14:39938250..39938831,2	MCF-7	breast:
4	chr14:39638891..39641141-chr14:39697742..39700523,2	MCF-7	breast:
5	chr14:39700567..39701347-chr14:39837621..39838221,3	MCF-7	breast:
6	chr14:39571162..39573957-chr14:39700069..39703541,3	MCF-7	breast:
7	chr14:39698773..39700516-chr14:39704009..39706576,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000258941	TF binding region
MIA2	TF binding region
ENSG00000258941	CpG island
MIA2	CpG island
ENSG00000258941	chromatin interactions
ENSG00000259083	chromatin interactions
ENSG00000258940	chromatin interactions
ENSG00000258651	chromatin interactions
ENSG00000100941	chromatin interactions
ENSG00000182400	chromatin interactions
ENSG00000150526	chromatin interactions
ENSG00000100934	chromatin interactions
ENSG00000150527	chromatin interactions

Extended variants
information (count: 311 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:311 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184149268	chr14:39698455-39698456	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs17109021	chr14:39698466-39698467	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs187594878	chr14:39698573-39698574	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs559749999	chr14:39698579-39698580	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs147713305	chr14:39698591-39698592	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs527269103	chr14:39698631-39698632	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs540738311	chr14:39698667-39698668	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs560281485	chr14:39698689-39698690	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs529488490	chr14:39698694-39698695	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs77611527	chr14:39698713-39698714	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs17109028	chr14:39698778-39698779	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs569438035	chr14:39698803-39698804	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs532076559	chr14:39698805-39698806	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs199692138	chr14:39698815-39698816	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs551751286	chr14:39698850-39698851	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs571676209	chr14:39698853-39698854	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs562208226	chr14:39698875-39698876	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs529498045	chr14:39698908-39698909	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs73275062	chr14:39698947-39698948	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs554328352	chr14:39698951-39698952	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs188482641	chr14:39698965-39698966	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs142436501	chr14:39698969-39698970	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs556364094	chr14:39698973-39698974	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs373436539	chr14:39699032-39699033	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs544906582	chr14:39699044-39699045	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs558091254	chr14:39699075-39699076	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs17692639	chr14:39699099-39699100	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs12886542	chr14:39699151-39699152	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs79354268	chr14:39699156-39699157	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs61998507	chr14:39699190-39699191	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs542847145	chr14:39699214-39699215	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs551886532	chr14:39699226-39699227	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs566893846	chr14:39699328-39699329	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs534150118	chr14:39699360-39699361	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs563098119	chr14:39699367-39699368	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs151327695	chr14:39699435-39699436	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs17109030	chr14:39699470-39699471	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs539479328	chr14:39699491-39699492	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs536804524	chr14:39699493-39699494	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs571639490	chr14:39699549-39699550	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs527664264	chr14:39699556-39699557	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs573807675	chr14:39699561-39699562	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs538138668	chr14:39699568-39699569	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs114620766	chr14:39699574-39699575	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs567646182	chr14:39699606-39699607	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs577398916	chr14:39699785-39699786	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs79515250	chr14:39699840-39699841	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs569842863	chr14:39699873-39699874	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs538514029	chr14:39699926-39699927	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs544731211	chr14:39699940-39699941	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Colorectal cancer	16774939	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
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Thyroid cancer	19470727	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:39674000-39705400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr14:39696400-39698800	Enhancers	Fetal Intestine Large	intestine
3	chr14:39696600-39699200	Enhancers	Fetal Intestine Small	intestine
4	chr14:39696600-39700600	Enhancers	HepG2	liver
5	chr14:39696800-39702400	Enhancers	Primary T cells fromperipheralblood	blood
6	chr14:39697000-39702600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
7	chr14:39697200-39699000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
8	chr14:39697200-39699400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr14:39697200-39699400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
10	chr14:39697200-39699400	Enhancers	Primary T killer memory cells from peripheral blood	blood
11	chr14:39697200-39699400	Enhancers	NH-A	brain
12	chr14:39697200-39701200	Enhancers	K562	blood
13	chr14:39697400-39699000	Enhancers	Primary T cells from cord blood	blood
14	chr14:39697400-39699400	Enhancers	Primary T helper naive cells from peripheral blood	blood
15	chr14:39697400-39699400	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr14:39697400-39699400	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr14:39697600-39699200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
18	chr14:39697600-39699200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr14:39697600-39699200	Enhancers	NHEK	skin
20	chr14:39697600-39699800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
21	chr14:39698000-39699000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr14:39698200-39702000	Weak transcription	Stomach Mucosa	stomach
23	chr14:39698400-39698800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
24	chr14:39698600-39698800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr14:39698600-39698800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
26	chr14:39698600-39698800	Enhancers	A549	lung
27	chr14:39698600-39698800	Enhancers	Osteobl	bone
28	chr14:39698800-39699000	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr14:39698800-39699200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
30	chr14:39698800-39700800	Weak transcription	A549	lung
31	chr14:39698800-39701000	Weak transcription	Fetal Intestine Large	intestine
32	chr14:39698800-39702200	Weak transcription	Osteobl	bone
33	chr14:39699000-39699800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr14:39699000-39700600	Weak transcription	HUES6 Cell Line	embryonic stem cell
35	chr14:39699000-39702200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
36	chr14:39699200-39699800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr14:39699200-39700600	Weak transcription	Fetal Intestine Small	intestine
38	chr14:39699200-39702400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr14:39699200-39702400	Weak transcription	NHEK	skin
40	chr14:39699400-39700600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr14:39699400-39700600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
42	chr14:39699400-39702000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
43	chr14:39699400-39702200	Weak transcription	Primary T helper cells fromperipheralblood	blood
44	chr14:39699400-39702200	Weak transcription	NH-A	brain
45	chr14:39699400-39702400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
46	chr14:39699400-39703200	Weak transcription	Primary T helper cells PMA-I stimulated	--
47	chr14:39699800-39700800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr14:39699800-39702400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
49	chr14:39699800-39702400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr14:39700600-39700800	Enhancers	HSMMtube	muscle

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