Variant report

Variant	nsv1055102
Chromosome Location	chr14:20687007-20743269
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:20730858-20731162	K562	blood:	n/a	n/a
2	ATF1	chr14:20724352-20724489	K562	blood:	n/a	n/a
3	ATF1	chr14:20730830-20731218	K562	blood:	n/a	n/a
4	ATF3	chr14:20730820-20731074	K562	blood:	n/a	n/a
5	BACH1	chr14:20687322-20687431	H1-hESC	embryonic stem cell:	n/a	chr14:20687387-20687401
6	BACH1	chr14:20687217-20687569	K562	blood:	n/a	chr14:20687387-20687401
7	BCL11A	chr14:20730703-20731061	GM12878	blood:	n/a	n/a
8	BHLHE40	chr14:20730754-20731222	GM12878	blood:	n/a	n/a
9	BHLHE40	chr14:20730817-20731297	K562	blood:	n/a	n/a
10	BRCA1	chr14:20716040-20716061	H1-hESC	embryonic stem cell:	n/a	n/a
11	CCNT2	chr14:20730801-20731127	K562	blood:	n/a	n/a
12	CEBPB	chr14:20730857-20731158	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr14:20730821-20731202	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr14:20741552-20741617	A549	lung:	n/a	n/a
15	CEBPB	chr14:20730819-20731174	IMR90	lung:	n/a	n/a
16	CEBPB	chr14:20730826-20731185	K562	blood:	n/a	n/a
17	CHD1	chr14:20730821-20730930	GM12878	blood:	n/a	n/a
18	CHD2	chr14:20730845-20731006	GM12878	blood:	n/a	n/a
19	CHD2	chr14:20730792-20731109	Hela-S3	cervix:	n/a	n/a
20	CTCF	chr14:20715921-20716058	Lung_OC	lung:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
21	CTCF	chr14:20715920-20716070	HRPEpiC	eye:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
22	CTCF	chr14:20715880-20716030	HFF-Myc	foreskin:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
23	CTCF	chr14:20715920-20716070	HRE	kidney:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
24	CTCF	chr14:20715900-20716146	MCF-7	breast:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
25	CTCF	chr14:20715976-20716063	GM19239	blood:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
26	CTCF	chr14:20715960-20716110	WERI-Rb-1	eye:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
27	CTCF	chr14:20715879-20716148	LNCaP	prostate:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
28	CTCF	chr14:20715880-20716030	HL-60	blood:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
29	CTCF	chr14:20715920-20716070	HMF	breast:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
30	CTCF	chr14:20715891-20716095	SK-N-SH_RA	brain:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
31	CTCF	chr14:20715900-20716050	GM12875	blood:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
32	CTCF	chr14:20715884-20716139	K562	blood:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
33	CTCF	chr14:20715900-20716050	GM12865	blood:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
34	CTCF	chr14:20715940-20716090	K562	blood:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
35	CTCF	chr14:20718697-20718758	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr14:20715940-20716090	GM12878	blood:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
37	CTCF	chr14:20715880-20716030	HEEpiC	esophagus:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
38	CTCF	chr14:20715940-20716090	GM12869	blood:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
39	CTCF	chr14:20715820-20716181	K562	blood:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
40	CTCF	chr14:20715920-20716070	HCFaa	heart:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
41	CTCF	chr14:20715940-20716090	GM12871	blood:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
42	CTCF	chr14:20715971-20716124	ProgFib	skin:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
43	CTCF	chr14:20715747-20716204	MCF-7	breast:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
44	CTCF	chr14:20715920-20716070	Hela-S3	cervix:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
45	CTCF	chr14:20715914-20716107	Pancreas_OC	pancreas:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
46	CTCF	chr14:20715940-20716090	GM12870	blood:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
47	CTCF	chr14:20715892-20716120	Hela-S3	cervix:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
48	CTCF	chr14:20715940-20716090	GM12873	blood:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
49	CTCF	chr14:20715762-20716127	MCF-7	breast:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
50	CTCF	chr14:20715940-20716090	SAEC	small airway:	n/a	chr14:20715990-20716008 chr14:20715985-20716006

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:20710881-20710931	A549	lung:	n/a
2	chr14:20704361-20704411	NH-A	brain:	n/a
3	chr14:20691777-20691827	NB4	blood:	n/a
4	chr14:20691777-20691827	SK-N-SH	brain:	n/a
5	chr14:20710905-20710955	SK-N-MC	brain:	n/a
6	chr14:20710315-20710365	GM12892	blood:	n/a
7	chr14:20710315-20710365	SKMC	muscle:	n/a
8	chr14:20710315-20710365	NH-A	brain:	n/a
9	chr14:20691777-20691827	HEEpiC	esophagus:	n/a
10	chr14:20704361-20704411	HAEpiC	amniotic membrane:	n/a
11	chr14:20711344-20711394	BJ	skin:	n/a
12	chr14:20691777-20691827	BJ	skin:	n/a
13	chr14:20711344-20711394	HCPEpiC	choroid plexus:	n/a
14	chr14:20710905-20710955	HUVEC	blood vessel:	n/a
15	chr14:20711344-20711394	AG09309	skin:	n/a
16	chr14:20704361-20704411	AG04449	skin:	fetal
17	chr14:20710881-20710931	CMK	blood:	n/a
18	chr14:20711344-20711394	MCF-7	breast:	n/a
19	chr14:20691777-20691827	GM12891	blood:	n/a
20	chr14:20711344-20711394	Hela-S3	cervix:	n/a
21	chr14:20692622-20692672	HepG2	liver:	n/a
22	chr14:20710905-20710955	HIPEpiC	eye:	n/a
23	chr14:20710905-20710955	K562	blood:	n/a
24	chr14:20692622-20692672	BJ	skin:	n/a
25	chr14:20704361-20704411	RPTEC	kidney:	n/a
26	chr14:20692622-20692672	NT2-D1	testis:	n/a
27	chr14:20710881-20710931	Jurkat	blood:	n/a
28	chr14:20691777-20691827	NHBE	bronchial:	n/a
29	chr14:20704361-20704411	HepG2	liver:	n/a
30	chr14:20711344-20711394	HNPCEpiC	eye:	n/a
31	chr14:20710881-20710931	BE2_C	brain:	n/a
32	chr14:20692622-20692672	HEK293	kidney:	embryo
33	chr14:20710881-20710931	GM12892	blood:	n/a
34	chr14:20710315-20710365	PANC-1	pancreas:	n/a
35	chr14:20710315-20710365	ECC-1	luminal epithelium:	n/a
36	chr14:20711344-20711394	NT2-D1	testis:	n/a
37	chr14:20710905-20710955	HL-60	blood:	n/a
38	chr14:20711344-20711394	SKMC	muscle:	n/a
39	chr14:20710315-20710365	T-47D	breast:	n/a
40	chr14:20710881-20710931	SAEC	small airway:	n/a
41	chr14:20710905-20710955	HMEC	breast:	n/a
42	chr14:20710881-20710931	HCM	heart:	n/a
43	chr14:20710315-20710365	ovcar-3	ovarian:	n/a
44	chr14:20692622-20692672	HRCEpiC	kidney:	n/a
45	chr14:20691777-20691827	SAEC	small airway:	n/a
46	chr14:20704361-20704411	NB4	blood:	n/a
47	chr14:20710905-20710955	Jurkat	blood:	n/a
48	chr14:20710315-20710365	SAEC	small airway:	n/a
49	chr14:20710315-20710365	K562	blood:	n/a
50	chr14:20691777-20691827	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:20691139..20693631-chr14:20695657..20698105,2	K562	blood:
2	chr14:20721089..20723559-chr14:20745289..20746790,2	K562	blood:
3	chr14:20716993..20719012-chr14:20810406..20812740,2	MCF-7	breast:
4	chr14:20691139..20693631-chr14:20695657..20698105,2	K562	blood:
5	chr14:20674085..20677001-chr14:20687478..20690164,2	MCF-7	breast:
6	chr14:20738427..20740825-chr14:20746566..20748519,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TTC5-2	chr14:20728743-20729137	NONHSAT035558
2	lnc-TTC5-3	chr14:20738080-20742354	ucscGeneNc_uc001vzu_1
3	lnc-TTC5-2	chr14:20726344-20726358	NONHSAT035556
4	lnc-TTC5-2	chr14:20729548-20729773	NONHSAT035558
5	lnc-TTC5-2	chr14:20724717-20724844	NONHSAT035556
6	lnc-TTC5-2	chr14:20728639-20732467	ENSG00000258768.2
7	lnc-TTC5-2	chr14:20729772-20729892	NONHSAT035556
8	lnc-TTC5-2	chr14:20725877-20725934	NONHSAT035556

Variant related genes	Relation type
ENSG00000266336	TF binding region
ENSG00000258768	TF binding region
OR11H6	TF binding region
TTC5	TF binding region
OR11H4	TF binding region
OR11H7	TF binding region
ENSG00000266336	CpG island
ENSG00000258768	CpG island
OR11H6	CpG island
TTC5	CpG island
OR11H4	CpG island
OR11H7	CpG island
ENSG00000176219	chromatin interactions
ENSG00000259001	chromatin interactions
ENSG00000258806	chromatin interactions
ENSG00000129484	chromatin interactions

Extended variants
information (count: 1623 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1623 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573987450	chr14:20687052-20687053	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs571416091	chr14:20687059-20687060	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs78068126	chr14:20687107-20687108	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs115138842	chr14:20687132-20687133	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs115656238	chr14:20687134-20687135	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs567040881	chr14:20687176-20687177	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs545593556	chr14:20687261-20687262	Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs555648073	chr14:20687262-20687263	Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs563982747	chr14:20687267-20687268	Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs190557726	chr14:20687294-20687295	Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs541255030	chr14:20687350-20687351	Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs538018294	chr14:20687419-20687420	Flanking Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs78353735	chr14:20687477-20687478	Flanking Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs2318889	chr14:20687506-20687507	Flanking Active TSS Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs114760764	chr14:20687517-20687518	Flanking Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs544957647	chr14:20687521-20687522	Flanking Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs76639655	chr14:20687585-20687586	Flanking Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs2873832	chr14:20687586-20687587	Flanking Active TSS Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs181073708	chr14:20687603-20687604	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs372190051	chr14:20687604-20687605	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs375511533	chr14:20687619-20687620	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs4569165	chr14:20687628-20687629	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs185281290	chr14:20687646-20687647	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs546860245	chr14:20687658-20687659	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs10149766	chr14:20687666-20687667	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs112186906	chr14:20687706-20687707	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs550568082	chr14:20687715-20687716	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs370858021	chr14:20687752-20687753	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs117800771	chr14:20687770-20687771	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs542846133	chr14:20687786-20687787	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs535904171	chr14:20687787-20687788	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs78922110	chr14:20687788-20687789	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs556003073	chr14:20687789-20687790	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs113241362	chr14:20687791-20687792	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs574298187	chr14:20687792-20687793	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs60893732	chr14:20687862-20687863	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs534336087	chr14:20687914-20687915	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs533499545	chr14:20687921-20687922	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369138269	chr14:20687945-20687946	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs8014956	chr14:20687978-20687979	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs377342507	chr14:20687981-20687982	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545119830	chr14:20688017-20688018	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs189691521	chr14:20688035-20688036	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs573671643	chr14:20688074-20688075	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs146967649	chr14:20688079-20688080	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs8015147	chr14:20688109-20688110	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs139202135	chr14:20688121-20688122	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs545149596	chr14:20688132-20688133	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542823743	chr14:20688135-20688136	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528405559	chr14:20688203-20688204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:140 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:20686000-20687200	Enhancers	A549	lung
2	chr14:20687000-20687200	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr14:20687000-20687200	Enhancers	K562	blood
4	chr14:20687000-20687400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr14:20687000-20687600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr14:20687200-20687400	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr14:20687200-20687800	Flanking Active TSS	A549	lung
8	chr14:20687200-20687800	Enhancers	Hela-S3	cervix
9	chr14:20687200-20687800	Flanking Active TSS	K562	blood
10	chr14:20687400-20687600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
11	chr14:20687600-20687800	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr14:20687800-20688200	Enhancers	A549	lung
13	chr14:20687800-20691200	Weak transcription	K562	blood
14	chr14:20691200-20692600	Enhancers	K562	blood
15	chr14:20695400-20695600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr14:20698000-20698400	Active TSS	Fetal Heart	heart
17	chr14:20704000-20704400	Active TSS	HepG2	liver
18	chr14:20707000-20707200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr14:20718600-20719200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
20	chr14:20718800-20724200	Weak transcription	Ovary	ovary
21	chr14:20719200-20719400	ZNF genes & repeats	Aorta	Aorta
22	chr14:20719400-20741000	Weak transcription	Aorta	Aorta
23	chr14:20720800-20721400	ZNF genes & repeats	Liver	Liver
24	chr14:20721400-20730400	Weak transcription	Liver	Liver
25	chr14:20722600-20755000	Weak transcription	Stomach Smooth Muscle	stomach
26	chr14:20722800-20723000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
27	chr14:20723000-20739400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr14:20724000-20724400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
29	chr14:20724200-20724600	ZNF genes & repeats	Ovary	ovary
30	chr14:20724400-20755200	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr14:20724600-20725200	Weak transcription	Ovary	ovary
32	chr14:20725200-20725400	ZNF genes & repeats	Ovary	ovary
33	chr14:20725400-20748200	Weak transcription	Ovary	ovary
34	chr14:20728800-20730400	Weak transcription	Fetal Brain Male	brain
35	chr14:20729600-20732200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr14:20729600-20732800	Enhancers	NHEK	skin
37	chr14:20730000-20732000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr14:20730000-20732600	Enhancers	HMEC	breast
39	chr14:20730000-20732800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr14:20730200-20731200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr14:20730200-20731400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr14:20730200-20731800	Enhancers	Hela-S3	cervix
43	chr14:20730400-20730600	Enhancers	Osteobl	bone
44	chr14:20730400-20731200	Enhancers	NHDF-Ad	bronchial
45	chr14:20730400-20731400	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr14:20730400-20731400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr14:20730400-20731600	Enhancers	HSMM	muscle
48	chr14:20730400-20732000	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr14:20730400-20732000	Enhancers	K562	blood
50	chr14:20730600-20730800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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