Variant report

Variant	nsv521915
Chromosome Location	chr14:24915383-24992619
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:457)
CpG islands
(count:183)
Chromatin interactive
region (count:28)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:457 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:24950760-24951183	HepG2	liver:	n/a	n/a
2	ATF2	chr14:24932426-24932919	GM12878	blood:	n/a	n/a
3	BCLAF1	chr14:24932394-24932853	GM12878	blood:	n/a	chr14:24932495-24932504
4	BHLHE40	chr14:24950918-24951048	K562	blood:	n/a	n/a
5	BHLHE40	chr14:24988161-24988425	GM12878	blood:	n/a	chr14:24988285-24988298 chr14:24988287-24988296 chr14:24988287-24988296 chr14:24988288-24988297
6	BHLHE40	chr14:24977363-24977725	GM12878	blood:	n/a	n/a
7	BHLHE40	chr14:24950873-24951083	GM12878	blood:	n/a	n/a
8	CEBPB	chr14:24925409-24925575	A549	lung:	n/a	chr14:24925447-24925460 chr14:24925447-24925458
9	CEBPB	chr14:24933380-24933633	A549	lung:	n/a	chr14:24933477-24933488
10	CEBPB	chr14:24961288-24961606	HepG2	liver:	n/a	n/a
11	CEBPB	chr14:24961363-24961489	HepG2	liver:	n/a	n/a
12	CEBPB	chr14:24961460-24961471	A549	lung:	n/a	n/a
13	CEBPB	chr14:24991135-24991276	HepG2	liver:	n/a	n/a
14	CEBPB	chr14:24961253-24961544	HepG2	liver:	n/a	n/a
15	CEBPB	chr14:24925313-24925621	HepG2	liver:	n/a	chr14:24925447-24925460 chr14:24925447-24925458
16	CEBPB	chr14:24936466-24936680	HepG2	liver:	n/a	chr14:24936570-24936581
17	CEBPB	chr14:24985169-24985265	HepG2	liver:	n/a	n/a
18	CEBPB	chr14:24936556-24936597	IMR90	lung:	n/a	chr14:24936570-24936581
19	CEBPB	chr14:24984093-24984194	HepG2	liver:	n/a	chr14:24984150-24984161
20	CEBPB	chr14:24933331-24933629	HepG2	liver:	n/a	chr14:24933477-24933488
21	CEBPB	chr14:24961365-24961539	MCF-7	breast:	n/a	n/a
22	CEBPB	chr14:24933322-24933646	K562	blood:	n/a	chr14:24933477-24933488
23	CEBPB	chr14:24933358-24933637	IMR90	lung:	n/a	chr14:24933477-24933488
24	CEBPB	chr14:24991550-24991602	HepG2	liver:	n/a	chr14:24991553-24991564
25	CHD2	chr14:24950846-24951061	HepG2	liver:	n/a	n/a
26	CHD2	chr14:24950790-24951053	H1-hESC	embryonic stem cell:	n/a	n/a
27	CREB1	chr14:24934957-24935508	GM12878	blood:	n/a	n/a
28	CREB1	chr14:24935061-24935433	GM12878	blood:	n/a	n/a
29	CREB1	chr14:24953109-24953480	GM12878	blood:	n/a	n/a
30	CTCF	chr14:24950860-24951010	HepG2	liver:	n/a	chr14:24950940-24950958
31	CTCF	chr14:24950820-24950970	K562	blood:	n/a	chr14:24950940-24950958
32	CTCF	chr14:24950825-24951067	Spleen_OC	spleen:	n/a	chr14:24950940-24950958
33	CTCF	chr14:24950900-24951050	WERI-Rb-1	eye:	n/a	chr14:24950940-24950958
34	CTCF	chr14:24950840-24950990	NHEK	skin:	n/a	chr14:24950940-24950958
35	CTCF	chr14:24950860-24951010	Caco-2	colon:	n/a	chr14:24950940-24950958
36	CTCF	chr14:24950773-24951137	K562	blood:	n/a	chr14:24950940-24950958
37	CTCF	chr14:24992040-24992190	AG04450	lung:	n/a	n/a
38	CTCF	chr14:24950840-24950990	HCT-116	colon:	n/a	chr14:24950940-24950958
39	CTCF	chr14:24950808-24951114	GM12878	blood:	n/a	chr14:24950940-24950958
40	CTCF	chr14:24950818-24951074	HUVEC	blood vessel:	n/a	chr14:24950940-24950958
41	CTCF	chr14:24950900-24951050	HCM	heart:	n/a	chr14:24950940-24950958
42	CTCF	chr14:24950785-24950991	A549	lung:	n/a	chr14:24950940-24950958
43	CTCF	chr14:24950900-24951050	HFF-Myc	foreskin:	n/a	chr14:24950940-24950958
44	CTCF	chr14:24950762-24951080	ECC-1	luminal epithelium:	n/a	chr14:24950940-24950958
45	CTCF	chr14:24950860-24951010	AG04449	skin:	n/a	chr14:24950940-24950958
46	CTCF	chr14:24950860-24951010	GM12878	blood:	n/a	chr14:24950940-24950958
47	CTCF	chr14:24950860-24951010	AoAF	blood vessel:	n/a	chr14:24950940-24950958
48	CTCF	chr14:24950860-24951010	GM12875	blood:	n/a	chr14:24950940-24950958
49	CTCF	chr14:24951260-24951410	HCT-116	colon:	n/a	n/a
50	CTCF	chr14:24950817-24951113	GM12891	blood:	n/a	chr14:24950940-24950958

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:24974804-24974854	RPTEC	kidney:	n/a
2	chr14:24978681-24978731	HRE	kidney:	n/a
3	chr14:24977773-24977823	HL-60	blood:	n/a
4	chr14:24974804-24974854	HCPEpiC	choroid plexus:	n/a
5	chr14:24978681-24978731	HCF	heart:	n/a
6	chr14:24977773-24977823	HUVEC	blood vessel:	n/a
7	chr14:24974804-24974854	HNPCEpiC	eye:	n/a
8	chr14:24978681-24978731	HCM	heart:	n/a
9	chr14:24977773-24977823	ProgFib	skin:	n/a
10	chr14:24978681-24978731	GM12891	blood:	n/a
11	chr14:24977773-24977823	PANC-1	pancreas:	n/a
12	chr14:24974804-24974854	SK-N-MC	brain:	n/a
13	chr14:24977773-24977823	K562	blood:	n/a
14	chr14:24977773-24977823	AG04449	skin:	fetal
15	chr14:24978681-24978731	CMK	blood:	n/a
16	chr14:24978681-24978731	AG04449	skin:	fetal
17	chr14:24974804-24974854	HepG2	liver:	n/a
18	chr14:24978681-24978731	NB4	blood:	n/a
19	chr14:24977773-24977823	SAEC	small airway:	n/a
20	chr14:24974804-24974854	ECC-1	luminal epithelium:	n/a
21	chr14:24974804-24974854	SAEC	small airway:	n/a
22	chr14:24977773-24977823	GM06990	blood:	n/a
23	chr14:24974804-24974854	NT2-D1	testis:	n/a
24	chr14:24977773-24977823	BJ	skin:	n/a
25	chr14:24974804-24974854	AG09309	skin:	n/a
26	chr14:24974804-24974854	NHBE	bronchial:	n/a
27	chr14:24977773-24977823	SK-N-SH_RA	brain:	n/a
28	chr14:24977773-24977823	HRPEpiC	eye:	n/a
29	chr14:24978681-24978731	GM12878	blood:	n/a
30	chr14:24974804-24974854	NHDF-neo	bronchial:	n/a
31	chr14:24974804-24974854	HRCEpiC	kidney:	n/a
32	chr14:24978681-24978731	NHDF-neo	bronchial:	n/a
33	chr14:24977773-24977823	HEEpiC	esophagus:	n/a
34	chr14:24977773-24977823	AG04450	lung:	fetal
35	chr14:24977773-24977823	SK-N-MC	brain:	n/a
36	chr14:24977773-24977823	BE2_C	brain:	n/a
37	chr14:24974804-24974854	HMEC	breast:	n/a
38	chr14:24974804-24974854	HUVEC	blood vessel:	n/a
39	chr14:24978681-24978731	HRPEpiC	eye:	n/a
40	chr14:24977773-24977823	SKMC	muscle:	n/a
41	chr14:24978681-24978731	NT2-D1	testis:	n/a
42	chr14:24977773-24977823	Caco-2	colon:	n/a
43	chr14:24978681-24978731	RPTEC	kidney:	n/a
44	chr14:24974804-24974854	GM12892	blood:	n/a
45	chr14:24974804-24974854	GM12891	blood:	n/a
46	chr14:24974804-24974854	U87	brain:	n/a
47	chr14:24974804-24974854	HIPEpiC	eye:	n/a
48	chr14:24978681-24978731	LNCaP	prostate:	n/a
49	chr14:24977773-24977823	Jurkat	blood:	n/a
50	chr14:24977773-24977823	AG09319	gingival:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:24952643..24955226-chr14:24957985..24960918,2	K562	blood:
2	chr14:24950901..24951428-chr14:25147948..25148704,2	K562	blood:
3	chr14:24977730..24979918-chr14:24980024..24982313,2	MCF-7	breast:
4	chr14:24922420..24924852-chr14:24926664..24928247,2	K562	blood:
5	chr14:24911857..24913696-chr14:24915123..24916800,2	MCF-7	breast:
6	chr14:24925537..24927679-chr14:24931012..24933705,2	MCF-7	breast:
7	chr14:24940138..24941029-chr14:24952690..24953556,3	MCF-7	breast:
8	chr14:24977730..24979918-chr14:24980024..24982313,2	MCF-7	breast:
9	chr14:24911430..24913240-chr14:24948207..24950557,2	K562	blood:
10	chr14:24987134..24988670-chr14:24989655..24991180,2	K562	blood:
11	chr14:24911289..24913259-chr14:24923385..24925782,2	MCF-7	breast:
12	chr14:24950446..24951536-chr14:25147799..25148973,31	MCF-7	breast:
13	chr14:24910451..24913467-chr14:24926014..24930297,6	MCF-7	breast:
14	chr14:24911704..24914258-chr14:24948506..24950947,2	MCF-7	breast:
15	chr14:24941879..24943792-chr14:24944086..24946470,2	MCF-7	breast:
16	chr14:24940138..24941029-chr14:24952690..24953556,3	MCF-7	breast:
17	chr14:24960817..24963613-chr14:24965277..24968190,2	K562	blood:
18	chr14:24923545..24925251-chr14:24928583..24930504,2	MCF-7	breast:
19	chr14:24923545..24925251-chr14:24928583..24930504,2	MCF-7	breast:
20	chr14:24929358..24930887-chr8:102503029..102505102,2	MCF-7	breast:
21	chr14:24960817..24963613-chr14:24965277..24968190,2	K562	blood:
22	chr14:24987134..24988670-chr14:24989655..24991180,2	K562	blood:
23	chr14:24950851..24951362-chr14:25074499..25075225,3	MCF-7	breast:
24	chr14:24922420..24924852-chr14:24926664..24928247,2	K562	blood:
25	chr14:24952643..24955226-chr14:24957985..24960918,2	K562	blood:
26	chr14:24950478..24951496-chr14:25147845..25148826,8	MCF-7	breast:
27	chr14:24941879..24943792-chr14:24944086..24946470,2	MCF-7	breast:
28	chr14:24925537..24927679-chr14:24931012..24933705,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-80A15.1.1-1	chr14:24970766-24971403	NR_110032
2	lnc-RP11-80A15.1.1-1	chr14:24970766-24971403	ENSG00000251021

No data

Variant related genes	Relation type
CMA1	TF binding region
SDR39U1	TF binding region
ENSG00000258744	TF binding region
CMA1	CpG island
SDR39U1	CpG island
ENSG00000258744	CpG island
ENSG00000100445	chromatin interactions
ENSG00000083307	chromatin interactions
ENSG00000254024	chromatin interactions
CYP2C8	miRNA target sites

Extended variants
information (count: 2459 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:2459 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10140911	chr14:24915383-24915384	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs150908924	chr14:24915419-24915420	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs565074581	chr14:24915427-24915428	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs186050313	chr14:24915481-24915482	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs550618663	chr14:24915543-24915544	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs113315699	chr14:24915565-24915566	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs370005014	chr14:24915691-24915692	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs528319549	chr14:24915705-24915706	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs375431851	chr14:24915745-24915746	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs201211329	chr14:24915759-24915760	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs549013722	chr14:24915767-24915768	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs145045308	chr14:24915817-24915818	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs77240427	chr14:24915818-24915819	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs142027181	chr14:24915827-24915828	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs144621226	chr14:24915828-24915829	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs74805728	chr14:24915837-24915838	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs534804174	chr14:24915868-24915869	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs551415996	chr14:24915880-24915881	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs569039871	chr14:24915897-24915898	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs80123144	chr14:24915898-24915899	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs189586023	chr14:24915936-24915937	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs202067375	chr14:24915968-24915969	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs199663027	chr14:24915976-24915977	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs386775691	chr14:24915978-24915979	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs1956901	chr14:24915980-24915981	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs386775692	chr14:24915998-24915999	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs1956899	chr14:24915999-24916000	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs180778066	chr14:24916052-24916053	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs532807501	chr14:24916069-24916070	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs572827890	chr14:24916093-24916094	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs569653260	chr14:24916101-24916102	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs537009251	chr14:24916108-24916109	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs200544747	chr14:24916110-24916111	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs200578368	chr14:24916280-24916281	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs77956369	chr14:24916282-24916283	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs397745519	chr14:24916283-24916284	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs373606390	chr14:24916284-24916285	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs545144870	chr14:24916300-24916301	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs533452267	chr14:24916301-24916302	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs1956898	chr14:24916304-24916305	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs186436404	chr14:24916322-24916323	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs190845825	chr14:24916341-24916342	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs72696330	chr14:24916355-24916356	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs139427884	chr14:24916361-24916362	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs185681565	chr14:24916378-24916379	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs559326241	chr14:24916426-24916427	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs528434102	chr14:24916437-24916438	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs578127097	chr14:24916528-24916529	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs571741803	chr14:24916529-24916530	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs191266451	chr14:24916558-24916559	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
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
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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Cancer	21183584	CNVD
Leukoplakia	24403051	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
Chronic myeloid leukemia	16756668	CNVD
Sudden cardiac death	19188705	CNVD
Pilocytic astrocytoma	18670637	CNVD
Multiple myeloma	16616336	CNVD

Chromatin state (count:293 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:24912000-24925800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr14:24912400-24922400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr14:24912600-24925800	Weak transcription	Ovary	ovary
4	chr14:24912800-24915800	Weak transcription	Aorta	Aorta
5	chr14:24912800-24922800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr14:24912800-24950800	Weak transcription	Gastric	stomach
7	chr14:24913000-24915600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr14:24913000-24917000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr14:24913000-24917400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr14:24913000-24917600	Weak transcription	Placenta	Placenta
11	chr14:24913000-24917800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr14:24913000-24918000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr14:24913000-24922200	Weak transcription	Fetal Intestine Small	intestine
14	chr14:24913000-24922400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr14:24913000-24922800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr14:24913000-24923600	Weak transcription	NHEK	skin
17	chr14:24913000-24925400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr14:24913000-24925800	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr14:24913000-24926400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr14:24913000-24930000	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr14:24913000-24931600	Weak transcription	Fetal Kidney	kidney
22	chr14:24913000-24932400	Weak transcription	Primary B cells from cord blood	blood
23	chr14:24913000-24932800	Weak transcription	Primary T cells from cord blood	blood
24	chr14:24913200-24916000	Weak transcription	HSMM	muscle
25	chr14:24913200-24921800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr14:24913200-24925400	Weak transcription	HMEC	breast
27	chr14:24913600-24923600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr14:24914000-24923200	Weak transcription	HepG2	liver
29	chr14:24920800-24927400	Weak transcription	Spleen	Spleen
30	chr14:24921800-24923600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr14:24922000-24925800	Weak transcription	Liver	Liver
32	chr14:24922200-24924200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr14:24922200-24924200	ZNF genes & repeats	Fetal Intestine Small	intestine
34	chr14:24922200-24946000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr14:24922400-24922800	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
36	chr14:24922400-24923000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
37	chr14:24922400-24924600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr14:24922800-24924200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr14:24922800-24924200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr14:24922800-24951000	Weak transcription	Pancreas	Pancrea
41	chr14:24923000-24925800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr14:24923200-24924000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr14:24923200-24924600	ZNF genes & repeats	HepG2	liver
44	chr14:24923200-24937400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr14:24923600-24923800	ZNF genes & repeats	NHEK	skin
46	chr14:24923600-24924200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr14:24923600-24924200	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr14:24923600-24932600	Weak transcription	Right Ventricle	heart
49	chr14:24923800-24924000	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr14:24923800-24924800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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