Variant report

Variant	nsv1039955
Chromosome Location	chr14:24927313-24993666
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:448)
CpG islands
(count:183)
Chromatin interactive
region (count:24)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:448 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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	chr14:24988161-24988425	GM12878	blood:	n/a	chr14:24988285-24988298 chr14:24988287-24988296 chr14:24988287-24988296 chr14:24988288-24988297
5	BHLHE40	chr14:24950873-24951083	GM12878	blood:	n/a	n/a
6	BHLHE40	chr14:24950918-24951048	K562	blood:	n/a	n/a
7	BHLHE40	chr14:24977363-24977725	GM12878	blood:	n/a	n/a
8	CEBPB	chr14:24961363-24961489	HepG2	liver:	n/a	n/a
9	CEBPB	chr14:24936556-24936597	IMR90	lung:	n/a	chr14:24936570-24936581
10	CEBPB	chr14:24961288-24961606	HepG2	liver:	n/a	n/a
11	CEBPB	chr14:24961460-24961471	A549	lung:	n/a	n/a
12	CEBPB	chr14:24933322-24933646	K562	blood:	n/a	chr14:24933477-24933488
13	CEBPB	chr14:24984093-24984194	HepG2	liver:	n/a	chr14:24984150-24984161
14	CEBPB	chr14:24991550-24991602	HepG2	liver:	n/a	chr14:24991553-24991564
15	CEBPB	chr14:24985169-24985265	HepG2	liver:	n/a	n/a
16	CEBPB	chr14:24961253-24961544	HepG2	liver:	n/a	n/a
17	CEBPB	chr14:24961365-24961539	MCF-7	breast:	n/a	n/a
18	CEBPB	chr14:24933331-24933629	HepG2	liver:	n/a	chr14:24933477-24933488
19	CEBPB	chr14:24933380-24933633	A549	lung:	n/a	chr14:24933477-24933488
20	CEBPB	chr14:24933358-24933637	IMR90	lung:	n/a	chr14:24933477-24933488
21	CEBPB	chr14:24936466-24936680	HepG2	liver:	n/a	chr14:24936570-24936581
22	CEBPB	chr14:24991135-24991276	HepG2	liver:	n/a	n/a
23	CHD2	chr14:24950790-24951053	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr14:24950846-24951061	HepG2	liver:	n/a	n/a
25	CREB1	chr14:24934957-24935508	GM12878	blood:	n/a	n/a
26	CREB1	chr14:24953109-24953480	GM12878	blood:	n/a	n/a
27	CREB1	chr14:24935061-24935433	GM12878	blood:	n/a	n/a
28	CTCF	chr14:24943340-24943490	K562	blood:	n/a	n/a
29	CTCF	chr14:24950840-24950990	HRPEpiC	eye:	n/a	chr14:24950940-24950958
30	CTCF	chr14:24950860-24951010	GM12870	blood:	n/a	chr14:24950940-24950958
31	CTCF	chr14:24950880-24951030	HVMF	connective:	n/a	chr14:24950940-24950958
32	CTCF	chr14:24950880-24951030	HEK293	kidney:	n/a	chr14:24950940-24950958
33	CTCF	chr14:24950900-24951050	HCT-116	colon:	n/a	chr14:24950940-24950958
34	CTCF	chr14:24950825-24951081	GM19239	blood:	n/a	chr14:24950940-24950958
35	CTCF	chr14:24950820-24950970	HL-60	blood:	n/a	chr14:24950940-24950958
36	CTCF	chr14:24950860-24951010	BE2_C	brain:	n/a	chr14:24950940-24950958
37	CTCF	chr14:24950880-24951030	BJ	skin:	n/a	chr14:24950940-24950958
38	CTCF	chr14:24950860-24951010	WERI-Rb-1	eye:	n/a	chr14:24950940-24950958
39	CTCF	chr14:24950200-24950350	HepG2	liver:	n/a	n/a
40	CTCF	chr14:24950704-24951229	MCF-7	breast:	n/a	chr14:24950940-24950958
41	CTCF	chr14:24951440-24951590	HepG2	liver:	n/a	chr14:24951464-24951482
42	CTCF	chr14:24950752-24951054	T-47D	breast:	n/a	chr14:24950940-24950958
43	CTCF	chr14:24950822-24951088	MCF-7	breast:	n/a	chr14:24950940-24950958
44	CTCF	chr14:24950840-24950990	HVMF	connective:	n/a	chr14:24950940-24950958
45	CTCF	chr14:24950787-24951103	T-47D	breast:	n/a	chr14:24950940-24950958
46	CTCF	chr14:24950716-24951155	K562	blood:	n/a	chr14:24950940-24950958
47	CTCF	chr14:24950842-24951023	SK-N-SH_RA	brain:	n/a	chr14:24950940-24950958
48	CTCF	chr14:24950880-24951030	NHDF-neo	bronchial:	n/a	chr14:24950940-24950958
49	CTCF	chr14:24950900-24951050	HMF	breast:	n/a	chr14:24950940-24950958
50	CTCF	chr14:24950900-24951050	Caco-2	colon:	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	chr14:24977773-24977823	AG04450	lung:	fetal
2	chr14:24977773-24977823	NH-A	brain:	n/a
3	chr14:24977773-24977823	Jurkat	blood:	n/a
4	chr14:24978681-24978731	BE2_C	brain:	n/a
5	chr14:24977773-24977823	BE2_C	brain:	n/a
6	chr14:24978681-24978731	SKMC	muscle:	n/a
7	chr14:24974804-24974854	HepG2	liver:	n/a
8	chr14:24977773-24977823	AG09309	skin:	n/a
9	chr14:24974804-24974854	NH-A	brain:	n/a
10	chr14:24974804-24974854	CMK	blood:	n/a
11	chr14:24977773-24977823	HMEC	breast:	n/a
12	chr14:24977773-24977823	SAEC	small airway:	n/a
13	chr14:24974804-24974854	GM19239	blood:	n/a
14	chr14:24977773-24977823	HEEpiC	esophagus:	n/a
15	chr14:24977773-24977823	CMK	blood:	n/a
16	chr14:24974804-24974854	U87	brain:	n/a
17	chr14:24977773-24977823	PrEC	prostate:	n/a
18	chr14:24974804-24974854	GM12891	blood:	n/a
19	chr14:24977773-24977823	Caco-2	colon:	n/a
20	chr14:24974804-24974854	AoSMC	blood vessel:	n/a
21	chr14:24978681-24978731	ECC-1	luminal epithelium:	n/a
22	chr14:24977773-24977823	SK-N-SH_RA	brain:	n/a
23	chr14:24977773-24977823	NB4	blood:	n/a
24	chr14:24977773-24977823	HUVEC	blood vessel:	n/a
25	chr14:24977773-24977823	SK-N-SH	brain:	n/a
26	chr14:24978681-24978731	K562	blood:	n/a
27	chr14:24978681-24978731	HEEpiC	esophagus:	n/a
28	chr14:24974804-24974854	ProgFib	skin:	n/a
29	chr14:24974804-24974854	HCM	heart:	n/a
30	chr14:24977773-24977823	A549	lung:	n/a
31	chr14:24977773-24977823	HIPEpiC	eye:	n/a
32	chr14:24978681-24978731	MCF-7	breast:	n/a
33	chr14:24978681-24978731	HPAEpiC	pulmonary alveolar:	n/a
34	chr14:24978681-24978731	HCF	heart:	n/a
35	chr14:24978681-24978731	PANC-1	pancreas:	n/a
36	chr14:24974804-24974854	HMEC	breast:	n/a
37	chr14:24974804-24974854	HCT-116	colon:	n/a
38	chr14:24978681-24978731	GM19239	blood:	n/a
39	chr14:24974804-24974854	AG09309	skin:	n/a
40	chr14:24977773-24977823	HCF	heart:	n/a
41	chr14:24978681-24978731	A549	lung:	n/a
42	chr14:24974804-24974854	AG09319	gingival:	n/a
43	chr14:24974804-24974854	NT2-D1	testis:	n/a
44	chr14:24978681-24978731	HL-60	blood:	n/a
45	chr14:24974804-24974854	SK-N-SH	brain:	n/a
46	chr14:24974804-24974854	AG04450	lung:	fetal
47	chr14:24974804-24974854	HPAEpiC	pulmonary alveolar:	n/a
48	chr14:24978681-24978731	HNPCEpiC	eye:	n/a
49	chr14:24977773-24977823	LNCaP	prostate:	n/a
50	chr14:24974804-24974854	H1-hESC	embryonic stem cell:	embryo

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:24911430..24913240-chr14:24948207..24950557,2	K562	blood:
2	chr14:24910451..24913467-chr14:24926014..24930297,6	MCF-7	breast:
3	chr14:24925537..24927679-chr14:24931012..24933705,2	MCF-7	breast:
4	chr14:24977730..24979918-chr14:24980024..24982313,2	MCF-7	breast:
5	chr14:24987134..24988670-chr14:24989655..24991180,2	K562	blood:
6	chr14:24911704..24914258-chr14:24948506..24950947,2	MCF-7	breast:
7	chr14:24929358..24930887-chr8:102503029..102505102,2	MCF-7	breast:
8	chr14:24960817..24963613-chr14:24965277..24968190,2	K562	blood:
9	chr14:24952643..24955226-chr14:24957985..24960918,2	K562	blood:
10	chr14:24950446..24951536-chr14:25147799..25148973,31	MCF-7	breast:
11	chr14:24950478..24951496-chr14:25147845..25148826,8	MCF-7	breast:
12	chr14:24941879..24943792-chr14:24944086..24946470,2	MCF-7	breast:
13	chr14:24922420..24924852-chr14:24926664..24928247,2	K562	blood:
14	chr14:24923545..24925251-chr14:24928583..24930504,2	MCF-7	breast:
15	chr14:24960817..24963613-chr14:24965277..24968190,2	K562	blood:
16	chr14:24940138..24941029-chr14:24952690..24953556,3	MCF-7	breast:
17	chr14:24950901..24951428-chr14:25147948..25148704,2	K562	blood:
18	chr14:24950851..24951362-chr14:25074499..25075225,3	MCF-7	breast:
19	chr14:24977730..24979918-chr14:24980024..24982313,2	MCF-7	breast:
20	chr14:24987134..24988670-chr14:24989655..24991180,2	K562	blood:
21	chr14:24952643..24955226-chr14:24957985..24960918,2	K562	blood:
22	chr14:24941879..24943792-chr14:24944086..24946470,2	MCF-7	breast:
23	chr14:24925537..24927679-chr14:24931012..24933705,2	MCF-7	breast:
24	chr14:24940138..24941029-chr14:24952690..24953556,3	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
ENSG00000258744	TF binding region
CMA1	CpG island
ENSG00000258744	CpG island
ENSG00000100445	chromatin interactions
ENSG00000083307	chromatin interactions
ENSG00000254024	chromatin interactions
CYP2C8	miRNA target sites

Extended variants
information (count: 1918 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1918 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs737246	chr14:24927313-24927314	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs117236728	chr14:24927319-24927320	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs573156236	chr14:24927350-24927351	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs911369	chr14:24927359-24927360	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs74036657	chr14:24927364-24927365	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs737245	chr14:24927382-24927383	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs544859052	chr14:24927383-24927384	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs561427516	chr14:24927406-24927407	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs737248	chr14:24927408-24927409	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs540894471	chr14:24927409-24927410	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs34117084	chr14:24927412-24927413	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs572808118	chr14:24927426-24927427	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs559909357	chr14:24927454-24927455	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs533701883	chr14:24927492-24927493	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs188985948	chr14:24927541-24927542	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs143585616	chr14:24927545-24927546	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs551735389	chr14:24927580-24927581	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs149327301	chr14:24927660-24927661	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs144523935	chr14:24927668-24927669	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs547981244	chr14:24927706-24927707	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs568215979	chr14:24927739-24927740	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs386775695	chr14:24927816-24927817	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs58483508	chr14:24927817-24927818	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs570633944	chr14:24927847-24927848	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs147165753	chr14:24927858-24927859	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs59552231	chr14:24927860-24927861	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs568246482	chr14:24927886-24927887	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs1473725	chr14:24927935-24927936	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs114286320	chr14:24927938-24927939	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs575817698	chr14:24928012-24928013	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs77165598	chr14:24928019-24928020	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs113252072	chr14:24928041-24928042	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs1473724	chr14:24928071-24928072	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs540455639	chr14:24928094-24928095	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs560869688	chr14:24928116-24928117	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs1473723	chr14:24928128-24928129	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs190606151	chr14:24928129-24928130	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs182879869	chr14:24928133-24928134	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs531324454	chr14:24928165-24928166	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs116516583	chr14:24928166-24928167	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs2332332	chr14:24928206-24928207	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs527507340	chr14:24928294-24928295	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs2332333	chr14:24928308-24928309	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs112888821	chr14:24928397-24928398	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs367739421	chr14:24928403-24928404	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs17103960	chr14:24928413-24928414	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs574217372	chr14:24928429-24928430	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs2332334	chr14:24928432-24928433	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs59448251	chr14:24928452-24928453	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs533442533	chr14:24928471-24928472	Weak transcription Enhancers Strong 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:233 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:24912800-24950800	Weak transcription	Gastric	stomach
2	chr14:24913000-24930000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr14:24913000-24931600	Weak transcription	Fetal Kidney	kidney
4	chr14:24913000-24932400	Weak transcription	Primary B cells from cord blood	blood
5	chr14:24913000-24932800	Weak transcription	Primary T cells from cord blood	blood
6	chr14:24920800-24927400	Weak transcription	Spleen	Spleen
7	chr14:24922200-24946000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr14:24922800-24951000	Weak transcription	Pancreas	Pancrea
9	chr14:24923200-24937400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr14:24923600-24932600	Weak transcription	Right Ventricle	heart
11	chr14:24924000-24929400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr14:24924200-24928000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr14:24924200-24932000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr14:24924600-24927600	Weak transcription	HepG2	liver
15	chr14:24925200-24929600	Weak transcription	Fetal Stomach	stomach
16	chr14:24925800-24928200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
17	chr14:24925800-24933400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr14:24926000-24927400	Weak transcription	Placenta	Placenta
19	chr14:24926000-24936000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr14:24926200-24929400	Weak transcription	Ovary	ovary
21	chr14:24926400-24927400	Weak transcription	Liver	Liver
22	chr14:24926400-24929600	Weak transcription	Aorta	Aorta
23	chr14:24926400-24930800	Weak transcription	Fetal Intestine Small	intestine
24	chr14:24926400-24934200	Weak transcription	Lung	lung
25	chr14:24926800-24929800	Weak transcription	Placenta Amnion	Placenta Amnion
26	chr14:24927200-24927600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr14:24927400-24928400	Strong transcription	Liver	Liver
28	chr14:24927400-24928400	Genic enhancers	Spleen	Spleen
29	chr14:24927400-24928600	Strong transcription	Placenta	Placenta
30	chr14:24927400-24929200	Enhancers	Adipose Nuclei	Adipose
31	chr14:24927400-24929200	Enhancers	Fetal Muscle Trunk	muscle
32	chr14:24927600-24928200	Strong transcription	HepG2	liver
33	chr14:24927600-24928600	Enhancers	HUVEC	blood vessel
34	chr14:24927600-24930400	Weak transcription	Esophagus	oesophagus
35	chr14:24927600-24951000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr14:24927800-24928200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr14:24927800-24929400	Enhancers	Fetal Muscle Leg	muscle
38	chr14:24928000-24928800	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr14:24928200-24934400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr14:24928200-24950400	Weak transcription	HepG2	liver
41	chr14:24928400-24928800	Enhancers	Spleen	Spleen
42	chr14:24928400-24936000	Weak transcription	Liver	Liver
43	chr14:24928600-24951000	Weak transcription	Placenta	Placenta
44	chr14:24928800-24951000	Weak transcription	Spleen	Spleen
45	chr14:24929600-24929800	ZNF genes & repeats	Aorta	Aorta
46	chr14:24929800-24932400	Weak transcription	Primary T helper cells PMA-I stimulated	--
47	chr14:24929800-24934600	Weak transcription	Aorta	Aorta
48	chr14:24930200-24931200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr14:24930400-24930600	Enhancers	Esophagus	oesophagus
50	chr14:24930400-24930800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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