Variant report

Variant	nsv563829
Chromosome Location	chr14:20445370-20694968
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:742)
CpG islands
(count:856)
Chromatin interactive
region (count:32)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:742 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:20645562-20646086	K562	blood:	n/a	n/a
2	ARID3A	chr14:20512405-20512844	K562	blood:	n/a	n/a
3	ARID3A	chr14:20644582-20645133	K562	blood:	n/a	n/a
4	ARID3A	chr14:20584982-20585271	K562	blood:	n/a	n/a
5	ATF1	chr14:20561670-20561913	K562	blood:	n/a	n/a
6	ATF1	chr14:20584956-20585164	K562	blood:	n/a	n/a
7	ATF1	chr14:20645594-20645932	K562	blood:	n/a	n/a
8	ATF1	chr14:20608626-20608778	K562	blood:	n/a	n/a
9	ATF3	chr14:20638032-20638356	K562	blood:	n/a	n/a
10	ATF3	chr14:20584968-20585229	K562	blood:	n/a	n/a
11	ATF3	chr14:20512489-20512787	K562	blood:	n/a	n/a
12	ATF3	chr14:20645584-20645910	K562	blood:	n/a	n/a
13	BACH1	chr14:20584638-20585505	K562	blood:	n/a	n/a
14	BACH1	chr14:20687322-20687431	H1-hESC	embryonic stem cell:	n/a	chr14:20687387-20687401
15	BACH1	chr14:20687217-20687569	K562	blood:	n/a	chr14:20687387-20687401
16	BHLHE40	chr14:20653018-20653080	K562	blood:	n/a	n/a
17	BHLHE40	chr14:20645542-20646303	K562	blood:	n/a	n/a
18	CBX3	chr14:20645492-20645863	K562	blood:	n/a	n/a
19	CBX3	chr14:20584916-20585201	K562	blood:	n/a	n/a
20	CBX3	chr14:20450329-20450560	K562	blood:	n/a	n/a
21	CBX3	chr14:20586942-20587293	K562	blood:	n/a	n/a
22	CBX3	chr14:20645515-20645980	K562	blood:	n/a	n/a
23	CBX3	chr14:20632656-20632932	K562	blood:	n/a	n/a
24	CBX3	chr14:20512416-20512761	K562	blood:	n/a	n/a
25	CBX3	chr14:20632642-20632904	K562	blood:	n/a	n/a
26	CBX3	chr14:20586982-20587337	K562	blood:	n/a	n/a
27	CCNT2	chr14:20677752-20678071	K562	blood:	n/a	n/a
28	CCNT2	chr14:20516381-20516636	K562	blood:	n/a	n/a
29	CCNT2	chr14:20645714-20646195	K562	blood:	n/a	n/a
30	CEBPB	chr14:20683376-20683687	A549	lung:	n/a	chr14:20683523-20683534
31	CEBPB	chr14:20683431-20683747	MCF-7	breast:	n/a	chr14:20683523-20683534
32	CEBPB	chr14:20622449-20622660	HepG2	liver:	n/a	chr14:20622561-20622572
33	CEBPB	chr14:20578626-20578939	A549	lung:	n/a	n/a
34	CEBPB	chr14:20667315-20667568	K562	blood:	n/a	chr14:20667443-20667454
35	CEBPB	chr14:20659063-20659394	HepG2	liver:	n/a	chr14:20659228-20659241 chr14:20659229-20659240 chr14:20659227-20659244
36	CEBPB	chr14:20578635-20578967	HepG2	liver:	n/a	n/a
37	CEBPB	chr14:20644548-20644852	K562	blood:	n/a	chr14:20644780-20644791 chr14:20644718-20644735 chr14:20644780-20644791
38	CEBPB	chr14:20546411-20546602	K562	blood:	n/a	n/a
39	CEBPB	chr14:20683384-20683692	Hela-S3	cervix:	n/a	chr14:20683523-20683534
40	CEBPB	chr14:20667271-20667577	Hela-S3	cervix:	n/a	chr14:20667443-20667454
41	CEBPB	chr14:20668608-20668745	K562	blood:	n/a	n/a
42	CEBPB	chr14:20470478-20470832	HepG2	liver:	n/a	chr14:20470615-20470626
43	CEBPB	chr14:20470519-20470853	K562	blood:	n/a	chr14:20470615-20470626
44	CEBPB	chr14:20645527-20645985	K562	blood:	n/a	n/a
45	CEBPB	chr14:20524789-20524910	A549	lung:	n/a	n/a
46	CEBPB	chr14:20578686-20578922	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr14:20645573-20645988	K562	blood:	n/a	n/a
48	CEBPB	chr14:20659170-20659372	K562	blood:	n/a	chr14:20659228-20659241 chr14:20659229-20659240 chr14:20659227-20659244
49	CEBPB	chr14:20578612-20578943	IMR90	lung:	n/a	n/a
50	CEBPB	chr14:20683466-20683657	K562	blood:	n/a	chr14:20683523-20683534

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:20502658-20502708	SKMC	muscle:	n/a
2	chr14:20611779-20611829	GM12878	blood:	n/a
3	chr14:20502658-20502708	SKMC	muscle:	n/a
4	chr14:20611779-20611829	GM12878	blood:	n/a
5	chr14:20611696-20611746	AG09319	gingival:	n/a
6	chr14:20585753-20585803	GM19239	blood:	n/a
7	chr14:20611779-20611829	ovcar-3	ovarian:	n/a
8	chr14:20611696-20611746	HRPEpiC	eye:	n/a
9	chr14:20664021-20664071	PANC-1	pancreas:	n/a
10	chr14:20482899-20482949	GM19239	blood:	n/a
11	chr14:20585753-20585803	AG09319	gingival:	n/a
12	chr14:20502658-20502708	AG04449	skin:	fetal
13	chr14:20666088-20666138	IMR90	lung:	fetal
14	chr14:20664021-20664071	SK-N-SH	brain:	n/a
15	chr14:20611696-20611746	ProgFib	skin:	n/a
16	chr14:20584239-20584289	HMEC	breast:	n/a
17	chr14:20691777-20691827	HEEpiC	esophagus:	n/a
18	chr14:20502658-20502708	Jurkat	blood:	n/a
19	chr14:20585753-20585803	AG04449	skin:	fetal
20	chr14:20482899-20482949	NH-A	brain:	n/a
21	chr14:20586367-20586417	GM12891	blood:	n/a
22	chr14:20482899-20482949	HEK293	kidney:	embryo
23	chr14:20611779-20611829	HCPEpiC	choroid plexus:	n/a
24	chr14:20611696-20611746	CMK	blood:	n/a
25	chr14:20692622-20692672	SAEC	small airway:	n/a
26	chr14:20502658-20502708	LNCaP	prostate:	n/a
27	chr14:20584239-20584289	GM12878	blood:	n/a
28	chr14:20664580-20664630	RPTEC	kidney:	n/a
29	chr14:20502658-20502708	NB4	blood:	n/a
30	chr14:20528812-20528862	ovcar-3	ovarian:	n/a
31	chr14:20612220-20612270	K562	blood:	n/a
32	chr14:20611779-20611829	RPTEC	kidney:	n/a
33	chr14:20502658-20502708	AG09309	skin:	n/a
34	chr14:20585753-20585803	HepG2	liver:	n/a
35	chr14:20586367-20586417	Hepatocyte	liver:	n/a
36	chr14:20666088-20666138	HCT-116	colon:	n/a
37	chr14:20584239-20584289	NHDF-neo	bronchial:	n/a
38	chr14:20611696-20611746	Hepatocyte	liver:	n/a
39	chr14:20586367-20586417	NB4	blood:	n/a
40	chr14:20584239-20584289	HRE	kidney:	n/a
41	chr14:20585753-20585803	HRPEpiC	eye:	n/a
42	chr14:20611779-20611829	HCF	heart:	n/a
43	chr14:20611696-20611746	GM12892	blood:	n/a
44	chr14:20482899-20482949	PANC-1	pancreas:	n/a
45	chr14:20482899-20482949	BJ	skin:	n/a
46	chr14:20691777-20691827	MCF-7	breast:	n/a
47	chr14:20586367-20586417	Caco-2	colon:	n/a
48	chr14:20664580-20664630	PrEC	prostate:	n/a
49	chr14:20612220-20612270	NT2-D1	testis:	n/a
50	chr14:20585753-20585803	PANC-1	pancreas:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:20653449..20656373-chr14:20661305..20663533,2	MCF-7	breast:
2	chr14:20691139..20693631-chr14:20695657..20698105,2	K562	blood:
3	chr14:20518924..20521802-chr14:20525808..20527615,2	K562	blood:
4	chr14:20649377..20653239-chr14:20653513..20656414,3	K562	blood:
5	chr14:20518924..20521802-chr14:20525808..20527615,2	K562	blood:
6	chr14:20615947..20618319-chr14:20622650..20625017,2	K562	blood:
7	chr14:20642540..20645135-chr14:20796578..20798741,2	K562	blood:
8	chr14:20611730..20613442-chr14:20616450..20619196,2	K562	blood:
9	chr14:20653650..20655621-chr14:20656798..20658985,2	K562	blood:
10	chr14:20623640..20625607-chr14:20644962..20647182,2	K562	blood:
11	chr14:20479309..20481272-chr14:20484820..20486760,2	K562	blood:
12	chr14:20583619..20586533-chr14:20649310..20650931,2	K562	blood:
13	chr14:20645666..20648683-chr14:20649468..20653312,5	K562	blood:
14	chr14:20578711..20580377-chr14:20580738..20583327,2	K562	blood:
15	chr14:20623957..20624479-chr3:64655642..64656615,2	MCF-7	breast:
16	chr14:20530040..20532845-chr14:20547946..20550280,2	K562	blood:
17	chr14:20623640..20625607-chr14:20644962..20647182,2	K562	blood:
18	chr14:20674085..20677001-chr14:20687478..20690164,2	MCF-7	breast:
19	chr14:20645875..20648132-chr14:20651152..20653312,3	K562	blood:
20	chr14:20611730..20613442-chr14:20616450..20619196,2	K562	blood:
21	chr14:20649377..20653239-chr14:20653513..20656414,3	K562	blood:
22	chr14:20582658..20584245-chr14:20584576..20586426,2	K562	blood:
23	chr14:20657790..20659854-chr14:20660139..20662743,2	K562	blood:
24	chr14:20453392..20455779-chr14:20560575..20562246,2	K562	blood:
25	chr14:20615947..20618319-chr14:20622650..20625486,3	K562	blood:
26	chr14:20653650..20655621-chr14:20656798..20658985,2	K562	blood:
27	chr14:20530040..20532845-chr14:20547946..20550280,2	K562	blood:
28	chr14:20657790..20659854-chr14:20660139..20662743,2	K562	blood:
29	chr14:20674085..20677001-chr14:20687478..20690164,2	MCF-7	breast:
30	chr14:20653449..20656373-chr14:20661305..20663533,2	MCF-7	breast:
31	chr14:20578711..20580377-chr14:20580738..20583327,2	K562	blood:
32	chr14:20479309..20481272-chr14:20484820..20486760,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR4N5-1	chr14:20617391-20617904	NONHSAT035552

No data

Variant related genes	Relation type
RNA5SP380	TF binding region
OR4K13	TF binding region
OR4N5	TF binding region
OR4K17	TF binding region
OR11H5P	TF binding region
OR4K14	TF binding region
RNA5SP381	TF binding region
ENSG00000266336	TF binding region
OR11G1P	TF binding region
ENSG00000265199	TF binding region
OR4T1P	TF binding region
OR11G2	TF binding region
OR4L1	TF binding region
OR4Q2	TF binding region
OR11H6	TF binding region
OR4U1P	TF binding region
ENSG00000259095	TF binding region
OR11H7	TF binding region
PSMB7P1	TF binding region
RNA5SP380	CpG island
OR4K13	CpG island
OR4N5	CpG island
OR4K17	CpG island
OR11H5P	CpG island
OR4K14	CpG island
RNA5SP381	CpG island
ENSG00000266336	CpG island
OR11G1P	CpG island
ENSG00000265199	CpG island
OR4T1P	CpG island
OR11G2	CpG island
OR4L1	CpG island
OR4Q2	CpG island
OR11H6	CpG island
OR4U1P	CpG island
ENSG00000259095	CpG island
OR11H7	CpG island
PSMB7P1	CpG island
ENSG00000100814	chromatin interactions
ENSG00000259074	chromatin interactions
ENSG00000258468	chromatin interactions
ENSG00000258806	chromatin interactions
ENSG00000176230	chromatin interactions
ENSG00000184394	chromatin interactions
ENSG00000258641	chromatin interactions

Extended variants
information (count: 3269 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:3269 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1972373	chr14:20445370-20445371	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs532563527	chr14:20445382-20445383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs368893588	chr14:20445460-20445461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs569346249	chr14:20445491-20445492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs530094186	chr14:20445499-20445500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs56371129	chr14:20445521-20445522	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs566321350	chr14:20445550-20445551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs7157946	chr14:20445558-20445559	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs149562113	chr14:20445607-20445608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs1972372	chr14:20445618-20445619	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs144249449	chr14:20445660-20445661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555839240	chr14:20445672-20445673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs546552951	chr14:20445695-20445696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs574522257	chr14:20445698-20445699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs541548591	chr14:20445712-20445713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs3928337	chr14:20445768-20445769	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs541738103	chr14:20445770-20445771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs573452196	chr14:20445783-20445784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs540799834	chr14:20445804-20445805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs529067244	chr14:20445814-20445815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs7150745	chr14:20445845-20445846	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs34896701	chr14:20445902-20445903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs7149721	chr14:20445905-20445906	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs544601098	chr14:20445908-20445909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs567872763	chr14:20445951-20445952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs562740031	chr14:20445967-20445968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs7145945	chr14:20445995-20445996	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs148740138	chr14:20445996-20445997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs192028679	chr14:20448821-20448822	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs184221678	chr14:20448836-20448837	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs371269369	chr14:20448955-20448956	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs72667627	chr14:20448964-20448965	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs577899023	chr14:20448966-20448967	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs374297720	chr14:20453392-20453393	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs184901646	chr14:20453401-20453402	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs530515129	chr14:20453416-20453417	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs1974320	chr14:20453427-20453428	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs190148792	chr14:20453461-20453462	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs529571142	chr14:20453471-20453472	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs370496332	chr14:20453508-20453509	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs548089985	chr14:20453510-20453511	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs566206933	chr14:20453517-20453518	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs539831090	chr14:20453553-20453554	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs551441415	chr14:20453556-20453557	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs570210875	chr14:20453607-20453608	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs537534052	chr14:20453633-20453634	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs182487599	chr14:20453663-20453664	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs573861514	chr14:20453718-20453719	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs71410206	chr14:20453722-20453723	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs553249555	chr14:20453762-20453763	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:20444600-20445800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr14:20445800-20446000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
3	chr14:20448800-20449000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr14:20461200-20461600	Enhancers	Dnd41	blood
5	chr14:20461600-20462400	ZNF genes & repeats	Dnd41	blood
6	chr14:20470000-20471200	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr14:20470600-20471000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr14:20478800-20479000	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr14:20479600-20479800	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr14:20482600-20483200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr14:20485000-20485600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
12	chr14:20487800-20488200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
13	chr14:20496200-20499200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
14	chr14:20496600-20496800	Enhancers	Small Intestine	intestine
15	chr14:20500000-20500400	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr14:20502200-20502400	Enhancers	Pancreas	Pancrea
17	chr14:20502400-20504200	Weak transcription	Pancreas	Pancrea
18	chr14:20512200-20512400	Enhancers	K562	blood
19	chr14:20512400-20512800	Flanking Active TSS	K562	blood
20	chr14:20512800-20513200	Enhancers	K562	blood
21	chr14:20513200-20515800	Weak transcription	K562	blood
22	chr14:20514600-20515000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr14:20515000-20517000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
24	chr14:20515800-20517600	Enhancers	K562	blood
25	chr14:20520400-20521400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
26	chr14:20533000-20533400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
27	chr14:20542800-20543400	Active TSS	Fetal Heart	heart
28	chr14:20561600-20562000	Enhancers	Primary neutrophils fromperipheralblood	blood
29	chr14:20574400-20574600	Enhancers	Pancreatic Islets	Pancreatic Islet
30	chr14:20580400-20580800	Enhancers	K562	blood
31	chr14:20580800-20584200	Weak transcription	K562	blood
32	chr14:20584200-20584600	Enhancers	K562	blood
33	chr14:20584600-20585000	Flanking Active TSS	K562	blood
34	chr14:20585000-20585200	Enhancers	K562	blood
35	chr14:20585200-20585400	Flanking Active TSS	K562	blood
36	chr14:20585400-20585600	Enhancers	K562	blood
37	chr14:20585400-20585800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr14:20585600-20585800	ZNF genes & repeats	K562	blood
39	chr14:20585800-20586400	Genic enhancers	K562	blood
40	chr14:20586200-20586600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr14:20586400-20586600	Enhancers	K562	blood
42	chr14:20611200-20612600	Enhancers	K562	blood
43	chr14:20612400-20612800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr14:20613200-20613400	Enhancers	Pancreatic Islets	Pancreatic Islet
45	chr14:20613600-20621000	Weak transcription	Pancreatic Islets	Pancreatic Islet
46	chr14:20622200-20622400	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr14:20623000-20624000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
48	chr14:20630600-20630800	ZNF genes & repeats	Pancreas	Pancrea
49	chr14:20638000-20638800	Enhancers	K562	blood
50	chr14:20638400-20638600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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