Variant report

Variant	nsv832739
Chromosome Location	chr14:20604126-20734222
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:766)
CpG islands
(count:793)
Chromatin interactive
region (count:25)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:766 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:20644582-20645133	K562	blood:	n/a	n/a
2	ARID3A	chr14:20645562-20646086	K562	blood:	n/a	n/a
3	ARID3A	chr14:20730858-20731162	K562	blood:	n/a	n/a
4	ATF1	chr14:20724352-20724489	K562	blood:	n/a	n/a
5	ATF1	chr14:20608626-20608778	K562	blood:	n/a	n/a
6	ATF1	chr14:20730830-20731218	K562	blood:	n/a	n/a
7	ATF1	chr14:20645594-20645932	K562	blood:	n/a	n/a
8	ATF3	chr14:20730820-20731074	K562	blood:	n/a	n/a
9	ATF3	chr14:20645584-20645910	K562	blood:	n/a	n/a
10	ATF3	chr14:20638032-20638356	K562	blood:	n/a	n/a
11	BACH1	chr14:20687217-20687569	K562	blood:	n/a	chr14:20687387-20687401
12	BACH1	chr14:20687322-20687431	H1-hESC	embryonic stem cell:	n/a	chr14:20687387-20687401
13	BCL11A	chr14:20730703-20731061	GM12878	blood:	n/a	n/a
14	BHLHE40	chr14:20645542-20646303	K562	blood:	n/a	n/a
15	BHLHE40	chr14:20730754-20731222	GM12878	blood:	n/a	n/a
16	BHLHE40	chr14:20730817-20731297	K562	blood:	n/a	n/a
17	BHLHE40	chr14:20653018-20653080	K562	blood:	n/a	n/a
18	BRCA1	chr14:20716040-20716061	H1-hESC	embryonic stem cell:	n/a	n/a
19	CBX3	chr14:20645515-20645980	K562	blood:	n/a	n/a
20	CBX3	chr14:20645492-20645863	K562	blood:	n/a	n/a
21	CBX3	chr14:20632642-20632904	K562	blood:	n/a	n/a
22	CBX3	chr14:20632656-20632932	K562	blood:	n/a	n/a
23	CCNT2	chr14:20730801-20731127	K562	blood:	n/a	n/a
24	CCNT2	chr14:20645714-20646195	K562	blood:	n/a	n/a
25	CCNT2	chr14:20677752-20678071	K562	blood:	n/a	n/a
26	CEBPB	chr14:20643233-20643506	K562	blood:	n/a	chr14:20643311-20643324
27	CEBPB	chr14:20644555-20644849	K562	blood:	n/a	chr14:20644780-20644791 chr14:20644718-20644735 chr14:20644780-20644791
28	CEBPB	chr14:20683376-20683687	A549	lung:	n/a	chr14:20683523-20683534
29	CEBPB	chr14:20730857-20731158	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr14:20638951-20639274	A549	lung:	n/a	chr14:20639103-20639114
31	CEBPB	chr14:20659063-20659394	HepG2	liver:	n/a	chr14:20659228-20659241 chr14:20659229-20659240 chr14:20659227-20659244
32	CEBPB	chr14:20683358-20683686	HepG2	liver:	n/a	chr14:20683523-20683534
33	CEBPB	chr14:20638926-20639276	K562	blood:	n/a	chr14:20639103-20639114
34	CEBPB	chr14:20622449-20622660	HepG2	liver:	n/a	chr14:20622561-20622572
35	CEBPB	chr14:20683431-20683747	MCF-7	breast:	n/a	chr14:20683523-20683534
36	CEBPB	chr14:20667315-20667568	K562	blood:	n/a	chr14:20667443-20667454
37	CEBPB	chr14:20730826-20731185	K562	blood:	n/a	n/a
38	CEBPB	chr14:20667315-20667616	A549	lung:	n/a	chr14:20667443-20667454
39	CEBPB	chr14:20683384-20683692	Hela-S3	cervix:	n/a	chr14:20683523-20683534
40	CEBPB	chr14:20639049-20639270	IMR90	lung:	n/a	chr14:20639103-20639114
41	CEBPB	chr14:20667271-20667577	Hela-S3	cervix:	n/a	chr14:20667443-20667454
42	CEBPB	chr14:20644548-20644852	K562	blood:	n/a	chr14:20644780-20644791 chr14:20644718-20644735 chr14:20644780-20644791
43	CEBPB	chr14:20645527-20645985	K562	blood:	n/a	n/a
44	CEBPB	chr14:20631110-20631224	HepG2	liver:	n/a	chr14:20631171-20631182
45	CEBPB	chr14:20668608-20668745	K562	blood:	n/a	n/a
46	CEBPB	chr14:20618584-20618626	A549	lung:	n/a	n/a
47	CEBPB	chr14:20634808-20635061	HepG2	liver:	n/a	chr14:20634950-20634963 chr14:20634951-20634962 chr14:20634950-20634961 chr14:20634952-20634961
48	CEBPB	chr14:20668546-20668738	A549	lung:	n/a	n/a
49	CEBPB	chr14:20638948-20639275	HepG2	liver:	n/a	chr14:20639103-20639114
50	CEBPB	chr14:20730821-20731202	Hela-S3	cervix:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:20664580-20664630	HCPEpiC	choroid plexus:	n/a
2	chr14:20711344-20711394	AoSMC	blood vessel:	n/a
3	chr14:20710905-20710955	HEK293	kidney:	embryo
4	chr14:20611696-20611746	ProgFib	skin:	n/a
5	chr14:20664580-20664630	GM19239	blood:	n/a
6	chr14:20710905-20710955	U87	brain:	n/a
7	chr14:20691777-20691827	ECC-1	luminal epithelium:	n/a
8	chr14:20704361-20704411	MCF10A-Er-Src	breast:	n/a
9	chr14:20710315-20710365	HAEpiC	amniotic membrane:	n/a
10	chr14:20664580-20664630	AG09319	gingival:	n/a
11	chr14:20710315-20710365	H1-hESC	embryonic stem cell:	embryo
12	chr14:20710905-20710955	LNCaP	prostate:	n/a
13	chr14:20704361-20704411	AG10803	skin:	n/a
14	chr14:20612220-20612270	SAEC	small airway:	n/a
15	chr14:20666088-20666138	GM12892	blood:	n/a
16	chr14:20710881-20710931	AG09309	skin:	n/a
17	chr14:20611779-20611829	HIPEpiC	eye:	n/a
18	chr14:20692622-20692672	HepG2	liver:	n/a
19	chr14:20612220-20612270	AG10803	skin:	n/a
20	chr14:20666088-20666138	HEK293	kidney:	embryo
21	chr14:20664021-20664071	GM12891	blood:	n/a
22	chr14:20691777-20691827	U87	brain:	n/a
23	chr14:20612220-20612270	Jurkat	blood:	n/a
24	chr14:20710905-20710955	AG04450	lung:	fetal
25	chr14:20611779-20611829	NT2-D1	testis:	n/a
26	chr14:20710881-20710931	SK-N-SH	brain:	n/a
27	chr14:20666088-20666138	HMEC	breast:	n/a
28	chr14:20612220-20612270	AG09319	gingival:	n/a
29	chr14:20710905-20710955	MCF10A-Er-Src	breast:	n/a
30	chr14:20710905-20710955	HUVEC	blood vessel:	n/a
31	chr14:20691777-20691827	ovcar-3	ovarian:	n/a
32	chr14:20711344-20711394	GM12892	blood:	n/a
33	chr14:20664021-20664071	AG04450	lung:	fetal
34	chr14:20710905-20710955	GM19239	blood:	n/a
35	chr14:20611779-20611829	H1-hESC	embryonic stem cell:	embryo
36	chr14:20691777-20691827	HEEpiC	esophagus:	n/a
37	chr14:20691777-20691827	HPAEpiC	pulmonary alveolar:	n/a
38	chr14:20704361-20704411	AG09319	gingival:	n/a
39	chr14:20664021-20664071	PFSK-1	brain:	n/a
40	chr14:20664580-20664630	T-47D	breast:	n/a
41	chr14:20691777-20691827	HCF	heart:	n/a
42	chr14:20710905-20710955	K562	blood:	n/a
43	chr14:20664021-20664071	H1-hESC	embryonic stem cell:	embryo
44	chr14:20611779-20611829	GM12892	blood:	n/a
45	chr14:20612220-20612270	NHDF-neo	bronchial:	n/a
46	chr14:20710905-20710955	AG04449	skin:	fetal
47	chr14:20691777-20691827	IMR90	lung:	fetal
48	chr14:20666088-20666138	RPTEC	kidney:	n/a
49	chr14:20710905-20710955	Hela-S3	cervix:	n/a
50	chr14:20704361-20704411	HL-60	blood:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:20649377..20653239-chr14:20653513..20656414,3	K562	blood:
2	chr14:20657790..20659854-chr14:20660139..20662743,2	K562	blood:
3	chr14:20615947..20618319-chr14:20622650..20625486,3	K562	blood:
4	chr14:20645875..20648132-chr14:20651152..20653312,3	K562	blood:
5	chr14:20623640..20625607-chr14:20644962..20647182,2	K562	blood:
6	chr14:20653650..20655621-chr14:20656798..20658985,2	K562	blood:
7	chr14:20657790..20659854-chr14:20660139..20662743,2	K562	blood:
8	chr14:20653449..20656373-chr14:20661305..20663533,2	MCF-7	breast:
9	chr14:20653449..20656373-chr14:20661305..20663533,2	MCF-7	breast:
10	chr14:20674085..20677001-chr14:20687478..20690164,2	MCF-7	breast:
11	chr14:20642540..20645135-chr14:20796578..20798741,2	K562	blood:
12	chr14:20615947..20618319-chr14:20622650..20625017,2	K562	blood:
13	chr14:20721089..20723559-chr14:20745289..20746790,2	K562	blood:
14	chr14:20645666..20648683-chr14:20649468..20653312,5	K562	blood:
15	chr14:20674085..20677001-chr14:20687478..20690164,2	MCF-7	breast:
16	chr14:20716993..20719012-chr14:20810406..20812740,2	MCF-7	breast:
17	chr14:20649377..20653239-chr14:20653513..20656414,3	K562	blood:
18	chr14:20583619..20586533-chr14:20649310..20650931,2	K562	blood:
19	chr14:20623957..20624479-chr3:64655642..64656615,2	MCF-7	breast:
20	chr14:20691139..20693631-chr14:20695657..20698105,2	K562	blood:
21	chr14:20653650..20655621-chr14:20656798..20658985,2	K562	blood:
22	chr14:20623640..20625607-chr14:20644962..20647182,2	K562	blood:
23	chr14:20691139..20693631-chr14:20695657..20698105,2	K562	blood:
24	chr14:20611730..20613442-chr14:20616450..20619196,2	K562	blood:
25	chr14:20611730..20613442-chr14:20616450..20619196,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TTC5-2	chr14:20725877-20725934	NONHSAT035556
2	lnc-OR4N5-1	chr14:20617391-20617904	NONHSAT035552
3	lnc-TTC5-2	chr14:20728743-20729137	NONHSAT035558
4	lnc-TTC5-2	chr14:20729548-20729773	NONHSAT035558
5	lnc-TTC5-2	chr14:20729772-20729892	NONHSAT035556
6	lnc-TTC5-2	chr14:20726344-20726358	NONHSAT035556
7	lnc-TTC5-2	chr14:20724717-20724844	NONHSAT035556
8	lnc-TTC5-2	chr14:20728639-20732467	ENSG00000258768.2

No data

Variant related genes	Relation type
OR4N5	TF binding region
OR11H5P	TF binding region
RNA5SP381	TF binding region
ENSG00000266336	TF binding region
OR11G1P	TF binding region
OR11G2	TF binding region
ENSG00000258768	TF binding region
OR11H6	TF binding region
TTC5	TF binding region
OR11H4	TF binding region
ENSG00000259095	TF binding region
OR11H7	TF binding region
PSMB7P1	TF binding region
OR4N5	CpG island
OR11H5P	CpG island
RNA5SP381	CpG island
ENSG00000266336	CpG island
OR11G1P	CpG island
OR11G2	CpG island
ENSG00000258768	CpG island
OR11H6	CpG island
TTC5	CpG island
OR11H4	CpG island
ENSG00000259095	CpG island
OR11H7	CpG island
PSMB7P1	CpG island
ENSG00000176219	chromatin interactions
ENSG00000258468	chromatin interactions
ENSG00000259001	chromatin interactions
ENSG00000258806	chromatin interactions
ENSG00000100814	chromatin interactions
ENSG00000176230	chromatin interactions
ENSG00000259074	chromatin interactions
ENSG00000184394	chromatin interactions
ENSG00000129484	chromatin interactions

Extended variants
information (count: 2873 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:2873 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560140297	chr14:20608107-20608108	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs532205950	chr14:20608594-20608595	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs116145770	chr14:20608663-20608664	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs151020598	chr14:20608684-20608685	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs139440291	chr14:20608694-20608695	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs547752768	chr14:20608706-20608707	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs182732715	chr14:20608708-20608709	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs187064288	chr14:20608730-20608731	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs553253949	chr14:20608747-20608748	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs578228791	chr14:20608754-20608755	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs538848730	chr14:20608765-20608766	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs149666743	chr14:20608777-20608778	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs192179031	chr14:20608778-20608779	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs145497076	chr14:20608788-20608789	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs185020945	chr14:20608793-20608794	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs540679841	chr14:20608839-20608840	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs190807406	chr14:20608854-20608855	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs193095617	chr14:20608875-20608876	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs544052755	chr14:20608877-20608878	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs370409172	chr14:20608883-20608884	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs562679334	chr14:20608895-20608896	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs562722851	chr14:20608914-20608915	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs201244848	chr14:20608918-20608919	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs529719680	chr14:20608937-20608938	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs145385318	chr14:20608942-20608943	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs527717041	chr14:20609403-20609404	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs60332994	chr14:20609405-20609406	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs74462357	chr14:20609436-20609437	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs529840545	chr14:20609451-20609452	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs115313364	chr14:20609457-20609458	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs559804784	chr14:20609506-20609507	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs577808095	chr14:20611209-20611210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs568122832	chr14:20611227-20611228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs140642790	chr14:20611285-20611286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs150456909	chr14:20611302-20611303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs145393232	chr14:20611360-20611361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs539602672	chr14:20611377-20611378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs187247411	chr14:20611378-20611379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs74322083	chr14:20611385-20611386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs543165831	chr14:20611465-20611466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs149222852	chr14:20611618-20611619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs573684773	chr14:20611626-20611627	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs376160792	chr14:20611673-20611674	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs10137715	chr14:20611676-20611677	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs386775263	chr14:20611689-20611690	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs375782256	chr14:20611690-20611691	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs189935711	chr14:20611692-20611693	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs564546677	chr14:20611711-20611712	Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs531790031	chr14:20611736-20611737	Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs182104496	chr14:20611776-20611777	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

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

Chromatin state (count:133 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:20611200-20612600	Enhancers	K562	blood
2	chr14:20612400-20612800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr14:20613200-20613400	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr14:20613600-20621000	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr14:20622200-20622400	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr14:20623000-20624000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
7	chr14:20630600-20630800	ZNF genes & repeats	Pancreas	Pancrea
8	chr14:20638000-20638800	Enhancers	K562	blood
9	chr14:20638400-20638600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr14:20638400-20638800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr14:20638800-20643000	Weak transcription	K562	blood
12	chr14:20643000-20644000	Enhancers	K562	blood
13	chr14:20643400-20643600	Enhancers	Pancreas	Pancrea
14	chr14:20643400-20643800	Enhancers	Stomach Mucosa	stomach
15	chr14:20643800-20645200	Weak transcription	Pancreas	Pancrea
16	chr14:20644000-20644200	Flanking Active TSS	K562	blood
17	chr14:20644200-20644400	Enhancers	Stomach Mucosa	stomach
18	chr14:20644200-20644600	Enhancers	K562	blood
19	chr14:20644600-20644800	Flanking Active TSS	K562	blood
20	chr14:20644800-20645000	Enhancers	K562	blood
21	chr14:20645000-20645200	Flanking Active TSS	K562	blood
22	chr14:20645200-20645800	Enhancers	K562	blood
23	chr14:20645200-20646400	Enhancers	Pancreas	Pancrea
24	chr14:20645800-20646400	Flanking Active TSS	K562	blood
25	chr14:20646000-20648200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr14:20646000-20649000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr14:20646200-20646400	Enhancers	Primary hematopoietic stem cells	blood
28	chr14:20646400-20647400	Weak transcription	Pancreas	Pancrea
29	chr14:20646400-20648400	Enhancers	K562	blood
30	chr14:20646800-20647400	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr14:20647000-20647800	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr14:20647400-20647600	ZNF genes & repeats	Pancreas	Pancrea
33	chr14:20647400-20648200	Enhancers	Primary neutrophils fromperipheralblood	blood
34	chr14:20647400-20648400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
35	chr14:20647600-20648200	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr14:20647600-20650400	Weak transcription	Pancreas	Pancrea
37	chr14:20647800-20648200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
38	chr14:20648000-20648400	Enhancers	Primary hematopoietic stem cells	blood
39	chr14:20648200-20649800	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr14:20648400-20648800	Weak transcription	K562	blood
41	chr14:20648400-20648800	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr14:20648800-20649000	Enhancers	K562	blood
43	chr14:20648800-20649200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
44	chr14:20649000-20650400	Weak transcription	K562	blood
45	chr14:20649200-20649600	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr14:20650000-20650400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr14:20650400-20651000	Enhancers	K562	blood
48	chr14:20651000-20652400	Weak transcription	K562	blood
49	chr14:20652400-20653200	Enhancers	K562	blood
50	chr14:20663200-20664600	Enhancers	K562	blood

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