Variant report

Variant	nsv510650
Chromosome Location	chr14:97238489-97325221
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1290)
CpG islands
(count:1038)
Chromatin interactive
region (count:104)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1290 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:97297247-97298040	K562	blood:	n/a	chr14:97297827-97297843
2	ARID3A	chr14:97294291-97294540	K562	blood:	n/a	n/a
3	ARID3A	chr14:97263366-97263797	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:97268957-97269728	K562	blood:	n/a	n/a
5	ARID3A	chr14:97275339-97275687	K562	blood:	n/a	n/a
6	ARID3A	chr14:97300621-97300849	K562	blood:	n/a	chr14:97300643-97300659 chr14:97300646-97300662
7	ATF1	chr14:97263386-97263812	K562	blood:	n/a	n/a
8	ATF1	chr14:97268987-97269670	K562	blood:	n/a	n/a
9	ATF1	chr14:97273223-97273549	K562	blood:	n/a	n/a
10	ATF1	chr14:97297370-97297756	K562	blood:	n/a	n/a
11	ATF1	chr14:97275339-97275756	K562	blood:	n/a	n/a
12	ATF1	chr14:97241267-97241530	K562	blood:	n/a	n/a
13	ATF1	chr14:97270459-97270522	K562	blood:	n/a	n/a
14	ATF2	chr14:97263404-97263855	GM12878	blood:	n/a	n/a
15	ATF3	chr14:97263389-97263682	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr14:97273176-97273463	K562	blood:	n/a	n/a
17	ATF3	chr14:97269265-97269726	K562	blood:	n/a	n/a
18	ATF3	chr14:97263414-97263815	K562	blood:	n/a	n/a
19	BACH1	chr14:97263683-97264115	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr14:97303655-97303683	K562	blood:	n/a	n/a
21	BACH1	chr14:97266062-97266100	H1-hESC	embryonic stem cell:	n/a	n/a
22	BCL3	chr14:97263288-97263788	A549	lung:	n/a	chr14:97263703-97263716 chr14:97263610-97263619 chr14:97263569-97263577
23	BCLAF1	chr14:97269163-97269669	K562	blood:	n/a	n/a
24	BCLAF1	chr14:97263285-97263986	GM12878	blood:	n/a	chr14:97263703-97263716 chr14:97263932-97263945 chr14:97263610-97263619 chr14:97263569-97263577 chr14:97263946-97263955
25	BHLHE40	chr14:97284308-97284991	GM12878	blood:	n/a	n/a
26	BHLHE40	chr14:97265995-97266355	HepG2	liver:	n/a	chr14:97266181-97266190 chr14:97266179-97266192 chr14:97266182-97266191 chr14:97266181-97266190 chr14:97266175-97266196
27	BHLHE40	chr14:97282966-97283111	K562	blood:	n/a	n/a
28	BHLHE40	chr14:97265035-97265041	GM12878	blood:	n/a	n/a
29	BHLHE40	chr14:97263450-97263858	HepG2	liver:	n/a	chr14:97263701-97263717
30	BHLHE40	chr14:97263378-97263838	GM12878	blood:	n/a	chr14:97263701-97263717
31	BHLHE40	chr14:97269256-97269696	K562	blood:	n/a	n/a
32	BHLHE40	chr14:97293719-97293841	K562	blood:	n/a	n/a
33	BHLHE40	chr14:97266018-97266257	K562	blood:	n/a	chr14:97266181-97266190 chr14:97266179-97266192 chr14:97266182-97266191 chr14:97266181-97266190 chr14:97266175-97266196
34	BHLHE40	chr14:97241283-97241626	K562	blood:	n/a	n/a
35	BHLHE40	chr14:97263346-97263997	K562	blood:	n/a	chr14:97263701-97263717
36	BHLHE40	chr14:97275335-97275592	K562	blood:	n/a	n/a
37	BHLHE40	chr14:97264255-97264566	K562	blood:	n/a	n/a
38	BHLHE40	chr14:97261688-97261700	K562	blood:	n/a	n/a
39	BHLHE40	chr14:97299291-97299440	K562	blood:	n/a	n/a
40	BRCA1	chr14:97263474-97263823	HepG2	liver:	n/a	n/a
41	BRCA1	chr14:97263456-97263813	GM12878	blood:	n/a	n/a
42	BRCA1	chr14:97263390-97263840	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr14:97264263-97264463	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr14:97263476-97263804	H1-hESC	embryonic stem cell:	n/a	n/a
45	CBX3	chr14:97259873-97260217	K562	blood:	n/a	n/a
46	CBX3	chr14:97296048-97296875	K562	blood:	n/a	n/a
47	CBX3	chr14:97269258-97269852	K562	blood:	n/a	n/a
48	CBX3	chr14:97263290-97263911	K562	blood:	n/a	n/a
49	CBX3	chr14:97296163-97296501	K562	blood:	n/a	n/a
50	CBX3	chr14:97304773-97305157	K562	blood:	n/a	n/a

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:97271313-97271363	NH-A	brain:	n/a
2	chr14:97271313-97271363	NH-A	brain:	n/a
3	chr14:97264415-97264465	MCF10A-Er-Src	breast:	n/a
4	chr14:97263716-97263766	MCF-7	breast:	n/a
5	chr14:97260744-97260794	RPTEC	kidney:	n/a
6	chr14:97263710-97263760	RPTEC	kidney:	n/a
7	chr14:97263710-97263760	H1-hESC	embryonic stem cell:	embryo
8	chr14:97263801-97263851	AoSMC	blood vessel:	n/a
9	chr14:97263801-97263851	HL-60	blood:	n/a
10	chr14:97282535-97282585	PANC-1	pancreas:	n/a
11	chr14:97264415-97264465	IMR90	lung:	fetal
12	chr14:97263524-97263574	LNCaP	prostate:	n/a
13	chr14:97260744-97260794	HAEpiC	amniotic membrane:	n/a
14	chr14:97263710-97263760	Jurkat	blood:	n/a
15	chr14:97263716-97263766	NHBE	bronchial:	n/a
16	chr14:97271313-97271363	HPAEpiC	pulmonary alveolar:	n/a
17	chr14:97282535-97282585	AG09309	skin:	n/a
18	chr14:97271313-97271363	HMEC	breast:	n/a
19	chr14:97263710-97263760	SAEC	small airway:	n/a
20	chr14:97267126-97267176	HAEpiC	amniotic membrane:	n/a
21	chr14:97286215-97286265	RPTEC	kidney:	n/a
22	chr14:97262871-97262921	NHBE	bronchial:	n/a
23	chr14:97263716-97263766	ECC-1	luminal epithelium:	n/a
24	chr14:97263710-97263760	HCT-116	colon:	n/a
25	chr14:97264166-97264216	HIPEpiC	eye:	n/a
26	chr14:97264013-97264063	A549	lung:	n/a
27	chr14:97264013-97264063	AG09309	skin:	n/a
28	chr14:97263710-97263760	AG04449	skin:	fetal
29	chr14:97263524-97263574	SK-N-MC	brain:	n/a
30	chr14:97264166-97264216	MCF10A-Er-Src	breast:	n/a
31	chr14:97286215-97286265	GM06990	blood:	n/a
32	chr14:97264166-97264216	HMEC	breast:	n/a
33	chr14:97267126-97267176	SKMC	muscle:	n/a
34	chr14:97264013-97264063	HEEpiC	esophagus:	n/a
35	chr14:97282535-97282585	BJ	skin:	n/a
36	chr14:97263560-97263610	ProgFib	skin:	n/a
37	chr14:97263801-97263851	AG10803	skin:	n/a
38	chr14:97263716-97263766	HRCEpiC	kidney:	n/a
39	chr14:97282535-97282585	NHBE	bronchial:	n/a
40	chr14:97260744-97260794	SKMC	muscle:	n/a
41	chr14:97263560-97263610	SK-N-MC	brain:	n/a
42	chr14:97282535-97282585	T-47D	breast:	n/a
43	chr14:97263801-97263851	CMK	blood:	n/a
44	chr14:97264415-97264465	A549	lung:	n/a
45	chr14:97267126-97267176	ovcar-3	ovarian:	n/a
46	chr14:97271313-97271363	BJ	skin:	n/a
47	chr14:97267126-97267176	Jurkat	blood:	n/a
48	chr14:97264013-97264063	SK-N-SH_RA	brain:	n/a
49	chr14:97271313-97271363	GM12891	blood:	n/a
50	chr14:97264013-97264063	BE2_C	brain:	n/a

(count:104 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr14:97303558..97306091-chr14:97311531..97314081,2	K562	blood:
2	chr14:97262824..97265554-chr14:97270271..97273136,2	MCF-7	breast:
3	chr14:97273377..97275528-chr14:97290757..97293307,2	K562	blood:
4	chr14:97050419..97051179-chr14:97313148..97314310,4	MCF-7	breast:
5	chr14:97265880..97270207-chr14:97278911..97281407,6	K562	blood:
6	chr14:97264592..97266800-chr14:97290033..97292350,2	K562	blood:
7	chr14:97266936..97268792-chr14:97269139..97271889,2	MCF-7	breast:
8	chr14:97263568..97264375-chr16:68119668..68120573,2	Hela-S3	cervix:
9	chr14:97270310..97272481-chr14:97294425..97296809,2	K562	blood:
10	chr14:97301564..97304982-chr14:97305349..97308383,3	K562	blood:
11	chr14:97295418..97297368-chr14:97301033..97303820,2	K562	blood:
12	chr14:97293055..97295755-chr14:97296835..97300397,4	MCF-7	breast:
13	chr14:97278908..97281500-chr14:97284326..97286978,2	MCF-7	breast:
14	chr14:97265289..97269463-chr14:97278304..97281407,5	K562	blood:
15	chr14:97300473..97303064-chr14:97305409..97307983,2	K562	blood:
16	chr14:97265289..97269463-chr14:97278304..97281407,5	K562	blood:
17	chr14:97199537..97202098-chr14:97275666..97277302,2	K562	blood:
18	chr14:97319882..97321804-chr14:97324094..97326598,3	K562	blood:
19	chr14:97240702..97243220-chr14:97263599..97265114,2	MCF-7	breast:
20	chr14:97300473..97303064-chr14:97305409..97307983,2	K562	blood:
21	chr14:97264592..97266800-chr14:97290033..97292350,2	K562	blood:
22	chr14:97263932..97266038-chr14:97266708..97268317,2	MCF-7	breast:
23	chr14:97272734..97276764-chr14:97276840..97280627,4	K562	blood:
24	chr14:97246983..97249194-chr14:97251275..97253607,2	K562	blood:
25	chr14:97265808..97269390-chr14:97269409..97272897,4	MCF-7	breast:
26	chr14:97271567..97274016-chr14:97278732..97280457,2	K562	blood:
27	chr14:97263731..97266819-chr14:97323461..97326778,3	K562	blood:
28	chr14:97297616..97299303-chr14:97302743..97305605,2	K562	blood:
29	chr14:97299339..97301771-chr14:97302252..97306278,3	MCF-7	breast:
30	chr14:97293502..97295046-chr14:97299094..97301646,2	MCF-7	breast:
31	chr14:97050550..97051166-chr14:97319962..97320604,2	MCF-7	breast:
32	chr14:97309879..97311402-chr14:97317013..97319777,2	K562	blood:
33	chr14:96966745..96968586-chr14:97263969..97266226,2	K562	blood:
34	chr14:97263932..97266038-chr14:97266708..97268317,2	MCF-7	breast:
35	chr14:97279153..97281602-chr14:97281672..97284139,2	MCF-7	breast:
36	chr14:97262147..97265294-chr14:97268571..97271608,4	MCF-7	breast:
37	chr14:97285108..97286873-chr14:97288100..97291000,2	MCF-7	breast:
38	chr14:97266936..97268792-chr14:97269139..97271889,2	MCF-7	breast:
39	chr14:97263901..97269146-chr14:97273376..97277295,5	K562	blood:
40	chr14:97241501..97244095-chr14:97245630..97248366,2	MCF-7	breast:
41	chr14:97271958..97274868-chr14:97298626..97301164,2	MCF-7	breast:
42	chr14:97263501..97264052-chr2:189157381..189157997,2	Hela-S3	cervix:
43	chr14:97297616..97299303-chr14:97302743..97305605,2	K562	blood:
44	chr14:97274260..97276872-chr14:97281847..97286316,3	K562	blood:
45	chr14:97274614..97276764-chr14:97277663..97279518,2	K562	blood:
46	chr14:97265880..97270207-chr14:97278911..97281407,6	K562	blood:
47	chr14:97303558..97306091-chr14:97311531..97314081,2	K562	blood:
48	chr14:97256997..97259190-chr14:97264213..97266084,2	K562	blood:
49	chr14:97295429..97297910-chr14:97313409..97315091,2	K562	blood:
50	chr14:97306347..97308005-chr14:97316727..97319636,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VRK1-2	chr14:97256709-97256950	ENSG00000258979
2	lnc-VRK1-2	chr14:97256709-97257011	XLOC_010921

No data

Variant related genes	Relation type
VRK1	TF binding region
VRK1	CpG island
ENSG00000144366	chromatin interactions
ENSG00000090060	chromatin interactions
ENSG00000100749	chromatin interactions
ENSG00000072736	chromatin interactions
ENSG00000270141	chromatin interactions

Extended variants
information (count: 3046 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:3046 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540706228	chr14:97238626-97238627	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs61078535	chr14:97238647-97238648	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs532789549	chr14:97238719-97238720	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs528043927	chr14:97238772-97238773	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs546211487	chr14:97238787-97238788	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs8015153	chr14:97238803-97238804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs76738121	chr14:97238804-97238805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs145590480	chr14:97238817-97238818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs8015437	chr14:97238831-97238832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs568961307	chr14:97238843-97238844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs532421619	chr14:97238844-97238845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs8015183	chr14:97238856-97238857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs982748	chr14:97238897-97238898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs8020536	chr14:97239014-97239015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs202114163	chr14:97239020-97239021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs34787675	chr14:97239021-97239022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs548175477	chr14:97239029-97239030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs566298134	chr14:97239034-97239035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs533909003	chr14:97239036-97239037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs374940144	chr14:97239054-97239055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs551819306	chr14:97239075-97239076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs537970241	chr14:97239086-97239087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs373211644	chr14:97239136-97239137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs570192138	chr14:97239141-97239142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs34403763	chr14:97239147-97239148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs537695591	chr14:97239158-97239159	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs189917715	chr14:97239166-97239167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs367607249	chr14:97239173-97239174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs2369898	chr14:97239216-97239217	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs554972066	chr14:97239260-97239261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs148900838	chr14:97239266-97239267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs375525726	chr14:97239269-97239270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs369770082	chr14:97239271-97239272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs565404217	chr14:97239276-97239277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs35541393	chr14:97239282-97239283	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs13379443	chr14:97239312-97239313	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs35729279	chr14:97239343-97239344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs544857012	chr14:97239350-97239351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs13379239	chr14:97239365-97239366	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs182558620	chr14:97239383-97239384	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs8019917	chr14:97239388-97239389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs185041010	chr14:97239399-97239400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs189887961	chr14:97239400-97239401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs8021219	chr14:97239424-97239425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs74076105	chr14:97239430-97239431	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs527321826	chr14:97239431-97239432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs551753843	chr14:97239442-97239443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs183952980	chr14:97239462-97239463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs531265823	chr14:97239471-97239472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs8017557	chr14:97240711-97240712	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:74)

Disease	PMID	Source
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
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
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	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
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Glioblastoma	21080181	CNVD
Cancer	20164920	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Breast cancer	21509527	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	17426248	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:1593 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:97230600-97238800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr14:97237800-97238800	Enhancers	Colon Smooth Muscle	Colon
3	chr14:97238600-97238800	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr14:97238600-97238800	Bivalent Enhancer	Right Atrium	heart
5	chr14:97238800-97239000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr14:97238800-97239200	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr14:97238800-97239400	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr14:97238800-97239600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr14:97246800-97250000	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr14:97248800-97249400	Enhancers	NHEK	skin
11	chr14:97248800-97249600	Enhancers	HMEC	breast
12	chr14:97248800-97250000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr14:97248800-97251400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr14:97249000-97249400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr14:97249000-97252600	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr14:97249400-97249800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr14:97249400-97250600	Flanking Active TSS	NHEK	skin
18	chr14:97249400-97251000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
19	chr14:97249600-97249800	Flanking Active TSS	HMEC	breast
20	chr14:97249600-97250200	Enhancers	Osteobl	bone
21	chr14:97249600-97250800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr14:97249800-97250000	Enhancers	HMEC	breast
23	chr14:97249800-97250200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr14:97249800-97251400	Enhancers	Primary B cells from cord blood	blood
25	chr14:97249800-97251400	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr14:97249800-97251400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr14:97250000-97250200	Flanking Active TSS	HMEC	breast
28	chr14:97250000-97250400	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr14:97250000-97250400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr14:97250000-97250800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr14:97250000-97251400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
32	chr14:97250200-97251000	Enhancers	HMEC	breast
33	chr14:97250200-97254400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr14:97250400-97251400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr14:97250600-97251200	Enhancers	NHEK	skin
36	chr14:97251000-97251200	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr14:97251200-97251400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
38	chr14:97251400-97251600	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr14:97251400-97253400	Enhancers	Primary neutrophils fromperipheralblood	blood
40	chr14:97251600-97252000	Weak transcription	Monocytes-CD14+_RO01746	blood
41	chr14:97251800-97252400	Enhancers	Brain Hippocampus Middle	brain
42	chr14:97252000-97252200	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr14:97252200-97255000	Weak transcription	Monocytes-CD14+_RO01746	blood
44	chr14:97252600-97254800	Weak transcription	Primary monocytes fromperipheralblood	blood
45	chr14:97253400-97254400	Weak transcription	Primary neutrophils fromperipheralblood	blood
46	chr14:97254400-97255800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr14:97254400-97261400	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr14:97254800-97260200	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr14:97255000-97257600	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr14:97255800-97258000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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