Variant report

Variant	nsv508566
Chromosome Location	chr10:5256836-5321354
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:357)
CpG islands
(count:122)
Chromatin interactive
region (count:13)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:357 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:5285389-5285941	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:5275365-5275665	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:5276009-5276456	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:5261272-5261624	HepG2	liver:	n/a	n/a
5	ATF1	chr10:5300425-5300441	K562	blood:	n/a	n/a
6	ATF1	chr10:5276143-5276340	K562	blood:	n/a	n/a
7	BACH1	chr10:5314040-5314410	K562	blood:	n/a	chr10:5314219-5314233
8	BACH1	chr10:5314029-5314452	H1-hESC	embryonic stem cell:	n/a	chr10:5314219-5314233
9	BHLHE40	chr10:5276097-5276402	HepG2	liver:	n/a	n/a
10	CEBPB	chr10:5275837-5276578	A549	lung:	n/a	chr10:5276210-5276221 chr10:5276211-5276222
11	CEBPB	chr10:5283675-5283701	A549	lung:	n/a	n/a
12	CEBPB	chr10:5276032-5276421	K562	blood:	n/a	chr10:5276210-5276221 chr10:5276211-5276222
13	CEBPB	chr10:5276004-5276566	MCF-7	breast:	n/a	chr10:5276210-5276221 chr10:5276211-5276222
14	CEBPB	chr10:5285358-5285791	HepG2	liver:	n/a	n/a
15	CEBPB	chr10:5276086-5276358	HepG2	liver:	n/a	chr10:5276210-5276221 chr10:5276211-5276222
16	CEBPB	chr10:5276098-5276385	Hela-S3	cervix:	n/a	chr10:5276210-5276221 chr10:5276211-5276222
17	CEBPB	chr10:5320571-5320633	A549	lung:	n/a	n/a
18	CEBPB	chr10:5276021-5276478	HepG2	liver:	n/a	chr10:5276210-5276221 chr10:5276211-5276222
19	CEBPB	chr10:5283605-5283805	K562	blood:	n/a	chr10:5283712-5283723
20	CEBPB	chr10:5276106-5276400	IMR90	lung:	n/a	chr10:5276210-5276221 chr10:5276211-5276222
21	CEBPB	chr10:5285396-5285741	HepG2	liver:	n/a	n/a
22	CEBPB	chr10:5275967-5276495	HepG2	liver:	n/a	chr10:5276210-5276221 chr10:5276211-5276222
23	CEBPB	chr10:5276044-5276405	K562	blood:	n/a	chr10:5276210-5276221 chr10:5276211-5276222
24	CEBPB	chr10:5283692-5283767	HepG2	liver:	n/a	chr10:5283712-5283723
25	CEBPB	chr10:5285419-5285640	HepG2	liver:	n/a	n/a
26	CEBPB	chr10:5294450-5294655	HepG2	liver:	n/a	n/a
27	CEBPB	chr10:5276049-5276449	HepG2	liver:	n/a	chr10:5276210-5276221 chr10:5276211-5276222
28	CEBPB	chr10:5294448-5294773	A549	lung:	n/a	n/a
29	CEBPB	chr10:5275974-5276527	MCF-7	breast:	n/a	chr10:5276210-5276221 chr10:5276211-5276222
30	CEBPB	chr10:5275982-5276498	A549	lung:	n/a	chr10:5276210-5276221 chr10:5276211-5276222
31	CEBPB	chr10:5275567-5275767	HepG2	liver:	n/a	n/a
32	CEBPB	chr10:5276037-5276457	A549	lung:	n/a	chr10:5276210-5276221 chr10:5276211-5276222
33	CEBPB	chr10:5276115-5276258	K562	blood:	n/a	chr10:5276210-5276221 chr10:5276211-5276222
34	CEBPD	chr10:5276049-5276296	HepG2	liver:	n/a	chr10:5276210-5276221
35	CEBPD	chr10:5285464-5285697	HepG2	liver:	n/a	n/a
36	CEBPD	chr10:5294655-5294915	HepG2	liver:	n/a	n/a
37	CEBPD	chr10:5276048-5276356	HepG2	liver:	n/a	chr10:5276210-5276221
38	CHD2	chr10:5285507-5285744	HepG2	liver:	n/a	n/a
39	CTCF	chr10:5294720-5294870	HCT-116	colon:	n/a	n/a
40	CTCF	chr10:5294800-5294950	A549	lung:	n/a	n/a
41	CTCF	chr10:5308420-5308570	HepG2	liver:	n/a	n/a
42	CTCF	chr10:5272074-5272126	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr10:5294380-5294530	HRE	kidney:	n/a	n/a
44	CTCF	chr10:5303703-5303793	A549	lung:	n/a	chr10:5303735-5303745 chr10:5303734-5303747 chr10:5303732-5303750
45	CTCF	chr10:5294280-5294430	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr10:5294701-5294870	MCF-7	breast:	n/a	n/a
47	CTCF	chr10:5294215-5294402	K562	blood:	n/a	n/a
48	CTCF	chr10:5294260-5294410	MCF-7	breast:	n/a	n/a
49	CTCF	chr10:5294224-5294472	A549	lung:	n/a	n/a
50	CTCF	chr10:5303631-5303856	MCF-7	breast:	n/a	chr10:5303735-5303745 chr10:5303734-5303747 chr10:5303732-5303750

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:5302629-5302679	HCM	heart:	n/a
2	chr10:5260740-5260790	SK-N-SH_RA	brain:	n/a
3	chr10:5260740-5260790	HNPCEpiC	eye:	n/a
4	chr10:5302629-5302679	PrEC	prostate:	n/a
5	chr10:5260740-5260790	RPTEC	kidney:	n/a
6	chr10:5260740-5260790	AG09319	gingival:	n/a
7	chr10:5260740-5260790	AoSMC	blood vessel:	n/a
8	chr10:5302629-5302679	NT2-D1	testis:	n/a
9	chr10:5302629-5302679	SK-N-MC	brain:	n/a
10	chr10:5260740-5260790	Hela-S3	cervix:	n/a
11	chr10:5260740-5260790	AG04450	lung:	fetal
12	chr10:5302629-5302679	GM12891	blood:	n/a
13	chr10:5260740-5260790	LNCaP	prostate:	n/a
14	chr10:5260740-5260790	HMEC	breast:	n/a
15	chr10:5260740-5260790	HepG2	liver:	n/a
16	chr10:5302629-5302679	Hela-S3	cervix:	n/a
17	chr10:5260740-5260790	PANC-1	pancreas:	n/a
18	chr10:5260740-5260790	Caco-2	colon:	n/a
19	chr10:5260740-5260790	HAEpiC	amniotic membrane:	n/a
20	chr10:5302629-5302679	NB4	blood:	n/a
21	chr10:5302629-5302679	GM12878	blood:	n/a
22	chr10:5260740-5260790	HL-60	blood:	n/a
23	chr10:5302629-5302679	AG09309	skin:	n/a
24	chr10:5260740-5260790	HEK293	kidney:	embryo
25	chr10:5302629-5302679	ECC-1	luminal epithelium:	n/a
26	chr10:5302629-5302679	IMR90	lung:	fetal
27	chr10:5302629-5302679	HPAEpiC	pulmonary alveolar:	n/a
28	chr10:5260740-5260790	BJ	skin:	n/a
29	chr10:5302629-5302679	HRPEpiC	eye:	n/a
30	chr10:5302629-5302679	PFSK-1	brain:	n/a
31	chr10:5260740-5260790	GM12892	blood:	n/a
32	chr10:5260740-5260790	HEEpiC	esophagus:	n/a
33	chr10:5302629-5302679	ProgFib	skin:	n/a
34	chr10:5260740-5260790	SKMC	muscle:	n/a
35	chr10:5260740-5260790	HCF	heart:	n/a
36	chr10:5260740-5260790	HRE	kidney:	n/a
37	chr10:5302629-5302679	RPTEC	kidney:	n/a
38	chr10:5302629-5302679	U87	brain:	n/a
39	chr10:5260740-5260790	H1-hESC	embryonic stem cell:	embryo
40	chr10:5260740-5260790	GM12891	blood:	n/a
41	chr10:5260740-5260790	HUVEC	blood vessel:	n/a
42	chr10:5302629-5302679	HUVEC	blood vessel:	n/a
43	chr10:5260740-5260790	K562	blood:	n/a
44	chr10:5260740-5260790	SK-N-SH	brain:	n/a
45	chr10:5260740-5260790	HPAEpiC	pulmonary alveolar:	n/a
46	chr10:5302629-5302679	HCPEpiC	choroid plexus:	n/a
47	chr10:5260740-5260790	ovcar-3	ovarian:	n/a
48	chr10:5302629-5302679	NHDF-neo	bronchial:	n/a
49	chr10:5260740-5260790	NT2-D1	testis:	n/a
50	chr10:5302629-5302679	HCT-116	colon:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:5308367..5310948-chr10:5323905..5325582,2	K562	blood:
2	chr10:5300898..5303251-chr10:5486479..5488838,2	K562	blood:
3	chr10:5285994..5288790-chr10:5292059..5294701,2	MCF-7	breast:
4	chr10:5256183..5258752-chr10:5259686..5261941,2	K562	blood:
5	chr10:5254857..5257683-chr10:5259686..5261466,3	K562	blood:
6	chr10:5285721..5288092-chr10:5296102..5298963,2	K562	blood:
7	chr10:5314790..5316685-chr10:5325493..5327295,2	K562	blood:
8	chr10:5256183..5258752-chr10:5259686..5261941,2	K562	blood:
9	chr10:5285721..5288092-chr10:5296102..5298963,2	K562	blood:
10	chr10:5309166..5310938-chr10:5312604..5314202,2	K562	blood:
11	chr10:5285994..5288790-chr10:5292059..5294701,2	MCF-7	breast:
12	chr10:5254857..5257683-chr10:5259686..5261466,3	K562	blood:
13	chr10:5210740..5212996-chr10:5319959..5322251,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AKR1CL1-3	chr10:5297996-5298648	NONHSAT011146
2	lnc-AKR1C4-1	chr10:5276321-5276555	XLOC_008363
3	lnc-AKR1C4-3	chr10:5266321-5266555	NONHSAT011143
4	lnc-AKR1C4-1	chr10:5304924-5305165	XLOC_008363
5	lnc-AKR1C4-1	chr10:5304928-5305371	ENSG00000231039.2
6	lnc-AKR1C4-1	chr10:5276321-5276556	ENSG00000231039.2
7	lnc-AKR1CL1-1	chr10:5313161-5313199	XLOC_008706
8	lnc-AKR1CL1-3	chr10:5303161-5303199	NONHSAT011146
9	lnc-AKR1CL1-1	chr10:5307996-5308648	XLOC_008706
10	lnc-AKR1C4-3	chr10:5294924-5295165	NONHSAT011143

No data

Variant related genes	Relation type
ENSG00000224034	TF binding region
ENSG00000231039	TF binding region
ENSG00000224034	CpG island
ENSG00000231039	CpG island
ENSG00000173848	chromatin interactions
ENSG00000224034	chromatin interactions
OLIG3	miRNA target sites
LRP1B	miRNA target sites

Extended variants
information (count: 3049 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:3049 , 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	rs571795307	chr10:5256842-5256843	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs146442054	chr10:5256865-5256866	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573420000	chr10:5256929-5256930	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs180822515	chr10:5256935-5256936	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs369889516	chr10:5256948-5256949	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs566342231	chr10:5256993-5256994	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs536950377	chr10:5257004-5257005	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs77560553	chr10:5257006-5257007	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs76256923	chr10:5257021-5257022	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs78585347	chr10:5257097-5257098	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs375597122	chr10:5257098-5257099	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs185807801	chr10:5257133-5257134	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs80075460	chr10:5257135-5257136	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs577291045	chr10:5257198-5257199	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs191501348	chr10:5257240-5257241	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs534807722	chr10:5257261-5257262	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs4350268	chr10:5257273-5257274	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs182498797	chr10:5257282-5257283	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs11253046	chr10:5257342-5257343	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs150164929	chr10:5257345-5257346	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs370026786	chr10:5257353-5257354	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs575986049	chr10:5257356-5257357	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs532499089	chr10:5257408-5257409	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs183556738	chr10:5257459-5257460	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs531464291	chr10:5257512-5257513	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564800877	chr10:5257513-5257514	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs532260421	chr10:5257553-5257554	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs547964343	chr10:5257560-5257561	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs139345312	chr10:5257576-5257577	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs369690133	chr10:5257578-5257579	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs548636997	chr10:5257589-5257590	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs535738919	chr10:5257601-5257602	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs537023829	chr10:5257610-5257611	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs565068293	chr10:5257616-5257617	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs373849242	chr10:5257620-5257621	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs547103523	chr10:5257633-5257634	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs143344380	chr10:5257646-5257647	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs75406471	chr10:5257647-5257648	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs188992089	chr10:5257655-5257656	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs571949325	chr10:5257659-5257660	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs536123823	chr10:5257665-5257666	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs76072956	chr10:5257720-5257721	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546353081	chr10:5257737-5257738	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs558087426	chr10:5257738-5257739	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs543016501	chr10:5257783-5257784	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564905466	chr10:5257792-5257793	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs78686304	chr10:5257797-5257798	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs80350946	chr10:5257901-5257902	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559971294	chr10:5257902-5257903	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs193034511	chr10:5257932-5257933	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Cancer	21129771	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Rheumatoid arthritis	23223014	CNVD

Chromatin state (count:159 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5253800-5263200	Strong transcription	Liver	Liver
2	chr10:5255400-5258800	Weak transcription	A549	lung
3	chr10:5258600-5259200	Enhancers	HepG2	liver
4	chr10:5258800-5259200	Enhancers	A549	lung
5	chr10:5259200-5260200	Weak transcription	HepG2	liver
6	chr10:5259200-5263000	Weak transcription	A549	lung
7	chr10:5260200-5262400	Enhancers	HepG2	liver
8	chr10:5261200-5261600	Enhancers	Gastric	stomach
9	chr10:5262000-5262400	Enhancers	Small Intestine	intestine
10	chr10:5262000-5262400	Enhancers	Stomach Mucosa	stomach
11	chr10:5263000-5264200	Strong transcription	A549	lung
12	chr10:5263200-5263800	Weak transcription	Liver	Liver
13	chr10:5264200-5275600	Weak transcription	A549	lung
14	chr10:5271000-5271200	Enhancers	Gastric	stomach
15	chr10:5271000-5271400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr10:5271200-5276600	Weak transcription	Gastric	stomach
17	chr10:5275000-5277800	Enhancers	HepG2	liver
18	chr10:5275400-5276000	Enhancers	Primary neutrophils fromperipheralblood	blood
19	chr10:5275400-5276400	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr10:5275400-5277800	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr10:5275600-5276200	Enhancers	Monocytes-CD14+_RO01746	blood
22	chr10:5275600-5276400	Genic enhancers	A549	lung
23	chr10:5275600-5276800	Enhancers	Liver	Liver
24	chr10:5275600-5277000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr10:5275600-5277600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr10:5275600-5278000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr10:5275800-5276000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr10:5275800-5276000	Enhancers	Primary B cells from cord blood	blood
29	chr10:5275800-5276600	Enhancers	HMEC	breast
30	chr10:5275800-5276600	Enhancers	NHEK	skin
31	chr10:5275800-5276800	Enhancers	Duodenum Mucosa	Duodenum
32	chr10:5275800-5277000	Enhancers	Primary hematopoietic stem cells	blood
33	chr10:5276000-5276400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr10:5276000-5276600	Active TSS	Primary B cells from cord blood	blood
35	chr10:5276000-5276800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr10:5276000-5276800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr10:5276000-5276800	Enhancers	Fetal Intestine Large	intestine
38	chr10:5276000-5277000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
39	chr10:5276000-5277000	Enhancers	Stomach Mucosa	stomach
40	chr10:5276200-5277000	Enhancers	Adipose Nuclei	Adipose
41	chr10:5276200-5277000	Enhancers	Fetal Lung	lung
42	chr10:5276200-5277000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
43	chr10:5276400-5276800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr10:5276400-5276800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
45	chr10:5276400-5277000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr10:5276400-5277200	Enhancers	Placenta	Placenta
47	chr10:5276400-5283600	Weak transcription	A549	lung
48	chr10:5276600-5276800	Enhancers	Gastric	stomach
49	chr10:5276600-5277000	Enhancers	Esophagus	oesophagus
50	chr10:5276600-5277000	Enhancers	Lung	lung

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