Variant report

Variant	nsv894793
Chromosome Location	chr10:4935482-4988818
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:486)
CpG islands
(count:122)
Chromatin interactive
region (count:27)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:486 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:4983798-4984189	K562	blood:	n/a	n/a
2	ARID3A	chr10:4981876-4982269	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:4983858-4984031	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:4944990-4945093	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:4988718-4988794	HepG2	liver:	n/a	n/a
6	ARID3A	chr10:4984981-4985181	HepG2	liver:	n/a	n/a
7	ATF1	chr10:4944820-4945103	K562	blood:	n/a	n/a
8	ATF1	chr10:4983770-4984175	K562	blood:	n/a	n/a
9	ATF1	chr10:4959638-4959671	K562	blood:	n/a	n/a
10	BACH1	chr10:4950244-4950301	K562	blood:	n/a	n/a
11	BACH1	chr10:4983782-4984060	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr10:4983742-4984064	K562	blood:	n/a	n/a
13	BHLHE40	chr10:4985134-4985328	A549	lung:	n/a	n/a
14	BHLHE40	chr10:4983738-4984235	K562	blood:	n/a	n/a
15	BHLHE40	chr10:4981632-4982232	HepG2	liver:	n/a	n/a
16	BHLHE40	chr10:4982007-4982229	K562	blood:	n/a	n/a
17	BRCA1	chr10:4944963-4945066	HepG2	liver:	n/a	n/a
18	CBX3	chr10:4952816-4953115	K562	blood:	n/a	n/a
19	CBX3	chr10:4968600-4969011	K562	blood:	n/a	n/a
20	CBX3	chr10:4968629-4968983	K562	blood:	n/a	n/a
21	CBX3	chr10:4952855-4953096	K562	blood:	n/a	n/a
22	CBX3	chr10:4983718-4984199	K562	blood:	n/a	n/a
23	CCNT2	chr10:4983812-4984110	K562	blood:	n/a	chr10:4983980-4983989 chr10:4983909-4983929
24	CEBPB	chr10:4948072-4948352	K562	blood:	n/a	chr10:4948213-4948224
25	CEBPB	chr10:4961716-4961873	Hela-S3	cervix:	n/a	chr10:4961841-4961852 chr10:4961778-4961789
26	CEBPB	chr10:4948135-4948323	HepG2	liver:	n/a	chr10:4948213-4948224
27	CEBPB	chr10:4961718-4961949	HepG2	liver:	n/a	chr10:4961841-4961852 chr10:4961778-4961789
28	CEBPB	chr10:4961752-4961882	K562	blood:	n/a	chr10:4961841-4961852 chr10:4961778-4961789
29	CEBPB	chr10:4958485-4958540	K562	blood:	n/a	n/a
30	CEBPB	chr10:4982145-4982396	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr10:4961709-4961851	HepG2	liver:	n/a	chr10:4961778-4961789
32	CEBPB	chr10:4988667-4988883	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr10:4960198-4960337	K562	blood:	n/a	n/a
34	CEBPB	chr10:4981808-4982210	HepG2	liver:	n/a	n/a
35	CEBPB	chr10:4981882-4982386	A549	lung:	n/a	n/a
36	CEBPB	chr10:4968670-4968923	K562	blood:	n/a	n/a
37	CEBPB	chr10:4988692-4988886	A549	lung:	n/a	n/a
38	CEBPB	chr10:4961758-4961791	IMR90	lung:	n/a	chr10:4961778-4961789
39	CEBPB	chr10:4985631-4985753	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr10:4944928-4945128	HepG2	liver:	n/a	n/a
41	CEBPB	chr10:4963346-4963627	K562	blood:	n/a	chr10:4963483-4963496 chr10:4963485-4963494 chr10:4963483-4963494 chr10:4963485-4963494 chr10:4963485-4963494 chr10:4963483-4963496 chr10:4963485-4963494
42	CHD2	chr10:4983858-4984127	Hela-S3	cervix:	n/a	n/a
43	CHD2	chr10:4981969-4982213	HepG2	liver:	n/a	n/a
44	CHD2	chr10:4987627-4987809	HepG2	liver:	n/a	n/a
45	CHD2	chr10:4981491-4981533	HepG2	liver:	n/a	n/a
46	CTCF	chr10:4985119-4985377	MCF-7	breast:	n/a	n/a
47	CTCF	chr10:4985080-4985230	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr10:4966766-4966975	MCF-7	breast:	n/a	n/a
49	CTCF	chr10:4985340-4985490	HCM	heart:	n/a	n/a
50	CTCF	chr10:4985120-4985270	NHLF	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:4979658-4979708	H1-hESC	embryonic stem cell:	embryo
2	chr10:4979614-4979664	ProgFib	skin:	n/a
3	chr10:4979658-4979708	PFSK-1	brain:	n/a
4	chr10:4979658-4979708	SKMC	muscle:	n/a
5	chr10:4979614-4979664	GM12891	blood:	n/a
6	chr10:4979614-4979664	ovcar-3	ovarian:	n/a
7	chr10:4979614-4979664	Hepatocyte	liver:	n/a
8	chr10:4979614-4979664	MCF-7	breast:	n/a
9	chr10:4979614-4979664	GM06990	blood:	n/a
10	chr10:4979658-4979708	HRPEpiC	eye:	n/a
11	chr10:4979614-4979664	AG09309	skin:	n/a
12	chr10:4979658-4979708	AoSMC	blood vessel:	n/a
13	chr10:4979614-4979664	BE2_C	brain:	n/a
14	chr10:4979658-4979708	HAEpiC	amniotic membrane:	n/a
15	chr10:4979658-4979708	HPAEpiC	pulmonary alveolar:	n/a
16	chr10:4979658-4979708	SAEC	small airway:	n/a
17	chr10:4979658-4979708	ProgFib	skin:	n/a
18	chr10:4979658-4979708	HCM	heart:	n/a
19	chr10:4979614-4979664	AG04449	skin:	fetal
20	chr10:4979614-4979664	PFSK-1	brain:	n/a
21	chr10:4979658-4979708	HUVEC	blood vessel:	n/a
22	chr10:4979658-4979708	PANC-1	pancreas:	n/a
23	chr10:4979614-4979664	HIPEpiC	eye:	n/a
24	chr10:4979614-4979664	SAEC	small airway:	n/a
25	chr10:4979614-4979664	SK-N-MC	brain:	n/a
26	chr10:4979658-4979708	AG04449	skin:	fetal
27	chr10:4979658-4979708	GM12891	blood:	n/a
28	chr10:4979614-4979664	AoSMC	blood vessel:	n/a
29	chr10:4979658-4979708	Hela-S3	cervix:	n/a
30	chr10:4979658-4979708	PrEC	prostate:	n/a
31	chr10:4979658-4979708	HEEpiC	esophagus:	n/a
32	chr10:4979658-4979708	LNCaP	prostate:	n/a
33	chr10:4979614-4979664	U87	brain:	n/a
34	chr10:4979614-4979664	H1-hESC	embryonic stem cell:	embryo
35	chr10:4979614-4979664	PrEC	prostate:	n/a
36	chr10:4979658-4979708	Hepatocyte	liver:	n/a
37	chr10:4979614-4979664	HPAEpiC	pulmonary alveolar:	n/a
38	chr10:4979614-4979664	HMEC	breast:	n/a
39	chr10:4979614-4979664	MCF10A-Er-Src	breast:	n/a
40	chr10:4979614-4979664	GM19239	blood:	n/a
41	chr10:4979658-4979708	GM12878	blood:	n/a
42	chr10:4979614-4979664	CMK	blood:	n/a
43	chr10:4979658-4979708	RPTEC	kidney:	n/a
44	chr10:4979658-4979708	ovcar-3	ovarian:	n/a
45	chr10:4979658-4979708	GM19239	blood:	n/a
46	chr10:4979614-4979664	HRCEpiC	kidney:	n/a
47	chr10:4979658-4979708	NH-A	brain:	n/a
48	chr10:4979614-4979664	ECC-1	luminal epithelium:	n/a
49	chr10:4979658-4979708	BJ	skin:	n/a
50	chr10:4979614-4979664	AG04450	lung:	fetal

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:4953662..4955307-chr10:4957981..4959719,2	MCF-7	breast:
2	chr10:4944287..4946415-chr10:4947566..4950260,2	K562	blood:
3	chr10:4973639..4975791-chr10:5115008..5116577,2	K562	blood:
4	chr10:4952930..4955597-chr10:4957156..4959069,3	K562	blood:
5	chr10:4984238..4986431-chr10:4987413..4989346,2	MCF-7	breast:
6	chr10:4944889..4947267-chr10:4947876..4949644,2	MCF-7	breast:
7	chr10:4891706..4892505-chr10:4984690..4985498,3	MCF-7	breast:
8	chr10:4947891..4950201-chr10:4952537..4954922,2	K562	blood:
9	chr10:4975051..4976698-chr10:4977001..4978571,2	K562	blood:
10	chr10:4944889..4947267-chr10:4947876..4949644,2	MCF-7	breast:
11	chr10:4975051..4976698-chr10:4977001..4978571,2	K562	blood:
12	chr10:4953562..4955597-chr10:4956461..4959069,2	K562	blood:
13	chr10:4944287..4946415-chr10:4947566..4950260,2	K562	blood:
14	chr10:4984421..4986595-chr10:4988529..4991058,2	K562	blood:
15	chr10:4924404..4926925-chr10:4947394..4949303,2	K562	blood:
16	chr10:4947891..4950201-chr10:4952537..4954922,2	K562	blood:
17	chr10:4984421..4986363-chr10:4988529..4990778,2	K562	blood:
18	chr10:4957459..4960472-chr10:4974097..4976295,3	K562	blood:
19	chr10:4952930..4955597-chr10:4957156..4959069,3	K562	blood:
20	chr10:4943122..4945399-chr10:6203684..6206362,2	K562	blood:
21	chr10:4953562..4955597-chr10:4956461..4959069,2	K562	blood:
22	chr10:4953662..4955307-chr10:4957981..4959719,2	MCF-7	breast:
23	chr10:4984238..4986431-chr10:4987413..4989346,2	MCF-7	breast:
24	chr10:4984421..4986363-chr10:4988529..4990778,2	K562	blood:
25	chr10:4930274..4933075-chr10:4935096..4936648,2	K562	blood:
26	chr10:4957459..4960472-chr10:4974097..4976295,3	K562	blood:
27	chr10:4984421..4986595-chr10:4988529..4991058,2	K562	blood:

No data

Variant related genes	Relation type
AKR1C6P	TF binding region
AKR1C6P	CpG island

Extended variants
information (count: 2170 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:2170 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9888112	chr10:4935482-4935483	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs369163936	chr10:4935569-4935570	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs188813392	chr10:4935626-4935627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs7477630	chr10:4935656-4935657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs369546798	chr10:4935766-4935767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs372970783	chr10:4935846-4935847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs397695368	chr10:4935849-4935850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs368320331	chr10:4935851-4935852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs192869360	chr10:4935893-4935894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs538408087	chr10:4935947-4935948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs79641116	chr10:4935975-4935976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs145238701	chr10:4936095-4936096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs560792932	chr10:4936096-4936097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs182941267	chr10:4936168-4936169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs573090251	chr10:4936203-4936204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs540113488	chr10:4936224-4936225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs75625406	chr10:4936225-4936226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs529066980	chr10:4936257-4936258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs550317350	chr10:4936285-4936286	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs77144500	chr10:4936297-4936298	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs533462196	chr10:4936335-4936336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs568133882	chr10:4936381-4936382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs149172067	chr10:4936399-4936400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs77369278	chr10:4936442-4936443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs566841063	chr10:4936449-4936450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs527660023	chr10:4936460-4936461	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs76299042	chr10:4936469-4936470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs187964458	chr10:4936472-4936473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs567918624	chr10:4936525-4936526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs550509674	chr10:4936593-4936594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs538444809	chr10:4936607-4936608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs373083323	chr10:4936610-4936611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs192394132	chr10:4936626-4936627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs78178256	chr10:4936684-4936685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs539506031	chr10:4936710-4936711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs183798047	chr10:4936725-4936726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs572525382	chr10:4936733-4936734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs539806997	chr10:4936774-4936775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs555249362	chr10:4936836-4936837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs4488103	chr10:4936837-4936838	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs74586131	chr10:4936881-4936882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs112437373	chr10:4936894-4936895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs533297975	chr10:4936899-4936900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs372512877	chr10:4936904-4936905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs148078047	chr10:4936906-4936907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs566964487	chr10:4936929-4936930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs545461317	chr10:4936930-4936931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs560350397	chr10:4936932-4936933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs55860913	chr10:4936935-4936936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs11252814	chr10:4936936-4936937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

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
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:432 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:4908800-4944200	Weak transcription	Adipose Nuclei	Adipose
2	chr10:4910400-4936400	Weak transcription	Left Ventricle	heart
3	chr10:4915800-4943600	Weak transcription	Aorta	Aorta
4	chr10:4916800-4936400	Weak transcription	Pancreas	Pancrea
5	chr10:4918400-4968000	Weak transcription	Primary T cells from cord blood	blood
6	chr10:4919200-4936800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr10:4925800-4936400	Weak transcription	Right Atrium	heart
8	chr10:4927800-4936200	Weak transcription	Lung	lung
9	chr10:4931200-4944200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr10:4932200-4936000	Weak transcription	Fetal Stomach	stomach
11	chr10:4932600-4936200	Weak transcription	Liver	Liver
12	chr10:4933400-4936000	Weak transcription	HepG2	liver
13	chr10:4935800-4937000	Enhancers	Fetal Heart	heart
14	chr10:4936000-4936400	Enhancers	Fetal Stomach	stomach
15	chr10:4936000-4936400	Enhancers	Stomach Mucosa	stomach
16	chr10:4936200-4936400	Enhancers	Small Intestine	intestine
17	chr10:4936200-4936800	Enhancers	Liver	Liver
18	chr10:4936200-4936800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr10:4936200-4936800	Enhancers	Fetal Lung	lung
20	chr10:4936200-4937000	Enhancers	Gastric	stomach
21	chr10:4936200-4937000	Enhancers	Lung	lung
22	chr10:4936400-4936800	Enhancers	Left Ventricle	heart
23	chr10:4936400-4937000	Enhancers	Ovary	ovary
24	chr10:4936400-4937000	Enhancers	Pancreas	Pancrea
25	chr10:4936400-4937000	Enhancers	Right Atrium	heart
26	chr10:4936800-4943600	Weak transcription	Left Ventricle	heart
27	chr10:4943600-4944200	Enhancers	Left Ventricle	heart
28	chr10:4943600-4944200	Enhancers	Lung	lung
29	chr10:4943600-4944200	Enhancers	Right Atrium	heart
30	chr10:4943600-4944400	Enhancers	Aorta	Aorta
31	chr10:4943600-4946000	Enhancers	Pancreas	Pancrea
32	chr10:4943600-4946400	Enhancers	K562	blood
33	chr10:4944200-4944400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr10:4944200-4944400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr10:4944200-4944400	Enhancers	Stomach Smooth Muscle	stomach
36	chr10:4944200-4944800	Weak transcription	Left Ventricle	heart
37	chr10:4944200-4944800	Weak transcription	Right Atrium	heart
38	chr10:4944200-4945200	Enhancers	Skeletal Muscle Male	skeletal muscle
39	chr10:4944200-4945400	Enhancers	Adipose Nuclei	Adipose
40	chr10:4944200-4945800	Enhancers	Liver	Liver
41	chr10:4944400-4944800	Enhancers	Brain Anterior Caudate	brain
42	chr10:4944400-4944800	Flanking Active TSS	Fetal Heart	heart
43	chr10:4944400-4944800	Flanking Active TSS	Stomach Smooth Muscle	stomach
44	chr10:4944400-4944800	Enhancers	HepG2	liver
45	chr10:4944400-4945000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr10:4944400-4945000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr10:4944400-4945200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr10:4944400-4945200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
49	chr10:4944400-4945200	Enhancers	Colon Smooth Muscle	Colon
50	chr10:4944400-4945200	Enhancers	GM12878-XiMat	blood

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