Variant report

Variant	nsv1042940
Chromosome Location	chr10:4916614-4974581
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:298)
CpG islands
(count:61)
Chromatin interactive
region (count:30)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:298 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:4925039-4925872	K562	blood:	n/a	n/a
2	ARID3A	chr10:4944990-4945093	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:4932162-4932695	HepG2	liver:	n/a	n/a
4	ATF1	chr10:4959638-4959671	K562	blood:	n/a	n/a
5	ATF1	chr10:4944820-4945103	K562	blood:	n/a	n/a
6	ATF1	chr10:4925204-4925856	K562	blood:	n/a	n/a
7	ATF3	chr10:4925496-4925910	K562	blood:	n/a	n/a
8	BACH1	chr10:4950244-4950301	K562	blood:	n/a	n/a
9	BHLHE40	chr10:4925299-4926371	K562	blood:	n/a	n/a
10	BRCA1	chr10:4944963-4945066	HepG2	liver:	n/a	n/a
11	CBX3	chr10:4925100-4926020	K562	blood:	n/a	n/a
12	CBX3	chr10:4952855-4953096	K562	blood:	n/a	n/a
13	CBX3	chr10:4952816-4953115	K562	blood:	n/a	n/a
14	CBX3	chr10:4968600-4969011	K562	blood:	n/a	n/a
15	CBX3	chr10:4968629-4968983	K562	blood:	n/a	n/a
16	CEBPB	chr10:4961716-4961873	Hela-S3	cervix:	n/a	chr10:4961841-4961852 chr10:4961778-4961789
17	CEBPB	chr10:4961718-4961949	HepG2	liver:	n/a	chr10:4961841-4961852 chr10:4961778-4961789
18	CEBPB	chr10:4961758-4961791	IMR90	lung:	n/a	chr10:4961778-4961789
19	CEBPB	chr10:4958485-4958540	K562	blood:	n/a	n/a
20	CEBPB	chr10:4948135-4948323	HepG2	liver:	n/a	chr10:4948213-4948224
21	CEBPB	chr10:4961709-4961851	HepG2	liver:	n/a	chr10:4961778-4961789
22	CEBPB	chr10:4961752-4961882	K562	blood:	n/a	chr10:4961841-4961852 chr10:4961778-4961789
23	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
24	CEBPB	chr10:4925328-4925869	K562	blood:	n/a	n/a
25	CEBPB	chr10:4948072-4948352	K562	blood:	n/a	chr10:4948213-4948224
26	CEBPB	chr10:4968670-4968923	K562	blood:	n/a	n/a
27	CEBPB	chr10:4932230-4932568	HepG2	liver:	n/a	chr10:4932444-4932455 chr10:4932444-4932455 chr10:4932549-4932560
28	CEBPB	chr10:4944928-4945128	HepG2	liver:	n/a	n/a
29	CEBPB	chr10:4960198-4960337	K562	blood:	n/a	n/a
30	CHD2	chr10:4925317-4925539	K562	blood:	n/a	n/a
31	CTCF	chr10:4951320-4951470	HMEC	breast:	n/a	n/a
32	CTCF	chr10:4951440-4951590	SAEC	small airway:	n/a	n/a
33	CTCF	chr10:4951434-4951615	NHEK	skin:	n/a	n/a
34	CTCF	chr10:4925662-4925706	NHEK	skin:	n/a	n/a
35	CTCF	chr10:4966842-4966900	GM20000	blood:	n/a	n/a
36	CTCF	chr10:4951500-4951650	Caco-2	colon:	n/a	n/a
37	CTCF	chr10:4951460-4951610	HepG2	liver:	n/a	n/a
38	CTCF	chr10:4925383-4925820	K562	blood:	n/a	n/a
39	CTCF	chr10:4951486-4951586	K562	blood:	n/a	n/a
40	CTCF	chr10:4951502-4951579	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr10:4951430-4951606	HepG2	liver:	n/a	n/a
42	CTCF	chr10:4966766-4966975	MCF-7	breast:	n/a	n/a
43	CTCF	chr10:4953516-4953579	MCF-7	breast:	n/a	n/a
44	CTCF	chr10:4951475-4951520	Fibrobl	skin:	n/a	n/a
45	CTCF	chr10:4951460-4951610	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr10:4951459-4951590	A549	lung:	n/a	n/a
47	CTCF	chr10:4966785-4966995	GM19239	blood:	n/a	n/a
48	CTCF	chr10:4951942-4951983	Fibrobl	skin:	n/a	n/a
49	CTCF	chr10:4973477-4973574	MCF-7	breast:	n/a	n/a
50	CTCF	chr10:4951460-4951610	AG04450	lung:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:4925586-4925636	AG04450	lung:	fetal
2	chr10:4925586-4925636	HCPEpiC	choroid plexus:	n/a
3	chr10:4925586-4925636	ovcar-3	ovarian:	n/a
4	chr10:4925586-4925636	HAEpiC	amniotic membrane:	n/a
5	chr10:4925586-4925636	SKMC	muscle:	n/a
6	chr10:4925586-4925636	HRE	kidney:	n/a
7	chr10:4925586-4925636	PANC-1	pancreas:	n/a
8	chr10:4925586-4925636	HEK293	kidney:	embryo
9	chr10:4925586-4925636	Caco-2	colon:	n/a
10	chr10:4925586-4925636	PFSK-1	brain:	n/a
11	chr10:4925586-4925636	HRCEpiC	kidney:	n/a
12	chr10:4925586-4925636	MCF-7	breast:	n/a
13	chr10:4925586-4925636	NH-A	brain:	n/a
14	chr10:4925586-4925636	HMEC	breast:	n/a
15	chr10:4925586-4925636	U87	brain:	n/a
16	chr10:4925586-4925636	HEEpiC	esophagus:	n/a
17	chr10:4925586-4925636	AG09309	skin:	n/a
18	chr10:4925586-4925636	HUVEC	blood vessel:	n/a
19	chr10:4925586-4925636	GM06990	blood:	n/a
20	chr10:4925586-4925636	Hela-S3	cervix:	n/a
21	chr10:4925586-4925636	T-47D	breast:	n/a
22	chr10:4925586-4925636	H1-hESC	embryonic stem cell:	embryo
23	chr10:4925586-4925636	RPTEC	kidney:	n/a
24	chr10:4925586-4925636	ECC-1	luminal epithelium:	n/a
25	chr10:4925586-4925636	SK-N-SH_RA	brain:	n/a
26	chr10:4925586-4925636	HL-60	blood:	n/a
27	chr10:4925586-4925636	HPAEpiC	pulmonary alveolar:	n/a
28	chr10:4925586-4925636	Hepatocyte	liver:	n/a
29	chr10:4925586-4925636	A549	lung:	n/a
30	chr10:4925586-4925636	NT2-D1	testis:	n/a
31	chr10:4925586-4925636	SK-N-MC	brain:	n/a
32	chr10:4925586-4925636	GM12892	blood:	n/a
33	chr10:4925586-4925636	HIPEpiC	eye:	n/a
34	chr10:4925586-4925636	K562	blood:	n/a
35	chr10:4925586-4925636	MCF10A-Er-Src	breast:	n/a
36	chr10:4925586-4925636	HCF	heart:	n/a
37	chr10:4925586-4925636	CMK	blood:	n/a
38	chr10:4925586-4925636	PrEC	prostate:	n/a
39	chr10:4925586-4925636	AoSMC	blood vessel:	n/a
40	chr10:4925586-4925636	GM12878	blood:	n/a
41	chr10:4925586-4925636	SK-N-SH	brain:	n/a
42	chr10:4925586-4925636	NB4	blood:	n/a
43	chr10:4925586-4925636	AG04449	skin:	fetal
44	chr10:4925586-4925636	HepG2	liver:	n/a
45	chr10:4925586-4925636	BJ	skin:	n/a
46	chr10:4925586-4925636	HCT-116	colon:	n/a
47	chr10:4925586-4925636	AG10803	skin:	n/a
48	chr10:4925586-4925636	NHBE	bronchial:	n/a
49	chr10:4925586-4925636	HNPCEpiC	eye:	n/a
50	chr10:4925586-4925636	ProgFib	skin:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:4925269..4926860-chr10:4926881..4928457,2	K562	blood:
2	chr10:4920221..4922762-chr10:4924634..4927281,2	K562	blood:
3	chr10:4957459..4960472-chr10:4974097..4976295,3	K562	blood:
4	chr10:4909631..4911744-chr10:4926137..4927768,2	K562	blood:
5	chr10:4924021..4926769-chr10:4926839..4928381,2	K562	blood:
6	chr10:4947891..4950201-chr10:4952537..4954922,2	K562	blood:
7	chr10:4953662..4955307-chr10:4957981..4959719,2	MCF-7	breast:
8	chr10:4947891..4950201-chr10:4952537..4954922,2	K562	blood:
9	chr10:4973639..4975791-chr10:5115008..5116577,2	K562	blood:
10	chr10:4952930..4955597-chr10:4957156..4959069,3	K562	blood:
11	chr10:4924404..4926925-chr10:4947394..4949303,2	K562	blood:
12	chr10:4924404..4926925-chr10:4947394..4949303,2	K562	blood:
13	chr10:4943122..4945399-chr10:6203684..6206362,2	K562	blood:
14	chr10:4908339..4911131-chr10:4925316..4927637,3	K562	blood:
15	chr10:4924021..4926769-chr10:4926839..4928381,2	K562	blood:
16	chr10:4957459..4960472-chr10:4974097..4976295,3	K562	blood:
17	chr10:4953662..4955307-chr10:4957981..4959719,2	MCF-7	breast:
18	chr10:4930274..4933075-chr10:4935096..4936648,2	K562	blood:
19	chr10:4953562..4955597-chr10:4956461..4959069,2	K562	blood:
20	chr10:4944287..4946415-chr10:4947566..4950260,2	K562	blood:
21	chr10:4952930..4955597-chr10:4957156..4959069,3	K562	blood:
22	chr10:4944287..4946415-chr10:4947566..4950260,2	K562	blood:
23	chr10:4944889..4947267-chr10:4947876..4949644,2	MCF-7	breast:
24	chr10:4930274..4933075-chr10:4935096..4936648,2	K562	blood:
25	chr10:4953562..4955597-chr10:4956461..4959069,2	K562	blood:
26	chr10:4910829..4913220-chr10:4919618..4922612,2	K562	blood:
27	chr10:4913150..4915341-chr10:4916191..4918470,2	K562	blood:
28	chr10:4920221..4922762-chr10:4924634..4927281,2	K562	blood:
29	chr10:4925269..4926860-chr10:4926881..4928457,2	K562	blood:
30	chr10:4944889..4947267-chr10:4947876..4949644,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AKR1C2-7	chr10:4918829-4919605	NONHSAT011119
2	lnc-AKR1C2-7	chr10:4918144-4918245	NONHSAT011119

No data

Variant related genes	Relation type
AKR1C6P	TF binding region
AKR1C1	TF binding region
AKR1C6P	CpG island
AKR1C1	CpG island

Extended variants
information (count: 2218 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:2218 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4880699	chr10:4916614-4916615	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs550819524	chr10:4916615-4916616	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs568980872	chr10:4916643-4916644	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs539650005	chr10:4916645-4916646	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs557516561	chr10:4916666-4916667	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs573044177	chr10:4916674-4916675	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs112523474	chr10:4916688-4916689	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs371540514	chr10:4916750-4916751	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs555348161	chr10:4916773-4916774	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs201072039	chr10:4916841-4916842	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs187492472	chr10:4916882-4916883	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs192864371	chr10:4916913-4916914	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs185173847	chr10:4916960-4916961	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs34718170	chr10:4916990-4916991	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs578175619	chr10:4917032-4917033	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs545622377	chr10:4917043-4917044	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs539183244	chr10:4917110-4917111	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs560665871	chr10:4917151-4917152	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs578099990	chr10:4917175-4917176	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs546678861	chr10:4917180-4917181	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs561682965	chr10:4917200-4917201	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs190454635	chr10:4917230-4917231	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs79465576	chr10:4917291-4917292	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs182227701	chr10:4917401-4917402	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs539345486	chr10:4917402-4917403	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs557691189	chr10:4917432-4917433	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs35433691	chr10:4917436-4917437	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs113654658	chr10:4917535-4917536	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs375890442	chr10:4917544-4917545	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs149680566	chr10:4917619-4917620	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs534041013	chr10:4917630-4917631	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs555411322	chr10:4917658-4917659	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs566356061	chr10:4917669-4917670	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs183787293	chr10:4917685-4917686	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs538270475	chr10:4917707-4917708	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs368414271	chr10:4917719-4917720	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs60237330	chr10:4917767-4917768	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs188272883	chr10:4917780-4917781	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs540714502	chr10:4917843-4917844	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs181407524	chr10:4917862-4917863	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs77118024	chr10:4917916-4917917	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs545329925	chr10:4917940-4917941	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs147795291	chr10:4917949-4917950	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs572642891	chr10:4917950-4917951	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs141264902	chr10:4917960-4917961	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs555218778	chr10:4917961-4917962	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs190744195	chr10:4917964-4917965	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs528967154	chr10:4917967-4917968	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs201198314	chr10:4918014-4918015	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs11252808	chr10:4918016-4918017	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

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
Breast cancer	22522925	CNVD

Chromatin state (count:299 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:4892200-4917800	Weak transcription	Primary T cells from cord blood	blood
2	chr10:4893000-4925000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr10:4903400-4924800	Weak transcription	A549	lung
4	chr10:4908800-4944200	Weak transcription	Adipose Nuclei	Adipose
5	chr10:4910200-4920400	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr10:4910400-4917800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr10:4910400-4936400	Weak transcription	Left Ventricle	heart
8	chr10:4914000-4920000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr10:4914600-4920600	Strong transcription	Liver	Liver
10	chr10:4915400-4919200	Strong transcription	Primary hematopoietic stem cells	blood
11	chr10:4915800-4925000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr10:4915800-4943600	Weak transcription	Aorta	Aorta
13	chr10:4916400-4918400	Enhancers	HepG2	liver
14	chr10:4916400-4918800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr10:4916400-4924600	Weak transcription	K562	blood
16	chr10:4916600-4925000	Weak transcription	Fetal Stomach	stomach
17	chr10:4916800-4936400	Weak transcription	Pancreas	Pancrea
18	chr10:4917600-4925600	Weak transcription	Spleen	Spleen
19	chr10:4917800-4918400	Strong transcription	Primary T cells from cord blood	blood
20	chr10:4917800-4919600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr10:4918400-4968000	Weak transcription	Primary T cells from cord blood	blood
22	chr10:4918800-4919200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
23	chr10:4918800-4931400	Weak transcription	Duodenum Mucosa	Duodenum
24	chr10:4919200-4924800	Weak transcription	Primary hematopoietic stem cells	blood
25	chr10:4919200-4936800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr10:4919600-4924800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr10:4920000-4924800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr10:4920600-4921400	Weak transcription	Liver	Liver
29	chr10:4921200-4929400	Weak transcription	Fetal Muscle Leg	muscle
30	chr10:4921400-4923600	Strong transcription	Liver	Liver
31	chr10:4921600-4930800	Weak transcription	Stomach Smooth Muscle	stomach
32	chr10:4922000-4924600	Weak transcription	Ovary	ovary
33	chr10:4922000-4924800	Weak transcription	Fetal Lung	lung
34	chr10:4923600-4925600	Weak transcription	Liver	Liver
35	chr10:4924600-4925000	Enhancers	K562	blood
36	chr10:4924600-4926000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr10:4924600-4926000	Enhancers	Ovary	ovary
38	chr10:4924600-4926200	Enhancers	NHEK	skin
39	chr10:4924800-4925400	Strong transcription	A549	lung
40	chr10:4924800-4925600	Enhancers	Fetal Lung	lung
41	chr10:4924800-4926800	Enhancers	Primary hematopoietic stem cells	blood
42	chr10:4924800-4929200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr10:4924800-4929600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr10:4925000-4925200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr10:4925000-4925400	Enhancers	Fetal Stomach	stomach
46	chr10:4925000-4925800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr10:4925000-4926000	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr10:4925000-4926000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr10:4925000-4926000	Flanking Active TSS	K562	blood
50	chr10:4925000-4926200	Enhancers	HepG2	liver

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