Variant report

Variant	nsv947581
Chromosome Location	chr10:4925629-4933637
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:102)
CpG islands
(count:62)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:102 , 50 per page) page: 1 2 3

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	chr10:4932162-4932695	HepG2	liver:	n/a	n/a
3	ATF1	chr10:4925204-4925856	K562	blood:	n/a	n/a
4	ATF3	chr10:4925496-4925910	K562	blood:	n/a	n/a
5	BHLHE40	chr10:4925299-4926371	K562	blood:	n/a	n/a
6	CBX3	chr10:4925100-4926020	K562	blood:	n/a	n/a
7	CEBPB	chr10:4932230-4932568	HepG2	liver:	n/a	chr10:4932444-4932455 chr10:4932444-4932455 chr10:4932549-4932560
8	CEBPB	chr10:4925328-4925869	K562	blood:	n/a	n/a
9	CTCF	chr10:4925383-4925820	K562	blood:	n/a	n/a
10	CTCF	chr10:4925560-4925710	HMF	breast:	n/a	n/a
11	CTCF	chr10:4925540-4925690	HCFaa	heart:	n/a	n/a
12	CTCF	chr10:4926035-4926081	GM20000	blood:	n/a	n/a
13	CTCF	chr10:4925662-4925706	NHEK	skin:	n/a	n/a
14	CTCF	chr10:4925560-4925710	HCPEpiC	choroid plexus:	n/a	n/a
15	CTCF	chr10:4925600-4925750	SAEC	small airway:	n/a	n/a
16	CUX1	chr10:4924902-4926288	K562	blood:	n/a	chr10:4925860-4925876
17	E2F6	chr10:4925526-4925777	K562	blood:	n/a	n/a
18	EGR1	chr10:4925241-4925797	K562	blood:	n/a	n/a
19	EGR1	chr10:4925494-4925827	K562	blood:	n/a	n/a
20	EP300	chr10:4932091-4932496	HepG2	liver:	n/a	n/a
21	EP300	chr10:4925030-4926333	K562	blood:	n/a	chr10:4925738-4925748
22	EP300	chr10:4932095-4932577	HepG2	liver:	n/a	n/a
23	EP300	chr10:4925548-4925807	HepG2	liver:	n/a	chr10:4925738-4925748
24	FOS	chr10:4925512-4925898	MCF10A-Er-Src	breast:	n/a	chr10:4925689-4925701
25	FOS	chr10:4925509-4925916	MCF10A-Er-Src	breast:	n/a	chr10:4925689-4925701
26	FOS	chr10:4925498-4925900	MCF10A-Er-Src	breast:	n/a	chr10:4925689-4925701
27	FOS	chr10:4925492-4925915	MCF10A-Er-Src	breast:	n/a	chr10:4925689-4925701
28	FOSL1	chr10:4925496-4925795	K562	blood:	n/a	chr10:4925689-4925701
29	FOSL1	chr10:4925445-4925938	K562	blood:	n/a	chr10:4925921-4925930 chr10:4925689-4925701
30	FOXA1	chr10:4931924-4932619	HepG2	liver:	n/a	n/a
31	FOXA1	chr10:4931943-4932559	HepG2	liver:	n/a	n/a
32	FOXA1	chr10:4931990-4932560	HepG2	liver:	n/a	n/a
33	FOXA1	chr10:4925535-4925867	HepG2	liver:	n/a	chr10:4925735-4925747
34	FOXA1	chr10:4931912-4932646	HepG2	liver:	n/a	n/a
35	FOXA2	chr10:4931979-4932556	HepG2	liver:	n/a	n/a
36	FOXA2	chr10:4925571-4925795	HepG2	liver:	n/a	chr10:4925735-4925747
37	FOXA2	chr10:4931898-4932805	HepG2	liver:	n/a	n/a
38	HCFC1	chr10:4926653-4926774	K562	blood:	n/a	n/a
39	HDAC2	chr10:4932160-4932546	HepG2	liver:	n/a	n/a
40	HDAC2	chr10:4932092-4932635	HepG2	liver:	n/a	n/a
41	HDAC2	chr10:4925497-4925781	K562	blood:	n/a	chr10:4925738-4925747
42	HMGN3	chr10:4925225-4925741	K562	blood:	n/a	n/a
43	HNF4A	chr10:4932262-4932492	HepG2	liver:	n/a	n/a
44	JUN	chr10:4931498-4931611	HepG2	liver:	n/a	chr10:4931519-4931532
45	JUN	chr10:4924813-4926992	K562	blood:	n/a	chr10:4925921-4925930 chr10:4925689-4925701
46	JUN	chr10:4925194-4925897	K562	blood:	n/a	chr10:4925689-4925701
47	JUND	chr10:4925145-4925916	K562	blood:	n/a	chr10:4925689-4925700 chr10:4925689-4925701
48	JUND	chr10:4926629-4926759	K562	blood:	n/a	n/a
49	JUND	chr10:4925581-4925797	HepG2	liver:	n/a	chr10:4925689-4925700 chr10:4925689-4925701
50	JUND	chr10:4925579-4925815	HepG2	liver:	n/a	chr10:4925689-4925700 chr10:4925689-4925701

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:4925586-4925636	NT2-D1	testis:	n/a
2	chr10:4925586-4925636	NT2-D1	testis:	n/a
3	chr10:4925586-4925636	HEK293	kidney:	embryo
4	chr10:4925586-4925636	ovcar-3	ovarian:	n/a
5	chr10:4925586-4925636	GM06990	blood:	n/a
6	chr10:4925586-4925636	Hepatocyte	liver:	n/a
7	chr10:4925586-4925636	AG04450	lung:	fetal
8	chr10:4925586-4925636	T-47D	breast:	n/a
9	chr10:4925586-4925636	PFSK-1	brain:	n/a
10	chr10:4925586-4925636	HRPEpiC	eye:	n/a
11	chr10:4925586-4925636	PANC-1	pancreas:	n/a
12	chr10:4925586-4925636	HCM	heart:	n/a
13	chr10:4925586-4925636	K562	blood:	n/a
14	chr10:4925586-4925636	NH-A	brain:	n/a
15	chr10:4925586-4925636	LNCaP	prostate:	n/a
16	chr10:4925586-4925636	PrEC	prostate:	n/a
17	chr10:4925586-4925636	BJ	skin:	n/a
18	chr10:4925586-4925636	HMEC	breast:	n/a
19	chr10:4925586-4925636	SKMC	muscle:	n/a
20	chr10:4925586-4925636	HIPEpiC	eye:	n/a
21	chr10:4925586-4925636	HepG2	liver:	n/a
22	chr10:4925586-4925636	HUVEC	blood vessel:	n/a
23	chr10:4925586-4925636	HRCEpiC	kidney:	n/a
24	chr10:4925586-4925636	NHDF-neo	bronchial:	n/a
25	chr10:4925586-4925636	SK-N-MC	brain:	n/a
26	chr10:4925586-4925636	NB4	blood:	n/a
27	chr10:4925586-4925636	ECC-1	luminal epithelium:	n/a
28	chr10:4925586-4925636	AG09319	gingival:	n/a
29	chr10:4925586-4925636	SK-N-SH	brain:	n/a
30	chr10:4925586-4925636	AG04449	skin:	fetal
31	chr10:4925586-4925636	Jurkat	blood:	n/a
32	chr10:4925586-4925636	GM19239	blood:	n/a
33	chr10:4925586-4925636	H1-hESC	embryonic stem cell:	embryo
34	chr10:4925586-4925636	RPTEC	kidney:	n/a
35	chr10:4925586-4925636	AoSMC	blood vessel:	n/a
36	chr10:4925586-4925636	HRE	kidney:	n/a
37	chr10:4925586-4925636	SK-N-SH_RA	brain:	n/a
38	chr10:4925586-4925636	HCT-116	colon:	n/a
39	chr10:4925586-4925636	GM12892	blood:	n/a
40	chr10:4925586-4925636	HEEpiC	esophagus:	n/a
41	chr10:4925586-4925636	U87	brain:	n/a
42	chr10:4925586-4925636	HAEpiC	amniotic membrane:	n/a
43	chr10:4925586-4925636	AG10803	skin:	n/a
44	chr10:4925586-4925636	GM12891	blood:	n/a
45	chr10:4925586-4925636	SAEC	small airway:	n/a
46	chr10:4925586-4925636	AG09309	skin:	n/a
47	chr10:4925586-4925636	GM12878	blood:	n/a
48	chr10:4925586-4925636	Caco-2	colon:	n/a
49	chr10:4925586-4925636	CMK	blood:	n/a
50	chr10:4925586-4925636	HCF	heart:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:4908339..4911131-chr10:4925316..4927637,3	K562	blood:
2	chr10:4925269..4926860-chr10:4926881..4928457,2	K562	blood:
3	chr10:4924021..4926769-chr10:4926839..4928381,2	K562	blood:
4	chr10:4909631..4911744-chr10:4926137..4927768,2	K562	blood:
5	chr10:4920221..4922762-chr10:4924634..4927281,2	K562	blood:
6	chr10:4925269..4926860-chr10:4926881..4928457,2	K562	blood:
7	chr10:4924404..4926925-chr10:4947394..4949303,2	K562	blood:
8	chr10:4930274..4933075-chr10:4935096..4936648,2	K562	blood:
9	chr10:4924021..4926769-chr10:4926839..4928381,2	K562	blood:

No data

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

Extended variants
information (count: 334 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:334 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544579559	chr10:4925648-4925649	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs369020377	chr10:4925664-4925665	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs186146169	chr10:4925678-4925679	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs553429049	chr10:4925707-4925708	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs4881369	chr10:4925714-4925715	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs561133808	chr10:4925739-4925740	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs34530369	chr10:4925766-4925767	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs531752678	chr10:4925790-4925791	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs376531122	chr10:4925835-4925836	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs565306023	chr10:4925880-4925881	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs532572188	chr10:4925912-4925913	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs547776338	chr10:4925933-4925934	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs566250948	chr10:4925934-4925935	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs190996621	chr10:4925956-4925957	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs7071257	chr10:4926008-4926009	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs555569762	chr10:4926053-4926054	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs567914365	chr10:4926057-4926058	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs376006494	chr10:4926058-4926059	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs570217926	chr10:4926107-4926108	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537580311	chr10:4926187-4926188	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs555864597	chr10:4926236-4926237	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs570978031	chr10:4926246-4926247	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs566991928	chr10:4926263-4926264	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs386740272	chr10:4926264-4926265	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs4406725	chr10:4926266-4926267	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs374690720	chr10:4926274-4926275	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs76363861	chr10:4926280-4926281	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs542899454	chr10:4926314-4926315	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs564899448	chr10:4926328-4926329	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs75030570	chr10:4926341-4926342	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs576282247	chr10:4926371-4926372	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs181413249	chr10:4926379-4926380	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs73594917	chr10:4926382-4926383	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs532609922	chr10:4926399-4926400	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs74330352	chr10:4926419-4926420	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs75018551	chr10:4926437-4926438	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs117865028	chr10:4926463-4926464	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs10904365	chr10:4926511-4926512	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs75815384	chr10:4926586-4926587	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs570226559	chr10:4926619-4926620	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531027125	chr10:4926667-4926668	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186424302	chr10:4926671-4926672	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191065743	chr10:4926719-4926720	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs74111791	chr10:4926748-4926749	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs553528818	chr10:4926802-4926803	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs565654440	chr10:4926805-4926806	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183079717	chr10:4926820-4926821	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554869292	chr10:4926830-4926831	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs576369269	chr10:4926877-4926878	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543649722	chr10:4926891-4926892	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

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

Chromatin state (count:74 , 50 per page) page: 1 2

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	chr10:4918800-4931400	Weak transcription	Duodenum Mucosa	Duodenum
7	chr10:4919200-4936800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr10:4921200-4929400	Weak transcription	Fetal Muscle Leg	muscle
9	chr10:4921600-4930800	Weak transcription	Stomach Smooth Muscle	stomach
10	chr10:4924600-4926000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr10:4924600-4926000	Enhancers	Ovary	ovary
12	chr10:4924600-4926200	Enhancers	NHEK	skin
13	chr10:4924800-4926800	Enhancers	Primary hematopoietic stem cells	blood
14	chr10:4924800-4929200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr10:4924800-4929600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr10:4925000-4925800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr10:4925000-4926000	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr10:4925000-4926000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr10:4925000-4926000	Flanking Active TSS	K562	blood
20	chr10:4925000-4926200	Enhancers	HepG2	liver
21	chr10:4925000-4926200	Enhancers	HMEC	breast
22	chr10:4925200-4925800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr10:4925200-4925800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr10:4925200-4925800	Enhancers	NH-A	brain
25	chr10:4925200-4926000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr10:4925400-4925800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr10:4925400-4925800	Enhancers	NHDF-Ad	bronchial
28	chr10:4925400-4926000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr10:4925400-4929200	Weak transcription	Fetal Stomach	stomach
30	chr10:4925600-4925800	Enhancers	Esophagus	oesophagus
31	chr10:4925600-4925800	Enhancers	Right Atrium	heart
32	chr10:4925600-4925800	Enhancers	Spleen	Spleen
33	chr10:4925600-4925800	Enhancers	HSMM	muscle
34	chr10:4925600-4926200	Enhancers	A549	lung
35	chr10:4925600-4930200	Strong transcription	Liver	Liver
36	chr10:4925800-4927600	Weak transcription	Lung	lung
37	chr10:4925800-4936400	Weak transcription	Right Atrium	heart
38	chr10:4926000-4926400	Enhancers	K562	blood
39	chr10:4926000-4927600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr10:4926000-4929800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr10:4926200-4929400	Weak transcription	A549	lung
42	chr10:4926200-4931400	Weak transcription	HepG2	liver
43	chr10:4926800-4927400	Weak transcription	Primary hematopoietic stem cells	blood
44	chr10:4927400-4930200	Enhancers	Primary hematopoietic stem cells	blood
45	chr10:4927600-4927800	ZNF genes & repeats	Lung	lung
46	chr10:4927600-4928000	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr10:4927800-4936200	Weak transcription	Lung	lung
48	chr10:4928000-4929200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
49	chr10:4929200-4929800	Enhancers	Primary B cells from peripheral blood	blood
50	chr10:4929200-4930000	Enhancers	Primary hematopoietic stem cells short term culture	blood

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