Variant report

Variant	nsv540570
Chromosome Location	chr10:38696654-38728292
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:54)
CpG islands
(count:183)
Chromatin interactive
region (count:0)
LncRNA
region (count:27)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:54 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr10:38726503-38726522	HepG2	liver:	n/a	chr10:38726511-38726522
2	CEBPB	chr10:38726323-38726688	IMR90	lung:	n/a	chr10:38726511-38726522
3	CTCF	chr10:38705100-38705250	HEK293	kidney:	n/a	n/a
4	CTCF	chr10:38705100-38705250	GM12875	blood:	n/a	n/a
5	CTCF	chr10:38705080-38705230	GM12869	blood:	n/a	n/a
6	CTCF	chr10:38705080-38705230	HMF	breast:	n/a	n/a
7	CTCF	chr10:38705136-38705221	MCF-7	breast:	n/a	n/a
8	CTCF	chr10:38705080-38705230	GM12872	blood:	n/a	n/a
9	CTCF	chr10:38705040-38705190	GM12864	blood:	n/a	n/a
10	CTCF	chr10:38705060-38705210	HBMEC	blood vessel:	n/a	n/a
11	CTCF	chr10:38705145-38705198	MCF-7	breast:	n/a	n/a
12	CTCF	chr10:38705080-38705230	GM12874	blood:	n/a	n/a
13	CTCF	chr10:38705040-38705190	GM12871	blood:	n/a	n/a
14	CTCF	chr10:38705035-38705083	LNCaP	prostate:	n/a	n/a
15	CTCF	chr10:38705040-38705190	A549	lung:	n/a	n/a
16	CTCF	chr10:38705135-38705209	MCF-7	breast:	n/a	n/a
17	CTCF	chr10:38705133-38705217	MCF-7	breast:	n/a	n/a
18	CTCF	chr10:38705040-38705190	MCF-7	breast:	n/a	n/a
19	CTCF	chr10:38705100-38705250	GM12878	blood:	n/a	n/a
20	CTCF	chr10:38705000-38705150	HPAF	blood vessel:	n/a	n/a
21	CTCF	chr10:38705140-38705173	GM19238	blood:	n/a	n/a
22	FOXA1	chr10:38708693-38709071	HepG2	liver:	n/a	n/a
23	FOXA2	chr10:38719087-38719519	A549	lung:	n/a	n/a
24	GABPA	chr10:38726408-38726608	Hela-S3	cervix:	n/a	n/a
25	JUND	chr10:38702267-38702478	HepG2	liver:	n/a	n/a
26	POLR2A	chr10:38696637-38696682	HepG2	liver:	n/a	n/a
27	POLR2A	chr10:38726202-38726708	U87	brain:	n/a	n/a
28	POLR2A	chr10:38726198-38726710	U87	brain:	n/a	n/a
29	REST	chr10:38719073-38719448	H1-hESC	embryonic stem cell:	n/a	n/a
30	REST	chr10:38718955-38719121	SK-N-SH	brain:	n/a	n/a
31	REST	chr10:38719192-38719395	U87	brain:	n/a	n/a
32	REST	chr10:38719191-38719312	PFSK-1	brain:	n/a	n/a
33	REST	chr10:38719191-38719314	HepG2	liver:	n/a	n/a
34	REST	chr10:38719202-38719308	GM12878	blood:	n/a	n/a
35	REST	chr10:38719174-38719496	U87	brain:	n/a	n/a
36	REST	chr10:38719235-38719483	K562	blood:	n/a	n/a
37	REST	chr10:38719190-38719523	SK-N-SH	brain:	n/a	n/a
38	REST	chr10:38719173-38719510	HepG2	liver:	n/a	n/a
39	REST	chr10:38719230-38719535	PFSK-1	brain:	n/a	n/a
40	REST	chr10:38719339-38719516	HepG2	liver:	n/a	n/a
41	REST	chr10:38719235-38719500	PFSK-1	brain:	n/a	n/a
42	REST	chr10:38719160-38719312	HepG2	liver:	n/a	n/a
43	REST	chr10:38719191-38719403	H1-hESC	embryonic stem cell:	n/a	n/a
44	REST	chr10:38719170-38719309	PANC-1	pancreas:	n/a	n/a
45	REST	chr10:38719133-38719332	PFSK-1	brain:	n/a	n/a
46	REST	chr10:38719191-38719392	PANC-1	pancreas:	n/a	n/a
47	REST	chr10:38719150-38719571	SK-N-SH	brain:	n/a	n/a
48	REST	chr10:38719129-38719560	HepG2	liver:	n/a	n/a
49	REST	chr10:38719025-38719656	U87	brain:	n/a	n/a
50	REST	chr10:38719083-38719620	GM12878	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:38715824-38715874	BJ	skin:	n/a
2	chr10:38716268-38716318	IMR90	lung:	fetal
3	chr10:38716268-38716318	NHDF-neo	bronchial:	n/a
4	chr10:38716291-38716341	ECC-1	luminal epithelium:	n/a
5	chr10:38716291-38716341	SK-N-SH	brain:	n/a
6	chr10:38716268-38716318	HCM	heart:	n/a
7	chr10:38715824-38715874	SKMC	muscle:	n/a
8	chr10:38716291-38716341	MCF10A-Er-Src	breast:	n/a
9	chr10:38716268-38716318	HEEpiC	esophagus:	n/a
10	chr10:38716268-38716318	Hepatocyte	liver:	n/a
11	chr10:38716268-38716318	SK-N-SH_RA	brain:	n/a
12	chr10:38716291-38716341	AoSMC	blood vessel:	n/a
13	chr10:38715824-38715874	AG09309	skin:	n/a
14	chr10:38716291-38716341	HCM	heart:	n/a
15	chr10:38716291-38716341	GM06990	blood:	n/a
16	chr10:38715824-38715874	HRE	kidney:	n/a
17	chr10:38716291-38716341	IMR90	lung:	fetal
18	chr10:38716268-38716318	HNPCEpiC	eye:	n/a
19	chr10:38716268-38716318	HCF	heart:	n/a
20	chr10:38715824-38715874	AG04450	lung:	fetal
21	chr10:38716291-38716341	HRPEpiC	eye:	n/a
22	chr10:38716268-38716318	GM19239	blood:	n/a
23	chr10:38715824-38715874	HEK293	kidney:	embryo
24	chr10:38716291-38716341	HCPEpiC	choroid plexus:	n/a
25	chr10:38716291-38716341	GM12878	blood:	n/a
26	chr10:38716268-38716318	HepG2	liver:	n/a
27	chr10:38715824-38715874	AG04449	skin:	fetal
28	chr10:38716291-38716341	SAEC	small airway:	n/a
29	chr10:38715824-38715874	HAEpiC	amniotic membrane:	n/a
30	chr10:38716268-38716318	A549	lung:	n/a
31	chr10:38716268-38716318	Hela-S3	cervix:	n/a
32	chr10:38716291-38716341	NHDF-neo	bronchial:	n/a
33	chr10:38716291-38716341	NB4	blood:	n/a
34	chr10:38715824-38715874	GM12891	blood:	n/a
35	chr10:38716291-38716341	SKMC	muscle:	n/a
36	chr10:38715824-38715874	K562	blood:	n/a
37	chr10:38715824-38715874	Hela-S3	cervix:	n/a
38	chr10:38716268-38716318	ovcar-3	ovarian:	n/a
39	chr10:38715824-38715874	HRCEpiC	kidney:	n/a
40	chr10:38715824-38715874	HRPEpiC	eye:	n/a
41	chr10:38716291-38716341	K562	blood:	n/a
42	chr10:38716268-38716318	SK-N-SH	brain:	n/a
43	chr10:38716291-38716341	HepG2	liver:	n/a
44	chr10:38715824-38715874	NHDF-neo	bronchial:	n/a
45	chr10:38716268-38716318	HCPEpiC	choroid plexus:	n/a
46	chr10:38715824-38715874	HL-60	blood:	n/a
47	chr10:38716268-38716318	AG09309	skin:	n/a
48	chr10:38716268-38716318	LNCaP	prostate:	n/a
49	chr10:38715824-38715874	T-47D	breast:	n/a
50	chr10:38716268-38716318	Caco-2	colon:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF37A-3	chr10:38702255-38702320	ENSG00000225119.2
2	lnc-ZNF37A-3	chr10:38727786-38727850	ENSG00000225119.2
3	lnc-ZNF37A-3	chr10:38701657-38701810	ENSG00000225119.2
4	lnc-ZNF37A-3	chr10:38726018-38726134	ENSG00000225119.2
5	lnc-ZNF37A-3	chr10:38716834-38717224	XLOC_008461
6	lnc-ZNF37A-3	chr10:38724228-38724691	XLOC_008461
7	lnc-ZNF37A-3	chr10:38717035-38717224	XLOC_008461
8	lnc-ZNF37A-3	chr10:38726276-38726679	NONHSAT012824
9	lnc-ZNF37A-3	chr10:38724058-38724184	XLOC_008461
10	lnc-ZNF37A-3	chr10:38717074-38717224	ENSG00000225119.2
11	lnc-ZNF37A-3	chr10:38711696-38711926	ENSG00000225119.2
12	lnc-ZNF37A-3	chr10:38726472-38726679	ENSG00000225119.2
13	lnc-ZNF37A-3	chr10:38714747-38714811	ENSG00000225119.2
14	lnc-ZNF37A-3	chr10:38704472-38704530	ENSG00000225119.2
15	lnc-ZNF37A-3	chr10:38714747-38714811	XLOC_008461
16	lnc-ZNF37A-3	chr10:38726472-38726668	ENSG00000225119.2
17	lnc-ZNF37A-3	chr10:38727786-38727798	NONHSAT012824
18	lnc-ZNF37A-3	chr10:38697731-38697862	ENSG00000225119.2
19	lnc-ZNF37A-3	chr10:38727786-38727954	ENSG00000225119.2
20	lnc-ZNF37A-3	chr10:38696559-38696668	ENSG00000225119.2
21	lnc-ZNF37A-3	chr10:38726018-38726134	ENSG00000225119.2
22	lnc-ZNF37A-3	chr10:38724058-38724181	ENSG00000225119.2
23	lnc-ZNF37A-3	chr10:38725679-38725788	ENSG00000225119.2
24	lnc-ZNF37A-3	chr10:38701156-38701371	ENSG00000225119.2
25	lnc-ZNF37A-3	chr10:38705610-38706132	ENSG00000225119.2
26	lnc-ZNF37A-3	chr10:38724058-38724486	XLOC_008461
27	lnc-ZNF37A-3	chr10:38714788-38714811	XLOC_008461

No data

Variant related genes	Relation type
RNU6-1118P	TF binding region
SEPT7P9	TF binding region
LINC00999	TF binding region
RNU6-1118P	CpG island
SEPT7P9	CpG island
LINC00999	CpG island

Extended variants
information (count: 1012 )
Associated
traits (count: 40 )

Variant overlapped rSNPs/rCNVs (count:1012 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564205744	chr10:38696671-38696672	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs3932487	chr10:38696744-38696745	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs540057226	chr10:38696770-38696771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs186474650	chr10:38696858-38696859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs191356632	chr10:38696868-38696869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs528568591	chr10:38696894-38696895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs182726407	chr10:38696923-38696924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs562151659	chr10:38696944-38696945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs186070417	chr10:38696946-38696947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs201748756	chr10:38696962-38696963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs189663752	chr10:38696973-38696974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs551284566	chr10:38697007-38697008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs183404197	chr10:38697017-38697018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs187756605	chr10:38697037-38697038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs373880989	chr10:38697124-38697125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs373517463	chr10:38697235-38697236	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs540100625	chr10:38697240-38697241	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs547222214	chr10:38697250-38697251	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs567021838	chr10:38697284-38697285	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs200666502	chr10:38697285-38697286	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs377417660	chr10:38697358-38697359	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs199543847	chr10:38697398-38697399	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs555155941	chr10:38697447-38697448	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs372883212	chr10:38697545-38697546	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs377275318	chr10:38697547-38697548	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs575226279	chr10:38697566-38697567	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537467369	chr10:38697631-38697632	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs557299579	chr10:38697716-38697717	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs577525505	chr10:38697721-38697722	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs540091137	chr10:38697740-38697741	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs553597627	chr10:38697762-38697763	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs11498336	chr10:38697786-38697787	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs573746729	chr10:38697796-38697797	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs542343019	chr10:38697812-38697813	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs562018330	chr10:38697905-38697906	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531005302	chr10:38697943-38697944	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564396455	chr10:38697992-38697993	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564430012	chr10:38697993-38697994	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs533668361	chr10:38697994-38697995	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs533487946	chr10:38697995-38697996	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs567109288	chr10:38698016-38698017	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs1810631	chr10:38698042-38698043	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546278740	chr10:38698043-38698044	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs192252657	chr10:38698065-38698066	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529445668	chr10:38698075-38698076	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs4079819	chr10:38698093-38698094	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs549529700	chr10:38698135-38698136	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531004785	chr10:38698160-38698161	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs568877841	chr10:38698180-38698181	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs537909155	chr10:38698201-38698202	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:40)

Disease	PMID	Source
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
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
T-cell lymphomas	19863542	CNVD
Esophageal cancer	21851588	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Lung cancer	21569311	CNVD
Colorectal cancer	20459617	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Central neurocytomas	17123091	CNVD
Neurocytoma	17123091	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:38691800-38698000	Weak transcription	Spleen	Spleen
2	chr10:38692200-38741000	Weak transcription	Aorta	Aorta
3	chr10:38692400-38739600	Weak transcription	Gastric	stomach
4	chr10:38692600-38698000	Weak transcription	Ovary	ovary
5	chr10:38692600-38699400	Weak transcription	Duodenum Mucosa	Duodenum
6	chr10:38692600-38716400	Weak transcription	Primary T cells from cord blood	blood
7	chr10:38692600-38736800	Weak transcription	Pancreas	Pancrea
8	chr10:38692600-38737200	Weak transcription	Esophagus	oesophagus
9	chr10:38692800-38698000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr10:38692800-38698000	Weak transcription	Lung	lung
11	chr10:38692800-38699800	Weak transcription	Fetal Stomach	stomach
12	chr10:38692800-38700000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr10:38692800-38700200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr10:38692800-38701800	Weak transcription	Fetal Intestine Small	intestine
15	chr10:38692800-38703200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr10:38692800-38709200	Weak transcription	Adipose Nuclei	Adipose
17	chr10:38692800-38714600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr10:38692800-38728800	Weak transcription	Brain Substantia Nigra	brain
19	chr10:38692800-38736800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr10:38692800-38736800	Weak transcription	Brain Anterior Caudate	brain
21	chr10:38692800-38736800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr10:38692800-38737200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr10:38692800-38737200	Weak transcription	Brain Hippocampus Middle	brain
24	chr10:38692800-38737400	Weak transcription	Fetal Intestine Large	intestine
25	chr10:38692800-38737600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr10:38692800-38741200	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr10:38693000-38697200	Weak transcription	Liver	Liver
28	chr10:38693000-38698000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr10:38693000-38698000	Weak transcription	Left Ventricle	heart
30	chr10:38693000-38700000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr10:38693000-38700200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr10:38693000-38714000	Weak transcription	Right Ventricle	heart
33	chr10:38693000-38716000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr10:38693000-38736800	Weak transcription	Stomach Smooth Muscle	stomach
35	chr10:38693000-38737200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr10:38693000-38737200	Weak transcription	Brain Cingulate Gyrus	brain
37	chr10:38693000-38737200	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr10:38693000-38737200	Weak transcription	Fetal Muscle Leg	muscle
39	chr10:38693000-38737400	Weak transcription	Placenta	Placenta
40	chr10:38693000-38739200	Weak transcription	Primary B cells from peripheral blood	blood
41	chr10:38693200-38698000	Weak transcription	Fetal Muscle Trunk	muscle
42	chr10:38693200-38699800	Weak transcription	Skeletal Muscle Male	skeletal muscle
43	chr10:38697200-38700600	Strong transcription	Liver	Liver
44	chr10:38698000-38698600	Genic enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr10:38698000-38698600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr10:38698000-38698600	Strong transcription	Ovary	ovary
47	chr10:38698000-38698600	Strong transcription	Spleen	Spleen
48	chr10:38698000-38698800	Strong transcription	Fetal Muscle Trunk	muscle
49	chr10:38698000-38698800	Strong transcription	Left Ventricle	heart
50	chr10:38698000-38698800	Strong transcription	Lung	lung

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