Variant report

Variant	nsv6132
Chromosome Location	chr10:27066081-27075522
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:141)
CpG islands
(count:61)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:141 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr10:27069978-27070519	GM12878	blood:	n/a	n/a
2	BATF	chr10:27072771-27073010	GM12878	blood:	n/a	chr10:27072862-27072873
3	CBX3	chr10:27069786-27070637	HCT-116	colon:	n/a	n/a
4	CCNT2	chr10:27068228-27068542	K562	blood:	n/a	n/a
5	CEBPB	chr10:27069982-27070428	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr10:27073858-27074371	MCF-7	breast:	n/a	chr10:27074099-27074110
7	CEBPB	chr10:27073928-27074275	K562	blood:	n/a	chr10:27074099-27074110
8	CEBPB	chr10:27069967-27070389	IMR90	lung:	n/a	n/a
9	CEBPB	chr10:27073920-27074259	A549	lung:	n/a	chr10:27074099-27074110
10	CEBPB	chr10:27073919-27074276	IMR90	lung:	n/a	chr10:27074099-27074110
11	CEBPB	chr10:27073915-27074274	Hela-S3	cervix:	n/a	chr10:27074099-27074110
12	CEBPB	chr10:27073967-27074172	H1-hESC	embryonic stem cell:	n/a	chr10:27074099-27074110
13	CEBPB	chr10:27070805-27071155	IMR90	lung:	n/a	n/a
14	CEBPB	chr10:27073943-27074197	HepG2	liver:	n/a	chr10:27074099-27074110
15	CTCF	chr10:27070200-27070350	HPAF	blood vessel:	n/a	n/a
16	CTCF	chr10:27070200-27070350	HMF	breast:	n/a	n/a
17	CTCF	chr10:27070200-27070350	HEEpiC	esophagus:	n/a	n/a
18	CTCF	chr10:27070240-27070390	AoAF	blood vessel:	n/a	n/a
19	CTCF	chr10:27074220-27074370	SAEC	small airway:	n/a	n/a
20	CTCF	chr10:27070340-27070490	HMEC	breast:	n/a	n/a
21	CTCF	chr10:27070201-27070375	GM12878	blood:	n/a	n/a
22	CTCF	chr10:27068200-27068350	GM12866	blood:	n/a	n/a
23	CTCF	chr10:27075220-27075256	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr10:27070430-27070463	Spleen_OC	spleen:	n/a	n/a
25	EBF1	chr10:27069942-27070858	GM12878	blood:	n/a	n/a
26	EBF1	chr10:27070228-27070628	GM12878	blood:	n/a	n/a
27	EBF1	chr10:27070105-27070585	GM12878	blood:	n/a	n/a
28	ELF1	chr10:27068108-27068423	K562	blood:	n/a	chr10:27068231-27068244 chr10:27068253-27068266
29	EP300	chr10:27070045-27070630	GM12878	blood:	n/a	n/a
30	FOS	chr10:27069989-27070376	HUVEC	blood vessel:	n/a	chr10:27070156-27070167 chr10:27070175-27070186
31	FOS	chr10:27069867-27070758	MCF10A-Er-Src	breast:	n/a	chr10:27070156-27070167 chr10:27070175-27070186
32	FOS	chr10:27073564-27074402	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr10:27073828-27074386	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr10:27069990-27070381	Hela-S3	cervix:	n/a	chr10:27070156-27070167 chr10:27070175-27070186
35	FOS	chr10:27069897-27070990	MCF10A-Er-Src	breast:	n/a	chr10:27070156-27070167 chr10:27070175-27070186
36	FOS	chr10:27073547-27074397	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr10:27069875-27070658	MCF10A-Er-Src	breast:	n/a	chr10:27070156-27070167 chr10:27070175-27070186
38	FOS	chr10:27073559-27074383	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr10:27069864-27071038	MCF10A-Er-Src	breast:	n/a	chr10:27070156-27070167 chr10:27070175-27070186
40	FOS	chr10:27070912-27071039	MCF10A-Er-Src	breast:	n/a	n/a
41	FOSL1	chr10:27069746-27070652	HCT-116	colon:	n/a	n/a
42	FOSL1	chr10:27069873-27070551	HCT-116	colon:	n/a	n/a
43	FOSL2	chr10:27069908-27070362	SK-N-SH	brain:	n/a	n/a
44	FOSL2	chr10:27069966-27070489	A549	lung:	n/a	n/a
45	FOSL2	chr10:27069791-27070566	A549	lung:	n/a	n/a
46	FOSL2	chr10:27069991-27070459	MCF-7	breast:	n/a	n/a
47	FOSL2	chr10:27070004-27070486	MCF-7	breast:	n/a	n/a
48	FOSL2	chr10:27069849-27070590	SK-N-SH	brain:	n/a	n/a
49	GATA3	chr10:27074031-27074635	MCF-7	breast:	n/a	n/a
50	GTF2F1	chr10:27070028-27070636	Hela-S3	cervix:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:27070113-27070163	Hepatocyte	liver:	n/a
2	chr10:27070113-27070163	RPTEC	kidney:	n/a
3	chr10:27070113-27070163	ovcar-3	ovarian:	n/a
4	chr10:27070113-27070163	HCT-116	colon:	n/a
5	chr10:27070113-27070163	PrEC	prostate:	n/a
6	chr10:27070113-27070163	HEEpiC	esophagus:	n/a
7	chr10:27070113-27070163	GM12891	blood:	n/a
8	chr10:27070113-27070163	SK-N-SH	brain:	n/a
9	chr10:27070113-27070163	HCF	heart:	n/a
10	chr10:27070113-27070163	NHDF-neo	bronchial:	n/a
11	chr10:27070113-27070163	AG09319	gingival:	n/a
12	chr10:27070113-27070163	HCPEpiC	choroid plexus:	n/a
13	chr10:27070113-27070163	NT2-D1	testis:	n/a
14	chr10:27070113-27070163	AG04449	skin:	fetal
15	chr10:27070113-27070163	K562	blood:	n/a
16	chr10:27070113-27070163	U87	brain:	n/a
17	chr10:27070113-27070163	MCF-7	breast:	n/a
18	chr10:27070113-27070163	AG04450	lung:	fetal
19	chr10:27070113-27070163	SKMC	muscle:	n/a
20	chr10:27070113-27070163	HIPEpiC	eye:	n/a
21	chr10:27070113-27070163	BE2_C	brain:	n/a
22	chr10:27070113-27070163	NH-A	brain:	n/a
23	chr10:27070113-27070163	LNCaP	prostate:	n/a
24	chr10:27070113-27070163	HCM	heart:	n/a
25	chr10:27070113-27070163	AG10803	skin:	n/a
26	chr10:27070113-27070163	IMR90	lung:	fetal
27	chr10:27070113-27070163	PFSK-1	brain:	n/a
28	chr10:27070113-27070163	SK-N-MC	brain:	n/a
29	chr10:27070113-27070163	T-47D	breast:	n/a
30	chr10:27070113-27070163	CMK	blood:	n/a
31	chr10:27070113-27070163	HRPEpiC	eye:	n/a
32	chr10:27070113-27070163	HAEpiC	amniotic membrane:	n/a
33	chr10:27070113-27070163	A549	lung:	n/a
34	chr10:27070113-27070163	NB4	blood:	n/a
35	chr10:27070113-27070163	HL-60	blood:	n/a
36	chr10:27070113-27070163	HUVEC	blood vessel:	n/a
37	chr10:27070113-27070163	NHBE	bronchial:	n/a
38	chr10:27070113-27070163	AoSMC	blood vessel:	n/a
39	chr10:27070113-27070163	HRCEpiC	kidney:	n/a
40	chr10:27070113-27070163	GM19239	blood:	n/a
41	chr10:27070113-27070163	GM12878	blood:	n/a
42	chr10:27070113-27070163	BJ	skin:	n/a
43	chr10:27070113-27070163	HRE	kidney:	n/a
44	chr10:27070113-27070163	AG09309	skin:	n/a
45	chr10:27070113-27070163	GM12892	blood:	n/a
46	chr10:27070113-27070163	HMEC	breast:	n/a
47	chr10:27070113-27070163	SK-N-SH_RA	brain:	n/a
48	chr10:27070113-27070163	HNPCEpiC	eye:	n/a
49	chr10:27070113-27070163	SAEC	small airway:	n/a
50	chr10:27070113-27070163	HEK293	kidney:	embryo

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:27074245..27076242-chr10:27078041..27079548,2	MCF-7	breast:
2	chr10:27057922..27061577-chr10:27062885..27066099,3	K562	blood:
3	chr10:27070974..27073894-chr10:27148134..27150716,3	MCF-7	breast:
4	chr10:27074239..27077172-chr10:27148340..27151224,5	MCF-7	breast:
5	chr10:27050958..27053361-chr10:27064664..27066891,2	K562	blood:
6	chr10:27064202..27066612-chr10:27068536..27071634,3	K562	blood:
7	chr10:27071993..27074236-chr10:27148436..27150093,2	MCF-7	breast:
8	chr10:27054901..27057514-chr10:27069095..27071711,3	MCF-7	breast:
9	chr10:27066132..27067920-chr10:27074183..27076184,2	K562	blood:
10	chr10:27066132..27067920-chr10:27074183..27076184,2	K562	blood:
11	chr10:27061393..27062937-chr10:27066179..27068006,2	MCF-7	breast:
12	chr10:27067079..27070597-chr10:27072640..27074844,4	K562	blood:
13	chr10:27073078..27074935-chr10:27148333..27150643,2	K562	blood:
14	chr10:27064202..27066612-chr10:27068536..27071634,3	K562	blood:
15	chr10:27068463..27071008-chr10:27149449..27152029,3	K562	blood:
16	chr10:27067079..27070597-chr10:27072640..27074844,4	K562	blood:
17	chr10:27063322..27065877-chr10:27068617..27071382,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000223027	TF binding region
ENSG00000223027	CpG island
ENSG00000136754	chromatin interactions

Extended variants
information (count: 354 )
Associated
traits (count: 45 )

Variant overlapped rSNPs/rCNVs (count:354 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200435060	chr10:27066106-27066107	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs201251251	chr10:27066107-27066108	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs544190583	chr10:27066144-27066145	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs181326046	chr10:27066184-27066185	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs367856868	chr10:27066216-27066217	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs10829062	chr10:27066379-27066380	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs532250921	chr10:27066398-27066399	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs150163724	chr10:27066413-27066414	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs72485032	chr10:27066417-27066418	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528643996	chr10:27066431-27066432	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs545219840	chr10:27066433-27066434	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs75955675	chr10:27066481-27066482	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs530897522	chr10:27066487-27066488	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs4448587	chr10:27066513-27066514	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs184585404	chr10:27066523-27066524	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs567650811	chr10:27066564-27066565	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs530653533	chr10:27066578-27066579	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs530083536	chr10:27066581-27066582	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs550656011	chr10:27066636-27066637	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs370263112	chr10:27066638-27066639	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs544311246	chr10:27066679-27066680	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs1853685	chr10:27066732-27066733	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs566653726	chr10:27066737-27066738	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs561135118	chr10:27066782-27066783	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs11015280	chr10:27066942-27066943	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs558798608	chr10:27066943-27066944	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs532980905	chr10:27066944-27066945	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs569104900	chr10:27066950-27066951	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs116017048	chr10:27066966-27066967	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs540280413	chr10:27066993-27066994	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs368368501	chr10:27066995-27066996	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs546877268	chr10:27067019-27067020	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs117038549	chr10:27067035-27067036	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs574364812	chr10:27067040-27067041	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs539857049	chr10:27067045-27067046	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs111764320	chr10:27067047-27067048	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs377099722	chr10:27067060-27067061	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368473704	chr10:27067065-27067066	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs552225443	chr10:27067096-27067097	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs553603005	chr10:27067114-27067115	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs566610592	chr10:27067205-27067206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs573474049	chr10:27067220-27067221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs565057199	chr10:27067224-27067225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs545329022	chr10:27067271-27067272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs565116092	chr10:27067282-27067283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs531057901	chr10:27067309-27067310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs565656112	chr10:27067356-27067357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs529269823	chr10:27067389-27067390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs141693286	chr10:27067395-27067396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs201187734	chr10:27067427-27067428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:45)

Disease	PMID	Source
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
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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
T-cell lymphomas	19863542	CNVD
Esophageal cancer	21851588	CNVD
Behavioral abnormalities	21522184	CNVD
Dysmorphic features	21522184	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Autism	21439084	CNVD
Maculopathy	20981449	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Adrenocortical carcinoma	18281524	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	17440070	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:480 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26988000-27069600	Weak transcription	Colon Smooth Muscle	Colon
2	chr10:27021600-27069600	Weak transcription	Esophagus	oesophagus
3	chr10:27023400-27070000	Weak transcription	Pancreas	Pancrea
4	chr10:27025600-27069600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr10:27025800-27068200	Weak transcription	Spleen	Spleen
6	chr10:27025800-27070800	Weak transcription	Aorta	Aorta
7	chr10:27026000-27069600	Weak transcription	Brain Angular Gyrus	brain
8	chr10:27027400-27069400	Weak transcription	Brain Hippocampus Middle	brain
9	chr10:27027800-27069600	Weak transcription	Rectal Smooth Muscle	rectum
10	chr10:27028200-27068600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr10:27028400-27069800	Weak transcription	NHLF	lung
12	chr10:27029800-27069600	Weak transcription	HSMMtube	muscle
13	chr10:27032000-27068200	Weak transcription	Small Intestine	intestine
14	chr10:27032000-27069600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr10:27032400-27069400	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr10:27032400-27069600	Weak transcription	Lung	lung
17	chr10:27032600-27069800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr10:27033600-27069200	Weak transcription	Psoas Muscle	Psoas
19	chr10:27034000-27069000	Weak transcription	Colonic Mucosa	Colon
20	chr10:27034000-27069600	Weak transcription	Ovary	ovary
21	chr10:27034000-27069800	Weak transcription	Stomach Smooth Muscle	stomach
22	chr10:27034400-27069600	Weak transcription	Right Ventricle	heart
23	chr10:27036800-27068400	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr10:27044800-27068000	Weak transcription	K562	blood
25	chr10:27044800-27068400	Weak transcription	A549	lung
26	chr10:27044800-27069000	Weak transcription	Brain Cingulate Gyrus	brain
27	chr10:27044800-27069600	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr10:27044800-27070400	Weak transcription	HUVEC	blood vessel
29	chr10:27044800-27082000	Weak transcription	Fetal Lung	lung
30	chr10:27048200-27069400	Weak transcription	NHDF-Ad	bronchial
31	chr10:27051400-27082000	Weak transcription	Fetal Stomach	stomach
32	chr10:27054200-27066800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr10:27054400-27068400	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr10:27054600-27068400	Weak transcription	Thymus	Thymus
35	chr10:27054800-27067400	Weak transcription	Fetal Muscle Trunk	muscle
36	chr10:27054800-27069000	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr10:27055400-27069000	Weak transcription	HSMM	muscle
38	chr10:27055600-27070200	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr10:27056600-27067000	Weak transcription	GM12878-XiMat	blood
40	chr10:27056600-27068400	Weak transcription	Duodenum Mucosa	Duodenum
41	chr10:27056600-27069200	Weak transcription	Placenta	Placenta
42	chr10:27057000-27067600	Weak transcription	Primary hematopoietic stem cells	blood
43	chr10:27057200-27069600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr10:27057600-27068600	Weak transcription	Fetal Intestine Small	intestine
45	chr10:27057800-27067800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr10:27057800-27072000	Weak transcription	Cortex derived primary cultured neurospheres	brain
47	chr10:27058000-27067800	Weak transcription	Fetal Intestine Large	intestine
48	chr10:27058000-27067800	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr10:27058000-27068200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
50	chr10:27058000-27072200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links