Variant report

Variant	nsv550044
Chromosome Location	chr10:18839350-18905935
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1044)
CpG islands
(count:366)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1044 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:18852867-18853155	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:18843485-18843910	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:18854097-18854130	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:18883708-18883996	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:18899277-18899936	HepG2	liver:	n/a	n/a
6	ARID3A	chr10:18872609-18872929	K562	blood:	n/a	n/a
7	ARID3A	chr10:18855015-18855499	HepG2	liver:	n/a	n/a
8	ARID3A	chr10:18871855-18872156	K562	blood:	n/a	n/a
9	ARID3A	chr10:18905265-18905558	HepG2	liver:	n/a	n/a
10	ARID3A	chr10:18847006-18847183	HepG2	liver:	n/a	n/a
11	ARID3A	chr10:18904510-18904940	HepG2	liver:	n/a	n/a
12	ARID3A	chr10:18850803-18851483	HepG2	liver:	n/a	n/a
13	ATF1	chr10:18871829-18872244	K562	blood:	n/a	n/a
14	ATF3	chr10:18899422-18899773	K562	blood:	n/a	n/a
15	ATF3	chr10:18899316-18899918	A549	lung:	n/a	n/a
16	BCL3	chr10:18899399-18899889	A549	lung:	n/a	chr10:18899618-18899627 chr10:18899617-18899626
17	BCL3	chr10:18899259-18899915	A549	lung:	n/a	chr10:18899618-18899627 chr10:18899617-18899626
18	BHLHE40	chr10:18883841-18883953	K562	blood:	n/a	n/a
19	BHLHE40	chr10:18899416-18899774	HepG2	liver:	n/a	n/a
20	BRCA1	chr10:18848238-18848611	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr10:18899413-18899828	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr10:18860126-18860500	GM12878	blood:	n/a	n/a
23	BRCA1	chr10:18860127-18860500	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr10:18866717-18867121	K562	blood:	n/a	n/a
25	CBX3	chr10:18899306-18899911	HCT-116	colon:	n/a	n/a
26	CBX3	chr10:18866819-18867030	K562	blood:	n/a	n/a
27	CEBPB	chr10:18905332-18905616	K562	blood:	n/a	chr10:18905467-18905478 chr10:18905467-18905480
28	CEBPB	chr10:18896887-18898030	A549	lung:	n/a	n/a
29	CEBPB	chr10:18905057-18905636	A549	lung:	n/a	chr10:18905467-18905478 chr10:18905467-18905480
30	CEBPB	chr10:18905280-18905585	MCF-7	breast:	n/a	chr10:18905467-18905478 chr10:18905467-18905480
31	CEBPB	chr10:18899297-18899950	A549	lung:	n/a	n/a
32	CEBPB	chr10:18899478-18899822	IMR90	lung:	n/a	n/a
33	CEBPB	chr10:18884993-18885181	A549	lung:	n/a	chr10:18885082-18885095
34	CEBPB	chr10:18899142-18899339	K562	blood:	n/a	n/a
35	CEBPB	chr10:18905155-18905787	A549	lung:	n/a	chr10:18905467-18905478 chr10:18905467-18905480
36	CEBPB	chr10:18896414-18896838	A549	lung:	n/a	n/a
37	CEBPB	chr10:18899449-18899705	HepG2	liver:	n/a	n/a
38	CEBPB	chr10:18899123-18899850	HepG2	liver:	n/a	n/a
39	CEBPB	chr10:18899357-18899980	HCT-116	colon:	n/a	n/a
40	CEBPB	chr10:18899369-18899850	A549	lung:	n/a	n/a
41	CEBPB	chr10:18872595-18872894	K562	blood:	n/a	n/a
42	CEBPB	chr10:18899349-18899886	A549	lung:	n/a	n/a
43	CEBPB	chr10:18905239-18905623	HepG2	liver:	n/a	chr10:18905467-18905478 chr10:18905467-18905480
44	CEBPB	chr10:18899386-18899890	MCF-7	breast:	n/a	n/a
45	CEBPB	chr10:18890991-18891113	HepG2	liver:	n/a	chr10:18891048-18891059
46	CEBPB	chr10:18904547-18904932	HepG2	liver:	n/a	n/a
47	CEBPB	chr10:18899351-18899802	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr10:18897524-18897856	A549	lung:	n/a	n/a
49	CEBPB	chr10:18854245-18854618	K562	blood:	n/a	n/a
50	CEBPB	chr10:18905309-18905644	A549	lung:	n/a	chr10:18905467-18905478 chr10:18905467-18905480

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:18875548-18875598	HAEpiC	amniotic membrane:	n/a
2	chr10:18895474-18895524	SK-N-SH_RA	brain:	n/a
3	chr10:18895474-18895524	PFSK-1	brain:	n/a
4	chr10:18898790-18898840	HRCEpiC	kidney:	n/a
5	chr10:18895474-18895524	NH-A	brain:	n/a
6	chr10:18898790-18898840	PrEC	prostate:	n/a
7	chr10:18875381-18875431	SKMC	muscle:	n/a
8	chr10:18875548-18875598	AG04449	skin:	fetal
9	chr10:18877005-18877055	K562	blood:	n/a
10	chr10:18875381-18875431	NHDF-neo	bronchial:	n/a
11	chr10:18898790-18898840	HMEC	breast:	n/a
12	chr10:18875473-18875523	BE2_C	brain:	n/a
13	chr10:18898790-18898840	HUVEC	blood vessel:	n/a
14	chr10:18877005-18877055	CMK	blood:	n/a
15	chr10:18875381-18875431	MCF10A-Er-Src	breast:	n/a
16	chr10:18875548-18875598	HRE	kidney:	n/a
17	chr10:18877005-18877055	NB4	blood:	n/a
18	chr10:18875548-18875598	SK-N-MC	brain:	n/a
19	chr10:18875381-18875431	GM19239	blood:	n/a
20	chr10:18895474-18895524	A549	lung:	n/a
21	chr10:18877005-18877055	HEK293	kidney:	embryo
22	chr10:18875548-18875598	PANC-1	pancreas:	n/a
23	chr10:18875473-18875523	LNCaP	prostate:	n/a
24	chr10:18877005-18877055	AG04450	lung:	fetal
25	chr10:18875473-18875523	Jurkat	blood:	n/a
26	chr10:18875473-18875523	AG04449	skin:	fetal
27	chr10:18875381-18875431	Hepatocyte	liver:	n/a
28	chr10:18875548-18875598	HCT-116	colon:	n/a
29	chr10:18898790-18898840	HL-60	blood:	n/a
30	chr10:18898790-18898840	SAEC	small airway:	n/a
31	chr10:18875548-18875598	GM19239	blood:	n/a
32	chr10:18898790-18898840	ProgFib	skin:	n/a
33	chr10:18875381-18875431	AG04449	skin:	fetal
34	chr10:18898790-18898840	HEEpiC	esophagus:	n/a
35	chr10:18875381-18875431	A549	lung:	n/a
36	chr10:18875381-18875431	NB4	blood:	n/a
37	chr10:18875548-18875598	HEEpiC	esophagus:	n/a
38	chr10:18898790-18898840	HRPEpiC	eye:	n/a
39	chr10:18875473-18875523	Hepatocyte	liver:	n/a
40	chr10:18875548-18875598	HepG2	liver:	n/a
41	chr10:18875473-18875523	HepG2	liver:	n/a
42	chr10:18877005-18877055	PFSK-1	brain:	n/a
43	chr10:18898790-18898840	BE2_C	brain:	n/a
44	chr10:18875548-18875598	SKMC	muscle:	n/a
45	chr10:18875381-18875431	HPAEpiC	pulmonary alveolar:	n/a
46	chr10:18877005-18877055	SK-N-SH	brain:	n/a
47	chr10:18898790-18898840	Jurkat	blood:	n/a
48	chr10:18895474-18895524	HRCEpiC	kidney:	n/a
49	chr10:18877005-18877055	SAEC	small airway:	n/a
50	chr10:18877005-18877055	PANC-1	pancreas:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:18893160..18894729-chr10:18899323..18901039,2	K562	blood:
2	chr10:18882733..18884546-chr10:18887488..18889531,2	MCF-7	breast:
3	chr10:18893160..18894729-chr10:18899323..18901039,2	K562	blood:
4	chr10:18892806..18896035-chr10:18901171..18903670,3	K562	blood:
5	chr10:18900986..18902692-chr10:18906814..18908491,2	MCF-7	breast:
6	chr10:18872028..18874928-chr10:18946049..18948722,4	K562	blood:
7	chr10:18897158..18899309-chr10:18901969..18904753,2	K562	blood:
8	chr10:18891764..18894660-chr10:18898788..18901660,3	K562	blood:
9	chr10:18891764..18894660-chr10:18898788..18901660,3	K562	blood:
10	chr10:18883515..18884111-chr10:18904979..18905887,2	MCF-7	breast:
11	chr10:18871041..18872755-chr10:18938799..18941399,2	K562	blood:
12	chr10:18832497..18833999-chr10:18887489..18889225,2	K562	blood:
13	chr1:1025004..1026004-chr10:18883636..18884321,2	MCF-7	breast:
14	chr10:18896603..18898658-chr10:18901969..18903863,2	K562	blood:
15	chr10:18892806..18896035-chr10:18901171..18903670,3	K562	blood:
16	chr10:18881247..18884169-chr10:18946476..18949026,2	K562	blood:
17	chr10:18904719..18906384-chr10:18907466..18910292,2	K562	blood:
18	chr10:18881247..18884193-chr10:18945949..18949026,3	K562	blood:
19	chr10:18901454..18904568-chr10:18946720..18950711,3	K562	blood:
20	chr10:18897158..18899309-chr10:18901969..18904753,2	K562	blood:
21	chr10:18882733..18884546-chr10:18887488..18889531,2	MCF-7	breast:
22	chr10:18896603..18898658-chr10:18901969..18903863,2	K562	blood:
23	chr10:18883515..18884111-chr10:18904979..18905887,2	MCF-7	breast:
24	chr10:18902407..18904405-chr10:18907032..18908667,2	K562	blood:

No data

Variant related genes	Relation type
NSUN6	TF binding region
ENSG00000240291	TF binding region
NSUN6	CpG island
ENSG00000240291	CpG island
ENSG00000165997	chromatin interactions
ENSG00000240291	chromatin interactions
ENSG00000241058	chromatin interactions
ENSG00000152487	chromatin interactions

Extended variants
information (count: 3587 )
Associated
traits (count: 41 )

Variant overlapped rSNPs/rCNVs (count:3587 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6482516	chr10:18839350-18839351	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs551794236	chr10:18839363-18839364	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs80054254	chr10:18839383-18839384	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs113524377	chr10:18839450-18839451	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371510115	chr10:18839451-18839452	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs184980957	chr10:18839452-18839453	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs188706686	chr10:18839453-18839454	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs535198745	chr10:18839483-18839484	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs61683342	chr10:18839487-18839488	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs146933805	chr10:18839640-18839641	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs577914407	chr10:18839643-18839644	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs202103632	chr10:18839647-18839648	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs66875630	chr10:18839658-18839659	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs368680742	chr10:18839659-18839660	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs373897642	chr10:18839672-18839673	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs368530000	chr10:18839673-18839674	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs538900581	chr10:18839680-18839681	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs549994540	chr10:18839723-18839724	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs181128995	chr10:18839730-18839731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs372615550	chr10:18839746-18839747	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs4328135	chr10:18839748-18839749	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs542282314	chr10:18839765-18839766	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs200050602	chr10:18839767-18839768	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200672877	chr10:18839772-18839773	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs7901598	chr10:18839779-18839780	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs572888844	chr10:18839813-18839814	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs183863784	chr10:18839827-18839828	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs199993908	chr10:18839843-18839844	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188394974	chr10:18839844-18839845	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs532348852	chr10:18839870-18839871	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs11014825	chr10:18839902-18839903	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs180803779	chr10:18839970-18839971	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs7097001	chr10:18839971-18839972	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs549136961	chr10:18839976-18839977	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs567739832	chr10:18839985-18839986	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs534853031	chr10:18839993-18839994	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546692933	chr10:18839994-18839995	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs187640977	chr10:18840054-18840055	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs190367168	chr10:18840064-18840065	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs557205732	chr10:18840082-18840083	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569739328	chr10:18840143-18840144	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs536232385	chr10:18840165-18840166	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs35396134	chr10:18840173-18840174	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs3223172	chr10:18840174-18840175	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs79238813	chr10:18840220-18840221	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs34031704	chr10:18840221-18840222	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs148243290	chr10:18840285-18840286	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs141272487	chr10:18840299-18840300	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs201273551	chr10:18840336-18840337	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs540282563	chr10:18840408-18840409	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:41)

Disease	PMID	Source
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
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
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal cancer	21851588	CNVD
Intracranial aneurysm	16715129	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	16616336	CNVD
T-cell lymphomas	19863542	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	22083797	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Olfactory neuroblastoma	18408657	CNVD

Chromatin state (count:1590 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:18815200-18843600	Weak transcription	A549	lung
2	chr10:18816400-18841800	Strong transcription	Liver	Liver
3	chr10:18820800-18841600	Weak transcription	Hela-S3	cervix
4	chr10:18822000-18840400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr10:18822000-18848000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr10:18822800-18841800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr10:18824200-18846200	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr10:18824200-18850600	Weak transcription	NHLF	lung
9	chr10:18825600-18841800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr10:18827200-18842000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr10:18827200-18845200	Weak transcription	NHEK	skin
12	chr10:18827400-18841600	Weak transcription	HMEC	breast
13	chr10:18827600-18839400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr10:18828600-18841600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr10:18828600-18841600	Weak transcription	Primary neutrophils fromperipheralblood	blood
16	chr10:18828600-18841800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr10:18828600-18841800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr10:18828600-18841800	Weak transcription	Pancreas	Pancrea
19	chr10:18828600-18843000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr10:18828600-18843400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr10:18828600-18844400	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr10:18828600-18845400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr10:18828800-18846000	Weak transcription	Spleen	Spleen
24	chr10:18829000-18840400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr10:18829000-18841800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr10:18829200-18851200	Weak transcription	Esophagus	oesophagus
27	chr10:18829800-18844000	Weak transcription	Brain Angular Gyrus	brain
28	chr10:18830000-18842000	Weak transcription	Fetal Brain Female	brain
29	chr10:18830000-18842400	Weak transcription	Brain Germinal Matrix	brain
30	chr10:18830200-18841400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr10:18830200-18841800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr10:18830200-18841800	Weak transcription	Aorta	Aorta
33	chr10:18830200-18851000	Weak transcription	Thymus	Thymus
34	chr10:18830400-18840000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr10:18830400-18840200	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr10:18830400-18840400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr10:18830400-18840400	Weak transcription	Brain Anterior Caudate	brain
38	chr10:18830400-18840400	Weak transcription	HSMMtube	muscle
39	chr10:18830400-18841600	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr10:18830400-18841800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr10:18830400-18841800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr10:18830400-18841800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
43	chr10:18830400-18841800	Weak transcription	Brain Cingulate Gyrus	brain
44	chr10:18830400-18841800	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr10:18830400-18841800	Weak transcription	Brain Substantia Nigra	brain
46	chr10:18830400-18841800	Weak transcription	Stomach Smooth Muscle	stomach
47	chr10:18830400-18843000	Weak transcription	Rectal Smooth Muscle	rectum
48	chr10:18830400-18856600	Weak transcription	Skeletal Muscle Male	skeletal muscle
49	chr10:18830600-18840200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr10:18830600-18840200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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