Variant report

Variant	nsv895113
Chromosome Location	chr10:46134013-46167847
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:391)
CpG islands
(count:244)
Chromatin interactive
region (count:9)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:391 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:46150304-46150339	HepG2	liver:	n/a	n/a
2	ATF1	chr10:46156450-46156572	K562	blood:	n/a	n/a
3	ATF1	chr10:46152214-46152277	K562	blood:	n/a	n/a
4	ATF2	chr10:46148813-46149349	GM12878	blood:	n/a	n/a
5	BACH1	chr10:46167812-46168617	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr10:46157638-46157843	GM12878	blood:	n/a	chr10:46157746-46157757
7	BATF	chr10:46157597-46157840	GM12878	blood:	n/a	chr10:46157746-46157757
8	BCLAF1	chr10:46167390-46168501	GM12878	blood:	n/a	chr10:46168230-46168239 chr10:46168224-46168237
9	BCLAF1	chr10:46167595-46168410	GM12878	blood:	n/a	chr10:46168230-46168239 chr10:46168224-46168237
10	BHLHE40	chr10:46167662-46168605	HepG2	liver:	n/a	chr10:46168224-46168240
11	BHLHE40	chr10:46167585-46168551	GM12878	blood:	n/a	chr10:46168224-46168240
12	CCNT2	chr10:46167817-46168282	K562	blood:	n/a	chr10:46168238-46168247
13	CEBPB	chr10:46167682-46168406	IMR90	lung:	n/a	n/a
14	CEBPB	chr10:46152546-46152811	ECC-1	luminal epithelium:	n/a	n/a
15	CEBPB	chr10:46135637-46135875	K562	blood:	n/a	chr10:46135761-46135772
16	CEBPB	chr10:46157190-46157394	IMR90	lung:	n/a	n/a
17	CEBPB	chr10:46152562-46152769	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr10:46167842-46168114	HepG2	liver:	n/a	n/a
19	CEBPB	chr10:46167682-46168448	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr10:46160272-46160420	HepG2	liver:	n/a	chr10:46160329-46160340
21	CEBPB	chr10:46152497-46152834	ECC-1	luminal epithelium:	n/a	n/a
22	CEBPB	chr10:46160234-46160477	K562	blood:	n/a	chr10:46160329-46160340
23	CEBPB	chr10:46160295-46160513	IMR90	lung:	n/a	chr10:46160329-46160340
24	CEBPB	chr10:46135741-46135795	A549	lung:	n/a	chr10:46135761-46135772
25	CEBPB	chr10:46167847-46168384	HepG2	liver:	n/a	n/a
26	CEBPB	chr10:46148631-46148831	HepG2	liver:	n/a	chr10:46148721-46148732
27	CEBPB	chr10:46152455-46152828	K562	blood:	n/a	n/a
28	CEBPB	chr10:46135650-46135806	HepG2	liver:	n/a	chr10:46135761-46135772
29	CEBPB	chr10:46149925-46150122	HepG2	liver:	n/a	n/a
30	CEBPB	chr10:46157182-46157527	K562	blood:	n/a	n/a
31	CEBPB	chr10:46160373-46160393	A549	lung:	n/a	n/a
32	CEBPB	chr10:46152582-46152790	K562	blood:	n/a	n/a
33	CEBPB	chr10:46152566-46152838	HepG2	liver:	n/a	n/a
34	CEBPB	chr10:46167847-46168212	A549	lung:	n/a	n/a
35	CEBPB	chr10:46167616-46168260	MCF-7	breast:	n/a	n/a
36	CEBPB	chr10:46157241-46157495	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr10:46152487-46152846	IMR90	lung:	n/a	n/a
38	CEBPB	chr10:46152503-46152839	A549	lung:	n/a	n/a
39	CEBPB	chr10:46152480-46152825	MCF-7	breast:	n/a	n/a
40	CEBPB	chr10:46167675-46169013	HepG2	liver:	n/a	n/a
41	CEBPB	chr10:46152485-46152850	K562	blood:	n/a	n/a
42	CEBPB	chr10:46157329-46157384	A549	lung:	n/a	n/a
43	CEBPB	chr10:46152532-46152732	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr10:46152521-46152851	A549	lung:	n/a	n/a
45	CEBPB	chr10:46167613-46168447	A549	lung:	n/a	n/a
46	CEBPB	chr10:46152590-46152879	A549	lung:	n/a	n/a
47	CEBPD	chr10:46167664-46168106	HepG2	liver:	n/a	n/a
48	CHD1	chr10:46167419-46168031	H1-hESC	embryonic stem cell:	n/a	chr10:46167673-46167683
49	CHD1	chr10:46167424-46168273	GM12878	blood:	n/a	chr10:46168236-46168246 chr10:46167673-46167683
50	CHD2	chr10:46167716-46168523	GM12878	blood:	n/a	chr10:46168236-46168246

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:46167678-46167728	BJ	skin:	n/a
2	chr10:46158095-46158145	NB4	blood:	n/a
3	chr10:46167626-46167676	MCF-7	breast:	n/a
4	chr10:46167678-46167728	NT2-D1	testis:	n/a
5	chr10:46164062-46164112	LNCaP	prostate:	n/a
6	chr10:46167626-46167676	BJ	skin:	n/a
7	chr10:46167678-46167728	MCF-7	breast:	n/a
8	chr10:46158095-46158145	BE2_C	brain:	n/a
9	chr10:46158095-46158145	GM06990	blood:	n/a
10	chr10:46167626-46167676	HIPEpiC	eye:	n/a
11	chr10:46167678-46167728	AG09309	skin:	n/a
12	chr10:46167626-46167676	IMR90	lung:	fetal
13	chr10:46167678-46167728	HPAEpiC	pulmonary alveolar:	n/a
14	chr10:46164062-46164112	AG09319	gingival:	n/a
15	chr10:46158095-46158145	NT2-D1	testis:	n/a
16	chr10:46167678-46167728	HAEpiC	amniotic membrane:	n/a
17	chr10:46167626-46167676	HL-60	blood:	n/a
18	chr10:46164062-46164112	BJ	skin:	n/a
19	chr10:46167626-46167676	HAEpiC	amniotic membrane:	n/a
20	chr10:46164062-46164112	HepG2	liver:	n/a
21	chr10:46158095-46158145	IMR90	lung:	fetal
22	chr10:46164062-46164112	GM06990	blood:	n/a
23	chr10:46167678-46167728	SAEC	small airway:	n/a
24	chr10:46164062-46164112	HL-60	blood:	n/a
25	chr10:46167626-46167676	PANC-1	pancreas:	n/a
26	chr10:46167678-46167728	AG10803	skin:	n/a
27	chr10:46158095-46158145	HRPEpiC	eye:	n/a
28	chr10:46164062-46164112	HNPCEpiC	eye:	n/a
29	chr10:46167626-46167676	SK-N-SH_RA	brain:	n/a
30	chr10:46167626-46167676	GM12891	blood:	n/a
31	chr10:46158095-46158145	HIPEpiC	eye:	n/a
32	chr10:46167678-46167728	GM12892	blood:	n/a
33	chr10:46167626-46167676	AG09319	gingival:	n/a
34	chr10:46164062-46164112	RPTEC	kidney:	n/a
35	chr10:46167678-46167728	CMK	blood:	n/a
36	chr10:46164062-46164112	ECC-1	luminal epithelium:	n/a
37	chr10:46164062-46164112	HRPEpiC	eye:	n/a
38	chr10:46167678-46167728	SK-N-SH_RA	brain:	n/a
39	chr10:46167678-46167728	ProgFib	skin:	n/a
40	chr10:46167626-46167676	AG10803	skin:	n/a
41	chr10:46164062-46164112	NHDF-neo	bronchial:	n/a
42	chr10:46167678-46167728	BE2_C	brain:	n/a
43	chr10:46167626-46167676	AG09309	skin:	n/a
44	chr10:46164062-46164112	HEEpiC	esophagus:	n/a
45	chr10:46167678-46167728	NHBE	bronchial:	n/a
46	chr10:46164062-46164112	ovcar-3	ovarian:	n/a
47	chr10:46167678-46167728	HL-60	blood:	n/a
48	chr10:46158095-46158145	PrEC	prostate:	n/a
49	chr10:46167678-46167728	ECC-1	luminal epithelium:	n/a
50	chr10:46167678-46167728	SKMC	muscle:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr10:46133340..46134958-chr10:46138632..46141400,2	K562	blood:
2	chr10:46167759..46168599-chr16:3450730..3451510,2	HCT-116	colon:
3	chr10:46154690..46156464-chr10:46158011..46159852,2	K562	blood:
4	chr10:46102379..46105047-chr10:46138813..46141083,2	K562	blood:
5	chr10:46133340..46134958-chr10:46138632..46141400,2	K562	blood:
6	chr10:46135491..46137232-chr10:46139389..46142363,2	K562	blood:
7	chr10:46163208..46166100-chr10:46169984..46171505,2	K562	blood:
8	chr10:46154690..46156464-chr10:46158011..46159852,2	K562	blood:
9	chr10:46135491..46137232-chr10:46139389..46142363,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MARCH8-3	chr10:46147414-46147481	NR_104256
2	lnc-MARCH8-3	chr10:46158990-46159290	NR_104256
3	lnc-MARCH8-3	chr10:46143742-46143982	NR_104256
4	lnc-MARCH8-3	chr10:46148432-46148507	NR_104256
5	lnc-MARCH8-3	chr10:46135689-46135869	NR_104256
6	lnc-MARCH8-3	chr10:46135154-46135411	NR_104256

No data

Variant related genes	Relation type
ZFAND4	TF binding region
ZFAND4	CpG island
ENSG00000103343	chromatin interactions
ENSG00000140987	chromatin interactions

Extended variants
information (count: 1280 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1280 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs386743357	chr10:46134013-46134014	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs182137644	chr10:46134014-46134015	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
3	rs201920449	chr10:46134015-46134016	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs113969208	chr10:46134016-46134017	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
5	rs146317496	chr10:46134035-46134036	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs114433908	chr10:46134038-46134039	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs182777872	chr10:46134118-46134119	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs78230012	chr10:46134208-46134209	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
9	rs527842656	chr10:46134239-46134240	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs551497383	chr10:46134304-46134305	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563095612	chr10:46134319-46134320	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs571094150	chr10:46134367-46134368	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs576151819	chr10:46134398-46134399	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538143887	chr10:46134559-46134560	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs567379767	chr10:46134647-46134648	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs139628770	chr10:46134662-46134663	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs376084000	chr10:46134684-46134685	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs567714110	chr10:46134688-46134689	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs535119430	chr10:46134692-46134693	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs188738164	chr10:46134699-46134700	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs192833282	chr10:46134705-46134706	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs369774838	chr10:46134710-46134711	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs35599803	chr10:46134784-46134785	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs117692917	chr10:46134820-46134821	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs185817830	chr10:46134896-46134897	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555674947	chr10:46134908-46134909	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs574846677	chr10:46134940-46134941	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs542248147	chr10:46134950-46134951	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs79050563	chr10:46134980-46134981	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
30	rs150626550	chr10:46135012-46135013	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs372939282	chr10:46135017-46135018	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201653168	chr10:46135052-46135053	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200016388	chr10:46135056-46135057	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs111587270	chr10:46135059-46135060	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200902405	chr10:46135060-46135061	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs113200519	chr10:46135061-46135062	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546316087	chr10:46135117-46135118	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs112606631	chr10:46135162-46135163	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs531976575	chr10:46135207-46135208	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs41301629	chr10:46135215-46135216	Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs199626254	chr10:46135221-46135222	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs372721395	chr10:46135291-46135292	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs149209361	chr10:46135305-46135306	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs201853061	chr10:46135316-46135317	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs371565449	chr10:46135366-46135367	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs143924829	chr10:46135376-46135377	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs199995795	chr10:46135407-46135408	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs370008256	chr10:46135424-46135425	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs530371917	chr10:46135472-46135473	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs139963952	chr10:46135563-46135564	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	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
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Glioblastoma multiforme	21138945	CNVD
Autism	19287141	CNVD
Intellectual disability	21948486	CNVD
Glioblastoma multiforme	21525872	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
early-passage human iPS cells	21368824	CNVD
Acute myeloid leukemia	19651601	CNVD
Breast cancer	20409316	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Rett syndrome	21593744	CNVD
Glioblastoma multiforme	22286061	CNVD
Neuroblastoma	21899760	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:771 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:46090600-46167600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr10:46096200-46142000	Weak transcription	Brain Anterior Caudate	brain
3	chr10:46098200-46153400	Weak transcription	HSMM	muscle
4	chr10:46100200-46142600	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr10:46103400-46142200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr10:46103800-46134600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr10:46104400-46151400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr10:46105600-46141600	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr10:46106400-46137000	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr10:46106400-46141400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr10:46106400-46142000	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr10:46106800-46142000	Weak transcription	Fetal Kidney	kidney
13	chr10:46106800-46146400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr10:46107800-46141800	Weak transcription	Colon Smooth Muscle	Colon
15	chr10:46107800-46142000	Weak transcription	Esophagus	oesophagus
16	chr10:46108000-46155800	Weak transcription	Brain Angular Gyrus	brain
17	chr10:46108200-46142000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr10:46108400-46142000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr10:46108400-46149400	Weak transcription	Rectal Smooth Muscle	rectum
20	chr10:46108400-46167000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr10:46108600-46149200	Weak transcription	Brain Hippocampus Middle	brain
22	chr10:46108600-46155400	Weak transcription	Fetal Intestine Small	intestine
23	chr10:46108800-46142000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr10:46110200-46153800	Weak transcription	NH-A	brain
25	chr10:46110800-46156800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr10:46112200-46152400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
27	chr10:46118800-46142400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr10:46119800-46137000	Weak transcription	Primary hematopoietic stem cells	blood
29	chr10:46119800-46148200	Weak transcription	Colonic Mucosa	Colon
30	chr10:46120000-46157800	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr10:46120200-46148400	Weak transcription	Small Intestine	intestine
32	chr10:46122200-46142000	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr10:46122200-46154600	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr10:46122200-46157200	Weak transcription	Gastric	stomach
35	chr10:46122400-46137200	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr10:46122400-46141800	Weak transcription	Rectal Mucosa Donor 31	rectum
37	chr10:46122400-46142000	Weak transcription	Fetal Lung	lung
38	chr10:46122400-46142200	Weak transcription	Fetal Muscle Trunk	muscle
39	chr10:46122400-46149000	Weak transcription	Brain Substantia Nigra	brain
40	chr10:46122400-46156400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr10:46122600-46136400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr10:46122600-46139400	Weak transcription	Duodenum Mucosa	Duodenum
43	chr10:46122600-46140600	Weak transcription	Primary monocytes fromperipheralblood	blood
44	chr10:46122600-46141400	Weak transcription	Primary neutrophils fromperipheralblood	blood
45	chr10:46122600-46141800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr10:46122600-46142000	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr10:46122600-46142000	Weak transcription	Fetal Muscle Leg	muscle
48	chr10:46122600-46142000	Weak transcription	Stomach Smooth Muscle	stomach
49	chr10:46122600-46142400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
50	chr10:46122600-46142400	Weak transcription	Primary T helper naive cells from peripheral blood	blood

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