Variant report

Variant	nsv7506
Chromosome Location	chr10:98902440-98940209
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:98939729-98939731	HepG2	liver:	n/a	n/a
2	ATF1	chr10:98920686-98920872	K562	blood:	n/a	n/a
3	BHLHE40	chr10:98917393-98917956	GM12878	blood:	n/a	n/a
4	BHLHE40	chr10:98917398-98917659	HepG2	liver:	n/a	n/a
5	BRCA1	chr10:98939895-98939926	HepG2	liver:	n/a	n/a
6	CEBPB	chr10:98915492-98915971	HepG2	liver:	n/a	chr10:98915541-98915550 chr10:98915541-98915550 chr10:98915541-98915552 chr10:98915541-98915550 chr10:98915539-98915552 chr10:98915541-98915550
7	CEBPB	chr10:98915482-98915923	A549	lung:	n/a	chr10:98915541-98915550 chr10:98915541-98915550 chr10:98915541-98915552 chr10:98915541-98915550 chr10:98915539-98915552 chr10:98915541-98915550
8	CEBPB	chr10:98915557-98915926	IMR90	lung:	n/a	n/a
9	CEBPB	chr10:98911401-98911670	A549	lung:	n/a	n/a
10	CEBPB	chr10:98906981-98907184	HepG2	liver:	n/a	chr10:98907041-98907052
11	CEBPB	chr10:98906963-98907192	K562	blood:	n/a	chr10:98907041-98907052
12	CEBPB	chr10:98905789-98905838	HepG2	liver:	n/a	n/a
13	CEBPB	chr10:98915721-98915885	HepG2	liver:	n/a	n/a
14	CEBPD	chr10:98917277-98917600	HepG2	liver:	n/a	n/a
15	CHD2	chr10:98927414-98927695	K562	blood:	n/a	n/a
16	CHD2	chr10:98917432-98917667	HepG2	liver:	n/a	n/a
17	CHD2	chr10:98917333-98917693	GM12878	blood:	n/a	n/a
18	CTCF	chr10:98939720-98939870	HVMF	connective:	n/a	chr10:98939793-98939802 chr10:98939789-98939802 chr10:98939792-98939805
19	CTCF	chr10:98939640-98939790	HFF-Myc	foreskin:	n/a	n/a
20	CTCF	chr10:98930160-98930310	MCF-7	breast:	n/a	chr10:98930241-98930254
21	CTCF	chr10:98930171-98930237	Hela-S3	cervix:	n/a	n/a
22	CTCF	chr10:98939680-98939830	GM12870	blood:	n/a	chr10:98939793-98939802 chr10:98939789-98939802 chr10:98939792-98939805
23	CTCF	chr10:98940140-98940290	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr10:98913000-98913150	SK-N-SH_RA	brain:	n/a	n/a
25	CTCF	chr10:98939720-98939870	BE2_C	brain:	n/a	chr10:98939793-98939802 chr10:98939789-98939802 chr10:98939792-98939805
26	CTCF	chr10:98939680-98939830	GM12865	blood:	n/a	chr10:98939793-98939802 chr10:98939789-98939802 chr10:98939792-98939805
27	CTCF	chr10:98939620-98939920	HepG2	liver:	n/a	chr10:98939793-98939802 chr10:98939789-98939802 chr10:98939792-98939805
28	CTCF	chr10:98917420-98917570	GM06990	blood:	n/a	n/a
29	CTCF	chr10:98939720-98939870	HAc	cerebellar:	n/a	chr10:98939793-98939802 chr10:98939789-98939802 chr10:98939792-98939805
30	CTCF	chr10:98939640-98939790	GM12869	blood:	n/a	n/a
31	CTCF	chr10:98939737-98939849	Spleen_OC	spleen:	n/a	chr10:98939793-98939802 chr10:98939789-98939802 chr10:98939792-98939805
32	CTCF	chr10:98939700-98939850	GM12865	blood:	n/a	chr10:98939793-98939802 chr10:98939789-98939802 chr10:98939792-98939805
33	CTCF	chr10:98939760-98939910	HPF	lung:	n/a	chr10:98939793-98939802 chr10:98939789-98939802 chr10:98939792-98939805
34	CTCF	chr10:98939700-98939850	HCPEpiC	choroid plexus:	n/a	chr10:98939793-98939802 chr10:98939789-98939802 chr10:98939792-98939805
35	CTCF	chr10:98939620-98939770	HFF-Myc	foreskin:	n/a	n/a
36	CTCF	chr10:98939185-98940750	SK-N-SH	brain:	n/a	chr10:98939793-98939802 chr10:98939453-98939461 chr10:98939789-98939802 chr10:98939792-98939805
37	CTCF	chr10:98917503-98917578	GM19240	blood:	n/a	n/a
38	CTCF	chr10:98939660-98939810	SAEC	small airway:	n/a	chr10:98939793-98939802 chr10:98939789-98939802 chr10:98939792-98939805
39	CTCF	chr10:98939747-98939866	MCF-7	breast:	n/a	chr10:98939793-98939802 chr10:98939789-98939802 chr10:98939792-98939805
40	CTCF	chr10:98939700-98939850	NHDF-neo	bronchial:	n/a	chr10:98939793-98939802 chr10:98939789-98939802 chr10:98939792-98939805
41	CTCF	chr10:98917530-98917585	GM19238	blood:	n/a	n/a
42	CTCF	chr10:98930140-98930290	Caco-2	colon:	n/a	chr10:98930241-98930254
43	CTCF	chr10:98930940-98931090	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr10:98939700-98939850	GM12874	blood:	n/a	chr10:98939793-98939802 chr10:98939789-98939802 chr10:98939792-98939805
45	CTCF	chr10:98939680-98939830	GM12864	blood:	n/a	chr10:98939793-98939802 chr10:98939789-98939802 chr10:98939792-98939805
46	CTCF	chr10:98940200-98940350	BE2_C	brain:	n/a	n/a
47	CTCF	chr10:98926540-98926690	HepG2	liver:	n/a	n/a
48	CTCF	chr10:98939720-98939870	SK-N-SH_RA	brain:	n/a	chr10:98939793-98939802 chr10:98939789-98939802 chr10:98939792-98939805
49	CTCF	chr10:98939700-98939850	AG09319	gingival:	n/a	chr10:98939793-98939802 chr10:98939789-98939802 chr10:98939792-98939805
50	CTCF	chr10:98939680-98939830	HRE	kidney:	n/a	chr10:98939793-98939802 chr10:98939789-98939802 chr10:98939792-98939805

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:98939742-98939792	BE2_C	brain:	n/a
2	chr10:98908962-98909012	HRCEpiC	kidney:	n/a
3	chr10:98939742-98939792	HL-60	blood:	n/a
4	chr10:98939742-98939792	HPAEpiC	pulmonary alveolar:	n/a
5	chr10:98908962-98909012	T-47D	breast:	n/a
6	chr10:98909007-98909057	HL-60	blood:	n/a
7	chr10:98909007-98909057	SK-N-MC	brain:	n/a
8	chr10:98924236-98924286	SK-N-SH	brain:	n/a
9	chr10:98908962-98909012	NH-A	brain:	n/a
10	chr10:98939912-98939962	HEEpiC	esophagus:	n/a
11	chr10:98908962-98909012	HRPEpiC	eye:	n/a
12	chr10:98909007-98909057	MCF10A-Er-Src	breast:	n/a
13	chr10:98939912-98939962	BJ	skin:	n/a
14	chr10:98908755-98908805	HPAEpiC	pulmonary alveolar:	n/a
15	chr10:98939742-98939792	RPTEC	kidney:	n/a
16	chr10:98910008-98910058	HEK293	kidney:	embryo
17	chr10:98924236-98924286	MCF-7	breast:	n/a
18	chr10:98910008-98910058	MCF-7	breast:	n/a
19	chr10:98939912-98939962	Hepatocyte	liver:	n/a
20	chr10:98910008-98910058	HPAEpiC	pulmonary alveolar:	n/a
21	chr10:98908962-98909012	HEK293	kidney:	embryo
22	chr10:98910008-98910058	MCF10A-Er-Src	breast:	n/a
23	chr10:98924236-98924286	AG04450	lung:	fetal
24	chr10:98908755-98908805	H1-hESC	embryonic stem cell:	embryo
25	chr10:98908755-98908805	HEEpiC	esophagus:	n/a
26	chr10:98910008-98910058	SAEC	small airway:	n/a
27	chr10:98939742-98939792	PrEC	prostate:	n/a
28	chr10:98924236-98924286	HRPEpiC	eye:	n/a
29	chr10:98908962-98909012	BE2_C	brain:	n/a
30	chr10:98910008-98910058	A549	lung:	n/a
31	chr10:98908962-98909012	LNCaP	prostate:	n/a
32	chr10:98924236-98924286	HRCEpiC	kidney:	n/a
33	chr10:98939912-98939962	HUVEC	blood vessel:	n/a
34	chr10:98939742-98939792	GM19239	blood:	n/a
35	chr10:98939742-98939792	IMR90	lung:	fetal
36	chr10:98908755-98908805	Hela-S3	cervix:	n/a
37	chr10:98939912-98939962	MCF10A-Er-Src	breast:	n/a
38	chr10:98908962-98909012	Caco-2	colon:	n/a
39	chr10:98908755-98908805	AoSMC	blood vessel:	n/a
40	chr10:98924236-98924286	PANC-1	pancreas:	n/a
41	chr10:98910008-98910058	SK-N-MC	brain:	n/a
42	chr10:98924236-98924286	AoSMC	blood vessel:	n/a
43	chr10:98939742-98939792	MCF10A-Er-Src	breast:	n/a
44	chr10:98909007-98909057	HepG2	liver:	n/a
45	chr10:98908962-98909012	HCF	heart:	n/a
46	chr10:98939742-98939792	NH-A	brain:	n/a
47	chr10:98924236-98924286	HRE	kidney:	n/a
48	chr10:98908962-98909012	AG09309	skin:	n/a
49	chr10:98909007-98909057	AG09319	gingival:	n/a
50	chr10:98909007-98909057	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:98929149..98931128-chr10:98946131..98948627,2	MCF-7	breast:
2	chr10:98920381..98922540-chr10:98922773..98924441,2	K562	blood:
3	chr10:98891626..98893262-chr10:98910638..98912795,2	K562	blood:
4	chr10:98923298..98925502-chr10:98954215..98957162,2	MCF-7	breast:
5	chr10:98920381..98922540-chr10:98922773..98924441,2	K562	blood:
6	chr10:98929224..98932105-chr10:98943480..98945226,2	MCF-7	breast:
7	chr10:98895047..98897356-chr10:98912806..98914743,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FRAT2-3	chr10:98912802-98915190	NONHSAT015848

Variant related genes	Relation type
ARHGAP19-SLIT1	TF binding region
ARHGAP19-SLIT1	CpG island

Extended variants
information (count: 1432 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1432 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181066528	chr10:98902484-98902485	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs71486111	chr10:98902526-98902527	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs115628081	chr10:98902533-98902534	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs540118688	chr10:98902553-98902554	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs551934265	chr10:98902582-98902583	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs570093704	chr10:98902598-98902599	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs537586381	chr10:98902599-98902600	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs4917757	chr10:98902606-98902607	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs555852577	chr10:98902622-98902623	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs185944935	chr10:98902637-98902638	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs535292785	chr10:98902648-98902649	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs553890045	chr10:98902649-98902650	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs190407892	chr10:98902718-98902719	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs201695824	chr10:98902719-98902720	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs138967867	chr10:98902789-98902790	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs181988361	chr10:98902889-98902890	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs373300955	chr10:98902903-98902904	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs543811182	chr10:98902912-98902913	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs562166808	chr10:98902915-98902916	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs186219387	chr10:98902989-98902990	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs12258466	chr10:98903017-98903018	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs559892123	chr10:98903153-98903154	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs533483260	chr10:98903240-98903241	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs552032825	chr10:98903283-98903284	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs529422806	chr10:98903307-98903308	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs191215221	chr10:98903332-98903333	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs562505653	chr10:98903394-98903395	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs549322273	chr10:98903395-98903396	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs116137330	chr10:98903457-98903458	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs535526979	chr10:98903462-98903463	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs142095267	chr10:98903474-98903475	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs565847459	chr10:98903476-98903477	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs146407308	chr10:98903511-98903512	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs558100648	chr10:98903516-98903517	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs2817654	chr10:98903521-98903522	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs543847394	chr10:98903522-98903523	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs555787660	chr10:98903575-98903576	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs182588587	chr10:98903598-98903599	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs55656826	chr10:98903609-98903610	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs185926459	chr10:98903614-98903615	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530170911	chr10:98903618-98903619	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs35137327	chr10:98903679-98903680	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs571649717	chr10:98903730-98903731	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs139751554	chr10:98903760-98903761	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs545241348	chr10:98903769-98903770	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs142826205	chr10:98903772-98903773	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs150608805	chr10:98903815-98903816	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs139676507	chr10:98903824-98903825	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567717174	chr10:98903879-98903880	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs149803047	chr10:98903880-98903881	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
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
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
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	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
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Paraganglioma	17535989	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21364760	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Glioblastoma multiforme	22286061	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16912164	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Autosomal dominant partial epilepsy	18472482	CNVD
Breast cancer	16397240	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ependymoma	20639864	CNVD
Lung adenocarcinoma	21935476	CNVD

Chromatin state (count:383 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:98880200-98912800	Weak transcription	Thymus	Thymus
2	chr10:98892400-98911400	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr10:98901000-98907400	Strong transcription	Fetal Thymus	thymus
4	chr10:98901000-98923200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr10:98901200-98909000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr10:98901200-98910400	Weak transcription	Brain Germinal Matrix	brain
7	chr10:98901400-98904000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr10:98901400-98908600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr10:98901400-98909800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr10:98901400-98911200	Weak transcription	Fetal Brain Female	brain
11	chr10:98901400-98918400	Weak transcription	Brain Angular Gyrus	brain
12	chr10:98901600-98906400	Enhancers	Fetal Lung	lung
13	chr10:98901800-98902600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr10:98902000-98904000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr10:98902200-98909800	Weak transcription	HepG2	liver
16	chr10:98902400-98904600	Enhancers	Fetal Brain Male	brain
17	chr10:98902600-98903600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr10:98902600-98903600	Bivalent Enhancer	Fetal Heart	heart
19	chr10:98903600-98905000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr10:98904000-98904600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr10:98904000-98904800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr10:98904200-98904400	Bivalent Enhancer	Right Ventricle	heart
23	chr10:98904200-98904600	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
24	chr10:98904200-98904600	Enhancers	Brain Anterior Caudate	brain
25	chr10:98904600-98908600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr10:98904600-98917400	Weak transcription	Brain Anterior Caudate	brain
27	chr10:98904600-98922800	Weak transcription	Fetal Brain Male	brain
28	chr10:98904800-98905200	Weak transcription	Spleen	Spleen
29	chr10:98904800-98906600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr10:98905000-98905600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr10:98905200-98905400	Enhancers	Spleen	Spleen
32	chr10:98905400-98910000	Weak transcription	Spleen	Spleen
33	chr10:98905600-98908200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr10:98907400-98909200	Weak transcription	Fetal Thymus	thymus
35	chr10:98907800-98922800	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr10:98908200-98911400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr10:98908600-98908800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr10:98908600-98910400	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr10:98908600-98911000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr10:98908600-98912400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr10:98908600-98913400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr10:98908800-98909000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
43	chr10:98908800-98909800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr10:98908800-98910200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
45	chr10:98908800-98911000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr10:98909000-98909200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr10:98909000-98910200	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr10:98909000-98910400	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr10:98909200-98909600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr10:98909200-98910400	Enhancers	iPS-15b Cell Line	embryonic stem cell

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