Variant report

Variant	nsv971896
Chromosome Location	chr10:99338341-99349551
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:191)
CpG islands
(count:732)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:191 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr10:99344873-99345110	K562	blood:	n/a	chr10:99345024-99345037
2	BHLHE40	chr10:99344884-99345251	HepG2	liver:	n/a	chr10:99345024-99345037
3	BHLHE40	chr10:99343814-99344124	HepG2	liver:	n/a	n/a
4	BRCA1	chr10:99346591-99346673	HepG2	liver:	n/a	n/a
5	CEBPB	chr10:99343895-99344056	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr10:99339069-99339161	HepG2	liver:	n/a	n/a
7	CEBPB	chr10:99343903-99344134	Hela-S3	cervix:	n/a	chr10:99344057-99344065
8	CEBPB	chr10:99348281-99348455	HepG2	liver:	n/a	n/a
9	CEBPB	chr10:99343853-99344155	HepG2	liver:	n/a	chr10:99344057-99344065
10	CEBPB	chr10:99339051-99339157	K562	blood:	n/a	n/a
11	CEBPB	chr10:99339046-99339222	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr10:99348246-99348525	HepG2	liver:	n/a	n/a
13	CEBPD	chr10:99343710-99344267	HepG2	liver:	n/a	n/a
14	CHD2	chr10:99344058-99344063	Hela-S3	cervix:	n/a	n/a
15	CHD2	chr10:99343993-99344155	HepG2	liver:	n/a	n/a
16	CTCF	chr10:99346440-99346590	GM12867	blood:	n/a	n/a
17	CTCF	chr10:99343740-99343890	HBMEC	blood vessel:	n/a	n/a
18	CTCF	chr10:99346191-99346290	MCF-7	breast:	n/a	n/a
19	CTCF	chr10:99343902-99343905	Kidney_OC	kidney:	n/a	n/a
20	CTCF	chr10:99343112-99343229	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr10:99343820-99343970	HMEC	breast:	n/a	n/a
22	CTCF	chr10:99343820-99343970	GM12872	blood:	n/a	n/a
23	CTCF	chr10:99343760-99343910	HepG2	liver:	n/a	n/a
24	CTCF	chr10:99343108-99343195	HUVEC	blood vessel:	n/a	n/a
25	CTCF	chr10:99343760-99343910	AoAF	blood vessel:	n/a	n/a
26	CTCF	chr10:99343040-99343190	GM12872	blood:	n/a	n/a
27	CTCF	chr10:99339601-99339638	GM20000	blood:	n/a	n/a
28	CTCF	chr10:99344280-99344430	RPTEC	kidney:	n/a	n/a
29	CTCF	chr10:99343740-99343890	SK-N-SH_RA	brain:	n/a	n/a
30	CTCF	chr10:99343700-99343850	HCT-116	colon:	n/a	n/a
31	CTCF	chr10:99346154-99346281	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr10:99344160-99344310	GM12872	blood:	n/a	n/a
33	CTCF	chr10:99344300-99344450	HepG2	liver:	n/a	n/a
34	CTCF	chr10:99343760-99343910	BE2_C	brain:	n/a	n/a
35	CTCF	chr10:99346189-99346285	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr10:99343640-99343790	NHEK	skin:	n/a	n/a
37	CTCF	chr10:99343808-99343884	Kidney_OC	kidney:	n/a	n/a
38	CTCF	chr10:99343886-99343896	Kidney_OC	kidney:	n/a	n/a
39	E2F6	chr10:99344907-99345153	K562	blood:	n/a	chr10:99345052-99345063
40	E2F6	chr10:99344924-99345159	K562	blood:	n/a	chr10:99345052-99345063
41	E2F6	chr10:99344877-99345206	K562	blood:	n/a	chr10:99345052-99345063
42	EBF1	chr10:99344164-99344422	GM12878	blood:	n/a	chr10:99344269-99344280
43	ELF1	chr10:99343630-99344185	HepG2	liver:	n/a	n/a
44	ELF1	chr10:99343706-99344185	HepG2	liver:	n/a	n/a
45	EP300	chr10:99343869-99344246	SK-N-SH_RA	brain:	n/a	n/a
46	EP300	chr10:99343874-99343980	HepG2	liver:	n/a	n/a
47	ESR1	chr10:99340046-99340384	T-47D	breast:	n/a	n/a
48	ESR1	chr10:99340054-99340430	T-47D	breast:	n/a	n/a
49	ESR1	chr10:99340027-99340472	T-47D	breast:	n/a	n/a
50	ESR1	chr10:99345131-99345517	T-47D	breast:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:99344969-99345019	HNPCEpiC	eye:	n/a
2	chr10:99344969-99345019	HMEC	breast:	n/a
3	chr10:99343486-99343536	AG09319	gingival:	n/a
4	chr10:99343486-99343536	HRE	kidney:	n/a
5	chr10:99343486-99343536	HCT-116	colon:	n/a
6	chr10:99349361-99349411	HRPEpiC	eye:	n/a
7	chr10:99349003-99349053	SKMC	muscle:	n/a
8	chr10:99344164-99344214	HepG2	liver:	n/a
9	chr10:99348244-99348294	GM19239	blood:	n/a
10	chr10:99344164-99344214	ECC-1	luminal epithelium:	n/a
11	chr10:99339736-99339786	HRPEpiC	eye:	n/a
12	chr10:99344969-99345019	Jurkat	blood:	n/a
13	chr10:99348862-99348912	NHBE	bronchial:	n/a
14	chr10:99344164-99344214	GM12892	blood:	n/a
15	chr10:99343942-99343992	SK-N-MC	brain:	n/a
16	chr10:99348862-99348912	AG04450	lung:	fetal
17	chr10:99348244-99348294	HNPCEpiC	eye:	n/a
18	chr10:99343486-99343536	PrEC	prostate:	n/a
19	chr10:99349003-99349053	HMEC	breast:	n/a
20	chr10:99348244-99348294	CMK	blood:	n/a
21	chr10:99348244-99348294	Caco-2	colon:	n/a
22	chr10:99349395-99349445	AG09309	skin:	n/a
23	chr10:99348244-99348294	GM12878	blood:	n/a
24	chr10:99349395-99349445	ECC-1	luminal epithelium:	n/a
25	chr10:99339736-99339786	PFSK-1	brain:	n/a
26	chr10:99349395-99349445	NHBE	bronchial:	n/a
27	chr10:99344969-99345019	HEK293	kidney:	embryo
28	chr10:99348862-99348912	T-47D	breast:	n/a
29	chr10:99344164-99344214	AG10803	skin:	n/a
30	chr10:99344164-99344214	LNCaP	prostate:	n/a
31	chr10:99348244-99348294	Jurkat	blood:	n/a
32	chr10:99339736-99339786	HPAEpiC	pulmonary alveolar:	n/a
33	chr10:99339736-99339786	AG04450	lung:	fetal
34	chr10:99341525-99341575	Hepatocyte	liver:	n/a
35	chr10:99343450-99343500	T-47D	breast:	n/a
36	chr10:99343450-99343500	SK-N-SH_RA	brain:	n/a
37	chr10:99349395-99349445	HCF	heart:	n/a
38	chr10:99348862-99348912	U87	brain:	n/a
39	chr10:99349003-99349053	HL-60	blood:	n/a
40	chr10:99343942-99343992	HCPEpiC	choroid plexus:	n/a
41	chr10:99349003-99349053	NT2-D1	testis:	n/a
42	chr10:99349003-99349053	HRE	kidney:	n/a
43	chr10:99349361-99349411	HRCEpiC	kidney:	n/a
44	chr10:99343486-99343536	PANC-1	pancreas:	n/a
45	chr10:99349395-99349445	SK-N-SH	brain:	n/a
46	chr10:99348244-99348294	ProgFib	skin:	n/a
47	chr10:99339736-99339786	HRCEpiC	kidney:	n/a
48	chr10:99349003-99349053	MCF-7	breast:	n/a
49	chr10:99349395-99349445	ProgFib	skin:	n/a
50	chr10:99344969-99345019	GM19239	blood:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:99341781..99343970-chr10:99356673..99358698,2	MCF-7	breast:
2	chr10:99330995..99332069-chr10:99339678..99340684,16	MCF-7	breast:
3	chr10:99331112..99332069-chr10:99339738..99340684,9	MCF-7	breast:
4	chr10:99338261..99340049-chr10:99343345..99345050,2	K562	blood:
5	chr10:99331295..99331846-chr10:99344716..99345312,2	MCF-7	breast:
6	chr10:99331113..99332849-chr10:99340895..99343387,2	MCF-7	breast:
7	chr10:99326165..99327172-chr10:99339740..99340648,3	MCF-7	breast:
8	chr10:99342912..99345937-chr10:99348140..99351473,3	K562	blood:
9	chr10:99342912..99345937-chr10:99348140..99351473,3	K562	blood:
10	chr10:99331139..99331795-chr10:99344716..99345483,2	MCF-7	breast:
11	chr10:99345242..99348489-chr10:99349078..99351813,3	K562	blood:
12	chr10:99331048..99332027-chr10:99339659..99340637,7	MCF-7	breast:
13	chr10:99257383..99259278-chr10:99348125..99351802,3	MCF-7	breast:
14	chr10:99341160..99342712-chr10:99360184..99361949,2	MCF-7	breast:
15	chr10:99329733..99337149-chr10:99338392..99346753,19	MCF-7	breast:

No data

Variant related genes	Relation type
C10orf62	TF binding region
ENSG00000249967	TF binding region
PI4K2A	TF binding region
HOGA1	TF binding region
C10orf62	CpG island
ENSG00000249967	CpG island
PI4K2A	CpG island
HOGA1	CpG island
ENSG00000165887	chromatin interactions
ENSG00000249967	chromatin interactions
ENSG00000165886	chromatin interactions
ENSG00000203942	chromatin interactions
ENSG00000241935	chromatin interactions
ENSG00000155229	chromatin interactions

Extended variants
information (count: 487 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:487 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140424419	chr10:99338347-99338348	Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs555582146	chr10:99338363-99338364	Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs373353644	chr10:99338386-99338387	Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs111984454	chr10:99338397-99338398	Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs74155506	chr10:99338422-99338423	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs370751698	chr10:99338450-99338451	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs559894456	chr10:99338557-99338558	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs192167040	chr10:99338581-99338582	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs551971957	chr10:99338673-99338674	Weak transcription Enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs57069102	chr10:99338706-99338707	Weak transcription Enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs531717789	chr10:99338719-99338720	Weak transcription Enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs183927812	chr10:99338786-99338787	Weak transcription Enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs11189287	chr10:99338795-99338796	Weak transcription Enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs375550907	chr10:99338807-99338808	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs568406946	chr10:99338812-99338813	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs116482187	chr10:99338813-99338814	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs138365017	chr10:99338847-99338848	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs566389156	chr10:99338891-99338892	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs59319014	chr10:99338901-99338902	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs7922873	chr10:99338902-99338903	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs374983802	chr10:99338907-99338908	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs73332755	chr10:99338921-99338922	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs556122418	chr10:99338926-99338927	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs80215603	chr10:99338930-99338931	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs200455140	chr10:99338931-99338932	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs77545511	chr10:99338932-99338933	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs61861959	chr10:99338947-99338948	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs574377920	chr10:99338951-99338952	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs142852169	chr10:99338968-99338969	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs74403757	chr10:99339080-99339081	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs59132098	chr10:99339081-99339082	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs559981719	chr10:99339084-99339085	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs527605152	chr10:99339125-99339126	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs372937894	chr10:99339158-99339159	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs564138617	chr10:99339164-99339165	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs7908668	chr10:99339178-99339179	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs187919610	chr10:99339218-99339219	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs549187037	chr10:99339256-99339257	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs529266842	chr10:99339292-99339293	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs547832162	chr10:99339310-99339311	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs112450717	chr10:99339353-99339354	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs143252764	chr10:99339365-99339366	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs367777744	chr10:99339385-99339386	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs566330008	chr10:99339398-99339399	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs190489293	chr10:99339403-99339404	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs558320946	chr10:99339407-99339408	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs570201921	chr10:99339408-99339409	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs537925665	chr10:99339494-99339495	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs556019292	chr10:99339496-99339497	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs574210497	chr10:99339503-99339504	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
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
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD

Chromatin state (count:261 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:99334800-99343400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr10:99335000-99343400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr10:99335200-99343400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr10:99335400-99340200	Weak transcription	Pancreas	Pancrea
5	chr10:99336000-99342000	Weak transcription	Right Ventricle	heart
6	chr10:99336000-99348800	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr10:99336200-99339800	Weak transcription	Hela-S3	cervix
8	chr10:99336200-99340200	Weak transcription	Placenta	Placenta
9	chr10:99336200-99340800	Weak transcription	Right Atrium	heart
10	chr10:99336200-99342000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr10:99336200-99343400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr10:99336200-99343400	Weak transcription	Psoas Muscle	Psoas
13	chr10:99337200-99338600	Genic enhancers	Skeletal Muscle Male	skeletal muscle
14	chr10:99337400-99338800	Strong transcription	Left Ventricle	heart
15	chr10:99337800-99340000	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr10:99337800-99343000	Weak transcription	A549	lung
17	chr10:99338000-99338400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr10:99338000-99338400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr10:99338000-99338400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr10:99338000-99338400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr10:99338000-99338400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr10:99338000-99338400	Active TSS	Brain Germinal Matrix	brain
23	chr10:99338000-99338400	Bivalent/Poised TSS	Fetal Brain Female	brain
24	chr10:99338000-99338400	Bivalent/Poised TSS	Fetal Intestine Small	intestine
25	chr10:99338000-99338400	Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr10:99338000-99338400	Bivalent Enhancer	Fetal Stomach	stomach
27	chr10:99338000-99338600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr10:99338200-99338400	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
29	chr10:99338200-99338400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
30	chr10:99338200-99338400	Active TSS	Fetal Muscle Leg	muscle
31	chr10:99338200-99338400	Enhancers	Lung	lung
32	chr10:99338200-99338600	Enhancers	Primary hematopoietic stem cells	blood
33	chr10:99338200-99338600	Active TSS	Brain Inferior Temporal Lobe	brain
34	chr10:99338200-99338600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
35	chr10:99338400-99338600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr10:99338400-99338600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr10:99338400-99338800	Bivalent Enhancer	Fetal Muscle Leg	muscle
38	chr10:99338400-99343400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr10:99338400-99343800	Weak transcription	Lung	lung
40	chr10:99338600-99338800	Enhancers	Brain Inferior Temporal Lobe	brain
41	chr10:99338600-99340000	Strong transcription	Skeletal Muscle Male	skeletal muscle
42	chr10:99338600-99343800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr10:99338800-99340400	Weak transcription	Left Ventricle	heart
44	chr10:99338800-99343200	Weak transcription	Fetal Muscle Leg	muscle
45	chr10:99338800-99343400	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr10:99339800-99340600	Enhancers	Hela-S3	cervix
47	chr10:99340000-99343000	Genic enhancers	Skeletal Muscle Female	skeletal muscle
48	chr10:99340000-99343600	Genic enhancers	Skeletal Muscle Male	skeletal muscle
49	chr10:99340200-99340400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr10:99340200-99340400	Enhancers	Pancreas	Pancrea

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