Variant report

Variant	nsv895882
Chromosome Location	chr10:91002927-91021645
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	chr10:91011635-91012246	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:91020118-91020501	HepG2	liver:	n/a	n/a
3	ATF2	chr10:91002490-91003007	GM12878	blood:	n/a	n/a
4	ATF2	chr10:91020060-91020637	GM12878	blood:	n/a	n/a
5	BATF	chr10:91020156-91020475	GM12878	blood:	n/a	n/a
6	BATF	chr10:91008901-91009157	GM12878	blood:	n/a	chr10:91009024-91009035 chr10:91009025-91009035
7	BATF	chr10:91008922-91009145	GM12878	blood:	n/a	chr10:91009024-91009035 chr10:91009025-91009035
8	BCLAF1	chr10:91020030-91020552	GM12878	blood:	n/a	n/a
9	BHLHE40	chr10:91020062-91020456	K562	blood:	n/a	n/a
10	BHLHE40	chr10:91020144-91020484	GM12878	blood:	n/a	n/a
11	BHLHE40	chr10:91011304-91012040	GM12878	blood:	n/a	chr10:91011458-91011474
12	CEBPB	chr10:91020124-91020456	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr10:91011306-91011428	HepG2	liver:	n/a	n/a
14	CEBPB	chr10:91015720-91015782	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr10:91011667-91011901	Hela-S3	cervix:	n/a	n/a
16	CEBPD	chr10:91020057-91020477	K562	blood:	n/a	n/a
17	CEBPD	chr10:91011253-91011611	HepG2	liver:	n/a	n/a
18	CHD1	chr10:91011882-91011885	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr10:91011152-91011563	HepG2	liver:	n/a	n/a
20	CHD2	chr10:91011436-91011858	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr10:91011333-91011988	Hela-S3	cervix:	n/a	n/a
22	CHD2	chr10:91020167-91020482	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr10:91020147-91020605	GM12878	blood:	n/a	n/a
24	CHD2	chr10:91011329-91011980	GM12878	blood:	n/a	n/a
25	CREB1	chr10:91011341-91011993	HepG2	liver:	n/a	n/a
26	CREB1	chr10:91011306-91011897	A549	lung:	n/a	n/a
27	CREB1	chr10:91011354-91012019	GM12878	blood:	n/a	n/a
28	CTCF	chr10:91020175-91020397	GM13976	blood:	n/a	chr10:91020286-91020295 chr10:91020283-91020301 chr10:91020286-91020299 chr10:91020285-91020306
29	CTCF	chr10:91011440-91011590	SK-N-SH_RA	brain:	n/a	chr10:91011566-91011574
30	CTCF	chr10:91011557-91011589	NHEK	skin:	n/a	chr10:91011566-91011574
31	CTCF	chr10:91005700-91005850	GM12872	blood:	n/a	chr10:91005741-91005757
32	CTCF	chr10:91005640-91005790	GM12864	blood:	n/a	chr10:91005741-91005757
33	CTCF	chr10:91011460-91011610	GM12866	blood:	n/a	chr10:91011566-91011574
34	CTCF	chr10:91005620-91005770	HMF	breast:	n/a	chr10:91005741-91005757
35	CTCF	chr10:91005727-91005786	GM19239	blood:	n/a	chr10:91005741-91005757
36	CTCF	chr10:91020045-91020517	A549	lung:	n/a	chr10:91020286-91020295 chr10:91020283-91020301 chr10:91020286-91020299 chr10:91020285-91020306
37	CTCF	chr10:91005640-91005790	GM12869	blood:	n/a	chr10:91005741-91005757
38	CTCF	chr10:91020200-91020350	GM12867	blood:	n/a	chr10:91020286-91020295 chr10:91020283-91020301 chr10:91020286-91020299 chr10:91020285-91020306
39	CTCF	chr10:91005680-91005830	AG09309	skin:	n/a	chr10:91005741-91005757
40	CTCF	chr10:91019672-91021147	SK-N-SH	brain:	n/a	chr10:91020286-91020295 chr10:91020283-91020301 chr10:91020286-91020299 chr10:91020285-91020306
41	CTCF	chr10:91020079-91020526	K562	blood:	n/a	chr10:91020286-91020295 chr10:91020283-91020301 chr10:91020286-91020299 chr10:91020285-91020306
42	CTCF	chr10:91005680-91005830	GM12869	blood:	n/a	chr10:91005741-91005757
43	CTCF	chr10:91011540-91011690	HBMEC	blood vessel:	n/a	chr10:91011566-91011574
44	CTCF	chr10:91020153-91020408	HepG2	liver:	n/a	chr10:91020286-91020295 chr10:91020283-91020301 chr10:91020286-91020299 chr10:91020285-91020306
45	CTCF	chr10:91020151-91020437	K562	blood:	n/a	chr10:91020286-91020295 chr10:91020283-91020301 chr10:91020286-91020299 chr10:91020285-91020306
46	CTCF	chr10:91020260-91020410	Caco-2	colon:	n/a	chr10:91020286-91020295 chr10:91020283-91020301 chr10:91020286-91020299 chr10:91020285-91020306
47	CTCF	chr10:91015020-91015094	GM10248	blood:	n/a	n/a
48	CTCF	chr10:91011380-91011530	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr10:91020200-91020350	GM12875	blood:	n/a	chr10:91020286-91020295 chr10:91020283-91020301 chr10:91020286-91020299 chr10:91020285-91020306
50	CTCF	chr10:91020160-91020310	GM12870	blood:	n/a	chr10:91020286-91020295 chr10:91020283-91020301 chr10:91020286-91020299 chr10:91020285-91020306

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:91020653-91020703	MCF10A-Er-Src	breast:	n/a
2	chr10:91008159-91008209	BJ	skin:	n/a
3	chr10:91011863-91011913	PANC-1	pancreas:	n/a
4	chr10:91011618-91011668	LNCaP	prostate:	n/a
5	chr10:91011695-91011745	LNCaP	prostate:	n/a
6	chr10:91011802-91011852	HPAEpiC	pulmonary alveolar:	n/a
7	chr10:91020653-91020703	MCF-7	breast:	n/a
8	chr10:91015046-91015096	HEK293	kidney:	embryo
9	chr10:91011802-91011852	NT2-D1	testis:	n/a
10	chr10:91011667-91011717	T-47D	breast:	n/a
11	chr10:91011618-91011668	RPTEC	kidney:	n/a
12	chr10:91011183-91011233	NT2-D1	testis:	n/a
13	chr10:91012862-91012912	AoSMC	blood vessel:	n/a
14	chr10:91011689-91011739	NB4	blood:	n/a
15	chr10:91012862-91012912	PrEC	prostate:	n/a
16	chr10:91011183-91011233	HEK293	kidney:	embryo
17	chr10:91011804-91011854	HRE	kidney:	n/a
18	chr10:91020653-91020703	Hela-S3	cervix:	n/a
19	chr10:91011695-91011745	HAEpiC	amniotic membrane:	n/a
20	chr10:91015046-91015096	AG10803	skin:	n/a
21	chr10:91020653-91020703	HNPCEpiC	eye:	n/a
22	chr10:91020653-91020703	NB4	blood:	n/a
23	chr10:91011618-91011668	HUVEC	blood vessel:	n/a
24	chr10:91015046-91015096	K562	blood:	n/a
25	chr10:91011183-91011233	BJ	skin:	n/a
26	chr10:91011676-91011726	HAEpiC	amniotic membrane:	n/a
27	chr10:91011593-91011643	AG10803	skin:	n/a
28	chr10:91012862-91012912	GM19239	blood:	n/a
29	chr10:91011892-91011942	SK-N-SH	brain:	n/a
30	chr10:91011618-91011668	SKMC	muscle:	n/a
31	chr10:91011676-91011726	GM19239	blood:	n/a
32	chr10:91011618-91011668	MCF-7	breast:	n/a
33	chr10:91011892-91011942	Jurkat	blood:	n/a
34	chr10:91015046-91015096	SK-N-SH_RA	brain:	n/a
35	chr10:91011689-91011739	HCPEpiC	choroid plexus:	n/a
36	chr10:91011863-91011913	LNCaP	prostate:	n/a
37	chr10:91011863-91011913	Hela-S3	cervix:	n/a
38	chr10:91011676-91011726	AG04449	skin:	fetal
39	chr10:91011618-91011668	HCT-116	colon:	n/a
40	chr10:91020653-91020703	H1-hESC	embryonic stem cell:	embryo
41	chr10:91011892-91011942	PANC-1	pancreas:	n/a
42	chr10:91011593-91011643	K562	blood:	n/a
43	chr10:91011183-91011233	CMK	blood:	n/a
44	chr10:91020653-91020703	HRPEpiC	eye:	n/a
45	chr10:91012862-91012912	RPTEC	kidney:	n/a
46	chr10:91011667-91011717	AoSMC	blood vessel:	n/a
47	chr10:91020653-91020703	HEK293	kidney:	embryo
48	chr10:91011695-91011745	NHBE	bronchial:	n/a
49	chr10:91011892-91011942	SK-N-MC	brain:	n/a
50	chr10:91020653-91020703	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:91001026..91003568-chr10:91009679..91012651,2	MCF-7	breast:
2	chr10:91003937..91005930-chr10:91020803..91022906,2	K562	blood:
3	chr10:91004556..91008070-chr10:91009861..91011850,3	MCF-7	breast:
4	chr10:91003937..91005930-chr10:91020803..91022906,2	K562	blood:
5	chr10:91004556..91008070-chr10:91009861..91011850,3	MCF-7	breast:
6	chr10:91010532..91012655-chr10:91015052..91017566,2	MCF-7	breast:
7	chr10:91009631..91012227-chr10:91174311..91176643,2	MCF-7	breast:
8	chr10:91019806..91020344-chr10:91323334..91324234,2	MCF-7	breast:
9	chr10:91019777..91020866-chr10:91128531..91129985,10	MCF-7	breast:
10	chr10:91019839..91020750-chr10:91128976..91129904,3	K562	blood:
11	chr10:90610616..90613278-chr10:91010263..91012632,2	MCF-7	breast:
12	chr10:91020387..91022060-chr10:91024157..91025732,2	MCF-7	breast:
13	chr10:91019908..91020478-chr10:91148791..91149465,2	K562	blood:
14	chr10:91019602..91020678-chr10:91148799..91149709,3	MCF-7	breast:
15	chr10:91019711..91020808-chr10:91128397..91129939,7	MCF-7	breast:

Variant related genes	Relation type
LIPA	TF binding region
LIPA	CpG island
ENSG00000266769	chromatin interactions
ENSG00000152766	chromatin interactions
ENSG00000152778	chromatin interactions
ENSG00000107798	chromatin interactions

Extended variants
information (count: 693 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:693 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1412444	chr10:91002927-91002928	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
2	rs564346648	chr10:91002933-91002934	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs528232099	chr10:91002949-91002950	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs540326331	chr10:91002995-91002996	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs574671239	chr10:91003038-91003039	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs561600366	chr10:91003090-91003091	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs113170756	chr10:91003220-91003221	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs528874786	chr10:91003279-91003280	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs187315486	chr10:91003281-91003282	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs140677191	chr10:91003289-91003290	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs61302111	chr10:91003322-91003323	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs531158366	chr10:91003333-91003334	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs5786865	chr10:91003350-91003351	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs552588648	chr10:91003361-91003362	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs571036559	chr10:91003362-91003363	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs374654146	chr10:91003376-91003377	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs542955671	chr10:91003388-91003389	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs145314792	chr10:91003403-91003404	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs1332329	chr10:91003419-91003420	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs535929093	chr10:91003486-91003487	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs191407307	chr10:91003492-91003493	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs184250799	chr10:91003510-91003511	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs533691587	chr10:91003522-91003523	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs539752124	chr10:91003585-91003586	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs146465104	chr10:91003587-91003588	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs573015904	chr10:91003664-91003665	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs540020469	chr10:91003849-91003850	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs561906575	chr10:91003851-91003852	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs573431392	chr10:91003853-91003854	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs140859865	chr10:91003870-91003871	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs563884233	chr10:91003900-91003901	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs12240489	chr10:91003903-91003904	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs199763852	chr10:91003935-91003936	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs189198583	chr10:91003937-91003938	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs566197051	chr10:91003986-91003987	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs546130481	chr10:91004029-91004030	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs193219390	chr10:91004088-91004089	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551774651	chr10:91004114-91004115	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528764837	chr10:91004159-91004160	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs79594176	chr10:91004217-91004218	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs546904435	chr10:91004238-91004239	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs75402299	chr10:91004245-91004246	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535993126	chr10:91004266-91004267	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551054072	chr10:91004271-91004272	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs7922536	chr10:91004297-91004298	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs569276692	chr10:91004334-91004335	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539814423	chr10:91004335-91004336	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs11203048	chr10:91004343-91004344	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs77414759	chr10:91004346-91004347	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs534073214	chr10:91004430-91004431	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
Endometrioid adenocarcinoma	16974079	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	18645599	CNVD
Polyposis syndrome	18645599	CNVD
Prostate cancer	17245344	CNVD
Glioblastoma multiforme	17369134	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Colorectal cancer	19359472	CNVD
Neurocytoma	17123091	CNVD
Prostate cancer	16461572	CNVD
Basal-like breast cancer	18066063	CNVD
Effusion lymphoma	18079361	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	22048815	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Glioblastoma multiforme	22286061	CNVD
Intracranial ependymoma	16609018	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Sezary syndrome	18413736	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:837 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:90977400-91010400	Weak transcription	Fetal Thymus	thymus
2	chr10:90977400-91010800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr10:90977600-91008800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr10:90977600-91009400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr10:90977600-91010400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr10:90977600-91010800	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr10:90979400-91003600	Strong transcription	Primary T cells from cord blood	blood
8	chr10:90985200-91010600	Weak transcription	Thymus	Thymus
9	chr10:90987400-91010800	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr10:90987600-91010800	Weak transcription	Pancreas	Pancrea
11	chr10:90987800-91010600	Weak transcription	HSMM	muscle
12	chr10:90988000-91010600	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr10:90989200-91003200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr10:90994800-91010800	Weak transcription	Esophagus	oesophagus
15	chr10:90995600-91003000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr10:90998600-91004200	Strong transcription	Primary T cells fromperipheralblood	blood
17	chr10:90998800-91003200	Strong transcription	Stomach Smooth Muscle	stomach
18	chr10:90999000-91004200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr10:90999600-91005400	Weak transcription	Brain Angular Gyrus	brain
20	chr10:90999600-91010400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr10:90999800-91010000	Weak transcription	Dnd41	blood
22	chr10:90999800-91010400	Weak transcription	Colon Smooth Muscle	Colon
23	chr10:90999800-91010400	Weak transcription	Duodenum Smooth Muscle	Duodenum
24	chr10:90999800-91010600	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr10:90999800-91010600	Weak transcription	Rectal Smooth Muscle	rectum
26	chr10:90999800-91010800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr10:90999800-91010800	Weak transcription	Ovary	ovary
28	chr10:91000000-91004800	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr10:91000000-91010400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
30	chr10:91000000-91010600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
31	chr10:91000200-91003200	Enhancers	Placenta	Placenta
32	chr10:91000200-91010600	Weak transcription	Brain Germinal Matrix	brain
33	chr10:91000200-91010600	Weak transcription	Fetal Brain Female	brain
34	chr10:91000400-91003600	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr10:91000600-91003000	Enhancers	Liver	Liver
36	chr10:91000600-91010400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
37	chr10:91000600-91010800	Weak transcription	Fetal Muscle Trunk	muscle
38	chr10:91000800-91003200	Genic enhancers	Brain Anterior Caudate	brain
39	chr10:91000800-91003600	Enhancers	H9 Cell Line	embryonic stem cell
40	chr10:91000800-91004200	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr10:91001000-91003000	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr10:91001000-91003600	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr10:91001000-91003800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr10:91001000-91010600	Weak transcription	Fetal Stomach	stomach
45	chr10:91001000-91010600	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr10:91001200-91003200	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr10:91001200-91003200	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr10:91001200-91006400	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr10:91001200-91009400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
50	chr10:91001200-91010600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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