Variant report

Variant	nsv1051921
Chromosome Location	chr10:44378011-44458880
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:542)
CpG islands
(count:610)
Chromatin interactive
region (count:24)
LncRNA
region (count:51)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:542 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:44381451-44381506	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:44398330-44398798	HepG2	liver:	n/a	n/a
3	BHLHE40	chr10:44435748-44436100	GM12878	blood:	n/a	n/a
4	BHLHE40	chr10:44417515-44417772	K562	blood:	n/a	chr10:44417664-44417673 chr10:44417664-44417673
5	BHLHE40	chr10:44397274-44397437	GM12878	blood:	n/a	n/a
6	CBX3	chr10:44448262-44448520	K562	blood:	n/a	n/a
7	CBX3	chr10:44448251-44448532	K562	blood:	n/a	n/a
8	CEBPB	chr10:44435684-44436278	IMR90	lung:	n/a	n/a
9	CEBPB	chr10:44390275-44390626	IMR90	lung:	n/a	chr10:44390434-44390445
10	CEBPB	chr10:44398359-44398706	HepG2	liver:	n/a	n/a
11	CEBPB	chr10:44387530-44387910	IMR90	lung:	n/a	n/a
12	CEBPB	chr10:44383920-44384598	IMR90	lung:	n/a	chr10:44384191-44384204 chr10:44384193-44384204 chr10:44384413-44384424 chr10:44384193-44384204 chr10:44384415-44384424
13	CEBPB	chr10:44398393-44398540	HepG2	liver:	n/a	n/a
14	CEBPB	chr10:44393592-44393727	HepG2	liver:	n/a	n/a
15	CEBPB	chr10:44426669-44427096	IMR90	lung:	n/a	n/a
16	CEBPB	chr10:44390274-44390585	A549	lung:	n/a	chr10:44390434-44390445
17	CEBPB	chr10:44383944-44384598	Hela-S3	cervix:	n/a	chr10:44384191-44384204 chr10:44384193-44384204 chr10:44384413-44384424 chr10:44384193-44384204 chr10:44384415-44384424
18	CEBPB	chr10:44390289-44390619	HepG2	liver:	n/a	chr10:44390434-44390445
19	CEBPB	chr10:44393532-44393792	HepG2	liver:	n/a	n/a
20	CHD2	chr10:44435457-44435596	GM12878	blood:	n/a	n/a
21	CHD2	chr10:44398387-44398564	HepG2	liver:	n/a	n/a
22	CTCF	chr10:44381400-44381550	GM12874	blood:	n/a	n/a
23	CTCF	chr10:44381431-44381514	GM10248	blood:	n/a	n/a
24	CTCF	chr10:44399781-44399993	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr10:44418307-44418409	GM12892	blood:	n/a	n/a
26	CTCF	chr10:44381409-44381560	GM10266	blood:	n/a	n/a
27	CTCF	chr10:44381380-44381530	HRE	kidney:	n/a	n/a
28	CTCF	chr10:44381342-44381639	T-47D	breast:	n/a	n/a
29	CTCF	chr10:44390980-44391130	HPF	lung:	n/a	n/a
30	CTCF	chr10:44404640-44404790	GM06990	blood:	n/a	n/a
31	CTCF	chr10:44396803-44397108	IMR90	lung:	n/a	n/a
32	CTCF	chr10:44390960-44391110	HepG2	liver:	n/a	n/a
33	CTCF	chr10:44396740-44396890	HVMF	connective:	n/a	n/a
34	CTCF	chr10:44404660-44404810	GM12873	blood:	n/a	n/a
35	CTCF	chr10:44396900-44397050	AG04449	skin:	n/a	n/a
36	CTCF	chr10:44404740-44404890	AG09309	skin:	n/a	n/a
37	CTCF	chr10:44418310-44418323	K562	blood:	n/a	n/a
38	CTCF	chr10:44396860-44397010	GM12873	blood:	n/a	n/a
39	CTCF	chr10:44404680-44404830	HepG2	liver:	n/a	n/a
40	CTCF	chr10:44380800-44380950	Caco-2	colon:	n/a	n/a
41	CTCF	chr10:44397060-44397210	HVMF	connective:	n/a	n/a
42	CTCF	chr10:44381208-44381772	MCF-7	breast:	n/a	n/a
43	CTCF	chr10:44381400-44381550	GM12867	blood:	n/a	n/a
44	CTCF	chr10:44396860-44397010	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr10:44396400-44396550	HCM	heart:	n/a	n/a
46	CTCF	chr10:44381340-44381490	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr10:44381380-44381530	GM12868	blood:	n/a	n/a
48	CTCF	chr10:44418226-44418385	HepG2	liver:	n/a	n/a
49	CTCF	chr10:44400300-44400450	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr10:44396840-44396990	HA-sp	spinal cord:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:44387291-44387341	MCF-7	breast:	n/a
2	chr10:44434381-44434431	GM12891	blood:	n/a
3	chr10:44432979-44433029	HEEpiC	esophagus:	n/a
4	chr10:44458167-44458217	SK-N-SH_RA	brain:	n/a
5	chr10:44426803-44426853	SK-N-SH	brain:	n/a
6	chr10:44387291-44387341	HUVEC	blood vessel:	n/a
7	chr10:44432979-44433029	NHBE	bronchial:	n/a
8	chr10:44426803-44426853	GM12878	blood:	n/a
9	chr10:44458167-44458217	AG04449	skin:	fetal
10	chr10:44394566-44394616	SK-N-SH_RA	brain:	n/a
11	chr10:44400532-44400582	HL-60	blood:	n/a
12	chr10:44458167-44458217	HEEpiC	esophagus:	n/a
13	chr10:44450977-44451027	SK-N-SH_RA	brain:	n/a
14	chr10:44434410-44434460	PrEC	prostate:	n/a
15	chr10:44400532-44400582	H1-hESC	embryonic stem cell:	embryo
16	chr10:44426803-44426853	Hepatocyte	liver:	n/a
17	chr10:44434381-44434431	SK-N-MC	brain:	n/a
18	chr10:44436485-44436535	Caco-2	colon:	n/a
19	chr10:44394566-44394616	HCM	heart:	n/a
20	chr10:44400532-44400582	Hepatocyte	liver:	n/a
21	chr10:44426803-44426853	HMEC	breast:	n/a
22	chr10:44434410-44434460	PANC-1	pancreas:	n/a
23	chr10:44450977-44451027	NT2-D1	testis:	n/a
24	chr10:44387291-44387341	A549	lung:	n/a
25	chr10:44400532-44400582	Hela-S3	cervix:	n/a
26	chr10:44436485-44436535	AG09309	skin:	n/a
27	chr10:44434410-44434460	AG04450	lung:	fetal
28	chr10:44434410-44434460	SK-N-SH	brain:	n/a
29	chr10:44432979-44433029	AG04450	lung:	fetal
30	chr10:44436485-44436535	MCF-7	breast:	n/a
31	chr10:44387291-44387341	IMR90	lung:	fetal
32	chr10:44426803-44426853	AoSMC	blood vessel:	n/a
33	chr10:44434381-44434431	U87	brain:	n/a
34	chr10:44387291-44387341	GM12891	blood:	n/a
35	chr10:44436485-44436535	SK-N-MC	brain:	n/a
36	chr10:44400532-44400582	RPTEC	kidney:	n/a
37	chr10:44432979-44433029	RPTEC	kidney:	n/a
38	chr10:44436485-44436535	Jurkat	blood:	n/a
39	chr10:44394566-44394616	GM12892	blood:	n/a
40	chr10:44434381-44434431	K562	blood:	n/a
41	chr10:44436485-44436535	GM12878	blood:	n/a
42	chr10:44387291-44387341	RPTEC	kidney:	n/a
43	chr10:44450977-44451027	ECC-1	luminal epithelium:	n/a
44	chr10:44426803-44426853	HRE	kidney:	n/a
45	chr10:44434410-44434460	AoSMC	blood vessel:	n/a
46	chr10:44400532-44400582	MCF10A-Er-Src	breast:	n/a
47	chr10:44434381-44434431	HNPCEpiC	eye:	n/a
48	chr10:44400532-44400582	PFSK-1	brain:	n/a
49	chr10:44426803-44426853	Hela-S3	cervix:	n/a
50	chr10:44434381-44434431	NT2-D1	testis:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr10:44453236..44456147-chr10:44456397..44460102,3	MCF-7	breast:
2	chr10:44387546..44389292-chr10:44394424..44396340,2	MCF-7	breast:
3	chr10:44387546..44389292-chr10:44394424..44396340,2	MCF-7	breast:
4	chr10:44432654..44435706-chr10:44438627..44441733,3	K562	blood:
5	chr10:44431204..44432720-chr10:44436776..44439206,2	MCF-7	breast:
6	chr10:44404441..44407159-chr10:44407657..44409247,2	K562	blood:
7	chr10:44436082..44438732-chr10:44441086..44443148,2	K562	blood:
8	chr10:44436249..44437922-chr10:44454148..44455778,2	MCF-7	breast:
9	chr10:44436249..44437922-chr10:44454148..44455778,2	MCF-7	breast:
10	chr10:44436082..44438732-chr10:44441086..44443148,2	K562	blood:
11	chr10:44431204..44432720-chr10:44436776..44439206,2	MCF-7	breast:
12	chr10:44380951..44381611-chr10:44881527..44882115,2	MCF-7	breast:
13	chr10:44453236..44456147-chr10:44456397..44460102,3	MCF-7	breast:
14	chr10:44381279..44384529-chr10:44386530..44388753,3	K562	blood:
15	chr10:44387084..44390446-chr10:44391009..44393507,3	MCF-7	breast:
16	chr10:44432874..44435706-chr10:44438627..44440384,2	K562	blood:
17	chr10:44379146..44381291-chr10:44381939..44383905,2	K562	blood:
18	chr10:44446026..44447976-chr10:44454993..44457895,2	K562	blood:
19	chr10:44380961..44382076-chr10:44525328..44526058,4	MCF-7	breast:
20	chr10:44387084..44390446-chr10:44391009..44393507,3	MCF-7	breast:
21	chr10:44381279..44384529-chr10:44386530..44388753,3	K562	blood:
22	chr10:44446026..44447976-chr10:44454993..44457895,2	K562	blood:
23	chr10:44355270..44357315-chr10:44376908..44378969,2	MCF-7	breast:
24	chr10:44379146..44381291-chr10:44381939..44383905,2	K562	blood:

(count:51 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF32-4	chr10:44409598-44409954	XLOC_008793
2	lnc-C10orf136-1	chr10:44438643-44438729	NONHSAT013008
3	lnc-C10orf136-1	chr10:44439305-44439439	XLOC_008473
4	lnc-ZNF32-3	chr10:44398995-44399037	XLOC_008792
5	lnc-C10orf136-1	chr10:44404727-44404817	XLOC_008473
6	lnc-ZNF32-9	chr10:44457648-44457786	NONHSAT013020
7	lnc-ZNF32-3	chr10:44398876-44399048	XLOC_008792
8	lnc-ZNF32-3	chr10:44396819-44397271	XLOC_008792
9	lnc-C10orf136-1	chr10:44438643-44438729	XLOC_008473
10	lnc-ZNF32-3	chr10:44398876-44399037	XLOC_008792
11	lnc-C10orf136-1	chr10:44390313-44390881	XLOC_008473
12	lnc-C10orf136-1	chr10:44409207-44409860	XLOC_008473
13	lnc-C10orf136-1	chr10:44439810-44439914	XLOC_008473
14	lnc-C10orf136-1	chr10:44404752-44404817	NONHSAT013008
15	lnc-C10orf136-1	chr10:44438640-44438729	XLOC_008473
16	lnc-ZNF32-8	chr10:44417404-44417558	NONHSAT013010
17	lnc-C10orf136-1	chr10:44404752-44404817	XLOC_008473
18	lnc-C10orf136-1	chr10:44409207-44409914	XLOC_008473
19	lnc-ZNF32-8	chr10:44406662-44407238	NONHSAT013010
20	lnc-ZNF32-3	chr10:44407741-44407774	XLOC_008792
21	lnc-ZNF32-3	chr10:44396813-44397271	XLOC_008792
22	lnc-C10orf136-1	chr10:44439305-44439481	NONHSAT013008
23	lnc-C10orf136-1	chr10:44439305-44439481	XLOC_008473
24	lnc-C10orf136-1	chr10:44439305-44439439	XLOC_008473
25	lnc-ZNF32-3	chr10:44396819-44397271	XLOC_008792
26	lnc-C10orf136-1	chr10:44404991-44405107	XLOC_008473
27	lnc-C10orf136-1	chr10:44404757-44405107	XLOC_008473
28	lnc-C10orf136-1	chr10:44404991-44405107	XLOC_008473
29	lnc-ZNF32-3	chr10:44398876-44398897	XLOC_008792
30	lnc-C10orf136-1	chr10:44441442-44441598	NONHSAT013008
31	lnc-C10orf136-1	chr10:44438685-44438729	XLOC_008473
32	lnc-C10orf136-1	chr10:44434451-44435990	XLOC_008473
33	lnc-C10orf136-1	chr10:44439305-44439413	XLOC_008473
34	lnc-ZNF32-3	chr10:44396819-44397271	XLOC_008792
35	lnc-C10orf136-1	chr10:44404727-44404817	XLOC_008473
36	lnc-C10orf136-1	chr10:44404991-44405107	NONHSAT013008
37	lnc-C10orf136-1	chr10:44441442-44441598	XLOC_008473
38	lnc-C10orf136-1	chr10:44438640-44438729	XLOC_008473
39	lnc-C10orf136-1	chr10:44404991-44405107	XLOC_008473
40	lnc-C10orf136-1	chr10:44407797-44407926	XLOC_008473
41	lnc-ZNF32-3	chr10:44407741-44407791	XLOC_008792
42	lnc-C10orf136-1	chr10:44439305-44439481	XLOC_008473
43	lnc-C10orf136-1	chr10:44438640-44438729	XLOC_008473
44	lnc-ZNF32-3	chr10:44407741-44407791	XLOC_008792
45	lnc-C10orf136-1	chr10:44407892-44407926	XLOC_008473
46	lnc-ZNF32-4	chr10:44409347-44409454	XLOC_008793
47	lnc-ZNF32-3	chr10:44407741-44407926	XLOC_008792
48	lnc-C10orf136-1	chr10:44407894-44407926	XLOC_008473
49	lnc-C10orf136-1	chr10:44409207-44409684	XLOC_008473
50	lnc-C10orf136-1	chr10:44436170-44436425	XLOC_008473

No data

Variant related genes	Relation type
ENSG00000236769	TF binding region
ENSG00000227029	TF binding region
LINC00841	TF binding region
ENSG00000236769	CpG island
ENSG00000227029	CpG island
LINC00841	CpG island
ENSG00000236769	chromatin interactions
ENSG00000227029	chromatin interactions
ENSG00000107562	chromatin interactions
ENSG00000233395	chromatin interactions
REEP3	miRNA target sites
SYNCRIP	miRNA target sites
HOXA5	miRNA target sites
AFF4	miRNA target sites
CASP7	miRNA target sites
SYNC	miRNA target sites
ABI2	miRNA target sites
NOL4	miRNA target sites
NME6	miRNA target sites
YIPF3	miRNA target sites

Extended variants
information (count: 3233 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:3233 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529639346	chr10:44378060-44378061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs182373446	chr10:44378071-44378072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs566300049	chr10:44378112-44378113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs539663551	chr10:44378121-44378122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs532342262	chr10:44378192-44378193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs570218498	chr10:44378226-44378227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs34209136	chr10:44378252-44378253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs68039047	chr10:44378266-44378267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs375297252	chr10:44378381-44378382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs574736347	chr10:44378403-44378404	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs188266209	chr10:44378433-44378434	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555778823	chr10:44378482-44378483	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs574344753	chr10:44378519-44378520	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs535766990	chr10:44378523-44378524	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553767067	chr10:44378540-44378541	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs372941808	chr10:44378564-44378565	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs74138919	chr10:44378591-44378592	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs192793477	chr10:44378609-44378610	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs564225299	chr10:44378632-44378633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs184134205	chr10:44378662-44378663	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543932293	chr10:44378670-44378671	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554338922	chr10:44378673-44378674	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs72781128	chr10:44378684-44378685	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs1540965	chr10:44378689-44378690	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs189213591	chr10:44378714-44378715	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569191607	chr10:44378727-44378728	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs141419959	chr10:44378730-44378731	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs547738710	chr10:44378735-44378736	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs374437886	chr10:44378736-44378737	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs7097453	chr10:44378740-44378741	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs137898710	chr10:44378787-44378788	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs386743224	chr10:44378795-44378796	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs192079794	chr10:44378799-44378800	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs369919744	chr10:44378840-44378841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs551569887	chr10:44378866-44378867	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs185007384	chr10:44378874-44378875	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs556916051	chr10:44378928-44378929	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs537594270	chr10:44378939-44378940	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs547849007	chr10:44378950-44378951	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189340724	chr10:44378968-44378969	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs180940786	chr10:44378969-44378970	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs7080468	chr10:44378999-44379000	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs185769048	chr10:44379013-44379014	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552983849	chr10:44379016-44379017	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs12259570	chr10:44379017-44379018	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs189447154	chr10:44379020-44379021	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs56067768	chr10:44379021-44379022	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs371334669	chr10:44379035-44379036	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539736261	chr10:44379048-44379049	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs558031503	chr10:44379058-44379059	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

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
Mental retardation	21062444	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
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	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
small cell lung cancer	20016488	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:692 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:44360000-44392200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr10:44374400-44378400	Weak transcription	HUVEC	blood vessel
3	chr10:44374400-44383400	Weak transcription	NHLF	lung
4	chr10:44375200-44378400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr10:44375800-44387400	Weak transcription	Left Ventricle	heart
6	chr10:44377000-44378200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr10:44377200-44378600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr10:44377400-44378200	Enhancers	Muscle Satellite Cultured Cells	--
9	chr10:44377400-44379000	Enhancers	Osteobl	bone
10	chr10:44377600-44378400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr10:44377600-44378800	Weak transcription	Right Ventricle	heart
12	chr10:44377600-44387600	Weak transcription	Right Atrium	heart
13	chr10:44377800-44383800	Weak transcription	HSMMtube	muscle
14	chr10:44378000-44380000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr10:44378000-44382600	Weak transcription	NHDF-Ad	bronchial
16	chr10:44378000-44383800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr10:44378200-44383200	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr10:44378200-44387000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr10:44378400-44378600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr10:44378400-44378800	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr10:44378400-44378800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr10:44378400-44378800	Enhancers	HUVEC	blood vessel
23	chr10:44378400-44379000	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr10:44378400-44379000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr10:44378400-44379200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr10:44378600-44378800	Enhancers	Gastric	stomach
27	chr10:44378600-44380200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr10:44378600-44383000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr10:44378800-44379000	Enhancers	Right Ventricle	heart
30	chr10:44378800-44380000	Weak transcription	Gastric	stomach
31	chr10:44379000-44383200	Weak transcription	Osteobl	bone
32	chr10:44379800-44381200	Enhancers	Stomach Mucosa	stomach
33	chr10:44380000-44380200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr10:44380000-44380600	Enhancers	Gastric	stomach
35	chr10:44380000-44381200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr10:44380200-44380400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr10:44380200-44380400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr10:44380200-44380600	Enhancers	Fetal Muscle Trunk	muscle
39	chr10:44380400-44386800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr10:44381200-44384600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr10:44381400-44381600	Enhancers	Fetal Muscle Trunk	muscle
42	chr10:44382200-44382400	Enhancers	Hela-S3	cervix
43	chr10:44382400-44384400	Weak transcription	Hela-S3	cervix
44	chr10:44382600-44389000	Enhancers	NHDF-Ad	bronchial
45	chr10:44383000-44383200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr10:44383200-44383400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr10:44383200-44385200	Enhancers	Muscle Satellite Cultured Cells	--
48	chr10:44383200-44388800	Enhancers	Osteobl	bone
49	chr10:44383400-44384800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr10:44383400-44388600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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