Variant report

Variant	nsv831874
Chromosome Location	chr10:53010357-53195508
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	chr10:53182465-53182665	HepG2	liver:	n/a	n/a
2	BACH1	chr10:53182381-53182667	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr10:53141090-53141352	GM12878	blood:	n/a	n/a
4	BATF	chr10:53141142-53141352	GM12878	blood:	n/a	n/a
5	BCLAF1	chr10:53149066-53149376	GM12878	blood:	n/a	n/a
6	BHLHE40	chr10:53182482-53182774	GM12878	blood:	n/a	n/a
7	BHLHE40	chr10:53116577-53116594	A549	lung:	n/a	n/a
8	BHLHE40	chr10:53149192-53149350	K562	blood:	n/a	n/a
9	BRCA1	chr10:53163856-53163891	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr10:53141091-53141633	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr10:53081791-53081924	HepG2	liver:	n/a	chr10:53081860-53081869 chr10:53081860-53081869 chr10:53081860-53081869 chr10:53081860-53081869 chr10:53081859-53081870
12	CEBPB	chr10:53182825-53183196	A549	lung:	n/a	chr10:53183010-53183023 chr10:53183011-53183022 chr10:53183012-53183021 chr10:53183012-53183021 chr10:53183010-53183023 chr10:53183012-53183021
13	CEBPB	chr10:53182828-53183198	HepG2	liver:	n/a	chr10:53183010-53183023 chr10:53183011-53183022 chr10:53183012-53183021 chr10:53183012-53183021 chr10:53183010-53183023 chr10:53183012-53183021
14	CEBPB	chr10:53178462-53178713	IMR90	lung:	n/a	n/a
15	CEBPB	chr10:53041681-53041940	A549	lung:	n/a	chr10:53041816-53041827
16	CEBPB	chr10:53020902-53020958	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr10:53010343-53010615	HepG2	liver:	n/a	chr10:53010468-53010479 chr10:53010467-53010478 chr10:53010467-53010480 chr10:53010467-53010480
18	CEBPB	chr10:53182516-53183198	Hela-S3	cervix:	n/a	chr10:53183010-53183023 chr10:53183011-53183022 chr10:53183012-53183021 chr10:53183012-53183021 chr10:53183010-53183023 chr10:53183012-53183021
19	CEBPB	chr10:53178445-53178635	HepG2	liver:	n/a	n/a
20	CEBPB	chr10:53020687-53021132	HepG2	liver:	n/a	chr10:53021033-53021044 chr10:53020810-53020823
21	CEBPB	chr10:53010319-53010589	K562	blood:	n/a	chr10:53010468-53010479 chr10:53010467-53010478 chr10:53010467-53010480 chr10:53010467-53010480
22	CEBPB	chr10:53010312-53010600	A549	lung:	n/a	chr10:53010468-53010479 chr10:53010467-53010478 chr10:53010467-53010480 chr10:53010467-53010480
23	CEBPB	chr10:53081673-53082098	MCF-7	breast:	n/a	chr10:53081860-53081869 chr10:53081860-53081869 chr10:53081860-53081869 chr10:53081860-53081869 chr10:53081859-53081870
24	CEBPB	chr10:53081676-53082033	A549	lung:	n/a	chr10:53081860-53081869 chr10:53081860-53081869 chr10:53081860-53081869 chr10:53081860-53081869 chr10:53081859-53081870
25	CEBPB	chr10:53041673-53042000	HepG2	liver:	n/a	chr10:53041816-53041827
26	CEBPB	chr10:53129672-53129981	IMR90	lung:	n/a	n/a
27	CEBPB	chr10:53149260-53150433	IMR90	lung:	n/a	chr10:53149689-53149701 chr10:53150212-53150225
28	CEBPB	chr10:53057215-53057551	IMR90	lung:	n/a	n/a
29	CEBPB	chr10:53182717-53183191	MCF-7	breast:	n/a	chr10:53183010-53183023 chr10:53183011-53183022 chr10:53183012-53183021 chr10:53183012-53183021 chr10:53183010-53183023 chr10:53183012-53183021
30	CEBPB	chr10:53050265-53050585	IMR90	lung:	n/a	chr10:53050417-53050428
31	CEBPB	chr10:53182136-53182259	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr10:53159620-53159938	HepG2	liver:	n/a	n/a
33	CEBPB	chr10:53104142-53104419	IMR90	lung:	n/a	n/a
34	CEBPB	chr10:53144714-53145155	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr10:53010289-53010617	IMR90	lung:	n/a	chr10:53010468-53010479 chr10:53010467-53010478 chr10:53010467-53010480 chr10:53010467-53010480
36	CEBPB	chr10:53020688-53021076	IMR90	lung:	n/a	chr10:53021033-53021044 chr10:53020810-53020823
37	CEBPB	chr10:53081674-53082048	HepG2	liver:	n/a	chr10:53081860-53081869 chr10:53081860-53081869 chr10:53081860-53081869 chr10:53081860-53081869 chr10:53081859-53081870
38	CEBPB	chr10:53081677-53082071	Hela-S3	cervix:	n/a	chr10:53081860-53081869 chr10:53081860-53081869 chr10:53081860-53081869 chr10:53081860-53081869 chr10:53081859-53081870
39	CEBPB	chr10:53182866-53183222	ECC-1	luminal epithelium:	n/a	chr10:53183010-53183023 chr10:53183011-53183022 chr10:53183012-53183021 chr10:53183012-53183021 chr10:53183010-53183023 chr10:53183012-53183021
40	CEBPB	chr10:53182817-53183206	IMR90	lung:	n/a	chr10:53183010-53183023 chr10:53183011-53183022 chr10:53183012-53183021 chr10:53183012-53183021 chr10:53183010-53183023 chr10:53183012-53183021
41	CEBPB	chr10:53141070-53141763	Hela-S3	cervix:	n/a	chr10:53141351-53141359
42	CEBPB	chr10:53062042-53062364	IMR90	lung:	n/a	n/a
43	CEBPB	chr10:53081605-53082063	IMR90	lung:	n/a	chr10:53081860-53081869 chr10:53081860-53081869 chr10:53081860-53081869 chr10:53081860-53081869 chr10:53081859-53081870
44	CEBPB	chr10:53159615-53159922	A549	lung:	n/a	n/a
45	CEBPB	chr10:53074170-53074419	HepG2	liver:	n/a	chr10:53074290-53074301 chr10:53074288-53074305
46	CEBPB	chr10:53159605-53159963	IMR90	lung:	n/a	n/a
47	CEBPB	chr10:53182821-53183259	H1-hESC	embryonic stem cell:	n/a	chr10:53183010-53183023 chr10:53183011-53183022 chr10:53183012-53183021 chr10:53183012-53183021 chr10:53183010-53183023 chr10:53183012-53183021
48	CEBPB	chr10:53182745-53183169	A549	lung:	n/a	chr10:53183010-53183023 chr10:53183011-53183022 chr10:53183012-53183021 chr10:53183012-53183021 chr10:53183010-53183023 chr10:53183012-53183021
49	CEBPB	chr10:53010310-53010619	Hela-S3	cervix:	n/a	chr10:53010468-53010479 chr10:53010467-53010478 chr10:53010467-53010480 chr10:53010467-53010480
50	CEBPB	chr10:53141061-53141757	IMR90	lung:	n/a	chr10:53141351-53141359

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:53165239-53165289	AG04450	lung:	fetal
2	chr10:53182118-53182168	HCT-116	colon:	n/a
3	chr10:53058473-53058523	PrEC	prostate:	n/a
4	chr10:53060815-53060865	RPTEC	kidney:	n/a
5	chr10:53071348-53071398	PANC-1	pancreas:	n/a
6	chr10:53143287-53143337	HRPEpiC	eye:	n/a
7	chr10:53071348-53071398	MCF-7	breast:	n/a
8	chr10:53011793-53011843	HCT-116	colon:	n/a
9	chr10:53071348-53071398	Hela-S3	cervix:	n/a
10	chr10:53149243-53149293	HEK293	kidney:	embryo
11	chr10:53058473-53058523	AG09309	skin:	n/a
12	chr10:53143287-53143337	HCPEpiC	choroid plexus:	n/a
13	chr10:53011793-53011843	ovcar-3	ovarian:	n/a
14	chr10:53137547-53137597	ProgFib	skin:	n/a
15	chr10:53011793-53011843	PANC-1	pancreas:	n/a
16	chr10:53058473-53058523	ECC-1	luminal epithelium:	n/a
17	chr10:53182118-53182168	MCF10A-Er-Src	breast:	n/a
18	chr10:53011793-53011843	BJ	skin:	n/a
19	chr10:53071348-53071398	A549	lung:	n/a
20	chr10:53149243-53149293	HCM	heart:	n/a
21	chr10:53149243-53149293	GM12892	blood:	n/a
22	chr10:53058473-53058523	BE2_C	brain:	n/a
23	chr10:53165239-53165289	SK-N-SH_RA	brain:	n/a
24	chr10:53182118-53182168	GM12878	blood:	n/a
25	chr10:53011793-53011843	HL-60	blood:	n/a
26	chr10:53058473-53058523	PFSK-1	brain:	n/a
27	chr10:53011793-53011843	AG10803	skin:	n/a
28	chr10:53182118-53182168	ECC-1	luminal epithelium:	n/a
29	chr10:53060815-53060865	NT2-D1	testis:	n/a
30	chr10:53149243-53149293	AoSMC	blood vessel:	n/a
31	chr10:53143287-53143337	NB4	blood:	n/a
32	chr10:53011793-53011843	SK-N-MC	brain:	n/a
33	chr10:53058473-53058523	HIPEpiC	eye:	n/a
34	chr10:53165239-53165289	GM19239	blood:	n/a
35	chr10:53182118-53182168	AG04450	lung:	fetal
36	chr10:53011793-53011843	BE2_C	brain:	n/a
37	chr10:53143287-53143337	IMR90	lung:	fetal
38	chr10:53149243-53149293	HPAEpiC	pulmonary alveolar:	n/a
39	chr10:53060815-53060865	HRE	kidney:	n/a
40	chr10:53058473-53058523	AG04449	skin:	fetal
41	chr10:53149243-53149293	ProgFib	skin:	n/a
42	chr10:53143287-53143337	T-47D	breast:	n/a
43	chr10:53182118-53182168	HPAEpiC	pulmonary alveolar:	n/a
44	chr10:53143287-53143337	AG09319	gingival:	n/a
45	chr10:53058473-53058523	ProgFib	skin:	n/a
46	chr10:53071348-53071398	SKMC	muscle:	n/a
47	chr10:53143287-53143337	AG10803	skin:	n/a
48	chr10:53071348-53071398	ProgFib	skin:	n/a
49	chr10:53149243-53149293	HNPCEpiC	eye:	n/a
50	chr10:53149243-53149293	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:53098772..53100977-chr10:53116314..53119071,2	K562	blood:
2	chr10:53008618..53010801-chr10:53013381..53015189,3	K562	blood:
3	chr10:53134398..53136579-chr10:53137759..53139607,2	K562	blood:
4	chr10:53098772..53100977-chr10:53116314..53119071,2	K562	blood:
5	chr10:53091191..53095808-chr10:53099838..53103049,4	K562	blood:
6	chr10:53008618..53010640-chr10:53013381..53015189,2	K562	blood:
7	chr10:53091191..53095808-chr10:53099838..53103049,4	K562	blood:
8	chr10:53150184..53151965-chr10:53152581..53154476,2	K562	blood:
9	chr10:53146560..53148101-chr10:53149083..53151252,2	MCF-7	breast:
10	chr10:52984696..52986392-chr10:53018336..53020821,2	K562	blood:
11	chr1:152369716..152370381-chr10:53149139..53149795,2	MCF-7	breast:
12	chr10:53008618..53010640-chr10:53013381..53015189,2	K562	blood:
13	chr10:52823455..52824113-chr10:53182409..53182910,2	MCF-7	breast:
14	chr10:53149203..53149747-chr10:53635097..53636033,2	MCF-7	breast:
15	chr10:53150184..53151965-chr10:53152581..53154476,2	K562	blood:
16	chr10:53148841..53149455-chr10:53652709..53653694,2	MCF-7	breast:
17	chr10:53008618..53010801-chr10:53013381..53015189,3	K562	blood:
18	chr10:53148869..53149613-chr10:53763797..53764717,2	MCF-7	breast:
19	chr10:53134398..53136579-chr10:53137759..53139607,2	K562	blood:
20	chr10:53145130..53146653-chr10:54068648..54071560,2	K562	blood:
21	chr10:53146560..53148101-chr10:53149083..53151252,2	MCF-7	breast:
22	chr10:53149205..53149730-chr10:53720127..53720824,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASAH2B-4	chr10:53066329-53066469	ENSG00000235279.1
2	lnc-ASAH2B-4	chr10:53062326-53062584	ENSG00000235279.1
3	lnc-ASAH2B-6	chr10:53079586-53080420	NONHSAT013412

miRNA name	Chromosome Location	mirBase accession
hsa-miR-605-3p	chr10:53059383-53059404	MIMAT0026621
hsa-miR-605-5p	chr10:53059348-53059370	MIMAT0003273

Variant related genes	Relation type
ENSG00000231132	TF binding region
ENSG00000235279	TF binding region
ENSG00000266591	TF binding region
MIR605	TF binding region
RSU1P3	TF binding region
ENSG00000231132	CpG island
ENSG00000235279	CpG island
ENSG00000266591	CpG island
MIR605	CpG island
RSU1P3	CpG island
TMEM64	Mature miRNA region
YBX1	Mature miRNA region
DRG1	Mature miRNA region
TP53	Mature miRNA region
MDM2	Mature miRNA region
KDM5C	Mature miRNA region
BCL9	Mature miRNA region
TCEAL1	Mature miRNA region
SEC24D	Mature miRNA region
TRAF4	Mature miRNA region

Extended variants
information (count: 6863 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:6863 , 50 per page) page: 1 2 3 4 5 6 7 ... 138

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553566204	chr10:53010379-53010380	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs377441470	chr10:53010388-53010389	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs572161737	chr10:53010405-53010406	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs189373968	chr10:53010409-53010410	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs564176946	chr10:53010439-53010440	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs569925876	chr10:53010449-53010450	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs61849746	chr10:53010489-53010490	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs184621208	chr10:53010499-53010500	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs529219925	chr10:53010536-53010537	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs555925293	chr10:53010586-53010587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs190120694	chr10:53010610-53010611	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs56307542	chr10:53010635-53010636	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs181789209	chr10:53010641-53010642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs532353351	chr10:53010704-53010705	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs184966549	chr10:53010711-53010712	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs189671352	chr10:53010717-53010718	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs142313798	chr10:53010750-53010751	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs180912128	chr10:53010776-53010777	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs567849074	chr10:53010787-53010788	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs34750163	chr10:53010803-53010804	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536993206	chr10:53010806-53010807	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs113445401	chr10:53010826-53010827	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs374618218	chr10:53010864-53010865	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs111773109	chr10:53010878-53010879	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs10996331	chr10:53010887-53010888	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs191130353	chr10:53010923-53010924	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs182016025	chr10:53010969-53010970	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs145945350	chr10:53011003-53011004	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs61849751	chr10:53011011-53011012	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs564559001	chr10:53011093-53011094	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs563333205	chr10:53011173-53011174	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs573847695	chr10:53011196-53011197	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs114508599	chr10:53011217-53011218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs73337554	chr10:53011238-53011239	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs187333387	chr10:53011246-53011247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs544005042	chr10:53011250-53011251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs551182839	chr10:53011305-53011306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs191767506	chr10:53011316-53011317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs183468830	chr10:53011320-53011321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs7097901	chr10:53011341-53011342	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs11392065	chr10:53011363-53011364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs67011771	chr10:53011364-53011365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs58368756	chr10:53011371-53011372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs550690070	chr10:53011372-53011373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs7094420	chr10:53011387-53011388	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs556543084	chr10:53011559-53011560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs149827862	chr10:53011596-53011597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs202005984	chr10:53011597-53011598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs547233624	chr10:53011599-53011600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs147948016	chr10:53011617-53011618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
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
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Cancer	20164920	CNVD
Ollier disease	21235737	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Mental retardation	17124404	CNVD
Epilepsy	20923578	CNVD
Prostate cancer	16573809	CNVD
Schizophrenia	19329560	CNVD
Heart failure	18772530	CNVD
Heart failure	18854381	CNVD
Hyperglycemia	19060297	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1236 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:53003600-53010400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr10:53004800-53010600	Weak transcription	Psoas Muscle	Psoas
3	chr10:53006200-53015800	Weak transcription	Colon Smooth Muscle	Colon
4	chr10:53006400-53010400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr10:53006600-53010400	Weak transcription	Primary hematopoietic stem cells	blood
6	chr10:53006800-53017000	Weak transcription	Aorta	Aorta
7	chr10:53006800-53017600	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr10:53007000-53010400	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr10:53007000-53010600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr10:53007400-53016600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr10:53007800-53010400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr10:53007800-53012600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr10:53008000-53010400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr10:53008000-53012400	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr10:53008000-53012800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr10:53009400-53011800	Enhancers	Skeletal Muscle Female	skeletal muscle
17	chr10:53009400-53012000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr10:53009400-53012000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr10:53009600-53010400	Enhancers	Stomach Smooth Muscle	stomach
20	chr10:53009600-53011800	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr10:53009600-53013600	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr10:53009800-53011000	Enhancers	Skeletal Muscle Male	skeletal muscle
23	chr10:53009800-53011200	Enhancers	Duodenum Smooth Muscle	Duodenum
24	chr10:53009800-53011400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr10:53009800-53011800	Enhancers	Rectal Smooth Muscle	rectum
26	chr10:53010000-53010600	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr10:53010000-53011200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr10:53010000-53011200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr10:53010000-53011800	Enhancers	HUVEC	blood vessel
30	chr10:53010200-53010600	Enhancers	H1 Cell Line	embryonic stem cell
31	chr10:53010200-53010800	Enhancers	Fetal Muscle Leg	muscle
32	chr10:53010200-53011200	Enhancers	Sigmoid Colon	Sigmoid Colon
33	chr10:53010400-53010800	Enhancers	H9 Cell Line	embryonic stem cell
34	chr10:53010400-53011000	Enhancers	HSMMtube	muscle
35	chr10:53010400-53011200	Enhancers	Primary hematopoietic stem cells	blood
36	chr10:53010400-53011200	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr10:53010400-53011200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr10:53010400-53012000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr10:53010400-53013600	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr10:53010600-53010800	Enhancers	Psoas Muscle	Psoas
41	chr10:53010600-53011200	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr10:53010600-53012400	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr10:53010600-53017200	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr10:53010800-53011600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr10:53010800-53015000	Weak transcription	Fetal Muscle Leg	muscle
46	chr10:53010800-53015200	Weak transcription	H9 Cell Line	embryonic stem cell
47	chr10:53010800-53015200	Weak transcription	Psoas Muscle	Psoas
48	chr10:53011200-53012200	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr10:53011200-53016200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr10:53011200-53017200	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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