Variant report

Variant	nsv825206
Chromosome Location	chr10:688018-818192
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:986)
CpG islands
(count:6114)
Chromatin interactive
region (count:53)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:986 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:695549-696087	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:727897-728114	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:758256-758463	HepG2	liver:	n/a	n/a
4	ATF1	chr10:813001-813370	K562	blood:	n/a	n/a
5	ATF1	chr10:691655-691733	K562	blood:	n/a	n/a
6	ATF1	chr10:729319-729702	K562	blood:	n/a	n/a
7	BACH1	chr10:734911-735245	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr10:718041-718363	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr10:699656-699670	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr10:736069-736281	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr10:723859-724161	GM12878	blood:	n/a	n/a
12	BATF	chr10:722135-722417	GM12878	blood:	n/a	n/a
13	BATF	chr10:722079-722448	GM12878	blood:	n/a	n/a
14	BATF	chr10:705986-706335	GM12878	blood:	n/a	n/a
15	BCL11A	chr10:722144-722453	GM12878	blood:	n/a	n/a
16	BCL11A	chr10:811979-812582	GM12878	blood:	n/a	n/a
17	BCL11A	chr10:723812-724184	GM12878	blood:	n/a	chr10:723831-723839 chr10:724070-724079 chr10:723932-723945
18	BCL11A	chr10:769301-769535	GM12878	blood:	n/a	n/a
19	BCL11A	chr10:743024-743363	GM12878	blood:	n/a	chr10:743188-743197
20	BCL11A	chr10:705958-706431	GM12878	blood:	n/a	n/a
21	BCL3	chr10:745959-746729	GM12878	blood:	n/a	n/a
22	BCL3	chr10:812586-812912	GM12878	blood:	n/a	n/a
23	BCL3	chr10:746085-746825	GM12878	blood:	n/a	n/a
24	BHLHE40	chr10:695485-697003	HepG2	liver:	n/a	n/a
25	BHLHE40	chr10:711494-711760	K562	blood:	n/a	chr10:711672-711681 chr10:711670-711683 chr10:711666-711687 chr10:711558-711571 chr10:711673-711682 chr10:711671-711680 chr10:711672-711681
26	BHLHE40	chr10:769894-770344	K562	blood:	n/a	n/a
27	BHLHE40	chr10:764330-764448	K562	blood:	n/a	n/a
28	BHLHE40	chr10:695707-696007	HepG2	liver:	n/a	n/a
29	BHLHE40	chr10:769085-769382	K562	blood:	n/a	n/a
30	BHLHE40	chr10:743220-743294	GM12878	blood:	n/a	n/a
31	CBX3	chr10:806640-806884	K562	blood:	n/a	n/a
32	CBX3	chr10:769860-770105	K562	blood:	n/a	n/a
33	CEBPB	chr10:695464-696050	IMR90	lung:	n/a	n/a
34	CEBPB	chr10:758430-759010	A549	lung:	n/a	n/a
35	CEBPB	chr10:776512-776828	A549	lung:	n/a	chr10:776667-776678
36	CEBPB	chr10:799560-799705	K562	blood:	n/a	n/a
37	CEBPB	chr10:733032-733346	IMR90	lung:	n/a	n/a
38	CEBPB	chr10:697228-697554	IMR90	lung:	n/a	n/a
39	CEBPB	chr10:695388-696030	A549	lung:	n/a	n/a
40	CEBPB	chr10:758593-758726	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr10:735751-735902	HepG2	liver:	n/a	n/a
42	CEBPB	chr10:758111-758888	Hela-S3	cervix:	n/a	chr10:758290-758301
43	CEBPB	chr10:758153-758435	HepG2	liver:	n/a	chr10:758290-758301
44	CEBPB	chr10:695403-696085	HepG2	liver:	n/a	n/a
45	CEBPB	chr10:776542-776771	H1-hESC	embryonic stem cell:	n/a	chr10:776667-776678
46	CEBPB	chr10:776582-776736	Hela-S3	cervix:	n/a	chr10:776667-776678
47	CEBPB	chr10:729197-729907	IMR90	lung:	n/a	n/a
48	CEBPB	chr10:799626-799733	HepG2	liver:	n/a	n/a
49	CEBPB	chr10:732595-732615	HepG2	liver:	n/a	n/a
50	CEBPB	chr10:758539-758922	MCF-7	breast:	n/a	n/a

(count:6114 , 50 per page) page: 1 2 3 4 5 6 7 ... 123

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:693439-693489	HUVEC	blood vessel:	n/a
2	chr10:695844-695894	HCPEpiC	choroid plexus:	n/a
3	chr10:711944-711994	SK-N-SH	brain:	n/a
4	chr10:717486-717536	AG04450	lung:	fetal
5	chr10:729226-729276	HEK293	kidney:	embryo
6	chr10:817083-817133	PANC-1	pancreas:	n/a
7	chr10:697055-697105	HRE	kidney:	n/a
8	chr10:742858-742908	PFSK-1	brain:	n/a
9	chr10:766041-766091	SAEC	small airway:	n/a
10	chr10:743478-743528	NT2-D1	testis:	n/a
11	chr10:743761-743811	AG04449	skin:	fetal
12	chr10:711556-711606	HL-60	blood:	n/a
13	chr10:689995-690045	GM12891	blood:	n/a
14	chr10:710082-710132	HEK293	kidney:	embryo
15	chr10:693439-693489	HUVEC	blood vessel:	n/a
16	chr10:695844-695894	HCPEpiC	choroid plexus:	n/a
17	chr10:711944-711994	SK-N-SH	brain:	n/a
18	chr10:717486-717536	AG04450	lung:	fetal
19	chr10:729226-729276	HEK293	kidney:	embryo
20	chr10:817083-817133	PANC-1	pancreas:	n/a
21	chr10:697055-697105	HRE	kidney:	n/a
22	chr10:742858-742908	PFSK-1	brain:	n/a
23	chr10:766041-766091	SAEC	small airway:	n/a
24	chr10:743478-743528	NT2-D1	testis:	n/a
25	chr10:743761-743811	AG04449	skin:	fetal
26	chr10:711556-711606	HL-60	blood:	n/a
27	chr10:689995-690045	GM12891	blood:	n/a
28	chr10:710082-710132	HEK293	kidney:	embryo
29	chr10:712442-712492	U87	brain:	n/a
30	chr10:709839-709889	HCPEpiC	choroid plexus:	n/a
31	chr10:697055-697105	AoSMC	blood vessel:	n/a
32	chr10:698258-698308	PFSK-1	brain:	n/a
33	chr10:729226-729276	NH-A	brain:	n/a
34	chr10:782282-782332	SK-N-SH_RA	brain:	n/a
35	chr10:783591-783641	H1-hESC	embryonic stem cell:	embryo
36	chr10:768541-768591	Caco-2	colon:	n/a
37	chr10:743392-743442	HUVEC	blood vessel:	n/a
38	chr10:766431-766481	U87	brain:	n/a
39	chr10:717091-717141	HL-60	blood:	n/a
40	chr10:743392-743442	HIPEpiC	eye:	n/a
41	chr10:743286-743336	HRE	kidney:	n/a
42	chr10:783591-783641	HEEpiC	esophagus:	n/a
43	chr10:710082-710132	BJ	skin:	n/a
44	chr10:773141-773191	AoSMC	blood vessel:	n/a
45	chr10:706006-706056	CMK	blood:	n/a
46	chr10:693439-693489	ECC-1	luminal epithelium:	n/a
47	chr10:743931-743981	MCF10A-Er-Src	breast:	n/a
48	chr10:724510-724560	HRCEpiC	kidney:	n/a
49	chr10:697901-697951	HMEC	breast:	n/a
50	chr10:697771-697821	HCF	heart:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:735855..737615-chr10:818949..821134,2	MCF-7	breast:
2	chr10:778218..778962-chr10:824579..825446,5	MCF-7	breast:
3	chr10:731969..737087-chr10:747564..751327,5	MCF-7	breast:
4	chr10:723887..725590-chr10:731403..733656,2	MCF-7	breast:
5	chr10:733710..735507-chr10:754476..756731,2	MCF-7	breast:
6	chr10:734188..737067-chr10:751931..753657,2	MCF-7	breast:
7	chr10:739447..741646-chr10:745969..747507,2	MCF-7	breast:
8	chr10:674481..678808-chr10:734028..737251,4	MCF-7	breast:
9	chr10:735546..737660-chr10:741311..743613,2	MCF-7	breast:
10	chr10:734436..736142-chr10:751742..753613,2	MCF-7	breast:
11	chr10:705629..708619-chr10:732652..734638,2	MCF-7	breast:
12	chr10:656339..658937-chr10:722531..724771,2	MCF-7	breast:
13	chr10:698785..701781-chr10:833421..835495,2	MCF-7	breast:
14	chr10:719611..721837-chr10:748749..751307,2	K562	blood:
15	chr10:762176..765127-chr10:765238..767512,2	MCF-7	breast:
16	chr10:705629..708619-chr10:732652..734638,2	MCF-7	breast:
17	chr10:692009..694331-chr10:706518..708449,2	MCF-7	breast:
18	chr10:721854..725155-chr10:733736..736400,3	MCF-7	breast:
19	chr10:583403..585208-chr10:714450..715956,2	K562	blood:
20	chr10:687008..688714-chr10:699568..702258,2	MCF-7	breast:
21	chr10:692009..694331-chr10:706518..708449,2	MCF-7	breast:
22	chr10:732975..736358-chr10:737675..743965,7	MCF-7	breast:
23	chr10:750983..753337-chr10:755498..757369,2	MCF-7	breast:
24	chr10:603209..605062-chr10:710188..713086,2	MCF-7	breast:
25	chr10:692996..695820-chr10:700101..701896,2	MCF-7	breast:
26	chr10:719611..721837-chr10:748749..751307,2	K562	blood:
27	chr10:736863..738900-chr10:740136..742469,2	MCF-7	breast:
28	chr10:762176..765127-chr10:765238..767512,2	MCF-7	breast:
29	chr10:817104..818718-chr10:820025..821722,2	MCF-7	breast:
30	chr10:783561..786479-chr10:789093..790752,2	MCF-7	breast:
31	chr10:725778..731472-chr10:731586..738263,11	MCF-7	breast:
32	chr10:750983..753337-chr10:755498..757369,2	MCF-7	breast:
33	chr10:733710..735507-chr10:754476..756731,2	MCF-7	breast:
34	chr10:739447..741646-chr10:745969..747507,2	MCF-7	breast:
35	chr10:739318..742202-chr10:834057..836421,2	MCF-7	breast:
36	chr10:723887..725590-chr10:731403..733656,2	MCF-7	breast:
37	chr10:736863..738900-chr10:740136..742469,2	MCF-7	breast:
38	chr10:757872..760729-chr10:776939..779568,2	MCF-7	breast:
39	chr10:717115..720273-chr10:724564..727281,3	MCF-7	breast:
40	chr10:733954..737075-chr10:737496..740853,6	MCF-7	breast:
41	chr10:701409..702201-chr19:4341065..4341565,2	MCF-7	breast:
42	chr10:736326..739216-chr10:743425..745379,3	K562	blood:
43	chr10:733897..735933-chr10:814143..815828,2	MCF-7	breast:
44	chr10:756021..758273-chr10:765053..767183,2	MCF-7	breast:
45	chr10:712816..715288-chr10:723469..725023,2	MCF-7	breast:
46	chr10:756021..758273-chr10:765053..767183,2	MCF-7	breast:
47	chr10:717115..720273-chr10:724564..727281,3	MCF-7	breast:
48	chr10:734350..736432-chr10:761399..763324,2	MCF-7	breast:
49	chr10:691751..694285-chr10:694356..695999,2	K562	blood:
50	chr10:736326..739216-chr10:743425..745379,3	K562	blood:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C10orf108-1	chr10:709498-709642	ENSG00000242357.1
2	lnc-C10orf108-1	chr10:696231-696382	NONHSAT010867
3	lnc-C10orf108-1	chr10:695888-696118	NONHSAT010867
4	lnc-C10orf108-5	chr10:714400-715521	ENSG00000272992.1
5	lnc-C10orf108-6	chr10:779932-779973	NONHSAT010872
6	lnc-LARP4B-3	chr10:724715-724736	NONHSAT010869
7	lnc-C10orf108-3	chr10:737256-737679	NONHSAT010870
8	lnc-C10orf108-1	chr10:707966-708058	NR_027152
9	lnc-C10orf108-4	chr10:789932-789973	XLOC_008335
10	lnc-C10orf108-1	chr10:696017-696382	NR_027152
11	lnc-LARP4B-3	chr10:724395-724591	NONHSAT010869
12	lnc-C10orf108-4	chr10:790517-790898	XLOC_008335
13	lnc-C10orf108-3	chr10:736183-736265	NONHSAT010870
14	lnc-C10orf108-3	chr10:737257-737679	XLOC_008334
15	lnc-C10orf108-1	chr10:708731-711109	NR_027152
16	lnc-C10orf108-6	chr10:780517-780898	NONHSAT010872
17	lnc-C10orf108-3	chr10:736184-736265	XLOC_008334
18	lnc-C10orf108-1	chr10:712158-712562	ENSG00000242357.1
19	lnc-C10orf108-1	chr10:697051-698595	NONHSAT010867

No data

Variant related genes	Relation type
MIR5699	TF binding region
PRR26	TF binding region
ENSG00000231601	TF binding region
ENSG00000242357	TF binding region
DIP2C	TF binding region
ENSG00000272992	TF binding region
MIR5699	CpG island
PRR26	CpG island
ENSG00000231601	CpG island
ENSG00000242357	CpG island
DIP2C	CpG island
ENSG00000272992	CpG island
ENSG00000225140	chromatin interactions
ENSG00000231601	chromatin interactions
ENSG00000151240	chromatin interactions
ENSG00000180525	chromatin interactions
ENSG00000263511	chromatin interactions
ENSG00000272992	chromatin interactions
SEC23IP	miRNA target sites
PTK2	miRNA target sites
SEC24A	miRNA target sites
PTGS2	miRNA target sites

Extended variants
information (count: 6040 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:6040 , 50 per page) page: 1 2 3 4 5 6 7 ... 121

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538991241	chr10:688044-688045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs563140450	chr10:688046-688047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs181910247	chr10:688069-688070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs532065313	chr10:688160-688161	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs187119395	chr10:688196-688197	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs531810330	chr10:688224-688225	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs12412997	chr10:688239-688240	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs575243758	chr10:688243-688244	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs527774708	chr10:688253-688254	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs547917392	chr10:688278-688279	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs370674779	chr10:688316-688317	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs570737139	chr10:688379-688380	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs139165465	chr10:688401-688402	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs560638042	chr10:688416-688417	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs189909232	chr10:688418-688419	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs10795292	chr10:688424-688425	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs537755252	chr10:688436-688437	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs554331136	chr10:688441-688442	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs78961929	chr10:688451-688452	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs533118985	chr10:688458-688459	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs11815644	chr10:688484-688485	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs181705548	chr10:688524-688525	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs537520597	chr10:688525-688526	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs144002044	chr10:688609-688610	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs539390116	chr10:688616-688617	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs186441726	chr10:688623-688624	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs369429904	chr10:688627-688628	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372303762	chr10:688640-688641	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs146416688	chr10:688647-688648	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs567929042	chr10:688661-688662	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs189947879	chr10:688713-688714	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs564437527	chr10:688714-688715	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373677399	chr10:688723-688724	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564572540	chr10:688782-688783	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs367605276	chr10:688801-688802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs182214710	chr10:688804-688805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs371869195	chr10:688824-688825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs548328723	chr10:688834-688835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs140200454	chr10:688844-688845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs7071528	chr10:688914-688915	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs531495881	chr10:688919-688920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs113798138	chr10:688932-688933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs568130712	chr10:688976-688977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs151313506	chr10:689007-689008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs7074927	chr10:689018-689019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs372361295	chr10:689050-689051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs547294821	chr10:689113-689114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs377156649	chr10:689114-689115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs539548495	chr10:689127-689128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs559696806	chr10:689158-689159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	20409316	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Breast cancer	17133270	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Cancer	21129771	CNVD
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21525872	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21858162	CNVD
Obesity	19966786	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Aortic dissecting aneurysms	22263138	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Breast cancer	21364760	CNVD
Glioma	20126413	CNVD

Chromatin state (count:2403 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:672000-700000	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr10:672200-690600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr10:672600-695800	Weak transcription	NHLF	lung
4	chr10:680200-690600	Weak transcription	Aorta	Aorta
5	chr10:680400-688400	Weak transcription	Stomach Mucosa	stomach
6	chr10:680400-690400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr10:680400-690600	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr10:680400-690600	Weak transcription	Fetal Lung	lung
9	chr10:681200-688400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr10:681800-688400	Weak transcription	Right Atrium	heart
11	chr10:681800-688600	Weak transcription	Psoas Muscle	Psoas
12	chr10:681800-690800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr10:681800-696200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr10:682400-690800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr10:683000-696000	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr10:683600-688400	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr10:683600-688400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr10:684000-690600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr10:684200-700000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr10:685000-688400	Weak transcription	Fetal Muscle Trunk	muscle
21	chr10:685200-690200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr10:685400-688400	Weak transcription	Lung	lung
23	chr10:685600-690400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr10:685600-690800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr10:685600-699800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr10:685800-690400	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr10:685800-695200	Weak transcription	Rectal Smooth Muscle	rectum
28	chr10:686000-688200	Weak transcription	Fetal Heart	heart
29	chr10:686000-688400	Weak transcription	Fetal Intestine Small	intestine
30	chr10:686000-688400	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr10:686000-690400	Weak transcription	Fetal Brain Female	brain
32	chr10:686000-690800	Weak transcription	Ovary	ovary
33	chr10:686200-688400	Weak transcription	Pancreas	Pancrea
34	chr10:686200-690400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr10:686200-696200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr10:686400-690000	Weak transcription	Fetal Stomach	stomach
37	chr10:686400-690800	Weak transcription	Brain Substantia Nigra	brain
38	chr10:686600-688400	Weak transcription	Gastric	stomach
39	chr10:687000-688200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr10:687000-688600	Weak transcription	Fetal Brain Male	brain
41	chr10:687200-688800	Enhancers	Left Ventricle	heart
42	chr10:687400-688400	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chr10:687400-689000	Enhancers	Colon Smooth Muscle	Colon
44	chr10:687400-700000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr10:687600-688800	Enhancers	Rectal Mucosa Donor 29	rectum
46	chr10:687600-690600	Weak transcription	Brain Angular Gyrus	brain
47	chr10:687600-690600	Weak transcription	Brain Cingulate Gyrus	brain
48	chr10:687600-690600	Weak transcription	Brain Inferior Temporal Lobe	brain
49	chr10:687600-690600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
50	chr10:687600-695200	Weak transcription	Right Ventricle	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links