Variant report

Variant	esv3693445
Chromosome Location	chr2:183542825-183725221
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1679)
CpG islands
(count:1222)
Chromatin interactive
region (count:124)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:1679 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:183679569-183679767	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:183648439-183648583	K562	blood:	n/a	n/a
3	ARID3A	chr2:183580474-183581183	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:183593463-183593469	K562	blood:	n/a	n/a
5	ARID3A	chr2:183649467-183649783	K562	blood:	n/a	n/a
6	ARID3A	chr2:183668859-183669300	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:183649459-183649762	HepG2	liver:	n/a	n/a
8	ATF1	chr2:183647473-183647647	K562	blood:	n/a	n/a
9	ATF2	chr2:183580660-183581085	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr2:183580338-183581152	GM12878	blood:	n/a	n/a
11	ATF2	chr2:183580660-183581148	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr2:183580790-183581114	K562	blood:	n/a	chr2:183580978-183580987
13	BACH1	chr2:183580525-183581202	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr2:183581406-183581577	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr2:183581032-183581106	K562	blood:	n/a	n/a
16	BATF	chr2:183591303-183591561	GM12878	blood:	n/a	n/a
17	BATF	chr2:183591221-183591595	GM12878	blood:	n/a	n/a
18	BCL11A	chr2:183683644-183683969	H1-hESC	embryonic stem cell:	n/a	n/a
19	BCL3	chr2:183580410-183581093	A549	lung:	n/a	chr2:183580912-183580925 chr2:183580685-183580694 chr2:183580748-183580761 chr2:183580903-183580916 chr2:183580753-183580766
20	BCLAF1	chr2:183580322-183581201	GM12878	blood:	n/a	chr2:183580912-183580925 chr2:183580685-183580694 chr2:183580748-183580761 chr2:183580903-183580916 chr2:183580753-183580766
21	BHLHE40	chr2:183580447-183581508	GM12878	blood:	n/a	chr2:183580750-183580766 chr2:183580968-183580984 chr2:183580900-183580916 chr2:183580742-183580758 chr2:183580753-183580769 chr2:183580910-183580926
22	BHLHE40	chr2:183583365-183583528	GM12878	blood:	n/a	n/a
23	BHLHE40	chr2:183580177-183581631	K562	blood:	n/a	chr2:183580750-183580766 chr2:183580968-183580984 chr2:183580900-183580916 chr2:183580742-183580758 chr2:183580753-183580769 chr2:183580910-183580926
24	BHLHE40	chr2:183580015-183581390	HepG2	liver:	n/a	chr2:183580750-183580766 chr2:183580968-183580984 chr2:183580900-183580916 chr2:183580742-183580758 chr2:183580753-183580769 chr2:183580910-183580926
25	BHLHE40	chr2:183581895-183581916	GM12878	blood:	n/a	n/a
26	BRCA1	chr2:183580727-183581109	HepG2	liver:	n/a	n/a
27	BRCA1	chr2:183679511-183679776	HepG2	liver:	n/a	n/a
28	BRCA1	chr2:183580850-183581133	H1-hESC	embryonic stem cell:	n/a	n/a
29	BRCA1	chr2:183576504-183576579	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr2:183580321-183581659	K562	blood:	n/a	n/a
31	CCNT2	chr2:183580601-183581535	K562	blood:	n/a	n/a
32	CCNT2	chr2:183650940-183651109	K562	blood:	n/a	n/a
33	CEBPB	chr2:183651455-183651655	A549	lung:	n/a	n/a
34	CEBPB	chr2:183626516-183626971	ECC-1	luminal epithelium:	n/a	chr2:183626725-183626736
35	CEBPB	chr2:183658874-183659067	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr2:183623123-183623469	A549	lung:	n/a	n/a
37	CEBPB	chr2:183676829-183676918	K562	blood:	n/a	chr2:183676879-183676890
38	CEBPB	chr2:183623298-183623480	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr2:183626538-183626940	HCT-116	colon:	n/a	chr2:183626725-183626736
40	CEBPB	chr2:183647103-183647312	HepG2	liver:	n/a	chr2:183647245-183647256
41	CEBPB	chr2:183623136-183623452	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr2:183579897-183580654	A549	lung:	n/a	n/a
43	CEBPB	chr2:183626540-183626927	A549	lung:	n/a	chr2:183626725-183626736
44	CEBPB	chr2:183679659-183679922	HepG2	liver:	n/a	chr2:183679810-183679823 chr2:183679811-183679822
45	CEBPB	chr2:183626580-183626883	MCF-7	breast:	n/a	chr2:183626725-183626736
46	CEBPB	chr2:183626536-183626923	HepG2	liver:	n/a	chr2:183626725-183626736
47	CEBPB	chr2:183647241-183647259	K562	blood:	n/a	chr2:183647245-183647256
48	CEBPB	chr2:183626539-183626936	IMR90	lung:	n/a	chr2:183626725-183626736
49	CEBPB	chr2:183626540-183626926	Hela-S3	cervix:	n/a	chr2:183626725-183626736
50	CEBPB	chr2:183685030-183685198	A549	lung:	n/a	chr2:183685096-183685107

(count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:183580841-183580891	SK-N-SH	brain:	n/a
2	chr2:183580574-183580624	LNCaP	prostate:	n/a
3	chr2:183580841-183580891	SK-N-SH	brain:	n/a
4	chr2:183580574-183580624	LNCaP	prostate:	n/a
5	chr2:183580523-183580573	HCPEpiC	choroid plexus:	n/a
6	chr2:183584043-183584093	PANC-1	pancreas:	n/a
7	chr2:183580818-183580868	GM19239	blood:	n/a
8	chr2:183580818-183580868	GM06990	blood:	n/a
9	chr2:183658977-183659027	HRCEpiC	kidney:	n/a
10	chr2:183723096-183723146	HCT-116	colon:	n/a
11	chr2:183581591-183581641	NH-A	brain:	n/a
12	chr2:183580463-183580513	MCF10A-Er-Src	breast:	n/a
13	chr2:183580841-183580891	Jurkat	blood:	n/a
14	chr2:183658977-183659027	IMR90	lung:	fetal
15	chr2:183580829-183580879	HAEpiC	amniotic membrane:	n/a
16	chr2:183580950-183581000	T-47D	breast:	n/a
17	chr2:183642235-183642285	AG09309	skin:	n/a
18	chr2:183580950-183581000	HMEC	breast:	n/a
19	chr2:183580829-183580879	HMEC	breast:	n/a
20	chr2:183580463-183580513	HNPCEpiC	eye:	n/a
21	chr2:183580523-183580573	SAEC	small airway:	n/a
22	chr2:183580910-183580960	GM12891	blood:	n/a
23	chr2:183580841-183580891	PANC-1	pancreas:	n/a
24	chr2:183580910-183580960	AG04449	skin:	fetal
25	chr2:183581591-183581641	HNPCEpiC	eye:	n/a
26	chr2:183580910-183580960	HCF	heart:	n/a
27	chr2:183580950-183581000	CMK	blood:	n/a
28	chr2:183580694-183580744	NHBE	bronchial:	n/a
29	chr2:183580574-183580624	HNPCEpiC	eye:	n/a
30	chr2:183683268-183683318	AG09309	skin:	n/a
31	chr2:183577625-183577675	ovcar-3	ovarian:	n/a
32	chr2:183580841-183580891	AG09319	gingival:	n/a
33	chr2:183580841-183580891	Caco-2	colon:	n/a
34	chr2:183577625-183577675	HEEpiC	esophagus:	n/a
35	chr2:183584043-183584093	HCM	heart:	n/a
36	chr2:183580841-183580891	HCT-116	colon:	n/a
37	chr2:183683268-183683318	CMK	blood:	n/a
38	chr2:183580829-183580879	HRPEpiC	eye:	n/a
39	chr2:183584043-183584093	HEK293	kidney:	embryo
40	chr2:183577625-183577675	HCM	heart:	n/a
41	chr2:183699153-183699203	Caco-2	colon:	n/a
42	chr2:183580829-183580879	IMR90	lung:	fetal
43	chr2:183658977-183659027	CMK	blood:	n/a
44	chr2:183658977-183659027	HMEC	breast:	n/a
45	chr2:183580841-183580891	HMEC	breast:	n/a
46	chr2:183580829-183580879	LNCaP	prostate:	n/a
47	chr2:183658977-183659027	LNCaP	prostate:	n/a
48	chr2:183580906-183580956	AG09319	gingival:	n/a
49	chr2:183667124-183667174	Hepatocyte	liver:	n/a
50	chr2:183580910-183580960	IMR90	lung:	fetal

(count:124 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr2:183598562..183601239-chr2:183604490..183606088,2	K562	blood:
2	chr2:183569800..183572698-chr2:183572719..183574437,2	MCF-7	breast:
3	chr2:183600722..183602612-chr2:183608045..183610895,3	K562	blood:
4	chr2:183695751..183697908-chr2:183701079..183703543,2	K562	blood:
5	chr17:57914325..57916942-chr2:183579945..183582060,2	MCF-7	breast:
6	chr2:183706383..183709007-chr2:183718084..183719976,2	K562	blood:
7	chr2:183668592..183670850-chr2:183672599..183674882,2	K562	blood:
8	chr2:183600490..183602060-chr2:183603873..183605839,2	K562	blood:
9	chr2:183648396..183651176-chr2:183657370..183660801,3	K562	blood:
10	chr2:183585145..183587372-chr2:183598804..183601047,2	K562	blood:
11	chr2:183568340..183570140-chr2:183571899..183573989,2	K562	blood:
12	chr2:183700483..183702944-chr2:183767110..183769629,2	K562	blood:
13	chr2:183619535..183621999-chr2:183651493..183653388,2	K562	blood:
14	chr2:183666474..183669367-chr2:183675559..183677309,2	K562	blood:
15	chr2:183618431..183622157-chr2:183625093..183627097,3	K562	blood:
16	chr2:183632424..183632937-chr2:183844464..183845026,2	K562	blood:
17	chr2:183605695..183607908-chr2:183711047..183713446,2	K562	blood:
18	chr2:183668592..183670850-chr2:183672599..183674882,2	K562	blood:
19	chr2:183603082..183605652-chr2:183608398..183611324,2	K562	blood:
20	chr2:183676117..183678247-chr2:183702144..183703855,2	MCF-7	breast:
21	chr2:183706094..183709034-chr2:183715040..183717717,2	K562	blood:
22	chr2:183591742..183594215-chr2:183596337..183599496,3	MCF-7	breast:
23	chr2:183691013..183692579-chr2:183710091..183711908,2	MCF-7	breast:
24	chr2:182756746..182758830-chr2:183579706..183581743,2	K562	blood:
25	chr2:183659213..183661128-chr2:183664377..183666463,2	MCF-7	breast:
26	chr2:183562956..183565340-chr2:183578999..183580676,2	MCF-7	breast:
27	chr2:183648162..183650730-chr2:183663988..183666770,2	K562	blood:
28	chr2:183546308..183548876-chr2:183579294..183581951,2	MCF-7	breast:
29	chr2:183622731..183624252-chr2:183625888..183627970,2	K562	blood:
30	chr2:183568184..183572232-chr2:183575375..183579342,4	K562	blood:
31	chr2:183615250..183618246-chr2:183622533..183624342,2	K562	blood:
32	chr2:183615250..183618246-chr2:183622533..183624342,2	K562	blood:
33	chr2:183587075..183588639-chr2:183597814..183600510,2	MCF-7	breast:
34	chr2:183615854..183617746-chr2:183618708..183621163,2	K562	blood:
35	chr2:183664890..183667245-chr2:183673485..183675403,2	K562	blood:
36	chr2:183579526..183582519-chr2:183598356..183600848,2	K562	blood:
37	chr2:183600490..183602060-chr2:183603873..183605839,2	K562	blood:
38	chr2:183579526..183582484-chr2:183598917..183600848,2	K562	blood:
39	chr2:183706094..183709034-chr2:183715040..183717717,2	K562	blood:
40	chr2:183676835..183678660-chr2:183680847..183683198,2	K562	blood:
41	chr2:183570034..183572518-chr2:183580411..183582264,3	K562	blood:
42	chr2:183596118..183599197-chr2:183620167..183622183,3	K562	blood:
43	chr2:183616174..183617713-chr2:183625030..183626585,2	MCF-7	breast:
44	chr2:183561976..183564805-chr2:183566522..183568031,2	K562	blood:
45	chr2:183658306..183660291-chr2:183661982..183664789,2	K562	blood:
46	chr1:228644091..228645688-chr2:183578348..183580384,2	K562	blood:
47	chr2:183653144..183655094-chr2:183658549..183660271,2	K562	blood:
48	chr2:183585145..183587372-chr2:183598804..183601047,2	K562	blood:
49	chr2:183580214..183582247-chr2:183600795..183602847,2	MCF-7	breast:
50	chr2:183568340..183570140-chr2:183571899..183573989,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DNAJC10-2	chr2:183654087-183659706	NONHSAT075921
2	lnc-DUSP19-3	chr2:183652825-183653162	NONHSAT075920
3	lnc-DUSP19-4	chr2:183650679-183652638	NONHSAT075919

No data

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	FRZB	hsa-miR-30b-5p	chr2:183699467-183699488
2	FRZB	hsa-miR-30b-5p	chr2:183699473-183699467
3	FRZB	hsa-miR-30b-5p	chr2:183699080-183699101

Variant related genes	Relation type
RPL31P15	TF binding region
ENSG00000212404	TF binding region
DNAJC10	TF binding region
RPL31P15	CpG island
ENSG00000212404	CpG island
DNAJC10	CpG island
ENSG00000061676	chromatin interactions
ENSG00000181218	chromatin interactions
ENSG00000212404	chromatin interactions
ENSG00000122545	chromatin interactions
ENSG00000138434	chromatin interactions
ENSG00000260742	chromatin interactions
ENSG00000078487	chromatin interactions
ENSG00000148335	chromatin interactions
ENSG00000232430	chromatin interactions
ENSG00000142230	chromatin interactions
ENSG00000230658	chromatin interactions
ENSG00000077232	chromatin interactions
ENSG00000122550	chromatin interactions
ENSG00000146834	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000130749	chromatin interactions

Extended variants
information (count: 6126 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:6126 , 50 per page) page: 1 2 3 4 5 6 7 ... 123

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs71427861	chr2:183544207-183544208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs573523922	chr2:183544223-183544224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs145086353	chr2:183544224-183544225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs11903020	chr2:183544235-183544236	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs575665228	chr2:183544238-183544239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs544303665	chr2:183544269-183544270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535136237	chr2:183544311-183544312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs555318064	chr2:183544394-183544395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530123535	chr2:183544409-183544410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs547102916	chr2:183544427-183544428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs559914994	chr2:183544432-183544433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs139028689	chr2:183544435-183544436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs552004395	chr2:183544484-183544485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs568831563	chr2:183544593-183544594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs535277878	chr2:183544603-183544604	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs547861218	chr2:183544629-183544630	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs568074222	chr2:183544637-183544638	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs533647139	chr2:183544713-183544714	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs564943575	chr2:183544752-183544753	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs552704720	chr2:183544853-183544854	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs539238070	chr2:183544878-183544879	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs35033718	chr2:183544902-183544903	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs192801288	chr2:183544907-183544908	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs532004350	chr2:183544939-183544940	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs72514885	chr2:183544943-183544944	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs182609542	chr2:183544963-183544964	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs187262565	chr2:183545095-183545096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs288337	chr2:183545110-183545111	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs191848389	chr2:183545121-183545122	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560213391	chr2:183545213-183545214	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184392963	chr2:183545219-183545220	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551966052	chr2:183545226-183545227	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562376389	chr2:183545267-183545268	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs563398969	chr2:183545279-183545280	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs142213022	chr2:183545300-183545301	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs546036056	chr2:183545337-183545338	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547320733	chr2:183545338-183545339	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs190272682	chr2:183545354-183545355	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567953409	chr2:183545387-183545388	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs193005652	chr2:183545421-183545422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs185873687	chr2:183545428-183545429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs189133029	chr2:183545449-183545450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs111463996	chr2:183545461-183545462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs539202848	chr2:183545577-183545578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs559182140	chr2:183545584-183545585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs185164281	chr2:183545586-183545587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs557144323	chr2:183545637-183545638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs144036490	chr2:183545641-183545642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs569463708	chr2:183545649-183545650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs369767670	chr2:183545687-183545688	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	18522746	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2753 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:183544200-183545400	Weak transcription	Brain Cingulate Gyrus	brain
2	chr2:183544400-183546800	Enhancers	Monocytes-CD14+_RO01746	blood
3	chr2:183544600-183548200	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr2:183546800-183547400	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr2:183546800-183547400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
6	chr2:183546800-183547600	Enhancers	Primary B cells from peripheral blood	blood
7	chr2:183546800-183547800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr2:183546800-183547800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr2:183547000-183547600	Enhancers	Adipose Nuclei	Adipose
10	chr2:183547400-183547800	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr2:183551200-183551800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
12	chr2:183559000-183559400	Enhancers	Pancreatic Islets	Pancreatic Islet
13	chr2:183563400-183563800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr2:183569000-183571000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr2:183569400-183571000	Enhancers	Primary hematopoietic stem cells	blood
16	chr2:183569400-183571000	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr2:183569600-183571000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr2:183570000-183570600	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr2:183570200-183570600	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr2:183570600-183571000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr2:183571200-183571600	Enhancers	Brain Substantia Nigra	brain
22	chr2:183571400-183571600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr2:183577200-183580000	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr2:183577400-183578200	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr2:183577600-183577800	Enhancers	Primary T killer memory cells from peripheral blood	blood
26	chr2:183577600-183578000	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr2:183577600-183579600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr2:183577600-183579800	Enhancers	Primary B cells from cord blood	blood
29	chr2:183577600-183579800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr2:183577800-183579800	Enhancers	Primary hematopoietic stem cells	blood
31	chr2:183577800-183580000	Enhancers	Primary B cells from peripheral blood	blood
32	chr2:183577800-183580000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
33	chr2:183577800-183580200	Enhancers	Primary neutrophils fromperipheralblood	blood
34	chr2:183578000-183580000	Enhancers	HUVEC	blood vessel
35	chr2:183578000-183580600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
36	chr2:183578200-183578600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
37	chr2:183578400-183578600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr2:183578400-183578600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr2:183578400-183578600	Enhancers	Primary T cells from cord blood	blood
40	chr2:183578400-183578600	Enhancers	Spleen	Spleen
41	chr2:183578400-183578800	Enhancers	Primary T helper cells fromperipheralblood	blood
42	chr2:183578600-183578800	Enhancers	K562	blood
43	chr2:183578600-183579000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr2:183578600-183579200	Weak transcription	Primary T cells from cord blood	blood
45	chr2:183578600-183579400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr2:183578600-183579600	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr2:183578600-183580000	Enhancers	Adipose Nuclei	Adipose
48	chr2:183578600-183580400	Weak transcription	Spleen	Spleen
49	chr2:183578800-183579800	Weak transcription	Primary T helper cells fromperipheralblood	blood
50	chr2:183578800-183579800	Weak transcription	K562	blood

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