Variant report

Variant	esv1851152
Chromosome Location	chr2:40393223-40512023
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1058)
CpG islands
(count:673)
Chromatin interactive
region (count:24)
LncRNA
region (count:41)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1058 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:40507954-40508037	K562	blood:	n/a	n/a
2	ATF2	chr2:40509517-40510007	GM12878	blood:	n/a	n/a
3	BACH1	chr2:40483228-40483237	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr2:40471896-40472050	H1-hESC	embryonic stem cell:	n/a	n/a
5	BRCA1	chr2:40510392-40510459	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr2:40472149-40472230	HepG2	liver:	n/a	chr2:40472203-40472216 chr2:40472204-40472215
7	CEBPB	chr2:40469533-40469684	HepG2	liver:	n/a	n/a
8	CEBPB	chr2:40500916-40501465	HepG2	liver:	n/a	chr2:40500947-40500958
9	CEBPB	chr2:40419947-40420519	MCF-7	breast:	n/a	n/a
10	CEBPB	chr2:40395205-40395325	HepG2	liver:	n/a	n/a
11	CEBPB	chr2:40450723-40451027	A549	lung:	n/a	n/a
12	CEBPB	chr2:40466291-40466553	A549	lung:	n/a	chr2:40466400-40466411 chr2:40466398-40466409
13	CEBPB	chr2:40465541-40465724	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr2:40453304-40453460	HepG2	liver:	n/a	n/a
15	CEBPB	chr2:40476489-40477104	Hela-S3	cervix:	n/a	chr2:40476580-40476591 chr2:40476580-40476591
16	CEBPB	chr2:40503147-40503403	A549	lung:	n/a	chr2:40503275-40503286 chr2:40503246-40503257 chr2:40503246-40503259 chr2:40503275-40503286
17	CEBPB	chr2:40420016-40420342	A549	lung:	n/a	n/a
18	CEBPB	chr2:40419954-40420391	MCF-7	breast:	n/a	n/a
19	CEBPB	chr2:40503236-40503347	IMR90	lung:	n/a	chr2:40503275-40503286 chr2:40503246-40503257 chr2:40503246-40503259 chr2:40503275-40503286
20	CEBPB	chr2:40439848-40440209	IMR90	lung:	n/a	n/a
21	CEBPB	chr2:40450707-40451000	HepG2	liver:	n/a	n/a
22	CEBPB	chr2:40419972-40420423	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr2:40486609-40486751	HepG2	liver:	n/a	chr2:40486676-40486687
24	CEBPB	chr2:40420145-40420217	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr2:40471869-40472315	IMR90	lung:	n/a	chr2:40472203-40472216 chr2:40472204-40472215
26	CEBPB	chr2:40406197-40406487	IMR90	lung:	n/a	n/a
27	CEBPB	chr2:40471863-40472183	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr2:40441546-40441737	IMR90	lung:	n/a	n/a
29	CEBPB	chr2:40466272-40466571	IMR90	lung:	n/a	chr2:40466400-40466411 chr2:40466398-40466409
30	CEBPB	chr2:40467096-40467749	IMR90	lung:	n/a	n/a
31	CEBPB	chr2:40500793-40501325	IMR90	lung:	n/a	chr2:40500947-40500958
32	CEBPB	chr2:40420027-40420346	HepG2	liver:	n/a	n/a
33	CEBPB	chr2:40466268-40466570	HepG2	liver:	n/a	chr2:40466400-40466411 chr2:40466398-40466409
34	CEBPB	chr2:40419994-40420352	IMR90	lung:	n/a	n/a
35	CEBPB	chr2:40441588-40441717	A549	lung:	n/a	n/a
36	CEBPB	chr2:40450688-40450982	IMR90	lung:	n/a	n/a
37	CEBPB	chr2:40447311-40448036	IMR90	lung:	n/a	n/a
38	CEBPB	chr2:40447451-40447538	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr2:40440440-40440590	BE2_C	brain:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
40	CTCF	chr2:40457940-40458090	AG09309	skin:	n/a	n/a
41	CTCF	chr2:40470940-40471090	AG10803	skin:	n/a	n/a
42	CTCF	chr2:40512020-40512170	HVMF	connective:	n/a	n/a
43	CTCF	chr2:40483900-40484050	MCF-7	breast:	n/a	n/a
44	CTCF	chr2:40440400-40440550	HCFaa	heart:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
45	CTCF	chr2:40471806-40472075	GM12878	blood:	n/a	chr2:40471927-40471943 chr2:40471926-40471944 chr2:40471928-40471949
46	CTCF	chr2:40471840-40471990	GM12867	blood:	n/a	chr2:40471927-40471943 chr2:40471926-40471944 chr2:40471928-40471949
47	CTCF	chr2:40440420-40440570	WI-38	lung:	n/a	chr2:40440472-40440493 chr2:40440470-40440488 chr2:40440471-40440487
48	CTCF	chr2:40483920-40484070	AG04449	skin:	n/a	n/a
49	CTCF	chr2:40471745-40472125	GM12878	blood:	n/a	chr2:40471927-40471943 chr2:40471926-40471944 chr2:40471928-40471949
50	CTCF	chr2:40471789-40472055	ProgFib	skin:	n/a	chr2:40471927-40471943 chr2:40471926-40471944 chr2:40471928-40471949

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:40429179-40429229	Jurkat	blood:	n/a
2	chr2:40452795-40452845	NB4	blood:	n/a
3	chr2:40429179-40429229	Jurkat	blood:	n/a
4	chr2:40452795-40452845	NB4	blood:	n/a
5	chr2:40436843-40436893	NH-A	brain:	n/a
6	chr2:40452795-40452845	NHDF-neo	bronchial:	n/a
7	chr2:40465453-40465503	PFSK-1	brain:	n/a
8	chr2:40470864-40470914	CMK	blood:	n/a
9	chr2:40465453-40465503	Hela-S3	cervix:	n/a
10	chr2:40472772-40472822	SKMC	muscle:	n/a
11	chr2:40468548-40468598	AG04449	skin:	fetal
12	chr2:40465453-40465503	SAEC	small airway:	n/a
13	chr2:40468548-40468598	GM06990	blood:	n/a
14	chr2:40437698-40437748	BJ	skin:	n/a
15	chr2:40472772-40472822	GM12892	blood:	n/a
16	chr2:40440949-40440999	ECC-1	luminal epithelium:	n/a
17	chr2:40436843-40436893	SK-N-MC	brain:	n/a
18	chr2:40440949-40440999	PrEC	prostate:	n/a
19	chr2:40437698-40437748	AoSMC	blood vessel:	n/a
20	chr2:40452795-40452845	AG09319	gingival:	n/a
21	chr2:40508306-40508356	GM12892	blood:	n/a
22	chr2:40437698-40437748	HCF	heart:	n/a
23	chr2:40470864-40470914	HUVEC	blood vessel:	n/a
24	chr2:40429179-40429229	HIPEpiC	eye:	n/a
25	chr2:40508306-40508356	HPAEpiC	pulmonary alveolar:	n/a
26	chr2:40470864-40470914	NHBE	bronchial:	n/a
27	chr2:40472772-40472822	AG04450	lung:	fetal
28	chr2:40436843-40436893	Hela-S3	cervix:	n/a
29	chr2:40468548-40468598	SAEC	small airway:	n/a
30	chr2:40436843-40436893	HEEpiC	esophagus:	n/a
31	chr2:40452795-40452845	IMR90	lung:	fetal
32	chr2:40468548-40468598	PANC-1	pancreas:	n/a
33	chr2:40452795-40452845	SKMC	muscle:	n/a
34	chr2:40470864-40470914	BJ	skin:	n/a
35	chr2:40508306-40508356	BE2_C	brain:	n/a
36	chr2:40436843-40436893	GM06990	blood:	n/a
37	chr2:40447561-40447611	NH-A	brain:	n/a
38	chr2:40447561-40447611	NHDF-neo	bronchial:	n/a
39	chr2:40437698-40437748	ovcar-3	ovarian:	n/a
40	chr2:40440949-40440999	AoSMC	blood vessel:	n/a
41	chr2:40437698-40437748	AG10803	skin:	n/a
42	chr2:40447561-40447611	T-47D	breast:	n/a
43	chr2:40437698-40437748	GM12878	blood:	n/a
44	chr2:40447561-40447611	GM12878	blood:	n/a
45	chr2:40436843-40436893	RPTEC	kidney:	n/a
46	chr2:40436843-40436893	HNPCEpiC	eye:	n/a
47	chr2:40440949-40440999	Hepatocyte	liver:	n/a
48	chr2:40437698-40437748	RPTEC	kidney:	n/a
49	chr2:40472772-40472822	SK-N-SH	brain:	n/a
50	chr2:40429179-40429229	MCF10A-Er-Src	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:40395306..40398028-chr2:40400733..40404513,4	K562	blood:
2	chr2:40430449..40432032-chr2:40434397..40435947,2	K562	blood:
3	chr2:40390508..40393940-chr2:40401107..40404487,3	MCF-7	breast:
4	chr2:40472223..40475000-chr2:40477866..40479502,2	K562	blood:
5	chr2:40419927..40421772-chr2:40425195..40428157,2	MCF-7	breast:
6	chr2:40419927..40421772-chr2:40425195..40428157,2	MCF-7	breast:
7	chr2:40440009..40440862-chr2:40987001..40987610,3	MCF-7	breast:
8	chr2:40395306..40398028-chr2:40400733..40404513,3	K562	blood:
9	chr2:40471470..40472428-chr2:40781584..40782502,3	MCF-7	breast:
10	chr2:40439962..40440629-chr2:40781631..40782440,3	MCF-7	breast:
11	chr2:40440228..40440936-chr2:40471245..40471990,2	MCF-7	breast:
12	chr2:40440053..40440830-chr2:40675706..40676650,2	MCF-7	breast:
13	chr2:40457676..40460307-chr2:40464951..40466510,2	K562	blood:
14	chr2:40440228..40440936-chr2:40471245..40471990,2	MCF-7	breast:
15	chr2:40395306..40398028-chr2:40400733..40404513,4	K562	blood:
16	chr2:40457676..40460307-chr2:40464951..40466510,2	K562	blood:
17	chr2:40401909..40404574-chr3:16441893..16443396,2	MCF-7	breast:
18	chr2:40390508..40393940-chr2:40401107..40404487,3	MCF-7	breast:
19	chr2:40395306..40398028-chr2:40400733..40404513,3	K562	blood:
20	chr2:40430449..40432032-chr2:40434397..40435947,2	K562	blood:
21	chr2:40502917..40505648-chr2:40506490..40508382,2	MCF-7	breast:
22	chr2:40502917..40505648-chr2:40506490..40508382,2	MCF-7	breast:
23	chr2:40140472..40141253-chr2:40471871..40472400,2	MCF-7	breast:
24	chr2:40427590..40429513-chr2:40436431..40438074,2	MCF-7	breast:

(count:41 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM178-2	chr2:40450770-40450891	ENSG00000227028.2
2	lnc-TMEM178-2	chr2:40440309-40440619	ENSG00000227028.2
3	lnc-TMEM178-2	chr2:40437107-40437164	ENSG00000227028.2
4	lnc-TMEM178-2	chr2:40478824-40478897	ENSG00000227028.2
5	lnc-TMEM178-2	chr2:40437107-40437164	ENSG00000227028.2
6	lnc-TMEM178-2	chr2:40450770-40450891	ENSG00000227028.2
7	lnc-TMEM178-2	chr2:40450770-40450891	ENSG00000227028.2
8	lnc-TMEM178-2	chr2:40481560-40481718	ENSG00000227028.1
9	lnc-TMEM178-2	chr2:40478824-40478889	ENSG00000227028.2
10	lnc-TMEM178-2	chr2:40481560-40481903	ENSG00000227028.1
11	lnc-TMEM178-2	chr2:40450770-40450891	ENSG00000227028.2
12	lnc-TMEM178-2	chr2:40481560-40482349	ENSG00000227028.1
13	lnc-TMEM178-2	chr2:40478824-40478889	ENSG00000227028.2
14	lnc-TMEM178-2	chr2:40437107-40437164	ENSG00000227028.2
15	lnc-TMEM178-2	chr2:40478563-40478688	ENSG00000227028.1
16	lnc-TMEM178-2	chr2:40478824-40478889	ENSG00000227028.2
17	lnc-TMEM178-2	chr2:40450770-40450891	ENSG00000227028.2
18	lnc-TMEM178-2	chr2:40478824-40478889	ENSG00000227028.2
19	lnc-TMEM178-2	chr2:40478824-40478897	ENSG00000227028.2
20	lnc-TMEM178-2	chr2:40478824-40478914	NONHSAT070261
21	lnc-TMEM178-2	chr2:40478824-40478889	ENSG00000227028.2
22	lnc-TMEM178-2	chr2:40450770-40450891	ENSG00000227028.2
23	lnc-TMEM178-2	chr2:40478824-40478889	ENSG00000227028.2
24	lnc-TMEM178-2	chr2:40478824-40478914	ENSG00000227028.1
25	lnc-TMEM178-2	chr2:40437105-40437164	ENSG00000227028.1
26	lnc-TMEM178-2	chr2:40478824-40478914	ENSG00000227028.1
27	lnc-TMEM178-2	chr2:40450770-40450891	ENSG00000227028.1
28	lnc-TMEM178-2	chr2:40481560-40482342	NONHSAT070263
29	lnc-TMEM178-2	chr2:40478824-40478889	ENSG00000227028.2
30	lnc-TMEM178-2	chr2:40450770-40450891	ENSG00000227028.2
31	lnc-TMEM178-2	chr2:40450770-40450891	ENSG00000227028.2
32	lnc-TMEM178-2	chr2:40478824-40478914	ENSG00000227028.1
33	lnc-TMEM178-2	chr2:40481560-40482349	NONHSAT070261
34	lnc-TMEM178-2	chr2:40481560-40481686	ENSG00000227028.1
35	lnc-TMEM178-2	chr2:40478824-40478914	ENSG00000227028.1
36	lnc-TMEM178-2	chr2:40478824-40478914	NONHSAT070263
37	lnc-TMEM178-2	chr2:40481560-40482198	ENSG00000227028.1
38	lnc-TMEM178-2	chr2:40435515-40435591	ENSG00000227028.2
39	lnc-TMEM178-2	chr2:40478824-40478914	ENSG00000227028.1
40	lnc-TMEM178-2	chr2:40447283-40447525	ENSG00000227028.1
41	lnc-TMEM178-2	chr2:40450770-40450891	ENSG00000227028.1

No data

Variant related genes	Relation type
SLC8A1-AS1	TF binding region
ENSG00000268898	TF binding region
SLC8A1-AS1	CpG island
ENSG00000268898	CpG island
ENSG00000227028	chromatin interactions

Extended variants
information (count: 5677 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:5677 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs440056	chr2:40393223-40393224	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs368283580	chr2:40393258-40393259	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs142337622	chr2:40393329-40393330	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs28628343	chr2:40393344-40393345	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs191414669	chr2:40393348-40393349	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs551835806	chr2:40393390-40393391	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs534847758	chr2:40393393-40393394	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182499660	chr2:40393413-40393414	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs141138692	chr2:40393414-40393415	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534400073	chr2:40393435-40393436	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs571569033	chr2:40393438-40393439	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs440387	chr2:40393447-40393448	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs145948856	chr2:40393526-40393527	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs549513840	chr2:40393532-40393533	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs78209137	chr2:40393536-40393537	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs441413	chr2:40393539-40393540	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs554282086	chr2:40393542-40393543	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs368772057	chr2:40393556-40393557	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs115201446	chr2:40393587-40393588	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs541275891	chr2:40393612-40393613	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs577697419	chr2:40393644-40393645	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs139469922	chr2:40393654-40393655	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577924572	chr2:40393778-40393779	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs545340122	chr2:40393839-40393840	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs557347691	chr2:40393842-40393843	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs78832928	chr2:40393849-40393850	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs79809966	chr2:40393898-40393899	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs187188586	chr2:40393911-40393912	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs192810879	chr2:40393939-40393940	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs528549604	chr2:40393991-40393992	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs61295272	chr2:40394016-40394017	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185324581	chr2:40394069-40394070	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs2192919	chr2:40394140-40394141	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs376675982	chr2:40394225-40394226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs538946520	chr2:40394238-40394239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs13404013	chr2:40394270-40394271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188651413	chr2:40394293-40394294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572189158	chr2:40394348-40394349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs112592812	chr2:40394362-40394363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs569121383	chr2:40394366-40394367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373309244	chr2:40394375-40394376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs535910347	chr2:40394381-40394382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs35786980	chr2:40394424-40394425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs116458990	chr2:40394492-40394493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs367922220	chr2:40394494-40394495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs543606993	chr2:40394506-40394507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs572605520	chr2:40394524-40394525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs575504625	chr2:40394553-40394554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs193278127	chr2:40394604-40394605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs578088169	chr2:40394659-40394660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Non-small cell lung cancer	18927303	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22522925	CNVD
Williams Syndrome	20824207	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1659 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:40357800-40406400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:40365200-40396200	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr2:40366600-40403000	Weak transcription	Brain Germinal Matrix	brain
4	chr2:40375600-40401800	Weak transcription	HSMMtube	muscle
5	chr2:40376800-40394200	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr2:40378000-40399000	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr2:40379200-40393400	Strong transcription	Primary monocytes fromperipheralblood	blood
8	chr2:40381600-40398800	Weak transcription	Brain Angular Gyrus	brain
9	chr2:40381800-40395200	Weak transcription	Spleen	Spleen
10	chr2:40386000-40395200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr2:40386000-40395200	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr2:40386400-40395200	Weak transcription	Fetal Intestine Large	intestine
13	chr2:40388400-40396400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr2:40388600-40395200	Weak transcription	Duodenum Mucosa	Duodenum
15	chr2:40389400-40396200	Weak transcription	Placenta	Placenta
16	chr2:40390600-40395200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr2:40390800-40395200	Weak transcription	Fetal Intestine Small	intestine
18	chr2:40391400-40393400	Enhancers	Fetal Muscle Leg	muscle
19	chr2:40391600-40393400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr2:40391600-40397600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr2:40391800-40393400	Enhancers	Fetal Lung	lung
22	chr2:40391800-40393400	Enhancers	Skeletal Muscle Male	skeletal muscle
23	chr2:40391800-40393400	Enhancers	NHDF-Ad	bronchial
24	chr2:40391800-40393600	Enhancers	Right Ventricle	heart
25	chr2:40392000-40393600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr2:40392000-40393600	Weak transcription	Brain Anterior Caudate	brain
27	chr2:40392000-40393600	Enhancers	Gastric	stomach
28	chr2:40392000-40393600	Enhancers	Left Ventricle	heart
29	chr2:40392000-40393600	Enhancers	Right Atrium	heart
30	chr2:40392000-40393800	Enhancers	Rectal Smooth Muscle	rectum
31	chr2:40392000-40394200	Enhancers	Colon Smooth Muscle	Colon
32	chr2:40392000-40395200	Weak transcription	Small Intestine	intestine
33	chr2:40392000-40413200	Weak transcription	Fetal Brain Female	brain
34	chr2:40392200-40393400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr2:40392200-40393400	Enhancers	Aorta	Aorta
36	chr2:40392200-40393400	Enhancers	Lung	lung
37	chr2:40392200-40393400	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr2:40392200-40393600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr2:40392200-40393600	Enhancers	Fetal Stomach	stomach
40	chr2:40392200-40394000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr2:40392400-40393400	Enhancers	Stomach Mucosa	stomach
42	chr2:40392400-40396200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr2:40392600-40396000	Weak transcription	HSMM	muscle
44	chr2:40392600-40405200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr2:40392800-40393400	Enhancers	Adipose Nuclei	Adipose
46	chr2:40392800-40394200	Enhancers	Fetal Heart	heart
47	chr2:40392800-40395600	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr2:40392800-40397400	Weak transcription	Dnd41	blood
49	chr2:40393000-40393600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr2:40393000-40393600	Enhancers	Cortex derived primary cultured neurospheres	brain

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