Variant report

Variant	nsv826357
Chromosome Location	chr12:45691091-45740769
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:479)
CpG islands
(count:244)
Chromatin interactive
region (count:49)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:479 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:45730875-45731557	K562	blood:	n/a	n/a
2	ARID3A	chr12:45692463-45693343	K562	blood:	n/a	n/a
3	ARID3A	chr12:45709249-45709839	K562	blood:	n/a	n/a
4	ARID3A	chr12:45718325-45718408	K562	blood:	n/a	n/a
5	ATF1	chr12:45709151-45709760	K562	blood:	n/a	n/a
6	ATF1	chr12:45730824-45731237	K562	blood:	n/a	n/a
7	ATF1	chr12:45718225-45718509	K562	blood:	n/a	n/a
8	ATF1	chr12:45730154-45730511	K562	blood:	n/a	n/a
9	ATF3	chr12:45730201-45730481	K562	blood:	n/a	n/a
10	BACH1	chr12:45730848-45731127	K562	blood:	n/a	n/a
11	BACH1	chr12:45732675-45732756	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr12:45709115-45709130	K562	blood:	n/a	n/a
13	BACH1	chr12:45692679-45692699	K562	blood:	n/a	n/a
14	BHLHE40	chr12:45718187-45718455	K562	blood:	n/a	n/a
15	BHLHE40	chr12:45730957-45731155	K562	blood:	n/a	n/a
16	BHLHE40	chr12:45709123-45709516	K562	blood:	n/a	n/a
17	BRCA1	chr12:45729927-45730521	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr12:45709001-45709629	K562	blood:	n/a	n/a
19	CBX3	chr12:45718133-45718630	K562	blood:	n/a	n/a
20	CCNT2	chr12:45691914-45693077	K562	blood:	n/a	chr12:45692672-45692692
21	CCNT2	chr12:45709178-45709720	K562	blood:	n/a	n/a
22	CCNT2	chr12:45731422-45731697	K562	blood:	n/a	n/a
23	CEBPB	chr12:45730899-45731413	K562	blood:	n/a	n/a
24	CEBPB	chr12:45727137-45727261	H1-hESC	embryonic stem cell:	n/a	chr12:45727191-45727204 chr12:45727191-45727202 chr12:45727191-45727204 chr12:45727192-45727203
25	CEBPB	chr12:45714893-45715150	A549	lung:	n/a	chr12:45715028-45715039
26	CEBPB	chr12:45701886-45702097	HepG2	liver:	n/a	chr12:45701981-45701992
27	CEBPB	chr12:45723141-45723407	HepG2	liver:	n/a	chr12:45723236-45723247
28	CEBPB	chr12:45714900-45715176	HepG2	liver:	n/a	chr12:45715028-45715039
29	CEBPB	chr12:45696508-45696732	IMR90	lung:	n/a	n/a
30	CEBPB	chr12:45703647-45703925	IMR90	lung:	n/a	chr12:45703691-45703702
31	CEBPB	chr12:45727109-45727265	HepG2	liver:	n/a	chr12:45727191-45727204 chr12:45727191-45727202 chr12:45727191-45727204 chr12:45727192-45727203
32	CEBPB	chr12:45716452-45716727	Hela-S3	cervix:	n/a	chr12:45716567-45716578 chr12:45716565-45716578 chr12:45716565-45716578
33	CEBPB	chr12:45696459-45696753	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr12:45730134-45730507	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr12:45730819-45731369	IMR90	lung:	n/a	n/a
36	CEBPB	chr12:45723090-45723348	IMR90	lung:	n/a	chr12:45723236-45723247
37	CEBPB	chr12:45692929-45693207	MCF-7	breast:	n/a	chr12:45693127-45693138
38	CEBPB	chr12:45701876-45702131	H1-hESC	embryonic stem cell:	n/a	chr12:45701981-45701992
39	CEBPB	chr12:45723069-45723385	A549	lung:	n/a	chr12:45723236-45723247
40	CEBPB	chr12:45692809-45693170	MCF-7	breast:	n/a	chr12:45693127-45693138
41	CEBPB	chr12:45730085-45730534	IMR90	lung:	n/a	n/a
42	CEBPB	chr12:45701815-45702152	IMR90	lung:	n/a	chr12:45701981-45701992
43	CEBPB	chr12:45730154-45730439	A549	lung:	n/a	n/a
44	CEBPD	chr12:45709246-45709712	K562	blood:	n/a	n/a
45	CEBPD	chr12:45692494-45693234	K562	blood:	n/a	n/a
46	CEBPD	chr12:45692428-45693183	K562	blood:	n/a	n/a
47	CEBPD	chr12:45709318-45709768	K562	blood:	n/a	n/a
48	CHD1	chr12:45730556-45731575	IMR90	lung:	n/a	n/a
49	CHD2	chr12:45731001-45731105	K562	blood:	n/a	n/a
50	CREB1	chr12:45718094-45718636	GM12878	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:45721125-45721175	NH-A	brain:	n/a
2	chr12:45736875-45736925	NHBE	bronchial:	n/a
3	chr12:45697809-45697859	SK-N-SH_RA	brain:	n/a
4	chr12:45721125-45721175	NT2-D1	testis:	n/a
5	chr12:45703832-45703882	AG09319	gingival:	n/a
6	chr12:45721125-45721175	NHDF-neo	bronchial:	n/a
7	chr12:45703832-45703882	AG04450	lung:	fetal
8	chr12:45697809-45697859	NHDF-neo	bronchial:	n/a
9	chr12:45703832-45703882	H1-hESC	embryonic stem cell:	embryo
10	chr12:45697809-45697859	PrEC	prostate:	n/a
11	chr12:45697809-45697859	GM12878	blood:	n/a
12	chr12:45721125-45721175	HRE	kidney:	n/a
13	chr12:45736875-45736925	HL-60	blood:	n/a
14	chr12:45736875-45736925	HEEpiC	esophagus:	n/a
15	chr12:45703832-45703882	HUVEC	blood vessel:	n/a
16	chr12:45697809-45697859	SAEC	small airway:	n/a
17	chr12:45697809-45697859	GM19239	blood:	n/a
18	chr12:45697809-45697859	T-47D	breast:	n/a
19	chr12:45736875-45736925	AG10803	skin:	n/a
20	chr12:45697809-45697859	NH-A	brain:	n/a
21	chr12:45697809-45697859	GM12892	blood:	n/a
22	chr12:45736875-45736925	PANC-1	pancreas:	n/a
23	chr12:45697809-45697859	Caco-2	colon:	n/a
24	chr12:45721125-45721175	GM12892	blood:	n/a
25	chr12:45697809-45697859	K562	blood:	n/a
26	chr12:45721125-45721175	SK-N-MC	brain:	n/a
27	chr12:45736875-45736925	GM19239	blood:	n/a
28	chr12:45703832-45703882	NB4	blood:	n/a
29	chr12:45721125-45721175	Caco-2	colon:	n/a
30	chr12:45736875-45736925	HNPCEpiC	eye:	n/a
31	chr12:45736875-45736925	Caco-2	colon:	n/a
32	chr12:45703832-45703882	Caco-2	colon:	n/a
33	chr12:45721125-45721175	GM12891	blood:	n/a
34	chr12:45736875-45736925	HCPEpiC	choroid plexus:	n/a
35	chr12:45703832-45703882	NT2-D1	testis:	n/a
36	chr12:45703832-45703882	HCT-116	colon:	n/a
37	chr12:45736875-45736925	HRE	kidney:	n/a
38	chr12:45721125-45721175	AG09319	gingival:	n/a
39	chr12:45721125-45721175	SAEC	small airway:	n/a
40	chr12:45721125-45721175	H1-hESC	embryonic stem cell:	embryo
41	chr12:45703832-45703882	HPAEpiC	pulmonary alveolar:	n/a
42	chr12:45721125-45721175	T-47D	breast:	n/a
43	chr12:45703832-45703882	AG04449	skin:	fetal
44	chr12:45703832-45703882	GM12878	blood:	n/a
45	chr12:45736875-45736925	ECC-1	luminal epithelium:	n/a
46	chr12:45721125-45721175	ECC-1	luminal epithelium:	n/a
47	chr12:45736875-45736925	HCT-116	colon:	n/a
48	chr12:45721125-45721175	HL-60	blood:	n/a
49	chr12:45736875-45736925	BE2_C	brain:	n/a
50	chr12:45736875-45736925	AoSMC	blood vessel:	n/a

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:45718807..45721001-chr12:45724956..45727389,2	K562	blood:
2	chr12:45688734..45691523-chr12:45698194..45700456,2	K562	blood:
3	chr12:45716663..45719500-chr12:45720743..45723305,3	K562	blood:
4	chr12:45698045..45699853-chr12:45702122..45704712,2	K562	blood:
5	chr12:45700222..45702386-chr12:45704412..45706326,2	K562	blood:
6	chr12:45716663..45719500-chr12:45720743..45723305,3	K562	blood:
7	chr12:45690191..45692024-chr12:45717586..45719684,2	MCF-7	breast:
8	chr12:45720984..45722682-chr12:45761329..45763104,2	K562	blood:
9	chr12:45690191..45692024-chr12:45717586..45719684,2	MCF-7	breast:
10	chr12:45725602..45727901-chr12:45729137..45731156,2	K562	blood:
11	chr12:45700222..45702386-chr12:45704412..45706326,2	K562	blood:
12	chr12:45729696..45732550-chr12:46121531..46124261,2	K562	blood:
13	chr12:45734789..45737221-chr12:45742624..45745362,2	MCF-7	breast:
14	chr12:45708234..45709954-chr12:45714015..45715994,2	K562	blood:
15	chr12:45736486..45738721-chr12:45739577..45741327,2	K562	blood:
16	chr12:45721123..45723044-chr12:45725966..45727904,2	K562	blood:
17	chr12:45686804..45689610-chr12:45698349..45700960,2	MCF-7	breast:
18	chr12:45684442..45687788-chr12:45687793..45692076,3	MCF-7	breast:
19	chr12:45698045..45699853-chr12:45702122..45704712,2	K562	blood:
20	chr12:33134639..33136187-chr12:45734034..45735761,2	MCF-7	breast:
21	chr12:45693359..45695379-chr12:45698618..45700511,2	K562	blood:
22	chr12:45708234..45709954-chr12:45714015..45715994,2	K562	blood:
23	chr12:45606663..45609233-chr12:45722642..45725122,2	K562	blood:
24	chr12:45609373..45612977-chr12:45689152..45693084,3	MCF-7	breast:
25	chr12:45690992..45693119-chr12:45698128..45699673,2	MCF-7	breast:
26	chr12:45732454..45735038-chr12:45737600..45739582,2	K562	blood:
27	chr12:45687856..45690300-chr12:45690892..45693312,2	K562	blood:
28	chr12:45702436..45704266-chr12:45707505..45709646,2	K562	blood:
29	chr12:45717384..45719924-chr12:45748264..45750670,2	MCF-7	breast:
30	chr12:45685386..45687801-chr12:45690061..45692281,2	K562	blood:
31	chr12:45608976..45610914-chr12:45699677..45701678,2	MCF-7	breast:
32	chr12:45701143..45702936-chr12:46121606..46123908,2	K562	blood:
33	chr12:45723096..45724748-chr12:45811796..45814001,2	MCF-7	breast:
34	chr12:45690992..45693119-chr12:45698128..45699673,2	MCF-7	breast:
35	chr12:45737306..45740256-chr12:45740506..45742097,2	MCF-7	breast:
36	chr12:45732454..45735038-chr12:45737600..45739582,2	K562	blood:
37	chr12:45734366..45736886-chr12:45747224..45749604,2	K562	blood:
38	chr12:45718807..45721001-chr12:45724956..45727389,2	K562	blood:
39	chr12:45736486..45738721-chr12:45739577..45741327,2	K562	blood:
40	chr12:45721123..45723044-chr12:45725966..45727904,2	K562	blood:
41	chr12:45606867..45609787-chr12:45691582..45693288,2	K562	blood:
42	chr12:45693359..45695379-chr12:45698618..45700511,2	K562	blood:
43	chr12:45688734..45691523-chr12:45698194..45700456,2	K562	blood:
44	chr12:45702436..45704266-chr12:45707505..45709646,2	K562	blood:
45	chr12:45737306..45740256-chr12:45740506..45742097,2	MCF-7	breast:
46	chr12:45701919..45704723-chr12:45708246..45711469,3	K562	blood:
47	chr12:45686301..45689290-chr12:45690781..45693334,2	K562	blood:
48	chr12:45701919..45704723-chr12:45708246..45711469,3	K562	blood:
49	chr12:45728847..45732311-chr12:45733300..45736387,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARID2-9	chr12:45729332-45729411	NONHSAT027825

No data

Variant related genes	Relation type
ANO6	TF binding region
ANO6	CpG island
ENSG00000177119	chromatin interactions
ENSG00000273015	chromatin interactions
ENSG00000189079	chromatin interactions
ENSG00000134297	chromatin interactions

Extended variants
information (count: 1731 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:1731 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545427198	chr12:45691137-45691138	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs548590310	chr12:45691168-45691169	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs560719070	chr12:45691186-45691187	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs568381276	chr12:45691206-45691207	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs536156967	chr12:45691212-45691213	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs144556288	chr12:45691256-45691257	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs528009850	chr12:45691259-45691260	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs377416723	chr12:45691280-45691281	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs549517647	chr12:45691323-45691324	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs547631270	chr12:45691356-45691357	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs147819983	chr12:45691376-45691377	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs6582541	chr12:45691420-45691421	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs558319809	chr12:45691434-45691435	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs576629678	chr12:45691453-45691454	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs373471339	chr12:45691513-45691514	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs116605565	chr12:45691530-45691531	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs555805951	chr12:45691582-45691583	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs143694041	chr12:45691738-45691739	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs531962428	chr12:45691742-45691743	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs148117417	chr12:45691774-45691775	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs559272905	chr12:45691779-45691780	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs577802078	chr12:45691785-45691786	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs190110650	chr12:45691812-45691813	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs76298004	chr12:45691823-45691824	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs530535960	chr12:45691835-45691836	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs548531729	chr12:45691837-45691838	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs181782463	chr12:45691859-45691860	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs185646012	chr12:45691860-45691861	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs572207535	chr12:45691873-45691874	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs190109365	chr12:45691928-45691929	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs571362007	chr12:45691931-45691932	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs181049649	chr12:45691933-45691934	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs185134715	chr12:45691996-45691997	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs190919519	chr12:45692043-45692044	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs570120328	chr12:45692080-45692081	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs184007424	chr12:45692098-45692099	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs140914861	chr12:45692138-45692139	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs12302718	chr12:45692152-45692153	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs574017610	chr12:45692184-45692185	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs73281450	chr12:45692185-45692186	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs538208142	chr12:45692205-45692206	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs546992994	chr12:45692224-45692225	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs561638177	chr12:45692268-45692269	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs114858844	chr12:45692299-45692300	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs75998317	chr12:45692305-45692306	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs565611124	chr12:45692318-45692319	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs35631328	chr12:45692332-45692333	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs188991820	chr12:45692437-45692438	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs4768600	chr12:45692459-45692460	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs542362971	chr12:45692460-45692461	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Gastric cancer	18160780	CNVD
Myelofibrosis	22110671	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Bladder cancer	21909424	CNVD

Chromatin state (count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:45654400-45725600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr12:45662800-45696800	Weak transcription	Primary T cells fromperipheralblood	blood
3	chr12:45666200-45709200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr12:45668400-45697800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr12:45668600-45693000	Weak transcription	Pancreas	Pancrea
6	chr12:45674200-45706800	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr12:45674400-45692200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr12:45675800-45709000	Weak transcription	Lung	lung
9	chr12:45676200-45693000	Weak transcription	Fetal Stomach	stomach
10	chr12:45676400-45696000	Weak transcription	Fetal Thymus	thymus
11	chr12:45676400-45697800	Weak transcription	Dnd41	blood
12	chr12:45676400-45740400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr12:45677000-45696000	Weak transcription	Primary monocytes fromperipheralblood	blood
14	chr12:45677600-45698200	Weak transcription	Primary T cells from cord blood	blood
15	chr12:45677800-45691800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr12:45677800-45696000	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr12:45678600-45691800	Weak transcription	HUVEC	blood vessel
18	chr12:45679200-45692200	Weak transcription	NHDF-Ad	bronchial
19	chr12:45679800-45692200	Weak transcription	NH-A	brain
20	chr12:45680000-45736800	Weak transcription	Fetal Intestine Small	intestine
21	chr12:45680200-45692600	Weak transcription	Fetal Intestine Large	intestine
22	chr12:45680400-45697600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr12:45680800-45693000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr12:45681000-45698200	Weak transcription	Primary hematopoietic stem cells	blood
25	chr12:45681200-45697800	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr12:45683600-45709400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr12:45684400-45692200	Weak transcription	Osteobl	bone
28	chr12:45684400-45693000	Weak transcription	Small Intestine	intestine
29	chr12:45684400-45721800	Weak transcription	Esophagus	oesophagus
30	chr12:45684600-45692400	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr12:45684800-45691800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr12:45685000-45693400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr12:45685800-45697800	Weak transcription	GM12878-XiMat	blood
34	chr12:45685800-45698200	Weak transcription	Primary B cells from peripheral blood	blood
35	chr12:45686000-45692200	Weak transcription	Rectal Smooth Muscle	rectum
36	chr12:45686200-45707000	Weak transcription	Primary B cells from cord blood	blood
37	chr12:45686800-45692200	Weak transcription	NHLF	lung
38	chr12:45686800-45693000	Weak transcription	Left Ventricle	heart
39	chr12:45686800-45693200	Weak transcription	Ovary	ovary
40	chr12:45687000-45691800	Weak transcription	Fetal Lung	lung
41	chr12:45687000-45692200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr12:45687000-45692800	Weak transcription	HSMMtube	muscle
43	chr12:45687000-45697200	Weak transcription	Aorta	Aorta
44	chr12:45687200-45692200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr12:45687200-45692200	Weak transcription	Adipose Nuclei	Adipose
46	chr12:45687200-45692600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr12:45687200-45693600	Enhancers	Fetal Heart	heart
48	chr12:45688000-45693000	Weak transcription	HMEC	breast
49	chr12:45688400-45692000	Weak transcription	Colon Smooth Muscle	Colon
50	chr12:45688400-45694200	Weak transcription	Stomach Smooth Muscle	stomach

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