Variant report

Variant	esv999028
Chromosome Location	chr12:48199301-48209132
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	chr12:48206873-48207044	K562	blood:	n/a	n/a
2	ARID3A	chr12:48202743-48202860	K562	blood:	n/a	n/a
3	ATF2	chr12:48206626-48207234	GM12878	blood:	n/a	n/a
4	ATF2	chr12:48206492-48207290	GM12878	blood:	n/a	n/a
5	ATF2	chr12:48207502-48208063	GM12878	blood:	n/a	n/a
6	ATF2	chr12:48201659-48202220	GM12878	blood:	n/a	n/a
7	ATF2	chr12:48201777-48202145	GM12878	blood:	n/a	n/a
8	ATF3	chr12:48206583-48206994	K562	blood:	n/a	chr12:48206872-48206881
9	BACH1	chr12:48206660-48207177	H1-hESC	embryonic stem cell:	n/a	chr12:48206807-48206821
10	BATF	chr12:48206511-48207233	GM12878	blood:	n/a	chr12:48206811-48206821
11	BATF	chr12:48208597-48208921	GM12878	blood:	n/a	n/a
12	BATF	chr12:48201942-48202241	GM12878	blood:	n/a	n/a
13	BATF	chr12:48206841-48207213	GM12878	blood:	n/a	n/a
14	BCL11A	chr12:48206750-48207076	GM12878	blood:	n/a	chr12:48206979-48206992 chr12:48206985-48206994
15	BCL11A	chr12:48206656-48207240	GM12878	blood:	n/a	chr12:48206979-48206992 chr12:48206681-48206694 chr12:48206985-48206994
16	BCL3	chr12:48206533-48207320	GM12878	blood:	n/a	chr12:48206979-48206992 chr12:48206681-48206694 chr12:48206985-48206994
17	BCL3	chr12:48206748-48207120	GM12878	blood:	n/a	chr12:48206979-48206992 chr12:48206985-48206994
18	BCL3	chr12:48206299-48207005	A549	lung:	n/a	chr12:48206979-48206992 chr12:48206681-48206694 chr12:48206985-48206994
19	BCLAF1	chr12:48206488-48207407	GM12878	blood:	n/a	chr12:48206979-48206992 chr12:48206681-48206694 chr12:48206985-48206994
20	BCLAF1	chr12:48207537-48208078	GM12878	blood:	n/a	n/a
21	BCLAF1	chr12:48201714-48202275	GM12878	blood:	n/a	n/a
22	BCLAF1	chr12:48206623-48207506	GM12878	blood:	n/a	chr12:48206979-48206992 chr12:48206681-48206694 chr12:48206985-48206994
23	BHLHE40	chr12:48205408-48205585	K562	blood:	n/a	n/a
24	BHLHE40	chr12:48206658-48207196	GM12878	blood:	n/a	n/a
25	BHLHE40	chr12:48207669-48207923	GM12878	blood:	n/a	n/a
26	BHLHE40	chr12:48204911-48204917	GM12878	blood:	n/a	n/a
27	BHLHE40	chr12:48206508-48207745	K562	blood:	n/a	n/a
28	CBX3	chr12:48206471-48207290	K562	blood:	n/a	n/a
29	CBX3	chr12:48202553-48203062	K562	blood:	n/a	n/a
30	CCNT2	chr12:48206596-48207199	K562	blood:	n/a	chr12:48206979-48206988 chr12:48206768-48206777 chr12:48207132-48207141
31	CEBPB	chr12:48204402-48204705	H1-hESC	embryonic stem cell:	n/a	chr12:48204518-48204529
32	CEBPB	chr12:48206661-48207452	GM12878	blood:	n/a	n/a
33	CEBPB	chr12:48206459-48206948	IMR90	lung:	n/a	n/a
34	CEBPB	chr12:48204352-48204701	IMR90	lung:	n/a	chr12:48204518-48204529
35	CEBPB	chr12:48199220-48199523	IMR90	lung:	n/a	n/a
36	CEBPB	chr12:48204437-48204555	HepG2	liver:	n/a	chr12:48204518-48204529
37	CEBPB	chr12:48204451-48204625	K562	blood:	n/a	chr12:48204518-48204529
38	CHD1	chr12:48206613-48206832	H1-hESC	embryonic stem cell:	n/a	chr12:48206755-48206765 chr12:48206735-48206745
39	CHD1	chr12:48207071-48207465	GM12878	blood:	n/a	n/a
40	CHD1	chr12:48207213-48207358	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD1	chr12:48206647-48206834	GM12878	blood:	n/a	chr12:48206755-48206765 chr12:48206735-48206745
42	CHD2	chr12:48206575-48207559	H1-hESC	embryonic stem cell:	n/a	chr12:48206755-48206765 chr12:48206735-48206745
43	CHD2	chr12:48206590-48206991	K562	blood:	n/a	chr12:48206755-48206765 chr12:48206735-48206745
44	CHD2	chr12:48206408-48207896	GM12878	blood:	n/a	chr12:48206755-48206765 chr12:48206735-48206745
45	CHD2	chr12:48201830-48202285	GM12878	blood:	n/a	n/a
46	CHD2	chr12:48202832-48202913	K562	blood:	n/a	n/a
47	CREB1	chr12:48206508-48207061	A549	lung:	n/a	n/a
48	CTBP2	chr12:48206586-48207713	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTBP2	chr12:48204691-48205086	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr12:48202840-48202990	HPF	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:48206848-48206898	HCT-116	colon:	n/a
2	chr12:48206848-48206898	HCT-116	colon:	n/a
3	chr12:48207063-48207113	HPAEpiC	pulmonary alveolar:	n/a
4	chr12:48204680-48204730	HRCEpiC	kidney:	n/a
5	chr12:48207862-48207912	AG04450	lung:	fetal
6	chr12:48207044-48207094	HUVEC	blood vessel:	n/a
7	chr12:48201852-48201902	Caco-2	colon:	n/a
8	chr12:48206848-48206898	NT2-D1	testis:	n/a
9	chr12:48204680-48204730	HPAEpiC	pulmonary alveolar:	n/a
10	chr12:48207063-48207113	ECC-1	luminal epithelium:	n/a
11	chr12:48201852-48201902	ovcar-3	ovarian:	n/a
12	chr12:48201852-48201902	GM19239	blood:	n/a
13	chr12:48205446-48205496	NH-A	brain:	n/a
14	chr12:48205446-48205496	SAEC	small airway:	n/a
15	chr12:48206848-48206898	HIPEpiC	eye:	n/a
16	chr12:48206783-48206833	AoSMC	blood vessel:	n/a
17	chr12:48204680-48204730	HCT-116	colon:	n/a
18	chr12:48206848-48206898	HCM	heart:	n/a
19	chr12:48205446-48205496	PFSK-1	brain:	n/a
20	chr12:48201852-48201902	PFSK-1	brain:	n/a
21	chr12:48205446-48205496	Hela-S3	cervix:	n/a
22	chr12:48204680-48204730	RPTEC	kidney:	n/a
23	chr12:48206783-48206833	HIPEpiC	eye:	n/a
24	chr12:48205446-48205496	MCF10A-Er-Src	breast:	n/a
25	chr12:48207862-48207912	U87	brain:	n/a
26	chr12:48207044-48207094	SK-N-SH	brain:	n/a
27	chr12:48201852-48201902	A549	lung:	n/a
28	chr12:48207063-48207113	AoSMC	blood vessel:	n/a
29	chr12:48207862-48207912	Jurkat	blood:	n/a
30	chr12:48207044-48207094	MCF-7	breast:	n/a
31	chr12:48199277-48199327	ECC-1	luminal epithelium:	n/a
32	chr12:48206783-48206833	MCF-7	breast:	n/a
33	chr12:48201852-48201902	HMEC	breast:	n/a
34	chr12:48199277-48199327	GM12878	blood:	n/a
35	chr12:48206848-48206898	HCPEpiC	choroid plexus:	n/a
36	chr12:48201852-48201902	SK-N-MC	brain:	n/a
37	chr12:48204680-48204730	PANC-1	pancreas:	n/a
38	chr12:48206848-48206898	IMR90	lung:	fetal
39	chr12:48205446-48205496	Jurkat	blood:	n/a
40	chr12:48207862-48207912	HL-60	blood:	n/a
41	chr12:48201852-48201902	Hepatocyte	liver:	n/a
42	chr12:48207063-48207113	AG09309	skin:	n/a
43	chr12:48205446-48205496	NHDF-neo	bronchial:	n/a
44	chr12:48204680-48204730	Hela-S3	cervix:	n/a
45	chr12:48206848-48206898	HMEC	breast:	n/a
46	chr12:48201852-48201902	HCT-116	colon:	n/a
47	chr12:48207044-48207094	SK-N-MC	brain:	n/a
48	chr12:48207044-48207094	AG04450	lung:	fetal
49	chr12:48207063-48207113	SK-N-SH	brain:	n/a
50	chr12:48204680-48204730	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:48202920..48205906-chr12:48322070..48325166,3	MCF-7	breast:
2	chr12:48180173..48182557-chr12:48208551..48210308,2	MCF-7	breast:
3	chr12:48193420..48195604-chr12:48198612..48200670,2	K562	blood:
4	chr12:48194244..48196196-chr12:48197765..48200382,2	MCF-7	breast:
5	chr12:48194186..48196955-chr12:48205034..48206864,2	K562	blood:
6	chr12:48206611..48207329-chr15:90744144..90745049,2	NB4	blood:
7	chr12:48198197..48199976-chr17:58677533..58679720,2	MCF-7	breast:
8	chr12:48200947..48203542-chr12:48208832..48210426,2	K562	blood:
9	chr12:48173557..48179365-chr12:48198461..48203449,6	K562	blood:
10	chr12:48200516..48204856-chr12:48204984..48208825,6	K562	blood:
11	chr12:48099357..48101447-chr12:48205677..48208435,2	K562	blood:
12	chr12:48165044..48167093-chr12:48206926..48209042,2	K562	blood:
13	chr12:48196446..48198672-chr12:48203077..48204827,2	K562	blood:
14	chr12:48153014..48156848-chr12:48203481..48206772,3	K562	blood:
15	chr12:48099357..48102097-chr12:48206829..48208435,2	K562	blood:
16	chr12:48185550..48187276-chr12:48201475..48205028,3	K562	blood:
17	chr12:48208028..48210618-chr17:57914996..57917527,2	MCF-7	breast:
18	chr12:48189907..48192102-chr12:48197745..48199769,2	MCF-7	breast:
19	chr12:48200947..48203542-chr12:48208832..48210426,2	K562	blood:
20	chr12:48101224..48103938-chr12:48201884..48203806,2	MCF-7	breast:
21	chr12:48194186..48197622-chr12:48205034..48208393,5	K562	blood:

Variant related genes	Relation type
HDAC7	TF binding region
HDAC7	CpG island
ENSG00000257433	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000268069	chromatin interactions
ENSG00000005175	chromatin interactions
ENSG00000211584	chromatin interactions
ENSG00000061273	chromatin interactions
ENSG00000170836	chromatin interactions
ENSG00000185033	chromatin interactions

Extended variants
information (count: 358 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:358 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115405472	chr12:48199309-48199310	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs559867638	chr12:48199315-48199316	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs115983511	chr12:48199358-48199359	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs76422001	chr12:48199448-48199449	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs565241366	chr12:48199514-48199515	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs530811261	chr12:48199519-48199520	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs550601700	chr12:48199573-48199574	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs567638008	chr12:48199595-48199596	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs536781674	chr12:48199663-48199664	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs561183938	chr12:48199667-48199668	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs376869505	chr12:48199684-48199685	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs546802080	chr12:48199695-48199696	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs17122326	chr12:48199739-48199740	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs140210814	chr12:48199848-48199849	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs145229737	chr12:48199853-48199854	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs571618648	chr12:48199855-48199856	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs376221999	chr12:48199898-48199899	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs181358129	chr12:48199908-48199909	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs556952785	chr12:48199910-48199911	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs573576007	chr12:48199950-48199951	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs34149349	chr12:48200006-48200007	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs74338394	chr12:48200056-48200057	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs186891962	chr12:48200057-48200058	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs545242777	chr12:48200062-48200063	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs148068460	chr12:48200083-48200084	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs531142190	chr12:48200084-48200085	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs544256914	chr12:48200118-48200119	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs561308534	chr12:48200122-48200123	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs530057584	chr12:48200178-48200179	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs546531975	chr12:48200179-48200180	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs564801739	chr12:48200180-48200181	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs191742373	chr12:48200186-48200187	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs35741403	chr12:48200260-48200261	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs371119746	chr12:48200263-48200264	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs141780254	chr12:48200290-48200291	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs79738995	chr12:48200341-48200342	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs150567059	chr12:48200375-48200376	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs541768772	chr12:48200404-48200405	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs113056781	chr12:48200451-48200452	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs567210923	chr12:48200480-48200481	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs74888637	chr12:48200516-48200517	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs117549626	chr12:48200578-48200579	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs565414466	chr12:48200606-48200607	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs572642269	chr12:48200615-48200616	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs545181072	chr12:48200628-48200629	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs143115200	chr12:48200636-48200637	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs112409134	chr12:48200650-48200651	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs376611942	chr12:48200654-48200655	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs56077617	chr12:48200695-48200696	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs372208072	chr12:48200729-48200730	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	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
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
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Breast cancer	21785460	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1142 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:48179800-48201000	Weak transcription	Dnd41	blood
2	chr12:48181200-48199800	Strong transcription	Fetal Intestine Small	intestine
3	chr12:48182000-48206400	Weak transcription	HepG2	liver
4	chr12:48182400-48202000	Weak transcription	Fetal Brain Male	brain
5	chr12:48183000-48204000	Weak transcription	Fetal Kidney	kidney
6	chr12:48189000-48201000	Weak transcription	NH-A	brain
7	chr12:48190800-48201400	Genic enhancers	Fetal Thymus	thymus
8	chr12:48191000-48201200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr12:48191400-48200000	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr12:48191400-48200200	Genic enhancers	Primary T cells fromperipheralblood	blood
11	chr12:48191400-48200600	Genic enhancers	Fetal Muscle Trunk	muscle
12	chr12:48191400-48201400	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr12:48191400-48202800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr12:48191600-48201600	Genic enhancers	Thymus	Thymus
15	chr12:48192200-48200200	Genic enhancers	Lung	lung
16	chr12:48192400-48201000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr12:48192400-48201600	Enhancers	Duodenum Smooth Muscle	Duodenum
18	chr12:48192400-48203200	Enhancers	Right Atrium	heart
19	chr12:48192600-48201400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
20	chr12:48192800-48200200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr12:48192800-48200200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
22	chr12:48193000-48200400	Genic enhancers	Fetal Muscle Leg	muscle
23	chr12:48193200-48200000	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr12:48193200-48200200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
25	chr12:48193200-48200200	Enhancers	Pancreas	Pancrea
26	chr12:48193400-48200200	Enhancers	Brain Substantia Nigra	brain
27	chr12:48193400-48203000	Enhancers	Fetal Heart	heart
28	chr12:48193400-48205000	Weak transcription	Brain Germinal Matrix	brain
29	chr12:48193600-48201400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr12:48193800-48201600	Enhancers	Skeletal Muscle Female	skeletal muscle
31	chr12:48194000-48200400	Enhancers	Brain Hippocampus Middle	brain
32	chr12:48194200-48200200	Strong transcription	Hela-S3	cervix
33	chr12:48194400-48201400	Enhancers	Primary T killer memory cells from peripheral blood	blood
34	chr12:48194800-48199800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
35	chr12:48195200-48201600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
36	chr12:48195400-48199600	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr12:48195400-48200400	Genic enhancers	Esophagus	oesophagus
38	chr12:48195400-48200400	Genic enhancers	Fetal Stomach	stomach
39	chr12:48195600-48200200	Enhancers	Colonic Mucosa	Colon
40	chr12:48195800-48200600	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr12:48196200-48200400	Strong transcription	NHEK	skin
42	chr12:48196200-48201600	Enhancers	Primary hematopoietic stem cells	blood
43	chr12:48196600-48199800	Genic enhancers	NHLF	lung
44	chr12:48196600-48201200	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr12:48196800-48200200	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
46	chr12:48196800-48201600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr12:48196800-48201600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr12:48197000-48199400	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr12:48197000-48200000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr12:48197000-48201200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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