Variant report

Variant	esv2760274
Chromosome Location	chr12:57335481-57377509
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:383)
CpG islands
(count:428)
Chromatin interactive
region (count:41)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:383 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:57335445-57335829	HepG2	liver:	n/a	n/a
2	ATF1	chr12:57362833-57363005	K562	blood:	n/a	n/a
3	BACH1	chr12:57335314-57335674	K562	blood:	n/a	n/a
4	BATF	chr12:57335348-57335706	GM12878	blood:	n/a	chr12:57335532-57335543
5	BATF	chr12:57335428-57335611	GM12878	blood:	n/a	chr12:57335532-57335543
6	CBX3	chr12:57337124-57337565	K562	blood:	n/a	n/a
7	CBX3	chr12:57352149-57352446	K562	blood:	n/a	n/a
8	CBX3	chr12:57337230-57337416	K562	blood:	n/a	n/a
9	CBX3	chr12:57359798-57360321	K562	blood:	n/a	n/a
10	CEBPB	chr12:57349466-57349757	K562	blood:	n/a	n/a
11	CEBPB	chr12:57349413-57349754	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr12:57341747-57341956	HepG2	liver:	n/a	n/a
13	CEBPB	chr12:57349459-57349683	HepG2	liver:	n/a	n/a
14	CEBPB	chr12:57372206-57372347	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr12:57344131-57344381	MCF-7	breast:	n/a	n/a
16	CEBPB	chr12:57335495-57335737	HepG2	liver:	n/a	n/a
17	CEBPB	chr12:57335437-57335773	HepG2	liver:	n/a	n/a
18	CEBPB	chr12:57349354-57349829	MCF-7	breast:	n/a	n/a
19	CEBPB	chr12:57344105-57344290	K562	blood:	n/a	n/a
20	CEBPB	chr12:57349345-57349760	HepG2	liver:	n/a	n/a
21	CEBPB	chr12:57349377-57349777	A549	lung:	n/a	n/a
22	CEBPB	chr12:57372221-57372421	HepG2	liver:	n/a	n/a
23	CEBPB	chr12:57344063-57344363	HepG2	liver:	n/a	n/a
24	CEBPB	chr12:57344148-57344348	A549	lung:	n/a	n/a
25	CEBPB	chr12:57349434-57349654	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr12:57349426-57349758	IMR90	lung:	n/a	n/a
27	CEBPB	chr12:57349414-57349774	HepG2	liver:	n/a	n/a
28	CEBPB	chr12:57349273-57349896	A549	lung:	n/a	chr12:57349277-57349289
29	CEBPB	chr12:57349395-57349785	A549	lung:	n/a	n/a
30	CEBPD	chr12:57335484-57335715	HepG2	liver:	n/a	n/a
31	CEBPD	chr12:57335487-57335862	HepG2	liver:	n/a	n/a
32	CEBPZ	chr12:57349503-57349558	HepG2	liver:	n/a	n/a
33	CEBPZ	chr12:57335613-57335694	HepG2	liver:	n/a	n/a
34	CHD2	chr12:57335484-57335763	HepG2	liver:	n/a	n/a
35	CTCF	chr12:57341540-57341690	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr12:57341600-57341750	GM06990	blood:	n/a	n/a
37	CTCF	chr12:57341500-57341650	Caco-2	colon:	n/a	n/a
38	CTCF	chr12:57351159-57351294	MCF-7	breast:	n/a	n/a
39	CTCF	chr12:57341543-57341657	Gliobla	brain:	n/a	n/a
40	CTCF	chr12:57341410-57341937	MCF-7	breast:	n/a	n/a
41	CTCF	chr12:57341540-57341690	HCT-116	colon:	n/a	n/a
42	CTCF	chr12:57341557-57341674	NHEK	skin:	n/a	n/a
43	CTCF	chr12:57341560-57341710	A549	lung:	n/a	n/a
44	CTCF	chr12:57341540-57341690	GM12874	blood:	n/a	n/a
45	CTCF	chr12:57341520-57341670	NHDF-neo	bronchial:	n/a	n/a
46	CTCF	chr12:57341499-57341721	MCF-7	breast:	n/a	n/a
47	CTCF	chr12:57341540-57341690	RPTEC	kidney:	n/a	n/a
48	CTCF	chr12:57341540-57341690	GM06990	blood:	n/a	n/a
49	CTCF	chr12:57344740-57344890	WI-38	lung:	n/a	n/a
50	CTCF	chr12:57341510-57341702	Hela-S3	cervix:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:57345407-57345457	PrEC	prostate:	n/a
2	chr12:57345407-57345457	PrEC	prostate:	n/a
3	chr12:57351856-57351906	Hepatocyte	liver:	n/a
4	chr12:57345407-57345457	ECC-1	luminal epithelium:	n/a
5	chr12:57345407-57345457	MCF-7	breast:	n/a
6	chr12:57351191-57351241	ECC-1	luminal epithelium:	n/a
7	chr12:57335615-57335665	HAEpiC	amniotic membrane:	n/a
8	chr12:57351732-57351782	SK-N-SH	brain:	n/a
9	chr12:57351191-57351241	NH-A	brain:	n/a
10	chr12:57335615-57335665	HEEpiC	esophagus:	n/a
11	chr12:57335615-57335665	HRCEpiC	kidney:	n/a
12	chr12:57351191-57351241	HCT-116	colon:	n/a
13	chr12:57335615-57335665	ovcar-3	ovarian:	n/a
14	chr12:57351191-57351241	SAEC	small airway:	n/a
15	chr12:57352514-57352564	AG04449	skin:	fetal
16	chr12:57351191-57351241	Jurkat	blood:	n/a
17	chr12:57351732-57351782	Hepatocyte	liver:	n/a
18	chr12:57351856-57351906	AG09309	skin:	n/a
19	chr12:57351191-57351241	ProgFib	skin:	n/a
20	chr12:57351856-57351906	HEEpiC	esophagus:	n/a
21	chr12:57351856-57351906	GM19239	blood:	n/a
22	chr12:57351732-57351782	HAEpiC	amniotic membrane:	n/a
23	chr12:57352514-57352564	Caco-2	colon:	n/a
24	chr12:57351856-57351906	LNCaP	prostate:	n/a
25	chr12:57335615-57335665	MCF10A-Er-Src	breast:	n/a
26	chr12:57352514-57352564	AG09319	gingival:	n/a
27	chr12:57345407-57345457	AG10803	skin:	n/a
28	chr12:57351732-57351782	NH-A	brain:	n/a
29	chr12:57351856-57351906	HL-60	blood:	n/a
30	chr12:57351191-57351241	NB4	blood:	n/a
31	chr12:57351191-57351241	HRPEpiC	eye:	n/a
32	chr12:57345934-57345984	ECC-1	luminal epithelium:	n/a
33	chr12:57351191-57351241	SK-N-SH_RA	brain:	n/a
34	chr12:57351191-57351241	Hela-S3	cervix:	n/a
35	chr12:57351732-57351782	NHDF-neo	bronchial:	n/a
36	chr12:57351856-57351906	NHDF-neo	bronchial:	n/a
37	chr12:57345934-57345984	SKMC	muscle:	n/a
38	chr12:57345407-57345457	HCM	heart:	n/a
39	chr12:57351856-57351906	AG04449	skin:	fetal
40	chr12:57351856-57351906	HRE	kidney:	n/a
41	chr12:57345407-57345457	NH-A	brain:	n/a
42	chr12:57345407-57345457	HCT-116	colon:	n/a
43	chr12:57345934-57345984	Hepatocyte	liver:	n/a
44	chr12:57352514-57352564	GM12878	blood:	n/a
45	chr12:57351191-57351241	H1-hESC	embryonic stem cell:	embryo
46	chr12:57351856-57351906	MCF-7	breast:	n/a
47	chr12:57345934-57345984	PANC-1	pancreas:	n/a
48	chr12:57335615-57335665	AG10803	skin:	n/a
49	chr12:57351856-57351906	ECC-1	luminal epithelium:	n/a
50	chr12:57345407-57345457	A549	lung:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:57347864..57350577-chr12:57381566..57383920,2	MCF-7	breast:
2	chr12:57349108..57350665-chr12:57479276..57481586,2	MCF-7	breast:
3	chr12:57347630..57349531-chr12:57349740..57351878,2	MCF-7	breast:
4	chr12:57326664..57330911-chr12:57334392..57337503,4	K562	blood:
5	chr12:57144393..57147298-chr12:57377477..57379944,2	MCF-7	breast:
6	chr12:57374244..57376394-chr12:57378626..57381125,2	MCF-7	breast:
7	chr12:57341397..57342171-chr12:57399982..57400550,2	MCF-7	breast:
8	chr12:57325236..57327206-chr12:57341575..57344080,3	MCF-7	breast:
9	chr12:57349736..57351385-chr12:57380003..57382609,2	MCF-7	breast:
10	chr12:57351085..57351674-chr12:57381073..57381575,2	MCF-7	breast:
11	chr12:57341072..57342721-chr12:57384674..57386261,2	K562	blood:
12	chr12:57327540..57330418-chr12:57347371..57350395,3	K562	blood:
13	chr12:57350025..57351752-chr12:57359432..57361772,2	MCF-7	breast:
14	chr12:57324104..57327319-chr12:57348172..57351129,3	MCF-7	breast:
15	chr12:57326673..57329540-chr12:57347284..57349028,2	MCF-7	breast:
16	chr12:57370332..57372734-chr12:57384660..57386537,2	K562	blood:
17	chr12:57321673..57323369-chr12:57347515..57349644,2	MCF-7	breast:
18	chr12:57347630..57349531-chr12:57349740..57351878,2	MCF-7	breast:
19	chr12:57347121..57349496-chr12:57383085..57384758,2	MCF-7	breast:
20	chr12:57328840..57330584-chr12:57335451..57337263,2	MCF-7	breast:
21	chr12:57338428..57340285-chr12:57349754..57351660,2	MCF-7	breast:
22	chr12:57319841..57322040-chr12:57335776..57337907,3	MCF-7	breast:
23	chr12:57351472..57353366-chr12:57371615..57374205,2	MCF-7	breast:
24	chr12:57341090..57342031-chr12:57380872..57381968,6	MCF-7	breast:
25	chr12:57081337..57084055-chr12:57347595..57351157,3	MCF-7	breast:
26	chr12:57233379..57233935-chr12:57351193..57351985,2	MCF-7	breast:
27	chr12:57327126..57329472-chr12:57342749..57346552,3	MCF-7	breast:
28	chr12:57333897..57335886-chr12:57347612..57349669,2	MCF-7	breast:
29	chr12:57349241..57352181-chr12:57373731..57375876,2	MCF-7	breast:
30	chr12:57341567..57342147-chr12:57381088..57381948,3	MCF-7	breast:
31	chr12:57319872..57321581-chr12:57347777..57350711,2	MCF-7	breast:
32	chr12:57342671..57345733-chr12:57481207..57484376,3	MCF-7	breast:
33	chr12:57340605..57343794-chr12:57388280..57390645,3	MCF-7	breast:
34	chr12:57333897..57335886-chr12:57347612..57349669,2	MCF-7	breast:
35	chr12:57211985..57213673-chr12:57349961..57351583,2	MCF-7	breast:
36	chr12:57327918..57330814-chr12:57348513..57351502,2	MCF-7	breast:
37	chr12:57345020..57348622-chr12:57399414..57401826,4	MCF-7	breast:
38	chr12:57338428..57340285-chr12:57349754..57351660,2	MCF-7	breast:
39	chr12:57347827..57349628-chr12:57379616..57381539,3	MCF-7	breast:
40	chr12:57330845..57332526-chr12:57336068..57338551,2	MCF-7	breast:
41	chr12:57350025..57351752-chr12:57359432..57361772,2	MCF-7	breast:

No data

Variant related genes	Relation type
RDH16	TF binding region
RDH16	CpG island
ENSG00000170426	chromatin interactions
ENSG00000166881	chromatin interactions
ENSG00000139547	chromatin interactions
ENSG00000025423	chromatin interactions
ENSG00000258442	chromatin interactions
ENSG00000110958	chromatin interactions
ENSG00000198056	chromatin interactions
ENSG00000166886	chromatin interactions
ENSG00000166860	chromatin interactions

Extended variants
information (count: 1487 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1487 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs117136342	chr12:57335540-57335541	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs55707312	chr12:57335541-57335542	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs115562488	chr12:57335608-57335609	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs557179275	chr12:57335631-57335632	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs575752036	chr12:57335639-57335640	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs546338824	chr12:57335668-57335669	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs73330530	chr12:57335670-57335671	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs573457045	chr12:57335689-57335690	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs187146534	chr12:57335768-57335769	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs191998665	chr12:57335838-57335839	Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs529041411	chr12:57335876-57335877	Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs184407530	chr12:57335896-57335897	Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs188634853	chr12:57335898-57335899	Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs561743277	chr12:57335914-57335915	Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs140253848	chr12:57335994-57335995	Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs536316527	chr12:57336010-57336011	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs193260575	chr12:57336015-57336016	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs566679768	chr12:57336032-57336033	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs534077165	chr12:57336067-57336068	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs546629529	chr12:57336076-57336077	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs184117261	chr12:57336088-57336089	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs58009868	chr12:57336098-57336099	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs557044364	chr12:57336115-57336116	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs150360211	chr12:57336215-57336216	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs569792072	chr12:57336223-57336224	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs539667756	chr12:57336241-57336242	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs375261737	chr12:57336242-57336243	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs538551371	chr12:57336278-57336279	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs558310972	chr12:57336327-57336328	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs573493907	chr12:57336337-57336338	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs540922366	chr12:57336338-57336339	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs59665366	chr12:57336387-57336388	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs189431628	chr12:57336397-57336398	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs527713861	chr12:57336444-57336445	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs572002479	chr12:57336451-57336452	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs544192244	chr12:57336465-57336466	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs562463345	chr12:57336556-57336557	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs572407688	chr12:57336634-57336635	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs137979526	chr12:57336645-57336646	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs551319121	chr12:57336747-57336748	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs547470523	chr12:57336748-57336749	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs555433441	chr12:57336756-57336757	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs541063097	chr12:57336790-57336791	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs560285735	chr12:57336839-57336840	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs372091203	chr12:57336900-57336901	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs527634963	chr12:57336901-57336902	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs548869929	chr12:57336960-57336961	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs567183207	chr12:57336968-57336969	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs535473749	chr12:57336971-57336972	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs537924393	chr12:57337025-57337026	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
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
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	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
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
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Bladder cancer	21909424	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Autism	20531469	CNVD
Rhabdomyosarcoma	16790082	CNVD
Renal cell carcinoma	18765545	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21138945	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glycogen storage disease	18421352	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:218 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:57334600-57336400	Enhancers	HMEC	breast
2	chr12:57335000-57335600	Enhancers	GM12878-XiMat	blood
3	chr12:57335000-57336200	Enhancers	Skeletal Muscle Male	skeletal muscle
4	chr12:57335000-57336400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr12:57335000-57336400	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr12:57335000-57336400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr12:57335000-57336400	Enhancers	HSMM	muscle
8	chr12:57335000-57337200	Enhancers	Liver	Liver
9	chr12:57335200-57335600	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr12:57335200-57335600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
11	chr12:57335200-57335600	Enhancers	Duodenum Mucosa	Duodenum
12	chr12:57335200-57335800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr12:57335200-57335800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr12:57335200-57335800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr12:57335200-57335800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr12:57335200-57335800	Enhancers	Right Atrium	heart
17	chr12:57335200-57335800	Enhancers	Sigmoid Colon	Sigmoid Colon
18	chr12:57335200-57335800	Flanking Active TSS	Hela-S3	cervix
19	chr12:57335200-57335800	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr12:57335200-57335800	Flanking Active TSS	NHEK	skin
21	chr12:57335200-57336000	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr12:57335200-57336000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr12:57335200-57336000	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr12:57335200-57336000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr12:57335200-57336000	Enhancers	Adipose Nuclei	Adipose
26	chr12:57335200-57336000	Enhancers	Brain Inferior Temporal Lobe	brain
27	chr12:57335200-57336000	Enhancers	Fetal Intestine Small	intestine
28	chr12:57335200-57336000	Enhancers	Placenta	Placenta
29	chr12:57335200-57336000	Enhancers	Placenta Amnion	Placenta Amnion
30	chr12:57335200-57336000	Enhancers	NH-A	brain
31	chr12:57335200-57336000	Enhancers	Osteobl	bone
32	chr12:57335200-57336200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr12:57335200-57336200	Enhancers	Primary hematopoietic stem cells	blood
34	chr12:57335200-57336200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
35	chr12:57335200-57336200	Enhancers	Colon Smooth Muscle	Colon
36	chr12:57335200-57336200	Enhancers	Duodenum Smooth Muscle	Duodenum
37	chr12:57335200-57336200	Enhancers	Rectal Smooth Muscle	rectum
38	chr12:57335200-57336200	Enhancers	Spleen	Spleen
39	chr12:57335200-57336200	Flanking Active TSS	A549	lung
40	chr12:57335200-57336200	Flanking Active TSS	HepG2	liver
41	chr12:57335200-57336200	Enhancers	NHDF-Ad	bronchial
42	chr12:57335200-57336200	Enhancers	NHLF	lung
43	chr12:57335200-57336400	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr12:57335200-57336400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr12:57335200-57336400	Enhancers	Esophagus	oesophagus
46	chr12:57335200-57336400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr12:57335200-57336400	Enhancers	Fetal Intestine Large	intestine
48	chr12:57335200-57336400	Enhancers	HSMMtube	muscle
49	chr12:57335200-57336400	Enhancers	K562	blood
50	chr12:57335400-57335600	Enhancers	Muscle Satellite Cultured Cells	--

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