Variant report

Variant	esv3413076
Chromosome Location	chr11:72349804-72353302
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:33)
CpG islands
(count:244)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:33 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr11:72351828-72352216	GM12878	blood:	n/a	n/a
2	BHLHE40	chr11:72350609-72350647	K562	blood:	n/a	n/a
3	BHLHE40	chr11:72350539-72350654	HepG2	liver:	n/a	n/a
4	CCNT2	chr11:72353214-72353753	K562	blood:	n/a	n/a
5	CTCF	chr11:72352298-72352365	GM12892	blood:	n/a	n/a
6	CTCF	chr11:72352311-72352327	GM19239	blood:	n/a	n/a
7	CTCF	chr11:72352277-72352346	GM12891	blood:	n/a	n/a
8	CTCF	chr11:72351913-72351939	GM19239	blood:	n/a	n/a
9	HMGN3	chr11:72353291-72354496	K562	blood:	n/a	n/a
10	MAX	chr11:72353192-72355118	A549	lung:	n/a	chr11:72353938-72353948
11	MAX	chr11:72353163-72353822	H1-hESC	embryonic stem cell:	n/a	n/a
12	MAX	chr11:72350419-72350791	K562	blood:	n/a	chr11:72350647-72350656 chr11:72350648-72350655
13	MAX	chr11:72353206-72355001	A549	lung:	n/a	chr11:72353938-72353948
14	MAX	chr11:72353254-72353485	K562	blood:	n/a	n/a
15	MAX	chr11:72353292-72354393	K562	blood:	n/a	chr11:72353938-72353948
16	MAX	chr11:72353210-72353836	ECC-1	luminal epithelium:	n/a	n/a
17	MAZ	chr11:72351396-72351450	Hela-S3	cervix:	n/a	n/a
18	MXI1	chr11:72353152-72354771	SK-N-SH	brain:	n/a	n/a
19	MXI1	chr11:72352861-72352913	Hela-S3	cervix:	n/a	n/a
20	NFYB	chr11:72352181-72352296	GM12878	blood:	n/a	n/a
21	POLR2A	chr11:72353199-72353510	HCT-116	colon:	n/a	n/a
22	POLR2A	chr11:72353247-72353520	Hela-S3	cervix:	n/a	n/a
23	POLR2A	chr11:72353101-72354971	Hela-S3	cervix:	n/a	n/a
24	POLR2A	chr11:72353160-72353703	HUVEC	blood vessel:	n/a	n/a
25	POLR2A	chr11:72353230-72353507	HUVEC	blood vessel:	n/a	n/a
26	POLR2A	chr11:72352824-72352826	MCF10A-Er-Src	breast:	n/a	n/a
27	POLR2A	chr11:72351222-72351231	MCF-7	breast:	n/a	n/a
28	POLR2A	chr11:72353302-72353757	K562	blood:	n/a	n/a
29	POLR2A	chr11:72351225-72351472	MCF-7	breast:	n/a	n/a
30	POLR2A	chr11:72353234-72353504	HCT-116	colon:	n/a	n/a
31	SIN3A	chr11:72352918-72353118	H1-hESC	embryonic stem cell:	n/a	n/a
32	SMARCB1	chr11:72352741-72355028	Hela-S3	cervix:	n/a	chr11:72354667-72354676
33	UBTF	chr11:72353269-72354453	K562	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	chr11:72350553-72350603	HRCEpiC	kidney:	n/a
2	chr11:72353157-72353207	MCF10A-Er-Src	breast:	n/a
3	chr11:72353049-72353099	HEK293	kidney:	embryo
4	chr11:72353157-72353207	PrEC	prostate:	n/a
5	chr11:72350651-72350701	GM12891	blood:	n/a
6	chr11:72353157-72353207	HRCEpiC	kidney:	n/a
7	chr11:72350553-72350603	NT2-D1	testis:	n/a
8	chr11:72353157-72353207	RPTEC	kidney:	n/a
9	chr11:72353049-72353099	A549	lung:	n/a
10	chr11:72353049-72353099	RPTEC	kidney:	n/a
11	chr11:72353157-72353207	AG04450	lung:	fetal
12	chr11:72350651-72350701	SK-N-SH_RA	brain:	n/a
13	chr11:72353049-72353099	HMEC	breast:	n/a
14	chr11:72350553-72350603	ECC-1	luminal epithelium:	n/a
15	chr11:72350651-72350701	BE2_C	brain:	n/a
16	chr11:72353049-72353099	SAEC	small airway:	n/a
17	chr11:72350553-72350603	HCM	heart:	n/a
18	chr11:72350651-72350701	HUVEC	blood vessel:	n/a
19	chr11:72353157-72353207	SK-N-SH_RA	brain:	n/a
20	chr11:72353157-72353207	NB4	blood:	n/a
21	chr11:72350651-72350701	GM06990	blood:	n/a
22	chr11:72350651-72350701	PrEC	prostate:	n/a
23	chr11:72353049-72353099	HepG2	liver:	n/a
24	chr11:72353049-72353099	BE2_C	brain:	n/a
25	chr11:72353157-72353207	PFSK-1	brain:	n/a
26	chr11:72350651-72350701	NHBE	bronchial:	n/a
27	chr11:72350651-72350701	NT2-D1	testis:	n/a
28	chr11:72350553-72350603	Jurkat	blood:	n/a
29	chr11:72350553-72350603	A549	lung:	n/a
30	chr11:72353049-72353099	ECC-1	luminal epithelium:	n/a
31	chr11:72350553-72350603	NHBE	bronchial:	n/a
32	chr11:72350651-72350701	GM12878	blood:	n/a
33	chr11:72350651-72350701	T-47D	breast:	n/a
34	chr11:72353157-72353207	HPAEpiC	pulmonary alveolar:	n/a
35	chr11:72350651-72350701	NB4	blood:	n/a
36	chr11:72350553-72350603	HL-60	blood:	n/a
37	chr11:72353157-72353207	BE2_C	brain:	n/a
38	chr11:72350651-72350701	AG04450	lung:	fetal
39	chr11:72350553-72350603	HUVEC	blood vessel:	n/a
40	chr11:72350553-72350603	SK-N-MC	brain:	n/a
41	chr11:72350651-72350701	BJ	skin:	n/a
42	chr11:72350553-72350603	HIPEpiC	eye:	n/a
43	chr11:72353157-72353207	BJ	skin:	n/a
44	chr11:72353049-72353099	ProgFib	skin:	n/a
45	chr11:72353049-72353099	NB4	blood:	n/a
46	chr11:72350651-72350701	AG09309	skin:	n/a
47	chr11:72353049-72353099	K562	blood:	n/a
48	chr11:72350553-72350603	IMR90	lung:	fetal
49	chr11:72353157-72353207	NT2-D1	testis:	n/a
50	chr11:72353157-72353207	HEK293	kidney:	embryo

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:72352692..72354361-chr11:72368071..72370416,2	K562	blood:
2	chr11:72340095..72342278-chr11:72348258..72351014,2	MCF-7	breast:
3	chr11:72308196..72310111-chr11:72350959..72352581,2	MCF-7	breast:
4	chr11:72342072..72343913-chr11:72348665..72350291,3	K562	blood:
5	chr1:9294464..9295463-chr11:72353109..72353947,2	Hela-S3	cervix:
6	chr11:72345729..72347708-chr11:72348323..72351528,4	K562	blood:
7	chr11:72352379..72355272-chr11:72384070..72386668,2	K562	blood:
8	chr11:72300263..72302231-chr11:72352736..72355134,2	K562	blood:
9	chr11:72341497..72343932-chr11:72350783..72352444,2	K562	blood:
10	chr11:72350202..72352070-chr11:72353672..72355954,2	K562	blood:

No data

Variant related genes	Relation type
PDE2A	TF binding region
ENSG00000255808	TF binding region
PDE2A	CpG island
ENSG00000255808	CpG island
ENSG00000049239	chromatin interactions
ENSG00000255808	chromatin interactions
ENSG00000186642	chromatin interactions

Extended variants
information (count: 143 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:143 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs80060303	chr11:72349812-72349813	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs372694915	chr11:72349815-72349816	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs543807696	chr11:72349828-72349829	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs78688103	chr11:72349829-72349830	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs575861111	chr11:72349886-72349887	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs543176442	chr11:72349927-72349928	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs561349651	chr11:72349937-72349938	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs528579765	chr11:72349939-72349940	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs540773241	chr11:72349942-72349943	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs376935504	chr11:72349978-72349979	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs191105260	chr11:72349986-72349987	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs552485504	chr11:72349996-72349997	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs550711736	chr11:72350003-72350004	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs61580813	chr11:72350021-72350022	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs531349546	chr11:72350042-72350043	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs529966810	chr11:72350058-72350059	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs550383324	chr11:72350072-72350073	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs548345269	chr11:72350078-72350079	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs566368047	chr11:72350097-72350098	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs533638067	chr11:72350107-72350108	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs182409280	chr11:72350179-72350180	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs34273765	chr11:72350214-72350215	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs74905558	chr11:72350232-72350233	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs187034829	chr11:72350233-72350234	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs548125301	chr11:72350243-72350244	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs7941968	chr11:72350326-72350327	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs575870043	chr11:72350352-72350353	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs191678338	chr11:72350368-72350369	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs111372391	chr11:72350376-72350377	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs529551141	chr11:72350403-72350404	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs77304990	chr11:72350462-72350463	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs112133349	chr11:72350478-72350479	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs536654263	chr11:72350552-72350553	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs540832842	chr11:72350554-72350555	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs570652762	chr11:72350588-72350589	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs539064184	chr11:72350592-72350593	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs3781926	chr11:72350595-72350596	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs544568699	chr11:72350601-72350602	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs562773760	chr11:72350648-72350649	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs529986852	chr11:72350651-72350652	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs548232558	chr11:72350747-72350748	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs566431038	chr11:72350759-72350760	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs527441703	chr11:72350767-72350768	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs551965867	chr11:72350776-72350777	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs370820755	chr11:72350835-72350836	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs72962134	chr11:72350846-72350847	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs146509279	chr11:72350935-72350936	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs183033696	chr11:72350941-72350942	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs368504129	chr11:72350968-72350969	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs187319614	chr11:72350980-72350981	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	19153074	CNVD
Acute myeloid leukemia	21251322	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:302 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:72334800-72350200	Enhancers	Left Ventricle	heart
2	chr11:72335800-72350600	Enhancers	Brain Hippocampus Middle	brain
3	chr11:72336000-72350400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
4	chr11:72339000-72350600	Enhancers	Brain Cingulate Gyrus	brain
5	chr11:72343400-72350200	Enhancers	Right Atrium	heart
6	chr11:72343400-72351000	Weak transcription	Esophagus	oesophagus
7	chr11:72343600-72350800	Weak transcription	Brain Substantia Nigra	brain
8	chr11:72343600-72351000	Enhancers	Skeletal Muscle Female	skeletal muscle
9	chr11:72344600-72351600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
10	chr11:72345800-72350400	Enhancers	Colon Smooth Muscle	Colon
11	chr11:72346600-72350400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
12	chr11:72346800-72351600	Bivalent Enhancer	Fetal Muscle Leg	muscle
13	chr11:72347000-72350800	Enhancers	Spleen	Spleen
14	chr11:72347200-72351000	Enhancers	Brain Angular Gyrus	brain
15	chr11:72347600-72351000	Enhancers	Right Ventricle	heart
16	chr11:72348200-72351000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
17	chr11:72348600-72352600	Enhancers	Lung	lung
18	chr11:72348800-72352800	Weak transcription	Gastric	stomach
19	chr11:72349000-72350800	Weak transcription	Fetal Brain Male	brain
20	chr11:72349000-72352200	Weak transcription	Pancreas	Pancrea
21	chr11:72349400-72350200	Weak transcription	Brain Anterior Caudate	brain
22	chr11:72349400-72350200	Weak transcription	Hela-S3	cervix
23	chr11:72349400-72350400	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr11:72349400-72352000	Weak transcription	Liver	Liver
25	chr11:72349600-72350000	Weak transcription	Stomach Smooth Muscle	stomach
26	chr11:72349600-72350200	Bivalent Enhancer	Adipose Nuclei	Adipose
27	chr11:72349600-72351000	Weak transcription	Psoas Muscle	Psoas
28	chr11:72349800-72350400	Bivalent Enhancer	Fetal Stomach	stomach
29	chr11:72350000-72350400	Genic enhancers	Stomach Smooth Muscle	stomach
30	chr11:72350200-72350400	Flanking Active TSS	Left Ventricle	heart
31	chr11:72350200-72350600	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
32	chr11:72350200-72351000	Enhancers	Brain Anterior Caudate	brain
33	chr11:72350200-72351000	Weak transcription	Right Atrium	heart
34	chr11:72350200-72351000	Active TSS	Hela-S3	cervix
35	chr11:72350200-72351400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr11:72350400-72350600	Enhancers	Brain Inferior Temporal Lobe	brain
37	chr11:72350400-72350600	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
38	chr11:72350400-72350600	Weak transcription	Stomach Smooth Muscle	stomach
39	chr11:72350400-72350800	Weak transcription	Colon Smooth Muscle	Colon
40	chr11:72350400-72351000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr11:72350400-72351000	Weak transcription	Left Ventricle	heart
42	chr11:72350400-72351200	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr11:72350400-72352000	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
44	chr11:72350600-72350800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
45	chr11:72350600-72351000	Bivalent Enhancer	Adipose Nuclei	Adipose
46	chr11:72350600-72351000	Enhancers	Stomach Smooth Muscle	stomach
47	chr11:72350600-72351200	Flanking Active TSS	Brain Hippocampus Middle	brain
48	chr11:72350600-72351600	Flanking Active TSS	Brain Cingulate Gyrus	brain
49	chr11:72350600-72352800	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
50	chr11:72350800-72351200	Enhancers	Colon Smooth Muscle	Colon

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