Variant report

Variant	esv3416094
Chromosome Location	chr11:33408518-33511658
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:482)
CpG islands
(count:244)
Chromatin interactive
region (count:32)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:482 , 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	chr11:33467294-33467606	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:33499524-33499864	HepG2	liver:	n/a	n/a
3	ATF2	chr11:33409013-33410089	GM12878	blood:	n/a	n/a
4	ATF2	chr11:33409042-33410013	GM12878	blood:	n/a	n/a
5	ATF2	chr11:33411036-33411671	GM12878	blood:	n/a	n/a
6	BATF	chr11:33411172-33411511	GM12878	blood:	n/a	n/a
7	BATF	chr11:33408990-33409983	GM12878	blood:	n/a	n/a
8	BATF	chr11:33409566-33409855	GM12878	blood:	n/a	n/a
9	BCL11A	chr11:33409572-33409836	GM12878	blood:	n/a	n/a
10	BCL11A	chr11:33409034-33409543	GM12878	blood:	n/a	n/a
11	BCL11A	chr11:33409556-33409888	GM12878	blood:	n/a	n/a
12	BCL3	chr11:33409282-33409904	GM12878	blood:	n/a	n/a
13	BCLAF1	chr11:33409061-33410037	GM12878	blood:	n/a	n/a
14	BCLAF1	chr11:33409067-33410001	GM12878	blood:	n/a	n/a
15	BHLHE40	chr11:33484666-33484886	K562	blood:	n/a	n/a
16	BHLHE40	chr11:33427892-33427983	K562	blood:	n/a	n/a
17	CEBPB	chr11:33417955-33418250	K562	blood:	n/a	chr11:33418096-33418109 chr11:33418098-33418107 chr11:33418096-33418107 chr11:33418098-33418107 chr11:33418098-33418107
18	CEBPB	chr11:33417956-33418181	Hela-S3	cervix:	n/a	chr11:33418096-33418109 chr11:33418098-33418107 chr11:33418096-33418107 chr11:33418098-33418107 chr11:33418098-33418107
19	CEBPB	chr11:33425244-33425411	IMR90	lung:	n/a	n/a
20	CEBPB	chr11:33474376-33474661	IMR90	lung:	n/a	n/a
21	CEBPB	chr11:33483885-33484074	HepG2	liver:	n/a	chr11:33483952-33483963
22	CEBPB	chr11:33499570-33499963	HepG2	liver:	n/a	chr11:33499751-33499762
23	CEBPB	chr11:33468792-33469028	HepG2	liver:	n/a	chr11:33468877-33468890 chr11:33468878-33468889
24	CEBPB	chr11:33499603-33499920	H1-hESC	embryonic stem cell:	n/a	chr11:33499751-33499762
25	CEBPB	chr11:33499657-33499869	Hela-S3	cervix:	n/a	chr11:33499751-33499762
26	CEBPB	chr11:33499528-33499927	HepG2	liver:	n/a	chr11:33499751-33499762
27	CEBPB	chr11:33422567-33422729	HepG2	liver:	n/a	chr11:33422604-33422615
28	CEBPB	chr11:33488219-33488245	HepG2	liver:	n/a	n/a
29	CEBPB	chr11:33499578-33499951	HepG2	liver:	n/a	chr11:33499751-33499762
30	CEBPB	chr11:33488148-33488342	A549	lung:	n/a	n/a
31	CEBPB	chr11:33488188-33488247	IMR90	lung:	n/a	n/a
32	CEBPB	chr11:33499621-33499855	HepG2	liver:	n/a	chr11:33499751-33499762
33	CEBPB	chr11:33418045-33418213	H1-hESC	embryonic stem cell:	n/a	chr11:33418096-33418109 chr11:33418098-33418107 chr11:33418096-33418107 chr11:33418098-33418107 chr11:33418098-33418107
34	CEBPB	chr11:33468747-33468988	IMR90	lung:	n/a	chr11:33468877-33468890 chr11:33468878-33468889
35	CEBPB	chr11:33417928-33418277	IMR90	lung:	n/a	chr11:33418096-33418109 chr11:33418098-33418107 chr11:33418096-33418107 chr11:33418098-33418107 chr11:33418098-33418107
36	CEBPB	chr11:33417941-33418267	HepG2	liver:	n/a	chr11:33418096-33418109 chr11:33418098-33418107 chr11:33418096-33418107 chr11:33418098-33418107 chr11:33418098-33418107
37	CEBPB	chr11:33468723-33468936	A549	lung:	n/a	chr11:33468877-33468890 chr11:33468878-33468889
38	CEBPB	chr11:33417934-33418273	A549	lung:	n/a	chr11:33418096-33418109 chr11:33418098-33418107 chr11:33418096-33418107 chr11:33418098-33418107 chr11:33418098-33418107
39	CEBPB	chr11:33408954-33410112	GM12878	blood:	n/a	n/a
40	CEBPB	chr11:33498761-33499059	IMR90	lung:	n/a	n/a
41	CEBPB	chr11:33499567-33499966	MCF-7	breast:	n/a	chr11:33499751-33499762
42	CHD2	chr11:33499726-33499731	HepG2	liver:	n/a	n/a
43	CTCF	chr11:33479714-33479736	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr11:33411740-33411890	GM12872	blood:	n/a	n/a
45	CTCF	chr11:33467200-33467350	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr11:33425055-33425138	GM19239	blood:	n/a	n/a
47	CTCF	chr11:33499520-33499670	GM12873	blood:	n/a	n/a
48	CTCF	chr11:33479620-33479770	HEK293	kidney:	n/a	n/a
49	CTCF	chr11:33479600-33479750	GM12869	blood:	n/a	n/a
50	CTCF	chr11:33479580-33479730	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	chr11:33442321-33442371	GM19239	blood:	n/a
2	chr11:33442321-33442371	U87	brain:	n/a
3	chr11:33474484-33474534	HCF	heart:	n/a
4	chr11:33506184-33506234	ECC-1	luminal epithelium:	n/a
5	chr11:33474484-33474534	HMEC	breast:	n/a
6	chr11:33453389-33453439	AG09309	skin:	n/a
7	chr11:33453389-33453439	PANC-1	pancreas:	n/a
8	chr11:33474484-33474534	AG04449	skin:	fetal
9	chr11:33442321-33442371	T-47D	breast:	n/a
10	chr11:33442321-33442371	GM06990	blood:	n/a
11	chr11:33442321-33442371	GM12892	blood:	n/a
12	chr11:33506184-33506234	PFSK-1	brain:	n/a
13	chr11:33442321-33442371	SK-N-SH_RA	brain:	n/a
14	chr11:33453389-33453439	BJ	skin:	n/a
15	chr11:33453389-33453439	GM06990	blood:	n/a
16	chr11:33474484-33474534	IMR90	lung:	fetal
17	chr11:33442321-33442371	HPAEpiC	pulmonary alveolar:	n/a
18	chr11:33474484-33474534	HEEpiC	esophagus:	n/a
19	chr11:33453389-33453439	T-47D	breast:	n/a
20	chr11:33474484-33474534	CMK	blood:	n/a
21	chr11:33442321-33442371	MCF-7	breast:	n/a
22	chr11:33453389-33453439	HCPEpiC	choroid plexus:	n/a
23	chr11:33506184-33506234	HCF	heart:	n/a
24	chr11:33474484-33474534	U87	brain:	n/a
25	chr11:33453389-33453439	H1-hESC	embryonic stem cell:	embryo
26	chr11:33506184-33506234	HEK293	kidney:	embryo
27	chr11:33506184-33506234	HL-60	blood:	n/a
28	chr11:33506184-33506234	HepG2	liver:	n/a
29	chr11:33453389-33453439	HRE	kidney:	n/a
30	chr11:33453389-33453439	IMR90	lung:	fetal
31	chr11:33442321-33442371	A549	lung:	n/a
32	chr11:33506184-33506234	HNPCEpiC	eye:	n/a
33	chr11:33453389-33453439	U87	brain:	n/a
34	chr11:33506184-33506234	NH-A	brain:	n/a
35	chr11:33453389-33453439	GM19239	blood:	n/a
36	chr11:33474484-33474534	NH-A	brain:	n/a
37	chr11:33453389-33453439	HEEpiC	esophagus:	n/a
38	chr11:33474484-33474534	BE2_C	brain:	n/a
39	chr11:33453389-33453439	HIPEpiC	eye:	n/a
40	chr11:33453389-33453439	A549	lung:	n/a
41	chr11:33442321-33442371	AoSMC	blood vessel:	n/a
42	chr11:33474484-33474534	PrEC	prostate:	n/a
43	chr11:33474484-33474534	AG04450	lung:	fetal
44	chr11:33506184-33506234	Jurkat	blood:	n/a
45	chr11:33474484-33474534	Caco-2	colon:	n/a
46	chr11:33442321-33442371	NHBE	bronchial:	n/a
47	chr11:33506184-33506234	SK-N-SH_RA	brain:	n/a
48	chr11:33506184-33506234	Hela-S3	cervix:	n/a
49	chr11:33506184-33506234	HEEpiC	esophagus:	n/a
50	chr11:33506184-33506234	HRE	kidney:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:33495157..33498013-chr11:33505516..33507926,2	K562	blood:
2	chr11:33433824..33436288-chr11:33439074..33441301,2	K562	blood:
3	chr11:33475872..33478381-chr11:33480677..33482697,2	MCF-7	breast:
4	chr11:33432981..33435559-chr11:33436354..33439310,2	K562	blood:
5	chr11:33497434..33499618-chr11:33502949..33504703,2	K562	blood:
6	chr11:33429478..33432664-chr11:33434233..33436615,3	K562	blood:
7	chr11:33474719..33477394-chr11:33482084..33484055,2	K562	blood:
8	chr11:33475872..33478381-chr11:33480677..33482697,2	MCF-7	breast:
9	chr11:33413545..33415997-chr11:33484077..33486158,2	K562	blood:
10	chr11:33422636..33425023-chr11:33427111..33429775,2	MCF-7	breast:
11	chr11:33403805..33405903-chr11:33414463..33417062,2	MCF-7	breast:
12	chr11:33464022..33465573-chr11:33469227..33471332,2	K562	blood:
13	chr11:33419522..33421501-chr11:33424149..33426108,2	K562	blood:
14	chr11:33432981..33435559-chr11:33436354..33439310,2	K562	blood:
15	chr11:33412811..33414591-chr11:33744029..33746622,2	K562	blood:
16	chr11:33428202..33430119-chr11:33432481..33434506,2	MCF-7	breast:
17	chr11:33429478..33432664-chr11:33434233..33436615,3	K562	blood:
18	chr11:33497434..33499618-chr11:33502949..33504703,2	K562	blood:
19	chr11:33464022..33465573-chr11:33469227..33471332,2	K562	blood:
20	chr11:33421417..33423758-chr11:33435787..33437817,2	K562	blood:
21	chr11:33428202..33430119-chr11:33432481..33434506,2	MCF-7	breast:
22	chr11:33450480..33453431-chr11:33470843..33473158,2	MCF-7	breast:
23	chr11:33495157..33498013-chr11:33505516..33507926,2	K562	blood:
24	chr11:33416676..33419367-chr11:33423190..33425357,2	K562	blood:
25	chr11:33404576..33406306-chr11:33408202..33410856,2	MCF-7	breast:
26	chr11:33421417..33423758-chr11:33435787..33437817,2	K562	blood:
27	chr11:33426996..33428983-chr11:33431666..33434178,3	K562	blood:
28	chr11:33426996..33428983-chr11:33431666..33434178,3	K562	blood:
29	chr11:33413545..33415997-chr11:33484077..33486158,2	K562	blood:
30	chr11:33433824..33436288-chr11:33439074..33441301,2	K562	blood:
31	chr11:33492401..33495030-chr11:33579028..33581044,2	K562	blood:
32	chr11:33474719..33477394-chr11:33482084..33484055,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C11orf41-5	chr11:33472192-33472489	NONHSAT018701
2	lnc-HIPK3-2	chr11:33424762-33425151	NONHSAT018700

No data

Variant related genes	Relation type
ENSG00000255207	TF binding region
ENSG00000254537	TF binding region
ENSG00000255207	CpG island
ENSG00000254537	CpG island
ENSG00000254537	chromatin interactions
ENSG00000085063	chromatin interactions
ENSG00000255207	chromatin interactions

Extended variants
information (count: 3935 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:3935 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552465683	chr11:33408523-33408524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs565988357	chr11:33408538-33408539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs534761643	chr11:33408545-33408546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs554849881	chr11:33408548-33408549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs375169539	chr11:33408602-33408603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs140659612	chr11:33408718-33408719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs144212132	chr11:33408737-33408738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs577133093	chr11:33408753-33408754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs545805256	chr11:33408779-33408780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs553207015	chr11:33408786-33408787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs187043340	chr11:33408795-33408796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs569023882	chr11:33408816-33408817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs192379350	chr11:33408844-33408845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs562179881	chr11:33408920-33408921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529775980	chr11:33408961-33408962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs549532985	chr11:33408964-33408965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs543123572	chr11:33408969-33408970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs563412782	chr11:33408974-33408975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs12363895	chr11:33409021-33409022	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs531971800	chr11:33409050-33409051	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs552205222	chr11:33409139-33409140	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs144239791	chr11:33409152-33409153	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs17346987	chr11:33409235-33409236	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs147789153	chr11:33409243-33409244	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs141250949	chr11:33409250-33409251	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs568187653	chr11:33409355-33409356	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs375221602	chr11:33409357-33409358	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs200953578	chr11:33409371-33409372	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs568391491	chr11:33409422-33409423	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs3886336	chr11:33409441-33409442	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs558226098	chr11:33409444-33409445	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs113411412	chr11:33409453-33409454	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs113181346	chr11:33409471-33409472	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs11032251	chr11:33409508-33409509	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs541132860	chr11:33409549-33409550	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs573186300	chr11:33409551-33409552	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs181478251	chr11:33409615-33409616	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs535778914	chr11:33409662-33409663	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs575715157	chr11:33409678-33409679	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs544800854	chr11:33409687-33409688	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs12280218	chr11:33409701-33409702	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs532292132	chr11:33409733-33409734	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs187002428	chr11:33409755-33409756	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs12293290	chr11:33409783-33409784	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs190648490	chr11:33409887-33409888	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs548155550	chr11:33409888-33409889	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs143621973	chr11:33409892-33409893	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs568355864	chr11:33409897-33409898	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs112305602	chr11:33410109-33410110	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs78196612	chr11:33410117-33410118	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	22286061	CNVD
Aniridia syndrome	21572526	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Retinoblastoma	22278416	CNVD
Denys-drash syndrome	21085971	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
WAGR syndrome	16773131	CNVD
Disorders of sex development	22290220	CNVD
Aniridia syndrome	17204608	CNVD
Mental retardation	17204608	CNVD
WAGR syndrome	19617690	CNVD
genitourinary abnormalities	17204608	CNVD
Breast cancer	16397240	CNVD
Mental retardation	16773131	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Cancer	21183584	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
WAGR syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Denys-drash syndrome	19566914	CNVD
Familial wilms tumor	19566914	CNVD
Frasier syndrome	19566914	CNVD
Non-small cell lung cancer	21829676	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:516 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33401800-33414400	Weak transcription	Fetal Brain Female	brain
2	chr11:33404800-33422000	Weak transcription	NH-A	brain
3	chr11:33407800-33411200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr11:33408000-33409000	Enhancers	GM12878-XiMat	blood
5	chr11:33408000-33414800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr11:33408200-33409000	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr11:33408200-33411400	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr11:33408800-33411800	Enhancers	Primary B cells from peripheral blood	blood
9	chr11:33409000-33409400	Enhancers	HUVEC	blood vessel
10	chr11:33409000-33409400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
11	chr11:33409000-33409600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr11:33409000-33411800	Flanking Active TSS	GM12878-XiMat	blood
13	chr11:33409200-33410000	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr11:33409400-33409600	Active TSS	Monocytes-CD14+_RO01746	blood
15	chr11:33409600-33409800	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr11:33409800-33410000	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr11:33410000-33410600	Enhancers	Primary B cells from cord blood	blood
18	chr11:33410000-33411400	Enhancers	Monocytes-CD14+_RO01746	blood
19	chr11:33411200-33413400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr11:33411800-33412200	Enhancers	GM12878-XiMat	blood
21	chr11:33412000-33413200	Enhancers	Brain Germinal Matrix	brain
22	chr11:33412600-33414000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr11:33413000-33413800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr11:33413200-33423600	Weak transcription	Brain Germinal Matrix	brain
25	chr11:33413400-33466200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr11:33413800-33422400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr11:33414000-33423200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr11:33414400-33415600	Strong transcription	Fetal Brain Female	brain
29	chr11:33414800-33415400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr11:33415400-33424800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr11:33415600-33434000	Weak transcription	Fetal Brain Female	brain
32	chr11:33417000-33423400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr11:33419800-33420000	Enhancers	Brain Inferior Temporal Lobe	brain
34	chr11:33420000-33425000	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr11:33422400-33422600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr11:33422600-33423000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr11:33423000-33423800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr11:33423200-33423800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr11:33423200-33424000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr11:33423400-33423800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr11:33423400-33424000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr11:33423400-33424000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr11:33423600-33423800	Enhancers	Brain Germinal Matrix	brain
44	chr11:33423600-33424400	Enhancers	GM12878-XiMat	blood
45	chr11:33423800-33433000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr11:33423800-33433400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr11:33423800-33434000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr11:33424000-33424800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr11:33424000-33432400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr11:33424000-33440200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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