Variant report

Variant	esv3352884
Chromosome Location	chr11:67182326-67184374
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:30)
CpG islands
(count:673)
Chromatin interactive
region (count:5)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:30 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr11:67184060-67184210	HepG2	liver:	n/a	chr11:67184123-67184132 chr11:67184117-67184135
2	CTCF	chr11:67184120-67184270	A549	lung:	n/a	chr11:67184123-67184132
3	CTCF	chr11:67184060-67184210	HBMEC	blood vessel:	n/a	chr11:67184123-67184132 chr11:67184117-67184135
4	EGR1	chr11:67183578-67183761	K562	blood:	n/a	n/a
5	FOXA1	chr11:67184335-67184627	T-47D	breast:	n/a	n/a
6	FOXA1	chr11:67184288-67184612	T-47D	breast:	n/a	n/a
7	FOXA1	chr11:67184321-67184712	HepG2	liver:	n/a	n/a
8	FOXA2	chr11:67184275-67184775	A549	lung:	n/a	n/a
9	FOXA2	chr11:67184345-67184662	HepG2	liver:	n/a	n/a
10	FOXA2	chr11:67184298-67184829	A549	lung:	n/a	n/a
11	FOXP2	chr11:67184293-67184886	SK-N-MC	brain:	n/a	n/a
12	MAX	chr11:67184352-67184837	NB4	blood:	n/a	n/a
13	NFIC	chr11:67184313-67184796	ECC-1	luminal epithelium:	n/a	n/a
14	POLR2A	chr11:67183054-67183295	MCF-7	breast:	n/a	n/a
15	POLR2A	chr11:67182658-67182900	HCT-116	colon:	n/a	n/a
16	POLR2A	chr11:67182865-67182871	MCF-7	breast:	n/a	n/a
17	POLR2A	chr11:67183567-67183576	MCF-7	breast:	n/a	n/a
18	POLR2A	chr11:67183577-67183620	MCF-7	breast:	n/a	n/a
19	POLR2A	chr11:67183117-67183283	HCT-116	colon:	n/a	n/a
20	POLR2A	chr11:67183521-67183738	K562	blood:	n/a	n/a
21	POLR2A	chr11:67183432-67183476	H1-hESC	embryonic stem cell:	n/a	n/a
22	POLR2A	chr11:67183402-67183641	H1-hESC	embryonic stem cell:	n/a	n/a
23	POLR2A	chr11:67183166-67183281	ProgFib	skin:	n/a	n/a
24	POLR2A	chr11:67183493-67183555	H1-hESC	embryonic stem cell:	n/a	n/a
25	SIN3A	chr11:67182738-67182982	H1-hESC	embryonic stem cell:	n/a	chr11:67182803-67182813
26	SP1	chr11:67184332-67184813	A549	lung:	n/a	n/a
27	TBP	chr11:67182598-67182850	H1-hESC	embryonic stem cell:	n/a	n/a
28	ZBTB7A	chr11:67182470-67182596	HepG2	liver:	n/a	n/a
29	ZBTB7A	chr11:67182414-67182818	K562	blood:	n/a	n/a
30	ZKSCAN1	chr11:67184173-67184563	Hela-S3	cervix:	n/a	n/a

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:67182672-67182722	HEEpiC	esophagus:	n/a
2	chr11:67183498-67183548	MCF-7	breast:	n/a
3	chr11:67182672-67182722	HEEpiC	esophagus:	n/a
4	chr11:67183498-67183548	MCF-7	breast:	n/a
5	chr11:67182488-67182538	AoSMC	blood vessel:	n/a
6	chr11:67183148-67183198	PrEC	prostate:	n/a
7	chr11:67183498-67183548	HRPEpiC	eye:	n/a
8	chr11:67183083-67183133	Caco-2	colon:	n/a
9	chr11:67182672-67182722	NH-A	brain:	n/a
10	chr11:67182488-67182538	SK-N-SH_RA	brain:	n/a
11	chr11:67183330-67183380	HRCEpiC	kidney:	n/a
12	chr11:67183083-67183133	NHBE	bronchial:	n/a
13	chr11:67183498-67183548	RPTEC	kidney:	n/a
14	chr11:67182488-67182538	HNPCEpiC	eye:	n/a
15	chr11:67183546-67183596	K562	blood:	n/a
16	chr11:67183616-67183666	RPTEC	kidney:	n/a
17	chr11:67183616-67183666	BE2_C	brain:	n/a
18	chr11:67183078-67183128	AG09309	skin:	n/a
19	chr11:67183148-67183198	SK-N-MC	brain:	n/a
20	chr11:67183083-67183133	GM12878	blood:	n/a
21	chr11:67183148-67183198	NHDF-neo	bronchial:	n/a
22	chr11:67183546-67183596	HepG2	liver:	n/a
23	chr11:67183616-67183666	HRPEpiC	eye:	n/a
24	chr11:67183330-67183380	NB4	blood:	n/a
25	chr11:67183083-67183133	AoSMC	blood vessel:	n/a
26	chr11:67183616-67183666	HepG2	liver:	n/a
27	chr11:67183080-67183130	GM06990	blood:	n/a
28	chr11:67183148-67183198	HUVEC	blood vessel:	n/a
29	chr11:67183078-67183128	Jurkat	blood:	n/a
30	chr11:67182672-67182722	ECC-1	luminal epithelium:	n/a
31	chr11:67183546-67183596	HRPEpiC	eye:	n/a
32	chr11:67183616-67183666	SK-N-SH	brain:	n/a
33	chr11:67182488-67182538	PrEC	prostate:	n/a
34	chr11:67183083-67183133	Hepatocyte	liver:	n/a
35	chr11:67183546-67183596	HUVEC	blood vessel:	n/a
36	chr11:67183080-67183130	BE2_C	brain:	n/a
37	chr11:67183083-67183133	SK-N-SH	brain:	n/a
38	chr11:67182724-67182774	Caco-2	colon:	n/a
39	chr11:67182672-67182722	GM12892	blood:	n/a
40	chr11:67183078-67183128	NH-A	brain:	n/a
41	chr11:67183616-67183666	GM06990	blood:	n/a
42	chr11:67182672-67182722	NB4	blood:	n/a
43	chr11:67183546-67183596	AoSMC	blood vessel:	n/a
44	chr11:67183148-67183198	BJ	skin:	n/a
45	chr11:67182724-67182774	PFSK-1	brain:	n/a
46	chr11:67183546-67183596	RPTEC	kidney:	n/a
47	chr11:67182724-67182774	T-47D	breast:	n/a
48	chr11:67183148-67183198	ECC-1	luminal epithelium:	n/a
49	chr11:67183546-67183596	GM12891	blood:	n/a
50	chr11:67183080-67183130	Caco-2	colon:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:67054592..67057284-chr11:67183944..67185616,2	MCF-7	breast:
2	chr11:67180570..67183103-chr11:67271029..67272927,2	K562	blood:
3	chr11:67182567..67190511-chr11:67270739..67276166,13	MCF-7	breast:
4	chr11:67181921..67184734-chr11:67234626..67236825,2	K562	blood:
5	chr11:67184311..67187046-chr11:67307232..67309565,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CARNS1-2	chr11:67182839-67182957	NONHSAT022419
2	lnc-CARNS1-2	chr11:67182439-67182687	NONHSAT022419

No data

Variant related genes	Relation type
CARNS1	TF binding region
CARNS1	CpG island
ENSG00000110697	chromatin interactions
ENSG00000172663	chromatin interactions
ENSG00000167797	chromatin interactions
ENSG00000244152	chromatin interactions
ENSG00000172932	chromatin interactions

Extended variants
information (count: 73 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:73 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183450398	chr11:67182340-67182341	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs529593606	chr11:67182361-67182362	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs61891594	chr11:67182367-67182368	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs1115052	chr11:67182371-67182372	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs1115051	chr11:67182383-67182384	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs533787805	chr11:67182401-67182402	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs558343080	chr11:67182454-67182455	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
8	rs570577543	chr11:67182474-67182475	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
9	rs538024496	chr11:67182488-67182489	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
10	rs556442891	chr11:67182527-67182528	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
11	rs56389755	chr11:67182581-67182582	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs535347047	chr11:67182611-67182612	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
13	rs186547584	chr11:67182672-67182673	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
14	rs572319986	chr11:67182714-67182715	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs546191883	chr11:67182725-67182726	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs564405283	chr11:67182758-67182759	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs367923335	chr11:67182814-67182815	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs576160017	chr11:67182844-67182845	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
19	rs543608003	chr11:67182858-67182859	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
20	rs561988175	chr11:67182896-67182897	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
21	rs373099699	chr11:67182910-67182911	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
22	rs529457776	chr11:67182911-67182912	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
23	rs547727269	chr11:67182912-67182913	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
24	rs560017062	chr11:67182915-67182916	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
25	rs527259362	chr11:67182921-67182922	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
26	rs552186361	chr11:67182957-67182958	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
27	rs570558824	chr11:67183014-67183015	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs537978327	chr11:67183025-67183026	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs372062759	chr11:67183052-67183053	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs549910782	chr11:67183090-67183091	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs568214379	chr11:67183115-67183116	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs535658233	chr11:67183165-67183166	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs35899279	chr11:67183193-67183194	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs34690275	chr11:67183196-67183197	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs34637876	chr11:67183259-67183260	Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs572336990	chr11:67183298-67183299	Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs368225452	chr11:67183330-67183331	Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs183628051	chr11:67183343-67183344	Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs188622906	chr11:67183384-67183385	Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs543473150	chr11:67183390-67183391	Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs561852079	chr11:67183463-67183464	Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs573298040	chr11:67183466-67183467	Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs34596169	chr11:67183492-67183493	Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs559781971	chr11:67183507-67183508	Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs533710074	chr11:67183544-67183545	Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs551874960	chr11:67183559-67183560	Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs529696284	chr11:67183588-67183589	Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs531335277	chr11:67183698-67183699	Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs376009203	chr11:67183700-67183701	Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs75477179	chr11:67183742-67183743	Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	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
Acute myeloid leukemia	21251322	CNVD
Lung cancer	19153074	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	22860045	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	21399695	CNVD
Ovarian clear cell carcinoma	19293255	CNVD

Chromatin state (count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67170000-67182800	Weak transcription	Right Atrium	heart
2	chr11:67176400-67182400	Enhancers	Primary hematopoietic stem cells	blood
3	chr11:67177800-67182400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
4	chr11:67177800-67182600	Enhancers	Primary T helper cells PMA-I stimulated	--
5	chr11:67177800-67182600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr11:67177800-67183400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr11:67178000-67182400	Enhancers	Primary B cells from peripheral blood	blood
8	chr11:67178000-67182400	Enhancers	Primary T cells fromperipheralblood	blood
9	chr11:67178000-67182400	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr11:67178000-67182600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
11	chr11:67178200-67182400	Weak transcription	Lung	lung
12	chr11:67178400-67182400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
13	chr11:67178400-67182400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
14	chr11:67178400-67182600	Enhancers	Primary B cells from cord blood	blood
15	chr11:67178400-67182600	Enhancers	Primary T killer memory cells from peripheral blood	blood
16	chr11:67178400-67184200	Enhancers	Primary T helper naive cells from peripheral blood	blood
17	chr11:67178600-67182400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr11:67178600-67182600	Enhancers	Primary T helper cells fromperipheralblood	blood
19	chr11:67178800-67182600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr11:67179000-67182400	Enhancers	Fetal Thymus	thymus
21	chr11:67179400-67182400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
22	chr11:67180200-67182400	Weak transcription	Esophagus	oesophagus
23	chr11:67180200-67182600	Weak transcription	Hela-S3	cervix
24	chr11:67180200-67182600	Weak transcription	HMEC	breast
25	chr11:67180400-67182600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr11:67180600-67182400	Weak transcription	Pancreas	Pancrea
27	chr11:67180800-67182600	Weak transcription	Spleen	Spleen
28	chr11:67181000-67182400	Weak transcription	Gastric	stomach
29	chr11:67181200-67182400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr11:67181200-67182600	Weak transcription	Dnd41	blood
31	chr11:67181200-67183400	Weak transcription	HSMMtube	muscle
32	chr11:67181400-67182400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr11:67182000-67182400	Enhancers	Stomach Mucosa	stomach
34	chr11:67182000-67182400	Enhancers	Thymus	Thymus
35	chr11:67182200-67182400	Enhancers	Primary T cells from cord blood	blood
36	chr11:67182200-67182400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr11:67182200-67182400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr11:67182200-67182400	Active TSS	Brain Anterior Caudate	brain
39	chr11:67182200-67182600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
40	chr11:67182200-67182600	Flanking Active TSS	Brain Hippocampus Middle	brain
41	chr11:67182200-67182600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
42	chr11:67182200-67183600	Active TSS	Brain Angular Gyrus	brain
43	chr11:67182200-67183600	Active TSS	Brain Inferior Temporal Lobe	brain
44	chr11:67182200-67183600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
45	chr11:67182200-67183800	Active TSS	Brain Cingulate Gyrus	brain
46	chr11:67182200-67183800	Active TSS	Brain Substantia Nigra	brain
47	chr11:67182400-67182600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
48	chr11:67182400-67182600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
49	chr11:67182400-67182600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
50	chr11:67182400-67182600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell

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