Variant report

Variant	nsv825952
Chromosome Location	chr11:65776517-65779832
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:70)
CpG islands
(count:672)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:70 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr11:65779620-65779770	SAEC	small airway:	n/a	n/a
2	CTCF	chr11:65779560-65779710	NHEK	skin:	n/a	n/a
3	E2F6	chr11:65778947-65779943	H1-hESC	embryonic stem cell:	n/a	chr11:65779761-65779770 chr11:65779329-65779338
4	E2F6	chr11:65779278-65779825	H1-hESC	embryonic stem cell:	n/a	chr11:65779761-65779770 chr11:65779329-65779338
5	EGR1	chr11:65779235-65779507	K562	blood:	n/a	chr11:65779333-65779346 chr11:65779333-65779343 chr11:65779407-65779420 chr11:65779333-65779346
6	EP300	chr11:65778483-65779710	ECC-1	luminal epithelium:	n/a	chr11:65779397-65779413 chr11:65779332-65779341
7	EP300	chr11:65778734-65779597	ECC-1	luminal epithelium:	n/a	chr11:65779397-65779413 chr11:65779332-65779341
8	ESR1	chr11:65776269-65776658	ECC-1	luminal epithelium:	n/a	n/a
9	ESR1	chr11:65776265-65776603	ECC-1	luminal epithelium:	n/a	n/a
10	ESR1	chr11:65778711-65779528	ECC-1	luminal epithelium:	n/a	n/a
11	ESR1	chr11:65778649-65779542	ECC-1	luminal epithelium:	n/a	n/a
12	ESR1	chr11:65779214-65779513	ECC-1	luminal epithelium:	n/a	n/a
13	ESR1	chr11:65778602-65779173	ECC-1	luminal epithelium:	n/a	n/a
14	ESR1	chr11:65778802-65779083	ECC-1	luminal epithelium:	n/a	n/a
15	ESR1	chr11:65778719-65779063	ECC-1	luminal epithelium:	n/a	n/a
16	FOS	chr11:65778739-65779127	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr11:65778794-65779110	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr11:65778717-65779105	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr11:65778705-65779156	MCF10A-Er-Src	breast:	n/a	n/a
20	FOXM1	chr11:65778682-65779494	ECC-1	luminal epithelium:	n/a	n/a
21	GABPA	chr11:65779261-65779865	H1-hESC	embryonic stem cell:	n/a	chr11:65779761-65779770
22	JUND	chr11:65778990-65778992	HepG2	liver:	n/a	n/a
23	JUND	chr11:65778843-65779252	H1-hESC	embryonic stem cell:	n/a	chr11:65778953-65778964
24	MAX	chr11:65779049-65779958	H1-hESC	embryonic stem cell:	n/a	n/a
25	MAX	chr11:65778569-65780136	HCT-116	colon:	n/a	n/a
26	MAX	chr11:65778662-65780019	HCT-116	colon:	n/a	n/a
27	MAX	chr11:65778669-65779820	ECC-1	luminal epithelium:	n/a	n/a
28	MAX	chr11:65779068-65779926	H1-hESC	embryonic stem cell:	n/a	n/a
29	MAX	chr11:65778683-65779779	ECC-1	luminal epithelium:	n/a	n/a
30	MAX	chr11:65779462-65779775	H1-hESC	embryonic stem cell:	n/a	n/a
31	MXI1	chr11:65779479-65779692	H1-hESC	embryonic stem cell:	n/a	n/a
32	MYC	chr11:65779478-65779724	H1-hESC	embryonic stem cell:	n/a	n/a
33	MYC	chr11:65778743-65779091	MCF10A-Er-Src	breast:	n/a	n/a
34	MYC	chr11:65778748-65779056	MCF10A-Er-Src	breast:	n/a	n/a
35	NFIC	chr11:65778568-65779546	ECC-1	luminal epithelium:	n/a	n/a
36	NFIC	chr11:65778666-65779714	ECC-1	luminal epithelium:	n/a	n/a
37	POLR2A	chr11:65778731-65779305	HCT-116	colon:	n/a	n/a
38	POLR2A	chr11:65776379-65776563	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr11:65775806-65776703	Hela-S3	cervix:	n/a	n/a
40	POLR2A	chr11:65778719-65779876	HCT-116	colon:	n/a	n/a
41	POLR2A	chr11:65779709-65779744	H1-hESC	embryonic stem cell:	n/a	n/a
42	POLR2A	chr11:65779449-65779872	HCT-116	colon:	n/a	n/a
43	POLR2A	chr11:65772803-65776533	Hela-S3	cervix:	n/a	n/a
44	POLR2A	chr11:65778721-65779273	ECC-1	luminal epithelium:	n/a	n/a
45	RAD21	chr11:65778720-65779253	ECC-1	luminal epithelium:	n/a	n/a
46	SIN3A	chr11:65779508-65779743	H1-hESC	embryonic stem cell:	n/a	n/a
47	SRF	chr11:65778671-65779183	ECC-1	luminal epithelium:	n/a	n/a
48	STAT3	chr11:65778741-65779123	MCF10A-Er-Src	breast:	n/a	n/a
49	STAT3	chr11:65778749-65779123	MCF10A-Er-Src	breast:	n/a	n/a
50	STAT3	chr11:65778911-65779097	MCF10A-Er-Src	breast:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:65779330-65779380	HCM	heart:	n/a
2	chr11:65779330-65779380	HCM	heart:	n/a
3	chr11:65779343-65779393	AG09319	gingival:	n/a
4	chr11:65779332-65779382	SKMC	muscle:	n/a
5	chr11:65779343-65779393	AG09309	skin:	n/a
6	chr11:65779330-65779380	HCPEpiC	choroid plexus:	n/a
7	chr11:65779192-65779242	RPTEC	kidney:	n/a
8	chr11:65778210-65778260	AG10803	skin:	n/a
9	chr11:65778967-65779017	NT2-D1	testis:	n/a
10	chr11:65779667-65779717	ECC-1	luminal epithelium:	n/a
11	chr11:65779335-65779385	AG10803	skin:	n/a
12	chr11:65779332-65779382	K562	blood:	n/a
13	chr11:65779263-65779313	NH-A	brain:	n/a
14	chr11:65778967-65779017	HUVEC	blood vessel:	n/a
15	chr11:65779192-65779242	HRE	kidney:	n/a
16	chr11:65779263-65779313	H1-hESC	embryonic stem cell:	embryo
17	chr11:65779335-65779385	HEK293	kidney:	embryo
18	chr11:65779676-65779726	PrEC	prostate:	n/a
19	chr11:65779332-65779382	PFSK-1	brain:	n/a
20	chr11:65779332-65779382	HIPEpiC	eye:	n/a
21	chr11:65779332-65779382	AoSMC	blood vessel:	n/a
22	chr11:65779330-65779380	NT2-D1	testis:	n/a
23	chr11:65778967-65779017	GM12892	blood:	n/a
24	chr11:65779330-65779380	AG04449	skin:	fetal
25	chr11:65779263-65779313	AG09309	skin:	n/a
26	chr11:65779526-65779576	HCT-116	colon:	n/a
27	chr11:65779192-65779242	H1-hESC	embryonic stem cell:	embryo
28	chr11:65779676-65779726	HCF	heart:	n/a
29	chr11:65779676-65779726	T-47D	breast:	n/a
30	chr11:65779667-65779717	GM06990	blood:	n/a
31	chr11:65779676-65779726	Hepatocyte	liver:	n/a
32	chr11:65779330-65779380	PFSK-1	brain:	n/a
33	chr11:65779263-65779313	AG10803	skin:	n/a
34	chr11:65779343-65779393	HMEC	breast:	n/a
35	chr11:65779335-65779385	Hepatocyte	liver:	n/a
36	chr11:65779343-65779393	IMR90	lung:	fetal
37	chr11:65779667-65779717	HRPEpiC	eye:	n/a
38	chr11:65779332-65779382	AG10803	skin:	n/a
39	chr11:65779676-65779726	NHBE	bronchial:	n/a
40	chr11:65779263-65779313	IMR90	lung:	fetal
41	chr11:65779676-65779726	CMK	blood:	n/a
42	chr11:65779330-65779380	HCT-116	colon:	n/a
43	chr11:65778967-65779017	GM06990	blood:	n/a
44	chr11:65778967-65779017	HEEpiC	esophagus:	n/a
45	chr11:65778210-65778260	HL-60	blood:	n/a
46	chr11:65779526-65779576	HRCEpiC	kidney:	n/a
47	chr11:65779263-65779313	AG04449	skin:	fetal
48	chr11:65779667-65779717	K562	blood:	n/a
49	chr11:65778967-65779017	K562	blood:	n/a
50	chr11:65778210-65778260	HRCEpiC	kidney:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:65650838..65654244-chr11:65778689..65782514,4	MCF-7	breast:
2	chr11:65779081..65782393-chr11:65836476..65839425,3	MCF-7	breast:
3	chr11:65764589..65766874-chr11:65774811..65776588,2	K562	blood:
4	chr11:65775918..65778029-chr11:65787513..65790456,2	MCF-7	breast:
5	chr11:65188418..65191702-chr11:65777424..65780862,3	MCF-7	breast:
6	chr11:65728544..65730713-chr11:65775327..65777524,2	K562	blood:
7	chr11:65774068..65777028-chr11:65792820..65794659,2	MCF-7	breast:
8	chr11:65776357..65777958-chr11:65817705..65819655,2	K562	blood:
9	chr11:65725324..65726831-chr11:65776264..65777958,2	MCF-7	breast:
10	chr11:65624293..65627593-chr11:65778197..65781174,3	MCF-7	breast:
11	chr11:65727748..65729468-chr11:65777688..65780268,2	MCF-7	breast:
12	chr11:65655400..65657605-chr11:65778805..65780715,2	MCF-7	breast:
13	chr11:65775333..65777143-chr11:65814393..65815931,2	K562	blood:
14	chr11:65624802..65627661-chr11:65779805..65782359,2	MCF-7	breast:
15	chr11:65778738..65782540-chr11:65791690..65794306,3	MCF-7	breast:
16	chr11:65778958..65780961-chr11:65818944..65820828,4	MCF-7	breast:
17	chr11:65684023..65687163-chr11:65778751..65782457,4	MCF-7	breast:
18	chr11:65727829..65730713-chr11:65776024..65777968,2	K562	blood:
19	chr11:65682118..65684018-chr11:65775122..65778045,2	MCF-7	breast:
20	chr11:65769812..65778104-chr11:65786537..65794453,15	K562	blood:

No data

Variant related genes	Relation type
CST6	TF binding region
CST6	CpG island
ENSG00000175550	chromatin interactions
ENSG00000175115	chromatin interactions
ENSG00000175467	chromatin interactions
ENSG00000087365	chromatin interactions
ENSG00000238752	chromatin interactions
ENSG00000175294	chromatin interactions
ENSG00000172732	chromatin interactions
ENSG00000175573	chromatin interactions
ENSG00000245532	chromatin interactions
ENSG00000255038	chromatin interactions
ENSG00000172500	chromatin interactions
ENSG00000172757	chromatin interactions

Extended variants
information (count: 112 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:112 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559903054	chr11:65776540-65776541	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs655744	chr11:65776585-65776586	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs549121363	chr11:65776599-65776600	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs140102334	chr11:65776657-65776658	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs115145684	chr11:65776658-65776659	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs528203420	chr11:65776707-65776708	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs551076013	chr11:65776719-65776720	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs534201	chr11:65776728-65776729	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs113820242	chr11:65776814-65776815	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs537918008	chr11:65776889-65776890	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs369291042	chr11:65776891-65776892	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs200943545	chr11:65776898-65776899	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs539731686	chr11:65776900-65776901	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs185793104	chr11:65776948-65776949	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs374544554	chr11:65777009-65777010	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs566551355	chr11:65777076-65777077	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs535426209	chr11:65777093-65777094	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs555477341	chr11:65777110-65777111	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs575313935	chr11:65777111-65777112	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs530529878	chr11:65777165-65777166	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs537695573	chr11:65777172-65777173	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs557659702	chr11:65777202-65777203	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs191045507	chr11:65777224-65777225	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs142612371	chr11:65777256-65777257	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs560367017	chr11:65777257-65777258	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs35911045	chr11:65777310-65777311	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs573693227	chr11:65777315-65777316	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs398097589	chr11:65777319-65777320	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs183744606	chr11:65777350-65777351	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs1624999	chr11:65777377-65777378	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs373562981	chr11:65777393-65777394	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs551194556	chr11:65777398-65777399	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs616073	chr11:65777460-65777461	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs34903372	chr11:65777487-65777488	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs533544788	chr11:65777493-65777494	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs546996314	chr11:65777538-65777539	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs187460338	chr11:65777539-65777540	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs615646	chr11:65777544-65777545	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs548964469	chr11:65777617-65777618	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs538828686	chr11:65777647-65777648	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs7113661	chr11:65777665-65777666	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs537963061	chr11:65777745-65777746	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs190570159	chr11:65777746-65777747	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs79077546	chr11:65777754-65777755	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs569444146	chr11:65777764-65777765	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs187133487	chr11:65777782-65777783	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs573960679	chr11:65777784-65777785	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs542689936	chr11:65777788-65777789	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs538482261	chr11:65777792-65777793	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs576096904	chr11:65777809-65777810	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Pituitary adenoma	18645599	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
ovarian endometriomas	16273235	CNVD
Breast cancer	16417655	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	17217626	CNVD
T-cell acute lymphoblastic leukemia	19406988	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
Anaplastic thyroid cancer	18753363	CNVD
Prostate cancer	18779856	CNVD
Cancer	17160897	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	22522925	CNVD

Chromatin state (count:276 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65771000-65779000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr11:65771000-65779000	Weak transcription	Aorta	Aorta
3	chr11:65771200-65779000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr11:65771200-65779200	Weak transcription	Right Atrium	heart
5	chr11:65772000-65776600	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr11:65772200-65778800	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr11:65772200-65779200	Weak transcription	Gastric	stomach
8	chr11:65772200-65779400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr11:65772200-65779400	Weak transcription	Psoas Muscle	Psoas
10	chr11:65772400-65778200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr11:65772600-65777200	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr11:65772600-65778400	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr11:65772800-65779200	Weak transcription	Right Ventricle	heart
14	chr11:65773000-65776800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr11:65773200-65776600	Weak transcription	Left Ventricle	heart
16	chr11:65773200-65776800	Weak transcription	NHDF-Ad	bronchial
17	chr11:65773200-65778000	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr11:65773200-65778200	Weak transcription	NH-A	brain
19	chr11:65773200-65779000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr11:65773200-65779200	Weak transcription	Colon Smooth Muscle	Colon
21	chr11:65773400-65777600	Weak transcription	Duodenum Mucosa	Duodenum
22	chr11:65773400-65778800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr11:65773400-65779000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr11:65773400-65779000	Weak transcription	Brain Hippocampus Middle	brain
25	chr11:65773400-65779000	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr11:65773400-65779000	Weak transcription	Rectal Smooth Muscle	rectum
27	chr11:65773400-65779400	Weak transcription	Ovary	ovary
28	chr11:65773400-65780200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr11:65773600-65776600	Weak transcription	Fetal Kidney	kidney
30	chr11:65773600-65777000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr11:65773600-65777000	Weak transcription	Liver	Liver
32	chr11:65773600-65778600	Weak transcription	Brain Anterior Caudate	brain
33	chr11:65773600-65778800	Weak transcription	Primary B cells from peripheral blood	blood
34	chr11:65773600-65778800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
35	chr11:65773600-65778800	Weak transcription	Osteobl	bone
36	chr11:65773600-65779200	Weak transcription	Brain Cingulate Gyrus	brain
37	chr11:65773800-65777800	Weak transcription	Primary T helper cells PMA-I stimulated	--
38	chr11:65773800-65778800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr11:65773800-65779000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr11:65774000-65777000	Weak transcription	Primary hematopoietic stem cells	blood
41	chr11:65774000-65777200	Weak transcription	Primary B cells from cord blood	blood
42	chr11:65774000-65777400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr11:65774000-65777400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
44	chr11:65774000-65778000	Weak transcription	Fetal Lung	lung
45	chr11:65774000-65779000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr11:65774000-65779200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
47	chr11:65774200-65777200	Weak transcription	Adipose Nuclei	Adipose
48	chr11:65774200-65777400	Weak transcription	Brain Germinal Matrix	brain
49	chr11:65774200-65778000	Weak transcription	Primary T cells from cord blood	blood
50	chr11:65774200-65778200	Weak transcription	Pancreas	Pancrea

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