Variant report

Variant	nsv521451
Chromosome Location	chr11:76053527-76087844
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:276)
CpG islands
(count:61)
Chromatin interactive
region (count:36)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:76082249-76082675	K562	blood:	n/a	n/a
2	ATF1	chr11:76082276-76082583	K562	blood:	n/a	n/a
3	ATF2	chr11:76087662-76088332	GM12878	blood:	n/a	n/a
4	ATF2	chr11:76082183-76082653	GM12878	blood:	n/a	n/a
5	ATF2	chr11:76082106-76082638	GM12878	blood:	n/a	n/a
6	ATF2	chr11:76087666-76088315	GM12878	blood:	n/a	n/a
7	BATF	chr11:76082219-76082568	GM12878	blood:	n/a	chr11:76082403-76082414
8	BATF	chr11:76082227-76082561	GM12878	blood:	n/a	chr11:76082403-76082414
9	BATF	chr11:76087646-76088280	GM12878	blood:	n/a	n/a
10	BATF	chr11:76087720-76088052	GM12878	blood:	n/a	n/a
11	BCL11A	chr11:76087765-76088024	GM12878	blood:	n/a	chr11:76087931-76087940
12	BCL11A	chr11:76087730-76088105	GM12878	blood:	n/a	chr11:76087931-76087940
13	BCL3	chr11:76082183-76082622	GM12878	blood:	n/a	n/a
14	BCL3	chr11:76087716-76088064	GM12878	blood:	n/a	chr11:76087931-76087940
15	BCL3	chr11:76087768-76087958	GM12878	blood:	n/a	chr11:76087931-76087940
16	BCLAF1	chr11:76087716-76088203	GM12878	blood:	n/a	chr11:76087931-76087940
17	BHLHE40	chr11:76076174-76076282	K562	blood:	n/a	n/a
18	CCNT2	chr11:76076267-76076412	K562	blood:	n/a	n/a
19	CEBPB	chr11:76077573-76077776	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr11:76086327-76086403	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr11:76077565-76077823	K562	blood:	n/a	n/a
22	CEBPB	chr11:76086992-76087349	K562	blood:	n/a	chr11:76087178-76087189
23	CEBPB	chr11:76087143-76087313	H1-hESC	embryonic stem cell:	n/a	chr11:76087178-76087189
24	CEBPB	chr11:76087007-76087345	IMR90	lung:	n/a	chr11:76087178-76087189
25	CEBPB	chr11:76086998-76087316	HepG2	liver:	n/a	chr11:76087178-76087189
26	CEBPB	chr11:76087022-76087303	A549	lung:	n/a	chr11:76087178-76087189
27	CEBPB	chr11:76086994-76087321	Hela-S3	cervix:	n/a	chr11:76087178-76087189
28	CEBPB	chr11:76086198-76086535	MCF-7	breast:	n/a	chr11:76086395-76086412
29	CEBPD	chr11:76076039-76076471	K562	blood:	n/a	n/a
30	CEBPD	chr11:76075983-76076497	K562	blood:	n/a	n/a
31	CTCF	chr11:76058720-76058870	HMEC	breast:	n/a	n/a
32	CTCF	chr11:76058540-76058690	BE2_C	brain:	n/a	n/a
33	CTCF	chr11:76058460-76058610	RPTEC	kidney:	n/a	n/a
34	CTCF	chr11:76058800-76058950	RPTEC	kidney:	n/a	n/a
35	CTCF	chr11:76074674-76074789	GM10248	blood:	n/a	n/a
36	CTCF	chr11:76058568-76058650	K562	blood:	n/a	n/a
37	CTCF	chr11:76058540-76058690	MCF-7	breast:	n/a	n/a
38	CTCF	chr11:76058396-76058801	MCF-7	breast:	n/a	n/a
39	CTCF	chr11:76058559-76058670	Medullo	brain:	n/a	n/a
40	CTCF	chr11:76061868-76061944	Lung_OC	lung:	n/a	n/a
41	CTCF	chr11:76086300-76086450	NHEK	skin:	n/a	chr11:76086329-76086350
42	CTCF	chr11:76086315-76086422	MCF-7	breast:	n/a	chr11:76086329-76086350
43	CTCF	chr11:76058520-76058670	HEEpiC	esophagus:	n/a	n/a
44	CTCF	chr11:76058560-76058710	HAc	cerebellar:	n/a	n/a
45	CTCF	chr11:76058560-76058710	GM12872	blood:	n/a	n/a
46	CTCF	chr11:76063223-76063294	GM13977	blood:	n/a	n/a
47	CTCF	chr11:76058440-76058590	HMEC	breast:	n/a	n/a
48	CTCF	chr11:76054541-76054597	GM10248	blood:	n/a	n/a
49	CTCF	chr11:76086320-76086470	HEEpiC	esophagus:	n/a	chr11:76086329-76086350
50	CTCF	chr11:76058520-76058670	AG10803	skin:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:76061438-76061488	NHBE	bronchial:	n/a
2	chr11:76061438-76061488	NT2-D1	testis:	n/a
3	chr11:76061438-76061488	NB4	blood:	n/a
4	chr11:76061438-76061488	NH-A	brain:	n/a
5	chr11:76061438-76061488	SK-N-MC	brain:	n/a
6	chr11:76061438-76061488	LNCaP	prostate:	n/a
7	chr11:76061438-76061488	ovcar-3	ovarian:	n/a
8	chr11:76061438-76061488	PrEC	prostate:	n/a
9	chr11:76061438-76061488	AoSMC	blood vessel:	n/a
10	chr11:76061438-76061488	BJ	skin:	n/a
11	chr11:76061438-76061488	A549	lung:	n/a
12	chr11:76061438-76061488	K562	blood:	n/a
13	chr11:76061438-76061488	HEEpiC	esophagus:	n/a
14	chr11:76061438-76061488	AG09309	skin:	n/a
15	chr11:76061438-76061488	GM12891	blood:	n/a
16	chr11:76061438-76061488	Caco-2	colon:	n/a
17	chr11:76061438-76061488	HPAEpiC	pulmonary alveolar:	n/a
18	chr11:76061438-76061488	SK-N-SH	brain:	n/a
19	chr11:76061438-76061488	GM12892	blood:	n/a
20	chr11:76061438-76061488	U87	brain:	n/a
21	chr11:76061438-76061488	HCM	heart:	n/a
22	chr11:76061438-76061488	HCT-116	colon:	n/a
23	chr11:76061438-76061488	HRPEpiC	eye:	n/a
24	chr11:76061438-76061488	PANC-1	pancreas:	n/a
25	chr11:76061438-76061488	GM19239	blood:	n/a
26	chr11:76061438-76061488	AG10803	skin:	n/a
27	chr11:76061438-76061488	GM12878	blood:	n/a
28	chr11:76061438-76061488	CMK	blood:	n/a
29	chr11:76061438-76061488	BE2_C	brain:	n/a
30	chr11:76061438-76061488	HAEpiC	amniotic membrane:	n/a
31	chr11:76061438-76061488	ProgFib	skin:	n/a
32	chr11:76061438-76061488	MCF10A-Er-Src	breast:	n/a
33	chr11:76061438-76061488	AG09319	gingival:	n/a
34	chr11:76061438-76061488	AG04450	lung:	fetal
35	chr11:76061438-76061488	HRCEpiC	kidney:	n/a
36	chr11:76061438-76061488	HEK293	kidney:	embryo
37	chr11:76061438-76061488	Jurkat	blood:	n/a
38	chr11:76061438-76061488	RPTEC	kidney:	n/a
39	chr11:76061438-76061488	SKMC	muscle:	n/a
40	chr11:76061438-76061488	PFSK-1	brain:	n/a
41	chr11:76061438-76061488	HNPCEpiC	eye:	n/a
42	chr11:76061438-76061488	HUVEC	blood vessel:	n/a
43	chr11:76061438-76061488	T-47D	breast:	n/a
44	chr11:76061438-76061488	ECC-1	luminal epithelium:	n/a
45	chr11:76061438-76061488	HCPEpiC	choroid plexus:	n/a
46	chr11:76061438-76061488	HIPEpiC	eye:	n/a
47	chr11:76061438-76061488	IMR90	lung:	fetal
48	chr11:76061438-76061488	HRE	kidney:	n/a
49	chr11:76061438-76061488	HL-60	blood:	n/a
50	chr11:76061438-76061488	GM06990	blood:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:76067003..76068670-chr11:76071732..76073278,2	K562	blood:
2	chr11:76075524..76077894-chr11:76154235..76156946,2	MCF-7	breast:
3	chr11:76055513..76058854-chr11:76089772..76093547,5	MCF-7	breast:
4	chr11:76063211..76065578-chr11:76066978..76069387,2	K562	blood:
5	chr11:76082898..76084920-chr11:76155032..76156868,3	MCF-7	breast:
6	chr11:76051537..76054007-chr11:76054724..76057312,2	K562	blood:
7	chr11:76070486..76072111-chr11:76154139..76156807,2	MCF-7	breast:
8	chr11:76072573..76074969-chr11:76078510..76081231,2	K562	blood:
9	chr11:76071533..76073218-chr11:76090981..76092790,2	K562	blood:
10	chr11:76073015..76075782-chr11:76080642..76082701,2	MCF-7	breast:
11	chr11:76077209..76079970-chr11:76081805..76083752,2	MCF-7	breast:
12	chr11:76074979..76076498-chr11:76155898..76158207,2	K562	blood:
13	chr11:76054270..76056421-chr11:76059241..76061034,2	MCF-7	breast:
14	chr11:76051537..76053648-chr11:76054724..76056266,2	K562	blood:
15	chr11:76069995..76071951-chr11:76081817..76083551,2	K562	blood:
16	chr11:76054270..76056421-chr11:76059241..76061034,2	MCF-7	breast:
17	chr11:76064413..76068190-chr11:76071048..76073540,4	MCF-7	breast:
18	chr11:76063904..76066072-chr11:76155439..76156956,2	MCF-7	breast:
19	chr11:76054481..76057332-chr11:76090389..76092075,2	MCF-7	breast:
20	chr11:76079303..76082514-chr11:76090617..76092781,5	K562	blood:
21	chr11:76063211..76065578-chr11:76066978..76069387,2	K562	blood:
22	chr11:76079440..76082067-chr11:76086701..76088711,2	MCF-7	breast:
23	chr11:76051537..76054007-chr11:76054724..76057312,2	K562	blood:
24	chr11:76080958..76083908-chr11:76090335..76092803,5	MCF-7	breast:
25	chr11:76081076..76084141-chr11:76087124..76089011,3	K562	blood:
26	chr11:76086256..76087973-chr11:76154460..76156663,2	MCF-7	breast:
27	chr11:76063211..76065578-chr11:76066828..76069387,3	K562	blood:
28	chr11:76083976..76087668-chr11:76154688..76156969,3	K562	blood:
29	chr11:76066083..76068514-chr11:76079264..76081458,2	K562	blood:
30	chr11:76063211..76065578-chr11:76066828..76069387,3	K562	blood:
31	chr11:76074770..76077133-chr11:76087640..76089591,2	K562	blood:
32	chr11:76051537..76053648-chr11:76054724..76056266,2	K562	blood:
33	chr11:76087147..76089667-chr11:76096180..76097746,2	MCF-7	breast:
34	chr11:76074770..76077133-chr11:76087640..76089591,2	K562	blood:
35	chr11:76081076..76084141-chr11:76087124..76089011,3	K562	blood:
36	chr11:76073015..76075782-chr11:76080642..76082701,2	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PRKRIR	hsa-miR-34a-5p	chr11:76061153-76061174

Variant related genes	Relation type
ENSG00000179240	TF binding region
PRKRIR	TF binding region
ENSG00000179240	CpG island
PRKRIR	CpG island
ENSG00000158636	chromatin interactions
ENSG00000137492	chromatin interactions
ENSG00000255135	chromatin interactions
ENSG00000179240	chromatin interactions

Extended variants
information (count: 1348 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:1348 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11236720	chr11:76053527-76053528	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs554334142	chr11:76053547-76053548	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs530921320	chr11:76053554-76053555	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs547536329	chr11:76053558-76053559	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs564522172	chr11:76053618-76053619	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs374554161	chr11:76053619-76053620	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs549743128	chr11:76053620-76053621	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs115255886	chr11:76053656-76053657	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs537745324	chr11:76053692-76053693	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs34153441	chr11:76053696-76053697	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs547983144	chr11:76053706-76053707	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs568121873	chr11:76053720-76053721	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs367548775	chr11:76053721-76053722	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs533901010	chr11:76053792-76053793	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs552294314	chr11:76053803-76053804	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs114212325	chr11:76053836-76053837	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs184995885	chr11:76053846-76053847	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs576847778	chr11:76053850-76053851	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs187436214	chr11:76053870-76053871	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs556188282	chr11:76053896-76053897	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs576858515	chr11:76053917-76053918	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs375563525	chr11:76053939-76053940	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs562278804	chr11:76053974-76053975	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs371466708	chr11:76053995-76053996	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs201101736	chr11:76053997-76053998	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs201276802	chr11:76053998-76053999	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs10666121	chr11:76054009-76054010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs56198824	chr11:76054012-76054013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs373344479	chr11:76054013-76054014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs376461349	chr11:76054014-76054015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs572513826	chr11:76054021-76054022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs12270671	chr11:76054043-76054044	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs564451585	chr11:76054060-76054061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs34794249	chr11:76054061-76054062	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs549809083	chr11:76054086-76054087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs563295362	chr11:76054119-76054120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs192288644	chr11:76054134-76054135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs548045870	chr11:76054155-76054156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs568266461	chr11:76054184-76054185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs2851475	chr11:76054257-76054258	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs547550986	chr11:76054289-76054290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs570491979	chr11:76054314-76054315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs369338608	chr11:76054324-76054325	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs112511631	chr11:76054327-76054328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs114405339	chr11:76054331-76054332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs576068658	chr11:76054345-76054346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs536174221	chr11:76054412-76054413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs369820851	chr11:76054544-76054545	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs555757863	chr11:76054565-76054566	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs11236721	chr11:76054568-76054569	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

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
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
Melanoma	18172304	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
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21482786	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	16608533	CNVD
Usher syndrome	18421352	CNVD
Breast cancer	21858162	CNVD
Ovarian cancer	21240255	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1130 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:76046600-76054600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:76048000-76060000	Weak transcription	Spleen	Spleen
3	chr11:76048000-76061400	Weak transcription	Primary B cells from peripheral blood	blood
4	chr11:76048000-76064800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr11:76048200-76064000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr11:76048400-76061800	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr11:76048600-76059800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr11:76050000-76064600	Weak transcription	Rectal Smooth Muscle	rectum
9	chr11:76050400-76060000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr11:76050400-76060000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr11:76050400-76060400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr11:76050400-76060400	Weak transcription	Stomach Smooth Muscle	stomach
13	chr11:76050400-76064000	Weak transcription	Fetal Stomach	stomach
14	chr11:76050400-76064200	Weak transcription	Left Ventricle	heart
15	chr11:76050400-76064200	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr11:76050400-76064200	Weak transcription	Thymus	Thymus
17	chr11:76050400-76064200	Weak transcription	NHLF	lung
18	chr11:76050400-76065000	Weak transcription	Colonic Mucosa	Colon
19	chr11:76050600-76054400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr11:76050600-76059600	Weak transcription	Primary B cells from cord blood	blood
21	chr11:76050600-76060000	Weak transcription	Placenta	Placenta
22	chr11:76050600-76064200	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr11:76050600-76064600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr11:76050800-76059000	Weak transcription	Liver	Liver
25	chr11:76050800-76059800	Weak transcription	Primary neutrophils fromperipheralblood	blood
26	chr11:76050800-76063800	Weak transcription	Primary T helper cells PMA-I stimulated	--
27	chr11:76050800-76063800	Weak transcription	Osteobl	bone
28	chr11:76050800-76064200	Weak transcription	Primary hematopoietic stem cells	blood
29	chr11:76051000-76060000	Weak transcription	Fetal Thymus	thymus
30	chr11:76051000-76063800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr11:76051000-76064200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
32	chr11:76051000-76064400	Weak transcription	Aorta	Aorta
33	chr11:76051200-76056200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr11:76051200-76056800	Weak transcription	Lung	lung
35	chr11:76051200-76059800	Weak transcription	Primary T cells fromperipheralblood	blood
36	chr11:76051200-76059800	Weak transcription	Fetal Muscle Trunk	muscle
37	chr11:76051200-76061600	Weak transcription	Duodenum Mucosa	Duodenum
38	chr11:76051200-76065000	Weak transcription	Gastric	stomach
39	chr11:76051200-76065200	Weak transcription	Right Ventricle	heart
40	chr11:76051200-76066200	Weak transcription	NHDF-Ad	bronchial
41	chr11:76051400-76056800	Weak transcription	Fetal Muscle Leg	muscle
42	chr11:76051400-76059400	Weak transcription	Primary monocytes fromperipheralblood	blood
43	chr11:76051400-76059400	Weak transcription	Adipose Nuclei	Adipose
44	chr11:76051400-76060000	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr11:76051400-76063800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr11:76052200-76058200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr11:76052200-76058400	Weak transcription	Skeletal Muscle Male	skeletal muscle
48	chr11:76052400-76054400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr11:76052600-76060000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr11:76052600-76065200	Weak transcription	HSMM	muscle

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