Variant report

Variant	nsv520130
Chromosome Location	chr11:73183598-73223776
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:73198981-73199164	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:73204974-73205389	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:73189857-73190129	HepG2	liver:	n/a	n/a
4	BATF	chr11:73221608-73221898	GM12878	blood:	n/a	n/a
5	BCL11A	chr11:73221643-73221988	GM12878	blood:	n/a	n/a
6	BCL11A	chr11:73221636-73221890	GM12878	blood:	n/a	n/a
7	BHLHE40	chr11:73221660-73221910	HepG2	liver:	n/a	n/a
8	BHLHE40	chr11:73192132-73192280	K562	blood:	n/a	n/a
9	CBX3	chr11:73205142-73205830	HCT-116	colon:	n/a	n/a
10	CEBPB	chr11:73189816-73190185	A549	lung:	n/a	n/a
11	CEBPB	chr11:73218941-73219241	IMR90	lung:	n/a	n/a
12	CEBPB	chr11:73191753-73192065	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr11:73189837-73190190	IMR90	lung:	n/a	n/a
14	CEBPB	chr11:73189853-73190147	K562	blood:	n/a	n/a
15	CEBPB	chr11:73189829-73190192	HepG2	liver:	n/a	n/a
16	CEBPB	chr11:73189827-73190178	HepG2	liver:	n/a	n/a
17	CEBPB	chr11:73192357-73192530	A549	lung:	n/a	n/a
18	CEBPB	chr11:73189805-73190221	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr11:73189834-73190197	K562	blood:	n/a	n/a
20	CEBPB	chr11:73189729-73190293	A549	lung:	n/a	n/a
21	CEBPB	chr11:73189821-73190241	A549	lung:	n/a	n/a
22	CEBPB	chr11:73189818-73190174	K562	blood:	n/a	n/a
23	CEBPB	chr11:73191720-73192077	IMR90	lung:	n/a	n/a
24	CEBPB	chr11:73204918-73205431	HepG2	liver:	n/a	n/a
25	CEBPB	chr11:73217270-73217542	IMR90	lung:	n/a	n/a
26	CEBPB	chr11:73189774-73190242	ECC-1	luminal epithelium:	n/a	n/a
27	CEBPB	chr11:73191754-73192027	K562	blood:	n/a	n/a
28	CEBPB	chr11:73189747-73190266	MCF-7	breast:	n/a	n/a
29	CEBPB	chr11:73189840-73190195	ECC-1	luminal epithelium:	n/a	n/a
30	CEBPB	chr11:73188229-73188372	A549	lung:	n/a	n/a
31	CEBPB	chr11:73189801-73190228	MCF-7	breast:	n/a	n/a
32	CEBPB	chr11:73189819-73190162	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPD	chr11:73221657-73221916	K562	blood:	n/a	n/a
34	CHD2	chr11:73185858-73185902	HepG2	liver:	n/a	n/a
35	CTCF	chr11:73189607-73190328	HCT-116	colon:	n/a	chr11:73189969-73189987 chr11:73189971-73189992 chr11:73189974-73189982 chr11:73189970-73189986
36	CTCF	chr11:73189920-73190070	NHLF	lung:	n/a	chr11:73189969-73189987 chr11:73189971-73189992 chr11:73189974-73189982 chr11:73189970-73189986
37	CTCF	chr11:73189900-73190050	AG09319	gingival:	n/a	chr11:73189969-73189987 chr11:73189971-73189992 chr11:73189974-73189982 chr11:73189970-73189986
38	CTCF	chr11:73189880-73190030	GM12873	blood:	n/a	chr11:73189969-73189987 chr11:73189971-73189992 chr11:73189974-73189982 chr11:73189970-73189986
39	CTCF	chr11:73189920-73190070	HepG2	liver:	n/a	chr11:73189969-73189987 chr11:73189971-73189992 chr11:73189974-73189982 chr11:73189970-73189986
40	CTCF	chr11:73189865-73190040	Pancreas_OC	pancreas:	n/a	chr11:73189969-73189987 chr11:73189971-73189992 chr11:73189974-73189982 chr11:73189970-73189986
41	CTCF	chr11:73189843-73190044	SK-N-SH_RA	brain:	n/a	chr11:73189969-73189987 chr11:73189971-73189992 chr11:73189974-73189982 chr11:73189970-73189986
42	CTCF	chr11:73189900-73190050	GM12869	blood:	n/a	chr11:73189969-73189987 chr11:73189971-73189992 chr11:73189974-73189982 chr11:73189970-73189986
43	CTCF	chr11:73189816-73190132	MCF-7	breast:	n/a	chr11:73189969-73189987 chr11:73189971-73189992 chr11:73189974-73189982 chr11:73189970-73189986
44	CTCF	chr11:73189900-73190050	HRPEpiC	eye:	n/a	chr11:73189969-73189987 chr11:73189971-73189992 chr11:73189974-73189982 chr11:73189970-73189986
45	CTCF	chr11:73189860-73190010	GM12870	blood:	n/a	chr11:73189969-73189987 chr11:73189971-73189992 chr11:73189974-73189982 chr11:73189970-73189986
46	CTCF	chr11:73189880-73190030	GM12872	blood:	n/a	chr11:73189969-73189987 chr11:73189971-73189992 chr11:73189974-73189982 chr11:73189970-73189986
47	CTCF	chr11:73189480-73189630	Caco-2	colon:	n/a	n/a
48	CTCF	chr11:73189876-73190068	GM12891	blood:	n/a	chr11:73189969-73189987 chr11:73189971-73189992 chr11:73189974-73189982 chr11:73189970-73189986
49	CTCF	chr11:73189834-73190073	Lung_OC	lung:	n/a	chr11:73189969-73189987 chr11:73189971-73189992 chr11:73189974-73189982 chr11:73189970-73189986
50	CTCF	chr11:73189562-73190332	SK-N-SH	brain:	n/a	chr11:73189969-73189987 chr11:73189971-73189992 chr11:73189974-73189982 chr11:73189970-73189986

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:73202336-73202386	AoSMC	blood vessel:	n/a
2	chr11:73202336-73202386	GM12891	blood:	n/a
3	chr11:73202336-73202386	HCM	heart:	n/a
4	chr11:73202336-73202386	H1-hESC	embryonic stem cell:	embryo
5	chr11:73202336-73202386	PANC-1	pancreas:	n/a
6	chr11:73202336-73202386	AG04450	lung:	fetal
7	chr11:73202336-73202386	ECC-1	luminal epithelium:	n/a
8	chr11:73202336-73202386	HCPEpiC	choroid plexus:	n/a
9	chr11:73202336-73202386	A549	lung:	n/a
10	chr11:73202336-73202386	SK-N-MC	brain:	n/a
11	chr11:73202336-73202386	ProgFib	skin:	n/a
12	chr11:73202336-73202386	Hepatocyte	liver:	n/a
13	chr11:73202336-73202386	BE2_C	brain:	n/a
14	chr11:73202336-73202386	PrEC	prostate:	n/a
15	chr11:73202336-73202386	GM12892	blood:	n/a
16	chr11:73202336-73202386	HepG2	liver:	n/a
17	chr11:73202336-73202386	AG04449	skin:	fetal
18	chr11:73202336-73202386	GM06990	blood:	n/a
19	chr11:73202336-73202386	IMR90	lung:	fetal
20	chr11:73202336-73202386	NHDF-neo	bronchial:	n/a
21	chr11:73202336-73202386	Jurkat	blood:	n/a
22	chr11:73202336-73202386	Caco-2	colon:	n/a
23	chr11:73202336-73202386	HNPCEpiC	eye:	n/a
24	chr11:73202336-73202386	HRE	kidney:	n/a
25	chr11:73202336-73202386	AG09309	skin:	n/a
26	chr11:73202336-73202386	NT2-D1	testis:	n/a
27	chr11:73202336-73202386	NB4	blood:	n/a
28	chr11:73202336-73202386	SKMC	muscle:	n/a
29	chr11:73202336-73202386	NH-A	brain:	n/a
30	chr11:73202336-73202386	HCT-116	colon:	n/a
31	chr11:73202336-73202386	LNCaP	prostate:	n/a
32	chr11:73202336-73202386	HUVEC	blood vessel:	n/a
33	chr11:73202336-73202386	HRCEpiC	kidney:	n/a
34	chr11:73202336-73202386	HMEC	breast:	n/a
35	chr11:73202336-73202386	AG10803	skin:	n/a
36	chr11:73202336-73202386	SK-N-SH_RA	brain:	n/a
37	chr11:73202336-73202386	CMK	blood:	n/a
38	chr11:73202336-73202386	RPTEC	kidney:	n/a
39	chr11:73202336-73202386	ovcar-3	ovarian:	n/a
40	chr11:73202336-73202386	HEEpiC	esophagus:	n/a
41	chr11:73202336-73202386	AG09319	gingival:	n/a
42	chr11:73202336-73202386	MCF-7	breast:	n/a
43	chr11:73202336-73202386	HIPEpiC	eye:	n/a
44	chr11:73202336-73202386	GM12878	blood:	n/a
45	chr11:73202336-73202386	HEK293	kidney:	embryo
46	chr11:73202336-73202386	Hela-S3	cervix:	n/a
47	chr11:73202336-73202386	HRPEpiC	eye:	n/a
48	chr11:73202336-73202386	HL-60	blood:	n/a
49	chr11:73202336-73202386	MCF10A-Er-Src	breast:	n/a
50	chr11:73202336-73202386	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:73189484..73190492-chr11:73371669..73372682,5	K562	blood:
2	chr11:73192780..73195868-chr11:73198299..73201993,3	MCF-7	breast:
3	chr11:73195983..73198212-chr11:73208729..73211318,2	MCF-7	breast:
4	chr11:73216954..73219144-chr11:73356797..73358531,2	K562	blood:
5	chr11:73216345..73218979-chr11:73223737..73225348,2	MCF-7	breast:
6	chr11:73189399..73190555-chr11:73372006..73372626,3	MCF-7	breast:
7	chr11:73216604..73218199-chr11:73221678..73223626,3	MCF-7	breast:
8	chr11:73182923..73184833-chr12:110717693..110719478,2	MCF-7	breast:
9	chr11:73188697..73191006-chr11:73192840..73195131,3	MCF-7	breast:
10	chr11:73183792..73185927-chr11:73188418..73190143,2	K562	blood:
11	chr11:73189355..73190472-chr11:73336415..73337167,5	MCF-7	breast:
12	chr11:73183792..73185927-chr11:73188418..73190143,2	K562	blood:
13	chr11:73216345..73218979-chr11:73223737..73225348,2	MCF-7	breast:
14	chr11:73188446..73190226-chr11:73307611..73309619,2	MCF-7	breast:
15	chr11:73189539..73190279-chr11:73371425..73372555,3	MCF-7	breast:
16	chr11:73195983..73198212-chr11:73208729..73211318,2	MCF-7	breast:
17	chr11:73222148..73225498-chr11:73227399..73230635,3	K562	blood:
18	chr11:73192780..73195868-chr11:73198299..73201993,3	MCF-7	breast:
19	chr11:73188697..73191006-chr11:73192840..73195131,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000256148	TF binding region
FAM168A	TF binding region
ENSG00000256148	CpG island
FAM168A	CpG island
ENSG00000256148	chromatin interactions
ENSG00000174437	chromatin interactions
ENSG00000054965	chromatin interactions
ENSG00000021300	chromatin interactions

Extended variants
information (count: 1425 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:1425 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4944841	chr11:73183598-73183599	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs115614699	chr11:73183656-73183657	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs112930464	chr11:73183678-73183679	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs190288438	chr11:73183712-73183713	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs373316339	chr11:73183715-73183716	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs151249596	chr11:73183717-73183718	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs376399481	chr11:73183807-73183808	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs576005576	chr11:73183883-73183884	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs544959784	chr11:73183886-73183887	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs561574913	chr11:73183900-73183901	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs142642592	chr11:73183952-73183953	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs183086855	chr11:73183983-73183984	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs11235770	chr11:73184002-73184003	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs12277462	chr11:73184004-73184005	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs34862145	chr11:73184064-73184065	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs113691923	chr11:73184073-73184074	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs551534098	chr11:73184205-73184206	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs564980478	chr11:73184232-73184233	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs10047427	chr11:73184370-73184371	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs150981675	chr11:73184376-73184377	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs370844823	chr11:73184394-73184395	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs567228181	chr11:73184409-73184410	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs536210143	chr11:73184419-73184420	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs546710380	chr11:73184420-73184421	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs76647471	chr11:73184434-73184435	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs538802946	chr11:73184446-73184447	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs140941929	chr11:73184509-73184510	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs537545998	chr11:73184529-73184530	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs575864219	chr11:73184560-73184561	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs116971697	chr11:73184575-73184576	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs143246380	chr11:73184594-73184595	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs77761753	chr11:73184613-73184614	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs570470435	chr11:73184639-73184640	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs577783671	chr11:73184650-73184651	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs542593282	chr11:73184696-73184697	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs116403203	chr11:73184698-73184699	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs35014290	chr11:73184707-73184708	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs572894161	chr11:73184790-73184791	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs544818230	chr11:73184799-73184800	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs564647854	chr11:73184822-73184823	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs538529926	chr11:73184833-73184834	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs191683978	chr11:73184863-73184864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550382978	chr11:73184908-73184909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs11235771	chr11:73184962-73184963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs11600327	chr11:73184995-73184996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs184025334	chr11:73185103-73185104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs554018765	chr11:73185145-73185146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs529964266	chr11:73185146-73185147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs546969290	chr11:73185150-73185151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs566792521	chr11:73185152-73185153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	19153074	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	17142309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:446 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:73123800-73209600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr11:73131000-73190000	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr11:73141800-73231600	Weak transcription	Thymus	Thymus
4	chr11:73151000-73187000	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr11:73156000-73187800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr11:73163800-73225600	Weak transcription	Fetal Stomach	stomach
7	chr11:73165200-73186600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr11:73168600-73189800	Weak transcription	Hela-S3	cervix
9	chr11:73170400-73185800	Weak transcription	HepG2	liver
10	chr11:73172800-73218800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr11:73173800-73184400	Weak transcription	Spleen	Spleen
12	chr11:73174200-73186800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr11:73174600-73187800	Weak transcription	Primary T cells from cord blood	blood
14	chr11:73176400-73186600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr11:73177000-73189800	Weak transcription	Fetal Heart	heart
16	chr11:73177400-73189800	Weak transcription	HMEC	breast
17	chr11:73177400-73190000	Weak transcription	Osteobl	bone
18	chr11:73177400-73191400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr11:73177400-73191800	Weak transcription	NHDF-Ad	bronchial
20	chr11:73177600-73186800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr11:73178000-73184600	Weak transcription	Fetal Thymus	thymus
22	chr11:73178600-73190000	Weak transcription	Fetal Brain Male	brain
23	chr11:73178800-73186600	Weak transcription	Monocytes-CD14+_RO01746	blood
24	chr11:73179600-73183800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr11:73179600-73192400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr11:73180000-73188000	Weak transcription	Primary B cells from cord blood	blood
27	chr11:73180000-73191800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr11:73180200-73186600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr11:73180600-73186800	Weak transcription	Brain Substantia Nigra	brain
30	chr11:73180600-73189600	Weak transcription	Brain Cingulate Gyrus	brain
31	chr11:73180800-73186800	Weak transcription	Right Ventricle	heart
32	chr11:73181600-73188000	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr11:73181600-73189800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr11:73181800-73184400	Weak transcription	Left Ventricle	heart
35	chr11:73181800-73186800	Weak transcription	Primary hematopoietic stem cells	blood
36	chr11:73181800-73186800	Weak transcription	Right Atrium	heart
37	chr11:73182000-73185800	Weak transcription	Gastric	stomach
38	chr11:73182000-73230000	Weak transcription	Dnd41	blood
39	chr11:73182200-73185800	Weak transcription	Psoas Muscle	Psoas
40	chr11:73182200-73189400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr11:73184400-73184600	Enhancers	Spleen	Spleen
42	chr11:73184400-73184800	Enhancers	Left Ventricle	heart
43	chr11:73184800-73186000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr11:73184800-73186800	Weak transcription	Left Ventricle	heart
45	chr11:73185400-73186000	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr11:73185800-73186000	Enhancers	Gastric	stomach
47	chr11:73185800-73186400	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr11:73185800-73186400	Enhancers	HepG2	liver
49	chr11:73185800-73187000	Enhancers	Psoas Muscle	Psoas
50	chr11:73186000-73186200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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