Variant report

Variant	esv3383733
Chromosome Location	chr11:76186353-76225544
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:290)
CpG islands
(count:61)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:290 , 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	BACH1	chr11:76215563-76215651	K562	blood:	n/a	n/a
2	CEBPB	chr11:76212856-76213158	IMR90	lung:	n/a	n/a
3	CEBPB	chr11:76214044-76214280	HepG2	liver:	n/a	chr11:76214160-76214171
4	CEBPB	chr11:76212864-76213191	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr11:76214033-76214244	IMR90	lung:	n/a	chr11:76214160-76214171
6	CEBPB	chr11:76214072-76214266	H1-hESC	embryonic stem cell:	n/a	chr11:76214160-76214171
7	CEBPB	chr11:76212884-76213186	ECC-1	luminal epithelium:	n/a	n/a
8	CEBPB	chr11:76212885-76213176	A549	lung:	n/a	n/a
9	CEBPB	chr11:76212909-76213167	K562	blood:	n/a	n/a
10	CEBPB	chr11:76212908-76213196	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr11:76212863-76213181	HepG2	liver:	n/a	n/a
12	CEBPB	chr11:76212954-76213141	MCF-7	breast:	n/a	n/a
13	CEBPB	chr11:76195905-76195947	K562	blood:	n/a	n/a
14	CTCF	chr11:76224280-76224430	AG04450	lung:	n/a	n/a
15	CTCF	chr11:76224157-76224461	A549	lung:	n/a	n/a
16	CTCF	chr11:76224240-76224390	GM12878	blood:	n/a	n/a
17	CTCF	chr11:76201320-76201470	HBMEC	blood vessel:	n/a	n/a
18	CTCF	chr11:76224200-76224350	BE2_C	brain:	n/a	n/a
19	CTCF	chr11:76224320-76224470	AG09309	skin:	n/a	n/a
20	CTCF	chr11:76224300-76224450	HCFaa	heart:	n/a	n/a
21	CTCF	chr11:76202880-76203030	Caco-2	colon:	n/a	n/a
22	CTCF	chr11:76224280-76224430	HAc	cerebellar:	n/a	n/a
23	CTCF	chr11:76224260-76224410	GM12865	blood:	n/a	n/a
24	CTCF	chr11:76224338-76224406	Kidney_OC	kidney:	n/a	n/a
25	CTCF	chr11:76224260-76224410	HMF	breast:	n/a	n/a
26	CTCF	chr11:76202760-76202910	HepG2	liver:	n/a	n/a
27	CTCF	chr11:76224241-76224400	A549	lung:	n/a	n/a
28	CTCF	chr11:76224280-76224430	GM12869	blood:	n/a	n/a
29	CTCF	chr11:76201320-76201470	HCT-116	colon:	n/a	n/a
30	CTCF	chr11:76224320-76224470	HEEpiC	esophagus:	n/a	n/a
31	CTCF	chr11:76224560-76224710	HRPEpiC	eye:	n/a	n/a
32	CTCF	chr11:76224313-76224425	GM10248	blood:	n/a	n/a
33	CTCF	chr11:76224260-76224410	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr11:76223973-76224933	A549	lung:	n/a	n/a
35	CTCF	chr11:76224280-76224430	Caco-2	colon:	n/a	n/a
36	CTCF	chr11:76224280-76224430	NHDF-neo	bronchial:	n/a	n/a
37	CTCF	chr11:76202760-76202910	HVMF	connective:	n/a	n/a
38	CTCF	chr11:76224234-76224629	MCF-7	breast:	n/a	n/a
39	CTCF	chr11:76224300-76224450	HUVEC	blood vessel:	n/a	n/a
40	CTCF	chr11:76202896-76202951	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr11:76224280-76224430	HRE	kidney:	n/a	n/a
42	CTCF	chr11:76203260-76203410	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr11:76224180-76224330	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr11:76202760-76202910	MCF-7	breast:	n/a	n/a
45	CTCF	chr11:76224280-76224430	AG10803	skin:	n/a	n/a
46	CTCF	chr11:76224240-76224390	HPF	lung:	n/a	n/a
47	CTCF	chr11:76224320-76224470	WI-38	lung:	n/a	n/a
48	CTCF	chr11:76202700-76202850	HFF-Myc	foreskin:	n/a	n/a
49	CTCF	chr11:76224240-76224390	HepG2	liver:	n/a	n/a
50	CTCF	chr11:76224251-76224469	Hela-S3	cervix:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:76222035-76222085	MCF-7	breast:	n/a
2	chr11:76222035-76222085	HCM	heart:	n/a
3	chr11:76222035-76222085	AG04449	skin:	fetal
4	chr11:76222035-76222085	HRPEpiC	eye:	n/a
5	chr11:76222035-76222085	SAEC	small airway:	n/a
6	chr11:76222035-76222085	NT2-D1	testis:	n/a
7	chr11:76222035-76222085	AG09309	skin:	n/a
8	chr11:76222035-76222085	U87	brain:	n/a
9	chr11:76222035-76222085	AoSMC	blood vessel:	n/a
10	chr11:76222035-76222085	PANC-1	pancreas:	n/a
11	chr11:76222035-76222085	BJ	skin:	n/a
12	chr11:76222035-76222085	IMR90	lung:	fetal
13	chr11:76222035-76222085	HRCEpiC	kidney:	n/a
14	chr11:76222035-76222085	HIPEpiC	eye:	n/a
15	chr11:76222035-76222085	HRE	kidney:	n/a
16	chr11:76222035-76222085	RPTEC	kidney:	n/a
17	chr11:76222035-76222085	NHDF-neo	bronchial:	n/a
18	chr11:76222035-76222085	AG09319	gingival:	n/a
19	chr11:76222035-76222085	HUVEC	blood vessel:	n/a
20	chr11:76222035-76222085	NH-A	brain:	n/a
21	chr11:76222035-76222085	HCT-116	colon:	n/a
22	chr11:76222035-76222085	Jurkat	blood:	n/a
23	chr11:76222035-76222085	GM12878	blood:	n/a
24	chr11:76222035-76222085	Caco-2	colon:	n/a
25	chr11:76222035-76222085	A549	lung:	n/a
26	chr11:76222035-76222085	Hela-S3	cervix:	n/a
27	chr11:76222035-76222085	SK-N-SH_RA	brain:	n/a
28	chr11:76222035-76222085	HEK293	kidney:	embryo
29	chr11:76222035-76222085	HPAEpiC	pulmonary alveolar:	n/a
30	chr11:76222035-76222085	HCPEpiC	choroid plexus:	n/a
31	chr11:76222035-76222085	PFSK-1	brain:	n/a
32	chr11:76222035-76222085	H1-hESC	embryonic stem cell:	embryo
33	chr11:76222035-76222085	BE2_C	brain:	n/a
34	chr11:76222035-76222085	GM19239	blood:	n/a
35	chr11:76222035-76222085	GM06990	blood:	n/a
36	chr11:76222035-76222085	NHBE	bronchial:	n/a
37	chr11:76222035-76222085	Hepatocyte	liver:	n/a
38	chr11:76222035-76222085	NB4	blood:	n/a
39	chr11:76222035-76222085	HNPCEpiC	eye:	n/a
40	chr11:76222035-76222085	ECC-1	luminal epithelium:	n/a
41	chr11:76222035-76222085	CMK	blood:	n/a
42	chr11:76222035-76222085	AG10803	skin:	n/a
43	chr11:76222035-76222085	PrEC	prostate:	n/a
44	chr11:76222035-76222085	SKMC	muscle:	n/a
45	chr11:76222035-76222085	HepG2	liver:	n/a
46	chr11:76222035-76222085	K562	blood:	n/a
47	chr11:76222035-76222085	HEEpiC	esophagus:	n/a
48	chr11:76222035-76222085	GM12892	blood:	n/a
49	chr11:76222035-76222085	SK-N-MC	brain:	n/a
50	chr11:76222035-76222085	ProgFib	skin:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:76202482..76203428-chr11:76391378..76392425,4	MCF-7	breast:
2	chr11:76206276..76208160-chr11:76208743..76210293,2	MCF-7	breast:
3	chr11:76190688..76192947-chr11:76198433..76201383,2	K562	blood:
4	chr11:76181244..76183930-chr11:76199565..76201178,2	K562	blood:
5	chr11:76176649..76178412-chr11:76202103..76204664,2	K562	blood:
6	chr11:76185002..76188138-chr11:76188501..76191147,3	K562	blood:
7	chr11:76206276..76208160-chr11:76208743..76210293,2	MCF-7	breast:
8	chr11:76182591..76185058-chr11:76186358..76187920,2	K562	blood:
9	chr11:76154099..76155966-chr11:76212379..76214386,2	K562	blood:
10	chr11:76217657..76219893-chr11:76220860..76223168,2	K562	blood:
11	chr11:76210981..76212652-chr11:76215333..76217549,2	K562	blood:
12	chr11:76190688..76192947-chr11:76198433..76201383,2	K562	blood:
13	chr11:76215740..76218864-chr11:76222952..76226299,3	K562	blood:
14	chr11:76154330..76156315-chr11:76215728..76217827,2	MCF-7	breast:
15	chr11:76217657..76219893-chr11:76220860..76223168,2	K562	blood:
16	chr11:76177261..76180116-chr11:76185767..76188611,2	MCF-7	breast:
17	chr11:76154766..76157535-chr11:76206262..76208406,2	K562	blood:
18	chr11:76210981..76212652-chr11:76215333..76217549,2	K562	blood:
19	chr11:76191502..76194293-chr11:76198687..76201522,2	MCF-7	breast:
20	chr11:76191502..76194293-chr11:76198687..76201522,2	MCF-7	breast:
21	chr11:76185002..76188138-chr11:76188501..76191147,3	K562	blood:
22	chr11:76154636..76157268-chr11:76209424..76211012,2	MCF-7	breast:

No data

Variant related genes	Relation type
C11orf30	TF binding region
C11orf30	CpG island
ENSG00000255135	chromatin interactions
ENSG00000158636	chromatin interactions

Extended variants
information (count: 1330 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:1330 , 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	rs570890736	chr11:76186354-76186355	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs182210141	chr11:76186405-76186406	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs556354076	chr11:76186438-76186439	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs141390889	chr11:76186470-76186471	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs187567082	chr11:76186509-76186510	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554484380	chr11:76186526-76186527	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs78451175	chr11:76186575-76186576	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs371749442	chr11:76186621-76186622	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs372024426	chr11:76186647-76186648	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs533776981	chr11:76186649-76186650	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553920692	chr11:76186660-76186661	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs7949258	chr11:76186668-76186669	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs545908280	chr11:76186723-76186724	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs539483882	chr11:76186734-76186735	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs576146147	chr11:76186773-76186774	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs376618203	chr11:76186796-76186797	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs139297599	chr11:76186837-76186838	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs112288178	chr11:76186845-76186846	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs527973375	chr11:76186959-76186960	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs543540384	chr11:76187062-76187063	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs547739327	chr11:76187080-76187081	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566427919	chr11:76187136-76187137	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs75671395	chr11:76187150-76187151	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs533316529	chr11:76187204-76187205	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs550258505	chr11:76187284-76187285	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569805819	chr11:76187316-76187317	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185198559	chr11:76187356-76187357	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs202073840	chr11:76187416-76187417	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs190129417	chr11:76187506-76187507	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs568050821	chr11:76187606-76187607	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs150016263	chr11:76187630-76187631	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs533780104	chr11:76187632-76187633	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs368019430	chr11:76187643-76187644	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371654569	chr11:76187669-76187670	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs555442933	chr11:76187707-76187708	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs114224171	chr11:76187739-76187740	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs576975091	chr11:76187786-76187787	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs146583300	chr11:76187793-76187794	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs574384383	chr11:76187851-76187852	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs576182908	chr11:76187914-76187915	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs140111672	chr11:76187918-76187919	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs79734564	chr11:76188094-76188095	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs375061295	chr11:76188104-76188105	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs571917903	chr11:76188119-76188120	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs541712843	chr11:76188127-76188128	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs538567302	chr11:76188129-76188130	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs564584088	chr11:76188286-76188287	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs529328999	chr11:76188314-76188315	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs368486191	chr11:76188315-76188316	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs556703238	chr11:76188320-76188321	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1232 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:76157200-76190200	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr11:76157200-76191200	Weak transcription	Stomach Mucosa	stomach
3	chr11:76157400-76190200	Weak transcription	Colonic Mucosa	Colon
4	chr11:76158200-76190200	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr11:76159800-76190400	Weak transcription	Colon Smooth Muscle	Colon
6	chr11:76164800-76188600	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr11:76166800-76219400	Weak transcription	Small Intestine	intestine
8	chr11:76167200-76190200	Weak transcription	NHLF	lung
9	chr11:76167800-76192000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr11:76168600-76187000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr11:76168800-76234800	Weak transcription	Psoas Muscle	Psoas
12	chr11:76171200-76221200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr11:76171400-76190200	Weak transcription	Fetal Heart	heart
14	chr11:76172400-76187800	Strong transcription	Primary B cells from peripheral blood	blood
15	chr11:76173200-76187000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr11:76173400-76187200	Strong transcription	Primary neutrophils fromperipheralblood	blood
17	chr11:76173400-76188000	Strong transcription	Primary B cells from cord blood	blood
18	chr11:76173400-76191400	Strong transcription	Primary monocytes fromperipheralblood	blood
19	chr11:76173400-76191600	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr11:76173600-76191600	Strong transcription	Primary T helper cells fromperipheralblood	blood
21	chr11:76173800-76190000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr11:76174800-76187000	Strong transcription	HUES48 Cell Line	embryonic stem cell
23	chr11:76174800-76188000	Strong transcription	HUES64 Cell Line	embryonic stem cell
24	chr11:76174800-76191400	Strong transcription	Primary T helper cells PMA-I stimulated	--
25	chr11:76175200-76190200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr11:76175400-76190400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr11:76175800-76190200	Weak transcription	Brain Substantia Nigra	brain
28	chr11:76177200-76187600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr11:76177400-76195400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr11:76178000-76187800	Weak transcription	K562	blood
31	chr11:76178000-76190200	Weak transcription	A549	lung
32	chr11:76179600-76187600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
33	chr11:76180200-76204200	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr11:76180400-76191000	Weak transcription	HSMMtube	muscle
35	chr11:76181600-76187000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr11:76181600-76187400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr11:76182000-76187800	Strong transcription	Cortex derived primary cultured neurospheres	brain
38	chr11:76182200-76187000	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
39	chr11:76182200-76187400	Strong transcription	Placenta	Placenta
40	chr11:76182200-76188000	Strong transcription	Duodenum Mucosa	Duodenum
41	chr11:76182400-76187200	Strong transcription	Primary hematopoietic stem cells	blood
42	chr11:76182400-76187600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
43	chr11:76182400-76187800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr11:76182400-76189200	Strong transcription	Brain Germinal Matrix	brain
45	chr11:76182600-76186400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr11:76182600-76187400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr11:76182600-76187400	Strong transcription	Primary T cells fromperipheralblood	blood
48	chr11:76182600-76187800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
49	chr11:76182600-76187800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr11:76182600-76187800	Strong transcription	Fetal Thymus	thymus

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