Variant report

Variant	esv2757477
Chromosome Location	chr11:121473598-121540642
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	chr11:121532722-121532870	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:121526244-121527300	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:121525601-121525850	HepG2	liver:	n/a	n/a
4	BACH1	chr11:121525996-121526967	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr11:121505572-121505937	GM12878	blood:	n/a	n/a
6	BHLHE40	chr11:121526219-121527120	GM12878	blood:	n/a	n/a
7	BHLHE40	chr11:121526190-121527541	HepG2	liver:	n/a	n/a
8	BHLHE40	chr11:121526179-121527010	K562	blood:	n/a	n/a
9	BRCA1	chr11:121526207-121526407	HepG2	liver:	n/a	n/a
10	BRCA1	chr11:121526704-121526980	H1-hESC	embryonic stem cell:	n/a	n/a
11	BRCA1	chr11:121526282-121527099	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr11:121526642-121526987	K562	blood:	n/a	n/a
13	CCNT2	chr11:121526746-121527053	K562	blood:	n/a	n/a
14	CEBPB	chr11:121507532-121507823	Hela-S3	cervix:	n/a	chr11:121507681-121507692 chr11:121507683-121507692 chr11:121507683-121507692
15	CEBPB	chr11:121507502-121507874	IMR90	lung:	n/a	chr11:121507681-121507692 chr11:121507683-121507692 chr11:121507683-121507692
16	CEBPB	chr11:121526144-121526538	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr11:121526243-121527132	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr11:121507662-121507700	K562	blood:	n/a	chr11:121507681-121507692 chr11:121507683-121507692 chr11:121507683-121507692
19	CEBPB	chr11:121496593-121496818	HepG2	liver:	n/a	chr11:121496701-121496714 chr11:121496701-121496712 chr11:121496702-121496713 chr11:121496701-121496714
20	CEBPB	chr11:121526855-121527503	HepG2	liver:	n/a	n/a
21	CEBPB	chr11:121489858-121490108	IMR90	lung:	n/a	n/a
22	CEBPB	chr11:121532595-121532877	HepG2	liver:	n/a	chr11:121532718-121532729
23	CEBPB	chr11:121474109-121474344	IMR90	lung:	n/a	chr11:121474263-121474274
24	CEBPB	chr11:121504169-121504450	IMR90	lung:	n/a	n/a
25	CEBPB	chr11:121505463-121505723	A549	lung:	n/a	chr11:121505621-121505632
26	CEBPB	chr11:121474996-121475222	HepG2	liver:	n/a	chr11:121475135-121475146
27	CEBPB	chr11:121507500-121507871	HepG2	liver:	n/a	chr11:121507681-121507692 chr11:121507683-121507692 chr11:121507683-121507692
28	CEBPB	chr11:121474954-121475312	HepG2	liver:	n/a	chr11:121475135-121475146
29	CEBPB	chr11:121505452-121505709	HepG2	liver:	n/a	chr11:121505621-121505632
30	CEBPB	chr11:121496550-121496852	IMR90	lung:	n/a	chr11:121496701-121496714 chr11:121496701-121496712 chr11:121496702-121496713 chr11:121496701-121496714
31	CEBPB	chr11:121532524-121533248	IMR90	lung:	n/a	chr11:121532718-121532729
32	CEBPB	chr11:121474987-121475185	HepG2	liver:	n/a	chr11:121475135-121475146
33	CEBPB	chr11:121507459-121507768	ECC-1	luminal epithelium:	n/a	chr11:121507681-121507692 chr11:121507683-121507692 chr11:121507683-121507692
34	CEBPB	chr11:121526311-121526562	HepG2	liver:	n/a	n/a
35	CEBPB	chr11:121474225-121474321	HepG2	liver:	n/a	chr11:121474263-121474274
36	CEBPB	chr11:121507500-121507859	A549	lung:	n/a	chr11:121507681-121507692 chr11:121507683-121507692 chr11:121507683-121507692
37	CEBPB	chr11:121518624-121518891	IMR90	lung:	n/a	chr11:121518754-121518765
38	CEBPB	chr11:121505487-121505767	K562	blood:	n/a	chr11:121505621-121505632
39	CEBPB	chr11:121505335-121505941	IMR90	lung:	n/a	chr11:121505621-121505632
40	CEBPB	chr11:121526125-121527177	IMR90	lung:	n/a	n/a
41	CEBPB	chr11:121518640-121518877	HepG2	liver:	n/a	chr11:121518754-121518765
42	CEBPB	chr11:121507554-121507832	H1-hESC	embryonic stem cell:	n/a	chr11:121507681-121507692 chr11:121507683-121507692 chr11:121507683-121507692
43	CEBPD	chr11:121527136-121527621	HepG2	liver:	n/a	n/a
44	CHD1	chr11:121525300-121527770	IMR90	lung:	n/a	n/a
45	CHD2	chr11:121526293-121526604	HepG2	liver:	n/a	n/a
46	CHD2	chr11:121526233-121527004	GM12878	blood:	n/a	n/a
47	CHD2	chr11:121526148-121526924	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr11:121526849-121526905	K562	blood:	n/a	n/a
49	CHD2	chr11:121527278-121527537	HepG2	liver:	n/a	n/a
50	CHD2	chr11:121526846-121527017	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:121485684-121485734	SAEC	small airway:	n/a
2	chr11:121485684-121485734	SAEC	small airway:	n/a
3	chr11:121519649-121519699	K562	blood:	n/a
4	chr11:121533431-121533481	ECC-1	luminal epithelium:	n/a
5	chr11:121533431-121533481	HNPCEpiC	eye:	n/a
6	chr11:121533431-121533481	PFSK-1	brain:	n/a
7	chr11:121477737-121477787	HMEC	breast:	n/a
8	chr11:121477655-121477705	ECC-1	luminal epithelium:	n/a
9	chr11:121474197-121474247	GM12892	blood:	n/a
10	chr11:121526609-121526659	GM12892	blood:	n/a
11	chr11:121507724-121507774	A549	lung:	n/a
12	chr11:121526840-121526890	BE2_C	brain:	n/a
13	chr11:121507724-121507774	SK-N-MC	brain:	n/a
14	chr11:121526609-121526659	AG10803	skin:	n/a
15	chr11:121485684-121485734	HepG2	liver:	n/a
16	chr11:121502395-121502445	ECC-1	luminal epithelium:	n/a
17	chr11:121526840-121526890	HepG2	liver:	n/a
18	chr11:121507724-121507774	SAEC	small airway:	n/a
19	chr11:121519649-121519699	Caco-2	colon:	n/a
20	chr11:121519649-121519699	PFSK-1	brain:	n/a
21	chr11:121526609-121526659	LNCaP	prostate:	n/a
22	chr11:121526264-121526314	HRPEpiC	eye:	n/a
23	chr11:121519649-121519699	AG04449	skin:	fetal
24	chr11:121526840-121526890	MCF10A-Er-Src	breast:	n/a
25	chr11:121502395-121502445	HEK293	kidney:	embryo
26	chr11:121502395-121502445	RPTEC	kidney:	n/a
27	chr11:121502395-121502445	K562	blood:	n/a
28	chr11:121507724-121507774	LNCaP	prostate:	n/a
29	chr11:121526840-121526890	SK-N-SH	brain:	n/a
30	chr11:121502395-121502445	BE2_C	brain:	n/a
31	chr11:121515019-121515069	Hela-S3	cervix:	n/a
32	chr11:121485684-121485734	HCT-116	colon:	n/a
33	chr11:121533431-121533481	AG04450	lung:	fetal
34	chr11:121524538-121524588	Caco-2	colon:	n/a
35	chr11:121533431-121533481	Hela-S3	cervix:	n/a
36	chr11:121485684-121485734	AG09309	skin:	n/a
37	chr11:121474197-121474247	NHDF-neo	bronchial:	n/a
38	chr11:121526840-121526890	HCT-116	colon:	n/a
39	chr11:121526840-121526890	ECC-1	luminal epithelium:	n/a
40	chr11:121507724-121507774	NT2-D1	testis:	n/a
41	chr11:121507724-121507774	U87	brain:	n/a
42	chr11:121515019-121515069	PANC-1	pancreas:	n/a
43	chr11:121507724-121507774	HEEpiC	esophagus:	n/a
44	chr11:121485684-121485734	GM12878	blood:	n/a
45	chr11:121526609-121526659	U87	brain:	n/a
46	chr11:121485684-121485734	PFSK-1	brain:	n/a
47	chr11:121477737-121477787	HCPEpiC	choroid plexus:	n/a
48	chr11:121477655-121477705	K562	blood:	n/a
49	chr11:121515019-121515069	ovcar-3	ovarian:	n/a
50	chr11:121533431-121533481	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:121526442..121527320-chr11:122376172..122377075,6	MCF-7	breast:
2	chr11:121536053..121538911-chr11:121546218..121548406,2	K562	blood:
3	chr11:121526799..121527341-chr11:122073257..122073852,3	K562	blood:
4	chr11:121540015..121542237-chr11:121544199..121546981,2	K562	blood:
5	chr11:121515868..121518433-chr11:121526478..121527992,2	K562	blood:
6	chr11:121512816..121514316-chr17:41399595..41402548,2	MCF-7	breast:
7	chr11:121515868..121518433-chr11:121526478..121527992,2	K562	blood:
8	chr11:121488832..121492923-chr11:121494735..121499119,4	K562	blood:
9	chr11:121492728..121494563-chr11:121521550..121524030,2	K562	blood:
10	chr11:121526110..121526861-chr11:122376172..122377002,2	K562	blood:
11	chr11:121524308..121528407-chr11:121529156..121532838,3	K562	blood:
12	chr11:121492728..121494563-chr11:121521550..121524030,2	K562	blood:
13	chr11:121525946..121527352-chr11:122073329..122074247,11	MCF-7	breast:
14	chr11:121512836..121514336-chr17:41466392..41468507,2	K562	blood:
15	chr11:121526136..121527320-chr11:122073409..122074417,3	MCF-7	breast:
16	chr11:121525458..121528227-chr11:122072456..122075011,2	MCF-7	breast:
17	chr11:121524308..121528407-chr11:121529156..121532838,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BLID-6	chr11:121471818-121474271	ucscGeneNc_uc001pye_1
2	lnc-BLID-7	chr11:121476292-121476369	ucscGeneNc_uc001pya_2

Variant related genes	Relation type
SORL1	TF binding region
SORL1	CpG island
ENSG00000255090	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000137642	chromatin interactions

Extended variants
information (count: 2643 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:2643 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7128608	chr11:121473598-121473599	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs147344309	chr11:121473605-121473606	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs555006148	chr11:121473720-121473721	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs566823487	chr11:121473762-121473763	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs534155188	chr11:121473874-121473875	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs558713652	chr11:121473949-121473950	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs180779638	chr11:121473996-121473997	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs12287339	chr11:121474025-121474026	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs556578497	chr11:121474026-121474027	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs536335135	chr11:121474070-121474071	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs377076487	chr11:121474075-121474076	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs554994764	chr11:121474087-121474088	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs372011226	chr11:121474123-121474124	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs117466188	chr11:121474189-121474190	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs542202984	chr11:121474197-121474198	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs561193642	chr11:121474198-121474199	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs17125523	chr11:121474239-121474240	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs540498940	chr11:121474281-121474282	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs565099279	chr11:121474485-121474486	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs559296120	chr11:121474513-121474514	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs372944091	chr11:121474532-121474533	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs532287395	chr11:121474557-121474558	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs55859116	chr11:121474603-121474604	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs562596509	chr11:121474760-121474761	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs529705428	chr11:121474762-121474763	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs544832374	chr11:121474803-121474804	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs556463442	chr11:121474807-121474808	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs529774964	chr11:121474810-121474811	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs566860590	chr11:121474855-121474856	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs370514109	chr11:121474861-121474862	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs552404655	chr11:121474871-121474872	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs138026768	chr11:121474872-121474873	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs538423188	chr11:121474875-121474876	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs575324925	chr11:121474880-121474881	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs375073678	chr11:121474911-121474912	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs138099155	chr11:121474930-121474931	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs201415809	chr11:121474952-121474953	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs374387449	chr11:121474972-121474973	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs542356147	chr11:121474974-121474975	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs368373709	chr11:121474975-121474976	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs376141881	chr11:121474979-121474980	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs372370099	chr11:121474984-121474985	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs376240326	chr11:121474987-121474988	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs199717181	chr11:121474988-121474989	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs142508034	chr11:121475014-121475015	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs144784010	chr11:121475020-121475021	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs372675140	chr11:121475026-121475027	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs77049486	chr11:121475043-121475044	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs368987974	chr11:121475049-121475050	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs371654759	chr11:121475057-121475058	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	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
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Hepatocellular carcinoma	16785998	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Ovarian cancer	21720365	CNVD
Neuroblastoma	17327916	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Renal cell carcinoma	21668985	CNVD
Developmental delay	21147756	CNVD
Squamous cell cancer	20885788	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Hepatocellular carcinoma	16750200	CNVD
Multiple myeloma	17550852	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Heart disease	20551144	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	21509527	CNVD
Barrett''s syndrome	19417022	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21385341	CNVD
Multiple myeloma	16461302	CNVD
Burkitt''s lymphoma	18698080	CNVD
Prostate cancer	23792589	CNVD
Effusion lymphoma	18079361	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:1619 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:121440600-121485000	Strong transcription	HUES48 Cell Line	embryonic stem cell
2	chr11:121448800-121495600	Weak transcription	Stomach Mucosa	stomach
3	chr11:121451200-121488200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
4	chr11:121453200-121504200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr11:121453400-121491200	Weak transcription	Small Intestine	intestine
6	chr11:121453400-121505400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr11:121454000-121503800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr11:121454400-121504000	Strong transcription	Primary T cells fromperipheralblood	blood
9	chr11:121454800-121503600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr11:121455600-121503800	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr11:121456600-121501200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr11:121458000-121495000	Weak transcription	Right Ventricle	heart
13	chr11:121459200-121501400	Strong transcription	Rectal Mucosa Donor 31	rectum
14	chr11:121460400-121491800	Weak transcription	Left Ventricle	heart
15	chr11:121461000-121491200	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr11:121461400-121506200	Strong transcription	Primary neutrophils fromperipheralblood	blood
17	chr11:121461800-121505400	Strong transcription	Primary T helper cells fromperipheralblood	blood
18	chr11:121462200-121474800	Weak transcription	Lung	lung
19	chr11:121462200-121475800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr11:121462200-121484400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr11:121462200-121490400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr11:121462200-121500400	Strong transcription	Fetal Thymus	thymus
23	chr11:121462200-121503600	Strong transcription	Primary B cells from cord blood	blood
24	chr11:121462200-121504200	Strong transcription	Dnd41	blood
25	chr11:121462200-121505600	Strong transcription	Monocytes-CD14+_RO01746	blood
26	chr11:121462200-121505800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr11:121462400-121505200	Strong transcription	Primary monocytes fromperipheralblood	blood
28	chr11:121462600-121495200	Weak transcription	Fetal Brain Male	brain
29	chr11:121462600-121503400	Strong transcription	Primary T helper cells PMA-I stimulated	--
30	chr11:121463000-121525400	Weak transcription	Fetal Kidney	kidney
31	chr11:121463200-121504000	Strong transcription	Primary hematopoietic stem cells	blood
32	chr11:121463400-121505200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
33	chr11:121463600-121487000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr11:121464600-121475800	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr11:121464600-121506000	Strong transcription	GM12878-XiMat	blood
36	chr11:121465400-121486800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr11:121466600-121477200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr11:121466800-121475800	Weak transcription	Ovary	ovary
39	chr11:121467000-121475800	Weak transcription	Adipose Nuclei	Adipose
40	chr11:121467200-121476200	Weak transcription	Rectal Smooth Muscle	rectum
41	chr11:121467200-121477200	Weak transcription	Brain Germinal Matrix	brain
42	chr11:121467400-121474800	Weak transcription	Aorta	Aorta
43	chr11:121467400-121475200	Weak transcription	H9 Cell Line	embryonic stem cell
44	chr11:121467400-121475800	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr11:121467400-121476200	Weak transcription	Esophagus	oesophagus
46	chr11:121467400-121476200	Weak transcription	Pancreas	Pancrea
47	chr11:121467400-121478000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr11:121467400-121485200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr11:121467400-121488200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr11:121467600-121474800	Weak transcription	Stomach Smooth Muscle	stomach

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