Variant report

Variant	esv3475420
Chromosome Location	chr11:10464352-10470454
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	BHLHE40	chr11:10466353-10466876	K562	blood:	n/a	n/a
2	CBX3	chr11:10466037-10466421	K562	blood:	n/a	n/a
3	CEBPB	chr11:10465277-10465602	HepG2	liver:	n/a	chr11:10465455-10465466
4	CEBPB	chr11:10469308-10469561	Hela-S3	cervix:	n/a	chr11:10469415-10469426
5	CEBPB	chr11:10465389-10465593	MCF-7	breast:	n/a	chr11:10465455-10465466
6	CEBPB	chr11:10465284-10465652	K562	blood:	n/a	chr11:10465455-10465466
7	CEBPB	chr11:10469327-10469560	A549	lung:	n/a	chr11:10469415-10469426
8	CEBPB	chr11:10465306-10465682	A549	lung:	n/a	chr11:10465455-10465466
9	CEBPB	chr11:10465287-10465645	IMR90	lung:	n/a	chr11:10465455-10465466
10	CEBPB	chr11:10465228-10465743	A549	lung:	n/a	chr11:10465455-10465466
11	CEBPB	chr11:10467160-10467387	HepG2	liver:	n/a	chr11:10467303-10467312 chr11:10467301-10467314 chr11:10467302-10467313
12	CEBPB	chr11:10465288-10465625	H1-hESC	embryonic stem cell:	n/a	chr11:10465455-10465466
13	CEBPB	chr11:10465347-10465630	K562	blood:	n/a	chr11:10465455-10465466
14	CEBPB	chr11:10469305-10469512	IMR90	lung:	n/a	chr11:10469415-10469426
15	CEBPB	chr11:10469256-10469605	K562	blood:	n/a	chr11:10469415-10469426
16	CEBPB	chr11:10467260-10467445	A549	lung:	n/a	chr11:10467303-10467312 chr11:10467301-10467314 chr11:10467302-10467313
17	CEBPB	chr11:10469338-10469518	K562	blood:	n/a	chr11:10469415-10469426
18	CEBPB	chr11:10465383-10465611	ECC-1	luminal epithelium:	n/a	chr11:10465455-10465466
19	CEBPB	chr11:10469309-10469580	K562	blood:	n/a	chr11:10469415-10469426
20	CEBPB	chr11:10465298-10465642	Hela-S3	cervix:	n/a	chr11:10465455-10465466
21	CEBPB	chr11:10469290-10469588	HepG2	liver:	n/a	chr11:10469415-10469426
22	CEBPB	chr11:10465291-10465643	A549	lung:	n/a	chr11:10465455-10465466
23	CEBPB	chr11:10465305-10465616	ECC-1	luminal epithelium:	n/a	chr11:10465455-10465466
24	CHD2	chr11:10466493-10466511	K562	blood:	n/a	n/a
25	CTCF	chr11:10467200-10467350	HEEpiC	esophagus:	n/a	n/a
26	CUX1	chr11:10466215-10466227	K562	blood:	n/a	n/a
27	E2F4	chr11:10465256-10465361	MCF10A-Er-Src	breast:	n/a	n/a
28	GATA2	chr11:10466737-10467312	SH-SY5Y	brain:	n/a	chr11:10466792-10466803 chr11:10466767-10466778
29	GATA3	chr11:10466738-10466958	T-47D	breast:	n/a	chr11:10466792-10466803 chr11:10466767-10466778
30	GATA3	chr11:10466779-10467307	SH-SY5Y	brain:	n/a	chr11:10466792-10466803
31	MAX	chr11:10467380-10467454	HepG2	liver:	n/a	n/a
32	MAX	chr11:10469313-10469516	NB4	blood:	n/a	chr11:10469456-10469466
33	MAX	chr11:10466268-10466814	K562	blood:	n/a	chr11:10466496-10466507
34	MAZ	chr11:10466400-10466876	K562	blood:	n/a	chr11:10466496-10466507
35	MXI1	chr11:10464884-10464954	K562	blood:	n/a	n/a
36	MYC	chr11:10469320-10469511	NB4	blood:	n/a	chr11:10469456-10469466
37	MYC	chr11:10466718-10466865	NB4	blood:	n/a	n/a
38	MYC	chr11:10466394-10466603	K562	blood:	n/a	chr11:10466496-10466507
39	MYC	chr11:10468317-10468359	MCF10A-Er-Src	breast:	n/a	n/a
40	MYC	chr11:10466671-10466770	K562	blood:	n/a	n/a
41	POLR2A	chr11:10468715-10468730	K562	blood:	n/a	n/a
42	RCOR1	chr11:10466411-10466887	K562	blood:	n/a	n/a
43	STAT3	chr11:10465410-10465574	MCF10A-Er-Src	breast:	n/a	n/a
44	STAT3	chr11:10465131-10465164	MCF10A-Er-Src	breast:	n/a	n/a
45	TAL1	chr11:10466302-10466619	K562	blood:	n/a	n/a
46	YY1	chr11:10466363-10466557	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:10469707-10469757	AG09309	skin:	n/a
2	chr11:10469317-10469367	HNPCEpiC	eye:	n/a
3	chr11:10469317-10469367	HIPEpiC	eye:	n/a
4	chr11:10469317-10469367	HCT-116	colon:	n/a
5	chr11:10469317-10469367	SK-N-MC	brain:	n/a
6	chr11:10469317-10469367	PFSK-1	brain:	n/a
7	chr11:10469317-10469367	U87	brain:	n/a
8	chr11:10469707-10469757	HCPEpiC	choroid plexus:	n/a
9	chr11:10469707-10469757	HNPCEpiC	eye:	n/a
10	chr11:10469317-10469367	Caco-2	colon:	n/a
11	chr11:10469707-10469757	HRPEpiC	eye:	n/a
12	chr11:10469317-10469367	Hela-S3	cervix:	n/a
13	chr11:10469317-10469367	HL-60	blood:	n/a
14	chr11:10469317-10469367	SK-N-SH	brain:	n/a
15	chr11:10469707-10469757	HPAEpiC	pulmonary alveolar:	n/a
16	chr11:10469317-10469367	LNCaP	prostate:	n/a
17	chr11:10469317-10469367	HUVEC	blood vessel:	n/a
18	chr11:10469707-10469757	HEK293	kidney:	embryo
19	chr11:10469317-10469367	HRE	kidney:	n/a
20	chr11:10469317-10469367	SAEC	small airway:	n/a
21	chr11:10469317-10469367	ECC-1	luminal epithelium:	n/a
22	chr11:10469707-10469757	AG04449	skin:	fetal
23	chr11:10469317-10469367	IMR90	lung:	fetal
24	chr11:10469707-10469757	Hepatocyte	liver:	n/a
25	chr11:10469317-10469367	ProgFib	skin:	n/a
26	chr11:10469707-10469757	SK-N-SH	brain:	n/a
27	chr11:10469707-10469757	HAEpiC	amniotic membrane:	n/a
28	chr11:10469317-10469367	ovcar-3	ovarian:	n/a
29	chr11:10469317-10469367	RPTEC	kidney:	n/a
30	chr11:10469707-10469757	PFSK-1	brain:	n/a
31	chr11:10469707-10469757	HepG2	liver:	n/a
32	chr11:10469707-10469757	AoSMC	blood vessel:	n/a
33	chr11:10469317-10469367	SKMC	muscle:	n/a
34	chr11:10469317-10469367	AG09319	gingival:	n/a
35	chr11:10469707-10469757	NH-A	brain:	n/a
36	chr11:10469707-10469757	T-47D	breast:	n/a
37	chr11:10469317-10469367	PANC-1	pancreas:	n/a
38	chr11:10469707-10469757	NB4	blood:	n/a
39	chr11:10469317-10469367	MCF10A-Er-Src	breast:	n/a
40	chr11:10469317-10469367	NB4	blood:	n/a
41	chr11:10469707-10469757	ovcar-3	ovarian:	n/a
42	chr11:10469317-10469367	PrEC	prostate:	n/a
43	chr11:10469707-10469757	H1-hESC	embryonic stem cell:	embryo
44	chr11:10469317-10469367	NH-A	brain:	n/a
45	chr11:10469707-10469757	GM12891	blood:	n/a
46	chr11:10469317-10469367	GM06990	blood:	n/a
47	chr11:10469317-10469367	HRPEpiC	eye:	n/a
48	chr11:10469707-10469757	NHDF-neo	bronchial:	n/a
49	chr11:10469707-10469757	SK-N-MC	brain:	n/a
50	chr11:10469707-10469757	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:10465504..10467220-chr11:10470212..10471987,2	K562	blood:
2	chr11:10466561..10468211-chr11:10473032..10475120,2	K562	blood:
3	chr11:10467512..10469886-chr11:10470093..10472685,2	K562	blood:
4	chr11:10466744..10468864-chr11:10475908..10478177,3	K562	blood:
5	chr11:10449274..10451855-chr11:10466562..10468948,2	K562	blood:
6	chr11:10464906..10468864-chr11:10475520..10479355,5	K562	blood:
7	chr11:10459654..10465823-chr11:10469269..10473470,7	MCF-7	breast:
8	chr11:10469398..10472547-chr11:10473380..10477623,4	K562	blood:
9	chr11:10466009..10469840-chr11:10470987..10473326,3	MCF-7	breast:
10	chr11:10464794..10466976-chr11:10476133..10477728,2	MCF-7	breast:

Variant related genes	Relation type
AMPD3	TF binding region
AMPD3	CpG island
ENSG00000133805	chromatin interactions

Extended variants
information (count: 243 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:243 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368462636	chr11:10464368-10464369	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs573763754	chr11:10464382-10464383	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs542723420	chr11:10464397-10464398	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs556091350	chr11:10464399-10464400	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs12280618	chr11:10464407-10464408	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs545427741	chr11:10464438-10464439	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs565426575	chr11:10464442-10464443	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs528018656	chr11:10464491-10464492	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs541240392	chr11:10464506-10464507	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs561539256	chr11:10464545-10464546	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs191365505	chr11:10464564-10464565	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs11042806	chr11:10464582-10464583	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs569804935	chr11:10464583-10464584	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs532128812	chr11:10464595-10464596	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs9971562	chr11:10464659-10464660	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs117637042	chr11:10464761-10464762	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs145378222	chr11:10464763-10464764	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs16907826	chr11:10464795-10464796	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs372643162	chr11:10464802-10464803	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs147687354	chr11:10464814-10464815	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs149171205	chr11:10464826-10464827	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs576166179	chr11:10464886-10464887	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs568781817	chr11:10464894-10464895	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs10840415	chr11:10464912-10464913	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs182849363	chr11:10464931-10464932	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs142386449	chr11:10464932-10464933	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs561611983	chr11:10464994-10464995	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs58465473	chr11:10465012-10465013	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs117349250	chr11:10465045-10465046	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs563350017	chr11:10465088-10465089	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs532264892	chr11:10465105-10465106	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs551852811	chr11:10465109-10465110	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs16907828	chr11:10465125-10465126	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs528329901	chr11:10465136-10465137	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs187240392	chr11:10465143-10465144	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs376820465	chr11:10465158-10465159	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs562256136	chr11:10465195-10465196	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs552531853	chr11:10465208-10465209	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs7109302	chr11:10465212-10465213	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs569789284	chr11:10465228-10465229	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs138560094	chr11:10465238-10465239	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs539141224	chr11:10465264-10465265	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs111728167	chr11:10465329-10465330	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs145894642	chr11:10465365-10465366	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs75597492	chr11:10465386-10465387	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs115522561	chr11:10465387-10465388	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs373383038	chr11:10465412-10465413	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs56125701	chr11:10465420-10465421	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs575237888	chr11:10465433-10465434	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs184598586	chr11:10465462-10465463	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:10457600-10471800	Weak transcription	NHDF-Ad	bronchial
2	chr11:10459400-10465600	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr11:10460400-10464800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr11:10462600-10464600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
5	chr11:10462600-10467400	Enhancers	Primary B cells from peripheral blood	blood
6	chr11:10462600-10467600	Enhancers	Fetal Thymus	thymus
7	chr11:10462800-10464400	Enhancers	GM12878-XiMat	blood
8	chr11:10462800-10467600	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr11:10463000-10464600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
10	chr11:10463000-10467000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr11:10463000-10467000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr11:10463200-10465400	Enhancers	Primary B cells from cord blood	blood
13	chr11:10463400-10464800	Enhancers	Thymus	Thymus
14	chr11:10463400-10465000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr11:10463400-10466400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr11:10463600-10465400	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr11:10463800-10465600	Weak transcription	Primary hematopoietic stem cells	blood
18	chr11:10464000-10465600	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr11:10464000-10465600	Weak transcription	Primary T cells from cord blood	blood
20	chr11:10464000-10466200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr11:10464000-10466200	Weak transcription	Primary T helper cells PMA-I stimulated	--
22	chr11:10464000-10466200	Weak transcription	Dnd41	blood
23	chr11:10464000-10466400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
24	chr11:10464000-10466600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr11:10464000-10466600	Weak transcription	Primary T helper cells fromperipheralblood	blood
26	chr11:10464000-10467000	Weak transcription	Adipose Nuclei	Adipose
27	chr11:10464000-10471000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr11:10464000-10471000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr11:10464200-10464600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
30	chr11:10464200-10466400	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr11:10464400-10464800	Flanking Active TSS	GM12878-XiMat	blood
32	chr11:10464600-10464800	Enhancers	Primary T helper naive cells from peripheral blood	blood
33	chr11:10464600-10465800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
34	chr11:10464600-10471600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr11:10464800-10465000	Enhancers	GM12878-XiMat	blood
36	chr11:10464800-10465200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr11:10464800-10466200	Weak transcription	Thymus	Thymus
38	chr11:10464800-10466400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
39	chr11:10465000-10465800	Weak transcription	Aorta	Aorta
40	chr11:10465000-10466400	Weak transcription	GM12878-XiMat	blood
41	chr11:10465400-10465800	Weak transcription	Primary neutrophils fromperipheralblood	blood
42	chr11:10465400-10471000	Weak transcription	Primary B cells from cord blood	blood
43	chr11:10465600-10466000	Enhancers	Spleen	Spleen
44	chr11:10465600-10466800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr11:10465600-10466800	Enhancers	Primary hematopoietic stem cells	blood
46	chr11:10465600-10467200	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr11:10465600-10467400	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr11:10465600-10468200	Enhancers	Primary T cells from cord blood	blood
49	chr11:10465600-10472000	Weak transcription	Right Atrium	heart
50	chr11:10465800-10466000	Enhancers	Primary neutrophils fromperipheralblood	blood

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