Variant report

Variant	nsv1040278
Chromosome Location	chr11:4440162-4530349
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:593)
CpG islands
(count:490)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:593 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:4514547-4514747	K562	blood:	n/a	n/a
2	ATF1	chr11:4502329-4502511	K562	blood:	n/a	n/a
3	ATF3	chr11:4494239-4494395	K562	blood:	n/a	n/a
4	ATF3	chr11:4502231-4502443	K562	blood:	n/a	n/a
5	BATF	chr11:4514210-4514762	GM12878	blood:	n/a	n/a
6	BATF	chr11:4514308-4514557	GM12878	blood:	n/a	n/a
7	BCL11A	chr11:4514325-4514757	GM12878	blood:	n/a	n/a
8	BCL11A	chr11:4514425-4514768	GM12878	blood:	n/a	n/a
9	BHLHE40	chr11:4514262-4514648	GM12878	blood:	n/a	n/a
10	BHLHE40	chr11:4494212-4494443	K562	blood:	n/a	n/a
11	BHLHE40	chr11:4514088-4514588	K562	blood:	n/a	n/a
12	CEBPB	chr11:4455134-4455441	HepG2	liver:	n/a	chr11:4455291-4455304 chr11:4455291-4455302 chr11:4455292-4455303
13	CEBPB	chr11:4464273-4464473	HepG2	liver:	n/a	chr11:4464335-4464348 chr11:4464336-4464347
14	CEBPB	chr11:4455124-4455430	A549	lung:	n/a	chr11:4455291-4455304 chr11:4455291-4455302 chr11:4455292-4455303
15	CEBPB	chr11:4521600-4521789	H1-hESC	embryonic stem cell:	n/a	chr11:4521689-4521700
16	CEBPB	chr11:4455143-4455440	IMR90	lung:	n/a	chr11:4455291-4455304 chr11:4455291-4455302 chr11:4455292-4455303
17	CEBPB	chr11:4506243-4506344	K562	blood:	n/a	n/a
18	CEBPB	chr11:4511844-4512110	HepG2	liver:	n/a	chr11:4511948-4511959
19	CEBPB	chr11:4485526-4486025	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr11:4480878-4481078	H1-hESC	embryonic stem cell:	n/a	chr11:4480932-4480943
21	CEBPB	chr11:4511852-4512146	A549	lung:	n/a	chr11:4511948-4511959
22	CEBPB	chr11:4511868-4512046	K562	blood:	n/a	chr11:4511948-4511959
23	CEBPB	chr11:4521640-4521844	A549	lung:	n/a	chr11:4521689-4521700
24	CEBPB	chr11:4511930-4511964	H1-hESC	embryonic stem cell:	n/a	chr11:4511948-4511959
25	CEBPB	chr11:4521549-4521828	K562	blood:	n/a	chr11:4521689-4521700
26	CEBPB	chr11:4455223-4455382	K562	blood:	n/a	chr11:4455291-4455304 chr11:4455291-4455302 chr11:4455292-4455303
27	CEBPB	chr11:4480790-4481073	HepG2	liver:	n/a	chr11:4480932-4480943
28	CEBPB	chr11:4516863-4517063	K562	blood:	n/a	n/a
29	CEBPB	chr11:4511807-4512092	IMR90	lung:	n/a	chr11:4511948-4511959
30	CEBPB	chr11:4480768-4481058	Hela-S3	cervix:	n/a	chr11:4480932-4480943
31	CEBPB	chr11:4512084-4512518	MCF-7	breast:	n/a	n/a
32	CEBPB	chr11:4484563-4484620	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr11:4521534-4521859	HepG2	liver:	n/a	chr11:4521689-4521700
34	CEBPB	chr11:4521334-4521828	IMR90	lung:	n/a	chr11:4521689-4521700
35	CEBPB	chr11:4480816-4481016	K562	blood:	n/a	chr11:4480932-4480943
36	CHD1	chr11:4485864-4486172	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr11:4485610-4486013	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr11:4514580-4514730	GM12878	blood:	n/a	n/a
39	CTCF	chr11:4514480-4514630	HEEpiC	esophagus:	n/a	n/a
40	CTCF	chr11:4515000-4515150	AG04450	lung:	n/a	n/a
41	CTCF	chr11:4514580-4514730	K562	blood:	n/a	n/a
42	CTCF	chr11:4514500-4514650	GM12873	blood:	n/a	n/a
43	CTCF	chr11:4514580-4514730	GM12872	blood:	n/a	n/a
44	CTCF	chr11:4514560-4514710	GM06990	blood:	n/a	n/a
45	CTCF	chr11:4514444-4514776	K562	blood:	n/a	n/a
46	CTCF	chr11:4514420-4514793	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr11:4514480-4514630	AG09309	skin:	n/a	n/a
48	CTCF	chr11:4514500-4514650	BE2_C	brain:	n/a	n/a
49	CTCF	chr11:4471780-4471930	GM12868	blood:	n/a	n/a
50	CTCF	chr11:4514480-4514630	GM12872	blood:	n/a	n/a

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:4509357-4509407	MCF10A-Er-Src	breast:	n/a
2	chr11:4471362-4471412	Caco-2	colon:	n/a
3	chr11:4509357-4509407	MCF10A-Er-Src	breast:	n/a
4	chr11:4471362-4471412	Caco-2	colon:	n/a
5	chr11:4456403-4456453	NHBE	bronchial:	n/a
6	chr11:4509357-4509407	HL-60	blood:	n/a
7	chr11:4469073-4469123	MCF10A-Er-Src	breast:	n/a
8	chr11:4469894-4469944	H1-hESC	embryonic stem cell:	embryo
9	chr11:4469894-4469944	ovcar-3	ovarian:	n/a
10	chr11:4471362-4471412	HepG2	liver:	n/a
11	chr11:4469894-4469944	NHDF-neo	bronchial:	n/a
12	chr11:4456403-4456453	H1-hESC	embryonic stem cell:	embryo
13	chr11:4510366-4510416	NH-A	brain:	n/a
14	chr11:4469604-4469654	T-47D	breast:	n/a
15	chr11:4469073-4469123	GM19239	blood:	n/a
16	chr11:4469894-4469944	HEK293	kidney:	embryo
17	chr11:4508841-4508891	U87	brain:	n/a
18	chr11:4469604-4469654	SKMC	muscle:	n/a
19	chr11:4508841-4508891	SK-N-SH	brain:	n/a
20	chr11:4509357-4509407	ProgFib	skin:	n/a
21	chr11:4469894-4469944	SAEC	small airway:	n/a
22	chr11:4469894-4469944	MCF10A-Er-Src	breast:	n/a
23	chr11:4508841-4508891	NT2-D1	testis:	n/a
24	chr11:4469604-4469654	HEEpiC	esophagus:	n/a
25	chr11:4509357-4509407	GM19239	blood:	n/a
26	chr11:4471362-4471412	BE2_C	brain:	n/a
27	chr11:4456403-4456453	Jurkat	blood:	n/a
28	chr11:4469604-4469654	H1-hESC	embryonic stem cell:	embryo
29	chr11:4508841-4508891	LNCaP	prostate:	n/a
30	chr11:4469604-4469654	HCM	heart:	n/a
31	chr11:4510366-4510416	SK-N-SH_RA	brain:	n/a
32	chr11:4509357-4509407	BE2_C	brain:	n/a
33	chr11:4469073-4469123	CMK	blood:	n/a
34	chr11:4469073-4469123	HRPEpiC	eye:	n/a
35	chr11:4469073-4469123	HCM	heart:	n/a
36	chr11:4509357-4509407	IMR90	lung:	fetal
37	chr11:4471362-4471412	HMEC	breast:	n/a
38	chr11:4509357-4509407	AG04450	lung:	fetal
39	chr11:4469604-4469654	NH-A	brain:	n/a
40	chr11:4510366-4510416	HCPEpiC	choroid plexus:	n/a
41	chr11:4469073-4469123	PFSK-1	brain:	n/a
42	chr11:4471362-4471412	T-47D	breast:	n/a
43	chr11:4469894-4469944	Hela-S3	cervix:	n/a
44	chr11:4469073-4469123	SAEC	small airway:	n/a
45	chr11:4469604-4469654	HUVEC	blood vessel:	n/a
46	chr11:4469604-4469654	GM12878	blood:	n/a
47	chr11:4510366-4510416	SAEC	small airway:	n/a
48	chr11:4456403-4456453	BJ	skin:	n/a
49	chr11:4469604-4469654	AG04450	lung:	fetal
50	chr11:4469604-4469654	BJ	skin:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:4451655..4453436-chr11:4454768..4456529,2	K562	blood:
2	chr11:4208123..4209247-chr11:4514343..4515119,4	MCF-7	breast:
3	chr11:4441835..4444233-chr11:4445411..4447480,2	K562	blood:
4	chr11:4441835..4444233-chr11:4445411..4447480,2	K562	blood:
5	chr11:4453118..4455290-chr11:4455987..4457955,2	MCF-7	breast:
6	chr11:4402110..4404126-chr11:4484207..4486605,2	K562	blood:
7	chr11:4451655..4453436-chr11:4454768..4456529,2	K562	blood:
8	chr11:4208460..4209382-chr11:4513705..4515541,8	MCF-7	breast:

No data

Variant related genes	Relation type
OR52P2P	TF binding region
ENSG00000221030	TF binding region
OR52K2	TF binding region
OR52K1	TF binding region
OR52K3P	TF binding region
OR52P2P	CpG island
ENSG00000221030	CpG island
OR52K2	CpG island
OR52K1	CpG island
OR52K3P	CpG island
ENSG00000254480	chromatin interactions
ENSG00000171999	chromatin interactions

Extended variants
information (count: 4078 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:4078 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566447723	chr11:4440164-4440165	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs539505101	chr11:4440175-4440176	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs527556784	chr11:4440229-4440230	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs546706228	chr11:4440265-4440266	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs568427105	chr11:4440280-4440281	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs535617354	chr11:4440300-4440301	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs186005125	chr11:4440304-4440305	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs149024181	chr11:4440305-4440306	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs540052795	chr11:4440327-4440328	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558355613	chr11:4440354-4440355	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs10500599	chr11:4440380-4440381	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs540902841	chr11:4440402-4440403	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs555106902	chr11:4440442-4440443	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573576672	chr11:4440448-4440449	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs543812305	chr11:4440482-4440483	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs10500600	chr11:4440483-4440484	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs372513312	chr11:4440502-4440503	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs111308540	chr11:4440567-4440568	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs577287153	chr11:4440580-4440581	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs76968066	chr11:4440584-4440585	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs1376685	chr11:4440617-4440618	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs189582837	chr11:4440627-4440628	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552585181	chr11:4440655-4440656	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs117776270	chr11:4440663-4440664	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs1823633	chr11:4440692-4440693	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs550665760	chr11:4440698-4440699	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577195988	chr11:4440712-4440713	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs181921713	chr11:4440751-4440752	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539918894	chr11:4440767-4440768	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs11032215	chr11:4440781-4440782	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs1839800	chr11:4440784-4440785	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs534269715	chr11:4440785-4440786	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs561560420	chr11:4440813-4440814	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs374828829	chr11:4440816-4440817	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371372206	chr11:4440832-4440833	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs1823634	chr11:4440838-4440839	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs1839801	chr11:4440885-4440886	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs537864409	chr11:4440894-4440895	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs555715350	chr11:4440938-4440939	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs115767554	chr11:4440970-4440971	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs186571994	chr11:4440990-4440991	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs371347051	chr11:4440994-4440995	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190484310	chr11:4441019-4441020	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs183055123	chr11:4441050-4441051	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs544907855	chr11:4441052-4441053	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs542411352	chr11:4441132-4441133	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561251516	chr11:4441216-4441217	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs375054501	chr11:4441226-4441227	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs563887218	chr11:4441243-4441244	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369515522	chr11:4441366-4441367	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Esophageal adenocarcinoma	18519675	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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:327 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:4438200-4441200	Weak transcription	Fetal Intestine Small	intestine
2	chr11:4438600-4441600	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr11:4439200-4440200	Strong transcription	Primary monocytes fromperipheralblood	blood
4	chr11:4439400-4440200	Enhancers	Pancreas	Pancrea
5	chr11:4440000-4440200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr11:4440200-4442800	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr11:4441600-4444600	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr11:4442800-4443200	Strong transcription	Primary monocytes fromperipheralblood	blood
9	chr11:4443200-4444800	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr11:4444600-4444800	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr11:4444800-4445400	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
12	chr11:4444800-4445600	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
13	chr11:4445400-4453000	Weak transcription	Primary monocytes fromperipheralblood	blood
14	chr11:4445600-4447200	Strong transcription	Monocytes-CD14+_RO01746	blood
15	chr11:4447200-4447800	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr11:4447800-4448400	Strong transcription	Monocytes-CD14+_RO01746	blood
17	chr11:4448400-4453400	Weak transcription	Monocytes-CD14+_RO01746	blood
18	chr11:4450600-4453400	Enhancers	Fetal Intestine Small	intestine
19	chr11:4450600-4453600	Enhancers	Fetal Intestine Large	intestine
20	chr11:4450800-4451600	Enhancers	Stomach Mucosa	stomach
21	chr11:4453000-4459600	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr11:4453200-4453400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr11:4453400-4454800	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr11:4454400-4454800	Enhancers	Primary neutrophils fromperipheralblood	blood
25	chr11:4454800-4455200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
26	chr11:4454800-4455800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
27	chr11:4454800-4464800	Weak transcription	Pancreas	Pancrea
28	chr11:4455200-4459200	Enhancers	Primary neutrophils fromperipheralblood	blood
29	chr11:4455600-4456200	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr11:4455800-4456600	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr11:4455800-4456800	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr11:4455800-4457400	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr11:4456000-4456400	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr11:4456600-4456800	Enhancers	Primary B cells from cord blood	blood
35	chr11:4457400-4458200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
36	chr11:4458200-4458400	Enhancers	Primary B cells from cord blood	blood
37	chr11:4458200-4459600	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr11:4458400-4458800	Weak transcription	Primary B cells from cord blood	blood
39	chr11:4459200-4461200	Weak transcription	Primary neutrophils fromperipheralblood	blood
40	chr11:4459600-4460000	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr11:4459600-4462600	Weak transcription	Monocytes-CD14+_RO01746	blood
42	chr11:4460000-4460200	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr11:4460200-4461800	Weak transcription	Primary monocytes fromperipheralblood	blood
44	chr11:4461200-4462800	Enhancers	Primary neutrophils fromperipheralblood	blood
45	chr11:4461800-4466400	Enhancers	Primary monocytes fromperipheralblood	blood
46	chr11:4462600-4463600	Enhancers	Primary B cells from cord blood	blood
47	chr11:4462600-4465400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
48	chr11:4462800-4463200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
49	chr11:4463200-4464800	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr11:4464000-4464600	Enhancers	Fetal Intestine Small	intestine

The 2.0 version of rSNPBase

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