Variant report

Variant	nsv1039640
Chromosome Location	chr11:4476167-4541813
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:543)
CpG islands
(count:183)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:543 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

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	chr11:4514088-4514588	K562	blood:	n/a	n/a
10	BHLHE40	chr11:4494212-4494443	K562	blood:	n/a	n/a
11	BHLHE40	chr11:4514262-4514648	GM12878	blood:	n/a	n/a
12	CEBPB	chr11:4511807-4512092	IMR90	lung:	n/a	chr11:4511948-4511959
13	CEBPB	chr11:4521334-4521828	IMR90	lung:	n/a	chr11:4521689-4521700
14	CEBPB	chr11:4480790-4481073	HepG2	liver:	n/a	chr11:4480932-4480943
15	CEBPB	chr11:4516863-4517063	K562	blood:	n/a	n/a
16	CEBPB	chr11:4521640-4521844	A549	lung:	n/a	chr11:4521689-4521700
17	CEBPB	chr11:4511868-4512046	K562	blood:	n/a	chr11:4511948-4511959
18	CEBPB	chr11:4485526-4486025	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr11:4521549-4521828	K562	blood:	n/a	chr11:4521689-4521700
20	CEBPB	chr11:4480878-4481078	H1-hESC	embryonic stem cell:	n/a	chr11:4480932-4480943
21	CEBPB	chr11:4512084-4512518	MCF-7	breast:	n/a	n/a
22	CEBPB	chr11:4506243-4506344	K562	blood:	n/a	n/a
23	CEBPB	chr11:4521600-4521789	H1-hESC	embryonic stem cell:	n/a	chr11:4521689-4521700
24	CEBPB	chr11:4521534-4521859	HepG2	liver:	n/a	chr11:4521689-4521700
25	CEBPB	chr11:4480816-4481016	K562	blood:	n/a	chr11:4480932-4480943
26	CEBPB	chr11:4511844-4512110	HepG2	liver:	n/a	chr11:4511948-4511959
27	CEBPB	chr11:4480768-4481058	Hela-S3	cervix:	n/a	chr11:4480932-4480943
28	CEBPB	chr11:4511930-4511964	H1-hESC	embryonic stem cell:	n/a	chr11:4511948-4511959
29	CEBPB	chr11:4511852-4512146	A549	lung:	n/a	chr11:4511948-4511959
30	CEBPB	chr11:4540065-4540287	HepG2	liver:	n/a	chr11:4540117-4540130
31	CEBPB	chr11:4484563-4484620	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD1	chr11:4485864-4486172	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr11:4485610-4486013	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr11:4514580-4514870	HA-sp	spinal cord:	n/a	n/a
35	CTCF	chr11:4514940-4515090	HMEC	breast:	n/a	n/a
36	CTCF	chr11:4514980-4515130	RPTEC	kidney:	n/a	n/a
37	CTCF	chr11:4514580-4514730	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr11:4514487-4514772	HepG2	liver:	n/a	n/a
39	CTCF	chr11:4514384-4514446	GM19238	blood:	n/a	n/a
40	CTCF	chr11:4514500-4514650	GM12867	blood:	n/a	n/a
41	CTCF	chr11:4514528-4514802	NHEK	skin:	n/a	n/a
42	CTCF	chr11:4514553-4514778	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr11:4514480-4514630	GM12871	blood:	n/a	n/a
44	CTCF	chr11:4514460-4514610	HCT-116	colon:	n/a	n/a
45	CTCF	chr11:4514600-4514750	NHEK	skin:	n/a	n/a
46	CTCF	chr11:4514720-4514870	A549	lung:	n/a	n/a
47	CTCF	chr11:4514560-4514710	GM12801	blood:	n/a	n/a
48	CTCF	chr11:4514480-4514630	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr11:4514535-4514785	GM20000	blood:	n/a	n/a
50	CTCF	chr11:4514391-4514767	A549	lung:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:4508841-4508891	HEEpiC	esophagus:	n/a
2	chr11:4509357-4509407	HEK293	kidney:	embryo
3	chr11:4508841-4508891	MCF-7	breast:	n/a
4	chr11:4510366-4510416	ovcar-3	ovarian:	n/a
5	chr11:4509357-4509407	IMR90	lung:	fetal
6	chr11:4508841-4508891	HCF	heart:	n/a
7	chr11:4508841-4508891	GM12878	blood:	n/a
8	chr11:4509357-4509407	GM12878	blood:	n/a
9	chr11:4508841-4508891	A549	lung:	n/a
10	chr11:4509357-4509407	HPAEpiC	pulmonary alveolar:	n/a
11	chr11:4509357-4509407	GM12891	blood:	n/a
12	chr11:4509357-4509407	T-47D	breast:	n/a
13	chr11:4510366-4510416	RPTEC	kidney:	n/a
14	chr11:4509357-4509407	AG04449	skin:	fetal
15	chr11:4508841-4508891	CMK	blood:	n/a
16	chr11:4508841-4508891	HIPEpiC	eye:	n/a
17	chr11:4508841-4508891	Jurkat	blood:	n/a
18	chr11:4508841-4508891	HepG2	liver:	n/a
19	chr11:4510366-4510416	HCF	heart:	n/a
20	chr11:4510366-4510416	SK-N-SH	brain:	n/a
21	chr11:4509357-4509407	HAEpiC	amniotic membrane:	n/a
22	chr11:4508841-4508891	GM12891	blood:	n/a
23	chr11:4510366-4510416	HEK293	kidney:	embryo
24	chr11:4510366-4510416	GM19239	blood:	n/a
25	chr11:4510366-4510416	HL-60	blood:	n/a
26	chr11:4508841-4508891	GM12892	blood:	n/a
27	chr11:4510366-4510416	MCF10A-Er-Src	breast:	n/a
28	chr11:4510366-4510416	U87	brain:	n/a
29	chr11:4509357-4509407	HIPEpiC	eye:	n/a
30	chr11:4508841-4508891	AG04450	lung:	fetal
31	chr11:4508841-4508891	SK-N-MC	brain:	n/a
32	chr11:4510366-4510416	SK-N-MC	brain:	n/a
33	chr11:4509357-4509407	PFSK-1	brain:	n/a
34	chr11:4508841-4508891	HCM	heart:	n/a
35	chr11:4510366-4510416	HRCEpiC	kidney:	n/a
36	chr11:4509357-4509407	SAEC	small airway:	n/a
37	chr11:4509357-4509407	HMEC	breast:	n/a
38	chr11:4510366-4510416	PANC-1	pancreas:	n/a
39	chr11:4509357-4509407	Caco-2	colon:	n/a
40	chr11:4510366-4510416	NHDF-neo	bronchial:	n/a
41	chr11:4508841-4508891	GM06990	blood:	n/a
42	chr11:4509357-4509407	NT2-D1	testis:	n/a
43	chr11:4510366-4510416	K562	blood:	n/a
44	chr11:4509357-4509407	SK-N-MC	brain:	n/a
45	chr11:4509357-4509407	Hepatocyte	liver:	n/a
46	chr11:4508841-4508891	AG04449	skin:	fetal
47	chr11:4508841-4508891	HCPEpiC	choroid plexus:	n/a
48	chr11:4510366-4510416	SAEC	small airway:	n/a
49	chr11:4510366-4510416	MCF-7	breast:	n/a
50	chr11:4509357-4509407	HRE	kidney:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:4531179..4533009-chr11:4535130..4536667,2	K562	blood:
2	chr11:4535006..4537782-chr11:4538961..4542552,3	K562	blood:
3	chr11:4531179..4533009-chr11:4535130..4536667,2	K562	blood:
4	chr11:4208460..4209382-chr11:4513705..4515541,8	MCF-7	breast:
5	chr11:4402110..4404126-chr11:4484207..4486605,2	K562	blood:
6	chr11:4208123..4209247-chr11:4514343..4515119,4	MCF-7	breast:

No data

Variant related genes	Relation type
OR52M2P	TF binding region
OR52K1	TF binding region
OR52K3P	TF binding region
OR52M2P	CpG island
OR52K1	CpG island
OR52K3P	CpG island
ENSG00000226616	chromatin interactions
ENSG00000254480	chromatin interactions

Extended variants
information (count: 2793 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:2793 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73432785	chr11:4476181-4476182	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs181921818	chr11:4476182-4476183	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs374706206	chr11:4476196-4476197	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs555090449	chr11:4476205-4476206	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs575369837	chr11:4476207-4476208	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs373531450	chr11:4476209-4476210	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567850784	chr11:4476215-4476216	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538100952	chr11:4476223-4476224	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs185087805	chr11:4476231-4476232	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs58815310	chr11:4476245-4476246	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs571398527	chr11:4476261-4476262	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs1292642	chr11:4476267-4476268	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs368044557	chr11:4476272-4476273	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs11032316	chr11:4476273-4476274	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs572334089	chr11:4476311-4476312	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs542920048	chr11:4476316-4476317	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs554424553	chr11:4476360-4476361	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs576184204	chr11:4476365-4476366	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs189118	chr11:4476397-4476398	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs373171247	chr11:4476407-4476408	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs562627406	chr11:4476409-4476410	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs562064169	chr11:4476434-4476435	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs533280461	chr11:4476441-4476442	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs189829235	chr11:4476452-4476453	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs117476757	chr11:4476504-4476505	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs11032318	chr11:4476526-4476527	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs529199112	chr11:4476528-4476529	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs549646576	chr11:4476559-4476560	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs142922656	chr11:4476615-4476616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs531916581	chr11:4476618-4476619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs181935356	chr11:4476625-4476626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs533864822	chr11:4476646-4476647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs368532882	chr11:4476658-4476659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs538751350	chr11:4476666-4476667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs147752676	chr11:4476693-4476694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs331535	chr11:4476699-4476700	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs568370233	chr11:4476720-4476721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs72854374	chr11:4476731-4476732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs530863629	chr11:4476773-4476774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs548194957	chr11:4476777-4476778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs533348798	chr11:4476786-4476787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs186243413	chr11:4476788-4476789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs576293581	chr11:4476791-4476792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs142624201	chr11:4476823-4476824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs139583036	chr11:4476855-4476856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs112432995	chr11:4476860-4476861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs11032319	chr11:4476880-4476881	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs545101581	chr11:4476894-4476895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs73432791	chr11:4476916-4476917	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs386749995	chr11:4476942-4476943	Weak transcription Enhancers	n/a	n/a	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
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
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:262 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:4470800-4480800	Weak transcription	Ovary	ovary
2	chr11:4471600-4481800	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr11:4473400-4476600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
4	chr11:4475400-4476200	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
5	chr11:4475400-4478000	Enhancers	Primary B cells from cord blood	blood
6	chr11:4475600-4476200	ZNF genes & repeats	NHEK	skin
7	chr11:4475800-4476200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
8	chr11:4475800-4476400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
9	chr11:4475800-4476600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr11:4476000-4476400	Enhancers	Spleen	Spleen
11	chr11:4476200-4477400	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr11:4476400-4477000	Enhancers	Primary neutrophils fromperipheralblood	blood
13	chr11:4476600-4477000	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr11:4476600-4480200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr11:4477000-4477400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
16	chr11:4477000-4478000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
17	chr11:4477200-4477400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr11:4477400-4480600	Enhancers	Primary neutrophils fromperipheralblood	blood
19	chr11:4478000-4481800	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr11:4479400-4483800	Enhancers	Fetal Intestine Small	intestine
21	chr11:4480000-4483600	Enhancers	Fetal Intestine Large	intestine
22	chr11:4480200-4481000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr11:4480200-4481000	Enhancers	Adipose Nuclei	Adipose
24	chr11:4480400-4480600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
25	chr11:4480400-4481000	Enhancers	Primary B cells from peripheral blood	blood
26	chr11:4480600-4481200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
27	chr11:4480600-4481200	Enhancers	HMEC	breast
28	chr11:4480800-4481000	Enhancers	Ovary	ovary
29	chr11:4480800-4481000	Enhancers	Pancreas	Pancrea
30	chr11:4480800-4481800	Enhancers	Left Ventricle	heart
31	chr11:4481000-4481400	Weak transcription	Ovary	ovary
32	chr11:4481000-4485200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr11:4481200-4482200	Enhancers	Primary neutrophils fromperipheralblood	blood
34	chr11:4481400-4482400	Enhancers	Ovary	ovary
35	chr11:4481600-4481800	Enhancers	Pancreas	Pancrea
36	chr11:4481800-4483400	Weak transcription	Monocytes-CD14+_RO01746	blood
37	chr11:4482200-4484400	Weak transcription	Primary neutrophils fromperipheralblood	blood
38	chr11:4483400-4484200	Strong transcription	Monocytes-CD14+_RO01746	blood
39	chr11:4484200-4486200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr11:4484200-4487000	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
41	chr11:4484400-4484600	Enhancers	H1 Cell Line	embryonic stem cell
42	chr11:4484400-4486400	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
43	chr11:4484600-4485600	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr11:4484800-4486400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
45	chr11:4485200-4487200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr11:4485600-4485800	ZNF genes & repeats	NHEK	skin
47	chr11:4485600-4487800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
48	chr11:4485600-4488600	Enhancers	H1 Cell Line	embryonic stem cell
49	chr11:4485800-4486000	Enhancers	H9 Cell Line	embryonic stem cell
50	chr11:4486000-4490000	Enhancers	Fetal Intestine Small	intestine

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