Variant report

Variant	nsv898068
Chromosome Location	chr11:86930270-87005969
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:576)
CpG islands
(count:61)
Chromatin interactive
region (count:21)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:576 , 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	ARID3A	chr11:87001268-87001774	K562	blood:	n/a	chr11:87001403-87001419
2	ARID3A	chr11:86944770-86944904	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:87001358-87001863	HepG2	liver:	n/a	chr11:87001403-87001419
4	ATF1	chr11:86977830-86978145	K562	blood:	n/a	n/a
5	ATF1	chr11:87001481-87001810	K562	blood:	n/a	n/a
6	ATF1	chr11:86992567-86992847	K562	blood:	n/a	n/a
7	ATF3	chr11:86977766-86978150	K562	blood:	n/a	n/a
8	BACH1	chr11:86950832-86950861	K562	blood:	n/a	n/a
9	CBX3	chr11:86943417-86943753	K562	blood:	n/a	n/a
10	CEBPB	chr11:86992591-86992884	ECC-1	luminal epithelium:	n/a	n/a
11	CEBPB	chr11:86970973-86971267	K562	blood:	n/a	chr11:86971129-86971142 chr11:86971129-86971140 chr11:86971129-86971142
12	CEBPB	chr11:86992611-86992934	A549	lung:	n/a	n/a
13	CEBPB	chr11:86992542-86992851	K562	blood:	n/a	n/a
14	CEBPB	chr11:86992557-86993003	MCF-7	breast:	n/a	n/a
15	CEBPB	chr11:86973934-86974184	K562	blood:	n/a	n/a
16	CEBPB	chr11:86992654-86992869	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr11:86974061-86974261	HepG2	liver:	n/a	n/a
18	CEBPB	chr11:86943439-86943477	A549	lung:	n/a	n/a
19	CEBPB	chr11:86977827-86978105	MCF-7	breast:	n/a	n/a
20	CEBPB	chr11:86992544-86992955	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr11:86977736-86978248	HCT-116	colon:	n/a	n/a
22	CEBPB	chr11:86974581-86974794	Hela-S3	cervix:	n/a	chr11:86974644-86974655
23	CEBPB	chr11:86974464-86974806	IMR90	lung:	n/a	chr11:86974644-86974655
24	CEBPB	chr11:86943362-86943506	K562	blood:	n/a	n/a
25	CEBPB	chr11:86977825-86978102	HepG2	liver:	n/a	n/a
26	CEBPB	chr11:86992567-86992933	K562	blood:	n/a	n/a
27	CEBPB	chr11:86974570-86974776	H1-hESC	embryonic stem cell:	n/a	chr11:86974644-86974655
28	CEBPB	chr11:86974550-86974809	A549	lung:	n/a	chr11:86974644-86974655
29	CEBPB	chr11:87001596-87001812	H1-hESC	embryonic stem cell:	n/a	chr11:87001779-87001790 chr11:87001778-87001791 chr11:87001778-87001791
30	CEBPB	chr11:86992442-86993035	A549	lung:	n/a	n/a
31	CEBPB	chr11:86977783-86978174	K562	blood:	n/a	n/a
32	CEBPB	chr11:86977861-86978136	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr11:86977749-86978195	K562	blood:	n/a	n/a
34	CEBPB	chr11:86974537-86974813	HepG2	liver:	n/a	chr11:86974644-86974655
35	CEBPB	chr11:87001609-87001929	HepG2	liver:	n/a	chr11:87001779-87001790 chr11:87001778-87001791 chr11:87001778-87001791
36	CEBPB	chr11:86947578-86947620	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr11:86993291-86993456	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr11:87001405-87001933	Hela-S3	cervix:	n/a	chr11:87001779-87001790 chr11:87001778-87001791 chr11:87001778-87001791
39	CEBPB	chr11:86974494-86974836	K562	blood:	n/a	chr11:86974644-86974655
40	CEBPB	chr11:86994770-86994961	K562	blood:	n/a	n/a
41	CEBPB	chr11:86992559-86992923	IMR90	lung:	n/a	n/a
42	CEBPB	chr11:87001595-87001911	A549	lung:	n/a	chr11:87001779-87001790 chr11:87001778-87001791 chr11:87001778-87001791
43	CEBPB	chr11:86991276-86991459	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr11:87001530-87001960	K562	blood:	n/a	chr11:87001779-87001790 chr11:87001778-87001791 chr11:87001778-87001791
45	CEBPB	chr11:86977799-86978091	K562	blood:	n/a	n/a
46	CEBPB	chr11:86993269-86993392	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr11:86992560-86992710	HRE	kidney:	n/a	n/a
48	CTCF	chr11:87001420-87001570	HCT-116	colon:	n/a	chr11:87001524-87001545 chr11:87001530-87001546 chr11:87001529-87001547
49	CTCF	chr11:87001380-87001530	GM12870	blood:	n/a	n/a
50	CTCF	chr11:86992720-86992870	NHDF-neo	bronchial:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:87002864-87002914	GM19239	blood:	n/a
2	chr11:87002864-87002914	BE2_C	brain:	n/a
3	chr11:87002864-87002914	MCF10A-Er-Src	breast:	n/a
4	chr11:87002864-87002914	AG10803	skin:	n/a
5	chr11:87002864-87002914	HCT-116	colon:	n/a
6	chr11:87002864-87002914	HEEpiC	esophagus:	n/a
7	chr11:87002864-87002914	SK-N-MC	brain:	n/a
8	chr11:87002864-87002914	SK-N-SH	brain:	n/a
9	chr11:87002864-87002914	LNCaP	prostate:	n/a
10	chr11:87002864-87002914	AG09319	gingival:	n/a
11	chr11:87002864-87002914	HCF	heart:	n/a
12	chr11:87002864-87002914	CMK	blood:	n/a
13	chr11:87002864-87002914	AG09309	skin:	n/a
14	chr11:87002864-87002914	NHBE	bronchial:	n/a
15	chr11:87002864-87002914	U87	brain:	n/a
16	chr11:87002864-87002914	HL-60	blood:	n/a
17	chr11:87002864-87002914	K562	blood:	n/a
18	chr11:87002864-87002914	HCPEpiC	choroid plexus:	n/a
19	chr11:87002864-87002914	HMEC	breast:	n/a
20	chr11:87002864-87002914	RPTEC	kidney:	n/a
21	chr11:87002864-87002914	GM12892	blood:	n/a
22	chr11:87002864-87002914	SAEC	small airway:	n/a
23	chr11:87002864-87002914	PFSK-1	brain:	n/a
24	chr11:87002864-87002914	AoSMC	blood vessel:	n/a
25	chr11:87002864-87002914	SKMC	muscle:	n/a
26	chr11:87002864-87002914	NB4	blood:	n/a
27	chr11:87002864-87002914	HNPCEpiC	eye:	n/a
28	chr11:87002864-87002914	HRPEpiC	eye:	n/a
29	chr11:87002864-87002914	A549	lung:	n/a
30	chr11:87002864-87002914	HRCEpiC	kidney:	n/a
31	chr11:87002864-87002914	Caco-2	colon:	n/a
32	chr11:87002864-87002914	HepG2	liver:	n/a
33	chr11:87002864-87002914	SK-N-SH_RA	brain:	n/a
34	chr11:87002864-87002914	ECC-1	luminal epithelium:	n/a
35	chr11:87002864-87002914	HIPEpiC	eye:	n/a
36	chr11:87002864-87002914	AG04450	lung:	fetal
37	chr11:87002864-87002914	HUVEC	blood vessel:	n/a
38	chr11:87002864-87002914	HPAEpiC	pulmonary alveolar:	n/a
39	chr11:87002864-87002914	NT2-D1	testis:	n/a
40	chr11:87002864-87002914	Jurkat	blood:	n/a
41	chr11:87002864-87002914	PrEC	prostate:	n/a
42	chr11:87002864-87002914	NH-A	brain:	n/a
43	chr11:87002864-87002914	Hepatocyte	liver:	n/a
44	chr11:87002864-87002914	PANC-1	pancreas:	n/a
45	chr11:87002864-87002914	BJ	skin:	n/a
46	chr11:87002864-87002914	ProgFib	skin:	n/a
47	chr11:87002864-87002914	GM06990	blood:	n/a
48	chr11:87002864-87002914	HAEpiC	amniotic membrane:	n/a
49	chr11:87002864-87002914	Hela-S3	cervix:	n/a
50	chr11:87002864-87002914	ovcar-3	ovarian:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:86936889..86939702-chr11:86940206..86942335,2	K562	blood:
2	chr11:86977540..86979356-chr11:86980303..86982155,2	MCF-7	breast:
3	chr11:86664953..86668319-chr11:86999800..87002548,3	MCF-7	breast:
4	chr11:86166836..86167387-chr11:87001058..87001771,2	K562	blood:
5	chr11:86664990..86667056-chr11:86996903..86999848,2	K562	blood:
6	chr11:86664855..86666701-chr11:87000839..87002926,2	MCF-7	breast:
7	chr11:86972962..86974479-chr11:86976089..86977632,2	MCF-7	breast:
8	chr11:86650138..86651130-chr11:87001040..87002269,8	K562	blood:
9	chr11:86665223..86667347-chr11:87003604..87005762,3	MCF-7	breast:
10	chr11:86806619..86807569-chr11:86992272..86993052,3	MCF-7	breast:
11	chr11:87001464..87002001-chr7:75943410..75944161,2	K562	blood:
12	chr11:86996729..86999242-chr11:87005313..87006882,2	MCF-7	breast:
13	chr11:86641346..86643236-chr11:86990430..86992858,2	K562	blood:
14	chr11:86996729..86999242-chr11:87005313..87006882,2	MCF-7	breast:
15	chr11:86977540..86979356-chr11:86980303..86982155,2	MCF-7	breast:
16	chr11:86924206..86926245-chr11:86930378..86932580,2	K562	blood:
17	chr11:86580752..86581690-chr11:87001116..87001998,4	K562	blood:
18	chr11:86936889..86939702-chr11:86940206..86942335,2	K562	blood:
19	chr11:86710137..86711956-chr11:86990366..86992245,2	MCF-7	breast:
20	chr11:86972962..86974479-chr11:86976089..86977632,2	MCF-7	breast:
21	chr11:86991946..86992672-chr5:176296643..176297235,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FZD4-8	chr11:86969893-86970301	NONHSAT023515

No data

Variant related genes	Relation type
ENSG00000213287	TF binding region
ENSG00000213287	CpG island
ENSG00000246523	chromatin interactions
ENSG00000174804	chromatin interactions

Extended variants
information (count: 2887 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:2887 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542279	chr11:86930270-86930271	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs113349987	chr11:86930285-86930286	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs151248072	chr11:86930286-86930287	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs112219151	chr11:86930326-86930327	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs187137869	chr11:86930332-86930333	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs79403926	chr11:86930340-86930341	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs76787607	chr11:86930362-86930363	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs201507479	chr11:86930407-86930408	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs559977630	chr11:86930416-86930417	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs564568038	chr11:86930440-86930441	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs140468431	chr11:86930508-86930509	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs189899337	chr11:86930509-86930510	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs369231240	chr11:86930515-86930516	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs552287435	chr11:86930520-86930521	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs570518063	chr11:86930524-86930525	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs529286751	chr11:86930526-86930527	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs528714688	chr11:86930544-86930545	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs563070689	chr11:86930581-86930582	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs531931190	chr11:86930601-86930602	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs551601163	chr11:86930621-86930622	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs539246120	chr11:86930631-86930632	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs518787	chr11:86930637-86930638	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs539097008	chr11:86930688-86930689	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs149986408	chr11:86930693-86930694	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs59448049	chr11:86930705-86930706	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs76852557	chr11:86930757-86930758	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555613818	chr11:86930776-86930777	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs113273597	chr11:86930781-86930782	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs552168187	chr11:86930814-86930815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs538028707	chr11:86930852-86930853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs576425622	chr11:86930910-86930911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs557938918	chr11:86930934-86930935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs577935365	chr11:86930957-86930958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs181694857	chr11:86930963-86930964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs540696403	chr11:86930980-86930981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs186405238	chr11:86931006-86931007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs145916157	chr11:86931024-86931025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs190081074	chr11:86931035-86931036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs368864846	chr11:86931083-86931084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs182299658	chr11:86931084-86931085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs185289397	chr11:86931132-86931133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs551659676	chr11:86931168-86931169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs558628663	chr11:86931181-86931182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs141434392	chr11:86931215-86931216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs76810357	chr11:86931237-86931238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs191190241	chr11:86931247-86931248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs566473467	chr11:86931295-86931296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs373100353	chr11:86931379-86931380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs183812377	chr11:86931402-86931403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs568838721	chr11:86931442-86931443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	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
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	21364760	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	16608533	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Sudden cardiac death	19188705	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ductal carcinoma	22052326	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Attention deficit hyperactivity disorder	22241247	CNVD
Breast cancer	21958427	CNVD
Breast cancer	17133270	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Obesity	20622171	CNVD
Renal cell carcinoma	18194544	CNVD

Chromatin state (count:449 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:86906000-86931000	Weak transcription	Fetal Lung	lung
2	chr11:86915400-86942000	Weak transcription	HepG2	liver
3	chr11:86916000-86931000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr11:86924800-86934800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr11:86926600-86935200	Weak transcription	Fetal Stomach	stomach
6	chr11:86926800-86934600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr11:86927000-86933800	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr11:86929600-86942000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr11:86929800-86930600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr11:86930200-86930800	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr11:86930200-86930800	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr11:86930200-86930800	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr11:86930200-86931000	Enhancers	GM12878-XiMat	blood
14	chr11:86930200-86932600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr11:86930400-86931800	Enhancers	Colon Smooth Muscle	Colon
16	chr11:86930600-86930800	Enhancers	Rectal Smooth Muscle	rectum
17	chr11:86930600-86931200	Enhancers	Osteobl	bone
18	chr11:86930800-86934000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr11:86931000-86931600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr11:86931200-86934600	Weak transcription	Osteobl	bone
21	chr11:86931200-86935600	Weak transcription	Fetal Lung	lung
22	chr11:86931400-86931600	Enhancers	Rectal Smooth Muscle	rectum
23	chr11:86931400-86931800	Enhancers	HSMMtube	muscle
24	chr11:86931600-86935000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr11:86931800-86935000	Weak transcription	Colon Smooth Muscle	Colon
26	chr11:86932600-86935000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr11:86933000-86942800	Weak transcription	Primary B cells from cord blood	blood
28	chr11:86933800-86934200	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr11:86934000-86934200	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr11:86934000-86943600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr11:86934600-86935400	Enhancers	Osteobl	bone
32	chr11:86934600-86935800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr11:86934800-86935800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr11:86935000-86935400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr11:86935000-86935400	Enhancers	Colon Smooth Muscle	Colon
36	chr11:86935000-86935600	Enhancers	Muscle Satellite Cultured Cells	--
37	chr11:86935000-86935600	Enhancers	K562	blood
38	chr11:86935000-86935600	Enhancers	NHLF	lung
39	chr11:86935000-86935800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr11:86935000-86935800	Enhancers	Adipose Nuclei	Adipose
41	chr11:86935000-86935800	Enhancers	NHDF-Ad	bronchial
42	chr11:86935000-86936600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr11:86935200-86935400	Enhancers	Fetal Stomach	stomach
44	chr11:86935200-86935400	Enhancers	Ovary	ovary
45	chr11:86935200-86935800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr11:86935400-86939200	Weak transcription	Colon Smooth Muscle	Colon
47	chr11:86935600-86936400	Enhancers	Fetal Lung	lung
48	chr11:86935800-86937000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr11:86935800-86943000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr11:86936600-86936800	Enhancers	Small Intestine	intestine

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