Variant report

Variant	nsv555712
Chromosome Location	chr11:86961994-87007030
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:495)
CpG islands
(count:61)
Chromatin interactive
region (count:19)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:495 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:87001358-87001863	HepG2	liver:	n/a	chr11:87001403-87001419
2	ARID3A	chr11:87001268-87001774	K562	blood:	n/a	chr11:87001403-87001419
3	ATF1	chr11:87001481-87001810	K562	blood:	n/a	n/a
4	ATF1	chr11:86977830-86978145	K562	blood:	n/a	n/a
5	ATF1	chr11:86992567-86992847	K562	blood:	n/a	n/a
6	ATF3	chr11:86977766-86978150	K562	blood:	n/a	n/a
7	BCL11A	chr11:87006356-87006585	GM12878	blood:	n/a	n/a
8	CEBPB	chr11:86977861-86978136	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr11:86974061-86974261	HepG2	liver:	n/a	n/a
10	CEBPB	chr11:86974570-86974776	H1-hESC	embryonic stem cell:	n/a	chr11:86974644-86974655
11	CEBPB	chr11:86977827-86978105	MCF-7	breast:	n/a	n/a
12	CEBPB	chr11:87001405-87001933	Hela-S3	cervix:	n/a	chr11:87001779-87001790 chr11:87001778-87001791 chr11:87001778-87001791
13	CEBPB	chr11:86992567-86992933	K562	blood:	n/a	n/a
14	CEBPB	chr11:86993269-86993392	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr11:86970973-86971267	K562	blood:	n/a	chr11:86971129-86971142 chr11:86971129-86971140 chr11:86971129-86971142
16	CEBPB	chr11:86992611-86992934	A549	lung:	n/a	n/a
17	CEBPB	chr11:86977799-86978091	K562	blood:	n/a	n/a
18	CEBPB	chr11:86992591-86992884	ECC-1	luminal epithelium:	n/a	n/a
19	CEBPB	chr11:87001530-87001960	K562	blood:	n/a	chr11:87001779-87001790 chr11:87001778-87001791 chr11:87001778-87001791
20	CEBPB	chr11:87001609-87001929	HepG2	liver:	n/a	chr11:87001779-87001790 chr11:87001778-87001791 chr11:87001778-87001791
21	CEBPB	chr11:87001595-87001911	A549	lung:	n/a	chr11:87001779-87001790 chr11:87001778-87001791 chr11:87001778-87001791
22	CEBPB	chr11:86977783-86978174	K562	blood:	n/a	n/a
23	CEBPB	chr11:86992544-86992955	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr11:86974537-86974813	HepG2	liver:	n/a	chr11:86974644-86974655
25	CEBPB	chr11:86977749-86978195	K562	blood:	n/a	n/a
26	CEBPB	chr11:86977736-86978248	HCT-116	colon:	n/a	n/a
27	CEBPB	chr11:86993291-86993456	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr11:86974464-86974806	IMR90	lung:	n/a	chr11:86974644-86974655
29	CEBPB	chr11:86977825-86978102	HepG2	liver:	n/a	n/a
30	CEBPB	chr11:86992654-86992869	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr11:86991276-86991459	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr11:86994770-86994961	K562	blood:	n/a	n/a
33	CEBPB	chr11:86992557-86993003	MCF-7	breast:	n/a	n/a
34	CEBPB	chr11:86992442-86993035	A549	lung:	n/a	n/a
35	CEBPB	chr11:86974494-86974836	K562	blood:	n/a	chr11:86974644-86974655
36	CEBPB	chr11:86992559-86992923	IMR90	lung:	n/a	n/a
37	CEBPB	chr11:86974581-86974794	Hela-S3	cervix:	n/a	chr11:86974644-86974655
38	CEBPB	chr11:86973934-86974184	K562	blood:	n/a	n/a
39	CEBPB	chr11:87001596-87001812	H1-hESC	embryonic stem cell:	n/a	chr11:87001779-87001790 chr11:87001778-87001791 chr11:87001778-87001791
40	CEBPB	chr11:86992542-86992851	K562	blood:	n/a	n/a
41	CEBPB	chr11:86974550-86974809	A549	lung:	n/a	chr11:86974644-86974655
42	CTCF	chr11:87001440-87001590	HVMF	connective:	n/a	chr11:87001524-87001545 chr11:87001530-87001546 chr11:87001529-87001547
43	CTCF	chr11:87001319-87001774	MCF-7	breast:	n/a	chr11:87001524-87001545 chr11:87001530-87001546 chr11:87001529-87001547
44	CTCF	chr11:86992680-86992830	HVMF	connective:	n/a	n/a
45	CTCF	chr11:87001408-87001661	HUVEC	blood vessel:	n/a	chr11:87001524-87001545 chr11:87001530-87001546 chr11:87001529-87001547
46	CTCF	chr11:87002240-87002390	BE2_C	brain:	n/a	n/a
47	CTCF	chr11:86991820-86991970	AG10803	skin:	n/a	n/a
48	CTCF	chr11:86992620-86992770	A549	lung:	n/a	n/a
49	CTCF	chr11:87001491-87001538	MCF-7	breast:	n/a	n/a
50	CTCF	chr11:87001480-87001630	AG09309	skin:	n/a	chr11:87001524-87001545 chr11:87001530-87001546 chr11:87001529-87001547

(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	T-47D	breast:	n/a
3	chr11:87002864-87002914	NH-A	brain:	n/a
4	chr11:87002864-87002914	HUVEC	blood vessel:	n/a
5	chr11:87002864-87002914	Jurkat	blood:	n/a
6	chr11:87002864-87002914	HCT-116	colon:	n/a
7	chr11:87002864-87002914	HRPEpiC	eye:	n/a
8	chr11:87002864-87002914	GM12892	blood:	n/a
9	chr11:87002864-87002914	U87	brain:	n/a
10	chr11:87002864-87002914	BJ	skin:	n/a
11	chr11:87002864-87002914	MCF-7	breast:	n/a
12	chr11:87002864-87002914	NB4	blood:	n/a
13	chr11:87002864-87002914	HPAEpiC	pulmonary alveolar:	n/a
14	chr11:87002864-87002914	RPTEC	kidney:	n/a
15	chr11:87002864-87002914	PANC-1	pancreas:	n/a
16	chr11:87002864-87002914	AG04449	skin:	fetal
17	chr11:87002864-87002914	HEK293	kidney:	embryo
18	chr11:87002864-87002914	HAEpiC	amniotic membrane:	n/a
19	chr11:87002864-87002914	SK-N-MC	brain:	n/a
20	chr11:87002864-87002914	HCM	heart:	n/a
21	chr11:87002864-87002914	HRE	kidney:	n/a
22	chr11:87002864-87002914	ECC-1	luminal epithelium:	n/a
23	chr11:87002864-87002914	HMEC	breast:	n/a
24	chr11:87002864-87002914	LNCaP	prostate:	n/a
25	chr11:87002864-87002914	ProgFib	skin:	n/a
26	chr11:87002864-87002914	GM12878	blood:	n/a
27	chr11:87002864-87002914	NHBE	bronchial:	n/a
28	chr11:87002864-87002914	BE2_C	brain:	n/a
29	chr11:87002864-87002914	NHDF-neo	bronchial:	n/a
30	chr11:87002864-87002914	HCPEpiC	choroid plexus:	n/a
31	chr11:87002864-87002914	HEEpiC	esophagus:	n/a
32	chr11:87002864-87002914	Hepatocyte	liver:	n/a
33	chr11:87002864-87002914	HL-60	blood:	n/a
34	chr11:87002864-87002914	CMK	blood:	n/a
35	chr11:87002864-87002914	NT2-D1	testis:	n/a
36	chr11:87002864-87002914	H1-hESC	embryonic stem cell:	embryo
37	chr11:87002864-87002914	AG10803	skin:	n/a
38	chr11:87002864-87002914	ovcar-3	ovarian:	n/a
39	chr11:87002864-87002914	AG09309	skin:	n/a
40	chr11:87002864-87002914	HCF	heart:	n/a
41	chr11:87002864-87002914	SK-N-SH_RA	brain:	n/a
42	chr11:87002864-87002914	HIPEpiC	eye:	n/a
43	chr11:87002864-87002914	GM12891	blood:	n/a
44	chr11:87002864-87002914	A549	lung:	n/a
45	chr11:87002864-87002914	Caco-2	colon:	n/a
46	chr11:87002864-87002914	GM06990	blood:	n/a
47	chr11:87002864-87002914	PFSK-1	brain:	n/a
48	chr11:87002864-87002914	AoSMC	blood vessel:	n/a
49	chr11:87002864-87002914	HRCEpiC	kidney:	n/a
50	chr11:87002864-87002914	SKMC	muscle:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:86991946..86992672-chr5:176296643..176297235,2	MCF-7	breast:
2	chr11:86977540..86979356-chr11:86980303..86982155,2	MCF-7	breast:
3	chr11:86664990..86667056-chr11:86996903..86999848,2	K562	blood:
4	chr11:86664953..86668319-chr11:86999800..87002548,3	MCF-7	breast:
5	chr11:87001464..87002001-chr7:75943410..75944161,2	K562	blood:
6	chr11:86166836..86167387-chr11:87001058..87001771,2	K562	blood:
7	chr11:86996729..86999242-chr11:87005313..87006882,2	MCF-7	breast:
8	chr11:86710137..86711956-chr11:86990366..86992245,2	MCF-7	breast:
9	chr11:86972962..86974479-chr11:86976089..86977632,2	MCF-7	breast:
10	chr11:86641346..86643236-chr11:86990430..86992858,2	K562	blood:
11	chr11:86996729..86999242-chr11:87005313..87006882,2	MCF-7	breast:
12	chr11:86665223..86667347-chr11:87003604..87005762,3	MCF-7	breast:
13	chr11:86806619..86807569-chr11:86992272..86993052,3	MCF-7	breast:
14	chr11:86580752..86581690-chr11:87001116..87001998,4	K562	blood:
15	chr11:86977540..86979356-chr11:86980303..86982155,2	MCF-7	breast:
16	chr11:87006858..87009141-chr11:87011283..87013131,2	K562	blood:
17	chr11:86664855..86666701-chr11:87000839..87002926,2	MCF-7	breast:
18	chr11:86972962..86974479-chr11:86976089..86977632,2	MCF-7	breast:
19	chr11:86650138..86651130-chr11:87001040..87002269,8	K562	blood:

(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: 1944 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1944 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs470706	chr11:86961994-86961995	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs561524233	chr11:86962011-86962012	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530431478	chr11:86962037-86962038	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs371598664	chr11:86962041-86962042	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs550368864	chr11:86962054-86962055	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs470751	chr11:86962071-86962072	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs531289194	chr11:86962183-86962184	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs551492979	chr11:86962194-86962195	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs571150655	chr11:86962199-86962200	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs533731429	chr11:86962229-86962230	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs11427194	chr11:86962245-86962246	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs67968550	chr11:86962246-86962247	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547096407	chr11:86962282-86962283	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567197691	chr11:86962288-86962289	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554554	chr11:86962312-86962313	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs35867886	chr11:86962325-86962326	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs555925952	chr11:86962342-86962343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs575874846	chr11:86962368-86962369	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs657917	chr11:86962378-86962379	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs188942100	chr11:86962379-86962380	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs191642619	chr11:86962413-86962414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs34706284	chr11:86962433-86962434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs541380683	chr11:86962480-86962481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs183492256	chr11:86962486-86962487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs575162374	chr11:86962502-86962503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs658369	chr11:86962505-86962506	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs187987146	chr11:86962519-86962520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs531240438	chr11:86962547-86962548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs369356867	chr11:86962575-86962576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs373496198	chr11:86962623-86962624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs532146516	chr11:86962624-86962625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs56719759	chr11:86962641-86962642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs67208988	chr11:86962644-86962645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs201308006	chr11:86962645-86962646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs470777	chr11:86962663-86962664	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs527420254	chr11:86962742-86962743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs487427	chr11:86962750-86962751	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs191671742	chr11:86962772-86962773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs149652180	chr11:86962796-86962797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs536133893	chr11:86962816-86962817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs376352354	chr11:86962817-86962818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs117859220	chr11:86962855-86962856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs528069	chr11:86962871-86962872	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs183765977	chr11:86962914-86962915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs531938066	chr11:86962927-86962928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs660930	chr11:86962985-86962986	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs571807767	chr11:86962997-86962998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs373740799	chr11:86963052-86963053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs79575736	chr11:86963059-86963060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs112428526	chr11:86963104-86963105	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:336 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:86960600-86962000	Weak transcription	Rectal Smooth Muscle	rectum
2	chr11:86961400-86967800	Weak transcription	NHDF-Ad	bronchial
3	chr11:86962000-86962600	Enhancers	Rectal Smooth Muscle	rectum
4	chr11:86962000-86963000	Enhancers	Colon Smooth Muscle	Colon
5	chr11:86962200-86962400	Enhancers	Primary T cells from cord blood	blood
6	chr11:86962200-86962400	Enhancers	Aorta	Aorta
7	chr11:86962200-86962600	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr11:86962400-86972000	Weak transcription	Primary T cells from cord blood	blood
9	chr11:86962600-86963000	Weak transcription	Rectal Smooth Muscle	rectum
10	chr11:86962600-86963600	Weak transcription	Aorta	Aorta
11	chr11:86962800-86963000	Enhancers	HUVEC	blood vessel
12	chr11:86962800-86963200	Enhancers	Adipose Nuclei	Adipose
13	chr11:86962800-86977600	Weak transcription	K562	blood
14	chr11:86963000-86963200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr11:86963000-86963200	Enhancers	Rectal Smooth Muscle	rectum
16	chr11:86963000-86963600	Weak transcription	HUVEC	blood vessel
17	chr11:86963000-86976200	Weak transcription	Colon Smooth Muscle	Colon
18	chr11:86963200-86963400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr11:86963200-86965800	Weak transcription	Rectal Smooth Muscle	rectum
20	chr11:86963200-86969400	Weak transcription	Adipose Nuclei	Adipose
21	chr11:86963400-86963800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
22	chr11:86963400-86963800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr11:86963600-86964400	Enhancers	HUVEC	blood vessel
24	chr11:86963800-86964400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr11:86963800-86964600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr11:86964000-86964200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr11:86964000-86964400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr11:86964400-86966200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr11:86964400-86969400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr11:86964400-86969400	Weak transcription	HUVEC	blood vessel
31	chr11:86964400-86970800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr11:86964600-86970800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr11:86965800-86966600	Enhancers	Rectal Smooth Muscle	rectum
34	chr11:86965800-86966600	Enhancers	Right Atrium	heart
35	chr11:86966200-86966600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr11:86966200-86966600	Enhancers	Pancreas	Pancrea
37	chr11:86966200-86966800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr11:86966200-86966800	Enhancers	Thymus	Thymus
39	chr11:86966200-86967000	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr11:86966400-86966800	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr11:86966400-86966800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr11:86966400-86966800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr11:86966600-86969400	Weak transcription	Right Atrium	heart
44	chr11:86966600-86970400	Weak transcription	Pancreas	Pancrea
45	chr11:86966800-86968400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr11:86966800-86968800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr11:86966800-86970800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr11:86967000-86968000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
49	chr11:86967000-86975400	Weak transcription	HepG2	liver
50	chr11:86967800-86968000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links