Variant report

Variant	nsv898073
Chromosome Location	chr11:86963330-87013438
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:555)
CpG islands
(count:61)
Chromatin interactive
region (count:22)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:555 , 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	chr11:87011415-87011637	K562	blood:	n/a	n/a
2	ARID3A	chr11:87001268-87001774	K562	blood:	n/a	chr11:87001403-87001419
3	ARID3A	chr11:87001358-87001863	HepG2	liver:	n/a	chr11:87001403-87001419
4	ATF1	chr11:86992567-86992847	K562	blood:	n/a	n/a
5	ATF1	chr11:86977830-86978145	K562	blood:	n/a	n/a
6	ATF1	chr11:87001481-87001810	K562	blood:	n/a	n/a
7	ATF3	chr11:86977766-86978150	K562	blood:	n/a	n/a
8	BACH1	chr11:87013438-87013541	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL11A	chr11:87006356-87006585	GM12878	blood:	n/a	n/a
10	CCNT2	chr11:87011981-87012237	K562	blood:	n/a	n/a
11	CEBPB	chr11:86992654-86992869	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr11:87010057-87010151	K562	blood:	n/a	n/a
13	CEBPB	chr11:87001596-87001812	H1-hESC	embryonic stem cell:	n/a	chr11:87001779-87001790 chr11:87001778-87001791 chr11:87001778-87001791
14	CEBPB	chr11:86974464-86974806	IMR90	lung:	n/a	chr11:86974644-86974655
15	CEBPB	chr11:86974570-86974776	H1-hESC	embryonic stem cell:	n/a	chr11:86974644-86974655
16	CEBPB	chr11:86992567-86992933	K562	blood:	n/a	n/a
17	CEBPB	chr11:86992557-86993003	MCF-7	breast:	n/a	n/a
18	CEBPB	chr11:86974550-86974809	A549	lung:	n/a	chr11:86974644-86974655
19	CEBPB	chr11:86994770-86994961	K562	blood:	n/a	n/a
20	CEBPB	chr11:87001595-87001911	A549	lung:	n/a	chr11:87001779-87001790 chr11:87001778-87001791 chr11:87001778-87001791
21	CEBPB	chr11:86992442-86993035	A549	lung:	n/a	n/a
22	CEBPB	chr11:86992559-86992923	IMR90	lung:	n/a	n/a
23	CEBPB	chr11:86993269-86993392	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr11:86974581-86974794	Hela-S3	cervix:	n/a	chr11:86974644-86974655
25	CEBPB	chr11:86977799-86978091	K562	blood:	n/a	n/a
26	CEBPB	chr11:86992542-86992851	K562	blood:	n/a	n/a
27	CEBPB	chr11:86970973-86971267	K562	blood:	n/a	chr11:86971129-86971142 chr11:86971129-86971140 chr11:86971129-86971142
28	CEBPB	chr11:87001609-87001929	HepG2	liver:	n/a	chr11:87001779-87001790 chr11:87001778-87001791 chr11:87001778-87001791
29	CEBPB	chr11:86977749-86978195	K562	blood:	n/a	n/a
30	CEBPB	chr11:86992591-86992884	ECC-1	luminal epithelium:	n/a	n/a
31	CEBPB	chr11:87001530-87001960	K562	blood:	n/a	chr11:87001779-87001790 chr11:87001778-87001791 chr11:87001778-87001791
32	CEBPB	chr11:86974061-86974261	HepG2	liver:	n/a	n/a
33	CEBPB	chr11:86977783-86978174	K562	blood:	n/a	n/a
34	CEBPB	chr11:87008727-87009034	HepG2	liver:	n/a	n/a
35	CEBPB	chr11:86977825-86978102	HepG2	liver:	n/a	n/a
36	CEBPB	chr11:87008716-87009063	A549	lung:	n/a	n/a
37	CEBPB	chr11:86992611-86992934	A549	lung:	n/a	n/a
38	CEBPB	chr11:86977861-86978136	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr11:86992544-86992955	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr11:86974494-86974836	K562	blood:	n/a	chr11:86974644-86974655
41	CEBPB	chr11:86977827-86978105	MCF-7	breast:	n/a	n/a
42	CEBPB	chr11:86991276-86991459	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr11:86973934-86974184	K562	blood:	n/a	n/a
44	CEBPB	chr11:86993291-86993456	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr11:87001405-87001933	Hela-S3	cervix:	n/a	chr11:87001779-87001790 chr11:87001778-87001791 chr11:87001778-87001791
46	CEBPB	chr11:86977736-86978248	HCT-116	colon:	n/a	n/a
47	CEBPB	chr11:86974537-86974813	HepG2	liver:	n/a	chr11:86974644-86974655
48	CTCF	chr11:86992560-86992710	HRE	kidney:	n/a	n/a
49	CTCF	chr11:87001460-87001610	HPF	lung:	n/a	chr11:87001524-87001545 chr11:87001530-87001546 chr11:87001529-87001547
50	CTCF	chr11:87001460-87001610	HPAF	blood vessel:	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	T-47D	breast:	n/a
2	chr11:87002864-87002914	GM12878	blood:	n/a
3	chr11:87002864-87002914	ovcar-3	ovarian:	n/a
4	chr11:87002864-87002914	HNPCEpiC	eye:	n/a
5	chr11:87002864-87002914	NT2-D1	testis:	n/a
6	chr11:87002864-87002914	HRE	kidney:	n/a
7	chr11:87002864-87002914	HMEC	breast:	n/a
8	chr11:87002864-87002914	GM12892	blood:	n/a
9	chr11:87002864-87002914	ProgFib	skin:	n/a
10	chr11:87002864-87002914	GM19239	blood:	n/a
11	chr11:87002864-87002914	Hepatocyte	liver:	n/a
12	chr11:87002864-87002914	GM12891	blood:	n/a
13	chr11:87002864-87002914	HRPEpiC	eye:	n/a
14	chr11:87002864-87002914	SK-N-SH	brain:	n/a
15	chr11:87002864-87002914	SK-N-SH_RA	brain:	n/a
16	chr11:87002864-87002914	AG09309	skin:	n/a
17	chr11:87002864-87002914	HAEpiC	amniotic membrane:	n/a
18	chr11:87002864-87002914	NHBE	bronchial:	n/a
19	chr11:87002864-87002914	RPTEC	kidney:	n/a
20	chr11:87002864-87002914	PANC-1	pancreas:	n/a
21	chr11:87002864-87002914	PrEC	prostate:	n/a
22	chr11:87002864-87002914	SKMC	muscle:	n/a
23	chr11:87002864-87002914	NH-A	brain:	n/a
24	chr11:87002864-87002914	Hela-S3	cervix:	n/a
25	chr11:87002864-87002914	PFSK-1	brain:	n/a
26	chr11:87002864-87002914	HRCEpiC	kidney:	n/a
27	chr11:87002864-87002914	HUVEC	blood vessel:	n/a
28	chr11:87002864-87002914	SK-N-MC	brain:	n/a
29	chr11:87002864-87002914	CMK	blood:	n/a
30	chr11:87002864-87002914	K562	blood:	n/a
31	chr11:87002864-87002914	AoSMC	blood vessel:	n/a
32	chr11:87002864-87002914	GM06990	blood:	n/a
33	chr11:87002864-87002914	IMR90	lung:	fetal
34	chr11:87002864-87002914	LNCaP	prostate:	n/a
35	chr11:87002864-87002914	H1-hESC	embryonic stem cell:	embryo
36	chr11:87002864-87002914	HCF	heart:	n/a
37	chr11:87002864-87002914	AG09319	gingival:	n/a
38	chr11:87002864-87002914	HCPEpiC	choroid plexus:	n/a
39	chr11:87002864-87002914	Caco-2	colon:	n/a
40	chr11:87002864-87002914	A549	lung:	n/a
41	chr11:87002864-87002914	HIPEpiC	eye:	n/a
42	chr11:87002864-87002914	BE2_C	brain:	n/a
43	chr11:87002864-87002914	HCM	heart:	n/a
44	chr11:87002864-87002914	ECC-1	luminal epithelium:	n/a
45	chr11:87002864-87002914	HCT-116	colon:	n/a
46	chr11:87002864-87002914	HL-60	blood:	n/a
47	chr11:87002864-87002914	BJ	skin:	n/a
48	chr11:87002864-87002914	HEK293	kidney:	embryo
49	chr11:87002864-87002914	AG04449	skin:	fetal
50	chr11:87002864-87002914	HPAEpiC	pulmonary alveolar:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:86664953..86668319-chr11:86999800..87002548,3	MCF-7	breast:
2	chr11:86996729..86999242-chr11:87005313..87006882,2	MCF-7	breast:
3	chr11:86664990..86667056-chr11:86996903..86999848,2	K562	blood:
4	chr11:86641346..86643236-chr11:86990430..86992858,2	K562	blood:
5	chr11:86972962..86974479-chr11:86976089..86977632,2	MCF-7	breast:
6	chr11:86972962..86974479-chr11:86976089..86977632,2	MCF-7	breast:
7	chr11:86805484..86807360-chr11:87007311..87009404,2	MCF-7	breast:
8	chr11:86996729..86999242-chr11:87005313..87006882,2	MCF-7	breast:
9	chr11:86977540..86979356-chr11:86980303..86982155,2	MCF-7	breast:
10	chr11:87006858..87009141-chr11:87011283..87013131,2	K562	blood:
11	chr11:86665223..86667347-chr11:87003604..87005762,3	MCF-7	breast:
12	chr11:86977540..86979356-chr11:86980303..86982155,2	MCF-7	breast:
13	chr11:86689677..86690529-chr11:87011689..87012195,2	MCF-7	breast:
14	chr11:86806619..86807569-chr11:86992272..86993052,3	MCF-7	breast:
15	chr11:86664855..86666701-chr11:87000839..87002926,2	MCF-7	breast:
16	chr11:87006858..87009141-chr11:87011283..87013131,2	K562	blood:
17	chr11:86710137..86711956-chr11:86990366..86992245,2	MCF-7	breast:
18	chr11:86580752..86581690-chr11:87001116..87001998,4	K562	blood:
19	chr11:86650138..86651130-chr11:87001040..87002269,8	K562	blood:
20	chr11:86166836..86167387-chr11:87001058..87001771,2	K562	blood:
21	chr11:87001464..87002001-chr7:75943410..75944161,2	K562	blood:
22	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: 2135 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:2135 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55804852	chr11:86963330-86963331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs185651624	chr11:86963351-86963352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs529597560	chr11:86963363-86963364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs575837604	chr11:86963391-86963392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs200092538	chr11:86963435-86963436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs558445693	chr11:86963445-86963446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs549375133	chr11:86963484-86963485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs190508952	chr11:86963497-86963498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577037539	chr11:86963504-86963505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs117022469	chr11:86963535-86963536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs552326099	chr11:86963540-86963541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs565769503	chr11:86963575-86963576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs535110634	chr11:86963585-86963586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs555144910	chr11:86963591-86963592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs568569028	chr11:86963665-86963666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs138694253	chr11:86963670-86963671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs557416135	chr11:86963695-86963696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs181762821	chr11:86963706-86963707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs185101460	chr11:86963709-86963710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs546215543	chr11:86963711-86963712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs149268891	chr11:86963727-86963728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs1996498	chr11:86963730-86963731	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs542022829	chr11:86963735-86963736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs10898645	chr11:86963750-86963751	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs541991054	chr11:86963779-86963780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs71460028	chr11:86963807-86963808	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs3936715	chr11:86963808-86963809	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs147892243	chr11:86963830-86963831	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs375507776	chr11:86963833-86963834	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs201923278	chr11:86963835-86963836	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558272693	chr11:86963840-86963841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs68000889	chr11:86963841-86963842	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs11235043	chr11:86963842-86963843	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs374948513	chr11:86963921-86963922	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs563164094	chr11:86963930-86963931	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs10501633	chr11:86963938-86963939	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs571929678	chr11:86964001-86964002	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200256074	chr11:86964075-86964076	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs532728434	chr11:86964076-86964077	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs141736806	chr11:86964078-86964079	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs495847	chr11:86964118-86964119	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs35501796	chr11:86964159-86964160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs369964037	chr11:86964166-86964167	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs528247052	chr11:86964177-86964178	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs188830283	chr11:86964199-86964200	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs114075643	chr11:86964246-86964247	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs377645513	chr11:86964338-86964339	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs687197	chr11:86964357-86964358	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs199705600	chr11:86964386-86964387	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs666043	chr11:86964415-86964416	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:493 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:86961400-86967800	Weak transcription	NHDF-Ad	bronchial
2	chr11:86962400-86972000	Weak transcription	Primary T cells from cord blood	blood
3	chr11:86962600-86963600	Weak transcription	Aorta	Aorta
4	chr11:86962800-86977600	Weak transcription	K562	blood
5	chr11:86963000-86963600	Weak transcription	HUVEC	blood vessel
6	chr11:86963000-86976200	Weak transcription	Colon Smooth Muscle	Colon
7	chr11:86963200-86963400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr11:86963200-86965800	Weak transcription	Rectal Smooth Muscle	rectum
9	chr11:86963200-86969400	Weak transcription	Adipose Nuclei	Adipose
10	chr11:86963400-86963800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
11	chr11:86963400-86963800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr11:86963600-86964400	Enhancers	HUVEC	blood vessel
13	chr11:86963800-86964400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr11:86963800-86964600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr11:86964000-86964200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr11:86964000-86964400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr11:86964400-86966200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr11:86964400-86969400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr11:86964400-86969400	Weak transcription	HUVEC	blood vessel
20	chr11:86964400-86970800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr11:86964600-86970800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr11:86965800-86966600	Enhancers	Rectal Smooth Muscle	rectum
23	chr11:86965800-86966600	Enhancers	Right Atrium	heart
24	chr11:86966200-86966600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr11:86966200-86966600	Enhancers	Pancreas	Pancrea
26	chr11:86966200-86966800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr11:86966200-86966800	Enhancers	Thymus	Thymus
28	chr11:86966200-86967000	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr11:86966400-86966800	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr11:86966400-86966800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr11:86966400-86966800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr11:86966600-86969400	Weak transcription	Right Atrium	heart
33	chr11:86966600-86970400	Weak transcription	Pancreas	Pancrea
34	chr11:86966800-86968400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr11:86966800-86968800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr11:86966800-86970800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr11:86967000-86968000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr11:86967000-86975400	Weak transcription	HepG2	liver
39	chr11:86967800-86968000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr11:86967800-86968200	Enhancers	Osteobl	bone
41	chr11:86967800-86968400	Enhancers	NHDF-Ad	bronchial
42	chr11:86968000-86970000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr11:86968000-86971400	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr11:86968200-86969400	Weak transcription	Aorta	Aorta
45	chr11:86968200-86971800	Weak transcription	Osteobl	bone
46	chr11:86968400-86969400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr11:86968400-86972000	Weak transcription	NHDF-Ad	bronchial
48	chr11:86968800-86970400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr11:86968800-86971000	Weak transcription	Fetal Lung	lung
50	chr11:86969200-86972200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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