Variant report

Variant	nsv555713
Chromosome Location	chr11:86971548-87013438
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:525)
CpG islands
(count:61)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:525 , 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	ARID3A	chr11:87001268-87001774	K562	blood:	n/a	chr11:87001403-87001419
2	ARID3A	chr11:87011415-87011637	K562	blood:	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	chr11:86992567-86992847	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	chr11:86974464-86974806	IMR90	lung:	n/a	chr11:86974644-86974655
12	CEBPB	chr11:87001530-87001960	K562	blood:	n/a	chr11:87001779-87001790 chr11:87001778-87001791 chr11:87001778-87001791
13	CEBPB	chr11:86992559-86992923	IMR90	lung:	n/a	n/a
14	CEBPB	chr11:86974550-86974809	A549	lung:	n/a	chr11:86974644-86974655
15	CEBPB	chr11:87008727-87009034	HepG2	liver:	n/a	n/a
16	CEBPB	chr11:86991276-86991459	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr11:86977799-86978091	K562	blood:	n/a	n/a
18	CEBPB	chr11:86977825-86978102	HepG2	liver:	n/a	n/a
19	CEBPB	chr11:86992654-86992869	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr11:87008716-87009063	A549	lung:	n/a	n/a
21	CEBPB	chr11:86992442-86993035	A549	lung:	n/a	n/a
22	CEBPB	chr11:87001405-87001933	Hela-S3	cervix:	n/a	chr11:87001779-87001790 chr11:87001778-87001791 chr11:87001778-87001791
23	CEBPB	chr11:87010057-87010151	K562	blood:	n/a	n/a
24	CEBPB	chr11:86974570-86974776	H1-hESC	embryonic stem cell:	n/a	chr11:86974644-86974655
25	CEBPB	chr11:86992591-86992884	ECC-1	luminal epithelium:	n/a	n/a
26	CEBPB	chr11:86992557-86993003	MCF-7	breast:	n/a	n/a
27	CEBPB	chr11:86974537-86974813	HepG2	liver:	n/a	chr11:86974644-86974655
28	CEBPB	chr11:86992544-86992955	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr11:86992611-86992934	A549	lung:	n/a	n/a
30	CEBPB	chr11:86977861-86978136	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr11:87001595-87001911	A549	lung:	n/a	chr11:87001779-87001790 chr11:87001778-87001791 chr11:87001778-87001791
32	CEBPB	chr11:86992542-86992851	K562	blood:	n/a	n/a
33	CEBPB	chr11:86977736-86978248	HCT-116	colon:	n/a	n/a
34	CEBPB	chr11:86992567-86992933	K562	blood:	n/a	n/a
35	CEBPB	chr11:86977827-86978105	MCF-7	breast:	n/a	n/a
36	CEBPB	chr11:86973934-86974184	K562	blood:	n/a	n/a
37	CEBPB	chr11:86993269-86993392	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr11:87001609-87001929	HepG2	liver:	n/a	chr11:87001779-87001790 chr11:87001778-87001791 chr11:87001778-87001791
39	CEBPB	chr11:87001596-87001812	H1-hESC	embryonic stem cell:	n/a	chr11:87001779-87001790 chr11:87001778-87001791 chr11:87001778-87001791
40	CEBPB	chr11:86993291-86993456	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr11:86974581-86974794	Hela-S3	cervix:	n/a	chr11:86974644-86974655
42	CEBPB	chr11:86974494-86974836	K562	blood:	n/a	chr11:86974644-86974655
43	CEBPB	chr11:86994770-86994961	K562	blood:	n/a	n/a
44	CEBPB	chr11:86977783-86978174	K562	blood:	n/a	n/a
45	CEBPB	chr11:86974061-86974261	HepG2	liver:	n/a	n/a
46	CEBPB	chr11:86977749-86978195	K562	blood:	n/a	n/a
47	CTCF	chr11:87001500-87001650	GM12864	blood:	n/a	chr11:87001524-87001545 chr11:87001530-87001546 chr11:87001529-87001547
48	CTCF	chr11:87001460-87001610	HPAF	blood vessel:	n/a	chr11:87001524-87001545 chr11:87001530-87001546 chr11:87001529-87001547
49	CTCF	chr11:87001339-87001652	ECC-1	luminal epithelium:	n/a	chr11:87001524-87001545 chr11:87001530-87001546 chr11:87001529-87001547
50	CTCF	chr11:87001480-87001630	GM12871	blood:	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	AG04449	skin:	fetal
2	chr11:87002864-87002914	GM12878	blood:	n/a
3	chr11:87002864-87002914	ECC-1	luminal epithelium:	n/a
4	chr11:87002864-87002914	HMEC	breast:	n/a
5	chr11:87002864-87002914	HRCEpiC	kidney:	n/a
6	chr11:87002864-87002914	PrEC	prostate:	n/a
7	chr11:87002864-87002914	AG10803	skin:	n/a
8	chr11:87002864-87002914	MCF-7	breast:	n/a
9	chr11:87002864-87002914	HCF	heart:	n/a
10	chr11:87002864-87002914	NT2-D1	testis:	n/a
11	chr11:87002864-87002914	HCPEpiC	choroid plexus:	n/a
12	chr11:87002864-87002914	MCF10A-Er-Src	breast:	n/a
13	chr11:87002864-87002914	GM06990	blood:	n/a
14	chr11:87002864-87002914	SK-N-SH_RA	brain:	n/a
15	chr11:87002864-87002914	Hepatocyte	liver:	n/a
16	chr11:87002864-87002914	HUVEC	blood vessel:	n/a
17	chr11:87002864-87002914	CMK	blood:	n/a
18	chr11:87002864-87002914	HAEpiC	amniotic membrane:	n/a
19	chr11:87002864-87002914	GM12892	blood:	n/a
20	chr11:87002864-87002914	Hela-S3	cervix:	n/a
21	chr11:87002864-87002914	HEK293	kidney:	embryo
22	chr11:87002864-87002914	HEEpiC	esophagus:	n/a
23	chr11:87002864-87002914	GM12891	blood:	n/a
24	chr11:87002864-87002914	AG04450	lung:	fetal
25	chr11:87002864-87002914	GM19239	blood:	n/a
26	chr11:87002864-87002914	HRPEpiC	eye:	n/a
27	chr11:87002864-87002914	HRE	kidney:	n/a
28	chr11:87002864-87002914	SK-N-MC	brain:	n/a
29	chr11:87002864-87002914	NH-A	brain:	n/a
30	chr11:87002864-87002914	PFSK-1	brain:	n/a
31	chr11:87002864-87002914	PANC-1	pancreas:	n/a
32	chr11:87002864-87002914	ProgFib	skin:	n/a
33	chr11:87002864-87002914	BJ	skin:	n/a
34	chr11:87002864-87002914	Jurkat	blood:	n/a
35	chr11:87002864-87002914	T-47D	breast:	n/a
36	chr11:87002864-87002914	AG09319	gingival:	n/a
37	chr11:87002864-87002914	LNCaP	prostate:	n/a
38	chr11:87002864-87002914	HCM	heart:	n/a
39	chr11:87002864-87002914	SAEC	small airway:	n/a
40	chr11:87002864-87002914	NB4	blood:	n/a
41	chr11:87002864-87002914	AoSMC	blood vessel:	n/a
42	chr11:87002864-87002914	AG09309	skin:	n/a
43	chr11:87002864-87002914	HIPEpiC	eye:	n/a
44	chr11:87002864-87002914	Caco-2	colon:	n/a
45	chr11:87002864-87002914	U87	brain:	n/a
46	chr11:87002864-87002914	ovcar-3	ovarian:	n/a
47	chr11:87002864-87002914	BE2_C	brain:	n/a
48	chr11:87002864-87002914	HPAEpiC	pulmonary alveolar:	n/a
49	chr11:87002864-87002914	HepG2	liver:	n/a
50	chr11:87002864-87002914	SKMC	muscle:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:86996729..86999242-chr11:87005313..87006882,2	MCF-7	breast:
2	chr11:86991946..86992672-chr5:176296643..176297235,2	MCF-7	breast:
3	chr11:86972962..86974479-chr11:86976089..86977632,2	MCF-7	breast:
4	chr11:86710137..86711956-chr11:86990366..86992245,2	MCF-7	breast:
5	chr11:86977540..86979356-chr11:86980303..86982155,2	MCF-7	breast:
6	chr11:86664855..86666701-chr11:87000839..87002926,2	MCF-7	breast:
7	chr11:87001464..87002001-chr7:75943410..75944161,2	K562	blood:
8	chr11:86996729..86999242-chr11:87005313..87006882,2	MCF-7	breast:
9	chr11:86665223..86667347-chr11:87003604..87005762,3	MCF-7	breast:
10	chr11:86972962..86974479-chr11:86976089..86977632,2	MCF-7	breast:
11	chr11:87006858..87009141-chr11:87011283..87013131,2	K562	blood:
12	chr11:86664953..86668319-chr11:86999800..87002548,3	MCF-7	breast:
13	chr11:86650138..86651130-chr11:87001040..87002269,8	K562	blood:
14	chr11:86166836..86167387-chr11:87001058..87001771,2	K562	blood:
15	chr11:86805484..86807360-chr11:87007311..87009404,2	MCF-7	breast:
16	chr11:86977540..86979356-chr11:86980303..86982155,2	MCF-7	breast:
17	chr11:86664990..86667056-chr11:86996903..86999848,2	K562	blood:
18	chr11:86689677..86690529-chr11:87011689..87012195,2	MCF-7	breast:
19	chr11:87006858..87009141-chr11:87011283..87013131,2	K562	blood:
20	chr11:86580752..86581690-chr11:87001116..87001998,4	K562	blood:
21	chr11:86641346..86643236-chr11:86990430..86992858,2	K562	blood:
22	chr11:86806619..86807569-chr11:86992272..86993052,3	MCF-7	breast:

No data

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

Extended variants
information (count: 1760 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1760 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577675	chr11:86971548-86971549	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs11338743	chr11:86971574-86971575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs7951097	chr11:86971627-86971628	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs549695185	chr11:86971640-86971641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs563040783	chr11:86971653-86971654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs548675591	chr11:86971656-86971657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs551696980	chr11:86971661-86971662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs566986278	chr11:86971688-86971689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs369459879	chr11:86971735-86971736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs539579428	chr11:86971755-86971756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs11436074	chr11:86971773-86971774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs528123356	chr11:86971774-86971775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs199851055	chr11:86971785-86971786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs546611715	chr11:86971791-86971792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs377369368	chr11:86971820-86971821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs527929563	chr11:86971831-86971832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542403404	chr11:86971835-86971836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs566523939	chr11:86971849-86971850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs370163279	chr11:86971899-86971900	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs535672698	chr11:86971920-86971921	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs145501653	chr11:86971933-86971934	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs7936587	chr11:86971949-86971950	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs575466496	chr11:86971958-86971959	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs7939286	chr11:86971975-86971976	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs10444376	chr11:86971988-86971989	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs374248091	chr11:86971989-86971990	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs2459958	chr11:86972018-86972019	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs2451055	chr11:86972049-86972050	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs2459957	chr11:86972065-86972066	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs2459956	chr11:86972073-86972074	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs192757	chr11:86972081-86972082	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs577698956	chr11:86972129-86972130	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs115586297	chr11:86972140-86972141	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs560111215	chr11:86972153-86972154	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs10444377	chr11:86972157-86972158	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs17821201	chr11:86972160-86972161	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs540598707	chr11:86972186-86972187	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs75901695	chr11:86972270-86972271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs551936929	chr11:86972284-86972285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs565522090	chr11:86972289-86972290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs562187286	chr11:86972290-86972291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs533060613	chr11:86972312-86972313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs546671027	chr11:86972315-86972316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs372216334	chr11:86972329-86972330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs188854978	chr11:86972371-86972372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs11235053	chr11:86972372-86972373	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs192892890	chr11:86972396-86972397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs533556449	chr11:86972403-86972404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs111753306	chr11:86972500-86972501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs544704191	chr11:86972552-86972553	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:416 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:86962400-86972000	Weak transcription	Primary T cells from cord blood	blood
2	chr11:86962800-86977600	Weak transcription	K562	blood
3	chr11:86963000-86976200	Weak transcription	Colon Smooth Muscle	Colon
4	chr11:86967000-86975400	Weak transcription	HepG2	liver
5	chr11:86968200-86971800	Weak transcription	Osteobl	bone
6	chr11:86968400-86972000	Weak transcription	NHDF-Ad	bronchial
7	chr11:86969200-86972200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr11:86969400-86972000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr11:86969600-86972800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr11:86969600-86976000	Weak transcription	Fetal Kidney	kidney
11	chr11:86969800-86971600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr11:86969800-86972200	Enhancers	Brain Inferior Temporal Lobe	brain
13	chr11:86969800-86995400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr11:86970200-86971600	Enhancers	Brain Substantia Nigra	brain
15	chr11:86970200-86971600	Enhancers	Fetal Heart	heart
16	chr11:86970200-86971800	Weak transcription	Right Atrium	heart
17	chr11:86970200-86974200	Weak transcription	Adipose Nuclei	Adipose
18	chr11:86970400-86972000	Enhancers	Brain Anterior Caudate	brain
19	chr11:86970400-86972200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr11:86970400-86973600	Weak transcription	Left Ventricle	heart
21	chr11:86970800-86972000	Enhancers	Brain Cingulate Gyrus	brain
22	chr11:86970800-86972400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr11:86970800-86972400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr11:86970800-86972800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr11:86970800-86972800	Enhancers	HUVEC	blood vessel
26	chr11:86971000-86971600	Enhancers	Pancreatic Islets	Pancreatic Islet
27	chr11:86971000-86972600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr11:86971200-86971600	Weak transcription	Fetal Lung	lung
29	chr11:86971200-86972000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr11:86971400-86973600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr11:86971400-86973600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr11:86971400-86975200	Weak transcription	Brain Hippocampus Middle	brain
33	chr11:86971400-86975600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr11:86971600-86972200	Enhancers	Fetal Lung	lung
35	chr11:86971600-86976200	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr11:86971800-86972000	Enhancers	Right Atrium	heart
37	chr11:86971800-86972200	Enhancers	Osteobl	bone
38	chr11:86971800-86972400	Enhancers	NH-A	brain
39	chr11:86972000-86972200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr11:86972000-86972400	Weak transcription	Right Atrium	heart
41	chr11:86972000-86972400	Enhancers	NHDF-Ad	bronchial
42	chr11:86972200-86975000	Weak transcription	Osteobl	bone
43	chr11:86972200-86976000	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr11:86972200-86976200	Weak transcription	Fetal Lung	lung
45	chr11:86972400-86973800	Enhancers	Right Atrium	heart
46	chr11:86972400-86974400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr11:86972400-86974400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr11:86972400-86975400	Weak transcription	NHDF-Ad	bronchial
49	chr11:86972400-86975600	Weak transcription	NH-A	brain
50	chr11:86972600-86974200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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