Variant report

Variant	esv3367089
Chromosome Location	chr11:58872776-58875774
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:508)
CpG islands
(count:672)
Chromatin interactive
region (count:11)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:508 , 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	chr11:58874268-58874746	HepG2	liver:	n/a	n/a
2	ATF2	chr11:58874367-58874899	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr11:58874015-58875031	GM12878	blood:	n/a	n/a
4	ATF2	chr11:58874344-58874770	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr11:58874286-58874870	GM12878	blood:	n/a	n/a
6	BACH1	chr11:58873974-58874757	H1-hESC	embryonic stem cell:	n/a	chr11:58874543-58874557
7	BATF	chr11:58875555-58875818	GM12878	blood:	n/a	chr11:58875662-58875670
8	BATF	chr11:58874419-58874727	GM12878	blood:	n/a	chr11:58874543-58874553 chr11:58874547-58874557 chr11:58874542-58874553
9	BATF	chr11:58875256-58875548	GM12878	blood:	n/a	n/a
10	BCL11A	chr11:58875271-58875606	GM12878	blood:	n/a	n/a
11	BCLAF1	chr11:58873883-58874436	GM12878	blood:	n/a	chr11:58874084-58874097
12	BHLHE40	chr11:58873768-58874942	GM12878	blood:	n/a	chr11:58874078-58874094 chr11:58874166-58874182 chr11:58873986-58874002 chr11:58874149-58874165 chr11:58873949-58873965
13	BHLHE40	chr11:58874184-58874825	HepG2	liver:	n/a	n/a
14	BHLHE40	chr11:58874616-58874646	K562	blood:	n/a	n/a
15	BHLHE40	chr11:58874518-58874815	A549	lung:	n/a	n/a
16	BRCA1	chr11:58874209-58874272	HepG2	liver:	n/a	n/a
17	CEBPB	chr11:58874293-58874354	HepG2	liver:	n/a	n/a
18	CEBPB	chr11:58874028-58874716	Hela-S3	cervix:	n/a	n/a
19	CHD1	chr11:58875131-58875137	GM12878	blood:	n/a	n/a
20	CHD2	chr11:58873992-58874907	Hela-S3	cervix:	n/a	chr11:58874166-58874176
21	CHD2	chr11:58873777-58874777	GM12878	blood:	n/a	chr11:58874166-58874176
22	CHD2	chr11:58874239-58874796	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr11:58874218-58874295	HepG2	liver:	n/a	n/a
24	CREB1	chr11:58874038-58874827	HepG2	liver:	n/a	n/a
25	CREB1	chr11:58874417-58874830	A549	lung:	n/a	n/a
26	CREB1	chr11:58873993-58874372	A549	lung:	n/a	n/a
27	CTCF	chr11:58874201-58874318	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr11:58874180-58874330	HMEC	breast:	n/a	n/a
29	CTCF	chr11:58874101-58874363	GM12878	blood:	n/a	chr11:58874168-58874181
30	CTCF	chr11:58874200-58874350	HMEC	breast:	n/a	n/a
31	CTCF	chr11:58874240-58874390	GM12873	blood:	n/a	n/a
32	CTCF	chr11:58874256-58874317	GM12878	blood:	n/a	n/a
33	CTCF	chr11:58874160-58874310	HRPEpiC	eye:	n/a	chr11:58874168-58874181
34	CTCF	chr11:58874200-58874350	GM12871	blood:	n/a	n/a
35	CTCF	chr11:58874200-58874350	AG10803	skin:	n/a	n/a
36	CTCF	chr11:58873780-58873930	HBMEC	blood vessel:	n/a	chr11:58873857-58873875 chr11:58873859-58873872
37	CTCF	chr11:58874200-58874350	NHEK	skin:	n/a	n/a
38	CTCF	chr11:58874160-58874310	AoAF	blood vessel:	n/a	chr11:58874168-58874181
39	CTCF	chr11:58873760-58873910	BJ	skin:	n/a	chr11:58873857-58873875 chr11:58873859-58873872
40	CTCF	chr11:58874120-58874270	GM12865	blood:	n/a	chr11:58874168-58874181
41	CTCF	chr11:58874220-58874370	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr11:58874160-58874310	GM12866	blood:	n/a	chr11:58874168-58874181
43	CTCF	chr11:58874241-58874286	GM19238	blood:	n/a	n/a
44	CTCF	chr11:58873800-58873950	HPAF	blood vessel:	n/a	chr11:58873857-58873875 chr11:58873859-58873872
45	CTCF	chr11:58873834-58873877	Hela-S3	cervix:	n/a	chr11:58873857-58873875 chr11:58873859-58873872
46	CTCF	chr11:58874200-58874350	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr11:58874264-58874342	Lung_OC	lung:	n/a	n/a
48	CTCF	chr11:58874180-58874330	HEK293	kidney:	n/a	n/a
49	CTCF	chr11:58874217-58874322	MCF-7	breast:	n/a	n/a
50	CTCF	chr11:58873815-58873917	MCF-7	breast:	n/a	chr11:58873857-58873875 chr11:58873859-58873872

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:58874723-58874773	Hela-S3	cervix:	n/a
2	chr11:58874723-58874773	Hela-S3	cervix:	n/a
3	chr11:58874641-58874691	NH-A	brain:	n/a
4	chr11:58874641-58874691	H1-hESC	embryonic stem cell:	embryo
5	chr11:58874733-58874783	HRCEpiC	kidney:	n/a
6	chr11:58873823-58873873	MCF-7	breast:	n/a
7	chr11:58874645-58874695	LNCaP	prostate:	n/a
8	chr11:58873955-58874005	LNCaP	prostate:	n/a
9	chr11:58874641-58874691	GM19239	blood:	n/a
10	chr11:58874641-58874691	HUVEC	blood vessel:	n/a
11	chr11:58874723-58874773	ECC-1	luminal epithelium:	n/a
12	chr11:58874637-58874687	HEK293	kidney:	embryo
13	chr11:58874608-58874658	AoSMC	blood vessel:	n/a
14	chr11:58874637-58874687	PFSK-1	brain:	n/a
15	chr11:58874637-58874687	HCM	heart:	n/a
16	chr11:58874635-58874685	GM12878	blood:	n/a
17	chr11:58874637-58874687	PrEC	prostate:	n/a
18	chr11:58874645-58874695	HCPEpiC	choroid plexus:	n/a
19	chr11:58874733-58874783	HL-60	blood:	n/a
20	chr11:58874635-58874685	NB4	blood:	n/a
21	chr11:58874207-58874257	NHBE	bronchial:	n/a
22	chr11:58874645-58874695	SKMC	muscle:	n/a
23	chr11:58874348-58874398	AoSMC	blood vessel:	n/a
24	chr11:58874635-58874685	BJ	skin:	n/a
25	chr11:58873823-58873873	AG09309	skin:	n/a
26	chr11:58874733-58874783	AG09309	skin:	n/a
27	chr11:58874637-58874687	ProgFib	skin:	n/a
28	chr11:58873955-58874005	SKMC	muscle:	n/a
29	chr11:58874635-58874685	NT2-D1	testis:	n/a
30	chr11:58874348-58874398	MCF-7	breast:	n/a
31	chr11:58874733-58874783	NT2-D1	testis:	n/a
32	chr11:58874723-58874773	BJ	skin:	n/a
33	chr11:58874645-58874695	BJ	skin:	n/a
34	chr11:58874635-58874685	PANC-1	pancreas:	n/a
35	chr11:58874733-58874783	PANC-1	pancreas:	n/a
36	chr11:58873955-58874005	AoSMC	blood vessel:	n/a
37	chr11:58874348-58874398	HAEpiC	amniotic membrane:	n/a
38	chr11:58874207-58874257	SK-N-MC	brain:	n/a
39	chr11:58874723-58874773	HRPEpiC	eye:	n/a
40	chr11:58874645-58874695	Caco-2	colon:	n/a
41	chr11:58874645-58874695	GM19239	blood:	n/a
42	chr11:58873955-58874005	T-47D	breast:	n/a
43	chr11:58874608-58874658	SK-N-SH_RA	brain:	n/a
44	chr11:58874635-58874685	K562	blood:	n/a
45	chr11:58874637-58874687	Hepatocyte	liver:	n/a
46	chr11:58874645-58874695	MCF-7	breast:	n/a
47	chr11:58874723-58874773	HepG2	liver:	n/a
48	chr11:58874637-58874687	SKMC	muscle:	n/a
49	chr11:58874645-58874695	Hepatocyte	liver:	n/a
50	chr11:58874207-58874257	ECC-1	luminal epithelium:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:58869769..58871706-chr11:58872515..58874019,2	MCF-7	breast:
2	chr11:58869975..58872858-chr11:58877240..58880132,2	MCF-7	breast:
3	chr11:58874735..58876453-chr11:58878007..58880480,2	MCF-7	breast:
4	chr11:58873805..58875305-chr17:41466179..41467880,2	MCF-7	breast:
5	chr11:58869989..58871867-chr11:58872289..58874332,2	MCF-7	breast:
6	chr11:58873805..58876804-chr17:41466274..41467888,2	K562	blood:
7	chr11:58875233..58875940-chr12:49657802..49658323,2	Hela-S3	cervix:
8	chr11:58875510..58878300-chr11:58880309..58883300,3	MCF-7	breast:
9	chr11:58873861..58874546-chr5:111496427..111496981,2	Hela-S3	cervix:
10	chr11:58872425..58874544-chr11:58888169..58890358,2	MCF-7	breast:
11	chr11:58873708..58874686-chr11:63448916..63449711,2	Hela-S3	cervix:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM111A-1	chr11:58874709-58874769	NONHSAT021500

No data

Variant related genes	Relation type
FAM111B	TF binding region
FAM111B	CpG island
ENSG00000188825	chromatin interactions
ENSG00000224032	chromatin interactions
ENSG00000133318	chromatin interactions
CNOT6	miRNA target sites

Extended variants
information (count: 124 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:124 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566833074	chr11:58872798-58872799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs373727222	chr11:58872801-58872802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs377025493	chr11:58872814-58872815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs534064103	chr11:58872818-58872819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs555794395	chr11:58872860-58872861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs567368503	chr11:58872937-58872938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs10896919	chr11:58872960-58872961	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs556508114	chr11:58872962-58872963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs185153184	chr11:58872964-58872965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs190344845	chr11:58872965-58872966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs553516611	chr11:58872972-58872973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs560021414	chr11:58872976-58872977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs571993046	chr11:58872984-58872985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs528763889	chr11:58872989-58872990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs552016520	chr11:58872997-58872998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs542374356	chr11:58873003-58873004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs560990298	chr11:58873004-58873005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs529453776	chr11:58873019-58873020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs182031764	chr11:58873073-58873074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs562739643	chr11:58873114-58873115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs187462769	chr11:58873124-58873125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs552032710	chr11:58873129-58873130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs565359548	chr11:58873157-58873158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs527655028	chr11:58873163-58873164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs552806592	chr11:58873180-58873181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs376851845	chr11:58873262-58873263	Weak transcription Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs530965563	chr11:58873273-58873274	Weak transcription Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs113199129	chr11:58873321-58873322	Weak transcription Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs188164337	chr11:58873341-58873342	Weak transcription Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs548119557	chr11:58873373-58873374	Weak transcription Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs550270476	chr11:58873397-58873398	Weak transcription Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs567014302	chr11:58873398-58873399	Weak transcription Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs185537031	chr11:58873431-58873432	Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs571445344	chr11:58873449-58873450	Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs538969895	chr11:58873481-58873482	Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs201533773	chr11:58873491-58873492	Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs112454387	chr11:58873492-58873493	Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs375249838	chr11:58873494-58873495	Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs190199131	chr11:58873497-58873498	Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs143149154	chr11:58873522-58873523	Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs571968961	chr11:58873566-58873567	Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs183460057	chr11:58873623-58873624	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs143499813	chr11:58873648-58873649	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs575778569	chr11:58873688-58873689	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs34816453	chr11:58873703-58873704	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs543091258	chr11:58873730-58873731	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs562773457	chr11:58873761-58873762	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs546168638	chr11:58873833-58873834	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs186672335	chr11:58873872-58873873	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs566794128	chr11:58873879-58873880	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:51)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Autism	22495309	CNVD
Autism	20808228	CNVD
Cancer	20164919	CNVD

Chromatin state (count:523 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:58868200-58873800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr11:58870000-58873400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr11:58870000-58873600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr11:58870000-58873600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr11:58870000-58873600	Weak transcription	Fetal Heart	heart
6	chr11:58870000-58873600	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr11:58870000-58873600	Weak transcription	Pancreas	Pancrea
8	chr11:58870000-58873600	Weak transcription	Spleen	Spleen
9	chr11:58870000-58873600	Weak transcription	HSMM	muscle
10	chr11:58870000-58873600	Weak transcription	HUVEC	blood vessel
11	chr11:58870000-58873600	Weak transcription	NHEK	skin
12	chr11:58870000-58873800	Weak transcription	Esophagus	oesophagus
13	chr11:58870000-58873800	Weak transcription	Gastric	stomach
14	chr11:58870000-58873800	Weak transcription	Ovary	ovary
15	chr11:58870200-58873000	Weak transcription	Primary T cells from cord blood	blood
16	chr11:58870200-58873000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
17	chr11:58870200-58873200	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr11:58870200-58873400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr11:58870200-58873400	Weak transcription	Brain Germinal Matrix	brain
20	chr11:58870200-58873600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr11:58870200-58873600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr11:58870200-58873600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr11:58870200-58873600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr11:58870200-58873600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr11:58870200-58873600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr11:58870200-58873600	Weak transcription	Primary monocytes fromperipheralblood	blood
27	chr11:58870200-58873600	Enhancers	Primary B cells from peripheral blood	blood
28	chr11:58870200-58873600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr11:58870200-58873600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr11:58870200-58873600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr11:58870200-58873600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr11:58870200-58873600	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr11:58870200-58873600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr11:58870200-58873600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr11:58870200-58873600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr11:58870200-58873600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr11:58870200-58873600	Weak transcription	Adipose Nuclei	Adipose
38	chr11:58870200-58873600	Weak transcription	Liver	Liver
39	chr11:58870200-58873600	Weak transcription	Duodenum Mucosa	Duodenum
40	chr11:58870200-58873600	Weak transcription	Fetal Brain Male	brain
41	chr11:58870200-58873600	Weak transcription	Fetal Brain Female	brain
42	chr11:58870200-58873600	Weak transcription	Fetal Intestine Large	intestine
43	chr11:58870200-58873600	Weak transcription	Fetal Intestine Small	intestine
44	chr11:58870200-58873600	Weak transcription	Fetal Kidney	kidney
45	chr11:58870200-58873600	Weak transcription	Fetal Thymus	thymus
46	chr11:58870200-58873600	Weak transcription	Placenta Amnion	Placenta Amnion
47	chr11:58870200-58873600	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr11:58870200-58873600	Weak transcription	Rectal Smooth Muscle	rectum
49	chr11:58870200-58873600	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr11:58870200-58873600	Weak transcription	Thymus	Thymus

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links