Variant report

Variant	esv1001380
Chromosome Location	chr11:73680052-73684451
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:255)
CpG islands
(count:62)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:255 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr11:73682343-73682802	GM12878	blood:	n/a	n/a
2	BCL3	chr11:73682099-73682922	A549	lung:	n/a	n/a
3	BCL3	chr11:73683146-73684091	A549	lung:	n/a	n/a
4	BCL3	chr11:73683046-73684019	A549	lung:	n/a	n/a
5	BCL3	chr11:73682152-73683018	A549	lung:	n/a	n/a
6	BCL3	chr11:73682238-73682683	GM12878	blood:	n/a	n/a
7	BCLAF1	chr11:73681111-73681724	GM12878	blood:	n/a	n/a
8	BCLAF1	chr11:73683050-73684671	GM12878	blood:	n/a	n/a
9	BCLAF1	chr11:73682155-73682887	GM12878	blood:	n/a	n/a
10	CCNT2	chr11:73682404-73682566	K562	blood:	n/a	n/a
11	CHD2	chr11:73682417-73682617	GM12878	blood:	n/a	n/a
12	CHD2	chr11:73683823-73684048	K562	blood:	n/a	n/a
13	CTCF	chr11:73681857-73681921	Lung_OC	lung:	n/a	n/a
14	ELF1	chr11:73682151-73682961	GM12878	blood:	n/a	n/a
15	FOXA1	chr11:73680729-73680874	T-47D	breast:	n/a	n/a
16	FOXM1	chr11:73682176-73682627	GM12878	blood:	n/a	n/a
17	GATA1	chr11:73680884-73681533	PBDE	blood:	n/a	n/a
18	HEY1	chr11:73683678-73684072	HepG2	liver:	n/a	n/a
19	JUN	chr11:73680308-73680404	HepG2	liver:	n/a	chr11:73680354-73680367
20	JUND	chr11:73680183-73680507	HepG2	liver:	n/a	n/a
21	MAX	chr11:73682445-73682573	GM12878	blood:	n/a	n/a
22	MAZ	chr11:73682629-73682687	Hela-S3	cervix:	n/a	chr11:73682668-73682675
23	MAZ	chr11:73684017-73684160	K562	blood:	n/a	n/a
24	MTA3	chr11:73680507-73681807	GM12878	blood:	n/a	n/a
25	MTA3	chr11:73683042-73684552	GM12878	blood:	n/a	n/a
26	MTA3	chr11:73681116-73681664	GM12878	blood:	n/a	n/a
27	MTA3	chr11:73681985-73682988	GM12878	blood:	n/a	n/a
28	NFATC1	chr11:73683045-73684257	GM12878	blood:	n/a	n/a
29	NFATC1	chr11:73681042-73681656	GM12878	blood:	n/a	n/a
30	NFATC1	chr11:73680816-73681459	GM12878	blood:	n/a	n/a
31	NFATC1	chr11:73682105-73682948	GM12878	blood:	n/a	chr11:73682766-73682779
32	NFATC1	chr11:73682122-73682929	GM12878	blood:	n/a	chr11:73682766-73682779
33	NFATC1	chr11:73683059-73684372	GM12878	blood:	n/a	n/a
34	NFIC	chr11:73682191-73682669	GM12878	blood:	n/a	n/a
35	PML	chr11:73683029-73684770	GM12878	blood:	n/a	n/a
36	PML	chr11:73682256-73682756	GM12878	blood:	n/a	n/a
37	PML	chr11:73682220-73682819	K562	blood:	n/a	n/a
38	PML	chr11:73683102-73684818	K562	blood:	n/a	n/a
39	PML	chr11:73682099-73682997	GM12878	blood:	n/a	n/a
40	PML	chr11:73683509-73683930	GM12878	blood:	n/a	n/a
41	PML	chr11:73681363-73681850	GM12878	blood:	n/a	n/a
42	POLR2A	chr11:73680621-73683005	PANC-1	pancreas:	n/a	n/a
43	POLR2A	chr11:73683171-73684745	K562	blood:	n/a	n/a
44	POLR2A	chr11:73682245-73682850	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr11:73681546-73681950	Hela-S3	cervix:	n/a	n/a
46	POLR2A	chr11:73684420-73684427	MCF-7	breast:	n/a	n/a
47	POLR2A	chr11:73682214-73682721	Hela-S3	cervix:	n/a	n/a
48	POLR2A	chr11:73683122-73684072	HepG2	liver:	n/a	n/a
49	POLR2A	chr11:73679259-73680053	ECC-1	luminal epithelium:	n/a	n/a
50	POLR2A	chr11:73680952-73681960	Hela-S3	cervix:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:73681281-73681331	BJ	skin:	n/a
2	chr11:73681281-73681331	BJ	skin:	n/a
3	chr11:73681281-73681331	HEEpiC	esophagus:	n/a
4	chr11:73681281-73681331	HL-60	blood:	n/a
5	chr11:73681281-73681331	Hepatocyte	liver:	n/a
6	chr11:73681281-73681331	K562	blood:	n/a
7	chr11:73681281-73681331	HNPCEpiC	eye:	n/a
8	chr11:73681281-73681331	HIPEpiC	eye:	n/a
9	chr11:73681281-73681331	HUVEC	blood vessel:	n/a
10	chr11:73681281-73681331	GM06990	blood:	n/a
11	chr11:73681281-73681331	SK-N-SH_RA	brain:	n/a
12	chr11:73681281-73681331	RPTEC	kidney:	n/a
13	chr11:73681281-73681331	HCF	heart:	n/a
14	chr11:73681281-73681331	AG09319	gingival:	n/a
15	chr11:73681281-73681331	HEK293	kidney:	embryo
16	chr11:73681281-73681331	BE2_C	brain:	n/a
17	chr11:73681281-73681331	PrEC	prostate:	n/a
18	chr11:73681281-73681331	LNCaP	prostate:	n/a
19	chr11:73681281-73681331	AG10803	skin:	n/a
20	chr11:73681281-73681331	GM12892	blood:	n/a
21	chr11:73681281-73681331	ProgFib	skin:	n/a
22	chr11:73681281-73681331	IMR90	lung:	fetal
23	chr11:73681281-73681331	Jurkat	blood:	n/a
24	chr11:73681281-73681331	AG09309	skin:	n/a
25	chr11:73681281-73681331	NT2-D1	testis:	n/a
26	chr11:73681281-73681331	HMEC	breast:	n/a
27	chr11:73681281-73681331	NHDF-neo	bronchial:	n/a
28	chr11:73681281-73681331	GM12891	blood:	n/a
29	chr11:73681281-73681331	HCPEpiC	choroid plexus:	n/a
30	chr11:73681281-73681331	AoSMC	blood vessel:	n/a
31	chr11:73681281-73681331	ECC-1	luminal epithelium:	n/a
32	chr11:73681281-73681331	Caco-2	colon:	n/a
33	chr11:73681281-73681331	PANC-1	pancreas:	n/a
34	chr11:73681281-73681331	AG04449	skin:	fetal
35	chr11:73681281-73681331	HRCEpiC	kidney:	n/a
36	chr11:73681281-73681331	NH-A	brain:	n/a
37	chr11:73681281-73681331	T-47D	breast:	n/a
38	chr11:73681281-73681331	HPAEpiC	pulmonary alveolar:	n/a
39	chr11:73681281-73681331	U87	brain:	n/a
40	chr11:73681281-73681331	GM12878	blood:	n/a
41	chr11:73681281-73681331	H1-hESC	embryonic stem cell:	embryo
42	chr11:73681281-73681331	NB4	blood:	n/a
43	chr11:73681281-73681331	NHBE	bronchial:	n/a
44	chr11:73681281-73681331	HRE	kidney:	n/a
45	chr11:73681281-73681331	MCF10A-Er-Src	breast:	n/a
46	chr11:73681281-73681331	HRPEpiC	eye:	n/a
47	chr11:73681281-73681331	ovcar-3	ovarian:	n/a
48	chr11:73681281-73681331	SKMC	muscle:	n/a
49	chr11:73681281-73681331	HAEpiC	amniotic membrane:	n/a
50	chr11:73681281-73681331	A549	lung:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:73679005..73682645-chr11:73778281..73782136,5	MCF-7	breast:
2	chr11:73679655..73681254-chr11:73938042..73940266,2	MCF-7	breast:
3	chr1:6295909..6296442-chr11:73684076..73684675,2	NB4	blood:
4	chr11:73681017..73683540-chr11:75108485..75110869,2	MCF-7	breast:
5	chr11:73684220..73687035-chr11:73766877..73770022,3	MCF-7	breast:
6	chr11:73678390..73681142-chr11:73802316..73803896,2	MCF-7	breast:
7	chr11:73681943..73683569-chr11:73889681..73892326,2	K562	blood:
8	chr11:73679561..73684546-chr11:73778723..73783416,5	MCF-7	breast:
9	chr11:73681646..73684288-chr11:73745260..73748147,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000255847	TF binding region
ENSG00000255847	CpG island
ENSG00000116237	chromatin interactions
ENSG00000225077	chromatin interactions
ENSG00000149273	chromatin interactions
ENSG00000168014	chromatin interactions

Extended variants
information (count: 233 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:233 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs599277	chr11:73680063-73680064	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs111799892	chr11:73680065-73680066	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs624096	chr11:73680082-73680083	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs78189778	chr11:73680086-73680087	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs545809424	chr11:73680087-73680088	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs72982970	chr11:73680128-73680129	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs77465317	chr11:73680138-73680139	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs573016287	chr11:73680141-73680142	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs577181207	chr11:73680158-73680159	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs74517954	chr11:73680176-73680177	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs531054789	chr11:73680192-73680193	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs79398991	chr11:73680195-73680196	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs561511879	chr11:73680212-73680213	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs71465904	chr11:73680277-73680278	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs181353808	chr11:73680283-73680284	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs35989550	chr11:73680285-73680286	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs369843758	chr11:73680304-73680305	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs185627938	chr11:73680311-73680312	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs140556652	chr11:73680327-73680328	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs150416952	chr11:73680365-73680366	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs532664812	chr11:73680386-73680387	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs551382903	chr11:73680452-73680453	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs149049180	chr11:73680456-73680457	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs141783955	chr11:73680465-73680466	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs536788561	chr11:73680496-73680497	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs556637441	chr11:73680545-73680546	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs566978211	chr11:73680559-73680560	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs190783079	chr11:73680561-73680562	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs386754969	chr11:73680626-73680627	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs115599075	chr11:73680627-73680628	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs544954390	chr11:73680678-73680679	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs558945372	chr11:73680708-73680709	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs112348704	chr11:73680709-73680710	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs544570876	chr11:73680741-73680742	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs114530185	chr11:73680750-73680751	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs34163970	chr11:73680754-73680755	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs72982971	chr11:73680776-73680777	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs540841360	chr11:73680782-73680783	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs560457215	chr11:73680784-73680785	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs34820619	chr11:73680791-73680792	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs373197281	chr11:73680794-73680795	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs532872226	chr11:73680818-73680819	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs143049341	chr11:73680892-73680893	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs570959608	chr11:73680895-73680896	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs138207403	chr11:73681016-73681017	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs373291047	chr11:73681050-73681051	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs199708737	chr11:73681051-73681052	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs550121287	chr11:73681059-73681060	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs2306819	chr11:73681090-73681091	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs535916675	chr11:73681091-73681092	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
Acute myeloid leukemia	20729466	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
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	21364760	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	17142309	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:209 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:73669000-73685800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:73669800-73681000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:73672800-73684200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr11:73672800-73684800	Weak transcription	HSMM	muscle
5	chr11:73672800-73693200	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr11:73674000-73685000	Weak transcription	Brain Hippocampus Middle	brain
7	chr11:73674600-73684200	Weak transcription	Right Atrium	heart
8	chr11:73675000-73680200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
9	chr11:73675200-73684400	Enhancers	Primary T helper cells PMA-I stimulated	--
10	chr11:73675200-73685400	Enhancers	Primary T helper cells fromperipheralblood	blood
11	chr11:73675400-73692600	Weak transcription	Psoas Muscle	Psoas
12	chr11:73675800-73680400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr11:73675800-73681200	Weak transcription	Dnd41	blood
14	chr11:73675800-73683800	Weak transcription	GM12878-XiMat	blood
15	chr11:73675800-73685400	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr11:73675800-73685400	Weak transcription	Fetal Brain Female	brain
17	chr11:73676000-73681000	Weak transcription	Thymus	Thymus
18	chr11:73676000-73684200	Weak transcription	Primary neutrophils fromperipheralblood	blood
19	chr11:73676000-73684200	Weak transcription	Duodenum Mucosa	Duodenum
20	chr11:73676000-73684400	Enhancers	Primary T cells fromperipheralblood	blood
21	chr11:73676000-73685000	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr11:73676000-73685400	Weak transcription	Rectal Smooth Muscle	rectum
23	chr11:73676000-73685600	Weak transcription	HepG2	liver
24	chr11:73676000-73686000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr11:73676000-73686200	Weak transcription	Brain Cingulate Gyrus	brain
26	chr11:73676000-73686200	Weak transcription	Brain Substantia Nigra	brain
27	chr11:73676000-73686400	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr11:73676000-73687400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr11:73676200-73680800	Weak transcription	K562	blood
30	chr11:73676200-73681200	Weak transcription	Stomach Mucosa	stomach
31	chr11:73676200-73682600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr11:73676200-73685000	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr11:73676200-73685000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr11:73676200-73685200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr11:73676200-73685400	Weak transcription	Brain Anterior Caudate	brain
36	chr11:73676200-73687600	Weak transcription	Brain Angular Gyrus	brain
37	chr11:73676400-73681000	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr11:73676400-73685400	Weak transcription	Hela-S3	cervix
39	chr11:73676400-73685800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr11:73676400-73693200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr11:73676600-73680800	Weak transcription	HSMMtube	muscle
42	chr11:73676600-73682400	Weak transcription	Skeletal Muscle Male	skeletal muscle
43	chr11:73676600-73684600	Weak transcription	A549	lung
44	chr11:73676600-73684800	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr11:73676600-73685200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr11:73676600-73685200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr11:73676600-73685600	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr11:73676600-73691000	Weak transcription	Fetal Heart	heart
49	chr11:73677400-73680200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr11:73677600-73680400	Weak transcription	Placenta	Placenta

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