Variant report

Variant	nsv975202
Chromosome Location	chr11:73289057-73294849
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:68)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:68 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:73290809-73290822	K562	blood:	n/a	n/a
2	ATF2	chr11:73289691-73290216	GM12878	blood:	n/a	n/a
3	ATF2	chr11:73289783-73290212	GM12878	blood:	n/a	n/a
4	BATF	chr11:73289721-73290174	GM12878	blood:	n/a	n/a
5	BATF	chr11:73289763-73290084	GM12878	blood:	n/a	n/a
6	BCLAF1	chr11:73289736-73290299	GM12878	blood:	n/a	n/a
7	BHLHE40	chr11:73294641-73294830	K562	blood:	n/a	n/a
8	BHLHE40	chr11:73289897-73290217	GM12878	blood:	n/a	n/a
9	BHLHE40	chr11:73289862-73290125	HepG2	liver:	n/a	n/a
10	CEBPB	chr11:73290859-73290879	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr11:73290811-73290972	K562	blood:	n/a	n/a
12	CHD2	chr11:73289951-73290096	GM12878	blood:	n/a	n/a
13	CTCF	chr11:73293260-73293376	Kidney_OC	kidney:	n/a	n/a
14	CUX1	chr11:73289808-73290008	GM12878	blood:	n/a	n/a
15	EBF1	chr11:73291781-73292155	GM12878	blood:	n/a	n/a
16	EBF1	chr11:73291886-73292120	GM12878	blood:	n/a	n/a
17	EBF1	chr11:73291909-73292092	GM12878	blood:	n/a	n/a
18	ELF1	chr11:73289841-73290275	GM12878	blood:	n/a	chr11:73290065-73290078
19	ELF1	chr11:73289902-73290190	K562	blood:	n/a	chr11:73290065-73290078
20	ELF1	chr11:73289968-73290242	HepG2	liver:	n/a	chr11:73290065-73290078
21	EP300	chr11:73292081-73292111	GM12878	blood:	n/a	n/a
22	EP300	chr11:73289803-73290118	GM12878	blood:	n/a	n/a
23	FOXA1	chr11:73289708-73290136	T-47D	breast:	n/a	n/a
24	FOXA1	chr11:73289792-73290130	T-47D	breast:	n/a	n/a
25	FOXA1	chr11:73289818-73290257	HepG2	liver:	n/a	n/a
26	FOXA1	chr11:73289798-73290162	HepG2	liver:	n/a	n/a
27	FOXA1	chr11:73289747-73290127	HepG2	liver:	n/a	n/a
28	FOXA1	chr11:73289675-73290238	HepG2	liver:	n/a	n/a
29	FOXA2	chr11:73289824-73290123	HepG2	liver:	n/a	n/a
30	FOXA2	chr11:73289745-73290152	A549	lung:	n/a	n/a
31	FOXP2	chr11:73288621-73289068	SK-N-MC	brain:	n/a	n/a
32	GATA3	chr11:73289632-73290240	SK-N-SH	brain:	n/a	n/a
33	GATA3	chr11:73289754-73290133	T-47D	breast:	n/a	n/a
34	GATA3	chr11:73289710-73290243	SK-N-SH	brain:	n/a	n/a
35	GATA3	chr11:73289766-73290148	T-47D	breast:	n/a	n/a
36	GATA3	chr11:73289756-73290209	MCF-7	breast:	n/a	n/a
37	MAFK	chr11:73293121-73293303	HepG2	liver:	n/a	chr11:73293234-73293250 chr11:73293237-73293251 chr11:73293239-73293250
38	MEF2A	chr11:73289727-73290253	GM12878	blood:	n/a	n/a
39	NFIC	chr11:73289407-73290215	GM12878	blood:	n/a	n/a
40	PBX3	chr11:73289818-73290035	GM12878	blood:	n/a	n/a
41	PBX3	chr11:73289673-73290184	SK-N-SH	brain:	n/a	n/a
42	POLR2A	chr11:73291253-73291357	MCF-7	breast:	n/a	n/a
43	POLR2A	chr11:73288494-73289092	SK-N-MC	brain:	n/a	n/a
44	POLR2A	chr11:73290826-73290839	ProgFib	skin:	n/a	n/a
45	PRDM1	chr11:73289921-73290110	Hela-S3	cervix:	n/a	n/a
46	RCOR1	chr11:73294813-73294883	HepG2	liver:	n/a	n/a
47	RELA	chr11:73291693-73292152	GM12891	blood:	n/a	n/a
48	RFX5	chr11:73290325-73290447	K562	blood:	n/a	n/a
49	RUNX3	chr11:73289392-73290344	GM12878	blood:	n/a	n/a
50	RUNX3	chr11:73289757-73290270	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:73289224-73289274	SK-N-SH_RA	brain:	n/a
2	chr11:73289224-73289274	AG04449	skin:	fetal
3	chr11:73289224-73289274	NT2-D1	testis:	n/a
4	chr11:73289224-73289274	HNPCEpiC	eye:	n/a
5	chr11:73289224-73289274	GM12892	blood:	n/a
6	chr11:73289224-73289274	NH-A	brain:	n/a
7	chr11:73289224-73289274	BE2_C	brain:	n/a
8	chr11:73289224-73289274	HCT-116	colon:	n/a
9	chr11:73289224-73289274	PFSK-1	brain:	n/a
10	chr11:73289224-73289274	PrEC	prostate:	n/a
11	chr11:73289224-73289274	ProgFib	skin:	n/a
12	chr11:73289224-73289274	HMEC	breast:	n/a
13	chr11:73289224-73289274	HL-60	blood:	n/a
14	chr11:73289224-73289274	NB4	blood:	n/a
15	chr11:73289224-73289274	MCF-7	breast:	n/a
16	chr11:73289224-73289274	Hela-S3	cervix:	n/a
17	chr11:73289224-73289274	PANC-1	pancreas:	n/a
18	chr11:73289224-73289274	IMR90	lung:	fetal
19	chr11:73289224-73289274	Jurkat	blood:	n/a
20	chr11:73289224-73289274	HRCEpiC	kidney:	n/a
21	chr11:73289224-73289274	ovcar-3	ovarian:	n/a
22	chr11:73289224-73289274	CMK	blood:	n/a
23	chr11:73289224-73289274	NHBE	bronchial:	n/a
24	chr11:73289224-73289274	HEEpiC	esophagus:	n/a
25	chr11:73289224-73289274	GM12878	blood:	n/a
26	chr11:73289224-73289274	HIPEpiC	eye:	n/a
27	chr11:73289224-73289274	AG10803	skin:	n/a
28	chr11:73289224-73289274	HEK293	kidney:	embryo
29	chr11:73289224-73289274	HPAEpiC	pulmonary alveolar:	n/a
30	chr11:73289224-73289274	Hepatocyte	liver:	n/a
31	chr11:73289224-73289274	NHDF-neo	bronchial:	n/a
32	chr11:73289224-73289274	K562	blood:	n/a
33	chr11:73289224-73289274	HCM	heart:	n/a
34	chr11:73289224-73289274	AG09309	skin:	n/a
35	chr11:73289224-73289274	GM19239	blood:	n/a
36	chr11:73289224-73289274	GM06990	blood:	n/a
37	chr11:73289224-73289274	HCPEpiC	choroid plexus:	n/a
38	chr11:73289224-73289274	LNCaP	prostate:	n/a
39	chr11:73289224-73289274	HepG2	liver:	n/a
40	chr11:73289224-73289274	HUVEC	blood vessel:	n/a
41	chr11:73289224-73289274	MCF10A-Er-Src	breast:	n/a
42	chr11:73289224-73289274	RPTEC	kidney:	n/a
43	chr11:73289224-73289274	HRE	kidney:	n/a
44	chr11:73289224-73289274	AoSMC	blood vessel:	n/a
45	chr11:73289224-73289274	H1-hESC	embryonic stem cell:	embryo
46	chr11:73289224-73289274	AG09319	gingival:	n/a
47	chr11:73289224-73289274	HCF	heart:	n/a
48	chr11:73289224-73289274	ECC-1	luminal epithelium:	n/a
49	chr11:73289224-73289274	Caco-2	colon:	n/a
50	chr11:73289224-73289274	GM12891	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:73289699..73292318-chr11:73308150..73310462,2	K562	blood:
2	chr11:73287100..73289867-chr11:73302120..73304102,3	K562	blood:

No data

Variant related genes	Relation type
HMGN2P38	TF binding region
HMGN2P38	CpG island
ENSG00000054965	chromatin interactions

Extended variants
information (count: 210 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:210 , 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	rs551523704	chr11:73289172-73289173	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs565047464	chr11:73289192-73289193	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs59043881	chr11:73289225-73289226	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs550702199	chr11:73289295-73289296	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs7102738	chr11:73289305-73289306	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs536231019	chr11:73289330-73289331	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs546717388	chr11:73289394-73289395	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs117695266	chr11:73289406-73289407	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs373436756	chr11:73289438-73289439	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs370019686	chr11:73289460-73289461	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs190187925	chr11:73289464-73289465	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs182239855	chr11:73289480-73289481	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs546922651	chr11:73289567-73289568	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs568724471	chr11:73289589-73289590	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs575852977	chr11:73289637-73289638	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs186244853	chr11:73289654-73289655	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs555294194	chr11:73289676-73289677	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs535776731	chr11:73289763-73289764	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs573711400	chr11:73289766-73289767	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs542620483	chr11:73289778-73289779	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs540360070	chr11:73289819-73289820	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs559509950	chr11:73289847-73289848	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs572859451	chr11:73289854-73289855	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs544883935	chr11:73289889-73289890	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs149289360	chr11:73289922-73289923	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs530615490	chr11:73289928-73289929	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs189876144	chr11:73289937-73289938	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs143504656	chr11:73289949-73289950	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs182235182	chr11:73289976-73289977	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs530059147	chr11:73289990-73289991	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs137964253	chr11:73289993-73289994	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs184898282	chr11:73290011-73290012	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs539077487	chr11:73290111-73290112	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs552389795	chr11:73290131-73290132	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs11235809	chr11:73290163-73290164	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs7107719	chr11:73290168-73290169	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs568879079	chr11:73290199-73290200	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs575155816	chr11:73290223-73290224	Weak transcription Strong transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs536266507	chr11:73290292-73290293	Weak transcription Strong transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs77469108	chr11:73290355-73290356	Weak transcription Strong transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs572853956	chr11:73290454-73290455	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs545135605	chr11:73290456-73290457	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs574360226	chr11:73290458-73290459	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs11235810	chr11:73290487-73290488	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs575424309	chr11:73290606-73290607	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs543975033	chr11:73290630-73290631	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs541025263	chr11:73290722-73290723	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs78251133	chr11:73290733-73290734	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs573304534	chr11:73290826-73290827	Weak transcription Strong transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs529899244	chr11:73290861-73290862	Weak transcription Strong transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	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
Lung cancer	18438408	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
Lung cancer	19153074	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	17142309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Lung cancer	21203850	CNVD

Chromatin state (count:179 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:73250000-73307800	Weak transcription	Stomach Smooth Muscle	stomach
2	chr11:73253800-73307000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr11:73263200-73306000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr11:73266600-73307800	Weak transcription	Fetal Intestine Small	intestine
5	chr11:73272200-73307600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr11:73274800-73290800	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr11:73275400-73307000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr11:73276400-73289800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr11:73276400-73296800	Weak transcription	Fetal Muscle Leg	muscle
10	chr11:73276400-73299200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr11:73276400-73307000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr11:73277200-73299600	Weak transcription	Primary B cells from peripheral blood	blood
13	chr11:73277400-73307800	Weak transcription	Fetal Intestine Large	intestine
14	chr11:73277600-73293800	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr11:73279400-73289200	Weak transcription	Primary hematopoietic stem cells	blood
16	chr11:73279400-73307000	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr11:73279600-73291200	Weak transcription	Ovary	ovary
18	chr11:73280000-73289800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
19	chr11:73280000-73299400	Weak transcription	Fetal Stomach	stomach
20	chr11:73280600-73289200	Weak transcription	Primary B cells from cord blood	blood
21	chr11:73280600-73296200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr11:73281600-73307800	Weak transcription	Hela-S3	cervix
23	chr11:73281800-73295400	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr11:73282000-73296800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr11:73282200-73296400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr11:73282200-73296600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr11:73282200-73297000	Weak transcription	HMEC	breast
28	chr11:73282200-73297200	Weak transcription	NH-A	brain
29	chr11:73282400-73293800	Weak transcription	HSMM	muscle
30	chr11:73285200-73292400	Weak transcription	Right Atrium	heart
31	chr11:73285200-73294600	Weak transcription	Right Ventricle	heart
32	chr11:73285200-73303600	Weak transcription	Left Ventricle	heart
33	chr11:73285200-73306600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr11:73285600-73289800	Weak transcription	Fetal Lung	lung
35	chr11:73285800-73289800	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr11:73286000-73289200	Strong transcription	Dnd41	blood
37	chr11:73286000-73294800	Weak transcription	Primary neutrophils fromperipheralblood	blood
38	chr11:73286200-73295000	Weak transcription	Primary monocytes fromperipheralblood	blood
39	chr11:73286800-73290200	Enhancers	Brain Germinal Matrix	brain
40	chr11:73286800-73307600	Weak transcription	Lung	lung
41	chr11:73287000-73289200	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr11:73287000-73289200	Enhancers	Brain Substantia Nigra	brain
43	chr11:73287400-73289200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr11:73287400-73290000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr11:73287800-73290000	Enhancers	Brain Hippocampus Middle	brain
46	chr11:73287800-73306200	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr11:73288000-73289400	Enhancers	Skeletal Muscle Female	skeletal muscle
48	chr11:73288000-73289600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr11:73288000-73289800	Weak transcription	Brain Angular Gyrus	brain
50	chr11:73288000-73290000	Enhancers	NHDF-Ad	bronchial

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