Variant report

Variant	esv3351862
Chromosome Location	chr11:101897791-101931442
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr11:101918085-101918425	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr11:101897618-101898114	IMR90	lung:	n/a	chr11:101897676-101897689 chr11:101897676-101897687 chr11:101897676-101897687 chr11:101897676-101897689 chr11:101897970-101897983
3	CHD1	chr11:101918487-101918490	H1-hESC	embryonic stem cell:	n/a	n/a
4	CREB1	chr11:101917900-101918376	A549	lung:	n/a	n/a
5	CREB1	chr11:101917933-101918348	ECC-1	luminal epithelium:	n/a	n/a
6	CREB1	chr11:101917909-101918365	H1-hESC	embryonic stem cell:	n/a	n/a
7	CREB1	chr11:101917984-101918259	A549	lung:	n/a	n/a
8	CREB1	chr11:101917830-101918437	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr11:101918180-101918330	AG09319	gingival:	n/a	n/a
10	CTCF	chr11:101918460-101918610	NHLF	lung:	n/a	n/a
11	CTCF	chr11:101918200-101918350	NHEK	skin:	n/a	n/a
12	CTCF	chr11:101918240-101918390	HCPEpiC	choroid plexus:	n/a	n/a
13	CTCF	chr11:101918180-101918330	HEEpiC	esophagus:	n/a	n/a
14	CTCF	chr11:101918140-101918290	HCM	heart:	n/a	n/a
15	CTCF	chr11:101918280-101918430	AoAF	blood vessel:	n/a	n/a
16	CTCF	chr11:101918300-101918450	AG04450	lung:	n/a	n/a
17	CTCF	chr11:101918280-101918430	HAc	cerebellar:	n/a	n/a
18	CTCF	chr11:101918200-101918350	HUVEC	blood vessel:	n/a	n/a
19	CTCF	chr11:101918260-101918410	HPAF	blood vessel:	n/a	n/a
20	CTCF	chr11:101918300-101918450	AG04449	skin:	n/a	n/a
21	CTCF	chr11:101918220-101918370	HBMEC	blood vessel:	n/a	n/a
22	E2F4	chr11:101918707-101918868	MCF10A-Er-Src	breast:	n/a	n/a
23	E2F4	chr11:101917939-101918462	MCF10A-Er-Src	breast:	n/a	chr11:101918118-101918127
24	E2F6	chr11:101917970-101918619	H1-hESC	embryonic stem cell:	n/a	chr11:101918118-101918127
25	E2F6	chr11:101918000-101918570	A549	lung:	n/a	chr11:101918118-101918127
26	E2F6	chr11:101917858-101918746	A549	lung:	n/a	chr11:101918118-101918127
27	E2F6	chr11:101917906-101918718	H1-hESC	embryonic stem cell:	n/a	chr11:101918118-101918127
28	EBF1	chr11:101917937-101918266	GM12878	blood:	n/a	chr11:101918100-101918111 chr11:101918100-101918110
29	EBF1	chr11:101917904-101918247	GM12878	blood:	n/a	chr11:101918100-101918111 chr11:101918100-101918110
30	EBF1	chr11:101918003-101918266	GM12878	blood:	n/a	chr11:101918100-101918111 chr11:101918100-101918110
31	EGR1	chr11:101917960-101918311	ECC-1	luminal epithelium:	n/a	chr11:101918120-101918130 chr11:101918114-101918136 chr11:101918118-101918132 chr11:101918120-101918130 chr11:101918119-101918132 chr11:101918119-101918132 chr11:101918119-101918129 chr11:101918118-101918133 chr11:101918120-101918131 chr11:101918117-101918127 chr11:101918119-101918132 chr11:101918120-101918129 chr11:101918119-101918132
32	EGR1	chr11:101917947-101918300	H1-hESC	embryonic stem cell:	n/a	chr11:101918120-101918130 chr11:101918114-101918136 chr11:101918118-101918132 chr11:101918120-101918130 chr11:101918119-101918132 chr11:101918119-101918132 chr11:101918119-101918129 chr11:101918118-101918133 chr11:101918120-101918131 chr11:101918117-101918127 chr11:101918119-101918132 chr11:101918120-101918129 chr11:101918119-101918132
33	EGR1	chr11:101917989-101918240	K562	blood:	n/a	chr11:101918120-101918130 chr11:101918114-101918136 chr11:101918118-101918132 chr11:101918120-101918130 chr11:101918119-101918132 chr11:101918119-101918132 chr11:101918119-101918129 chr11:101918118-101918133 chr11:101918120-101918131 chr11:101918117-101918127 chr11:101918119-101918132 chr11:101918120-101918129 chr11:101918119-101918132
34	ELK4	chr11:101917973-101918282	HEK293	kidney:	n/a	n/a
35	EP300	chr11:101897622-101898011	SK-N-SH_RA	brain:	n/a	chr11:101897674-101897688
36	EP300	chr11:101897684-101898035	SK-N-SH_RA	brain:	n/a	n/a
37	FOS	chr11:101925915-101926028	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr11:101925849-101926039	MCF10A-Er-Src	breast:	n/a	n/a
39	FOXP2	chr11:101917942-101918216	PFSK-1	brain:	n/a	n/a
40	FOXP2	chr11:101917937-101918271	SK-N-MC	brain:	n/a	n/a
41	GATA3	chr11:101924355-101924779	MCF-7	breast:	n/a	chr11:101924582-101924589 chr11:101924583-101924600 chr11:101924580-101924592 chr11:101924582-101924591
42	GTF2F1	chr11:101917978-101918077	H1-hESC	embryonic stem cell:	n/a	n/a
43	HDAC2	chr11:101917877-101918256	H1-hESC	embryonic stem cell:	n/a	n/a
44	JUN	chr11:101921707-101922020	HepG2	liver:	n/a	chr11:101921855-101921868
45	JUN	chr11:101916758-101916793	HepG2	liver:	n/a	n/a
46	JUND	chr11:101921678-101922015	HepG2	liver:	n/a	n/a
47	JUND	chr11:101929658-101929883	HepG2	liver:	n/a	chr11:101929778-101929785 chr11:101929776-101929787 chr11:101929778-101929786 chr11:101929776-101929788 chr11:101929777-101929786 chr11:101929778-101929787
48	MAFF	chr11:101927563-101927840	HepG2	liver:	n/a	n/a
49	MAFF	chr11:101920895-101921060	HepG2	liver:	n/a	chr11:101920934-101920952
50	MAFF	chr11:101899529-101899530	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:101918403-101918453	HAEpiC	amniotic membrane:	n/a
2	chr11:101918157-101918207	LNCaP	prostate:	n/a
3	chr11:101916810-101916860	HNPCEpiC	eye:	n/a
4	chr11:101918171-101918221	MCF10A-Er-Src	breast:	n/a
5	chr11:101916810-101916860	HCM	heart:	n/a
6	chr11:101918145-101918195	SAEC	small airway:	n/a
7	chr11:101917981-101918031	HRPEpiC	eye:	n/a
8	chr11:101918152-101918202	A549	lung:	n/a
9	chr11:101918403-101918453	Caco-2	colon:	n/a
10	chr11:101918403-101918453	CMK	blood:	n/a
11	chr11:101917847-101917897	GM06990	blood:	n/a
12	chr11:101918152-101918202	H1-hESC	embryonic stem cell:	embryo
13	chr11:101918710-101918760	HRPEpiC	eye:	n/a
14	chr11:101918710-101918760	U87	brain:	n/a
15	chr11:101918140-101918190	PANC-1	pancreas:	n/a
16	chr11:101918140-101918190	GM12878	blood:	n/a
17	chr11:101921849-101921899	PANC-1	pancreas:	n/a
18	chr11:101918304-101918354	GM12878	blood:	n/a
19	chr11:101921849-101921899	NH-A	brain:	n/a
20	chr11:101915387-101915437	Jurkat	blood:	n/a
21	chr11:101918145-101918195	AG04449	skin:	fetal
22	chr11:101918710-101918760	Hepatocyte	liver:	n/a
23	chr11:101918152-101918202	Hepatocyte	liver:	n/a
24	chr11:101918157-101918207	NB4	blood:	n/a
25	chr11:101921849-101921899	SK-N-SH	brain:	n/a
26	chr11:101915387-101915437	Hela-S3	cervix:	n/a
27	chr11:101918575-101918625	AG10803	skin:	n/a
28	chr11:101918152-101918202	HRE	kidney:	n/a
29	chr11:101918157-101918207	Hela-S3	cervix:	n/a
30	chr11:101921849-101921899	HUVEC	blood vessel:	n/a
31	chr11:101918304-101918354	AG10803	skin:	n/a
32	chr11:101915387-101915437	BJ	skin:	n/a
33	chr11:101918575-101918625	PFSK-1	brain:	n/a
34	chr11:101915387-101915437	NB4	blood:	n/a
35	chr11:101918710-101918760	GM06990	blood:	n/a
36	chr11:101918145-101918195	AG09319	gingival:	n/a
37	chr11:101918171-101918221	HCM	heart:	n/a
38	chr11:101918171-101918221	NHBE	bronchial:	n/a
39	chr11:101917981-101918031	PrEC	prostate:	n/a
40	chr11:101918403-101918453	LNCaP	prostate:	n/a
41	chr11:101918403-101918453	HNPCEpiC	eye:	n/a
42	chr11:101918171-101918221	IMR90	lung:	fetal
43	chr11:101918575-101918625	CMK	blood:	n/a
44	chr11:101918157-101918207	BE2_C	brain:	n/a
45	chr11:101918157-101918207	GM12891	blood:	n/a
46	chr11:101916810-101916860	AoSMC	blood vessel:	n/a
47	chr11:101918403-101918453	RPTEC	kidney:	n/a
48	chr11:101918157-101918207	K562	blood:	n/a
49	chr11:101918140-101918190	SAEC	small airway:	n/a
50	chr11:101918171-101918221	HMEC	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:101923063..101925584-chr11:101978678..101981062,2	MCF-7	breast:
2	chr11:101907253..101909356-chr11:101914990..101916981,2	MCF-7	breast:
3	chr11:101907563..101909226-chr11:101910658..101913238,2	K562	blood:
4	chr11:101894694..101896719-chr11:101899860..101902314,2	K562	blood:
5	chr11:101907563..101909226-chr11:101910658..101913238,2	K562	blood:
6	chr11:101907253..101909356-chr11:101914990..101916981,2	MCF-7	breast:

Variant related genes	Relation type
C11orf70	TF binding region
ENSG00000252679	TF binding region
ENSG00000239154	TF binding region
C11orf70	CpG island
ENSG00000252679	CpG island
ENSG00000239154	CpG island

Extended variants
information (count: 1275 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1275 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555898089	chr11:101897798-101897799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs544606392	chr11:101897832-101897833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs572557503	chr11:101897835-101897836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs541290298	chr11:101897876-101897877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs558360669	chr11:101897898-101897899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs139700051	chr11:101897918-101897919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs544138622	chr11:101897926-101897927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs79645794	chr11:101898020-101898021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs528862473	chr11:101898089-101898090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs531308250	chr11:101898206-101898207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs542275273	chr11:101898259-101898260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs113905481	chr11:101898271-101898272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs528261530	chr11:101898310-101898311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs7924710	chr11:101898318-101898319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs566912459	chr11:101898331-101898332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs529320594	chr11:101898407-101898408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs549391862	chr11:101898423-101898424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs184541234	chr11:101898447-101898448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs530704630	chr11:101898454-101898455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs189437271	chr11:101898496-101898497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs151055579	chr11:101898547-101898548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs535857094	chr11:101898562-101898563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs555860945	chr11:101898832-101898833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs369156075	chr11:101898877-101898878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs535155535	chr11:101898921-101898922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs558061148	chr11:101898937-101898938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs374081335	chr11:101898947-101898948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs578158243	chr11:101898955-101898956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs140998357	chr11:101898956-101898957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs557242313	chr11:101898969-101898970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs573267755	chr11:101898993-101898994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs542238220	chr11:101899023-101899024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs373105010	chr11:101899041-101899042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs528158689	chr11:101899067-101899068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs542970640	chr11:101899110-101899111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs568399057	chr11:101899136-101899137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs564926967	chr11:101899137-101899138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs78753380	chr11:101899143-101899144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs4754830	chr11:101899146-101899147	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs567579348	chr11:101899218-101899219	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs530047916	chr11:101899222-101899223	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs549385708	chr11:101899225-101899226	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs377040287	chr11:101899239-101899240	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs566109086	chr11:101899298-101899299	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs534807235	chr11:101899301-101899302	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs182036745	chr11:101899328-101899329	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs557265625	chr11:101899335-101899336	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs571710616	chr11:101899503-101899504	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs542824730	chr11:101899595-101899596	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs117181739	chr11:101899610-101899611	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	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
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	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	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	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
Melanoma	22183965	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Mantle cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal cancer	21851588	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:101895200-101899200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr11:101896000-101898000	Enhancers	Fetal Brain Female	brain
3	chr11:101896000-101898000	Enhancers	Placenta Amnion	Placenta Amnion
4	chr11:101896200-101898000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr11:101896400-101898000	Enhancers	Duodenum Smooth Muscle	Duodenum
6	chr11:101896400-101898000	Enhancers	NHEK	skin
7	chr11:101896600-101898000	Enhancers	Sigmoid Colon	Sigmoid Colon
8	chr11:101897000-101898000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr11:101897000-101898000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr11:101897000-101898000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr11:101897000-101898000	Enhancers	Placenta	Placenta
12	chr11:101897200-101897800	Enhancers	Fetal Lung	lung
13	chr11:101897200-101898000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr11:101897200-101898000	Enhancers	Fetal Intestine Small	intestine
15	chr11:101897200-101898200	Enhancers	Fetal Intestine Large	intestine
16	chr11:101897200-101898200	Enhancers	Rectal Smooth Muscle	rectum
17	chr11:101897200-101900000	Enhancers	HepG2	liver
18	chr11:101897400-101898000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr11:101897400-101898000	Enhancers	Rectal Mucosa Donor 29	rectum
20	chr11:101897800-101898000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr11:101898000-101899200	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr11:101898000-101899600	Weak transcription	Fetal Intestine Small	intestine
23	chr11:101898000-101901000	Weak transcription	Placenta	Placenta
24	chr11:101899200-101899800	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr11:101899200-101900200	Enhancers	Placenta Amnion	Placenta Amnion
26	chr11:101899600-101900000	Enhancers	Fetal Intestine Small	intestine
27	chr11:101899800-101900000	Enhancers	Fetal Intestine Large	intestine
28	chr11:101899800-101900000	Enhancers	Sigmoid Colon	Sigmoid Colon
29	chr11:101899800-101918000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr11:101901000-101901200	Enhancers	Placenta	Placenta
31	chr11:101917200-101917600	Enhancers	NHDF-Ad	bronchial
32	chr11:101917400-101917600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr11:101917400-101917800	Enhancers	Osteobl	bone
34	chr11:101917600-101917800	Enhancers	Muscle Satellite Cultured Cells	--
35	chr11:101917600-101917800	Enhancers	NHEK	skin
36	chr11:101917600-101918000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr11:101917600-101918400	Active TSS	iPS-20b Cell Line	embryonic stem cell
38	chr11:101917600-101918600	Active TSS	HUES48 Cell Line	embryonic stem cell
39	chr11:101917600-101918600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr11:101917600-101919000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr11:101917600-101919000	Active TSS	Pancreatic Islets	Pancreatic Islet
42	chr11:101917600-101919000	Active TSS	NHDF-Ad	bronchial
43	chr11:101917600-101919200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr11:101917800-101918000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr11:101917800-101918000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr11:101917800-101918000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr11:101917800-101918000	Active TSS	Primary T helper naive cells fromperipheralblood	blood
48	chr11:101917800-101918000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr11:101917800-101918000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
50	chr11:101917800-101918000	Active TSS	Cortex derived primary cultured neurospheres	brain

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