Variant report

Variant	nsv541202
Chromosome Location	chr11:127423435-127637119
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	chr11:127497816-127498224	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr11:127497898-127498053	K562	blood:	n/a	n/a
3	BHLHE40	chr11:127501964-127502188	GM12878	blood:	n/a	chr11:127502054-127502063 chr11:127502052-127502065 chr11:127502048-127502069 chr11:127502055-127502064 chr11:127502054-127502063
4	CEBPB	chr11:127538023-127538326	A549	lung:	n/a	n/a
5	CEBPB	chr11:127479484-127479571	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr11:127576997-127577326	IMR90	lung:	n/a	chr11:127577148-127577159
7	CEBPB	chr11:127538008-127538289	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr11:127519979-127520189	H1-hESC	embryonic stem cell:	n/a	chr11:127520081-127520092
9	CEBPB	chr11:127484451-127484769	IMR90	lung:	n/a	chr11:127484600-127484611 chr11:127484598-127484611 chr11:127484600-127484609 chr11:127484598-127484609 chr11:127484598-127484611 chr11:127484600-127484609 chr11:127484600-127484609 chr11:127484598-127484611 chr11:127484600-127484611 chr11:127484600-127484609
10	CEBPB	chr11:127449779-127449939	H1-hESC	embryonic stem cell:	n/a	chr11:127449805-127449816
11	CEBPB	chr11:127449724-127449935	K562	blood:	n/a	chr11:127449805-127449816
12	CEBPB	chr11:127547813-127548084	K562	blood:	n/a	chr11:127547925-127547934 chr11:127547925-127547934 chr11:127547924-127547935 chr11:127547923-127547936 chr11:127547925-127547934 chr11:127547923-127547936 chr11:127547925-127547934 chr11:127547923-127547934
13	CEBPB	chr11:127519999-127520205	HepG2	liver:	n/a	chr11:127520081-127520092
14	CEBPB	chr11:127525098-127525432	IMR90	lung:	n/a	chr11:127525255-127525266 chr11:127525253-127525266 chr11:127525253-127525264
15	CEBPB	chr11:127547728-127548105	HepG2	liver:	n/a	chr11:127547925-127547934 chr11:127547925-127547934 chr11:127547924-127547935 chr11:127547923-127547936 chr11:127547925-127547934 chr11:127547923-127547936 chr11:127547925-127547934 chr11:127547923-127547934
16	CEBPB	chr11:127547753-127548103	IMR90	lung:	n/a	chr11:127547925-127547934 chr11:127547925-127547934 chr11:127547924-127547935 chr11:127547923-127547936 chr11:127547925-127547934 chr11:127547923-127547936 chr11:127547925-127547934 chr11:127547923-127547934
17	CEBPB	chr11:127502993-127503524	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr11:127576981-127577332	HepG2	liver:	n/a	chr11:127577148-127577159
19	CEBPB	chr11:127525106-127525389	HepG2	liver:	n/a	chr11:127525255-127525266 chr11:127525253-127525266 chr11:127525253-127525264
20	CEBPB	chr11:127547774-127547968	H1-hESC	embryonic stem cell:	n/a	chr11:127547925-127547934 chr11:127547925-127547934 chr11:127547924-127547935 chr11:127547923-127547936 chr11:127547925-127547934 chr11:127547923-127547936 chr11:127547925-127547934 chr11:127547923-127547934
21	CEBPB	chr11:127516129-127516224	HepG2	liver:	n/a	chr11:127516175-127516186
22	CEBPB	chr11:127520898-127521437	IMR90	lung:	n/a	n/a
23	CEBPB	chr11:127449629-127449976	HepG2	liver:	n/a	chr11:127449805-127449816
24	CEBPB	chr11:127577005-127577298	A549	lung:	n/a	chr11:127577148-127577159
25	CEBPB	chr11:127501384-127501691	HepG2	liver:	n/a	n/a
26	CEBPB	chr11:127484446-127484767	HepG2	liver:	n/a	chr11:127484600-127484611 chr11:127484598-127484611 chr11:127484600-127484609 chr11:127484598-127484609 chr11:127484598-127484611 chr11:127484600-127484609 chr11:127484600-127484609 chr11:127484598-127484611 chr11:127484600-127484611 chr11:127484600-127484609
27	CEBPB	chr11:127577007-127577222	H1-hESC	embryonic stem cell:	n/a	chr11:127577148-127577159
28	CEBPB	chr11:127501431-127501660	A549	lung:	n/a	n/a
29	CEBPB	chr11:127538014-127538299	IMR90	lung:	n/a	n/a
30	CEBPB	chr11:127449634-127449970	IMR90	lung:	n/a	chr11:127449805-127449816
31	CEBPB	chr11:127484451-127484756	A549	lung:	n/a	chr11:127484600-127484611 chr11:127484598-127484611 chr11:127484600-127484609 chr11:127484598-127484609 chr11:127484598-127484611 chr11:127484600-127484609 chr11:127484600-127484609 chr11:127484598-127484611 chr11:127484600-127484611 chr11:127484600-127484609
32	CEBPB	chr11:127547755-127548077	A549	lung:	n/a	chr11:127547925-127547934 chr11:127547925-127547934 chr11:127547924-127547935 chr11:127547923-127547936 chr11:127547925-127547934 chr11:127547923-127547936 chr11:127547925-127547934 chr11:127547923-127547934
33	CHD2	chr11:127482493-127482777	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr11:127540320-127540470	GM12864	blood:	n/a	n/a
35	CTCF	chr11:127488150-127488291	GM12891	blood:	n/a	n/a
36	CTCF	chr11:127537214-127537276	GM20000	blood:	n/a	n/a
37	CTCF	chr11:127479463-127479542	MCF-7	breast:	n/a	n/a
38	CTCF	chr11:127479421-127479583	MCF-7	breast:	n/a	n/a
39	CTCF	chr11:127465380-127465530	WI-38	lung:	n/a	n/a
40	CTCF	chr11:127479435-127479562	MCF-7	breast:	n/a	n/a
41	CTCF	chr11:127488192-127488273	ProgFib	skin:	n/a	n/a
42	CTCF	chr11:127600400-127600550	Caco-2	colon:	n/a	n/a
43	CTCF	chr11:127624638-127624701	GM13977	blood:	n/a	n/a
44	CTCF	chr11:127488180-127488330	Caco-2	colon:	n/a	n/a
45	CTCF	chr11:127600380-127600530	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr11:127479403-127479568	MCF-7	breast:	n/a	n/a
47	CTCF	chr11:127488161-127488291	GM19239	blood:	n/a	n/a
48	CTCF	chr11:127500428-127500461	Fibrobl	skin:	n/a	n/a
49	CTCF	chr11:127509418-127509480	GM13976	blood:	n/a	n/a
50	CTCF	chr11:127600440-127600590	Caco-2	colon:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:127481918-127481968	HUVEC	blood vessel:	n/a
2	chr11:127445168-127445218	A549	lung:	n/a
3	chr11:127471623-127471673	LNCaP	prostate:	n/a
4	chr11:127481918-127481968	PANC-1	pancreas:	n/a
5	chr11:127471623-127471673	SK-N-SH_RA	brain:	n/a
6	chr11:127547963-127548013	Jurkat	blood:	n/a
7	chr11:127471623-127471673	HCPEpiC	choroid plexus:	n/a
8	chr11:127471623-127471673	SAEC	small airway:	n/a
9	chr11:127547963-127548013	HRCEpiC	kidney:	n/a
10	chr11:127481918-127481968	GM19239	blood:	n/a
11	chr11:127471623-127471673	HCM	heart:	n/a
12	chr11:127547963-127548013	H1-hESC	embryonic stem cell:	embryo
13	chr11:127481918-127481968	ovcar-3	ovarian:	n/a
14	chr11:127481918-127481968	Caco-2	colon:	n/a
15	chr11:127445168-127445218	AG09319	gingival:	n/a
16	chr11:127547963-127548013	BJ	skin:	n/a
17	chr11:127445168-127445218	HCF	heart:	n/a
18	chr11:127547963-127548013	MCF10A-Er-Src	breast:	n/a
19	chr11:127445168-127445218	HepG2	liver:	n/a
20	chr11:127471623-127471673	GM12892	blood:	n/a
21	chr11:127445168-127445218	ProgFib	skin:	n/a
22	chr11:127471623-127471673	NHBE	bronchial:	n/a
23	chr11:127547963-127548013	U87	brain:	n/a
24	chr11:127547963-127548013	ECC-1	luminal epithelium:	n/a
25	chr11:127547963-127548013	Hepatocyte	liver:	n/a
26	chr11:127445168-127445218	HIPEpiC	eye:	n/a
27	chr11:127547963-127548013	PrEC	prostate:	n/a
28	chr11:127471623-127471673	NH-A	brain:	n/a
29	chr11:127481918-127481968	HRE	kidney:	n/a
30	chr11:127471623-127471673	U87	brain:	n/a
31	chr11:127481918-127481968	SK-N-SH_RA	brain:	n/a
32	chr11:127481918-127481968	AG04449	skin:	fetal
33	chr11:127445168-127445218	NT2-D1	testis:	n/a
34	chr11:127481918-127481968	SAEC	small airway:	n/a
35	chr11:127481918-127481968	Hela-S3	cervix:	n/a
36	chr11:127547963-127548013	T-47D	breast:	n/a
37	chr11:127547963-127548013	GM12892	blood:	n/a
38	chr11:127481918-127481968	AG09319	gingival:	n/a
39	chr11:127445168-127445218	GM06990	blood:	n/a
40	chr11:127481918-127481968	AG04450	lung:	fetal
41	chr11:127547963-127548013	HCT-116	colon:	n/a
42	chr11:127547963-127548013	Hela-S3	cervix:	n/a
43	chr11:127481918-127481968	NB4	blood:	n/a
44	chr11:127481918-127481968	CMK	blood:	n/a
45	chr11:127481918-127481968	A549	lung:	n/a
46	chr11:127445168-127445218	HRPEpiC	eye:	n/a
47	chr11:127445168-127445218	IMR90	lung:	fetal
48	chr11:127481918-127481968	HNPCEpiC	eye:	n/a
49	chr11:127471623-127471673	BJ	skin:	n/a
50	chr11:127445168-127445218	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:127471349..127474677-chr11:127481414..127484937,3	K562	blood:
2	chr11:127561976..127564649-chr11:127569398..127572641,3	K562	blood:
3	chr11:127561976..127565555-chr11:127568028..127572641,4	K562	blood:
4	chr11:127561976..127564649-chr11:127569398..127572641,3	K562	blood:
5	chr11:127580769..127582770-chr11:127586879..127588885,2	MCF-7	breast:
6	chr11:127580769..127582770-chr11:127586879..127588885,2	MCF-7	breast:
7	chr11:127561976..127565555-chr11:127568028..127572641,4	K562	blood:
8	chr11:127471349..127474677-chr11:127481414..127484937,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-168K9.2.1-7	chr11:127527463-127527772	NONHSAT025058

Variant related genes	Relation type
ENSG00000254591	TF binding region
ENSG00000254591	CpG island

Extended variants
information (count: 4609 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:4609 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571919941	chr11:127424220-127424221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs541002615	chr11:127424266-127424267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs7122870	chr11:127424310-127424311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs556510828	chr11:127424325-127424326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs533672203	chr11:127424339-127424340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs145307836	chr11:127424381-127424382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs550496499	chr11:127424415-127424416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs563830845	chr11:127424421-127424422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs370944343	chr11:127424477-127424478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs188145184	chr11:127424500-127424501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs549469878	chr11:127424503-127424504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs566142052	chr11:127424504-127424505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs7122824	chr11:127424537-127424538	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs551744148	chr11:127424589-127424590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs568614920	chr11:127424607-127424608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs373319493	chr11:127424615-127424616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs180942449	chr11:127424629-127424630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs73029669	chr11:127424650-127424651	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs556050378	chr11:127424651-127424652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs77688747	chr11:127424685-127424686	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs35617006	chr11:127424686-127424687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs369931645	chr11:127424696-127424697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs535291376	chr11:127424737-127424738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs555302873	chr11:127424742-127424743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs544285455	chr11:127424752-127424753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs545795211	chr11:127424755-127424756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs374620912	chr11:127424783-127424784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs150708954	chr11:127424792-127424793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs35371328	chr11:127424852-127424853	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs139533751	chr11:127424868-127424869	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs11220969	chr11:127424889-127424890	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs117053122	chr11:127424937-127424938	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs142826666	chr11:127424961-127424962	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs563993053	chr11:127425045-127425046	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs376735602	chr11:127425066-127425067	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs529641771	chr11:127425096-127425097	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs544480467	chr11:127425097-127425098	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs76669489	chr11:127425143-127425144	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs543226842	chr11:127425187-127425188	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs146093417	chr11:127425227-127425228	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs528583503	chr11:127425228-127425229	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs551587901	chr11:127425239-127425240	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs571577861	chr11:127425303-127425304	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs185507981	chr11:127425309-127425310	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs545639980	chr11:127425331-127425332	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs569596109	chr11:127425347-127425348	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs368801762	chr11:127425367-127425368	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs191234547	chr11:127425398-127425399	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs183436618	chr11:127425430-127425431	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs565736777	chr11:127425486-127425487	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	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
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Hepatocellular carcinoma	16785998	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Ovarian cancer	21720365	CNVD
Neuroblastoma	17327916	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Renal cell carcinoma	21668985	CNVD
Developmental delay	21147756	CNVD
Squamous cell cancer	20885788	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Multiple myeloma	17550852	CNVD
Heart disease	20551144	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	21509527	CNVD
Barrett''s syndrome	19417022	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21385341	CNVD
Multiple myeloma	16461302	CNVD
Burkitt''s lymphoma	18698080	CNVD
Prostate cancer	23792589	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Burkitt''s lymphoma	20823134	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	19571808	CNVD
Multiple myeloma	16616336	CNVD
Myelodysplastic syndrome	18663149	CNVD
Autism	20858243	CNVD
Cancer	20164919	CNVD
Autism	20531469	CNVD
Urothelial carcinoma	21177765	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21045282	CNVD
Glioblastoma	21080181	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:514 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:127424200-127424600	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr11:127424200-127425400	Enhancers	Fetal Kidney	kidney
3	chr11:127424400-127424600	Enhancers	Fetal Muscle Leg	muscle
4	chr11:127424400-127424800	Enhancers	Fetal Stomach	stomach
5	chr11:127424400-127425000	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr11:127424800-127425200	Weak transcription	Fetal Stomach	stomach
7	chr11:127425000-127425400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
8	chr11:127425200-127425400	Enhancers	Fetal Stomach	stomach
9	chr11:127425400-127425600	Enhancers	Fetal Muscle Leg	muscle
10	chr11:127425400-127425800	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr11:127425400-127430000	Weak transcription	Fetal Stomach	stomach
12	chr11:127425400-127430600	Weak transcription	Fetal Kidney	kidney
13	chr11:127429600-127430600	Enhancers	Fetal Brain Male	brain
14	chr11:127429800-127430200	Enhancers	Fetal Brain Female	brain
15	chr11:127430000-127431200	Enhancers	Fetal Stomach	stomach
16	chr11:127430600-127431000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr11:127430600-127431000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr11:127430600-127431000	Enhancers	Fetal Kidney	kidney
19	chr11:127430800-127431200	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr11:127430800-127431200	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr11:127430800-127431400	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr11:127431200-127437200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr11:127431400-127436800	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr11:127434200-127435400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr11:127434400-127435400	Enhancers	NH-A	brain
26	chr11:127434600-127434800	Enhancers	H1 Cell Line	embryonic stem cell
27	chr11:127434600-127434800	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr11:127434600-127435000	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr11:127434800-127436800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr11:127434800-127437200	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr11:127434800-127438200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr11:127435000-127437000	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr11:127435400-127436400	Enhancers	Fetal Intestine Large	intestine
34	chr11:127436200-127436400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr11:127436400-127437600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr11:127436400-127438000	Weak transcription	Fetal Intestine Large	intestine
37	chr11:127436800-127437800	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr11:127436800-127438000	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr11:127436800-127438200	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr11:127437000-127438000	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr11:127437200-127437600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr11:127437200-127438000	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr11:127437200-127438200	Enhancers	H1 Cell Line	embryonic stem cell
44	chr11:127437200-127438200	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr11:127437200-127438800	Enhancers	Fetal Intestine Small	intestine
46	chr11:127437400-127438000	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr11:127437400-127438400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr11:127437600-127437800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
49	chr11:127437600-127438000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr11:127437600-127438200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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