Variant report

Variant	nsv468866
Chromosome Location	chr11:107472733-107566585
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	ATF1	chr11:107559172-107559178	K562	blood:	n/a	n/a
2	ATF1	chr11:107537932-107538032	K562	blood:	n/a	n/a
3	BATF	chr11:107549940-107550117	GM12878	blood:	n/a	chr11:107550057-107550068
4	BATF	chr11:107549940-107550234	GM12878	blood:	n/a	chr11:107550057-107550068
5	BCL11A	chr11:107549860-107550416	GM12878	blood:	n/a	chr11:107550355-107550364
6	BHLHE40	chr11:107542618-107542879	K562	blood:	n/a	n/a
7	BRCA1	chr11:107476939-107476971	GM12878	blood:	n/a	n/a
8	BRCA1	chr11:107487918-107488014	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr11:107522375-107522732	HCT-116	colon:	n/a	n/a
10	CEBPB	chr11:107560412-107560635	A549	lung:	n/a	n/a
11	CEBPB	chr11:107495458-107495625	K562	blood:	n/a	chr11:107495501-107495512
12	CEBPB	chr11:107548781-107548947	HepG2	liver:	n/a	chr11:107548864-107548875
13	CEBPB	chr11:107498665-107498928	IMR90	lung:	n/a	chr11:107498802-107498813 chr11:107498800-107498813 chr11:107498800-107498811 chr11:107498800-107498813
14	CEBPB	chr11:107475812-107476144	H1-hESC	embryonic stem cell:	n/a	chr11:107475822-107475833 chr11:107475981-107475992
15	CEBPB	chr11:107475891-107476093	MCF-7	breast:	n/a	chr11:107475981-107475992
16	CEBPB	chr11:107475899-107476029	HepG2	liver:	n/a	chr11:107475981-107475992
17	CEBPB	chr11:107498773-107498861	HepG2	liver:	n/a	chr11:107498802-107498813 chr11:107498800-107498813 chr11:107498800-107498811 chr11:107498800-107498813
18	CEBPB	chr11:107475735-107476116	HCT-116	colon:	n/a	chr11:107475822-107475833 chr11:107475981-107475992
19	CEBPB	chr11:107498752-107498856	H1-hESC	embryonic stem cell:	n/a	chr11:107498802-107498813 chr11:107498800-107498813 chr11:107498800-107498811 chr11:107498800-107498813
20	CEBPB	chr11:107523899-107524111	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr11:107498700-107498900	K562	blood:	n/a	chr11:107498802-107498813 chr11:107498800-107498813 chr11:107498800-107498811 chr11:107498800-107498813
22	CEBPB	chr11:107522057-107522063	K562	blood:	n/a	n/a
23	CEBPB	chr11:107527338-107527485	K562	blood:	n/a	chr11:107527401-107527414 chr11:107527403-107527414
24	CEBPB	chr11:107560366-107560714	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr11:107475839-107476051	K562	blood:	n/a	chr11:107475981-107475992
26	CEBPB	chr11:107475924-107476134	A549	lung:	n/a	chr11:107475981-107475992
27	CEBPB	chr11:107480617-107480956	HepG2	liver:	n/a	n/a
28	CEBPB	chr11:107475829-107476152	K562	blood:	n/a	chr11:107475981-107475992
29	CEBPB	chr11:107475817-107476087	A549	lung:	n/a	chr11:107475822-107475833 chr11:107475981-107475992
30	CEBPB	chr11:107560353-107560632	HepG2	liver:	n/a	n/a
31	CEBPB	chr11:107495427-107495616	H1-hESC	embryonic stem cell:	n/a	chr11:107495501-107495512
32	CEBPB	chr11:107495424-107495579	HepG2	liver:	n/a	chr11:107495501-107495512
33	CEBPB	chr11:107475936-107476030	HepG2	liver:	n/a	chr11:107475981-107475992
34	CEBPD	chr11:107517461-107517916	K562	blood:	n/a	n/a
35	CHD2	chr11:107480244-107480343	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr11:107549866-107550355	GM12878	blood:	n/a	n/a
37	CTCF	chr11:107554620-107554770	WERI-Rb-1	eye:	n/a	chr11:107554651-107554664
38	CTCF	chr11:107522535-107522577	ProgFib	skin:	n/a	n/a
39	CTCF	chr11:107554640-107554790	HPAF	blood vessel:	n/a	chr11:107554651-107554664
40	CTCF	chr11:107560480-107560630	GM12874	blood:	n/a	chr11:107560517-107560530 chr11:107560510-107560531 chr11:107560515-107560533
41	CTCF	chr11:107560440-107560590	HEEpiC	esophagus:	n/a	chr11:107560517-107560530 chr11:107560510-107560531 chr11:107560515-107560533
42	CTCF	chr11:107560440-107560590	HMF	breast:	n/a	chr11:107560517-107560530 chr11:107560510-107560531 chr11:107560515-107560533
43	CTCF	chr11:107554620-107554770	HL-60	blood:	n/a	chr11:107554651-107554664
44	CTCF	chr11:107533700-107533850	GM12869	blood:	n/a	n/a
45	CTCF	chr11:107560680-107560830	WI-38	lung:	n/a	n/a
46	CTCF	chr11:107560400-107560550	GM12866	blood:	n/a	chr11:107560517-107560530 chr11:107560510-107560531 chr11:107560515-107560533
47	CTCF	chr11:107560409-107560596	SK-N-SH_RA	brain:	n/a	chr11:107560517-107560530 chr11:107560510-107560531 chr11:107560515-107560533
48	CTCF	chr11:107476940-107477090	NHDF-neo	bronchial:	n/a	chr11:107477008-107477029
49	CTCF	chr11:107560840-107560990	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr11:107475808-107476064	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:107519203-107519253	HNPCEpiC	eye:	n/a
2	chr11:107540995-107541045	HUVEC	blood vessel:	n/a
3	chr11:107519203-107519253	AG04450	lung:	fetal
4	chr11:107537213-107537263	HCF	heart:	n/a
5	chr11:107540995-107541045	SK-N-MC	brain:	n/a
6	chr11:107540995-107541045	ProgFib	skin:	n/a
7	chr11:107496475-107496525	GM12892	blood:	n/a
8	chr11:107540995-107541045	PANC-1	pancreas:	n/a
9	chr11:107537213-107537263	Hepatocyte	liver:	n/a
10	chr11:107496475-107496525	GM06990	blood:	n/a
11	chr11:107496475-107496525	SK-N-SH	brain:	n/a
12	chr11:107537213-107537263	ECC-1	luminal epithelium:	n/a
13	chr11:107537213-107537263	GM19239	blood:	n/a
14	chr11:107519203-107519253	AG09319	gingival:	n/a
15	chr11:107537213-107537263	GM12878	blood:	n/a
16	chr11:107537213-107537263	HCM	heart:	n/a
17	chr11:107537213-107537263	HPAEpiC	pulmonary alveolar:	n/a
18	chr11:107496475-107496525	HPAEpiC	pulmonary alveolar:	n/a
19	chr11:107519203-107519253	K562	blood:	n/a
20	chr11:107537213-107537263	HNPCEpiC	eye:	n/a
21	chr11:107519203-107519253	HRCEpiC	kidney:	n/a
22	chr11:107496475-107496525	LNCaP	prostate:	n/a
23	chr11:107537213-107537263	NH-A	brain:	n/a
24	chr11:107537213-107537263	PANC-1	pancreas:	n/a
25	chr11:107540995-107541045	HPAEpiC	pulmonary alveolar:	n/a
26	chr11:107537213-107537263	HAEpiC	amniotic membrane:	n/a
27	chr11:107537213-107537263	PrEC	prostate:	n/a
28	chr11:107540995-107541045	GM12878	blood:	n/a
29	chr11:107496475-107496525	AG10803	skin:	n/a
30	chr11:107519203-107519253	HMEC	breast:	n/a
31	chr11:107537213-107537263	GM12891	blood:	n/a
32	chr11:107519203-107519253	NB4	blood:	n/a
33	chr11:107496475-107496525	PrEC	prostate:	n/a
34	chr11:107537213-107537263	HUVEC	blood vessel:	n/a
35	chr11:107537213-107537263	NHBE	bronchial:	n/a
36	chr11:107537213-107537263	AG09319	gingival:	n/a
37	chr11:107496475-107496525	AG04450	lung:	fetal
38	chr11:107519203-107519253	PFSK-1	brain:	n/a
39	chr11:107519203-107519253	AG10803	skin:	n/a
40	chr11:107496475-107496525	NH-A	brain:	n/a
41	chr11:107540995-107541045	HCT-116	colon:	n/a
42	chr11:107537213-107537263	T-47D	breast:	n/a
43	chr11:107537213-107537263	NHDF-neo	bronchial:	n/a
44	chr11:107496475-107496525	AoSMC	blood vessel:	n/a
45	chr11:107537213-107537263	ovcar-3	ovarian:	n/a
46	chr11:107540995-107541045	T-47D	breast:	n/a
47	chr11:107496475-107496525	ECC-1	luminal epithelium:	n/a
48	chr11:107496475-107496525	HMEC	breast:	n/a
49	chr11:107540995-107541045	HepG2	liver:	n/a
50	chr11:107519203-107519253	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:107560069..107560995-chr11:107641497..107642096,3	MCF-7	breast:
2	chr11:107435466..107437505-chr11:107558141..107560561,3	K562	blood:
3	chr11:107499538..107501877-chr11:107503729..107506113,2	K562	blood:
4	chr11:107435466..107437371-chr11:107558528..107560561,2	K562	blood:
5	chr11:107433924..107437606-chr11:107557431..107561019,4	MCF-7	breast:
6	chr11:106189939..106190500-chr11:107560120..107561021,2	K562	blood:
7	chr11:107492917..107496514-chr11:107496948..107499847,3	K562	blood:
8	chr11:107533663..107536332-chr11:107539088..107541417,2	K562	blood:
9	chr11:107434249..107434771-chr11:107560082..107560724,2	MCF-7	breast:
10	chr11:107447431..107448148-chr11:107560127..107560783,2	MCF-7	breast:
11	chr11:107499538..107501621-chr11:107504588..107506113,2	K562	blood:
12	chr11:107473623..107475571-chr11:107491521..107493538,2	MCF-7	breast:
13	chr11:107447551..107449731-chr11:107476688..107479043,2	MCF-7	breast:
14	chr11:107420177..107420684-chr11:107560050..107560867,2	MCF-7	breast:
15	chr11:107545277..107546932-chr11:107553541..107555478,2	K562	blood:
16	chr11:107499538..107501621-chr11:107504588..107506113,2	K562	blood:
17	chr11:107473623..107475571-chr11:107491521..107493538,2	MCF-7	breast:
18	chr11:107492917..107496514-chr11:107496948..107499847,3	K562	blood:
19	chr11:107434069..107435069-chr11:107559704..107560955,5	K562	blood:
20	chr11:107499538..107501877-chr11:107503729..107506113,2	K562	blood:
21	chr11:107545277..107546932-chr11:107553541..107555478,2	K562	blood:
22	chr11:107553206..107555890-chr11:107557656..107559672,2	K562	blood:
23	chr11:107553206..107555890-chr11:107557656..107559672,2	K562	blood:
24	chr11:107518067..107520406-chr11:107522750..107524559,2	K562	blood:
25	chr11:107533663..107536332-chr11:107539088..107541417,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AP001024.2-2	chr11:107488831-107488932	NONHSAT023996
2	lnc-AP001024.2-2	chr11:107488831-107488932	NONHSAT023998
3	lnc-AP001024.2-2	chr11:107494005-107494590	NONHSAT023996
4	lnc-SLN-1	chr11:107513613-107513761	NONHSAT024000
5	lnc-AP001024.2-2	chr11:107490762-107491196	NONHSAT023998
6	lnc-SLN-1	chr11:107514087-107514597	NONHSAT024000

Variant related genes	Relation type
ENSG00000254758	TF binding region
ELMOD1	TF binding region
ENSG00000255483	TF binding region
ENSG00000254758	CpG island
ELMOD1	CpG island
ENSG00000255483	CpG island
ENSG00000110675	chromatin interactions
ENSG00000137760	chromatin interactions

Extended variants
information (count: 3279 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:3279 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs670446	chr11:107472733-107472734	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs148724749	chr11:107472751-107472752	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs571872962	chr11:107472794-107472795	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs548762714	chr11:107472855-107472856	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs567259027	chr11:107472865-107472866	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs112614190	chr11:107472888-107472889	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs188861101	chr11:107472909-107472910	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs369995771	chr11:107472954-107472955	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs181643491	chr11:107472971-107472972	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs502537	chr11:107472988-107472989	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs572169613	chr11:107472998-107472999	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs184662672	chr11:107473048-107473049	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs202035804	chr11:107473053-107473054	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs139918582	chr11:107473054-107473055	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs567489340	chr11:107473061-107473062	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs576674321	chr11:107473079-107473080	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs544116394	chr11:107473089-107473090	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs12271970	chr11:107473116-107473117	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs190813450	chr11:107473170-107473171	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs550806756	chr11:107473175-107473176	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs541054580	chr11:107473326-107473327	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs143381456	chr11:107473399-107473400	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553106850	chr11:107473403-107473404	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs146744854	chr11:107473414-107473415	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs541889665	chr11:107473437-107473438	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs71047612	chr11:107473452-107473453	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs398115801	chr11:107473464-107473465	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs561800	chr11:107473480-107473481	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs180671750	chr11:107473507-107473508	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs377171110	chr11:107473519-107473520	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs186120865	chr11:107473543-107473544	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs571442159	chr11:107473595-107473596	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371162804	chr11:107473598-107473599	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375471882	chr11:107473600-107473601	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs368442600	chr11:107473601-107473602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs200177422	chr11:107473602-107473603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs57329522	chr11:107473603-107473604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs200666235	chr11:107473604-107473605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs370276198	chr11:107473606-107473607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs373730016	chr11:107473607-107473608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs140402739	chr11:107473619-107473620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs149870188	chr11:107473665-107473666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs536368385	chr11:107473693-107473694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs367816222	chr11:107473709-107473710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs144880273	chr11:107473733-107473734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs12293060	chr11:107473825-107473826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs570234182	chr11:107473833-107473834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs537205130	chr11:107473836-107473837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs73557730	chr11:107473935-107473936	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs577463081	chr11:107473944-107473945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	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
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mantle cell lymphoma	19029149	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Obesity	19966786	CNVD
Renal cell carcinoma	21668985	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD

Chromatin state (count:461 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:107463200-107482600	Weak transcription	HSMMtube	muscle
2	chr11:107469400-107476400	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr11:107469800-107472800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr11:107469800-107479000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr11:107470000-107476400	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr11:107470000-107479000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr11:107472600-107473600	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr11:107472600-107473600	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr11:107472600-107473800	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr11:107472800-107473800	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr11:107473000-107473400	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr11:107473600-107474600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr11:107473800-107476200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr11:107473800-107476200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr11:107474600-107475200	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr11:107474800-107475200	Enhancers	Fetal Kidney	kidney
17	chr11:107475200-107476600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr11:107476200-107476600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr11:107476200-107476800	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr11:107476200-107477000	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr11:107476200-107477200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr11:107476400-107477000	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr11:107476400-107477200	Enhancers	H1 Cell Line	embryonic stem cell
24	chr11:107476400-107477200	Enhancers	H9 Cell Line	embryonic stem cell
25	chr11:107476400-107477200	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr11:107476600-107477000	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr11:107476800-107477200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr11:107476800-107478800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr11:107477000-107478800	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr11:107477000-107479000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr11:107477000-107479000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr11:107477200-107478800	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr11:107477200-107479400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr11:107477200-107479600	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr11:107477200-107480400	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr11:107478400-107481000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr11:107478600-107481000	Enhancers	HUVEC	blood vessel
38	chr11:107478800-107479200	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr11:107478800-107480400	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr11:107478800-107480400	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr11:107479000-107479200	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr11:107479000-107480000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr11:107479000-107480600	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr11:107479000-107480600	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr11:107479000-107481000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr11:107479200-107479600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
47	chr11:107479200-107479800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
48	chr11:107479200-107481000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
49	chr11:107479400-107480200	Enhancers	Liver	Liver
50	chr11:107479400-107481200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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