Variant report

Variant	nsv898331
Chromosome Location	chr11:101436689-101492630
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:164)
CpG islands
(count:918)
Chromatin interactive
region (count:3)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:164 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr11:101453804-101454530	H1-hESC	embryonic stem cell:	n/a	n/a
2	BRCA1	chr11:101448053-101448058	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr11:101479664-101480027	K562	blood:	n/a	chr11:101479836-101479847
4	CEBPB	chr11:101479691-101480023	Hela-S3	cervix:	n/a	chr11:101479836-101479847
5	CEBPB	chr11:101447538-101447615	A549	lung:	n/a	chr11:101447539-101447552 chr11:101447539-101447550 chr11:101447539-101447550 chr11:101447539-101447552
6	CEBPB	chr11:101479653-101480027	IMR90	lung:	n/a	chr11:101479836-101479847
7	CEBPB	chr11:101479738-101480000	ECC-1	luminal epithelium:	n/a	chr11:101479836-101479847
8	CEBPB	chr11:101479658-101480030	HepG2	liver:	n/a	chr11:101479836-101479847
9	CEBPB	chr11:101479661-101480026	A549	lung:	n/a	chr11:101479836-101479847
10	CEBPB	chr11:101489534-101489734	IMR90	lung:	n/a	n/a
11	CEBPB	chr11:101479694-101480015	H1-hESC	embryonic stem cell:	n/a	chr11:101479836-101479847
12	CEBPB	chr11:101479637-101480107	A549	lung:	n/a	chr11:101479836-101479847
13	CEBPB	chr11:101479703-101480053	MCF-7	breast:	n/a	chr11:101479836-101479847
14	CHD1	chr11:101454054-101454582	H1-hESC	embryonic stem cell:	n/a	chr11:101454269-101454279
15	CHD2	chr11:101437815-101438108	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTBP2	chr11:101453612-101454851	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr11:101457680-101457830	GM12867	blood:	n/a	n/a
18	CTCF	chr11:101490920-101491070	GM12865	blood:	n/a	chr11:101490955-101490973
19	CTCF	chr11:101490880-101491030	GM12868	blood:	n/a	chr11:101490955-101490973
20	CTCF	chr11:101490860-101491010	GM12865	blood:	n/a	chr11:101490955-101490973
21	CTCF	chr11:101490940-101491090	GM06990	blood:	n/a	chr11:101490955-101490973
22	CTCF	chr11:101454540-101454690	AG04450	lung:	n/a	n/a
23	CTCF	chr11:101454060-101454210	SAEC	small airway:	n/a	n/a
24	CTCF	chr11:101440502-101440575	Kidney_OC	kidney:	n/a	n/a
25	CTCF	chr11:101490907-101491034	GM12878	blood:	n/a	chr11:101490955-101490973
26	CTCF	chr11:101454141-101454226	MCF-7	breast:	n/a	n/a
27	CTCF	chr11:101490960-101491110	GM12864	blood:	n/a	n/a
28	CTCF	chr11:101490880-101491030	Caco-2	colon:	n/a	chr11:101490955-101490973
29	CTCF	chr11:101441195-101441294	GM20000	blood:	n/a	n/a
30	CTCF	chr11:101454117-101454317	IMR90	lung:	n/a	n/a
31	CTCF	chr11:101490840-101491098	H1-hESC	embryonic stem cell:	n/a	chr11:101490955-101490973
32	CTCF	chr11:101490880-101491030	HEEpiC	esophagus:	n/a	chr11:101490955-101490973
33	CTCF	chr11:101454145-101454188	A549	lung:	n/a	n/a
34	CTCF	chr11:101490868-101491042	LNCaP	prostate:	n/a	chr11:101490955-101490973
35	CTCF	chr11:101454600-101454750	HRE	kidney:	n/a	n/a
36	CTCF	chr11:101490867-101491128	GM12878	blood:	n/a	chr11:101490955-101490973
37	CTCF	chr11:101490847-101491062	LNCaP	prostate:	n/a	chr11:101490955-101490973
38	CTCF	chr11:101454122-101454157	MCF-7	breast:	n/a	n/a
39	CTCF	chr11:101490860-101491010	WERI-Rb-1	eye:	n/a	chr11:101490955-101490973
40	CTCF	chr11:101490931-101490981	MCF-7	breast:	n/a	chr11:101490955-101490973
41	CTCF	chr11:101490920-101491070	Caco-2	colon:	n/a	chr11:101490955-101490973
42	CTCF	chr11:101490900-101491050	GM12873	blood:	n/a	chr11:101490955-101490973
43	CTCF	chr11:101490920-101491070	GM12867	blood:	n/a	chr11:101490955-101490973
44	CTCF	chr11:101490919-101490999	NHEK	skin:	n/a	chr11:101490955-101490973
45	CTCF	chr11:101446820-101446970	NHDF-neo	bronchial:	n/a	n/a
46	CTCF	chr11:101445705-101445729	Lung_OC	lung:	n/a	n/a
47	CTCF	chr11:101454040-101454190	SAEC	small airway:	n/a	n/a
48	CTCF	chr11:101490930-101490967	GM13977	blood:	n/a	n/a
49	CTCF	chr11:101490939-101491008	MCF-7	breast:	n/a	chr11:101490955-101490973
50	CUX1	chr11:101469898-101469985	GM12878	blood:	n/a	n/a

(count:918 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:101454823-101454873	AoSMC	blood vessel:	n/a
2	chr11:101453358-101453408	AG10803	skin:	n/a
3	chr11:101454676-101454726	HRE	kidney:	n/a
4	chr11:101454823-101454873	AoSMC	blood vessel:	n/a
5	chr11:101453358-101453408	AG10803	skin:	n/a
6	chr11:101454676-101454726	HRE	kidney:	n/a
7	chr11:101458233-101458283	SK-N-SH	brain:	n/a
8	chr11:101454626-101454676	Hela-S3	cervix:	n/a
9	chr11:101454733-101454783	RPTEC	kidney:	n/a
10	chr11:101454996-101455046	ECC-1	luminal epithelium:	n/a
11	chr11:101454317-101454367	GM12891	blood:	n/a
12	chr11:101453106-101453156	PFSK-1	brain:	n/a
13	chr11:101454765-101454815	PANC-1	pancreas:	n/a
14	chr11:101454733-101454783	AG04449	skin:	fetal
15	chr11:101454765-101454815	HIPEpiC	eye:	n/a
16	chr11:101454676-101454726	HNPCEpiC	eye:	n/a
17	chr11:101455225-101455275	HCF	heart:	n/a
18	chr11:101454683-101454733	PFSK-1	brain:	n/a
19	chr11:101453871-101453921	AG04450	lung:	fetal
20	chr11:101454676-101454726	NH-A	brain:	n/a
21	chr11:101454626-101454676	HPAEpiC	pulmonary alveolar:	n/a
22	chr11:101453358-101453408	T-47D	breast:	n/a
23	chr11:101454317-101454367	HCM	heart:	n/a
24	chr11:101454680-101454730	BE2_C	brain:	n/a
25	chr11:101454680-101454730	HCT-116	colon:	n/a
26	chr11:101455225-101455275	A549	lung:	n/a
27	chr11:101450197-101450247	RPTEC	kidney:	n/a
28	chr11:101454823-101454873	PFSK-1	brain:	n/a
29	chr11:101458233-101458283	K562	blood:	n/a
30	chr11:101454996-101455046	HepG2	liver:	n/a
31	chr11:101455225-101455275	RPTEC	kidney:	n/a
32	chr11:101454765-101454815	NH-A	brain:	n/a
33	chr11:101458233-101458283	HEK293	kidney:	embryo
34	chr11:101453358-101453408	NB4	blood:	n/a
35	chr11:101458233-101458283	Hepatocyte	liver:	n/a
36	chr11:101458233-101458283	Caco-2	colon:	n/a
37	chr11:101453358-101453408	A549	lung:	n/a
38	chr11:101454823-101454873	HMEC	breast:	n/a
39	chr11:101454683-101454733	HepG2	liver:	n/a
40	chr11:101458233-101458283	ProgFib	skin:	n/a
41	chr11:101453106-101453156	HEEpiC	esophagus:	n/a
42	chr11:101453358-101453408	HEEpiC	esophagus:	n/a
43	chr11:101454680-101454730	ECC-1	luminal epithelium:	n/a
44	chr11:101454683-101454733	CMK	blood:	n/a
45	chr11:101454683-101454733	HRCEpiC	kidney:	n/a
46	chr11:101458233-101458283	AG04449	skin:	fetal
47	chr11:101454676-101454726	NHDF-neo	bronchial:	n/a
48	chr11:101458233-101458283	HepG2	liver:	n/a
49	chr11:101454683-101454733	SAEC	small airway:	n/a
50	chr11:101458233-101458283	ovcar-3	ovarian:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:101491591..101493827-chr11:101495085..101497074,2	K562	blood:
2	chr11:101453489..101455397-chr11:101455802..101458009,2	MCF-7	breast:
3	chr11:101488247..101490096-chr11:101496460..101499129,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIAA1377-2	chr11:101464411-101465887	NONHSAT023860
2	lnc-KIAA1377-2	chr11:101464751-101465665	NONHSAT023861
3	lnc-KIAA1377-1	chr11:101483827-101485776	ucscGeneNc_uc001pgr_2
4	lnc-KIAA1377-2	chr11:101455026-101455855	NONHSAT023860
5	lnc-KIAA1377-2	chr11:101456456-101456519	NONHSAT023860

No data

Variant related genes	Relation type
ENSG00000254506	TF binding region
TRPC6	TF binding region
ENSG00000254506	CpG island
TRPC6	CpG island
ENSG00000254506	chromatin interactions
ENSG00000137672	chromatin interactions

Extended variants
information (count: 1641 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1641 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10791504	chr11:101436689-101436690	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs577078615	chr11:101436696-101436697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs386756871	chr11:101436721-101436722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs10895141	chr11:101436741-101436742	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs12796392	chr11:101436789-101436790	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs373650473	chr11:101436791-101436792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs541620906	chr11:101436801-101436802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs34025615	chr11:101436832-101436833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs10895142	chr11:101436882-101436883	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs180729745	chr11:101436970-101436971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs140478409	chr11:101436972-101436973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs535761425	chr11:101436996-101436997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs4754779	chr11:101436997-101436998	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs575444788	chr11:101437000-101437001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs544087143	chr11:101437033-101437034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs563964173	chr11:101437048-101437049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs551084161	chr11:101437070-101437071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs150430464	chr11:101437130-101437131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs549535962	chr11:101437177-101437178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs145169385	chr11:101437190-101437191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs564593399	chr11:101437206-101437207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs528551442	chr11:101437221-101437222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs149142754	chr11:101437235-101437236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs145019809	chr11:101437281-101437282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs117229108	chr11:101437288-101437289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs73584483	chr11:101437296-101437297	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs569590448	chr11:101437317-101437318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs535324074	chr11:101437347-101437348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs564168687	chr11:101437348-101437349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs7932338	chr11:101437364-101437365	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs572065085	chr11:101437369-101437370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs139014473	chr11:101437403-101437404	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs6590888	chr11:101437415-101437416	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs185590056	chr11:101437435-101437436	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs190048094	chr11:101437496-101437497	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs183029673	chr11:101437513-101437514	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs35712546	chr11:101437524-101437525	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs529599217	chr11:101437532-101437533	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs542869238	chr11:101437571-101437572	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs67536177	chr11:101437606-101437607	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs187357284	chr11:101437645-101437646	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs551813343	chr11:101437725-101437726	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs10895143	chr11:101437729-101437730	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs191653396	chr11:101437792-101437793	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs550544889	chr11:101437800-101437801	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371959897	chr11:101437802-101437803	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs567974743	chr11:101437803-101437804	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs569629597	chr11:101437805-101437806	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs535711162	chr11:101437808-101437809	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs183931080	chr11:101437809-101437810	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
Myelofibrosis	22110671	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	20164919	CNVD
Breast cancer	22522925	CNVD
Cancer	20164920	CNVD
Breast cancer	17142309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:414 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:101416400-101437400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr11:101424400-101437200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr11:101426400-101447600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr11:101429600-101437400	Weak transcription	Ovary	ovary
5	chr11:101431400-101437400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr11:101434600-101438000	Weak transcription	NHLF	lung
7	chr11:101436000-101437200	Weak transcription	Fetal Lung	lung
8	chr11:101436600-101437000	Enhancers	NHDF-Ad	bronchial
9	chr11:101437000-101444400	Weak transcription	NHDF-Ad	bronchial
10	chr11:101437200-101437400	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr11:101437200-101437400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr11:101437200-101437400	Enhancers	Fetal Lung	lung
13	chr11:101437400-101437600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
14	chr11:101437400-101437600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr11:101437400-101437600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr11:101437400-101437600	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr11:101437400-101437600	Enhancers	Ovary	ovary
18	chr11:101437400-101438000	Active TSS	iPS-15b Cell Line	embryonic stem cell
19	chr11:101437400-101438000	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr11:101437400-101438000	Weak transcription	Fetal Lung	lung
21	chr11:101437400-101438200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr11:101437400-101438400	Enhancers	H1 Cell Line	embryonic stem cell
23	chr11:101437400-101438400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
24	chr11:101437400-101438400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr11:101437400-101438400	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr11:101437400-101438600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr11:101437600-101437800	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr11:101437600-101437800	Weak transcription	Ovary	ovary
29	chr11:101437600-101438000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr11:101437600-101438000	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr11:101437600-101438000	Active TSS	iPS-18 Cell Line	embryonic stem cell
32	chr11:101437600-101438200	Active TSS	ES-I3 Cell Line	embryonic stem cell
33	chr11:101437800-101438400	Enhancers	Fetal Stomach	stomach
34	chr11:101438000-101438200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr11:101438000-101438200	Enhancers	Fetal Lung	lung
36	chr11:101438000-101438400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
37	chr11:101438000-101438400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
38	chr11:101438000-101438400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
39	chr11:101438000-101438400	Enhancers	Fetal Muscle Trunk	muscle
40	chr11:101438000-101438400	Enhancers	HepG2	liver
41	chr11:101438000-101438400	Enhancers	NHLF	lung
42	chr11:101438000-101438600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
43	chr11:101438200-101438400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
44	chr11:101438200-101438400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr11:101438200-101438400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr11:101438400-101438800	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr11:101438400-101443400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr11:101438400-101445400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr11:101438600-101438800	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr11:101443400-101443800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast

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