Variant report

Variant	esv34253
Chromosome Location	chr11:48402752-48930132
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3009)
CpG islands
(count:977)
Chromatin interactive
region (count:5)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3009 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:48600198-48600306	K562	blood:	n/a	n/a
2	ARID3A	chr11:48895975-48896341	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:48880376-48880748	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:48892892-48893269	HepG2	liver:	n/a	n/a
5	ATF1	chr11:48796111-48796444	K562	blood:	n/a	n/a
6	ATF1	chr11:48859189-48859770	K562	blood:	n/a	n/a
7	ATF1	chr11:48845364-48845733	K562	blood:	n/a	n/a
8	ATF1	chr11:48883351-48883720	K562	blood:	n/a	n/a
9	ATF1	chr11:48896850-48897050	K562	blood:	n/a	n/a
10	ATF1	chr11:48867583-48867993	K562	blood:	n/a	n/a
11	ATF1	chr11:48880374-48880748	K562	blood:	n/a	n/a
12	ATF1	chr11:48895825-48896343	K562	blood:	n/a	n/a
13	ATF1	chr11:48849264-48849333	K562	blood:	n/a	n/a
14	ATF1	chr11:48892890-48893270	K562	blood:	n/a	n/a
15	ATF3	chr11:48892858-48893151	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr11:48845439-48845653	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr11:48881669-48882080	K562	blood:	n/a	n/a
18	BACH1	chr11:48814467-48814498	K562	blood:	n/a	n/a
19	BATF	chr11:48775367-48775560	GM12878	blood:	n/a	n/a
20	BATF	chr11:48844232-48844479	GM12878	blood:	n/a	n/a
21	BATF	chr11:48844167-48844436	GM12878	blood:	n/a	n/a
22	BATF	chr11:48741581-48741798	GM12878	blood:	n/a	n/a
23	BATF	chr11:48856700-48857102	GM12878	blood:	n/a	n/a
24	BATF	chr11:48916722-48917006	GM12878	blood:	n/a	chr11:48916904-48916914
25	BATF	chr11:48810099-48810738	GM12878	blood:	n/a	n/a
26	BATF	chr11:48894524-48895290	GM12878	blood:	n/a	n/a
27	BATF	chr11:48898982-48899252	GM12878	blood:	n/a	n/a
28	BATF	chr11:48831050-48831447	GM12878	blood:	n/a	n/a
29	BATF	chr11:48883213-48883919	GM12878	blood:	n/a	n/a
30	BATF	chr11:48856704-48856991	GM12878	blood:	n/a	n/a
31	BATF	chr11:48861740-48862096	GM12878	blood:	n/a	n/a
32	BATF	chr11:48895950-48896265	GM12878	blood:	n/a	n/a
33	BATF	chr11:48854717-48855191	GM12878	blood:	n/a	n/a
34	BATF	chr11:48877878-48878291	GM12878	blood:	n/a	n/a
35	BATF	chr11:48885664-48885889	GM12878	blood:	n/a	n/a
36	BATF	chr11:48834403-48834545	GM12878	blood:	n/a	n/a
37	BATF	chr11:48842846-48843034	GM12878	blood:	n/a	n/a
38	BATF	chr11:48877883-48878085	GM12878	blood:	n/a	n/a
39	BATF	chr11:48775372-48775512	GM12878	blood:	n/a	n/a
40	BATF	chr11:48804986-48805223	GM12878	blood:	n/a	n/a
41	BATF	chr11:48892880-48893156	GM12878	blood:	n/a	n/a
42	BATF	chr11:48887996-48888565	GM12878	blood:	n/a	n/a
43	BATF	chr11:48883215-48883597	GM12878	blood:	n/a	n/a
44	BATF	chr11:48828245-48828584	GM12878	blood:	n/a	n/a
45	BATF	chr11:48866749-48866988	GM12878	blood:	n/a	n/a
46	BATF	chr11:48776572-48776725	GM12878	blood:	n/a	n/a
47	BATF	chr11:48895948-48896327	GM12878	blood:	n/a	n/a
48	BATF	chr11:48898958-48899437	GM12878	blood:	n/a	n/a
49	BATF	chr11:48906491-48906775	GM12878	blood:	n/a	chr11:48906618-48906628
50	BATF	chr11:48776576-48776723	GM12878	blood:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:48922674-48922724	K562	blood:	n/a
2	chr11:48922674-48922724	K562	blood:	n/a
3	chr11:48923668-48923718	GM06990	blood:	n/a
4	chr11:48922035-48922085	SK-N-SH_RA	brain:	n/a
5	chr11:48922741-48922791	HRPEpiC	eye:	n/a
6	chr11:48510647-48510697	HMEC	breast:	n/a
7	chr11:48901914-48901964	HCT-116	colon:	n/a
8	chr11:48509488-48509538	NHBE	bronchial:	n/a
9	chr11:48922269-48922319	HRPEpiC	eye:	n/a
10	chr11:48922271-48922321	U87	brain:	n/a
11	chr11:48510647-48510697	HL-60	blood:	n/a
12	chr11:48922674-48922724	AG10803	skin:	n/a
13	chr11:48923392-48923442	HMEC	breast:	n/a
14	chr11:48922035-48922085	HNPCEpiC	eye:	n/a
15	chr11:48922269-48922319	PFSK-1	brain:	n/a
16	chr11:48922741-48922791	HEEpiC	esophagus:	n/a
17	chr11:48923392-48923442	BE2_C	brain:	n/a
18	chr11:48901705-48901755	GM12891	blood:	n/a
19	chr11:48923668-48923718	HepG2	liver:	n/a
20	chr11:48510647-48510697	HCF	heart:	n/a
21	chr11:48923392-48923442	NT2-D1	testis:	n/a
22	chr11:48509778-48509828	HRCEpiC	kidney:	n/a
23	chr11:48923668-48923718	HCM	heart:	n/a
24	chr11:48509778-48509828	SK-N-SH_RA	brain:	n/a
25	chr11:48922269-48922319	GM12891	blood:	n/a
26	chr11:48509488-48509538	CMK	blood:	n/a
27	chr11:48922271-48922321	AG10803	skin:	n/a
28	chr11:48923577-48923627	MCF10A-Er-Src	breast:	n/a
29	chr11:48923668-48923718	HMEC	breast:	n/a
30	chr11:48880009-48880059	GM12892	blood:	n/a
31	chr11:48922741-48922791	GM19239	blood:	n/a
32	chr11:48923392-48923442	AG09319	gingival:	n/a
33	chr11:48923577-48923627	U87	brain:	n/a
34	chr11:48922035-48922085	HCT-116	colon:	n/a
35	chr11:48901914-48901964	HEEpiC	esophagus:	n/a
36	chr11:48922674-48922724	SK-N-SH_RA	brain:	n/a
37	chr11:48922271-48922321	CMK	blood:	n/a
38	chr11:48922271-48922321	BE2_C	brain:	n/a
39	chr11:48901914-48901964	IMR90	lung:	fetal
40	chr11:48922674-48922724	RPTEC	kidney:	n/a
41	chr11:48902014-48902064	PANC-1	pancreas:	n/a
42	chr11:48922269-48922319	NH-A	brain:	n/a
43	chr11:48901914-48901964	MCF-7	breast:	n/a
44	chr11:48923392-48923442	MCF-7	breast:	n/a
45	chr11:48901705-48901755	GM19239	blood:	n/a
46	chr11:48902014-48902064	AG04449	skin:	fetal
47	chr11:48509488-48509538	SK-N-SH_RA	brain:	n/a
48	chr11:48923392-48923442	Hepatocyte	liver:	n/a
49	chr11:48922674-48922724	HCT-116	colon:	n/a
50	chr11:48510647-48510697	T-47D	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:121484496..121485051-chr11:48865024..48865528,2	K562	blood:
2	chr11:48862246..48863766-chr12:38036979..38038502,2	MCF-7	breast:
3	chr11:48478071..48478587-chr11:49191267..49191777,2	MCF-7	breast:
4	chr11:48811378..48811898-chr8:46850618..46851141,2	MCF-7	breast:
5	chr1:121484040..121484766-chr11:48865024..48865526,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC084851.1-5	chr11:48919940-48920255	NONHSAT021301
2	lnc-AC084851.1-5	chr11:48919540-48919822	NONHSAT021301
3	lnc-AC084851.1-5	chr11:48916513-48916636	NONHSAT021301
4	lnc-OR4C5-1	chr11:48507915-48508377	NONHSAT021297
5	lnc-AC084851.1-5	chr11:48914808-48914900	NONHSAT021301
6	lnc-AC084851.1-4	chr11:48929840-48930498	NONHSAT021302
7	lnc-AC084851.1-4	chr11:48928655-48928750	NONHSAT021302

No data

Variant related genes	Relation type
OR4C9P	TF binding region
ENSG00000255527	TF binding region
OR4C10P	TF binding region
OR4A47	TF binding region
OR4C2P	TF binding region
OR4A41P	TF binding region
OR4A40P	TF binding region
OR4A46P	TF binding region
OR4A44P	TF binding region
ENSG00000255551	TF binding region
OR4A45P	TF binding region
OR4A48P	TF binding region
ENSG00000254920	TF binding region
ENSG00000254728	TF binding region
OR4R1P	TF binding region
OR4A42P	TF binding region
OR4A43P	TF binding region
OR4C9P	CpG island
ENSG00000255527	CpG island
OR4C10P	CpG island
OR4A47	CpG island
OR4C2P	CpG island
OR4A41P	CpG island
OR4A40P	CpG island
OR4A46P	CpG island
OR4A44P	CpG island
ENSG00000255551	CpG island
OR4A45P	CpG island
OR4A48P	CpG island
ENSG00000254920	CpG island
ENSG00000254728	CpG island
OR4R1P	CpG island
OR4A42P	CpG island
OR4A43P	CpG island

Extended variants
information (count: 16463 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:16463 , 50 per page) page: 1 2 3 4 5 6 7 ... 330

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114348014	chr11:48404602-48404603	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs192631262	chr11:48404616-48404617	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs574287342	chr11:48404618-48404619	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs567755019	chr11:48404656-48404657	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs536892814	chr11:48404707-48404708	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs543335047	chr11:48404708-48404709	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs143431708	chr11:48404729-48404730	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs528652224	chr11:48404741-48404742	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs545529984	chr11:48404742-48404743	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs565346822	chr11:48404750-48404751	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs147985960	chr11:48404765-48404766	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs183543369	chr11:48404798-48404799	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs115021051	chr11:48404801-48404802	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs529217329	chr11:48404838-48404839	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs188336121	chr11:48404856-48404857	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs115708351	chr11:48404896-48404897	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs534476094	chr11:48404897-48404898	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs557453422	chr11:48404945-48404946	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs11500522	chr11:48404946-48404947	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs537136023	chr11:48404956-48404957	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs368827241	chr11:48404962-48404963	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs556722932	chr11:48404979-48404980	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs566652430	chr11:48405021-48405022	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs573580684	chr11:48405032-48405033	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs181162894	chr11:48405040-48405041	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs112704118	chr11:48405081-48405082	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs553666214	chr11:48405087-48405088	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs114979147	chr11:48405106-48405107	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs371526300	chr11:48405115-48405116	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs12099288	chr11:48405148-48405149	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs184801210	chr11:48405210-48405211	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs670559	chr11:48405289-48405290	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs561128450	chr11:48405303-48405304	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs530062658	chr11:48405304-48405305	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs548880526	chr11:48405341-48405342	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs118031150	chr11:48405408-48405409	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs528348911	chr11:48405411-48405412	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs190051910	chr11:48405420-48405421	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs577830710	chr11:48405462-48405463	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs571412692	chr11:48405486-48405487	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs536794184	chr11:48405494-48405495	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs556973580	chr11:48405533-48405534	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs181811767	chr11:48405540-48405541	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs536223729	chr11:48405580-48405581	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs147115569	chr11:48405581-48405582	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs111382568	chr11:48405601-48405602	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs545703594	chr11:48405615-48405616	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs138598551	chr11:48405631-48405632	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs190324592	chr11:48405643-48405644	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs182017438	chr11:48405644-48405645	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Breast cancer	21990379	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	20967226	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioma	20126413	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Medulloblastoma	21163964	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD
Intellectual disability	22045946	CNVD

Chromatin state (count:755 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:48404600-48405800	ZNF genes & repeats	Adipose Nuclei	Adipose
2	chr11:48413000-48413400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
3	chr11:48515600-48516600	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr11:48569000-48569600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
5	chr11:48569200-48569600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
6	chr11:48576800-48577000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr11:48632800-48633200	Active TSS	Fetal Heart	heart
8	chr11:48670600-48672800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
9	chr11:48671600-48672200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
10	chr11:48671600-48674000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
11	chr11:48679800-48680400	ZNF genes & repeats	Adipose Nuclei	Adipose
12	chr11:48680200-48688400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr11:48681200-48684000	ZNF genes & repeats	Liver	Liver
14	chr11:48685000-48686400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr11:48686800-48688000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
16	chr11:48688200-48691800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
17	chr11:48694000-48695400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
18	chr11:48694200-48695800	ZNF genes & repeats	Adipose Nuclei	Adipose
19	chr11:48695400-48695800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr11:48696800-48698200	ZNF genes & repeats	Liver	Liver
21	chr11:48697200-48699000	ZNF genes & repeats	Adipose Nuclei	Adipose
22	chr11:48698200-48698800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr11:48704600-48705400	ZNF genes & repeats	Adipose Nuclei	Adipose
24	chr11:48711000-48712200	ZNF genes & repeats	Liver	Liver
25	chr11:48717600-48718400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
26	chr11:48718000-48718200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
27	chr11:48718000-48718200	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr11:48718000-48718200	ZNF genes & repeats	HUVEC	blood vessel
29	chr11:48718000-48718200	ZNF genes & repeats	NH-A	brain
30	chr11:48718000-48718400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
31	chr11:48718000-48718400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
32	chr11:48718000-48718600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
33	chr11:48718000-48719000	ZNF genes & repeats	Adipose Nuclei	Adipose
34	chr11:48718200-48718400	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
35	chr11:48728000-48728800	ZNF genes & repeats	Liver	Liver
36	chr11:48728400-48728800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
37	chr11:48731000-48732600	ZNF genes & repeats	Liver	Liver
38	chr11:48731400-48733000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
39	chr11:48731400-48735600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr11:48732600-48733400	Weak transcription	Liver	Liver
41	chr11:48733200-48734600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
42	chr11:48733200-48735800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
43	chr11:48733400-48734200	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
44	chr11:48733400-48734200	ZNF genes & repeats	Liver	Liver
45	chr11:48733400-48734400	ZNF genes & repeats	Adipose Nuclei	Adipose
46	chr11:48733800-48734200	Active TSS	Right Atrium	heart
47	chr11:48734200-48738400	Weak transcription	Right Atrium	heart
48	chr11:48736600-48742600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr11:48738000-48739600	ZNF genes & repeats	Adipose Nuclei	Adipose
50	chr11:48738400-48739200	Active TSS	Right Atrium	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links