Variant report

Variant	esv1812230
Chromosome Location	chr11:48387275-48765567
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:481)
CpG islands
(count:183)
Chromatin interactive
region (count:1)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:481 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

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	BATF	chr11:48741581-48741798	GM12878	blood:	n/a	n/a
3	BCL3	chr11:48393835-48394182	GM12878	blood:	n/a	n/a
4	BCL3	chr11:48649085-48649287	GM12878	blood:	n/a	n/a
5	CEBPB	chr11:48477483-48477823	HepG2	liver:	n/a	n/a
6	CEBPB	chr11:48641584-48641785	HepG2	liver:	n/a	n/a
7	CEBPB	chr11:48477500-48477793	IMR90	lung:	n/a	n/a
8	CEBPB	chr11:48477590-48477827	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr11:48628746-48628791	HepG2	liver:	n/a	chr11:48628766-48628779 chr11:48628767-48628778 chr11:48628766-48628777
10	CEBPB	chr11:48641582-48641875	IMR90	lung:	n/a	n/a
11	CEBPB	chr11:48727879-48728005	K562	blood:	n/a	n/a
12	CEBPB	chr11:48477613-48477707	K562	blood:	n/a	n/a
13	CEBPB	chr11:48727818-48727993	A549	lung:	n/a	n/a
14	CEBPB	chr11:48477506-48477722	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr11:48477489-48477840	A549	lung:	n/a	n/a
16	CEBPB	chr11:48641711-48641734	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr11:48497081-48497188	IMR90	lung:	n/a	n/a
18	CTCF	chr11:48406380-48406530	HL-60	blood:	n/a	n/a
19	CTCF	chr11:48387500-48387650	HepG2	liver:	n/a	n/a
20	CTCF	chr11:48406348-48406520	MCF-7	breast:	n/a	n/a
21	CTCF	chr11:48406340-48406490	GM06990	blood:	n/a	n/a
22	CTCF	chr11:48478040-48478190	MCF-7	breast:	n/a	n/a
23	CTCF	chr11:48406340-48406490	AG04449	skin:	n/a	n/a
24	CTCF	chr11:48670490-48670521	GM13976	blood:	n/a	n/a
25	CTCF	chr11:48406380-48406530	GM12872	blood:	n/a	n/a
26	CTCF	chr11:48406340-48406490	HCT-116	colon:	n/a	n/a
27	CTCF	chr11:48406360-48406510	GM12871	blood:	n/a	n/a
28	CTCF	chr11:48492470-48492503	GM20000	blood:	n/a	n/a
29	CTCF	chr11:48518266-48518294	Fibrobl	skin:	n/a	n/a
30	CTCF	chr11:48405768-48405851	LNCaP	prostate:	n/a	n/a
31	CTCF	chr11:48445392-48445457	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr11:48387519-48387561	HepG2	liver:	n/a	n/a
33	CTCF	chr11:48643117-48643153	GM10266	blood:	n/a	n/a
34	CTCF	chr11:48406380-48406530	GM12874	blood:	n/a	n/a
35	CTCF	chr11:48406371-48406513	GM19240	blood:	n/a	n/a
36	CTCF	chr11:48406380-48406530	NHEK	skin:	n/a	n/a
37	CTCF	chr11:48634700-48634706	GM10248	blood:	n/a	n/a
38	CTCF	chr11:48478059-48478158	HepG2	liver:	n/a	n/a
39	CTCF	chr11:48406400-48406550	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr11:48387460-48387610	Caco-2	colon:	n/a	n/a
41	CTCF	chr11:48406380-48406530	GM12875	blood:	n/a	n/a
42	CTCF	chr11:48652535-48652571	Lung_OC	lung:	n/a	n/a
43	CTCF	chr11:48406340-48406490	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr11:48661873-48661916	LNCaP	prostate:	n/a	n/a
45	CTCF	chr11:48406380-48406530	GM12866	blood:	n/a	n/a
46	CTCF	chr11:48664030-48664131	LNCaP	prostate:	n/a	n/a
47	CTCF	chr11:48477977-48478225	LNCaP	prostate:	n/a	n/a
48	CTCF	chr11:48517944-48518015	Lung_OC	lung:	n/a	n/a
49	CTCF	chr11:48588680-48588719	LNCaP	prostate:	n/a	n/a
50	CTCF	chr11:48555880-48556030	MCF-7	breast:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:48510647-48510697	AG09309	skin:	n/a
2	chr11:48510647-48510697	PFSK-1	brain:	n/a
3	chr11:48510647-48510697	PANC-1	pancreas:	n/a
4	chr11:48509778-48509828	AG04450	lung:	fetal
5	chr11:48510647-48510697	HRE	kidney:	n/a
6	chr11:48509488-48509538	HL-60	blood:	n/a
7	chr11:48509778-48509828	LNCaP	prostate:	n/a
8	chr11:48509488-48509538	BJ	skin:	n/a
9	chr11:48510647-48510697	ProgFib	skin:	n/a
10	chr11:48510647-48510697	AG10803	skin:	n/a
11	chr11:48509778-48509828	HIPEpiC	eye:	n/a
12	chr11:48510647-48510697	AoSMC	blood vessel:	n/a
13	chr11:48509488-48509538	ovcar-3	ovarian:	n/a
14	chr11:48510647-48510697	HCPEpiC	choroid plexus:	n/a
15	chr11:48509778-48509828	HEK293	kidney:	embryo
16	chr11:48509488-48509538	IMR90	lung:	fetal
17	chr11:48510647-48510697	HCM	heart:	n/a
18	chr11:48510647-48510697	MCF10A-Er-Src	breast:	n/a
19	chr11:48509778-48509828	HRE	kidney:	n/a
20	chr11:48509778-48509828	ProgFib	skin:	n/a
21	chr11:48509488-48509538	AG09309	skin:	n/a
22	chr11:48509778-48509828	NT2-D1	testis:	n/a
23	chr11:48509778-48509828	HCT-116	colon:	n/a
24	chr11:48509778-48509828	Jurkat	blood:	n/a
25	chr11:48509488-48509538	HRPEpiC	eye:	n/a
26	chr11:48509778-48509828	HCF	heart:	n/a
27	chr11:48509778-48509828	Hela-S3	cervix:	n/a
28	chr11:48509778-48509828	RPTEC	kidney:	n/a
29	chr11:48509778-48509828	AoSMC	blood vessel:	n/a
30	chr11:48509778-48509828	AG09319	gingival:	n/a
31	chr11:48510647-48510697	Caco-2	colon:	n/a
32	chr11:48510647-48510697	HRCEpiC	kidney:	n/a
33	chr11:48509488-48509538	GM06990	blood:	n/a
34	chr11:48510647-48510697	HCF	heart:	n/a
35	chr11:48510647-48510697	T-47D	breast:	n/a
36	chr11:48510647-48510697	HepG2	liver:	n/a
37	chr11:48510647-48510697	HEK293	kidney:	embryo
38	chr11:48510647-48510697	HUVEC	blood vessel:	n/a
39	chr11:48510647-48510697	SK-N-SH_RA	brain:	n/a
40	chr11:48509488-48509538	HRE	kidney:	n/a
41	chr11:48509488-48509538	MCF-7	breast:	n/a
42	chr11:48509488-48509538	AG04450	lung:	fetal
43	chr11:48510647-48510697	GM12892	blood:	n/a
44	chr11:48509778-48509828	SAEC	small airway:	n/a
45	chr11:48509488-48509538	AG10803	skin:	n/a
46	chr11:48509488-48509538	GM12892	blood:	n/a
47	chr11:48509488-48509538	HNPCEpiC	eye:	n/a
48	chr11:48509778-48509828	H1-hESC	embryonic stem cell:	embryo
49	chr11:48509488-48509538	Jurkat	blood:	n/a
50	chr11:48510647-48510697	HCT-116	colon:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:48478071..48478587-chr11:49191267..49191777,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR4C5-1	chr11:48507915-48508377	NONHSAT021297

No data

Variant related genes	Relation type
OR4C9P	TF binding region
OR4C10P	TF binding region
OR4A47	TF binding region
OR4C2P	TF binding region
OR4A41P	TF binding region
OR4A46P	TF binding region
OR4A45P	TF binding region
OR4R1P	TF binding region
OR4A43P	TF binding region
OR4C5	TF binding region
OR4A40P	TF binding region
OR4A44P	TF binding region
OR4A48P	TF binding region
OR4A42P	TF binding region
OR4C9P	CpG island
OR4C10P	CpG island
OR4A47	CpG island
OR4C2P	CpG island
OR4A41P	CpG island
OR4A46P	CpG island
OR4A45P	CpG island
OR4R1P	CpG island
OR4A43P	CpG island
OR4C5	CpG island
OR4A40P	CpG island
OR4A44P	CpG island
OR4A48P	CpG island
OR4A42P	CpG island

Extended variants
information (count: 3421 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:3421 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10838881	chr11:48387275-48387276	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs139139147	chr11:48387278-48387279	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs76306144	chr11:48387279-48387280	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs369896820	chr11:48387285-48387286	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs76220342	chr11:48387301-48387302	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs540969683	chr11:48387307-48387308	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs73460769	chr11:48387335-48387336	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs560621031	chr11:48387343-48387344	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs73460771	chr11:48387354-48387355	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs73460772	chr11:48387370-48387371	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs546041572	chr11:48387376-48387377	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs563015644	chr11:48387412-48387413	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs61917478	chr11:48387424-48387425	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs77144540	chr11:48387490-48387491	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs72898882	chr11:48387506-48387507	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs531718545	chr11:48387518-48387519	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs78378263	chr11:48387526-48387527	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs72898883	chr11:48387535-48387536	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs72898885	chr11:48387540-48387541	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs527674874	chr11:48387569-48387570	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs78299098	chr11:48387580-48387581	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs75027745	chr11:48387582-48387583	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs75821991	chr11:48387584-48387585	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs146834236	chr11:48387590-48387591	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs75297075	chr11:48387591-48387592	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs554773218	chr11:48387595-48387596	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs72898886	chr11:48387604-48387605	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs569015234	chr11:48387627-48387628	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs140665145	chr11:48387628-48387629	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs73460777	chr11:48387630-48387631	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs554698444	chr11:48387632-48387633	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs75615667	chr11:48387647-48387648	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs533724202	chr11:48387656-48387657	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs151060469	chr11:48387663-48387664	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs10769651	chr11:48387668-48387669	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs76209049	chr11:48387679-48387680	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs67755516	chr11:48387684-48387685	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs79526328	chr11:48387687-48387688	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs75371569	chr11:48387689-48387690	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs34926479	chr11:48387705-48387706	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs577432467	chr11:48387724-48387725	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs546454963	chr11:48387736-48387737	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs73460780	chr11:48387737-48387738	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs74557904	chr11:48387757-48387758	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs76329018	chr11:48387780-48387781	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs80222485	chr11:48387789-48387790	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs75650204	chr11:48387825-48387826	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs79515387	chr11:48387833-48387834	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs73460781	chr11:48387850-48387851	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs556514578	chr11:48387855-48387856	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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

Chromatin state (count:68 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:48382200-48388400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
2	chr11:48400000-48401600	ZNF genes & repeats	Liver	Liver
3	chr11:48404600-48405800	ZNF genes & repeats	Adipose Nuclei	Adipose
4	chr11:48413000-48413400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
5	chr11:48515600-48516600	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr11:48569000-48569600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
7	chr11:48569200-48569600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
8	chr11:48576800-48577000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr11:48632800-48633200	Active TSS	Fetal Heart	heart
10	chr11:48670600-48672800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
11	chr11:48671600-48672200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
12	chr11:48671600-48674000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
13	chr11:48679800-48680400	ZNF genes & repeats	Adipose Nuclei	Adipose
14	chr11:48680200-48688400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr11:48681200-48684000	ZNF genes & repeats	Liver	Liver
16	chr11:48685000-48686400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr11:48686800-48688000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
18	chr11:48688200-48691800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
19	chr11:48694000-48695400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
20	chr11:48694200-48695800	ZNF genes & repeats	Adipose Nuclei	Adipose
21	chr11:48695400-48695800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr11:48696800-48698200	ZNF genes & repeats	Liver	Liver
23	chr11:48697200-48699000	ZNF genes & repeats	Adipose Nuclei	Adipose
24	chr11:48698200-48698800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr11:48704600-48705400	ZNF genes & repeats	Adipose Nuclei	Adipose
26	chr11:48711000-48712200	ZNF genes & repeats	Liver	Liver
27	chr11:48717600-48718400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
28	chr11:48718000-48718200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
29	chr11:48718000-48718200	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr11:48718000-48718200	ZNF genes & repeats	HUVEC	blood vessel
31	chr11:48718000-48718200	ZNF genes & repeats	NH-A	brain
32	chr11:48718000-48718400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
33	chr11:48718000-48718400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
34	chr11:48718000-48718600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
35	chr11:48718000-48719000	ZNF genes & repeats	Adipose Nuclei	Adipose
36	chr11:48718200-48718400	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
37	chr11:48728000-48728800	ZNF genes & repeats	Liver	Liver
38	chr11:48728400-48728800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
39	chr11:48731000-48732600	ZNF genes & repeats	Liver	Liver
40	chr11:48731400-48733000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
41	chr11:48731400-48735600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr11:48732600-48733400	Weak transcription	Liver	Liver
43	chr11:48733200-48734600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
44	chr11:48733200-48735800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
45	chr11:48733400-48734200	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
46	chr11:48733400-48734200	ZNF genes & repeats	Liver	Liver
47	chr11:48733400-48734400	ZNF genes & repeats	Adipose Nuclei	Adipose
48	chr11:48733800-48734200	Active TSS	Right Atrium	heart
49	chr11:48734200-48738400	Weak transcription	Right Atrium	heart
50	chr11:48736600-48742600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links