Variant report

Variant	esv3409893
Chromosome Location	chr11:48775434-48957952
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3253)
CpG islands
(count:793)
Chromatin interactive
region (count:5)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3253 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:48892892-48893269	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:48880376-48880748	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:48895975-48896341	HepG2	liver:	n/a	n/a
4	ATF1	chr11:48883351-48883720	K562	blood:	n/a	n/a
5	ATF1	chr11:48895825-48896343	K562	blood:	n/a	n/a
6	ATF1	chr11:48940082-48940286	K562	blood:	n/a	n/a
7	ATF1	chr11:48849264-48849333	K562	blood:	n/a	n/a
8	ATF1	chr11:48859189-48859770	K562	blood:	n/a	n/a
9	ATF1	chr11:48796111-48796444	K562	blood:	n/a	n/a
10	ATF1	chr11:48896850-48897050	K562	blood:	n/a	n/a
11	ATF1	chr11:48845364-48845733	K562	blood:	n/a	n/a
12	ATF1	chr11:48892890-48893270	K562	blood:	n/a	n/a
13	ATF1	chr11:48880374-48880748	K562	blood:	n/a	n/a
14	ATF1	chr11:48867583-48867993	K562	blood:	n/a	n/a
15	ATF3	chr11:48845439-48845653	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr11:48892858-48893151	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr11:48814467-48814498	K562	blood:	n/a	n/a
18	BACH1	chr11:48881669-48882080	K562	blood:	n/a	n/a
19	BACH1	chr11:48956270-48956471	K562	blood:	n/a	n/a
20	BATF	chr11:48934117-48934343	GM12878	blood:	n/a	n/a
21	BATF	chr11:48953209-48953631	GM12878	blood:	n/a	n/a
22	BATF	chr11:48934428-48934662	GM12878	blood:	n/a	n/a
23	BATF	chr11:48839569-48839852	GM12878	blood:	n/a	n/a
24	BATF	chr11:48805015-48805320	GM12878	blood:	n/a	n/a
25	BATF	chr11:48885554-48885939	GM12878	blood:	n/a	n/a
26	BATF	chr11:48894524-48895290	GM12878	blood:	n/a	n/a
27	BATF	chr11:48935181-48935425	GM12878	blood:	n/a	n/a
28	BATF	chr11:48776572-48776725	GM12878	blood:	n/a	n/a
29	BATF	chr11:48940420-48940720	GM12878	blood:	n/a	n/a
30	BATF	chr11:48810174-48810367	GM12878	blood:	n/a	n/a
31	BATF	chr11:48828245-48828584	GM12878	blood:	n/a	n/a
32	BATF	chr11:48867136-48868238	GM12878	blood:	n/a	n/a
33	BATF	chr11:48856700-48857102	GM12878	blood:	n/a	n/a
34	BATF	chr11:48887996-48888565	GM12878	blood:	n/a	n/a
35	BATF	chr11:48854637-48855193	GM12878	blood:	n/a	n/a
36	BATF	chr11:48877878-48878291	GM12878	blood:	n/a	n/a
37	BATF	chr11:48810099-48810738	GM12878	blood:	n/a	n/a
38	BATF	chr11:48934181-48934321	GM12878	blood:	n/a	n/a
39	BATF	chr11:48943793-48944288	GM12878	blood:	n/a	n/a
40	BATF	chr11:48861796-48862105	GM12878	blood:	n/a	n/a
41	BATF	chr11:48877883-48878085	GM12878	blood:	n/a	n/a
42	BATF	chr11:48834286-48834608	GM12878	blood:	n/a	n/a
43	BATF	chr11:48877440-48877803	GM12878	blood:	n/a	n/a
44	BATF	chr11:48883213-48883919	GM12878	blood:	n/a	n/a
45	BATF	chr11:48945011-48945390	GM12878	blood:	n/a	n/a
46	BATF	chr11:48898982-48899252	GM12878	blood:	n/a	n/a
47	BATF	chr11:48906491-48906775	GM12878	blood:	n/a	chr11:48906618-48906628
48	BATF	chr11:48916722-48917006	GM12878	blood:	n/a	chr11:48916904-48916914
49	BATF	chr11:48775367-48775560	GM12878	blood:	n/a	n/a
50	BATF	chr11:48953227-48953611	GM12878	blood:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:48922741-48922791	BJ	skin:	n/a
2	chr11:48922741-48922791	U87	brain:	n/a
3	chr11:48924804-48924854	MCF10A-Er-Src	breast:	n/a
4	chr11:48922271-48922321	Hela-S3	cervix:	n/a
5	chr11:48902014-48902064	HNPCEpiC	eye:	n/a
6	chr11:48922271-48922321	HRCEpiC	kidney:	n/a
7	chr11:48923668-48923718	MCF10A-Er-Src	breast:	n/a
8	chr11:48924804-48924854	HRCEpiC	kidney:	n/a
9	chr11:48922269-48922319	LNCaP	prostate:	n/a
10	chr11:48902014-48902064	PFSK-1	brain:	n/a
11	chr11:48922741-48922791	Hepatocyte	liver:	n/a
12	chr11:48923392-48923442	GM12878	blood:	n/a
13	chr11:48923577-48923627	HRCEpiC	kidney:	n/a
14	chr11:48901914-48901964	GM12892	blood:	n/a
15	chr11:48901914-48901964	AG04450	lung:	fetal
16	chr11:48880009-48880059	AoSMC	blood vessel:	n/a
17	chr11:48880009-48880059	PFSK-1	brain:	n/a
18	chr11:48922269-48922319	HRE	kidney:	n/a
19	chr11:48902014-48902064	AG09309	skin:	n/a
20	chr11:48880009-48880059	ProgFib	skin:	n/a
21	chr11:48922269-48922319	HCT-116	colon:	n/a
22	chr11:48922035-48922085	ECC-1	luminal epithelium:	n/a
23	chr11:48901705-48901755	HepG2	liver:	n/a
24	chr11:48880009-48880059	HAEpiC	amniotic membrane:	n/a
25	chr11:48922741-48922791	A549	lung:	n/a
26	chr11:48922674-48922724	HUVEC	blood vessel:	n/a
27	chr11:48922674-48922724	U87	brain:	n/a
28	chr11:48902014-48902064	HepG2	liver:	n/a
29	chr11:48922674-48922724	LNCaP	prostate:	n/a
30	chr11:48924804-48924854	Hepatocyte	liver:	n/a
31	chr11:48922035-48922085	AG09309	skin:	n/a
32	chr11:48923577-48923627	HCPEpiC	choroid plexus:	n/a
33	chr11:48880009-48880059	NHBE	bronchial:	n/a
34	chr11:48901705-48901755	HAEpiC	amniotic membrane:	n/a
35	chr11:48923577-48923627	AG04449	skin:	fetal
36	chr11:48923392-48923442	AG10803	skin:	n/a
37	chr11:48922271-48922321	GM19239	blood:	n/a
38	chr11:48924804-48924854	HCPEpiC	choroid plexus:	n/a
39	chr11:48922269-48922319	AG10803	skin:	n/a
40	chr11:48880009-48880059	Jurkat	blood:	n/a
41	chr11:48924804-48924854	GM12891	blood:	n/a
42	chr11:48902014-48902064	RPTEC	kidney:	n/a
43	chr11:48922271-48922321	BE2_C	brain:	n/a
44	chr11:48922035-48922085	NT2-D1	testis:	n/a
45	chr11:48922269-48922319	RPTEC	kidney:	n/a
46	chr11:48902014-48902064	BE2_C	brain:	n/a
47	chr11:48901914-48901964	ProgFib	skin:	n/a
48	chr11:48923392-48923442	NHBE	bronchial:	n/a
49	chr11:48880009-48880059	PrEC	prostate:	n/a
50	chr11:48901705-48901755	AG04449	skin:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr1:121484040..121484766-chr11:48865024..48865526,2	MCF-7	breast:
2	chr11:48862246..48863766-chr12:38036979..38038502,2	MCF-7	breast:
3	chr1:121484902..121485419-chr11:48946286..48946806,2	MCF-7	breast:
4	chr1:121484496..121485051-chr11:48865024..48865528,2	K562	blood:
5	chr11:48811378..48811898-chr8:46850618..46851141,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

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

No data

Variant related genes	Relation type
ENSG00000255551	TF binding region
ENSG00000254920	TF binding region
ENSG00000255527	TF binding region
ENSG00000254728	TF binding region
ENSG00000255551	CpG island
ENSG00000254920	CpG island
ENSG00000255527	CpG island
ENSG00000254728	CpG island

Extended variants
information (count: 16267 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:16267 , 50 per page) page: 1 2 3 4 5 6 7 ... 326

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs61930818	chr11:48775444-48775445	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs192801406	chr11:48775449-48775450	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs202196561	chr11:48775469-48775470	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs112257357	chr11:48775478-48775479	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs554375162	chr11:48775488-48775489	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs545295059	chr11:48775495-48775496	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs557830286	chr11:48775499-48775500	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs61930819	chr11:48775507-48775508	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs577986263	chr11:48775515-48775516	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs571275984	chr11:48775518-48775519	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs112402484	chr11:48775520-48775521	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs36144428	chr11:48775566-48775567	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs111998292	chr11:48775582-48775583	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs563805683	chr11:48775591-48775592	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs529501527	chr11:48775614-48775615	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs184904664	chr11:48775616-48775617	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs543290073	chr11:48775633-48775634	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs375564981	chr11:48775641-48775642	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs528745613	chr11:48775646-48775647	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs78685135	chr11:48775652-48775653	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs76993359	chr11:48775659-48775660	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs72643505	chr11:48775663-48775664	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs113796001	chr11:48775671-48775672	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs78494802	chr11:48775687-48775688	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs552075445	chr11:48775697-48775698	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs571134671	chr11:48775700-48775701	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs554192959	chr11:48775709-48775710	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs34001083	chr11:48775720-48775721	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs397759514	chr11:48775726-48775727	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs397754945	chr11:48775727-48775728	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs530459523	chr11:48775732-48775733	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs550253992	chr11:48775735-48775736	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs540052060	chr11:48775737-48775738	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs78012647	chr11:48775742-48775743	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs73461429	chr11:48775749-48775750	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs369312667	chr11:48775758-48775759	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs189672259	chr11:48775759-48775760	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs145786352	chr11:48775784-48775785	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs566672061	chr11:48775812-48775813	Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs182618701	chr11:48775813-48775814	Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs538526158	chr11:48775822-48775823	Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs556366791	chr11:48775834-48775835	Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs576521985	chr11:48775845-48775846	Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs60764175	chr11:48775856-48775857	Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs577941828	chr11:48775880-48775881	Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs188220630	chr11:48775881-48775882	Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs192794206	chr11:48775926-48775927	Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs183570990	chr11:48775931-48775932	Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs187481001	chr11:48775944-48775945	Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs140500832	chr11:48775946-48775947	Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
Non-syndromic sensorineural hearing loss	19587683	CNVD
Medulloblastoma	21163964	CNVD
early-passage human iPS cells	21368824	CNVD
Intellectual disability	22045946	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
small cell lung cancer	17426248	CNVD

Chromatin state (count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:48774800-48776400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:48775400-48776000	Active TSS	Aorta	Aorta
3	chr11:48775800-48776600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr11:48776400-48776600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr11:48777400-48780800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
6	chr11:48778200-48781800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
7	chr11:48779600-48782600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr11:48787200-48792800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr11:48789200-48789800	Active TSS	Fetal Heart	heart
10	chr11:48789800-48796200	Weak transcription	Fetal Heart	heart
11	chr11:48791000-48791200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr11:48791200-48796200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr11:48793000-48793200	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr11:48793200-48793400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr11:48793200-48796200	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr11:48794800-48796200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr11:48795400-48796200	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr11:48796000-48797600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
19	chr11:48796000-48802600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr11:48796200-48796400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
21	chr11:48796200-48796400	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr11:48796200-48796400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr11:48796200-48796400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
24	chr11:48796200-48796400	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
25	chr11:48796200-48796400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr11:48796200-48796400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr11:48796200-48796400	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr11:48796200-48796400	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr11:48796200-48796400	ZNF genes & repeats	Primary B cells from peripheral blood	blood
30	chr11:48796200-48796400	ZNF genes & repeats	Primary T cells fromperipheralblood	blood
31	chr11:48796200-48796400	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 2	blood
32	chr11:48796200-48796400	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
33	chr11:48796200-48796400	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
34	chr11:48796200-48796400	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
35	chr11:48796200-48796400	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
36	chr11:48796200-48796400	ZNF genes & repeats	Primary T helper 17 cells PMA-I stimulated	--
37	chr11:48796200-48796400	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
38	chr11:48796200-48796400	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr11:48796200-48796400	ZNF genes & repeats	Primary T killer naive cells fromperipheralblood	blood
40	chr11:48796200-48796400	ZNF genes & repeats	Primary T killer memory cells from peripheral blood	blood
41	chr11:48796200-48796400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr11:48796200-48796400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr11:48796200-48796400	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
44	chr11:48796200-48796400	ZNF genes & repeats	Adipose Nuclei	Adipose
45	chr11:48796200-48796400	Enhancers	Aorta	Aorta
46	chr11:48796200-48796400	ZNF genes & repeats	Liver	Liver
47	chr11:48796200-48796400	Flanking Bivalent TSS/Enh	Brain Angular Gyrus	brain
48	chr11:48796200-48796400	ZNF genes & repeats	Brain Anterior Caudate	brain
49	chr11:48796200-48796400	ZNF genes & repeats	Brain Hippocampus Middle	brain
50	chr11:48796200-48796400	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain

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