Variant report

Variant	esv2759828
Chromosome Location	chr11:55222420-55638112
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	ATF2	chr11:55425450-55425874	GM12878	blood:	n/a	n/a
2	BATF	chr11:55627832-55628094	GM12878	blood:	n/a	n/a
3	BATF	chr11:55425468-55425815	GM12878	blood:	n/a	n/a
4	BATF	chr11:55425431-55426129	GM12878	blood:	n/a	n/a
5	BATF	chr11:55426940-55427106	GM12878	blood:	n/a	chr11:55427071-55427081
6	BATF	chr11:55634919-55635279	GM12878	blood:	n/a	chr11:55635206-55635216
7	BATF	chr11:55634940-55635308	GM12878	blood:	n/a	chr11:55635206-55635216
8	BATF	chr11:55627814-55628095	GM12878	blood:	n/a	n/a
9	BCL11A	chr11:55425504-55425830	GM12878	blood:	n/a	n/a
10	BCL11A	chr11:55634987-55635226	GM12878	blood:	n/a	n/a
11	BCL11A	chr11:55425496-55426197	GM12878	blood:	n/a	n/a
12	BHLHE40	chr11:55634894-55635260	GM12878	blood:	n/a	chr11:55635049-55635062 chr11:55634927-55634943
13	BHLHE40	chr11:55427039-55427080	GM12878	blood:	n/a	n/a
14	BHLHE40	chr11:55425502-55426161	GM12878	blood:	n/a	n/a
15	CCNT2	chr11:55598241-55598440	K562	blood:	n/a	n/a
16	CEBPB	chr11:55591978-55592114	HepG2	liver:	n/a	chr11:55592043-55592056 chr11:55592042-55592059 chr11:55592043-55592056 chr11:55592043-55592054 chr11:55592044-55592055
17	CEBPB	chr11:55397830-55398153	IMR90	lung:	n/a	n/a
18	CEBPB	chr11:55484570-55484826	K562	blood:	n/a	chr11:55484684-55484695 chr11:55484682-55484695 chr11:55484684-55484695 chr11:55484682-55484693 chr11:55484682-55484695
19	CEBPB	chr11:55225032-55225273	A549	lung:	n/a	n/a
20	CEBPB	chr11:55290616-55290841	HepG2	liver:	n/a	chr11:55290662-55290673
21	CEBPB	chr11:55237118-55237419	HepG2	liver:	n/a	chr11:55237275-55237286
22	CEBPB	chr11:55486845-55487046	A549	lung:	n/a	n/a
23	CEBPB	chr11:55407050-55407358	IMR90	lung:	n/a	chr11:55407201-55407212
24	CEBPB	chr11:55460766-55460962	A549	lung:	n/a	n/a
25	CEBPB	chr11:55237138-55237399	A549	lung:	n/a	chr11:55237275-55237286
26	CEBPB	chr11:55531894-55532015	HepG2	liver:	n/a	n/a
27	CEBPB	chr11:55436863-55437223	HepG2	liver:	n/a	chr11:55437045-55437056
28	CEBPB	chr11:55541048-55541310	A549	lung:	n/a	n/a
29	CEBPB	chr11:55436866-55437227	IMR90	lung:	n/a	chr11:55437045-55437056
30	CEBPB	chr11:55436869-55437201	A549	lung:	n/a	chr11:55437045-55437056
31	CEBPB	chr11:55268173-55268348	K562	blood:	n/a	n/a
32	CEBPB	chr11:55535621-55535901	HepG2	liver:	n/a	chr11:55535727-55535738
33	CEBPB	chr11:55407077-55407277	HepG2	liver:	n/a	chr11:55407201-55407212
34	CEBPB	chr11:55407058-55407336	A549	lung:	n/a	chr11:55407201-55407212
35	CEBPB	chr11:55436916-55437222	K562	blood:	n/a	chr11:55437045-55437056
36	CEBPB	chr11:55567730-55568064	A549	lung:	n/a	chr11:55567868-55567879 chr11:55567908-55567919
37	CEBPB	chr11:55312931-55313225	HepG2	liver:	n/a	chr11:55313093-55313104
38	CEBPB	chr11:55479060-55479320	HepG2	liver:	n/a	chr11:55479150-55479161
39	CEBPB	chr11:55397893-55398090	HepG2	liver:	n/a	n/a
40	CEBPB	chr11:55484586-55484848	HepG2	liver:	n/a	chr11:55484684-55484695 chr11:55484682-55484695 chr11:55484684-55484695 chr11:55484682-55484693 chr11:55484682-55484695
41	CEBPB	chr11:55567767-55568076	HepG2	liver:	n/a	chr11:55567868-55567879 chr11:55567908-55567919
42	CEBPB	chr11:55397950-55398078	A549	lung:	n/a	n/a
43	CHD2	chr11:55425350-55426118	GM12878	blood:	n/a	n/a
44	CREB1	chr11:55461401-55461644	A549	lung:	n/a	n/a
45	CTCF	chr11:55482880-55483030	GM06990	blood:	n/a	chr11:55482946-55482967 chr11:55482947-55482960 chr11:55482945-55482961 chr11:55482947-55482960 chr11:55482944-55482962
46	CTCF	chr11:55482860-55483010	GM12864	blood:	n/a	chr11:55482946-55482967 chr11:55482947-55482960 chr11:55482945-55482961 chr11:55482947-55482960 chr11:55482944-55482962
47	CTCF	chr11:55482860-55483010	HCPEpiC	choroid plexus:	n/a	chr11:55482946-55482967 chr11:55482947-55482960 chr11:55482945-55482961 chr11:55482947-55482960 chr11:55482944-55482962
48	CTCF	chr11:55271050-55271261	Gliobla	brain:	n/a	n/a
49	CTCF	chr11:55474600-55474750	HCM	heart:	n/a	chr11:55474686-55474707 chr11:55474691-55474709 chr11:55474696-55474704 chr11:55474693-55474706
50	CTCF	chr11:55482867-55483088	GM12892	blood:	n/a	chr11:55482946-55482967 chr11:55482947-55482960 chr11:55482945-55482961 chr11:55482947-55482960 chr11:55482944-55482962

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:55577775-55577825	HCF	heart:	n/a
2	chr11:55227646-55227696	SK-N-SH	brain:	n/a
3	chr11:55322753-55322803	SAEC	small airway:	n/a
4	chr11:55406191-55406241	ECC-1	luminal epithelium:	n/a
5	chr11:55577775-55577825	HCF	heart:	n/a
6	chr11:55227646-55227696	SK-N-SH	brain:	n/a
7	chr11:55322753-55322803	SAEC	small airway:	n/a
8	chr11:55406191-55406241	ECC-1	luminal epithelium:	n/a
9	chr11:55577775-55577825	Hela-S3	cervix:	n/a
10	chr11:55227646-55227696	AG04450	lung:	fetal
11	chr11:55433005-55433055	Hepatocyte	liver:	n/a
12	chr11:55321480-55321530	HRE	kidney:	n/a
13	chr11:55563401-55563451	HAEpiC	amniotic membrane:	n/a
14	chr11:55322753-55322803	Caco-2	colon:	n/a
15	chr11:55579363-55579413	HMEC	breast:	n/a
16	chr11:55605161-55605211	LNCaP	prostate:	n/a
17	chr11:55406191-55406241	GM06990	blood:	n/a
18	chr11:55541018-55541068	Hepatocyte	liver:	n/a
19	chr11:55418816-55418866	AG09309	skin:	n/a
20	chr11:55322753-55322803	GM12892	blood:	n/a
21	chr11:55606710-55606760	K562	blood:	n/a
22	chr11:55433005-55433055	HAEpiC	amniotic membrane:	n/a
23	chr11:55594854-55594904	HAEpiC	amniotic membrane:	n/a
24	chr11:55371077-55371127	K562	blood:	n/a
25	chr11:55606710-55606760	Hela-S3	cervix:	n/a
26	chr11:55587764-55587814	HCM	heart:	n/a
27	chr11:55431152-55431202	PrEC	prostate:	n/a
28	chr11:55594854-55594904	HepG2	liver:	n/a
29	chr11:55321480-55321530	SK-N-MC	brain:	n/a
30	chr11:55594854-55594904	BE2_C	brain:	n/a
31	chr11:55606216-55606266	NHDF-neo	bronchial:	n/a
32	chr11:55227646-55227696	Hepatocyte	liver:	n/a
33	chr11:55431152-55431202	HRPEpiC	eye:	n/a
34	chr11:55606710-55606760	MCF10A-Er-Src	breast:	n/a
35	chr11:55433005-55433055	SAEC	small airway:	n/a
36	chr11:55593465-55593515	HL-60	blood:	n/a
37	chr11:55541018-55541068	AoSMC	blood vessel:	n/a
38	chr11:55561545-55561595	Caco-2	colon:	n/a
39	chr11:55579363-55579413	AG09309	skin:	n/a
40	chr11:55418816-55418866	A549	lung:	n/a
41	chr11:55594854-55594904	HCPEpiC	choroid plexus:	n/a
42	chr11:55541018-55541068	IMR90	lung:	fetal
43	chr11:55587764-55587814	PrEC	prostate:	n/a
44	chr11:55541269-55541319	HCM	heart:	n/a
45	chr11:55321480-55321530	ProgFib	skin:	n/a
46	chr11:55586293-55586343	T-47D	breast:	n/a
47	chr11:55227718-55227768	H1-hESC	embryonic stem cell:	embryo
48	chr11:55586293-55586343	Jurkat	blood:	n/a
49	chr11:55637839-55637889	AG04449	skin:	fetal
50	chr11:55561545-55561595	LNCaP	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:55575230..55577016-chr11:55600877..55602678,2	K562	blood:
2	chr11:55569608..55571383-chr11:55587513..55589076,2	K562	blood:
3	chr11:55575230..55577016-chr11:55600877..55602678,2	K562	blood:
4	chr11:55599784..55601500-chr11:55669222..55671222,2	K562	blood:
5	chr11:55491735..55492235-chr19:6736783..6737284,2	NB4	blood:
6	chr11:55569608..55571383-chr11:55587513..55589076,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR4C11-1	chr11:55453377-55453636	ENSG00000254804
2	lnc-OR4C11-1	chr11:55451617-55451701	ENSG00000254804
3	lnc-SPRYD5-1	chr11:55631408-55631812	NONHSAT021372

Variant related genes	Relation type
OR4S2	TF binding region
OR4C11	TF binding region
OR5L1	TF binding region
OR4A13P	TF binding region
OR5L2	TF binding region
OR5D13	TF binding region
OR5D15P	TF binding region
OR5D2P	TF binding region
OR5D18	TF binding region
ENSG00000255204	TF binding region
OR4C16	TF binding region
OR4A21P	TF binding region
OR9M1P	TF binding region
OR4P4	TF binding region
OR4A50P	TF binding region
ENSG00000255499	TF binding region
OR4A14P	TF binding region
OR5D17P	TF binding region
OR4C1P	TF binding region
OR5D14	TF binding region
OR4C15	TF binding region
OR5D16	TF binding region
OR4C14P	TF binding region
OR4V1P	TF binding region
OR4P1P	TF binding region
OR4C6	TF binding region
OR5D3P	TF binding region
ENSG00000254804	TF binding region
OR4S2	CpG island
OR4C11	CpG island
OR5L1	CpG island
OR4A13P	CpG island
OR5L2	CpG island
OR5D13	CpG island
OR5D15P	CpG island
OR5D2P	CpG island
OR5D18	CpG island
ENSG00000255204	CpG island
OR4C16	CpG island
OR4A21P	CpG island
OR9M1P	CpG island
OR4P4	CpG island
OR4A50P	CpG island
ENSG00000255499	CpG island
OR4A14P	CpG island
OR5D17P	CpG island
OR4C1P	CpG island
OR5D14	CpG island
OR4C15	CpG island
OR5D16	CpG island
OR4C14P	CpG island
OR4V1P	CpG island
OR4P1P	CpG island
OR4C6	CpG island
OR5D3P	CpG island
ENSG00000254804	CpG island
ENSG00000125734	chromatin interactions

Extended variants
information (count: 2635 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:2635 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112470357	chr11:55225406-55225407	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs386753659	chr11:55225416-55225417	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs76046642	chr11:55225417-55225418	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs530301924	chr11:55225428-55225429	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs531604399	chr11:55225429-55225430	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs548500859	chr11:55225461-55225462	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs570193323	chr11:55225465-55225466	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs190431630	chr11:55225477-55225478	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs369464046	chr11:55225478-55225479	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs116926639	chr11:55225481-55225482	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs571293037	chr11:55225485-55225486	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs538620496	chr11:55225511-55225512	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs377249980	chr11:55225546-55225547	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs553764769	chr11:55225557-55225558	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs142697330	chr11:55225559-55225560	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs536502703	chr11:55225567-55225568	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs554475939	chr11:55225578-55225579	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs616461	chr11:55225598-55225599	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs562026585	chr11:55225611-55225612	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs543598880	chr11:55225613-55225614	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs558987004	chr11:55225618-55225619	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs113937651	chr11:55225702-55225703	Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs541048835	chr11:55225710-55225711	Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs181253373	chr11:55225722-55225723	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs112520692	chr11:55225723-55225724	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs115237326	chr11:55225724-55225725	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs542502503	chr11:55225749-55225750	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs530336945	chr11:55225768-55225769	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs563778074	chr11:55225775-55225776	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs67920343	chr11:55225807-55225808	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs571178180	chr11:55225811-55225812	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs140009122	chr11:55225816-55225817	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs189637969	chr11:55225817-55225818	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs116966729	chr11:55225831-55225832	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs182085699	chr11:55225834-55225835	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs185108809	chr11:55225846-55225847	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs142273600	chr11:55225862-55225863	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs74625780	chr11:55225873-55225874	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs569682206	chr11:55225886-55225887	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs549403644	chr11:55225892-55225893	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs537268230	chr11:55225900-55225901	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs535097333	chr11:55225906-55225907	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs36126519	chr11:55225920-55225921	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs76426677	chr11:55225921-55225922	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs75498743	chr11:55225924-55225925	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs552992417	chr11:55225934-55225935	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs565761076	chr11:55225940-55225941	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs534849228	chr11:55225942-55225943	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs191788014	chr11:55225969-55225970	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs557488301	chr11:55226016-55226017	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	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
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21990379	CNVD
small cell lung cancer	20016488	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	17142309	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	20067559	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
Multiple myeloma	16616336	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
Alcoholism	21790672	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	20967226	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:55225400-55225800	Active TSS	HSMMtube	muscle
2	chr11:55225800-55227600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
3	chr11:55227400-55227800	Active TSS	ES-I3 Cell Line	embryonic stem cell
4	chr11:55243200-55243600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
5	chr11:55260600-55262800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
6	chr11:55263400-55263600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
7	chr11:55268600-55270400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr11:55269600-55277400	Weak transcription	Pancreas	Pancrea
9	chr11:55277400-55277800	ZNF genes & repeats	Pancreas	Pancrea
10	chr11:55277400-55278000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
11	chr11:55282000-55282400	Active TSS	Fetal Heart	heart
12	chr11:55312200-55315800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
13	chr11:55325800-55326000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
14	chr11:55337800-55338200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr11:55338000-55338400	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr11:55340200-55340400	Bivalent Enhancer	Aorta	Aorta
17	chr11:55353800-55354600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
18	chr11:55366800-55367200	ZNF genes & repeats	Esophagus	oesophagus
19	chr11:55395800-55397000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
20	chr11:55411800-55412000	Active TSS	Fetal Brain Male	brain
21	chr11:55412000-55421200	Weak transcription	Fetal Brain Male	brain
22	chr11:55414600-55415000	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
23	chr11:55415000-55416200	Weak transcription	Rectal Mucosa Donor 29	rectum
24	chr11:55416200-55416400	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
25	chr11:55421200-55421600	Active TSS	Fetal Brain Male	brain
26	chr11:55425800-55426600	Enhancers	GM12878-XiMat	blood
27	chr11:55426200-55426400	Enhancers	Rectal Mucosa Donor 29	rectum
28	chr11:55451200-55453000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
29	chr11:55453400-55454000	Active TSS	ES-I3 Cell Line	embryonic stem cell
30	chr11:55500200-55500800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr11:55508400-55508600	Enhancers	Esophagus	oesophagus
32	chr11:55508400-55508600	ZNF genes & repeats	Pancreas	Pancrea
33	chr11:55545600-55547200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
34	chr11:55589400-55590400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
35	chr11:55633200-55633600	Active TSS	Breast Myoepithelial Primary Cells	Breast
36	chr11:55638000-55640200	Weak transcription	Brain Inferior Temporal Lobe	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links