Variant report

Variant	esv1815338
Chromosome Location	chr4:1052100-1063187
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:59)
CpG islands
(count:489)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:59 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr4:1056984-1057312	K562	blood:	n/a	n/a
2	CBX3	chr4:1056947-1057365	K562	blood:	n/a	n/a
3	CEBPB	chr4:1059610-1059827	IMR90	lung:	n/a	chr4:1059720-1059731
4	CEBPB	chr4:1059560-1059843	HepG2	liver:	n/a	chr4:1059720-1059731
5	CEBPB	chr4:1059679-1059786	H1-hESC	embryonic stem cell:	n/a	chr4:1059720-1059731
6	CEBPB	chr4:1059589-1059882	HepG2	liver:	n/a	chr4:1059720-1059731
7	CEBPB	chr4:1059601-1059846	K562	blood:	n/a	chr4:1059720-1059731
8	CEBPB	chr4:1059648-1059806	A549	lung:	n/a	chr4:1059720-1059731
9	CEBPB	chr4:1059586-1059870	HepG2	liver:	n/a	chr4:1059720-1059731
10	CEBPB	chr4:1059624-1059865	K562	blood:	n/a	chr4:1059720-1059731
11	CEBPB	chr4:1059616-1059816	Hela-S3	cervix:	n/a	chr4:1059720-1059731
12	CEBPB	chr4:1059641-1059801	HepG2	liver:	n/a	chr4:1059720-1059731
13	CTCF	chr4:1052820-1052970	HepG2	liver:	n/a	n/a
14	CTCF	chr4:1052323-1052411	MCF-7	breast:	n/a	n/a
15	CTCF	chr4:1052360-1052510	HMEC	breast:	n/a	n/a
16	CTCF	chr4:1052339-1052448	MCF-7	breast:	n/a	n/a
17	CTCF	chr4:1058540-1058690	AG09309	skin:	n/a	n/a
18	CTCF	chr4:1052302-1052426	MCF-7	breast:	n/a	n/a
19	CTCF	chr4:1058700-1058850	K562	blood:	n/a	n/a
20	CTCF	chr4:1052295-1052414	MCF-7	breast:	n/a	n/a
21	CTCF	chr4:1052260-1052410	HEEpiC	esophagus:	n/a	n/a
22	CTCF	chr4:1052300-1052450	SAEC	small airway:	n/a	n/a
23	CTCF	chr4:1052980-1053130	WERI-Rb-1	eye:	n/a	n/a
24	CTCF	chr4:1052351-1052446	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr4:1052280-1052430	HMEC	breast:	n/a	n/a
26	CTCF	chr4:1054252-1054315	MCF-7	breast:	n/a	n/a
27	E2F6	chr4:1052145-1052260	K562	blood:	n/a	n/a
28	FOS	chr4:1057976-1058176	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr4:1057957-1058248	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr4:1057958-1058216	MCF10A-Er-Src	breast:	n/a	n/a
31	FOSL2	chr4:1052083-1052345	HepG2	liver:	n/a	n/a
32	JUND	chr4:1052128-1052338	HepG2	liver:	n/a	n/a
33	KAP1	chr4:1057013-1057317	K562	blood:	n/a	n/a
34	MAFF	chr4:1056788-1057166	K562	blood:	n/a	chr4:1056966-1056984
35	MAFF	chr4:1056789-1057147	HepG2	liver:	n/a	chr4:1056966-1056984
36	MAFK	chr4:1056797-1057161	IMR90	lung:	n/a	chr4:1056967-1056982
37	MAFK	chr4:1056829-1057095	Hela-S3	cervix:	n/a	chr4:1056967-1056982
38	MAFK	chr4:1056796-1057156	HepG2	liver:	n/a	chr4:1056967-1056982
39	MAFK	chr4:1056845-1057138	HepG2	liver:	n/a	chr4:1056967-1056982
40	MAFK	chr4:1056806-1057135	K562	blood:	n/a	chr4:1056967-1056982
41	MAX	chr4:1052154-1052327	HepG2	liver:	n/a	n/a
42	MAX	chr4:1052152-1052396	K562	blood:	n/a	n/a
43	MYC	chr4:1057909-1058198	MCF10A-Er-Src	breast:	n/a	n/a
44	MYC	chr4:1052275-1052360	MCF-7	breast:	n/a	n/a
45	POLR2A	chr4:1058836-1058916	Hela-S3	cervix:	n/a	n/a
46	POLR2A	chr4:1052020-1052443	H1-neurons	neurons:	n/a	n/a
47	RAD21	chr4:1052333-1052533	Hela-S3	cervix:	n/a	n/a
48	RAD21	chr4:1052977-1053021	H1-hESC	embryonic stem cell:	n/a	n/a
49	RCOR1	chr4:1052271-1052287	K562	blood:	n/a	n/a
50	SMC3	chr4:1052278-1052493	Hela-S3	cervix:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:1052676-1052726	AoSMC	blood vessel:	n/a
2	chr4:1052676-1052726	AoSMC	blood vessel:	n/a
3	chr4:1062280-1062330	HIPEpiC	eye:	n/a
4	chr4:1060445-1060495	BE2_C	brain:	n/a
5	chr4:1052372-1052422	HepG2	liver:	n/a
6	chr4:1052372-1052422	HRCEpiC	kidney:	n/a
7	chr4:1052717-1052767	Hela-S3	cervix:	n/a
8	chr4:1052138-1052188	ECC-1	luminal epithelium:	n/a
9	chr4:1052372-1052422	HRPEpiC	eye:	n/a
10	chr4:1052717-1052767	NHBE	bronchial:	n/a
11	chr4:1052138-1052188	AG04449	skin:	fetal
12	chr4:1052676-1052726	HCPEpiC	choroid plexus:	n/a
13	chr4:1052138-1052188	LNCaP	prostate:	n/a
14	chr4:1052717-1052767	AoSMC	blood vessel:	n/a
15	chr4:1052138-1052188	HNPCEpiC	eye:	n/a
16	chr4:1052717-1052767	GM12892	blood:	n/a
17	chr4:1062280-1062330	GM12892	blood:	n/a
18	chr4:1052676-1052726	GM12878	blood:	n/a
19	chr4:1060445-1060495	HPAEpiC	pulmonary alveolar:	n/a
20	chr4:1052560-1052610	GM19239	blood:	n/a
21	chr4:1052717-1052767	ProgFib	skin:	n/a
22	chr4:1052676-1052726	SK-N-SH	brain:	n/a
23	chr4:1052158-1052208	HUVEC	blood vessel:	n/a
24	chr4:1060445-1060495	U87	brain:	n/a
25	chr4:1052372-1052422	MCF-7	breast:	n/a
26	chr4:1052717-1052767	K562	blood:	n/a
27	chr4:1052717-1052767	RPTEC	kidney:	n/a
28	chr4:1052372-1052422	HL-60	blood:	n/a
29	chr4:1052158-1052208	ECC-1	luminal epithelium:	n/a
30	chr4:1052717-1052767	U87	brain:	n/a
31	chr4:1052372-1052422	SK-N-MC	brain:	n/a
32	chr4:1060445-1060495	AG09319	gingival:	n/a
33	chr4:1052372-1052422	HAEpiC	amniotic membrane:	n/a
34	chr4:1052560-1052610	T-47D	breast:	n/a
35	chr4:1060445-1060495	PANC-1	pancreas:	n/a
36	chr4:1062280-1062330	GM12891	blood:	n/a
37	chr4:1052158-1052208	IMR90	lung:	fetal
38	chr4:1052717-1052767	AG09319	gingival:	n/a
39	chr4:1052717-1052767	HPAEpiC	pulmonary alveolar:	n/a
40	chr4:1052717-1052767	HCM	heart:	n/a
41	chr4:1060445-1060495	SK-N-SH	brain:	n/a
42	chr4:1060445-1060495	AG10803	skin:	n/a
43	chr4:1052372-1052422	PFSK-1	brain:	n/a
44	chr4:1052372-1052422	HCPEpiC	choroid plexus:	n/a
45	chr4:1052138-1052188	NB4	blood:	n/a
46	chr4:1060445-1060495	HL-60	blood:	n/a
47	chr4:1060445-1060495	BJ	skin:	n/a
48	chr4:1052560-1052610	SKMC	muscle:	n/a
49	chr4:1060445-1060495	Hepatocyte	liver:	n/a
50	chr4:1060445-1060495	HCM	heart:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:1054268..1056865-chr4:1058331..1059927,2	MCF-7	breast:
2	chr4:1052002..1052766-chr4:1359397..1360108,2	MCF-7	breast:
3	chr4:1058468..1061069-chr4:1080892..1083707,2	K562	blood:
4	chr4:1036349..1037985-chr4:1063186..1065162,2	MCF-7	breast:
5	chr4:1045118..1048090-chr4:1052343..1053975,2	K562	blood:
6	chr4:1048335..1050594-chr4:1053315..1054904,2	K562	blood:
7	chr4:1052199..1054974-chr4:1055597..1057652,2	MCF-7	breast:
8	chr4:1061442..1063759-chr4:1126141..1128093,2	MCF-7	breast:
9	chr4:1029606..1032234-chr4:1052650..1054698,2	K562	blood:
10	chr4:1054268..1056865-chr4:1058331..1059927,2	MCF-7	breast:

No data

Variant related genes	Relation type
RNF212	TF binding region
RNF212	CpG island
ENSG00000163945	chromatin interactions
ENSG00000178222	chromatin interactions

Extended variants
information (count: 509 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:509 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs57186616	chr4:1052100-1052101	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
2	rs11724371	chr4:1052125-1052126	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs536957567	chr4:1052138-1052139	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs548722321	chr4:1052144-1052145	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs57452522	chr4:1052159-1052160	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs386670456	chr4:1052164-1052165	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs2248083	chr4:1052166-1052167	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs534541270	chr4:1052176-1052177	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs371748322	chr4:1052177-1052178	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs2045069	chr4:1052206-1052207	Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs2045068	chr4:1052212-1052213	Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs77924371	chr4:1052230-1052231	Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs556690062	chr4:1052231-1052232	Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs561099527	chr4:1052299-1052300	Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs576627275	chr4:1052336-1052337	Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs2045067	chr4:1052355-1052356	Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs543699529	chr4:1052398-1052399	Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs2045066	chr4:1052401-1052402	Weak transcription Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs372950668	chr4:1052408-1052409	Weak transcription Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs574272447	chr4:1052409-1052410	Weak transcription Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs192343182	chr4:1052440-1052441	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs559860091	chr4:1052458-1052459	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs2045065	chr4:1052488-1052489	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs149097918	chr4:1052509-1052510	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs563537343	chr4:1052515-1052516	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs530981635	chr4:1052542-1052543	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs548856027	chr4:1052544-1052545	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs6852246	chr4:1052556-1052557	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs534482239	chr4:1052565-1052566	Weak transcription Bivalent Enhancer Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs546404444	chr4:1052574-1052575	Weak transcription Bivalent Enhancer Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs55943351	chr4:1052577-1052578	Weak transcription Bivalent Enhancer Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs571279103	chr4:1052597-1052598	Weak transcription Bivalent Enhancer Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs34881651	chr4:1052602-1052603	Weak transcription Enhancers Bivalent Enhancer	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs143127061	chr4:1052615-1052616	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs557063871	chr4:1052623-1052624	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs113061374	chr4:1052662-1052663	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs529774372	chr4:1052663-1052664	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs79067760	chr4:1052671-1052672	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs536290754	chr4:1052676-1052677	Weak transcription Enhancers Bivalent Enhancer	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs547983894	chr4:1052677-1052678	Weak transcription Enhancers Bivalent Enhancer	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs556075915	chr4:1052718-1052719	Weak transcription Enhancers Bivalent Enhancer	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs570227692	chr4:1052731-1052732	Weak transcription Enhancers Bivalent Enhancer	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs574409910	chr4:1052734-1052735	Weak transcription Enhancers Bivalent Enhancer	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs111572776	chr4:1052762-1052763	Weak transcription Enhancers Bivalent Enhancer	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs559186579	chr4:1052770-1052771	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs555192134	chr4:1052784-1052785	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs200835789	chr4:1052806-1052807	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs184143819	chr4:1052809-1052810	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs115610563	chr4:1052821-1052822	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs530792801	chr4:1052828-1052829	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17142309	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD
Breast cancer	20932292	CNVD
Cancer	20164919	CNVD
Type 2 diabetes	21754918	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:75 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:1042200-1052200	Weak transcription	Gastric	stomach
2	chr4:1049600-1054600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:1049800-1056200	Weak transcription	Right Atrium	heart
4	chr4:1050000-1052200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr4:1050000-1052200	Weak transcription	Esophagus	oesophagus
6	chr4:1050000-1052400	Weak transcription	Left Ventricle	heart
7	chr4:1050000-1052800	Weak transcription	Spleen	Spleen
8	chr4:1050000-1054600	Weak transcription	Pancreas	Pancrea
9	chr4:1050000-1055400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr4:1050200-1052400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr4:1050200-1054200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr4:1050400-1055600	Weak transcription	GM12878-XiMat	blood
13	chr4:1051000-1052800	Bivalent Enhancer	Stomach Mucosa	stomach
14	chr4:1051200-1052400	Bivalent Enhancer	HepG2	liver
15	chr4:1051800-1053400	Enhancers	Fetal Heart	heart
16	chr4:1052000-1052200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
17	chr4:1052000-1052600	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr4:1052000-1053000	Enhancers	Right Ventricle	heart
19	chr4:1052000-1053600	Bivalent Enhancer	Fetal Muscle Leg	muscle
20	chr4:1052200-1052400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
21	chr4:1052200-1052400	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr4:1052200-1052400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr4:1052200-1052400	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr4:1052200-1052400	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
25	chr4:1052200-1052400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr4:1052200-1052400	Flanking Bivalent TSS/Enh	Sigmoid Colon	Sigmoid Colon
27	chr4:1052200-1052600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr4:1052200-1052800	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr4:1052200-1052800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr4:1052200-1052800	Enhancers	Esophagus	oesophagus
31	chr4:1052200-1053000	Enhancers	Gastric	stomach
32	chr4:1052200-1053400	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr4:1052400-1052800	Enhancers	Left Ventricle	heart
34	chr4:1052400-1053000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr4:1052400-1053000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr4:1052400-1053000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
37	chr4:1052400-1053000	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
38	chr4:1052400-1053000	Bivalent Enhancer	HMEC	breast
39	chr4:1052400-1053200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr4:1052400-1053400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
41	chr4:1052400-1053400	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
42	chr4:1052800-1053000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr4:1052800-1053000	Bivalent Enhancer	Duodenum Mucosa	Duodenum
44	chr4:1052800-1053000	Flanking Bivalent TSS/Enh	Stomach Mucosa	stomach
45	chr4:1052800-1053000	ZNF genes & repeats	Spleen	Spleen
46	chr4:1052800-1053400	Bivalent Enhancer	Esophagus	oesophagus
47	chr4:1053000-1053200	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
48	chr4:1053000-1053400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr4:1053000-1053400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr4:1053000-1053600	Bivalent Enhancer	Stomach Mucosa	stomach

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