Variant report

Variant	nsv461543
Chromosome Location	chr4:68797380-68877026
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	ATF1	chr4:68799641-68799825	K562	blood:	n/a	n/a
2	CEBPB	chr4:68854260-68854618	IMR90	lung:	n/a	chr4:68854428-68854439 chr4:68854428-68854441 chr4:68854428-68854441 chr4:68854429-68854440
3	CEBPB	chr4:68867081-68867455	MCF-7	breast:	n/a	chr4:68867240-68867257
4	CEBPB	chr4:68861899-68862052	HepG2	liver:	n/a	chr4:68861967-68861980 chr4:68861968-68861979
5	CEBPB	chr4:68854296-68854552	K562	blood:	n/a	chr4:68854428-68854439 chr4:68854428-68854441 chr4:68854428-68854441 chr4:68854429-68854440
6	CEBPB	chr4:68867136-68867337	Hela-S3	cervix:	n/a	chr4:68867240-68867257
7	CEBPB	chr4:68855216-68855371	HepG2	liver:	n/a	chr4:68855246-68855257 chr4:68855292-68855300 chr4:68855247-68855258
8	CEBPB	chr4:68867077-68867408	HepG2	liver:	n/a	chr4:68867240-68867257
9	CEBPB	chr4:68813237-68813501	HepG2	liver:	n/a	chr4:68813348-68813359
10	CEBPB	chr4:68867062-68867417	IMR90	lung:	n/a	chr4:68867240-68867257
11	CEBPB	chr4:68855215-68855252	K562	blood:	n/a	n/a
12	CEBPB	chr4:68856229-68856393	HepG2	liver:	n/a	chr4:68856321-68856332 chr4:68856323-68856334 chr4:68856323-68856332
13	CEBPB	chr4:68856283-68856483	K562	blood:	n/a	chr4:68856321-68856332 chr4:68856323-68856334 chr4:68856323-68856332
14	CEBPB	chr4:68855153-68855430	MCF-7	breast:	n/a	chr4:68855246-68855257 chr4:68855292-68855300 chr4:68855247-68855258
15	CEBPB	chr4:68867084-68867396	A549	lung:	n/a	chr4:68867240-68867257
16	CEBPB	chr4:68854270-68854590	HepG2	liver:	n/a	chr4:68854428-68854439 chr4:68854428-68854441 chr4:68854428-68854441 chr4:68854429-68854440
17	CEBPB	chr4:68854301-68854524	A549	lung:	n/a	chr4:68854428-68854439 chr4:68854428-68854441 chr4:68854428-68854441 chr4:68854429-68854440
18	CEBPB	chr4:68867138-68867338	H1-hESC	embryonic stem cell:	n/a	chr4:68867240-68867257
19	CEBPB	chr4:68857875-68858075	H1-hESC	embryonic stem cell:	n/a	chr4:68857997-68858014
20	CEBPB	chr4:68853094-68853163	HepG2	liver:	n/a	n/a
21	CEBPB	chr4:68854271-68854605	Hela-S3	cervix:	n/a	chr4:68854428-68854439 chr4:68854428-68854441 chr4:68854428-68854441 chr4:68854429-68854440
22	CTCF	chr4:68854119-68854489	H1-hESC	embryonic stem cell:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
23	CTCF	chr4:68854140-68854270	MCF-7	breast:	n/a	n/a
24	CTCF	chr4:68854266-68854271	GM12892	blood:	n/a	n/a
25	CTCF	chr4:68854300-68854450	HPF	lung:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
26	CTCF	chr4:68854181-68854466	T-47D	breast:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
27	CTCF	chr4:68854220-68854370	GM12871	blood:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
28	CTCF	chr4:68857900-68858050	NHEK	skin:	n/a	n/a
29	CTCF	chr4:68854241-68854397	Spleen_OC	spleen:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
30	CTCF	chr4:68854280-68854430	GM12864	blood:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
31	CTCF	chr4:68854260-68854410	AG04449	skin:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
32	CTCF	chr4:68854182-68854411	HepG2	liver:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
33	CTCF	chr4:68854240-68854390	GM06990	blood:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
34	CTCF	chr4:68866932-68866990	ProgFib	skin:	n/a	n/a
35	CTCF	chr4:68854219-68854417	GM13977	blood:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
36	CTCF	chr4:68854223-68854449	HUVEC	blood vessel:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
37	CTCF	chr4:68854220-68854370	Hela-S3	cervix:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
38	CTCF	chr4:68854280-68854430	NHLF	lung:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
39	CTCF	chr4:68854191-68854429	MCF-7	breast:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
40	CTCF	chr4:68854260-68854410	HCPEpiC	choroid plexus:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
41	CTCF	chr4:68854300-68854450	GM12878	blood:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
42	CTCF	chr4:68854260-68854410	HPAF	blood vessel:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
43	CTCF	chr4:68854299-68854342	MCF-7	breast:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
44	CTCF	chr4:68854172-68854387	A549	lung:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
45	CTCF	chr4:68854300-68854450	HL-60	blood:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
46	CTCF	chr4:68854240-68854390	AG09309	skin:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
47	CTCF	chr4:68854240-68854390	GM12870	blood:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
48	CTCF	chr4:68854217-68854438	HepG2	liver:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
49	CTCF	chr4:68854260-68854410	HepG2	liver:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
50	CTCF	chr4:68854126-68854438	A549	lung:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:68801145-68801195	AoSMC	blood vessel:	n/a
2	chr4:68801145-68801195	AoSMC	blood vessel:	n/a
3	chr4:68829101-68829151	MCF10A-Er-Src	breast:	n/a
4	chr4:68801145-68801195	HRE	kidney:	n/a
5	chr4:68801145-68801195	HCF	heart:	n/a
6	chr4:68829101-68829151	Hepatocyte	liver:	n/a
7	chr4:68830227-68830277	HepG2	liver:	n/a
8	chr4:68829101-68829151	PFSK-1	brain:	n/a
9	chr4:68830227-68830277	A549	lung:	n/a
10	chr4:68801145-68801195	HIPEpiC	eye:	n/a
11	chr4:68829101-68829151	Caco-2	colon:	n/a
12	chr4:68801145-68801195	ovcar-3	ovarian:	n/a
13	chr4:68801145-68801195	HepG2	liver:	n/a
14	chr4:68801145-68801195	U87	brain:	n/a
15	chr4:68830227-68830277	SKMC	muscle:	n/a
16	chr4:68829101-68829151	ovcar-3	ovarian:	n/a
17	chr4:68801145-68801195	HMEC	breast:	n/a
18	chr4:68829101-68829151	AG09319	gingival:	n/a
19	chr4:68830227-68830277	HMEC	breast:	n/a
20	chr4:68829101-68829151	NH-A	brain:	n/a
21	chr4:68830227-68830277	HL-60	blood:	n/a
22	chr4:68829101-68829151	Jurkat	blood:	n/a
23	chr4:68801145-68801195	NHBE	bronchial:	n/a
24	chr4:68830227-68830277	AG09319	gingival:	n/a
25	chr4:68829101-68829151	GM19239	blood:	n/a
26	chr4:68830227-68830277	AG10803	skin:	n/a
27	chr4:68801145-68801195	NH-A	brain:	n/a
28	chr4:68830227-68830277	HIPEpiC	eye:	n/a
29	chr4:68829101-68829151	A549	lung:	n/a
30	chr4:68830227-68830277	HRCEpiC	kidney:	n/a
31	chr4:68830227-68830277	Caco-2	colon:	n/a
32	chr4:68829101-68829151	GM12878	blood:	n/a
33	chr4:68829101-68829151	PANC-1	pancreas:	n/a
34	chr4:68829101-68829151	MCF-7	breast:	n/a
35	chr4:68801145-68801195	NHDF-neo	bronchial:	n/a
36	chr4:68830227-68830277	Jurkat	blood:	n/a
37	chr4:68830227-68830277	SK-N-SH	brain:	n/a
38	chr4:68829101-68829151	BE2_C	brain:	n/a
39	chr4:68801145-68801195	RPTEC	kidney:	n/a
40	chr4:68829101-68829151	BJ	skin:	n/a
41	chr4:68801145-68801195	BE2_C	brain:	n/a
42	chr4:68829101-68829151	AG04449	skin:	fetal
43	chr4:68801145-68801195	HNPCEpiC	eye:	n/a
44	chr4:68829101-68829151	T-47D	breast:	n/a
45	chr4:68830227-68830277	SK-N-SH_RA	brain:	n/a
46	chr4:68830227-68830277	K562	blood:	n/a
47	chr4:68801145-68801195	MCF-7	breast:	n/a
48	chr4:68830227-68830277	SAEC	small airway:	n/a
49	chr4:68801145-68801195	AG10803	skin:	n/a
50	chr4:68829101-68829151	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:68854585..68857401-chr4:68944516..68946087,2	MCF-7	breast:
2	chr4:68801891..68804770-chr4:68805510..68808424,3	K562	blood:
3	chr4:68791805..68794624-chr4:68798478..68800793,2	K562	blood:
4	chr4:68565498..68567091-chr4:68824885..68827731,2	K562	blood:
5	chr4:68796679..68798591-chr4:68806253..68807881,2	MCF-7	breast:
6	chr4:68796679..68798591-chr4:68806253..68807881,2	MCF-7	breast:
7	chr4:68853837..68854799-chr4:69040919..69041918,3	MCF-7	breast:
8	chr4:68784089..68784796-chr4:68853790..68854411,2	MCF-7	breast:
9	chr4:68802859..68804770-chr4:68805510..68807108,2	K562	blood:
10	chr4:68798924..68801314-chr4:68932123..68934294,2	MCF-7	breast:
11	chr4:68801891..68804770-chr4:68805510..68808424,3	K562	blood:
12	chr4:68854785..68855326-chr4:69041026..69041997,2	MCF-7	breast:
13	chr4:68853962..68854562-chr4:69041076..69041834,2	K562	blood:
14	chr4:68787068..68789277-chr4:68795494..68798392,2	MCF-7	breast:
15	chr4:68802859..68804770-chr4:68805510..68807108,2	K562	blood:

Variant related genes	Relation type
TMPRSS11A	TF binding region
RNU6-95P	TF binding region
TMPRSS11GP	TF binding region
TMPRSS11A	CpG island
RNU6-95P	CpG island
TMPRSS11GP	CpG island
ENSG00000248049	chromatin interactions
ENSG00000033178	chromatin interactions

Extended variants
information (count: 1483 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1483 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs353176	chr4:68797380-68797381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs543742727	chr4:68797393-68797394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs557338716	chr4:68797412-68797413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs577195480	chr4:68797502-68797503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs546008068	chr4:68797504-68797505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs373495749	chr4:68797548-68797549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs150589169	chr4:68797562-68797563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs190772151	chr4:68797566-68797567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs182309325	chr4:68797634-68797635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs530085196	chr4:68797643-68797644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs529825761	chr4:68797649-68797650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs75592724	chr4:68797664-68797665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs138571655	chr4:68797675-68797676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs371040022	chr4:68797703-68797704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs142955442	chr4:68797710-68797711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs151094571	chr4:68797711-68797712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs370242991	chr4:68797727-68797728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs112827609	chr4:68797740-68797741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs376258886	chr4:68797791-68797792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs374454980	chr4:68797806-68797807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs552757290	chr4:68797808-68797809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs73823321	chr4:68797827-68797828	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs534724742	chr4:68797851-68797852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs554657884	chr4:68797887-68797888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs538913317	chr4:68797920-68797921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs537083701	chr4:68797949-68797950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs10518046	chr4:68797982-68797983	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs373440493	chr4:68797984-68797985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs149301743	chr4:68797991-68797992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs186924350	chr4:68797992-68797993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs553141358	chr4:68798028-68798029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs191765351	chr4:68798065-68798066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs144723929	chr4:68798134-68798135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs561088223	chr4:68798141-68798142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs375721556	chr4:68798180-68798181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs140008305	chr4:68798213-68798214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs569150092	chr4:68798329-68798330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs543438051	chr4:68798377-68798378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs563311700	chr4:68798380-68798381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs28469855	chr4:68798413-68798414	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs549216049	chr4:68798444-68798445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs566265662	chr4:68798480-68798481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs147234931	chr4:68798494-68798495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs548789133	chr4:68798506-68798507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs140717177	chr4:68798531-68798532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs182760708	chr4:68798533-68798534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs142442568	chr4:68798536-68798537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs151330778	chr4:68798629-68798630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs188404420	chr4:68798630-68798631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs553042051	chr4:68798648-68798649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	20369283	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Graft versus host disease	20877625	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Osteoporosis	20877625	CNVD
Osteoporosis	19737800	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Glioblastoma multiforme	21138945	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:68793400-68806600	Weak transcription	Esophagus	oesophagus
2	chr4:68793600-68799800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr4:68794200-68799000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr4:68794400-68797800	Enhancers	NHEK	skin
5	chr4:68794800-68799200	Weak transcription	Primary hematopoietic stem cells	blood
6	chr4:68794800-68799400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr4:68794800-68799400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr4:68794800-68799800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr4:68795200-68800000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr4:68796000-68799400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr4:68796200-68797400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr4:68797400-68797800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr4:68797800-68800200	Weak transcription	NHEK	skin
14	chr4:68797800-68800400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr4:68798600-68802000	Enhancers	Dnd41	blood
16	chr4:68798800-68799000	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr4:68799000-68799400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr4:68799000-68800000	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr4:68799200-68802200	Enhancers	Primary hematopoietic stem cells	blood
20	chr4:68799400-68799600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr4:68799400-68800000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr4:68799400-68800200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr4:68799400-68801000	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr4:68799400-68801000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr4:68799600-68800000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr4:68799800-68801000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr4:68799800-68801000	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr4:68799800-68801000	Enhancers	Fetal Heart	heart
29	chr4:68799800-68801200	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr4:68800000-68800600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr4:68800000-68800800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr4:68800000-68801000	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr4:68800000-68801200	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr4:68800000-68801200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr4:68800200-68800400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr4:68800200-68800800	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr4:68800200-68800800	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr4:68800200-68800800	Enhancers	NHEK	skin
39	chr4:68800200-68801200	Enhancers	Fetal Intestine Small	intestine
40	chr4:68800400-68800600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr4:68800400-68800800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr4:68800400-68800800	Enhancers	Brain Germinal Matrix	brain
43	chr4:68800400-68800800	Enhancers	Thymus	Thymus
44	chr4:68800400-68801000	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr4:68800600-68800800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr4:68800600-68801000	Enhancers	H1 Cell Line	embryonic stem cell
47	chr4:68800800-68801200	Enhancers	H9 Cell Line	embryonic stem cell
48	chr4:68800800-68801200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr4:68800800-68801200	Enhancers	Fetal Kidney	kidney
50	chr4:68800800-68801800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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