Variant report

Variant	nsv879657
Chromosome Location	chr4:100082154-100139366
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	ARID3A	chr4:100087752-100088164	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:100126236-100127065	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:100089099-100089294	HepG2	liver:	n/a	n/a
4	BATF	chr4:100113638-100113790	GM12878	blood:	n/a	n/a
5	CEBPB	chr4:100111081-100111438	MCF-7	breast:	n/a	chr4:100111245-100111256
6	CEBPB	chr4:100126313-100127116	HepG2	liver:	n/a	chr4:100126944-100126955 chr4:100126486-100126497 chr4:100126944-100126955 chr4:100126888-100126900
7	CEBPB	chr4:100128569-100128934	IMR90	lung:	n/a	chr4:100128748-100128759
8	CEBPB	chr4:100111062-100111435	HepG2	liver:	n/a	chr4:100111245-100111256
9	CEBPB	chr4:100126297-100127136	HepG2	liver:	n/a	chr4:100126944-100126955 chr4:100126486-100126497 chr4:100126944-100126955 chr4:100126888-100126900
10	CEBPB	chr4:100126346-100126581	HepG2	liver:	n/a	chr4:100126486-100126497
11	CEBPB	chr4:100128587-100128935	HepG2	liver:	n/a	chr4:100128748-100128759
12	CEBPB	chr4:100128604-100128837	K562	blood:	n/a	chr4:100128748-100128759
13	CEBPB	chr4:100111142-100111424	Hela-S3	cervix:	n/a	chr4:100111245-100111256
14	CEBPB	chr4:100111070-100111428	K562	blood:	n/a	chr4:100111245-100111256
15	CEBPB	chr4:100126335-100126686	MCF-7	breast:	n/a	chr4:100126486-100126497
16	CEBPB	chr4:100128629-100128898	A549	lung:	n/a	chr4:100128748-100128759
17	CEBPB	chr4:100126828-100127018	HepG2	liver:	n/a	chr4:100126944-100126955 chr4:100126944-100126955 chr4:100126888-100126900
18	CEBPB	chr4:100111109-100111357	HepG2	liver:	n/a	chr4:100111245-100111256
19	CEBPB	chr4:100101641-100101813	A549	lung:	n/a	chr4:100101697-100101708
20	CEBPB	chr4:100125099-100125246	K562	blood:	n/a	n/a
21	CEBPB	chr4:100111165-100111376	MCF-7	breast:	n/a	chr4:100111245-100111256
22	CEBPB	chr4:100125068-100125268	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr4:100101627-100101836	HepG2	liver:	n/a	chr4:100101697-100101708
24	CEBPB	chr4:100111069-100111432	IMR90	lung:	n/a	chr4:100111245-100111256
25	CEBPB	chr4:100123717-100123973	IMR90	lung:	n/a	chr4:100123756-100123767 chr4:100123756-100123767
26	CEBPB	chr4:100126778-100127013	HepG2	liver:	n/a	chr4:100126944-100126955 chr4:100126944-100126955 chr4:100126888-100126900
27	CEBPB	chr4:100125038-100125274	IMR90	lung:	n/a	n/a
28	CEBPB	chr4:100082376-100082606	HepG2	liver:	n/a	n/a
29	CEBPB	chr4:100126333-100127073	IMR90	lung:	n/a	chr4:100126944-100126955 chr4:100126486-100126497 chr4:100126944-100126955 chr4:100126888-100126900
30	CEBPB	chr4:100101529-100101897	IMR90	lung:	n/a	chr4:100101697-100101708
31	CEBPB	chr4:100126305-100126657	HepG2	liver:	n/a	chr4:100126486-100126497
32	CEBPB	chr4:100111078-100111370	H1-hESC	embryonic stem cell:	n/a	chr4:100111245-100111256
33	CEBPB	chr4:100126351-100126650	H1-hESC	embryonic stem cell:	n/a	chr4:100126486-100126497
34	CEBPB	chr4:100128577-100128913	H1-hESC	embryonic stem cell:	n/a	chr4:100128748-100128759
35	CEBPB	chr4:100128570-100128804	HepG2	liver:	n/a	chr4:100128748-100128759
36	CEBPB	chr4:100111077-100111427	A549	lung:	n/a	chr4:100111245-100111256
37	CEBPB	chr4:100125021-100125340	HepG2	liver:	n/a	n/a
38	CTCF	chr4:100122960-100123110	AG04449	skin:	n/a	chr4:100123012-100123033
39	CTCF	chr4:100126340-100126490	AoAF	blood vessel:	n/a	n/a
40	CTCF	chr4:100126180-100126330	MCF-7	breast:	n/a	n/a
41	CTCF	chr4:100122940-100123090	HEEpiC	esophagus:	n/a	chr4:100123012-100123033
42	CTCF	chr4:100126380-100126530	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr4:100122920-100123070	NHDF-neo	bronchial:	n/a	chr4:100123012-100123033
44	CTCF	chr4:100122969-100123075	Kidney_OC	kidney:	n/a	chr4:100123012-100123033
45	CTCF	chr4:100101700-100101850	BJ	skin:	n/a	n/a
46	CTCF	chr4:100126340-100126490	BJ	skin:	n/a	n/a
47	CTCF	chr4:100123020-100123170	HFF	foreskin:	n/a	n/a
48	CTCF	chr4:100101540-100101690	HMF	breast:	n/a	n/a
49	CTCF	chr4:100126260-100126410	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr4:100101019-100101087	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:100082970-100083020	ProgFib	skin:	n/a
2	chr4:100128186-100128236	RPTEC	kidney:	n/a
3	chr4:100083331-100083381	GM19239	blood:	n/a
4	chr4:100125999-100126049	AG10803	skin:	n/a
5	chr4:100128186-100128236	SK-N-SH	brain:	n/a
6	chr4:100128186-100128236	HPAEpiC	pulmonary alveolar:	n/a
7	chr4:100101289-100101339	GM12892	blood:	n/a
8	chr4:100083121-100083171	HL-60	blood:	n/a
9	chr4:100083331-100083381	SK-N-SH	brain:	n/a
10	chr4:100128186-100128236	GM12892	blood:	n/a
11	chr4:100083121-100083171	PFSK-1	brain:	n/a
12	chr4:100101289-100101339	HEEpiC	esophagus:	n/a
13	chr4:100083331-100083381	GM12878	blood:	n/a
14	chr4:100083331-100083381	A549	lung:	n/a
15	chr4:100101289-100101339	HCT-116	colon:	n/a
16	chr4:100083331-100083381	Jurkat	blood:	n/a
17	chr4:100083121-100083171	T-47D	breast:	n/a
18	chr4:100130470-100130520	K562	blood:	n/a
19	chr4:100125999-100126049	ProgFib	skin:	n/a
20	chr4:100125999-100126049	A549	lung:	n/a
21	chr4:100083331-100083381	AG09309	skin:	n/a
22	chr4:100125999-100126049	MCF10A-Er-Src	breast:	n/a
23	chr4:100083121-100083171	HEK293	kidney:	embryo
24	chr4:100101289-100101339	HCF	heart:	n/a
25	chr4:100101289-100101339	HPAEpiC	pulmonary alveolar:	n/a
26	chr4:100083121-100083171	HCPEpiC	choroid plexus:	n/a
27	chr4:100128186-100128236	AG04449	skin:	fetal
28	chr4:100128186-100128236	ProgFib	skin:	n/a
29	chr4:100125999-100126049	SAEC	small airway:	n/a
30	chr4:100082970-100083020	PFSK-1	brain:	n/a
31	chr4:100082970-100083020	SAEC	small airway:	n/a
32	chr4:100125999-100126049	HEK293	kidney:	embryo
33	chr4:100101289-100101339	AG09319	gingival:	n/a
34	chr4:100101289-100101339	Caco-2	colon:	n/a
35	chr4:100101289-100101339	ECC-1	luminal epithelium:	n/a
36	chr4:100125999-100126049	H1-hESC	embryonic stem cell:	embryo
37	chr4:100128186-100128236	GM06990	blood:	n/a
38	chr4:100128186-100128236	SAEC	small airway:	n/a
39	chr4:100130470-100130520	NB4	blood:	n/a
40	chr4:100128186-100128236	U87	brain:	n/a
41	chr4:100125999-100126049	PFSK-1	brain:	n/a
42	chr4:100083331-100083381	T-47D	breast:	n/a
43	chr4:100083331-100083381	AG09319	gingival:	n/a
44	chr4:100083121-100083171	HNPCEpiC	eye:	n/a
45	chr4:100125999-100126049	HRCEpiC	kidney:	n/a
46	chr4:100082970-100083020	NT2-D1	testis:	n/a
47	chr4:100083331-100083381	HNPCEpiC	eye:	n/a
48	chr4:100083331-100083381	HMEC	breast:	n/a
49	chr4:100128186-100128236	HUVEC	blood vessel:	n/a
50	chr4:100130470-100130520	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:99916019..99918646-chr4:100083097..100084598,2	K562	blood:
2	chr4:100122531..100123516-chr4:100326382..100326915,3	MCF-7	breast:
3	chr4:100122648..100123636-chr4:100326377..100326984,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADH4-1	chr4:100081671-100082422	NONHSAT097522
2	lnc-METAP1-3	chr4:100125514-100125588	ENSG00000246090
3	lnc-METAP1-3	chr4:100082967-100083061	ENSG00000246090
4	lnc-ADH4-1	chr4:100082094-100082802	NONHSAT097524
5	lnc-ADH4-1	chr4:100081751-100082804	NONHSAT097523
6	lnc-METAP1-3	chr4:100109802-100110012	ENSG00000246090
7	lnc-METAP1-3	chr4:100125514-100125588	ENSG00000246090
8	lnc-ADH1A-1	chr4:100136952-100137419	NONHSAT097527
9	lnc-METAP1-6	chr4:100103643-100103769	l_2690_chr4:100101302-100104555_testes
10	lnc-METAP1-3	chr4:100125514-100125584	ENSG00000246090
11	lnc-METAP1-3	chr4:100082941-100083061	ENSG00000246090
12	lnc-METAP1-6	chr4:100101303-100101330	l_2690_chr4:100101302-100104555_testes
13	lnc-METAP1-6	chr4:100104128-100104555	l_2690_chr4:100101302-100104555_testes

Variant related genes	Relation type
ADH6	TF binding region
PCNAP1	TF binding region
ADH4	TF binding region
ENSG00000246090	TF binding region
ADH6	CpG island
PCNAP1	CpG island
ADH4	CpG island
ENSG00000246090	CpG island
ENSG00000265213	chromatin interactions
ENSG00000164024	chromatin interactions

Extended variants
information (count: 2010 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:2010 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1540053	chr4:100082154-100082155	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs187095724	chr4:100082173-100082174	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs541597290	chr4:100082183-100082184	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs534848276	chr4:100082203-100082204	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs147512026	chr4:100082304-100082305	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs191984360	chr4:100082347-100082348	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs34743543	chr4:100082368-100082369	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs545463246	chr4:100082408-100082409	Weak transcription Enhancers	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
9	rs563667566	chr4:100082485-100082486	Weak transcription Enhancers	TF binding region lncRNA	3 gene(s)	Overlapped CNVs	n/a
10	rs183314710	chr4:100082500-100082501	Weak transcription Enhancers	TF binding region lncRNA	3 gene(s)	Overlapped CNVs	n/a
11	rs140124446	chr4:100082515-100082516	Weak transcription Enhancers	TF binding region lncRNA	3 gene(s)	Overlapped CNVs	n/a
12	rs561920340	chr4:100082568-100082569	Weak transcription Enhancers	TF binding region lncRNA	3 gene(s)	Overlapped CNVs	n/a
13	rs567796832	chr4:100082591-100082592	Weak transcription Enhancers	TF binding region lncRNA	3 gene(s)	Overlapped CNVs	n/a
14	rs529216438	chr4:100082625-100082626	Enhancers Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs4141887	chr4:100082632-100082633	Enhancers Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs559475277	chr4:100082633-100082634	Enhancers Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs189112023	chr4:100082763-100082764	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region lncRNA	3 gene(s)	Overlapped CNVs	n/a
18	rs551419690	chr4:100082798-100082799	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region lncRNA	3 gene(s)	Overlapped CNVs	n/a
19	rs569432474	chr4:100082799-100082800	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region lncRNA	3 gene(s)	Overlapped CNVs	n/a
20	rs112808368	chr4:100082861-100082862	Enhancers Weak transcription Strong transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
21	rs193018899	chr4:100082898-100082899	Enhancers Weak transcription Strong transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
22	rs566964040	chr4:100082973-100082974	Enhancers Weak transcription Strong transcription	CpG island lncRNA	2 gene(s)	Overlapped CNVs	n/a
23	rs535323245	chr4:100083013-100083014	Weak transcription Strong transcription Enhancers	CpG island lncRNA	2 gene(s)	Overlapped CNVs	n/a
24	rs79242815	chr4:100083030-100083031	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
25	rs79241219	chr4:100083031-100083032	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
26	rs12648974	chr4:100083128-100083129	Weak transcription Strong transcription Enhancers	CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs557464998	chr4:100083276-100083277	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs183630574	chr4:100083331-100083332	Weak transcription Strong transcription	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs150008287	chr4:100083332-100083333	Weak transcription Strong transcription	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs561260708	chr4:100083397-100083398	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs186800141	chr4:100083415-100083416	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs191222972	chr4:100083468-100083469	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs184098317	chr4:100083489-100083490	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs189464983	chr4:100083610-100083611	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs370730198	chr4:100083630-100083631	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs182048728	chr4:100083647-100083648	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs563011178	chr4:100083683-100083684	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs145269181	chr4:100083704-100083705	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs548697791	chr4:100083736-100083737	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs148712772	chr4:100083741-100083742	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs375585733	chr4:100083748-100083749	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs528114820	chr4:100083772-100083773	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs113649176	chr4:100083785-100083786	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs564818938	chr4:100083811-100083812	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs376877362	chr4:100083824-100083825	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs571848494	chr4:100083839-100083840	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs539194130	chr4:100083856-100083857	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs557601714	chr4:100083882-100083883	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs4699723	chr4:100083937-100083938	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs536718825	chr4:100083970-100083971	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	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
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Gastric cancer	16891809	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:360 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:100035000-100098200	Weak transcription	Ovary	ovary
2	chr4:100056800-100082600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr4:100064000-100082600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr4:100065600-100096600	Weak transcription	Fetal Lung	lung
5	chr4:100066200-100083200	Enhancers	Liver	Liver
6	chr4:100066600-100082600	Weak transcription	Pancreas	Pancrea
7	chr4:100072200-100101400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr4:100074600-100085400	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr4:100075600-100083200	Enhancers	HepG2	liver
10	chr4:100078800-100088400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr4:100079800-100082600	Weak transcription	Aorta	Aorta
12	chr4:100082000-100082800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr4:100082000-100083200	Enhancers	Fetal Intestine Large	intestine
14	chr4:100082600-100082800	Genic enhancers	Aorta	Aorta
15	chr4:100082600-100083000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr4:100082600-100083200	Enhancers	Pancreas	Pancrea
17	chr4:100082600-100083800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
18	chr4:100082800-100083000	Strong transcription	Aorta	Aorta
19	chr4:100082800-100101200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr4:100083000-100098200	Weak transcription	Aorta	Aorta
21	chr4:100083200-100084200	Weak transcription	Liver	Liver
22	chr4:100083200-100087000	Weak transcription	HepG2	liver
23	chr4:100083200-100088400	Weak transcription	Pancreas	Pancrea
24	chr4:100083800-100086400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr4:100084200-100085600	Enhancers	Liver	Liver
26	chr4:100085600-100086400	Weak transcription	Liver	Liver
27	chr4:100086400-100087800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
28	chr4:100086400-100090400	Enhancers	Liver	Liver
29	chr4:100087000-100087400	Enhancers	HMEC	breast
30	chr4:100087000-100089600	Enhancers	HepG2	liver
31	chr4:100087200-100087400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr4:100087200-100087600	Enhancers	NHEK	skin
33	chr4:100088000-100088600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr4:100088400-100088600	Enhancers	Pancreas	Pancrea
35	chr4:100088400-100089200	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr4:100089200-100101000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr4:100090400-100100800	Weak transcription	Liver	Liver
38	chr4:100095600-100096600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr4:100095600-100100000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
40	chr4:100096600-100096800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr4:100096600-100097400	ZNF genes & repeats	Fetal Lung	lung
42	chr4:100097400-100098000	Weak transcription	Fetal Lung	lung
43	chr4:100098000-100099400	ZNF genes & repeats	Fetal Lung	lung
44	chr4:100098200-100098600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr4:100098200-100098600	ZNF genes & repeats	Aorta	Aorta
46	chr4:100098200-100098600	ZNF genes & repeats	Ovary	ovary
47	chr4:100098400-100098600	ZNF genes & repeats	Lung	lung
48	chr4:100098600-100099000	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
49	chr4:100098600-100101400	Weak transcription	Lung	lung
50	chr4:100098600-100102200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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