Variant report

Variant	esv2752360
Chromosome Location	chr4:102790822-102888822
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:570)
CpG islands
(count:122)
Chromatin interactive
region (count:29)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:570 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:102806719-102807095	HepG2	liver:	n/a	n/a
2	ATF2	chr4:102875018-102875480	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr4:102874997-102875510	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr4:102806799-102807077	HepG2	liver:	n/a	n/a
5	BRCA1	chr4:102875169-102875556	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr4:102864499-102864545	GM12878	blood:	n/a	n/a
7	CEBPB	chr4:102862850-102863632	ECC-1	luminal epithelium:	n/a	n/a
8	CEBPB	chr4:102808030-102808318	A549	lung:	n/a	chr4:102808169-102808180
9	CEBPB	chr4:102859976-102860454	ECC-1	luminal epithelium:	n/a	chr4:102860203-102860214 chr4:102860253-102860266
10	CEBPB	chr4:102842528-102842874	MCF-7	breast:	n/a	n/a
11	CEBPB	chr4:102819100-102819300	HepG2	liver:	n/a	chr4:102819215-102819228 chr4:102819215-102819226
12	CEBPB	chr4:102821191-102821414	HepG2	liver:	n/a	chr4:102821287-102821298 chr4:102821286-102821299
13	CEBPB	chr4:102806635-102807206	MCF-7	breast:	n/a	chr4:102806919-102806930
14	CEBPB	chr4:102806586-102807173	A549	lung:	n/a	chr4:102806919-102806930
15	CEBPB	chr4:102806761-102807122	HepG2	liver:	n/a	chr4:102806919-102806930
16	CEBPB	chr4:102806740-102807126	HepG2	liver:	n/a	chr4:102806919-102806930
17	CEBPB	chr4:102859908-102860460	ECC-1	luminal epithelium:	n/a	chr4:102860203-102860214 chr4:102860253-102860266
18	CEBPB	chr4:102815807-102815871	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr4:102806691-102807169	MCF-7	breast:	n/a	chr4:102806919-102806930
20	CEBPB	chr4:102808053-102808294	HepG2	liver:	n/a	chr4:102808169-102808180
21	CEBPB	chr4:102806702-102807108	A549	lung:	n/a	chr4:102806919-102806930
22	CEBPB	chr4:102806816-102807010	HepG2	liver:	n/a	chr4:102806919-102806930
23	CEBPB	chr4:102859965-102860440	Hela-S3	cervix:	n/a	chr4:102860203-102860214 chr4:102860253-102860266
24	CEBPB	chr4:102875003-102875504	A549	lung:	n/a	n/a
25	CEBPB	chr4:102806741-102807114	A549	lung:	n/a	chr4:102806919-102806930
26	CEBPB	chr4:102806689-102807087	HepG2	liver:	n/a	chr4:102806919-102806930
27	CEBPB	chr4:102874953-102875505	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr4:102876021-102876528	ECC-1	luminal epithelium:	n/a	n/a
29	CEBPD	chr4:102806773-102807041	HepG2	liver:	n/a	n/a
30	CHD2	chr4:102875127-102875493	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr4:102874141-102874215	LNCaP	prostate:	n/a	chr4:102874182-102874203
32	CTCF	chr4:102874157-102874242	Pancreas_OC	pancreas:	n/a	chr4:102874182-102874203
33	CTCF	chr4:102793859-102793947	Fibrobl	skin:	n/a	n/a
34	CTCF	chr4:102874184-102874190	LNCaP	prostate:	n/a	n/a
35	CTCF	chr4:102874113-102874278	MCF-7	breast:	n/a	chr4:102874182-102874203
36	CTCF	chr4:102849920-102850070	Caco-2	colon:	n/a	n/a
37	CTCF	chr4:102874100-102874250	MCF-7	breast:	n/a	chr4:102874182-102874203
38	CTCF	chr4:102874091-102874293	MCF-7	breast:	n/a	chr4:102874182-102874203
39	CTCF	chr4:102874191-102874219	LNCaP	prostate:	n/a	n/a
40	CTCF	chr4:102874080-102874230	MCF-7	breast:	n/a	chr4:102874182-102874203
41	CTCF	chr4:102879940-102880090	MCF-7	breast:	n/a	n/a
42	E2F4	chr4:102837788-102837897	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr4:102843778-102843890	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr4:102810261-102810441	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr4:102875901-102876076	MCF10A-Er-Src	breast:	n/a	n/a
46	EBF1	chr4:102855824-102856034	GM12878	blood:	n/a	chr4:102855886-102855899 chr4:102855888-102855897 chr4:102855887-102855897 chr4:102855888-102855898 chr4:102855886-102855897
47	ELK1	chr4:102875070-102875423	Hela-S3	cervix:	n/a	n/a
48	EP300	chr4:102874886-102875655	A549	lung:	n/a	chr4:102874915-102874924
49	EP300	chr4:102874995-102875636	ECC-1	luminal epithelium:	n/a	n/a
50	EP300	chr4:102835931-102836382	T-47D	breast:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:102878132-102878182	HNPCEpiC	eye:	n/a
2	chr4:102875309-102875359	HMEC	breast:	n/a
3	chr4:102875309-102875359	HRCEpiC	kidney:	n/a
4	chr4:102878132-102878182	AG09319	gingival:	n/a
5	chr4:102875309-102875359	NH-A	brain:	n/a
6	chr4:102878132-102878182	HCM	heart:	n/a
7	chr4:102878132-102878182	HPAEpiC	pulmonary alveolar:	n/a
8	chr4:102878132-102878182	HRCEpiC	kidney:	n/a
9	chr4:102875309-102875359	HCT-116	colon:	n/a
10	chr4:102878132-102878182	T-47D	breast:	n/a
11	chr4:102878132-102878182	HEK293	kidney:	embryo
12	chr4:102875309-102875359	HNPCEpiC	eye:	n/a
13	chr4:102878132-102878182	PFSK-1	brain:	n/a
14	chr4:102875309-102875359	BE2_C	brain:	n/a
15	chr4:102878132-102878182	HMEC	breast:	n/a
16	chr4:102875309-102875359	HEK293	kidney:	embryo
17	chr4:102878132-102878182	Hepatocyte	liver:	n/a
18	chr4:102875309-102875359	HCPEpiC	choroid plexus:	n/a
19	chr4:102878132-102878182	HRPEpiC	eye:	n/a
20	chr4:102878132-102878182	ProgFib	skin:	n/a
21	chr4:102878132-102878182	AG10803	skin:	n/a
22	chr4:102875309-102875359	K562	blood:	n/a
23	chr4:102875309-102875359	LNCaP	prostate:	n/a
24	chr4:102878132-102878182	HCT-116	colon:	n/a
25	chr4:102875309-102875359	HRE	kidney:	n/a
26	chr4:102875309-102875359	HEEpiC	esophagus:	n/a
27	chr4:102875309-102875359	HAEpiC	amniotic membrane:	n/a
28	chr4:102878132-102878182	SK-N-SH_RA	brain:	n/a
29	chr4:102875309-102875359	RPTEC	kidney:	n/a
30	chr4:102875309-102875359	HL-60	blood:	n/a
31	chr4:102878132-102878182	BE2_C	brain:	n/a
32	chr4:102875309-102875359	AG04450	lung:	fetal
33	chr4:102875309-102875359	NHBE	bronchial:	n/a
34	chr4:102878132-102878182	AG09309	skin:	n/a
35	chr4:102878132-102878182	NH-A	brain:	n/a
36	chr4:102878132-102878182	HL-60	blood:	n/a
37	chr4:102878132-102878182	GM12891	blood:	n/a
38	chr4:102878132-102878182	HUVEC	blood vessel:	n/a
39	chr4:102875309-102875359	PFSK-1	brain:	n/a
40	chr4:102878132-102878182	NHBE	bronchial:	n/a
41	chr4:102878132-102878182	HEEpiC	esophagus:	n/a
42	chr4:102878132-102878182	A549	lung:	n/a
43	chr4:102875309-102875359	AoSMC	blood vessel:	n/a
44	chr4:102878132-102878182	PrEC	prostate:	n/a
45	chr4:102878132-102878182	NT2-D1	testis:	n/a
46	chr4:102875309-102875359	MCF10A-Er-Src	breast:	n/a
47	chr4:102878132-102878182	ovcar-3	ovarian:	n/a
48	chr4:102878132-102878182	PANC-1	pancreas:	n/a
49	chr4:102878132-102878182	HCF	heart:	n/a
50	chr4:102875309-102875359	HRPEpiC	eye:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:102842276..102843131-chr4:102874015..102874871,3	MCF-7	breast:
2	chr4:102853526..102855448-chr4:102860047..102862482,2	K562	blood:
3	chr4:102846487..102848228-chr4:102853686..102856013,2	MCF-7	breast:
4	chr4:102874020..102874843-chr4:102891401..102892080,2	MCF-7	breast:
5	chr4:102872789..102875813-chr4:102887302..102889181,3	MCF-7	breast:
6	chr3:64045097..64045973-chr4:102874042..102874640,2	MCF-7	breast:
7	chr4:102842276..102843131-chr4:102874015..102874871,3	MCF-7	breast:
8	chr4:102880000..102881759-chr4:102886736..102889314,2	MCF-7	breast:
9	chr4:102842214..102843068-chr4:102854874..102855625,2	MCF-7	breast:
10	chr4:102842214..102843068-chr4:102854874..102855625,2	MCF-7	breast:
11	chr4:102842702..102843248-chr4:102855080..102855669,2	MCF-7	breast:
12	chr4:102791636..102793550-chr4:102797262..102799640,2	K562	blood:
13	chr4:102846487..102848228-chr4:102853686..102856013,2	MCF-7	breast:
14	chr4:102840186..102841875-chr4:102843846..102845982,2	K562	blood:
15	chr4:102872789..102875813-chr4:102887302..102889181,3	MCF-7	breast:
16	chr4:102880000..102881759-chr4:102886736..102889314,2	MCF-7	breast:
17	chr4:102842702..102843248-chr4:102855080..102855669,2	MCF-7	breast:
18	chr4:102819220..102821914-chr4:102824309..102827008,2	MCF-7	breast:
19	chr4:102792418..102794710-chr4:102794751..102797672,2	MCF-7	breast:
20	chr4:102840186..102841875-chr4:102843846..102845982,2	K562	blood:
21	chr4:102860897..102862820-chr4:102873982..102876353,2	MCF-7	breast:
22	chr4:102792418..102794710-chr4:102794751..102797672,2	MCF-7	breast:
23	chr4:102860897..102862820-chr4:102873982..102876353,2	MCF-7	breast:
24	chr4:102791636..102793550-chr4:102797262..102799640,2	K562	blood:
25	chr4:102853526..102855448-chr4:102860047..102862482,2	K562	blood:
26	chr4:102831487..102833404-chr4:102833922..102836733,2	MCF-7	breast:
27	chr4:102831487..102833404-chr4:102833922..102836733,2	MCF-7	breast:
28	chr4:102842819..102843467-chr4:133460108..133460904,2	MCF-7	breast:
29	chr4:102819220..102821914-chr4:102824309..102827008,2	MCF-7	breast:

No data

Variant related genes	Relation type
MTND5P5	TF binding region
MTND5P5	CpG island

Extended variants
information (count: 3411 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:3411 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs77383330	chr4:102790851-102790852	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs532867657	chr4:102790891-102790892	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs77078113	chr4:102790894-102790895	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs569313128	chr4:102790900-102790901	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs533394160	chr4:102790912-102790913	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs182899889	chr4:102790931-102790932	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs56268659	chr4:102790942-102790943	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs188398735	chr4:102790973-102790974	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs143664676	chr4:102791006-102791007	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs558747043	chr4:102791067-102791068	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs577049705	chr4:102791081-102791082	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs148076178	chr4:102791122-102791123	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs7662572	chr4:102791185-102791186	Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs533014527	chr4:102791190-102791191	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs141790290	chr4:102791208-102791209	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs200005743	chr4:102791242-102791243	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs559830997	chr4:102791243-102791244	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs397994745	chr4:102791247-102791248	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs182367282	chr4:102791342-102791343	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs555827006	chr4:102791373-102791374	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs377663599	chr4:102791383-102791384	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs567804033	chr4:102791386-102791387	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs71597110	chr4:102791430-102791431	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs573072795	chr4:102791551-102791552	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs540447750	chr4:102791590-102791591	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs565508592	chr4:102791636-102791637	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs113019518	chr4:102791641-102791642	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538417382	chr4:102791657-102791658	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs150903005	chr4:102791695-102791696	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs532683237	chr4:102791706-102791707	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs201930891	chr4:102791707-102791708	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs139390646	chr4:102791708-102791709	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs145555039	chr4:102791709-102791710	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs370508926	chr4:102791725-102791726	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs73836621	chr4:102791797-102791798	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs377468246	chr4:102791819-102791820	Enhancers Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs72686742	chr4:102791830-102791831	Enhancers Strong transcription Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs17031750	chr4:102791864-102791865	Enhancers Strong transcription Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs566952323	chr4:102791888-102791889	Enhancers Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs10516483	chr4:102791905-102791906	Enhancers Strong transcription Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs544618545	chr4:102791917-102791918	Enhancers Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs552079055	chr4:102791984-102791985	Enhancers Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs199950152	chr4:102791986-102791987	Enhancers Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs28538316	chr4:102791992-102791993	Enhancers Strong transcription Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs556048410	chr4:102792026-102792027	Enhancers Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs571808864	chr4:102792030-102792031	Enhancers Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs535102824	chr4:102792033-102792034	Enhancers Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs10516484	chr4:102792085-102792086	Enhancers Strong transcription Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs138921183	chr4:102792095-102792096	Enhancers Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs371373460	chr4:102792154-102792155	Enhancers Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
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
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
Breast cancer	16397240	CNVD
Acute myeloid leukemia	18000384	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
myeloid cancer	21057493	CNVD
Chronic lymphocytic leukemia	21546498	CNVD

Chromatin state (count:287 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:102784000-102793200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr4:102787000-102793800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr4:102787200-102792000	Weak transcription	Primary hematopoietic stem cells	blood
4	chr4:102787200-102797200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr4:102787800-102791800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr4:102788000-102791000	Strong transcription	Primary B cells from peripheral blood	blood
7	chr4:102790600-102791600	Weak transcription	Primary B cells from cord blood	blood
8	chr4:102791000-102792000	Genic enhancers	Primary B cells from peripheral blood	blood
9	chr4:102791400-102792200	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr4:102791600-102792000	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr4:102791600-102792200	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr4:102791600-102792400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr4:102791600-102792400	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr4:102791600-102792800	Genic enhancers	Primary B cells from cord blood	blood
15	chr4:102791800-102792400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr4:102792000-102792200	Enhancers	GM12878-XiMat	blood
17	chr4:102792000-102793200	Strong transcription	Primary B cells from peripheral blood	blood
18	chr4:102792200-102792400	Enhancers	Primary hematopoietic stem cells	blood
19	chr4:102792400-102794600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr4:102792400-102796800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr4:102792800-102793400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr4:102792800-102793800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr4:102792800-102796600	Strong transcription	Primary B cells from cord blood	blood
24	chr4:102793200-102793600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr4:102793200-102793800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr4:102793200-102794200	Genic enhancers	Primary B cells from peripheral blood	blood
27	chr4:102793800-102794200	Enhancers	Fetal Thymus	thymus
28	chr4:102794200-102797000	Strong transcription	Primary B cells from peripheral blood	blood
29	chr4:102794600-102795400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr4:102795400-102795600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr4:102795600-102796000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr4:102796600-102797400	ZNF genes & repeats	Primary B cells from cord blood	blood
33	chr4:102796800-102797200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr4:102797000-102798000	Genic enhancers	Primary B cells from peripheral blood	blood
35	chr4:102797200-102797400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr4:102797200-102798400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr4:102797400-102800200	Strong transcription	Primary B cells from cord blood	blood
38	chr4:102798000-102809200	Strong transcription	Primary B cells from peripheral blood	blood
39	chr4:102800200-102801600	Weak transcription	Primary B cells from cord blood	blood
40	chr4:102801600-102811200	Strong transcription	Primary B cells from cord blood	blood
41	chr4:102806200-102807600	Enhancers	Stomach Mucosa	stomach
42	chr4:102806400-102807000	Enhancers	Gastric	stomach
43	chr4:102806400-102807000	Enhancers	HepG2	liver
44	chr4:102806400-102807600	Enhancers	A549	lung
45	chr4:102809000-102809400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr4:102809200-102809600	Enhancers	Fetal Lung	lung
47	chr4:102809200-102813000	ZNF genes & repeats	Primary B cells from peripheral blood	blood
48	chr4:102809400-102809600	Enhancers	A549	lung
49	chr4:102810400-102822600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr4:102811200-102812800	ZNF genes & repeats	Primary B cells from cord blood	blood

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