Variant report

Variant	nsv879518
Chromosome Location	chr4:86739805-86778943
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:366)
CpG islands
(count:244)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr4:86747365-86747701	A549	lung:	n/a	chr4:86747501-86747522
2	BHLHE40	chr4:86747332-86747692	K562	blood:	n/a	chr4:86747501-86747522
3	BHLHE40	chr4:86747358-86747692	GM12878	blood:	n/a	chr4:86747501-86747522
4	BHLHE40	chr4:86747314-86747693	HepG2	liver:	n/a	chr4:86747501-86747522
5	BHLHE40	chr4:86750600-86750697	A549	lung:	n/a	n/a
6	BHLHE40	chr4:86761532-86761752	K562	blood:	n/a	n/a
7	BRCA1	chr4:86763874-86763922	GM12878	blood:	n/a	n/a
8	CEBPB	chr4:86744382-86744708	HepG2	liver:	n/a	chr4:86744532-86744543
9	CEBPB	chr4:86744347-86744732	IMR90	lung:	n/a	chr4:86744532-86744543
10	CEBPB	chr4:86748530-86748856	MCF-7	breast:	n/a	n/a
11	CEBPB	chr4:86744453-86744671	H1-hESC	embryonic stem cell:	n/a	chr4:86744532-86744543
12	CEBPB	chr4:86744230-86744931	HCT-116	colon:	n/a	chr4:86744532-86744543
13	CEBPB	chr4:86744394-86744731	Hela-S3	cervix:	n/a	chr4:86744532-86744543
14	CEBPB	chr4:86744413-86744712	A549	lung:	n/a	chr4:86744532-86744543
15	CEBPB	chr4:86748430-86748982	A549	lung:	n/a	chr4:86748482-86748493
16	CEBPB	chr4:86744363-86744732	K562	blood:	n/a	chr4:86744532-86744543
17	CEBPB	chr4:86748517-86748793	A549	lung:	n/a	n/a
18	CEBPB	chr4:86744249-86744989	HCT-116	colon:	n/a	chr4:86744532-86744543
19	CEBPB	chr4:86748545-86749240	IMR90	lung:	n/a	n/a
20	CEBPB	chr4:86750768-86751156	IMR90	lung:	n/a	n/a
21	CTCF	chr4:86747410-86747778	MCF-7	breast:	n/a	n/a
22	CTCF	chr4:86755783-86755865	Kidney_OC	kidney:	n/a	n/a
23	CTCF	chr4:86747458-86747708	K562	blood:	n/a	n/a
24	CTCF	chr4:86747522-86747630	MCF-7	breast:	n/a	n/a
25	CTCF	chr4:86747440-86747590	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr4:86747420-86747570	HRPEpiC	eye:	n/a	n/a
27	CTCF	chr4:86747460-86747610	GM12871	blood:	n/a	n/a
28	CTCF	chr4:86748840-86748990	HBMEC	blood vessel:	n/a	n/a
29	CTCF	chr4:86747460-86747610	BJ	skin:	n/a	n/a
30	CTCF	chr4:86747449-86747666	ProgFib	skin:	n/a	n/a
31	CTCF	chr4:86747440-86747590	AoAF	blood vessel:	n/a	n/a
32	CTCF	chr4:86748800-86748950	AG04450	lung:	n/a	n/a
33	CTCF	chr4:86747440-86747590	HPF	lung:	n/a	n/a
34	CTCF	chr4:86747480-86747630	GM12878	blood:	n/a	n/a
35	CTCF	chr4:86747459-86747664	MCF-7	breast:	n/a	n/a
36	CTCF	chr4:86747540-86747690	NHLF	lung:	n/a	n/a
37	CTCF	chr4:86747256-86747815	A549	lung:	n/a	n/a
38	CTCF	chr4:86747440-86747590	RPTEC	kidney:	n/a	n/a
39	CTCF	chr4:86747440-86747590	NHDF-neo	bronchial:	n/a	n/a
40	CTCF	chr4:86748760-86748910	HRE	kidney:	n/a	n/a
41	CTCF	chr4:86747501-86747648	A549	lung:	n/a	n/a
42	CTCF	chr4:86747540-86747690	GM12874	blood:	n/a	n/a
43	CTCF	chr4:86748920-86749070	NHLF	lung:	n/a	n/a
44	CTCF	chr4:86747427-86747691	GM12878	blood:	n/a	n/a
45	CTCF	chr4:86747460-86747610	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr4:86748922-86748962	Fibrobl	skin:	n/a	n/a
47	CTCF	chr4:86770979-86771063	LNCaP	prostate:	n/a	n/a
48	CTCF	chr4:86747420-86747570	HCFaa	heart:	n/a	n/a
49	CTCF	chr4:86747458-86747668	A549	lung:	n/a	n/a
50	CTCF	chr4:86747408-86747649	H1-hESC	embryonic stem cell:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:86745824-86745874	HNPCEpiC	eye:	n/a
2	chr4:86745824-86745874	AG04450	lung:	fetal
3	chr4:86749040-86749090	AG09309	skin:	n/a
4	chr4:86745824-86745874	RPTEC	kidney:	n/a
5	chr4:86748944-86748994	AG10803	skin:	n/a
6	chr4:86748944-86748994	HEK293	kidney:	embryo
7	chr4:86748944-86748994	T-47D	breast:	n/a
8	chr4:86749040-86749090	Hepatocyte	liver:	n/a
9	chr4:86749040-86749090	GM12892	blood:	n/a
10	chr4:86745824-86745874	IMR90	lung:	fetal
11	chr4:86748944-86748994	K562	blood:	n/a
12	chr4:86749040-86749090	AG09319	gingival:	n/a
13	chr4:86748949-86748999	AG09309	skin:	n/a
14	chr4:86749040-86749090	ovcar-3	ovarian:	n/a
15	chr4:86749040-86749090	NHBE	bronchial:	n/a
16	chr4:86749040-86749090	Jurkat	blood:	n/a
17	chr4:86745824-86745874	HPAEpiC	pulmonary alveolar:	n/a
18	chr4:86745824-86745874	SK-N-SH	brain:	n/a
19	chr4:86749040-86749090	HRE	kidney:	n/a
20	chr4:86748949-86748999	U87	brain:	n/a
21	chr4:86748944-86748994	Jurkat	blood:	n/a
22	chr4:86748944-86748994	HepG2	liver:	n/a
23	chr4:86749040-86749090	MCF-7	breast:	n/a
24	chr4:86749040-86749090	A549	lung:	n/a
25	chr4:86745824-86745874	LNCaP	prostate:	n/a
26	chr4:86748944-86748994	SAEC	small airway:	n/a
27	chr4:86749040-86749090	SAEC	small airway:	n/a
28	chr4:86749040-86749090	HCT-116	colon:	n/a
29	chr4:86748949-86748999	HEEpiC	esophagus:	n/a
30	chr4:86745824-86745874	AG09309	skin:	n/a
31	chr4:86745824-86745874	GM12891	blood:	n/a
32	chr4:86745824-86745874	PFSK-1	brain:	n/a
33	chr4:86745824-86745874	U87	brain:	n/a
34	chr4:86745824-86745874	NHDF-neo	bronchial:	n/a
35	chr4:86748944-86748994	AG04449	skin:	fetal
36	chr4:86748944-86748994	SKMC	muscle:	n/a
37	chr4:86748944-86748994	NHBE	bronchial:	n/a
38	chr4:86748949-86748999	HL-60	blood:	n/a
39	chr4:86748949-86748999	A549	lung:	n/a
40	chr4:86748944-86748994	GM12892	blood:	n/a
41	chr4:86748944-86748994	GM06990	blood:	n/a
42	chr4:86748949-86748999	HMEC	breast:	n/a
43	chr4:86748949-86748999	HCT-116	colon:	n/a
44	chr4:86749040-86749090	HRCEpiC	kidney:	n/a
45	chr4:86748949-86748999	HAEpiC	amniotic membrane:	n/a
46	chr4:86748949-86748999	HUVEC	blood vessel:	n/a
47	chr4:86748949-86748999	AG04449	skin:	fetal
48	chr4:86745824-86745874	HCT-116	colon:	n/a
49	chr4:86748949-86748999	MCF-7	breast:	n/a
50	chr4:86745824-86745874	Hela-S3	cervix:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:86762784..86764294-chr4:86767286..86769112,2	MCF-7	breast:
2	chr4:86747130..86748178-chr4:86885197..86886140,3	MCF-7	breast:
3	chr4:86758093..86760173-chr4:86804562..86807184,2	MCF-7	breast:
4	chr4:86747317..86749374-chr4:86754151..86756768,2	MCF-7	breast:
5	chr4:86762784..86764294-chr4:86767286..86769112,2	MCF-7	breast:

No data

Variant related genes	Relation type
ARHGAP24	TF binding region
ARHGAP24	CpG island
ENSG00000138639	chromatin interactions

Extended variants
information (count: 1426 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:1426 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12498568	chr4:86739805-86739806	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs550006446	chr4:86739808-86739809	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs140682254	chr4:86739829-86739830	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs539157548	chr4:86739839-86739840	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150080426	chr4:86739880-86739881	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs10014188	chr4:86739890-86739891	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs12506184	chr4:86739901-86739902	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs565262470	chr4:86739902-86739903	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs77147853	chr4:86740024-86740025	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs75544922	chr4:86740075-86740076	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs538030595	chr4:86740090-86740091	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs6842326	chr4:86740104-86740105	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs577646388	chr4:86740106-86740107	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs138601467	chr4:86740139-86740140	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs141591759	chr4:86740140-86740141	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs374142615	chr4:86740144-86740145	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571665375	chr4:86740161-86740162	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs146257092	chr4:86740200-86740201	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs60665690	chr4:86740446-86740447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs189178525	chr4:86740483-86740484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs115040418	chr4:86740491-86740492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs377161450	chr4:86740559-86740560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs376427314	chr4:86740560-86740561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs565502474	chr4:86740614-86740615	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs370846906	chr4:86740660-86740661	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs547829921	chr4:86740683-86740684	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs566045080	chr4:86740700-86740701	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs561211393	chr4:86740720-86740721	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs529819850	chr4:86740803-86740804	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs574086949	chr4:86740842-86740843	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374156895	chr4:86740845-86740846	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs138014322	chr4:86740870-86740871	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs149545637	chr4:86740903-86740904	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs566579653	chr4:86740917-86740918	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs57129466	chr4:86740933-86740934	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs372537369	chr4:86740943-86740944	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs371556241	chr4:86740944-86740945	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556208955	chr4:86740989-86740990	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs529167963	chr4:86741004-86741005	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs148683979	chr4:86741030-86741031	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs193121651	chr4:86741031-86741032	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs61163122	chr4:86741050-86741051	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs571852924	chr4:86741089-86741090	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs142815222	chr4:86741110-86741111	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs185551862	chr4:86741116-86741117	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs150605002	chr4:86741159-86741160	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189116534	chr4:86741174-86741175	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs191970755	chr4:86741187-86741188	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112274615	chr4:86741205-86741206	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs66596399	chr4:86741214-86741215	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:76)

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
lymphocytic leukemia	21291569	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
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
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
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Prostate cancer	16573809	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:868 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:86728200-86747200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr4:86729000-86744600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr4:86729400-86747400	Weak transcription	Colon Smooth Muscle	Colon
4	chr4:86729800-86743600	Weak transcription	HSMMtube	muscle
5	chr4:86729800-86744600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr4:86730200-86741400	Weak transcription	HSMM	muscle
7	chr4:86734400-86741000	Weak transcription	Primary B cells from peripheral blood	blood
8	chr4:86734600-86741200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr4:86734600-86741200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr4:86734600-86743000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr4:86734600-86743200	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr4:86734600-86743400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr4:86734600-86743400	Weak transcription	Aorta	Aorta
14	chr4:86734600-86743400	Weak transcription	Osteobl	bone
15	chr4:86736200-86748600	Weak transcription	Fetal Muscle Trunk	muscle
16	chr4:86737000-86740600	Weak transcription	HUVEC	blood vessel
17	chr4:86737400-86741200	Weak transcription	Fetal Muscle Leg	muscle
18	chr4:86737600-86744600	Weak transcription	K562	blood
19	chr4:86737600-86763200	Weak transcription	Primary B cells from cord blood	blood
20	chr4:86737800-86741200	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr4:86738800-86741200	Weak transcription	Fetal Kidney	kidney
22	chr4:86739200-86740200	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr4:86739400-86740200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr4:86739400-86740200	Enhancers	H9 Cell Line	embryonic stem cell
25	chr4:86739400-86740200	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr4:86739400-86740200	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr4:86739400-86740200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr4:86739600-86740200	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr4:86739600-86740200	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr4:86739600-86740600	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr4:86739800-86740000	Weak transcription	Fetal Lung	lung
32	chr4:86739800-86740200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr4:86739800-86740200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr4:86739800-86740600	Weak transcription	Fetal Brain Male	brain
35	chr4:86739800-86741200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr4:86740000-86740200	Enhancers	Fetal Lung	lung
37	chr4:86740000-86742600	Weak transcription	Monocytes-CD14+_RO01746	blood
38	chr4:86740200-86742400	Weak transcription	NHDF-Ad	bronchial
39	chr4:86740200-86743200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr4:86740200-86744600	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr4:86740200-86744600	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr4:86740200-86744800	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr4:86740200-86745000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr4:86740200-86747000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr4:86740200-86747200	Weak transcription	Fetal Lung	lung
46	chr4:86740200-86748600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr4:86740200-86748800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr4:86740600-86740800	Enhancers	Fetal Brain Male	brain
49	chr4:86740600-86741800	Strong transcription	HUVEC	blood vessel
50	chr4:86740800-86743800	Weak transcription	Fetal Brain Male	brain

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