Variant report

Variant	nsv1004408
Chromosome Location	chr4:55124471-55179212
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:189)
CpG islands
(count:610)
Chromatin interactive
region (count:7)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:7)

(count:189 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:55162862-55163089	HepG2	liver:	n/a	n/a
2	BACH1	chr4:55143445-55143674	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr4:55143891-55144132	GM12878	blood:	n/a	chr4:55144109-55144120
4	BATF	chr4:55143876-55144294	GM12878	blood:	n/a	chr4:55144109-55144120
5	BATF	chr4:55141318-55141540	GM12878	blood:	n/a	n/a
6	BATF	chr4:55142251-55142554	GM12878	blood:	n/a	n/a
7	CEBPB	chr4:55131571-55131910	HepG2	liver:	n/a	n/a
8	CEBPB	chr4:55142669-55142969	IMR90	lung:	n/a	chr4:55142791-55142802
9	CEBPB	chr4:55131574-55131910	IMR90	lung:	n/a	n/a
10	CEBPB	chr4:55134357-55134635	IMR90	lung:	n/a	n/a
11	CEBPB	chr4:55142615-55142975	H1-hESC	embryonic stem cell:	n/a	chr4:55142791-55142802
12	CEBPB	chr4:55131590-55131850	A549	lung:	n/a	n/a
13	CEBPB	chr4:55147486-55147838	IMR90	lung:	n/a	chr4:55147567-55147578
14	CEBPB	chr4:55142705-55142836	HepG2	liver:	n/a	chr4:55142791-55142802
15	CEBPB	chr4:55142786-55142870	K562	blood:	n/a	chr4:55142791-55142802
16	CEBPB	chr4:55144434-55144651	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr4:55134157-55134167	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTBP2	chr4:55143144-55143717	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr4:55126020-55126170	NHDF-neo	bronchial:	n/a	n/a
20	CTCF	chr4:55142760-55142910	HMEC	breast:	n/a	n/a
21	CTCF	chr4:55138118-55138149	Pancreas_OC	pancreas:	n/a	n/a
22	CTCF	chr4:55142771-55142891	NHEK	skin:	n/a	n/a
23	CTCF	chr4:55138072-55138159	Lung_OC	lung:	n/a	n/a
24	CTCF	chr4:55167180-55167330	GM12878	blood:	n/a	n/a
25	CTCF	chr4:55172260-55172410	HCFaa	heart:	n/a	n/a
26	CTCF	chr4:55141192-55141225	GM20000	blood:	n/a	n/a
27	CTCF	chr4:55162962-55163044	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr4:55172260-55172410	BJ	skin:	n/a	n/a
29	CTCF	chr4:55166200-55166350	HMF	breast:	n/a	n/a
30	CTCF	chr4:55142753-55142827	Kidney_OC	kidney:	n/a	n/a
31	E2F4	chr4:55127679-55127878	MCF10A-Er-Src	breast:	n/a	n/a
32	E2F4	chr4:55175407-55175479	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr4:55129713-55129918	MCF10A-Er-Src	breast:	n/a	n/a
34	E2F4	chr4:55147517-55147916	MCF10A-Er-Src	breast:	n/a	n/a
35	EBF1	chr4:55143138-55143547	GM12878	blood:	n/a	chr4:55143248-55143259
36	EBF1	chr4:55144047-55144240	GM12878	blood:	n/a	n/a
37	ELF1	chr4:55143744-55144264	SK-N-SH	brain:	n/a	chr4:55144008-55144019
38	EP300	chr4:55157389-55157503	K562	blood:	n/a	n/a
39	EP300	chr4:55155624-55155747	K562	blood:	n/a	n/a
40	EP300	chr4:55147368-55148095	SK-N-SH	brain:	n/a	chr4:55147564-55147574
41	EP300	chr4:55143815-55144195	SK-N-SH_RA	brain:	n/a	chr4:55144010-55144019
42	EP300	chr4:55147545-55147897	SK-N-SH_RA	brain:	n/a	chr4:55147564-55147574
43	EP300	chr4:55143812-55144198	SK-N-SH_RA	brain:	n/a	chr4:55144010-55144019
44	EP300	chr4:55143705-55144397	SK-N-SH	brain:	n/a	chr4:55144010-55144019
45	EP300	chr4:55148141-55148197	K562	blood:	n/a	n/a
46	FOS	chr4:55134333-55134649	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr4:55135929-55136200	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr4:55136000-55136200	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr4:55134319-55134666	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr4:55143840-55144251	MCF10A-Er-Src	breast:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:55125798-55125848	HMEC	breast:	n/a
2	chr4:55128515-55128565	T-47D	breast:	n/a
3	chr4:55139873-55139923	HAEpiC	amniotic membrane:	n/a
4	chr4:55143285-55143335	ProgFib	skin:	n/a
5	chr4:55129115-55129165	PANC-1	pancreas:	n/a
6	chr4:55134316-55134366	AG04449	skin:	fetal
7	chr4:55142142-55142192	HEEpiC	esophagus:	n/a
8	chr4:55144066-55144116	AG09309	skin:	n/a
9	chr4:55129115-55129165	HL-60	blood:	n/a
10	chr4:55143557-55143607	HRE	kidney:	n/a
11	chr4:55128515-55128565	AG09319	gingival:	n/a
12	chr4:55143557-55143607	A549	lung:	n/a
13	chr4:55143269-55143319	LNCaP	prostate:	n/a
14	chr4:55143557-55143607	HCM	heart:	n/a
15	chr4:55143269-55143319	HCPEpiC	choroid plexus:	n/a
16	chr4:55143269-55143319	ECC-1	luminal epithelium:	n/a
17	chr4:55143269-55143319	NB4	blood:	n/a
18	chr4:55143285-55143335	HRE	kidney:	n/a
19	chr4:55144066-55144116	NT2-D1	testis:	n/a
20	chr4:55129115-55129165	MCF-7	breast:	n/a
21	chr4:55142142-55142192	PANC-1	pancreas:	n/a
22	chr4:55142142-55142192	A549	lung:	n/a
23	chr4:55139873-55139923	NT2-D1	testis:	n/a
24	chr4:55128515-55128565	NH-A	brain:	n/a
25	chr4:55134316-55134366	HEK293	kidney:	embryo
26	chr4:55143285-55143335	HNPCEpiC	eye:	n/a
27	chr4:55144066-55144116	MCF10A-Er-Src	breast:	n/a
28	chr4:55144066-55144116	GM12878	blood:	n/a
29	chr4:55129115-55129165	HepG2	liver:	n/a
30	chr4:55125798-55125848	AG09319	gingival:	n/a
31	chr4:55143285-55143335	ECC-1	luminal epithelium:	n/a
32	chr4:55143557-55143607	PANC-1	pancreas:	n/a
33	chr4:55143285-55143335	LNCaP	prostate:	n/a
34	chr4:55142142-55142192	ProgFib	skin:	n/a
35	chr4:55129115-55129165	K562	blood:	n/a
36	chr4:55134316-55134366	HRPEpiC	eye:	n/a
37	chr4:55139873-55139923	HCF	heart:	n/a
38	chr4:55129115-55129165	HEEpiC	esophagus:	n/a
39	chr4:55142142-55142192	GM06990	blood:	n/a
40	chr4:55139873-55139923	T-47D	breast:	n/a
41	chr4:55134316-55134366	NHBE	bronchial:	n/a
42	chr4:55143269-55143319	HMEC	breast:	n/a
43	chr4:55128515-55128565	SAEC	small airway:	n/a
44	chr4:55143557-55143607	AG10803	skin:	n/a
45	chr4:55144066-55144116	AG10803	skin:	n/a
46	chr4:55143557-55143607	SAEC	small airway:	n/a
47	chr4:55125798-55125848	A549	lung:	n/a
48	chr4:55125798-55125848	BJ	skin:	n/a
49	chr4:55125798-55125848	HepG2	liver:	n/a
50	chr4:55129115-55129165	BJ	skin:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:55130972..55133707-chr4:55137155..55139847,2	MCF-7	breast:
2	chr4:55135740..55138560-chr4:55139917..55141829,2	MCF-7	breast:
3	chr4:55133319..55135360-chr4:55145191..55147587,2	MCF-7	breast:
4	chr4:55130972..55133707-chr4:55137155..55139847,2	MCF-7	breast:
5	chr4:55133319..55135360-chr4:55145191..55147587,2	MCF-7	breast:
6	chr4:55135740..55138560-chr4:55139917..55141829,2	MCF-7	breast:
7	chr4:55139472..55141383-chr4:55141730..55143677,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHIC2-5	chr4:55167807-55168055	ucscGeneNc_uc003hap_2
2	lnc-CHIC2-5	chr4:55164137-55166101	ucscGeneNc_uc003hap_2

No data

(count:7 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	PDGFRA	hsa-miR-34a-5p	chr4:55164095-55164115
2	PDGFRA	hsa-miR-34a-5p	chr4:55164124-55164145
3	PDGFRA	hsa-miR-34a-5p	chr4:55164138-55164144
4	PDGFRA	hsa-miR-26b-5p	chr4:55163465-55163485
5	PDGFRA	hsa-miR-140-5p	chr4:55161498-55161504
6	PDGFRA	hsa-miR-34a-5p	chr4:55164109-55164115
7	PDGFRA	hsa-miR-140-5p	chr4:55161485-55161505

Variant related genes	Relation type
PDGFRA	TF binding region
PDGFRA	CpG island
ENSG00000134853	chromatin interactions

Extended variants
information (count: 2014 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:2014 , 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	rs535772034	chr4:55124557-55124558	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs9991165	chr4:55124591-55124592	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs577949817	chr4:55124618-55124619	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs184657642	chr4:55124730-55124731	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs371629218	chr4:55124764-55124765	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs73151433	chr4:55124767-55124768	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs374858199	chr4:55124771-55124772	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs541600633	chr4:55124806-55124807	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs9993826	chr4:55124827-55124828	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs559947792	chr4:55124831-55124832	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs9991421	chr4:55124834-55124835	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs139339216	chr4:55124848-55124849	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs148968049	chr4:55124862-55124863	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs2303429	chr4:55124870-55124871	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs367592917	chr4:55124899-55124900	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs138929755	chr4:55124946-55124947	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs200090515	chr4:55124956-55124957	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs375117626	chr4:55124960-55124961	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs369607686	chr4:55124989-55124990	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs372348389	chr4:55124993-55124994	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs377310679	chr4:55124994-55124995	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs538602084	chr4:55124996-55124997	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs369839746	chr4:55125009-55125010	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs2303430	chr4:55125058-55125059	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs2303431	chr4:55125087-55125088	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs377542283	chr4:55125133-55125134	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs185907393	chr4:55125139-55125140	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs530843896	chr4:55125151-55125152	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs550039823	chr4:55125169-55125170	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs569898610	chr4:55125192-55125193	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs529044810	chr4:55125195-55125196	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs149586813	chr4:55125200-55125201	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs548782639	chr4:55125234-55125235	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs565409862	chr4:55125237-55125238	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs73252945	chr4:55125253-55125254	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs538923079	chr4:55125307-55125308	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs564097165	chr4:55125322-55125323	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs33988725	chr4:55125323-55125324	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs35322593	chr4:55125389-55125390	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs191214203	chr4:55125436-55125437	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs369845941	chr4:55125448-55125449	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs536697199	chr4:55125476-55125477	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs116727309	chr4:55125479-55125480	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs574258179	chr4:55125488-55125489	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs181218264	chr4:55125528-55125529	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs186263843	chr4:55125538-55125539	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs143705595	chr4:55125595-55125596	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs530763897	chr4:55125596-55125597	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs79853560	chr4:55125651-55125652	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs148037111	chr4:55125680-55125681	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
Hodgkin''s lymphoma	17606441	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	22183965	CNVD
Cancer	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	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
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	19435819	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
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
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian neoplasms	16753589	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Glioblastoma multiforme	21569311	CNVD
Glioblastoma	17504929	CNVD
Glioblastoma	16823502	CNVD
Melanoma	16908931	CNVD
Glioblastoma	20031968	CNVD
Medulloblastoma	19270706	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Olfactory neuroblastoma	18408657	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Rhabdomyosarcoma	16790082	CNVD
Gastrointestinal stromal cancer	17438095	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	19115005	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	20164920	CNVD
Rhabdomyosarcoma	20807811	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:784 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:55105600-55124800	Weak transcription	Aorta	Aorta
2	chr4:55117200-55129600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr4:55118000-55129800	Weak transcription	Fetal Muscle Trunk	muscle
4	chr4:55119000-55127200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr4:55119000-55138600	Weak transcription	Fetal Intestine Small	intestine
6	chr4:55119400-55148000	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr4:55120400-55126800	Weak transcription	Fetal Stomach	stomach
8	chr4:55120600-55129600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr4:55120800-55125800	Weak transcription	Fetal Lung	lung
10	chr4:55121000-55147600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr4:55121000-55153200	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr4:55121200-55125000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr4:55121200-55125400	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr4:55121200-55130400	Weak transcription	Fetal Kidney	kidney
15	chr4:55121200-55133400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr4:55121200-55147200	Weak transcription	Rectal Smooth Muscle	rectum
17	chr4:55121600-55125000	Weak transcription	Osteobl	bone
18	chr4:55121600-55128600	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr4:55122200-55124800	Enhancers	Ovary	ovary
20	chr4:55122400-55125000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr4:55122400-55133400	Weak transcription	Fetal Muscle Leg	muscle
22	chr4:55122400-55142600	Strong transcription	Cortex derived primary cultured neurospheres	brain
23	chr4:55124000-55124800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr4:55124200-55124600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr4:55124400-55125000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr4:55124400-55125000	Weak transcription	NHDF-Ad	bronchial
27	chr4:55124400-55125200	Enhancers	NHLF	lung
28	chr4:55124400-55140400	Weak transcription	Placenta	Placenta
29	chr4:55124400-55147800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr4:55124600-55124800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr4:55124800-55125000	Enhancers	Aorta	Aorta
32	chr4:55124800-55125000	Bivalent Enhancer	HUVEC	blood vessel
33	chr4:55124800-55125200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr4:55124800-55125400	Genic enhancers	Ovary	ovary
35	chr4:55124800-55125600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr4:55124800-55134000	Weak transcription	Fetal Brain Male	brain
37	chr4:55124800-55138600	Weak transcription	NH-A	brain
38	chr4:55125000-55125400	Genic enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr4:55125000-55125400	Bivalent Enhancer	HepG2	liver
40	chr4:55125000-55125600	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr4:55125000-55126000	Genic enhancers	Osteobl	bone
42	chr4:55125000-55126400	Genic enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr4:55125000-55126400	Weak transcription	Aorta	Aorta
44	chr4:55125000-55130400	Strong transcription	NHDF-Ad	bronchial
45	chr4:55125200-55126000	Genic enhancers	NHLF	lung
46	chr4:55125200-55126200	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr4:55125400-55125600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr4:55125400-55126800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr4:55125400-55140600	Strong transcription	Ovary	ovary
50	chr4:55125600-55126000	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin

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