Variant report

Variant	nsv594583
Chromosome Location	chr4:69928642-69988378
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	chr4:69960997-69962638	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:69968302-69968701	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:69981638-69981898	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:69964127-69964803	HepG2	liver:	n/a	n/a
5	ATF1	chr4:69932559-69932881	K562	blood:	n/a	n/a
6	ATF3	chr4:69961016-69961540	A549	lung:	n/a	n/a
7	ATF3	chr4:69961043-69961523	A549	lung:	n/a	n/a
8	BATF	chr4:69988219-69988511	GM12878	blood:	n/a	n/a
9	BATF	chr4:69988190-69988541	GM12878	blood:	n/a	n/a
10	BATF	chr4:69958781-69959019	GM12878	blood:	n/a	n/a
11	BCL3	chr4:69960907-69962340	A549	lung:	n/a	n/a
12	BCL3	chr4:69961801-69962281	A549	lung:	n/a	n/a
13	BHLHE40	chr4:69984332-69984392	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:69932682-69932824	K562	blood:	n/a	n/a
15	BHLHE40	chr4:69959220-69959407	GM12878	blood:	n/a	n/a
16	CEBPB	chr4:69961654-69962398	A549	lung:	n/a	chr4:69961952-69961965 chr4:69961952-69961963 chr4:69961949-69961966 chr4:69961952-69961965
17	CEBPB	chr4:69968429-69968717	HepG2	liver:	n/a	n/a
18	CEBPB	chr4:69961787-69962551	HepG2	liver:	n/a	chr4:69961952-69961965 chr4:69961952-69961963 chr4:69961949-69961966 chr4:69961952-69961965
19	CEBPB	chr4:69961026-69961496	A549	lung:	n/a	n/a
20	CEBPB	chr4:69932857-69933596	IMR90	lung:	n/a	n/a
21	CEBPB	chr4:69932884-69933620	HepG2	liver:	n/a	n/a
22	CEBPB	chr4:69960967-69961605	A549	lung:	n/a	n/a
23	CEBPB	chr4:69961795-69962072	HepG2	liver:	n/a	chr4:69961952-69961965 chr4:69961952-69961963 chr4:69961949-69961966 chr4:69961952-69961965
24	CEBPB	chr4:69961749-69962164	A549	lung:	n/a	chr4:69961952-69961965 chr4:69961952-69961963 chr4:69961949-69961966 chr4:69961952-69961965
25	CEBPB	chr4:69961861-69962033	HepG2	liver:	n/a	chr4:69961952-69961965 chr4:69961952-69961963 chr4:69961949-69961966 chr4:69961952-69961965
26	CEBPB	chr4:69961802-69962387	A549	lung:	n/a	chr4:69961952-69961965 chr4:69961952-69961963 chr4:69961949-69961966 chr4:69961952-69961965
27	CEBPB	chr4:69964210-69964437	HepG2	liver:	n/a	n/a
28	CEBPB	chr4:69962103-69962398	HepG2	liver:	n/a	n/a
29	CEBPB	chr4:69980567-69980672	HepG2	liver:	n/a	n/a
30	CEBPB	chr4:69968440-69968803	HepG2	liver:	n/a	n/a
31	CEBPB	chr4:69964211-69964793	A549	lung:	n/a	chr4:69964654-69964665 chr4:69964655-69964666 chr4:69964654-69964667
32	CEBPB	chr4:69931931-69931986	A549	lung:	n/a	n/a
33	CEBPB	chr4:69962157-69962338	HepG2	liver:	n/a	n/a
34	CEBPB	chr4:69968407-69968710	HepG2	liver:	n/a	n/a
35	CEBPB	chr4:69964189-69964841	HepG2	liver:	n/a	chr4:69964654-69964665 chr4:69964655-69964666 chr4:69964654-69964667
36	CEBPB	chr4:69968322-69968816	HepG2	liver:	n/a	n/a
37	CEBPB	chr4:69961159-69961453	A549	lung:	n/a	n/a
38	CEBPB	chr4:69945882-69946082	HepG2	liver:	n/a	chr4:69945930-69945943 chr4:69945931-69945942
39	CEBPB	chr4:69964243-69964585	HepG2	liver:	n/a	n/a
40	CEBPB	chr4:69961869-69962048	Hela-S3	cervix:	n/a	chr4:69961952-69961965 chr4:69961952-69961963 chr4:69961949-69961966 chr4:69961952-69961965
41	CREB1	chr4:69964151-69964530	HepG2	liver:	n/a	n/a
42	CTCF	chr4:69943296-69943316	GM10248	blood:	n/a	n/a
43	CTCF	chr4:69938820-69938970	HepG2	liver:	n/a	n/a
44	CTCF	chr4:69939945-69939997	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr4:69933180-69933330	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr4:69973871-69973986	GM10248	blood:	n/a	n/a
47	CTCF	chr4:69976680-69976830	GM06990	blood:	n/a	n/a
48	CTCF	chr4:69954360-69954510	HCT-116	colon:	n/a	n/a
49	CTCF	chr4:69942923-69942962	GM10248	blood:	n/a	n/a
50	CTCF	chr4:69939860-69940010	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69960869-69960919	GM19239	blood:	n/a
2	chr4:69959004-69959054	Hepatocyte	liver:	n/a
3	chr4:69960869-69960919	AG09309	skin:	n/a
4	chr4:69976406-69976456	T-47D	breast:	n/a
5	chr4:69976406-69976456	HCT-116	colon:	n/a
6	chr4:69976406-69976456	HCPEpiC	choroid plexus:	n/a
7	chr4:69960869-69960919	HRCEpiC	kidney:	n/a
8	chr4:69959004-69959054	GM12891	blood:	n/a
9	chr4:69976406-69976456	GM12878	blood:	n/a
10	chr4:69959004-69959054	SKMC	muscle:	n/a
11	chr4:69962676-69962726	K562	blood:	n/a
12	chr4:69959004-69959054	ProgFib	skin:	n/a
13	chr4:69960869-69960919	U87	brain:	n/a
14	chr4:69962676-69962726	PANC-1	pancreas:	n/a
15	chr4:69959004-69959054	HepG2	liver:	n/a
16	chr4:69959004-69959054	PFSK-1	brain:	n/a
17	chr4:69976406-69976456	NH-A	brain:	n/a
18	chr4:69959004-69959054	HRE	kidney:	n/a
19	chr4:69960869-69960919	SKMC	muscle:	n/a
20	chr4:69962676-69962726	BJ	skin:	n/a
21	chr4:69976406-69976456	HRE	kidney:	n/a
22	chr4:69960869-69960919	PANC-1	pancreas:	n/a
23	chr4:69960869-69960919	T-47D	breast:	n/a
24	chr4:69960869-69960919	IMR90	lung:	fetal
25	chr4:69976406-69976456	A549	lung:	n/a
26	chr4:69976406-69976456	SKMC	muscle:	n/a
27	chr4:69959004-69959054	NHDF-neo	bronchial:	n/a
28	chr4:69959004-69959054	AG04450	lung:	fetal
29	chr4:69960869-69960919	AoSMC	blood vessel:	n/a
30	chr4:69959004-69959054	BJ	skin:	n/a
31	chr4:69976406-69976456	K562	blood:	n/a
32	chr4:69959004-69959054	HCM	heart:	n/a
33	chr4:69962676-69962726	NB4	blood:	n/a
34	chr4:69959004-69959054	Jurkat	blood:	n/a
35	chr4:69960869-69960919	A549	lung:	n/a
36	chr4:69960869-69960919	Jurkat	blood:	n/a
37	chr4:69959004-69959054	PrEC	prostate:	n/a
38	chr4:69960869-69960919	BJ	skin:	n/a
39	chr4:69962676-69962726	HNPCEpiC	eye:	n/a
40	chr4:69976406-69976456	HNPCEpiC	eye:	n/a
41	chr4:69962676-69962726	HepG2	liver:	n/a
42	chr4:69959004-69959054	HRCEpiC	kidney:	n/a
43	chr4:69962676-69962726	U87	brain:	n/a
44	chr4:69962676-69962726	ECC-1	luminal epithelium:	n/a
45	chr4:69959004-69959054	AG04449	skin:	fetal
46	chr4:69976406-69976456	ECC-1	luminal epithelium:	n/a
47	chr4:69959004-69959054	IMR90	lung:	fetal
48	chr4:69976406-69976456	GM12891	blood:	n/a
49	chr4:69976406-69976456	HEK293	kidney:	embryo
50	chr4:69976406-69976456	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:69964055..69967936-chr4:69969110..69971498,3	K562	blood:
2	chr4:69964055..69967936-chr4:69969110..69971498,3	K562	blood:
3	chr4:69925736..69927833-chr4:69929000..69931725,2	MCF-7	breast:
4	chr4:69981403..69984275-chr4:69989733..69991990,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2B28-8	chr4:69932113-69932198	NONHSAT096752
2	lnc-UGT2B28-8	chr4:69933121-69933337	NONHSAT096752
3	lnc-UGT2B28-8	chr4:69935360-69935606	NONHSAT096752

Variant related genes	Relation type
UGT2B7	TF binding region
ENSG00000248763	TF binding region
ENSG00000251284	TF binding region
UGT2B7	CpG island
ENSG00000248763	CpG island
ENSG00000251284	CpG island
ENSG00000251284	chromatin interactions

Extended variants
information (count: 2595 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2595 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6820734	chr4:69928642-69928643	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs181649675	chr4:69928650-69928651	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs148553865	chr4:69928665-69928666	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs542753762	chr4:69928762-69928763	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs562639384	chr4:69928798-69928799	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531648702	chr4:69928808-69928809	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs34438793	chr4:69928813-69928814	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs6834855	chr4:69928820-69928821	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs545197335	chr4:69928821-69928822	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs564898131	chr4:69928850-69928851	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs527607294	chr4:69928853-69928854	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370310508	chr4:69928879-69928880	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs554770702	chr4:69928897-69928898	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567306630	chr4:69928905-69928906	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs529707112	chr4:69928955-69928956	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs549951602	chr4:69928958-69928959	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs569774107	chr4:69928961-69928962	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs11249521	chr4:69928964-69928965	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs558350250	chr4:69928976-69928977	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs112627510	chr4:69928985-69928986	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs534542543	chr4:69929015-69929016	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs111503495	chr4:69929024-69929025	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
23	rs79851694	chr4:69929036-69929037	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs79310750	chr4:69929038-69929039	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs77137913	chr4:69929040-69929041	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs556109411	chr4:69929043-69929044	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs370628678	chr4:69929044-69929045	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372751997	chr4:69929054-69929055	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs74940828	chr4:69929058-69929059	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs185042807	chr4:69929085-69929086	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs542615000	chr4:69929117-69929118	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs556097466	chr4:69929147-69929148	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373223398	chr4:69929155-69929156	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs545143676	chr4:69929179-69929180	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565118324	chr4:69929189-69929190	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527481542	chr4:69929266-69929267	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541358163	chr4:69929294-69929295	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs189849145	chr4:69929348-69929349	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561166703	chr4:69929460-69929461	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs182455438	chr4:69929480-69929481	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs60814050	chr4:69929488-69929489	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs569640560	chr4:69929491-69929492	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs532260163	chr4:69929530-69929531	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs185358386	chr4:69929560-69929561	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571849943	chr4:69929565-69929566	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs73823805	chr4:69929567-69929568	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs550656152	chr4:69929584-69929585	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs553901802	chr4:69929591-69929592	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs530858717	chr4:69929605-69929606	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs569435598	chr4:69929631-69929632	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:227 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69923800-69932400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:69925000-69928800	Weak transcription	Fetal Kidney	kidney
3	chr4:69925000-69930000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr4:69925000-69932600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr4:69925800-69929600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr4:69927400-69934400	Weak transcription	Liver	Liver
7	chr4:69927800-69930400	Strong transcription	HepG2	liver
8	chr4:69929600-69930600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr4:69930000-69930600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr4:69930400-69936600	Weak transcription	HepG2	liver
11	chr4:69930600-69932600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr4:69930600-69944400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr4:69932400-69933000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr4:69932400-69933200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr4:69932600-69933000	Enhancers	Muscle Satellite Cultured Cells	--
16	chr4:69932600-69933000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr4:69932600-69933000	Enhancers	HMEC	breast
18	chr4:69932600-69933000	Enhancers	NHEK	skin
19	chr4:69932600-69933200	Enhancers	HSMM	muscle
20	chr4:69932600-69933400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr4:69932600-69933600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr4:69932800-69933400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr4:69933600-69936400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr4:69934400-69939200	Enhancers	Liver	Liver
25	chr4:69934800-69935000	Enhancers	HMEC	breast
26	chr4:69934800-69935000	Enhancers	NHEK	skin
27	chr4:69936400-69938200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr4:69936600-69937200	Enhancers	HepG2	liver
29	chr4:69938800-69957400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr4:69939200-69939600	Flanking Active TSS	Liver	Liver
31	chr4:69939600-69939800	Enhancers	Liver	Liver
32	chr4:69939800-69940000	Flanking Active TSS	Liver	Liver
33	chr4:69940000-69941200	Enhancers	Liver	Liver
34	chr4:69940800-69941200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr4:69940800-69941800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr4:69941000-69941400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr4:69941000-69941400	Enhancers	A549	lung
38	chr4:69941000-69941600	Enhancers	Muscle Satellite Cultured Cells	--
39	chr4:69941200-69944400	Weak transcription	Liver	Liver
40	chr4:69944400-69944800	Enhancers	Esophagus	oesophagus
41	chr4:69944400-69945000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr4:69944400-69945000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr4:69944400-69945000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr4:69944400-69945000	Enhancers	Liver	Liver
45	chr4:69944600-69945000	Enhancers	H1 Cell Line	embryonic stem cell
46	chr4:69944600-69945000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr4:69945000-69957200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr4:69950800-69951400	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr4:69954400-69955000	Enhancers	HepG2	liver
50	chr4:69955000-69955400	Weak transcription	HepG2	liver

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