Variant report

Variant	nsv965590
Chromosome Location	chr5:76061083-76081416
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	chr5:76070411-76070732	HepG2	liver:	n/a	n/a
2	ATF2	chr5:76070318-76070761	GM12878	blood:	n/a	n/a
3	ATF3	chr5:76067852-76068234	A549	lung:	n/a	n/a
4	ATF3	chr5:76081235-76081754	A549	lung:	n/a	n/a
5	ATF3	chr5:76081264-76081700	A549	lung:	n/a	n/a
6	BACH1	chr5:76070379-76070679	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr5:76081199-76081823	A549	lung:	n/a	n/a
8	BCL3	chr5:76081377-76081777	A549	lung:	n/a	n/a
9	BCL3	chr5:76067487-76068377	A549	lung:	n/a	n/a
10	BCLAF1	chr5:76070255-76070755	GM12878	blood:	n/a	n/a
11	BHLHE40	chr5:76078612-76078808	K562	blood:	n/a	n/a
12	BHLHE40	chr5:76070330-76070841	K562	blood:	n/a	n/a
13	BHLHE40	chr5:76070263-76070754	GM12878	blood:	n/a	n/a
14	BRCA1	chr5:76070354-76070712	H1-hESC	embryonic stem cell:	n/a	n/a
15	CBX3	chr5:76081269-76081862	HCT-116	colon:	n/a	n/a
16	CBX3	chr5:76062548-76063160	HCT-116	colon:	n/a	n/a
17	CEBPB	chr5:76067488-76068562	A549	lung:	n/a	chr5:76067990-76068003 chr5:76067712-76067723
18	CEBPB	chr5:76067833-76068210	A549	lung:	n/a	chr5:76067990-76068003
19	CEBPB	chr5:76067684-76068086	HepG2	liver:	n/a	chr5:76067990-76068003 chr5:76067712-76067723
20	CEBPB	chr5:76067832-76068165	IMR90	lung:	n/a	chr5:76067990-76068003
21	CEBPB	chr5:76078490-76078519	IMR90	lung:	n/a	n/a
22	CEBPB	chr5:76070427-76070718	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr5:76081230-76081845	HCT-116	colon:	n/a	n/a
24	CEBPB	chr5:76081321-76081705	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr5:76081402-76081705	A549	lung:	n/a	n/a
26	CEBPB	chr5:76067601-76068570	A549	lung:	n/a	chr5:76067990-76068003 chr5:76067712-76067723
27	CEBPZ	chr5:76070331-76070689	HepG2	liver:	n/a	n/a
28	CHD1	chr5:76070297-76070628	GM12878	blood:	n/a	n/a
29	CHD1	chr5:76062500-76063066	IMR90	lung:	n/a	n/a
30	CHD1	chr5:76070175-76071032	IMR90	lung:	n/a	n/a
31	CHD2	chr5:76070385-76070624	HepG2	liver:	n/a	n/a
32	CHD2	chr5:76081389-76081618	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr5:76070331-76070753	GM12878	blood:	n/a	n/a
34	CHD2	chr5:76075247-76075570	H1-hESC	embryonic stem cell:	n/a	n/a
35	CREB1	chr5:76070433-76070649	A549	lung:	n/a	n/a
36	CTCF	chr5:76070520-76070670	HPAF	blood vessel:	n/a	chr5:76070570-76070586 chr5:76070569-76070587 chr5:76070564-76070585
37	CTCF	chr5:76070480-76070630	GM12869	blood:	n/a	chr5:76070570-76070586 chr5:76070569-76070587 chr5:76070564-76070585
38	CTCF	chr5:76070420-76070570	HMEC	breast:	n/a	n/a
39	CTCF	chr5:76070458-76070651	A549	lung:	n/a	chr5:76070570-76070586 chr5:76070569-76070587 chr5:76070564-76070585
40	CTCF	chr5:76070540-76070690	GM12872	blood:	n/a	chr5:76070570-76070586 chr5:76070569-76070587 chr5:76070564-76070585
41	CTCF	chr5:76070446-76070705	HepG2	liver:	n/a	chr5:76070570-76070586 chr5:76070569-76070587 chr5:76070564-76070585
42	CTCF	chr5:76070480-76070630	GM12870	blood:	n/a	chr5:76070570-76070586 chr5:76070569-76070587 chr5:76070564-76070585
43	CTCF	chr5:76070500-76070650	AG10803	skin:	n/a	chr5:76070570-76070586 chr5:76070569-76070587 chr5:76070564-76070585
44	CTCF	chr5:76070425-76070718	GM19238	blood:	n/a	chr5:76070570-76070586 chr5:76070569-76070587 chr5:76070564-76070585
45	CTCF	chr5:76070831-76070932	GM10266	blood:	n/a	n/a
46	CTCF	chr5:76070460-76070610	GM12868	blood:	n/a	chr5:76070570-76070586 chr5:76070569-76070587 chr5:76070564-76070585
47	CTCF	chr5:76070500-76070650	NHEK	skin:	n/a	chr5:76070570-76070586 chr5:76070569-76070587 chr5:76070564-76070585
48	CTCF	chr5:76070500-76070650	GM12878	blood:	n/a	chr5:76070570-76070586 chr5:76070569-76070587 chr5:76070564-76070585
49	CTCF	chr5:76070540-76070690	GM06990	blood:	n/a	chr5:76070570-76070586 chr5:76070569-76070587 chr5:76070564-76070585
50	CTCF	chr5:76070500-76070650	HRPEpiC	eye:	n/a	chr5:76070570-76070586 chr5:76070569-76070587 chr5:76070564-76070585

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:76068752-76068802	SK-N-SH_RA	brain:	n/a
2	chr5:76068752-76068802	GM12878	blood:	n/a
3	chr5:76068752-76068802	GM19239	blood:	n/a
4	chr5:76068752-76068802	AG09309	skin:	n/a
5	chr5:76068752-76068802	ProgFib	skin:	n/a
6	chr5:76068752-76068802	GM06990	blood:	n/a
7	chr5:76068752-76068802	K562	blood:	n/a
8	chr5:76068752-76068802	SKMC	muscle:	n/a
9	chr5:76068752-76068802	ECC-1	luminal epithelium:	n/a
10	chr5:76068752-76068802	HepG2	liver:	n/a
11	chr5:76068752-76068802	HRPEpiC	eye:	n/a
12	chr5:76068752-76068802	HUVEC	blood vessel:	n/a
13	chr5:76068752-76068802	PrEC	prostate:	n/a
14	chr5:76068752-76068802	HRE	kidney:	n/a
15	chr5:76068752-76068802	HL-60	blood:	n/a
16	chr5:76068752-76068802	T-47D	breast:	n/a
17	chr5:76068752-76068802	HRCEpiC	kidney:	n/a
18	chr5:76068752-76068802	HEEpiC	esophagus:	n/a
19	chr5:76068752-76068802	IMR90	lung:	fetal
20	chr5:76068752-76068802	NB4	blood:	n/a
21	chr5:76068752-76068802	NHBE	bronchial:	n/a
22	chr5:76068752-76068802	SAEC	small airway:	n/a
23	chr5:76068752-76068802	HEK293	kidney:	embryo
24	chr5:76068752-76068802	HAEpiC	amniotic membrane:	n/a
25	chr5:76068752-76068802	HCM	heart:	n/a
26	chr5:76068752-76068802	CMK	blood:	n/a
27	chr5:76068752-76068802	GM12891	blood:	n/a
28	chr5:76068752-76068802	Jurkat	blood:	n/a
29	chr5:76068752-76068802	HCF	heart:	n/a
30	chr5:76068752-76068802	U87	brain:	n/a
31	chr5:76068752-76068802	NT2-D1	testis:	n/a
32	chr5:76068752-76068802	HPAEpiC	pulmonary alveolar:	n/a
33	chr5:76068752-76068802	LNCaP	prostate:	n/a
34	chr5:76068752-76068802	AoSMC	blood vessel:	n/a
35	chr5:76068752-76068802	AG10803	skin:	n/a
36	chr5:76068752-76068802	AG09319	gingival:	n/a
37	chr5:76068752-76068802	BE2_C	brain:	n/a
38	chr5:76068752-76068802	BJ	skin:	n/a
39	chr5:76068752-76068802	Caco-2	colon:	n/a
40	chr5:76068752-76068802	A549	lung:	n/a
41	chr5:76068752-76068802	HNPCEpiC	eye:	n/a
42	chr5:76068752-76068802	HMEC	breast:	n/a
43	chr5:76068752-76068802	HCPEpiC	choroid plexus:	n/a
44	chr5:76068752-76068802	MCF10A-Er-Src	breast:	n/a
45	chr5:76068752-76068802	HIPEpiC	eye:	n/a
46	chr5:76068752-76068802	SK-N-MC	brain:	n/a
47	chr5:76068752-76068802	PFSK-1	brain:	n/a
48	chr5:76068752-76068802	HCT-116	colon:	n/a
49	chr5:76068752-76068802	PANC-1	pancreas:	n/a
50	chr5:76068752-76068802	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:76011519..76012401-chr5:76070136..76070995,3	K562	blood:
2	chr5:75896999..75898252-chr5:76070091..76071474,10	K562	blood:
3	chr5:76042157..76044508-chr5:76060594..76062584,2	K562	blood:
4	chr5:76011366..76011912-chr5:76070358..76071019,2	MCF-7	breast:
5	chr5:76069360..76073048-chr5:76075455..76078776,4	K562	blood:
6	chr5:76054516..76057505-chr5:76058992..76061122,2	K562	blood:
7	chr5:76060733..76063470-chr5:76063980..76065939,2	K562	blood:
8	chr5:76069360..76073048-chr5:76075455..76078776,4	K562	blood:
9	chr5:75898209..75899288-chr5:76070136..76071088,4	MCF-7	breast:
10	chr5:76060733..76063470-chr5:76063980..76065939,2	K562	blood:
11	chr5:75896963..75898061-chr5:76070096..76071180,9	MCF-7	breast:
12	chr5:75897438..75897959-chr5:76070126..76070803,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000238688	TF binding region
ENSG00000238688	CpG island
ENSG00000181104	chromatin interactions
ENSG00000225407	chromatin interactions

Extended variants
information (count: 836 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:836 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573323308	chr5:76061084-76061085	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs17568753	chr5:76061099-76061100	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs564984666	chr5:76061108-76061109	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs552659957	chr5:76061124-76061125	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs374204223	chr5:76061153-76061154	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs559423527	chr5:76061158-76061159	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs544733699	chr5:76061186-76061187	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs565003600	chr5:76061238-76061239	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs250724	chr5:76061256-76061257	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs544868959	chr5:76061301-76061302	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs561547893	chr5:76061359-76061360	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs146397896	chr5:76061381-76061382	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560238441	chr5:76061399-76061400	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs377081093	chr5:76061474-76061475	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs139470606	chr5:76061537-76061538	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs144204112	chr5:76061549-76061550	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs569379508	chr5:76061555-76061556	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs146560876	chr5:76061598-76061599	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs4704361	chr5:76061638-76061639	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs185433626	chr5:76061666-76061667	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs4703718	chr5:76061671-76061672	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs149807841	chr5:76061672-76061673	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs572712533	chr5:76061675-76061676	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs190688750	chr5:76061707-76061708	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs145554596	chr5:76061717-76061718	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs173669	chr5:76061748-76061749	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs148882969	chr5:76061753-76061754	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555169498	chr5:76061784-76061785	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs575087021	chr5:76061787-76061788	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs540529189	chr5:76061799-76061800	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs560881656	chr5:76061826-76061827	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547850905	chr5:76061857-76061858	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs532398427	chr5:76061868-76061869	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs548409825	chr5:76061870-76061871	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs515362	chr5:76061924-76061925	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs531660735	chr5:76061929-76061930	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530057823	chr5:76061936-76061937	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs548299152	chr5:76062001-76062002	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs180813525	chr5:76062004-76062005	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs529850820	chr5:76062021-76062022	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs377262669	chr5:76062046-76062047	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs147001596	chr5:76062095-76062096	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs547247985	chr5:76062104-76062105	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs138212681	chr5:76062109-76062110	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs568335920	chr5:76062123-76062124	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs183734737	chr5:76062146-76062147	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs536605051	chr5:76062215-76062216	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs568891025	chr5:76062281-76062282	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs537890419	chr5:76062292-76062293	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs376373370	chr5:76062306-76062307	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17133270	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Schizophrenia	23813976	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Lung squamous cell carcinoma	22363434	CNVD

Chromatin state (count:242 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:76056200-76067000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:76059200-76061400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr5:76059200-76062600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr5:76059400-76067400	Weak transcription	HepG2	liver
5	chr5:76059600-76062600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr5:76059800-76061400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr5:76060400-76063000	Enhancers	Osteobl	bone
8	chr5:76060600-76061800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr5:76060600-76070200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr5:76060800-76061600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr5:76060800-76063400	Enhancers	NHDF-Ad	bronchial
12	chr5:76061000-76061200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr5:76061000-76061600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr5:76061000-76061600	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr5:76061000-76061600	Enhancers	Placenta Amnion	Placenta Amnion
16	chr5:76061000-76061600	Enhancers	NH-A	brain
17	chr5:76061200-76061600	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr5:76061200-76062600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr5:76061400-76062000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr5:76061400-76062600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr5:76061400-76062800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr5:76061400-76063000	Enhancers	NHLF	lung
23	chr5:76061600-76074800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr5:76062000-76062200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr5:76062000-76063200	Enhancers	NHEK	skin
26	chr5:76062000-76063800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr5:76062600-76062800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr5:76062600-76063000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr5:76062600-76063000	Enhancers	A549	lung
30	chr5:76062600-76063200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr5:76062600-76063200	Enhancers	HUVEC	blood vessel
32	chr5:76062600-76063800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr5:76062800-76067200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr5:76063000-76063400	Weak transcription	NHLF	lung
35	chr5:76063000-76067200	Weak transcription	A549	lung
36	chr5:76063000-76067600	Weak transcription	Osteobl	bone
37	chr5:76063400-76063600	Enhancers	NHLF	lung
38	chr5:76063400-76067800	Weak transcription	NHDF-Ad	bronchial
39	chr5:76063600-76067400	Weak transcription	NHLF	lung
40	chr5:76063800-76067400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr5:76067000-76067200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr5:76067200-76067400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr5:76067200-76068000	Enhancers	A549	lung
44	chr5:76067400-76067800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr5:76067400-76068200	Enhancers	HepG2	liver
46	chr5:76067400-76068200	Enhancers	NHLF	lung
47	chr5:76067400-76068400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr5:76067400-76068400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr5:76067400-76068800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr5:76067600-76068200	Enhancers	Muscle Satellite Cultured Cells	--

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