Variant report

Variant	nsv879503
Chromosome Location	chr4:79108589-79163162
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:200)
CpG islands
(count:305)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:200 , 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	chr4:79139434-79139814	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:79122109-79122522	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:79141036-79141685	HepG2	liver:	n/a	n/a
4	ATF1	chr4:79121235-79121392	K562	blood:	n/a	n/a
5	ATF1	chr4:79139582-79139790	K562	blood:	n/a	n/a
6	CEBPB	chr4:79128707-79129021	HepG2	liver:	n/a	chr4:79128871-79128882
7	CEBPB	chr4:79139499-79139697	HepG2	liver:	n/a	chr4:79139607-79139618
8	CEBPB	chr4:79124340-79124353	HepG2	liver:	n/a	n/a
9	CEBPB	chr4:79139578-79139759	H1-hESC	embryonic stem cell:	n/a	chr4:79139607-79139618
10	CEBPB	chr4:79131971-79132152	HepG2	liver:	n/a	chr4:79132046-79132057 chr4:79132046-79132059 chr4:79132047-79132058 chr4:79132048-79132057
11	CEBPB	chr4:79111859-79112039	HepG2	liver:	n/a	n/a
12	CEBPB	chr4:79139442-79139801	HepG2	liver:	n/a	chr4:79139607-79139618
13	CEBPB	chr4:79139321-79139891	HCT-116	colon:	n/a	chr4:79139607-79139618
14	CEBPB	chr4:79132786-79133065	HepG2	liver:	n/a	chr4:79132922-79132933
15	CEBPB	chr4:79158440-79158575	IMR90	lung:	n/a	chr4:79158469-79158480
16	CEBPB	chr4:79139433-79139713	HepG2	liver:	n/a	chr4:79139607-79139618
17	CEBPB	chr4:79139449-79139792	Hela-S3	cervix:	n/a	chr4:79139607-79139618
18	CEBPB	chr4:79122192-79122392	HepG2	liver:	n/a	n/a
19	CEBPB	chr4:79132890-79132972	K562	blood:	n/a	chr4:79132922-79132933
20	CEBPB	chr4:79158401-79158607	HepG2	liver:	n/a	chr4:79158469-79158480
21	CEBPB	chr4:79121226-79121605	HepG2	liver:	n/a	chr4:79121312-79121325
22	CEBPB	chr4:79132793-79133084	IMR90	lung:	n/a	chr4:79132922-79132933
23	CEBPB	chr4:79139454-79139763	IMR90	lung:	n/a	chr4:79139607-79139618
24	CEBPB	chr4:79139418-79139808	HepG2	liver:	n/a	chr4:79139607-79139618
25	CHD1	chr4:79149907-79150030	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr4:79109820-79109970	HCT-116	colon:	n/a	n/a
27	CTCF	chr4:79126860-79127010	HRE	kidney:	n/a	n/a
28	CTCF	chr4:79143600-79143750	HRE	kidney:	n/a	n/a
29	CTCF	chr4:79116440-79116590	GM12873	blood:	n/a	n/a
30	CTCF	chr4:79119233-79119354	K562	blood:	n/a	n/a
31	CTCF	chr4:79119170-79119403	K562	blood:	n/a	n/a
32	CTCF	chr4:79143740-79143890	BE2_C	brain:	n/a	n/a
33	CTCF	chr4:79153664-79153747	ProgFib	skin:	n/a	n/a
34	CTCF	chr4:79119222-79119421	GM12878	blood:	n/a	n/a
35	CTCF	chr4:79119220-79119370	GM12869	blood:	n/a	n/a
36	CTCF	chr4:79119220-79119370	GM12874	blood:	n/a	n/a
37	CTCF	chr4:79118104-79118120	GM13976	blood:	n/a	n/a
38	CTCF	chr4:79130204-79130235	ProgFib	skin:	n/a	n/a
39	CTCF	chr4:79143492-79143525	GM10248	blood:	n/a	n/a
40	CTCFL	chr4:79119172-79119322	K562	blood:	n/a	n/a
41	CUX1	chr4:79125330-79125685	GM12878	blood:	n/a	n/a
42	E2F4	chr4:79134412-79134514	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr4:79128598-79128794	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr4:79132857-79132973	MCF10A-Er-Src	breast:	n/a	n/a
45	EBF1	chr4:79125245-79125676	GM12878	blood:	n/a	n/a
46	EBF1	chr4:79120308-79120376	GM12878	blood:	n/a	chr4:79120346-79120357
47	EGR1	chr4:79129402-79129621	K562	blood:	n/a	n/a
48	EP300	chr4:79122037-79122442	HepG2	liver:	n/a	n/a
49	EP300	chr4:79144205-79144499	SK-N-SH_RA	brain:	n/a	n/a
50	EP300	chr4:79135267-79135710	SK-N-SH_RA	brain:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:79126719-79126769	HCM	heart:	n/a
2	chr4:79138888-79138938	HepG2	liver:	n/a
3	chr4:79149936-79149986	T-47D	breast:	n/a
4	chr4:79143682-79143732	NHBE	bronchial:	n/a
5	chr4:79143682-79143732	HRPEpiC	eye:	n/a
6	chr4:79119852-79119902	ovcar-3	ovarian:	n/a
7	chr4:79143682-79143732	GM19239	blood:	n/a
8	chr4:79149936-79149986	BJ	skin:	n/a
9	chr4:79119852-79119902	HIPEpiC	eye:	n/a
10	chr4:79143682-79143732	HEK293	kidney:	embryo
11	chr4:79143682-79143732	BE2_C	brain:	n/a
12	chr4:79119852-79119902	AG04449	skin:	fetal
13	chr4:79126719-79126769	Hepatocyte	liver:	n/a
14	chr4:79119852-79119902	SK-N-MC	brain:	n/a
15	chr4:79138888-79138938	HRCEpiC	kidney:	n/a
16	chr4:79138888-79138938	A549	lung:	n/a
17	chr4:79143682-79143732	HCPEpiC	choroid plexus:	n/a
18	chr4:79138888-79138938	PANC-1	pancreas:	n/a
19	chr4:79149936-79149986	SK-N-SH	brain:	n/a
20	chr4:79138888-79138938	HIPEpiC	eye:	n/a
21	chr4:79149936-79149986	HMEC	breast:	n/a
22	chr4:79143682-79143732	HEEpiC	esophagus:	n/a
23	chr4:79138888-79138938	U87	brain:	n/a
24	chr4:79126719-79126769	AG09319	gingival:	n/a
25	chr4:79138888-79138938	HCM	heart:	n/a
26	chr4:79143682-79143732	AG10803	skin:	n/a
27	chr4:79138888-79138938	HCT-116	colon:	n/a
28	chr4:79143682-79143732	K562	blood:	n/a
29	chr4:79138888-79138938	Caco-2	colon:	n/a
30	chr4:79119852-79119902	ECC-1	luminal epithelium:	n/a
31	chr4:79126719-79126769	SAEC	small airway:	n/a
32	chr4:79149936-79149986	PFSK-1	brain:	n/a
33	chr4:79149936-79149986	ProgFib	skin:	n/a
34	chr4:79138888-79138938	MCF-7	breast:	n/a
35	chr4:79143682-79143732	HPAEpiC	pulmonary alveolar:	n/a
36	chr4:79138888-79138938	LNCaP	prostate:	n/a
37	chr4:79143682-79143732	ECC-1	luminal epithelium:	n/a
38	chr4:79126719-79126769	RPTEC	kidney:	n/a
39	chr4:79149936-79149986	NHBE	bronchial:	n/a
40	chr4:79119852-79119902	HEEpiC	esophagus:	n/a
41	chr4:79149936-79149986	Hela-S3	cervix:	n/a
42	chr4:79119852-79119902	HCF	heart:	n/a
43	chr4:79119852-79119902	HAEpiC	amniotic membrane:	n/a
44	chr4:79126719-79126769	NHDF-neo	bronchial:	n/a
45	chr4:79149936-79149986	HCT-116	colon:	n/a
46	chr4:79126719-79126769	HMEC	breast:	n/a
47	chr4:79149936-79149986	Caco-2	colon:	n/a
48	chr4:79126719-79126769	HL-60	blood:	n/a
49	chr4:79138888-79138938	GM12892	blood:	n/a
50	chr4:79126719-79126769	NH-A	brain:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:79093805..79095382-chr4:79119242..79121206,2	K562	blood:
2	chr4:79116297..79118632-chr4:79121339..79123057,2	K562	blood:
3	chr4:79116297..79118632-chr4:79121339..79123057,2	K562	blood:
4	chr4:79143866..79146531-chr4:79146925..79148583,2	K562	blood:
5	chr4:79143866..79146531-chr4:79146925..79148583,2	K562	blood:
6	chr4:79153666..79155870-chr4:79187424..79190153,2	K562	blood:

No data

Variant related genes	Relation type
FRAS1	TF binding region
ENSG00000221183	TF binding region
FRAS1	CpG island
ENSG00000221183	CpG island

Extended variants
information (count: 1904 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1904 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11098085	chr4:79108589-79108590	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs531811049	chr4:79108594-79108595	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs184195767	chr4:79108601-79108602	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs140225958	chr4:79108604-79108605	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs534189267	chr4:79108686-79108687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs544939278	chr4:79108744-79108745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs564833552	chr4:79108798-79108799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs547707441	chr4:79108831-79108832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs188343535	chr4:79108844-79108845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs539482976	chr4:79108848-79108849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs145274472	chr4:79108852-79108853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs372482545	chr4:79108895-79108896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs576435817	chr4:79108958-79108959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs535586497	chr4:79108959-79108960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs138476799	chr4:79109042-79109043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs574706085	chr4:79109075-79109076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs17003036	chr4:79109081-79109082	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs533389012	chr4:79109090-79109091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs2866998	chr4:79109100-79109101	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs549889344	chr4:79109208-79109209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs17003037	chr4:79109241-79109242	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs545832841	chr4:79109247-79109248	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs568948515	chr4:79109319-79109320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs116355406	chr4:79109364-79109365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140199778	chr4:79109426-79109427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs60821257	chr4:79109433-79109434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs376707656	chr4:79109461-79109462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs144389522	chr4:79109465-79109466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs67743063	chr4:79109469-79109470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs200494366	chr4:79109473-79109474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs369024018	chr4:79109474-79109475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs371467087	chr4:79109475-79109476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs115735321	chr4:79109484-79109485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs145165986	chr4:79109488-79109489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs369949077	chr4:79109547-79109548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs547669345	chr4:79109562-79109563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs58661619	chr4:79109613-79109614	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs201010630	chr4:79109648-79109649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs75757647	chr4:79109657-79109658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs2866997	chr4:79109675-79109676	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs138860082	chr4:79109724-79109725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs555605395	chr4:79109739-79109740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs536406813	chr4:79109850-79109851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs529389859	chr4:79109858-79109859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs534016392	chr4:79109867-79109868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs372547258	chr4:79109888-79109889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs181113129	chr4:79109891-79109892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs79009323	chr4:79109922-79109923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs185721459	chr4:79109953-79109954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs575972365	chr4:79109957-79109958	Weak transcription Enhancers	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
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
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
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
small cell lung cancer	20016488	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
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
primary effusion lymphomas	17116491	CNVD
Gastric cancer	16891809	CNVD
Prostate cancer	16573809	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:79100200-79109200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:79100600-79111200	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr4:79101000-79112200	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr4:79103600-79116400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr4:79105200-79108800	Enhancers	Fetal Intestine Large	intestine
6	chr4:79105200-79108800	Enhancers	Fetal Intestine Small	intestine
7	chr4:79106600-79111200	Weak transcription	HepG2	liver
8	chr4:79106600-79115800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr4:79108200-79108800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr4:79108400-79108600	Enhancers	Pancreas	Pancrea
11	chr4:79108400-79109200	Enhancers	Psoas Muscle	Psoas
12	chr4:79108400-79111200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr4:79108400-79111400	Weak transcription	Fetal Kidney	kidney
14	chr4:79108400-79112200	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr4:79108800-79115800	Weak transcription	Fetal Intestine Small	intestine
16	chr4:79109200-79109600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr4:79109600-79109800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr4:79109800-79112000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr4:79109800-79115400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr4:79111200-79111400	Enhancers	H9 Cell Line	embryonic stem cell
21	chr4:79111200-79111600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr4:79111200-79111600	Enhancers	HepG2	liver
23	chr4:79111200-79111800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr4:79111400-79111600	Enhancers	Fetal Kidney	kidney
25	chr4:79111600-79118000	Weak transcription	HepG2	liver
26	chr4:79112200-79112600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
27	chr4:79112200-79112600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
28	chr4:79115800-79116400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr4:79116400-79116600	Weak transcription	Pancreas	Pancrea
30	chr4:79116400-79117000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr4:79116400-79117200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
32	chr4:79116400-79117600	ZNF genes & repeats	Fetal Intestine Small	intestine
33	chr4:79116600-79117000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
34	chr4:79116600-79117000	ZNF genes & repeats	Spleen	Spleen
35	chr4:79116600-79117200	ZNF genes & repeats	Fetal Intestine Large	intestine
36	chr4:79116800-79117000	ZNF genes & repeats	Pancreas	Pancrea
37	chr4:79117000-79126000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr4:79117000-79129000	Weak transcription	Pancreas	Pancrea
39	chr4:79117200-79120800	Weak transcription	Fetal Intestine Large	intestine
40	chr4:79117200-79121000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr4:79117600-79121400	Weak transcription	Fetal Intestine Small	intestine
42	chr4:79117600-79123600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr4:79117800-79118800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr4:79118000-79123600	Enhancers	HepG2	liver
45	chr4:79119200-79119400	Enhancers	H1 Cell Line	embryonic stem cell
46	chr4:79119400-79121400	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr4:79119600-79119800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr4:79119600-79120000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr4:79119600-79120000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr4:79119800-79121200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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