Variant report

Variant	nsv329560
Chromosome Location	chr5:147269326-147278710
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:78)
CpG islands
(count:62)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:78 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:147275521-147275631	K562	blood:	n/a	n/a
2	CEBPB	chr5:147272272-147272558	MCF-7	breast:	n/a	n/a
3	CEBPB	chr5:147275587-147275623	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr5:147277142-147277483	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr5:147278443-147278747	Hela-S3	cervix:	n/a	n/a
6	CHD2	chr5:147278534-147278763	Hela-S3	cervix:	n/a	n/a
7	CTCF	chr5:147272380-147272530	Caco-2	colon:	n/a	n/a
8	CTCF	chr5:147269660-147269810	GM12874	blood:	n/a	n/a
9	EP300	chr5:147272182-147272656	MCF-7	breast:	n/a	n/a
10	EP300	chr5:147278373-147278762	Hela-S3	cervix:	n/a	n/a
11	FOS	chr5:147272566-147272855	MCF10A-Er-Src	breast:	n/a	chr5:147272773-147272781 chr5:147272772-147272782
12	FOS	chr5:147278332-147278865	MCF10A-Er-Src	breast:	n/a	n/a
13	FOS	chr5:147273543-147273601	MCF10A-Er-Src	breast:	n/a	n/a
14	FOS	chr5:147278374-147278744	MCF10A-Er-Src	breast:	n/a	n/a
15	FOS	chr5:147272498-147272892	HUVEC	blood vessel:	n/a	chr5:147272773-147272781 chr5:147272772-147272782
16	FOS	chr5:147272623-147272836	MCF10A-Er-Src	breast:	n/a	chr5:147272773-147272781 chr5:147272772-147272782
17	FOS	chr5:147278360-147278712	Hela-S3	cervix:	n/a	n/a
18	FOS	chr5:147278332-147278859	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr5:147273497-147273678	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr5:147278396-147278903	HUVEC	blood vessel:	n/a	n/a
21	FOS	chr5:147278377-147278779	MCF10A-Er-Src	breast:	n/a	n/a
22	FOSL2	chr5:147278410-147278796	A549	lung:	n/a	n/a
23	FOXA1	chr5:147272289-147272553	T-47D	breast:	n/a	n/a
24	FOXA1	chr5:147272342-147272600	T-47D	breast:	n/a	chr5:147272562-147272574
25	GATA2	chr5:147270700-147271335	HUVEC	blood vessel:	n/a	n/a
26	GATA2	chr5:147273344-147274344	HUVEC	blood vessel:	n/a	chr5:147274118-147274139 chr5:147274173-147274183 chr5:147274125-147274132 chr5:147274125-147274134 chr5:147274124-147274134 chr5:147274125-147274132 chr5:147274125-147274132 chr5:147274325-147274336 chr5:147273795-147273805
27	GATA2	chr5:147272367-147272842	HUVEC	blood vessel:	n/a	n/a
28	GATA2	chr5:147276914-147277527	SH-SY5Y	brain:	n/a	n/a
29	GATA3	chr5:147278388-147278904	A549	lung:	n/a	chr5:147278706-147278717
30	GATA3	chr5:147272298-147272533	T-47D	breast:	n/a	n/a
31	GATA3	chr5:147270994-147271194	SH-SY5Y	brain:	n/a	n/a
32	GATA3	chr5:147272288-147272635	MCF-7	breast:	n/a	n/a
33	GATA3	chr5:147270988-147271405	MCF-7	breast:	n/a	n/a
34	GATA3	chr5:147276864-147277324	SH-SY5Y	brain:	n/a	n/a
35	GTF2F1	chr5:147278552-147278802	Hela-S3	cervix:	n/a	n/a
36	HDAC2	chr5:147272239-147272624	MCF-7	breast:	n/a	n/a
37	HDAC2	chr5:147272271-147272588	MCF-7	breast:	n/a	n/a
38	JUND	chr5:147278401-147278815	Hela-S3	cervix:	n/a	n/a
39	JUND	chr5:147272168-147272772	MCF-7	breast:	n/a	n/a
40	MAX	chr5:147272349-147272647	H1-hESC	embryonic stem cell:	n/a	n/a
41	MAX	chr5:147278529-147278643	Hela-S3	cervix:	n/a	n/a
42	MAX	chr5:147272225-147272665	MCF-7	breast:	n/a	n/a
43	MAX	chr5:147272299-147272669	H1-hESC	embryonic stem cell:	n/a	n/a
44	MYC	chr5:147272427-147272483	MCF-7	breast:	n/a	n/a
45	MYC	chr5:147278378-147278882	MCF10A-Er-Src	breast:	n/a	n/a
46	NFYB	chr5:147275434-147275700	Hela-S3	cervix:	n/a	chr5:147275529-147275544
47	NR2F2	chr5:147272302-147272662	MCF-7	breast:	n/a	n/a
48	POLR2A	chr5:147278659-147278706	Hela-S3	cervix:	n/a	n/a
49	POLR2A	chr5:147278675-147279059	MCF10A-Er-Src	breast:	n/a	n/a
50	POLR2A	chr5:147270591-147270766	GM12878	blood:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:147272300-147272350	HEEpiC	esophagus:	n/a
2	chr5:147272300-147272350	HEEpiC	esophagus:	n/a
3	chr5:147272300-147272350	HNPCEpiC	eye:	n/a
4	chr5:147272300-147272350	ECC-1	luminal epithelium:	n/a
5	chr5:147272300-147272350	AG04450	lung:	fetal
6	chr5:147272300-147272350	RPTEC	kidney:	n/a
7	chr5:147272300-147272350	NHBE	bronchial:	n/a
8	chr5:147272300-147272350	HCT-116	colon:	n/a
9	chr5:147272300-147272350	HIPEpiC	eye:	n/a
10	chr5:147272300-147272350	NT2-D1	testis:	n/a
11	chr5:147272300-147272350	AG04449	skin:	fetal
12	chr5:147272300-147272350	IMR90	lung:	fetal
13	chr5:147272300-147272350	BJ	skin:	n/a
14	chr5:147272300-147272350	PFSK-1	brain:	n/a
15	chr5:147272300-147272350	NHDF-neo	bronchial:	n/a
16	chr5:147272300-147272350	NB4	blood:	n/a
17	chr5:147272300-147272350	AG09319	gingival:	n/a
18	chr5:147272300-147272350	MCF-7	breast:	n/a
19	chr5:147272300-147272350	HEK293	kidney:	embryo
20	chr5:147272300-147272350	SK-N-SH	brain:	n/a
21	chr5:147272300-147272350	A549	lung:	n/a
22	chr5:147272300-147272350	HRPEpiC	eye:	n/a
23	chr5:147272300-147272350	NH-A	brain:	n/a
24	chr5:147272300-147272350	HCF	heart:	n/a
25	chr5:147272300-147272350	LNCaP	prostate:	n/a
26	chr5:147272300-147272350	GM06990	blood:	n/a
27	chr5:147272300-147272350	AG09309	skin:	n/a
28	chr5:147272300-147272350	GM12892	blood:	n/a
29	chr5:147272300-147272350	Hela-S3	cervix:	n/a
30	chr5:147272300-147272350	HMEC	breast:	n/a
31	chr5:147272300-147272350	SK-N-MC	brain:	n/a
32	chr5:147272300-147272350	HPAEpiC	pulmonary alveolar:	n/a
33	chr5:147272300-147272350	Jurkat	blood:	n/a
34	chr5:147272300-147272350	ovcar-3	ovarian:	n/a
35	chr5:147272300-147272350	GM12891	blood:	n/a
36	chr5:147272300-147272350	SK-N-SH_RA	brain:	n/a
37	chr5:147272300-147272350	ProgFib	skin:	n/a
38	chr5:147272300-147272350	GM19239	blood:	n/a
39	chr5:147272300-147272350	HL-60	blood:	n/a
40	chr5:147272300-147272350	PrEC	prostate:	n/a
41	chr5:147272300-147272350	HRE	kidney:	n/a
42	chr5:147272300-147272350	BE2_C	brain:	n/a
43	chr5:147272300-147272350	HCPEpiC	choroid plexus:	n/a
44	chr5:147272300-147272350	CMK	blood:	n/a
45	chr5:147272300-147272350	T-47D	breast:	n/a
46	chr5:147272300-147272350	GM12878	blood:	n/a
47	chr5:147272300-147272350	MCF10A-Er-Src	breast:	n/a
48	chr5:147272300-147272350	Caco-2	colon:	n/a
49	chr5:147272300-147272350	PANC-1	pancreas:	n/a
50	chr5:147272300-147272350	Hepatocyte	liver:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:147272144..147273653-chr5:147300672..147302249,2	MCF-7	breast:
2	chr5:147265148..147267409-chr5:147270950..147272492,2	MCF-7	breast:
3	chr5:147274656..147275267-chr9:127623855..127624555,2	Hela-S3	cervix:
4	chr5:147274175..147276959-chr5:147278370..147280406,2	MCF-7	breast:
5	chr5:147274175..147276959-chr5:147278370..147280406,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000248362	TF binding region
ENSG00000248362	CpG island
ENSG00000250346	chromatin interactions
ENSG00000248362	chromatin interactions
ENSG00000251320	chromatin interactions
ENSG00000136942	chromatin interactions
ENSG00000136950	chromatin interactions

Extended variants
information (count: 371 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:371 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145487376	chr5:147269335-147269336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs187591088	chr5:147269348-147269349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs370351932	chr5:147269359-147269360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs192800268	chr5:147269360-147269361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs77663222	chr5:147269391-147269392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs140949544	chr5:147269413-147269414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs565831442	chr5:147269439-147269440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs34430524	chr5:147269465-147269466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs114385440	chr5:147269515-147269516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs373796548	chr5:147269538-147269539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs185485990	chr5:147269541-147269542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs190740639	chr5:147269543-147269544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550109791	chr5:147269544-147269545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs78169046	chr5:147269551-147269552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs555757039	chr5:147269673-147269674	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs574105863	chr5:147269676-147269677	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs150184549	chr5:147269707-147269708	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs17703748	chr5:147269716-147269717	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs560262452	chr5:147269729-147269730	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs573635039	chr5:147269755-147269756	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs192578057	chr5:147269912-147269913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs532228511	chr5:147269945-147269946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs184211919	chr5:147269960-147269961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs188973008	chr5:147269974-147269975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs575495432	chr5:147269988-147269989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs542919632	chr5:147270004-147270005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs35547234	chr5:147270020-147270021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs561317207	chr5:147270050-147270051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs75544112	chr5:147270077-147270078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565671646	chr5:147270085-147270086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs116096614	chr5:147270092-147270093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs181038424	chr5:147270122-147270123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs551326823	chr5:147270167-147270168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs569874952	chr5:147270177-147270178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs534389508	chr5:147270193-147270194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs530777868	chr5:147270200-147270201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs549313882	chr5:147270201-147270202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs185650200	chr5:147270237-147270238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs189130809	chr5:147270244-147270245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs71580459	chr5:147270251-147270252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs114600591	chr5:147270254-147270255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs138092976	chr5:147270268-147270269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs115450190	chr5:147270273-147270274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs2163747	chr5:147270295-147270296	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs542876442	chr5:147270312-147270313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs554875027	chr5:147270322-147270323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs13355947	chr5:147270352-147270353	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs60783706	chr5:147270360-147270361	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs149099629	chr5:147270362-147270363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs13360221	chr5:147270374-147270375	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:76)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	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
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
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Renal cell carcinoma	18592004	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Hyperekplexia	16941485	CNVD
Myelofibrosis	22110671	CNVD
Crohn''s disease	20877625	CNVD
T-cell lymphomas	19863542	CNVD
Breast cancer	17603634	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:102 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:147262600-147272600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr5:147262800-147272200	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr5:147262800-147275600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr5:147266800-147272200	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr5:147267600-147272800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr5:147267800-147273000	Weak transcription	Right Ventricle	heart
7	chr5:147268000-147271400	Weak transcription	Hela-S3	cervix
8	chr5:147268000-147272200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr5:147268000-147272200	Weak transcription	NH-A	brain
10	chr5:147268200-147270200	Weak transcription	Aorta	Aorta
11	chr5:147268200-147271600	Weak transcription	HUVEC	blood vessel
12	chr5:147268200-147271800	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr5:147268200-147272200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr5:147268200-147272200	Weak transcription	NHEK	skin
15	chr5:147268200-147272400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr5:147268400-147271000	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr5:147268400-147272000	Weak transcription	HMEC	breast
18	chr5:147270200-147270400	Enhancers	Aorta	Aorta
19	chr5:147270400-147273000	Weak transcription	Aorta	Aorta
20	chr5:147271000-147272000	Enhancers	Placenta Amnion	Placenta Amnion
21	chr5:147271200-147272400	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr5:147271400-147274200	Enhancers	Hela-S3	cervix
23	chr5:147271600-147273200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr5:147271600-147273400	Enhancers	Osteobl	bone
25	chr5:147271600-147274600	Enhancers	HUVEC	blood vessel
26	chr5:147271800-147272200	Enhancers	Placenta	Placenta
27	chr5:147271800-147272800	Enhancers	Stomach Mucosa	stomach
28	chr5:147271800-147273400	Enhancers	Muscle Satellite Cultured Cells	--
29	chr5:147272000-147273800	Enhancers	HMEC	breast
30	chr5:147272000-147275200	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr5:147272200-147272600	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr5:147272200-147272600	Weak transcription	Placenta	Placenta
33	chr5:147272200-147272800	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr5:147272200-147272800	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr5:147272200-147272800	Enhancers	NH-A	brain
36	chr5:147272200-147273000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr5:147272200-147273200	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr5:147272200-147273600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr5:147272200-147274000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr5:147272200-147274200	Enhancers	NHEK	skin
41	chr5:147272400-147273000	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr5:147272400-147273200	Enhancers	Pancreas	Pancrea
43	chr5:147272400-147273600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr5:147272600-147273400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr5:147272600-147273400	Enhancers	Placenta	Placenta
46	chr5:147272800-147273000	Weak transcription	NH-A	brain
47	chr5:147272800-147273400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr5:147272800-147278400	Weak transcription	Stomach Mucosa	stomach
49	chr5:147272800-147279600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr5:147273000-147273200	Enhancers	Right Ventricle	heart

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