Variant report

Variant	nsv980103
Chromosome Location	chr3:132975869-132988869
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	ATF1	chr3:132985181-132985392	K562	blood:	n/a	n/a
2	CEBPB	chr3:132977968-132978184	HepG2	liver:	n/a	chr3:132978135-132978146
3	CTCF	chr3:132980573-132980678	K562	blood:	n/a	n/a
4	EP300	chr3:132987483-132988104	SK-N-SH_RA	brain:	n/a	n/a
5	EP300	chr3:132975786-132976309	SK-N-SH_RA	brain:	n/a	n/a
6	EP300	chr3:132983657-132984352	SK-N-SH	brain:	n/a	n/a
7	EP300	chr3:132975591-132976645	SK-N-SH	brain:	n/a	chr3:132976536-132976550
8	EP300	chr3:132982458-132985711	SK-N-SH	brain:	n/a	chr3:132982817-132982831
9	EP300	chr3:132985945-132990160	SK-N-SH	brain:	n/a	chr3:132988397-132988411 chr3:132988788-132988797
10	EP300	chr3:132976977-132977723	SK-N-SH	brain:	n/a	chr3:132977390-132977406
11	EP300	chr3:132983538-132984388	SK-N-SH	brain:	n/a	n/a
12	EP300	chr3:132988271-132988536	SK-N-SH_RA	brain:	n/a	chr3:132988397-132988411
13	EP300	chr3:132987486-132988104	SK-N-SH_RA	brain:	n/a	n/a
14	EP300	chr3:132975656-132976491	SK-N-SH	brain:	n/a	n/a
15	EP300	chr3:132977807-132978075	SK-N-SH_RA	brain:	n/a	chr3:132977827-132977841
16	EP300	chr3:132983679-132984273	SK-N-SH_RA	brain:	n/a	n/a
17	EP300	chr3:132975726-132976365	SK-N-SH_RA	brain:	n/a	n/a
18	EP300	chr3:132983706-132984257	SK-N-SH_RA	brain:	n/a	n/a
19	FOS	chr3:132975986-132976241	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr3:132975985-132976236	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr3:132985258-132985446	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr3:132985159-132985387	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr3:132976019-132976173	MCF10A-Er-Src	breast:	n/a	n/a
24	FOSL2	chr3:132977065-132977750	SK-N-SH	brain:	n/a	chr3:132977535-132977546 chr3:132977585-132977597
25	FOSL2	chr3:132975810-132976479	SK-N-SH	brain:	n/a	n/a
26	GATA2	chr3:132987533-132987985	SH-SY5Y	brain:	n/a	n/a
27	GATA2	chr3:132983621-132984374	SH-SY5Y	brain:	n/a	chr3:132984284-132984293
28	GATA2	chr3:132981150-132981608	SH-SY5Y	brain:	n/a	n/a
29	GATA3	chr3:132983253-132984404	SK-N-SH	brain:	n/a	chr3:132984284-132984293
30	GATA3	chr3:132987495-132987939	SH-SY5Y	brain:	n/a	n/a
31	GATA3	chr3:132976968-132977754	SK-N-SH	brain:	n/a	chr3:132977377-132977386 chr3:132977377-132977384 chr3:132977376-132977386
32	GATA3	chr3:132977022-132977792	SK-N-SH	brain:	n/a	chr3:132977377-132977386 chr3:132977377-132977384 chr3:132977376-132977386
33	GATA3	chr3:132985149-132985286	SH-SY5Y	brain:	n/a	n/a
34	GATA3	chr3:132983503-132984380	SK-N-SH	brain:	n/a	chr3:132984284-132984293
35	GATA3	chr3:132987420-132988089	SK-N-SH	brain:	n/a	n/a
36	GATA3	chr3:132983199-132984307	SH-SY5Y	brain:	n/a	chr3:132984284-132984293
37	GATA3	chr3:132982182-132982338	SH-SY5Y	brain:	n/a	n/a
38	GATA3	chr3:132979651-132979773	SH-SY5Y	brain:	n/a	n/a
39	GATA3	chr3:132975539-132976491	SK-N-SH	brain:	n/a	n/a
40	GATA3	chr3:132980900-132981523	SH-SY5Y	brain:	n/a	chr3:132981029-132981036 chr3:132981029-132981036 chr3:132981029-132981038 chr3:132981029-132981038 chr3:132981028-132981038 chr3:132981029-132981036
41	GATA3	chr3:132987340-132988118	SK-N-SH	brain:	n/a	n/a
42	GATA3	chr3:132975502-132976547	SK-N-SH	brain:	n/a	n/a
43	IRF1	chr3:132988204-132988600	K562	blood:	n/a	chr3:132988402-132988412 chr3:132988406-132988420 chr3:132988408-132988418 chr3:132988402-132988416 chr3:132988402-132988413 chr3:132988406-132988426 chr3:132988407-132988420 chr3:132988401-132988413 chr3:132988400-132988420 chr3:132988401-132988413 chr3:132988407-132988424 chr3:132988401-132988418 chr3:132988404-132988418 chr3:132988398-132988412
44	IRF1	chr3:132988308-132988560	K562	blood:	n/a	chr3:132988402-132988412 chr3:132988406-132988420 chr3:132988408-132988418 chr3:132988402-132988416 chr3:132988402-132988413 chr3:132988406-132988426 chr3:132988407-132988420 chr3:132988401-132988413 chr3:132988400-132988420 chr3:132988401-132988413 chr3:132988407-132988424 chr3:132988401-132988418 chr3:132988404-132988418 chr3:132988398-132988412
45	JUND	chr3:132975733-132976468	SK-N-SH	brain:	n/a	n/a
46	MAFK	chr3:132988854-132989054	HepG2	liver:	n/a	n/a
47	MYC	chr3:132975993-132976197	MCF10A-Er-Src	breast:	n/a	n/a
48	NFIC	chr3:132975656-132976544	SK-N-SH	brain:	n/a	n/a
49	NFIC	chr3:132975787-132976415	SK-N-SH	brain:	n/a	n/a
50	PBX3	chr3:132977058-132977762	SK-N-SH	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:132977031-132977081	RPTEC	kidney:	n/a
2	chr3:132977031-132977081	HCF	heart:	n/a
3	chr3:132977031-132977081	AG04450	lung:	fetal
4	chr3:132977031-132977081	SK-N-MC	brain:	n/a
5	chr3:132977031-132977081	SAEC	small airway:	n/a
6	chr3:132977031-132977081	IMR90	lung:	fetal
7	chr3:132977031-132977081	ECC-1	luminal epithelium:	n/a
8	chr3:132977031-132977081	NHDF-neo	bronchial:	n/a
9	chr3:132977031-132977081	LNCaP	prostate:	n/a
10	chr3:132977031-132977081	GM19239	blood:	n/a
11	chr3:132977031-132977081	NH-A	brain:	n/a
12	chr3:132977031-132977081	HRE	kidney:	n/a
13	chr3:132977031-132977081	HPAEpiC	pulmonary alveolar:	n/a
14	chr3:132977031-132977081	BE2_C	brain:	n/a
15	chr3:132977031-132977081	Hela-S3	cervix:	n/a
16	chr3:132977031-132977081	HRPEpiC	eye:	n/a
17	chr3:132977031-132977081	Caco-2	colon:	n/a
18	chr3:132977031-132977081	Jurkat	blood:	n/a
19	chr3:132977031-132977081	ProgFib	skin:	n/a
20	chr3:132977031-132977081	T-47D	breast:	n/a
21	chr3:132977031-132977081	HCM	heart:	n/a
22	chr3:132977031-132977081	AG10803	skin:	n/a
23	chr3:132977031-132977081	GM12878	blood:	n/a
24	chr3:132977031-132977081	HepG2	liver:	n/a
25	chr3:132977031-132977081	HAEpiC	amniotic membrane:	n/a
26	chr3:132977031-132977081	NT2-D1	testis:	n/a
27	chr3:132977031-132977081	HNPCEpiC	eye:	n/a
28	chr3:132977031-132977081	AoSMC	blood vessel:	n/a
29	chr3:132977031-132977081	K562	blood:	n/a
30	chr3:132977031-132977081	PANC-1	pancreas:	n/a
31	chr3:132977031-132977081	AG09319	gingival:	n/a
32	chr3:132977031-132977081	ovcar-3	ovarian:	n/a
33	chr3:132977031-132977081	MCF-7	breast:	n/a
34	chr3:132977031-132977081	BJ	skin:	n/a
35	chr3:132977031-132977081	HEK293	kidney:	embryo
36	chr3:132977031-132977081	NHBE	bronchial:	n/a
37	chr3:132977031-132977081	Hepatocyte	liver:	n/a
38	chr3:132977031-132977081	SKMC	muscle:	n/a
39	chr3:132977031-132977081	GM06990	blood:	n/a
40	chr3:132977031-132977081	A549	lung:	n/a
41	chr3:132977031-132977081	H1-hESC	embryonic stem cell:	embryo
42	chr3:132977031-132977081	HCPEpiC	choroid plexus:	n/a
43	chr3:132977031-132977081	GM12891	blood:	n/a
44	chr3:132977031-132977081	SK-N-SH	brain:	n/a
45	chr3:132977031-132977081	HEEpiC	esophagus:	n/a
46	chr3:132977031-132977081	HL-60	blood:	n/a
47	chr3:132977031-132977081	U87	brain:	n/a
48	chr3:132977031-132977081	MCF10A-Er-Src	breast:	n/a
49	chr3:132977031-132977081	SK-N-SH_RA	brain:	n/a
50	chr3:132977031-132977081	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:132983643..132985958-chr3:132988828..132991292,2	MCF-7	breast:
2	chr3:132983643..132985958-chr3:132988828..132991292,2	MCF-7	breast:
3	chr3:132972367..132974641-chr3:132976452..132979083,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TOPBP1-2	chr3:132975869-132976032	ENSG00000251011.1
2	lnc-TOPBP1-2	chr3:132975869-132975892	ENSG00000251011.1

Variant related genes	Relation type
ENSG00000251011	TF binding region
ENSG00000251011	CpG island

Extended variants
information (count: 498 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:498 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529038468	chr3:132975933-132975934	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
2	rs536333482	chr3:132975934-132975935	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs138739537	chr3:132975972-132975973	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs556648139	chr3:132976028-132976029	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs191310928	chr3:132976094-132976095	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs370591189	chr3:132976129-132976130	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs149374577	chr3:132976147-132976148	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs12495802	chr3:132976158-132976159	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs191753122	chr3:132976186-132976187	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs554081771	chr3:132976235-132976236	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs373687532	chr3:132976264-132976265	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs373370369	chr3:132976267-132976268	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs114422280	chr3:132976271-132976272	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs558540367	chr3:132976292-132976293	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs200887363	chr3:132976371-132976372	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs73217545	chr3:132976386-132976387	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs556756551	chr3:132976393-132976394	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs576618050	chr3:132976400-132976401	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs7641051	chr3:132976563-132976564	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs188237142	chr3:132976579-132976580	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs557303721	chr3:132976628-132976629	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs577235775	chr3:132976637-132976638	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs539876635	chr3:132976690-132976691	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs559794439	chr3:132976706-132976707	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs16840103	chr3:132976744-132976745	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs542449980	chr3:132976748-132976749	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562714725	chr3:132976773-132976774	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs6439397	chr3:132976782-132976783	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs147471171	chr3:132976799-132976800	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs77451427	chr3:132976813-132976814	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs527662115	chr3:132976842-132976843	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190294382	chr3:132976856-132976857	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs55719274	chr3:132976961-132976962	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs530220112	chr3:132976964-132976965	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs550058819	chr3:132976968-132976969	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs570254288	chr3:132976972-132976973	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs138402951	chr3:132976984-132976985	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs558808740	chr3:132977010-132977011	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs566061493	chr3:132977023-132977024	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs543127798	chr3:132977073-132977074	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs143594226	chr3:132977075-132977076	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
42	rs563443267	chr3:132977082-132977083	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs113973851	chr3:132977108-132977109	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs532135027	chr3:132977109-132977110	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs542711839	chr3:132977117-132977118	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs556049507	chr3:132977125-132977126	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs374214740	chr3:132977155-132977156	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs576169610	chr3:132977190-132977191	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs545249166	chr3:132977279-132977280	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs368123685	chr3:132977296-132977297	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Hailey-hailey disease	17597066	CNVD
Intracranial aneurysm	16715129	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:74 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:132957200-132981400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr3:132968000-132984200	Weak transcription	Psoas Muscle	Psoas
3	chr3:132971400-132977600	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr3:132974800-132980400	Weak transcription	Fetal Brain Male	brain
5	chr3:132975200-132977400	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr3:132975600-132976000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr3:132975600-132976000	Enhancers	GM12878-XiMat	blood
8	chr3:132975600-132976400	Enhancers	Fetal Lung	lung
9	chr3:132975600-132976800	Enhancers	Muscle Satellite Cultured Cells	--
10	chr3:132975600-132977600	Enhancers	NH-A	brain
11	chr3:132975600-132977800	Enhancers	Osteobl	bone
12	chr3:132975600-132979200	Enhancers	NHEK	skin
13	chr3:132975600-132979600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr3:132975800-132977200	Enhancers	HSMM	muscle
15	chr3:132975800-132977800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr3:132976000-132981200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr3:132976400-132987000	Weak transcription	Fetal Lung	lung
18	chr3:132977000-132977600	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr3:132977200-132977600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr3:132977200-132977600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr3:132977200-132982200	Weak transcription	HSMM	muscle
22	chr3:132977200-132983800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr3:132977400-132979600	Enhancers	Breast Myoepithelial Primary Cells	Breast
24	chr3:132977400-132986800	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr3:132977600-132978200	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr3:132977800-132978200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr3:132978200-132979200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr3:132980400-132982400	Enhancers	Fetal Brain Male	brain
29	chr3:132980800-132981600	Enhancers	Fetal Brain Female	brain
30	chr3:132981200-132981600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr3:132981400-132981600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr3:132981600-132986800	Weak transcription	Fetal Brain Female	brain
33	chr3:132982400-132984000	Enhancers	HSMMtube	muscle
34	chr3:132982400-132986800	Weak transcription	Fetal Brain Male	brain
35	chr3:132983800-132984600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr3:132984000-132994800	Weak transcription	HSMMtube	muscle
37	chr3:132984200-132984400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr3:132984200-132984400	Flanking Active TSS	Left Ventricle	heart
39	chr3:132984200-132984600	Enhancers	Psoas Muscle	Psoas
40	chr3:132984600-132988200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr3:132984600-132988200	Weak transcription	Psoas Muscle	Psoas
42	chr3:132984800-132985400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr3:132985400-133002800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr3:132986400-132989800	Weak transcription	Lung	lung
45	chr3:132986600-132988800	Enhancers	Fetal Stomach	stomach
46	chr3:132986800-132988400	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr3:132986800-132988400	Enhancers	Fetal Brain Male	brain
48	chr3:132986800-132989000	Enhancers	Right Atrium	heart
49	chr3:132986800-132989200	Enhancers	Fetal Brain Female	brain
50	chr3:132986800-132990000	Enhancers	Fetal Muscle Leg	muscle

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