Variant report

Variant	nsv875470
Chromosome Location	chr2:180400021-180432529
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:234)
CpG islands
(count:306)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:234 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:180422657-180423509	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:180414903-180415937	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:180407947-180409432	HepG2	liver:	n/a	chr2:180408148-180408164
4	ARID3A	chr2:180424909-180425355	HepG2	liver:	n/a	n/a
5	ATF2	chr2:180414802-180415273	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr2:180414915-180415345	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr2:180408098-180408686	HepG2	liver:	n/a	n/a
8	CEBPB	chr2:180408092-180408712	HepG2	liver:	n/a	n/a
9	CEBPB	chr2:180415621-180415943	IMR90	lung:	n/a	chr2:180415790-180415807
10	CEBPB	chr2:180415621-180415974	HepG2	liver:	n/a	chr2:180415790-180415807
11	CEBPB	chr2:180408111-180408446	HepG2	liver:	n/a	n/a
12	CEBPB	chr2:180406674-180406944	HepG2	liver:	n/a	n/a
13	CEBPB	chr2:180408058-180408677	HepG2	liver:	n/a	n/a
14	CEBPB	chr2:180414915-180415363	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr2:180414949-180415320	HepG2	liver:	n/a	n/a
16	CEBPB	chr2:180415654-180415891	H1-hESC	embryonic stem cell:	n/a	chr2:180415790-180415807
17	CEBPB	chr2:180408083-180408435	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr2:180407996-180408605	HepG2	liver:	n/a	n/a
19	CEBPB	chr2:180415684-180415899	A549	lung:	n/a	chr2:180415790-180415807
20	CEBPB	chr2:180408174-180408281	A549	lung:	n/a	n/a
21	CEBPB	chr2:180409119-180409481	HepG2	liver:	n/a	chr2:180409300-180409311 chr2:180409299-180409312 chr2:180409299-180409310 chr2:180409301-180409310
22	CEBPD	chr2:180408202-180408593	HepG2	liver:	n/a	n/a
23	CEBPD	chr2:180408126-180408435	HepG2	liver:	n/a	n/a
24	CHD2	chr2:180409549-180409839	HepG2	liver:	n/a	n/a
25	CHD2	chr2:180414966-180415352	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr2:180408170-180408689	HepG2	liver:	n/a	n/a
27	CTCF	chr2:180426500-180426650	RPTEC	kidney:	n/a	chr2:180426581-180426589
28	CTCF	chr2:180405457-180405488	Kidney_OC	kidney:	n/a	n/a
29	CTCF	chr2:180418956-180418998	K562	blood:	n/a	n/a
30	CTCF	chr2:180416185-180416214	Kidney_OC	kidney:	n/a	n/a
31	CUX1	chr2:180421082-180421112	GM12878	blood:	n/a	n/a
32	E2F4	chr2:180411568-180411602	GM12878	blood:	n/a	n/a
33	E2F4	chr2:180403206-180403483	MCF10A-Er-Src	breast:	n/a	n/a
34	E2F4	chr2:180404539-180404739	MCF10A-Er-Src	breast:	n/a	n/a
35	ELF1	chr2:180408122-180408639	HepG2	liver:	n/a	n/a
36	EP300	chr2:180424806-180425622	HepG2	liver:	n/a	chr2:180425122-180425132
37	EP300	chr2:180422487-180423450	HepG2	liver:	n/a	chr2:180422989-180423005 chr2:180423062-180423071
38	EP300	chr2:180403194-180403435	SK-N-SH_RA	brain:	n/a	n/a
39	EP300	chr2:180401266-180401534	SK-N-SH_RA	brain:	n/a	n/a
40	EP300	chr2:180407977-180408804	HepG2	liver:	n/a	n/a
41	EP300	chr2:180407898-180408892	HepG2	liver:	n/a	n/a
42	EP300	chr2:180403230-180403439	SK-N-SH_RA	brain:	n/a	n/a
43	EP300	chr2:180422602-180423464	HepG2	liver:	n/a	chr2:180422989-180423005 chr2:180423062-180423071
44	EP300	chr2:180408073-180408684	HepG2	liver:	n/a	n/a
45	EP300	chr2:180424699-180425571	HepG2	liver:	n/a	chr2:180425122-180425132
46	EP300	chr2:180414832-180415415	HepG2	liver:	n/a	n/a
47	EP300	chr2:180403015-180403714	SK-N-SH	brain:	n/a	n/a
48	FOS	chr2:180403109-180403540	MCF10A-Er-Src	breast:	n/a	chr2:180403277-180403289 chr2:180403279-180403287
49	FOS	chr2:180403013-180403672	MCF10A-Er-Src	breast:	n/a	chr2:180403277-180403289 chr2:180403279-180403287
50	FOS	chr2:180403105-180403533	MCF10A-Er-Src	breast:	n/a	chr2:180403277-180403289 chr2:180403279-180403287

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:180428696-180428746	HMEC	breast:	n/a
2	chr2:180428696-180428746	HMEC	breast:	n/a
3	chr2:180408380-180408430	T-47D	breast:	n/a
4	chr2:180427177-180427227	ECC-1	luminal epithelium:	n/a
5	chr2:180428696-180428746	MCF10A-Er-Src	breast:	n/a
6	chr2:180427325-180427375	AG10803	skin:	n/a
7	chr2:180427177-180427227	NHBE	bronchial:	n/a
8	chr2:180428745-180428795	ProgFib	skin:	n/a
9	chr2:180428696-180428746	SKMC	muscle:	n/a
10	chr2:180427325-180427375	ProgFib	skin:	n/a
11	chr2:180427325-180427375	LNCaP	prostate:	n/a
12	chr2:180428696-180428746	PFSK-1	brain:	n/a
13	chr2:180427177-180427227	AoSMC	blood vessel:	n/a
14	chr2:180427325-180427375	HEEpiC	esophagus:	n/a
15	chr2:180427177-180427227	GM12892	blood:	n/a
16	chr2:180428696-180428746	HIPEpiC	eye:	n/a
17	chr2:180427177-180427227	U87	brain:	n/a
18	chr2:180428745-180428795	BJ	skin:	n/a
19	chr2:180408380-180408430	HPAEpiC	pulmonary alveolar:	n/a
20	chr2:180427177-180427227	HEEpiC	esophagus:	n/a
21	chr2:180427177-180427227	CMK	blood:	n/a
22	chr2:180427325-180427375	A549	lung:	n/a
23	chr2:180408380-180408430	H1-hESC	embryonic stem cell:	embryo
24	chr2:180428745-180428795	PANC-1	pancreas:	n/a
25	chr2:180427177-180427227	HIPEpiC	eye:	n/a
26	chr2:180408380-180408430	SK-N-SH_RA	brain:	n/a
27	chr2:180428696-180428746	HCT-116	colon:	n/a
28	chr2:180428745-180428795	MCF10A-Er-Src	breast:	n/a
29	chr2:180428745-180428795	LNCaP	prostate:	n/a
30	chr2:180427177-180427227	GM06990	blood:	n/a
31	chr2:180427325-180427375	GM19239	blood:	n/a
32	chr2:180427325-180427375	HRPEpiC	eye:	n/a
33	chr2:180427177-180427227	GM12891	blood:	n/a
34	chr2:180427325-180427375	AG04450	lung:	fetal
35	chr2:180408380-180408430	NT2-D1	testis:	n/a
36	chr2:180428745-180428795	Caco-2	colon:	n/a
37	chr2:180408380-180408430	PFSK-1	brain:	n/a
38	chr2:180428696-180428746	HCM	heart:	n/a
39	chr2:180428696-180428746	HRCEpiC	kidney:	n/a
40	chr2:180427177-180427227	PFSK-1	brain:	n/a
41	chr2:180428745-180428795	GM12892	blood:	n/a
42	chr2:180428696-180428746	HNPCEpiC	eye:	n/a
43	chr2:180428745-180428795	NHDF-neo	bronchial:	n/a
44	chr2:180408380-180408430	HAEpiC	amniotic membrane:	n/a
45	chr2:180427177-180427227	HRPEpiC	eye:	n/a
46	chr2:180427325-180427375	Hepatocyte	liver:	n/a
47	chr2:180427177-180427227	HAEpiC	amniotic membrane:	n/a
48	chr2:180428696-180428746	NH-A	brain:	n/a
49	chr2:180428745-180428795	AG09319	gingival:	n/a
50	chr2:180428696-180428746	PANC-1	pancreas:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:180430735..180433402-chr2:180437315..180438959,2	K562	blood:
2	chr2:180396502..180399490-chr2:180403575..180405915,2	K562	blood:
3	chr2:180405427..180408122-chr2:180413189..180415887,2	MCF-7	breast:
4	chr2:180405427..180408122-chr2:180413189..180415887,2	MCF-7	breast:
5	chr2:180432423..180435401-chr2:180435886..180437761,2	MCF-7	breast:

No data

Variant related genes	Relation type
ZNF385B	TF binding region
ZNF385B	CpG island

Extended variants
information (count: 1159 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:1159 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10497541	chr2:180400021-180400022	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs535452243	chr2:180400072-180400073	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs566307557	chr2:180400091-180400092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs549931842	chr2:180400094-180400095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs548952072	chr2:180400104-180400105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs565675437	chr2:180400135-180400136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs71425631	chr2:180400186-180400187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs569997794	chr2:180400277-180400278	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs534458322	chr2:180400286-180400287	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs557817142	chr2:180400288-180400289	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs578128377	chr2:180400322-180400323	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs537620697	chr2:180400334-180400335	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs184910038	chr2:180400346-180400347	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs573951262	chr2:180400398-180400399	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs542913217	chr2:180400423-180400424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs552590426	chr2:180400465-180400466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs566173048	chr2:180400488-180400489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs115043675	chr2:180400583-180400584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs573176713	chr2:180400593-180400594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs147121906	chr2:180400600-180400601	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs189375566	chr2:180400605-180400606	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs374599241	chr2:180400606-180400607	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs199663310	chr2:180400684-180400685	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs113998393	chr2:180400703-180400704	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs549961442	chr2:180400725-180400726	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs138646770	chr2:180400739-180400740	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs191353077	chr2:180400755-180400756	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs549289056	chr2:180400773-180400774	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs6709838	chr2:180400813-180400814	Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs554788570	chr2:180400823-180400824	Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs534588491	chr2:180400845-180400846	Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs113261315	chr2:180400847-180400848	Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs571284984	chr2:180401046-180401047	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs537253181	chr2:180401072-180401073	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs144479408	chr2:180401091-180401092	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs376296311	chr2:180401103-180401104	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs548446299	chr2:180401128-180401129	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs148429249	chr2:180401162-180401163	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs553231388	chr2:180401181-180401182	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs573180361	chr2:180401184-180401185	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs545352871	chr2:180401205-180401206	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs6738933	chr2:180401233-180401234	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs183753140	chr2:180401248-180401249	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs188074614	chr2:180401254-180401255	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs368991533	chr2:180401350-180401351	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs576727734	chr2:180401351-180401352	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs16866768	chr2:180401369-180401370	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs6725869	chr2:180401424-180401425	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs56395909	chr2:180401449-180401450	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs182037184	chr2:180401481-180401482	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Sudden cardiac death	19188705	CNVD
Acute myeloid leukemia	20729466	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Mental retardation	21062444	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Schizophrenia	19348701	CNVD
Muscular dystrophy	17160897	CNVD
Cardiomyopathy	17576883	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Breast cancer	22522925	CNVD
Myelofibrosis	22110671	CNVD

Chromatin state (count:292 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:180394000-180401200	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr2:180397000-180401000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr2:180397800-180403600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr2:180398400-180402800	Weak transcription	Liver	Liver
5	chr2:180399600-180402200	Weak transcription	Psoas Muscle	Psoas
6	chr2:180399800-180400800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr2:180400000-180400200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr2:180400000-180401800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr2:180400200-180400400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr2:180400200-180401400	Enhancers	Osteobl	bone
11	chr2:180400400-180400600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr2:180400600-180401000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr2:180400600-180401600	Enhancers	Muscle Satellite Cultured Cells	--
14	chr2:180400800-180401200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr2:180400800-180401600	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr2:180401000-180401800	Enhancers	Skeletal Muscle Female	skeletal muscle
17	chr2:180401000-180402000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr2:180401000-180402000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr2:180401200-180401800	Enhancers	Skeletal Muscle Male	skeletal muscle
20	chr2:180401200-180402800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr2:180401400-180402600	Weak transcription	Osteobl	bone
22	chr2:180401600-180402800	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr2:180401600-180403400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr2:180401800-180402800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr2:180401800-180403400	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr2:180402000-180402400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr2:180402200-180402400	Enhancers	Psoas Muscle	Psoas
28	chr2:180402400-180403800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr2:180402600-180403800	Enhancers	Osteobl	bone
30	chr2:180402800-180403200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr2:180402800-180403600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr2:180402800-180403600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr2:180402800-180403600	Strong transcription	Liver	Liver
34	chr2:180402800-180403800	Enhancers	Muscle Satellite Cultured Cells	--
35	chr2:180403200-180408000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr2:180403400-180403800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr2:180403400-180403800	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr2:180403400-180403800	Enhancers	NHEK	skin
39	chr2:180403400-180407600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr2:180403600-180403800	ZNF genes & repeats	Fetal Kidney	kidney
41	chr2:180403600-180404000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr2:180403600-180404000	ZNF genes & repeats	Liver	Liver
43	chr2:180403800-180404200	ZNF genes & repeats	Gastric	stomach
44	chr2:180403800-180407400	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr2:180403800-180408000	Weak transcription	Osteobl	bone
46	chr2:180403800-180408600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr2:180403800-180408600	Weak transcription	Fetal Kidney	kidney
48	chr2:180403800-180409800	Weak transcription	Skeletal Muscle Male	skeletal muscle
49	chr2:180404000-180408000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr2:180404000-180410000	Strong transcription	Liver	Liver

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