Variant report

Variant	nsv523865
Chromosome Location	chr2:180403128-180426764
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:218)
CpG islands
(count:61)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:218 , 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	chr2:180407947-180409432	HepG2	liver:	n/a	chr2:180408148-180408164
2	ARID3A	chr2:180424909-180425355	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:180414903-180415937	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:180422657-180423509	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	chr2:180415684-180415899	A549	lung:	n/a	chr2:180415790-180415807
9	CEBPB	chr2:180408111-180408446	HepG2	liver:	n/a	n/a
10	CEBPB	chr2:180408058-180408677	HepG2	liver:	n/a	n/a
11	CEBPB	chr2:180407996-180408605	HepG2	liver:	n/a	n/a
12	CEBPB	chr2:180415621-180415943	IMR90	lung:	n/a	chr2:180415790-180415807
13	CEBPB	chr2:180406674-180406944	HepG2	liver:	n/a	n/a
14	CEBPB	chr2:180415654-180415891	H1-hESC	embryonic stem cell:	n/a	chr2:180415790-180415807
15	CEBPB	chr2:180415621-180415974	HepG2	liver:	n/a	chr2:180415790-180415807
16	CEBPB	chr2:180408083-180408435	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr2:180409119-180409481	HepG2	liver:	n/a	chr2:180409300-180409311 chr2:180409299-180409312 chr2:180409299-180409310 chr2:180409301-180409310
18	CEBPB	chr2:180408174-180408281	A549	lung:	n/a	n/a
19	CEBPB	chr2:180414949-180415320	HepG2	liver:	n/a	n/a
20	CEBPB	chr2:180408092-180408712	HepG2	liver:	n/a	n/a
21	CEBPB	chr2:180414915-180415363	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPD	chr2:180408126-180408435	HepG2	liver:	n/a	n/a
23	CEBPD	chr2:180408202-180408593	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	chr2:180416185-180416214	Kidney_OC	kidney:	n/a	n/a
29	CTCF	chr2:180418956-180418998	K562	blood:	n/a	n/a
30	CTCF	chr2:180405457-180405488	Kidney_OC	kidney:	n/a	n/a
31	CUX1	chr2:180421082-180421112	GM12878	blood:	n/a	n/a
32	E2F4	chr2:180403206-180403483	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr2:180404539-180404739	MCF10A-Er-Src	breast:	n/a	n/a
34	E2F4	chr2:180411568-180411602	GM12878	blood:	n/a	n/a
35	ELF1	chr2:180408122-180408639	HepG2	liver:	n/a	n/a
36	EP300	chr2:180422487-180423450	HepG2	liver:	n/a	chr2:180422989-180423005 chr2:180423062-180423071
37	EP300	chr2:180407898-180408892	HepG2	liver:	n/a	n/a
38	EP300	chr2:180403194-180403435	SK-N-SH_RA	brain:	n/a	n/a
39	EP300	chr2:180403015-180403714	SK-N-SH	brain:	n/a	n/a
40	EP300	chr2:180424806-180425622	HepG2	liver:	n/a	chr2:180425122-180425132
41	EP300	chr2:180407977-180408804	HepG2	liver:	n/a	n/a
42	EP300	chr2:180403230-180403439	SK-N-SH_RA	brain:	n/a	n/a
43	EP300	chr2:180414832-180415415	HepG2	liver:	n/a	n/a
44	EP300	chr2:180422602-180423464	HepG2	liver:	n/a	chr2:180422989-180423005 chr2:180423062-180423071
45	EP300	chr2:180424699-180425571	HepG2	liver:	n/a	chr2:180425122-180425132
46	EP300	chr2:180408073-180408684	HepG2	liver:	n/a	n/a
47	FOS	chr2:180403109-180403540	MCF10A-Er-Src	breast:	n/a	chr2:180403277-180403289 chr2:180403279-180403287
48	FOS	chr2:180403013-180403672	MCF10A-Er-Src	breast:	n/a	chr2:180403277-180403289 chr2:180403279-180403287
49	FOS	chr2:180403103-180403536	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:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:180408380-180408430	HCM	heart:	n/a
2	chr2:180408380-180408430	GM06990	blood:	n/a
3	chr2:180408380-180408430	HRE	kidney:	n/a
4	chr2:180408380-180408430	AG04449	skin:	fetal
5	chr2:180408380-180408430	BE2_C	brain:	n/a
6	chr2:180408380-180408430	GM12891	blood:	n/a
7	chr2:180408380-180408430	PANC-1	pancreas:	n/a
8	chr2:180408380-180408430	HRCEpiC	kidney:	n/a
9	chr2:180408380-180408430	AG04450	lung:	fetal
10	chr2:180408380-180408430	NT2-D1	testis:	n/a
11	chr2:180408380-180408430	NB4	blood:	n/a
12	chr2:180408380-180408430	NH-A	brain:	n/a
13	chr2:180408380-180408430	GM12878	blood:	n/a
14	chr2:180408380-180408430	SK-N-MC	brain:	n/a
15	chr2:180408380-180408430	LNCaP	prostate:	n/a
16	chr2:180408380-180408430	NHBE	bronchial:	n/a
17	chr2:180408380-180408430	CMK	blood:	n/a
18	chr2:180408380-180408430	AoSMC	blood vessel:	n/a
19	chr2:180408380-180408430	RPTEC	kidney:	n/a
20	chr2:180408380-180408430	HCF	heart:	n/a
21	chr2:180408380-180408430	SAEC	small airway:	n/a
22	chr2:180408380-180408430	BJ	skin:	n/a
23	chr2:180408380-180408430	AG09319	gingival:	n/a
24	chr2:180408380-180408430	Hela-S3	cervix:	n/a
25	chr2:180408380-180408430	K562	blood:	n/a
26	chr2:180408380-180408430	IMR90	lung:	fetal
27	chr2:180408380-180408430	PrEC	prostate:	n/a
28	chr2:180408380-180408430	HNPCEpiC	eye:	n/a
29	chr2:180408380-180408430	HRPEpiC	eye:	n/a
30	chr2:180408380-180408430	HEEpiC	esophagus:	n/a
31	chr2:180408380-180408430	HMEC	breast:	n/a
32	chr2:180408380-180408430	MCF10A-Er-Src	breast:	n/a
33	chr2:180408380-180408430	H1-hESC	embryonic stem cell:	embryo
34	chr2:180408380-180408430	AG09309	skin:	n/a
35	chr2:180408380-180408430	U87	brain:	n/a
36	chr2:180408380-180408430	HAEpiC	amniotic membrane:	n/a
37	chr2:180408380-180408430	HEK293	kidney:	embryo
38	chr2:180408380-180408430	ProgFib	skin:	n/a
39	chr2:180408380-180408430	HCT-116	colon:	n/a
40	chr2:180408380-180408430	GM19239	blood:	n/a
41	chr2:180408380-180408430	HL-60	blood:	n/a
42	chr2:180408380-180408430	SK-N-SH_RA	brain:	n/a
43	chr2:180408380-180408430	HCPEpiC	choroid plexus:	n/a
44	chr2:180408380-180408430	Hepatocyte	liver:	n/a
45	chr2:180408380-180408430	T-47D	breast:	n/a
46	chr2:180408380-180408430	Jurkat	blood:	n/a
47	chr2:180408380-180408430	HepG2	liver:	n/a
48	chr2:180408380-180408430	Caco-2	colon:	n/a
49	chr2:180408380-180408430	MCF-7	breast:	n/a
50	chr2:180408380-180408430	A549	lung:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:180405427..180408122-chr2:180413189..180415887,2	MCF-7	breast:
2	chr2:180405427..180408122-chr2:180413189..180415887,2	MCF-7	breast:
3	chr2:180396502..180399490-chr2:180403575..180405915,2	K562	blood:

No data

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

Extended variants
information (count: 821 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:821 , 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	rs11884072	chr2:180403128-180403129	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs71425634	chr2:180403179-180403180	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs143199346	chr2:180403214-180403215	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs540350861	chr2:180403216-180403217	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs112282494	chr2:180403245-180403246	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs559964258	chr2:180403246-180403247	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs532753332	chr2:180403258-180403259	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs552453569	chr2:180403354-180403355	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs188604028	chr2:180403367-180403368	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs568226673	chr2:180403384-180403385	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs11889308	chr2:180403390-180403391	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs371237274	chr2:180403402-180403403	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs191863038	chr2:180403459-180403460	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs558701966	chr2:180403493-180403494	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs114287278	chr2:180403539-180403540	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs533914929	chr2:180403561-180403562	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs547886366	chr2:180403610-180403611	ZNF genes & repeats Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs35638010	chr2:180403619-180403620	ZNF genes & repeats Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs570817041	chr2:180403621-180403622	ZNF genes & repeats Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs538831121	chr2:180403710-180403711	ZNF genes & repeats Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs560107662	chr2:180403742-180403743	ZNF genes & repeats Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558378014	chr2:180403751-180403752	ZNF genes & repeats Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs147924821	chr2:180403820-180403821	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs550901196	chr2:180403873-180403874	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs11901287	chr2:180403896-180403897	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs74663856	chr2:180403910-180403911	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs141790915	chr2:180403963-180403964	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs112608530	chr2:180404043-180404044	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs183308528	chr2:180404045-180404046	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs375915049	chr2:180404073-180404074	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs553837638	chr2:180404077-180404078	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs13424600	chr2:180404146-180404147	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs545909440	chr2:180404164-180404165	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs112220846	chr2:180404172-180404173	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs563111372	chr2:180404180-180404181	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs531921339	chr2:180404185-180404186	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs113885491	chr2:180404266-180404267	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs562212497	chr2:180404270-180404271	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs113866277	chr2:180404298-180404299	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs370261204	chr2:180404302-180404303	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs6722937	chr2:180404353-180404354	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs570824104	chr2:180404386-180404387	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535144961	chr2:180404411-180404412	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs570540999	chr2:180404497-180404498	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs533306268	chr2:180404500-180404501	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549847465	chr2:180404532-180404533	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs568739157	chr2:180404533-180404534	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs147106026	chr2:180404542-180404543	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs386653174	chr2:180404547-180404548	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs546555737	chr2:180404548-180404549	Weak transcription Strong transcription	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:214 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:180397800-180403600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:180401600-180403400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr2:180401800-180403400	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr2:180402400-180403800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr2:180402600-180403800	Enhancers	Osteobl	bone
6	chr2:180402800-180403200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr2:180402800-180403600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr2:180402800-180403600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr2:180402800-180403600	Strong transcription	Liver	Liver
10	chr2:180402800-180403800	Enhancers	Muscle Satellite Cultured Cells	--
11	chr2:180403200-180408000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr2:180403400-180403800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr2:180403400-180403800	Enhancers	Skeletal Muscle Male	skeletal muscle
14	chr2:180403400-180403800	Enhancers	NHEK	skin
15	chr2:180403400-180407600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr2:180403600-180403800	ZNF genes & repeats	Fetal Kidney	kidney
17	chr2:180403600-180404000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr2:180403600-180404000	ZNF genes & repeats	Liver	Liver
19	chr2:180403800-180404200	ZNF genes & repeats	Gastric	stomach
20	chr2:180403800-180407400	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr2:180403800-180408000	Weak transcription	Osteobl	bone
22	chr2:180403800-180408600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr2:180403800-180408600	Weak transcription	Fetal Kidney	kidney
24	chr2:180403800-180409800	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr2:180404000-180408000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr2:180404000-180410000	Strong transcription	Liver	Liver
27	chr2:180404200-180409800	Weak transcription	Gastric	stomach
28	chr2:180405400-180405800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr2:180405400-180410600	Enhancers	HepG2	liver
30	chr2:180405800-180408000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr2:180406400-180406600	Enhancers	Brain Germinal Matrix	brain
32	chr2:180406600-180406800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr2:180406800-180407800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr2:180407000-180411400	Weak transcription	Right Atrium	heart
35	chr2:180407400-180408800	Enhancers	Muscle Satellite Cultured Cells	--
36	chr2:180407600-180408400	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr2:180407800-180408400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr2:180407800-180408400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr2:180407800-180408800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr2:180407800-180410000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr2:180408000-180408400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr2:180408000-180408600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr2:180408000-180408600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr2:180408000-180408600	Enhancers	Osteobl	bone
45	chr2:180408000-180408800	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr2:180408000-180408800	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr2:180408000-180408800	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr2:180408000-180408800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr2:180408200-180408400	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr2:180408200-180408600	Enhancers	iPS-15b Cell Line	embryonic stem cell

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