Variant report

Variant	nsv962062
Chromosome Location	chr2:36920237-36925000
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	CEBPB	chr2:36921355-36921939	K562	blood:	n/a	chr2:36921564-36921575
2	CEBPB	chr2:36921404-36921745	HepG2	liver:	n/a	chr2:36921564-36921575
3	CEBPB	chr2:36924875-36925199	HepG2	liver:	n/a	chr2:36925033-36925044
4	CEBPB	chr2:36924860-36925191	A549	lung:	n/a	chr2:36925033-36925044
5	CEBPB	chr2:36921432-36921754	A549	lung:	n/a	chr2:36921564-36921575
6	CEBPB	chr2:36921492-36921657	Hela-S3	cervix:	n/a	chr2:36921564-36921575
7	CEBPB	chr2:36924508-36925275	Hela-S3	cervix:	n/a	chr2:36925033-36925044
8	CEBPB	chr2:36924860-36925201	IMR90	lung:	n/a	chr2:36925033-36925044
9	CTCF	chr2:36923040-36923190	NHLF	lung:	n/a	chr2:36923102-36923115
10	CTCF	chr2:36923040-36923190	HEK293	kidney:	n/a	chr2:36923102-36923115
11	CTCF	chr2:36923040-36923190	Caco-2	colon:	n/a	chr2:36923102-36923115
12	CTCF	chr2:36923020-36923170	AG04450	lung:	n/a	chr2:36923102-36923115
13	CTCF	chr2:36922964-36923234	Hela-S3	cervix:	n/a	chr2:36923102-36923115
14	CTCF	chr2:36923010-36923172	MCF-7	breast:	n/a	chr2:36923102-36923115
15	CTCF	chr2:36922980-36923130	HPF	lung:	n/a	chr2:36923102-36923115
16	CTCF	chr2:36923020-36923170	SAEC	small airway:	n/a	chr2:36923102-36923115
17	CTCF	chr2:36923060-36923210	HMEC	breast:	n/a	chr2:36923102-36923115
18	CTCF	chr2:36922340-36922490	AG10803	skin:	n/a	n/a
19	CTCF	chr2:36923000-36923150	NHDF-neo	bronchial:	n/a	chr2:36923102-36923115
20	CTCF	chr2:36923020-36923170	A549	lung:	n/a	chr2:36923102-36923115
21	CTCF	chr2:36922966-36923200	ProgFib	skin:	n/a	chr2:36923102-36923115
22	CTCF	chr2:36923040-36923190	AG09319	gingival:	n/a	chr2:36923102-36923115
23	CTCF	chr2:36923026-36923186	MCF-7	breast:	n/a	chr2:36923102-36923115
24	CTCF	chr2:36922985-36923256	IMR90	lung:	n/a	chr2:36923102-36923115
25	CTCF	chr2:36923020-36923170	NHEK	skin:	n/a	chr2:36923102-36923115
26	CTCF	chr2:36922935-36923281	MCF-7	breast:	n/a	chr2:36923102-36923115
27	CTCF	chr2:36923008-36923170	H1-hESC	embryonic stem cell:	n/a	chr2:36923102-36923115
28	CTCF	chr2:36922748-36923427	SK-N-SH	brain:	n/a	chr2:36923102-36923115
29	CTCF	chr2:36923160-36923310	MCF-7	breast:	n/a	n/a
30	CTCF	chr2:36922979-36923217	MCF-7	breast:	n/a	chr2:36923102-36923115
31	CTCF	chr2:36922940-36923090	HVMF	connective:	n/a	n/a
32	CTCF	chr2:36923020-36923170	HEEpiC	esophagus:	n/a	chr2:36923102-36923115
33	CTCF	chr2:36923040-36923190	AG10803	skin:	n/a	chr2:36923102-36923115
34	CTCF	chr2:36923000-36923150	AoAF	blood vessel:	n/a	chr2:36923102-36923115
35	CTCF	chr2:36922960-36923110	WI-38	lung:	n/a	n/a
36	CTCF	chr2:36923140-36923290	HAc	cerebellar:	n/a	n/a
37	CTCF	chr2:36923040-36923190	AG04450	lung:	n/a	chr2:36923102-36923115
38	CTCF	chr2:36922973-36923223	MCF-7	breast:	n/a	chr2:36923102-36923115
39	CTCF	chr2:36923087-36923107	GM19240	blood:	n/a	n/a
40	CTCF	chr2:36922980-36923130	HL-60	blood:	n/a	chr2:36923102-36923115
41	CTCF	chr2:36923040-36923190	HA-sp	spinal cord:	n/a	chr2:36923102-36923115
42	CTCF	chr2:36923000-36923150	K562	blood:	n/a	chr2:36923102-36923115
43	CTCF	chr2:36923040-36923190	HAc	cerebellar:	n/a	chr2:36923102-36923115
44	CTCF	chr2:36923040-36923190	HCFaa	heart:	n/a	chr2:36923102-36923115
45	CTCF	chr2:36923000-36923150	HVMF	connective:	n/a	chr2:36923102-36923115
46	CTCF	chr2:36923020-36923170	Hela-S3	cervix:	n/a	chr2:36923102-36923115
47	CTCF	chr2:36923000-36923150	HPF	lung:	n/a	chr2:36923102-36923115
48	CTCF	chr2:36923020-36923170	HUVEC	blood vessel:	n/a	chr2:36923102-36923115
49	CTCF	chr2:36923020-36923170	HMF	breast:	n/a	chr2:36923102-36923115
50	CTCF	chr2:36923045-36923164	HepG2	liver:	n/a	chr2:36923102-36923115

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:36922916-36922966	RPTEC	kidney:	n/a
2	chr2:36923086-36923136	SKMC	muscle:	n/a
3	chr2:36922916-36922966	GM12891	blood:	n/a
4	chr2:36923828-36923878	AG04450	lung:	fetal
5	chr2:36923828-36923878	MCF10A-Er-Src	breast:	n/a
6	chr2:36923828-36923878	AG09309	skin:	n/a
7	chr2:36922916-36922966	LNCaP	prostate:	n/a
8	chr2:36922916-36922966	HEK293	kidney:	embryo
9	chr2:36923828-36923878	HRE	kidney:	n/a
10	chr2:36923828-36923878	AG09319	gingival:	n/a
11	chr2:36923828-36923878	HCT-116	colon:	n/a
12	chr2:36923828-36923878	HMEC	breast:	n/a
13	chr2:36922916-36922966	NHDF-neo	bronchial:	n/a
14	chr2:36923828-36923878	HepG2	liver:	n/a
15	chr2:36923086-36923136	T-47D	breast:	n/a
16	chr2:36923828-36923878	LNCaP	prostate:	n/a
17	chr2:36923086-36923136	GM12892	blood:	n/a
18	chr2:36923086-36923136	NB4	blood:	n/a
19	chr2:36922916-36922966	HL-60	blood:	n/a
20	chr2:36922916-36922966	HCM	heart:	n/a
21	chr2:36923086-36923136	NT2-D1	testis:	n/a
22	chr2:36923828-36923878	HEK293	kidney:	embryo
23	chr2:36923828-36923878	SK-N-MC	brain:	n/a
24	chr2:36922916-36922966	HepG2	liver:	n/a
25	chr2:36923086-36923136	Hela-S3	cervix:	n/a
26	chr2:36923086-36923136	SAEC	small airway:	n/a
27	chr2:36923828-36923878	GM12891	blood:	n/a
28	chr2:36923086-36923136	BJ	skin:	n/a
29	chr2:36923086-36923136	AG10803	skin:	n/a
30	chr2:36923828-36923878	HNPCEpiC	eye:	n/a
31	chr2:36923086-36923136	AG04449	skin:	fetal
32	chr2:36923086-36923136	ovcar-3	ovarian:	n/a
33	chr2:36923828-36923878	SK-N-SH	brain:	n/a
34	chr2:36922916-36922966	BE2_C	brain:	n/a
35	chr2:36922916-36922966	AG04450	lung:	fetal
36	chr2:36922916-36922966	CMK	blood:	n/a
37	chr2:36923828-36923878	BE2_C	brain:	n/a
38	chr2:36923828-36923878	AG10803	skin:	n/a
39	chr2:36923828-36923878	AG04449	skin:	fetal
40	chr2:36922916-36922966	Caco-2	colon:	n/a
41	chr2:36923086-36923136	PANC-1	pancreas:	n/a
42	chr2:36923828-36923878	A549	lung:	n/a
43	chr2:36923086-36923136	GM19239	blood:	n/a
44	chr2:36923086-36923136	IMR90	lung:	fetal
45	chr2:36923828-36923878	HCF	heart:	n/a
46	chr2:36923828-36923878	HCPEpiC	choroid plexus:	n/a
47	chr2:36923828-36923878	HPAEpiC	pulmonary alveolar:	n/a
48	chr2:36923828-36923878	ProgFib	skin:	n/a
49	chr2:36923828-36923878	RPTEC	kidney:	n/a
50	chr2:36923828-36923878	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:36922543..36923508-chr2:37012076..37013001,3	MCF-7	breast:
2	chr2:36922695..36923609-chr2:36997471..36998399,4	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FEZ2-2	chr2:36924810-36925173	expReg_chr2_2321_-

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

Extended variants
information (count: 179 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:179 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571246232	chr2:36920247-36920248	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs7604443	chr2:36920273-36920274	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs550535819	chr2:36920274-36920275	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs116534799	chr2:36920309-36920310	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs536138341	chr2:36920322-36920323	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554351674	chr2:36920385-36920386	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs200289685	chr2:36920485-36920486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs79033655	chr2:36920487-36920488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs147188549	chr2:36920488-36920489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs534322410	chr2:36920521-36920522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs62132511	chr2:36920528-36920529	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs71437561	chr2:36920622-36920623	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs111738935	chr2:36920624-36920625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs562865824	chr2:36920635-36920636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs575210744	chr2:36920706-36920707	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs62132512	chr2:36920712-36920713	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs369998182	chr2:36920741-36920742	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs182543587	chr2:36920787-36920788	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs567155851	chr2:36920821-36920822	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs575553031	chr2:36920830-36920831	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs187288927	chr2:36920848-36920849	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs564865323	chr2:36920851-36920852	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs532227165	chr2:36920860-36920861	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs550209022	chr2:36920876-36920877	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs546032095	chr2:36920888-36920889	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs367951522	chr2:36920896-36920897	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs397984308	chr2:36920910-36920911	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs564125505	chr2:36920913-36920914	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs548052202	chr2:36920916-36920917	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs566737561	chr2:36920983-36920984	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs533778842	chr2:36920997-36920998	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs528213469	chr2:36921081-36921082	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs558706173	chr2:36921096-36921097	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs577312774	chr2:36921104-36921105	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs538288917	chr2:36921109-36921110	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs55939088	chr2:36921146-36921147	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs574853047	chr2:36921160-36921161	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs542564537	chr2:36921165-36921166	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs560798748	chr2:36921166-36921167	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs72801329	chr2:36921185-36921186	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs376773436	chr2:36921186-36921187	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs397729385	chr2:36921189-36921190	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs200511007	chr2:36921190-36921191	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs182757528	chr2:36921202-36921203	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs564700497	chr2:36921205-36921206	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs34638531	chr2:36921220-36921221	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs550225494	chr2:36921236-36921237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs10173131	chr2:36921255-36921256	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs529669269	chr2:36921290-36921291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs57922899	chr2:36921324-36921325	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:36918800-36920400	Enhancers	Fetal Lung	lung
2	chr2:36918800-36920800	Enhancers	Ovary	ovary
3	chr2:36918800-36922800	Weak transcription	Gastric	stomach
4	chr2:36920400-36920800	Enhancers	K562	blood
5	chr2:36920400-36922800	Weak transcription	Fetal Lung	lung
6	chr2:36920800-36921200	Flanking Active TSS	K562	blood
7	chr2:36920800-36922800	Weak transcription	Ovary	ovary
8	chr2:36921200-36921400	Enhancers	K562	blood
9	chr2:36922400-36925200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr2:36922600-36922800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr2:36922600-36922800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr2:36922600-36922800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr2:36922600-36922800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr2:36922600-36922800	Enhancers	Muscle Satellite Cultured Cells	--
15	chr2:36922600-36922800	Enhancers	NHDF-Ad	bronchial
16	chr2:36922600-36922800	Enhancers	Osteobl	bone
17	chr2:36922600-36923000	Enhancers	NHEK	skin
18	chr2:36922600-36923400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr2:36922600-36924600	Enhancers	Hela-S3	cervix
20	chr2:36922600-36924600	Enhancers	HSMM	muscle
21	chr2:36922800-36923000	Enhancers	Gastric	stomach
22	chr2:36922800-36923000	Enhancers	NHLF	lung
23	chr2:36922800-36923200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr2:36922800-36923200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr2:36922800-36923200	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr2:36922800-36923200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
27	chr2:36922800-36923200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr2:36922800-36923200	Enhancers	HSMMtube	muscle
29	chr2:36922800-36923200	Flanking Active TSS	NHDF-Ad	bronchial
30	chr2:36922800-36923400	Enhancers	Ovary	ovary
31	chr2:36922800-36923400	Enhancers	HUVEC	blood vessel
32	chr2:36922800-36923800	Enhancers	Adipose Nuclei	Adipose
33	chr2:36922800-36925000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr2:36922800-36925200	Enhancers	Fetal Lung	lung
35	chr2:36922800-36925200	Enhancers	NH-A	brain
36	chr2:36922800-36925400	Flanking Active TSS	Osteobl	bone
37	chr2:36922800-36925800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr2:36922800-36925800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr2:36923000-36923200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr2:36923000-36923200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr2:36923000-36923200	Flanking Active TSS	NHLF	lung
42	chr2:36923000-36923400	Enhancers	HMEC	breast
43	chr2:36923000-36924000	Flanking Active TSS	NHEK	skin
44	chr2:36923200-36923400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr2:36923200-36923600	Active TSS	Muscle Satellite Cultured Cells	--
46	chr2:36923200-36923800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr2:36923200-36924600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr2:36923200-36924600	Weak transcription	HSMMtube	muscle
49	chr2:36923200-36924800	Enhancers	NHLF	lung
50	chr2:36923200-36925000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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