Variant report

Variant	nsv976630
Chromosome Location	chr12:57332126-57335427
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	BACH1	chr12:57335314-57335674	K562	blood:	n/a	n/a
2	BATF	chr12:57335348-57335706	GM12878	blood:	n/a	chr12:57335532-57335543
3	CREB1	chr12:57335061-57335390	A549	lung:	n/a	n/a
4	CTCF	chr12:57335180-57335330	HMEC	breast:	n/a	chr12:57335245-57335263
5	CTCF	chr12:57333829-57333847	GM10266	blood:	n/a	n/a
6	CTCF	chr12:57335220-57335370	HCPEpiC	choroid plexus:	n/a	chr12:57335245-57335263
7	CTCF	chr12:57335220-57335370	HEEpiC	esophagus:	n/a	chr12:57335245-57335263
8	CTCF	chr12:57332723-57332793	LNCaP	prostate:	n/a	n/a
9	CTCF	chr12:57335160-57335310	NHEK	skin:	n/a	chr12:57335245-57335263
10	CTCF	chr12:57335200-57335350	HMEC	breast:	n/a	chr12:57335245-57335263
11	CTCF	chr12:57335220-57335370	A549	lung:	n/a	chr12:57335245-57335263
12	CTCF	chr12:57335160-57335310	MCF-7	breast:	n/a	chr12:57335245-57335263
13	E2F6	chr12:57335075-57335537	A549	lung:	n/a	n/a
14	ELF1	chr12:57335426-57335784	HepG2	liver:	n/a	n/a
15	EP300	chr12:57335378-57335796	HepG2	liver:	n/a	chr12:57335536-57335545
16	EP300	chr12:57335307-57335951	HepG2	liver:	n/a	chr12:57335536-57335545
17	EP300	chr12:57335015-57335935	A549	lung:	n/a	chr12:57335536-57335545
18	EP300	chr12:57335363-57335889	HepG2	liver:	n/a	chr12:57335536-57335545
19	FOS	chr12:57335374-57335647	HUVEC	blood vessel:	n/a	chr12:57335536-57335544 chr12:57335536-57335544 chr12:57335534-57335545 chr12:57335534-57335546 chr12:57335486-57335493 chr12:57335536-57335543
20	FOS	chr12:57335012-57335705	MCF10A-Er-Src	breast:	n/a	chr12:57335146-57335157 chr12:57335536-57335544 chr12:57335536-57335544 chr12:57335150-57335159 chr12:57335534-57335545 chr12:57335534-57335546 chr12:57335486-57335493 chr12:57335536-57335543
21	FOS	chr12:57334975-57335757	MCF10A-Er-Src	breast:	n/a	chr12:57335146-57335157 chr12:57335536-57335544 chr12:57335536-57335544 chr12:57335150-57335159 chr12:57335534-57335545 chr12:57335534-57335546 chr12:57335486-57335493 chr12:57335536-57335543
22	FOS	chr12:57335014-57335640	MCF10A-Er-Src	breast:	n/a	chr12:57335146-57335157 chr12:57335536-57335544 chr12:57335536-57335544 chr12:57335150-57335159 chr12:57335534-57335545 chr12:57335534-57335546 chr12:57335486-57335493 chr12:57335536-57335543
23	FOS	chr12:57334976-57335779	MCF10A-Er-Src	breast:	n/a	chr12:57335146-57335157 chr12:57335536-57335544 chr12:57335536-57335544 chr12:57335150-57335159 chr12:57335534-57335545 chr12:57335534-57335546 chr12:57335486-57335493 chr12:57335536-57335543
24	FOSL1	chr12:57335053-57335285	K562	blood:	n/a	chr12:57335146-57335157 chr12:57335150-57335159
25	FOSL2	chr12:57335039-57335951	A549	lung:	n/a	chr12:57335146-57335157 chr12:57335536-57335544 chr12:57335536-57335544 chr12:57335150-57335159 chr12:57335534-57335546 chr12:57335486-57335493 chr12:57335536-57335543
26	FOSL2	chr12:57335076-57335727	A549	lung:	n/a	chr12:57335146-57335157 chr12:57335536-57335544 chr12:57335536-57335544 chr12:57335150-57335159 chr12:57335534-57335546 chr12:57335486-57335493 chr12:57335536-57335543
27	FOSL2	chr12:57334835-57335941	HepG2	liver:	n/a	chr12:57335146-57335157 chr12:57335536-57335544 chr12:57335536-57335544 chr12:57335150-57335159 chr12:57335534-57335546 chr12:57335486-57335493 chr12:57335536-57335543
28	FOSL2	chr12:57334848-57335861	HepG2	liver:	n/a	chr12:57335146-57335157 chr12:57335536-57335544 chr12:57335536-57335544 chr12:57335150-57335159 chr12:57335534-57335546 chr12:57335486-57335493 chr12:57335536-57335543
29	FOSL2	chr12:57335082-57335314	MCF-7	breast:	n/a	chr12:57335146-57335157 chr12:57335150-57335159
30	FOXA1	chr12:57335304-57335874	HepG2	liver:	n/a	n/a
31	FOXA1	chr12:57335390-57335946	HepG2	liver:	n/a	n/a
32	FOXA1	chr12:57335375-57335940	HepG2	liver:	n/a	n/a
33	FOXA1	chr12:57335339-57335885	HepG2	liver:	n/a	n/a
34	FOXA2	chr12:57334900-57335910	A549	lung:	n/a	n/a
35	FOXA2	chr12:57335403-57335871	HepG2	liver:	n/a	n/a
36	FOXA2	chr12:57335016-57335903	HepG2	liver:	n/a	n/a
37	FOXA2	chr12:57334987-57335788	A549	lung:	n/a	n/a
38	GATA3	chr12:57335233-57335755	T-47D	breast:	n/a	n/a
39	GATA3	chr12:57335306-57335775	MCF-7	breast:	n/a	n/a
40	HDAC2	chr12:57335296-57335866	HepG2	liver:	n/a	n/a
41	HDAC2	chr12:57335323-57335839	HepG2	liver:	n/a	n/a
42	HNF4A	chr12:57335390-57335903	HepG2	liver:	n/a	chr12:57335685-57335699 chr12:57335686-57335698 chr12:57335684-57335699 chr12:57335687-57335699
43	HNF4A	chr12:57335427-57335878	HepG2	liver:	n/a	chr12:57335685-57335699 chr12:57335686-57335698 chr12:57335684-57335699 chr12:57335687-57335699
44	HNF4A	chr12:57335388-57335852	HepG2	liver:	n/a	chr12:57335685-57335699 chr12:57335686-57335698 chr12:57335684-57335699 chr12:57335687-57335699
45	HNF4G	chr12:57335425-57335886	HepG2	liver:	n/a	chr12:57335685-57335699 chr12:57335683-57335698 chr12:57335686-57335698 chr12:57335687-57335699
46	HNF4G	chr12:57335374-57335939	HepG2	liver:	n/a	chr12:57335685-57335699 chr12:57335683-57335698 chr12:57335686-57335698 chr12:57335687-57335699
47	JUND	chr12:57334936-57335295	HepG2	liver:	n/a	chr12:57335146-57335157 chr12:57335150-57335159
48	JUND	chr12:57335356-57335823	HepG2	liver:	n/a	chr12:57335536-57335544 chr12:57335536-57335544 chr12:57335534-57335545 chr12:57335534-57335546 chr12:57335486-57335493 chr12:57335536-57335543
49	JUND	chr12:57334927-57335376	A549	lung:	n/a	chr12:57335146-57335157 chr12:57335150-57335159
50	JUND	chr12:57335011-57335232	HepG2	liver:	n/a	chr12:57335146-57335157 chr12:57335150-57335159

No.	Distal block	Cell Line	Cell type
1	chr12:57326664..57330911-chr12:57334392..57337503,4	K562	blood:
2	chr12:57330845..57332526-chr12:57336068..57338551,2	MCF-7	breast:
3	chr12:57323485..57328382-chr12:57328704..57333004,6	K562	blood:
4	chr12:57325326..57326887-chr12:57330449..57332916,2	K562	blood:
5	chr12:57325090..57327714-chr12:57331602..57333568,3	MCF-7	breast:
6	chr12:57322265..57324003-chr12:57330480..57332983,2	MCF-7	breast:
7	chr12:57326942..57329124-chr12:57333812..57335374,2	MCF-7	breast:
8	chr12:57333897..57335886-chr12:57347612..57349669,2	MCF-7	breast:

Variant related genes	Relation type
SDR9C7	TF binding region
ENSG00000170426	chromatin interactions

Extended variants
information (count: 116 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:116 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539010624	chr12:57332141-57332142	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs725958	chr12:57332158-57332159	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs11829786	chr12:57332232-57332233	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs566204811	chr12:57332245-57332246	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs372921009	chr12:57332258-57332259	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs554118494	chr12:57332272-57332273	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs575763710	chr12:57332275-57332276	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs71459395	chr12:57332289-57332290	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs148806077	chr12:57332326-57332327	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs61939618	chr12:57332357-57332358	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs558375533	chr12:57332404-57332405	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs576968822	chr12:57332490-57332491	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs540827471	chr12:57332524-57332525	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs571218837	chr12:57332559-57332560	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs559614574	chr12:57332627-57332628	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs369358548	chr12:57332629-57332630	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs574615066	chr12:57332634-57332635	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs543070541	chr12:57332658-57332659	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs561252569	chr12:57332676-57332677	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs531883892	chr12:57332704-57332705	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs550295305	chr12:57332732-57332733	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs376852369	chr12:57332806-57332807	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs532753145	chr12:57332880-57332881	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs186379132	chr12:57332892-57332893	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs28584593	chr12:57332916-57332917	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs147153116	chr12:57332930-57332931	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs547820624	chr12:57332940-57332941	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs28470625	chr12:57332983-57332984	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs28621466	chr12:57332984-57332985	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs1813815	chr12:57333077-57333078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs1813814	chr12:57333114-57333115	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs192397060	chr12:57333132-57333133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534838130	chr12:57333159-57333160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs428206	chr12:57333168-57333169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200182685	chr12:57333171-57333172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs552870062	chr12:57333213-57333214	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs1813813	chr12:57333225-57333226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs542138001	chr12:57333231-57333232	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561313407	chr12:57333236-57333237	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576508192	chr12:57333242-57333243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs543801059	chr12:57333243-57333244	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs565397484	chr12:57333244-57333245	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs532474576	chr12:57333260-57333261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548000745	chr12:57333292-57333293	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs182437048	chr12:57333306-57333307	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs1813812	chr12:57333395-57333396	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs548473918	chr12:57333440-57333441	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs143347904	chr12:57333443-57333444	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs187908094	chr12:57333458-57333459	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs190992255	chr12:57333508-57333509	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Bladder cancer	21909424	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Autism	20531469	CNVD
Rhabdomyosarcoma	16790082	CNVD
Renal cell carcinoma	18765545	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21138945	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glycogen storage disease	18421352	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:83 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:57325800-57335200	Weak transcription	Fetal Intestine Large	intestine
2	chr12:57326400-57335200	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr12:57327000-57335200	Weak transcription	Spleen	Spleen
4	chr12:57328200-57335000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr12:57329400-57335200	Weak transcription	A549	lung
6	chr12:57329800-57335000	Weak transcription	NHEK	skin
7	chr12:57330000-57334600	Weak transcription	HMEC	breast
8	chr12:57330000-57335200	Weak transcription	K562	blood
9	chr12:57330200-57335200	Weak transcription	Esophagus	oesophagus
10	chr12:57333000-57335000	Weak transcription	Liver	Liver
11	chr12:57333200-57333800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr12:57333200-57333800	Enhancers	HepG2	liver
13	chr12:57333800-57335000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr12:57333800-57335000	Weak transcription	HepG2	liver
15	chr12:57334600-57336400	Enhancers	HMEC	breast
16	chr12:57335000-57335200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr12:57335000-57335200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr12:57335000-57335200	Enhancers	Muscle Satellite Cultured Cells	--
19	chr12:57335000-57335200	Enhancers	HepG2	liver
20	chr12:57335000-57335200	Enhancers	NHEK	skin
21	chr12:57335000-57335600	Enhancers	GM12878-XiMat	blood
22	chr12:57335000-57336200	Enhancers	Skeletal Muscle Male	skeletal muscle
23	chr12:57335000-57336400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr12:57335000-57336400	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr12:57335000-57336400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr12:57335000-57336400	Enhancers	HSMM	muscle
27	chr12:57335000-57337200	Enhancers	Liver	Liver
28	chr12:57335200-57335400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr12:57335200-57335400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
30	chr12:57335200-57335400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr12:57335200-57335400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr12:57335200-57335400	Flanking Active TSS	Stomach Smooth Muscle	stomach
33	chr12:57335200-57335600	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr12:57335200-57335600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
35	chr12:57335200-57335600	Enhancers	Duodenum Mucosa	Duodenum
36	chr12:57335200-57335800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr12:57335200-57335800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr12:57335200-57335800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr12:57335200-57335800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr12:57335200-57335800	Enhancers	Right Atrium	heart
41	chr12:57335200-57335800	Enhancers	Sigmoid Colon	Sigmoid Colon
42	chr12:57335200-57335800	Flanking Active TSS	Hela-S3	cervix
43	chr12:57335200-57335800	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr12:57335200-57335800	Flanking Active TSS	NHEK	skin
45	chr12:57335200-57336000	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr12:57335200-57336000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr12:57335200-57336000	Enhancers	Primary monocytes fromperipheralblood	blood
48	chr12:57335200-57336000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr12:57335200-57336000	Enhancers	Adipose Nuclei	Adipose
50	chr12:57335200-57336000	Enhancers	Brain Inferior Temporal Lobe	brain

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