Variant report

Variant	nsv1015031
Chromosome Location	chr1:120095922-120140011
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	chr1:120096485-120096507	K562	blood:	n/a	n/a
2	ATF1	chr1:120125462-120125747	K562	blood:	n/a	n/a
3	ATF2	chr1:120107169-120107553	GM12878	blood:	n/a	n/a
4	BATF	chr1:120107245-120107513	GM12878	blood:	n/a	n/a
5	BCL3	chr1:120107142-120107447	GM12878	blood:	n/a	chr1:120107299-120107308
6	BRCA1	chr1:120125543-120125709	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr1:120123093-120123321	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr1:120107540-120107630	K562	blood:	n/a	chr1:120107566-120107577 chr1:120107585-120107598
9	CEBPB	chr1:120107417-120107689	HepG2	liver:	n/a	chr1:120107566-120107577 chr1:120107585-120107598
10	CEBPB	chr1:120112719-120112961	K562	blood:	n/a	chr1:120112801-120112814
11	CEBPB	chr1:120112658-120112932	K562	blood:	n/a	chr1:120112801-120112814
12	CTCF	chr1:120112959-120113198	A549	lung:	n/a	chr1:120113079-120113092 chr1:120113077-120113093 chr1:120113076-120113094 chr1:120113078-120113099
13	CTCF	chr1:120125520-120125670	Caco-2	colon:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
14	CTCF	chr1:120112951-120113216	Gliobla	brain:	n/a	chr1:120113079-120113092 chr1:120113077-120113093 chr1:120113076-120113094 chr1:120113078-120113099
15	CTCF	chr1:120125560-120125710	GM06990	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
16	CTCF	chr1:120125540-120125690	GM12873	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
17	CTCF	chr1:120125580-120125730	BE2_C	brain:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
18	CTCF	chr1:120112989-120113061	SK-N-SH_RA	brain:	n/a	n/a
19	CTCF	chr1:120125560-120125710	SK-N-SH_RA	brain:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
20	CTCF	chr1:120125580-120125730	GM12874	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
21	CTCF	chr1:120112880-120113030	GM12870	blood:	n/a	n/a
22	CTCF	chr1:120125544-120125727	Kidney_OC	kidney:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
23	CTCF	chr1:120112900-120113050	GM12872	blood:	n/a	n/a
24	CTCF	chr1:120112880-120113030	GM12873	blood:	n/a	n/a
25	CTCF	chr1:120125520-120125670	AoAF	blood vessel:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
26	CTCF	chr1:120125540-120125690	WI-38	lung:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
27	CTCF	chr1:120125438-120125821	IMR90	lung:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
28	CTCF	chr1:120112955-120113100	H1-hESC	embryonic stem cell:	n/a	chr1:120113079-120113092 chr1:120113077-120113093 chr1:120113076-120113094 chr1:120113078-120113099
29	CTCF	chr1:120128467-120128522	GM13976	blood:	n/a	n/a
30	CTCF	chr1:120125476-120125869	MCF-7	breast:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
31	CTCF	chr1:120113012-120113216	K562	blood:	n/a	chr1:120113079-120113092 chr1:120113077-120113093 chr1:120113076-120113094 chr1:120113078-120113099
32	CTCF	chr1:120125445-120125799	K562	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
33	CTCF	chr1:120125580-120125730	HEEpiC	esophagus:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
34	CTCF	chr1:120125540-120125690	GM12878	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
35	CTCF	chr1:120125548-120125725	H1-hESC	embryonic stem cell:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
36	CTCF	chr1:120125540-120125690	HL-60	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
37	CTCF	chr1:120112900-120113050	HMEC	breast:	n/a	n/a
38	CTCF	chr1:120112880-120113030	GM12867	blood:	n/a	n/a
39	CTCF	chr1:120112942-120113208	GM19240	blood:	n/a	chr1:120113079-120113092 chr1:120113077-120113093 chr1:120113076-120113094 chr1:120113078-120113099
40	CTCF	chr1:120125560-120125710	HRE	kidney:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
41	CTCF	chr1:120112880-120113030	SAEC	small airway:	n/a	n/a
42	CTCF	chr1:120112972-120113135	A549	lung:	n/a	chr1:120113079-120113092 chr1:120113077-120113093 chr1:120113076-120113094 chr1:120113078-120113099
43	CTCF	chr1:120123434-120123473	GM12878	blood:	n/a	n/a
44	CTCF	chr1:120125560-120125710	NHEK	skin:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
45	CTCF	chr1:120112920-120113070	MCF-7	breast:	n/a	n/a
46	CTCF	chr1:120125532-120125689	Spleen_OC	spleen:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
47	CTCF	chr1:120125540-120125690	AG09309	skin:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
48	CTCF	chr1:120112920-120113070	HFF-Myc	foreskin:	n/a	n/a
49	CTCF	chr1:120125560-120125710	RPTEC	kidney:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
50	CTCF	chr1:120125458-120125732	LNCaP	prostate:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638

No.	Distal block	Cell Line	Cell type
1	chr1:120125219..120126121-chr1:120153919..120154547,2	MCF-7	breast:
2	chr1:120090713..120092396-chr1:120094225..120096675,2	MCF-7	breast:
3	chr1:120092305..120093953-chr1:120095014..120096664,2	MCF-7	breast:
4	chr1:120125200..120126107-chr1:120217588..120218409,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF697-3	chr1:120111655-120111668	NONHSAT005569

Variant related genes	Relation type
HSD3BP4	TF binding region
GAPDHP27	TF binding region
GAPDHP33	TF binding region
HSD3BP5	TF binding region

Extended variants
information (count: 1892 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1892 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17023814	chr1:120095922-120095923	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs587719407	chr1:120095967-120095968	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs587773395	chr1:120096002-120096003	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs587678337	chr1:120096010-120096011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs145910613	chr1:120096106-120096107	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs587768551	chr1:120096125-120096126	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs587643210	chr1:120096167-120096168	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs587704695	chr1:120096180-120096181	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs34709329	chr1:120096189-120096190	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs188270995	chr1:120096198-120096199	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs375057731	chr1:120096228-120096229	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs181053337	chr1:120096259-120096260	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs587720450	chr1:120096283-120096284	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs184585594	chr1:120096299-120096300	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs113599329	chr1:120096344-120096345	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs138490623	chr1:120096384-120096385	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs587734935	chr1:120096425-120096426	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs10157474	chr1:120096458-120096459	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs587657752	chr1:120096487-120096488	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs587743467	chr1:120096507-120096508	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs111810529	chr1:120096517-120096518	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs111727309	chr1:120096532-120096533	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs113352990	chr1:120096562-120096563	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs587715427	chr1:120096633-120096634	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs587746353	chr1:120096641-120096642	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs116070040	chr1:120096645-120096646	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs189932901	chr1:120096658-120096659	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs587765398	chr1:120096719-120096720	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs587640785	chr1:120096765-120096766	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs181523646	chr1:120096793-120096794	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs368291743	chr1:120096794-120096795	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs186906214	chr1:120096871-120096872	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs7539280	chr1:120096881-120096882	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs587710741	chr1:120096918-120096919	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs587603966	chr1:120096921-120096922	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs139830294	chr1:120096941-120096942	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs587742513	chr1:120097017-120097018	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs34361278	chr1:120097043-120097044	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs587604332	chr1:120097087-120097088	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs199880152	chr1:120097105-120097106	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs587698969	chr1:120097186-120097187	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs587756387	chr1:120097219-120097220	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs371042775	chr1:120097237-120097238	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs375124877	chr1:120097252-120097253	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs371813977	chr1:120097271-120097272	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs587725319	chr1:120097290-120097291	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs369253916	chr1:120097299-120097300	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs190613882	chr1:120097318-120097319	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs111499845	chr1:120097326-120097327	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs149495783	chr1:120097338-120097339	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
small cell lung cancer	20016488	CNVD
Aetanephric adenomas	20802469	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Systemic lupus erythematosus	21956041	CNVD
Breast cancer	21804112	CNVD
Mental retardation	21062444	CNVD
Myelofibrosis	22110671	CNVD
Emphysema	19352772	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21858162	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164920	CNVD
Cancer	21272361	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:357 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:120082800-120096000	Weak transcription	Lung	lung
2	chr1:120092400-120096000	Weak transcription	Fetal Heart	heart
3	chr1:120092400-120097000	Enhancers	Monocytes-CD14+_RO01746	blood
4	chr1:120092400-120097200	Enhancers	Pancreas	Pancrea
5	chr1:120092600-120097800	Enhancers	Fetal Lung	lung
6	chr1:120092800-120116600	Weak transcription	Spleen	Spleen
7	chr1:120093000-120096000	Weak transcription	Ovary	ovary
8	chr1:120093800-120096400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr1:120094200-120097000	Enhancers	Placenta	Placenta
10	chr1:120094200-120098000	Enhancers	Fetal Muscle Leg	muscle
11	chr1:120094400-120098000	Enhancers	Fetal Intestine Large	intestine
12	chr1:120094800-120098000	Enhancers	Fetal Intestine Small	intestine
13	chr1:120094800-120098800	Enhancers	HSMMtube	muscle
14	chr1:120095000-120096400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr1:120095000-120097200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr1:120095000-120098000	Enhancers	HSMM	muscle
17	chr1:120095200-120096800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr1:120095600-120096400	Weak transcription	Fetal Muscle Trunk	muscle
19	chr1:120095600-120097400	Enhancers	HMEC	breast
20	chr1:120095800-120097200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr1:120095800-120097200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr1:120095800-120099000	Weak transcription	Primary monocytes fromperipheralblood	blood
23	chr1:120096000-120096400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr1:120096000-120096800	Enhancers	HUVEC	blood vessel
25	chr1:120096000-120097200	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr1:120096000-120097200	Enhancers	Brain Germinal Matrix	brain
27	chr1:120096000-120097200	Enhancers	Lung	lung
28	chr1:120096000-120097200	Enhancers	Placenta Amnion	Placenta Amnion
29	chr1:120096000-120097200	Enhancers	K562	blood
30	chr1:120096000-120097400	Enhancers	Fetal Kidney	kidney
31	chr1:120096000-120097400	Enhancers	Ovary	ovary
32	chr1:120096000-120097400	Enhancers	NH-A	brain
33	chr1:120096000-120097600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr1:120096000-120097600	Enhancers	Liver	Liver
35	chr1:120096000-120097600	Enhancers	Fetal Heart	heart
36	chr1:120096000-120097800	Enhancers	Muscle Satellite Cultured Cells	--
37	chr1:120096200-120097200	Enhancers	Osteobl	bone
38	chr1:120096200-120097400	Enhancers	Right Atrium	heart
39	chr1:120096400-120096600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr1:120096400-120097000	Enhancers	Gastric	stomach
41	chr1:120096400-120097200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr1:120096400-120097200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr1:120096400-120097200	Enhancers	Brain Anterior Caudate	brain
44	chr1:120096400-120097200	Enhancers	Brain Substantia Nigra	brain
45	chr1:120096400-120097200	Enhancers	Fetal Stomach	stomach
46	chr1:120096400-120097400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr1:120096400-120097400	Enhancers	Brain Angular Gyrus	brain
48	chr1:120096400-120097400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
49	chr1:120096400-120097400	Enhancers	Fetal Muscle Trunk	muscle
50	chr1:120096400-120097400	Bivalent Enhancer	NHLF	lung

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