Variant report

Variant	nsv872171
Chromosome Location	chr1:120093312-120126990
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	chr1:120125462-120125747	K562	blood:	n/a	n/a
2	ATF1	chr1:120096485-120096507	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	chr1:120107417-120107689	HepG2	liver:	n/a	chr1:120107566-120107577 chr1:120107585-120107598
8	CEBPB	chr1:120112658-120112932	K562	blood:	n/a	chr1:120112801-120112814
9	CEBPB	chr1:120123093-120123321	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr1:120112719-120112961	K562	blood:	n/a	chr1:120112801-120112814
11	CEBPB	chr1:120107540-120107630	K562	blood:	n/a	chr1:120107566-120107577 chr1:120107585-120107598
12	CTCF	chr1:120125520-120125670	GM12801	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
13	CTCF	chr1:120112880-120113030	GM12867	blood:	n/a	n/a
14	CTCF	chr1:120112900-120113050	WERI-Rb-1	eye:	n/a	n/a
15	CTCF	chr1:120125560-120125710	HVMF	connective:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
16	CTCF	chr1:120125544-120125727	Kidney_OC	kidney:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
17	CTCF	chr1:120125540-120125690	GM06990	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
18	CTCF	chr1:120125840-120125990	WERI-Rb-1	eye:	n/a	n/a
19	CTCF	chr1:120125540-120125690	AG04449	skin:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
20	CTCF	chr1:120125560-120125710	HEK293	kidney:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
21	CTCF	chr1:120125520-120125670	GM12867	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
22	CTCF	chr1:120125508-120125750	A549	lung:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
23	CTCF	chr1:120116620-120116770	SAEC	small airway:	n/a	n/a
24	CTCF	chr1:120125600-120125750	AG09309	skin:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
25	CTCF	chr1:120125492-120125745	MCF-7	breast:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
26	CTCF	chr1:120125532-120125689	Spleen_OC	spleen:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
27	CTCF	chr1:120125580-120125730	BJ	skin:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
28	CTCF	chr1:120125520-120125670	NHEK	skin:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
29	CTCF	chr1:120125540-120125690	AG04450	lung:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
30	CTCF	chr1:120125560-120125710	RPTEC	kidney:	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	chr1:120125560-120125710	GM12868	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
33	CTCF	chr1:120112982-120113171	Kidney_OC	kidney:	n/a	chr1:120113079-120113092 chr1:120113077-120113093 chr1:120113076-120113094 chr1:120113078-120113099
34	CTCF	chr1:120125560-120125710	NHLF	lung:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
35	CTCF	chr1:120125560-120125710	HRE	kidney:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
36	CTCF	chr1:120112970-120113169	Pancreas_OC	pancreas:	n/a	chr1:120113079-120113092 chr1:120113077-120113093 chr1:120113076-120113094 chr1:120113078-120113099
37	CTCF	chr1:120125520-120125670	AoAF	blood vessel:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
38	CTCF	chr1:120125560-120125710	GM12872	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
39	CTCF	chr1:120125508-120125722	MCF-7	breast:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
40	CTCF	chr1:120125500-120125650	GM12867	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
41	CTCF	chr1:120125548-120125725	H1-hESC	embryonic stem cell:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
42	CTCF	chr1:120125520-120125670	GM12875	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
43	CTCF	chr1:120112880-120113030	K562	blood:	n/a	n/a
44	CTCF	chr1:120125560-120125710	K562	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
45	CTCF	chr1:120125560-120125710	GM06990	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
46	CTCF	chr1:120125560-120125710	SK-N-SH_RA	brain:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
47	CTCF	chr1:120112942-120113208	GM19240	blood:	n/a	chr1:120113079-120113092 chr1:120113077-120113093 chr1:120113076-120113094 chr1:120113078-120113099
48	CTCF	chr1:120125620-120125770	GM12871	blood:	n/a	n/a
49	CTCF	chr1:120125580-120125730	HAc	cerebellar:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
50	CTCF	chr1:120125520-120125670	HCT-116	colon:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638

No.	Distal block	Cell Line	Cell type
1	chr1:120092305..120093953-chr1:120095014..120096664,2	MCF-7	breast:
2	chr1:120092305..120093953-chr1:120095014..120096664,2	MCF-7	breast:
3	chr1:120090713..120092396-chr1:120094225..120096675,2	MCF-7	breast:
4	chr1:120125219..120126121-chr1:120153919..120154547,2	MCF-7	breast:
5	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

Extended variants
information (count: 1420 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1420 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12059477	chr1:120093312-120093313	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs587771008	chr1:120093386-120093387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs75461075	chr1:120093422-120093423	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs67601577	chr1:120093431-120093432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs587611559	chr1:120093437-120093438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs200276473	chr1:120093438-120093439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs587676957	chr1:120093440-120093441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs116612468	chr1:120093499-120093500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs587765131	chr1:120093539-120093540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs587646436	chr1:120093577-120093578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs148432486	chr1:120093638-120093639	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs190960279	chr1:120093643-120093644	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs183411218	chr1:120093654-120093655	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs186586352	chr1:120093665-120093666	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs587597365	chr1:120093674-120093675	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs201661664	chr1:120093688-120093689	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs587673675	chr1:120093709-120093710	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs587731080	chr1:120093769-120093770	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs587603830	chr1:120093801-120093802	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs139022556	chr1:120093839-120093840	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs587658700	chr1:120093901-120093902	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs36082019	chr1:120093918-120093919	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs372436281	chr1:120093923-120093924	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs375654406	chr1:120093929-120093930	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs587734167	chr1:120094037-120094038	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs35032419	chr1:120094092-120094093	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs12064519	chr1:120094125-120094126	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs369553329	chr1:120094143-120094144	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs587756328	chr1:120094158-120094159	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs189908170	chr1:120094162-120094163	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs182969440	chr1:120094171-120094172	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs587770161	chr1:120094174-120094175	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs115731041	chr1:120094327-120094328	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs587702349	chr1:120094342-120094343	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs7537695	chr1:120094362-120094363	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs142540618	chr1:120094370-120094371	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs147562619	chr1:120094396-120094397	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs141956211	chr1:120094400-120094401	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs73001116	chr1:120094463-120094464	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs587703691	chr1:120094512-120094513	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs147846738	chr1:120094552-120094553	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs6428831	chr1:120094575-120094576	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs587741280	chr1:120094652-120094653	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs587619135	chr1:120094658-120094659	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs587697156	chr1:120094741-120094742	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs73001118	chr1:120094752-120094753	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs73001120	chr1:120094771-120094772	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs73001123	chr1:120094779-120094780	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs140331261	chr1:120094789-120094790	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs587622093	chr1:120094806-120094807	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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

Chromatin state (count:259 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:120082800-120096000	Weak transcription	Lung	lung
2	chr1:120084200-120095000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr1:120092400-120093600	Enhancers	Fetal Muscle Leg	muscle
4	chr1:120092400-120096000	Weak transcription	Fetal Heart	heart
5	chr1:120092400-120097000	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr1:120092400-120097200	Enhancers	Pancreas	Pancrea
7	chr1:120092600-120094000	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr1:120092600-120097800	Enhancers	Fetal Lung	lung
9	chr1:120092800-120093800	Weak transcription	Fetal Muscle Trunk	muscle
10	chr1:120092800-120094200	Weak transcription	Placenta	Placenta
11	chr1:120092800-120116600	Weak transcription	Spleen	Spleen
12	chr1:120093000-120096000	Weak transcription	Ovary	ovary
13	chr1:120093600-120093800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
14	chr1:120093600-120094200	Bivalent Enhancer	Fetal Muscle Leg	muscle
15	chr1:120093800-120094400	Enhancers	Fetal Muscle Trunk	muscle
16	chr1:120093800-120096400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr1:120094000-120094400	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr1:120094200-120094600	Bivalent Enhancer	HSMMtube	muscle
19	chr1:120094200-120097000	Enhancers	Placenta	Placenta
20	chr1:120094200-120098000	Enhancers	Fetal Muscle Leg	muscle
21	chr1:120094400-120095000	Weak transcription	Fetal Muscle Trunk	muscle
22	chr1:120094400-120095400	Enhancers	Primary B cells from peripheral blood	blood
23	chr1:120094400-120095800	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr1:120094400-120098000	Enhancers	Fetal Intestine Large	intestine
25	chr1:120094600-120095000	Bivalent Enhancer	HSMM	muscle
26	chr1:120094800-120098000	Enhancers	Fetal Intestine Small	intestine
27	chr1:120094800-120098800	Enhancers	HSMMtube	muscle
28	chr1:120095000-120095600	Enhancers	Fetal Muscle Trunk	muscle
29	chr1:120095000-120096400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr1:120095000-120097200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr1:120095000-120098000	Enhancers	HSMM	muscle
32	chr1:120095200-120096800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr1:120095400-120095800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
34	chr1:120095600-120096400	Weak transcription	Fetal Muscle Trunk	muscle
35	chr1:120095600-120097400	Enhancers	HMEC	breast
36	chr1:120095800-120097200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr1:120095800-120097200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr1:120095800-120099000	Weak transcription	Primary monocytes fromperipheralblood	blood
39	chr1:120096000-120096400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr1:120096000-120096800	Enhancers	HUVEC	blood vessel
41	chr1:120096000-120097200	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr1:120096000-120097200	Enhancers	Brain Germinal Matrix	brain
43	chr1:120096000-120097200	Enhancers	Lung	lung
44	chr1:120096000-120097200	Enhancers	Placenta Amnion	Placenta Amnion
45	chr1:120096000-120097200	Enhancers	K562	blood
46	chr1:120096000-120097400	Enhancers	Fetal Kidney	kidney
47	chr1:120096000-120097400	Enhancers	Ovary	ovary
48	chr1:120096000-120097400	Enhancers	NH-A	brain
49	chr1:120096000-120097600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr1:120096000-120097600	Enhancers	Liver	Liver

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