Variant report

Variant	nsv1004359
Chromosome Location	chr1:120109113-120140011
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	chr1:120125462-120125747	K562	blood:	n/a	n/a
2	BRCA1	chr1:120125543-120125709	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr1:120123093-120123321	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr1:120112658-120112932	K562	blood:	n/a	chr1:120112801-120112814
5	CEBPB	chr1:120112719-120112961	K562	blood:	n/a	chr1:120112801-120112814
6	CTCF	chr1:120125475-120125714	T-47D	breast:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
7	CTCF	chr1:120125520-120125670	NHEK	skin:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
8	CTCF	chr1:120125560-120125710	HA-sp	spinal cord:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
9	CTCF	chr1:120112880-120113030	HA-sp	spinal cord:	n/a	n/a
10	CTCF	chr1:120112900-120113050	NHEK	skin:	n/a	n/a
11	CTCF	chr1:120125438-120125821	IMR90	lung:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
12	CTCF	chr1:120123450-120123473	GM12892	blood:	n/a	n/a
13	CTCF	chr1:120125600-120125750	HFF-Myc	foreskin:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
14	CTCF	chr1:120125580-120125730	GM12865	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
15	CTCF	chr1:120125600-120125750	GM12866	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
16	CTCF	chr1:120125560-120125710	HVMF	connective:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
17	CTCF	chr1:120125459-120125732	GM20000	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
18	CTCF	chr1:120125529-120125716	Lung_OC	lung:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
19	CTCF	chr1:120125660-120125810	HAc	cerebellar:	n/a	n/a
20	CTCF	chr1:120125560-120125710	SK-N-SH_RA	brain:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
21	CTCF	chr1:120112880-120113030	GM12869	blood:	n/a	n/a
22	CTCF	chr1:120112970-120113169	Pancreas_OC	pancreas:	n/a	chr1:120113079-120113092 chr1:120113077-120113093 chr1:120113076-120113094 chr1:120113078-120113099
23	CTCF	chr1:120125508-120125750	A549	lung:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
24	CTCF	chr1:120125540-120125690	GM12873	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
25	CTCF	chr1:120125520-120125670	GM12872	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
26	CTCF	chr1:120112969-120113164	GM13976	blood:	n/a	chr1:120113079-120113092 chr1:120113077-120113093 chr1:120113076-120113094 chr1:120113078-120113099
27	CTCF	chr1:120113016-120113216	GM12878	blood:	n/a	chr1:120113079-120113092 chr1:120113077-120113093 chr1:120113076-120113094 chr1:120113078-120113099
28	CTCF	chr1:120112951-120113203	GM10266	blood:	n/a	chr1:120113079-120113092 chr1:120113077-120113093 chr1:120113076-120113094 chr1:120113078-120113099
29	CTCF	chr1:120125280-120125430	HAc	cerebellar:	n/a	n/a
30	CTCF	chr1:120125560-120125710	HCM	heart:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
31	CTCF	chr1:120112880-120113030	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr1:120125528-120125716	Pancreas_OC	pancreas:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
33	CTCF	chr1:120125547-120125719	GM12891	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
34	CTCF	chr1:120112969-120113220	GM13977	blood:	n/a	chr1:120113079-120113092 chr1:120113077-120113093 chr1:120113076-120113094 chr1:120113078-120113099
35	CTCF	chr1:120112949-120113249	GM12878	blood:	n/a	chr1:120113079-120113092 chr1:120113077-120113093 chr1:120113076-120113094 chr1:120113078-120113099
36	CTCF	chr1:120125541-120125710	GM19239	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
37	CTCF	chr1:120112946-120113208	LNCaP	prostate:	n/a	chr1:120113079-120113092 chr1:120113077-120113093 chr1:120113076-120113094 chr1:120113078-120113099
38	CTCF	chr1:120125540-120125690	GM12872	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
39	CTCF	chr1:120125540-120125690	WERI-Rb-1	eye:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
40	CTCF	chr1:120125236-120125917	SK-N-SH	brain:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
41	CTCF	chr1:120125513-120125735	GM19238	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
42	CTCF	chr1:120112880-120113030	GM12873	blood:	n/a	n/a
43	CTCF	chr1:120125600-120125750	HCM	heart:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
44	CTCF	chr1:120125502-120125797	SK-N-SH_RA	brain:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
45	CTCF	chr1:120125540-120125690	K562	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
46	CTCF	chr1:120112920-120113070	HFF	foreskin:	n/a	n/a
47	CTCF	chr1:120125520-120125670	HCT-116	colon:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
48	CTCF	chr1:120125520-120125670	HepG2	liver:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
49	CTCF	chr1:120125540-120125690	AG04450	lung:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
50	CTCF	chr1:120125540-120125690	RPTEC	kidney:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:120125219..120126121-chr1:120153919..120154547,2	MCF-7	breast:
2	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
GAPDHP33	TF binding region
HSD3BP5	TF binding region

Extended variants
information (count: 1430 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1430 , 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	rs2008921	chr1:120109113-120109114	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs587671109	chr1:120109158-120109159	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs151289092	chr1:120109205-120109206	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs587725817	chr1:120109215-120109216	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs140777463	chr1:120109242-120109243	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs587658685	chr1:120109249-120109250	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs41427946	chr1:120109260-120109261	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs185521376	chr1:120109262-120109263	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs587661938	chr1:120109327-120109328	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs368822370	chr1:120109391-120109392	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs587747147	chr1:120109407-120109408	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs587622501	chr1:120109409-120109410	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs587700159	chr1:120109410-120109411	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs190393324	chr1:120109426-120109427	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs587622987	chr1:120109430-120109431	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs587686379	chr1:120109431-120109432	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs587759045	chr1:120109434-120109435	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs17023666	chr1:120109464-120109465	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs587715548	chr1:120109468-120109469	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs587771543	chr1:120109475-120109476	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs587669007	chr1:120109488-120109489	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs587727477	chr1:120109533-120109534	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs12123783	chr1:120109563-120109564	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs376811469	chr1:120109566-120109567	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs587714758	chr1:120109629-120109630	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs180759898	chr1:120109634-120109635	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs113136554	chr1:120109664-120109665	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs587722774	chr1:120109714-120109715	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs112746379	chr1:120109724-120109725	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs411346	chr1:120109729-120109730	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs372144509	chr1:120109759-120109760	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs2008694	chr1:120109785-120109786	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs116407496	chr1:120109801-120109802	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs145589232	chr1:120109827-120109828	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs587657519	chr1:120109884-120109885	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs587741271	chr1:120109904-120109905	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs183725548	chr1:120109917-120109918	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs188397118	chr1:120109918-120109919	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs138147668	chr1:120109929-120109930	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs587645639	chr1:120109970-120109971	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs587703068	chr1:120110003-120110004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs115859093	chr1:120110043-120110044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs4659202	chr1:120110074-120110075	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs78170381	chr1:120110087-120110088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs4659203	chr1:120110104-120110105	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs149527681	chr1:120110173-120110174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs4659204	chr1:120110175-120110176	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs369220000	chr1:120110184-120110185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs181274546	chr1:120110187-120110188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs186515081	chr1:120110195-120110196	Weak transcription Enhancers	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:230 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:120092800-120116600	Weak transcription	Spleen	Spleen
2	chr1:120106800-120111600	Weak transcription	Lung	lung
3	chr1:120106800-120112400	Enhancers	Placenta	Placenta
4	chr1:120107000-120109200	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr1:120107000-120109200	Enhancers	Primary B cells from peripheral blood	blood
6	chr1:120107200-120110000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
7	chr1:120107200-120110600	Enhancers	HMEC	breast
8	chr1:120107400-120109400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr1:120107400-120109600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr1:120107400-120110600	Enhancers	NHEK	skin
11	chr1:120107600-120109200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr1:120107600-120111400	Weak transcription	Primary hematopoietic stem cells	blood
13	chr1:120107800-120111200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr1:120107800-120111600	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr1:120108000-120109200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr1:120108000-120110400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr1:120108000-120111200	Weak transcription	Fetal Lung	lung
18	chr1:120108000-120111600	Weak transcription	Right Atrium	heart
19	chr1:120108200-120109200	Enhancers	GM12878-XiMat	blood
20	chr1:120108600-120111200	Weak transcription	Primary B cells from cord blood	blood
21	chr1:120108800-120111000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr1:120108800-120111800	Weak transcription	Ovary	ovary
23	chr1:120109000-120109200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr1:120109200-120110400	Weak transcription	Primary neutrophils fromperipheralblood	blood
25	chr1:120109200-120111400	Weak transcription	Primary B cells from peripheral blood	blood
26	chr1:120109200-120111400	Weak transcription	GM12878-XiMat	blood
27	chr1:120109400-120110400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr1:120109600-120117200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr1:120110000-120110400	Enhancers	Monocytes-CD14+_RO01746	blood
30	chr1:120110400-120110600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr1:120110400-120110600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
32	chr1:120110400-120111400	Enhancers	Primary neutrophils fromperipheralblood	blood
33	chr1:120110400-120111600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr1:120110400-120112800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr1:120110600-120111000	Enhancers	Monocytes-CD14+_RO01746	blood
36	chr1:120110600-120111600	Weak transcription	NHEK	skin
37	chr1:120111000-120112400	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr1:120111000-120112400	Enhancers	Fetal Thymus	thymus
39	chr1:120111000-120112800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
40	chr1:120111200-120112000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
41	chr1:120111200-120112400	Enhancers	Primary B cells from cord blood	blood
42	chr1:120111200-120112600	Enhancers	Fetal Lung	lung
43	chr1:120111400-120112000	Enhancers	Primary B cells from peripheral blood	blood
44	chr1:120111400-120112200	Enhancers	Adipose Nuclei	Adipose
45	chr1:120111400-120112200	Enhancers	Placenta Amnion	Placenta Amnion
46	chr1:120111400-120112400	Enhancers	Primary hematopoietic stem cells	blood
47	chr1:120111400-120112400	Enhancers	GM12878-XiMat	blood
48	chr1:120111400-120112800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
49	chr1:120111600-120111800	Enhancers	Left Ventricle	heart
50	chr1:120111600-120111800	Enhancers	NHEK	skin

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