Variant report

Variant	nsv1011721
Chromosome Location	chr1:120115285-120149517
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	chr1:120144827-120145081	Hela-S3	cervix:	n/a	chr1:120144889-120144900
4	CEBPB	chr1:120123093-120123321	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr1:120144741-120145077	HepG2	liver:	n/a	chr1:120144889-120144900
6	CEBPB	chr1:120142586-120142702	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr1:120144744-120145076	A549	lung:	n/a	chr1:120144889-120144900
8	CEBPB	chr1:120144888-120144965	H1-hESC	embryonic stem cell:	n/a	chr1:120144889-120144900
9	CTCF	chr1:120125535-120125679	GM13977	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
10	CTCF	chr1:120125540-120125690	A549	lung:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
11	CTCF	chr1:120125493-120125751	HepG2	liver:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
12	CTCF	chr1:120125580-120125730	HAc	cerebellar:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
13	CTCF	chr1:120125540-120125690	WERI-Rb-1	eye:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
14	CTCF	chr1:120125840-120125990	WERI-Rb-1	eye:	n/a	n/a
15	CTCF	chr1:120125540-120125690	GM12875	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
16	CTCF	chr1:120125397-120125921	HCT-116	colon:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
17	CTCF	chr1:120125477-120125728	Medullo	brain:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
18	CTCF	chr1:120125522-120125733	MCF-7	breast:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
19	CTCF	chr1:120125520-120125670	AG04450	lung:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
20	CTCF	chr1:120125560-120125710	HRE	kidney:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
21	CTCF	chr1:120125560-120125710	HCM	heart:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
22	CTCF	chr1:120123419-120123501	Gliobla	brain:	n/a	n/a
23	CTCF	chr1:120125527-120125706	GM10266	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
24	CTCF	chr1:120125540-120125690	BJ	skin:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
25	CTCF	chr1:120125500-120125750	HUVEC	blood vessel:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
26	CTCF	chr1:120125700-120125850	A549	lung:	n/a	n/a
27	CTCF	chr1:120125580-120125730	GM12866	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
28	CTCF	chr1:120125529-120125716	Lung_OC	lung:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
29	CTCF	chr1:120125600-120125750	GM12873	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
30	CTCF	chr1:120125540-120125690	HEEpiC	esophagus:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
31	CTCF	chr1:120125560-120125710	GM12872	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
32	CTCF	chr1:120125692-120125695	GM10248	blood:	n/a	n/a
33	CTCF	chr1:120125820-120125970	GM12864	blood:	n/a	n/a
34	CTCF	chr1:120125433-120125948	A549	lung:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
35	CTCF	chr1:120125502-120125797	SK-N-SH_RA	brain:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
36	CTCF	chr1:120125580-120125730	GM12865	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
37	CTCF	chr1:120125560-120125710	RPTEC	kidney:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
38	CTCF	chr1:120125540-120125690	NB4	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
39	CTCF	chr1:120125560-120125710	GM06990	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
40	CTCF	chr1:120125560-120125710	Hela-S3	cervix:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
41	CTCF	chr1:120125433-120125813	K562	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
42	CTCF	chr1:120125532-120125689	Spleen_OC	spleen:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
43	CTCF	chr1:120125433-120125744	A549	lung:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
44	CTCF	chr1:120125394-120125831	MCF-7	breast:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
45	CTCF	chr1:120125520-120125670	HepG2	liver:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
46	CTCF	chr1:120125560-120125710	HA-sp	spinal cord:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
47	CTCF	chr1:120125508-120125722	MCF-7	breast:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
48	CTCF	chr1:120125560-120125710	HPF	lung:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
49	CTCF	chr1:120130436-120130484	GM13976	blood:	n/a	n/a
50	CTCF	chr1:120125600-120125750	HFF-Myc	foreskin:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:120143242-120143292	HNPCEpiC	eye:	n/a
2	chr1:120143242-120143292	HMEC	breast:	n/a
3	chr1:120143242-120143292	CMK	blood:	n/a
4	chr1:120143242-120143292	ECC-1	luminal epithelium:	n/a
5	chr1:120143242-120143292	HRPEpiC	eye:	n/a
6	chr1:120143242-120143292	BJ	skin:	n/a
7	chr1:120143242-120143292	AG04450	lung:	fetal
8	chr1:120143242-120143292	GM12878	blood:	n/a
9	chr1:120143242-120143292	IMR90	lung:	fetal
10	chr1:120143242-120143292	ovcar-3	ovarian:	n/a
11	chr1:120143242-120143292	SK-N-SH	brain:	n/a
12	chr1:120143242-120143292	RPTEC	kidney:	n/a
13	chr1:120143242-120143292	AG10803	skin:	n/a
14	chr1:120143242-120143292	NHBE	bronchial:	n/a
15	chr1:120143242-120143292	PFSK-1	brain:	n/a
16	chr1:120143242-120143292	U87	brain:	n/a
17	chr1:120143242-120143292	PrEC	prostate:	n/a
18	chr1:120143242-120143292	ProgFib	skin:	n/a
19	chr1:120143242-120143292	HEK293	kidney:	embryo
20	chr1:120143242-120143292	NB4	blood:	n/a
21	chr1:120143242-120143292	SK-N-MC	brain:	n/a
22	chr1:120143242-120143292	HCF	heart:	n/a
23	chr1:120143242-120143292	T-47D	breast:	n/a
24	chr1:120143242-120143292	AG09309	skin:	n/a
25	chr1:120143242-120143292	HUVEC	blood vessel:	n/a
26	chr1:120143242-120143292	GM06990	blood:	n/a
27	chr1:120143242-120143292	K562	blood:	n/a
28	chr1:120143242-120143292	SAEC	small airway:	n/a
29	chr1:120143242-120143292	AG09319	gingival:	n/a
30	chr1:120143242-120143292	Hela-S3	cervix:	n/a
31	chr1:120143242-120143292	PANC-1	pancreas:	n/a
32	chr1:120143242-120143292	HCPEpiC	choroid plexus:	n/a
33	chr1:120143242-120143292	GM12892	blood:	n/a
34	chr1:120143242-120143292	HAEpiC	amniotic membrane:	n/a
35	chr1:120143242-120143292	AoSMC	blood vessel:	n/a
36	chr1:120143242-120143292	A549	lung:	n/a
37	chr1:120143242-120143292	HRCEpiC	kidney:	n/a
38	chr1:120143242-120143292	HEEpiC	esophagus:	n/a
39	chr1:120143242-120143292	Hepatocyte	liver:	n/a
40	chr1:120143242-120143292	HCM	heart:	n/a
41	chr1:120143242-120143292	HCT-116	colon:	n/a
42	chr1:120143242-120143292	HL-60	blood:	n/a
43	chr1:120143242-120143292	Caco-2	colon:	n/a
44	chr1:120143242-120143292	NT2-D1	testis:	n/a
45	chr1:120143242-120143292	SK-N-SH_RA	brain:	n/a
46	chr1:120143242-120143292	MCF10A-Er-Src	breast:	n/a
47	chr1:120143242-120143292	H1-hESC	embryonic stem cell:	embryo
48	chr1:120143242-120143292	HPAEpiC	pulmonary alveolar:	n/a
49	chr1:120143242-120143292	HIPEpiC	eye:	n/a
50	chr1:120143242-120143292	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:120125219..120126121-chr1:120153919..120154547,2	MCF-7	breast:
2	chr1:120145059..120147660-chr1:120162749..120165475,2	MCF-7	breast:
3	chr1:120125200..120126107-chr1:120217588..120218409,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHGDH-1	chr1:120144910-120145118	ENSG00000242959.1
2	lnc-PHGDH-1	chr1:120143780-120144107	ENSG00000242959.1
3	lnc-ZNF697-1	chr1:120140325-120141914	NONHSAT005570
4	lnc-ZNF697-1	chr1:120140325-120141894	ENSG00000260941.1
5	lnc-ZNF697-3	chr1:120148999-120149695	NONHSAT005569

Variant related genes	Relation type
LINC00622	TF binding region
GAPDHP33	TF binding region
HSD3BP5	TF binding region
LINC00622	CpG island
GAPDHP33	CpG island
HSD3BP5	CpG island

Extended variants
information (count: 1437 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1437 , 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	rs6701437	chr1:120115285-120115286	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs114903844	chr1:120115314-120115315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs146449859	chr1:120115321-120115322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs140739037	chr1:120115336-120115337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs12134798	chr1:120115384-120115385	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs114200559	chr1:120115450-120115451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs74114706	chr1:120115521-120115522	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs149672812	chr1:120115526-120115527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs587670526	chr1:120115528-120115529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs587721982	chr1:120115560-120115561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs587630041	chr1:120115561-120115562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs587680950	chr1:120115573-120115574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs10802114	chr1:120115654-120115655	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs188909306	chr1:120115685-120115686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs181579282	chr1:120115696-120115697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs186079238	chr1:120115718-120115719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs4021423	chr1:120115723-120115724	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs4021424	chr1:120115735-120115736	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs189413621	chr1:120115811-120115812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs180739617	chr1:120115884-120115885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs587613697	chr1:120115911-120115912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs35329802	chr1:120115912-120115913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs587707791	chr1:120115951-120115952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs185892672	chr1:120115997-120115998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs147260819	chr1:120115998-120115999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs191213385	chr1:120116047-120116048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs6677352	chr1:120116050-120116051	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs116807750	chr1:120116090-120116091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs187981488	chr1:120116118-120116119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs182954375	chr1:120116121-120116122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs587731182	chr1:120116141-120116142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs6668773	chr1:120116142-120116143	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs587662582	chr1:120116146-120116147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs587762282	chr1:120116161-120116162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs4659016	chr1:120116183-120116184	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs11369983	chr1:120116199-120116200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs67357609	chr1:120116200-120116201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs55929656	chr1:120116201-120116202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs185735262	chr1:120116205-120116206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs587619568	chr1:120116224-120116225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs587697569	chr1:120116226-120116227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs190449065	chr1:120116242-120116243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs369197429	chr1:120116256-120116257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs587649515	chr1:120116329-120116330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs112910328	chr1:120116338-120116339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs587689989	chr1:120116380-120116381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs183101880	chr1:120116404-120116405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs138706145	chr1:120116431-120116432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs587727194	chr1:120116432-120116433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs587614766	chr1:120116433-120116434	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
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:286 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:120092800-120116600	Weak transcription	Spleen	Spleen
2	chr1:120109600-120117200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr1:120111800-120129800	Weak transcription	Left Ventricle	heart
4	chr1:120112000-120116400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr1:120112000-120129600	Weak transcription	Right Atrium	heart
6	chr1:120112400-120115400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr1:120112400-120116600	Weak transcription	Placenta	Placenta
8	chr1:120112800-120116600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr1:120113800-120115600	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr1:120113800-120116200	Weak transcription	Primary neutrophils fromperipheralblood	blood
11	chr1:120115200-120117400	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr1:120115200-120160800	Weak transcription	Gastric	stomach
13	chr1:120115400-120115600	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr1:120115600-120116000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr1:120115600-120117200	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr1:120116000-120117200	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr1:120116200-120117400	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr1:120116400-120117000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
19	chr1:120116600-120117000	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr1:120116600-120117000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr1:120116600-120117000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr1:120116600-120117000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr1:120116600-120117000	Enhancers	Placenta	Placenta
24	chr1:120116600-120117000	Enhancers	Spleen	Spleen
25	chr1:120116600-120117200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr1:120116600-120117200	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr1:120116600-120117200	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr1:120116800-120117000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr1:120117000-120128200	Weak transcription	Placenta	Placenta
30	chr1:120117000-120128600	Weak transcription	Spleen	Spleen
31	chr1:120117400-120125400	Weak transcription	Primary monocytes fromperipheralblood	blood
32	chr1:120122000-120129000	Weak transcription	Ovary	ovary
33	chr1:120123000-120123400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr1:120123000-120123400	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chr1:120123000-120123600	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr1:120123000-120123600	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr1:120123000-120123600	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr1:120123000-120123800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr1:120123200-120123600	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr1:120123200-120123800	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr1:120123600-120125400	Weak transcription	Monocytes-CD14+_RO01746	blood
42	chr1:120123800-120125200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr1:120123800-120128200	Weak transcription	Fetal Intestine Small	intestine
44	chr1:120125400-120125600	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr1:120125400-120125600	Bivalent Enhancer	HSMMtube	muscle
46	chr1:120125400-120126000	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr1:120125400-120128200	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr1:120125600-120126200	Enhancers	Fetal Stomach	stomach
49	chr1:120125600-120126400	Enhancers	Fetal Lung	lung
50	chr1:120125600-120126800	Enhancers	Fetal Muscle Leg	muscle

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