Variant report

Variant	nsv872177
Chromosome Location	chr1:120099980-120152082
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	chr1:120151890-120151896	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	chr1:120112658-120112932	K562	blood:	n/a	chr1:120112801-120112814
9	CEBPB	chr1:120144741-120145077	HepG2	liver:	n/a	chr1:120144889-120144900
10	CEBPB	chr1:120144827-120145081	Hela-S3	cervix:	n/a	chr1:120144889-120144900
11	CEBPB	chr1:120107417-120107689	HepG2	liver:	n/a	chr1:120107566-120107577 chr1:120107585-120107598
12	CEBPB	chr1:120144744-120145076	A549	lung:	n/a	chr1:120144889-120144900
13	CEBPB	chr1:120107540-120107630	K562	blood:	n/a	chr1:120107566-120107577 chr1:120107585-120107598
14	CEBPB	chr1:120142586-120142702	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr1:120112719-120112961	K562	blood:	n/a	chr1:120112801-120112814
16	CEBPB	chr1:120144888-120144965	H1-hESC	embryonic stem cell:	n/a	chr1:120144889-120144900
17	CTCF	chr1:120125560-120125710	HA-sp	spinal cord:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
18	CTCF	chr1:120125560-120125710	RPTEC	kidney:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
19	CTCF	chr1:120125433-120125813	K562	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
20	CTCF	chr1:120125509-120125738	K562	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
21	CTCF	chr1:120101225-120101337	GM10248	blood:	n/a	n/a
22	CTCF	chr1:120125560-120125710	HPAF	blood vessel:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
23	CTCF	chr1:120112880-120113030	GM12869	blood:	n/a	n/a
24	CTCF	chr1:120150122-120150232	HepG2	liver:	n/a	n/a
25	CTCF	chr1:120125541-120125710	GM19239	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
26	CTCF	chr1:120130140-120130290	HCPEpiC	choroid plexus:	n/a	chr1:120130214-120130223
27	CTCF	chr1:120125560-120125710	Caco-2	colon:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
28	CTCF	chr1:120149740-120149890	GM12872	blood:	n/a	n/a
29	CTCF	chr1:120125480-120125630	GM12864	blood:	n/a	n/a
30	CTCF	chr1:120125520-120125670	HepG2	liver:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
31	CTCF	chr1:120112880-120113030	GM12873	blood:	n/a	n/a
32	CTCF	chr1:120112954-120113194	NHEK	skin:	n/a	chr1:120113079-120113092 chr1:120113077-120113093 chr1:120113076-120113094 chr1:120113078-120113099
33	CTCF	chr1:120125580-120125730	HAc	cerebellar:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
34	CTCF	chr1:120130436-120130484	GM13976	blood:	n/a	n/a
35	CTCF	chr1:120123439-120123494	GM19240	blood:	n/a	n/a
36	CTCF	chr1:120112970-120113169	Pancreas_OC	pancreas:	n/a	chr1:120113079-120113092 chr1:120113077-120113093 chr1:120113076-120113094 chr1:120113078-120113099
37	CTCF	chr1:120125540-120125690	HA-sp	spinal cord:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
38	CTCF	chr1:120125580-120125730	Hela-S3	cervix:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
39	CTCF	chr1:120125540-120125690	HPAF	blood vessel:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
40	CTCF	chr1:120125520-120125670	Caco-2	colon:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
41	CTCF	chr1:120150112-120150355	HUVEC	blood vessel:	n/a	chr1:120150241-120150262 chr1:120150240-120150256 chr1:120150239-120150257 chr1:120150242-120150255
42	CTCF	chr1:120112860-120113010	A549	lung:	n/a	n/a
43	CTCF	chr1:120116620-120116770	SAEC	small airway:	n/a	n/a
44	CTCF	chr1:120125520-120125670	AG04450	lung:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
45	CTCF	chr1:120125540-120125690	HEEpiC	esophagus:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
46	CTCF	chr1:120113016-120113216	GM12878	blood:	n/a	chr1:120113079-120113092 chr1:120113077-120113093 chr1:120113076-120113094 chr1:120113078-120113099
47	CTCF	chr1:120125548-120125725	H1-hESC	embryonic stem cell:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
48	CTCF	chr1:120125547-120125719	GM12891	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
49	CTCF	chr1:120125520-120125670	GM12878	blood:	n/a	chr1:120125618-120125631 chr1:120125615-120125633 chr1:120125617-120125638
50	CTCF	chr1:120112880-120113030	HA-sp	spinal cord:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:120143242-120143292	ovcar-3	ovarian:	n/a
2	chr1:120143242-120143292	H1-hESC	embryonic stem cell:	embryo
3	chr1:120143242-120143292	NHDF-neo	bronchial:	n/a
4	chr1:120143242-120143292	SK-N-MC	brain:	n/a
5	chr1:120143242-120143292	GM12878	blood:	n/a
6	chr1:120143242-120143292	SAEC	small airway:	n/a
7	chr1:120143242-120143292	HAEpiC	amniotic membrane:	n/a
8	chr1:120143242-120143292	HRCEpiC	kidney:	n/a
9	chr1:120143242-120143292	HUVEC	blood vessel:	n/a
10	chr1:120143242-120143292	HEEpiC	esophagus:	n/a
11	chr1:120143242-120143292	Jurkat	blood:	n/a
12	chr1:120143242-120143292	CMK	blood:	n/a
13	chr1:120143242-120143292	NHBE	bronchial:	n/a
14	chr1:120143242-120143292	AoSMC	blood vessel:	n/a
15	chr1:120143242-120143292	T-47D	breast:	n/a
16	chr1:120143242-120143292	HCM	heart:	n/a
17	chr1:120143242-120143292	HEK293	kidney:	embryo
18	chr1:120143242-120143292	SK-N-SH_RA	brain:	n/a
19	chr1:120143242-120143292	HL-60	blood:	n/a
20	chr1:120143242-120143292	PFSK-1	brain:	n/a
21	chr1:120143242-120143292	HCT-116	colon:	n/a
22	chr1:120143242-120143292	MCF10A-Er-Src	breast:	n/a
23	chr1:120143242-120143292	Caco-2	colon:	n/a
24	chr1:120143242-120143292	U87	brain:	n/a
25	chr1:120143242-120143292	Hela-S3	cervix:	n/a
26	chr1:120143242-120143292	HRE	kidney:	n/a
27	chr1:120143242-120143292	K562	blood:	n/a
28	chr1:120143242-120143292	NT2-D1	testis:	n/a
29	chr1:120143242-120143292	MCF-7	breast:	n/a
30	chr1:120143242-120143292	HPAEpiC	pulmonary alveolar:	n/a
31	chr1:120143242-120143292	HCF	heart:	n/a
32	chr1:120143242-120143292	HMEC	breast:	n/a
33	chr1:120143242-120143292	AG04450	lung:	fetal
34	chr1:120143242-120143292	HNPCEpiC	eye:	n/a
35	chr1:120143242-120143292	PANC-1	pancreas:	n/a
36	chr1:120143242-120143292	LNCaP	prostate:	n/a
37	chr1:120143242-120143292	BE2_C	brain:	n/a
38	chr1:120143242-120143292	HIPEpiC	eye:	n/a
39	chr1:120143242-120143292	HRPEpiC	eye:	n/a
40	chr1:120143242-120143292	A549	lung:	n/a
41	chr1:120143242-120143292	NB4	blood:	n/a
42	chr1:120143242-120143292	GM12892	blood:	n/a
43	chr1:120143242-120143292	IMR90	lung:	fetal
44	chr1:120143242-120143292	AG04449	skin:	fetal
45	chr1:120143242-120143292	AG09319	gingival:	n/a
46	chr1:120143242-120143292	BJ	skin:	n/a
47	chr1:120143242-120143292	NH-A	brain:	n/a
48	chr1:120143242-120143292	RPTEC	kidney:	n/a
49	chr1:120143242-120143292	GM12891	blood:	n/a
50	chr1:120143242-120143292	GM06990	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:120091982..120092921-chr1:120150180..120150935,3	MCF-7	breast:
2	chr1:120145059..120147660-chr1:120162749..120165475,2	MCF-7	breast:
3	chr1:120125219..120126121-chr1:120153919..120154547,2	MCF-7	breast:
4	chr1:120125200..120126107-chr1:120217588..120218409,3	K562	blood:
5	chr1:120151431..120154337-chr1:120190081..120192940,2	MCF-7	breast:

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	chr1:120140325-120141894	ENSG00000260941.1
4	lnc-ZNF697-3	chr1:120148999-120149695	NONHSAT005569
5	lnc-ZNF697-3	chr1:120111655-120111668	NONHSAT005569
6	lnc-ZNF697-1	chr1:120140325-120141914	NONHSAT005570

Variant related genes	Relation type
HSD3BP4	TF binding region
GAPDHP27	TF binding region
LINC00622	TF binding region
GAPDHP33	TF binding region
HSD3BP5	TF binding region
HSD3BP4	CpG island
GAPDHP27	CpG island
LINC00622	CpG island
GAPDHP33	CpG island
HSD3BP5	CpG island
ENSG00000143067	chromatin interactions

Extended variants
information (count: 2213 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:2213 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4659200	chr1:120099980-120099981	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs587716487	chr1:120099981-120099982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs114376025	chr1:120099994-120099995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs143390859	chr1:120100005-120100006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs587607463	chr1:120100017-120100018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs148360922	chr1:120100018-120100019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs587740133	chr1:120100032-120100033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs587617215	chr1:120100048-120100049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs112735111	chr1:120100057-120100058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs587735066	chr1:120100058-120100059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs186085353	chr1:120100109-120100110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs587668266	chr1:120100112-120100113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs114816294	chr1:120100239-120100240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs587624476	chr1:120100265-120100266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs587703959	chr1:120100269-120100270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs587763786	chr1:120100452-120100453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs189399036	chr1:120100454-120100455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs587614088	chr1:120100464-120100465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs587689368	chr1:120100509-120100510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs587750926	chr1:120100560-120100561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs59209220	chr1:120100576-120100577	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs371392746	chr1:120100752-120100753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs587706591	chr1:120100770-120100771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs180729919	chr1:120100792-120100793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs4433446	chr1:120100827-120100828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs587760872	chr1:120100828-120100829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs587660182	chr1:120100851-120100852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs2018370	chr1:120100945-120100946	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs116529414	chr1:120100960-120100961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs587675213	chr1:120100990-120100991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs587705596	chr1:120101036-120101037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs587612012	chr1:120101045-120101046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs147174434	chr1:120101091-120101092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs72469591	chr1:120101096-120101097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs111577499	chr1:120101116-120101117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs113648083	chr1:120101153-120101154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs143802297	chr1:120101164-120101165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs186012382	chr1:120101180-120101181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs142733306	chr1:120101201-120101202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs587616053	chr1:120101202-120101203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs587692580	chr1:120101228-120101229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs190883301	chr1:120101247-120101248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs183258127	chr1:120101279-120101280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs375384721	chr1:120101384-120101385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs147354973	chr1:120101391-120101392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs138987780	chr1:120101407-120101408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs57709343	chr1:120101412-120101413	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs115379210	chr1:120101429-120101430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs60415998	chr1:120101480-120101481	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs149969949	chr1:120101510-120101511	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:431 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:120092800-120116600	Weak transcription	Spleen	Spleen
2	chr1:120097000-120105400	Weak transcription	Placenta	Placenta
3	chr1:120097200-120101200	Weak transcription	Pancreas	Pancrea
4	chr1:120097200-120107400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr1:120097600-120107400	Weak transcription	Brain Hippocampus Middle	brain
6	chr1:120097800-120100000	Weak transcription	Fetal Lung	lung
7	chr1:120098000-120100600	Weak transcription	Ovary	ovary
8	chr1:120100000-120100800	Enhancers	Fetal Lung	lung
9	chr1:120100600-120102200	Enhancers	Ovary	ovary
10	chr1:120100800-120105000	Weak transcription	Fetal Lung	lung
11	chr1:120102200-120105400	Weak transcription	Ovary	ovary
12	chr1:120103200-120103400	Enhancers	GM12878-XiMat	blood
13	chr1:120103400-120106600	Weak transcription	GM12878-XiMat	blood
14	chr1:120104000-120104200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr1:120104200-120105400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr1:120105000-120108000	Enhancers	Fetal Lung	lung
17	chr1:120105000-120108800	Enhancers	Fetal Intestine Large	intestine
18	chr1:120105200-120105800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr1:120105200-120108600	Enhancers	Fetal Intestine Small	intestine
20	chr1:120105400-120105800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr1:120105400-120105800	Enhancers	Placenta	Placenta
22	chr1:120105400-120106800	Enhancers	Ovary	ovary
23	chr1:120105600-120106400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr1:120105800-120106800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr1:120105800-120106800	Weak transcription	Placenta	Placenta
26	chr1:120106200-120106800	Enhancers	Fetal Stomach	stomach
27	chr1:120106200-120107200	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr1:120106200-120107400	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr1:120106600-120106800	Enhancers	Lung	lung
30	chr1:120106600-120106800	Enhancers	Right Atrium	heart
31	chr1:120106600-120107400	Enhancers	GM12878-XiMat	blood
32	chr1:120106800-120107000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr1:120106800-120107600	Weak transcription	Right Atrium	heart
34	chr1:120106800-120108600	Weak transcription	Ovary	ovary
35	chr1:120106800-120111600	Weak transcription	Lung	lung
36	chr1:120106800-120112400	Enhancers	Placenta	Placenta
37	chr1:120107000-120107400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr1:120107000-120107600	Enhancers	Primary hematopoietic stem cells	blood
39	chr1:120107000-120109200	Enhancers	Primary neutrophils fromperipheralblood	blood
40	chr1:120107000-120109200	Enhancers	Primary B cells from peripheral blood	blood
41	chr1:120107200-120108600	Enhancers	Primary B cells from cord blood	blood
42	chr1:120107200-120108600	Enhancers	Brain Substantia Nigra	brain
43	chr1:120107200-120110000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
44	chr1:120107200-120110600	Enhancers	HMEC	breast
45	chr1:120107400-120107800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
46	chr1:120107400-120107800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
47	chr1:120107400-120108000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr1:120107400-120108200	Flanking Active TSS	GM12878-XiMat	blood
49	chr1:120107400-120108600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr1:120107400-120108600	Enhancers	Brain Cingulate Gyrus	brain

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