Variant report

Variant	nsv871606
Chromosome Location	chr1:92444125-92538104
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	ARID3A	chr1:92504254-92504757	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:92463047-92463494	K562	blood:	n/a	n/a
3	ARID3A	chr1:92463265-92463529	HepG2	liver:	n/a	n/a
4	ATF1	chr1:92530637-92530857	K562	blood:	n/a	n/a
5	BACH1	chr1:92494875-92495995	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr1:92458760-92458932	K562	blood:	n/a	n/a
7	BRCA1	chr1:92495150-92495489	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr1:92456028-92456242	K562	blood:	n/a	chr1:92456098-92456109
9	CEBPB	chr1:92496162-92496469	IMR90	lung:	n/a	chr1:92496303-92496314
10	CEBPB	chr1:92504657-92504803	H1-hESC	embryonic stem cell:	n/a	chr1:92504690-92504701 chr1:92504689-92504700 chr1:92504689-92504702
11	CEBPB	chr1:92448101-92448201	K562	blood:	n/a	n/a
12	CEBPB	chr1:92504525-92504861	K562	blood:	n/a	chr1:92504690-92504701 chr1:92504689-92504700 chr1:92504689-92504702
13	CEBPB	chr1:92467135-92467242	HepG2	liver:	n/a	n/a
14	CEBPB	chr1:92455981-92456236	Hela-S3	cervix:	n/a	chr1:92456098-92456109
15	CEBPB	chr1:92479574-92479774	K562	blood:	n/a	chr1:92479683-92479694 chr1:92479681-92479694 chr1:92479681-92479694
16	CEBPB	chr1:92504114-92504877	HepG2	liver:	n/a	chr1:92504690-92504701 chr1:92504689-92504700 chr1:92504689-92504702
17	CEBPB	chr1:92504579-92504830	Hela-S3	cervix:	n/a	chr1:92504690-92504701 chr1:92504689-92504700 chr1:92504689-92504702
18	CEBPB	chr1:92517024-92517137	HepG2	liver:	n/a	chr1:92517083-92517094
19	CEBPB	chr1:92504503-92504863	IMR90	lung:	n/a	chr1:92504690-92504701 chr1:92504689-92504700 chr1:92504689-92504702
20	CEBPB	chr1:92455971-92456232	HepG2	liver:	n/a	chr1:92456098-92456109
21	CEBPB	chr1:92504509-92504831	A549	lung:	n/a	chr1:92504690-92504701 chr1:92504689-92504700 chr1:92504689-92504702
22	CHD1	chr1:92495834-92495836	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr1:92495204-92495535	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr1:92495929-92495950	HepG2	liver:	n/a	n/a
25	CREB1	chr1:92495385-92495616	A549	lung:	n/a	n/a
26	CTBP2	chr1:92495345-92496141	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr1:92495520-92495670	AG09309	skin:	n/a	n/a
28	CTCF	chr1:92530780-92530930	HFF-Myc	foreskin:	n/a	n/a
29	CTCF	chr1:92530760-92530910	GM06990	blood:	n/a	n/a
30	CTCF	chr1:92495840-92495990	HMEC	breast:	n/a	chr1:92495961-92495977 chr1:92495955-92495976 chr1:92495960-92495978
31	CTCF	chr1:92463240-92463390	Hela-S3	cervix:	n/a	chr1:92463357-92463378 chr1:92463355-92463373 chr1:92463356-92463372
32	CTCF	chr1:92463300-92463450	HUVEC	blood vessel:	n/a	chr1:92463357-92463378 chr1:92463355-92463373 chr1:92463356-92463372
33	CTCF	chr1:92495880-92496030	HA-sp	spinal cord:	n/a	chr1:92495961-92495977 chr1:92495955-92495976 chr1:92495960-92495978
34	CTCF	chr1:92530720-92530870	RPTEC	kidney:	n/a	n/a
35	CTCF	chr1:92495891-92496005	HepG2	liver:	n/a	chr1:92495961-92495977 chr1:92495955-92495976 chr1:92495960-92495978
36	CTCF	chr1:92495860-92496010	AG04450	lung:	n/a	chr1:92495961-92495977 chr1:92495955-92495976 chr1:92495960-92495978
37	CTCF	chr1:92495820-92495970	HVMF	connective:	n/a	n/a
38	CTCF	chr1:92463300-92463450	HepG2	liver:	n/a	chr1:92463357-92463378 chr1:92463355-92463373 chr1:92463356-92463372
39	CTCF	chr1:92463211-92463511	Medullo	brain:	n/a	chr1:92463357-92463378 chr1:92463355-92463373 chr1:92463356-92463372
40	CTCF	chr1:92495916-92496060	NHEK	skin:	n/a	chr1:92495961-92495977 chr1:92495955-92495976 chr1:92495960-92495978
41	CTCF	chr1:92463273-92463424	GM13976	blood:	n/a	chr1:92463357-92463378 chr1:92463355-92463373 chr1:92463356-92463372
42	CTCF	chr1:92463260-92463410	HAc	cerebellar:	n/a	chr1:92463357-92463378 chr1:92463355-92463373 chr1:92463356-92463372
43	CTCF	chr1:92530700-92530850	HepG2	liver:	n/a	n/a
44	CTCF	chr1:92463202-92463550	MCF-7	breast:	n/a	chr1:92463357-92463378 chr1:92463355-92463373 chr1:92463356-92463372
45	CTCF	chr1:92530700-92530850	HL-60	blood:	n/a	n/a
46	CTCF	chr1:92495920-92496070	AG04449	skin:	n/a	chr1:92495961-92495977 chr1:92495955-92495976 chr1:92495960-92495978
47	CTCF	chr1:92452970-92453049	GM20000	blood:	n/a	n/a
48	CTCF	chr1:92463260-92463410	GM12878	blood:	n/a	chr1:92463357-92463378 chr1:92463355-92463373 chr1:92463356-92463372
49	CTCF	chr1:92463280-92463430	GM12867	blood:	n/a	chr1:92463357-92463378 chr1:92463355-92463373 chr1:92463356-92463372
50	CTCF	chr1:92495540-92495690	NHEK	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:92495877-92495927	AG04449	skin:	fetal
2	chr1:92495877-92495927	AG04449	skin:	fetal
3	chr1:92495877-92495927	HCF	heart:	n/a
4	chr1:92495729-92495779	Hepatocyte	liver:	n/a
5	chr1:92495083-92495133	HAEpiC	amniotic membrane:	n/a
6	chr1:92495720-92495770	RPTEC	kidney:	n/a
7	chr1:92491486-92491536	SK-N-SH	brain:	n/a
8	chr1:92495004-92495054	NHDF-neo	bronchial:	n/a
9	chr1:92494898-92494948	AG10803	skin:	n/a
10	chr1:92495729-92495779	U87	brain:	n/a
11	chr1:92495877-92495927	SK-N-MC	brain:	n/a
12	chr1:92491486-92491536	ECC-1	luminal epithelium:	n/a
13	chr1:92494898-92494948	IMR90	lung:	fetal
14	chr1:92502933-92502983	HMEC	breast:	n/a
15	chr1:92495877-92495927	HPAEpiC	pulmonary alveolar:	n/a
16	chr1:92502933-92502983	HCT-116	colon:	n/a
17	chr1:92494898-92494948	AG04450	lung:	fetal
18	chr1:92495720-92495770	Hela-S3	cervix:	n/a
19	chr1:92495004-92495054	HCPEpiC	choroid plexus:	n/a
20	chr1:92495004-92495054	HepG2	liver:	n/a
21	chr1:92495877-92495927	HEEpiC	esophagus:	n/a
22	chr1:92495342-92495392	HNPCEpiC	eye:	n/a
23	chr1:92494898-92494948	RPTEC	kidney:	n/a
24	chr1:92495877-92495927	HCPEpiC	choroid plexus:	n/a
25	chr1:92495877-92495927	RPTEC	kidney:	n/a
26	chr1:92495004-92495054	HUVEC	blood vessel:	n/a
27	chr1:92494898-92494948	BE2_C	brain:	n/a
28	chr1:92494997-92495047	HRCEpiC	kidney:	n/a
29	chr1:92491486-92491536	Jurkat	blood:	n/a
30	chr1:92495720-92495770	NH-A	brain:	n/a
31	chr1:92495342-92495392	SK-N-MC	brain:	n/a
32	chr1:92494898-92494948	HMEC	breast:	n/a
33	chr1:92495004-92495054	Hela-S3	cervix:	n/a
34	chr1:92495720-92495770	SK-N-MC	brain:	n/a
35	chr1:92495720-92495770	HUVEC	blood vessel:	n/a
36	chr1:92495720-92495770	H1-hESC	embryonic stem cell:	embryo
37	chr1:92491486-92491536	SK-N-SH_RA	brain:	n/a
38	chr1:92495342-92495392	HRPEpiC	eye:	n/a
39	chr1:92495342-92495392	Hela-S3	cervix:	n/a
40	chr1:92495342-92495392	HCM	heart:	n/a
41	chr1:92494898-92494948	HRCEpiC	kidney:	n/a
42	chr1:92494997-92495047	NT2-D1	testis:	n/a
43	chr1:92495720-92495770	NHBE	bronchial:	n/a
44	chr1:92495818-92495868	PFSK-1	brain:	n/a
45	chr1:92495818-92495868	GM19239	blood:	n/a
46	chr1:92495004-92495054	GM06990	blood:	n/a
47	chr1:92491486-92491536	HCPEpiC	choroid plexus:	n/a
48	chr1:92495342-92495392	NB4	blood:	n/a
49	chr1:92495083-92495133	NHDF-neo	bronchial:	n/a
50	chr1:92495083-92495133	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:92529998..92532866-chr1:92545519..92547678,2	MCF-7	breast:
2	chr1:91964010..91966765-chr1:92464590..92467417,2	K562	blood:
3	chr1:92500741..92502488-chr1:92762793..92765174,2	MCF-7	breast:
4	chr1:92493964..92495908-chr1:92496400..92499100,2	K562	blood:
5	chr1:92535153..92538093-chr1:92546590..92548474,2	K562	blood:
6	chr1:92531679..92534472-chr1:92536505..92538325,2	K562	blood:
7	chr1:92494787..92497358-chr1:92544717..92548251,3	MCF-7	breast:
8	chr1:92463193..92463783-chr1:92756674..92757244,2	MCF-7	breast:
9	chr1:92519730..92522449-chr1:92522597..92525189,3	K562	blood:
10	chr1:92506546..92509433-chr1:92514602..92517083,2	K562	blood:
11	chr1:92532650..92534894-chr1:92538818..92540475,2	K562	blood:
12	chr1:92506546..92509433-chr1:92514602..92517083,2	K562	blood:
13	chr1:92519730..92522449-chr1:92522597..92525189,3	K562	blood:
14	chr1:92493964..92495908-chr1:92496400..92499100,2	K562	blood:
15	chr1:92490161..92492607-chr1:92493368..92497617,3	K562	blood:
16	chr1:92494741..92496705-chr1:92764193..92766152,2	MCF-7	breast:
17	chr1:92529291..92531947-chr1:92544374..92546080,2	K562	blood:

Variant related genes	Relation type
LPCAT2BP	TF binding region
EPHX4	TF binding region
LPCAT2BP	CpG island
EPHX4	CpG island
ENSG00000172031	chromatin interactions
ENSG00000233228	chromatin interactions
ENSG00000174842	chromatin interactions
ENSG00000097046	chromatin interactions
ENSG00000189195	chromatin interactions
ENSG00000122484	chromatin interactions

Extended variants
information (count: 1852 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1852 , 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	rs55912588	chr1:92446609-92446610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs141699970	chr1:92446633-92446634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs538375718	chr1:92446639-92446640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs368253715	chr1:92446645-92446646	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs372543134	chr1:92446674-92446675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs145962253	chr1:92446678-92446679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs376776587	chr1:92446700-92446701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs369332056	chr1:92446721-92446722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs199871085	chr1:92446731-92446732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs571751506	chr1:92446761-92446762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs376484719	chr1:92446764-92446765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs370704432	chr1:92446765-92446766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs372154804	chr1:92446783-92446784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs542747184	chr1:92446820-92446821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs374841922	chr1:92446859-92446860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs561241613	chr1:92446871-92446872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs146154567	chr1:92446887-92446888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs35327986	chr1:92446888-92446889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs34755513	chr1:92446891-92446892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs145501619	chr1:92446896-92446897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs543622557	chr1:92446905-92446906	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs564957587	chr1:92446918-92446919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs140949811	chr1:92446927-92446928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs148496128	chr1:92446961-92446962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs372503180	chr1:92446962-92446963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs201663866	chr1:92446977-92446978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs560563543	chr1:92446982-92446983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs35241748	chr1:92446985-92446986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs550426173	chr1:92447887-92447888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs3767855	chr1:92448017-92448018	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs565469419	chr1:92448036-92448037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs535988042	chr1:92448061-92448062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs79303785	chr1:92448127-92448128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs528177822	chr1:92448129-92448130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs537006412	chr1:92448188-92448189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs558940137	chr1:92448201-92448202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs374950160	chr1:92448308-92448309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs192498518	chr1:92448368-92448369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs553181705	chr1:92448385-92448386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs148720952	chr1:92464659-92464660	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs6699466	chr1:92464661-92464662	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs3767854	chr1:92464663-92464664	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs567882663	chr1:92464681-92464682	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs369329647	chr1:92464706-92464707	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs376320832	chr1:92464732-92464733	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs142256540	chr1:92464772-92464773	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs189889442	chr1:92464792-92464793	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs569717730	chr1:92464794-92464795	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs537046140	chr1:92464812-92464813	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs12751778	chr1:92464864-92464865	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	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
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
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	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
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	16397240	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Prostate cancer	19156837	CNVD
Autism	17483303	CNVD
Malignant melanoma	17260012	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:516 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92446600-92447000	Enhancers	Fetal Lung	lung
2	chr1:92447800-92448400	Enhancers	A549	lung
3	chr1:92481800-92482200	Enhancers	Dnd41	blood
4	chr1:92481800-92483800	Enhancers	Primary T cells from cord blood	blood
5	chr1:92482000-92482400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
6	chr1:92482000-92482400	Enhancers	Fetal Thymus	thymus
7	chr1:92482000-92482600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr1:92482000-92482800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr1:92482000-92483200	Enhancers	Primary T cells fromperipheralblood	blood
10	chr1:92482000-92483600	Enhancers	Primary T helper naive cells from peripheral blood	blood
11	chr1:92482000-92483600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
12	chr1:92482000-92483600	Enhancers	Primary T helper cells fromperipheralblood	blood
13	chr1:92482000-92483600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
14	chr1:92482000-92483600	Enhancers	Primary T killer memory cells from peripheral blood	blood
15	chr1:92482000-92483600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr1:92482000-92483800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
17	chr1:92482000-92483800	Enhancers	Primary T helper cells PMA-I stimulated	--
18	chr1:92482000-92484200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
19	chr1:92482200-92482400	Flanking Active TSS	Dnd41	blood
20	chr1:92482200-92482600	Enhancers	Primary hematopoietic stem cells	blood
21	chr1:92482200-92482800	Enhancers	Thymus	Thymus
22	chr1:92482200-92483800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
23	chr1:92482400-92482600	Enhancers	Dnd41	blood
24	chr1:92482400-92482800	Enhancers	K562	blood
25	chr1:92482400-92483600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
26	chr1:92482600-92482800	Flanking Active TSS	Dnd41	blood
27	chr1:92482600-92483000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr1:92482600-92483600	Weak transcription	Primary hematopoietic stem cells	blood
29	chr1:92482800-92483800	Enhancers	Dnd41	blood
30	chr1:92483000-92483600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr1:92483600-92483800	Enhancers	Primary hematopoietic stem cells	blood
32	chr1:92491200-92491400	Enhancers	Duodenum Smooth Muscle	Duodenum
33	chr1:92491400-92491800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr1:92491800-92495000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr1:92492400-92492600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr1:92492600-92492800	Enhancers	Brain Cingulate Gyrus	brain
37	chr1:92492600-92494800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr1:92492800-92494800	Weak transcription	Brain Cingulate Gyrus	brain
39	chr1:92493600-92493800	Enhancers	Lung	lung
40	chr1:92493800-92494800	Weak transcription	Lung	lung
41	chr1:92494200-92494400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
42	chr1:92494200-92494600	Enhancers	Dnd41	blood
43	chr1:92494400-92497600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
44	chr1:92494600-92494800	Active TSS	Brain Angular Gyrus	brain
45	chr1:92494600-92494800	Enhancers	Brain Substantia Nigra	brain
46	chr1:92494600-92495400	Flanking Active TSS	Dnd41	blood
47	chr1:92494800-92495000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
48	chr1:92494800-92495000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr1:92494800-92495000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
50	chr1:92494800-92495000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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