Variant report

Variant	nsv546900
Chromosome Location	chr1:102376258-102473559
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	BACH1	chr1:102462480-102462684	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr1:102419814-102420160	HepG2	liver:	n/a	chr1:102419972-102419983
3	CEBPB	chr1:102419855-102420123	A549	lung:	n/a	chr1:102419972-102419983
4	CEBPB	chr1:102426046-102426246	A549	lung:	n/a	n/a
5	CEBPB	chr1:102458888-102459025	H1-hESC	embryonic stem cell:	n/a	chr1:102458998-102459011 chr1:102458998-102459009
6	CEBPB	chr1:102447627-102447928	IMR90	lung:	n/a	n/a
7	CEBPB	chr1:102419871-102420030	K562	blood:	n/a	chr1:102419972-102419983
8	CEBPB	chr1:102383891-102384166	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr1:102458849-102459202	Hela-S3	cervix:	n/a	chr1:102458998-102459011 chr1:102458998-102459009
10	CEBPB	chr1:102419807-102420140	IMR90	lung:	n/a	chr1:102419972-102419983
11	CHD2	chr1:102462364-102462764	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTBP2	chr1:102462052-102462804	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr1:102436984-102437129	Gliobla	brain:	n/a	n/a
14	CTCF	chr1:102459363-102459505	Pancreas_OC	pancreas:	n/a	chr1:102459441-102459459 chr1:102459442-102459458 chr1:102459443-102459464
15	CTCF	chr1:102459320-102459470	HPAF	blood vessel:	n/a	chr1:102459441-102459459 chr1:102459442-102459458 chr1:102459443-102459464
16	CTCF	chr1:102436960-102437110	HRE	kidney:	n/a	n/a
17	CTCF	chr1:102437000-102437150	HMEC	breast:	n/a	n/a
18	CTCF	chr1:102403900-102404050	GM12869	blood:	n/a	n/a
19	CTCF	chr1:102437000-102437150	BE2_C	brain:	n/a	n/a
20	CTCF	chr1:102404014-102404116	GM12878	blood:	n/a	chr1:102404072-102404093 chr1:102404070-102404088
21	CTCF	chr1:102437000-102437150	GM12872	blood:	n/a	n/a
22	CTCF	chr1:102459440-102459590	HCPEpiC	choroid plexus:	n/a	chr1:102459441-102459459 chr1:102459442-102459458 chr1:102459443-102459464
23	CTCF	chr1:102436900-102437050	HRPEpiC	eye:	n/a	n/a
24	CTCF	chr1:102458840-102458990	BE2_C	brain:	n/a	n/a
25	CTCF	chr1:102462500-102462650	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr1:102437048-102437059	Medullo	brain:	n/a	n/a
27	CTCF	chr1:102436940-102437090	HEK293	kidney:	n/a	n/a
28	CTCF	chr1:102458912-102458960	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr1:102411580-102411730	GM12866	blood:	n/a	n/a
30	CTCF	chr1:102436954-102437084	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr1:102403941-102404201	GM12878	blood:	n/a	chr1:102404072-102404093 chr1:102404070-102404088
32	CTCF	chr1:102437000-102437150	GM06990	blood:	n/a	n/a
33	CTCF	chr1:102437060-102437210	MCF-7	breast:	n/a	n/a
34	CTCF	chr1:102436980-102437130	GM12864	blood:	n/a	n/a
35	CTCF	chr1:102404006-102404127	MCF-7	breast:	n/a	chr1:102404072-102404093 chr1:102404070-102404088
36	CTCF	chr1:102436980-102437130	HPAF	blood vessel:	n/a	n/a
37	CTCF	chr1:102404008-102404120	Pancreas_OC	pancreas:	n/a	chr1:102404072-102404093 chr1:102404070-102404088
38	CTCF	chr1:102436880-102437170	HCT-116	colon:	n/a	n/a
39	CTCF	chr1:102459420-102459570	HMF	breast:	n/a	chr1:102459441-102459459 chr1:102459442-102459458 chr1:102459443-102459464
40	CTCF	chr1:102459280-102459430	RPTEC	kidney:	n/a	n/a
41	CTCF	chr1:102436940-102437090	GM12873	blood:	n/a	n/a
42	CTCF	chr1:102437020-102437170	GM12866	blood:	n/a	n/a
43	CTCF	chr1:102436960-102437110	HMF	breast:	n/a	n/a
44	CTCF	chr1:102459328-102459531	H1-hESC	embryonic stem cell:	n/a	chr1:102459441-102459459 chr1:102459442-102459458 chr1:102459443-102459464
45	CTCF	chr1:102437041-102437067	ProgFib	skin:	n/a	n/a
46	CTCF	chr1:102403990-102404152	LNCaP	prostate:	n/a	chr1:102404072-102404093 chr1:102404070-102404088
47	CTCF	chr1:102436904-102437178	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr1:102459279-102459620	GM12878	blood:	n/a	chr1:102459441-102459459 chr1:102459442-102459458 chr1:102459443-102459464
49	CTCF	chr1:102437020-102437170	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr1:102436989-102437128	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:102462855-102462905	HRCEpiC	kidney:	n/a
2	chr1:102462632-102462682	SKMC	muscle:	n/a
3	chr1:102462855-102462905	HRCEpiC	kidney:	n/a
4	chr1:102462632-102462682	SKMC	muscle:	n/a
5	chr1:102462590-102462640	K562	blood:	n/a
6	chr1:102462682-102462732	LNCaP	prostate:	n/a
7	chr1:102462877-102462927	HCM	heart:	n/a
8	chr1:102462043-102462093	K562	blood:	n/a
9	chr1:102462855-102462905	Caco-2	colon:	n/a
10	chr1:102462590-102462640	HIPEpiC	eye:	n/a
11	chr1:102462043-102462093	GM12878	blood:	n/a
12	chr1:102462445-102462495	HepG2	liver:	n/a
13	chr1:102462590-102462640	SKMC	muscle:	n/a
14	chr1:102462656-102462706	BE2_C	brain:	n/a
15	chr1:102462877-102462927	MCF10A-Er-Src	breast:	n/a
16	chr1:102462445-102462495	LNCaP	prostate:	n/a
17	chr1:102462043-102462093	SKMC	muscle:	n/a
18	chr1:102462877-102462927	HRPEpiC	eye:	n/a
19	chr1:102462632-102462682	AoSMC	blood vessel:	n/a
20	chr1:102462590-102462640	CMK	blood:	n/a
21	chr1:102462043-102462093	AG04449	skin:	fetal
22	chr1:102462855-102462905	Hela-S3	cervix:	n/a
23	chr1:102462175-102462225	U87	brain:	n/a
24	chr1:102462806-102462856	H1-hESC	embryonic stem cell:	embryo
25	chr1:102462175-102462225	PANC-1	pancreas:	n/a
26	chr1:102462656-102462706	PFSK-1	brain:	n/a
27	chr1:102462175-102462225	AG04450	lung:	fetal
28	chr1:102462175-102462225	K562	blood:	n/a
29	chr1:102462445-102462495	PFSK-1	brain:	n/a
30	chr1:102462445-102462495	AG04450	lung:	fetal
31	chr1:102462632-102462682	HEEpiC	esophagus:	n/a
32	chr1:102462877-102462927	IMR90	lung:	fetal
33	chr1:102462806-102462856	HUVEC	blood vessel:	n/a
34	chr1:102462590-102462640	A549	lung:	n/a
35	chr1:102462821-102462871	NT2-D1	testis:	n/a
36	chr1:102462855-102462905	U87	brain:	n/a
37	chr1:102462682-102462732	HEEpiC	esophagus:	n/a
38	chr1:102462821-102462871	SK-N-MC	brain:	n/a
39	chr1:102462682-102462732	SAEC	small airway:	n/a
40	chr1:102462855-102462905	PrEC	prostate:	n/a
41	chr1:102462821-102462871	HAEpiC	amniotic membrane:	n/a
42	chr1:102462445-102462495	H1-hESC	embryonic stem cell:	embryo
43	chr1:102462043-102462093	HCPEpiC	choroid plexus:	n/a
44	chr1:102462855-102462905	HAEpiC	amniotic membrane:	n/a
45	chr1:102462877-102462927	NT2-D1	testis:	n/a
46	chr1:102462821-102462871	HRCEpiC	kidney:	n/a
47	chr1:102462175-102462225	SK-N-SH_RA	brain:	n/a
48	chr1:102462855-102462905	GM12891	blood:	n/a
49	chr1:102462682-102462732	HCF	heart:	n/a
50	chr1:102462855-102462905	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr1:102451706..102453377-chr1:102456104..102458404,2	K562	blood:
2	chr1:102456863..102457700-chr7:19592037..19592862,2	MCF-7	breast:
3	chr1:102434316..102436694-chr1:102437372..102439039,2	K562	blood:
4	chr1:102434316..102436694-chr1:102437372..102439039,2	K562	blood:
5	chr1:102451706..102453377-chr1:102456104..102458404,2	K562	blood:
6	chr1:102310233..102312368-chr1:102385841..102387762,2	MCF-7	breast:
7	chr1:102459133..102459923-chr1:102657241..102657780,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OLFM3-3	chr1:102437883-102438141	NONHSAT004870

Variant related genes	Relation type
OLFM3	TF binding region
OLFM3	CpG island

Extended variants
information (count: 1627 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:1627 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2000150	chr1:102376258-102376259	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs370314931	chr1:102376312-102376313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs576373787	chr1:102376320-102376321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs75307044	chr1:102376341-102376342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs141637730	chr1:102376355-102376356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs574285291	chr1:102376365-102376366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541604137	chr1:102376377-102376378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs577941058	chr1:102376383-102376384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs560010210	chr1:102376447-102376448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs114863771	chr1:102376460-102376461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs191002522	chr1:102376496-102376497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs560875454	chr1:102376524-102376525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs2000149	chr1:102376563-102376564	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs552774771	chr1:102376568-102376569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112146095	chr1:102376624-102376625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs549542950	chr1:102376625-102376626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs531246771	chr1:102376629-102376630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs568331753	chr1:102376643-102376644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs529169611	chr1:102376692-102376693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs547140948	chr1:102376700-102376701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs565545721	chr1:102376730-102376731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs539286954	chr1:102376731-102376732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs557826722	chr1:102376732-102376733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs570079185	chr1:102376738-102376739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537437142	chr1:102376755-102376756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs374718653	chr1:102376756-102376757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs143736170	chr1:102376844-102376845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs182477404	chr1:102376857-102376858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs368776121	chr1:102376877-102376878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs553565119	chr1:102376890-102376891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs578211608	chr1:102376891-102376892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs545666469	chr1:102376901-102376902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564188867	chr1:102376907-102376908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs576093634	chr1:102376908-102376909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs543374012	chr1:102376912-102376913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs368770315	chr1:102376919-102376920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs561527201	chr1:102376920-102376921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs148114675	chr1:102376921-102376922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs6662872	chr1:102377028-102377029	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs74107128	chr1:102377044-102377045	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs185779186	chr1:102377088-102377089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs368052355	chr1:102377090-102377091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs551320771	chr1:102377096-102377097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs370552615	chr1:102377117-102377118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs374570921	chr1:102377351-102377352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs6668325	chr1:102377413-102377414	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs549312999	chr1:102377423-102377424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs191467857	chr1:102377435-102377436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs141715523	chr1:102377526-102377527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs114288393	chr1:102377527-102377528	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:108)

Disease	PMID	Source
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
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	16774939	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Lung cancer	17086460	CNVD
Gastric cancer	16891809	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:193 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:102373200-102377000	Weak transcription	Fetal Heart	heart
2	chr1:102377000-102378000	Enhancers	Fetal Heart	heart
3	chr1:102378000-102379200	Weak transcription	Fetal Heart	heart
4	chr1:102379000-102379200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr1:102379200-102380200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr1:102379200-102382000	Enhancers	Fetal Heart	heart
7	chr1:102380200-102380400	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr1:102380200-102382000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr1:102380600-102385600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr1:102381400-102382000	Enhancers	Brain Germinal Matrix	brain
11	chr1:102384000-102384400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr1:102385200-102385600	Enhancers	Fetal Intestine Large	intestine
13	chr1:102385600-102386000	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr1:102385800-102386600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr1:102386000-102386400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr1:102386000-102386600	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr1:102394600-102394800	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr1:102394800-102399000	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr1:102395000-102395200	Enhancers	Fetal Intestine Large	intestine
20	chr1:102395200-102396800	Weak transcription	Fetal Intestine Large	intestine
21	chr1:102396800-102397600	Enhancers	Fetal Intestine Large	intestine
22	chr1:102396800-102397600	Enhancers	Fetal Intestine Small	intestine
23	chr1:102399000-102399800	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr1:102410600-102411400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr1:102410800-102411400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr1:102411600-102412000	Enhancers	Fetal Lung	lung
27	chr1:102416400-102417200	Enhancers	Stomach Mucosa	stomach
28	chr1:102419000-102420200	Enhancers	Fetal Heart	heart
29	chr1:102423800-102424600	Enhancers	Dnd41	blood
30	chr1:102424600-102424800	Flanking Active TSS	Dnd41	blood
31	chr1:102424600-102425200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr1:102424600-102425400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr1:102424800-102425000	Enhancers	Dnd41	blood
34	chr1:102425000-102425200	Enhancers	Brain Angular Gyrus	brain
35	chr1:102425000-102425200	Flanking Active TSS	Dnd41	blood
36	chr1:102425200-102426000	Weak transcription	Brain Angular Gyrus	brain
37	chr1:102425200-102426000	Enhancers	Dnd41	blood
38	chr1:102425200-102427200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr1:102425400-102427000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr1:102425600-102426000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr1:102426000-102426200	Enhancers	Brain Angular Gyrus	brain
42	chr1:102426000-102427200	Weak transcription	Dnd41	blood
43	chr1:102427000-102428200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr1:102427200-102427600	Enhancers	Dnd41	blood
45	chr1:102427200-102428000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr1:102427600-102429000	Weak transcription	Dnd41	blood
47	chr1:102428200-102430400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr1:102429000-102431400	Enhancers	Dnd41	blood
49	chr1:102429600-102432000	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr1:102429800-102432400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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