Variant report

Variant	nsv532548
Chromosome Location	chr1:103381480-103431911
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:120)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:120 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:103424463-103424755	HepG2	liver:	n/a	n/a
2	CEBPB	chr1:103420205-103420542	A549	lung:	n/a	chr1:103420350-103420361
3	CEBPB	chr1:103424437-103424754	HepG2	liver:	n/a	n/a
4	CEBPB	chr1:103385285-103385812	IMR90	lung:	n/a	chr1:103385694-103385707 chr1:103385696-103385707 chr1:103385694-103385707 chr1:103385696-103385707 chr1:103385694-103385707
5	CEBPB	chr1:103420192-103420551	H1-hESC	embryonic stem cell:	n/a	chr1:103420350-103420361
6	CEBPB	chr1:103420192-103420500	IMR90	lung:	n/a	chr1:103420350-103420361
7	CEBPB	chr1:103385312-103385827	Hela-S3	cervix:	n/a	chr1:103385694-103385707 chr1:103385696-103385707 chr1:103385694-103385707 chr1:103385696-103385707 chr1:103385694-103385707
8	CEBPB	chr1:103420187-103420500	HepG2	liver:	n/a	chr1:103420350-103420361
9	CTCF	chr1:103404270-103404339	Lung_OC	lung:	n/a	n/a
10	CTCF	chr1:103420312-103420383	GM13976	blood:	n/a	n/a
11	CTCF	chr1:103410720-103410870	HBMEC	blood vessel:	n/a	n/a
12	CTCF	chr1:103399020-103399170	HCPEpiC	choroid plexus:	n/a	n/a
13	E2F4	chr1:103391721-103392041	MCF10A-Er-Src	breast:	n/a	n/a
14	EP300	chr1:103402654-103404134	SK-N-SH	brain:	n/a	chr1:103403952-103403966 chr1:103403932-103403946
15	EP300	chr1:103417847-103418374	SK-N-SH	brain:	n/a	n/a
16	EP300	chr1:103406825-103407218	T-47D	breast:	n/a	n/a
17	EP300	chr1:103384984-103385814	SK-N-SH	brain:	n/a	chr1:103385436-103385450 chr1:103385695-103385709
18	EP300	chr1:103385321-103385668	Hela-S3	cervix:	n/a	chr1:103385436-103385450
19	EP300	chr1:103384937-103385818	SK-N-SH	brain:	n/a	chr1:103385436-103385450 chr1:103385695-103385709
20	EP300	chr1:103406716-103407287	T-47D	breast:	n/a	n/a
21	EP300	chr1:103385102-103385703	SK-N-SH_RA	brain:	n/a	chr1:103385436-103385450
22	EP300	chr1:103385078-103385617	SK-N-SH_RA	brain:	n/a	chr1:103385436-103385450
23	ESR1	chr1:103406768-103407279	T-47D	breast:	n/a	n/a
24	ESR1	chr1:103406728-103407404	T-47D	breast:	n/a	n/a
25	ESR1	chr1:103406782-103407188	T-47D	breast:	n/a	n/a
26	ESR1	chr1:103406772-103407223	T-47D	breast:	n/a	n/a
27	FOS	chr1:103385258-103385757	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr1:103385318-103385576	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr1:103385386-103385621	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr1:103382753-103382792	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr1:103385269-103385691	MCF10A-Er-Src	breast:	n/a	n/a
32	FOSL2	chr1:103385021-103385804	SK-N-SH	brain:	n/a	n/a
33	FOXA1	chr1:103406820-103407307	T-47D	breast:	n/a	n/a
34	FOXA1	chr1:103424505-103424771	HepG2	liver:	n/a	n/a
35	FOXA1	chr1:103406727-103407125	T-47D	breast:	n/a	n/a
36	FOXA1	chr1:103424493-103424884	HepG2	liver:	n/a	n/a
37	FOXA1	chr1:103424453-103424703	HepG2	liver:	n/a	n/a
38	FOXA2	chr1:103424503-103424716	HepG2	liver:	n/a	n/a
39	FOXA2	chr1:103398852-103399557	A549	lung:	n/a	n/a
40	FOXM1	chr1:103384951-103385913	SK-N-SH	brain:	n/a	n/a
41	GATA3	chr1:103406718-103407367	T-47D	breast:	n/a	n/a
42	GATA3	chr1:103406811-103408528	SK-N-SH	brain:	n/a	n/a
43	GATA3	chr1:103430147-103430311	SH-SY5Y	brain:	n/a	n/a
44	GATA3	chr1:103406873-103407620	SK-N-SH	brain:	n/a	n/a
45	GATA3	chr1:103406716-103407302	MCF-7	breast:	n/a	n/a
46	GATA3	chr1:103384169-103384732	SK-N-SH	brain:	n/a	n/a
47	GATA3	chr1:103406801-103407148	MCF-7	breast:	n/a	n/a
48	GATA3	chr1:103406789-103407261	MCF-7	breast:	n/a	n/a
49	GATA3	chr1:103384972-103385821	SK-N-SH	brain:	n/a	n/a
50	GATA3	chr1:103406743-103407489	T-47D	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:103399388-103399438	HAEpiC	amniotic membrane:	n/a
2	chr1:103399388-103399438	PANC-1	pancreas:	n/a
3	chr1:103399388-103399438	GM06990	blood:	n/a
4	chr1:103399388-103399438	IMR90	lung:	fetal
5	chr1:103399388-103399438	GM12892	blood:	n/a
6	chr1:103399388-103399438	GM19239	blood:	n/a
7	chr1:103399388-103399438	NH-A	brain:	n/a
8	chr1:103399388-103399438	HIPEpiC	eye:	n/a
9	chr1:103399388-103399438	HepG2	liver:	n/a
10	chr1:103399388-103399438	NHDF-neo	bronchial:	n/a
11	chr1:103399388-103399438	NT2-D1	testis:	n/a
12	chr1:103399388-103399438	HCPEpiC	choroid plexus:	n/a
13	chr1:103399388-103399438	ovcar-3	ovarian:	n/a
14	chr1:103399388-103399438	AG04449	skin:	fetal
15	chr1:103399388-103399438	HRPEpiC	eye:	n/a
16	chr1:103399388-103399438	H1-hESC	embryonic stem cell:	embryo
17	chr1:103399388-103399438	RPTEC	kidney:	n/a
18	chr1:103399388-103399438	U87	brain:	n/a
19	chr1:103399388-103399438	HEEpiC	esophagus:	n/a
20	chr1:103399388-103399438	HCM	heart:	n/a
21	chr1:103399388-103399438	A549	lung:	n/a
22	chr1:103399388-103399438	AG04450	lung:	fetal
23	chr1:103399388-103399438	HCT-116	colon:	n/a
24	chr1:103399388-103399438	GM12878	blood:	n/a
25	chr1:103399388-103399438	HRCEpiC	kidney:	n/a
26	chr1:103399388-103399438	HMEC	breast:	n/a
27	chr1:103399388-103399438	K562	blood:	n/a
28	chr1:103399388-103399438	Jurkat	blood:	n/a
29	chr1:103399388-103399438	AoSMC	blood vessel:	n/a
30	chr1:103399388-103399438	MCF-7	breast:	n/a
31	chr1:103399388-103399438	AG09309	skin:	n/a
32	chr1:103399388-103399438	HNPCEpiC	eye:	n/a
33	chr1:103399388-103399438	MCF10A-Er-Src	breast:	n/a
34	chr1:103399388-103399438	HCF	heart:	n/a
35	chr1:103399388-103399438	NHBE	bronchial:	n/a
36	chr1:103399388-103399438	SAEC	small airway:	n/a
37	chr1:103399388-103399438	SK-N-SH_RA	brain:	n/a
38	chr1:103399388-103399438	CMK	blood:	n/a
39	chr1:103399388-103399438	SK-N-SH	brain:	n/a
40	chr1:103399388-103399438	SK-N-MC	brain:	n/a
41	chr1:103399388-103399438	NB4	blood:	n/a
42	chr1:103399388-103399438	HL-60	blood:	n/a
43	chr1:103399388-103399438	HRE	kidney:	n/a
44	chr1:103399388-103399438	PrEC	prostate:	n/a
45	chr1:103399388-103399438	SKMC	muscle:	n/a
46	chr1:103399388-103399438	BE2_C	brain:	n/a
47	chr1:103399388-103399438	PFSK-1	brain:	n/a
48	chr1:103399388-103399438	HPAEpiC	pulmonary alveolar:	n/a
49	chr1:103399388-103399438	HUVEC	blood vessel:	n/a
50	chr1:103399388-103399438	GM12891	blood:	n/a

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:103426177..103428144-chr1:103433364..103435643,2	K562	blood:
2	chr1:103303886..103305574-chr1:103404633..103406434,2	MCF-7	breast:

No data

Variant related genes	Relation type
COL11A1	TF binding region
COL11A1	CpG island

Extended variants
information (count: 2130 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:2130 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535953642	chr1:103381484-103381485	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs572106287	chr1:103381565-103381566	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs114880683	chr1:103381574-103381575	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs140600505	chr1:103381652-103381653	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs538871549	chr1:103381681-103381682	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs557497627	chr1:103381689-103381690	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189544889	chr1:103381723-103381724	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs577598978	chr1:103381769-103381770	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs9434362	chr1:103381780-103381781	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs180791385	chr1:103381835-103381836	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs114030620	chr1:103381862-103381863	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs12124674	chr1:103381873-103381874	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs113529225	chr1:103381903-103381904	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561382117	chr1:103381906-103381907	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs1241167	chr1:103381957-103381958	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs1261689	chr1:103381986-103381987	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs564764030	chr1:103382014-103382015	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs117233300	chr1:103382061-103382062	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs532269983	chr1:103382120-103382121	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs12121979	chr1:103382158-103382159	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs144250826	chr1:103382232-103382233	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs190217425	chr1:103382239-103382240	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181759371	chr1:103382263-103382264	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs533003838	chr1:103382277-103382278	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs566524760	chr1:103382281-103382282	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs551300330	chr1:103382285-103382286	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs12125550	chr1:103382299-103382300	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs12125551	chr1:103382302-103382303	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs76338391	chr1:103382311-103382312	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs571106962	chr1:103382318-103382319	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs369072183	chr1:103382338-103382339	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs538531342	chr1:103382375-103382376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs3835567	chr1:103382380-103382381	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200454540	chr1:103382381-103382382	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs67248624	chr1:103382390-103382391	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs115798322	chr1:103382398-103382399	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs186117938	chr1:103382418-103382419	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs542180507	chr1:103382425-103382426	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs151130571	chr1:103382451-103382452	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12118250	chr1:103382456-103382457	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs12118259	chr1:103382532-103382533	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs564727677	chr1:103382533-103382534	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs140205410	chr1:103382553-103382554	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs544002436	chr1:103382557-103382558	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs369931618	chr1:103382569-103382570	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529958968	chr1:103382573-103382574	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs116706683	chr1:103382615-103382616	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs114281325	chr1:103382628-103382629	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs12133116	chr1:103382678-103382679	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs149895454	chr1:103382724-103382725	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
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	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
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
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Lung cancer	17086460	CNVD
Gastric cancer	16891809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:158 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:103345600-103385600	Weak transcription	HSMMtube	muscle
2	chr1:103352600-103403200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr1:103363600-103384400	Weak transcription	HSMM	muscle
4	chr1:103363800-103385400	Weak transcription	NH-A	brain
5	chr1:103369600-103498600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr1:103371200-103385000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr1:103376000-103385800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr1:103376200-103381600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr1:103376200-103382200	Strong transcription	Cortex derived primary cultured neurospheres	brain
10	chr1:103378800-103400000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr1:103380000-103399000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr1:103380200-103382000	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr1:103380400-103384400	Weak transcription	Osteobl	bone
14	chr1:103380400-103384600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr1:103380800-103393000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr1:103381200-103399400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr1:103381400-103385800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr1:103381600-103384400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr1:103382200-103393000	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr1:103384400-103384600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr1:103384400-103385800	Enhancers	HSMM	muscle
22	chr1:103384400-103386200	Enhancers	Muscle Satellite Cultured Cells	--
23	chr1:103384400-103386200	Enhancers	Osteobl	bone
24	chr1:103384400-103387400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr1:103384600-103385200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr1:103384600-103386200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr1:103385000-103387000	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr1:103385200-103386000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr1:103385400-103385600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr1:103385400-103386000	Enhancers	NH-A	brain
31	chr1:103385600-103385800	Enhancers	HSMMtube	muscle
32	chr1:103385600-103386000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr1:103385800-103386000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr1:103385800-103388800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr1:103385800-103401000	Weak transcription	HSMM	muscle
36	chr1:103386000-103386200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr1:103386000-103407000	Weak transcription	NH-A	brain
38	chr1:103386200-103393000	Weak transcription	Osteobl	bone
39	chr1:103386200-103399600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr1:103386200-103482000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr1:103387000-103394400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr1:103387400-103392800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr1:103388800-103392800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr1:103392800-103394200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr1:103392800-103394200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr1:103393000-103393400	Active TSS	Osteobl	bone
47	chr1:103393000-103393600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr1:103393000-103394200	Strong transcription	Cortex derived primary cultured neurospheres	brain
49	chr1:103393400-103393600	Flanking Active TSS	Osteobl	bone
50	chr1:103393600-103399200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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