Variant report

Variant	nsv1040903
Chromosome Location	chr10:98986382-99047475
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	chr10:99038222-99039608	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:99038171-99038699	K562	blood:	n/a	n/a
3	ARID3A	chr10:98994217-98994515	HepG2	liver:	n/a	n/a
4	ATF3	chr10:99039088-99039522	K562	blood:	n/a	n/a
5	ATF3	chr10:99039246-99039441	K562	blood:	n/a	n/a
6	BACH1	chr10:99039478-99039637	K562	blood:	n/a	n/a
7	BACH1	chr10:99023131-99023176	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr10:98990092-98990302	GM12878	blood:	n/a	n/a
9	BRCA1	chr10:99038906-99039407	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr10:99030500-99030894	K562	blood:	n/a	n/a
11	CEBPB	chr10:99039156-99039429	ECC-1	luminal epithelium:	n/a	chr10:99039305-99039316
12	CEBPB	chr10:99039168-99039528	HepG2	liver:	n/a	chr10:99039305-99039316
13	CEBPB	chr10:99039139-99039498	HepG2	liver:	n/a	chr10:99039305-99039316
14	CEBPB	chr10:99039132-99039525	MCF-7	breast:	n/a	chr10:99039305-99039316
15	CEBPB	chr10:99039120-99039498	A549	lung:	n/a	chr10:99039305-99039316
16	CEBPB	chr10:99039120-99039504	HepG2	liver:	n/a	chr10:99039305-99039316
17	CEBPB	chr10:99039201-99039446	K562	blood:	n/a	chr10:99039305-99039316
18	CEBPB	chr10:99021342-99021463	K562	blood:	n/a	chr10:99021361-99021374 chr10:99021363-99021374
19	CEBPB	chr10:99039117-99039430	K562	blood:	n/a	chr10:99039305-99039316
20	CEBPB	chr10:99026991-99027231	HepG2	liver:	n/a	chr10:99027053-99027064
21	CEBPB	chr10:99038261-99038602	K562	blood:	n/a	n/a
22	CEBPB	chr10:98991022-98991230	K562	blood:	n/a	n/a
23	CEBPB	chr10:99026978-99027178	IMR90	lung:	n/a	chr10:99027053-99027064
24	CEBPB	chr10:99039163-99039409	HepG2	liver:	n/a	chr10:99039305-99039316
25	CEBPB	chr10:99027009-99027205	A549	lung:	n/a	chr10:99027053-99027064
26	CEBPB	chr10:99038918-99039616	A549	lung:	n/a	chr10:99039305-99039316
27	CEBPB	chr10:99039116-99039500	K562	blood:	n/a	chr10:99039305-99039316
28	CEBPB	chr10:99038323-99039525	Hela-S3	cervix:	n/a	chr10:99038662-99038673 chr10:99038662-99038673 chr10:99039305-99039316
29	CEBPB	chr10:99039123-99039497	IMR90	lung:	n/a	chr10:99039305-99039316
30	CEBPB	chr10:99039133-99039448	H1-hESC	embryonic stem cell:	n/a	chr10:99039305-99039316
31	CEBPB	chr10:99046182-99046360	HepG2	liver:	n/a	chr10:99046299-99046310
32	CEBPB	chr10:99039052-99039536	A549	lung:	n/a	chr10:99039305-99039316
33	CEBPD	chr10:99039199-99039407	HepG2	liver:	n/a	n/a
34	CEBPD	chr10:99039160-99039429	HepG2	liver:	n/a	n/a
35	CEBPD	chr10:99039079-99039547	K562	blood:	n/a	n/a
36	CEBPD	chr10:99039110-99039504	K562	blood:	n/a	n/a
37	CHD2	chr10:99039248-99039494	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr10:99038156-99038695	IMR90	lung:	n/a	chr10:99038419-99038437 chr10:99038420-99038436 chr10:99038424-99038432 chr10:99038421-99038442
39	CTCF	chr10:98994014-98994621	HCT-116	colon:	n/a	chr10:98994345-98994363 chr10:98994347-98994368 chr10:98994343-98994361 chr10:98994338-98994359
40	CTCF	chr10:98994280-98994430	GM12864	blood:	n/a	chr10:98994345-98994363 chr10:98994347-98994368 chr10:98994343-98994361 chr10:98994338-98994359
41	CTCF	chr10:98994221-98994472	GM12878	blood:	n/a	chr10:98994345-98994363 chr10:98994347-98994368 chr10:98994343-98994361 chr10:98994338-98994359
42	CTCF	chr10:98994280-98994430	GM06990	blood:	n/a	chr10:98994345-98994363 chr10:98994347-98994368 chr10:98994343-98994361 chr10:98994338-98994359
43	CTCF	chr10:98994540-98994690	GM12874	blood:	n/a	n/a
44	CTCF	chr10:98994360-98994510	RPTEC	kidney:	n/a	n/a
45	CTCF	chr10:98994260-98994410	HMF	breast:	n/a	chr10:98994345-98994363 chr10:98994347-98994368 chr10:98994343-98994361 chr10:98994338-98994359
46	CTCF	chr10:99038305-99038536	GM12878	blood:	n/a	chr10:99038419-99038437 chr10:99038420-99038436 chr10:99038424-99038432 chr10:99038421-99038442
47	CTCF	chr10:99038085-99038155	GM10266	blood:	n/a	n/a
48	CTCF	chr10:99038344-99038476	SK-N-SH_RA	brain:	n/a	chr10:99038419-99038437 chr10:99038420-99038436 chr10:99038424-99038432 chr10:99038421-99038442
49	CTCF	chr10:99038400-99038550	HRE	kidney:	n/a	chr10:99038419-99038437 chr10:99038420-99038436 chr10:99038424-99038432 chr10:99038421-99038442
50	CTCF	chr10:98994240-98994390	HVMF	connective:	n/a	chr10:98994345-98994363 chr10:98994347-98994368 chr10:98994343-98994361 chr10:98994338-98994359

No.	Distal block	Cell Line	Cell type
1	chr10:98980598..98984541-chr10:98986940..98989319,3	K562	blood:
2	chr10:98980948..98983777-chr10:98984731..98986586,2	K562	blood:
3	chr10:98970315..98970824-chr10:98993860..98994647,2	MCF-7	breast:
4	chr10:98970361..98971335-chr10:98994318..98994830,2	K562	blood:
5	chr10:98993826..98994564-chr10:99114704..99115929,4	MCF-7	breast:
6	chr10:99037958..99038944-chr10:99092338..99093941,8	MCF-7	breast:
7	chr10:98982062..98983736-chr10:98992807..98994462,2	K562	blood:
8	chr10:98994406..98995974-chr10:98996173..98997856,2	K562	blood:
9	chr10:99037940..99038860-chr10:99115149..99115993,4	MCF-7	breast:
10	chr10:99036915..99039794-chr10:99077195..99080138,2	MCF-7	breast:
11	chr10:98832712..98833218-chr10:98993851..98994375,2	MCF-7	breast:
12	chr10:98994406..98995974-chr10:98996173..98997856,2	K562	blood:
13	chr10:99002077..99004785-chr10:99007316..99010027,2	K562	blood:
14	chr10:99002077..99004456-chr10:99007278..99008816,2	K562	blood:
15	chr10:99019069..99020733-chr10:99024295..99026088,2	K562	blood:
16	chr10:98876999..98877834-chr10:98994252..98994779,2	MCF-7	breast:
17	chr10:99029216..99031729-chr10:99037036..99038703,2	K562	blood:
18	chr10:99028447..99031711-chr10:99092744..99094330,3	MCF-7	breast:
19	chr10:98986271..98988962-chr10:98994711..98997131,2	K562	blood:
20	chr10:99044514..99046643-chr10:99048334..99050746,3	K562	blood:
21	chr10:99019069..99020733-chr10:99024295..99026088,2	K562	blood:
22	chr10:99040697..99043641-chr10:99044330..99048505,4	K562	blood:
23	chr10:98976025..98978892-chr10:98984824..98987620,2	K562	blood:
24	chr10:99039203..99042240-chr10:99050005..99053012,5	K562	blood:
25	chr10:98986271..98988962-chr10:98994711..98997131,2	K562	blood:
26	chr10:99031855..99035094-chr10:99036519..99039061,3	K562	blood:
27	chr10:99030229..99033115-chr10:99036634..99039427,3	K562	blood:
28	chr10:99037600..99039792-chr10:99078754..99080411,2	K562	blood:
29	chr10:99038998..99042436-chr10:99050729..99053109,4	K562	blood:
30	chr10:99016160..99017870-chr10:99021990..99024984,2	MCF-7	breast:
31	chr10:99002077..99004785-chr10:99007316..99010027,2	K562	blood:
32	chr10:99034381..99036020-chr10:99036062..99037985,2	K562	blood:
33	chr10:99043100..99045603-chr10:99092696..99094572,2	MCF-7	breast:
34	chr10:99014050..99016184-chr10:99078788..99081522,2	K562	blood:
35	chr10:99040683..99043669-chr10:99044105..99045670,2	MCF-7	breast:
36	chr10:99002077..99004456-chr10:99007278..99008816,2	K562	blood:
37	chr10:99040697..99043641-chr10:99044330..99048505,4	K562	blood:
38	chr10:99038038..99038854-chr10:99093284..99094248,2	K562	blood:
39	chr10:99040683..99043669-chr10:99044105..99045670,2	MCF-7	breast:
40	chr10:99036931..99039171-chr10:99085750..99087329,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FRAT1-3	chr10:99037396-99037514	NONHSAT015852
2	lnc-FRAT1-3	chr10:99034769-99034864	NONHSAT015852
3	lnc-FRAT1-3	chr10:99037705-99037854	NONHSAT015852

Variant related genes	Relation type
ARHGAP19	TF binding region
ENSG00000231398	TF binding region
ENSG00000225850	chromatin interactions
ENSG00000231398	chromatin interactions
ENSG00000213390	chromatin interactions
ENSG00000165879	chromatin interactions
ENSG00000181274	chromatin interactions
ENSG00000269891	chromatin interactions

Extended variants
information (count: 2348 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:2348 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12244658	chr10:98986382-98986383	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs701820	chr10:98986472-98986473	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs534598277	chr10:98986494-98986495	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs553444532	chr10:98986519-98986520	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs578066455	chr10:98986526-98986527	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs372038936	chr10:98986566-98986567	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs545374312	chr10:98986590-98986591	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs11189044	chr10:98986624-98986625	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs11189045	chr10:98986666-98986667	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs148834885	chr10:98986686-98986687	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs543141704	chr10:98986691-98986692	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs561300285	chr10:98986723-98986724	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs11189046	chr10:98986754-98986755	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs116131019	chr10:98986797-98986798	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565193104	chr10:98986801-98986802	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs532776303	chr10:98986839-98986840	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs550928907	chr10:98986870-98986871	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs369426710	chr10:98986878-98986879	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs142502992	chr10:98986907-98986908	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs793518	chr10:98986970-98986971	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs72835306	chr10:98986988-98986989	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs78678772	chr10:98986999-98987000	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs567339585	chr10:98987041-98987042	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs534964321	chr10:98987059-98987060	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs562415893	chr10:98987060-98987061	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs553306085	chr10:98987117-98987118	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs116747972	chr10:98987196-98987197	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs528017029	chr10:98987201-98987202	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs150965243	chr10:98987294-98987295	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs547767482	chr10:98987311-98987312	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs111464059	chr10:98987315-98987316	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs552813716	chr10:98987323-98987324	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs371366614	chr10:98987371-98987372	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs570788355	chr10:98987399-98987400	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs575717780	chr10:98987407-98987408	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs190012870	chr10:98987419-98987420	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs550315743	chr10:98987429-98987430	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs555195104	chr10:98987445-98987446	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs140929805	chr10:98987458-98987459	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs183321287	chr10:98987488-98987489	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs793517	chr10:98987522-98987523	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs563352629	chr10:98987537-98987538	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs7088321	chr10:98987585-98987586	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs563122871	chr10:98987637-98987638	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs530670015	chr10:98987638-98987639	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs375547856	chr10:98987639-98987640	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs548801976	chr10:98987655-98987656	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs535046760	chr10:98987689-98987690	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs567305690	chr10:98987690-98987691	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs57924254	chr10:98987721-98987722	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Paraganglioma	17535989	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21364760	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Glioblastoma multiforme	22286061	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16912164	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Autosomal dominant partial epilepsy	18472482	CNVD
Breast cancer	16397240	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	22522925	CNVD
Ependymoma	20639864	CNVD
Lung adenocarcinoma	21935476	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1265 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:98972400-98988400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr10:98973800-99019000	Weak transcription	HepG2	liver
3	chr10:98976000-99011400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
4	chr10:98976400-98988200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr10:98976800-98988200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr10:98977200-99023800	Weak transcription	Colonic Mucosa	Colon
7	chr10:98977400-99027000	Weak transcription	Right Ventricle	heart
8	chr10:98978200-99003400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr10:98978200-99003600	Weak transcription	NHEK	skin
10	chr10:98978600-98988800	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr10:98978600-99019000	Weak transcription	HSMMtube	muscle
12	chr10:98978600-99030400	Weak transcription	NH-A	brain
13	chr10:98978600-99037400	Weak transcription	HSMM	muscle
14	chr10:98978600-99051800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr10:98979000-98990400	Strong transcription	Fetal Thymus	thymus
16	chr10:98979000-99027400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
17	chr10:98979200-98987200	Weak transcription	Fetal Intestine Large	intestine
18	chr10:98979400-98989600	Weak transcription	NHLF	lung
19	chr10:98979400-99000600	Strong transcription	Dnd41	blood
20	chr10:98979600-98990000	Strong transcription	Thymus	Thymus
21	chr10:98979600-99003400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr10:98980200-98987000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr10:98980200-98989600	Strong transcription	Primary T cells from cord blood	blood
24	chr10:98980200-98992800	Strong transcription	Primary T helper cells fromperipheralblood	blood
25	chr10:98980400-98988000	Weak transcription	Skeletal Muscle Female	skeletal muscle
26	chr10:98980600-98990400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr10:98980800-98987000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr10:98980800-98988800	Weak transcription	A549	lung
29	chr10:98981000-98987200	Strong transcription	Fetal Stomach	stomach
30	chr10:98981000-99018200	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr10:98981400-98989200	Strong transcription	Fetal Muscle Leg	muscle
32	chr10:98981400-98989600	Strong transcription	Primary hematopoietic stem cells	blood
33	chr10:98981400-98990400	Strong transcription	Fetal Muscle Trunk	muscle
34	chr10:98981400-99025400	Weak transcription	Colon Smooth Muscle	Colon
35	chr10:98982200-98988800	Strong transcription	Lung	lung
36	chr10:98982200-98990000	Strong transcription	Primary B cells from peripheral blood	blood
37	chr10:98982200-98990200	Strong transcription	Primary T cells fromperipheralblood	blood
38	chr10:98982200-98991600	Strong transcription	Primary B cells from cord blood	blood
39	chr10:98982400-98987200	Strong transcription	Duodenum Mucosa	Duodenum
40	chr10:98982400-98988600	Weak transcription	Fetal Kidney	kidney
41	chr10:98982400-98998800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr10:98982400-99003400	Weak transcription	Brain Inferior Temporal Lobe	brain
43	chr10:98982600-98987400	Strong transcription	GM12878-XiMat	blood
44	chr10:98982600-98992000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr10:98982600-98993200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr10:98982600-99007600	Weak transcription	Fetal Brain Female	brain
47	chr10:98982600-99007600	Weak transcription	Placenta	Placenta
48	chr10:98982600-99020800	Weak transcription	Brain Cingulate Gyrus	brain
49	chr10:98982800-98999200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr10:98983000-98986600	Weak transcription	Aorta	Aorta

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