Variant report

Variant	esv33964
Chromosome Location	chr10:46205719-46224333
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	chr10:46210671-46210703	HepG2	liver:	n/a	n/a
2	ATF1	chr10:46222606-46222787	K562	blood:	n/a	n/a
3	ATF2	chr10:46222436-46222747	GM12878	blood:	n/a	n/a
4	ATF3	chr10:46222527-46222928	K562	blood:	n/a	chr10:46222627-46222647 chr10:46222653-46222662 chr10:46222638-46222647
5	ATF3	chr10:46222288-46222805	A549	lung:	n/a	chr10:46222627-46222647 chr10:46222512-46222526 chr10:46222653-46222662 chr10:46222638-46222647
6	ATF3	chr10:46222330-46222832	A549	lung:	n/a	chr10:46222627-46222647 chr10:46222512-46222526 chr10:46222653-46222662 chr10:46222638-46222647
7	ATF3	chr10:46222421-46222856	H1-hESC	embryonic stem cell:	n/a	chr10:46222627-46222647 chr10:46222512-46222526 chr10:46222653-46222662 chr10:46222638-46222647
8	ATF3	chr10:46222266-46222810	K562	blood:	n/a	chr10:46222627-46222647 chr10:46222512-46222526 chr10:46222653-46222662 chr10:46222638-46222647
9	ATF3	chr10:46222449-46222782	GM12878	blood:	n/a	chr10:46222627-46222647 chr10:46222512-46222526 chr10:46222653-46222662 chr10:46222638-46222647
10	ATF3	chr10:46222280-46222898	HepG2	liver:	n/a	chr10:46222627-46222647 chr10:46222512-46222526 chr10:46222653-46222662 chr10:46222638-46222647
11	ATF3	chr10:46222432-46222836	HepG2	liver:	n/a	chr10:46222627-46222647 chr10:46222512-46222526 chr10:46222653-46222662 chr10:46222638-46222647
12	ATF3	chr10:46222444-46222821	H1-hESC	embryonic stem cell:	n/a	chr10:46222627-46222647 chr10:46222512-46222526 chr10:46222653-46222662 chr10:46222638-46222647
13	ATF3	chr10:46222356-46222895	GM12878	blood:	n/a	chr10:46222627-46222647 chr10:46222512-46222526 chr10:46222653-46222662 chr10:46222638-46222647
14	BACH1	chr10:46220491-46220500	K562	blood:	n/a	n/a
15	BACH1	chr10:46221092-46221228	K562	blood:	n/a	n/a
16	BATF	chr10:46222438-46222799	GM12878	blood:	n/a	n/a
17	BATF	chr10:46222450-46222764	GM12878	blood:	n/a	n/a
18	BATF	chr10:46205693-46205968	GM12878	blood:	n/a	n/a
19	BCL11A	chr10:46205588-46206013	GM12878	blood:	n/a	chr10:46205926-46205935 chr10:46205854-46205863 chr10:46205633-46205642
20	BCL11A	chr10:46205665-46206042	GM12878	blood:	n/a	chr10:46205926-46205935 chr10:46205854-46205863
21	BCL11A	chr10:46222384-46222798	GM12878	blood:	n/a	chr10:46222539-46222548
22	BCL11A	chr10:46222511-46222718	GM12878	blood:	n/a	chr10:46222539-46222548
23	BCL3	chr10:46222272-46222864	A549	lung:	n/a	chr10:46222802-46222815 chr10:46222347-46222355 chr10:46222539-46222548
24	BCLAF1	chr10:46222444-46222833	GM12878	blood:	n/a	chr10:46222802-46222815 chr10:46222539-46222548
25	BHLHE40	chr10:46222242-46222941	K562	blood:	n/a	chr10:46222638-46222647 chr10:46222651-46222664 chr10:46222474-46222490 chr10:46222637-46222646 chr10:46222653-46222662 chr10:46222616-46222637 chr10:46222636-46222649 chr10:46222632-46222653 chr10:46222620-46222633 chr10:46222639-46222648 chr10:46222653-46222662 chr10:46222652-46222661 chr10:46222638-46222647
26	BHLHE40	chr10:46205776-46206049	HepG2	liver:	n/a	n/a
27	BHLHE40	chr10:46222352-46222834	HepG2	liver:	n/a	chr10:46222638-46222647 chr10:46222651-46222664 chr10:46222474-46222490 chr10:46222637-46222646 chr10:46222653-46222662 chr10:46222616-46222637 chr10:46222636-46222649 chr10:46222632-46222653 chr10:46222620-46222633 chr10:46222639-46222648 chr10:46222653-46222662 chr10:46222652-46222661 chr10:46222638-46222647
28	BHLHE40	chr10:46222520-46222798	HepG2	liver:	n/a	chr10:46222638-46222647 chr10:46222651-46222664 chr10:46222637-46222646 chr10:46222653-46222662 chr10:46222616-46222637 chr10:46222636-46222649 chr10:46222632-46222653 chr10:46222620-46222633 chr10:46222639-46222648 chr10:46222653-46222662 chr10:46222652-46222661 chr10:46222638-46222647
29	BHLHE40	chr10:46221133-46221274	K562	blood:	n/a	n/a
30	BHLHE40	chr10:46222427-46222809	A549	lung:	n/a	chr10:46222638-46222647 chr10:46222651-46222664 chr10:46222474-46222490 chr10:46222637-46222646 chr10:46222653-46222662 chr10:46222616-46222637 chr10:46222636-46222649 chr10:46222632-46222653 chr10:46222620-46222633 chr10:46222639-46222648 chr10:46222653-46222662 chr10:46222652-46222661 chr10:46222638-46222647
31	BHLHE40	chr10:46222387-46222921	HepG2	liver:	n/a	chr10:46222638-46222647 chr10:46222651-46222664 chr10:46222474-46222490 chr10:46222637-46222646 chr10:46222653-46222662 chr10:46222616-46222637 chr10:46222636-46222649 chr10:46222632-46222653 chr10:46222620-46222633 chr10:46222639-46222648 chr10:46222653-46222662 chr10:46222652-46222661 chr10:46222638-46222647
32	BHLHE40	chr10:46222398-46222891	GM12878	blood:	n/a	chr10:46222638-46222647 chr10:46222651-46222664 chr10:46222474-46222490 chr10:46222637-46222646 chr10:46222653-46222662 chr10:46222616-46222637 chr10:46222636-46222649 chr10:46222632-46222653 chr10:46222620-46222633 chr10:46222639-46222648 chr10:46222653-46222662 chr10:46222652-46222661 chr10:46222638-46222647
33	BHLHE40	chr10:46206838-46207055	HepG2	liver:	n/a	n/a
34	BRCA1	chr10:46222591-46222722	Hela-S3	cervix:	n/a	n/a
35	CBX3	chr10:46222391-46222783	K562	blood:	n/a	n/a
36	CBX3	chr10:46221958-46223080	K562	blood:	n/a	n/a
37	CCNT2	chr10:46222610-46222780	K562	blood:	n/a	n/a
38	CEBPB	chr10:46222529-46222788	GM12878	blood:	n/a	n/a
39	CEBPB	chr10:46205793-46205994	IMR90	lung:	n/a	n/a
40	CEBPB	chr10:46222610-46222629	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr10:46222332-46222771	K562	blood:	n/a	n/a
42	CEBPB	chr10:46222311-46222916	GM12878	blood:	n/a	n/a
43	CEBPB	chr10:46205866-46205983	HepG2	liver:	n/a	n/a
44	CEBPD	chr10:46222336-46222870	K562	blood:	n/a	n/a
45	CEBPD	chr10:46222498-46222784	HepG2	liver:	n/a	n/a
46	CHD1	chr10:46222585-46222800	GM12878	blood:	n/a	n/a
47	CHD2	chr10:46222545-46222794	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr10:46222583-46222714	K562	blood:	n/a	n/a
49	CHD2	chr10:46222521-46222718	GM12878	blood:	n/a	n/a
50	CREB1	chr10:46222319-46222889	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:46222272-46222322	AG09319	gingival:	n/a
2	chr10:46222272-46222322	AG09319	gingival:	n/a
3	chr10:46221254-46221304	HNPCEpiC	eye:	n/a
4	chr10:46221684-46221734	HRPEpiC	eye:	n/a
5	chr10:46219381-46219431	HMEC	breast:	n/a
6	chr10:46222480-46222530	AG04449	skin:	fetal
7	chr10:46223127-46223177	HCPEpiC	choroid plexus:	n/a
8	chr10:46222487-46222537	ECC-1	luminal epithelium:	n/a
9	chr10:46221684-46221734	PANC-1	pancreas:	n/a
10	chr10:46219381-46219431	HRE	kidney:	n/a
11	chr10:46222474-46222524	HCT-116	colon:	n/a
12	chr10:46222272-46222322	PANC-1	pancreas:	n/a
13	chr10:46222875-46222925	HNPCEpiC	eye:	n/a
14	chr10:46222487-46222537	NHDF-neo	bronchial:	n/a
15	chr10:46221225-46221275	BE2_C	brain:	n/a
16	chr10:46222657-46222707	SK-N-SH	brain:	n/a
17	chr10:46223127-46223177	Jurkat	blood:	n/a
18	chr10:46221684-46221734	ProgFib	skin:	n/a
19	chr10:46222487-46222537	PANC-1	pancreas:	n/a
20	chr10:46221282-46221332	AG09319	gingival:	n/a
21	chr10:46221684-46221734	Hepatocyte	liver:	n/a
22	chr10:46221282-46221332	HEK293	kidney:	embryo
23	chr10:46222272-46222322	HAEpiC	amniotic membrane:	n/a
24	chr10:46222272-46222322	GM19239	blood:	n/a
25	chr10:46221684-46221734	HUVEC	blood vessel:	n/a
26	chr10:46222474-46222524	T-47D	breast:	n/a
27	chr10:46221254-46221304	SK-N-MC	brain:	n/a
28	chr10:46217976-46218026	Hela-S3	cervix:	n/a
29	chr10:46222272-46222322	PrEC	prostate:	n/a
30	chr10:46221254-46221304	HL-60	blood:	n/a
31	chr10:46222487-46222537	HepG2	liver:	n/a
32	chr10:46222657-46222707	HepG2	liver:	n/a
33	chr10:46221282-46221332	HEEpiC	esophagus:	n/a
34	chr10:46217976-46218026	GM06990	blood:	n/a
35	chr10:46219381-46219431	AoSMC	blood vessel:	n/a
36	chr10:46222474-46222524	HAEpiC	amniotic membrane:	n/a
37	chr10:46222487-46222537	HCM	heart:	n/a
38	chr10:46221684-46221734	HAEpiC	amniotic membrane:	n/a
39	chr10:46222272-46222322	AG04450	lung:	fetal
40	chr10:46221254-46221304	SK-N-SH	brain:	n/a
41	chr10:46223127-46223177	K562	blood:	n/a
42	chr10:46219381-46219431	Jurkat	blood:	n/a
43	chr10:46222272-46222322	NHBE	bronchial:	n/a
44	chr10:46221684-46221734	HCPEpiC	choroid plexus:	n/a
45	chr10:46221684-46221734	GM12891	blood:	n/a
46	chr10:46222272-46222322	HepG2	liver:	n/a
47	chr10:46222657-46222707	NH-A	brain:	n/a
48	chr10:46222272-46222322	HRPEpiC	eye:	n/a
49	chr10:46217976-46218026	NHBE	bronchial:	n/a
50	chr10:46222474-46222524	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:46222331..46222849-chr10:51827700..51828251,2	HCT-116	colon:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZFAND4-4	chr10:46218376-46218706	NONHSAT013114
2	lnc-ZFAND4-3	chr10:46221142-46221486	NONHSAT013115
3	lnc-ZFAND4-4	chr10:46219342-46219522	NONHSAT013114

Variant related genes	Relation type
FAM21C	TF binding region
ENSG00000228702	TF binding region
FAM21FP	TF binding region
FAM21C	CpG island
ENSG00000228702	CpG island
FAM21FP	CpG island
ENSG00000099290	chromatin interactions

Extended variants
information (count: 919 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:919 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554677030	chr10:46205726-46205727	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs572934304	chr10:46205734-46205735	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs540459321	chr10:46205801-46205802	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs558885641	chr10:46205810-46205811	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs183714031	chr10:46205816-46205817	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs57756590	chr10:46205863-46205864	Enhancers Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs57279747	chr10:46205872-46205873	Enhancers Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs59689764	chr10:46205876-46205877	Enhancers Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs531009208	chr10:46205878-46205879	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs542736411	chr10:46205883-46205884	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs561468644	chr10:46205896-46205897	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs528669652	chr10:46205936-46205937	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs57012350	chr10:46205941-46205942	Enhancers Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs187965477	chr10:46205998-46205999	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs532679880	chr10:46206003-46206004	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs550131307	chr10:46206016-46206017	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs192240869	chr10:46206035-46206036	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs372793232	chr10:46206051-46206052	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs536277843	chr10:46206081-46206082	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs547964727	chr10:46206089-46206090	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs566607437	chr10:46206095-46206096	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs533700923	chr10:46206114-46206115	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs566134116	chr10:46206123-46206124	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs577177185	chr10:46206141-46206142	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs538168054	chr10:46206167-46206168	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs556528508	chr10:46206194-46206195	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs535027080	chr10:46206198-46206199	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs6593489	chr10:46206231-46206232	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs543048887	chr10:46206249-46206250	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs4424627	chr10:46206272-46206273	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs183415572	chr10:46206281-46206282	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs116199003	chr10:46206307-46206308	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs7919110	chr10:46206312-46206313	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs4123568	chr10:46206321-46206322	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs114410128	chr10:46206324-46206325	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs577355601	chr10:46206344-46206345	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs186975636	chr10:46206347-46206348	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs199904801	chr10:46206351-46206352	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs116900409	chr10:46206365-46206366	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs376342481	chr10:46206373-46206374	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529652226	chr10:46206379-46206380	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs374708909	chr10:46206398-46206399	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs572560358	chr10:46206400-46206401	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs150803818	chr10:46206408-46206409	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
45	rs533891425	chr10:46206421-46206422	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs552374520	chr10:46206422-46206423	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561495374	chr10:46206425-46206426	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs575532158	chr10:46206431-46206432	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs192290600	chr10:46206462-46206463	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
50	rs139616278	chr10:46206463-46206464	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
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
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	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
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	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
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Glioblastoma multiforme	21138945	CNVD
Autism	19287141	CNVD
Intellectual disability	21948486	CNVD
Glioblastoma multiforme	21525872	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
early-passage human iPS cells	21368824	CNVD
Acute myeloid leukemia	19651601	CNVD
Breast cancer	20409316	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Rett syndrome	21593744	CNVD
Glioblastoma multiforme	22286061	CNVD
Neuroblastoma	21899760	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Schizophrenia	20967226	CNVD
Cognitive impairment	21505072	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:415 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:46199800-46221600	Weak transcription	Primary T cells from cord blood	blood
2	chr10:46200000-46210400	Weak transcription	Primary T helper cells fromperipheralblood	blood
3	chr10:46201400-46221000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr10:46202000-46206000	Weak transcription	Liver	Liver
5	chr10:46205200-46206600	Enhancers	GM12878-XiMat	blood
6	chr10:46205200-46207000	Enhancers	HepG2	liver
7	chr10:46205200-46207800	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr10:46205600-46206000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr10:46205600-46207800	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr10:46205800-46206000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr10:46205800-46206200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr10:46205800-46206200	Active TSS	Osteobl	bone
13	chr10:46206000-46206200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr10:46206000-46206400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr10:46206000-46206400	Enhancers	Primary B cells from peripheral blood	blood
16	chr10:46206000-46206400	Enhancers	Liver	Liver
17	chr10:46206000-46206600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr10:46206200-46206600	Enhancers	Left Ventricle	heart
19	chr10:46206400-46211000	Weak transcription	Primary B cells from peripheral blood	blood
20	chr10:46206400-46221000	Weak transcription	Liver	Liver
21	chr10:46206400-46221600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr10:46207000-46209600	Weak transcription	HepG2	liver
23	chr10:46208200-46212000	Weak transcription	Rectal Mucosa Donor 29	rectum
24	chr10:46209600-46211200	Enhancers	HepG2	liver
25	chr10:46210800-46212400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr10:46211000-46211200	Enhancers	Sigmoid Colon	Sigmoid Colon
27	chr10:46211000-46211200	Enhancers	HSMMtube	muscle
28	chr10:46211200-46212400	Weak transcription	HepG2	liver
29	chr10:46211200-46212800	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr10:46212000-46213000	Enhancers	Rectal Mucosa Donor 29	rectum
31	chr10:46212000-46213200	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr10:46212400-46213000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr10:46212400-46214000	Enhancers	HepG2	liver
34	chr10:46212800-46213200	Enhancers	Sigmoid Colon	Sigmoid Colon
35	chr10:46213000-46213200	Enhancers	Colonic Mucosa	Colon
36	chr10:46213000-46221000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr10:46219000-46220000	Enhancers	Primary neutrophils fromperipheralblood	blood
38	chr10:46219600-46220000	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr10:46219800-46220000	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr10:46219800-46222000	Weak transcription	Placenta Amnion	Placenta Amnion
41	chr10:46220000-46221200	Weak transcription	Monocytes-CD14+_RO01746	blood
42	chr10:46220000-46221600	Weak transcription	Primary monocytes fromperipheralblood	blood
43	chr10:46220000-46222200	Weak transcription	Primary neutrophils fromperipheralblood	blood
44	chr10:46220400-46222000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr10:46220600-46221200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr10:46220800-46221000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr10:46220800-46221000	Enhancers	Dnd41	blood
48	chr10:46220800-46221400	Enhancers	Pancreas	Pancrea
49	chr10:46221000-46221200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr10:46221000-46221200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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