Variant report

Variant	esv3360208
Chromosome Location	chr10:26861751-26915460
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:602)
CpG islands
(count:732)
Chromatin interactive
region (count:6)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:602 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:26895385-26895597	K562	blood:	n/a	n/a
2	ATF2	chr10:26863637-26864211	GM12878	blood:	n/a	n/a
3	ATF2	chr10:26863707-26864194	GM12878	blood:	n/a	n/a
4	ATF3	chr10:26863854-26863990	GM12878	blood:	n/a	n/a
5	BACH1	chr10:26910868-26911617	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr10:26911081-26911366	GM12878	blood:	n/a	chr10:26911109-26911117
7	BATF	chr10:26911106-26911298	GM12878	blood:	n/a	chr10:26911109-26911117
8	BATF	chr10:26895352-26895577	GM12878	blood:	n/a	n/a
9	BATF	chr10:26863751-26864136	GM12878	blood:	n/a	n/a
10	BATF	chr10:26862573-26862909	GM12878	blood:	n/a	n/a
11	BATF	chr10:26862524-26862900	GM12878	blood:	n/a	n/a
12	BATF	chr10:26863697-26864149	GM12878	blood:	n/a	n/a
13	BCL11A	chr10:26863793-26864021	GM12878	blood:	n/a	n/a
14	BCL11A	chr10:26863648-26864087	GM12878	blood:	n/a	n/a
15	BCL11A	chr10:26862584-26862977	GM12878	blood:	n/a	n/a
16	BCLAF1	chr10:26863717-26864158	GM12878	blood:	n/a	n/a
17	BCLAF1	chr10:26863786-26864104	GM12878	blood:	n/a	n/a
18	BHLHE40	chr10:26862634-26862906	GM12878	blood:	n/a	n/a
19	BHLHE40	chr10:26863731-26864167	GM12878	blood:	n/a	n/a
20	CCNT2	chr10:26882957-26883162	K562	blood:	n/a	n/a
21	CEBPB	chr10:26910907-26911238	K562	blood:	n/a	chr10:26911053-26911064 chr10:26910983-26910994
22	CEBPB	chr10:26894346-26894466	HepG2	liver:	n/a	chr10:26894416-26894427
23	CEBPB	chr10:26874087-26874199	A549	lung:	n/a	n/a
24	CEBPB	chr10:26910930-26911239	HepG2	liver:	n/a	chr10:26911053-26911064 chr10:26910983-26910994
25	CEBPB	chr10:26910882-26911209	A549	lung:	n/a	chr10:26911053-26911064 chr10:26910983-26910994
26	CHD1	chr10:26862678-26862878	GM12878	blood:	n/a	n/a
27	CHD1	chr10:26911280-26911380	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr10:26883116-26883294	GM12878	blood:	n/a	n/a
29	CHD2	chr10:26862700-26862938	GM12878	blood:	n/a	n/a
30	CHD2	chr10:26862199-26862219	GM12878	blood:	n/a	n/a
31	CREB1	chr10:26863824-26864151	GM12878	blood:	n/a	n/a
32	CTCF	chr10:26862700-26862850	AoAF	blood vessel:	n/a	n/a
33	CTCF	chr10:26895340-26895490	GM12865	blood:	n/a	n/a
34	CTCF	chr10:26895040-26895190	HRPEpiC	eye:	n/a	n/a
35	CTCF	chr10:26862740-26862890	HFF	foreskin:	n/a	n/a
36	CTCF	chr10:26862700-26862850	HepG2	liver:	n/a	n/a
37	CTCF	chr10:26862740-26862890	HPAF	blood vessel:	n/a	n/a
38	CTCF	chr10:26895280-26895430	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr10:26862743-26862900	MCF-7	breast:	n/a	n/a
40	CTCF	chr10:26895540-26895830	GM12864	blood:	n/a	n/a
41	CTCF	chr10:26894700-26894850	AG09319	gingival:	n/a	n/a
42	CTCF	chr10:26862710-26862896	GM12878	blood:	n/a	n/a
43	CTCF	chr10:26895540-26895690	NHDF-neo	bronchial:	n/a	n/a
44	CTCF	chr10:26862784-26862810	LNCaP	prostate:	n/a	n/a
45	CTCF	chr10:26895400-26895550	Caco-2	colon:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
46	CTCF	chr10:26862720-26862870	HepG2	liver:	n/a	n/a
47	CTCF	chr10:26895320-26895470	BE2_C	brain:	n/a	n/a
48	CTCF	chr10:26862660-26862810	GM12873	blood:	n/a	n/a
49	CTCF	chr10:26895320-26895470	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr10:26862780-26862930	HCFaa	heart:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:26911451-26911501	SK-N-SH	brain:	n/a
2	chr10:26883013-26883063	AG04450	lung:	fetal
3	chr10:26883165-26883215	HCT-116	colon:	n/a
4	chr10:26883165-26883215	GM12878	blood:	n/a
5	chr10:26911186-26911236	HCPEpiC	choroid plexus:	n/a
6	chr10:26883013-26883063	NT2-D1	testis:	n/a
7	chr10:26877716-26877766	HPAEpiC	pulmonary alveolar:	n/a
8	chr10:26877803-26877853	SK-N-SH	brain:	n/a
9	chr10:26911451-26911501	SKMC	muscle:	n/a
10	chr10:26877803-26877853	HAEpiC	amniotic membrane:	n/a
11	chr10:26881860-26881910	H1-hESC	embryonic stem cell:	embryo
12	chr10:26881860-26881910	HAEpiC	amniotic membrane:	n/a
13	chr10:26883165-26883215	H1-hESC	embryonic stem cell:	embryo
14	chr10:26911451-26911501	AG04449	skin:	fetal
15	chr10:26883165-26883215	HNPCEpiC	eye:	n/a
16	chr10:26877716-26877766	HepG2	liver:	n/a
17	chr10:26877803-26877853	Hela-S3	cervix:	n/a
18	chr10:26877803-26877853	ProgFib	skin:	n/a
19	chr10:26911186-26911236	HepG2	liver:	n/a
20	chr10:26877716-26877766	GM12891	blood:	n/a
21	chr10:26878629-26878679	T-47D	breast:	n/a
22	chr10:26911451-26911501	Hela-S3	cervix:	n/a
23	chr10:26911186-26911236	HPAEpiC	pulmonary alveolar:	n/a
24	chr10:26878627-26878677	NH-A	brain:	n/a
25	chr10:26911186-26911236	HCT-116	colon:	n/a
26	chr10:26877716-26877766	AG04449	skin:	fetal
27	chr10:26911186-26911236	GM06990	blood:	n/a
28	chr10:26877716-26877766	SK-N-MC	brain:	n/a
29	chr10:26877515-26877565	BJ	skin:	n/a
30	chr10:26878627-26878677	H1-hESC	embryonic stem cell:	embryo
31	chr10:26877716-26877766	LNCaP	prostate:	n/a
32	chr10:26878627-26878677	AoSMC	blood vessel:	n/a
33	chr10:26877716-26877766	BJ	skin:	n/a
34	chr10:26911186-26911236	Caco-2	colon:	n/a
35	chr10:26883013-26883063	LNCaP	prostate:	n/a
36	chr10:26911186-26911236	AoSMC	blood vessel:	n/a
37	chr10:26883079-26883129	HRPEpiC	eye:	n/a
38	chr10:26878627-26878677	SAEC	small airway:	n/a
39	chr10:26883013-26883063	ovcar-3	ovarian:	n/a
40	chr10:26878627-26878677	SK-N-SH	brain:	n/a
41	chr10:26911186-26911236	HRE	kidney:	n/a
42	chr10:26883079-26883129	PrEC	prostate:	n/a
43	chr10:26878629-26878679	NB4	blood:	n/a
44	chr10:26883013-26883063	GM06990	blood:	n/a
45	chr10:26881860-26881910	GM12892	blood:	n/a
46	chr10:26877515-26877565	RPTEC	kidney:	n/a
47	chr10:26878632-26878682	U87	brain:	n/a
48	chr10:26878632-26878682	PANC-1	pancreas:	n/a
49	chr10:26881860-26881910	Hepatocyte	liver:	n/a
50	chr10:26877803-26877853	A549	lung:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:26888726..26891002-chr10:26893312..26895569,2	K562	blood:
2	chr10:26911042..26911570-chr17:41400814..41401666,2	NB4	blood:
3	chr10:26895319..26895931-chr10:26973740..26974253,2	K562	blood:
4	chr10:26895059..26895568-chr10:27171114..27171693,2	K562	blood:
5	chr10:26895094..26895872-chr10:26973347..26973911,2	MCF-7	breast:
6	chr10:26888726..26891002-chr10:26893312..26895569,2	K562	blood:

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-APBB1IP-1	chr10:26878993-26879266	XLOC_008419
2	lnc-PDSS1-1	chr10:26880239-26880342	NR_026793
3	lnc-ABI1-8	chr10:26907771-26908030	NONHSAT011841
4	lnc-ABI1-8	chr10:26908129-26908315	l_271_chr10:26906510-26908315_testes
5	lnc-APBB1IP-1	chr10:26881779-26882156	XLOC_008419
6	lnc-APBB1IP-1	chr10:26879064-26879266	XLOC_008419
7	lnc-APBB1IP-1	chr10:26880239-26880342	XLOC_008419
8	lnc-PDSS1-1	chr10:26881779-26881895	NR_026793
9	lnc-PDSS1-1	chr10:26870673-26871754	NONHSAT011834
10	lnc-PDSS1-1	chr10:26878794-26879266	NR_026793
11	lnc-ABI1-8	chr10:26906611-26906782	NONHSAT011842
12	lnc-APBB1IP-1	chr10:26878993-26879266	XLOC_008419
13	lnc-ABI1-8	chr10:26907771-26907906	NONHSAT011842
14	lnc-APBB1IP-1	chr10:26882863-26883254	XLOC_008419
15	lnc-ABI1-8	chr10:26908129-26908242	NONHSAT011842
16	lnc-ABI1-8	chr10:26906511-26906782	l_271_chr10:26906510-26908315_testes
17	lnc-ABI1-8	chr10:26907771-26907837	l_271_chr10:26906510-26908315_testes
18	lnc-APBB1IP-1	chr10:26880239-26880342	XLOC_008419
19	lnc-APBB1IP-1	chr10:26880239-26880342	XLOC_008419
20	lnc-PDSS1-1	chr10:26882863-26883251	NR_026793
21	lnc-APBB1IP-1	chr10:26882863-26883254	XLOC_008419
22	lnc-ABI1-8	chr10:26906611-26906782	NONHSAT011841
23	lnc-APBB1IP-1	chr10:26876526-26877939	XLOC_008419
24	lnc-PDSS1-1	chr10:26879025-26879266	NONHSAT011840

No data

Variant related genes	Relation type
ENSG00000236894	TF binding region
LINC00264	TF binding region
ENSG00000236894	CpG island
LINC00264	CpG island
ZNF365	miRNA target sites
ZNF367	miRNA target sites

Extended variants
information (count: 2813 )
Associated
traits (count: 45 )

Variant overlapped rSNPs/rCNVs (count:2813 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183773964	chr10:26861762-26861763	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs114994494	chr10:26861769-26861770	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs201110926	chr10:26861780-26861781	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs10829028	chr10:26861784-26861785	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs571020844	chr10:26861813-26861814	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs10829029	chr10:26861828-26861829	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs537142088	chr10:26861855-26861856	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs556529042	chr10:26861869-26861870	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs570211559	chr10:26861870-26861871	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs11015182	chr10:26861904-26861905	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs11015183	chr10:26861940-26861941	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs72805233	chr10:26861974-26861975	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs377357837	chr10:26861978-26861979	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs78392833	chr10:26861994-26861995	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs556114438	chr10:26861999-26862000	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs199648354	chr10:26862004-26862005	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs374288146	chr10:26862042-26862043	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs186628456	chr10:26862098-26862099	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs531887292	chr10:26862101-26862102	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs77987124	chr10:26862115-26862116	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs115916685	chr10:26862126-26862127	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs578070159	chr10:26862149-26862150	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs543875209	chr10:26862194-26862195	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs117500441	chr10:26862211-26862212	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs74128358	chr10:26862238-26862239	Enhancers Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs542385619	chr10:26862242-26862243	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs192376690	chr10:26862277-26862278	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs200597051	chr10:26862310-26862311	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs528330502	chr10:26862335-26862336	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376418777	chr10:26862337-26862338	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs551004402	chr10:26862343-26862344	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs202209562	chr10:26862387-26862388	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200411277	chr10:26862390-26862391	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs542009555	chr10:26862424-26862425	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs563727805	chr10:26862434-26862435	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs185563439	chr10:26862477-26862478	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs117827611	chr10:26862497-26862498	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs550637789	chr10:26862566-26862567	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200347572	chr10:26862569-26862570	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs117575516	chr10:26862572-26862573	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs116329505	chr10:26862576-26862577	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs536055977	chr10:26862639-26862640	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs201484248	chr10:26862642-26862643	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs200693114	chr10:26862667-26862668	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs57722155	chr10:26862680-26862681	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs200935360	chr10:26862731-26862732	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs190496320	chr10:26862738-26862739	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs558211074	chr10:26862767-26862768	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs577952817	chr10:26862769-26862770	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs117356388	chr10:26862785-26862786	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:45)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	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
Oral cancer	21386901	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
T-cell lymphomas	19863542	CNVD
Esophageal cancer	21851588	CNVD
small cell lung cancer	20016488	CNVD
Behavioral abnormalities	21522184	CNVD
Dysmorphic features	21522184	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Autism	21439084	CNVD
Maculopathy	20981449	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Adrenocortical carcinoma	18281524	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17431168	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	chr10:26840200-26863200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr10:26845400-26863000	Strong transcription	Primary T helper cells fromperipheralblood	blood
3	chr10:26846800-26863000	Strong transcription	Primary neutrophils fromperipheralblood	blood
4	chr10:26848400-26863000	Strong transcription	Fetal Thymus	thymus
5	chr10:26856400-26864000	Weak transcription	Pancreas	Pancrea
6	chr10:26857600-26880200	Weak transcription	Adipose Nuclei	Adipose
7	chr10:26858400-26879400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr10:26859000-26862200	Weak transcription	GM12878-XiMat	blood
9	chr10:26860800-26862000	Weak transcription	Thymus	Thymus
10	chr10:26860800-26862000	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr10:26860800-26862200	Weak transcription	Primary T cells from cord blood	blood
12	chr10:26860800-26862600	Weak transcription	Primary T cells fromperipheralblood	blood
13	chr10:26860800-26863000	Strong transcription	Primary hematopoietic stem cells	blood
14	chr10:26860800-26881200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr10:26860800-26892600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr10:26861000-26862000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr10:26861000-26862000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr10:26861000-26862600	Strong transcription	Primary B cells from cord blood	blood
19	chr10:26861000-26862600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr10:26861000-26862800	Weak transcription	Primary B cells from peripheral blood	blood
21	chr10:26861000-26864200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr10:26861000-26864200	Weak transcription	Primary T helper cells PMA-I stimulated	--
23	chr10:26861000-26864200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr10:26861000-26874400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr10:26861000-26886600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
26	chr10:26861200-26862000	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr10:26861200-26862000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
28	chr10:26861200-26862600	Weak transcription	Dnd41	blood
29	chr10:26861200-26872000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
30	chr10:26861200-26884400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
31	chr10:26861200-26884800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr10:26861600-26862000	Weak transcription	Primary monocytes fromperipheralblood	blood
33	chr10:26862000-26862200	Enhancers	H1 Cell Line	embryonic stem cell
34	chr10:26862000-26862400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr10:26862000-26863000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr10:26862000-26863000	Strong transcription	Thymus	Thymus
37	chr10:26862000-26863200	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr10:26862000-26863200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr10:26862000-26863400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr10:26862000-26863600	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr10:26862000-26864600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr10:26862000-26864600	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr10:26862200-26863000	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr10:26862200-26863600	Enhancers	GM12878-XiMat	blood
45	chr10:26862200-26864400	Strong transcription	Primary T cells from cord blood	blood
46	chr10:26862400-26882400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr10:26862600-26863000	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr10:26862600-26863000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr10:26862600-26863000	Genic enhancers	Primary B cells from cord blood	blood
50	chr10:26862600-26863000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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