Variant report

Variant	esv3351582
Chromosome Location	chr10:26861352-26915063
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:604)
CpG islands
(count:732)
Chromatin interactive
region (count:6)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:604 , 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	chr10:26895352-26895577	GM12878	blood:	n/a	n/a
7	BATF	chr10:26911081-26911366	GM12878	blood:	n/a	chr10:26911109-26911117
8	BATF	chr10:26862573-26862909	GM12878	blood:	n/a	n/a
9	BATF	chr10:26863697-26864149	GM12878	blood:	n/a	n/a
10	BATF	chr10:26863751-26864136	GM12878	blood:	n/a	n/a
11	BATF	chr10:26911106-26911298	GM12878	blood:	n/a	chr10:26911109-26911117
12	BATF	chr10:26862524-26862900	GM12878	blood:	n/a	n/a
13	BCL11A	chr10:26863648-26864087	GM12878	blood:	n/a	n/a
14	BCL11A	chr10:26863793-26864021	GM12878	blood:	n/a	n/a
15	BCL11A	chr10:26862584-26862977	GM12878	blood:	n/a	n/a
16	BCLAF1	chr10:26863786-26864104	GM12878	blood:	n/a	n/a
17	BCLAF1	chr10:26863717-26864158	GM12878	blood:	n/a	n/a
18	BHLHE40	chr10:26863731-26864167	GM12878	blood:	n/a	n/a
19	BHLHE40	chr10:26862634-26862906	GM12878	blood:	n/a	n/a
20	CCNT2	chr10:26882957-26883162	K562	blood:	n/a	n/a
21	CEBPB	chr10:26894346-26894466	HepG2	liver:	n/a	chr10:26894416-26894427
22	CEBPB	chr10:26910930-26911239	HepG2	liver:	n/a	chr10:26911053-26911064 chr10:26910983-26910994
23	CEBPB	chr10:26910882-26911209	A549	lung:	n/a	chr10:26911053-26911064 chr10:26910983-26910994
24	CEBPB	chr10:26910907-26911238	K562	blood:	n/a	chr10:26911053-26911064 chr10:26910983-26910994
25	CEBPB	chr10:26874087-26874199	A549	lung:	n/a	n/a
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	chr10:26862199-26862219	GM12878	blood:	n/a	n/a
30	CHD2	chr10:26862700-26862938	GM12878	blood:	n/a	n/a
31	CREB1	chr10:26863824-26864151	GM12878	blood:	n/a	n/a
32	CTCF	chr10:26875103-26875180	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr10:26862720-26862870	GM12866	blood:	n/a	n/a
34	CTCF	chr10:26895560-26895710	GM12875	blood:	n/a	n/a
35	CTCF	chr10:26895540-26895690	GM06990	blood:	n/a	n/a
36	CTCF	chr10:26895480-26895630	GM12873	blood:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
37	CTCF	chr10:26895420-26895570	WERI-Rb-1	eye:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
38	CTCF	chr10:26892326-26892398	Gliobla	brain:	n/a	n/a
39	CTCF	chr10:26862660-26862810	GM12864	blood:	n/a	n/a
40	CTCF	chr10:26862720-26862870	HAc	cerebellar:	n/a	n/a
41	CTCF	chr10:26895400-26895550	AG09319	gingival:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
42	CTCF	chr10:26895400-26895550	HPAF	blood vessel:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
43	CTCF	chr10:26895540-26895690	NHDF-neo	bronchial:	n/a	n/a
44	CTCF	chr10:26875090-26875221	GM19240	blood:	n/a	n/a
45	CTCF	chr10:26895480-26895630	GM12871	blood:	n/a	chr10:26895492-26895500 chr10:26895490-26895503 chr10:26895488-26895504 chr10:26895487-26895505 chr10:26895489-26895510
46	CTCF	chr10:26895280-26895430	RPTEC	kidney:	n/a	n/a
47	CTCF	chr10:26862700-26862850	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr10:26895280-26895430	GM12866	blood:	n/a	n/a
49	CTCF	chr10:26875104-26875190	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr10:26895300-26895450	NHDF-neo	bronchial:	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	chr10:26878627-26878677	ECC-1	luminal epithelium:	n/a
2	chr10:26911451-26911501	HepG2	liver:	n/a
3	chr10:26878627-26878677	GM12878	blood:	n/a
4	chr10:26877803-26877853	Jurkat	blood:	n/a
5	chr10:26911451-26911501	HL-60	blood:	n/a
6	chr10:26877803-26877853	HPAEpiC	pulmonary alveolar:	n/a
7	chr10:26877716-26877766	HEEpiC	esophagus:	n/a
8	chr10:26883079-26883129	NHBE	bronchial:	n/a
9	chr10:26883013-26883063	NH-A	brain:	n/a
10	chr10:26878629-26878679	ovcar-3	ovarian:	n/a
11	chr10:26881860-26881910	AG04449	skin:	fetal
12	chr10:26911186-26911236	K562	blood:	n/a
13	chr10:26883079-26883129	HCT-116	colon:	n/a
14	chr10:26877716-26877766	GM19239	blood:	n/a
15	chr10:26877803-26877853	HCF	heart:	n/a
16	chr10:26883079-26883129	ECC-1	luminal epithelium:	n/a
17	chr10:26877716-26877766	GM12878	blood:	n/a
18	chr10:26878632-26878682	Caco-2	colon:	n/a
19	chr10:26881860-26881910	ProgFib	skin:	n/a
20	chr10:26881860-26881910	BE2_C	brain:	n/a
21	chr10:26877515-26877565	AG10803	skin:	n/a
22	chr10:26877716-26877766	SK-N-MC	brain:	n/a
23	chr10:26878629-26878679	SK-N-SH_RA	brain:	n/a
24	chr10:26877803-26877853	AoSMC	blood vessel:	n/a
25	chr10:26881860-26881910	GM06990	blood:	n/a
26	chr10:26878627-26878677	PrEC	prostate:	n/a
27	chr10:26911186-26911236	T-47D	breast:	n/a
28	chr10:26881860-26881910	MCF-7	breast:	n/a
29	chr10:26877803-26877853	HRCEpiC	kidney:	n/a
30	chr10:26877716-26877766	CMK	blood:	n/a
31	chr10:26883165-26883215	SK-N-SH	brain:	n/a
32	chr10:26877803-26877853	NB4	blood:	n/a
33	chr10:26878629-26878679	HepG2	liver:	n/a
34	chr10:26878629-26878679	AG10803	skin:	n/a
35	chr10:26883013-26883063	A549	lung:	n/a
36	chr10:26877515-26877565	MCF-7	breast:	n/a
37	chr10:26883013-26883063	ECC-1	luminal epithelium:	n/a
38	chr10:26877515-26877565	HepG2	liver:	n/a
39	chr10:26883013-26883063	SK-N-SH	brain:	n/a
40	chr10:26911186-26911236	ECC-1	luminal epithelium:	n/a
41	chr10:26878632-26878682	NT2-D1	testis:	n/a
42	chr10:26911186-26911236	HIPEpiC	eye:	n/a
43	chr10:26911451-26911501	Hela-S3	cervix:	n/a
44	chr10:26877716-26877766	HMEC	breast:	n/a
45	chr10:26877515-26877565	GM12878	blood:	n/a
46	chr10:26883165-26883215	HNPCEpiC	eye:	n/a
47	chr10:26883013-26883063	SK-N-MC	brain:	n/a
48	chr10:26878627-26878677	NB4	blood:	n/a
49	chr10:26881860-26881910	HRE	kidney:	n/a
50	chr10:26877515-26877565	LNCaP	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr10:26895319..26895931-chr10:26973740..26974253,2	K562	blood:
2	chr10:26888726..26891002-chr10:26893312..26895569,2	K562	blood:
3	chr10:26911042..26911570-chr17:41400814..41401666,2	NB4	blood:
4	chr10:26895094..26895872-chr10:26973347..26973911,2	MCF-7	breast:
5	chr10:26895059..26895568-chr10:27171114..27171693,2	K562	blood:
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-PDSS1-1	chr10:26879025-26879266	NONHSAT011840
2	lnc-PDSS1-1	chr10:26880239-26880342	NR_026793
3	lnc-APBB1IP-1	chr10:26879064-26879266	XLOC_008419
4	lnc-APBB1IP-1	chr10:26878993-26879266	XLOC_008419
5	lnc-PDSS1-1	chr10:26882863-26883251	NR_026793
6	lnc-APBB1IP-1	chr10:26881779-26882156	XLOC_008419
7	lnc-APBB1IP-1	chr10:26876526-26877939	XLOC_008419
8	lnc-APBB1IP-1	chr10:26882863-26883254	XLOC_008419
9	lnc-ABI1-8	chr10:26908129-26908242	NONHSAT011842
10	lnc-APBB1IP-1	chr10:26882863-26883254	XLOC_008419
11	lnc-ABI1-8	chr10:26906611-26906782	NONHSAT011841
12	lnc-PDSS1-1	chr10:26870673-26871754	NONHSAT011834
13	lnc-APBB1IP-1	chr10:26880239-26880342	XLOC_008419
14	lnc-APBB1IP-1	chr10:26880239-26880342	XLOC_008419
15	lnc-APBB1IP-1	chr10:26880239-26880342	XLOC_008419
16	lnc-PDSS1-1	chr10:26881779-26881895	NR_026793
17	lnc-ABI1-8	chr10:26906511-26906782	l_271_chr10:26906510-26908315_testes
18	lnc-ABI1-8	chr10:26907771-26907906	NONHSAT011842
19	lnc-PDSS1-1	chr10:26878794-26879266	NR_026793
20	lnc-ABI1-8	chr10:26906611-26906782	NONHSAT011842
21	lnc-ABI1-8	chr10:26907771-26907837	l_271_chr10:26906510-26908315_testes
22	lnc-ABI1-8	chr10:26907771-26908030	NONHSAT011841
23	lnc-APBB1IP-1	chr10:26878993-26879266	XLOC_008419
24	lnc-ABI1-8	chr10:26908129-26908315	l_271_chr10:26906510-26908315_testes

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: 2791 )
Associated
traits (count: 45 )

Variant overlapped rSNPs/rCNVs (count:2791 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs77858718	chr10:26861353-26861354	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs72805230	chr10:26861384-26861385	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs72805231	chr10:26861394-26861395	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs562095446	chr10:26861395-26861396	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs72805232	chr10:26861416-26861417	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs78594617	chr10:26861455-26861456	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs187115529	chr10:26861469-26861470	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs76636189	chr10:26861479-26861480	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs564572034	chr10:26861491-26861492	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs75048053	chr10:26861500-26861501	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs200800101	chr10:26861560-26861561	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191920615	chr10:26861568-26861569	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs563494452	chr10:26861598-26861599	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs149312961	chr10:26861627-26861628	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200915669	chr10:26861628-26861629	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs375991266	chr10:26861649-26861650	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs74128357	chr10:26861676-26861677	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs75037112	chr10:26861683-26861684	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370409358	chr10:26861705-26861706	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs35801387	chr10:26861706-26861707	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs75429155	chr10:26861707-26861708	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs59453295	chr10:26861726-26861727	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs373415671	chr10:26861727-26861728	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs11015181	chr10:26861730-26861731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs565604661	chr10:26861747-26861748	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs183773964	chr10:26861762-26861763	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs114994494	chr10:26861769-26861770	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs201110926	chr10:26861780-26861781	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs10829028	chr10:26861784-26861785	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs571020844	chr10:26861813-26861814	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs10829029	chr10:26861828-26861829	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs537142088	chr10:26861855-26861856	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs556529042	chr10:26861869-26861870	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs570211559	chr10:26861870-26861871	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs11015182	chr10:26861904-26861905	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs11015183	chr10:26861940-26861941	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs72805233	chr10:26861974-26861975	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs377357837	chr10:26861978-26861979	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs78392833	chr10:26861994-26861995	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs556114438	chr10:26861999-26862000	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs199648354	chr10:26862004-26862005	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs374288146	chr10:26862042-26862043	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs186628456	chr10:26862098-26862099	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs531887292	chr10:26862101-26862102	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs77987124	chr10:26862115-26862116	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs115916685	chr10:26862126-26862127	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs578070159	chr10:26862149-26862150	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs543875209	chr10:26862194-26862195	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs117500441	chr10:26862211-26862212	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs74128358	chr10:26862238-26862239	Enhancers Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:416 , 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	chr10:26846400-26861600	Strong transcription	Primary monocytes fromperipheralblood	blood
4	chr10:26846800-26863000	Strong transcription	Primary neutrophils fromperipheralblood	blood
5	chr10:26848400-26863000	Strong transcription	Fetal Thymus	thymus
6	chr10:26856400-26864000	Weak transcription	Pancreas	Pancrea
7	chr10:26857600-26880200	Weak transcription	Adipose Nuclei	Adipose
8	chr10:26858400-26879400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr10:26859000-26862200	Weak transcription	GM12878-XiMat	blood
10	chr10:26860800-26862000	Weak transcription	Thymus	Thymus
11	chr10:26860800-26862000	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr10:26860800-26862200	Weak transcription	Primary T cells from cord blood	blood
13	chr10:26860800-26862600	Weak transcription	Primary T cells fromperipheralblood	blood
14	chr10:26860800-26863000	Strong transcription	Primary hematopoietic stem cells	blood
15	chr10:26860800-26881200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr10:26860800-26892600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr10:26861000-26862000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr10:26861000-26862000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr10:26861000-26862600	Strong transcription	Primary B cells from cord blood	blood
20	chr10:26861000-26862600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr10:26861000-26862800	Weak transcription	Primary B cells from peripheral blood	blood
22	chr10:26861000-26864200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr10:26861000-26864200	Weak transcription	Primary T helper cells PMA-I stimulated	--
24	chr10:26861000-26864200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr10:26861000-26874400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr10:26861000-26886600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr10:26861200-26862000	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr10:26861200-26862000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr10:26861200-26862600	Weak transcription	Dnd41	blood
30	chr10:26861200-26872000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
31	chr10:26861200-26884400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
32	chr10:26861200-26884800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr10:26861600-26862000	Weak transcription	Primary monocytes fromperipheralblood	blood
34	chr10:26862000-26862200	Enhancers	H1 Cell Line	embryonic stem cell
35	chr10:26862000-26862400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr10:26862000-26863000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr10:26862000-26863000	Strong transcription	Thymus	Thymus
38	chr10:26862000-26863200	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr10:26862000-26863200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr10:26862000-26863400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr10:26862000-26863600	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr10:26862000-26864600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr10:26862000-26864600	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr10:26862200-26863000	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr10:26862200-26863600	Enhancers	GM12878-XiMat	blood
46	chr10:26862200-26864400	Strong transcription	Primary T cells from cord blood	blood
47	chr10:26862400-26882400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
48	chr10:26862600-26863000	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr10:26862600-26863000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr10:26862600-26863000	Genic enhancers	Primary B cells from cord blood	blood

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