Variant report

Variant	esv3364575
Chromosome Location	chr10:16236995-16272985
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:96)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:96 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr10:16237074-16237552	GM12878	blood:	n/a	n/a
2	ATF2	chr10:16237133-16237544	GM12878	blood:	n/a	n/a
3	BATF	chr10:16237321-16237585	GM12878	blood:	n/a	n/a
4	BATF	chr10:16237101-16237316	GM12878	blood:	n/a	chr10:16237239-16237250
5	BCL3	chr10:16237288-16237504	GM12878	blood:	n/a	n/a
6	BHLHE40	chr10:16237176-16237527	GM12878	blood:	n/a	n/a
7	CEBPB	chr10:16254419-16254431	A549	lung:	n/a	n/a
8	CEBPB	chr10:16237943-16238214	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr10:16237794-16238334	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD2	chr10:16237188-16237611	GM12878	blood:	n/a	n/a
11	CTCF	chr10:16245640-16245790	HCFaa	heart:	n/a	n/a
12	CTCF	chr10:16258575-16258666	GM10248	blood:	n/a	n/a
13	CTCF	chr10:16248960-16249015	GM10266	blood:	n/a	n/a
14	CTCF	chr10:16249540-16249690	Caco-2	colon:	n/a	n/a
15	CUX1	chr10:16237384-16237445	GM12878	blood:	n/a	n/a
16	E2F4	chr10:16272498-16272524	MCF10A-Er-Src	breast:	n/a	n/a
17	E2F4	chr10:16238966-16239225	MCF10A-Er-Src	breast:	n/a	n/a
18	E2F6	chr10:16238806-16239332	H1-hESC	embryonic stem cell:	n/a	n/a
19	E2F6	chr10:16238818-16239416	H1-hESC	embryonic stem cell:	n/a	n/a
20	EBF1	chr10:16237328-16237580	GM12878	blood:	n/a	n/a
21	EP300	chr10:16237034-16237859	GM12878	blood:	n/a	n/a
22	EP300	chr10:16237152-16237497	GM12878	blood:	n/a	n/a
23	EP300	chr10:16237073-16237588	GM12878	blood:	n/a	n/a
24	FOS	chr10:16238964-16238971	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr10:16237095-16237473	MCF10A-Er-Src	breast:	n/a	chr10:16237242-16237252 chr10:16237244-16237251 chr10:16237241-16237253 chr10:16237239-16237250 chr10:16237243-16237251
26	FOXM1	chr10:16237018-16237548	GM12878	blood:	n/a	chr10:16237240-16237248
27	GATA3	chr10:16236584-16237240	MCF-7	breast:	n/a	chr10:16237205-16237215 chr10:16236868-16236875
28	GTF2F1	chr10:16238031-16238205	H1-hESC	embryonic stem cell:	n/a	n/a
29	HDAC2	chr10:16236749-16237100	MCF-7	breast:	n/a	chr10:16236786-16236795 chr10:16236925-16236934
30	HEY1	chr10:16240412-16240596	HepG2	liver:	n/a	n/a
31	IKZF1	chr10:16237106-16237681	GM12878	blood:	n/a	chr10:16237660-16237668
32	JUN	chr10:16237921-16238192	H1-hESC	embryonic stem cell:	n/a	n/a
33	JUN	chr10:16267349-16267640	H1-hESC	embryonic stem cell:	n/a	chr10:16267440-16267453
34	JUN	chr10:16267345-16267555	HepG2	liver:	n/a	chr10:16267440-16267453
35	JUN	chr10:16243682-16243802	K562	blood:	n/a	n/a
36	JUND	chr10:16237775-16238122	H1-hESC	embryonic stem cell:	n/a	n/a
37	JUND	chr10:16267315-16267613	H1-hESC	embryonic stem cell:	n/a	n/a
38	JUND	chr10:16255849-16256085	HepG2	liver:	n/a	chr10:16256002-16256013
39	JUND	chr10:16267287-16267612	HepG2	liver:	n/a	n/a
40	KAP1	chr10:16264881-16265476	K562	blood:	n/a	n/a
41	KAP1	chr10:16264898-16265398	HEK293	kidney:	n/a	n/a
42	MAFK	chr10:16241650-16241762	HepG2	liver:	n/a	chr10:16241706-16241723
43	MAFK	chr10:16237636-16238116	H1-hESC	embryonic stem cell:	n/a	n/a
44	MAX	chr10:16237961-16238228	H1-hESC	embryonic stem cell:	n/a	n/a
45	MAX	chr10:16238988-16239246	H1-hESC	embryonic stem cell:	n/a	n/a
46	MEF2A	chr10:16237064-16237619	GM12878	blood:	n/a	chr10:16237205-16237213
47	MEF2A	chr10:16236972-16237649	GM12878	blood:	n/a	chr10:16237205-16237213
48	MEF2C	chr10:16237096-16237520	GM12878	blood:	n/a	chr10:16237205-16237213
49	MXI1	chr10:16262823-16262934	H1-hESC	embryonic stem cell:	n/a	n/a
50	MXI1	chr10:16237279-16237512	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:16238008-16238058	CMK	blood:	n/a
2	chr10:16238008-16238058	SAEC	small airway:	n/a
3	chr10:16238008-16238058	HRE	kidney:	n/a
4	chr10:16238008-16238058	HL-60	blood:	n/a
5	chr10:16238008-16238058	HPAEpiC	pulmonary alveolar:	n/a
6	chr10:16238008-16238058	AoSMC	blood vessel:	n/a
7	chr10:16238008-16238058	H1-hESC	embryonic stem cell:	embryo
8	chr10:16238008-16238058	HCF	heart:	n/a
9	chr10:16238008-16238058	AG09319	gingival:	n/a
10	chr10:16238008-16238058	NHBE	bronchial:	n/a
11	chr10:16238008-16238058	ProgFib	skin:	n/a
12	chr10:16238008-16238058	BJ	skin:	n/a
13	chr10:16238008-16238058	ovcar-3	ovarian:	n/a
14	chr10:16238008-16238058	HUVEC	blood vessel:	n/a
15	chr10:16238008-16238058	GM12878	blood:	n/a
16	chr10:16238008-16238058	PrEC	prostate:	n/a
17	chr10:16238008-16238058	MCF-7	breast:	n/a
18	chr10:16238008-16238058	NT2-D1	testis:	n/a
19	chr10:16238008-16238058	HCT-116	colon:	n/a
20	chr10:16238008-16238058	AG04449	skin:	fetal
21	chr10:16238008-16238058	A549	lung:	n/a
22	chr10:16238008-16238058	NHDF-neo	bronchial:	n/a
23	chr10:16238008-16238058	IMR90	lung:	fetal
24	chr10:16238008-16238058	HEK293	kidney:	embryo
25	chr10:16238008-16238058	PANC-1	pancreas:	n/a
26	chr10:16238008-16238058	AG04450	lung:	fetal
27	chr10:16238008-16238058	Hepatocyte	liver:	n/a
28	chr10:16238008-16238058	HMEC	breast:	n/a
29	chr10:16238008-16238058	HNPCEpiC	eye:	n/a
30	chr10:16238008-16238058	U87	brain:	n/a
31	chr10:16238008-16238058	GM06990	blood:	n/a
32	chr10:16238008-16238058	AG09309	skin:	n/a
33	chr10:16238008-16238058	SKMC	muscle:	n/a
34	chr10:16238008-16238058	HRCEpiC	kidney:	n/a
35	chr10:16238008-16238058	AG10803	skin:	n/a
36	chr10:16238008-16238058	SK-N-SH	brain:	n/a
37	chr10:16238008-16238058	SK-N-MC	brain:	n/a
38	chr10:16238008-16238058	T-47D	breast:	n/a
39	chr10:16238008-16238058	SK-N-SH_RA	brain:	n/a
40	chr10:16238008-16238058	PFSK-1	brain:	n/a
41	chr10:16238008-16238058	MCF10A-Er-Src	breast:	n/a
42	chr10:16238008-16238058	HepG2	liver:	n/a
43	chr10:16238008-16238058	HEEpiC	esophagus:	n/a
44	chr10:16238008-16238058	NH-A	brain:	n/a
45	chr10:16238008-16238058	Jurkat	blood:	n/a
46	chr10:16238008-16238058	GM19239	blood:	n/a
47	chr10:16238008-16238058	BE2_C	brain:	n/a
48	chr10:16238008-16238058	GM12892	blood:	n/a
49	chr10:16238008-16238058	K562	blood:	n/a
50	chr10:16238008-16238058	Hela-S3	cervix:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:16272567..16275355-chr10:16277483..16279973,2	K562	blood:

No data

Variant related genes	Relation type
RNU6-1075P	TF binding region
RNU6-1075P	CpG island

Extended variants
information (count: 668 )
Associated
traits (count: 47 )

Variant overlapped rSNPs/rCNVs (count:668 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183913727	chr10:16236995-16236996	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs544856080	chr10:16237032-16237033	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs116276866	chr10:16237115-16237116	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs530183497	chr10:16237127-16237128	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs145792008	chr10:16237130-16237131	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs560638609	chr10:16237138-16237139	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs369814519	chr10:16237186-16237187	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs138621777	chr10:16237191-16237192	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs190355136	chr10:16237207-16237208	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs546264720	chr10:16237279-16237280	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs547149411	chr10:16237321-16237322	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs182598864	chr10:16237386-16237387	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs184993565	chr10:16237392-16237393	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs372040545	chr10:16237422-16237423	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs7915627	chr10:16237425-16237426	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs536441654	chr10:16237436-16237437	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs35796610	chr10:16237438-16237439	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs10795358	chr10:16237439-16237440	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs12243102	chr10:16237599-16237600	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs190286986	chr10:16237630-16237631	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs577140205	chr10:16237664-16237665	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs544283325	chr10:16237715-16237716	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs556396343	chr10:16237724-16237725	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs35275894	chr10:16237725-16237726	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs181078279	chr10:16237742-16237743	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs537293125	chr10:16237772-16237773	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs560351147	chr10:16237775-16237776	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs546521161	chr10:16237800-16237801	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs558821689	chr10:16237804-16237805	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs527897382	chr10:16237824-16237825	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs540297748	chr10:16237841-16237842	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs115549794	chr10:16237862-16237863	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs550636399	chr10:16237890-16237891	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs185563252	chr10:16237940-16237941	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs190221106	chr10:16237946-16237947	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs57870435	chr10:16237959-16237960	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs548387508	chr10:16237996-16237997	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs566636626	chr10:16238000-16238001	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs370656552	chr10:16238008-16238009	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs376429845	chr10:16238050-16238051	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs180804490	chr10:16238083-16238084	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs570863903	chr10:16238093-16238094	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs373623344	chr10:16238099-16238100	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs556183156	chr10:16238124-16238125	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs556152294	chr10:16238129-16238130	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs574768652	chr10:16238158-16238159	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs542085936	chr10:16238229-16238230	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs143371069	chr10:16238241-16238242	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs80125244	chr10:16238351-16238352	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs576924822	chr10:16238374-16238375	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:47)

Disease	PMID	Source
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
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
small cell lung cancer	20016488	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
Renal cell carcinoma	18765545	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
DiGeorge-Velo cardiofacial	22470819	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
Esophageal cancer	21851588	CNVD
Adrenocortical carcinoma	18281524	CNVD
Digeorge syndrome	17576883	CNVD
Lung cancer	16773561	CNVD
Velocardiofacial syndrome	17576883	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	22048815	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Hepatocellular carcinoma	16750200	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Thymic lymphomas tumor	22700994	CNVD

Chromatin state (count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:16217400-16239000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr10:16234200-16237600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr10:16234400-16237000	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr10:16235400-16239000	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr10:16236000-16239000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr10:16236000-16239000	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr10:16236200-16237600	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr10:16236400-16238000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr10:16236800-16237200	Enhancers	HMEC	breast
10	chr10:16236800-16237600	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr10:16236800-16237600	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr10:16236800-16237600	Enhancers	HSMM	muscle
13	chr10:16236800-16237800	Enhancers	H9 Cell Line	embryonic stem cell
14	chr10:16236800-16239200	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr10:16236800-16239400	Enhancers	H1 Cell Line	embryonic stem cell
16	chr10:16237000-16237200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
17	chr10:16237200-16237400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr10:16237200-16237600	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr10:16237400-16237800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
20	chr10:16237600-16237800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
21	chr10:16237600-16237800	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
22	chr10:16237600-16238000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
23	chr10:16237600-16238000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
24	chr10:16237600-16238000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
25	chr10:16237600-16238000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
26	chr10:16237800-16238400	Active TSS	iPS-20b Cell Line	embryonic stem cell
27	chr10:16237800-16238800	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr10:16238000-16238200	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr10:16238000-16238400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
30	chr10:16238000-16238400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr10:16238000-16238800	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr10:16238000-16239000	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr10:16238200-16238400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
34	chr10:16238400-16238600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
35	chr10:16238400-16238800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
36	chr10:16238400-16239000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr10:16238400-16239200	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr10:16238600-16238800	Flanking Active TSS	ES-WA7 Cell Line	embryonic stem cell
39	chr10:16238800-16239000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
40	chr10:16238800-16239000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
41	chr10:16238800-16239200	Enhancers	H9 Cell Line	embryonic stem cell
42	chr10:16238800-16239200	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr10:16239000-16239200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr10:16239000-16239200	ZNF genes & repeats	Aorta	Aorta
45	chr10:16239000-16239400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr10:16239000-16239400	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
47	chr10:16239000-16239400	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr10:16239400-16239600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr10:16247200-16247400	Weak transcription	Aorta	Aorta
50	chr10:16257400-16257800	Enhancers	iPS-15b Cell Line	embryonic stem cell

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