Variant report

Variant	nsv894905
Chromosome Location	chr10:16410436-16483081
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:769)
CpG islands
(count:795)
Chromatin interactive
region (count:14)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:769 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:16478962-16479104	K562	blood:	n/a	n/a
2	ARID3A	chr10:16422969-16423559	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:16482831-16483096	K562	blood:	n/a	chr10:16483052-16483068
4	ATF2	chr10:16428721-16429282	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr10:16423065-16423602	A549	lung:	n/a	n/a
6	ATF3	chr10:16422975-16423561	A549	lung:	n/a	n/a
7	BACH1	chr10:16428775-16429371	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr10:16417933-16417987	K562	blood:	n/a	n/a
9	BACH1	chr10:16433607-16433807	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr10:16478713-16479279	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr10:16429609-16429851	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr10:16423103-16423406	GM12878	blood:	n/a	chr10:16423259-16423270 chr10:16423372-16423382 chr10:16423260-16423270
13	BCL11A	chr10:16423180-16423405	GM12878	blood:	n/a	chr10:16423263-16423272 chr10:16423262-16423271
14	BCL11A	chr10:16482643-16483040	GM12878	blood:	n/a	chr10:16482944-16482952
15	BCL3	chr10:16478787-16479306	A549	lung:	n/a	chr10:16479006-16479015
16	BCL3	chr10:16422924-16423596	A549	lung:	n/a	chr10:16422963-16422972 chr10:16423263-16423272 chr10:16423262-16423271
17	BCL3	chr10:16467511-16467767	GM12878	blood:	n/a	n/a
18	BCLAF1	chr10:16482772-16483182	GM12878	blood:	n/a	chr10:16482944-16482952
19	BCLAF1	chr10:16478815-16479269	GM12878	blood:	n/a	chr10:16479006-16479015
20	BHLHE40	chr10:16423085-16423417	HepG2	liver:	n/a	n/a
21	BHLHE40	chr10:16479355-16479644	HepG2	liver:	n/a	n/a
22	BHLHE40	chr10:16482677-16483181	GM12878	blood:	n/a	n/a
23	BHLHE40	chr10:16441669-16441861	K562	blood:	n/a	n/a
24	BHLHE40	chr10:16478599-16479910	GM12878	blood:	n/a	n/a
25	BHLHE40	chr10:16478783-16479924	K562	blood:	n/a	n/a
26	BHLHE40	chr10:16482581-16483012	K562	blood:	n/a	n/a
27	BHLHE40	chr10:16450532-16450677	K562	blood:	n/a	n/a
28	BRCA1	chr10:16479215-16479278	GM12878	blood:	n/a	n/a
29	CBX3	chr10:16422988-16423607	HCT-116	colon:	n/a	n/a
30	CBX3	chr10:16469654-16469960	K562	blood:	n/a	n/a
31	CBX3	chr10:16478636-16479568	K562	blood:	n/a	n/a
32	CCNT2	chr10:16478599-16479386	K562	blood:	n/a	chr10:16478933-16478942
33	CCNT2	chr10:16482745-16483001	K562	blood:	n/a	n/a
34	CEBPB	chr10:16479476-16479840	K562	blood:	n/a	n/a
35	CEBPB	chr10:16479538-16479736	K562	blood:	n/a	n/a
36	CEBPB	chr10:16423171-16423401	A549	lung:	n/a	n/a
37	CEBPB	chr10:16479190-16479367	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr10:16422960-16423579	A549	lung:	n/a	n/a
39	CEBPB	chr10:16427497-16427753	IMR90	lung:	n/a	chr10:16427529-16427540 chr10:16427657-16427670 chr10:16427531-16427542
40	CEBPB	chr10:16479539-16479836	HepG2	liver:	n/a	n/a
41	CEBPB	chr10:16427424-16427784	A549	lung:	n/a	chr10:16427529-16427540 chr10:16427657-16427670 chr10:16427531-16427542
42	CEBPB	chr10:16481336-16481701	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr10:16427385-16427804	HepG2	liver:	n/a	chr10:16427529-16427540 chr10:16427657-16427670 chr10:16427531-16427542
44	CEBPB	chr10:16456327-16456475	HepG2	liver:	n/a	n/a
45	CEBPB	chr10:16478737-16479855	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr10:16427522-16427992	H1-hESC	embryonic stem cell:	n/a	chr10:16427529-16427540 chr10:16427657-16427670 chr10:16427531-16427542
47	CEBPB	chr10:16479502-16479880	K562	blood:	n/a	n/a
48	CEBPB	chr10:16427542-16427813	K562	blood:	n/a	chr10:16427657-16427670
49	CEBPB	chr10:16428600-16429336	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr10:16413647-16413769	A549	lung:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:16479034-16479084	HAEpiC	amniotic membrane:	n/a
2	chr10:16478910-16478960	BE2_C	brain:	n/a
3	chr10:16479034-16479084	HAEpiC	amniotic membrane:	n/a
4	chr10:16478910-16478960	BE2_C	brain:	n/a
5	chr10:16479076-16479126	HCPEpiC	choroid plexus:	n/a
6	chr10:16478854-16478904	IMR90	lung:	fetal
7	chr10:16478919-16478969	AoSMC	blood vessel:	n/a
8	chr10:16481929-16481979	AG10803	skin:	n/a
9	chr10:16478471-16478521	MCF-7	breast:	n/a
10	chr10:16478471-16478521	AG04450	lung:	fetal
11	chr10:16478554-16478604	HCM	heart:	n/a
12	chr10:16479076-16479126	NHDF-neo	bronchial:	n/a
13	chr10:16478471-16478521	HCT-116	colon:	n/a
14	chr10:16478834-16478884	AoSMC	blood vessel:	n/a
15	chr10:16478613-16478663	HCF	heart:	n/a
16	chr10:16479192-16479242	NH-A	brain:	n/a
17	chr10:16478613-16478663	BJ	skin:	n/a
18	chr10:16479034-16479084	PANC-1	pancreas:	n/a
19	chr10:16478834-16478884	RPTEC	kidney:	n/a
20	chr10:16478854-16478904	HPAEpiC	pulmonary alveolar:	n/a
21	chr10:16478471-16478521	GM19239	blood:	n/a
22	chr10:16478554-16478604	HCT-116	colon:	n/a
23	chr10:16478471-16478521	SK-N-SH_RA	brain:	n/a
24	chr10:16481929-16481979	Hela-S3	cervix:	n/a
25	chr10:16478910-16478960	K562	blood:	n/a
26	chr10:16478834-16478884	GM12878	blood:	n/a
27	chr10:16478471-16478521	BJ	skin:	n/a
28	chr10:16479034-16479084	NHBE	bronchial:	n/a
29	chr10:16478471-16478521	AoSMC	blood vessel:	n/a
30	chr10:16478919-16478969	ovcar-3	ovarian:	n/a
31	chr10:16481929-16481979	ProgFib	skin:	n/a
32	chr10:16478854-16478904	HepG2	liver:	n/a
33	chr10:16481929-16481979	GM19239	blood:	n/a
34	chr10:16481929-16481979	HCM	heart:	n/a
35	chr10:16478471-16478521	GM12878	blood:	n/a
36	chr10:16479192-16479242	SK-N-MC	brain:	n/a
37	chr10:16478834-16478884	ovcar-3	ovarian:	n/a
38	chr10:16478471-16478521	HEK293	kidney:	embryo
39	chr10:16479192-16479242	HRE	kidney:	n/a
40	chr10:16480652-16480702	PrEC	prostate:	n/a
41	chr10:16478834-16478884	AG04449	skin:	fetal
42	chr10:16478471-16478521	HL-60	blood:	n/a
43	chr10:16478854-16478904	RPTEC	kidney:	n/a
44	chr10:16478554-16478604	CMK	blood:	n/a
45	chr10:16480652-16480702	H1-hESC	embryonic stem cell:	embryo
46	chr10:16478910-16478960	Hepatocyte	liver:	n/a
47	chr10:16480652-16480702	CMK	blood:	n/a
48	chr10:16478919-16478969	GM06990	blood:	n/a
49	chr10:16479192-16479242	K562	blood:	n/a
50	chr10:16478910-16478960	HNPCEpiC	eye:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:16478859..16479423-chrX:118602412..118603354,2	Hela-S3	cervix:
2	chr10:16449086..16451167-chr10:16822811..16824865,2	K562	blood:
3	chr10:16480336..16481883-chr10:16489217..16491093,2	K562	blood:
4	chr10:16474070..16475704-chr10:16478118..16480113,2	K562	blood:
5	chr10:16425069..16427084-chr10:16526700..16529577,2	K562	blood:
6	chr10:16456924..16458854-chr10:16459687..16461812,2	K562	blood:
7	chr10:16478731..16479259-chr9:110045655..110046403,2	Hela-S3	cervix:
8	chr10:16473600..16475647-chr10:16477202..16478707,2	K562	blood:
9	chr10:16481008..16482712-chr10:16490466..16492255,2	K562	blood:
10	chr10:16456924..16458854-chr10:16459687..16461812,2	K562	blood:
11	chr10:16406573..16409426-chr10:16416756..16418414,2	K562	blood:
12	chr10:16468825..16471153-chr10:16477248..16479431,2	K562	blood:
13	chr10:16473600..16475647-chr10:16477202..16478707,2	K562	blood:
14	chr10:16478865..16480731-chr6:26157879..26159983,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C1QL3-2	chr10:16428802-16429050	NONHSAT011594

No data

Variant related genes	Relation type
PTER	TF binding region
ENSG00000238552	TF binding region
PTER	CpG island
ENSG00000238552	CpG island
ENSG00000165983	chromatin interactions
ENSG00000005022	chromatin interactions
ENSG00000119318	chromatin interactions
ENSG00000158373	chromatin interactions
ENSG00000224281	chromatin interactions

Extended variants
information (count: 2590 )
Associated
traits (count: 47 )

Variant overlapped rSNPs/rCNVs (count:2590 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12219697	chr10:16410436-16410437	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs568203526	chr10:16410439-16410440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs556213930	chr10:16410458-16410459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs535502234	chr10:16410465-16410466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs190540889	chr10:16410518-16410519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs146377595	chr10:16410536-16410537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs182380211	chr10:16410543-16410544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs200096536	chr10:16410583-16410584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs187188815	chr10:16410596-16410597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs567825213	chr10:16410613-16410614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs576540356	chr10:16410633-16410634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs139694785	chr10:16410652-16410653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs556342866	chr10:16410726-16410727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs17138484	chr10:16410727-16410728	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs191253436	chr10:16410773-16410774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs147988307	chr10:16410800-16410801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs184497892	chr10:16410809-16410810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs560061779	chr10:16410818-16410819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs574112887	chr10:16410830-16410831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs188977726	chr10:16410841-16410842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs546028685	chr10:16410861-16410862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs564132897	chr10:16410862-16410863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs549563532	chr10:16410888-16410889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs549560950	chr10:16410915-16410916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs568241803	chr10:16410932-16410933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs144327018	chr10:16410933-16410934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs547401778	chr10:16410942-16410943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs566037592	chr10:16410984-16410985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs539754334	chr10:16410997-16410998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs558470174	chr10:16411001-16411002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374941946	chr10:16411007-16411008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs570250937	chr10:16411029-16411030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571366288	chr10:16411044-16411045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541634432	chr10:16411083-16411084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs193039633	chr10:16411091-16411092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574603877	chr10:16411125-16411126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs114976604	chr10:16411168-16411169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs553494309	chr10:16411247-16411248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571964175	chr10:16411328-16411329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs545470072	chr10:16411346-16411347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs538245284	chr10:16411378-16411379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564450467	chr10:16411420-16411421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185739827	chr10:16411450-16411451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs543246550	chr10:16411465-16411466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs151059466	chr10:16411490-16411491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529367903	chr10:16411527-16411528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547823476	chr10:16411535-16411536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs566032503	chr10:16411561-16411562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs140945289	chr10:16411614-16411615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs7080600	chr10:16411624-16411625	Weak transcription	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
Breast cancer	22522925	CNVD

Chromatin state (count:748 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:16403400-16428600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr10:16409800-16411000	Enhancers	Fetal Brain Female	brain
3	chr10:16409800-16428800	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr10:16410200-16411000	Enhancers	Brain Germinal Matrix	brain
5	chr10:16410400-16410600	Enhancers	Fetal Brain Male	brain
6	chr10:16412200-16412600	Enhancers	HepG2	liver
7	chr10:16416600-16417400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr10:16417400-16418200	Enhancers	A549	lung
9	chr10:16418200-16419400	Weak transcription	A549	lung
10	chr10:16419400-16419600	Enhancers	A549	lung
11	chr10:16419600-16422000	Weak transcription	A549	lung
12	chr10:16419800-16420000	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr10:16419800-16420000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
14	chr10:16419800-16420000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
15	chr10:16419800-16420000	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
16	chr10:16419800-16420000	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
17	chr10:16419800-16420000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
18	chr10:16419800-16420000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr10:16419800-16420000	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
20	chr10:16419800-16420000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr10:16419800-16420400	Enhancers	Placenta	Placenta
22	chr10:16420400-16420800	Weak transcription	Placenta	Placenta
23	chr10:16420800-16421200	Enhancers	Placenta	Placenta
24	chr10:16421400-16425200	Enhancers	HepG2	liver
25	chr10:16422000-16422800	Enhancers	A549	lung
26	chr10:16422800-16423200	Flanking Active TSS	A549	lung
27	chr10:16423200-16424000	Active TSS	A549	lung
28	chr10:16423200-16427000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr10:16424000-16424200	Flanking Active TSS	A549	lung
30	chr10:16424200-16424600	Enhancers	A549	lung
31	chr10:16424600-16424800	Enhancers	Fetal Brain Female	brain
32	chr10:16424800-16425800	Weak transcription	Fetal Brain Female	brain
33	chr10:16425600-16425800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr10:16425800-16426200	Enhancers	Brain Germinal Matrix	brain
35	chr10:16425800-16426400	Enhancers	Fetal Brain Female	brain
36	chr10:16425800-16426400	Enhancers	Fetal Muscle Leg	muscle
37	chr10:16426000-16426200	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
38	chr10:16426000-16426400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr10:16426000-16426400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr10:16426000-16427600	Enhancers	H1 Cell Line	embryonic stem cell
41	chr10:16426200-16426400	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr10:16426200-16426400	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr10:16426200-16426600	Bivalent Enhancer	Brain Cingulate Gyrus	brain
44	chr10:16426200-16426600	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
45	chr10:16426200-16427200	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr10:16426400-16427400	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr10:16426400-16428600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr10:16427000-16427200	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr10:16427200-16428000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
50	chr10:16427200-16428200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell

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