Variant report

Variant	nsv873640
Chromosome Location	chr2:10385097-10422342
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:935)
CpG islands
(count:244)
Chromatin interactive
region (count:126)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:935 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:10418584-10418795	K562	blood:	n/a	n/a
2	ARID3A	chr2:10415415-10415772	K562	blood:	n/a	n/a
3	ARID3A	chr2:10410744-10411204	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:10418323-10418786	HepG2	liver:	n/a	n/a
5	ATF1	chr2:10412562-10412818	K562	blood:	n/a	n/a
6	ATF1	chr2:10415442-10415835	K562	blood:	n/a	n/a
7	ATF3	chr2:10410755-10411243	A549	lung:	n/a	n/a
8	BACH1	chr2:10389636-10389730	K562	blood:	n/a	n/a
9	BACH1	chr2:10394865-10395052	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr2:10410798-10411074	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr2:10394612-10395418	K562	blood:	n/a	n/a
12	BCL3	chr2:10411569-10411911	GM12878	blood:	n/a	n/a
13	BCL3	chr2:10410565-10411163	A549	lung:	n/a	n/a
14	BCL3	chr2:10392265-10392784	GM12878	blood:	n/a	n/a
15	BCL3	chr2:10392412-10392681	GM12878	blood:	n/a	n/a
16	BHLHE40	chr2:10412605-10412933	K562	blood:	n/a	n/a
17	BHLHE40	chr2:10418418-10418917	HepG2	liver:	n/a	n/a
18	BHLHE40	chr2:10397051-10397251	K562	blood:	n/a	chr2:10397193-10397214
19	BHLHE40	chr2:10410818-10411199	HepG2	liver:	n/a	chr2:10410818-10410834
20	BHLHE40	chr2:10410647-10410988	K562	blood:	n/a	chr2:10410818-10410834
21	BHLHE40	chr2:10394330-10395085	K562	blood:	n/a	n/a
22	BHLHE40	chr2:10418559-10418816	GM12878	blood:	n/a	n/a
23	BHLHE40	chr2:10410727-10410890	GM12878	blood:	n/a	chr2:10410818-10410834
24	BHLHE40	chr2:10408292-10408379	HepG2	liver:	n/a	n/a
25	BHLHE40	chr2:10411770-10411877	K562	blood:	n/a	n/a
26	BHLHE40	chr2:10418496-10419147	K562	blood:	n/a	n/a
27	BRCA1	chr2:10410723-10410937	Hela-S3	cervix:	n/a	n/a
28	CBX3	chr2:10413618-10414092	K562	blood:	n/a	n/a
29	CBX3	chr2:10389900-10390243	K562	blood:	n/a	n/a
30	CBX3	chr2:10389934-10390243	K562	blood:	n/a	n/a
31	CBX3	chr2:10418272-10419464	K562	blood:	n/a	n/a
32	CBX3	chr2:10412632-10413096	K562	blood:	n/a	n/a
33	CBX3	chr2:10393543-10395118	K562	blood:	n/a	n/a
34	CCNT2	chr2:10418572-10418854	K562	blood:	n/a	n/a
35	CCNT2	chr2:10394708-10395106	K562	blood:	n/a	n/a
36	CCNT2	chr2:10412618-10412895	K562	blood:	n/a	n/a
37	CEBPB	chr2:10414553-10414720	K562	blood:	n/a	n/a
38	CEBPB	chr2:10410838-10411219	Hela-S3	cervix:	n/a	chr2:10411068-10411079
39	CEBPB	chr2:10410698-10411389	A549	lung:	n/a	chr2:10411068-10411079
40	CEBPB	chr2:10410819-10411289	MCF-7	breast:	n/a	chr2:10411068-10411079
41	CEBPB	chr2:10410942-10411171	IMR90	lung:	n/a	chr2:10411068-10411079
42	CEBPB	chr2:10418575-10418875	HepG2	liver:	n/a	n/a
43	CEBPB	chr2:10410937-10411128	K562	blood:	n/a	chr2:10411068-10411079
44	CEBPB	chr2:10410850-10411245	A549	lung:	n/a	chr2:10411068-10411079
45	CEBPB	chr2:10410805-10411302	A549	lung:	n/a	chr2:10411068-10411079
46	CEBPB	chr2:10417920-10417950	HepG2	liver:	n/a	n/a
47	CEBPB	chr2:10394142-10394590	K562	blood:	n/a	n/a
48	CEBPB	chr2:10410877-10411261	HepG2	liver:	n/a	chr2:10411068-10411079
49	CEBPD	chr2:10417779-10418725	HepG2	liver:	n/a	n/a
50	CHD1	chr2:10418571-10418625	GM12878	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:10395333-10395383	HEK293	kidney:	embryo
2	chr2:10395333-10395383	HPAEpiC	pulmonary alveolar:	n/a
3	chr2:10395189-10395239	HCPEpiC	choroid plexus:	n/a
4	chr2:10395195-10395245	HEEpiC	esophagus:	n/a
5	chr2:10406539-10406589	ovcar-3	ovarian:	n/a
6	chr2:10395189-10395239	Hela-S3	cervix:	n/a
7	chr2:10395189-10395239	AG04449	skin:	fetal
8	chr2:10395333-10395383	NT2-D1	testis:	n/a
9	chr2:10406539-10406589	PFSK-1	brain:	n/a
10	chr2:10395333-10395383	SKMC	muscle:	n/a
11	chr2:10395333-10395383	HUVEC	blood vessel:	n/a
12	chr2:10395333-10395383	Hepatocyte	liver:	n/a
13	chr2:10406539-10406589	K562	blood:	n/a
14	chr2:10395195-10395245	HRPEpiC	eye:	n/a
15	chr2:10406539-10406589	HPAEpiC	pulmonary alveolar:	n/a
16	chr2:10395333-10395383	Hela-S3	cervix:	n/a
17	chr2:10395195-10395245	HAEpiC	amniotic membrane:	n/a
18	chr2:10406539-10406589	RPTEC	kidney:	n/a
19	chr2:10395189-10395239	IMR90	lung:	fetal
20	chr2:10395333-10395383	HAEpiC	amniotic membrane:	n/a
21	chr2:10395189-10395239	PFSK-1	brain:	n/a
22	chr2:10395195-10395245	MCF10A-Er-Src	breast:	n/a
23	chr2:10395189-10395239	PrEC	prostate:	n/a
24	chr2:10395189-10395239	MCF-7	breast:	n/a
25	chr2:10395189-10395239	BE2_C	brain:	n/a
26	chr2:10406539-10406589	HNPCEpiC	eye:	n/a
27	chr2:10395333-10395383	Caco-2	colon:	n/a
28	chr2:10395189-10395239	NB4	blood:	n/a
29	chr2:10395189-10395239	T-47D	breast:	n/a
30	chr2:10406539-10406589	SK-N-MC	brain:	n/a
31	chr2:10406539-10406589	NHDF-neo	bronchial:	n/a
32	chr2:10406539-10406589	HIPEpiC	eye:	n/a
33	chr2:10395333-10395383	AG10803	skin:	n/a
34	chr2:10406539-10406589	GM19239	blood:	n/a
35	chr2:10406539-10406589	SAEC	small airway:	n/a
36	chr2:10406539-10406589	MCF-7	breast:	n/a
37	chr2:10406539-10406589	GM06990	blood:	n/a
38	chr2:10395333-10395383	GM19239	blood:	n/a
39	chr2:10395195-10395245	GM12878	blood:	n/a
40	chr2:10395195-10395245	Hepatocyte	liver:	n/a
41	chr2:10395333-10395383	AoSMC	blood vessel:	n/a
42	chr2:10406539-10406589	SK-N-SH	brain:	n/a
43	chr2:10395189-10395239	GM12878	blood:	n/a
44	chr2:10395195-10395245	NH-A	brain:	n/a
45	chr2:10395189-10395239	NHDF-neo	bronchial:	n/a
46	chr2:10406539-10406589	AG09309	skin:	n/a
47	chr2:10406539-10406589	BJ	skin:	n/a
48	chr2:10395195-10395245	HEK293	kidney:	embryo
49	chr2:10406539-10406589	Hepatocyte	liver:	n/a
50	chr2:10395189-10395239	HEEpiC	esophagus:	n/a

(count:126 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr2:10363646..10365657-chr2:10382522..10385441,2	K562	blood:
2	chr2:10411031..10415128-chr2:10415819..10419718,6	K562	blood:
3	chr2:10394375..10395994-chr2:10546875..10548738,2	K562	blood:
4	chr2:10390359..10393912-chr2:10395616..10397789,3	MCF-7	breast:
5	chr2:10410318..10412062-chr2:10423255..10425080,2	K562	blood:
6	chr2:10392904..10395765-chr2:10528915..10531340,2	K562	blood:
7	chr2:10409808..10412548-chr2:10436886..10439745,2	K562	blood:
8	chr2:10407684..10409187-chr2:10409189..10411668,2	K562	blood:
9	chr2:10379961..10381980-chr2:10382595..10386156,4	K562	blood:
10	chr2:10417267..10421526-chr2:10440124..10444517,8	K562	blood:
11	chr2:10412656..10415128-chr2:10415819..10419038,3	K562	blood:
12	chr2:10410359..10411311-chr2:10549026..10549739,3	MCF-7	breast:
13	chr2:10275519..10277436-chr2:10408432..10410415,2	K562	blood:
14	chr2:10393925..10395521-chr2:10443524..10445686,2	K562	blood:
15	chr2:10393925..10398726-chr2:10441942..10445686,4	K562	blood:
16	chr2:10390359..10393912-chr2:10395616..10397789,3	MCF-7	breast:
17	chr2:10393127..10396055-chr2:10588104..10589824,2	K562	blood:
18	chr2:10393709..10396218-chr2:10398784..10401137,2	MCF-7	breast:
19	chr2:10418589..10420185-chr2:10425009..10427268,2	MCF-7	breast:
20	chr2:10392345..10395188-chr2:10407318..10409008,2	K562	blood:
21	chr2:10393161..10396056-chr2:10408396..10410670,2	K562	blood:
22	chr2:10259903..10262300-chr2:10409674..10412836,3	K562	blood:
23	chr2:10392978..10395026-chr2:10400491..10403143,2	K562	blood:
24	chr2:10416266..10418182-chr2:10522791..10524644,2	K562	blood:
25	chr2:10393383..10395595-chr2:10425523..10427994,2	MCF-7	breast:
26	chr2:10393518..10395785-chr2:10396578..10398775,3	K562	blood:
27	chr2:10394157..10396963-chr2:10408123..10409745,2	MCF-7	breast:
28	chr2:10277542..10280020-chr2:10400338..10402509,2	MCF-7	breast:
29	chr2:10393987..10396865-chr2:10417626..10420147,4	K562	blood:
30	chr2:10402021..10404531-chr2:10418594..10421121,3	MCF-7	breast:
31	chr2:10411246..10413017-chr2:10487385..10489486,2	MCF-7	breast:
32	chr2:10410210..10413138-chr2:10413246..10415299,2	K562	blood:
33	chr2:10382224..10385160-chr2:10393761..10396666,3	K562	blood:
34	chr2:10400709..10402534-chr2:10403743..10407467,3	K562	blood:
35	chr2:10409240..10412523-chr2:10441653..10444866,3	MCF-7	breast:
36	chr2:10392294..10394554-chr2:10441498..10444201,2	MCF-7	breast:
37	chr2:10412424..10413935-chr2:10416602..10418723,2	MCF-7	breast:
38	chr2:10412868..10415493-chr2:10441728..10443510,2	MCF-7	breast:
39	chr2:10409606..10412546-chr2:10546766..10549181,2	MCF-7	breast:
40	chr2:10382224..10385160-chr2:10393761..10396666,3	K562	blood:
41	chr2:10403955..10406520-chr2:10410509..10412633,2	K562	blood:
42	chr2:10265893..10268828-chr2:10402718..10405251,2	K562	blood:
43	chr2:10408398..10410082-chr2:10581938..10584140,2	K562	blood:
44	chr2:10408428..10415108-chr2:10440417..10445284,9	MCF-7	breast:
45	chr2:10396329..10399682-chr2:10404983..10407952,4	K562	blood:
46	chr2:10394556..10396189-chr2:10409170..10411649,3	K562	blood:
47	chr2:10404445..10406499-chr2:10426749..10428741,2	K562	blood:
48	chr2:10402938..10406350-chr2:10406661..10410178,4	K562	blood:
49	chr2:10393987..10396865-chr2:10417626..10420147,4	K562	blood:
50	chr2:10394556..10396189-chr2:10409170..10411649,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HPCAL1-4	chr2:10420757-10421017	NONHSAT069094

No data

Variant related genes	Relation type
RN7SL66P	TF binding region
RN7SL66P	CpG island
ENSG00000163009	chromatin interactions
ENSG00000264030	chromatin interactions
ENSG00000272524	chromatin interactions
ENSG00000257135	chromatin interactions
ENSG00000206633	chromatin interactions
ENSG00000171848	chromatin interactions
ENSG00000115756	chromatin interactions
ENSG00000115758	chromatin interactions

Extended variants
information (count: 1745 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:1745 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10929646	chr2:10385097-10385098	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs573923697	chr2:10385106-10385107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555597554	chr2:10385108-10385109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs35253931	chr2:10385175-10385176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs114949190	chr2:10385180-10385181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs78743492	chr2:10385206-10385207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs397723229	chr2:10385207-10385208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs370730221	chr2:10385234-10385235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs578013054	chr2:10385263-10385264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs545103349	chr2:10385282-10385283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563502507	chr2:10385284-10385285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs531002636	chr2:10385285-10385286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs367981435	chr2:10385293-10385294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs549214087	chr2:10385338-10385339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs75822018	chr2:10385347-10385348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs186142383	chr2:10385354-10385355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs115274411	chr2:10385406-10385407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs565689115	chr2:10385411-10385412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs190557210	chr2:10385422-10385423	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs181484845	chr2:10385444-10385445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs551509995	chr2:10385467-10385468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs569807073	chr2:10385474-10385475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs11695140	chr2:10385480-10385481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs145976953	chr2:10385489-10385490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs186470255	chr2:10385519-10385520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs72771621	chr2:10385537-10385538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs368044447	chr2:10385563-10385564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs35516039	chr2:10385584-10385585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs10445710	chr2:10385654-10385655	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs577978126	chr2:10385670-10385671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs371376061	chr2:10385688-10385689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs376637560	chr2:10385695-10385696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs17379426	chr2:10385699-10385700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs75166578	chr2:10385732-10385733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574107316	chr2:10385747-10385748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs568887643	chr2:10385767-10385768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs143343155	chr2:10385797-10385798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs6715087	chr2:10385815-10385816	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs191398814	chr2:10385827-10385828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs528751358	chr2:10385828-10385829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs540921276	chr2:10385831-10385832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs559043319	chr2:10385832-10385833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs62127656	chr2:10385847-10385848	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs116181150	chr2:10385851-10385852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375851519	chr2:10385871-10385872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs569745822	chr2:10385895-10385896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs115225692	chr2:10385908-10385909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs548877766	chr2:10385922-10385923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs116804556	chr2:10386010-10386011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs73914011	chr2:10386032-10386033	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Mental retardation	17847001	CNVD
Glioblastoma multiforme	21080181	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Cancer	20164920	CNVD
Neuroblastoma	21508638	CNVD
Breast cancer	17603634	CNVD
Cancer	16751803	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Ependymoma	16718352	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Glioma	17123091	CNVD
Breast cancer	20409316	CNVD
Multiple myeloma	16616336	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	22522925	CNVD
Neuroblastoma	18923524	CNVD
Pancreatic cancer	17952125	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:515 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:10384400-10385400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:10385400-10385600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr2:10385600-10392400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr2:10386400-10387200	Enhancers	Primary B cells from peripheral blood	blood
5	chr2:10386400-10387400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr2:10386600-10386800	Bivalent Enhancer	Primary B cells from cord blood	blood
7	chr2:10386600-10387000	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
8	chr2:10386600-10387200	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
9	chr2:10386600-10387200	Enhancers	Primary hematopoietic stem cells	blood
10	chr2:10386600-10387200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr2:10386800-10387000	Enhancers	Primary B cells from cord blood	blood
12	chr2:10391600-10394400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr2:10392400-10392600	Enhancers	K562	blood
14	chr2:10392400-10392800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr2:10392400-10392800	Enhancers	Gastric	stomach
16	chr2:10392400-10393000	Enhancers	Stomach Mucosa	stomach
17	chr2:10392400-10393800	Enhancers	Primary hematopoietic stem cells	blood
18	chr2:10392400-10394200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr2:10392600-10393200	Weak transcription	K562	blood
20	chr2:10392600-10393800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr2:10392600-10395800	Enhancers	Primary hematopoietic stem cells short term culture	blood
22	chr2:10392800-10393600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr2:10392800-10394400	Enhancers	Placenta	Placenta
24	chr2:10392800-10399200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
25	chr2:10392800-10407600	Weak transcription	Gastric	stomach
26	chr2:10393000-10395000	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr2:10393000-10395200	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr2:10393200-10394200	Enhancers	K562	blood
29	chr2:10393400-10397800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
30	chr2:10393600-10393800	Enhancers	Spleen	Spleen
31	chr2:10393600-10394800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr2:10393600-10395200	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr2:10393800-10394400	Enhancers	Lung	lung
34	chr2:10393800-10394800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr2:10393800-10394800	Weak transcription	Spleen	Spleen
36	chr2:10393800-10395000	Enhancers	Fetal Muscle Leg	muscle
37	chr2:10393800-10395600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr2:10393800-10396200	Weak transcription	Primary hematopoietic stem cells	blood
39	chr2:10393800-10396200	Enhancers	Hela-S3	cervix
40	chr2:10394200-10394600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr2:10394200-10395200	Enhancers	Fetal Intestine Large	intestine
42	chr2:10394200-10395400	Flanking Active TSS	K562	blood
43	chr2:10394200-10395600	Enhancers	A549	lung
44	chr2:10394400-10395200	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr2:10394400-10395200	Enhancers	HSMM	muscle
46	chr2:10394400-10396000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr2:10394400-10396000	Bivalent Enhancer	Placenta	Placenta
48	chr2:10394600-10394800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
49	chr2:10394600-10394800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr2:10394600-10395000	Enhancers	H1 Cell Line	embryonic stem cell

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