Variant report

Variant	esv2762357
Chromosome Location	chr2:10401309-10426323
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1176)
CpG islands
(count:122)
Chromatin interactive
region (count:95)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1176 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:10425773-10425934	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:10423382-10423767	K562	blood:	n/a	n/a
3	ARID3A	chr2:10418584-10418795	K562	blood:	n/a	n/a
4	ARID3A	chr2:10418323-10418786	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:10410744-10411204	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:10415415-10415772	K562	blood:	n/a	n/a
7	ATF1	chr2:10415442-10415835	K562	blood:	n/a	n/a
8	ATF1	chr2:10412562-10412818	K562	blood:	n/a	n/a
9	ATF3	chr2:10425529-10426250	A549	lung:	n/a	chr2:10425759-10425768
10	ATF3	chr2:10423393-10423864	K562	blood:	n/a	n/a
11	ATF3	chr2:10423471-10423752	K562	blood:	n/a	n/a
12	ATF3	chr2:10410755-10411243	A549	lung:	n/a	n/a
13	BACH1	chr2:10410798-10411074	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr2:10423654-10423659	K562	blood:	n/a	n/a
15	BACH1	chr2:10425631-10426072	H1-hESC	embryonic stem cell:	n/a	chr2:10425816-10425830
16	BACH1	chr2:10425722-10425874	K562	blood:	n/a	chr2:10425816-10425830
17	BCL3	chr2:10410565-10411163	A549	lung:	n/a	n/a
18	BCL3	chr2:10411569-10411911	GM12878	blood:	n/a	n/a
19	BCL3	chr2:10424909-10426288	A549	lung:	n/a	n/a
20	BHLHE40	chr2:10418559-10418816	GM12878	blood:	n/a	n/a
21	BHLHE40	chr2:10410818-10411199	HepG2	liver:	n/a	chr2:10410818-10410834
22	BHLHE40	chr2:10423263-10423733	K562	blood:	n/a	chr2:10423335-10423351
23	BHLHE40	chr2:10425701-10426037	A549	lung:	n/a	n/a
24	BHLHE40	chr2:10418496-10419147	K562	blood:	n/a	n/a
25	BHLHE40	chr2:10412605-10412933	K562	blood:	n/a	n/a
26	BHLHE40	chr2:10408292-10408379	HepG2	liver:	n/a	n/a
27	BHLHE40	chr2:10425625-10426094	HepG2	liver:	n/a	n/a
28	BHLHE40	chr2:10410647-10410988	K562	blood:	n/a	chr2:10410818-10410834
29	BHLHE40	chr2:10411770-10411877	K562	blood:	n/a	n/a
30	BHLHE40	chr2:10418418-10418917	HepG2	liver:	n/a	n/a
31	BHLHE40	chr2:10410727-10410890	GM12878	blood:	n/a	chr2:10410818-10410834
32	BHLHE40	chr2:10425639-10426099	K562	blood:	n/a	n/a
33	BRCA1	chr2:10410723-10410937	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr2:10425541-10425979	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr2:10423370-10423682	Hela-S3	cervix:	n/a	n/a
36	CBX3	chr2:10418272-10419464	K562	blood:	n/a	n/a
37	CBX3	chr2:10423236-10423852	K562	blood:	n/a	n/a
38	CBX3	chr2:10412632-10413096	K562	blood:	n/a	n/a
39	CBX3	chr2:10413618-10414092	K562	blood:	n/a	n/a
40	CBX3	chr2:10425807-10426098	K562	blood:	n/a	n/a
41	CCNT2	chr2:10418572-10418854	K562	blood:	n/a	n/a
42	CCNT2	chr2:10412618-10412895	K562	blood:	n/a	n/a
43	CCNT2	chr2:10425747-10426039	K562	blood:	n/a	n/a
44	CCNT2	chr2:10423389-10423779	K562	blood:	n/a	chr2:10423589-10423598 chr2:10423594-10423603
45	CEBPB	chr2:10418575-10418875	HepG2	liver:	n/a	n/a
46	CEBPB	chr2:10410877-10411261	HepG2	liver:	n/a	chr2:10411068-10411079
47	CEBPB	chr2:10423339-10423853	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr2:10423465-10423818	K562	blood:	n/a	n/a
49	CEBPB	chr2:10414553-10414720	K562	blood:	n/a	n/a
50	CEBPB	chr2:10423455-10423848	A549	lung:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:10425661-10425711	MCF10A-Er-Src	breast:	n/a
2	chr2:10406539-10406589	AG09319	gingival:	n/a
3	chr2:10425661-10425711	HEK293	kidney:	embryo
4	chr2:10406539-10406589	AG04449	skin:	fetal
5	chr2:10425661-10425711	A549	lung:	n/a
6	chr2:10425661-10425711	AG10803	skin:	n/a
7	chr2:10425661-10425711	HRE	kidney:	n/a
8	chr2:10425661-10425711	Caco-2	colon:	n/a
9	chr2:10406539-10406589	MCF10A-Er-Src	breast:	n/a
10	chr2:10406539-10406589	HRPEpiC	eye:	n/a
11	chr2:10406539-10406589	HRCEpiC	kidney:	n/a
12	chr2:10406539-10406589	NH-A	brain:	n/a
13	chr2:10425661-10425711	HMEC	breast:	n/a
14	chr2:10406539-10406589	HRE	kidney:	n/a
15	chr2:10406539-10406589	NHDF-neo	bronchial:	n/a
16	chr2:10406539-10406589	NHBE	bronchial:	n/a
17	chr2:10425661-10425711	NHDF-neo	bronchial:	n/a
18	chr2:10406539-10406589	Hela-S3	cervix:	n/a
19	chr2:10425661-10425711	U87	brain:	n/a
20	chr2:10425661-10425711	HPAEpiC	pulmonary alveolar:	n/a
21	chr2:10425661-10425711	SKMC	muscle:	n/a
22	chr2:10425661-10425711	HCM	heart:	n/a
23	chr2:10425661-10425711	LNCaP	prostate:	n/a
24	chr2:10406539-10406589	K562	blood:	n/a
25	chr2:10425661-10425711	HNPCEpiC	eye:	n/a
26	chr2:10425661-10425711	NHBE	bronchial:	n/a
27	chr2:10406539-10406589	AG09309	skin:	n/a
28	chr2:10406539-10406589	SK-N-SH	brain:	n/a
29	chr2:10406539-10406589	CMK	blood:	n/a
30	chr2:10425661-10425711	GM12891	blood:	n/a
31	chr2:10425661-10425711	BE2_C	brain:	n/a
32	chr2:10406539-10406589	T-47D	breast:	n/a
33	chr2:10406539-10406589	HepG2	liver:	n/a
34	chr2:10425661-10425711	CMK	blood:	n/a
35	chr2:10425661-10425711	PrEC	prostate:	n/a
36	chr2:10406539-10406589	AG10803	skin:	n/a
37	chr2:10425661-10425711	SK-N-MC	brain:	n/a
38	chr2:10406539-10406589	HL-60	blood:	n/a
39	chr2:10425661-10425711	GM12878	blood:	n/a
40	chr2:10425661-10425711	H1-hESC	embryonic stem cell:	embryo
41	chr2:10406539-10406589	HEK293	kidney:	embryo
42	chr2:10406539-10406589	HCM	heart:	n/a
43	chr2:10406539-10406589	HUVEC	blood vessel:	n/a
44	chr2:10406539-10406589	GM06990	blood:	n/a
45	chr2:10425661-10425711	NB4	blood:	n/a
46	chr2:10425661-10425711	GM06990	blood:	n/a
47	chr2:10425661-10425711	HUVEC	blood vessel:	n/a
48	chr2:10425661-10425711	RPTEC	kidney:	n/a
49	chr2:10425661-10425711	ProgFib	skin:	n/a
50	chr2:10425661-10425711	HIPEpiC	eye:	n/a

(count:95 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:10412779..10415250-chr2:10424064..10426883,2	MCF-7	breast:
2	chr2:10424312..10426665-chr2:10442705..10445320,2	K562	blood:
3	chr2:10412424..10413935-chr2:10416602..10418723,2	MCF-7	breast:
4	chr2:10410506..10411312-chr2:10545626..10546272,2	MCF-7	breast:
5	chr2:10405314..10407272-chr2:10438185..10440055,2	K562	blood:
6	chr2:10406981..10409160-chr2:10410945..10413654,2	MCF-7	breast:
7	chr2:10406981..10409160-chr2:10410945..10413654,2	MCF-7	breast:
8	chr2:10408398..10410082-chr2:10581938..10584140,2	K562	blood:
9	chr2:10421994..10428607-chr2:10439137..10445249,17	MCF-7	breast:
10	chr2:10396329..10399682-chr2:10404983..10407952,4	K562	blood:
11	chr2:10407684..10409187-chr2:10409189..10411668,2	K562	blood:
12	chr2:10420712..10423243-chr2:10586890..10589076,2	K562	blood:
13	chr2:10423331..10426574-chr2:10438305..10440403,3	K562	blood:
14	chr2:10424782..10426457-chr2:10440963..10442554,2	K562	blood:
15	chr2:10261370..10264199-chr2:10417040..10418605,2	K562	blood:
16	chr2:10410343..10411295-chr2:10574815..10575700,7	K562	blood:
17	chr2:10403955..10406520-chr2:10410509..10412633,2	K562	blood:
18	chr2:10394556..10396189-chr2:10409170..10411649,3	K562	blood:
19	chr2:10416195..10418762-chr2:10425700..10428798,3	MCF-7	breast:
20	chr2:10412656..10415128-chr2:10415819..10419038,3	K562	blood:
21	chr2:10408428..10415108-chr2:10440417..10445284,9	MCF-7	breast:
22	chr2:10410318..10412062-chr2:10423255..10425080,2	K562	blood:
23	chr2:10409606..10412546-chr2:10546766..10549181,2	MCF-7	breast:
24	chr2:10416484..10418101-chr2:10547563..10549707,2	MCF-7	breast:
25	chr2:10416195..10418762-chr2:10425700..10428798,3	MCF-7	breast:
26	chr2:10410711..10412312-chr2:10545552..10547500,2	K562	blood:
27	chr2:10411031..10415128-chr2:10415819..10419718,6	K562	blood:
28	chr2:10392345..10395188-chr2:10407318..10409008,2	K562	blood:
29	chr2:10414107..10415744-chr2:10422290..10425033,2	K562	blood:
30	chr2:10401968..10404721-chr2:10588280..10589854,2	K562	blood:
31	chr2:10425416..10427502-chr2:10437383..10439645,2	K562	blood:
32	chr2:10402938..10406350-chr2:10406661..10410178,4	K562	blood:
33	chr2:10424760..10427362-chr2:10571844..10574068,2	MCF-7	breast:
34	chr2:10423354..10425763-chr2:10586960..10588617,2	K562	blood:
35	chr2:10412424..10413935-chr2:10416602..10418723,2	MCF-7	breast:
36	chr2:10274325..10277239-chr2:10417227..10419368,3	K562	blood:
37	chr2:10412779..10415250-chr2:10424064..10426883,2	MCF-7	breast:
38	chr2:10394157..10396963-chr2:10408123..10409745,2	MCF-7	breast:
39	chr2:10410210..10413138-chr2:10413246..10415299,2	K562	blood:
40	chr2:10407016..10409073-chr2:10423584..10425357,2	K562	blood:
41	chr2:10416266..10418182-chr2:10522791..10524644,2	K562	blood:
42	chr2:10411031..10415128-chr2:10415819..10419718,6	K562	blood:
43	chr2:10422162..10423929-chr2:10444657..10446996,2	K562	blood:
44	chr2:10425999..10428311-chr2:10434515..10436938,2	MCF-7	breast:
45	chr2:10392978..10395026-chr2:10400491..10403143,2	K562	blood:
46	chr2:10409756..10412116-chr2:10586894..10589733,2	K562	blood:
47	chr2:10265893..10268828-chr2:10402718..10405251,2	K562	blood:
48	chr2:10393383..10395595-chr2:10425523..10427994,2	MCF-7	breast:
49	chr2:10400941..10403372-chr2:10468145..10469648,2	K562	blood:
50	chr2:10277542..10280020-chr2:10400338..10402509,2	MCF-7	breast:

(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
ENSG00000115758	chromatin interactions
ENSG00000163009	chromatin interactions
ENSG00000171848	chromatin interactions
ENSG00000272524	chromatin interactions
ENSG00000115756	chromatin interactions
ENSG00000124151	chromatin interactions
ENSG00000206898	chromatin interactions
ENSG00000257135	chromatin interactions
ENSG00000264030	chromatin interactions
ENSG00000206633	chromatin interactions

Extended variants
information (count: 1229 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:1229 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544505209	chr2:10401331-10401332	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs562813192	chr2:10401356-10401357	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs574883743	chr2:10401403-10401404	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs144484708	chr2:10401416-10401417	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs573366783	chr2:10401423-10401424	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs560534874	chr2:10401505-10401506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs113141277	chr2:10401516-10401517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs372591710	chr2:10401536-10401537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs13399485	chr2:10401560-10401561	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs552447692	chr2:10401597-10401598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs564708856	chr2:10401600-10401601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs531847461	chr2:10401628-10401629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs7593936	chr2:10401629-10401630	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs568440479	chr2:10401634-10401635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529628758	chr2:10401674-10401675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs185902017	chr2:10401712-10401713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs190312349	chr2:10401761-10401762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs566204440	chr2:10401800-10401801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs533892992	chr2:10401808-10401809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs369809496	chr2:10401857-10401858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs58373925	chr2:10401872-10401873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs62128461	chr2:10401875-10401876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs558426594	chr2:10401880-10401881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs570616460	chr2:10401891-10401892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs115866594	chr2:10401928-10401929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs556477268	chr2:10401929-10401930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs574798803	chr2:10401933-10401934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs111775690	chr2:10401940-10401941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs554211478	chr2:10401943-10401944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs374905928	chr2:10401948-10401949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs369048439	chr2:10401963-10401964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs546266930	chr2:10401984-10401985	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs113315942	chr2:10402026-10402027	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs112601408	chr2:10402037-10402038	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs374852851	chr2:10402055-10402056	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs141444800	chr2:10402067-10402068	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs543641955	chr2:10402072-10402073	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs142485209	chr2:10402073-10402074	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs114683724	chr2:10402095-10402096	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs547740093	chr2:10402139-10402140	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs370616726	chr2:10402148-10402149	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs370109580	chr2:10402164-10402165	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs527337554	chr2:10402184-10402185	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs552247660	chr2:10402231-10402232	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs544571263	chr2:10402233-10402234	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs4668674	chr2:10402244-10402245	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs116290744	chr2:10402256-10402257	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs182603723	chr2:10402291-10402292	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs115027370	chr2:10402314-10402315	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs75953224	chr2:10402356-10402357	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	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:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:10392800-10407600	Weak transcription	Gastric	stomach
2	chr2:10396600-10407800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr2:10397800-10401400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr2:10398400-10401600	Enhancers	Rectal Mucosa Donor 31	rectum
5	chr2:10399600-10401600	Enhancers	Rectal Mucosa Donor 29	rectum
6	chr2:10400800-10402400	Weak transcription	Fetal Intestine Small	intestine
7	chr2:10400800-10405000	Weak transcription	HSMMtube	muscle
8	chr2:10400800-10406400	Weak transcription	HSMM	muscle
9	chr2:10401200-10401400	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr2:10401400-10402200	Enhancers	Fetal Stomach	stomach
11	chr2:10401400-10402400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr2:10401400-10403000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr2:10401600-10405800	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr2:10401600-10409600	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr2:10402800-10403000	Enhancers	Fetal Intestine Small	intestine
16	chr2:10403000-10407200	Weak transcription	Fetal Intestine Small	intestine
17	chr2:10404600-10405400	Weak transcription	Fetal Intestine Large	intestine
18	chr2:10404600-10405600	Bivalent Enhancer	Fetal Muscle Leg	muscle
19	chr2:10404600-10406000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
20	chr2:10404800-10406000	Bivalent Enhancer	HepG2	liver
21	chr2:10405000-10405200	Active TSS	Spleen	Spleen
22	chr2:10405000-10408200	Enhancers	HSMMtube	muscle
23	chr2:10405200-10410600	Weak transcription	Spleen	Spleen
24	chr2:10405400-10405600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr2:10405400-10406000	Enhancers	Fetal Intestine Large	intestine
26	chr2:10405600-10408800	Enhancers	Fetal Muscle Leg	muscle
27	chr2:10405600-10411000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr2:10405800-10406000	Enhancers	Rectal Mucosa Donor 31	rectum
29	chr2:10405800-10406400	Enhancers	Aorta	Aorta
30	chr2:10405800-10407400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr2:10406000-10406200	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
32	chr2:10406000-10406200	Flanking Bivalent TSS/Enh	HepG2	liver
33	chr2:10406000-10406400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr2:10406000-10406400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr2:10406000-10406400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr2:10406000-10406400	Enhancers	Fetal Lung	lung
37	chr2:10406000-10406400	Enhancers	Ovary	ovary
38	chr2:10406000-10406400	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr2:10406000-10407000	Enhancers	NHDF-Ad	bronchial
40	chr2:10406000-10407000	Enhancers	Osteobl	bone
41	chr2:10406000-10407200	Weak transcription	Fetal Intestine Large	intestine
42	chr2:10406000-10408600	Enhancers	Fetal Muscle Trunk	muscle
43	chr2:10406200-10406400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
44	chr2:10406200-10406400	Bivalent Enhancer	HepG2	liver
45	chr2:10406200-10406600	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr2:10406200-10406600	Enhancers	A549	lung
47	chr2:10406200-10406600	Enhancers	NH-A	brain
48	chr2:10406200-10406800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr2:10406200-10407200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr2:10406400-10406800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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