Variant report

Variant	esv3356298
Chromosome Location	chr2:10441526-10444374
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:937)
CpG islands
(count:1162)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:937 , 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	chr2:10441286-10441734	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:10442687-10442851	K562	blood:	n/a	n/a
3	BACH1	chr2:10444042-10444349	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr2:10442606-10442826	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr2:10443288-10443757	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr2:10442923-10443742	A549	lung:	n/a	chr2:10443143-10443156
7	BHLHE40	chr2:10442581-10443136	GM12878	blood:	n/a	chr2:10442856-10442872
8	BHLHE40	chr2:10442537-10442887	K562	blood:	n/a	chr2:10442856-10442872
9	BHLHE40	chr2:10443386-10443406	GM12878	blood:	n/a	n/a
10	BHLHE40	chr2:10443715-10443866	K562	blood:	n/a	n/a
11	BHLHE40	chr2:10443649-10444447	GM12878	blood:	n/a	n/a
12	BRCA1	chr2:10442616-10442896	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr2:10443238-10443655	K562	blood:	n/a	n/a
14	CBX3	chr2:10442182-10443186	K562	blood:	n/a	n/a
15	CCNT2	chr2:10442504-10444532	K562	blood:	n/a	chr2:10442588-10442597 chr2:10442568-10442577 chr2:10444311-10444320 chr2:10442574-10442583
16	CEBPB	chr2:10443955-10444510	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr2:10442638-10443174	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr2:10441584-10441627	HepG2	liver:	n/a	n/a
19	CEBPB	chr2:10442672-10442742	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPD	chr2:10442572-10442861	HepG2	liver:	n/a	n/a
21	CEBPD	chr2:10441202-10441834	HepG2	liver:	n/a	n/a
22	CEBPD	chr2:10442003-10443347	HepG2	liver:	n/a	n/a
23	CHD1	chr2:10443092-10443492	GM12878	blood:	n/a	n/a
24	CHD1	chr2:10443300-10443388	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD1	chr2:10443847-10444415	GM12878	blood:	n/a	n/a
26	CHD2	chr2:10443439-10444028	GM12878	blood:	n/a	n/a
27	CHD2	chr2:10442421-10443268	Hela-S3	cervix:	n/a	n/a
28	CHD2	chr2:10442662-10442921	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr2:10444263-10444463	GM12878	blood:	n/a	n/a
30	CHD2	chr2:10442429-10442883	HepG2	liver:	n/a	n/a
31	CHD2	chr2:10442444-10442884	K562	blood:	n/a	n/a
32	CHD2	chr2:10442233-10443171	GM12878	blood:	n/a	n/a
33	CHD2	chr2:10441429-10441922	HepG2	liver:	n/a	n/a
34	CHD2	chr2:10443900-10444472	Hela-S3	cervix:	n/a	n/a
35	CREB1	chr2:10442443-10443528	A549	lung:	n/a	n/a
36	CTBP2	chr2:10443094-10444822	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr2:10442498-10443072	K562	blood:	n/a	n/a
38	CTCF	chr2:10442603-10442875	MCF-7	breast:	n/a	n/a
39	CTCF	chr2:10442680-10442830	GM12873	blood:	n/a	n/a
40	CTCF	chr2:10442640-10442790	GM12869	blood:	n/a	n/a
41	CTCF	chr2:10442599-10442860	K562	blood:	n/a	n/a
42	CTCF	chr2:10444240-10444390	HA-sp	spinal cord:	n/a	n/a
43	CTCF	chr2:10442591-10442890	MCF-7	breast:	n/a	n/a
44	CTCF	chr2:10443840-10443990	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr2:10442640-10442790	NHEK	skin:	n/a	n/a
46	CTCF	chr2:10442680-10442830	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr2:10442631-10442846	Lung_OC	lung:	n/a	n/a
48	CTCF	chr2:10442780-10442930	AG04450	lung:	n/a	n/a
49	CTCF	chr2:10442594-10442865	GM13977	blood:	n/a	n/a
50	CTCF	chr2:10444219-10444417	GM10266	blood:	n/a	chr2:10444236-10444249

(count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:10442852-10442902	SK-N-SH_RA	brain:	n/a
2	chr2:10442521-10442571	HEK293	kidney:	embryo
3	chr2:10442817-10442867	NH-A	brain:	n/a
4	chr2:10442852-10442902	SK-N-SH_RA	brain:	n/a
5	chr2:10442521-10442571	HEK293	kidney:	embryo
6	chr2:10442817-10442867	NH-A	brain:	n/a
7	chr2:10443639-10443689	T-47D	breast:	n/a
8	chr2:10444156-10444206	HRCEpiC	kidney:	n/a
9	chr2:10442817-10442867	SK-N-MC	brain:	n/a
10	chr2:10443818-10443868	GM12878	blood:	n/a
11	chr2:10443138-10443188	T-47D	breast:	n/a
12	chr2:10443138-10443188	HNPCEpiC	eye:	n/a
13	chr2:10442836-10442886	HPAEpiC	pulmonary alveolar:	n/a
14	chr2:10442953-10443003	RPTEC	kidney:	n/a
15	chr2:10443745-10443795	ovcar-3	ovarian:	n/a
16	chr2:10444156-10444206	CMK	blood:	n/a
17	chr2:10443745-10443795	HIPEpiC	eye:	n/a
18	chr2:10442879-10442929	IMR90	lung:	fetal
19	chr2:10443138-10443188	HEK293	kidney:	embryo
20	chr2:10442953-10443003	HMEC	breast:	n/a
21	chr2:10442852-10442902	AG04450	lung:	fetal
22	chr2:10443745-10443795	SK-N-SH	brain:	n/a
23	chr2:10442521-10442571	AG09319	gingival:	n/a
24	chr2:10443138-10443188	HIPEpiC	eye:	n/a
25	chr2:10442040-10442090	NH-A	brain:	n/a
26	chr2:10443818-10443868	PrEC	prostate:	n/a
27	chr2:10443758-10443808	ProgFib	skin:	n/a
28	chr2:10442868-10442918	SK-N-MC	brain:	n/a
29	chr2:10442941-10442991	PFSK-1	brain:	n/a
30	chr2:10442521-10442571	LNCaP	prostate:	n/a
31	chr2:10441972-10442022	BE2_C	brain:	n/a
32	chr2:10442868-10442918	HEEpiC	esophagus:	n/a
33	chr2:10442521-10442571	BJ	skin:	n/a
34	chr2:10442953-10443003	BJ	skin:	n/a
35	chr2:10442953-10443003	HEK293	kidney:	embryo
36	chr2:10442941-10442991	HCT-116	colon:	n/a
37	chr2:10443138-10443188	NB4	blood:	n/a
38	chr2:10442879-10442929	AG04450	lung:	fetal
39	chr2:10442953-10443003	AoSMC	blood vessel:	n/a
40	chr2:10442817-10442867	Caco-2	colon:	n/a
41	chr2:10443758-10443808	PrEC	prostate:	n/a
42	chr2:10442953-10443003	HRCEpiC	kidney:	n/a
43	chr2:10442953-10443003	H1-hESC	embryonic stem cell:	embryo
44	chr2:10443632-10443682	Jurkat	blood:	n/a
45	chr2:10442817-10442867	SK-N-SH_RA	brain:	n/a
46	chr2:10442521-10442571	AG04450	lung:	fetal
47	chr2:10442953-10443003	GM06990	blood:	n/a
48	chr2:10442868-10442918	NHBE	bronchial:	n/a
49	chr2:10443758-10443808	GM19239	blood:	n/a
50	chr2:10442521-10442571	GM12892	blood:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:10444182..10445702-chr2:10452012..10454686,2	MCF-7	breast:
2	chr2:10440329..10443014-chr2:10447614..10450153,3	K562	blood:
3	chr2:10443037..10443588-chr8:26148654..26149361,2	Hela-S3	cervix:
4	chr2:10328421..10328930-chr2:10442179..10443004,2	MCF-7	breast:
5	chr2:10284792..10287057-chr2:10444307..10446479,2	K562	blood:
6	chr2:10424782..10426457-chr2:10440963..10442554,2	K562	blood:
7	chr2:10417102..10422487-chr2:10439870..10443532,9	K562	blood:
8	chr2:10442668..10443459-chr2:198317615..198318346,2	HCT-116	colon:
9	chr2:10441623..10444200-chr2:10586906..10588748,2	K562	blood:
10	chr2:10442628..10443339-chrX:153362706..153363466,2	Hela-S3	cervix:
11	chr2:10441623..10444177-chr2:10587166..10588748,2	K562	blood:
12	chr2:10438477..10441704-chr2:10442402..10444544,4	MCF-7	breast:
13	chr2:10261047..10264754-chr2:10441936..10445688,4	MCF-7	breast:
14	chr2:10261055..10262657-chr2:10441629..10443172,2	K562	blood:
15	chr2:10434745..10440361-chr2:10440769..10446494,13	MCF-7	breast:
16	chr11:108337866..108338745-chr2:10442140..10442929,2	Hela-S3	cervix:
17	chr2:10259191..10262555-chr2:10441232..10444497,4	K562	blood:
18	chr2:10417267..10421526-chr2:10440124..10444517,8	K562	blood:
19	chr2:10441262..10442820-chr2:10525916..10527574,2	MCF-7	breast:
20	chr2:10443130..10443758-chr22:47158091..47158932,2	Hela-S3	cervix:
21	chr2:10426724..10428299-chr2:10440170..10442093,2	K562	blood:
22	chr2:10259183..10262149-chr2:10441411..10444855,4	MCF-7	breast:
23	chr2:10183111..10185258-chr2:10441327..10442852,2	K562	blood:
24	chr2:10265405..10268289-chr2:10440877..10444021,3	K562	blood:

No data

Variant related genes	Relation type
HPCAL1	TF binding region
HPCAL1	CpG island
ENSG00000115520	chromatin interactions
ENSG00000115758	chromatin interactions
ENSG00000260708	chromatin interactions
ENSG00000206633	chromatin interactions
ENSG00000171848	chromatin interactions
ENSG00000054611	chromatin interactions
ENSG00000264030	chromatin interactions
ENSG00000115756	chromatin interactions
ENSG00000272524	chromatin interactions
ENSG00000172059	chromatin interactions
ENSG00000206898	chromatin interactions
ENSG00000169057	chromatin interactions
ENSG00000166323	chromatin interactions
ENSG00000221914	chromatin interactions

Extended variants
information (count: 110 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:110 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189307762	chr2:10441565-10441566	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs140007491	chr2:10441623-10441624	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
3	rs149865415	chr2:10441636-10441637	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
4	rs553525369	chr2:10441665-10441666	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
5	rs571760693	chr2:10441671-10441672	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
6	rs539274565	chr2:10441710-10441711	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs143876649	chr2:10441731-10441732	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs72771663	chr2:10441790-10441791	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs542999433	chr2:10441792-10441793	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs533718097	chr2:10441795-10441796	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs554990313	chr2:10441835-10441836	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs573390705	chr2:10441861-10441862	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs116312985	chr2:10441891-10441892	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs549710242	chr2:10441922-10441923	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs559451141	chr2:10442030-10442031	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs533000419	chr2:10442111-10442112	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs538907167	chr2:10442126-10442127	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs559083961	chr2:10442132-10442133	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs563419148	chr2:10442159-10442160	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs73161219	chr2:10442214-10442215	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs549397919	chr2:10442234-10442235	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs116172975	chr2:10442272-10442273	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs528558275	chr2:10442326-10442327	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs117138248	chr2:10442389-10442390	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs371605533	chr2:10442405-10442406	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs571784890	chr2:10442406-10442407	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs538875437	chr2:10442412-10442413	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs557568301	chr2:10442426-10442427	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs368425911	chr2:10442434-10442435	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs569187332	chr2:10442442-10442443	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs536587439	chr2:10442457-10442458	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs75848743	chr2:10442466-10442467	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs6723733	chr2:10442541-10442542	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs534686362	chr2:10442628-10442629	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
35	rs552806745	chr2:10442704-10442705	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
36	rs577698409	chr2:10442731-10442732	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
37	rs544853078	chr2:10442740-10442741	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
38	rs181665330	chr2:10442799-10442800	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
39	rs575603958	chr2:10442818-10442819	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
40	rs372817729	chr2:10442855-10442856	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
41	rs561222185	chr2:10442859-10442860	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
42	rs528517288	chr2:10442868-10442869	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
43	rs374841083	chr2:10442906-10442907	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
44	rs185903914	chr2:10442913-10442914	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
45	rs565220989	chr2:10442915-10442916	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
46	rs190059211	chr2:10443005-10443006	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
47	rs550883713	chr2:10443006-10443007	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
48	rs372411769	chr2:10443007-10443008	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
49	rs11556253	chr2:10443057-10443058	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
50	rs536500576	chr2:10443060-10443061	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

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

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	chr2:10436000-10442000	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr2:10436600-10442200	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr2:10437800-10441600	Weak transcription	Spleen	Spleen
4	chr2:10437800-10441800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr2:10438400-10442000	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr2:10438400-10442000	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr2:10438600-10441600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr2:10438600-10441800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr2:10438600-10441800	Weak transcription	Lung	lung
10	chr2:10438600-10442000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr2:10438600-10442000	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr2:10438600-10442000	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr2:10438600-10442000	Weak transcription	Adipose Nuclei	Adipose
14	chr2:10438600-10442000	Weak transcription	Dnd41	blood
15	chr2:10438600-10442200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr2:10438600-10442200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr2:10438600-10442200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
18	chr2:10438600-10442200	Weak transcription	Psoas Muscle	Psoas
19	chr2:10438600-10442200	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr2:10438800-10441600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr2:10438800-10442000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr2:10438800-10442000	Weak transcription	Colon Smooth Muscle	Colon
23	chr2:10438800-10442000	Weak transcription	Fetal Muscle Leg	muscle
24	chr2:10438800-10442200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr2:10438800-10442200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr2:10438800-10442200	Weak transcription	HMEC	breast
27	chr2:10438800-10442200	Weak transcription	HSMMtube	muscle
28	chr2:10438800-10442200	Weak transcription	NHDF-Ad	bronchial
29	chr2:10438800-10442200	Weak transcription	NHEK	skin
30	chr2:10438800-10442200	Weak transcription	Osteobl	bone
31	chr2:10438800-10442600	Weak transcription	NHLF	lung
32	chr2:10439000-10441800	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr2:10439000-10442000	Weak transcription	HUVEC	blood vessel
34	chr2:10439000-10442200	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr2:10439000-10442400	Weak transcription	HSMM	muscle
36	chr2:10439000-10442400	Weak transcription	NH-A	brain
37	chr2:10439800-10441600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr2:10440400-10441800	Enhancers	Primary T cells from cord blood	blood
39	chr2:10440400-10441800	Enhancers	Primary T helper cells fromperipheralblood	blood
40	chr2:10440400-10441800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr2:10440600-10441600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
42	chr2:10440600-10441600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chr2:10440600-10441800	Flanking Active TSS	HepG2	liver
44	chr2:10440600-10442000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
45	chr2:10440600-10442000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
46	chr2:10440600-10442000	Enhancers	A549	lung
47	chr2:10440600-10442200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
48	chr2:10440600-10442200	Enhancers	Fetal Thymus	thymus
49	chr2:10440800-10441600	Enhancers	Fetal Intestine Large	intestine
50	chr2:10440800-10441800	Enhancers	Primary T cells fromperipheralblood	blood

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