Variant report

Variant	esv3326017
Chromosome Location	chr2:10090726-10093274
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:420)
CpG islands
(count:611)
Chromatin interactive
region (count:21)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:420 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:10091981-10092024	HepG2	liver:	n/a	n/a
2	ATF3	chr2:10092367-10092770	K562	blood:	n/a	n/a
3	BACH1	chr2:10090910-10091402	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr2:10091928-10092548	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr2:10091078-10091363	K562	blood:	n/a	n/a
6	BHLHE40	chr2:10091050-10091462	GM12878	blood:	n/a	n/a
7	BRCA1	chr2:10092390-10092544	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr2:10091215-10091319	H1-hESC	embryonic stem cell:	n/a	n/a
9	CCNT2	chr2:10090860-10092444	K562	blood:	n/a	chr2:10092345-10092354
10	CEBPB	chr2:10092385-10092730	K562	blood:	n/a	n/a
11	CEBPB	chr2:10092421-10092710	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr2:10092488-10092682	K562	blood:	n/a	n/a
13	CEBPB	chr2:10092401-10092770	K562	blood:	n/a	n/a
14	CEBPD	chr2:10090968-10091418	HepG2	liver:	n/a	n/a
15	CEBPD	chr2:10091474-10092402	HepG2	liver:	n/a	n/a
16	CHD1	chr2:10091220-10091390	GM12878	blood:	n/a	chr2:10091371-10091381
17	CHD2	chr2:10091095-10091874	GM12878	blood:	n/a	chr2:10091738-10091748 chr2:10091371-10091381
18	CHD2	chr2:10091673-10091942	K562	blood:	n/a	chr2:10091738-10091748
19	CHD2	chr2:10092128-10092268	HepG2	liver:	n/a	n/a
20	CHD2	chr2:10092174-10092321	Hela-S3	cervix:	n/a	n/a
21	CHD2	chr2:10091477-10091937	Hela-S3	cervix:	n/a	chr2:10091738-10091748
22	CHD2	chr2:10091060-10091421	K562	blood:	n/a	chr2:10091371-10091381
23	CHD2	chr2:10091049-10091404	HepG2	liver:	n/a	chr2:10091371-10091381
24	CREB1	chr2:10091064-10091386	A549	lung:	n/a	n/a
25	CREB1	chr2:10091427-10092155	A549	lung:	n/a	n/a
26	CTCF	chr2:10091364-10091372	K562	blood:	n/a	n/a
27	CTCF	chr2:10091239-10091398	MCF-7	breast:	n/a	n/a
28	CTCF	chr2:10091460-10091610	SAEC	small airway:	n/a	n/a
29	CTCF	chr2:10091200-10091350	SK-N-SH_RA	brain:	n/a	n/a
30	CTCF	chr2:10091327-10091357	GM13976	blood:	n/a	n/a
31	CTCF	chr2:10091220-10091370	NHDF-neo	bronchial:	n/a	n/a
32	CTCF	chr2:10091235-10091347	GM10248	blood:	n/a	n/a
33	CTCF	chr2:10091240-10091390	GM12864	blood:	n/a	n/a
34	CTCF	chr2:10091492-10091578	Kidney_OC	kidney:	n/a	n/a
35	CTCF	chr2:10091900-10092050	GM12870	blood:	n/a	n/a
36	CTCF	chr2:10091232-10091417	MCF-7	breast:	n/a	n/a
37	CTCF	chr2:10091160-10091310	K562	blood:	n/a	n/a
38	CTCF	chr2:10091172-10091408	HepG2	liver:	n/a	n/a
39	CTCF	chr2:10091200-10091350	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr2:10091268-10091369	Pancreas_OC	pancreas:	n/a	n/a
41	CTCF	chr2:10091200-10091350	GM12875	blood:	n/a	n/a
42	CTCF	chr2:10091460-10091610	GM12866	blood:	n/a	n/a
43	CTCF	chr2:10091500-10091650	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr2:10091400-10091550	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr2:10091462-10091593	NHEK	skin:	n/a	n/a
46	CTCF	chr2:10091160-10091310	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr2:10091435-10091646	HepG2	liver:	n/a	n/a
48	CTCF	chr2:10091491-10091563	MCF-7	breast:	n/a	n/a
49	CTCF	chr2:10091260-10091410	GM12873	blood:	n/a	n/a
50	CTCF	chr2:10091267-10091269	ProgFib	skin:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:10091661-10091711	LNCaP	prostate:	n/a
2	chr2:10091661-10091711	LNCaP	prostate:	n/a
3	chr2:10092403-10092453	MCF10A-Er-Src	breast:	n/a
4	chr2:10091661-10091711	AG04449	skin:	fetal
5	chr2:10091721-10091771	HCT-116	colon:	n/a
6	chr2:10091665-10091715	SK-N-SH_RA	brain:	n/a
7	chr2:10091661-10091711	GM12891	blood:	n/a
8	chr2:10091270-10091320	Caco-2	colon:	n/a
9	chr2:10091721-10091771	AG04450	lung:	fetal
10	chr2:10092403-10092453	SK-N-SH	brain:	n/a
11	chr2:10092455-10092505	SKMC	muscle:	n/a
12	chr2:10091700-10091750	HepG2	liver:	n/a
13	chr2:10092403-10092453	HEEpiC	esophagus:	n/a
14	chr2:10092403-10092453	NT2-D1	testis:	n/a
15	chr2:10091661-10091711	BE2_C	brain:	n/a
16	chr2:10091270-10091320	AG04450	lung:	fetal
17	chr2:10091661-10091711	SAEC	small airway:	n/a
18	chr2:10091661-10091711	ovcar-3	ovarian:	n/a
19	chr2:10091897-10091947	Hepatocyte	liver:	n/a
20	chr2:10091688-10091738	PFSK-1	brain:	n/a
21	chr2:10090974-10091024	Caco-2	colon:	n/a
22	chr2:10091688-10091738	SKMC	muscle:	n/a
23	chr2:10091270-10091320	HEK293	kidney:	embryo
24	chr2:10091688-10091738	HepG2	liver:	n/a
25	chr2:10090974-10091024	HAEpiC	amniotic membrane:	n/a
26	chr2:10092403-10092453	ECC-1	luminal epithelium:	n/a
27	chr2:10091661-10091711	MCF10A-Er-Src	breast:	n/a
28	chr2:10091897-10091947	HCPEpiC	choroid plexus:	n/a
29	chr2:10091897-10091947	HRPEpiC	eye:	n/a
30	chr2:10091700-10091750	HRCEpiC	kidney:	n/a
31	chr2:10091721-10091771	Hepatocyte	liver:	n/a
32	chr2:10092455-10092505	ProgFib	skin:	n/a
33	chr2:10091270-10091320	SKMC	muscle:	n/a
34	chr2:10091700-10091750	T-47D	breast:	n/a
35	chr2:10091688-10091738	HIPEpiC	eye:	n/a
36	chr2:10092455-10092505	SAEC	small airway:	n/a
37	chr2:10091688-10091738	Caco-2	colon:	n/a
38	chr2:10091661-10091711	ECC-1	luminal epithelium:	n/a
39	chr2:10091700-10091750	MCF10A-Er-Src	breast:	n/a
40	chr2:10091661-10091711	HepG2	liver:	n/a
41	chr2:10091688-10091738	ECC-1	luminal epithelium:	n/a
42	chr2:10091721-10091771	U87	brain:	n/a
43	chr2:10091270-10091320	HCM	heart:	n/a
44	chr2:10092403-10092453	GM12891	blood:	n/a
45	chr2:10091897-10091947	SK-N-SH_RA	brain:	n/a
46	chr2:10091721-10091771	HRPEpiC	eye:	n/a
47	chr2:10091700-10091750	SK-N-SH	brain:	n/a
48	chr2:10090974-10091024	HNPCEpiC	eye:	n/a
49	chr2:10091700-10091750	SAEC	small airway:	n/a
50	chr2:10091270-10091320	NHDF-neo	bronchial:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:10090160..10094173-chr2:10181224..10185885,6	MCF-7	breast:
2	chr2:9982271..9986804-chr2:10090021..10093067,7	K562	blood:
3	chr2:10092110..10094474-chr2:10182208..10184991,2	K562	blood:
4	chr2:10080626..10083275-chr2:10089838..10091585,2	K562	blood:
5	chr2:10090913..10094433-chr2:10181887..10185131,5	K562	blood:
6	chr2:10091367..10094043-chr2:10260841..10262617,2	K562	blood:
7	chr2:10090078..10091613-chr2:10169348..10171878,2	K562	blood:
8	chr2:10090511..10093177-chr2:10182491..10184266,3	MCF-7	breast:
9	chr2:10085922..10087593-chr2:10089321..10091253,3	K562	blood:
10	chr2:9962243..9964669-chr2:10088779..10091216,2	MCF-7	breast:
11	chr2:9777094..9779295-chr2:10091033..10093180,2	MCF-7	breast:
12	chr2:9768803..9771575-chr2:10089760..10091656,2	MCF-7	breast:
13	chr2:9932897..9935597-chr2:10092783..10094532,2	MCF-7	breast:
14	chr2:10089749..10091694-chr2:10096424..10099200,2	K562	blood:
15	chr2:10090081..10091760-chr2:10195035..10197397,2	K562	blood:
16	chr2:9938284..9940065-chr2:10092605..10094538,2	MCF-7	breast:
17	chr2:9982271..9985181-chr2:10090033..10093358,4	K562	blood:
18	chr2:9770089..9772474-chr2:10090151..10092445,2	K562	blood:
19	chr2:9982092..9985559-chr2:10088577..10093200,6	MCF-7	breast:
20	chr2:10091739..10097867-chr2:10098252..10106254,13	K562	blood:
21	chr2:9983066..9987186-chr2:10091615..10095343,4	MCF-7	breast:

No data

Variant related genes	Relation type
GRHL1	TF binding region
GRHL1	CpG island
ENSG00000171848	chromatin interactions
ENSG00000115750	chromatin interactions
ENSG00000134308	chromatin interactions
ENSG00000272524	chromatin interactions
ENSG00000240687	chromatin interactions
ENSG00000134317	chromatin interactions
ENSG00000172059	chromatin interactions

Extended variants
information (count: 85 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:85 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565386935	chr2:10090732-10090733	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs1864542	chr2:10090761-10090762	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs554513668	chr2:10090788-10090789	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs574334853	chr2:10090796-10090797	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs543332588	chr2:10090807-10090808	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs556575989	chr2:10090815-10090816	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs576751628	chr2:10090816-10090817	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs545578711	chr2:10090818-10090819	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs149768720	chr2:10090839-10090840	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs60937990	chr2:10090851-10090852	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs541083196	chr2:10090862-10090863	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs561369452	chr2:10090922-10090923	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs116444873	chr2:10090925-10090926	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs550622758	chr2:10090967-10090968	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs573047505	chr2:10090972-10090973	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs78204084	chr2:10091038-10091039	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs532176598	chr2:10091126-10091127	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs113074022	chr2:10091144-10091145	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs373505866	chr2:10091194-10091195	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs565451113	chr2:10091209-10091210	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs534747841	chr2:10091222-10091223	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs186108653	chr2:10091301-10091302	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs568094310	chr2:10091323-10091324	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs536632700	chr2:10091372-10091373	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs556904360	chr2:10091379-10091380	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs191008206	chr2:10091381-10091382	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs545640088	chr2:10091382-10091383	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs559162065	chr2:10091418-10091419	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs115898376	chr2:10091422-10091423	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs533381656	chr2:10091448-10091449	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs541836159	chr2:10091457-10091458	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs4630741	chr2:10091472-10091473	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs541545263	chr2:10091506-10091507	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs561224756	chr2:10091523-10091524	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs183994067	chr2:10091585-10091586	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs543402866	chr2:10091689-10091690	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs563262826	chr2:10091776-10091777	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs532237257	chr2:10091820-10091821	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs552035405	chr2:10091849-10091850	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs565565956	chr2:10091855-10091856	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs528270541	chr2:10091858-10091859	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs548306371	chr2:10091871-10091872	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs568022995	chr2:10091887-10091888	Bivalent/Poised TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs374854604	chr2:10091923-10091924	Bivalent/Poised TSS Active TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs369304105	chr2:10091948-10091949	Bivalent/Poised TSS Active TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs550568054	chr2:10091951-10091952	Bivalent/Poised TSS Active TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs111645870	chr2:10091952-10091953	Bivalent/Poised TSS Active TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs539377124	chr2:10091975-10091976	Bivalent/Poised TSS Active TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs376559669	chr2:10091978-10091979	Bivalent/Poised TSS Active TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs369881446	chr2:10092013-10092014	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD

Chromatin state (count:415 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:10082000-10090800	Weak transcription	HMEC	breast
2	chr2:10086000-10090800	Weak transcription	Pancreas	Pancrea
3	chr2:10086200-10090800	Weak transcription	Right Atrium	heart
4	chr2:10088800-10090800	Enhancers	Spleen	Spleen
5	chr2:10089800-10091000	Enhancers	Lung	lung
6	chr2:10090000-10090800	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
7	chr2:10090000-10092800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr2:10090200-10090800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr2:10090200-10090800	Enhancers	Placenta Amnion	Placenta Amnion
10	chr2:10090200-10091000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
11	chr2:10090200-10091000	Flanking Bivalent TSS/Enh	HepG2	liver
12	chr2:10090200-10092600	Active TSS	Gastric	stomach
13	chr2:10090400-10090800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr2:10090400-10090800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
15	chr2:10090400-10090800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
16	chr2:10090400-10090800	Flanking Active TSS	Esophagus	oesophagus
17	chr2:10090400-10090800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
18	chr2:10090400-10090800	Enhancers	Right Ventricle	heart
19	chr2:10090400-10091000	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
20	chr2:10090400-10091200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr2:10090400-10091200	Flanking Active TSS	Placenta	Placenta
22	chr2:10090400-10091200	Bivalent Enhancer	Stomach Mucosa	stomach
23	chr2:10090400-10091400	Active TSS	Primary T killer memory cells from peripheral blood	blood
24	chr2:10090400-10093000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
25	chr2:10090600-10090800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
26	chr2:10090600-10090800	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
27	chr2:10090600-10090800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr2:10090600-10090800	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr2:10090600-10090800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr2:10090600-10090800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
31	chr2:10090600-10090800	Flanking Bivalent TSS/Enh	Primary T cells from cord blood	blood
32	chr2:10090600-10090800	Bivalent Enhancer	Primary hematopoietic stem cells	blood
33	chr2:10090600-10090800	Flanking Bivalent TSS/Enh	Primary T helper naive cells fromperipheralblood	blood
34	chr2:10090600-10090800	Enhancers	Primary T helper cells PMA-I stimulated	--
35	chr2:10090600-10090800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
36	chr2:10090600-10090800	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
37	chr2:10090600-10090800	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
38	chr2:10090600-10090800	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr2:10090600-10090800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr2:10090600-10090800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr2:10090600-10090800	Enhancers	Adipose Nuclei	Adipose
42	chr2:10090600-10090800	Enhancers	Liver	Liver
43	chr2:10090600-10090800	Bivalent/Poised TSS	Brain Germinal Matrix	brain
44	chr2:10090600-10090800	Enhancers	Brain Hippocampus Middle	brain
45	chr2:10090600-10090800	Bivalent Enhancer	Colonic Mucosa	Colon
46	chr2:10090600-10090800	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
47	chr2:10090600-10090800	Bivalent Enhancer	Fetal Stomach	stomach
48	chr2:10090600-10090800	Bivalent Enhancer	Fetal Thymus	thymus
49	chr2:10090600-10090800	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
50	chr2:10090600-10090800	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum

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