Variant report

Variant	esv3409926
Chromosome Location	chr2:179058531-179061079
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:528)
CpG islands
(count:427)
Chromatin interactive
region (count:12)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:528 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:179058147-179058700	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:179059192-179059308	K562	blood:	n/a	n/a
3	BACH1	chr2:179059663-179060261	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr2:179058627-179059213	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr2:179058869-179058966	K562	blood:	n/a	n/a
6	BHLHE40	chr2:179058252-179058609	HepG2	liver:	n/a	n/a
7	BHLHE40	chr2:179059725-179060345	K562	blood:	n/a	n/a
8	BHLHE40	chr2:179058398-179059517	K562	blood:	n/a	n/a
9	BRCA1	chr2:179060038-179060272	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr2:179059841-179060241	K562	blood:	n/a	n/a
11	CBX3	chr2:179058754-179059585	K562	blood:	n/a	n/a
12	CCNT2	chr2:179058576-179060455	K562	blood:	n/a	n/a
13	CEBPB	chr2:179058137-179058562	HepG2	liver:	n/a	n/a
14	CEBPB	chr2:179060223-179060508	K562	blood:	n/a	n/a
15	CEBPB	chr2:179059704-179059973	K562	blood:	n/a	n/a
16	CEBPB	chr2:179058590-179058717	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr2:179059649-179060530	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr2:179058072-179059362	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr2:179059757-179060042	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr2:179059697-179060389	IMR90	lung:	n/a	n/a
21	CEBPB	chr2:179058054-179058776	HepG2	liver:	n/a	n/a
22	CEBPB	chr2:179058152-179058608	HepG2	liver:	n/a	n/a
23	CEBPD	chr2:179058214-179058617	HepG2	liver:	n/a	n/a
24	CHD1	chr2:179058524-179059060	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD1	chr2:179059290-179059478	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr2:179059013-179059142	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr2:179059684-179060277	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr2:179058389-179060267	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr2:179058533-179058768	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr2:179058920-179060350	K562	blood:	n/a	n/a
31	CHD2	chr2:179059419-179059815	HepG2	liver:	n/a	n/a
32	CREB1	chr2:179058042-179058792	HepG2	liver:	n/a	n/a
33	CREB1	chr2:179058443-179058928	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr2:179058808-179059341	A549	lung:	n/a	n/a
35	CREB1	chr2:179058444-179058852	H1-hESC	embryonic stem cell:	n/a	n/a
36	CREB1	chr2:179058442-179059535	K562	blood:	n/a	n/a
37	CTBP2	chr2:179058381-179060303	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr2:179059117-179059399	NHEK	skin:	n/a	n/a
39	CTCF	chr2:179059560-179059710	HAc	cerebellar:	n/a	n/a
40	CTCF	chr2:179059132-179059362	MCF-7	breast:	n/a	n/a
41	CTCF	chr2:179059136-179059299	GM13977	blood:	n/a	n/a
42	CTCF	chr2:179059057-179059453	K562	blood:	n/a	n/a
43	CTCF	chr2:179059040-179059190	GM12864	blood:	n/a	chr2:179059040-179059053
44	CTCF	chr2:179059860-179060010	HCM	heart:	n/a	chr2:179059980-179059993
45	CTCF	chr2:179059139-179059335	MCF-7	breast:	n/a	n/a
46	CTCF	chr2:179059160-179059310	SAEC	small airway:	n/a	n/a
47	CTCF	chr2:179059143-179059350	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr2:179059920-179060070	NHEK	skin:	n/a	chr2:179059980-179059993
49	CTCF	chr2:179059160-179059310	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr2:179059640-179059790	HCPEpiC	choroid plexus:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:179058612-179058662	HEEpiC	esophagus:	n/a
2	chr2:179058612-179058662	GM12878	blood:	n/a
3	chr2:179060011-179060061	HMEC	breast:	n/a
4	chr2:179058698-179058748	MCF10A-Er-Src	breast:	n/a
5	chr2:179059440-179059490	ECC-1	luminal epithelium:	n/a
6	chr2:179058736-179058786	AG10803	skin:	n/a
7	chr2:179058612-179058662	Caco-2	colon:	n/a
8	chr2:179059440-179059490	HCF	heart:	n/a
9	chr2:179060117-179060167	MCF-7	breast:	n/a
10	chr2:179060117-179060167	PANC-1	pancreas:	n/a
11	chr2:179058612-179058662	NT2-D1	testis:	n/a
12	chr2:179059440-179059490	HL-60	blood:	n/a
13	chr2:179058736-179058786	CMK	blood:	n/a
14	chr2:179058736-179058786	HL-60	blood:	n/a
15	chr2:179060011-179060061	AoSMC	blood vessel:	n/a
16	chr2:179058698-179058748	U87	brain:	n/a
17	chr2:179059440-179059490	HRCEpiC	kidney:	n/a
18	chr2:179059452-179059502	AG04449	skin:	fetal
19	chr2:179059440-179059490	HEK293	kidney:	embryo
20	chr2:179059440-179059490	HRE	kidney:	n/a
21	chr2:179059452-179059502	HUVEC	blood vessel:	n/a
22	chr2:179058736-179058786	HNPCEpiC	eye:	n/a
23	chr2:179060117-179060167	AG09319	gingival:	n/a
24	chr2:179060011-179060061	BJ	skin:	n/a
25	chr2:179058698-179058748	PFSK-1	brain:	n/a
26	chr2:179060011-179060061	AG09319	gingival:	n/a
27	chr2:179059452-179059502	ECC-1	luminal epithelium:	n/a
28	chr2:179059452-179059502	IMR90	lung:	fetal
29	chr2:179060011-179060061	HRCEpiC	kidney:	n/a
30	chr2:179059452-179059502	HNPCEpiC	eye:	n/a
31	chr2:179058698-179058748	T-47D	breast:	n/a
32	chr2:179059452-179059502	PFSK-1	brain:	n/a
33	chr2:179060011-179060061	Caco-2	colon:	n/a
34	chr2:179058612-179058662	PrEC	prostate:	n/a
35	chr2:179060011-179060061	HCM	heart:	n/a
36	chr2:179060011-179060061	Hepatocyte	liver:	n/a
37	chr2:179060011-179060061	SK-N-SH_RA	brain:	n/a
38	chr2:179059440-179059490	HMEC	breast:	n/a
39	chr2:179060011-179060061	HRE	kidney:	n/a
40	chr2:179060011-179060061	AG09309	skin:	n/a
41	chr2:179058736-179058786	AoSMC	blood vessel:	n/a
42	chr2:179060117-179060167	HEEpiC	esophagus:	n/a
43	chr2:179058612-179058662	MCF-7	breast:	n/a
44	chr2:179058736-179058786	AG09319	gingival:	n/a
45	chr2:179059440-179059490	AG10803	skin:	n/a
46	chr2:179060117-179060167	BE2_C	brain:	n/a
47	chr2:179060011-179060061	AG04449	skin:	fetal
48	chr2:179059452-179059502	GM19239	blood:	n/a
49	chr2:179058612-179058662	HRCEpiC	kidney:	n/a
50	chr2:179058736-179058786	HMEC	breast:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:179060480..179062055-chr2:179072193..179074054,2	K562	blood:
2	chr2:178979115..178980922-chr2:179059390..179062250,2	K562	blood:
3	chr2:178940431..178942693-chr2:179060357..179062621,2	K562	blood:
4	chr2:178976797..178977610-chr2:179058506..179059074,2	MCF-7	breast:
5	chr2:179060830..179065562-chr2:179066300..179070960,4	K562	blood:
6	chr2:178937601..178939157-chr2:179060683..179062611,2	K562	blood:
7	chr2:179056933..179060923-chr2:179315358..179318702,4	MCF-7	breast:
8	chr2:178975761..178978600-chr2:179056476..179059620,3	K562	blood:
9	chr2:178978462..178980467-chr2:179057158..179058664,2	MCF-7	breast:
10	chr2:179059539..179061742-chr2:179114111..179116745,2	K562	blood:
11	chr2:179057756..179060082-chr2:179314891..179318046,3	MCF-7	breast:
12	chr2:178975067..178978289-chr2:179058254..179060575,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RBM45-9	chr2:179059216-179059401	NONHSAT075739

No data

Variant related genes	Relation type
OSBPL6	TF binding region
OSBPL6	CpG island
ENSG00000155636	chromatin interactions
ENSG00000204311	chromatin interactions
ENSG00000180228	chromatin interactions

Extended variants
information (count: 95 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:95 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571064217	chr2:179058545-179058546	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs117807540	chr2:179058559-179058560	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs556945300	chr2:179058566-179058567	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs16866156	chr2:179058577-179058578	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs535607284	chr2:179058597-179058598	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs112770858	chr2:179058639-179058640	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs148371931	chr2:179058646-179058647	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs573363868	chr2:179058655-179058656	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs12693155	chr2:179058714-179058715	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs531124646	chr2:179058717-179058718	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs35510522	chr2:179058739-179058740	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs117716086	chr2:179058748-179058749	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs62177189	chr2:179058803-179058804	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs544905656	chr2:179058813-179058814	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs561394726	chr2:179058842-179058843	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs187854145	chr2:179058872-179058873	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs375638797	chr2:179058914-179058915	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs548684768	chr2:179058916-179058917	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs334125	chr2:179058924-179058925	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs528177151	chr2:179058933-179058934	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs150883299	chr2:179058968-179058969	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs138440334	chr2:179058975-179058976	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs536825742	chr2:179059113-179059114	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs550882877	chr2:179059118-179059119	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs567435702	chr2:179059188-179059189	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs529728126	chr2:179059225-179059226	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
27	rs373036124	chr2:179059226-179059227	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
28	rs536693397	chr2:179059242-179059243	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
29	rs553087121	chr2:179059274-179059275	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
30	rs143920076	chr2:179059301-179059302	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
31	rs539141780	chr2:179059400-179059401	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
32	rs559060793	chr2:179059447-179059448	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs575930859	chr2:179059472-179059473	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs544455819	chr2:179059474-179059475	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs561659372	chr2:179059502-179059503	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs575030691	chr2:179059530-179059531	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs540875947	chr2:179059533-179059534	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs376739168	chr2:179059581-179059582	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs528043748	chr2:179059583-179059584	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs528969576	chr2:179059626-179059627	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs551086342	chr2:179059644-179059645	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs564618686	chr2:179059661-179059662	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs530769253	chr2:179059683-179059684	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs550494251	chr2:179059692-179059693	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs567595410	chr2:179059697-179059698	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs536157393	chr2:179059698-179059699	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs546872774	chr2:179059699-179059700	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs566885324	chr2:179059703-179059704	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs539006715	chr2:179059706-179059707	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs559122166	chr2:179059743-179059744	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Prostate cancer	18632612	CNVD
Sudden cardiac death	19188705	CNVD
Acute myeloid leukemia	20729466	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Mental retardation	21062444	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Schizophrenia	19348701	CNVD
Muscular dystrophy	17160897	CNVD
Cardiomyopathy	17576883	CNVD
Pancreatic cancer	17952125	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:460 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:179058000-179058600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
2	chr2:179058000-179058600	Enhancers	Fetal Brain Male	brain
3	chr2:179058000-179058600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
4	chr2:179058000-179058600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
5	chr2:179058000-179058800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr2:179058000-179058800	Flanking Active TSS	Adipose Nuclei	Adipose
7	chr2:179058000-179058800	Flanking Active TSS	Liver	Liver
8	chr2:179058000-179058800	Flanking Active TSS	Stomach Smooth Muscle	stomach
9	chr2:179058000-179058800	Flanking Active TSS	NHEK	skin
10	chr2:179058000-179059000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
11	chr2:179058000-179060800	Active TSS	NHLF	lung
12	chr2:179058000-179061200	Active TSS	Brain Angular Gyrus	brain
13	chr2:179058200-179058600	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr2:179058200-179058600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
15	chr2:179058200-179058600	Flanking Bivalent TSS/Enh	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr2:179058200-179058600	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr2:179058200-179058600	Flanking Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr2:179058200-179058600	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
19	chr2:179058200-179058600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr2:179058200-179058600	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
21	chr2:179058200-179058600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr2:179058200-179058600	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
23	chr2:179058200-179058600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
24	chr2:179058200-179058600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr2:179058200-179058600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
26	chr2:179058200-179058600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr2:179058200-179058600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr2:179058200-179058600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr2:179058200-179058600	Flanking Active TSS	Brain Anterior Caudate	brain
30	chr2:179058200-179058600	Flanking Active TSS	Brain Cingulate Gyrus	brain
31	chr2:179058200-179058600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
32	chr2:179058200-179058600	Flanking Active TSS	Brain Substantia Nigra	brain
33	chr2:179058200-179058600	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
34	chr2:179058200-179058600	Flanking Active TSS	Fetal Brain Female	brain
35	chr2:179058200-179058600	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
36	chr2:179058200-179058600	Enhancers	Gastric	stomach
37	chr2:179058200-179058600	Flanking Active TSS	Hela-S3	cervix
38	chr2:179058200-179058600	Flanking Active TSS	HSMMtube	muscle
39	chr2:179058200-179058600	Flanking Active TSS	NH-A	brain
40	chr2:179058200-179058600	Flanking Active TSS	Osteobl	bone
41	chr2:179058200-179058800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells	blood
42	chr2:179058200-179058800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr2:179058200-179058800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr2:179058200-179058800	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
45	chr2:179058200-179058800	Bivalent/Poised TSS	Small Intestine	intestine
46	chr2:179058200-179058800	Flanking Active TSS	HMEC	breast
47	chr2:179058200-179059000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
48	chr2:179058200-179059000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
49	chr2:179058200-179059200	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
50	chr2:179058200-179059400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin

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