Variant report

Variant	esv3332869
Chromosome Location	chr13:51795701-51797799
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:364)
CpG islands
(count:610)
Chromatin interactive
region (count:2)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:364 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr13:51796858-51797275	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr13:51795887-51796535	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr13:51796032-51796501	GM12878	blood:	n/a	n/a
4	BHLHE40	chr13:51796182-51796368	K562	blood:	n/a	n/a
5	CEBPB	chr13:51796196-51796274	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD1	chr13:51796947-51797452	H1-hESC	embryonic stem cell:	n/a	n/a
7	CREB1	chr13:51796185-51796795	A549	lung:	n/a	n/a
8	CTBP2	chr13:51795964-51797389	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr13:51796120-51796270	HA-sp	spinal cord:	n/a	n/a
10	CTCF	chr13:51796218-51796223	MCF-7	breast:	n/a	n/a
11	CTCF	chr13:51796360-51796510	GM12869	blood:	n/a	n/a
12	CTCF	chr13:51796955-51797053	ProgFib	skin:	n/a	n/a
13	CTCF	chr13:51796400-51796550	HUVEC	blood vessel:	n/a	n/a
14	CTCF	chr13:51796955-51797127	HUVEC	blood vessel:	n/a	chr13:51797054-51797072
15	CTCF	chr13:51796900-51797050	WERI-Rb-1	eye:	n/a	n/a
16	CTCF	chr13:51796920-51797070	GM06990	blood:	n/a	n/a
17	CTCF	chr13:51796860-51797010	GM12873	blood:	n/a	chr13:51796882-51796891
18	CTCF	chr13:51796980-51797130	HA-sp	spinal cord:	n/a	chr13:51797054-51797072
19	CTCF	chr13:51796363-51796589	GM13977	blood:	n/a	n/a
20	CTCF	chr13:51796980-51797130	HFF-Myc	foreskin:	n/a	chr13:51797054-51797072
21	CTCF	chr13:51795920-51796070	BE2_C	brain:	n/a	n/a
22	CTCF	chr13:51796358-51796560	GM19240	blood:	n/a	n/a
23	CTCF	chr13:51796350-51796707	K562	blood:	n/a	n/a
24	CTCF	chr13:51796940-51797090	GM12874	blood:	n/a	chr13:51797054-51797072
25	CTCF	chr13:51796940-51797090	HepG2	liver:	n/a	chr13:51797054-51797072
26	CTCF	chr13:51796435-51796494	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr13:51796960-51797110	HCPEpiC	choroid plexus:	n/a	chr13:51797054-51797072
28	CTCF	chr13:51796440-51796590	HAc	cerebellar:	n/a	n/a
29	CTCF	chr13:51796940-51797090	HCM	heart:	n/a	chr13:51797054-51797072
30	CTCF	chr13:51796674-51796811	A549	lung:	n/a	n/a
31	CTCF	chr13:51796400-51796550	GM12871	blood:	n/a	n/a
32	CTCF	chr13:51796992-51797117	Kidney_OC	kidney:	n/a	chr13:51797054-51797072
33	CTCF	chr13:51796420-51796570	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr13:51796960-51797110	SK-N-SH_RA	brain:	n/a	chr13:51797054-51797072
35	CTCF	chr13:51796306-51796643	GM12878	blood:	n/a	n/a
36	CTCF	chr13:51796686-51796805	GM12892	blood:	n/a	n/a
37	CTCF	chr13:51796400-51796550	HA-sp	spinal cord:	n/a	n/a
38	CTCF	chr13:51797000-51797150	HA-sp	spinal cord:	n/a	chr13:51797054-51797072
39	CTCF	chr13:51797020-51797170	HRPEpiC	eye:	n/a	chr13:51797054-51797072
40	CTCF	chr13:51796840-51796990	GM06990	blood:	n/a	chr13:51796882-51796891
41	CTCF	chr13:51796020-51796170	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr13:51796941-51796952	Spleen_OC	spleen:	n/a	n/a
43	CTCF	chr13:51796380-51796530	HCM	heart:	n/a	n/a
44	CTCF	chr13:51796360-51796510	HPF	lung:	n/a	n/a
45	CTCF	chr13:51796340-51796490	HCFaa	heart:	n/a	n/a
46	CTCF	chr13:51796885-51796940	Spleen_OC	spleen:	n/a	n/a
47	CTCF	chr13:51796399-51796568	Medullo	brain:	n/a	n/a
48	CTCF	chr13:51796420-51796570	K562	blood:	n/a	n/a
49	CTCF	chr13:51797035-51797119	MCF-7	breast:	n/a	chr13:51797054-51797072
50	CTCF	chr13:51796222-51796281	GM19240	blood:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:51796714-51796764	Caco-2	colon:	n/a
2	chr13:51795926-51795976	GM19239	blood:	n/a
3	chr13:51796223-51796273	GM12891	blood:	n/a
4	chr13:51796223-51796273	SKMC	muscle:	n/a
5	chr13:51797793-51797843	RPTEC	kidney:	n/a
6	chr13:51796265-51796315	HNPCEpiC	eye:	n/a
7	chr13:51796265-51796315	NB4	blood:	n/a
8	chr13:51795680-51795730	SK-N-SH	brain:	n/a
9	chr13:51796714-51796764	HUVEC	blood vessel:	n/a
10	chr13:51797793-51797843	HIPEpiC	eye:	n/a
11	chr13:51796887-51796937	HCF	heart:	n/a
12	chr13:51797793-51797843	BJ	skin:	n/a
13	chr13:51797793-51797843	HepG2	liver:	n/a
14	chr13:51796962-51797012	GM06990	blood:	n/a
15	chr13:51795680-51795730	Jurkat	blood:	n/a
16	chr13:51796887-51796937	ovcar-3	ovarian:	n/a
17	chr13:51795680-51795730	U87	brain:	n/a
18	chr13:51795926-51795976	PANC-1	pancreas:	n/a
19	chr13:51797139-51797189	PANC-1	pancreas:	n/a
20	chr13:51797793-51797843	AG09319	gingival:	n/a
21	chr13:51796962-51797012	SK-N-MC	brain:	n/a
22	chr13:51795926-51795976	SK-N-SH	brain:	n/a
23	chr13:51796265-51796315	HIPEpiC	eye:	n/a
24	chr13:51797139-51797189	PFSK-1	brain:	n/a
25	chr13:51797793-51797843	Hela-S3	cervix:	n/a
26	chr13:51796962-51797012	HRCEpiC	kidney:	n/a
27	chr13:51797646-51797696	U87	brain:	n/a
28	chr13:51797793-51797843	HCF	heart:	n/a
29	chr13:51797793-51797843	GM12878	blood:	n/a
30	chr13:51795926-51795976	IMR90	lung:	fetal
31	chr13:51795926-51795976	HCM	heart:	n/a
32	chr13:51795680-51795730	PrEC	prostate:	n/a
33	chr13:51796265-51796315	LNCaP	prostate:	n/a
34	chr13:51797646-51797696	AG09319	gingival:	n/a
35	chr13:51796714-51796764	ovcar-3	ovarian:	n/a
36	chr13:51796714-51796764	PANC-1	pancreas:	n/a
37	chr13:51795926-51795976	A549	lung:	n/a
38	chr13:51796887-51796937	AG10803	skin:	n/a
39	chr13:51796887-51796937	HAEpiC	amniotic membrane:	n/a
40	chr13:51795680-51795730	SK-N-MC	brain:	n/a
41	chr13:51795926-51795976	BE2_C	brain:	n/a
42	chr13:51796223-51796273	IMR90	lung:	fetal
43	chr13:51797646-51797696	HL-60	blood:	n/a
44	chr13:51795680-51795730	NHDF-neo	bronchial:	n/a
45	chr13:51796962-51797012	HRE	kidney:	n/a
46	chr13:51797793-51797843	AG04449	skin:	fetal
47	chr13:51797139-51797189	BE2_C	brain:	n/a
48	chr13:51796962-51797012	Caco-2	colon:	n/a
49	chr13:51796962-51797012	HEEpiC	esophagus:	n/a
50	chr13:51796714-51796764	MCF10A-Er-Src	breast:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:51793406..51795432-chr13:51797315..51800295,2	K562	blood:
2	chr13:51796898..51797532-chr13:51860320..51860855,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SERPINE3-4	chr13:51796513-51796705	NONHSAT033893
2	lnc-SERPINE3-4	chr13:51795151-51798286	ncRnaDb_ncrna_FR376720_3

No data

Variant related genes	Relation type
FAM124A	TF binding region
FAM124A	CpG island

Extended variants
information (count: 60 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:60 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547952116	chr13:51795746-51795747	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
2	rs61958529	chr13:51795784-51795785	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs570417756	chr13:51795834-51795835	Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs576761918	chr13:51795846-51795847	Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs35637975	chr13:51795847-51795848	Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs397705129	chr13:51795858-51795859	Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs377487822	chr13:51795859-51795860	Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs370897344	chr13:51795906-51795907	Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs539421582	chr13:51795913-51795914	Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs553109206	chr13:51796019-51796020	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs374234680	chr13:51796022-51796023	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs192358335	chr13:51796058-51796059	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs555927514	chr13:51796149-51796150	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs184951673	chr13:51796268-51796269	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs558144475	chr13:51796336-51796337	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs542150468	chr13:51796343-51796344	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs368808684	chr13:51796356-51796357	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs544830350	chr13:51796357-51796358	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs550278169	chr13:51796363-51796364	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs564721759	chr13:51796380-51796381	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs578254954	chr13:51796381-51796382	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs545779089	chr13:51796448-51796449	Bivalent/Poised TSS Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs7320388	chr13:51796468-51796469	Bivalent/Poised TSS Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs528167181	chr13:51796496-51796497	Bivalent/Poised TSS Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs7323665	chr13:51796524-51796525	Bivalent/Poised TSS Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
26	rs561909042	chr13:51796539-51796540	Bivalent/Poised TSS Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
27	rs530574093	chr13:51796722-51796723	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
28	rs35219766	chr13:51796843-51796844	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs570380200	chr13:51796871-51796872	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
30	rs539382879	chr13:51796889-51796890	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
31	rs561639475	chr13:51796919-51796920	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
32	rs9568553	chr13:51796974-51796975	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs574972078	chr13:51797024-51797025	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
34	rs555539796	chr13:51797060-51797061	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
35	rs189137332	chr13:51797075-51797076	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
36	rs9526734	chr13:51797094-51797095	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs5803559	chr13:51797332-51797333	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs78658254	chr13:51797342-51797343	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs76205626	chr13:51797344-51797345	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs61958531	chr13:51797346-51797347	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs538411843	chr13:51797368-51797369	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs9568554	chr13:51797393-51797394	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs578245350	chr13:51797409-51797410	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs192811296	chr13:51797419-51797420	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs149676607	chr13:51797432-51797433	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs1887161	chr13:51797437-51797438	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs184680972	chr13:51797480-51797481	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs574407219	chr13:51797508-51797509	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs56035793	chr13:51797550-51797551	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs368026798	chr13:51797567-51797568	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	19242612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Retinoblastoma	21504564	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Mental retardation	17502991	CNVD
Retinoblastoma	17502991	CNVD
Bipolar disorder	18458673	CNVD
Liposarcoma	21253554	CNVD
T-cell lymphomas	19863542	CNVD
Cervical cancer	21062161	CNVD
microdeletion syndrome	19284877	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Multiple myeloma	19135901	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	16461572	CNVD
Merkel cell carcinoma	19020549	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	19435819	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21858162	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	17237825	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Myelofibrosis	22110671	CNVD
Hereditary prostate cancer	22028916	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Prostate cancer	17217626	CNVD
Ovarian cancer	21781307	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21990379	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	17908304	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:403 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:51792800-51795800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr13:51794800-51795800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr13:51795200-51795800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr13:51795200-51796000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
5	chr13:51795400-51795800	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
6	chr13:51795400-51795800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr13:51795400-51795800	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr13:51795400-51795800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr13:51795400-51796000	Bivalent Enhancer	Fetal Thymus	thymus
10	chr13:51795400-51796200	Bivalent Enhancer	Stomach Mucosa	stomach
11	chr13:51795600-51795800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
12	chr13:51795600-51795800	Flanking Active TSS	H9 Cell Line	embryonic stem cell
13	chr13:51795600-51795800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr13:51795600-51795800	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
15	chr13:51795600-51795800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
16	chr13:51795600-51795800	Bivalent Enhancer	Primary hematopoietic stem cells	blood
17	chr13:51795600-51795800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells short term culture	blood
18	chr13:51795600-51795800	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
19	chr13:51795600-51795800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
20	chr13:51795600-51795800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr13:51795600-51795800	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr13:51795600-51795800	Enhancers	Colon Smooth Muscle	Colon
23	chr13:51795600-51795800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
24	chr13:51795600-51795800	Enhancers	Fetal Brain Male	brain
25	chr13:51795600-51795800	Flanking Active TSS	Fetal Brain Female	brain
26	chr13:51795600-51795800	Bivalent Enhancer	Fetal Intestine Small	intestine
27	chr13:51795600-51795800	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr13:51795600-51795800	Bivalent Enhancer	Fetal Muscle Leg	muscle
29	chr13:51795600-51795800	Enhancers	Right Ventricle	heart
30	chr13:51795600-51795800	Flanking Active TSS	Stomach Smooth Muscle	stomach
31	chr13:51795600-51795800	Bivalent Enhancer	Dnd41	blood
32	chr13:51795600-51795800	Bivalent Enhancer	NHLF	lung
33	chr13:51795600-51796000	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
34	chr13:51795600-51796000	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
35	chr13:51795600-51796000	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
36	chr13:51795600-51796000	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
37	chr13:51795600-51796000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr13:51795600-51796000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr13:51795600-51796000	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
40	chr13:51795600-51796000	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
41	chr13:51795600-51796000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
42	chr13:51795600-51796000	Bivalent Enhancer	Fetal Lung	lung
43	chr13:51795600-51796000	Enhancers	Pancreas	Pancrea
44	chr13:51795600-51796000	Enhancers	Rectal Smooth Muscle	rectum
45	chr13:51795600-51796200	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
46	chr13:51795600-51796200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr13:51795600-51796200	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
48	chr13:51795600-51796200	Active TSS	Esophagus	oesophagus
49	chr13:51795600-51796400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr13:51795600-51797200	Active TSS	A549	lung

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