Variant report

Variant	esv3427175
Chromosome Location	chr13:53773776-53776324
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:295)
CpG islands
(count:489)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:295 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr13:53776052-53776376	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr13:53775251-53775601	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr13:53774896-53775639	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr13:53776070-53776411	H1-hESC	embryonic stem cell:	n/a	n/a
5	BRCA1	chr13:53775324-53775536	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr13:53775300-53775500	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD2	chr13:53775202-53775571	H1-hESC	embryonic stem cell:	n/a	n/a
8	CREB1	chr13:53774857-53775718	H1-hESC	embryonic stem cell:	n/a	n/a
9	CREB1	chr13:53774843-53775729	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTBP2	chr13:53775318-53776314	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr13:53775380-53775530	GM12869	blood:	n/a	n/a
12	CTCF	chr13:53775400-53775550	HUVEC	blood vessel:	n/a	n/a
13	CTCF	chr13:53776200-53776350	NHEK	skin:	n/a	n/a
14	CTCF	chr13:53775340-53775490	HUVEC	blood vessel:	n/a	n/a
15	CTCF	chr13:53776220-53776370	HRE	kidney:	n/a	n/a
16	CTCF	chr13:53776200-53776350	HBMEC	blood vessel:	n/a	n/a
17	CTCF	chr13:53776200-53776350	AG09319	gingival:	n/a	n/a
18	CTCF	chr13:53775315-53775570	Pancreas_OC	pancreas:	n/a	n/a
19	CTCF	chr13:53775247-53775593	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr13:53775340-53775490	HBMEC	blood vessel:	n/a	n/a
21	CTCF	chr13:53775320-53775470	AG04450	lung:	n/a	n/a
22	CTCF	chr13:53775340-53775490	NHEK	skin:	n/a	n/a
23	CTCF	chr13:53775399-53775466	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr13:53775261-53775627	MCF-7	breast:	n/a	n/a
25	CTCF	chr13:53776200-53776350	HAc	cerebellar:	n/a	n/a
26	CTCF	chr13:53776220-53776370	HEEpiC	esophagus:	n/a	n/a
27	CTCF	chr13:53775420-53775570	GM12869	blood:	n/a	n/a
28	CTCF	chr13:53775340-53775590	RPTEC	kidney:	n/a	n/a
29	CTCF	chr13:53775380-53775530	GM12868	blood:	n/a	n/a
30	CTCF	chr13:53775360-53775510	HMF	breast:	n/a	n/a
31	CTCF	chr13:53776190-53776365	Pancreas_OC	pancreas:	n/a	n/a
32	CTCF	chr13:53775320-53775470	AG10803	skin:	n/a	n/a
33	CTCF	chr13:53776227-53776357	Kidney_OC	kidney:	n/a	n/a
34	CTCF	chr13:53775396-53775463	GM13976	blood:	n/a	n/a
35	CTCF	chr13:53775418-53775478	GM12892	blood:	n/a	n/a
36	CTCF	chr13:53775380-53775530	BJ	skin:	n/a	n/a
37	CTCF	chr13:53775268-53775619	MCF-7	breast:	n/a	n/a
38	CTCF	chr13:53775293-53775570	LNCaP	prostate:	n/a	n/a
39	CTCF	chr13:53776142-53776426	Medullo	brain:	n/a	n/a
40	CTCF	chr13:53775360-53775510	AG09319	gingival:	n/a	n/a
41	CTCF	chr13:53776140-53776290	GM12874	blood:	n/a	n/a
42	CTCF	chr13:53776220-53776370	AG09319	gingival:	n/a	n/a
43	CTCF	chr13:53776249-53776333	Lung_OC	lung:	n/a	n/a
44	CTCF	chr13:53776105-53776350	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr13:53776120-53776270	WI-38	lung:	n/a	n/a
46	CTCF	chr13:53775389-53775518	GM19240	blood:	n/a	n/a
47	CTCF	chr13:53775340-53775490	HMEC	breast:	n/a	n/a
48	CTCF	chr13:53776260-53776410	GM12871	blood:	n/a	n/a
49	CTCF	chr13:53776180-53776330	AG04449	skin:	n/a	n/a
50	CTCF	chr13:53775399-53775447	Spleen_OC	spleen:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:53776259-53776309	Hepatocyte	liver:	n/a
2	chr13:53776259-53776309	Hepatocyte	liver:	n/a
3	chr13:53774217-53774267	LNCaP	prostate:	n/a
4	chr13:53774359-53774409	BE2_C	brain:	n/a
5	chr13:53775108-53775158	K562	blood:	n/a
6	chr13:53775410-53775460	HRPEpiC	eye:	n/a
7	chr13:53776259-53776309	PANC-1	pancreas:	n/a
8	chr13:53774359-53774409	HEK293	kidney:	embryo
9	chr13:53775636-53775686	HRPEpiC	eye:	n/a
10	chr13:53776259-53776309	HCT-116	colon:	n/a
11	chr13:53774359-53774409	SKMC	muscle:	n/a
12	chr13:53776259-53776309	Caco-2	colon:	n/a
13	chr13:53775410-53775460	HPAEpiC	pulmonary alveolar:	n/a
14	chr13:53775410-53775460	NH-A	brain:	n/a
15	chr13:53775108-53775158	ECC-1	luminal epithelium:	n/a
16	chr13:53775035-53775085	GM06990	blood:	n/a
17	chr13:53775410-53775460	H1-hESC	embryonic stem cell:	embryo
18	chr13:53775636-53775686	HCM	heart:	n/a
19	chr13:53775108-53775158	Caco-2	colon:	n/a
20	chr13:53776259-53776309	AG09319	gingival:	n/a
21	chr13:53774359-53774409	HepG2	liver:	n/a
22	chr13:53775958-53776008	AG04450	lung:	fetal
23	chr13:53776259-53776309	AG04449	skin:	fetal
24	chr13:53775636-53775686	HIPEpiC	eye:	n/a
25	chr13:53775958-53776008	HUVEC	blood vessel:	n/a
26	chr13:53776259-53776309	CMK	blood:	n/a
27	chr13:53774359-53774409	BJ	skin:	n/a
28	chr13:53775035-53775085	HRCEpiC	kidney:	n/a
29	chr13:53774359-53774409	HL-60	blood:	n/a
30	chr13:53776259-53776309	HUVEC	blood vessel:	n/a
31	chr13:53775035-53775085	AG10803	skin:	n/a
32	chr13:53775108-53775158	HRPEpiC	eye:	n/a
33	chr13:53776259-53776309	GM12878	blood:	n/a
34	chr13:53775958-53776008	ovcar-3	ovarian:	n/a
35	chr13:53775636-53775686	Hela-S3	cervix:	n/a
36	chr13:53775035-53775085	AG04450	lung:	fetal
37	chr13:53775958-53776008	HAEpiC	amniotic membrane:	n/a
38	chr13:53775636-53775686	RPTEC	kidney:	n/a
39	chr13:53776259-53776309	HMEC	breast:	n/a
40	chr13:53775410-53775460	PrEC	prostate:	n/a
41	chr13:53774359-53774409	ovcar-3	ovarian:	n/a
42	chr13:53775410-53775460	NHDF-neo	bronchial:	n/a
43	chr13:53775958-53776008	AG09319	gingival:	n/a
44	chr13:53775035-53775085	HL-60	blood:	n/a
45	chr13:53776259-53776309	AG04450	lung:	fetal
46	chr13:53774359-53774409	ECC-1	luminal epithelium:	n/a
47	chr13:53775636-53775686	AG04450	lung:	fetal
48	chr13:53774217-53774267	HEK293	kidney:	embryo
49	chr13:53775636-53775686	CMK	blood:	n/a
50	chr13:53774359-53774409	HCPEpiC	choroid plexus:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:53541952..53542484-chr13:53774972..53775830,2	MCF-7	breast:
2	chr13:53726507..53727505-chr13:53774966..53775870,2	MCF-7	breast:
3	chr13:53239228..53240126-chr13:53775321..53776150,2	MCF-7	breast:
4	chr13:53541918..53542704-chr13:53775013..53775632,3	MCF-7	breast:
5	chr13:53436613..53437297-chr13:53775140..53775836,2	MCF-7	breast:

No data

Variant related genes	Relation type
PCDH8P1	TF binding region
PCDH8P1	CpG island

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

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	rs184881090	chr13:53773791-53773792	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs565584176	chr13:53773810-53773811	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs569295395	chr13:53773866-53773867	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs532736435	chr13:53773889-53773890	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs139457826	chr13:53773893-53773894	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs189771436	chr13:53773922-53773923	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs528188852	chr13:53773997-53773998	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs1322948	chr13:53774024-53774025	Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs192307800	chr13:53774040-53774041	Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs117236565	chr13:53774047-53774048	Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs575256160	chr13:53774197-53774198	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs544105012	chr13:53774217-53774218	ZNF genes & repeats Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs57694479	chr13:53774221-53774222	ZNF genes & repeats Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs184367221	chr13:53774248-53774249	ZNF genes & repeats Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs189514224	chr13:53774290-53774291	ZNF genes & repeats Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs546002914	chr13:53774376-53774377	ZNF genes & repeats Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs55813433	chr13:53774383-53774384	ZNF genes & repeats Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs117546956	chr13:53774388-53774389	ZNF genes & repeats Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs375437263	chr13:53774412-53774413	ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs114487777	chr13:53774437-53774438	ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs115140905	chr13:53774442-53774443	ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs369834701	chr13:53774451-53774452	ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs34942897	chr13:53774500-53774501	ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs529973139	chr13:53774501-53774502	ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs149748049	chr13:53774514-53774515	ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs569332358	chr13:53774534-53774535	ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs539381087	chr13:53774536-53774537	ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs558381424	chr13:53774537-53774538	ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565810646	chr13:53774541-53774542	ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs534418123	chr13:53774562-53774563	ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs74474805	chr13:53774607-53774608	Bivalent Enhancer ZNF genes & repeats Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs181823674	chr13:53774621-53774622	Bivalent Enhancer ZNF genes & repeats Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs147419086	chr13:53774626-53774627	Bivalent Enhancer ZNF genes & repeats Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs2004422	chr13:53774627-53774628	Bivalent Enhancer ZNF genes & repeats Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs557656804	chr13:53774632-53774633	Bivalent Enhancer ZNF genes & repeats Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs577312525	chr13:53774649-53774650	Bivalent Enhancer ZNF genes & repeats Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546138625	chr13:53774694-53774695	Bivalent Enhancer ZNF genes & repeats Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572154811	chr13:53774712-53774713	Bivalent Enhancer ZNF genes & repeats Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs139688378	chr13:53774718-53774719	Bivalent Enhancer ZNF genes & repeats Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs2015677	chr13:53774731-53774732	Bivalent Enhancer ZNF genes & repeats Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs541944334	chr13:53774810-53774811	Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs145202175	chr13:53774858-53774859	Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs202149035	chr13:53774873-53774874	Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529812223	chr13:53774899-53774900	Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs113244526	chr13:53774900-53774901	Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs543965773	chr13:53774920-53774921	Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs142466479	chr13:53774929-53774930	Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368774115	chr13:53774938-53774939	Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs183880895	chr13:53774950-53774951	Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs111759582	chr13:53775029-53775030	Bivalent/Poised TSS ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

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
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
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
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
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	18852474	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Urothelial carcinoma	21177765	CNVD

Chromatin state (count:129 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:53766400-53774200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr13:53770800-53774000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr13:53771200-53773800	Enhancers	Fetal Brain Female	brain
4	chr13:53771800-53774000	Enhancers	Brain Germinal Matrix	brain
5	chr13:53772800-53774000	Enhancers	Fetal Brain Male	brain
6	chr13:53773000-53773800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr13:53773400-53775400	Weak transcription	Brain Anterior Caudate	brain
8	chr13:53773600-53774000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr13:53773800-53774000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr13:53773800-53774800	Bivalent Enhancer	Fetal Brain Female	brain
11	chr13:53774000-53774200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr13:53774000-53774600	Bivalent Enhancer	Fetal Brain Male	brain
13	chr13:53774000-53774800	Bivalent Enhancer	Brain Germinal Matrix	brain
14	chr13:53774200-53774400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr13:53774200-53776200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr13:53774200-53776200	ZNF genes & repeats	Spleen	Spleen
17	chr13:53774200-53776600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr13:53774400-53774600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr13:53774400-53775200	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr13:53774400-53776600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr13:53774400-53776600	Enhancers	Pancreas	Pancrea
22	chr13:53774600-53774800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
23	chr13:53774600-53774800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr13:53774600-53775200	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
25	chr13:53774600-53775400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr13:53774600-53776000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
27	chr13:53774600-53776000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
28	chr13:53774800-53775000	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
29	chr13:53774800-53775000	Bivalent Enhancer	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr13:53774800-53775000	Flanking Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr13:53774800-53775000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr13:53774800-53775000	Bivalent Enhancer	Esophagus	oesophagus
33	chr13:53774800-53775200	Active TSS	H9 Cell Line	embryonic stem cell
34	chr13:53774800-53775200	Bivalent Enhancer	Primary hematopoietic stem cells	blood
35	chr13:53774800-53775200	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
36	chr13:53774800-53775200	Bivalent Enhancer	Fetal Brain Male	brain
37	chr13:53774800-53775200	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
38	chr13:53774800-53775400	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
39	chr13:53774800-53775400	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr13:53774800-53775400	Bivalent Enhancer	Fetal Stomach	stomach
41	chr13:53774800-53775600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
42	chr13:53774800-53775600	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
43	chr13:53774800-53775800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
44	chr13:53774800-53775800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
45	chr13:53774800-53775800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr13:53774800-53775800	Bivalent Enhancer	Fetal Muscle Leg	muscle
47	chr13:53774800-53775800	Enhancers	Gastric	stomach
48	chr13:53774800-53776000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
49	chr13:53774800-53776400	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
50	chr13:53774800-53776400	Bivalent Enhancer	Fetal Muscle Trunk	muscle

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