Variant report

Variant	esv2756368
Chromosome Location	chr13:53824599-53923599
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:53824410-53824767	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:53824458-53824849	K562	blood:	n/a	n/a
3	ATF2	chr13:53850266-53850825	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr13:53917422-53917944	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr13:53917374-53917879	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr13:53917408-53917886	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr13:53917483-53917885	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL11A	chr13:53917539-53917806	H1-hESC	embryonic stem cell:	n/a	n/a
9	BRCA1	chr13:53825799-53825882	H1-hESC	embryonic stem cell:	n/a	n/a
10	BRCA1	chr13:53884718-53884805	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr13:53855862-53856062	HepG2	liver:	n/a	chr13:53855977-53855990
12	CEBPB	chr13:53834705-53835040	HepG2	liver:	n/a	n/a
13	CEBPB	chr13:53834727-53834953	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr13:53850310-53850840	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr13:53917275-53917810	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr13:53830934-53831057	HepG2	liver:	n/a	chr13:53830977-53830990 chr13:53830978-53830989
17	CEBPB	chr13:53885090-53885296	HepG2	liver:	n/a	chr13:53885143-53885154 chr13:53885144-53885153 chr13:53885142-53885155 chr13:53885142-53885155 chr13:53885144-53885153 chr13:53885142-53885155 chr13:53885142-53885153 chr13:53885144-53885153 chr13:53885142-53885153 chr13:53885144-53885153
18	CEBPB	chr13:53851777-53852036	HepG2	liver:	n/a	chr13:53851894-53851905 chr13:53851896-53851907
19	CEBPB	chr13:53862693-53862986	A549	lung:	n/a	chr13:53862824-53862835
20	CEBPB	chr13:53862657-53862980	IMR90	lung:	n/a	chr13:53862824-53862835
21	CEBPB	chr13:53864064-53864255	HepG2	liver:	n/a	chr13:53864185-53864196 chr13:53864186-53864197 chr13:53864185-53864198
22	CEBPB	chr13:53862700-53862971	K562	blood:	n/a	chr13:53862824-53862835
23	CEBPB	chr13:53862674-53862990	HepG2	liver:	n/a	chr13:53862824-53862835
24	CEBPB	chr13:53862676-53862974	H1-hESC	embryonic stem cell:	n/a	chr13:53862824-53862835
25	CEBPB	chr13:53885032-53885172	H1-hESC	embryonic stem cell:	n/a	chr13:53885143-53885154 chr13:53885144-53885153 chr13:53885142-53885155 chr13:53885142-53885155 chr13:53885144-53885153 chr13:53885142-53885155 chr13:53885142-53885153 chr13:53885144-53885153 chr13:53885142-53885153 chr13:53885144-53885153
26	CEBPB	chr13:53885121-53885188	K562	blood:	n/a	chr13:53885143-53885154 chr13:53885144-53885153 chr13:53885142-53885155 chr13:53885142-53885155 chr13:53885144-53885153 chr13:53885142-53885155 chr13:53885142-53885153 chr13:53885144-53885153 chr13:53885142-53885153 chr13:53885144-53885153
27	CHD2	chr13:53917481-53917938	H1-hESC	embryonic stem cell:	n/a	n/a
28	CREB1	chr13:53917417-53917884	H1-hESC	embryonic stem cell:	n/a	n/a
29	CREB1	chr13:53917382-53917968	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr13:53885872-53886095	Medullo	brain:	n/a	n/a
31	CTCF	chr13:53879660-53879810	HEK293	kidney:	n/a	n/a
32	CTCF	chr13:53824521-53824721	Gliobla	brain:	n/a	chr13:53824575-53824591 chr13:53824579-53824587 chr13:53824574-53824592 chr13:53824671-53824684 chr13:53824576-53824597 chr13:53824670-53824691
33	CTCF	chr13:53824406-53824818	MCF-7	breast:	n/a	chr13:53824575-53824591 chr13:53824579-53824587 chr13:53824574-53824592 chr13:53824671-53824684 chr13:53824576-53824597 chr13:53824670-53824691
34	CTCF	chr13:53885900-53886050	GM12872	blood:	n/a	n/a
35	CTCF	chr13:53913000-53913150	HEK293	kidney:	n/a	chr13:53913093-53913109
36	CTCF	chr13:53824940-53825090	GM06990	blood:	n/a	n/a
37	CTCF	chr13:53824428-53824755	H1-hESC	embryonic stem cell:	n/a	chr13:53824575-53824591 chr13:53824579-53824587 chr13:53824574-53824592 chr13:53824671-53824684 chr13:53824576-53824597 chr13:53824670-53824691
38	CTCF	chr13:53917580-53917730	GM12864	blood:	n/a	n/a
39	CTCF	chr13:53824520-53824670	HCM	heart:	n/a	chr13:53824575-53824591 chr13:53824579-53824587 chr13:53824574-53824592 chr13:53824576-53824597
40	CTCF	chr13:53824520-53824670	HEEpiC	esophagus:	n/a	chr13:53824575-53824591 chr13:53824579-53824587 chr13:53824574-53824592 chr13:53824576-53824597
41	CTCF	chr13:53824480-53824630	GM12869	blood:	n/a	chr13:53824575-53824591 chr13:53824579-53824587 chr13:53824574-53824592 chr13:53824576-53824597
42	CTCF	chr13:53824520-53824670	HMEC	breast:	n/a	chr13:53824575-53824591 chr13:53824579-53824587 chr13:53824574-53824592 chr13:53824576-53824597
43	CTCF	chr13:53913080-53913230	HMF	breast:	n/a	chr13:53913093-53913109
44	CTCF	chr13:53885940-53886090	HepG2	liver:	n/a	n/a
45	CTCF	chr13:53824520-53824670	HFF	foreskin:	n/a	chr13:53824575-53824591 chr13:53824579-53824587 chr13:53824574-53824592 chr13:53824576-53824597
46	CTCF	chr13:53824441-53824769	HepG2	liver:	n/a	chr13:53824575-53824591 chr13:53824579-53824587 chr13:53824574-53824592 chr13:53824671-53824684 chr13:53824576-53824597 chr13:53824670-53824691
47	CTCF	chr13:53824520-53824670	SK-N-SH_RA	brain:	n/a	chr13:53824575-53824591 chr13:53824579-53824587 chr13:53824574-53824592 chr13:53824576-53824597
48	CTCF	chr13:53913040-53913190	GM12873	blood:	n/a	chr13:53913093-53913109
49	CTCF	chr13:53885900-53886050	GM12873	blood:	n/a	n/a
50	CTCF	chr13:53824560-53824710	HMF	breast:	n/a	chr13:53824575-53824591 chr13:53824579-53824587 chr13:53824574-53824592 chr13:53824671-53824684 chr13:53824576-53824597 chr13:53824670-53824691

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:53885252-53885302	GM06990	blood:	n/a
2	chr13:53885252-53885302	GM06990	blood:	n/a
3	chr13:53869898-53869948	SKMC	muscle:	n/a
4	chr13:53916476-53916526	ECC-1	luminal epithelium:	n/a
5	chr13:53916476-53916526	ProgFib	skin:	n/a
6	chr13:53916476-53916526	SK-N-SH_RA	brain:	n/a
7	chr13:53869898-53869948	HAEpiC	amniotic membrane:	n/a
8	chr13:53869898-53869948	GM12891	blood:	n/a
9	chr13:53916476-53916526	K562	blood:	n/a
10	chr13:53916476-53916526	T-47D	breast:	n/a
11	chr13:53916476-53916526	NT2-D1	testis:	n/a
12	chr13:53916476-53916526	BE2_C	brain:	n/a
13	chr13:53885252-53885302	ovcar-3	ovarian:	n/a
14	chr13:53885252-53885302	HUVEC	blood vessel:	n/a
15	chr13:53916476-53916526	HEK293	kidney:	embryo
16	chr13:53850898-53850948	GM19239	blood:	n/a
17	chr13:53850898-53850948	AG09319	gingival:	n/a
18	chr13:53885252-53885302	GM19239	blood:	n/a
19	chr13:53885252-53885302	Caco-2	colon:	n/a
20	chr13:53916476-53916526	PFSK-1	brain:	n/a
21	chr13:53916476-53916526	Hepatocyte	liver:	n/a
22	chr13:53885252-53885302	HRE	kidney:	n/a
23	chr13:53850898-53850948	SKMC	muscle:	n/a
24	chr13:53850898-53850948	GM12892	blood:	n/a
25	chr13:53850898-53850948	HUVEC	blood vessel:	n/a
26	chr13:53916476-53916526	Caco-2	colon:	n/a
27	chr13:53850898-53850948	PANC-1	pancreas:	n/a
28	chr13:53885252-53885302	HCPEpiC	choroid plexus:	n/a
29	chr13:53850898-53850948	GM06990	blood:	n/a
30	chr13:53916476-53916526	BJ	skin:	n/a
31	chr13:53869898-53869948	PANC-1	pancreas:	n/a
32	chr13:53916476-53916526	ovcar-3	ovarian:	n/a
33	chr13:53916476-53916526	GM19239	blood:	n/a
34	chr13:53869898-53869948	Caco-2	colon:	n/a
35	chr13:53850898-53850948	HCM	heart:	n/a
36	chr13:53869898-53869948	U87	brain:	n/a
37	chr13:53869898-53869948	ovcar-3	ovarian:	n/a
38	chr13:53916476-53916526	MCF-7	breast:	n/a
39	chr13:53916476-53916526	LNCaP	prostate:	n/a
40	chr13:53850898-53850948	CMK	blood:	n/a
41	chr13:53916476-53916526	AG09319	gingival:	n/a
42	chr13:53869898-53869948	HRCEpiC	kidney:	n/a
43	chr13:53916476-53916526	HepG2	liver:	n/a
44	chr13:53916476-53916526	HEEpiC	esophagus:	n/a
45	chr13:53916476-53916526	CMK	blood:	n/a
46	chr13:53885252-53885302	HL-60	blood:	n/a
47	chr13:53850898-53850948	AG10803	skin:	n/a
48	chr13:53916476-53916526	U87	brain:	n/a
49	chr13:53885252-53885302	AG10803	skin:	n/a
50	chr13:53885252-53885302	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:53824156..53824674-chr13:54349734..54350480,3	MCF-7	breast:
2	chr13:53824070..53825129-chr13:54355995..54357044,7	MCF-7	breast:
3	chr13:53824138..53824998-chr13:54353117..54353653,2	MCF-7	breast:
4	chr13:53915723..53916223-chr17:57970367..57971069,2	MCF-7	breast:
5	chr13:53824154..53825004-chr13:54349752..54350528,4	MCF-7	breast:
6	chr13:53917930..53919463-chr13:53919847..53922635,2	K562	blood:
7	chr13:53824325..53824988-chr13:58132042..58132595,2	MCF-7	breast:
8	chr13:53917930..53919463-chr13:53919847..53922635,2	K562	blood:
9	chr12:58153957..58154503-chr13:53901447..53902222,2	MCF-7	breast:
10	chr13:53824183..53825128-chr13:54355772..54356571,3	MCF-7	breast:
11	chr13:53824036..53825003-chr13:55819208..55820068,4	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OLFM4-8	chr13:53901537-53901605	NONHSAT034017
2	lnc-OLFM4-8	chr13:53900089-53900167	NONHSAT034017
3	lnc-OLFM4-8	chr13:53891266-53891339	NONHSAT034017
4	lnc-OLFM4-7	chr13:53832212-53832505	NONHSAT034016
5	lnc-OLFM4-9	chr13:53919346-53920093	NONHSAT034018

Variant related genes	Relation type
RN7SL618P	TF binding region
RN7SL618P	CpG island
ENSG00000108443	chromatin interactions

Extended variants
information (count: 1922 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:1922 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557654530	chr13:53824604-53824605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs563166806	chr13:53824613-53824614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs1555549	chr13:53824637-53824638	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs551755444	chr13:53824647-53824648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs370645275	chr13:53824650-53824651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs187940080	chr13:53824680-53824681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs539043030	chr13:53824694-53824695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs193199692	chr13:53824720-53824721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs77600715	chr13:53824729-53824730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs74686840	chr13:53824730-53824731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs63278861	chr13:53824731-53824732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs547855768	chr13:53824741-53824742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs185016737	chr13:53824742-53824743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs374062912	chr13:53824796-53824797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs140885558	chr13:53824820-53824821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs555280180	chr13:53824872-53824873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs575153198	chr13:53824881-53824882	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs1555548	chr13:53824938-53824939	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs557439803	chr13:53824939-53824940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs189530216	chr13:53825022-53825023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs539983685	chr13:53825041-53825042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs560190553	chr13:53825042-53825043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs568360418	chr13:53825136-53825137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs200552826	chr13:53825137-53825138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs386771083	chr13:53825144-53825145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs370191175	chr13:53825146-53825147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs1555547	chr13:53825147-53825148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs1555546	chr13:53825148-53825149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs1555545	chr13:53825149-53825150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs5803641	chr13:53825159-53825160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs386771084	chr13:53825161-53825162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs543202378	chr13:53825162-53825163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs563181247	chr13:53825167-53825168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs181835331	chr13:53825244-53825245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs545435908	chr13:53825251-53825252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs138599194	chr13:53825257-53825258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs73483520	chr13:53825270-53825271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs575058178	chr13:53825282-53825283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs78832557	chr13:53825316-53825317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs80269165	chr13:53825321-53825322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs375410290	chr13:53825343-53825344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs184837052	chr13:53825482-53825483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs564199852	chr13:53825487-53825488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs28573308	chr13:53825495-53825496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs537712013	chr13:53825501-53825502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs558016327	chr13:53825531-53825532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs571203016	chr13:53825554-53825555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs188429132	chr13:53825591-53825592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs553596267	chr13:53825601-53825602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs180831984	chr13:53825675-53825676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:113)

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
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:194 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:53823400-53825400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr13:53823800-53825000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr13:53825000-53827000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr13:53825200-53825400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr13:53825200-53825800	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr13:53825400-53826600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr13:53826600-53826800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr13:53826800-53834600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr13:53827000-53827200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr13:53833000-53834200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr13:53834000-53834600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
12	chr13:53834200-53835400	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr13:53834400-53834800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
14	chr13:53834600-53836000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr13:53835200-53836000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr13:53836000-53843800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr13:53840000-53840800	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr13:53840200-53840800	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr13:53840200-53840800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr13:53840400-53840800	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr13:53843600-53843800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
22	chr13:53843600-53843800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr13:53843800-53844000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
24	chr13:53843800-53844200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr13:53843800-53844200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
26	chr13:53843800-53844200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr13:53844000-53844200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
28	chr13:53844200-53844400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
29	chr13:53849400-53851200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
30	chr13:53849600-53849800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
31	chr13:53849600-53850000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
32	chr13:53849600-53850200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
33	chr13:53849600-53850800	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
34	chr13:53849600-53851000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
35	chr13:53849600-53851000	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
36	chr13:53849600-53851000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
37	chr13:53849600-53851200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr13:53849800-53851400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
39	chr13:53850000-53850600	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr13:53850200-53850400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
41	chr13:53850200-53850800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr13:53850200-53850800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr13:53850200-53850800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
44	chr13:53850400-53850600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
45	chr13:53850600-53850800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
46	chr13:53850600-53850800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr13:53850600-53851000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr13:53850600-53851000	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
49	chr13:53850600-53851000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
50	chr13:53850600-53851000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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