Variant report

Variant	nsv541777
Chromosome Location	chr13:54124103-54521120
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:844)
CpG islands
(count:183)
Chromatin interactive
region (count:27)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:844 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr13:54217880-54218136	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr13:54479603-54479849	GM12878	blood:	n/a	chr13:54479776-54479784
3	BCL11A	chr13:54479665-54479895	GM12878	blood:	n/a	chr13:54479779-54479788 chr13:54479742-54479751
4	BHLHE40	chr13:54202518-54202704	GM12878	blood:	n/a	chr13:54202577-54202590
5	BHLHE40	chr13:54475131-54475138	GM12878	blood:	n/a	n/a
6	BHLHE40	chr13:54356605-54356862	GM12878	blood:	n/a	n/a
7	BRCA1	chr13:54149773-54149781	GM12878	blood:	n/a	n/a
8	CEBPB	chr13:54356591-54356893	K562	blood:	n/a	n/a
9	CEBPB	chr13:54356588-54356906	A549	lung:	n/a	n/a
10	CEBPB	chr13:54404485-54404673	HepG2	liver:	n/a	chr13:54404618-54404629
11	CEBPB	chr13:54170589-54170783	HepG2	liver:	n/a	n/a
12	CEBPB	chr13:54356619-54356839	MCF-7	breast:	n/a	n/a
13	CEBPB	chr13:54478345-54478474	HepG2	liver:	n/a	n/a
14	CEBPB	chr13:54356576-54356912	IMR90	lung:	n/a	n/a
15	CEBPB	chr13:54165814-54166014	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr13:54356561-54356898	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr13:54356622-54356826	A549	lung:	n/a	n/a
18	CEBPB	chr13:54493442-54493716	IMR90	lung:	n/a	chr13:54493546-54493557
19	CEBPB	chr13:54356658-54356771	HepG2	liver:	n/a	n/a
20	CEBPB	chr13:54356551-54356967	ECC-1	luminal epithelium:	n/a	chr13:54356928-54356936
21	CEBPB	chr13:54361120-54361404	HepG2	liver:	n/a	chr13:54361258-54361269
22	CEBPB	chr13:54356561-54356901	HepG2	liver:	n/a	n/a
23	CEBPB	chr13:54356549-54356924	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr13:54376269-54376545	HepG2	liver:	n/a	chr13:54376521-54376534 chr13:54376318-54376331
25	CEBPB	chr13:54493406-54493731	HepG2	liver:	n/a	chr13:54493546-54493557
26	CEBPB	chr13:54235548-54235783	HepG2	liver:	n/a	chr13:54235670-54235681
27	CEBPB	chr13:54447335-54447587	H1-hESC	embryonic stem cell:	n/a	chr13:54447412-54447423
28	CHD1	chr13:54281102-54281120	GM12878	blood:	n/a	n/a
29	CHD1	chr13:54162299-54162343	GM12878	blood:	n/a	n/a
30	CHD1	chr13:54448302-54448308	GM12878	blood:	n/a	n/a
31	CHD1	chr13:54287148-54287163	GM12878	blood:	n/a	n/a
32	CHD2	chr13:54447886-54448044	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr13:54356639-54356857	K562	blood:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
34	CTCF	chr13:54356620-54356770	Hela-S3	cervix:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
35	CTCF	chr13:54356620-54356770	WERI-Rb-1	eye:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
36	CTCF	chr13:54356600-54356750	RPTEC	kidney:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
37	CTCF	chr13:54356640-54356790	GM12868	blood:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
38	CTCF	chr13:54356580-54356730	HCT-116	colon:	n/a	n/a
39	CTCF	chr13:54335840-54335990	GM12873	blood:	n/a	n/a
40	CTCF	chr13:54356176-54356368	LNCaP	prostate:	n/a	chr13:54356250-54356266
41	CTCF	chr13:54356640-54356790	GM12870	blood:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
42	CTCF	chr13:54356649-54356830	SK-N-SH_RA	brain:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
43	CTCF	chr13:54356640-54356790	HUVEC	blood vessel:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
44	CTCF	chr13:54356260-54356410	HMEC	breast:	n/a	n/a
45	CTCF	chr13:54356720-54356870	HVMF	connective:	n/a	n/a
46	CTCF	chr13:54356740-54356890	NHLF	lung:	n/a	n/a
47	CTCF	chr13:54356620-54356770	GM12873	blood:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
48	CTCF	chr13:54356620-54356770	AoAF	blood vessel:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
49	CTCF	chr13:54331720-54331870	GM12873	blood:	n/a	n/a
50	CTCF	chr13:54145700-54145850	AG09319	gingival:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:54265754-54265804	GM12892	blood:	n/a
2	chr13:54422912-54422962	NHBE	bronchial:	n/a
3	chr13:54265754-54265804	ECC-1	luminal epithelium:	n/a
4	chr13:54422912-54422962	A549	lung:	n/a
5	chr13:54265754-54265804	HMEC	breast:	n/a
6	chr13:54362844-54362894	T-47D	breast:	n/a
7	chr13:54362844-54362894	GM12891	blood:	n/a
8	chr13:54265754-54265804	RPTEC	kidney:	n/a
9	chr13:54422912-54422962	SK-N-MC	brain:	n/a
10	chr13:54362844-54362894	HCF	heart:	n/a
11	chr13:54422912-54422962	HEEpiC	esophagus:	n/a
12	chr13:54422912-54422962	HL-60	blood:	n/a
13	chr13:54362844-54362894	BJ	skin:	n/a
14	chr13:54362844-54362894	RPTEC	kidney:	n/a
15	chr13:54362844-54362894	LNCaP	prostate:	n/a
16	chr13:54362844-54362894	HL-60	blood:	n/a
17	chr13:54422912-54422962	HCT-116	colon:	n/a
18	chr13:54422912-54422962	SK-N-SH_RA	brain:	n/a
19	chr13:54362844-54362894	SK-N-MC	brain:	n/a
20	chr13:54362844-54362894	SK-N-SH_RA	brain:	n/a
21	chr13:54265754-54265804	SKMC	muscle:	n/a
22	chr13:54265754-54265804	HCF	heart:	n/a
23	chr13:54362844-54362894	HEK293	kidney:	embryo
24	chr13:54265754-54265804	Caco-2	colon:	n/a
25	chr13:54422912-54422962	GM12892	blood:	n/a
26	chr13:54362844-54362894	K562	blood:	n/a
27	chr13:54362844-54362894	AG09319	gingival:	n/a
28	chr13:54265754-54265804	IMR90	lung:	fetal
29	chr13:54362844-54362894	MCF10A-Er-Src	breast:	n/a
30	chr13:54265754-54265804	HPAEpiC	pulmonary alveolar:	n/a
31	chr13:54362844-54362894	HMEC	breast:	n/a
32	chr13:54422912-54422962	U87	brain:	n/a
33	chr13:54422912-54422962	Hela-S3	cervix:	n/a
34	chr13:54422912-54422962	HIPEpiC	eye:	n/a
35	chr13:54362844-54362894	H1-hESC	embryonic stem cell:	embryo
36	chr13:54265754-54265804	HRPEpiC	eye:	n/a
37	chr13:54362844-54362894	BE2_C	brain:	n/a
38	chr13:54265754-54265804	AG10803	skin:	n/a
39	chr13:54265754-54265804	U87	brain:	n/a
40	chr13:54362844-54362894	ECC-1	luminal epithelium:	n/a
41	chr13:54362844-54362894	HCT-116	colon:	n/a
42	chr13:54422912-54422962	SAEC	small airway:	n/a
43	chr13:54265754-54265804	SK-N-SH_RA	brain:	n/a
44	chr13:54362844-54362894	CMK	blood:	n/a
45	chr13:54265754-54265804	HIPEpiC	eye:	n/a
46	chr13:54422912-54422962	HPAEpiC	pulmonary alveolar:	n/a
47	chr13:54265754-54265804	HCM	heart:	n/a
48	chr13:54422912-54422962	NT2-D1	testis:	n/a
49	chr13:54265754-54265804	NT2-D1	testis:	n/a
50	chr13:54422912-54422962	BE2_C	brain:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:54262097..54264058-chr13:54265102..54267919,2	K562	blood:
2	chr13:53824070..53825129-chr13:54355995..54357044,7	MCF-7	breast:
3	chr13:53996660..53998932-chr13:54254094..54256636,2	MCF-7	breast:
4	chr13:54214945..54217343-chr13:54221329..54223882,2	K562	blood:
5	chr13:54454384..54456139-chr13:54459138..54461330,2	K562	blood:
6	chr13:54255787..54257307-chr8:43091408..43092931,2	MCF-7	breast:
7	chr13:54454384..54456447-chr13:54458357..54461330,3	K562	blood:
8	chr13:54454384..54456139-chr13:54459138..54461330,2	K562	blood:
9	chr13:53824138..53824998-chr13:54353117..54353653,2	MCF-7	breast:
10	chr13:54454384..54456447-chr13:54458357..54461330,3	K562	blood:
11	chr13:54222984..54225792-chr13:54226034..54227625,2	K562	blood:
12	chr13:54214945..54217343-chr13:54221329..54223882,2	K562	blood:
13	chr13:54128556..54131217-chr13:54185376..54186896,2	MCF-7	breast:
14	chr13:54215843..54218051-chr13:54222381..54223882,2	K562	blood:
15	chr13:54256787..54257307-chr8:43092259..43092930,2	MCF-7	breast:
16	chr13:53824156..53824674-chr13:54349734..54350480,3	MCF-7	breast:
17	chr13:53824154..53825004-chr13:54349752..54350528,4	MCF-7	breast:
18	chr13:54222984..54225792-chr13:54226034..54227625,2	K562	blood:
19	chr13:53824183..53825128-chr13:54355772..54356571,3	MCF-7	breast:
20	chr13:54359558..54362515-chr13:54378341..54380305,2	MCF-7	breast:
21	chr13:54411879..54413790-chr13:54440349..54442010,2	K562	blood:
22	chr13:54262097..54264058-chr13:54265102..54267919,2	K562	blood:
23	chr13:54128556..54131217-chr13:54185376..54186896,2	MCF-7	breast:
24	chr13:54215843..54218051-chr13:54222381..54223882,2	K562	blood:
25	chr13:54359558..54362515-chr13:54378341..54380305,2	MCF-7	breast:
26	chr13:54411879..54413790-chr13:54440349..54442010,2	K562	blood:
27	chr13:54256807..54257307-chr8:43092259..43092909,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OLFM4-2	chr13:54348953-54349119	XLOC_010398
2	lnc-OLFM4-3	chr13:54389554-54389628	ENSG00000261517.1
3	lnc-OLFM4-10	chr13:54452517-54452560	l_854_chr13:54424438-54458818_testes
4	lnc-OLFM4-10	chr13:54458356-54458818	l_854_chr13:54424438-54458818_testes
5	lnc-OLFM4-10	chr13:54451446-54451527	l_854_chr13:54424438-54458818_testes
6	lnc-OLFM4-3	chr13:54447587-54450254	ENSG00000261517.1
7	lnc-OLFM4-3	chr13:54444600-54444662	ENSG00000261517.1
8	lnc-OLFM4-3	chr13:54414818-54414945	ENSG00000261517.1
9	lnc-OLFM4-10	chr13:54424439-54424529	l_854_chr13:54424438-54458818_testes
10	lnc-OLFM4-3	chr13:54412874-54412924	ENSG00000261517.1
11	lnc-OLFM4-2	chr13:54334856-54334931	XLOC_010398
12	lnc-OLFM4-3	chr13:54418480-54418657	ENSG00000261517.1

No data

Variant related genes	Relation type
LINC00558	TF binding region
LINC00558	CpG island

Extended variants
information (count: 3856 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:3856 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189888846	chr13:54130616-54130617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs148280928	chr13:54130617-54130618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs563763865	chr13:54130662-54130663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs534528687	chr13:54130691-54130692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs181117340	chr13:54130750-54130751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs532729975	chr13:54130760-54130761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs552952479	chr13:54130803-54130804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs566381029	chr13:54130851-54130852	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs558811209	chr13:54130863-54130864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs528759314	chr13:54130874-54130875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs376284443	chr13:54130893-54130894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs71437901	chr13:54130897-54130898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs17061139	chr13:54130902-54130903	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs568420810	chr13:54130903-54130904	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs376930139	chr13:54130937-54130938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs537182739	chr13:54130947-54130948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs557415508	chr13:54130964-54130965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs1572478	chr13:54130976-54130977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs146262699	chr13:54130986-54130987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs139315709	chr13:54131016-54131017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs572027105	chr13:54131073-54131074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs540901585	chr13:54131078-54131079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs554299946	chr13:54131109-54131110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs187167954	chr13:54131160-54131161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs543194423	chr13:54131163-54131164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563394400	chr13:54131215-54131216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs532198473	chr13:54131216-54131217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs546433800	chr13:54131235-54131236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs559956970	chr13:54131255-54131256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs374189310	chr13:54131256-54131257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs142512074	chr13:54131264-54131265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs17061145	chr13:54131349-54131350	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs150653514	chr13:54131353-54131354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs371488527	chr13:54131361-54131362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs139766837	chr13:54131436-54131437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs570932074	chr13:54131568-54131569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs7983394	chr13:54131577-54131578	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs551977907	chr13:54131590-54131591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs565518707	chr13:54131600-54131601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs149781045	chr13:54131631-54131632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs145697574	chr13:54131653-54131654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs574396792	chr13:54131661-54131662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs189039260	chr13:54131696-54131697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs556644982	chr13:54131723-54131724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs543749350	chr13:54131745-54131746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs577034295	chr13:54131749-54131750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs542830017	chr13:54131771-54131772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs560022307	chr13:54131819-54131820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs573466449	chr13:54131833-54131834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs542202706	chr13:54131844-54131845	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:117)

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
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:54130600-54132200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr13:54142400-54142800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr13:54142800-54146800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr13:54143000-54144200	Enhancers	Colon Smooth Muscle	Colon
5	chr13:54146800-54149800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr13:54149000-54149600	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr13:54149000-54150000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr13:54162400-54162600	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr13:54162600-54162800	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr13:54162600-54163800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr13:54162800-54164400	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr13:54163800-54166200	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr13:54164400-54165600	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr13:54164800-54165000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr13:54164800-54166200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr13:54165000-54166200	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr13:54165000-54166200	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr13:54165200-54165800	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr13:54165200-54166000	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr13:54165200-54166200	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr13:54165600-54165800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
22	chr13:54165600-54165800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr13:54165600-54166000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr13:54165800-54166000	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr13:54166000-54166200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
26	chr13:54175400-54175600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr13:54175800-54176800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr13:54176800-54177200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr13:54182200-54183600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr13:54182800-54183600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr13:54184400-54184800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
32	chr13:54194400-54194600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr13:54195800-54196600	Enhancers	NH-A	brain
34	chr13:54195800-54198200	Enhancers	Fetal Brain Male	brain
35	chr13:54197600-54200000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr13:54201000-54201400	Enhancers	Fetal Heart	heart
37	chr13:54203000-54203200	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr13:54204800-54205800	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr13:54205000-54205400	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr13:54205000-54205600	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr13:54205800-54206000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr13:54210800-54211400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr13:54211200-54211800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr13:54211200-54212000	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr13:54211200-54212600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr13:54211800-54216400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr13:54216400-54216800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr13:54216400-54216800	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr13:54225200-54225600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr13:54225200-54225600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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