Variant report

Variant	nsv900919
Chromosome Location	chr13:93957816-94030693
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:535)
CpG islands
(count:244)
Chromatin interactive
region (count:117)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:535 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:93975346-93975650	K562	blood:	n/a	n/a
2	ARID3A	chr13:93981267-93981463	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:94016486-94020420	K562	blood:	n/a	n/a
4	ATF1	chr13:93969038-93969891	K562	blood:	n/a	n/a
5	ATF1	chr13:93992749-93993702	K562	blood:	n/a	n/a
6	ATF1	chr13:93958037-93958682	K562	blood:	n/a	n/a
7	ATF1	chr13:93970852-93971517	K562	blood:	n/a	n/a
8	ATF1	chr13:93964940-93966373	K562	blood:	n/a	n/a
9	ATF1	chr13:93961911-93963133	K562	blood:	n/a	n/a
10	ATF1	chr13:93972963-93974272	K562	blood:	n/a	n/a
11	ATF1	chr13:93968037-93968798	K562	blood:	n/a	n/a
12	ATF1	chr13:93981778-93983018	K562	blood:	n/a	n/a
13	ATF1	chr13:94016448-94019058	K562	blood:	n/a	n/a
14	ATF1	chr13:94002711-94006491	K562	blood:	n/a	n/a
15	ATF1	chr13:94010722-94015288	K562	blood:	n/a	n/a
16	BACH1	chr13:93962377-93962420	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr13:93957083-93958146	K562	blood:	n/a	n/a
18	BHLHE40	chr13:93995400-93995965	K562	blood:	n/a	n/a
19	BHLHE40	chr13:94006930-94013742	K562	blood:	n/a	n/a
20	BHLHE40	chr13:93962106-93963353	K562	blood:	n/a	n/a
21	BHLHE40	chr13:93975637-93976117	K562	blood:	n/a	n/a
22	BHLHE40	chr13:93990127-93992188	K562	blood:	n/a	n/a
23	BRCA1	chr13:93970044-93970136	Hela-S3	cervix:	n/a	n/a
24	CCNT2	chr13:93959343-93959445	K562	blood:	n/a	n/a
25	CCNT2	chr13:93996156-93996788	K562	blood:	n/a	n/a
26	CCNT2	chr13:93988584-93989325	K562	blood:	n/a	n/a
27	CCNT2	chr13:94018389-94019550	K562	blood:	n/a	n/a
28	CEBPB	chr13:94029504-94029777	A549	lung:	n/a	chr13:94029654-94029665 chr13:94029656-94029667 chr13:94029651-94029668 chr13:94029654-94029667
29	CEBPB	chr13:93973833-93974558	K562	blood:	n/a	chr13:93974085-93974098
30	CEBPB	chr13:94016455-94016741	IMR90	lung:	n/a	n/a
31	CEBPB	chr13:93970850-93971157	A549	lung:	n/a	chr13:93971022-93971033
32	CEBPB	chr13:94029625-94029805	H1-hESC	embryonic stem cell:	n/a	chr13:94029654-94029665 chr13:94029656-94029667 chr13:94029651-94029668 chr13:94029654-94029667
33	CEBPB	chr13:93970848-93971204	K562	blood:	n/a	chr13:93971022-93971033
34	CEBPB	chr13:93984367-93984731	K562	blood:	n/a	n/a
35	CEBPB	chr13:93961965-93963284	K562	blood:	n/a	chr13:93963088-93963099
36	CEBPB	chr13:93973310-93973578	K562	blood:	n/a	n/a
37	CEBPB	chr13:93970789-93971188	K562	blood:	n/a	chr13:93971022-93971033
38	CEBPB	chr13:94029506-94029812	HepG2	liver:	n/a	chr13:94029654-94029665 chr13:94029656-94029667 chr13:94029651-94029668 chr13:94029654-94029667
39	CEBPB	chr13:93970816-93971191	H1-hESC	embryonic stem cell:	n/a	chr13:93971022-93971033
40	CEBPB	chr13:93973209-93973617	K562	blood:	n/a	n/a
41	CEBPB	chr13:93962939-93963272	A549	lung:	n/a	chr13:93963088-93963099
42	CEBPB	chr13:93995536-93996206	K562	blood:	n/a	n/a
43	CEBPB	chr13:93982290-93982481	A549	lung:	n/a	n/a
44	CEBPB	chr13:93970837-93971513	K562	blood:	n/a	chr13:93971022-93971033
45	CEBPB	chr13:93973286-93973594	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr13:94004365-94004467	HepG2	liver:	n/a	chr13:94004416-94004427
47	CEBPB	chr13:93970866-93971176	IMR90	lung:	n/a	chr13:93971022-93971033
48	CEBPB	chr13:93962985-93963206	HepG2	liver:	n/a	chr13:93963088-93963099
49	CEBPB	chr13:94014025-94014435	HepG2	liver:	n/a	chr13:94014303-94014316
50	CEBPB	chr13:93973280-93973547	A549	lung:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:93969707-93969757	Jurkat	blood:	n/a
2	chr13:93990004-93990054	GM12878	blood:	n/a
3	chr13:94013507-94013557	SK-N-SH	brain:	n/a
4	chr13:93979371-93979421	AG09319	gingival:	n/a
5	chr13:93979371-93979421	AG04449	skin:	fetal
6	chr13:93969707-93969757	K562	blood:	n/a
7	chr13:93990004-93990054	NHDF-neo	bronchial:	n/a
8	chr13:93979371-93979421	T-47D	breast:	n/a
9	chr13:94013507-94013557	SK-N-SH_RA	brain:	n/a
10	chr13:93990004-93990054	NB4	blood:	n/a
11	chr13:93990004-93990054	K562	blood:	n/a
12	chr13:93990004-93990054	NT2-D1	testis:	n/a
13	chr13:93969707-93969757	NHBE	bronchial:	n/a
14	chr13:93990004-93990054	AG09319	gingival:	n/a
15	chr13:93969707-93969757	CMK	blood:	n/a
16	chr13:93979371-93979421	HAEpiC	amniotic membrane:	n/a
17	chr13:93979371-93979421	IMR90	lung:	fetal
18	chr13:94013507-94013557	BJ	skin:	n/a
19	chr13:93990004-93990054	SK-N-SH	brain:	n/a
20	chr13:93979371-93979421	HepG2	liver:	n/a
21	chr13:93979371-93979421	U87	brain:	n/a
22	chr13:93979371-93979421	HL-60	blood:	n/a
23	chr13:93990004-93990054	BE2_C	brain:	n/a
24	chr13:93990004-93990054	ProgFib	skin:	n/a
25	chr13:93979371-93979421	HUVEC	blood vessel:	n/a
26	chr13:93969707-93969757	SK-N-MC	brain:	n/a
27	chr13:93979371-93979421	GM06990	blood:	n/a
28	chr13:94013507-94013557	PFSK-1	brain:	n/a
29	chr13:93990004-93990054	HCM	heart:	n/a
30	chr13:93969707-93969757	A549	lung:	n/a
31	chr13:94013507-94013557	PrEC	prostate:	n/a
32	chr13:93979371-93979421	HMEC	breast:	n/a
33	chr13:94013507-94013557	SAEC	small airway:	n/a
34	chr13:93969707-93969757	NB4	blood:	n/a
35	chr13:94013507-94013557	Caco-2	colon:	n/a
36	chr13:94013507-94013557	AG09319	gingival:	n/a
37	chr13:93979371-93979421	ProgFib	skin:	n/a
38	chr13:93969707-93969757	SK-N-SH	brain:	n/a
39	chr13:93979371-93979421	HNPCEpiC	eye:	n/a
40	chr13:94013507-94013557	Hela-S3	cervix:	n/a
41	chr13:94013507-94013557	GM12892	blood:	n/a
42	chr13:93990004-93990054	HepG2	liver:	n/a
43	chr13:94013507-94013557	BE2_C	brain:	n/a
44	chr13:93990004-93990054	SK-N-MC	brain:	n/a
45	chr13:94013507-94013557	HCT-116	colon:	n/a
46	chr13:93990004-93990054	HL-60	blood:	n/a
47	chr13:94013507-94013557	HRE	kidney:	n/a
48	chr13:93969707-93969757	MCF-7	breast:	n/a
49	chr13:93979371-93979421	MCF10A-Er-Src	breast:	n/a
50	chr13:93990004-93990054	GM06990	blood:	n/a

(count:117 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr13:93977966..93980099-chr13:93991360..93994357,2	K562	blood:
2	chr13:94010780..94012995-chr13:108620575..108623194,2	K562	blood:
3	chr13:93960806..93963273-chr13:94011770..94013409,2	K562	blood:
4	chr13:94004779..94008809-chr13:94017437..94020691,3	K562	blood:
5	chr13:94017688..94019371-chr13:94020852..94022869,2	K562	blood:
6	chr13:93965717..93968015-chr13:108517543..108519565,2	K562	blood:
7	chr13:94004123..94006975-chr13:94011670..94013283,2	K562	blood:
8	chr13:93986499..93989486-chr13:94001279..94002915,2	K562	blood:
9	chr13:93948708..93950660-chr13:93986697..93989056,2	K562	blood:
10	chr13:93977629..93980676-chr13:93981025..93983333,3	K562	blood:
11	chr13:93960806..93963273-chr13:94011770..94013409,2	K562	blood:
12	chr13:93988036..93992700-chr13:93993487..93997832,6	K562	blood:
13	chr13:93971946..93973781-chr13:93991313..93994089,2	K562	blood:
14	chr13:93976016..93978454-chr13:94013289..94015025,2	K562	blood:
15	chr13:93982327..93985980-chr9:134148007..134150497,3	K562	blood:
16	chr13:94018136..94020866-chr13:94022567..94024673,2	K562	blood:
17	chr13:93962460..93964812-chr13:93979944..93982073,2	K562	blood:
18	chr13:93969120..93972348-chr13:93976896..93981024,5	K562	blood:
19	chr13:93975407..93977294-chr13:93983328..93985446,2	K562	blood:
20	chr13:94002904..94005207-chr13:94013306..94015512,2	K562	blood:
21	chr13:93987672..93989845-chr13:93991078..93993426,2	K562	blood:
22	chr13:93980175..93982832-chr13:93987646..93990345,3	K562	blood:
23	chr13:93977629..93980676-chr13:93981025..93983333,3	K562	blood:
24	chr13:93976016..93978454-chr13:94013289..94015025,2	K562	blood:
25	chr13:93975713..93977333-chr9:134000453..134002028,2	K562	blood:
26	chr13:93987223..93988872-chr9:134152571..134154570,2	K562	blood:
27	chr13:93963378..93968505-chr13:93974566..93977658,4	K562	blood:
28	chr13:94015507..94017999-chr13:108503926..108506561,2	K562	blood:
29	chr13:93970087..93972348-chr13:93976027..93978960,2	K562	blood:
30	chr13:93987672..93989845-chr13:93991078..93993426,2	K562	blood:
31	chr13:94014516..94016781-chr13:108501023..108503211,2	K562	blood:
32	chr13:93892932..93894807-chr13:94006312..94008534,2	MCF-7	breast:
33	chr13:93963826..93965366-chr13:93969759..93971609,2	K562	blood:
34	chr13:93968945..93970649-chr13:93985808..93988147,2	K562	blood:
35	chr13:93957288..93959129-chr13:93987026..93989631,2	K562	blood:
36	chr13:93971466..93973630-chr13:94008916..94010635,2	K562	blood:
37	chr13:93968945..93970649-chr13:93985808..93988147,2	K562	blood:
38	chr13:94010069..94012294-chr13:94018133..94019897,2	K562	blood:
39	chr13:93031583..93033539-chr13:94000749..94002746,2	K562	blood:
40	chr13:93969120..93972348-chr13:93976896..93981024,5	K562	blood:
41	chr13:93997163..93999865-chr13:94017680..94019331,2	MCF-7	breast:
42	chr13:93963378..93968505-chr13:93974566..93977658,4	K562	blood:
43	chr13:93971014..93972548-chr9:134153245..134155429,2	K562	blood:
44	chr13:94013815..94015574-chr9:134152986..134155025,2	K562	blood:
45	chr13:94011901..94014196-chr13:108499616..108501775,3	K562	blood:
46	chr13:93989647..93991913-chr13:93995033..93997878,2	K562	blood:
47	chr13:93975150..93977138-chr13:93989003..93991236,2	K562	blood:
48	chr13:94004779..94008809-chr13:94017437..94020691,3	K562	blood:
49	chr13:94003388..94006279-chr13:94018446..94020737,2	K562	blood:
50	chr13:93957288..93959129-chr13:93987026..93989631,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000252365	TF binding region
ENSG00000252365	CpG island
ENSG00000183098	chromatin interactions
ENSG00000252365	chromatin interactions
ENSG00000126882	chromatin interactions
ENSG00000204442	chromatin interactions
ENSG00000126883	chromatin interactions

Extended variants
information (count: 2849 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:2849 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2057525	chr13:93957816-93957817	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs190130296	chr13:93957862-93957863	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs551472638	chr13:93957870-93957871	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs527319094	chr13:93957876-93957877	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs375138628	chr13:93957886-93957887	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs140233377	chr13:93957890-93957891	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs74621198	chr13:93957901-93957902	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs183047378	chr13:93957936-93957937	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs149322104	chr13:93957942-93957943	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs569952705	chr13:93958023-93958024	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs529485197	chr13:93958045-93958046	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs72635701	chr13:93958059-93958060	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs566346740	chr13:93958107-93958108	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs527813162	chr13:93958134-93958135	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs187382423	chr13:93958140-93958141	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs558155935	chr13:93958163-93958164	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs192120989	chr13:93958166-93958167	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs74847135	chr13:93958217-93958218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs557481731	chr13:93958362-93958363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs556714547	chr13:93958412-93958413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs573668643	chr13:93958428-93958429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs2057524	chr13:93958432-93958433	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs374260411	chr13:93958463-93958464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs555410979	chr13:93958513-93958514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs572273248	chr13:93958516-93958517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs148054645	chr13:93958522-93958523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs141771949	chr13:93958532-93958533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs577206644	chr13:93958551-93958552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs553257073	chr13:93958574-93958575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs147151063	chr13:93958615-93958616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs184086940	chr13:93958651-93958652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs529496500	chr13:93958656-93958657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs549519684	chr13:93958662-93958663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs7325380	chr13:93958667-93958668	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs201161637	chr13:93958738-93958739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs577720777	chr13:93958743-93958744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs59971455	chr13:93958747-93958748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs188971953	chr13:93958753-93958754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs551808543	chr13:93958810-93958811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs192463279	chr13:93958898-93958899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs545196155	chr13:93958916-93958917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs537439798	chr13:93958941-93958942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs184314428	chr13:93958944-93958945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs4283093	chr13:93958955-93958956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs575684412	chr13:93958968-93958969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs188639703	chr13:93958987-93958988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs555513483	chr13:93959046-93959047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs572256712	chr13:93959134-93959135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs534637482	chr13:93959139-93959140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs557612140	chr13:93959165-93959166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
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
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Metanephric adenoma	20802469	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Mantle cell lymphoma	19690137	CNVD
Rhabdomyosarcoma	17210683	CNVD
Breast cancer	21364760	CNVD
Medulloblastoma	19270706	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	19651601	CNVD
Effusion lymphoma	18079361	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:357 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:93943600-93962200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr13:93952400-93965000	Weak transcription	Fetal Kidney	kidney
3	chr13:93955600-93958200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr13:93956600-93958000	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr13:93956600-93958400	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr13:93957000-93958000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr13:93957200-93958200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr13:93957400-93958000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr13:93957400-93958200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr13:93957400-93962000	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr13:93957600-93958000	Enhancers	NHLF	lung
12	chr13:93957600-93958200	Active TSS	Pancreatic Islets	Pancreatic Islet
13	chr13:93957600-93959200	Enhancers	Fetal Lung	lung
14	chr13:93957600-93960000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr13:93957600-93960000	Enhancers	Osteobl	bone
16	chr13:93957600-93968400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr13:93957800-93958000	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr13:93957800-93958200	Enhancers	Fetal Brain Female	brain
19	chr13:93957800-93959200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr13:93957800-93959400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr13:93957800-93960000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr13:93957800-93960000	Enhancers	Muscle Satellite Cultured Cells	--
23	chr13:93957800-93962000	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr13:93957800-93962200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr13:93958000-93958200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr13:93958000-93959000	Weak transcription	NHLF	lung
27	chr13:93958000-93960000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr13:93958000-93960200	Enhancers	HSMM	muscle
29	chr13:93958000-93960200	Enhancers	NH-A	brain
30	chr13:93958000-93962200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr13:93958200-93958600	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr13:93958200-93958800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr13:93958200-93959200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr13:93958200-93959600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr13:93958200-93960600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr13:93958200-93962400	Weak transcription	Fetal Brain Female	brain
37	chr13:93958200-93969800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr13:93958600-93962200	Weak transcription	Pancreatic Islets	Pancreatic Islet
39	chr13:93958800-93962000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr13:93959000-93959600	Enhancers	NHLF	lung
41	chr13:93959200-93961800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr13:93959400-93959600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr13:93959600-93960200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr13:93959600-93962000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr13:93960000-93962000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr13:93960000-93962000	Weak transcription	Osteobl	bone
47	chr13:93960200-93960400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr13:93960400-93962200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr13:93960600-93960800	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr13:93960600-93961000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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