Variant report

Variant	nsv1040320
Chromosome Location	chr13:96573646-96790859
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2064)
CpG islands
(count:2629)
Chromatin interactive
region (count:57)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2064 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:96705446-96705959	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:96710321-96710493	K562	blood:	n/a	n/a
3	ARID3A	chr13:96632838-96633002	K562	blood:	n/a	n/a
4	ARID3A	chr13:96624887-96625205	HepG2	liver:	n/a	n/a
5	ARID3A	chr13:96673132-96673488	HepG2	liver:	n/a	n/a
6	ATF1	chr13:96704862-96705264	K562	blood:	n/a	n/a
7	ATF1	chr13:96608880-96609099	K562	blood:	n/a	n/a
8	ATF2	chr13:96704875-96705211	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr13:96704708-96705377	GM12878	blood:	n/a	n/a
10	ATF2	chr13:96705443-96705765	GM12878	blood:	n/a	n/a
11	ATF2	chr13:96704761-96705830	GM12878	blood:	n/a	n/a
12	ATF2	chr13:96704816-96705230	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr13:96705437-96705791	A549	lung:	n/a	n/a
14	ATF3	chr13:96608777-96609107	K562	blood:	n/a	n/a
15	BACH1	chr13:96705010-96706104	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr13:96761376-96761557	K562	blood:	n/a	n/a
17	BACH1	chr13:96602381-96602390	K562	blood:	n/a	n/a
18	BACH1	chr13:96761604-96761614	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr13:96705515-96705712	K562	blood:	n/a	n/a
20	BCL11A	chr13:96606653-96606944	H1-hESC	embryonic stem cell:	n/a	n/a
21	BHLHE40	chr13:96705452-96705826	K562	blood:	n/a	n/a
22	BHLHE40	chr13:96673960-96673961	GM12878	blood:	n/a	n/a
23	BHLHE40	chr13:96705078-96705207	K562	blood:	n/a	n/a
24	BHLHE40	chr13:96632919-96632932	K562	blood:	n/a	n/a
25	BHLHE40	chr13:96704992-96706021	GM12878	blood:	n/a	n/a
26	BRCA1	chr13:96705537-96706241	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr13:96705530-96705786	GM12878	blood:	n/a	n/a
28	BRCA1	chr13:96705964-96706299	H1-hESC	embryonic stem cell:	n/a	n/a
29	BRCA1	chr13:96704813-96705240	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr13:96705801-96705964	HepG2	liver:	n/a	n/a
31	BRCA1	chr13:96608842-96609006	Hela-S3	cervix:	n/a	n/a
32	CBX3	chr13:96698869-96699225	K562	blood:	n/a	n/a
33	CBX3	chr13:96760389-96760640	K562	blood:	n/a	n/a
34	CBX3	chr13:96705479-96705930	K562	blood:	n/a	n/a
35	CBX3	chr13:96710079-96710563	HCT-116	colon:	n/a	n/a
36	CBX3	chr13:96612468-96612822	K562	blood:	n/a	n/a
37	CBX3	chr13:96760331-96760577	K562	blood:	n/a	n/a
38	CCNT2	chr13:96608827-96609027	K562	blood:	n/a	n/a
39	CCNT2	chr13:96704993-96706008	K562	blood:	n/a	n/a
40	CCNT2	chr13:96589983-96590394	K562	blood:	n/a	n/a
41	CEBPB	chr13:96706948-96707142	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr13:96626133-96626333	HepG2	liver:	n/a	chr13:96626229-96626240
43	CEBPB	chr13:96704865-96705219	HepG2	liver:	n/a	n/a
44	CEBPB	chr13:96704747-96705276	IMR90	lung:	n/a	n/a
45	CEBPB	chr13:96769285-96769451	A549	lung:	n/a	chr13:96769343-96769354 chr13:96769343-96769356
46	CEBPB	chr13:96576859-96577151	A549	lung:	n/a	n/a
47	CEBPB	chr13:96743490-96743639	HepG2	liver:	n/a	n/a
48	CEBPB	chr13:96673325-96673461	HepG2	liver:	n/a	n/a
49	CEBPB	chr13:96611029-96611416	MCF-7	breast:	n/a	chr13:96611218-96611229
50	CEBPB	chr13:96704922-96705192	H1-hESC	embryonic stem cell:	n/a	n/a

(count:2629 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:96640017-96640067	GM19239	blood:	n/a
2	chr13:96743492-96743542	HUVEC	blood vessel:	n/a
3	chr13:96706045-96706095	GM12892	blood:	n/a
4	chr13:96705123-96705173	AG04449	skin:	fetal
5	chr13:96583885-96583935	HRPEpiC	eye:	n/a
6	chr13:96583885-96583935	SAEC	small airway:	n/a
7	chr13:96640017-96640067	GM19239	blood:	n/a
8	chr13:96743492-96743542	HUVEC	blood vessel:	n/a
9	chr13:96706045-96706095	GM12892	blood:	n/a
10	chr13:96705123-96705173	AG04449	skin:	fetal
11	chr13:96583885-96583935	HRPEpiC	eye:	n/a
12	chr13:96583885-96583935	SAEC	small airway:	n/a
13	chr13:96705123-96705173	HEEpiC	esophagus:	n/a
14	chr13:96742056-96742106	NT2-D1	testis:	n/a
15	chr13:96707199-96707249	RPTEC	kidney:	n/a
16	chr13:96583970-96584020	H1-hESC	embryonic stem cell:	embryo
17	chr13:96743170-96743220	SAEC	small airway:	n/a
18	chr13:96581176-96581226	IMR90	lung:	fetal
19	chr13:96742421-96742471	T-47D	breast:	n/a
20	chr13:96738685-96738735	HepG2	liver:	n/a
21	chr13:96705929-96705979	Hela-S3	cervix:	n/a
22	chr13:96742413-96742463	IMR90	lung:	fetal
23	chr13:96624108-96624158	HEK293	kidney:	embryo
24	chr13:96743895-96743945	CMK	blood:	n/a
25	chr13:96672440-96672490	HRE	kidney:	n/a
26	chr13:96705786-96705836	Hela-S3	cervix:	n/a
27	chr13:96738685-96738735	GM06990	blood:	n/a
28	chr13:96705712-96705762	NT2-D1	testis:	n/a
29	chr13:96705929-96705979	HMEC	breast:	n/a
30	chr13:96706773-96706823	HUVEC	blood vessel:	n/a
31	chr13:96583885-96583935	HRE	kidney:	n/a
32	chr13:96743652-96743702	HRPEpiC	eye:	n/a
33	chr13:96743110-96743160	ProgFib	skin:	n/a
34	chr13:96705395-96705445	GM19239	blood:	n/a
35	chr13:96743492-96743542	GM06990	blood:	n/a
36	chr13:96672440-96672490	HL-60	blood:	n/a
37	chr13:96583885-96583935	SK-N-SH_RA	brain:	n/a
38	chr13:96651633-96651683	SK-N-SH_RA	brain:	n/a
39	chr13:96746650-96746700	ProgFib	skin:	n/a
40	chr13:96707199-96707249	GM12891	blood:	n/a
41	chr13:96744289-96744339	HCPEpiC	choroid plexus:	n/a
42	chr13:96651633-96651683	HMEC	breast:	n/a
43	chr13:96705908-96705958	NHDF-neo	bronchial:	n/a
44	chr13:96743492-96743542	SKMC	muscle:	n/a
45	chr13:96651633-96651683	HCM	heart:	n/a
46	chr13:96583751-96583801	BJ	skin:	n/a
47	chr13:96742421-96742471	HRE	kidney:	n/a
48	chr13:96706045-96706095	ECC-1	luminal epithelium:	n/a
49	chr13:96743170-96743220	BJ	skin:	n/a
50	chr13:96583885-96583935	GM06990	blood:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr13:96704503..96706630-chr13:96744009..96746380,2	MCF-7	breast:
2	chr13:96638885..96641405-chr13:96646337..96648047,2	K562	blood:
3	chr13:96705694..96707387-chr13:96740919..96743720,3	MCF-7	breast:
4	chr13:96642387..96644158-chr13:96654027..96655529,2	K562	blood:
5	chr13:96645821..96648157-chr13:96652865..96656450,3	K562	blood:
6	chr13:96672084..96672616-chr13:97469396..97470262,2	MCF-7	breast:
7	chr13:96705422..96706004-chr16:74337665..74338558,2	NB4	blood:
8	chr1:16970980..16971545-chr13:96704941..96705920,2	HCT-116	colon:
9	chr13:96623472..96625702-chr13:96633366..96635270,2	K562	blood:
10	chr13:96705694..96707387-chr13:96740919..96743720,3	MCF-7	breast:
11	chr13:96741913..96744664-chr13:96755780..96757951,2	MCF-7	breast:
12	chr13:96746204..96748627-chr13:96759326..96761567,2	K562	blood:
13	chr13:96705368..96706022-chr3:169482389..169482964,2	Hela-S3	cervix:
14	chr13:96742136..96745093-chr13:96745710..96749821,3	MCF-7	breast:
15	chr13:96705350..96706193-chr15:72520336..72521147,2	Hela-S3	cervix:
16	chr13:96705303..96706107-chr17:73775369..73775878,2	Hela-S3	cervix:
17	chr13:96666484..96668467-chr13:96672707..96674381,2	K562	blood:
18	chr13:96666484..96668467-chr13:96672707..96674381,2	K562	blood:
19	chr13:96632367..96634450-chr13:96637310..96639783,2	K562	blood:
20	chr13:96691444..96693305-chr13:96704321..96706823,2	MCF-7	breast:
21	chr13:96704367..96706595-chr13:96710468..96713623,3	MCF-7	breast:
22	chr13:96642387..96644158-chr13:96654027..96655529,2	K562	blood:
23	chr13:96676019..96678407-chr13:96704479..96707236,2	K562	blood:
24	chr13:96711531..96713496-chr13:96738453..96740111,2	MCF-7	breast:
25	chr13:96704058..96705666-chr13:96708973..96710836,2	K562	blood:
26	chr13:96632367..96634292-chr13:96635472..96638810,3	K562	blood:
27	chr13:96676638..96679476-chr13:96757318..96759037,2	MCF-7	breast:
28	chr13:96632367..96634292-chr13:96635472..96638810,3	K562	blood:
29	chr13:96623472..96625702-chr13:96633366..96635270,2	K562	blood:
30	chr13:96681222..96683044-chr13:96705277..96706981,2	MCF-7	breast:
31	chr13:96704511..96706638-chr13:96708531..96711999,4	MCF-7	breast:
32	chr1:236958210..236959010-chr13:96705467..96706161,2	Hela-S3	cervix:
33	chr13:96732215..96734781-chr13:96740954..96743608,2	MCF-7	breast:
34	chr13:96705761..96707656-chr13:96724280..96725801,2	MCF-7	breast:
35	chr13:96638885..96641405-chr13:96646337..96648047,2	K562	blood:
36	chr13:96725464..96726444-chr6:144512474..144513042,2	MCF-7	breast:
37	chr13:96575800..96578505-chr13:96580994..96583120,2	MCF-7	breast:
38	chr13:96646657..96649376-chr13:96653623..96656450,2	K562	blood:
39	chr13:96645463..96647410-chr13:96650803..96652749,2	K562	blood:
40	chr13:96575800..96578505-chr13:96580994..96583120,2	MCF-7	breast:
41	chr13:96703695..96705658-chr13:96724041..96726709,2	K562	blood:
42	chr13:96654618..96657100-chr13:96704216..96707114,2	MCF-7	breast:
43	chr13:96646657..96649376-chr13:96653623..96656450,2	K562	blood:
44	chr13:96676638..96679476-chr13:96757318..96759037,2	MCF-7	breast:
45	chr13:96757306..96759865-chr13:96763569..96765220,2	MCF-7	breast:
46	chr13:96645821..96648157-chr13:96652865..96656450,3	K562	blood:
47	chr13:96672513..96673053-chr13:97619391..97620229,2	K562	blood:
48	chr13:96632367..96634450-chr13:96637310..96639783,2	K562	blood:
49	chr13:96586030..96588095-chr13:96594403..96597240,2	MCF-7	breast:
50	chr13:96746204..96748627-chr13:96759326..96761567,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HS6ST3-1	chr13:96675417-96675649	expReg_chr13_3428_+
2	lnc-UGGT2-1	chr13:96737150-96737367	NONHSAT034782
3	lnc-UGGT2-1	chr13:96737151-96737367	XLOC_010699
4	lnc-DZIP1-9	chr13:96622724-96623119	NONHSAT034781
5	lnc-UGGT2-1	chr13:96739248-96739285	NONHSAT034782
6	lnc-DZIP1-9	chr13:96629582-96629877	NONHSAT034781
7	lnc-UGGT2-1	chr13:96739249-96739285	XLOC_010699

No data

Variant related genes	Relation type
UGGT2	TF binding region
HS6ST3	TF binding region
UGGT2	CpG island
HS6ST3	CpG island
ENSG00000270141	chromatin interactions
ENSG00000103035	chromatin interactions
ENSG00000215908	chromatin interactions
ENSG00000185352	chromatin interactions
ENSG00000102595	chromatin interactions
ENSG00000116984	chromatin interactions
ENSG00000132475	chromatin interactions
ENSG00000067225	chromatin interactions
ATP2A2	miRNA target sites
ATP13A3	miRNA target sites

Extended variants
information (count: 7548 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:7548 , 50 per page) page: 1 2 3 4 5 6 7 ... 151

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375498074	chr13:96573689-96573690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs556872622	chr13:96573714-96573715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs199859688	chr13:96573738-96573739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs573591481	chr13:96573764-96573765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs542463193	chr13:96573820-96573821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs185018620	chr13:96573834-96573835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs572515969	chr13:96573861-96573862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs143303445	chr13:96573881-96573882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs564580798	chr13:96574008-96574009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs78230300	chr13:96574018-96574019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs569647989	chr13:96574043-96574044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs189775888	chr13:96574080-96574081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs564017243	chr13:96574112-96574113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs529566466	chr13:96574123-96574124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs146702095	chr13:96574134-96574135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs369290910	chr13:96574152-96574153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs74988177	chr13:96574167-96574168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs566108133	chr13:96574195-96574196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs534739347	chr13:96574197-96574198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs535568106	chr13:96574277-96574278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs551218500	chr13:96574282-96574283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs373747475	chr13:96574301-96574302	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs571306992	chr13:96574322-96574323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs536692001	chr13:96574332-96574333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs369794928	chr13:96574334-96574335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs143452079	chr13:96574375-96574376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs77890700	chr13:96574381-96574382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs536104056	chr13:96574413-96574414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs140907850	chr13:96574475-96574476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs572979635	chr13:96574478-96574479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs183069798	chr13:96574498-96574499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs564461935	chr13:96574536-96574537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs578047322	chr13:96574574-96574575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs150161631	chr13:96574583-96574584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs78810542	chr13:96574588-96574589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs138863613	chr13:96574604-96574605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs371364850	chr13:96574606-96574607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529629533	chr13:96574642-96574643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549672259	chr13:96574683-96574684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs77115374	chr13:96574686-96574687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs528716622	chr13:96574698-96574699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs35233965	chr13:96574701-96574702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs558069005	chr13:96574710-96574711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs189088417	chr13:96574788-96574789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571304233	chr13:96574796-96574797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs202009378	chr13:96574900-96574901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs143271262	chr13:96574902-96574903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs536704222	chr13:96574903-96574904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs75865855	chr13:96574904-96574905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs77921736	chr13:96574906-96574907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Rhabdomyosarcoma	17210683	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Developmental delay	21147756	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
Acute myeloid leukemia	19651601	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Burkitt''s lymphoma	20823134	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2407 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:96495000-96590800	Weak transcription	Rectal Smooth Muscle	rectum
2	chr13:96503400-96580800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr13:96523200-96581800	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr13:96536200-96587200	Weak transcription	Stomach Smooth Muscle	stomach
5	chr13:96542400-96576800	Weak transcription	HSMMtube	muscle
6	chr13:96542400-96581600	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr13:96543000-96581600	Weak transcription	Fetal Lung	lung
8	chr13:96543000-96581800	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr13:96543000-96586800	Weak transcription	Brain Hippocampus Middle	brain
10	chr13:96543400-96576600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr13:96544600-96576800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr13:96549400-96586400	Weak transcription	Hela-S3	cervix
13	chr13:96558400-96586600	Weak transcription	Right Ventricle	heart
14	chr13:96558600-96579000	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr13:96559600-96576600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr13:96559600-96576800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr13:96559600-96580800	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr13:96559600-96583000	Weak transcription	Pancreas	Pancrea
19	chr13:96559600-96586400	Weak transcription	A549	lung
20	chr13:96559800-96580600	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr13:96559800-96580600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr13:96559800-96583400	Weak transcription	Esophagus	oesophagus
23	chr13:96559800-96588600	Weak transcription	Gastric	stomach
24	chr13:96560000-96581400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr13:96560000-96581600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr13:96560200-96581000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr13:96562600-96580600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr13:96566200-96576800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr13:96566400-96576200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr13:96566400-96581600	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr13:96566800-96587000	Weak transcription	Colon Smooth Muscle	Colon
32	chr13:96567600-96575400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr13:96567600-96581600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr13:96568200-96576600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr13:96568200-96576800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr13:96568200-96578400	Weak transcription	Fetal Kidney	kidney
37	chr13:96568400-96576400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr13:96568400-96577400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr13:96568400-96579600	Weak transcription	GM12878-XiMat	blood
40	chr13:96568400-96580600	Weak transcription	Fetal Intestine Large	intestine
41	chr13:96568400-96581600	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr13:96568600-96576800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr13:96568600-96576800	Weak transcription	Fetal Muscle Leg	muscle
44	chr13:96568600-96577000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr13:96568600-96577400	Weak transcription	Adipose Nuclei	Adipose
46	chr13:96568600-96580600	Weak transcription	Fetal Muscle Trunk	muscle
47	chr13:96568600-96580600	Weak transcription	Fetal Stomach	stomach
48	chr13:96568600-96580800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr13:96568600-96581600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr13:96568600-96582000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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