Variant report

Variant	nsv832689
Chromosome Location	chr13:95759073-95921308
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2627)
CpG islands
(count:611)
Chromatin interactive
region (count:121)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2627 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:95895419-95895845	K562	blood:	n/a	n/a
2	ARID3A	chr13:95844032-95844221	K562	blood:	n/a	n/a
3	ARID3A	chr13:95920014-95920195	HepG2	liver:	n/a	n/a
4	ARID3A	chr13:95775923-95776469	HepG2	liver:	n/a	n/a
5	ARID3A	chr13:95906602-95906921	K562	blood:	n/a	n/a
6	ARID3A	chr13:95919931-95920159	K562	blood:	n/a	n/a
7	ARID3A	chr13:95841672-95841952	K562	blood:	n/a	n/a
8	ARID3A	chr13:95910897-95911268	HepG2	liver:	n/a	n/a
9	ARID3A	chr13:95900202-95900486	K562	blood:	n/a	n/a
10	ARID3A	chr13:95854451-95854755	K562	blood:	n/a	n/a
11	ARID3A	chr13:95773320-95773616	HepG2	liver:	n/a	n/a
12	ARID3A	chr13:95812705-95813304	HepG2	liver:	n/a	chr13:95812897-95812913
13	ARID3A	chr13:95920491-95920517	K562	blood:	n/a	n/a
14	ARID3A	chr13:95841626-95841953	HepG2	liver:	n/a	n/a
15	ARID3A	chr13:95861449-95861751	K562	blood:	n/a	n/a
16	ATF1	chr13:95900089-95900504	K562	blood:	n/a	n/a
17	ATF1	chr13:95895413-95895960	K562	blood:	n/a	n/a
18	ATF1	chr13:95854370-95854781	K562	blood:	n/a	n/a
19	ATF1	chr13:95920455-95920690	K562	blood:	n/a	n/a
20	ATF2	chr13:95903741-95904329	GM12878	blood:	n/a	n/a
21	ATF2	chr13:95911930-95913003	GM12878	blood:	n/a	n/a
22	ATF2	chr13:95915014-95915440	GM12878	blood:	n/a	n/a
23	ATF2	chr13:95886487-95887002	GM12878	blood:	n/a	n/a
24	ATF2	chr13:95879547-95880052	GM12878	blood:	n/a	n/a
25	ATF2	chr13:95913116-95913879	GM12878	blood:	n/a	n/a
26	ATF2	chr13:95860013-95860633	GM12878	blood:	n/a	n/a
27	ATF2	chr13:95903692-95904322	GM12878	blood:	n/a	n/a
28	ATF2	chr13:95911992-95913092	GM12878	blood:	n/a	n/a
29	ATF2	chr13:95878779-95880120	GM12878	blood:	n/a	n/a
30	ATF2	chr13:95891968-95892606	GM12878	blood:	n/a	n/a
31	ATF3	chr13:95910861-95911290	A549	lung:	n/a	n/a
32	ATF3	chr13:95780228-95780994	A549	lung:	n/a	n/a
33	ATF3	chr13:95854346-95854772	K562	blood:	n/a	n/a
34	ATF3	chr13:95908294-95908927	HCT-116	colon:	n/a	n/a
35	ATF3	chr13:95812773-95813266	A549	lung:	n/a	n/a
36	ATF3	chr13:95908314-95908842	A549	lung:	n/a	n/a
37	ATF3	chr13:95919821-95920194	A549	lung:	n/a	n/a
38	ATF3	chr13:95908362-95908787	A549	lung:	n/a	n/a
39	ATF3	chr13:95919829-95920275	A549	lung:	n/a	n/a
40	ATF3	chr13:95912121-95912566	GM12878	blood:	n/a	n/a
41	ATF3	chr13:95912222-95912437	GM12878	blood:	n/a	n/a
42	BACH1	chr13:95844132-95844362	H1-hESC	embryonic stem cell:	n/a	n/a
43	BACH1	chr13:95788136-95788220	K562	blood:	n/a	n/a
44	BACH1	chr13:95880476-95880612	K562	blood:	n/a	n/a
45	BATF	chr13:95912417-95912798	GM12878	blood:	n/a	n/a
46	BATF	chr13:95903876-95904230	GM12878	blood:	n/a	n/a
47	BATF	chr13:95903925-95904207	GM12878	blood:	n/a	n/a
48	BATF	chr13:95789450-95789658	GM12878	blood:	n/a	n/a
49	BATF	chr13:95908387-95908685	GM12878	blood:	n/a	chr13:95908534-95908545
50	BATF	chr13:95836627-95836939	GM12878	blood:	n/a	chr13:95836760-95836771

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:95907745-95907795	PFSK-1	brain:	n/a
2	chr13:95907745-95907795	PFSK-1	brain:	n/a
3	chr13:95811931-95811981	HCT-116	colon:	n/a
4	chr13:95811931-95811981	HUVEC	blood vessel:	n/a
5	chr13:95844361-95844411	HRPEpiC	eye:	n/a
6	chr13:95846842-95846892	Hepatocyte	liver:	n/a
7	chr13:95826930-95826980	GM06990	blood:	n/a
8	chr13:95811931-95811981	HPAEpiC	pulmonary alveolar:	n/a
9	chr13:95907745-95907795	SKMC	muscle:	n/a
10	chr13:95834131-95834181	RPTEC	kidney:	n/a
11	chr13:95844361-95844411	SK-N-MC	brain:	n/a
12	chr13:95834131-95834181	GM06990	blood:	n/a
13	chr13:95844361-95844411	PFSK-1	brain:	n/a
14	chr13:95826994-95827044	NH-A	brain:	n/a
15	chr13:95844361-95844411	AG04449	skin:	fetal
16	chr13:95846842-95846892	HEK293	kidney:	embryo
17	chr13:95920671-95920721	AG09309	skin:	n/a
18	chr13:95920671-95920721	HEEpiC	esophagus:	n/a
19	chr13:95846842-95846892	IMR90	lung:	fetal
20	chr13:95844361-95844411	HUVEC	blood vessel:	n/a
21	chr13:95811931-95811981	Caco-2	colon:	n/a
22	chr13:95834131-95834181	CMK	blood:	n/a
23	chr13:95844361-95844411	HEEpiC	esophagus:	n/a
24	chr13:95920671-95920721	U87	brain:	n/a
25	chr13:95907745-95907795	HAEpiC	amniotic membrane:	n/a
26	chr13:95826930-95826980	AG04450	lung:	fetal
27	chr13:95907745-95907795	HNPCEpiC	eye:	n/a
28	chr13:95901718-95901768	HNPCEpiC	eye:	n/a
29	chr13:95834131-95834181	AG09309	skin:	n/a
30	chr13:95827029-95827079	HUVEC	blood vessel:	n/a
31	chr13:95811931-95811981	LNCaP	prostate:	n/a
32	chr13:95834131-95834181	LNCaP	prostate:	n/a
33	chr13:95907745-95907795	PrEC	prostate:	n/a
34	chr13:95901718-95901768	U87	brain:	n/a
35	chr13:95811931-95811981	AG04450	lung:	fetal
36	chr13:95846842-95846892	PANC-1	pancreas:	n/a
37	chr13:95907745-95907795	HCF	heart:	n/a
38	chr13:95846842-95846892	AoSMC	blood vessel:	n/a
39	chr13:95827029-95827079	NT2-D1	testis:	n/a
40	chr13:95920671-95920721	HEK293	kidney:	embryo
41	chr13:95901718-95901768	GM12878	blood:	n/a
42	chr13:95834131-95834181	HMEC	breast:	n/a
43	chr13:95844361-95844411	AG10803	skin:	n/a
44	chr13:95920671-95920721	PrEC	prostate:	n/a
45	chr13:95811931-95811981	BE2_C	brain:	n/a
46	chr13:95920671-95920721	MCF-7	breast:	n/a
47	chr13:95907745-95907795	Jurkat	blood:	n/a
48	chr13:95834131-95834181	SK-N-MC	brain:	n/a
49	chr13:95846842-95846892	MCF10A-Er-Src	breast:	n/a
50	chr13:95844361-95844411	HCT-116	colon:	n/a

(count:121 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr13:95752245..95755943-chr13:95774951..95780273,6	MCF-7	breast:
2	chr13:95752693..95755831-chr13:95780565..95782684,3	MCF-7	breast:
3	chr13:95766396..95768415-chr13:95805096..95807111,2	MCF-7	breast:
4	chr13:95858681..95860676-chr13:95871438..95873483,2	K562	blood:
5	chr13:95751490..95755868-chr13:95765298..95769920,8	MCF-7	breast:
6	chr13:95765198..95767036-chr13:95776278..95779037,2	MCF-7	breast:
7	chr13:95771772..95773594-chr13:95805832..95808411,2	MCF-7	breast:
8	chr13:95827296..95830102-chr13:95830426..95833781,3	K562	blood:
9	chr13:95911255..95914596-chr13:95915357..95918944,4	K562	blood:
10	chr13:95767278..95770224-chr13:95779723..95782766,3	MCF-7	breast:
11	chr13:95881851..95884038-chr13:95887592..95891206,3	K562	blood:
12	chr13:95863328..95866133-chr13:95869098..95871173,2	K562	blood:
13	chr13:95751186..95754744-chr13:95765427..95767632,4	MCF-7	breast:
14	chr13:95753163..95755993-chr13:95781109..95783183,3	MCF-7	breast:
15	chr13:95858681..95860676-chr13:95871438..95873483,2	K562	blood:
16	chr13:95912252..95914596-chr13:95915357..95918104,2	K562	blood:
17	chr13:95889668..95892228-chr13:95954506..95956697,2	K562	blood:
18	chr13:95775918..95777949-chr13:95804692..95806351,2	MCF-7	breast:
19	chr13:95757108..95759848-chr13:95767830..95770575,2	K562	blood:
20	chr13:95763899..95767263-chr13:95780210..95781935,3	MCF-7	breast:
21	chr13:95881832..95883914-chr13:95893087..95895290,2	K562	blood:
22	chr13:95765198..95767036-chr13:95776278..95779037,2	MCF-7	breast:
23	chr13:95889610..95892047-chr13:95952813..95954487,2	K562	blood:
24	chr13:95898930..95900924-chr13:95902230..95904877,2	K562	blood:
25	chr13:95880516..95882106-chr13:95884068..95886065,2	K562	blood:
26	chr13:95890021..95893385-chr13:95895054..95897743,4	K562	blood:
27	chr13:95763899..95767263-chr13:95780210..95781935,3	MCF-7	breast:
28	chr13:95782636..95784986-chr13:95795437..95796972,2	MCF-7	breast:
29	chr13:95753710..95755346-chr13:95758126..95760689,2	MCF-7	breast:
30	chr13:95783276..95785945-chr13:95785951..95788414,2	MCF-7	breast:
31	chr13:95807500..95810294-chr13:96058766..96060692,2	MCF-7	breast:
32	chr13:95843651..95844564-chr13:96056296..96057006,3	MCF-7	breast:
33	chr13:95779479..95782281-chr13:95805249..95807826,2	MCF-7	breast:
34	chr13:95875072..95877586-chr13:95879150..95881186,2	K562	blood:
35	chr13:95881832..95883914-chr13:95893087..95895290,2	K562	blood:
36	chr13:95863328..95866133-chr13:95869098..95871173,2	K562	blood:
37	chr13:95771772..95773594-chr13:95805832..95808411,2	MCF-7	breast:
38	chr13:95872874..95874567-chr13:95880822..95883621,2	K562	blood:
39	chr13:95773275..95777718-chr13:95779226..95784336,7	MCF-7	breast:
40	chr13:95752750..95754704-chr13:95772151..95774652,2	MCF-7	breast:
41	chr13:95782617..95784261-chr13:95786018..95787574,3	K562	blood:
42	chr13:95272320..95273164-chr13:95808439..95809049,2	MCF-7	breast:
43	chr13:95361893..95364519-chr13:95778634..95780154,2	MCF-7	breast:
44	chr13:95843758..95844705-chr13:96056220..96057135,5	MCF-7	breast:
45	chr13:95875072..95877586-chr13:95879150..95881186,2	K562	blood:
46	chr13:95767278..95770224-chr13:95779723..95782766,3	MCF-7	breast:
47	chr13:95841692..95842231-chr13:96032699..96033435,2	MCF-7	breast:
48	chr13:95843632..95844184-chr2:220506969..220507827,2	MCF-7	breast:
49	chr13:95906835..95908604-chr13:95908820..95911598,2	K562	blood:
50	chr13:95775051..95777791-chr13:95778708..95781627,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SOX21-8	chr13:95773454-95773862	NONHSAT034752

No data

Variant related genes	Relation type
ENSG00000238463	TF binding region
ENSG00000238463	CpG island
ENSG00000125257	chromatin interactions
ENSG00000238463	chromatin interactions
ENSG00000227640	chromatin interactions
ENSG00000125285	chromatin interactions

Extended variants
information (count: 6617 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:6617 , 50 per page) page: 1 2 3 4 5 6 7 ... 133

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566206319	chr13:95759142-95759143	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs143921382	chr13:95759175-95759176	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs548758715	chr13:95759185-95759186	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs143307090	chr13:95759188-95759189	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs201998710	chr13:95759190-95759191	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs529848670	chr13:95759267-95759268	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs11616490	chr13:95759363-95759364	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs370025059	chr13:95759403-95759404	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs375534202	chr13:95759404-95759405	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs199641651	chr13:95759425-95759426	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs141437502	chr13:95759459-95759460	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs554567779	chr13:95759460-95759461	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs190302836	chr13:95759472-95759473	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs536635101	chr13:95759487-95759488	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs373222835	chr13:95759533-95759534	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs553532753	chr13:95759542-95759543	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs573397398	chr13:95759567-95759568	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs558108742	chr13:95759633-95759634	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs369864416	chr13:95759638-95759639	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs559116721	chr13:95759666-95759667	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs575745740	chr13:95759682-95759683	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs577929639	chr13:95759710-95759711	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs182572784	chr13:95759721-95759722	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs544930190	chr13:95759731-95759732	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs543425810	chr13:95759761-95759762	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs561405722	chr13:95759842-95759843	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs114891233	chr13:95759852-95759853	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs539862204	chr13:95759950-95759951	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs1209126	chr13:95759978-95759979	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs1189432	chr13:95759987-95759988	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs532084685	chr13:95759997-95759998	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs551806751	chr13:95760084-95760085	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs376642113	chr13:95760093-95760094	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs569082869	chr13:95760097-95760098	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs1751060	chr13:95760109-95760110	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs143035479	chr13:95760136-95760137	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs372380013	chr13:95760137-95760138	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs146128589	chr13:95760171-95760172	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs140148523	chr13:95760179-95760180	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs561777052	chr13:95760180-95760181	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs566832344	chr13:95760193-95760194	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs539182442	chr13:95760225-95760226	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs375723731	chr13:95760293-95760294	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs558772547	chr13:95760350-95760351	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs149819828	chr13:95760376-95760377	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs538032349	chr13:95760381-95760382	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs555115406	chr13:95760385-95760386	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs370431037	chr13:95760418-95760419	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs574807105	chr13:95760612-95760613	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs143979927	chr13:95760616-95760617	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Intellectual disability	22102821	CNVD

Chromatin state (count:2607 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:95723800-95760000	Weak transcription	Colon Smooth Muscle	Colon
2	chr13:95724000-95760600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr13:95727000-95791600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr13:95727000-95812000	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr13:95727600-95761000	Weak transcription	K562	blood
6	chr13:95727800-95767800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr13:95728400-95778800	Weak transcription	Ovary	ovary
8	chr13:95728600-95776000	Weak transcription	Gastric	stomach
9	chr13:95731200-95791600	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr13:95740600-95772200	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr13:95740800-95791200	Weak transcription	NHLF	lung
12	chr13:95741400-95763400	Weak transcription	Left Ventricle	heart
13	chr13:95741600-95772600	Weak transcription	Primary hematopoietic stem cells	blood
14	chr13:95744200-95765200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr13:95749600-95761000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr13:95750400-95812400	Weak transcription	Duodenum Mucosa	Duodenum
17	chr13:95750400-95815400	Weak transcription	Fetal Intestine Large	intestine
18	chr13:95751000-95793400	Weak transcription	Fetal Kidney	kidney
19	chr13:95751400-95777600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr13:95751600-95795600	Weak transcription	Small Intestine	intestine
21	chr13:95752000-95789000	Weak transcription	Aorta	Aorta
22	chr13:95752200-95760600	Weak transcription	GM12878-XiMat	blood
23	chr13:95752200-95823200	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr13:95752200-95844200	Weak transcription	Rectal Smooth Muscle	rectum
25	chr13:95753400-95775400	Weak transcription	HSMMtube	muscle
26	chr13:95753600-95761000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr13:95753600-95767400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr13:95753600-95772600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr13:95754000-95766800	Weak transcription	Osteobl	bone
30	chr13:95754000-95777200	Weak transcription	NHDF-Ad	bronchial
31	chr13:95754000-95794800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr13:95754400-95768000	Weak transcription	NH-A	brain
33	chr13:95754400-95782600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr13:95754600-95764000	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr13:95755000-95774200	Weak transcription	Primary T cells fromperipheralblood	blood
36	chr13:95755400-95776400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr13:95756400-95759200	Strong transcription	A549	lung
38	chr13:95756400-95759800	Weak transcription	Psoas Muscle	Psoas
39	chr13:95756400-95828200	Weak transcription	HSMM	muscle
40	chr13:95756600-95766400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
41	chr13:95757600-95772800	Weak transcription	Lung	lung
42	chr13:95757600-95814400	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chr13:95757800-95760600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr13:95758000-95761600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr13:95758000-95764800	Weak transcription	Stomach Smooth Muscle	stomach
46	chr13:95758000-95766600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr13:95758000-95791600	Weak transcription	Duodenum Smooth Muscle	Duodenum
48	chr13:95758200-95760800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr13:95758200-95761000	Weak transcription	Fetal Intestine Small	intestine
50	chr13:95758200-95769200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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