Variant report

Variant	nsv562346
Chromosome Location	chr13:75972846-76090084
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2386)
CpG islands
(count:1343)
Chromatin interactive
region (count:72)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2386 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:76014191-76014675	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:76063855-76064507	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:76052864-76053526	HepG2	liver:	n/a	n/a
4	ARID3A	chr13:76033000-76033692	HepG2	liver:	n/a	n/a
5	ARID3A	chr13:76019801-76020008	HepG2	liver:	n/a	n/a
6	ARID3A	chr13:76007189-76007353	HepG2	liver:	n/a	n/a
7	ARID3A	chr13:75977140-75977324	HepG2	liver:	n/a	n/a
8	ARID3A	chr13:75986159-75987206	HepG2	liver:	n/a	n/a
9	ARID3A	chr13:75974906-75975645	HepG2	liver:	n/a	n/a
10	ARID3A	chr13:76014298-76014341	K562	blood:	n/a	n/a
11	ARID3A	chr13:76042691-76043136	HepG2	liver:	n/a	n/a
12	ARID3A	chr13:76056560-76056571	K562	blood:	n/a	n/a
13	ARID3A	chr13:76041061-76041519	HepG2	liver:	n/a	n/a
14	ARID3A	chr13:76026723-76026947	HepG2	liver:	n/a	n/a
15	ARID3A	chr13:76054914-76055180	HepG2	liver:	n/a	n/a
16	ARID3A	chr13:76049433-76049776	HepG2	liver:	n/a	n/a
17	ARID3A	chr13:76056172-76056962	HepG2	liver:	n/a	n/a
18	ARID3A	chr13:76018232-76018483	HepG2	liver:	n/a	n/a
19	ATF1	chr13:75999408-76000077	K562	blood:	n/a	n/a
20	ATF2	chr13:76056580-76057027	GM12878	blood:	n/a	n/a
21	ATF2	chr13:76023473-76023840	GM12878	blood:	n/a	n/a
22	ATF2	chr13:76086299-76086714	GM12878	blood:	n/a	n/a
23	ATF2	chr13:75990555-75991243	GM12878	blood:	n/a	n/a
24	ATF2	chr13:75999154-75999868	GM12878	blood:	n/a	n/a
25	ATF2	chr13:76056368-76057096	GM12878	blood:	n/a	n/a
26	ATF2	chr13:76086245-76086999	GM12878	blood:	n/a	n/a
27	ATF2	chr13:76088550-76089058	GM12878	blood:	n/a	n/a
28	ATF2	chr13:76023375-76023869	GM12878	blood:	n/a	n/a
29	ATF2	chr13:75988150-75988829	GM12878	blood:	n/a	n/a
30	ATF3	chr13:76066626-76066796	K562	blood:	n/a	n/a
31	ATF3	chr13:76056583-76056939	GM12878	blood:	n/a	n/a
32	ATF3	chr13:76066577-76066876	K562	blood:	n/a	n/a
33	BACH1	chr13:76014515-76014701	K562	blood:	n/a	n/a
34	BACH1	chr13:76054850-76056943	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr13:76057162-76057164	K562	blood:	n/a	n/a
36	BACH1	chr13:76059840-76060561	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr13:76042227-76042263	K562	blood:	n/a	n/a
38	BATF	chr13:76086386-76086750	GM12878	blood:	n/a	n/a
39	BATF	chr13:75990642-75991104	GM12878	blood:	n/a	n/a
40	BATF	chr13:76023530-76023780	GM12878	blood:	n/a	n/a
41	BATF	chr13:76056670-76056975	GM12878	blood:	n/a	n/a
42	BATF	chr13:76003421-76003671	GM12878	blood:	n/a	n/a
43	BATF	chr13:76079141-76079398	GM12878	blood:	n/a	chr13:76079240-76079251
44	BATF	chr13:75988378-75988640	GM12878	blood:	n/a	n/a
45	BATF	chr13:76086423-76086754	GM12878	blood:	n/a	n/a
46	BATF	chr13:76079101-76079335	GM12878	blood:	n/a	chr13:76079240-76079251
47	BATF	chr13:76041160-76041439	GM12878	blood:	n/a	n/a
48	BATF	chr13:75990737-75991015	GM12878	blood:	n/a	n/a
49	BCL11A	chr13:76056637-76056925	GM12878	blood:	n/a	chr13:76056873-76056882
50	BCL11A	chr13:76056610-76057003	GM12878	blood:	n/a	chr13:76056873-76056882

(count:1343 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:76056416-76056466	HPAEpiC	pulmonary alveolar:	n/a
2	chr13:76056416-76056466	HPAEpiC	pulmonary alveolar:	n/a
3	chr13:76056027-76056077	Hela-S3	cervix:	n/a
4	chr13:76016968-76017018	HEK293	kidney:	embryo
5	chr13:76056419-76056469	H1-hESC	embryonic stem cell:	embryo
6	chr13:76016968-76017018	SK-N-SH	brain:	n/a
7	chr13:76054909-76054959	AoSMC	blood vessel:	n/a
8	chr13:76055871-76055921	GM12891	blood:	n/a
9	chr13:76055871-76055921	HPAEpiC	pulmonary alveolar:	n/a
10	chr13:76056421-76056471	BE2_C	brain:	n/a
11	chr13:76056497-76056547	HCPEpiC	choroid plexus:	n/a
12	chr13:76056497-76056547	GM19239	blood:	n/a
13	chr13:76055871-76055921	HepG2	liver:	n/a
14	chr13:75991251-75991301	PFSK-1	brain:	n/a
15	chr13:76056030-76056080	MCF10A-Er-Src	breast:	n/a
16	chr13:76055871-76055921	AG09319	gingival:	n/a
17	chr13:76056030-76056080	HUVEC	blood vessel:	n/a
18	chr13:75991251-75991301	RPTEC	kidney:	n/a
19	chr13:76032565-76032615	SK-N-MC	brain:	n/a
20	chr13:76043069-76043119	AG09319	gingival:	n/a
21	chr13:76056490-76056540	PANC-1	pancreas:	n/a
22	chr13:76055293-76055343	GM12891	blood:	n/a
23	chr13:76052395-76052445	GM12891	blood:	n/a
24	chr13:75980679-75980729	PFSK-1	brain:	n/a
25	chr13:75991251-75991301	GM06990	blood:	n/a
26	chr13:76056027-76056077	T-47D	breast:	n/a
27	chr13:75991251-75991301	LNCaP	prostate:	n/a
28	chr13:76056416-76056466	SK-N-MC	brain:	n/a
29	chr13:76056336-76056386	SAEC	small airway:	n/a
30	chr13:76054909-76054959	RPTEC	kidney:	n/a
31	chr13:76056027-76056077	Caco-2	colon:	n/a
32	chr13:76056490-76056540	Caco-2	colon:	n/a
33	chr13:76056490-76056540	AG04449	skin:	fetal
34	chr13:75991251-75991301	NT2-D1	testis:	n/a
35	chr13:76056490-76056540	AoSMC	blood vessel:	n/a
36	chr13:76056336-76056386	LNCaP	prostate:	n/a
37	chr13:76056784-76056834	A549	lung:	n/a
38	chr13:76056490-76056540	HMEC	breast:	n/a
39	chr13:76056444-76056494	H1-hESC	embryonic stem cell:	embryo
40	chr13:76056027-76056077	AG10803	skin:	n/a
41	chr13:76055871-76055921	ECC-1	luminal epithelium:	n/a
42	chr13:75991251-75991301	Hela-S3	cervix:	n/a
43	chr13:75980679-75980729	ovcar-3	ovarian:	n/a
44	chr13:76056497-76056547	HRCEpiC	kidney:	n/a
45	chr13:76069242-76069292	Hepatocyte	liver:	n/a
46	chr13:76056497-76056547	GM12892	blood:	n/a
47	chr13:76052395-76052445	SK-N-SH_RA	brain:	n/a
48	chr13:76054909-76054959	AG10803	skin:	n/a
49	chr13:76060574-76060624	HCM	heart:	n/a
50	chr13:76056419-76056469	SK-N-SH	brain:	n/a

(count:72 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr13:76056169..76056921-chr13:76123095..76123971,5	MCF-7	breast:
2	chr13:76051274..76054795-chr13:76057453..76061221,3	K562	blood:
3	chr13:75998555..76000327-chr13:76013218..76015228,2	K562	blood:
4	chr13:76049737..76051578-chr13:76054500..76056677,3	MCF-7	breast:
5	chr13:76076405..76080634-chr13:76083700..76088829,4	K562	blood:
6	chr13:76075450..76077905-chr13:76087329..76089009,2	K562	blood:
7	chr13:76074591..76077298-chr13:76079207..76081950,2	K562	blood:
8	chr13:76013400..76015872-chr13:76018076..76020883,2	MCF-7	breast:
9	chr13:76076405..76080634-chr13:76083700..76088829,4	K562	blood:
10	chr13:76024363..76026211-chr13:76040160..76042265,2	K562	blood:
11	chr13:76074143..76076070-chr13:76123601..76125267,2	MCF-7	breast:
12	chr11:62608582..62609197-chr13:76054850..76055765,2	NB4	blood:
13	chr13:75967418..75969067-chr13:75972792..75975207,2	K562	blood:
14	chr13:76055194..76058369-chr13:76060502..76064078,3	K562	blood:
15	chr13:76060096..76062427-chr13:76067449..76070144,3	K562	blood:
16	chr13:76074591..76077298-chr13:76079207..76081950,2	K562	blood:
17	chr13:76024363..76026211-chr13:76040160..76042265,2	K562	blood:
18	chr13:76051274..76054795-chr13:76057453..76061221,3	K562	blood:
19	chr13:75946564..75947349-chr13:76056407..76057240,4	MCF-7	breast:
20	chr13:76055434..76058277-chr13:76123047..76126766,3	K562	blood:
21	chr13:76004463..76006060-chr13:76111032..76113406,2	MCF-7	breast:
22	chr13:76060096..76062427-chr13:76067449..76070144,3	K562	blood:
23	chr13:75995155..75997583-chr13:76008441..76010514,2	MCF-7	breast:
24	chr13:76035923..76038251-chr13:76040733..76043153,2	K562	blood:
25	chr13:76055137..76056712-chr13:76122225..76124650,2	MCF-7	breast:
26	chr13:76056486..76057156-chr16:7762589..7763109,2	MCF-7	breast:
27	chr13:75992093..75993846-chr13:76062771..76064533,2	K562	blood:
28	chr1:27191364..27192041-chr13:76054801..76055652,2	Hela-S3	cervix:
29	chr13:76016614..76019558-chr13:76031564..76033175,2	MCF-7	breast:
30	chr13:75996518..75998034-chr13:76000598..76003105,2	K562	blood:
31	chr13:76080347..76082551-chr13:76083582..76085785,4	K562	blood:
32	chr13:75902704..75905125-chr13:75993318..75996004,2	K562	blood:
33	chr13:75988028..75990689-chr13:75994977..75997792,3	K562	blood:
34	chr13:76003639..76004562-chr21:27304576..27305349,2	MCF-7	breast:
35	chr13:76053295..76053983-chr2:68978753..68979370,2	MCF-7	breast:
36	chr13:76080347..76082551-chr13:76083582..76085785,4	K562	blood:
37	chr13:75992093..75993846-chr13:76062771..76064533,2	K562	blood:
38	chr13:75987894..75988452-chr13:76055971..76056871,2	MCF-7	breast:
39	chr13:76060354..76062055-chr13:76103178..76106915,3	K562	blood:
40	chr13:76010975..76013895-chr13:76015597..76017378,2	K562	blood:
41	chr13:75998555..76000327-chr13:76013218..76015228,2	K562	blood:
42	chr13:76010975..76013105-chr13:76023574..76025826,2	K562	blood:
43	chr13:76048295..76050774-chr13:76052549..76054947,2	MCF-7	breast:
44	chr13:76039660..76041295-chr2:8817858..8820426,2	MCF-7	breast:
45	chr13:76041458..76043973-chr13:76054893..76056478,2	MCF-7	breast:
46	chr13:76056190..76058519-chr13:76061605..76064578,2	MCF-7	breast:
47	chr13:76010975..76013895-chr13:76015597..76017378,2	K562	blood:
48	chr13:75931707..75932464-chr13:76077700..76078200,2	MCF-7	breast:
49	chr13:75987952..75988694-chr13:76056057..76056871,2	MCF-7	breast:
50	chr13:76006248..76008169-chr13:76054948..76056743,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COMMD6-4	chr13:76072524-76072824	l_873_chr13:76072523-76201534_testes

No data

Variant related genes	Relation type
TBC1D4	TF binding region
TBC1D4	CpG island
ENSG00000136111	chromatin interactions
ENSG00000171159	chromatin interactions
ENSG00000235092	chromatin interactions
ENSG00000118939	chromatin interactions
ENSG00000261553	chromatin interactions
ENSG00000188243	chromatin interactions
ENSG00000115738	chromatin interactions

Extended variants
information (count: 4200 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:4200 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9285295	chr13:75972846-75972847	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs564780780	chr13:75972874-75972875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs532343915	chr13:75972894-75972895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs4129482	chr13:75972914-75972915	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs117133947	chr13:75972918-75972919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs529992494	chr13:75972975-75972976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs549430547	chr13:75973020-75973021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs567652211	chr13:75973032-75973033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs538003848	chr13:75973078-75973079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs118090171	chr13:75973125-75973126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs17064364	chr13:75973129-75973130	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs539240124	chr13:75973141-75973142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs554046000	chr13:75973162-75973163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs111376425	chr13:75973192-75973193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs370142225	chr13:75973200-75973201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs554190223	chr13:75973203-75973204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs575635723	chr13:75973204-75973205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs117786553	chr13:75973205-75973206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs73535658	chr13:75973206-75973207	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs532079623	chr13:75973234-75973235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs541247075	chr13:75973244-75973245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs73535660	chr13:75973253-75973254	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs558134272	chr13:75973259-75973260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs530054235	chr13:75973271-75973272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs576386936	chr13:75973287-75973288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs145160735	chr13:75973341-75973342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs6562893	chr13:75973361-75973362	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs528281479	chr13:75973362-75973363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs544896130	chr13:75973410-75973411	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs571276902	chr13:75973444-75973445	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs183907657	chr13:75973464-75973465	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs367960936	chr13:75973486-75973487	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs571735934	chr13:75973492-75973493	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs4427680	chr13:75973507-75973508	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs553980126	chr13:75973562-75973563	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs17064366	chr13:75973564-75973565	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs141512764	chr13:75973585-75973586	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs116315412	chr13:75973601-75973602	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs576292612	chr13:75973614-75973615	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs4396420	chr13:75973672-75973673	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs558243136	chr13:75973687-75973688	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs187785593	chr13:75973714-75973715	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs190321749	chr13:75973720-75973721	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs111460417	chr13:75973721-75973722	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs4640064	chr13:75973740-75973741	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs4334162	chr13:75973752-75973753	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs538568487	chr13:75973815-75973816	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs563591791	chr13:75973842-75973843	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs71417622	chr13:75973844-75973845	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs4393456	chr13:75973845-75973846	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:96)

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
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21858162	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	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
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hirschsprung''s Disease	21712996	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Intracranial aneurysm	16715129	CNVD
Non-small cell lung cancer	19010865	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	17002787	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:2198 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:75959600-75973400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr13:75966000-75977000	Weak transcription	Right Ventricle	heart
3	chr13:75966800-75973400	Weak transcription	Psoas Muscle	Psoas
4	chr13:75968400-75973400	Weak transcription	HSMMtube	muscle
5	chr13:75969200-75975000	Weak transcription	Fetal Kidney	kidney
6	chr13:75969400-75973200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr13:75969400-75974200	Weak transcription	Small Intestine	intestine
8	chr13:75970200-75975400	Weak transcription	Ovary	ovary
9	chr13:75971000-75979200	Enhancers	HepG2	liver
10	chr13:75971600-75973000	Enhancers	Fetal Heart	heart
11	chr13:75972000-75977000	Enhancers	Skeletal Muscle Female	skeletal muscle
12	chr13:75972200-75973400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr13:75972200-75977000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr13:75972600-75974000	Weak transcription	Left Ventricle	heart
15	chr13:75972600-75974000	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr13:75972800-75980000	Weak transcription	Osteobl	bone
17	chr13:75973000-75974000	Weak transcription	Fetal Heart	heart
18	chr13:75973400-75974000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr13:75973400-75974400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr13:75973400-75974400	Enhancers	Psoas Muscle	Psoas
21	chr13:75973400-75974400	Enhancers	HSMMtube	muscle
22	chr13:75973400-75977400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr13:75973400-75987200	Weak transcription	Gastric	stomach
24	chr13:75973600-75974200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr13:75973600-75975600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr13:75974000-75974200	Enhancers	Left Ventricle	heart
27	chr13:75974000-75975000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr13:75974000-75975400	Enhancers	Fetal Heart	heart
29	chr13:75974000-75977000	Enhancers	Skeletal Muscle Male	skeletal muscle
30	chr13:75974200-75974400	Enhancers	NH-A	brain
31	chr13:75974200-75974600	Weak transcription	Fetal Muscle Leg	muscle
32	chr13:75974200-75974800	Weak transcription	Left Ventricle	heart
33	chr13:75974200-75975800	Enhancers	Liver	Liver
34	chr13:75974200-75977000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr13:75974400-75974800	Weak transcription	Psoas Muscle	Psoas
36	chr13:75974400-75976800	Weak transcription	HSMMtube	muscle
37	chr13:75974400-75980200	Weak transcription	NH-A	brain
38	chr13:75974800-75977400	Enhancers	Left Ventricle	heart
39	chr13:75974800-75977400	Enhancers	Psoas Muscle	Psoas
40	chr13:75975000-75975200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr13:75975000-75975200	Enhancers	Pancreas	Pancrea
42	chr13:75975000-75976400	Enhancers	Fetal Kidney	kidney
43	chr13:75975200-75975600	Enhancers	A549	lung
44	chr13:75975200-75981000	Weak transcription	Pancreas	Pancrea
45	chr13:75975400-75975600	Enhancers	Right Atrium	heart
46	chr13:75975400-75976000	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr13:75975400-75976200	Flanking Active TSS	Fetal Heart	heart
48	chr13:75975400-75977400	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr13:75975400-75977400	Enhancers	Ovary	ovary
50	chr13:75975600-75977200	Weak transcription	A549	lung

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