Variant report

Variant	esv1823336
Chromosome Location	chr13:111329535-111360585
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1402)
CpG islands
(count:1652)
Chromatin interactive
region (count:41)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1402 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:111336891-111337374	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:111358502-111358688	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:111335600-111336012	HepG2	liver:	n/a	n/a
4	ATF2	chr13:111328300-111329671	GM12878	blood:	n/a	n/a
5	ATF2	chr13:111358404-111358906	GM12878	blood:	n/a	n/a
6	ATF2	chr13:111351013-111351470	GM12878	blood:	n/a	n/a
7	BACH1	chr13:111358564-111358921	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr13:111354174-111354255	K562	blood:	n/a	n/a
9	BACH1	chr13:111357933-111358316	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr13:111329690-111330085	GM12878	blood:	n/a	n/a
11	BCL11A	chr13:111329451-111330173	GM12878	blood:	n/a	n/a
12	BCL3	chr13:111359273-111359700	GM12878	blood:	n/a	n/a
13	BCL3	chr13:111358321-111358947	GM12878	blood:	n/a	chr13:111358653-111358662
14	BCLAF1	chr13:111358471-111359475	GM12878	blood:	n/a	chr13:111358653-111358662
15	BCLAF1	chr13:111358123-111358873	GM12878	blood:	n/a	chr13:111358653-111358662
16	BHLHE40	chr13:111357294-111357378	GM12878	blood:	n/a	n/a
17	BHLHE40	chr13:111358088-111359042	K562	blood:	n/a	chr13:111358181-111358197
18	BHLHE40	chr13:111358083-111359001	GM12878	blood:	n/a	chr13:111358181-111358197
19	BHLHE40	chr13:111358350-111359050	HepG2	liver:	n/a	n/a
20	BHLHE40	chr13:111328344-111329778	GM12878	blood:	n/a	chr13:111328790-111328806 chr13:111328782-111328798
21	BHLHE40	chr13:111359523-111359649	K562	blood:	n/a	n/a
22	BRCA1	chr13:111358426-111358827	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr13:111357097-111357890	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr13:111358559-111358744	HepG2	liver:	n/a	n/a
25	CBX3	chr13:111358407-111359006	K562	blood:	n/a	n/a
26	CCNT2	chr13:111358123-111358920	K562	blood:	n/a	n/a
27	CEBPB	chr13:111357234-111357545	MCF-7	breast:	n/a	n/a
28	CEBPB	chr13:111357252-111357498	K562	blood:	n/a	n/a
29	CEBPB	chr13:111355569-111355710	HepG2	liver:	n/a	chr13:111355645-111355658
30	CEBPB	chr13:111335784-111336094	A549	lung:	n/a	n/a
31	CEBPB	chr13:111357191-111357794	A549	lung:	n/a	chr13:111357227-111357238
32	CEBPB	chr13:111357166-111357640	IMR90	lung:	n/a	chr13:111357227-111357238
33	CEBPB	chr13:111356603-111356821	IMR90	lung:	n/a	n/a
34	CEBPB	chr13:111357213-111357523	HepG2	liver:	n/a	chr13:111357227-111357238
35	CEBPB	chr13:111356622-111356766	A549	lung:	n/a	n/a
36	CEBPB	chr13:111335776-111336154	HepG2	liver:	n/a	n/a
37	CEBPB	chr13:111336870-111336959	HepG2	liver:	n/a	n/a
38	CEBPB	chr13:111358060-111358836	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr13:111357218-111357414	HepG2	liver:	n/a	chr13:111357227-111357238
40	CEBPB	chr13:111357119-111357556	K562	blood:	n/a	chr13:111357227-111357238
41	CEBPB	chr13:111357100-111357696	HCT-116	colon:	n/a	chr13:111357227-111357238
42	CEBPB	chr13:111356593-111357855	Hela-S3	cervix:	n/a	chr13:111357227-111357238
43	CEBPB	chr13:111358752-111358816	K562	blood:	n/a	n/a
44	CEBPB	chr13:111357054-111357595	A549	lung:	n/a	chr13:111357227-111357238
45	CEBPB	chr13:111357102-111357884	HCT-116	colon:	n/a	chr13:111357227-111357238
46	CEBPB	chr13:111335778-111336129	K562	blood:	n/a	n/a
47	CEBPB	chr13:111355141-111355817	IMR90	lung:	n/a	chr13:111355645-111355658
48	CEBPB	chr13:111357163-111357524	K562	blood:	n/a	chr13:111357227-111357238
49	CEBPB	chr13:111355523-111355790	Hela-S3	cervix:	n/a	chr13:111355645-111355658
50	CEBPD	chr13:111359305-111359625	HepG2	liver:	n/a	n/a

(count:1652 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:111358522-111358572	HNPCEpiC	eye:	n/a
2	chr13:111334467-111334517	SK-N-SH_RA	brain:	n/a
3	chr13:111330802-111330852	BE2_C	brain:	n/a
4	chr13:111330699-111330749	HAEpiC	amniotic membrane:	n/a
5	chr13:111331324-111331374	SAEC	small airway:	n/a
6	chr13:111358522-111358572	HNPCEpiC	eye:	n/a
7	chr13:111334467-111334517	SK-N-SH_RA	brain:	n/a
8	chr13:111330802-111330852	BE2_C	brain:	n/a
9	chr13:111330699-111330749	HAEpiC	amniotic membrane:	n/a
10	chr13:111331324-111331374	SAEC	small airway:	n/a
11	chr13:111334467-111334517	HCT-116	colon:	n/a
12	chr13:111358924-111358974	U87	brain:	n/a
13	chr13:111358552-111358602	HL-60	blood:	n/a
14	chr13:111336430-111336480	GM12891	blood:	n/a
15	chr13:111358803-111358853	NB4	blood:	n/a
16	chr13:111340159-111340209	ECC-1	luminal epithelium:	n/a
17	chr13:111331104-111331154	HCPEpiC	choroid plexus:	n/a
18	chr13:111358532-111358582	HIPEpiC	eye:	n/a
19	chr13:111358538-111358588	HRE	kidney:	n/a
20	chr13:111358516-111358566	ProgFib	skin:	n/a
21	chr13:111358522-111358572	NT2-D1	testis:	n/a
22	chr13:111358532-111358582	K562	blood:	n/a
23	chr13:111340250-111340300	AG04449	skin:	fetal
24	chr13:111340250-111340300	SK-N-SH_RA	brain:	n/a
25	chr13:111358522-111358572	HMEC	breast:	n/a
26	chr13:111358803-111358853	NH-A	brain:	n/a
27	chr13:111358862-111358912	Jurkat	blood:	n/a
28	chr13:111330434-111330484	NT2-D1	testis:	n/a
29	chr13:111340350-111340400	PrEC	prostate:	n/a
30	chr13:111330434-111330484	AG09309	skin:	n/a
31	chr13:111331324-111331374	NHBE	bronchial:	n/a
32	chr13:111340159-111340209	GM06990	blood:	n/a
33	chr13:111330699-111330749	H1-hESC	embryonic stem cell:	embryo
34	chr13:111358532-111358582	HNPCEpiC	eye:	n/a
35	chr13:111333333-111333383	SK-N-MC	brain:	n/a
36	chr13:111358885-111358935	H1-hESC	embryonic stem cell:	embryo
37	chr13:111358803-111358853	PrEC	prostate:	n/a
38	chr13:111333333-111333383	HEEpiC	esophagus:	n/a
39	chr13:111334467-111334517	HEEpiC	esophagus:	n/a
40	chr13:111340159-111340209	HAEpiC	amniotic membrane:	n/a
41	chr13:111330434-111330484	AoSMC	blood vessel:	n/a
42	chr13:111358532-111358582	AG09319	gingival:	n/a
43	chr13:111358862-111358912	HNPCEpiC	eye:	n/a
44	chr13:111358862-111358912	HepG2	liver:	n/a
45	chr13:111358527-111358577	HRPEpiC	eye:	n/a
46	chr13:111355112-111355162	NH-A	brain:	n/a
47	chr13:111336430-111336480	MCF-7	breast:	n/a
48	chr13:111331255-111331305	ECC-1	luminal epithelium:	n/a
49	chr13:111334467-111334517	HUVEC	blood vessel:	n/a
50	chr13:111358862-111358912	HCM	heart:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:111334523..111337110-chr13:111337713..111340706,3	K562	blood:
2	chr13:111341464..111343204-chr13:111366168..111368327,2	MCF-7	breast:
3	chr1:179718648..179719326-chr13:111357431..111357953,2	Hela-S3	cervix:
4	chr13:111357509..111359061-chr13:111566329..111568110,2	MCF-7	breast:
5	chr13:111357144..111360099-chr13:111360341..111362234,3	K562	blood:
6	chr13:111341286..111343605-chr13:111352948..111355342,2	K562	blood:
7	chr13:111331059..111333327-chr13:111365310..111368139,4	MCF-7	breast:
8	chr13:111328800..111330834-chr13:111364440..111366788,2	K562	blood:
9	chr13:111354215..111355804-chr13:111356852..111360371,4	MCF-7	breast:
10	chr13:111333021..111335304-chr13:111366011..111368539,3	K562	blood:
11	chr13:111344285..111345813-chr13:111363151..111365831,2	MCF-7	breast:
12	chr13:111266746..111269387-chr13:111357064..111359748,3	MCF-7	breast:
13	chr13:111331878..111333857-chr13:111363101..111365113,2	MCF-7	breast:
14	chr13:111345499..111348039-chr13:111356467..111358973,3	K562	blood:
15	chr13:111328169..111330528-chr13:111354350..111356160,2	K562	blood:
16	chr13:111354377..111357375-chr13:111522032..111524115,2	K562	blood:
17	chr13:111332786..111335109-chr13:111356617..111359801,4	MCF-7	breast:
18	chr12:52444794..52445706-chr13:111357930..111358458,2	Hela-S3	cervix:
19	chr13:111339506..111342066-chr13:111350294..111353169,2	MCF-7	breast:
20	chr13:111336321..111339230-chr13:111365853..111367619,2	K562	blood:
21	chr13:111348126..111353752-chr13:111353903..111360039,12	K562	blood:
22	chr13:111348523..111351928-chr13:111363890..111366242,4	K562	blood:
23	chr13:111334321..111336628-chr13:111364897..111367415,3	MCF-7	breast:
24	chr13:111335534..111341041-chr13:111341252..111346282,8	K562	blood:
25	chr13:111340529..111343866-chr13:111358060..111360020,4	K562	blood:
26	chr13:111358233..111358789-chr17:61904375..61905309,2	HCT-116	colon:
27	chr13:111330512..111332280-chr13:111367075..111369007,2	K562	blood:
28	chr13:111344513..111346210-chr13:111366483..111368086,2	MCF-7	breast:
29	chr13:111339852..111341870-chr13:111364379..111365979,2	K562	blood:
30	chr13:111335534..111341041-chr13:111341252..111346282,8	K562	blood:
31	chr13:111341286..111343605-chr13:111352948..111355342,2	K562	blood:
32	chr13:111340758..111343844-chr13:111351055..111354448,3	K562	blood:
33	chr13:111340758..111343844-chr13:111351055..111354448,3	K562	blood:
34	chr13:111335461..111337308-chr13:111363462..111365716,2	MCF-7	breast:
35	chr13:111328800..111332502-chr13:111363272..111367932,6	K562	blood:
36	chr13:111332795..111333429-chr13:111365730..111366453,2	K562	blood:
37	chr13:111339867..111342003-chr13:111356640..111358659,2	MCF-7	breast:
38	chr13:111266587..111269692-chr13:111357018..111359356,4	K562	blood:
39	chr13:111335027..111337821-chr13:111366043..111367943,3	K562	blood:
40	chr13:111338558..111340999-chr13:111366379..111367908,2	MCF-7	breast:
41	chr13:111339506..111342066-chr13:111350294..111353169,2	MCF-7	breast:

No data

Variant related genes	Relation type
ING1	TF binding region
CARS2	TF binding region
ING1	CpG island
CARS2	CpG island
ENSG00000123358	chromatin interactions
ENSG00000213995	chromatin interactions
ENSG00000108592	chromatin interactions
ENSG00000088448	chromatin interactions
ENSG00000255874	chromatin interactions
ENSG00000153487	chromatin interactions
ENSG00000134905	chromatin interactions
ENSG00000087191	chromatin interactions

Extended variants
information (count: 1255 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1255 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113622654	chr13:111329579-111329580	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs74125032	chr13:111329589-111329590	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs56131494	chr13:111329596-111329597	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs76103038	chr13:111329610-111329611	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs78214217	chr13:111329612-111329613	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs56405935	chr13:111329613-111329614	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs56260830	chr13:111329619-111329620	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs11069862	chr13:111329632-111329633	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs80279244	chr13:111329655-111329656	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs11069863	chr13:111329665-111329666	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
11	rs372446455	chr13:111329673-111329674	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs369148346	chr13:111329679-111329680	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs386774764	chr13:111329680-111329681	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs151026419	chr13:111329686-111329687	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs12431291	chr13:111329688-111329689	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs12431292	chr13:111329689-111329690	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs112411948	chr13:111329731-111329732	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
18	rs116445785	chr13:111329741-111329742	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs375733871	chr13:111329749-111329750	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs111861692	chr13:111329762-111329763	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs555745014	chr13:111329790-111329791	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs573906307	chr13:111329792-111329793	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs111337923	chr13:111329806-111329807	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs535011932	chr13:111329807-111329808	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs553542826	chr13:111329812-111329813	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs56390422	chr13:111329813-111329814	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs559014010	chr13:111329830-111329831	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs55698523	chr13:111329855-111329856	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs371387530	chr13:111329865-111329866	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs56402184	chr13:111329867-111329868	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs56303604	chr13:111329874-111329875	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs113152490	chr13:111329877-111329878	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs55900054	chr13:111329879-111329880	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs56362560	chr13:111329885-111329886	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs56042147	chr13:111329893-111329894	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs56112855	chr13:111329899-111329900	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs55654030	chr13:111329900-111329901	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs534222517	chr13:111329914-111329915	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs578130793	chr13:111329916-111329917	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs544395733	chr13:111329918-111329919	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs547137033	chr13:111329939-111329940	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs367590116	chr13:111329953-111329954	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs544892193	chr13:111329974-111329975	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs113376408	chr13:111330024-111330025	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs188051054	chr13:111330046-111330047	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs61971608	chr13:111330052-111330053	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs61971609	chr13:111330058-111330059	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs142156861	chr13:111330066-111330067	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs374916590	chr13:111330069-111330070	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs145764371	chr13:111330072-111330073	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
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
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
Basal cell lymphoma	17053054	CNVD
Gastric cancer	17908304	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	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
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
Acute myeloid leukemia	21251322	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Burkitt''s lymphoma	20823134	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Burkitt''s lymphoma	19759907	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Medulloblastoma	19270706	CNVD
Mental retardation	17124404	CNVD
Leukemia	18688285	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21858162	CNVD
Melanoma	17363583	CNVD
Developmental delay	21147756	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	16608533	CNVD
Glioblastoma multiforme	22286061	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
abnormal development	18461090	CNVD
Malignant glioma	17146433	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Glioma	17123091	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	20409316	CNVD
Central neurocytomas	17123091	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Neurocytoma	17123091	CNVD
Mantle cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1781 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:111297800-111336400	Weak transcription	Small Intestine	intestine
2	chr13:111302200-111351400	Weak transcription	Stomach Mucosa	stomach
3	chr13:111310800-111352200	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr13:111311600-111352000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr13:111312800-111357400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr13:111316200-111330600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr13:111316600-111332800	Weak transcription	K562	blood
8	chr13:111319400-111337600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr13:111319800-111348400	Weak transcription	Fetal Brain Male	brain
10	chr13:111319800-111354600	Weak transcription	Fetal Heart	heart
11	chr13:111320200-111339200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr13:111321800-111332800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr13:111322000-111330000	Weak transcription	NHDF-Ad	bronchial
14	chr13:111322800-111333800	Weak transcription	Fetal Kidney	kidney
15	chr13:111322800-111349600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr13:111327600-111329600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr13:111327800-111331400	Strong transcription	Colonic Mucosa	Colon
18	chr13:111327800-111336000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr13:111327800-111344200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr13:111327800-111347400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr13:111327800-111355000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr13:111328000-111329600	Strong transcription	Brain Anterior Caudate	brain
23	chr13:111328000-111330400	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
24	chr13:111328000-111331000	Strong transcription	Fetal Lung	lung
25	chr13:111328000-111331200	Strong transcription	Fetal Muscle Trunk	muscle
26	chr13:111328000-111331600	Strong transcription	Duodenum Smooth Muscle	Duodenum
27	chr13:111328000-111331800	Strong transcription	Brain Inferior Temporal Lobe	brain
28	chr13:111328000-111331800	Strong transcription	Gastric	stomach
29	chr13:111328000-111331800	Strong transcription	Ovary	ovary
30	chr13:111328000-111331800	Strong transcription	Thymus	Thymus
31	chr13:111328000-111332400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr13:111328000-111333200	Strong transcription	NHLF	lung
33	chr13:111328000-111335200	Strong transcription	Brain Cingulate Gyrus	brain
34	chr13:111328000-111335200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr13:111328000-111335400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr13:111328000-111335400	Strong transcription	HepG2	liver
37	chr13:111328000-111335600	Strong transcription	Liver	Liver
38	chr13:111328000-111335600	Strong transcription	Duodenum Mucosa	Duodenum
39	chr13:111328000-111336000	Strong transcription	Fetal Intestine Large	intestine
40	chr13:111328000-111336600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
41	chr13:111328000-111336800	Strong transcription	Left Ventricle	heart
42	chr13:111328000-111337800	Strong transcription	Brain Germinal Matrix	brain
43	chr13:111328000-111338200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr13:111328000-111339800	Strong transcription	HUES6 Cell Line	embryonic stem cell
45	chr13:111328000-111340200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr13:111328000-111341000	Strong transcription	HUES64 Cell Line	embryonic stem cell
47	chr13:111328000-111342400	Strong transcription	Fetal Muscle Leg	muscle
48	chr13:111328000-111342400	Strong transcription	Osteobl	bone
49	chr13:111328000-111342800	Strong transcription	Primary T helper cells PMA-I stimulated	--
50	chr13:111328000-111343200	Strong transcription	Cortex derived primary cultured neurospheres	brain

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