Variant report

Variant	esv3359253
Chromosome Location	chr13:30168577-30171125
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:30170053-30170123	HepG2	liver:	n/a	n/a
2	ATF2	chr13:30168499-30169250	GM12878	blood:	n/a	n/a
3	ATF2	chr13:30168897-30169456	GM12878	blood:	n/a	n/a
4	ATF3	chr13:30168972-30169405	K562	blood:	n/a	chr13:30169089-30169098 chr13:30169217-30169226
5	BACH1	chr13:30169186-30170316	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr13:30168926-30169445	GM12878	blood:	n/a	n/a
7	BATF	chr13:30168512-30168904	GM12878	blood:	n/a	n/a
8	BCL3	chr13:30168831-30169399	GM12878	blood:	n/a	chr13:30169031-30169044 chr13:30169138-30169151 chr13:30169176-30169189 chr13:30169172-30169185 chr13:30169134-30169147
9	BCLAF1	chr13:30169824-30170286	GM12878	blood:	n/a	chr13:30169938-30169951 chr13:30170162-30170170 chr13:30169927-30169940 chr13:30169934-30169943 chr13:30169932-30169945 chr13:30169960-30169973 chr13:30169937-30169946
10	BCLAF1	chr13:30168706-30169467	GM12878	blood:	n/a	chr13:30169031-30169044 chr13:30169138-30169151 chr13:30169176-30169189 chr13:30169172-30169185 chr13:30169134-30169147
11	BHLHE40	chr13:30169634-30169789	K562	blood:	n/a	chr13:30169712-30169728
12	BHLHE40	chr13:30169164-30169386	K562	blood:	n/a	n/a
13	BHLHE40	chr13:30170060-30170172	K562	blood:	n/a	n/a
14	BHLHE40	chr13:30169596-30169809	GM12878	blood:	n/a	chr13:30169712-30169728
15	BHLHE40	chr13:30168371-30169369	GM12878	blood:	n/a	chr13:30169002-30169018
16	BHLHE40	chr13:30168414-30168770	HepG2	liver:	n/a	n/a
17	BRCA1	chr13:30168238-30168664	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr13:30169993-30170255	Hela-S3	cervix:	n/a	n/a
19	CCNT2	chr13:30168898-30170255	K562	blood:	n/a	n/a
20	CEBPB	chr13:30168313-30170146	Hela-S3	cervix:	n/a	chr13:30168508-30168521 chr13:30169284-30169295
21	CEBPB	chr13:30169023-30169548	MCF-7	breast:	n/a	chr13:30169284-30169295
22	CEBPB	chr13:30169208-30169401	ECC-1	luminal epithelium:	n/a	chr13:30169284-30169295
23	CEBPB	chr13:30169043-30169492	MCF-7	breast:	n/a	chr13:30169284-30169295
24	CEBPB	chr13:30169019-30169486	HepG2	liver:	n/a	chr13:30169284-30169295
25	CEBPB	chr13:30168935-30169486	IMR90	lung:	n/a	chr13:30169284-30169295
26	CEBPB	chr13:30168325-30168684	K562	blood:	n/a	chr13:30168508-30168521
27	CEBPB	chr13:30168343-30168621	K562	blood:	n/a	chr13:30168508-30168521
28	CEBPB	chr13:30169072-30169453	K562	blood:	n/a	chr13:30169284-30169295
29	CEBPB	chr13:30169042-30169478	HepG2	liver:	n/a	chr13:30169284-30169295
30	CEBPB	chr13:30169173-30169413	HepG2	liver:	n/a	chr13:30169284-30169295
31	CEBPB	chr13:30168334-30168752	A549	lung:	n/a	chr13:30168508-30168521
32	CEBPB	chr13:30169121-30169433	K562	blood:	n/a	chr13:30169284-30169295
33	CEBPB	chr13:30169002-30169477	ECC-1	luminal epithelium:	n/a	chr13:30169284-30169295
34	CEBPB	chr13:30168973-30169493	K562	blood:	n/a	chr13:30169284-30169295
35	CEBPB	chr13:30169078-30169587	A549	lung:	n/a	chr13:30169284-30169295
36	CEBPB	chr13:30168347-30168785	MCF-7	breast:	n/a	chr13:30168508-30168521
37	CEBPB	chr13:30169114-30169481	A549	lung:	n/a	chr13:30169284-30169295
38	CEBPB	chr13:30168325-30168754	HepG2	liver:	n/a	chr13:30168508-30168521
39	CEBPB	chr13:30168221-30168843	A549	lung:	n/a	chr13:30168508-30168521
40	CEBPB	chr13:30169755-30169796	HepG2	liver:	n/a	n/a
41	CEBPB	chr13:30170234-30170238	A549	lung:	n/a	n/a
42	CEBPB	chr13:30168320-30168725	IMR90	lung:	n/a	chr13:30168508-30168521
43	CEBPB	chr13:30169099-30169456	H1-hESC	embryonic stem cell:	n/a	chr13:30169284-30169295
44	CEBPB	chr13:30168369-30168725	A549	lung:	n/a	chr13:30168508-30168521
45	CEBPD	chr13:30169143-30169344	HepG2	liver:	n/a	n/a
46	CHD1	chr13:30169253-30169448	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD1	chr13:30168359-30169492	GM12878	blood:	n/a	chr13:30169129-30169139 chr13:30169090-30169100
48	CHD1	chr13:30168201-30168983	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD1	chr13:30167920-30170849	IMR90	lung:	n/a	chr13:30169129-30169139 chr13:30169090-30169100
50	CHD2	chr13:30168981-30169340	K562	blood:	n/a	chr13:30169129-30169139 chr13:30169090-30169100

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:30169727-30169777	PrEC	prostate:	n/a
2	chr13:30169249-30169299	AG10803	skin:	n/a
3	chr13:30169825-30169875	GM19239	blood:	n/a
4	chr13:30170094-30170144	BJ	skin:	n/a
5	chr13:30169482-30169532	GM19239	blood:	n/a
6	chr13:30169727-30169777	Caco-2	colon:	n/a
7	chr13:30169249-30169299	HCT-116	colon:	n/a
8	chr13:30170129-30170179	HepG2	liver:	n/a
9	chr13:30169249-30169299	H1-hESC	embryonic stem cell:	embryo
10	chr13:30170844-30170894	RPTEC	kidney:	n/a
11	chr13:30170129-30170179	HEK293	kidney:	embryo
12	chr13:30169727-30169777	HUVEC	blood vessel:	n/a
13	chr13:30169249-30169299	SAEC	small airway:	n/a
14	chr13:30170122-30170172	MCF-7	breast:	n/a
15	chr13:30170129-30170179	HUVEC	blood vessel:	n/a
16	chr13:30170122-30170172	A549	lung:	n/a
17	chr13:30169482-30169532	NHDF-neo	bronchial:	n/a
18	chr13:30169249-30169299	NH-A	brain:	n/a
19	chr13:30170844-30170894	AoSMC	blood vessel:	n/a
20	chr13:30170129-30170179	MCF-7	breast:	n/a
21	chr13:30169825-30169875	LNCaP	prostate:	n/a
22	chr13:30170844-30170894	A549	lung:	n/a
23	chr13:30170094-30170144	HEK293	kidney:	embryo
24	chr13:30170844-30170894	GM12891	blood:	n/a
25	chr13:30169727-30169777	HAEpiC	amniotic membrane:	n/a
26	chr13:30169482-30169532	ovcar-3	ovarian:	n/a
27	chr13:30170122-30170172	Hela-S3	cervix:	n/a
28	chr13:30170844-30170894	HL-60	blood:	n/a
29	chr13:30169482-30169532	AG09309	skin:	n/a
30	chr13:30169727-30169777	U87	brain:	n/a
31	chr13:30170122-30170172	ECC-1	luminal epithelium:	n/a
32	chr13:30170122-30170172	PrEC	prostate:	n/a
33	chr13:30169249-30169299	BE2_C	brain:	n/a
34	chr13:30170094-30170144	Jurkat	blood:	n/a
35	chr13:30170094-30170144	AoSMC	blood vessel:	n/a
36	chr13:30170094-30170144	HepG2	liver:	n/a
37	chr13:30169825-30169875	HUVEC	blood vessel:	n/a
38	chr13:30170844-30170894	BE2_C	brain:	n/a
39	chr13:30169249-30169299	LNCaP	prostate:	n/a
40	chr13:30170129-30170179	HCM	heart:	n/a
41	chr13:30170129-30170179	GM12891	blood:	n/a
42	chr13:30169482-30169532	AG04450	lung:	fetal
43	chr13:30169727-30169777	CMK	blood:	n/a
44	chr13:30169482-30169532	HEK293	kidney:	embryo
45	chr13:30170844-30170894	PrEC	prostate:	n/a
46	chr13:30170094-30170144	NT2-D1	testis:	n/a
47	chr13:30169825-30169875	AG04449	skin:	fetal
48	chr13:30170844-30170894	HRE	kidney:	n/a
49	chr13:30170094-30170144	BE2_C	brain:	n/a
50	chr13:30169482-30169532	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:30168293..30169921-chr13:31039031..31041940,2	K562	blood:
2	chr13:30091097..30092804-chr13:30167943..30169459,2	K562	blood:
3	chr13:30069723..30071518-chr13:30169502..30172461,2	MCF-7	breast:
4	chr12:49525036..49525582-chr13:30168706..30169410,2	Hela-S3	cervix:
5	chr13:30169260..30170181-chr14:23398301..23399025,2	HCT-116	colon:
6	chr13:30168942..30169620-chr2:220094024..220094805,2	Hela-S3	cervix:
7	chr13:30169255..30170193-chr3:73159968..73160573,2	Hela-S3	cervix:
8	chr13:30168290..30169281-chr3:119814085..119814597,2	Hela-S3	cervix:
9	chr13:30093611..30096522-chr13:30167989..30170777,2	MCF-7	breast:
10	chr13:30168902..30170623-chr13:47369921..47372567,2	MCF-7	breast:
11	chr13:30086955..30089041-chr13:30166781..30169428,2	MCF-7	breast:
12	chr13:30170246..30170891-chr4:53525300..53526271,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MTUS2-2	chr13:30170020-30170280	XLOC_010330
2	lnc-MTUS2-2	chr13:30170824-30170919	XLOC_010330

Variant related genes	Relation type
SLC7A1	TF binding region
SLC7A1	CpG island
ENSG00000100462	chromatin interactions
ENSG00000139514	chromatin interactions
ENSG00000258017	chromatin interactions
ENSG00000198925	chromatin interactions
ENSG00000132938	chromatin interactions
ENSG00000109189	chromatin interactions
ENSG00000123416	chromatin interactions
ENSG00000139684	chromatin interactions
ENSG00000163516	chromatin interactions
ENSG00000248866	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000242622	chromatin interactions
ENSG00000257285	chromatin interactions
ENSG00000189403	chromatin interactions

Extended variants
information (count: 78 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:78 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533844552	chr13:30168589-30168590	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs555206329	chr13:30168676-30168677	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs9508501	chr13:30168693-30168694	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs534335929	chr13:30168702-30168703	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs548790084	chr13:30168742-30168743	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs144079641	chr13:30168766-30168767	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs191355500	chr13:30168787-30168788	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs367940523	chr13:30168803-30168804	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs566630600	chr13:30168804-30168805	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs535518698	chr13:30168854-30168855	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs183811304	chr13:30168859-30168860	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs555290359	chr13:30168902-30168903	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs145014058	chr13:30168926-30168927	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs537779666	chr13:30168987-30168988	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs558018500	chr13:30169036-30169037	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs369331946	chr13:30169050-30169051	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs4769763	chr13:30169098-30169099	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs111324208	chr13:30169140-30169141	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs140166390	chr13:30169174-30169175	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs114917727	chr13:30169192-30169193	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs368867170	chr13:30169232-30169233	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs573796049	chr13:30169250-30169251	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs12872613	chr13:30169307-30169308	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
24	rs555731742	chr13:30169314-30169315	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
25	rs35499262	chr13:30169459-30169460	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs542678731	chr13:30169467-30169468	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs372160330	chr13:30169498-30169499	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs77871962	chr13:30169521-30169522	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs544617158	chr13:30169533-30169534	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs73454246	chr13:30169550-30169551	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs533397262	chr13:30169634-30169635	Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs546601066	chr13:30169638-30169639	Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs140060217	chr13:30169644-30169645	Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs555770903	chr13:30169662-30169663	Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs76676938	chr13:30169666-30169667	Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs566497537	chr13:30169799-30169800	Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs61947180	chr13:30169861-30169862	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs549436003	chr13:30169920-30169921	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs558575413	chr13:30170011-30170012	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs575151300	chr13:30170048-30170049	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
41	rs575641690	chr13:30170069-30170070	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
42	rs9579416	chr13:30170111-30170112	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
43	rs538035919	chr13:30170125-30170126	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
44	rs192051656	chr13:30170136-30170137	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
45	rs374785866	chr13:30170151-30170152	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
46	rs534044148	chr13:30170156-30170157	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
47	rs71427274	chr13:30170167-30170168	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs573656197	chr13:30170176-30170177	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
49	rs543816096	chr13:30170209-30170210	Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
50	rs73454247	chr13:30170211-30170212	Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	18698080	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	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
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	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
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Squamous cell cancer	20885788	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Malignant glioma	17146433	CNVD
Breast cancer	17899364	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Retinoblastoma	22278416	CNVD
Peters Plus syndrome	16909395	CNVD
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Ovarian cancer	19047089	CNVD
Alveolar rhabdomyosarcoma	16790082	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD

Chromatin state (count:379 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:30157800-30168600	Weak transcription	Ovary	ovary
2	chr13:30158000-30168600	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr13:30164000-30168600	Weak transcription	Right Atrium	heart
4	chr13:30164000-30168600	Weak transcription	Thymus	Thymus
5	chr13:30164400-30168600	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr13:30165400-30168600	Transcr. at gene 5' and 3'	NHEK	skin
7	chr13:30166800-30169000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr13:30167200-30168600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr13:30167200-30168600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
10	chr13:30167400-30168600	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr13:30167400-30170400	Active TSS	H1 Cell Line	embryonic stem cell
12	chr13:30167400-30170400	Active TSS	iPS-20b Cell Line	embryonic stem cell
13	chr13:30167600-30168600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr13:30167600-30168600	Enhancers	Fetal Heart	heart
15	chr13:30167600-30168600	Flanking Active TSS	Dnd41	blood
16	chr13:30167600-30168800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr13:30167600-30168800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr13:30167600-30170200	Active TSS	GM12878-XiMat	blood
19	chr13:30167600-30170400	Active TSS	HUES48 Cell Line	embryonic stem cell
20	chr13:30167600-30170400	Active TSS	A549	lung
21	chr13:30167600-30170400	Active TSS	Hela-S3	cervix
22	chr13:30167600-30170600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr13:30167800-30168600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
24	chr13:30167800-30168600	Active TSS	HSMMtube	muscle
25	chr13:30167800-30169000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr13:30167800-30169000	Flanking Active TSS	HUVEC	blood vessel
27	chr13:30167800-30170400	Active TSS	HUES64 Cell Line	embryonic stem cell
28	chr13:30167800-30170600	Active TSS	Pancreatic Islets	Pancreatic Islet
29	chr13:30168000-30168800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr13:30168000-30169000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
31	chr13:30168000-30169200	Enhancers	Fetal Brain Male	brain
32	chr13:30168000-30170000	Active TSS	Primary T helper cells PMA-I stimulated	--
33	chr13:30168000-30170000	Active TSS	HMEC	breast
34	chr13:30168000-30170200	Active TSS	Breast Myoepithelial Primary Cells	Breast
35	chr13:30168000-30170400	Active TSS	ES-I3 Cell Line	embryonic stem cell
36	chr13:30168000-30170400	Active TSS	K562	blood
37	chr13:30168200-30168600	Enhancers	Primary B cells from cord blood	blood
38	chr13:30168200-30168600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
39	chr13:30168200-30168600	Active TSS	Placenta	Placenta
40	chr13:30168200-30168600	Enhancers	Spleen	Spleen
41	chr13:30168200-30168800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr13:30168200-30168800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr13:30168200-30168800	Flanking Active TSS	Primary T cells from cord blood	blood
44	chr13:30168200-30168800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
45	chr13:30168200-30168800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
46	chr13:30168200-30168800	Flanking Active TSS	Osteobl	bone
47	chr13:30168200-30169000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr13:30168200-30169000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
49	chr13:30168200-30169000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
50	chr13:30168200-30169200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin

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