Variant report

Variant	esv3420595
Chromosome Location	chr19:19160552-19164950
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	chr19:19164616-19164816	K562	blood:	n/a	n/a
2	ATF2	chr19:19164618-19164894	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr19:19164691-19164877	GM12878	blood:	n/a	n/a
4	BHLHE40	chr19:19164780-19164804	GM12878	blood:	n/a	n/a
5	BHLHE40	chr19:19164668-19164953	K562	blood:	n/a	n/a
6	CEBPB	chr19:19160240-19160571	K562	blood:	n/a	chr19:19160404-19160415
7	CEBPB	chr19:19162774-19163015	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr19:19160239-19160591	IMR90	lung:	n/a	chr19:19160404-19160415
9	CHD2	chr19:19164778-19164817	GM12878	blood:	n/a	n/a
10	CTCF	chr19:19164643-19164910	HUVEC	blood vessel:	n/a	chr19:19164776-19164794 chr19:19164777-19164793 chr19:19164779-19164792 chr19:19164779-19164788 chr19:19164778-19164799
11	CTCF	chr19:19162480-19162630	WERI-Rb-1	eye:	n/a	n/a
12	CTCF	chr19:19164700-19164850	MCF-7	breast:	n/a	chr19:19164776-19164794 chr19:19164777-19164793 chr19:19164779-19164792 chr19:19164779-19164788 chr19:19164778-19164799
13	CTCF	chr19:19164653-19164956	GM19238	blood:	n/a	chr19:19164776-19164794 chr19:19164777-19164793 chr19:19164779-19164792 chr19:19164779-19164788 chr19:19164778-19164799
14	CTCF	chr19:19164720-19164870	BJ	skin:	n/a	chr19:19164776-19164794 chr19:19164777-19164793 chr19:19164779-19164792 chr19:19164779-19164788 chr19:19164778-19164799
15	CTCF	chr19:19164700-19164850	HRPEpiC	eye:	n/a	chr19:19164776-19164794 chr19:19164777-19164793 chr19:19164779-19164792 chr19:19164779-19164788 chr19:19164778-19164799
16	CTCF	chr19:19164692-19164881	LNCaP	prostate:	n/a	chr19:19164776-19164794 chr19:19164777-19164793 chr19:19164779-19164792 chr19:19164779-19164788 chr19:19164778-19164799
17	CTCF	chr19:19164540-19164690	A549	lung:	n/a	n/a
18	CTCF	chr19:19164700-19164850	HBMEC	blood vessel:	n/a	chr19:19164776-19164794 chr19:19164777-19164793 chr19:19164779-19164792 chr19:19164779-19164788 chr19:19164778-19164799
19	CTCF	chr19:19164660-19164810	MCF-7	breast:	n/a	chr19:19164776-19164794 chr19:19164777-19164793 chr19:19164779-19164792 chr19:19164779-19164788 chr19:19164778-19164799
20	CTCF	chr19:19164638-19164889	SK-N-SH_RA	brain:	n/a	chr19:19164776-19164794 chr19:19164777-19164793 chr19:19164779-19164792 chr19:19164779-19164788 chr19:19164778-19164799
21	CTCF	chr19:19164680-19164830	GM12873	blood:	n/a	chr19:19164776-19164794 chr19:19164777-19164793 chr19:19164779-19164792 chr19:19164779-19164788 chr19:19164778-19164799
22	CTCF	chr19:19164700-19164850	NHEK	skin:	n/a	chr19:19164776-19164794 chr19:19164777-19164793 chr19:19164779-19164792 chr19:19164779-19164788 chr19:19164778-19164799
23	CTCF	chr19:19164740-19164890	Caco-2	colon:	n/a	chr19:19164776-19164794 chr19:19164777-19164793 chr19:19164779-19164792 chr19:19164779-19164788 chr19:19164778-19164799
24	CTCF	chr19:19164584-19164965	IMR90	lung:	n/a	chr19:19164776-19164794 chr19:19164777-19164793 chr19:19164779-19164792 chr19:19164779-19164788 chr19:19164778-19164799
25	CTCF	chr19:19164720-19164870	BE2_C	brain:	n/a	chr19:19164776-19164794 chr19:19164777-19164793 chr19:19164779-19164792 chr19:19164779-19164788 chr19:19164778-19164799
26	CTCF	chr19:19164700-19164850	GM12869	blood:	n/a	chr19:19164776-19164794 chr19:19164777-19164793 chr19:19164779-19164792 chr19:19164779-19164788 chr19:19164778-19164799
27	CTCF	chr19:19164657-19164902	Lung_OC	lung:	n/a	chr19:19164776-19164794 chr19:19164777-19164793 chr19:19164779-19164792 chr19:19164779-19164788 chr19:19164778-19164799
28	CTCF	chr19:19164581-19165009	GM12878	blood:	n/a	chr19:19164776-19164794 chr19:19164777-19164793 chr19:19164779-19164792 chr19:19164779-19164788 chr19:19164778-19164799
29	CTCF	chr19:19164680-19164830	GM12870	blood:	n/a	chr19:19164776-19164794 chr19:19164777-19164793 chr19:19164779-19164792 chr19:19164779-19164788 chr19:19164778-19164799
30	CTCF	chr19:19164700-19164850	GM12878	blood:	n/a	chr19:19164776-19164794 chr19:19164777-19164793 chr19:19164779-19164792 chr19:19164779-19164788 chr19:19164778-19164799
31	CTCF	chr19:19164720-19164870	NHDF-neo	bronchial:	n/a	chr19:19164776-19164794 chr19:19164777-19164793 chr19:19164779-19164792 chr19:19164779-19164788 chr19:19164778-19164799
32	CTCF	chr19:19162366-19162702	K562	blood:	n/a	n/a
33	CTCF	chr19:19164680-19164830	GM12867	blood:	n/a	chr19:19164776-19164794 chr19:19164777-19164793 chr19:19164779-19164792 chr19:19164779-19164788 chr19:19164778-19164799
34	CTCF	chr19:19164935-19164936	GM12891	blood:	n/a	n/a
35	CTCF	chr19:19164480-19164630	GM12867	blood:	n/a	chr19:19164487-19164500
36	CTCF	chr19:19164660-19164810	HEEpiC	esophagus:	n/a	chr19:19164776-19164794 chr19:19164777-19164793 chr19:19164779-19164792 chr19:19164779-19164788 chr19:19164778-19164799
37	CTCF	chr19:19164700-19164850	HCPEpiC	choroid plexus:	n/a	chr19:19164776-19164794 chr19:19164777-19164793 chr19:19164779-19164792 chr19:19164779-19164788 chr19:19164778-19164799
38	CTCF	chr19:19164740-19164890	AG04449	skin:	n/a	chr19:19164777-19164793 chr19:19164778-19164799 chr19:19164776-19164794 chr19:19164779-19164792 chr19:19164779-19164788
39	CTCF	chr19:19164720-19164870	HEK293	kidney:	n/a	chr19:19164776-19164794 chr19:19164777-19164793 chr19:19164779-19164792 chr19:19164779-19164788 chr19:19164778-19164799
40	CTCF	chr19:19164667-19164913	H1-hESC	embryonic stem cell:	n/a	chr19:19164776-19164794 chr19:19164777-19164793 chr19:19164779-19164792 chr19:19164779-19164788 chr19:19164778-19164799
41	CTCF	chr19:19164551-19165070	MCF-7	breast:	n/a	chr19:19164776-19164794 chr19:19164777-19164793 chr19:19164779-19164792 chr19:19164779-19164788 chr19:19164778-19164799
42	CTCF	chr19:19164700-19164850	GM12865	blood:	n/a	chr19:19164776-19164794 chr19:19164777-19164793 chr19:19164779-19164792 chr19:19164779-19164788 chr19:19164778-19164799
43	CTCF	chr19:19164673-19164876	GM13976	blood:	n/a	chr19:19164776-19164794 chr19:19164777-19164793 chr19:19164779-19164792 chr19:19164779-19164788 chr19:19164778-19164799
44	CTCF	chr19:19162420-19162570	HepG2	liver:	n/a	n/a
45	CTCF	chr19:19164400-19164550	GM12874	blood:	n/a	chr19:19164487-19164500
46	CTCF	chr19:19164660-19164810	HFF-Myc	foreskin:	n/a	chr19:19164776-19164794 chr19:19164777-19164793 chr19:19164779-19164792 chr19:19164779-19164788 chr19:19164778-19164799
47	CTCF	chr19:19164324-19165133	SK-N-SH	brain:	n/a	chr19:19164776-19164794 chr19:19164777-19164793 chr19:19164779-19164792 chr19:19164779-19164788 chr19:19164487-19164500 chr19:19164778-19164799
48	CTCF	chr19:19164700-19164850	AG10803	skin:	n/a	chr19:19164776-19164794 chr19:19164777-19164793 chr19:19164779-19164792 chr19:19164779-19164788 chr19:19164778-19164799
49	CTCF	chr19:19164678-19164911	Gliobla	brain:	n/a	chr19:19164776-19164794 chr19:19164777-19164793 chr19:19164779-19164792 chr19:19164779-19164788 chr19:19164778-19164799
50	CTCF	chr19:19164700-19164850	GM12801	blood:	n/a	chr19:19164776-19164794 chr19:19164777-19164793 chr19:19164779-19164792 chr19:19164779-19164788 chr19:19164778-19164799

No.	Distal block	Cell Line	Cell type
1	chr19:19142741..19144460-chr19:19159670..19161319,2	MCF-7	breast:
2	chr19:19150556..19153646-chr19:19160742..19164221,4	K562	blood:
3	chr19:19158546..19161308-chr19:19161560..19163154,2	K562	blood:
4	chr19:19153804..19155400-chr19:19160958..19162912,2	K562	blood:
5	chr19:19162153..19163903-chr19:19245411..19247437,2	K562	blood:
6	chr19:19161417..19167211-chr19:19171135..19175299,5	MCF-7	breast:
7	chr19:19161171..19163416-chr19:19248764..19250387,2	K562	blood:
8	chr19:19164507..19166528-chr19:19249184..19251105,2	K562	blood:
9	chr19:19162360..19163114-chr19:19173888..19174551,2	MCF-7	breast:
10	chr19:19144430..19146064-chr19:19161561..19163477,2	MCF-7	breast:
11	chr19:19110147..19110942-chr19:19162265..19163244,7	MCF-7	breast:
12	chr19:19160117..19161662-chr19:19222753..19224886,2	K562	blood:
13	chr19:19164303..19165014-chr19:19226443..19227934,4	MCF-7	breast:
14	chr19:19161010..19164780-chr19:19249045..19252111,4	MCF-7	breast:
15	chr19:19161051..19163295-chr19:19164654..19166677,2	MCF-7	breast:
16	chr19:19110190..19110827-chr19:19162308..19163244,2	MCF-7	breast:
17	chr19:19042506..19044271-chr19:19163286..19165495,2	K562	blood:
18	chr19:19158546..19161308-chr19:19161560..19163154,2	K562	blood:
19	chr19:19163080..19165123-chr19:19247773..19249964,2	MCF-7	breast:

Variant related genes	Relation type
ARMC6	TF binding region
ENSG00000181035	chromatin interactions
ENSG00000064545	chromatin interactions
ENSG00000105676	chromatin interactions
ENSG00000051128	chromatin interactions
ENSG00000064607	chromatin interactions

Extended variants
information (count: 195 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:195 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201171438	chr19:19160605-19160606	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs534528838	chr19:19160638-19160639	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs554359033	chr19:19160659-19160660	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs376534715	chr19:19160689-19160690	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs181670979	chr19:19160706-19160707	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs185802443	chr19:19160715-19160716	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs576368327	chr19:19160731-19160732	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs149947614	chr19:19160738-19160739	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs544660277	chr19:19160763-19160764	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs537331939	chr19:19160785-19160786	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs190241444	chr19:19160802-19160803	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs558752632	chr19:19160827-19160828	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs8104754	chr19:19160842-19160843	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs541330687	chr19:19160843-19160844	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs76236499	chr19:19160850-19160851	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs560892352	chr19:19160860-19160861	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs376515983	chr19:19160897-19160898	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs529836780	chr19:19160904-19160905	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs549593735	chr19:19160905-19160906	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs116796770	chr19:19160939-19160940	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs185360560	chr19:19161042-19161043	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs563977821	chr19:19161096-19161097	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs571617862	chr19:19161114-19161115	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs534185590	chr19:19161150-19161151	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs527291709	chr19:19161156-19161157	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs548100990	chr19:19161169-19161170	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs568004005	chr19:19161178-19161179	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs79101888	chr19:19161180-19161181	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs556828415	chr19:19161190-19161191	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs576020423	chr19:19161195-19161196	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs190598995	chr19:19161223-19161224	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs558228729	chr19:19161233-19161234	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs572001006	chr19:19161274-19161275	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs184132299	chr19:19161286-19161287	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs560827240	chr19:19161316-19161317	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs73008949	chr19:19161319-19161320	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs543181004	chr19:19161524-19161525	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs144902741	chr19:19161537-19161538	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs188643186	chr19:19161570-19161571	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs559193795	chr19:19161634-19161635	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs551861260	chr19:19161636-19161637	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs567365052	chr19:19161690-19161691	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs192027152	chr19:19161717-19161718	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs527679835	chr19:19161845-19161846	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs75166692	chr19:19161991-19161992	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs574427800	chr19:19162010-19162011	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs4808180	chr19:19162057-19162058	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs550352630	chr19:19162059-19162060	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs570242361	chr19:19162074-19162075	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs369903143	chr19:19162075-19162076	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Follicular lymphoma	20505157	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	20179077	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Lung cancer	17297452	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Chordoma	18071362	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
ovarian endometriomas	16273235	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Cervical cancer	21063398	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Ovarian cancer	21720365	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Basal cell lymphoma	21115979	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21364760	CNVD
Mycobacterial infection	18421352	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute monocytic leukemia	16498392	CNVD
Lung cancer	18438408	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Liver carcinoma	19366792	CNVD
Colorectal cancer	19455253	CNVD
Lujan-Fryns syndrom	21521776	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Cancer	17440070	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Ependymoma	20639864	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:252 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:19145000-19174000	Weak transcription	Small Intestine	intestine
2	chr19:19145400-19165600	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr19:19145400-19171800	Weak transcription	Right Atrium	heart
4	chr19:19145600-19172200	Weak transcription	Stomach Mucosa	stomach
5	chr19:19145600-19173800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr19:19145600-19173800	Weak transcription	Fetal Kidney	kidney
7	chr19:19146600-19161800	Weak transcription	Psoas Muscle	Psoas
8	chr19:19148400-19161600	Weak transcription	Fetal Heart	heart
9	chr19:19149400-19164800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr19:19151000-19173800	Weak transcription	Fetal Brain Male	brain
11	chr19:19151400-19162000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr19:19151800-19166000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr19:19151800-19173800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr19:19151800-19173800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr19:19152600-19173200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
16	chr19:19152800-19161000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr19:19152800-19171400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr19:19153200-19171000	Strong transcription	Monocytes-CD14+_RO01746	blood
19	chr19:19153200-19171200	Strong transcription	HUES64 Cell Line	embryonic stem cell
20	chr19:19153200-19171400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr19:19153200-19172200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr19:19153200-19173600	Strong transcription	Fetal Stomach	stomach
23	chr19:19153400-19163800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr19:19153400-19167400	Strong transcription	Fetal Muscle Leg	muscle
25	chr19:19153400-19168400	Strong transcription	Fetal Intestine Small	intestine
26	chr19:19153400-19168600	Strong transcription	Fetal Intestine Large	intestine
27	chr19:19153400-19169800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr19:19153400-19170400	Strong transcription	H9 Cell Line	embryonic stem cell
29	chr19:19153400-19170800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr19:19153400-19170800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr19:19153400-19170800	Strong transcription	HUES48 Cell Line	embryonic stem cell
32	chr19:19153400-19171000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr19:19153400-19171200	Strong transcription	Cortex derived primary cultured neurospheres	brain
34	chr19:19154800-19161600	Strong transcription	Fetal Thymus	thymus
35	chr19:19155400-19161000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr19:19155400-19161600	Weak transcription	Brain Angular Gyrus	brain
37	chr19:19155400-19162400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr19:19155400-19162400	Weak transcription	Aorta	Aorta
39	chr19:19155400-19165200	Weak transcription	NHDF-Ad	bronchial
40	chr19:19155600-19161000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
41	chr19:19155600-19161400	Weak transcription	A549	lung
42	chr19:19155600-19161600	Weak transcription	Primary neutrophils fromperipheralblood	blood
43	chr19:19155600-19161600	Weak transcription	Right Ventricle	heart
44	chr19:19155600-19162000	Weak transcription	Pancreas	Pancrea
45	chr19:19155600-19162400	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr19:19155600-19162400	Weak transcription	Placenta Amnion	Placenta Amnion
47	chr19:19155600-19162600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr19:19155600-19162600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr19:19155600-19165000	Weak transcription	HUVEC	blood vessel
50	chr19:19155800-19161000	Weak transcription	HMEC	breast

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