Variant report

Variant	esv3345234
Chromosome Location	chr14:56045824-56048372
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:532)
CpG islands
(count:612)
Chromatin interactive
region (count:11)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:532 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:56045690-56045890	K562	blood:	n/a	n/a
2	ARID3A	chr14:56046048-56046085	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:56046597-56046900	HepG2	liver:	n/a	n/a
4	BACH1	chr14:56045735-56046148	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr14:56046476-56046887	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr14:56046380-56046864	A549	lung:	n/a	chr14:56046777-56046790
7	BCLAF1	chr14:56047551-56048158	GM12878	blood:	n/a	chr14:56047631-56047644
8	BCLAF1	chr14:56046273-56046733	GM12878	blood:	n/a	n/a
9	BHLHE40	chr14:56046392-56047138	GM12878	blood:	n/a	n/a
10	BHLHE40	chr14:56046499-56047013	HepG2	liver:	n/a	n/a
11	BHLHE40	chr14:56047504-56047657	K562	blood:	n/a	n/a
12	BHLHE40	chr14:56046497-56047036	K562	blood:	n/a	n/a
13	BRCA1	chr14:56047910-56048053	HepG2	liver:	n/a	n/a
14	BRCA1	chr14:56046449-56046836	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr14:56047798-56047932	GM12878	blood:	n/a	n/a
16	BRCA1	chr14:56046584-56046800	HepG2	liver:	n/a	n/a
17	BRCA1	chr14:56046498-56046765	GM12878	blood:	n/a	n/a
18	BRCA1	chr14:56047663-56048330	Hela-S3	cervix:	n/a	n/a
19	CCNT2	chr14:56046541-56047888	K562	blood:	n/a	n/a
20	CEBPB	chr14:56047415-56047938	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr14:56047522-56047722	HepG2	liver:	n/a	n/a
22	CEBPD	chr14:56046783-56047170	HepG2	liver:	n/a	n/a
23	CHD1	chr14:56046422-56046973	GM12878	blood:	n/a	chr14:56046914-56046924 chr14:56046909-56046919
24	CHD1	chr14:56046308-56046859	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD1	chr14:56045664-56048621	IMR90	lung:	n/a	chr14:56046914-56046924 chr14:56046909-56046919 chr14:56047666-56047676
26	CHD1	chr14:56047373-56048096	H1-hESC	embryonic stem cell:	n/a	chr14:56047666-56047676
27	CHD1	chr14:56047371-56047753	GM12878	blood:	n/a	chr14:56047666-56047676
28	CHD2	chr14:56046477-56046829	K562	blood:	n/a	n/a
29	CHD2	chr14:56046387-56047163	Hela-S3	cervix:	n/a	chr14:56046914-56046924 chr14:56046909-56046919
30	CHD2	chr14:56046435-56046924	GM12878	blood:	n/a	chr14:56046914-56046924 chr14:56046909-56046919
31	CHD2	chr14:56045736-56046095	GM12878	blood:	n/a	n/a
32	CHD2	chr14:56047210-56048298	GM12878	blood:	n/a	chr14:56047666-56047676
33	CHD2	chr14:56047368-56048028	Hela-S3	cervix:	n/a	chr14:56047666-56047676
34	CHD2	chr14:56046391-56046811	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr14:56047381-56047969	K562	blood:	n/a	chr14:56047666-56047676
36	CHD2	chr14:56046448-56046889	HepG2	liver:	n/a	n/a
37	CHD2	chr14:56047362-56047863	HepG2	liver:	n/a	chr14:56047666-56047676
38	CREB1	chr14:56046349-56047166	HepG2	liver:	n/a	n/a
39	CREB1	chr14:56046557-56047194	A549	lung:	n/a	n/a
40	CREB1	chr14:56047422-56047706	A549	lung:	n/a	n/a
41	CTCF	chr14:56047480-56047630	GM12873	blood:	n/a	chr14:56047590-56047603
42	CTCF	chr14:56047500-56047650	GM12865	blood:	n/a	chr14:56047590-56047603
43	CTCF	chr14:56047440-56047590	GM12874	blood:	n/a	n/a
44	CTCF	chr14:56047520-56047670	HEEpiC	esophagus:	n/a	chr14:56047590-56047603
45	CTCF	chr14:56047500-56047650	HCFaa	heart:	n/a	chr14:56047590-56047603
46	CTCF	chr14:56047540-56047690	GM12872	blood:	n/a	chr14:56047590-56047603
47	CTCF	chr14:56047380-56047530	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr14:56047840-56047990	HRE	kidney:	n/a	n/a
49	CTCF	chr14:56047740-56047890	HCM	heart:	n/a	n/a
50	CTCF	chr14:56047680-56047830	BJ	skin:	n/a	n/a

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:56045894-56045944	HMEC	breast:	n/a
2	chr14:56046001-56046051	H1-hESC	embryonic stem cell:	embryo
3	chr14:56045894-56045944	HMEC	breast:	n/a
4	chr14:56046001-56046051	H1-hESC	embryonic stem cell:	embryo
5	chr14:56046098-56046148	GM12892	blood:	n/a
6	chr14:56046685-56046735	HCPEpiC	choroid plexus:	n/a
7	chr14:56047964-56048014	LNCaP	prostate:	n/a
8	chr14:56046001-56046051	PFSK-1	brain:	n/a
9	chr14:56046697-56046747	K562	blood:	n/a
10	chr14:56046685-56046735	HepG2	liver:	n/a
11	chr14:56047471-56047521	HCM	heart:	n/a
12	chr14:56047471-56047521	A549	lung:	n/a
13	chr14:56046685-56046735	AG04449	skin:	fetal
14	chr14:56046098-56046148	SK-N-SH_RA	brain:	n/a
15	chr14:56047964-56048014	HUVEC	blood vessel:	n/a
16	chr14:56047964-56048014	HCM	heart:	n/a
17	chr14:56045827-56045877	HIPEpiC	eye:	n/a
18	chr14:56046098-56046148	SK-N-MC	brain:	n/a
19	chr14:56047964-56048014	AG10803	skin:	n/a
20	chr14:56047923-56047973	Jurkat	blood:	n/a
21	chr14:56046685-56046735	NB4	blood:	n/a
22	chr14:56046098-56046148	AG10803	skin:	n/a
23	chr14:56047471-56047521	PFSK-1	brain:	n/a
24	chr14:56047764-56047814	HepG2	liver:	n/a
25	chr14:56046685-56046735	LNCaP	prostate:	n/a
26	chr14:56046697-56046747	HRCEpiC	kidney:	n/a
27	chr14:56047964-56048014	T-47D	breast:	n/a
28	chr14:56047964-56048014	HIPEpiC	eye:	n/a
29	chr14:56046001-56046051	HRCEpiC	kidney:	n/a
30	chr14:56045827-56045877	NB4	blood:	n/a
31	chr14:56046697-56046747	Hepatocyte	liver:	n/a
32	chr14:56045827-56045877	ovcar-3	ovarian:	n/a
33	chr14:56047471-56047521	GM19239	blood:	n/a
34	chr14:56046685-56046735	HRPEpiC	eye:	n/a
35	chr14:56046697-56046747	SKMC	muscle:	n/a
36	chr14:56045894-56045944	AG04449	skin:	fetal
37	chr14:56046001-56046051	A549	lung:	n/a
38	chr14:56046098-56046148	HCT-116	colon:	n/a
39	chr14:56047923-56047973	HepG2	liver:	n/a
40	chr14:56047964-56048014	HCPEpiC	choroid plexus:	n/a
41	chr14:56046001-56046051	HEK293	kidney:	embryo
42	chr14:56046098-56046148	U87	brain:	n/a
43	chr14:56046685-56046735	HEK293	kidney:	embryo
44	chr14:56046098-56046148	IMR90	lung:	fetal
45	chr14:56045894-56045944	GM12892	blood:	n/a
46	chr14:56047471-56047521	Hela-S3	cervix:	n/a
47	chr14:56047764-56047814	HCPEpiC	choroid plexus:	n/a
48	chr14:56046697-56046747	PANC-1	pancreas:	n/a
49	chr14:56046098-56046148	MCF10A-Er-Src	breast:	n/a
50	chr14:56045894-56045944	LNCaP	prostate:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:151964961..151965492-chr14:56046820..56047820,2	Hela-S3	cervix:
2	chr14:56046559..56049206-chr14:56078372..56080917,2	MCF-7	breast:
3	chr14:56047540..56051954-chr14:56053859..56059782,6	K562	blood:
4	chr12:21654164..21654736-chr14:56046727..56047402,2	Hela-S3	cervix:
5	chr14:56047768..56050679-chr14:56060569..56062105,2	K562	blood:
6	chr14:56022620..56026445-chr14:56044953..56047966,3	MCF-7	breast:
7	chr14:56046884..56048461-chr14:56110849..56113567,2	K562	blood:
8	chr14:55737342..55739119-chr14:56046136..56048438,2	K562	blood:
9	chr14:55946573..55948131-chr14:56047906..56049458,2	K562	blood:
10	chr14:55905450..55907568-chr14:56045550..56047292,2	MCF-7	breast:
11	chr14:56046261..56047012-chr19:41869306..41870109,2	NB4	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TBPL2-1	chr14:56046654-56046810	XLOC_011036
2	lnc-TBPL2-1	chr14:56046654-56046792	ENSG00000186615.6
3	lnc-TBPL2-1	chr14:56046654-56046810	ENSG00000186615
4	lnc-TBPL2-1	chr14:56046654-56046828	ENSG00000186615
5	lnc-TBPL2-1	chr14:56046654-56046814	ENSG00000186615
6	lnc-TBPL2-1	chr14:56046654-56046810	ENSG00000186615.6
7	lnc-TBPL2-1	chr14:56046654-56046810	XLOC_011036

No data

Variant related genes	Relation type
KTN1-AS1	TF binding region
KTN1	TF binding region
KTN1-AS1	CpG island
KTN1	CpG island
ENSG00000178974	chromatin interactions
ENSG00000123810	chromatin interactions
ENSG00000182521	chromatin interactions
ENSG00000004700	chromatin interactions
ENSG00000197747	chromatin interactions
ENSG00000258413	chromatin interactions
ENSG00000111711	chromatin interactions
ENSG00000142046	chromatin interactions
ENSG00000126777	chromatin interactions
SRRM1	miRNA target sites
TRRAP	miRNA target sites
GPATCH8	miRNA target sites

Extended variants
information (count: 109 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:109 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79849469	chr14:56045886-56045887	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs544187224	chr14:56045919-56045920	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs186680625	chr14:56045925-56045926	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs10146870	chr14:56045932-56045933	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs534743241	chr14:56045933-56045934	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs149249262	chr14:56045938-56045939	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs568223403	chr14:56045949-56045950	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs535531259	chr14:56045988-56045989	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs554771092	chr14:56046003-56046004	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs146171031	chr14:56046009-56046010	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs10149408	chr14:56046075-56046076	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs191591781	chr14:56046104-56046105	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs35256757	chr14:56046115-56046116	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs538821493	chr14:56046124-56046125	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs111467375	chr14:56046159-56046160	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	mRNA abundance
16	rs371186580	chr14:56046174-56046175	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs577205504	chr14:56046175-56046176	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs541039018	chr14:56046184-56046185	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs559346829	chr14:56046188-56046189	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs560406944	chr14:56046285-56046286	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs138133948	chr14:56046317-56046318	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs541528358	chr14:56046325-56046326	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs374951134	chr14:56046358-56046359	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs563381892	chr14:56046395-56046396	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs182997571	chr14:56046404-56046405	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs186109770	chr14:56046418-56046419	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs189557383	chr14:56046422-56046423	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs79438225	chr14:56046423-56046424	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs549323761	chr14:56046441-56046442	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs373668966	chr14:56046457-56046458	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs538112162	chr14:56046467-56046468	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs567121539	chr14:56046498-56046499	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs183335303	chr14:56046501-56046502	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs568085777	chr14:56046538-56046539	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs10138893	chr14:56046561-56046562	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs550828153	chr14:56046584-56046585	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs569310739	chr14:56046716-56046717	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
38	rs111309189	chr14:56046798-56046799	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	mRNA abundance
39	rs558746705	chr14:56046815-56046816	Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
40	rs570765371	chr14:56046829-56046830	Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
41	rs534889870	chr14:56046830-56046831	Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
42	rs187641359	chr14:56046837-56046838	Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
43	rs574383918	chr14:56046839-56046840	Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
44	rs541788221	chr14:56046865-56046866	Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
45	rs556826941	chr14:56046883-56046884	Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
46	rs575290356	chr14:56046886-56046887	Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
47	rs545996105	chr14:56046913-56046914	Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
48	rs564293095	chr14:56046934-56046935	Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
49	rs528780810	chr14:56046948-56046949	Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
50	rs534439479	chr14:56046972-56046973	Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21633010	CNVD
Breast cancer	22032731	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Medulloblastoma	19270706	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	17603634	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	21163964	CNVD
Cancer	20164919	CNVD

Chromatin state (count:344 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:56034200-56046000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr14:56044600-56046000	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr14:56045000-56046200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr14:56045200-56046000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
5	chr14:56045200-56046000	Flanking Active TSS	HSMMtube	muscle
6	chr14:56045200-56048000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr14:56045200-56048200	Active TSS	NHDF-Ad	bronchial
8	chr14:56045200-56048400	Active TSS	Ovary	ovary
9	chr14:56045200-56048400	Active TSS	A549	lung
10	chr14:56045200-56050000	Active TSS	GM12878-XiMat	blood
11	chr14:56045400-56046000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr14:56045400-56046000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
13	chr14:56045400-56046000	Enhancers	Primary T killer memory cells from peripheral blood	blood
14	chr14:56045400-56046000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
15	chr14:56045400-56046000	Flanking Active TSS	Adipose Nuclei	Adipose
16	chr14:56045400-56046000	Flanking Active TSS	K562	blood
17	chr14:56045400-56046000	Flanking Active TSS	NHEK	skin
18	chr14:56045400-56046200	Active TSS	Stomach Smooth Muscle	stomach
19	chr14:56045400-56046400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr14:56045400-56046400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr14:56045400-56047200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr14:56045400-56047800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr14:56045400-56047800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr14:56045400-56048000	Active TSS	Brain Cingulate Gyrus	brain
25	chr14:56045400-56048000	Active TSS	Brain Hippocampus Middle	brain
26	chr14:56045400-56048000	Active TSS	Brain Inferior Temporal Lobe	brain
27	chr14:56045400-56048000	Active TSS	Duodenum Smooth Muscle	Duodenum
28	chr14:56045400-56048000	Active TSS	Right Ventricle	heart
29	chr14:56045400-56048200	Active TSS	HMEC	breast
30	chr14:56045400-56048400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr14:56045600-56046000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
32	chr14:56045600-56046000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
33	chr14:56045600-56046000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
34	chr14:56045600-56046000	Flanking Active TSS	Brain Angular Gyrus	brain
35	chr14:56045600-56046000	Flanking Active TSS	Fetal Intestine Small	intestine
36	chr14:56045600-56046000	Flanking Active TSS	Fetal Stomach	stomach
37	chr14:56045600-56046000	Flanking Active TSS	Left Ventricle	heart
38	chr14:56045600-56046000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
39	chr14:56045600-56046000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
40	chr14:56045600-56046000	Flanking Active TSS	HepG2	liver
41	chr14:56045600-56046000	Flanking Active TSS	HSMM	muscle
42	chr14:56045600-56046000	Flanking Active TSS	Osteobl	bone
43	chr14:56045600-56046200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
44	chr14:56045600-56046200	Flanking Active TSS	Primary T cells from cord blood	blood
45	chr14:56045600-56046200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
46	chr14:56045600-56046200	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
47	chr14:56045600-56046200	Flanking Active TSS	Fetal Brain Male	brain
48	chr14:56045600-56046200	Flanking Active TSS	Fetal Brain Female	brain
49	chr14:56045600-56046200	Flanking Active TSS	Hela-S3	cervix
50	chr14:56045600-56046400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--

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