Variant report

Variant	esv9830
Chromosome Location	chr14:24420325-24423668
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	chr14:24422800-24422908	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:24421080-24421116	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:24423178-24423574	HepG2	liver:	n/a	n/a
4	ATF3	chr14:24423153-24423533	A549	lung:	n/a	n/a
5	BCL11A	chr14:24423190-24423452	GM12878	blood:	n/a	n/a
6	BCL3	chr14:24422958-24423594	A549	lung:	n/a	n/a
7	BCLAF1	chr14:24422706-24423635	GM12878	blood:	n/a	n/a
8	BHLHE40	chr14:24422805-24422983	GM12878	blood:	n/a	n/a
9	BHLHE40	chr14:24423117-24423544	K562	blood:	n/a	n/a
10	BHLHE40	chr14:24422878-24423495	HepG2	liver:	n/a	n/a
11	BHLHE40	chr14:24422789-24422794	K562	blood:	n/a	n/a
12	BRCA1	chr14:24422911-24423016	HepG2	liver:	n/a	n/a
13	BRCA1	chr14:24423242-24423570	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr14:24423250-24423488	HepG2	liver:	n/a	n/a
15	CCNT2	chr14:24422729-24423159	K562	blood:	n/a	chr14:24422739-24422748
16	CEBPB	chr14:24423252-24423596	HepG2	liver:	n/a	chr14:24423462-24423473
17	CEBPB	chr14:24423214-24423650	Hela-S3	cervix:	n/a	chr14:24423462-24423473
18	CEBPB	chr14:24423302-24423566	IMR90	lung:	n/a	chr14:24423462-24423473
19	CEBPB	chr14:24423287-24423491	K562	blood:	n/a	chr14:24423462-24423473
20	CEBPB	chr14:24423255-24423518	HepG2	liver:	n/a	chr14:24423462-24423473
21	CEBPB	chr14:24423180-24423697	A549	lung:	n/a	chr14:24423462-24423473
22	CEBPB	chr14:24423347-24423547	K562	blood:	n/a	chr14:24423462-24423473
23	CEBPB	chr14:24422846-24423653	HepG2	liver:	n/a	chr14:24423462-24423473
24	CEBPD	chr14:24423163-24423525	HepG2	liver:	n/a	n/a
25	CEBPD	chr14:24422665-24423162	HepG2	liver:	n/a	n/a
26	CEBPD	chr14:24422642-24423596	HepG2	liver:	n/a	n/a
27	CHD1	chr14:24422741-24423601	IMR90	lung:	n/a	chr14:24422888-24422898
28	CHD1	chr14:24422828-24423012	GM12878	blood:	n/a	chr14:24422888-24422898
29	CHD1	chr14:24422790-24422885	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr14:24421057-24421194	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr14:24422857-24423550	Hela-S3	cervix:	n/a	chr14:24422888-24422898
32	CHD2	chr14:24422988-24423442	HepG2	liver:	n/a	n/a
33	CHD2	chr14:24422812-24422880	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr14:24423190-24423469	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr14:24422754-24423425	GM12878	blood:	n/a	chr14:24422888-24422898
36	CREB1	chr14:24422781-24423566	A549	lung:	n/a	n/a
37	CTBP2	chr14:24422733-24423440	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr14:24420980-24421130	HMF	breast:	n/a	chr14:24421108-24421124 chr14:24421107-24421125
39	CTCF	chr14:24423320-24423470	GM12864	blood:	n/a	chr14:24423405-24423426 chr14:24423411-24423427 chr14:24423410-24423428
40	CTCF	chr14:24423276-24423519	MCF-7	breast:	n/a	chr14:24423405-24423426 chr14:24423411-24423427 chr14:24423410-24423428
41	CTCF	chr14:24423167-24423688	A549	lung:	n/a	chr14:24423405-24423426 chr14:24423411-24423427 chr14:24423410-24423428
42	CTCF	chr14:24423252-24423522	T-47D	breast:	n/a	chr14:24423405-24423426 chr14:24423411-24423427 chr14:24423410-24423428
43	CTCF	chr14:24423280-24423430	WI-38	lung:	n/a	chr14:24423405-24423426 chr14:24423411-24423427 chr14:24423410-24423428
44	CTCF	chr14:24422980-24423130	HRPEpiC	eye:	n/a	n/a
45	CTCF	chr14:24421065-24421187	MCF-7	breast:	n/a	chr14:24421108-24421124 chr14:24421107-24421125
46	CTCF	chr14:24423320-24423470	GM12869	blood:	n/a	chr14:24423405-24423426 chr14:24423411-24423427 chr14:24423410-24423428
47	CTCF	chr14:24423320-24423470	GM06990	blood:	n/a	chr14:24423405-24423426 chr14:24423411-24423427 chr14:24423410-24423428
48	CTCF	chr14:24423340-24423490	HEEpiC	esophagus:	n/a	chr14:24423405-24423426 chr14:24423411-24423427 chr14:24423410-24423428
49	CTCF	chr14:24423320-24423470	NHEK	skin:	n/a	chr14:24423405-24423426 chr14:24423411-24423427 chr14:24423410-24423428
50	CTCF	chr14:24422620-24422770	GM12871	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:24420715-24420765	HEK293	kidney:	embryo
2	chr14:24423618-24423668	AoSMC	blood vessel:	n/a
3	chr14:24422928-24422978	HepG2	liver:	n/a
4	chr14:24422837-24422887	BJ	skin:	n/a
5	chr14:24422956-24423006	AoSMC	blood vessel:	n/a
6	chr14:24422419-24422469	ovcar-3	ovarian:	n/a
7	chr14:24423140-24423190	HEK293	kidney:	embryo
8	chr14:24423199-24423249	GM19239	blood:	n/a
9	chr14:24422419-24422469	Hepatocyte	liver:	n/a
10	chr14:24423199-24423249	SKMC	muscle:	n/a
11	chr14:24423199-24423249	T-47D	breast:	n/a
12	chr14:24422837-24422887	SK-N-SH	brain:	n/a
13	chr14:24423618-24423668	HEK293	kidney:	embryo
14	chr14:24423618-24423668	PrEC	prostate:	n/a
15	chr14:24420715-24420765	HPAEpiC	pulmonary alveolar:	n/a
16	chr14:24422368-24422418	HRCEpiC	kidney:	n/a
17	chr14:24422928-24422978	HEK293	kidney:	embryo
18	chr14:24422916-24422966	Hepatocyte	liver:	n/a
19	chr14:24423140-24423190	AG09309	skin:	n/a
20	chr14:24422956-24423006	ovcar-3	ovarian:	n/a
21	chr14:24422368-24422418	HepG2	liver:	n/a
22	chr14:24423031-24423081	Caco-2	colon:	n/a
23	chr14:24423140-24423190	GM12878	blood:	n/a
24	chr14:24423483-24423533	GM19239	blood:	n/a
25	chr14:24422916-24422966	IMR90	lung:	fetal
26	chr14:24422749-24422799	SK-N-MC	brain:	n/a
27	chr14:24422368-24422418	AG10803	skin:	n/a
28	chr14:24422956-24423006	AG09309	skin:	n/a
29	chr14:24422956-24423006	GM12892	blood:	n/a
30	chr14:24422837-24422887	NT2-D1	testis:	n/a
31	chr14:24423031-24423081	NH-A	brain:	n/a
32	chr14:24423031-24423081	HNPCEpiC	eye:	n/a
33	chr14:24422916-24422966	AG09319	gingival:	n/a
34	chr14:24422916-24422966	AG10803	skin:	n/a
35	chr14:24422749-24422799	HCPEpiC	choroid plexus:	n/a
36	chr14:24422916-24422966	HCT-116	colon:	n/a
37	chr14:24423199-24423249	HPAEpiC	pulmonary alveolar:	n/a
38	chr14:24422928-24422978	AG04449	skin:	fetal
39	chr14:24422928-24422978	HEEpiC	esophagus:	n/a
40	chr14:24422749-24422799	GM12878	blood:	n/a
41	chr14:24422749-24422799	NH-A	brain:	n/a
42	chr14:24422872-24422922	HCM	heart:	n/a
43	chr14:24422872-24422922	HepG2	liver:	n/a
44	chr14:24422837-24422887	MCF-7	breast:	n/a
45	chr14:24420715-24420765	HIPEpiC	eye:	n/a
46	chr14:24422419-24422469	AG09319	gingival:	n/a
47	chr14:24423483-24423533	HRPEpiC	eye:	n/a
48	chr14:24422956-24423006	K562	blood:	n/a
49	chr14:24423483-24423533	HCT-116	colon:	n/a
50	chr14:24423199-24423249	HRE	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:24421741..24423927-chr14:24582561..24584260,2	K562	blood:
2	chr14:24036767..24038500-chr14:24420729..24424068,4	MCF-7	breast:
3	chr14:24099084..24100809-chr14:24421080..24423663,2	MCF-7	breast:
4	chr14:24422551..24423442-chr5:180229136..180229785,2	HCT-116	colon:
5	chr14:24422701..24424551-chr14:24504249..24506129,2	MCF-7	breast:
6	chr14:24398247..24400471-chr14:24419661..24421717,2	MCF-7	breast:
7	chr14:24197895..24200996-chr14:24421897..24424681,3	MCF-7	breast:
8	chr14:24422915..24424427-chr14:24563237..24565374,2	MCF-7	breast:
9	chr1:186344468..186345047-chr14:24423051..24423847,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NRL-1	chr14:24422783-24423331	ENSG00000215256.3
2	lnc-NRL-1	chr14:24422518-24422578	ENSG00000215256.3
3	lnc-NRL-1	chr14:24422983-24423242	ENSG00000215256.3
4	lnc-NRL-1	chr14:24422983-24423242	NR_023923
5	lnc-NRL-1	chr14:24422783-24423392	NONHSAT035954
6	lnc-NRL-1	chr14:24422783-24423406	NR_023921
7	lnc-NRL-1	chr14:24423334-24423406	NR_023923
8	lnc-NRL-1	chr14:24422983-24423242	NONHSAT035952
9	lnc-NRL-1	chr14:24423334-24423392	NONHSAT035952
10	lnc-NRL-1	chr14:24422983-24423061	ENSG00000215256.3
11	lnc-NRL-1	chr14:24422983-24423406	ENSG00000215256.3
12	lnc-NRL-1	chr14:24422199-24422628	ENSG00000215256.3
13	lnc-NRL-1	chr14:24423334-24423375	ENSG00000215256.3

Variant related genes	Relation type
DHRS4	TF binding region
DHRS4-AS1	TF binding region
DHRS4	CpG island
DHRS4-AS1	CpG island
ENSG00000100897	chromatin interactions
ENSG00000100867	chromatin interactions
ENSG00000225766	chromatin interactions
ENSG00000129535	chromatin interactions
ENSG00000131446	chromatin interactions
ENSG00000157181	chromatin interactions
ENSG00000100889	chromatin interactions
ENSG00000047410	chromatin interactions
ENSG00000258464	chromatin interactions
ENSG00000213983	chromatin interactions

Extended variants
information (count: 233 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:233 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76872010	chr14:24420326-24420327	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs73600716	chr14:24420329-24420330	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs536072678	chr14:24420338-24420339	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs549689616	chr14:24420362-24420363	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs73600717	chr14:24420372-24420373	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs572711008	chr14:24420410-24420411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs74036727	chr14:24420427-24420428	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs368057416	chr14:24420457-24420458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs111437306	chr14:24420490-24420491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs201817119	chr14:24420491-24420492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs60177702	chr14:24420498-24420499	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs371769797	chr14:24420583-24420584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs575941039	chr14:24420589-24420590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs59434518	chr14:24420597-24420598	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs181119761	chr14:24420603-24420604	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs563409108	chr14:24420625-24420626	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs529057321	chr14:24420626-24420627	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs28693392	chr14:24420642-24420643	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs375385515	chr14:24420648-24420649	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs528388490	chr14:24420652-24420653	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs551309520	chr14:24420662-24420663	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs140633477	chr14:24420715-24420716	Weak transcription ZNF genes & repeats Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs533189370	chr14:24420730-24420731	Weak transcription ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs549839373	chr14:24420734-24420735	Weak transcription ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs369928051	chr14:24420752-24420753	Weak transcription ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs570153100	chr14:24420807-24420808	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs535638709	chr14:24420808-24420809	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs570266206	chr14:24420810-24420811	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs116764724	chr14:24420832-24420833	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs571261727	chr14:24420835-24420836	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs538580394	chr14:24420841-24420842	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs185691166	chr14:24420863-24420864	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs577699241	chr14:24420894-24420895	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs543471362	chr14:24420910-24420911	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs189958703	chr14:24420922-24420923	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs28670278	chr14:24420956-24420957	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs542417505	chr14:24420970-24420971	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs559495748	chr14:24420979-24420980	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs528313869	chr14:24421024-24421025	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs200200892	chr14:24421063-24421064	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs544887761	chr14:24421078-24421079	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs61710531	chr14:24421090-24421091	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs397975264	chr14:24421092-24421093	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs35183145	chr14:24421116-24421117	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs564863870	chr14:24421127-24421128	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs145631645	chr14:24421146-24421147	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs10148822	chr14:24421152-24421153	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs553134057	chr14:24421154-24421155	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs574736985	chr14:24421156-24421157	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs10148823	chr14:24421161-24421162	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:61)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Acute lymphoblastic leukemia	20067559	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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Cancer	21183584	CNVD
Leukoplakia	24403051	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Glioblastoma multiforme	21390271	CNVD

Chromatin state (count:529 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:24400600-24421000	Weak transcription	Colon Smooth Muscle	Colon
2	chr14:24402200-24421200	Weak transcription	Rectal Smooth Muscle	rectum
3	chr14:24405600-24422400	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr14:24405800-24421400	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr14:24405800-24422400	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr14:24407000-24421000	Weak transcription	Fetal Intestine Large	intestine
7	chr14:24407000-24421200	Weak transcription	Fetal Kidney	kidney
8	chr14:24407400-24422400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr14:24407600-24422200	Weak transcription	Primary B cells from cord blood	blood
10	chr14:24407800-24422400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr14:24408400-24421200	Weak transcription	Brain Substantia Nigra	brain
12	chr14:24409800-24421000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr14:24410200-24420800	Weak transcription	Spleen	Spleen
14	chr14:24410200-24421000	Weak transcription	Left Ventricle	heart
15	chr14:24410400-24421000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr14:24410400-24421000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr14:24410400-24421000	Weak transcription	Brain Hippocampus Middle	brain
18	chr14:24410400-24421000	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr14:24410400-24421200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr14:24410600-24420600	Weak transcription	Ovary	ovary
21	chr14:24410600-24420800	Weak transcription	Brain Cingulate Gyrus	brain
22	chr14:24410600-24421000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
23	chr14:24410600-24421200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr14:24410600-24421800	Weak transcription	Primary B cells from peripheral blood	blood
25	chr14:24410800-24420600	Weak transcription	Fetal Muscle Leg	muscle
26	chr14:24410800-24420800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr14:24410800-24421000	Weak transcription	Primary T cells fromperipheralblood	blood
28	chr14:24410800-24421000	Weak transcription	Primary T helper cells fromperipheralblood	blood
29	chr14:24410800-24421800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr14:24410800-24422000	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr14:24410800-24422400	Weak transcription	Aorta	Aorta
32	chr14:24411000-24420800	Weak transcription	Duodenum Smooth Muscle	Duodenum
33	chr14:24411000-24421000	Weak transcription	Fetal Muscle Trunk	muscle
34	chr14:24411400-24420800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr14:24412000-24420800	Weak transcription	Lung	lung
36	chr14:24412200-24422400	Weak transcription	Esophagus	oesophagus
37	chr14:24412400-24420800	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr14:24413600-24421400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
39	chr14:24414000-24420800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr14:24419200-24421200	Enhancers	Liver	Liver
41	chr14:24419200-24422200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr14:24419400-24420400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
43	chr14:24419600-24420400	ZNF genes & repeats	Primary T cells from cord blood	blood
44	chr14:24419600-24420400	ZNF genes & repeats	K562	blood
45	chr14:24419600-24421000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr14:24420000-24420400	ZNF genes & repeats	HSMM	muscle
47	chr14:24420000-24420800	Enhancers	Adipose Nuclei	Adipose
48	chr14:24420000-24420800	Weak transcription	Fetal Stomach	stomach
49	chr14:24420000-24421000	Enhancers	Brain Angular Gyrus	brain
50	chr14:24420200-24420600	Weak transcription	Skeletal Muscle Male	skeletal muscle

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