Variant report

Variant	esv3347717
Chromosome Location	chr14:55737449-55739397
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	chr14:55737680-55738264	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:55737609-55738095	K562	blood:	n/a	n/a
3	ATF1	chr14:55737763-55738251	K562	blood:	n/a	n/a
4	ATF1	chr14:55738654-55739054	K562	blood:	n/a	n/a
5	ATF2	chr14:55737673-55738269	GM12878	blood:	n/a	chr14:55738065-55738076
6	ATF2	chr14:55737728-55738297	H1-hESC	embryonic stem cell:	n/a	chr14:55738065-55738076
7	ATF2	chr14:55738548-55739095	GM12878	blood:	n/a	n/a
8	ATF2	chr14:55737735-55738254	GM12878	blood:	n/a	chr14:55738065-55738076
9	ATF2	chr14:55738647-55739082	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr14:55738582-55739097	GM12878	blood:	n/a	n/a
11	ATF2	chr14:55738659-55739066	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr14:55737660-55738235	H1-hESC	embryonic stem cell:	n/a	chr14:55738065-55738076
13	ATF3	chr14:55737859-55738214	K562	blood:	n/a	chr14:55738065-55738076 chr14:55738067-55738074 chr14:55738066-55738074 chr14:55738121-55738130 chr14:55738066-55738077 chr14:55738067-55738075 chr14:55738064-55738077 chr14:55738064-55738077
14	ATF3	chr14:55737723-55738107	H1-hESC	embryonic stem cell:	n/a	chr14:55738065-55738076 chr14:55738067-55738074 chr14:55738066-55738074 chr14:55738066-55738077 chr14:55738067-55738075 chr14:55738064-55738077 chr14:55738064-55738077
15	ATF3	chr14:55737720-55738262	K562	blood:	n/a	chr14:55738065-55738076 chr14:55738067-55738074 chr14:55738066-55738074 chr14:55738121-55738130 chr14:55738066-55738077 chr14:55738067-55738075 chr14:55738064-55738077 chr14:55738064-55738077
16	BACH1	chr14:55737881-55738303	H1-hESC	embryonic stem cell:	n/a	n/a
17	BCLAF1	chr14:55737739-55738333	GM12878	blood:	n/a	chr14:55738118-55738131 chr14:55738227-55738240 chr14:55738117-55738126 chr14:55737967-55737976 chr14:55738231-55738244 chr14:55738234-55738247 chr14:55738308-55738321 chr14:55738120-55738129 chr14:55737998-55738011
18	BCLAF1	chr14:55737630-55738306	GM12878	blood:	n/a	chr14:55738118-55738131 chr14:55738227-55738240 chr14:55738117-55738126 chr14:55737967-55737976 chr14:55738231-55738244 chr14:55738234-55738247 chr14:55738120-55738129 chr14:55737998-55738011
19	BCLAF1	chr14:55738676-55739262	GM12878	blood:	n/a	n/a
20	BHLHE40	chr14:55738725-55738966	K562	blood:	n/a	n/a
21	BHLHE40	chr14:55737754-55738214	K562	blood:	n/a	n/a
22	BHLHE40	chr14:55737507-55738243	GM12878	blood:	n/a	chr14:55738225-55738241
23	BHLHE40	chr14:55737789-55738228	HepG2	liver:	n/a	n/a
24	BRCA1	chr14:55738653-55738892	GM12878	blood:	n/a	n/a
25	BRCA1	chr14:55737790-55738211	HepG2	liver:	n/a	n/a
26	BRCA1	chr14:55737774-55738164	GM12878	blood:	n/a	n/a
27	BRCA1	chr14:55738499-55739046	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr14:55737698-55738241	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr14:55738625-55738626	HepG2	liver:	n/a	n/a
30	BRCA1	chr14:55737763-55738188	H1-hESC	embryonic stem cell:	n/a	n/a
31	CBX3	chr14:55737584-55738283	HCT-116	colon:	n/a	n/a
32	CBX3	chr14:55737835-55738139	K562	blood:	n/a	n/a
33	CBX3	chr14:55737655-55738180	K562	blood:	n/a	n/a
34	CBX3	chr14:55738633-55739015	K562	blood:	n/a	n/a
35	CCNT2	chr14:55737795-55738938	K562	blood:	n/a	chr14:55738031-55738040 chr14:55738330-55738339
36	CEBPB	chr14:55738655-55738977	IMR90	lung:	n/a	n/a
37	CEBPB	chr14:55737833-55738193	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr14:55738722-55738924	HepG2	liver:	n/a	n/a
39	CEBPB	chr14:55737723-55738214	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr14:55737810-55738091	K562	blood:	n/a	n/a
41	CEBPB	chr14:55738653-55738953	K562	blood:	n/a	n/a
42	CEBPB	chr14:55737895-55738172	K562	blood:	n/a	n/a
43	CEBPB	chr14:55737892-55738130	HepG2	liver:	n/a	n/a
44	CEBPB	chr14:55737914-55738107	HepG2	liver:	n/a	n/a
45	CEBPB	chr14:55738590-55739142	Hela-S3	cervix:	n/a	chr14:55739006-55739019
46	CEBPD	chr14:55737905-55738340	HepG2	liver:	n/a	n/a
47	CHD1	chr14:55737655-55738289	GM12878	blood:	n/a	n/a
48	CHD1	chr14:55737375-55739517	IMR90	lung:	n/a	chr14:55738328-55738338 chr14:55738641-55738651
49	CHD1	chr14:55738641-55739203	GM12878	blood:	n/a	chr14:55738641-55738651
50	CHD2	chr14:55737646-55738176	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:55738888-55738938	BE2_C	brain:	n/a
2	chr14:55738888-55738938	BE2_C	brain:	n/a
3	chr14:55737854-55737904	SAEC	small airway:	n/a
4	chr14:55737629-55737679	SK-N-SH_RA	brain:	n/a
5	chr14:55738283-55738333	SK-N-SH_RA	brain:	n/a
6	chr14:55738748-55738798	AG10803	skin:	n/a
7	chr14:55738124-55738174	HAEpiC	amniotic membrane:	n/a
8	chr14:55739068-55739118	RPTEC	kidney:	n/a
9	chr14:55737941-55737991	NB4	blood:	n/a
10	chr14:55738545-55738595	HMEC	breast:	n/a
11	chr14:55738748-55738798	HRCEpiC	kidney:	n/a
12	chr14:55738888-55738938	HMEC	breast:	n/a
13	chr14:55738852-55738902	CMK	blood:	n/a
14	chr14:55738283-55738333	AoSMC	blood vessel:	n/a
15	chr14:55738124-55738174	U87	brain:	n/a
16	chr14:55738888-55738938	SK-N-SH_RA	brain:	n/a
17	chr14:55739068-55739118	SK-N-MC	brain:	n/a
18	chr14:55737941-55737991	Hepatocyte	liver:	n/a
19	chr14:55738748-55738798	AG09309	skin:	n/a
20	chr14:55737629-55737679	SK-N-SH	brain:	n/a
21	chr14:55738852-55738902	AG10803	skin:	n/a
22	chr14:55738748-55738798	MCF-7	breast:	n/a
23	chr14:55737629-55737679	AoSMC	blood vessel:	n/a
24	chr14:55737854-55737904	BJ	skin:	n/a
25	chr14:55738124-55738174	AoSMC	blood vessel:	n/a
26	chr14:55738852-55738902	ovcar-3	ovarian:	n/a
27	chr14:55737941-55737991	PrEC	prostate:	n/a
28	chr14:55738888-55738938	SAEC	small airway:	n/a
29	chr14:55738852-55738902	NHBE	bronchial:	n/a
30	chr14:55737629-55737679	A549	lung:	n/a
31	chr14:55738748-55738798	HRPEpiC	eye:	n/a
32	chr14:55737854-55737904	NHBE	bronchial:	n/a
33	chr14:55737629-55737679	HEEpiC	esophagus:	n/a
34	chr14:55738748-55738798	HCPEpiC	choroid plexus:	n/a
35	chr14:55738783-55738833	GM12892	blood:	n/a
36	chr14:55737941-55737991	H1-hESC	embryonic stem cell:	embryo
37	chr14:55738748-55738798	PrEC	prostate:	n/a
38	chr14:55739068-55739118	PrEC	prostate:	n/a
39	chr14:55738124-55738174	NHDF-neo	bronchial:	n/a
40	chr14:55738888-55738938	HRE	kidney:	n/a
41	chr14:55738852-55738902	A549	lung:	n/a
42	chr14:55737854-55737904	NT2-D1	testis:	n/a
43	chr14:55737941-55737991	HPAEpiC	pulmonary alveolar:	n/a
44	chr14:55737854-55737904	NH-A	brain:	n/a
45	chr14:55738888-55738938	SK-N-SH	brain:	n/a
46	chr14:55737941-55737991	NHDF-neo	bronchial:	n/a
47	chr14:55738888-55738938	NH-A	brain:	n/a
48	chr14:55738783-55738833	HEK293	kidney:	embryo
49	chr14:55738545-55738595	GM12891	blood:	n/a
50	chr14:55738545-55738595	HRCEpiC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:55705409..55707823-chr14:55736627..55738832,2	K562	blood:
2	chr14:55664630..55666911-chr14:55737863..55740088,2	K562	blood:
3	chr14:55736450..55738716-chr14:55817481..55820238,2	K562	blood:
4	chr14:55736930..55738808-chr14:55763982..55767802,4	MCF-7	breast:
5	chr14:55737940..55739664-chr14:55764646..55766801,2	MCF-7	breast:
6	chr14:55737342..55739119-chr14:56046136..56048438,2	K562	blood:
7	chr14:55723404..55725998-chr14:55735499..55737800,2	K562	blood:
8	chr14:55737712..55738366-chr15:56285235..56286222,2	Hela-S3	cervix:
9	chr14:55738930..55742893-chr14:55754578..55757898,4	K562	blood:
10	chr14:55516892..55519791-chr14:55737278..55740152,4	K562	blood:
11	chr14:55739383..55741164-chr14:55767168..55768699,2	MCF-7	breast:
12	chr14:55736427..55740242-chr14:55801434..55807681,7	MCF-7	breast:
13	chr14:55517347..55519818-chr14:55736283..55739378,3	MCF-7	breast:
14	chr14:55736296..55738259-chr14:55878149..55880015,2	MCF-7	breast:
15	chr14:55736795..55740558-chr14:55765144..55770564,6	K562	blood:
16	chr14:55738930..55742893-chr14:55754578..55758061,4	K562	blood:
17	chr14:55706045..55707823-chr14:55736335..55738127,2	K562	blood:
18	chr14:55736665..55740457-chr14:55875135..55883763,10	K562	blood:
19	chr14:55657821..55660879-chr14:55735073..55739609,4	K562	blood:
20	chr12:77157369..77158369-chr14:55737768..55738541,2	Hela-S3	cervix:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LGALS3-2	chr14:55738929-55738999	NONHSAT036997
2	lnc-DLGAP5-4	chr14:55738600-55738793	ENSG00000258413
3	lnc-DLGAP5-4	chr14:55737863-55738026	ENSG00000258413
4	lnc-DLGAP5-4	chr14:55738600-55738835	NONHSAT036996

Variant related genes	Relation type
ENSG00000258413	TF binding region
FBXO34	TF binding region
ENSG00000258413	CpG island
FBXO34	CpG island
ENSG00000258050	chromatin interactions
ENSG00000168175	chromatin interactions
ENSG00000126775	chromatin interactions
ENSG00000258469	chromatin interactions
ENSG00000186615	chromatin interactions
ENSG00000126787	chromatin interactions
ENSG00000069869	chromatin interactions
ENSG00000126777	chromatin interactions
ENSG00000186908	chromatin interactions
ENSG00000271180	chromatin interactions
ENSG00000178974	chromatin interactions
ENSG00000239199	chromatin interactions
ENSG00000258455	chromatin interactions

Extended variants
information (count: 82 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:82 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191435916	chr14:55737490-55737491	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
2	rs534709540	chr14:55737508-55737509	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
3	rs183492497	chr14:55737522-55737523	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
4	rs72715740	chr14:55737552-55737553	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs542801631	chr14:55737596-55737597	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
6	rs182275573	chr14:55737615-55737616	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
7	rs576385322	chr14:55737629-55737630	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
8	rs544228175	chr14:55737637-55737638	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
9	rs563941877	chr14:55737639-55737640	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
10	rs565195764	chr14:55737652-55737653	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
11	rs532106057	chr14:55737653-55737654	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
12	rs185232446	chr14:55737724-55737725	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
13	rs559397767	chr14:55737742-55737743	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
14	rs79306172	chr14:55737745-55737746	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
15	rs142220188	chr14:55737766-55737767	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
16	rs570181445	chr14:55737805-55737806	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
17	rs146401491	chr14:55737812-55737813	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
18	rs531031171	chr14:55737827-55737828	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
19	rs2880103	chr14:55737832-55737833	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs570817425	chr14:55737833-55737834	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
21	rs534650902	chr14:55737875-55737876	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a
22	rs530614013	chr14:55737924-55737925	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a
23	rs550742094	chr14:55737926-55737927	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a
24	rs553137971	chr14:55737973-55737974	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a
25	rs56166765	chr14:55738018-55738019	Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	14 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs529140383	chr14:55738094-55738095	Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
27	rs535605226	chr14:55738099-55738100	Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
28	rs557452382	chr14:55738103-55738104	Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
29	rs576273862	chr14:55738124-55738125	Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
30	rs549197434	chr14:55738134-55738135	Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
31	rs71412676	chr14:55738154-55738155	Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
32	rs11547116	chr14:55738165-55738166	Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs558842993	chr14:55738185-55738186	Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
34	rs142999509	chr14:55738194-55738195	Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
35	rs541013045	chr14:55738265-55738266	Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
36	rs559119564	chr14:55738308-55738309	Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
37	rs943593	chr14:55738406-55738407	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
38	rs529772217	chr14:55738433-55738434	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
39	rs79163357	chr14:55738449-55738450	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
40	rs563059060	chr14:55738502-55738503	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
41	rs943592	chr14:55738513-55738514	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
42	rs943591	chr14:55738593-55738594	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
43	rs943590	chr14:55738596-55738597	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs552353530	chr14:55738644-55738645	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
45	rs564435617	chr14:55738650-55738651	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
46	rs570780083	chr14:55738651-55738652	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
47	rs190385205	chr14:55738659-55738660	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
48	rs568338044	chr14:55738681-55738682	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
49	rs535860616	chr14:55738732-55738733	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
50	rs116144984	chr14:55738744-55738745	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

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	16397240	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
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
Breast cancer	21364760	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:331 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:55734000-55737600	Weak transcription	Lung	lung
2	chr14:55734800-55737600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr14:55734800-55737800	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr14:55735000-55737600	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr14:55735000-55737600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr14:55735000-55737600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr14:55735000-55737800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr14:55735200-55737600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr14:55735200-55737600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr14:55735200-55737600	Weak transcription	Aorta	Aorta
11	chr14:55735200-55737600	Weak transcription	HSMMtube	muscle
12	chr14:55735200-55737800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr14:55735400-55737600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr14:55735400-55737600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr14:55737200-55737600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr14:55737200-55737600	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr14:55737200-55737600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
18	chr14:55737200-55737600	Enhancers	Dnd41	blood
19	chr14:55737200-55737600	Enhancers	Osteobl	bone
20	chr14:55737400-55737600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr14:55737400-55737600	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr14:55737400-55737600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr14:55737400-55737600	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr14:55737400-55737600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
25	chr14:55737400-55737600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr14:55737400-55737600	Enhancers	Muscle Satellite Cultured Cells	--
27	chr14:55737400-55737600	Enhancers	Liver	Liver
28	chr14:55737400-55737600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr14:55737400-55737600	Enhancers	Fetal Kidney	kidney
30	chr14:55737400-55737600	Weak transcription	Fetal Stomach	stomach
31	chr14:55737400-55737600	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr14:55737400-55737600	Enhancers	Skeletal Muscle Female	skeletal muscle
33	chr14:55737400-55737600	Enhancers	HUVEC	blood vessel
34	chr14:55737400-55737600	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr14:55737400-55737600	Enhancers	NHEK	skin
36	chr14:55737400-55737800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
37	chr14:55737400-55737800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr14:55737400-55737800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
39	chr14:55737400-55737800	Enhancers	Primary T helper cells fromperipheralblood	blood
40	chr14:55737400-55737800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
41	chr14:55737400-55737800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr14:55737400-55737800	Enhancers	Fetal Heart	heart
43	chr14:55737400-55737800	Flanking Active TSS	Rectal Smooth Muscle	rectum
44	chr14:55737400-55737800	Flanking Active TSS	A549	lung
45	chr14:55737400-55737800	Flanking Active TSS	GM12878-XiMat	blood
46	chr14:55737400-55737800	Flanking Active TSS	HepG2	liver
47	chr14:55737400-55737800	Flanking Active TSS	HMEC	breast
48	chr14:55737400-55737800	Flanking Active TSS	K562	blood
49	chr14:55737400-55738000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
50	chr14:55737400-55738000	Enhancers	Primary T helper naive cells from peripheral blood	blood

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