Variant report

Variant	esv3388575
Chromosome Location	chr14:70077224-70080072
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	ATF3	chr14:70077672-70077886	K562	blood:	n/a	n/a
2	ATF3	chr14:70078043-70078288	K562	blood:	n/a	n/a
3	BACH1	chr14:70078765-70079609	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCLAF1	chr14:70078274-70079248	GM12878	blood:	n/a	chr14:70078783-70078796 chr14:70079066-70079079 chr14:70078964-70078977 chr14:70078786-70078799
5	BHLHE40	chr14:70077965-70078539	GM12878	blood:	n/a	chr14:70078318-70078334 chr14:70078414-70078430
6	BHLHE40	chr14:70077364-70077711	K562	blood:	n/a	n/a
7	BHLHE40	chr14:70077916-70078221	HepG2	liver:	n/a	n/a
8	BHLHE40	chr14:70077931-70078480	K562	blood:	n/a	chr14:70078318-70078334 chr14:70078414-70078430
9	BRCA1	chr14:70078730-70078835	GM12878	blood:	n/a	n/a
10	BRCA1	chr14:70078440-70078453	Hela-S3	cervix:	n/a	n/a
11	CCNT2	chr14:70078003-70079019	K562	blood:	n/a	n/a
12	CEBPB	chr14:70077981-70078227	Hela-S3	cervix:	n/a	n/a
13	CHD1	chr14:70078269-70080696	IMR90	lung:	n/a	n/a
14	CHD1	chr14:70077870-70078196	GM12878	blood:	n/a	n/a
15	CHD1	chr14:70078406-70079070	GM12878	blood:	n/a	n/a
16	CHD1	chr14:70079298-70080173	GM12878	blood:	n/a	n/a
17	CHD2	chr14:70078265-70078505	K562	blood:	n/a	n/a
18	CHD2	chr14:70079397-70079486	GM12878	blood:	n/a	n/a
19	CHD2	chr14:70077819-70078597	Hela-S3	cervix:	n/a	n/a
20	CHD2	chr14:70077972-70078563	GM12878	blood:	n/a	n/a
21	CREB1	chr14:70077866-70078590	GM12878	blood:	n/a	n/a
22	CREB1	chr14:70077837-70079153	HepG2	liver:	n/a	n/a
23	CREB1	chr14:70077940-70078546	K562	blood:	n/a	n/a
24	CREB1	chr14:70077866-70078775	A549	lung:	n/a	n/a
25	CREB1	chr14:70077861-70078585	HepG2	liver:	n/a	n/a
26	CREB1	chr14:70077641-70078731	H1-hESC	embryonic stem cell:	n/a	n/a
27	CREB1	chr14:70077651-70078588	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr14:70079605-70079780	GM12878	blood:	n/a	chr14:70079686-70079704 chr14:70079691-70079699 chr14:70079681-70079702
29	CTCF	chr14:70079620-70079770	K562	blood:	n/a	chr14:70079686-70079704 chr14:70079691-70079699 chr14:70079681-70079702
30	CTCF	chr14:70079701-70079717	GM13977	blood:	n/a	n/a
31	CTCF	chr14:70079580-70079730	WI-38	lung:	n/a	chr14:70079686-70079704 chr14:70079691-70079699 chr14:70079681-70079702
32	CTCF	chr14:70079700-70079850	NHDF-neo	bronchial:	n/a	n/a
33	CTCF	chr14:70079620-70079770	HPAF	blood vessel:	n/a	chr14:70079686-70079704 chr14:70079691-70079699 chr14:70079681-70079702
34	CTCF	chr14:70079540-70079690	NHDF-neo	bronchial:	n/a	n/a
35	CTCF	chr14:70078300-70078450	GM12875	blood:	n/a	n/a
36	CTCF	chr14:70079588-70079788	MCF-7	breast:	n/a	chr14:70079686-70079704 chr14:70079691-70079699 chr14:70079681-70079702
37	CTCF	chr14:70079660-70079810	K562	blood:	n/a	chr14:70079686-70079704 chr14:70079691-70079699 chr14:70079681-70079702
38	CTCF	chr14:70079680-70079830	HRPEpiC	eye:	n/a	chr14:70079686-70079704 chr14:70079691-70079699 chr14:70079681-70079702
39	CTCF	chr14:70079576-70079809	MCF-7	breast:	n/a	chr14:70079686-70079704 chr14:70079691-70079699 chr14:70079681-70079702
40	CTCF	chr14:70079640-70079748	Fibrobl	skin:	n/a	chr14:70079686-70079704 chr14:70079691-70079699 chr14:70079681-70079702
41	CTCF	chr14:70079620-70079770	HMEC	breast:	n/a	chr14:70079686-70079704 chr14:70079691-70079699 chr14:70079681-70079702
42	CTCF	chr14:70079360-70079510	GM06990	blood:	n/a	n/a
43	CTCF	chr14:70079654-70079700	GM13977	blood:	n/a	chr14:70079691-70079699
44	CTCF	chr14:70079620-70079749	ProgFib	skin:	n/a	chr14:70079686-70079704 chr14:70079691-70079699 chr14:70079681-70079702
45	CTCF	chr14:70079600-70079750	HCT-116	colon:	n/a	chr14:70079686-70079704 chr14:70079691-70079699 chr14:70079681-70079702
46	CTCF	chr14:70079580-70079730	HMF	breast:	n/a	chr14:70079686-70079704 chr14:70079691-70079699 chr14:70079681-70079702
47	CTCF	chr14:70079560-70079710	HPF	lung:	n/a	chr14:70079686-70079704 chr14:70079691-70079699 chr14:70079681-70079702
48	CTCF	chr14:70079440-70079590	HRE	kidney:	n/a	n/a
49	CTCF	chr14:70078440-70078590	GM12874	blood:	n/a	n/a
50	CTCF	chr14:70079580-70079730	AoAF	blood vessel:	n/a	chr14:70079686-70079704 chr14:70079691-70079699 chr14:70079681-70079702

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:70077930-70077980	HCF	heart:	n/a
2	chr14:70077930-70077980	RPTEC	kidney:	n/a
3	chr14:70077930-70077980	AG04450	lung:	fetal
4	chr14:70078973-70079023	RPTEC	kidney:	n/a
5	chr14:70078336-70078386	HMEC	breast:	n/a
6	chr14:70077191-70077241	AG10803	skin:	n/a
7	chr14:70078336-70078386	AG04449	skin:	fetal
8	chr14:70079160-70079210	SK-N-SH_RA	brain:	n/a
9	chr14:70078336-70078386	Hela-S3	cervix:	n/a
10	chr14:70078336-70078386	ovcar-3	ovarian:	n/a
11	chr14:70078026-70078076	GM19239	blood:	n/a
12	chr14:70078336-70078386	ECC-1	luminal epithelium:	n/a
13	chr14:70078026-70078076	AG04449	skin:	fetal
14	chr14:70077191-70077241	HCT-116	colon:	n/a
15	chr14:70077191-70077241	ProgFib	skin:	n/a
16	chr14:70078026-70078076	ovcar-3	ovarian:	n/a
17	chr14:70079160-70079210	HCT-116	colon:	n/a
18	chr14:70077191-70077241	AG09319	gingival:	n/a
19	chr14:70077191-70077241	HCM	heart:	n/a
20	chr14:70078026-70078076	Hela-S3	cervix:	n/a
21	chr14:70078026-70078076	HIPEpiC	eye:	n/a
22	chr14:70079160-70079210	HRE	kidney:	n/a
23	chr14:70077930-70077980	HCPEpiC	choroid plexus:	n/a
24	chr14:70079160-70079210	HEK293	kidney:	embryo
25	chr14:70079160-70079210	T-47D	breast:	n/a
26	chr14:70077191-70077241	HAEpiC	amniotic membrane:	n/a
27	chr14:70077930-70077980	SKMC	muscle:	n/a
28	chr14:70078336-70078386	CMK	blood:	n/a
29	chr14:70077930-70077980	Caco-2	colon:	n/a
30	chr14:70079160-70079210	GM12878	blood:	n/a
31	chr14:70078026-70078076	HCF	heart:	n/a
32	chr14:70078973-70079023	GM12892	blood:	n/a
33	chr14:70078973-70079023	LNCaP	prostate:	n/a
34	chr14:70077930-70077980	ovcar-3	ovarian:	n/a
35	chr14:70078973-70079023	HRCEpiC	kidney:	n/a
36	chr14:70077191-70077241	NH-A	brain:	n/a
37	chr14:70079160-70079210	Jurkat	blood:	n/a
38	chr14:70078973-70079023	HMEC	breast:	n/a
39	chr14:70078336-70078386	LNCaP	prostate:	n/a
40	chr14:70079160-70079210	AG09309	skin:	n/a
41	chr14:70078026-70078076	GM12891	blood:	n/a
42	chr14:70079160-70079210	HRCEpiC	kidney:	n/a
43	chr14:70077930-70077980	PANC-1	pancreas:	n/a
44	chr14:70077930-70077980	HUVEC	blood vessel:	n/a
45	chr14:70078026-70078076	U87	brain:	n/a
46	chr14:70078973-70079023	AoSMC	blood vessel:	n/a
47	chr14:70077930-70077980	Jurkat	blood:	n/a
48	chr14:70078026-70078076	Hepatocyte	liver:	n/a
49	chr14:70078026-70078076	LNCaP	prostate:	n/a
50	chr14:70077930-70077980	HRE	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:70078750..70079338-chr14:70193348..70193999,2	MCF-7	breast:
2	chr14:70078972..70081003-chr14:70168060..70169859,2	MCF-7	breast:
3	chr14:70078362..70080995-chr14:70181831..70184954,3	MCF-7	breast:
4	chr14:70078651..70079377-chr18:12990690..12991548,2	Hela-S3	cervix:
5	chr14:70078352..70079224-chr16:2014382..2015342,3	Hela-S3	cervix:
6	chr14:70075659..70077569-chr14:70081813..70084609,2	K562	blood:
7	chr14:70077972..70078597-chr14:70233346..70233919,2	HCT-116	colon:
8	chr14:70069839..70070933-chr14:70079326..70080176,3	MCF-7	breast:
9	chr14:70079455..70080135-chr14:70193509..70194042,2	MCF-7	breast:
10	chr14:70075993..70078165-chr14:70168395..70170224,2	K562	blood:
11	chr14:70078032..70078862-chr2:54197449..54198389,2	Hela-S3	cervix:
12	chr14:70078320..70079096-chr5:10250566..10251194,2	Hela-S3	cervix:
13	chr14:70075878..70078294-chr14:70112470..70114213,2	K562	blood:
14	chr14:70076728..70078237-chr14:70177828..70179629,2	MCF-7	breast:
15	chr14:70075993..70078093-chr14:70168395..70170520,2	K562	blood:
16	chr14:70077094..70079754-chr14:70233044..70235632,2	K562	blood:
17	chr14:70078988..70081475-chr14:70103806..70105577,2	MCF-7	breast:
18	chr14:70076119..70078735-chr14:70193171..70195049,2	MCF-7	breast:
19	chr14:70077771..70080127-chr14:70232780..70235719,3	MCF-7	breast:
20	chr14:70078185..70080215-chr14:70232416..70234645,2	K562	blood:
21	chr14:70078354..70079913-chr14:70192981..70195416,2	K562	blood:
22	chr14:70079232..70080112-chr14:70175519..70176175,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLEKHD1-3	chr14:70078355-70078545	NONHSAT037535

Variant related genes	Relation type
KIAA0247	TF binding region
KIAA0247	CpG island
ENSG00000150753	chromatin interactions
ENSG00000140988	chromatin interactions
ENSG00000170634	chromatin interactions
ENSG00000101639	chromatin interactions
ENSG00000068878	chromatin interactions
ENSG00000100650	chromatin interactions
ENSG00000255198	chromatin interactions
ENSG00000266969	chromatin interactions

Extended variants
information (count: 100 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:100 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565012682	chr14:70077269-70077270	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs201625451	chr14:70077357-70077358	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs151078320	chr14:70077359-70077360	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs371655235	chr14:70077382-70077383	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs578224621	chr14:70077421-70077422	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs545266196	chr14:70077423-70077424	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs540885484	chr14:70077442-70077443	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs530881564	chr14:70077444-70077445	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs141064696	chr14:70077445-70077446	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs369457617	chr14:70077482-70077483	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs191239599	chr14:70077528-70077529	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs561251535	chr14:70077545-70077546	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs28758769	chr14:70077641-70077642	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs150269884	chr14:70077650-70077651	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs201165879	chr14:70077654-70077655	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs369888673	chr14:70077739-70077740	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs550576970	chr14:70077773-70077774	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs533260158	chr14:70077793-70077794	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs543435095	chr14:70077832-70077833	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs372972349	chr14:70077847-70077848	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs79721749	chr14:70077853-70077854	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs116754257	chr14:70077874-70077875	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs183490426	chr14:70077885-70077886	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs74352620	chr14:70077941-70077942	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs138968300	chr14:70077943-70077944	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs369639264	chr14:70077979-70077980	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs74060216	chr14:70078019-70078020	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs539432418	chr14:70078020-70078021	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs566286612	chr14:70078068-70078069	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs186759019	chr14:70078155-70078156	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs539337063	chr14:70078181-70078182	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs557107627	chr14:70078286-70078287	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs191012832	chr14:70078323-70078324	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs561038253	chr14:70078426-70078427	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
35	rs573334497	chr14:70078465-70078466	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
36	rs540215545	chr14:70078481-70078482	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
37	rs141877609	chr14:70078509-70078510	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
38	rs112303601	chr14:70078573-70078574	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs551722313	chr14:70078582-70078583	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs563601756	chr14:70078634-70078635	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs530707390	chr14:70078653-70078654	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs549237975	chr14:70078723-70078724	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs567244448	chr14:70078743-70078744	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs71423367	chr14:70078777-70078778	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs137879175	chr14:70078809-70078810	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs555867108	chr14:70078861-70078862	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs534716444	chr14:70078881-70078882	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs138667587	chr14:70078934-70078935	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs571246293	chr14:70078969-70078970	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs374311251	chr14:70078999-70079000	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
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
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
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD

Chromatin state (count:491 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:70073400-70077400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr14:70073400-70077400	Weak transcription	Small Intestine	intestine
3	chr14:70073400-70077400	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr14:70074200-70077400	Weak transcription	Gastric	stomach
5	chr14:70075600-70077400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr14:70076000-70077400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
7	chr14:70076600-70077400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr14:70076600-70077400	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr14:70076600-70077400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
10	chr14:70076600-70077400	Enhancers	Primary T helper naive cells from peripheral blood	blood
11	chr14:70076600-70077400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr14:70076600-70077400	Enhancers	Right Ventricle	heart
13	chr14:70076600-70077600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr14:70076600-70077600	Enhancers	Spleen	Spleen
15	chr14:70076600-70077800	Enhancers	Primary B cells from peripheral blood	blood
16	chr14:70076600-70077800	Flanking Active TSS	Primary T cells from cord blood	blood
17	chr14:70076800-70077400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr14:70076800-70077400	Enhancers	Primary hematopoietic stem cells	blood
19	chr14:70076800-70077400	Enhancers	Fetal Heart	heart
20	chr14:70076800-70077400	Enhancers	Fetal Intestine Small	intestine
21	chr14:70076800-70077400	Enhancers	Fetal Kidney	kidney
22	chr14:70076800-70077400	Enhancers	Placenta	Placenta
23	chr14:70076800-70077400	Enhancers	Left Ventricle	heart
24	chr14:70076800-70077600	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr14:70076800-70077600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
26	chr14:70076800-70077600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr14:70076800-70077600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr14:70076800-70077600	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
29	chr14:70076800-70077600	Enhancers	Fetal Intestine Large	intestine
30	chr14:70076800-70077600	Enhancers	Fetal Muscle Leg	muscle
31	chr14:70076800-70077800	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr14:70076800-70077800	Enhancers	Sigmoid Colon	Sigmoid Colon
33	chr14:70076800-70078000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
34	chr14:70076800-70078000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
35	chr14:70076800-70078000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
36	chr14:70076800-70078000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
37	chr14:70076800-70078000	Flanking Active TSS	Dnd41	blood
38	chr14:70076800-70078000	Flanking Active TSS	NHDF-Ad	bronchial
39	chr14:70076800-70079200	Active TSS	ES-I3 Cell Line	embryonic stem cell
40	chr14:70077000-70077400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
41	chr14:70077000-70077400	Enhancers	Brain Substantia Nigra	brain
42	chr14:70077000-70077400	Enhancers	Colonic Mucosa	Colon
43	chr14:70077000-70077400	Enhancers	Fetal Lung	lung
44	chr14:70077000-70077400	Enhancers	Psoas Muscle	Psoas
45	chr14:70077000-70077400	Active TSS	Rectal Smooth Muscle	rectum
46	chr14:70077000-70077400	Enhancers	Stomach Mucosa	stomach
47	chr14:70077000-70077400	Flanking Active TSS	HepG2	liver
48	chr14:70077000-70077600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
49	chr14:70077000-70077600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
50	chr14:70077000-70077600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

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