Variant report

Variant	esv1795887
Chromosome Location	chr10:94449271-94450334
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:364)
CpG islands
(count:244)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:364 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:94449642-94449923	K562	blood:	n/a	n/a
2	ARID3A	chr10:94449623-94449834	HepG2	liver:	n/a	n/a
3	BACH1	chr10:94449756-94450595	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr10:94450119-94450426	GM12878	blood:	n/a	chr10:94450279-94450290
5	BHLHE40	chr10:94449745-94450830	K562	blood:	n/a	chr10:94450146-94450162
6	BHLHE40	chr10:94448540-94450445	HepG2	liver:	n/a	chr10:94449270-94449286 chr10:94450146-94450162 chr10:94449642-94449658
7	BHLHE40	chr10:94449290-94449318	K562	blood:	n/a	n/a
8	BHLHE40	chr10:94450084-94450434	GM12878	blood:	n/a	chr10:94450146-94450162
9	BRCA1	chr10:94450090-94450104	HepG2	liver:	n/a	n/a
10	CCNT2	chr10:94448631-94451909	K562	blood:	n/a	chr10:94449521-94449530 chr10:94451255-94451264
11	CEBPB	chr10:94450237-94450353	HepG2	liver:	n/a	n/a
12	CEBPB	chr10:94450133-94450542	Hela-S3	cervix:	n/a	n/a
13	CEBPD	chr10:94449168-94449517	HepG2	liver:	n/a	n/a
14	CEBPD	chr10:94449571-94450015	HepG2	liver:	n/a	n/a
15	CEBPD	chr10:94449523-94449905	HepG2	liver:	n/a	n/a
16	CHD2	chr10:94449342-94449343	K562	blood:	n/a	n/a
17	CHD2	chr10:94449248-94450546	Hela-S3	cervix:	n/a	chr10:94449522-94449532 chr10:94449385-94449395
18	CREB1	chr10:94449053-94450362	A549	lung:	n/a	n/a
19	CTBP2	chr10:94448629-94449382	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTBP2	chr10:94449746-94452477	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr10:94449617-94449749	GM19240	blood:	n/a	n/a
22	CTCF	chr10:94449600-94449750	GM12871	blood:	n/a	n/a
23	CTCF	chr10:94449469-94449489	GM12878	blood:	n/a	n/a
24	CTCF	chr10:94449872-94449899	MCF-7	breast:	n/a	n/a
25	CTCF	chr10:94449940-94450090	HepG2	liver:	n/a	n/a
26	CTCF	chr10:94449880-94450030	AG04449	skin:	n/a	n/a
27	CTCF	chr10:94449860-94450010	AG04450	lung:	n/a	n/a
28	CTCF	chr10:94449900-94450050	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr10:94449659-94450015	IMR90	lung:	n/a	n/a
30	CTCF	chr10:94449937-94449948	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr10:94449900-94450050	HUVEC	blood vessel:	n/a	n/a
32	CTCF	chr10:94449820-94449970	GM12869	blood:	n/a	n/a
33	CTCF	chr10:94450100-94450250	GM12866	blood:	n/a	chr10:94450145-94450158 chr10:94450142-94450160
34	CTCF	chr10:94449320-94449470	GM12873	blood:	n/a	n/a
35	CTCF	chr10:94449901-94450029	MCF-7	breast:	n/a	n/a
36	CTCF	chr10:94449800-94449950	GM12865	blood:	n/a	n/a
37	CTCF	chr10:94450060-94450210	Hela-S3	cervix:	n/a	chr10:94450145-94450158 chr10:94450142-94450160
38	CTCF	chr10:94449900-94450050	A549	lung:	n/a	n/a
39	CTCF	chr10:94449820-94449970	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr10:94449662-94449817	MCF-7	breast:	n/a	n/a
41	CTCF	chr10:94449355-94449380	K562	blood:	n/a	n/a
42	CTCF	chr10:94449678-94449739	MCF-7	breast:	n/a	n/a
43	CTCF	chr10:94450000-94450150	GM12874	blood:	n/a	n/a
44	CTCF	chr10:94449720-94449870	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr10:94449394-94449519	GM12892	blood:	n/a	n/a
46	CTCF	chr10:94449220-94449370	HCM	heart:	n/a	n/a
47	CTCF	chr10:94449180-94449330	AG04450	lung:	n/a	n/a
48	CTCF	chr10:94450031-94450033	MCF-7	breast:	n/a	n/a
49	CTCF	chr10:94449800-94449950	GM12874	blood:	n/a	n/a
50	CTCF	chr10:94449600-94449750	GM12874	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:94449250-94449300	NHBE	bronchial:	n/a
2	chr10:94449567-94449617	HCM	heart:	n/a
3	chr10:94449250-94449300	IMR90	lung:	fetal
4	chr10:94449797-94449847	HCF	heart:	n/a
5	chr10:94450056-94450106	HCPEpiC	choroid plexus:	n/a
6	chr10:94449250-94449300	HNPCEpiC	eye:	n/a
7	chr10:94449797-94449847	MCF-7	breast:	n/a
8	chr10:94449797-94449847	HRCEpiC	kidney:	n/a
9	chr10:94449250-94449300	NB4	blood:	n/a
10	chr10:94449797-94449847	ECC-1	luminal epithelium:	n/a
11	chr10:94449797-94449847	ovcar-3	ovarian:	n/a
12	chr10:94449250-94449300	RPTEC	kidney:	n/a
13	chr10:94449797-94449847	HL-60	blood:	n/a
14	chr10:94449797-94449847	BE2_C	brain:	n/a
15	chr10:94449250-94449300	GM12878	blood:	n/a
16	chr10:94450056-94450106	A549	lung:	n/a
17	chr10:94450056-94450106	H1-hESC	embryonic stem cell:	embryo
18	chr10:94450056-94450106	AG09319	gingival:	n/a
19	chr10:94449797-94449847	NH-A	brain:	n/a
20	chr10:94450056-94450106	HRPEpiC	eye:	n/a
21	chr10:94449567-94449617	HNPCEpiC	eye:	n/a
22	chr10:94450056-94450106	ProgFib	skin:	n/a
23	chr10:94449567-94449617	NT2-D1	testis:	n/a
24	chr10:94449797-94449847	AG09309	skin:	n/a
25	chr10:94450056-94450106	HAEpiC	amniotic membrane:	n/a
26	chr10:94449250-94449300	ECC-1	luminal epithelium:	n/a
27	chr10:94449567-94449617	ProgFib	skin:	n/a
28	chr10:94449567-94449617	GM06990	blood:	n/a
29	chr10:94450056-94450106	HL-60	blood:	n/a
30	chr10:94449250-94449300	GM19239	blood:	n/a
31	chr10:94449250-94449300	HL-60	blood:	n/a
32	chr10:94450056-94450106	LNCaP	prostate:	n/a
33	chr10:94450056-94450106	Hepatocyte	liver:	n/a
34	chr10:94449567-94449617	PrEC	prostate:	n/a
35	chr10:94449567-94449617	GM12878	blood:	n/a
36	chr10:94450056-94450106	GM12891	blood:	n/a
37	chr10:94449250-94449300	T-47D	breast:	n/a
38	chr10:94449797-94449847	HCPEpiC	choroid plexus:	n/a
39	chr10:94449567-94449617	BE2_C	brain:	n/a
40	chr10:94450056-94450106	NH-A	brain:	n/a
41	chr10:94449567-94449617	HL-60	blood:	n/a
42	chr10:94449797-94449847	HAEpiC	amniotic membrane:	n/a
43	chr10:94449567-94449617	SK-N-SH_RA	brain:	n/a
44	chr10:94449250-94449300	CMK	blood:	n/a
45	chr10:94449567-94449617	LNCaP	prostate:	n/a
46	chr10:94450056-94450106	T-47D	breast:	n/a
47	chr10:94449250-94449300	LNCaP	prostate:	n/a
48	chr10:94450056-94450106	Hela-S3	cervix:	n/a
49	chr10:94449250-94449300	SAEC	small airway:	n/a
50	chr10:94449250-94449300	AG04449	skin:	fetal

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:94449475..94450112-chr19:14529907..14530785,2	Hela-S3	cervix:
2	chr10:94349533..94354628-chr10:94448059..94453493,12	K562	blood:
3	chr10:94449913..94450519-chr18:12990641..12991585,2	Hela-S3	cervix:
4	chr10:94333616..94336720-chr10:94448718..94451044,3	K562	blood:
5	chr10:94449237..94450232-chr6:27805942..27806496,2	NB4	blood:
6	chr10:94449678..94450357-chr11:62359130..62359860,2	Hela-S3	cervix:
7	chr10:94349533..94356622-chr10:94447410..94453498,11	K562	blood:
8	chr10:94450024..94450724-chr19:12901932..12902636,2	Hela-S3	cervix:
9	chr10:94449635..94450319-chr15:59396946..59397778,2	NB4	blood:
10	chr10:94449758..94450309-chr20:30192485..30193219,2	Hela-S3	cervix:
11	chr10:94449314..94450224-chr16:30388710..30389229,2	NB4	blood:
12	chr10:94448193..94452899-chr10:94604769..94609293,6	K562	blood:
13	chr10:94449603..94452740-chr10:94589464..94592452,3	K562	blood:

No data

Variant related genes	Relation type
HHEX	TF binding region
HHEX	CpG island
ENSG00000157456	chromatin interactions
ENSG00000180209	chromatin interactions
ENSG00000138190	chromatin interactions
ENSG00000233822	chromatin interactions
ENSG00000138160	chromatin interactions
ENSG00000125968	chromatin interactions
ENSG00000101639	chromatin interactions
ENSG00000149016	chromatin interactions
ENSG00000171223	chromatin interactions
ENSG00000184348	chromatin interactions
ENSG00000123136	chromatin interactions
ENSG00000266969	chromatin interactions
ENSG00000119912	chromatin interactions

Extended variants
information (count: 45 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:45 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555690607	chr10:94449286-94449287	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs575746087	chr10:94449287-94449288	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs375280193	chr10:94449305-94449306	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs544399912	chr10:94449334-94449335	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs558196263	chr10:94449416-94449417	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs578130983	chr10:94449438-94449439	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs540657123	chr10:94449448-94449449	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs7475059	chr10:94449469-94449470	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs367580592	chr10:94449475-94449476	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs560488859	chr10:94449496-94449497	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs4075563	chr10:94449550-94449551	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs528438935	chr10:94449606-94449607	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs542070126	chr10:94449680-94449681	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
14	rs561738313	chr10:94449692-94449693	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
15	rs191640546	chr10:94449698-94449699	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
16	rs558170145	chr10:94449720-94449721	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
17	rs117639730	chr10:94449733-94449734	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
18	rs532842622	chr10:94449739-94449740	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
19	rs546230628	chr10:94449766-94449767	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
20	rs566090388	chr10:94449788-94449789	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
21	rs535776260	chr10:94449794-94449795	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
22	rs555996923	chr10:94449854-94449855	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
23	rs34266926	chr10:94449926-94449927	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
24	rs2229328	chr10:94449932-94449933	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
25	rs142036619	chr10:94449934-94449935	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
26	rs377053008	chr10:94449947-94449948	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
27	rs1418387	chr10:94450012-94450013	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
28	rs199544448	chr10:94450016-94450017	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
29	rs558044709	chr10:94450019-94450020	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
30	rs370000570	chr10:94450039-94450040	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
31	rs113121942	chr10:94450061-94450062	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
32	rs540724252	chr10:94450081-94450082	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
33	rs554220013	chr10:94450103-94450104	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
34	rs2901618	chr10:94450126-94450127	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
35	rs2901619	chr10:94450127-94450128	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
36	rs574038551	chr10:94450137-94450138	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
37	rs569073176	chr10:94450227-94450228	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
38	rs34372348	chr10:94450229-94450230	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
39	rs9420589	chr10:94450233-94450234	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs561983167	chr10:94450238-94450239	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
41	rs530700567	chr10:94450249-94450250	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
42	rs200072506	chr10:94450254-94450255	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
43	rs372911659	chr10:94450268-94450269	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
44	rs117662920	chr10:94450281-94450282	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
45	rs532873184	chr10:94450316-94450317	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	18645599	CNVD
Polyposis syndrome	18645599	CNVD
Prostate cancer	17245344	CNVD
Glioblastoma multiforme	17369134	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21364760	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Sezary syndrome	18413736	CNVD
Intracranial aneurysm	16715129	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD

Chromatin state (count:212 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:94447800-94450600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
2	chr10:94448000-94449400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr10:94448200-94449400	Flanking Active TSS	Primary B cells from cord blood	blood
4	chr10:94448400-94449400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr10:94448400-94450000	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
6	chr10:94448400-94450600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
7	chr10:94448400-94450600	Active TSS	Osteobl	bone
8	chr10:94448400-94451600	Active TSS	NHLF	lung
9	chr10:94448400-94451800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
10	chr10:94448400-94452600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
11	chr10:94448400-94452600	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
12	chr10:94448400-94452800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
13	chr10:94448600-94449400	Flanking Active TSS	Primary hematopoietic stem cells	blood
14	chr10:94448600-94449400	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
15	chr10:94448600-94449400	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
16	chr10:94448600-94449400	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
17	chr10:94448600-94449400	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
18	chr10:94448600-94449400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr10:94448600-94449400	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
20	chr10:94448600-94449400	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
21	chr10:94448600-94449400	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
22	chr10:94448600-94449400	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
23	chr10:94448600-94449400	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
24	chr10:94448600-94449600	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr10:94448600-94449600	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
26	chr10:94448600-94449800	Active TSS	Right Atrium	heart
27	chr10:94448600-94449800	Bivalent/Poised TSS	Thymus	Thymus
28	chr10:94448600-94450000	Active TSS	HepG2	liver
29	chr10:94448600-94450200	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
30	chr10:94448600-94450200	Bivalent/Poised TSS	NHDF-Ad	bronchial
31	chr10:94448600-94450400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
32	chr10:94448600-94450400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr10:94448600-94450400	Active TSS	Breast Myoepithelial Primary Cells	Breast
34	chr10:94448600-94450600	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr10:94448600-94450600	Active TSS	Aorta	Aorta
36	chr10:94448600-94450600	Bivalent/Poised TSS	Brain Angular Gyrus	brain
37	chr10:94448600-94450600	Bivalent/Poised TSS	NHEK	skin
38	chr10:94448600-94450800	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
39	chr10:94448600-94451800	Active TSS	K562	blood
40	chr10:94448600-94451800	Active TSS	Monocytes-CD14+_RO01746	blood
41	chr10:94448600-94452400	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr10:94448600-94452400	Bivalent/Poised TSS	Brain Anterior Caudate	brain
43	chr10:94448600-94452400	Active TSS	Colon Smooth Muscle	Colon
44	chr10:94448600-94452400	Bivalent/Poised TSS	Psoas Muscle	Psoas
45	chr10:94448800-94449400	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
46	chr10:94448800-94449400	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
47	chr10:94448800-94449400	Flanking Bivalent TSS/Enh	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr10:94448800-94449400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr10:94448800-94449400	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr10:94448800-94449400	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon

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