Variant report

Variant	esv3441326
Chromosome Location	chr10:21805146-21807294
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:386)
CpG islands
(count:490)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:386 , 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	BHLHE40	chr10:21806378-21806764	K562	blood:	n/a	n/a
2	CCNT2	chr10:21805061-21806699	K562	blood:	n/a	n/a
3	CEBPB	chr10:21807080-21807466	Hela-S3	cervix:	n/a	chr10:21807274-21807285
4	CEBPB	chr10:21807169-21807430	K562	blood:	n/a	chr10:21807274-21807285
5	CEBPB	chr10:21806960-21807582	A549	lung:	n/a	chr10:21807274-21807285
6	CEBPB	chr10:21805790-21805957	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr10:21807102-21807608	H1-hESC	embryonic stem cell:	n/a	chr10:21807274-21807285
8	CEBPB	chr10:21807085-21807518	A549	lung:	n/a	chr10:21807274-21807285
9	CEBPB	chr10:21807088-21807457	A549	lung:	n/a	chr10:21807274-21807285
10	CEBPB	chr10:21807141-21807431	HepG2	liver:	n/a	chr10:21807274-21807285
11	CEBPB	chr10:21807105-21807460	IMR90	lung:	n/a	chr10:21807274-21807285
12	CEBPD	chr10:21806298-21806635	HepG2	liver:	n/a	n/a
13	CHD1	chr10:21805182-21805704	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD1	chr10:21806214-21808592	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr10:21806271-21806614	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr10:21806278-21806584	HepG2	liver:	n/a	n/a
17	CHD2	chr10:21805421-21805621	Hela-S3	cervix:	n/a	n/a
18	CHD2	chr10:21805565-21805626	K562	blood:	n/a	n/a
19	CHD2	chr10:21806104-21806708	Hela-S3	cervix:	n/a	n/a
20	CREB1	chr10:21806237-21806687	A549	lung:	n/a	n/a
21	CTBP2	chr10:21804821-21805873	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTBP2	chr10:21806180-21806743	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr10:21806304-21806583	MCF-7	breast:	n/a	n/a
24	CTCF	chr10:21805876-21805877	GM19239	blood:	n/a	n/a
25	CTCF	chr10:21806360-21806510	AG04449	skin:	n/a	n/a
26	CTCF	chr10:21806340-21806490	HUVEC	blood vessel:	n/a	n/a
27	CTCF	chr10:21806259-21806547	K562	blood:	n/a	n/a
28	CTCF	chr10:21806340-21806490	GM12865	blood:	n/a	n/a
29	CTCF	chr10:21806260-21806410	K562	blood:	n/a	n/a
30	CTCF	chr10:21806384-21806509	Fibrobl	skin:	n/a	n/a
31	CTCF	chr10:21805860-21805936	GM13976	blood:	n/a	n/a
32	CTCF	chr10:21806344-21806546	A549	lung:	n/a	n/a
33	CTCF	chr10:21806334-21806490	MCF-7	breast:	n/a	n/a
34	CTCF	chr10:21806245-21806505	K562	blood:	n/a	n/a
35	CTCF	chr10:21805739-21805965	GM12878	blood:	n/a	n/a
36	CTCF	chr10:21805200-21805350	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr10:21806347-21806461	GM19240	blood:	n/a	n/a
38	CTCF	chr10:21806420-21806570	SAEC	small airway:	n/a	n/a
39	CTCF	chr10:21806180-21806330	GM12866	blood:	n/a	n/a
40	CTCF	chr10:21805847-21805970	GM12892	blood:	n/a	n/a
41	CTCF	chr10:21805852-21805958	MCF-7	breast:	n/a	n/a
42	CTCF	chr10:21806500-21806650	GM12864	blood:	n/a	n/a
43	CTCF	chr10:21806355-21806473	GM19238	blood:	n/a	n/a
44	CTCF	chr10:21806420-21806570	GM12869	blood:	n/a	n/a
45	CTCF	chr10:21805800-21805950	Caco-2	colon:	n/a	n/a
46	CTCF	chr10:21805860-21805952	GM19240	blood:	n/a	n/a
47	CTCF	chr10:21806355-21806407	GM19239	blood:	n/a	n/a
48	CTCF	chr10:21805580-21805730	AG04449	skin:	n/a	n/a
49	CTCF	chr10:21806420-21806570	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr10:21806212-21806502	HepG2	liver:	n/a	n/a

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:21806139-21806189	U87	brain:	n/a
2	chr10:21805358-21805408	SK-N-SH	brain:	n/a
3	chr10:21806139-21806189	U87	brain:	n/a
4	chr10:21805358-21805408	SK-N-SH	brain:	n/a
5	chr10:21805800-21805850	NHBE	bronchial:	n/a
6	chr10:21806076-21806126	Hela-S3	cervix:	n/a
7	chr10:21807252-21807302	BE2_C	brain:	n/a
8	chr10:21805800-21805850	AG09319	gingival:	n/a
9	chr10:21805402-21805452	HAEpiC	amniotic membrane:	n/a
10	chr10:21806139-21806189	GM12892	blood:	n/a
11	chr10:21805800-21805850	AG04450	lung:	fetal
12	chr10:21807211-21807261	HRPEpiC	eye:	n/a
13	chr10:21806076-21806126	AG09309	skin:	n/a
14	chr10:21807166-21807216	AG09309	skin:	n/a
15	chr10:21807166-21807216	HRE	kidney:	n/a
16	chr10:21805358-21805408	A549	lung:	n/a
17	chr10:21806076-21806126	HNPCEpiC	eye:	n/a
18	chr10:21805800-21805850	AG09309	skin:	n/a
19	chr10:21806076-21806126	AG04450	lung:	fetal
20	chr10:21806139-21806189	HCM	heart:	n/a
21	chr10:21807211-21807261	GM19239	blood:	n/a
22	chr10:21807252-21807302	AoSMC	blood vessel:	n/a
23	chr10:21807166-21807216	HPAEpiC	pulmonary alveolar:	n/a
24	chr10:21806139-21806189	ECC-1	luminal epithelium:	n/a
25	chr10:21806076-21806126	IMR90	lung:	fetal
26	chr10:21805800-21805850	HCT-116	colon:	n/a
27	chr10:21806139-21806189	HUVEC	blood vessel:	n/a
28	chr10:21806139-21806189	RPTEC	kidney:	n/a
29	chr10:21805358-21805408	HL-60	blood:	n/a
30	chr10:21807252-21807302	A549	lung:	n/a
31	chr10:21806139-21806189	GM12878	blood:	n/a
32	chr10:21805800-21805850	H1-hESC	embryonic stem cell:	embryo
33	chr10:21805402-21805452	MCF10A-Er-Src	breast:	n/a
34	chr10:21805800-21805850	ovcar-3	ovarian:	n/a
35	chr10:21807211-21807261	PFSK-1	brain:	n/a
36	chr10:21806076-21806126	BJ	skin:	n/a
37	chr10:21806139-21806189	A549	lung:	n/a
38	chr10:21805358-21805408	Jurkat	blood:	n/a
39	chr10:21807211-21807261	HepG2	liver:	n/a
40	chr10:21805358-21805408	GM19239	blood:	n/a
41	chr10:21807166-21807216	IMR90	lung:	fetal
42	chr10:21805800-21805850	RPTEC	kidney:	n/a
43	chr10:21805358-21805408	HAEpiC	amniotic membrane:	n/a
44	chr10:21805402-21805452	AoSMC	blood vessel:	n/a
45	chr10:21807211-21807261	AG04450	lung:	fetal
46	chr10:21807211-21807261	AG09319	gingival:	n/a
47	chr10:21807252-21807302	Hela-S3	cervix:	n/a
48	chr10:21805358-21805408	HCM	heart:	n/a
49	chr10:21807166-21807216	SK-N-MC	brain:	n/a
50	chr10:21807166-21807216	HIPEpiC	eye:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:21624338..21627195-chr10:21803332..21806134,2	MCF-7	breast:
2	chr10:21794929..21798874-chr10:21803033..21806226,5	K562	blood:
3	chr10:21783306..21788486-chr10:21805319..21811721,9	K562	blood:
4	chr10:21784381..21785021-chr10:21806127..21806753,2	MCF-7	breast:
5	chr10:21789123..21792163-chr10:21802631..21806658,3	MCF-7	breast:
6	chr10:21799042..21801453-chr10:21803205..21806030,4	MCF-7	breast:
7	chr10:21783475..21788073-chr10:21802793..21808915,11	MCF-7	breast:
8	chr10:21805605..21807805-chr10:21851609..21854226,2	MCF-7	breast:

No data

Variant related genes	Relation type
SKIDA1	TF binding region
SKIDA1	CpG island
ENSG00000207347	chromatin interactions
ENSG00000222071	chromatin interactions
ENSG00000204682	chromatin interactions

Extended variants
information (count: 64 )
Associated
traits (count: 35 )

Variant overlapped rSNPs/rCNVs (count:64 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372042825	chr10:21805165-21805166	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs187865454	chr10:21805167-21805168	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs199786304	chr10:21805176-21805177	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs564628471	chr10:21805183-21805184	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs372139891	chr10:21805191-21805192	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs375502355	chr10:21805204-21805205	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs374968071	chr10:21805212-21805213	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs570307343	chr10:21805223-21805224	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs201812682	chr10:21805241-21805242	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs373742077	chr10:21805245-21805246	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs376500574	chr10:21805263-21805264	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs369319147	chr10:21805266-21805267	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs373816445	chr10:21805321-21805322	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs547752540	chr10:21805345-21805346	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs201628705	chr10:21805387-21805388	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs373195307	chr10:21805442-21805443	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs192157988	chr10:21805454-21805455	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs553562521	chr10:21805459-21805460	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs112207161	chr10:21805466-21805467	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs201836118	chr10:21805480-21805481	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs370380837	chr10:21805537-21805538	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs376037638	chr10:21805679-21805680	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs577009784	chr10:21805749-21805750	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs539596870	chr10:21805765-21805766	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs183835202	chr10:21805807-21805808	Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs187048263	chr10:21805810-21805811	Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs191856294	chr10:21805813-21805814	Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs184454408	chr10:21805819-21805820	Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs556217118	chr10:21805852-21805853	Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs576249151	chr10:21805908-21805909	Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs528652346	chr10:21806019-21806020	Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs541879371	chr10:21806047-21806048	Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs377557900	chr10:21806187-21806188	Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs370781497	chr10:21806206-21806207	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs562015153	chr10:21806213-21806214	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs374992267	chr10:21806223-21806224	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs572580223	chr10:21806317-21806318	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs7072980	chr10:21806321-21806322	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs564569965	chr10:21806333-21806334	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs533390342	chr10:21806337-21806338	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs550333279	chr10:21806350-21806351	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs563846320	chr10:21806443-21806444	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs200611548	chr10:21806446-21806447	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs547788272	chr10:21806688-21806689	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs371514617	chr10:21806692-21806693	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs567680362	chr10:21806696-21806697	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs533538345	chr10:21806698-21806699	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs374060542	chr10:21806704-21806705	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs946711	chr10:21806832-21806833	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs41277378	chr10:21806858-21806859	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:35)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Intracranial aneurysm	16715129	CNVD
Multiple myeloma	16616336	CNVD
T-cell lymphomas	19863542	CNVD
Esophageal cancer	21851588	CNVD
small cell lung cancer	20016488	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	21525872	CNVD

Chromatin state (count:390 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:21797400-21806600	Active TSS	Fetal Brain Female	brain
2	chr10:21800000-21805800	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr10:21800200-21805600	Transcr. at gene 5' and 3'	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr10:21801000-21805400	Transcr. at gene 5' and 3'	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr10:21801000-21809200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr10:21802000-21806600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr10:21802800-21807000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr10:21803000-21805600	Active TSS	Fetal Heart	heart
9	chr10:21803200-21805200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
10	chr10:21803200-21809200	Active TSS	Colon Smooth Muscle	Colon
11	chr10:21803400-21805200	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
12	chr10:21803400-21808200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr10:21803600-21805600	Flanking Active TSS	Liver	Liver
14	chr10:21803600-21808000	Active TSS	Fetal Lung	lung
15	chr10:21803600-21808600	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
16	chr10:21803800-21805200	Active TSS	Fetal Muscle Trunk	muscle
17	chr10:21804000-21805200	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr10:21804000-21805200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
19	chr10:21804000-21806800	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
20	chr10:21804000-21809600	Active TSS	Right Ventricle	heart
21	chr10:21804200-21805200	Enhancers	Esophagus	oesophagus
22	chr10:21804200-21806400	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
23	chr10:21804200-21809400	Active TSS	Brain Inferior Temporal Lobe	brain
24	chr10:21804200-21809400	Active TSS	Left Ventricle	heart
25	chr10:21804400-21805200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr10:21804400-21805200	Flanking Active TSS	Fetal Intestine Large	intestine
27	chr10:21804400-21805200	Flanking Active TSS	A549	lung
28	chr10:21804400-21805400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr10:21804400-21805600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr10:21804400-21808000	Active TSS	Brain Substantia Nigra	brain
31	chr10:21804400-21808000	Active TSS	Fetal Kidney	kidney
32	chr10:21804400-21808200	Active TSS	Placenta Amnion	Placenta Amnion
33	chr10:21804400-21809400	Active TSS	Brain Cingulate Gyrus	brain
34	chr10:21804400-21809600	Active TSS	Ovary	ovary
35	chr10:21804600-21805400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr10:21804600-21805600	Flanking Active TSS	Primary hematopoietic stem cells	blood
37	chr10:21804600-21805600	Active TSS	Fetal Brain Male	brain
38	chr10:21804600-21805600	Flanking Active TSS	NHEK	skin
39	chr10:21804600-21806400	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
40	chr10:21804600-21809600	Active TSS	Brain Germinal Matrix	brain
41	chr10:21804800-21805200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr10:21804800-21805200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr10:21804800-21805200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr10:21804800-21805200	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
45	chr10:21804800-21805200	Flanking Active TSS	Brain Hippocampus Middle	brain
46	chr10:21804800-21805200	Flanking Active TSS	HepG2	liver
47	chr10:21804800-21805400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
48	chr10:21804800-21805400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
49	chr10:21804800-21805400	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
50	chr10:21804800-21805400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood

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