Variant report

Variant	esv34779
Chromosome Location	chr21:40884871-40977473
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:729)
CpG islands
(count:122)
Chromatin interactive
region (count:99)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:729 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:40890351-40890549	HepG2	liver:	n/a	n/a
2	ARID3A	chr21:40899665-40899842	HepG2	liver:	n/a	n/a
3	ATF1	chr21:40903903-40904225	K562	blood:	n/a	n/a
4	ATF2	chr21:40909605-40910115	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr21:40909409-40910070	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr21:40890244-40890540	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr21:40909577-40910020	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL11A	chr21:40909414-40909781	H1-hESC	embryonic stem cell:	n/a	n/a
9	BHLHE40	chr21:40890245-40890518	GM12878	blood:	n/a	n/a
10	BHLHE40	chr21:40890323-40890515	K562	blood:	n/a	n/a
11	BRCA1	chr21:40970051-40970096	HepG2	liver:	n/a	n/a
12	CBX3	chr21:40960796-40961090	K562	blood:	n/a	n/a
13	CEBPB	chr21:40890687-40890980	A549	lung:	n/a	chr21:40890863-40890876
14	CEBPB	chr21:40900371-40900587	HepG2	liver:	n/a	chr21:40900441-40900452
15	CEBPB	chr21:40916233-40916264	HepG2	liver:	n/a	chr21:40916247-40916258
16	CEBPB	chr21:40951298-40952147	MCF-7	breast:	n/a	n/a
17	CEBPB	chr21:40895515-40895666	HepG2	liver:	n/a	n/a
18	CEBPB	chr21:40890749-40890981	HepG2	liver:	n/a	chr21:40890863-40890876
19	CEBPB	chr21:40920982-40921249	HepG2	liver:	n/a	chr21:40921130-40921141
20	CEBPB	chr21:40921105-40921163	IMR90	lung:	n/a	chr21:40921130-40921141
21	CEBPB	chr21:40951432-40952178	MCF-7	breast:	n/a	n/a
22	CEBPB	chr21:40890776-40890889	IMR90	lung:	n/a	chr21:40890863-40890876
23	CEBPB	chr21:40899453-40900662	MCF-7	breast:	n/a	chr21:40900441-40900452
24	CEBPB	chr21:40965231-40965706	MCF-7	breast:	n/a	n/a
25	CEBPB	chr21:40895398-40896206	MCF-7	breast:	n/a	n/a
26	CHD1	chr21:40890197-40890667	IMR90	lung:	n/a	n/a
27	CHD1	chr21:40918489-40918500	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr21:40890252-40890537	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr21:40940516-40940543	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr21:40890273-40890575	HUVEC	blood vessel:	n/a	chr21:40890407-40890428 chr21:40890406-40890422 chr21:40890405-40890423
31	CTCF	chr21:40953476-40953536	Pancreas_OC	pancreas:	n/a	n/a
32	CTCF	chr21:40890196-40890650	K562	blood:	n/a	chr21:40890407-40890428 chr21:40890406-40890422 chr21:40890405-40890423
33	CTCF	chr21:40890380-40890530	Caco-2	colon:	n/a	chr21:40890407-40890428 chr21:40890406-40890422 chr21:40890405-40890423
34	CTCF	chr21:40890420-40890570	HCT-116	colon:	n/a	n/a
35	CTCF	chr21:40890057-40890931	A549	lung:	n/a	chr21:40890407-40890428 chr21:40890406-40890422 chr21:40890405-40890423
36	CTCF	chr21:40890299-40890530	A549	lung:	n/a	chr21:40890407-40890428 chr21:40890406-40890422 chr21:40890405-40890423
37	CTCF	chr21:40890112-40890150	GM13976	blood:	n/a	n/a
38	CTCF	chr21:40953400-40953550	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr21:40891530-40891654	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr21:40890340-40890490	GM12865	blood:	n/a	chr21:40890407-40890428 chr21:40890406-40890422 chr21:40890405-40890423
41	CTCF	chr21:40890700-40890850	GM12865	blood:	n/a	n/a
42	CTCF	chr21:40890121-40890139	GM19240	blood:	n/a	n/a
43	CTCF	chr21:40890340-40890490	AG09309	skin:	n/a	chr21:40890407-40890428 chr21:40890406-40890422 chr21:40890405-40890423
44	CTCF	chr21:40890264-40890520	SK-N-SH_RA	brain:	n/a	chr21:40890407-40890428 chr21:40890406-40890422 chr21:40890405-40890423
45	CTCF	chr21:40903755-40903932	MCF-7	breast:	n/a	n/a
46	CTCF	chr21:40890208-40890566	Gliobla	brain:	n/a	chr21:40890407-40890428 chr21:40890406-40890422 chr21:40890405-40890423
47	CTCF	chr21:40910779-40910791	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr21:40890270-40890544	LNCaP	prostate:	n/a	chr21:40890407-40890428 chr21:40890406-40890422 chr21:40890405-40890423
49	CTCF	chr21:40890300-40890450	GM06990	blood:	n/a	chr21:40890407-40890428 chr21:40890406-40890422 chr21:40890405-40890423
50	CTCF	chr21:40890360-40890510	AG09309	skin:	n/a	chr21:40890407-40890428 chr21:40890406-40890422 chr21:40890405-40890423

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:40886418-40886468	HEK293	kidney:	embryo
2	chr21:40931914-40931964	HCM	heart:	n/a
3	chr21:40886418-40886468	T-47D	breast:	n/a
4	chr21:40886418-40886468	A549	lung:	n/a
5	chr21:40886418-40886468	HRCEpiC	kidney:	n/a
6	chr21:40931914-40931964	HCPEpiC	choroid plexus:	n/a
7	chr21:40931914-40931964	GM12878	blood:	n/a
8	chr21:40886418-40886468	MCF10A-Er-Src	breast:	n/a
9	chr21:40931914-40931964	MCF-7	breast:	n/a
10	chr21:40931914-40931964	HUVEC	blood vessel:	n/a
11	chr21:40886418-40886468	LNCaP	prostate:	n/a
12	chr21:40931914-40931964	ProgFib	skin:	n/a
13	chr21:40931914-40931964	NHDF-neo	bronchial:	n/a
14	chr21:40886418-40886468	BE2_C	brain:	n/a
15	chr21:40931914-40931964	HCT-116	colon:	n/a
16	chr21:40931914-40931964	SKMC	muscle:	n/a
17	chr21:40931914-40931964	SK-N-SH	brain:	n/a
18	chr21:40931914-40931964	IMR90	lung:	fetal
19	chr21:40886418-40886468	GM19239	blood:	n/a
20	chr21:40931914-40931964	HRPEpiC	eye:	n/a
21	chr21:40931914-40931964	HNPCEpiC	eye:	n/a
22	chr21:40886418-40886468	HCF	heart:	n/a
23	chr21:40886418-40886468	HRPEpiC	eye:	n/a
24	chr21:40931914-40931964	SAEC	small airway:	n/a
25	chr21:40931914-40931964	GM06990	blood:	n/a
26	chr21:40886418-40886468	ProgFib	skin:	n/a
27	chr21:40931914-40931964	ovcar-3	ovarian:	n/a
28	chr21:40886418-40886468	AG10803	skin:	n/a
29	chr21:40886418-40886468	AG09309	skin:	n/a
30	chr21:40931914-40931964	Caco-2	colon:	n/a
31	chr21:40931914-40931964	AG04450	lung:	fetal
32	chr21:40931914-40931964	Jurkat	blood:	n/a
33	chr21:40931914-40931964	GM19239	blood:	n/a
34	chr21:40931914-40931964	Hela-S3	cervix:	n/a
35	chr21:40886418-40886468	HCM	heart:	n/a
36	chr21:40931914-40931964	ECC-1	luminal epithelium:	n/a
37	chr21:40886418-40886468	K562	blood:	n/a
38	chr21:40886418-40886468	Hela-S3	cervix:	n/a
39	chr21:40886418-40886468	HPAEpiC	pulmonary alveolar:	n/a
40	chr21:40886418-40886468	NT2-D1	testis:	n/a
41	chr21:40886418-40886468	SK-N-MC	brain:	n/a
42	chr21:40886418-40886468	HCT-116	colon:	n/a
43	chr21:40931914-40931964	AG09319	gingival:	n/a
44	chr21:40931914-40931964	GM12891	blood:	n/a
45	chr21:40931914-40931964	NHBE	bronchial:	n/a
46	chr21:40886418-40886468	PFSK-1	brain:	n/a
47	chr21:40931914-40931964	RPTEC	kidney:	n/a
48	chr21:40931914-40931964	PrEC	prostate:	n/a
49	chr21:40886418-40886468	HNPCEpiC	eye:	n/a
50	chr21:40886418-40886468	HL-60	blood:	n/a

(count:99 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr21:40889961..40890860-chr21:41087398..41088395,10	MCF-7	breast:
2	chr21:40933376..40935680-chr21:40951136..40954071,2	MCF-7	breast:
3	chr21:40891710..40894102-chr21:40894328..40895948,2	MCF-7	breast:
4	chr21:40976514..40978882-chr21:40987659..40990131,2	MCF-7	breast:
5	chr21:40928238..40929752-chr21:40932007..40934794,2	MCF-7	breast:
6	chr21:40933376..40935680-chr21:40951136..40954071,2	MCF-7	breast:
7	chr21:40816623..40819045-chr21:40951462..40953239,2	MCF-7	breast:
8	chr21:40963714..40965931-chr21:40968819..40971403,2	K562	blood:
9	chr21:40889947..40890880-chr21:41084564..41085517,6	MCF-7	breast:
10	chr21:40966387..40968273-chr21:40975393..40977345,2	MCF-7	breast:
11	chr21:40901121..40903929-chr21:40907917..40910902,2	K562	blood:
12	chr21:40898411..40901316-chr21:40977081..40979354,2	MCF-7	breast:
13	chr21:40891069..40892721-chr21:40900987..40902576,2	MCF-7	breast:
14	chr21:40815529..40818322-chr21:40890161..40892801,2	MCF-7	breast:
15	chr21:40938920..40940719-chr21:40942034..40944243,2	MCF-7	breast:
16	chr21:40919721..40922141-chr21:40925056..40927590,2	MCF-7	breast:
17	chr21:40889992..40890995-chr21:41087409..41088601,6	MCF-7	breast:
18	chr21:40951149..40953987-chr21:41066958..41068611,2	MCF-7	breast:
19	chr21:40893231..40895228-chr21:40896960..40900223,3	MCF-7	breast:
20	chr21:40966387..40968273-chr21:40975393..40977345,2	MCF-7	breast:
21	chr21:40902475..40904077-chr21:40952462..40954060,2	MCF-7	breast:
22	chr21:40931124..40933238-chr21:40974685..40976833,2	MCF-7	breast:
23	chr21:40973024..40975835-chr21:41005421..41007852,2	MCF-7	breast:
24	chr21:40898411..40901316-chr21:40977081..40979354,2	MCF-7	breast:
25	chr21:40938677..40940816-chr21:41079572..41081840,2	MCF-7	breast:
26	chr21:40889928..40890908-chr21:41492573..41493506,3	K562	blood:
27	chr21:40938866..40941607-chr21:40942165..40944706,2	K562	blood:
28	chr21:40975922..40977945-chr21:40981394..40984393,2	MCF-7	breast:
29	chr21:40963714..40965931-chr21:40968819..40971403,2	K562	blood:
30	chr21:40936564..40938095-chr21:40947433..40949927,2	MCF-7	breast:
31	chr21:40951091..40953456-chr21:41032196..41036006,4	MCF-7	breast:
32	chr21:40895232..40897422-chr21:40987219..40990019,2	MCF-7	breast:
33	chr21:40950425..40953784-chr21:40975609..40978181,3	MCF-7	breast:
34	chr21:40918819..40921569-chr21:40925046..40926881,2	K562	blood:
35	chr21:40903746..40904291-chr21:41077595..41078460,2	MCF-7	breast:
36	chr21:40900284..40901980-chr21:41045530..41047230,2	MCF-7	breast:
37	chr21:40950925..40952824-chr21:40985213..40987161,2	MCF-7	breast:
38	chr21:40894588..40897351-chr21:41015543..41018234,2	MCF-7	breast:
39	chr21:40888055..40890382-chr21:41107871..41110600,2	MCF-7	breast:
40	chr21:40894704..40896899-chr21:40951352..40952979,2	MCF-7	breast:
41	chr21:40890554..40891390-chr21:41077384..41078170,2	MCF-7	breast:
42	chr21:40889881..40890913-chr21:41087416..41088456,10	K562	blood:
43	chr21:40931124..40933238-chr21:40974685..40976833,2	MCF-7	breast:
44	chr21:40943694..40945815-chr21:40949884..40952156,3	MCF-7	breast:
45	chr21:40890014..40890661-chr21:41083159..41083881,2	MCF-7	breast:
46	chr21:40891069..40892721-chr21:40900987..40902576,2	MCF-7	breast:
47	chr21:40936564..40938095-chr21:40947433..40949927,2	MCF-7	breast:
48	chr21:40895888..40897721-chr21:40949552..40952315,2	MCF-7	breast:
49	chr21:40902475..40904077-chr21:40952462..40954060,2	MCF-7	breast:
50	chr21:40889963..40891050-chr21:41077484..41078432,7	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SH3BGR-3	chr21:40934881-40935511	NONHSAT082199
2	lnc-C21orf88-1	chr21:40969074-40969916	NONHSAT082201
3	lnc-SH3BGR-5	chr21:40974740-40975257	NONHSAT082203
4	lnc-C21orf88-1	chr21:40969031-40972206	NONHSAT082200
5	lnc-SH3BGR-5	chr21:40975412-40975419	NONHSAT082203
6	lnc-C21orf88-1	chr21:40969075-40969916	NR_026542
7	lnc-C21orf88-1	chr21:40973346-40973473	NONHSAT082200
8	lnc-SH3BGR-3	chr21:40928411-40928437	NONHSAT082199
9	lnc-C21orf88-1	chr21:40976206-40976335	NONHSAT082200
10	lnc-SH3BGR-1	chr21:40898286-40901782	NONHSAT082198
11	lnc-C21orf88-1	chr21:40971268-40971583	NONHSAT082201
12	lnc-C21orf88-1	chr21:40976387-40978276	NONHSAT082200
13	lnc-SH3BGR-1	chr21:40897510-40897992	NONHSAT082198

No data

Variant related genes	Relation type
B3GALT5	TF binding region
C21orf88	TF binding region
ENSG00000235012	TF binding region
B3GALT5	CpG island
C21orf88	CpG island
ENSG00000235012	CpG island
ENSG00000235012	chromatin interactions
ENSG00000183778	chromatin interactions
ENSG00000185437	chromatin interactions
ENSG00000184809	chromatin interactions
ENSG00000157578	chromatin interactions
ENSG00000170836	chromatin interactions

Extended variants
information (count: 3535 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:3535 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7281425	chr21:40884871-40884872	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs116315105	chr21:40884924-40884925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs184798825	chr21:40884925-40884926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs145327246	chr21:40884938-40884939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs79263589	chr21:40884944-40884945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs188876968	chr21:40884994-40884995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs558426454	chr21:40884995-40884996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs181677096	chr21:40885036-40885037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs183980054	chr21:40885042-40885043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs533923015	chr21:40885093-40885094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs7281891	chr21:40885103-40885104	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs7282142	chr21:40885108-40885109	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs7281794	chr21:40885159-40885160	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs79638666	chr21:40885182-40885183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576231615	chr21:40885184-40885185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs80342760	chr21:40885199-40885200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs75043774	chr21:40885207-40885208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs75665121	chr21:40885281-40885282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs540648670	chr21:40885291-40885292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs144971946	chr21:40885295-40885296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs574552727	chr21:40885318-40885319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs76747482	chr21:40885320-40885321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs189671354	chr21:40885339-40885340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs62222775	chr21:40885379-40885380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs58689801	chr21:40885452-40885453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs397949055	chr21:40885456-40885457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs377527894	chr21:40885477-40885478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs532344676	chr21:40885496-40885497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs371084340	chr21:40885497-40885498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs552381300	chr21:40885511-40885512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs368908773	chr21:40885532-40885533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs559362521	chr21:40885539-40885540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs528406970	chr21:40885559-40885560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs181316308	chr21:40885646-40885647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs116808870	chr21:40885722-40885723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs536299463	chr21:40885739-40885740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs549858136	chr21:40885759-40885760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs34015367	chr21:40885779-40885780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs538708758	chr21:40885793-40885794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs574323	chr21:40885843-40885844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs556952362	chr21:40885893-40885894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs569854741	chr21:40885925-40885926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs538842895	chr21:40885997-40885998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs143082948	chr21:40886026-40886027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs572624340	chr21:40886034-40886035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs535342561	chr21:40886062-40886063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs76847003	chr21:40886069-40886070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs574491101	chr21:40886070-40886071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs540354148	chr21:40886165-40886166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs145090207	chr21:40886176-40886177	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Down syndrome	17412756	CNVD
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Renal cell carcinoma	19461508	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
lymphocytic leukemia	21291569	CNVD
Melanoma	18172304	CNVD
Autism	22958593	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Wilms tumour	21544195	CNVD
Ewing''s sarcoma	17952124	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute myeloid leukemia	16864856	CNVD
Mental retardation	21031080	CNVD
Polymicrogyria	21031080	CNVD
periventricular nodular heterotopia	21031080	CNVD
Myelodysplastic syndrome	21606161	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Autism	18414403	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21858162	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17899364	CNVD
Down syndrome	20877625	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Prostate cancer	21147910	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Prostate cancer	17245344	CNVD
Prostate cancer	20473283	CNVD
Chordoma	18071362	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:764 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:40836400-40894800	Weak transcription	Right Ventricle	heart
2	chr21:40848200-40895600	Weak transcription	Stomach Smooth Muscle	stomach
3	chr21:40874800-40887000	Weak transcription	Aorta	Aorta
4	chr21:40875200-40890400	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr21:40875400-40890200	Weak transcription	Brain Hippocampus Middle	brain
6	chr21:40875400-40890400	Weak transcription	Fetal Lung	lung
7	chr21:40875800-40895200	Weak transcription	Brain Substantia Nigra	brain
8	chr21:40875800-40898600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr21:40876400-40887600	Weak transcription	Left Ventricle	heart
10	chr21:40876400-40894600	Weak transcription	Gastric	stomach
11	chr21:40876400-40897400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr21:40876600-40885000	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr21:40877000-40891000	Weak transcription	Pancreas	Pancrea
14	chr21:40877200-40887000	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr21:40877400-40899600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr21:40878200-40889800	Weak transcription	Primary T cells from cord blood	blood
17	chr21:40880200-40899800	Weak transcription	Fetal Muscle Leg	muscle
18	chr21:40880600-40885000	Weak transcription	Psoas Muscle	Psoas
19	chr21:40883000-40885400	Enhancers	Fetal Heart	heart
20	chr21:40883200-40887800	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr21:40883400-40890400	Weak transcription	Fetal Kidney	kidney
22	chr21:40884400-40886400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr21:40884600-40887600	Weak transcription	Brain Anterior Caudate	brain
24	chr21:40885000-40885600	Enhancers	Skeletal Muscle Female	skeletal muscle
25	chr21:40885000-40886000	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr21:40885200-40885400	Enhancers	Fetal Brain Female	brain
27	chr21:40885200-40888200	Enhancers	Fetal Brain Male	brain
28	chr21:40885400-40885600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr21:40885400-40885800	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr21:40885400-40885800	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr21:40885400-40886800	Weak transcription	Fetal Brain Female	brain
32	chr21:40885400-40890600	Weak transcription	Fetal Heart	heart
33	chr21:40885600-40887600	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr21:40885600-40891000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr21:40885800-40887800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr21:40886400-40888200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
37	chr21:40886800-40888200	Enhancers	Fetal Brain Female	brain
38	chr21:40887000-40888000	Strong transcription	Aorta	Aorta
39	chr21:40887000-40888200	Strong transcription	Skeletal Muscle Male	skeletal muscle
40	chr21:40887000-40890600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr21:40887400-40888400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr21:40887400-40888600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr21:40887400-40890400	Weak transcription	Adipose Nuclei	Adipose
44	chr21:40887400-40895200	Weak transcription	Liver	Liver
45	chr21:40887600-40888000	Strong transcription	Left Ventricle	heart
46	chr21:40887600-40888200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr21:40887600-40888200	Strong transcription	Skeletal Muscle Female	skeletal muscle
48	chr21:40887600-40888400	Enhancers	Brain Anterior Caudate	brain
49	chr21:40887800-40888200	Enhancers	H9 Cell Line	embryonic stem cell
50	chr21:40887800-40888200	Enhancers	HUES48 Cell Line	embryonic stem cell

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