Variant report

Variant	esv3498615
Chromosome Location	chr21:47602674-47604872
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:441)
CpG islands
(count:367)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:441 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:47603955-47605670	K562	blood:	n/a	n/a
2	ATF1	chr21:47604322-47605322	K562	blood:	n/a	n/a
3	BACH1	chr21:47604648-47604803	K562	blood:	n/a	n/a
4	BACH1	chr21:47604533-47605159	H1-hESC	embryonic stem cell:	n/a	chr21:47604969-47604983
5	BACH1	chr21:47604094-47604170	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr21:47604305-47604771	GM12878	blood:	n/a	n/a
7	BATF	chr21:47604311-47604581	GM12878	blood:	n/a	n/a
8	BCL11A	chr21:47604284-47604707	GM12878	blood:	n/a	n/a
9	BCL11A	chr21:47604296-47604778	GM12878	blood:	n/a	n/a
10	BHLHE40	chr21:47604531-47604866	GM12878	blood:	n/a	n/a
11	BHLHE40	chr21:47602670-47602874	K562	blood:	n/a	n/a
12	BHLHE40	chr21:47603834-47605107	K562	blood:	n/a	n/a
13	BHLHE40	chr21:47603113-47603416	K562	blood:	n/a	n/a
14	BRCA1	chr21:47604496-47604500	GM12878	blood:	n/a	n/a
15	BRCA1	chr21:47604610-47604804	HepG2	liver:	n/a	n/a
16	BRCA1	chr21:47604617-47604806	H1-hESC	embryonic stem cell:	n/a	n/a
17	BRCA1	chr21:47604428-47604792	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr21:47603261-47605256	K562	blood:	n/a	n/a
19	CCNT2	chr21:47603783-47605058	K562	blood:	n/a	n/a
20	CCNT2	chr21:47602516-47603574	K562	blood:	n/a	n/a
21	CEBPB	chr21:47604664-47604999	H1-hESC	embryonic stem cell:	n/a	chr21:47604860-47604871
22	CEBPB	chr21:47604594-47605069	MCF-7	breast:	n/a	chr21:47604860-47604871
23	CEBPB	chr21:47603263-47603964	K562	blood:	n/a	n/a
24	CEBPB	chr21:47604151-47605207	K562	blood:	n/a	chr21:47604860-47604871
25	CEBPB	chr21:47604671-47605051	IMR90	lung:	n/a	chr21:47604860-47604871
26	CEBPB	chr21:47604639-47604980	K562	blood:	n/a	chr21:47604860-47604871
27	CEBPB	chr21:47604611-47605154	K562	blood:	n/a	chr21:47604860-47604871
28	CEBPB	chr21:47604625-47605036	HepG2	liver:	n/a	chr21:47604860-47604871
29	CEBPB	chr21:47604600-47605061	Hela-S3	cervix:	n/a	chr21:47604860-47604871
30	CEBPD	chr21:47603229-47604112	K562	blood:	n/a	n/a
31	CEBPZ	chr21:47604298-47604856	HepG2	liver:	n/a	n/a
32	CHD1	chr21:47604225-47604292	GM12878	blood:	n/a	n/a
33	CHD1	chr21:47604847-47605030	GM12878	blood:	n/a	n/a
34	CHD1	chr21:47604719-47604919	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr21:47604138-47604903	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr21:47603959-47605020	K562	blood:	n/a	n/a
37	CHD2	chr21:47604350-47604863	HepG2	liver:	n/a	n/a
38	CHD2	chr21:47603938-47605049	GM12878	blood:	n/a	n/a
39	CHD2	chr21:47604302-47605034	Hela-S3	cervix:	n/a	n/a
40	CREB1	chr21:47604524-47605208	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chr21:47604132-47605133	GM12878	blood:	n/a	n/a
42	CREB1	chr21:47604538-47605161	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr21:47604335-47604653	A549	lung:	n/a	n/a
44	CTCF	chr21:47602447-47602803	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr21:47604431-47604693	GM10248	blood:	n/a	n/a
46	CTCF	chr21:47604577-47604585	Pancreas_OC	pancreas:	n/a	n/a
47	CTCF	chr21:47604195-47604926	K562	blood:	n/a	n/a
48	CTCF	chr21:47602560-47602710	K562	blood:	n/a	n/a
49	CTCF	chr21:47602470-47602826	K562	blood:	n/a	n/a
50	CTCF	chr21:47604403-47604632	GM13977	blood:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:47604654-47604704	AoSMC	blood vessel:	n/a
2	chr21:47604654-47604704	AoSMC	blood vessel:	n/a
3	chr21:47604291-47604341	NHDF-neo	bronchial:	n/a
4	chr21:47604291-47604341	HCPEpiC	choroid plexus:	n/a
5	chr21:47604291-47604341	GM12891	blood:	n/a
6	chr21:47604291-47604341	HCF	heart:	n/a
7	chr21:47604291-47604341	SK-N-MC	brain:	n/a
8	chr21:47604052-47604102	SAEC	small airway:	n/a
9	chr21:47602702-47602752	Caco-2	colon:	n/a
10	chr21:47604654-47604704	HCF	heart:	n/a
11	chr21:47604052-47604102	BE2_C	brain:	n/a
12	chr21:47604654-47604704	GM06990	blood:	n/a
13	chr21:47604291-47604341	SK-N-SH	brain:	n/a
14	chr21:47604361-47604411	HRPEpiC	eye:	n/a
15	chr21:47604654-47604704	AG04449	skin:	fetal
16	chr21:47604291-47604341	MCF-7	breast:	n/a
17	chr21:47604291-47604341	Jurkat	blood:	n/a
18	chr21:47604052-47604102	Jurkat	blood:	n/a
19	chr21:47604291-47604341	AG09309	skin:	n/a
20	chr21:47604654-47604704	PFSK-1	brain:	n/a
21	chr21:47604291-47604341	HNPCEpiC	eye:	n/a
22	chr21:47604654-47604704	A549	lung:	n/a
23	chr21:47604361-47604411	HCM	heart:	n/a
24	chr21:47604361-47604411	ovcar-3	ovarian:	n/a
25	chr21:47604654-47604704	HPAEpiC	pulmonary alveolar:	n/a
26	chr21:47604052-47604102	NHBE	bronchial:	n/a
27	chr21:47604052-47604102	NHDF-neo	bronchial:	n/a
28	chr21:47604291-47604341	HIPEpiC	eye:	n/a
29	chr21:47604654-47604704	RPTEC	kidney:	n/a
30	chr21:47604052-47604102	AG04449	skin:	fetal
31	chr21:47604166-47604216	HNPCEpiC	eye:	n/a
32	chr21:47604166-47604216	RPTEC	kidney:	n/a
33	chr21:47604052-47604102	MCF-7	breast:	n/a
34	chr21:47604166-47604216	HepG2	liver:	n/a
35	chr21:47604361-47604411	H1-hESC	embryonic stem cell:	embryo
36	chr21:47604052-47604102	Caco-2	colon:	n/a
37	chr21:47604166-47604216	GM06990	blood:	n/a
38	chr21:47604052-47604102	SKMC	muscle:	n/a
39	chr21:47604361-47604411	HEK293	kidney:	embryo
40	chr21:47604166-47604216	HPAEpiC	pulmonary alveolar:	n/a
41	chr21:47604291-47604341	H1-hESC	embryonic stem cell:	embryo
42	chr21:47604052-47604102	PFSK-1	brain:	n/a
43	chr21:47604361-47604411	NHDF-neo	bronchial:	n/a
44	chr21:47602702-47602752	NB4	blood:	n/a
45	chr21:47604291-47604341	RPTEC	kidney:	n/a
46	chr21:47604361-47604411	Hepatocyte	liver:	n/a
47	chr21:47604361-47604411	GM12891	blood:	n/a
48	chr21:47604166-47604216	PFSK-1	brain:	n/a
49	chr21:47604166-47604216	NB4	blood:	n/a
50	chr21:47602702-47602752	MCF-7	breast:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:47604083..47605836-chr21:47704849..47706499,2	K562	blood:
2	chr21:47563716..47566123-chr21:47602803..47604796,2	K562	blood:
3	chr21:47600488..47602703-chr21:47632844..47634921,2	K562	blood:
4	chr21:47602595..47605401-chr21:47649000..47651929,3	K562	blood:
5	chr21:47602847..47606841-chr21:47742668..47745795,6	K562	blood:
6	chr21:47603167..47605215-chr21:47743246..47745709,3	K562	blood:
7	chr21:47600278..47602930-chr21:47743867..47746831,2	K562	blood:
8	chr21:47601827..47605045-chr21:47646095..47649627,4	MCF-7	breast:
9	chr21:47591887..47593806-chr21:47599783..47602845,3	K562	blood:
10	chr21:47563633..47565565-chr21:47603562..47606281,2	K562	blood:
11	chr21:47588823..47590462-chr21:47601081..47603080,2	MCF-7	breast:
12	chr21:47602452..47604357-chr21:47877079..47880272,3	K562	blood:
13	chr21:47571733..47573390-chr21:47601169..47604058,2	K562	blood:
14	chr21:47601203..47604335-chr21:47632751..47634921,3	K562	blood:
15	chr21:47602500..47604164-chr21:47614586..47616622,2	K562	blood:
16	chr21:47568990..47571521-chr21:47602008..47603891,2	K562	blood:

No data

Variant related genes	Relation type
SPATC1L	TF binding region
ENSG00000228404	TF binding region
SPATC1L	CpG island
ENSG00000228404	CpG island
ENSG00000160285	chromatin interactions
ENSG00000160282	chromatin interactions
ENSG00000160294	chromatin interactions
ENSG00000160299	chromatin interactions
ENSG00000215424	chromatin interactions
ENSG00000160298	chromatin interactions
ENSG00000160305	chromatin interactions
ENSG00000182362	chromatin interactions

Extended variants
information (count: 137 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:137 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557963450	chr21:47602686-47602687	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs143719440	chr21:47602691-47602692	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs544371646	chr21:47602692-47602693	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs114558842	chr21:47602701-47602702	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs534033767	chr21:47602715-47602716	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs55819909	chr21:47602719-47602720	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs35921830	chr21:47602745-47602746	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs113955394	chr21:47602750-47602751	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs546782709	chr21:47602758-47602759	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs149414972	chr21:47602773-47602774	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs560379686	chr21:47602774-47602775	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs566694792	chr21:47602812-47602813	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs138357031	chr21:47602824-47602825	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs554119745	chr21:47602842-47602843	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs532397772	chr21:47602854-47602855	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs552506545	chr21:47602881-47602882	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs2330407	chr21:47602907-47602908	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs549567840	chr21:47602920-47602921	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs568072065	chr21:47602985-47602986	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs535074321	chr21:47602993-47602994	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs369053734	chr21:47603040-47603041	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs538282798	chr21:47603069-47603070	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs554745368	chr21:47603071-47603072	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs547355148	chr21:47603089-47603090	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs55652162	chr21:47603099-47603100	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs534046367	chr21:47603192-47603193	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs57262496	chr21:47603199-47603200	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs62215188	chr21:47603202-47603203	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs558025460	chr21:47603264-47603265	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs576263972	chr21:47603333-47603334	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs35799958	chr21:47603352-47603353	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs538340113	chr21:47603362-47603363	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs143998500	chr21:47603374-47603375	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs556354162	chr21:47603383-47603384	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs56293013	chr21:47603413-47603414	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs141064018	chr21:47603426-47603427	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs55730748	chr21:47603465-47603466	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs556264500	chr21:47603500-47603501	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs541891340	chr21:47603502-47603503	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs35960150	chr21:47603509-47603510	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs572450358	chr21:47603514-47603515	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs554317959	chr21:47603532-47603533	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs546077816	chr21:47603533-47603534	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs564346349	chr21:47603535-47603536	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs531787297	chr21:47603582-47603583	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs373960010	chr21:47603636-47603637	Weak transcription Enhancers Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs28788544	chr21:47603640-47603641	Weak transcription Enhancers Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs28839323	chr21:47603657-47603658	Weak transcription Enhancers Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs561668170	chr21:47603658-47603659	Weak transcription Enhancers Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs528963626	chr21:47603663-47603664	Weak transcription Enhancers Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:36)

Disease	PMID	Source
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	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
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Autism	18414403	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Breast cancer	17899364	CNVD
Prostate cancer	20473283	CNVD
Chordoma	18071362	CNVD
Cholangiocarcinoma	16830362	CNVD
Down syndrome	17334655	CNVD
Neuroticism	17667963	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Autoimmune polyendocrine syndrome	18200029	CNVD
Prostate cancer	19363497	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Olfactory neuroblastoma	18408657	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Multiple myeloma	16616336	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:391 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:47573800-47603800	Weak transcription	Right Atrium	heart
2	chr21:47581400-47602800	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr21:47582000-47602800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr21:47582000-47602800	Weak transcription	Ovary	ovary
5	chr21:47582400-47603800	Weak transcription	Thymus	Thymus
6	chr21:47583000-47602800	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr21:47588600-47602800	Weak transcription	Lung	lung
8	chr21:47594200-47603800	Weak transcription	Fetal Intestine Small	intestine
9	chr21:47596800-47603000	Weak transcription	Brain Hippocampus Middle	brain
10	chr21:47597200-47602800	Weak transcription	Right Ventricle	heart
11	chr21:47597200-47603800	Weak transcription	Fetal Brain Female	brain
12	chr21:47598000-47602800	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr21:47598000-47603000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr21:47598000-47603400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr21:47598600-47603800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr21:47599200-47602800	Weak transcription	Pancreas	Pancrea
17	chr21:47599600-47602800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr21:47599600-47603000	Strong transcription	Fetal Stomach	stomach
19	chr21:47600200-47603600	Enhancers	H1 Cell Line	embryonic stem cell
20	chr21:47600600-47602800	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr21:47600600-47603000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr21:47600600-47603400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr21:47600800-47603000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr21:47600800-47603200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr21:47600800-47603800	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr21:47601000-47602800	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr21:47601000-47602800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr21:47601000-47603000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr21:47601000-47603200	Weak transcription	Primary hematopoietic stem cells	blood
30	chr21:47601000-47603200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr21:47601000-47603800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr21:47601200-47602800	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr21:47601200-47603800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr21:47601200-47603800	Weak transcription	Colon Smooth Muscle	Colon
35	chr21:47601200-47604000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
36	chr21:47601400-47602800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr21:47601400-47602800	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr21:47601400-47603000	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr21:47601400-47603200	Weak transcription	NHLF	lung
40	chr21:47601600-47602800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr21:47601600-47603000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr21:47601800-47602800	Weak transcription	Esophagus	oesophagus
43	chr21:47601800-47603000	Weak transcription	Brain Cingulate Gyrus	brain
44	chr21:47602000-47602800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr21:47602000-47603800	Enhancers	Gastric	stomach
46	chr21:47602000-47604000	Enhancers	Spleen	Spleen
47	chr21:47602200-47602800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr21:47602200-47603000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
49	chr21:47602200-47603000	Genic enhancers	Fetal Muscle Leg	muscle
50	chr21:47602200-47603200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain

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