Variant report

Variant	esv3491908
Chromosome Location	chr21:47608524-47612022
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:261)
CpG islands
(count:61)
Chromatin interactive
region (count:18)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:261 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:47608004-47608624	K562	blood:	n/a	n/a
2	ATF1	chr21:47608341-47609112	K562	blood:	n/a	n/a
3	ATF3	chr21:47609133-47609351	K562	blood:	n/a	n/a
4	ATF3	chr21:47608295-47608597	K562	blood:	n/a	n/a
5	ATF3	chr21:47608177-47608713	K562	blood:	n/a	n/a
6	BHLHE40	chr21:47608321-47609421	K562	blood:	n/a	n/a
7	CCNT2	chr21:47608340-47608752	K562	blood:	n/a	n/a
8	CEBPB	chr21:47608335-47608644	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr21:47611068-47611501	IMR90	lung:	n/a	n/a
10	CEBPB	chr21:47611120-47611390	A549	lung:	n/a	n/a
11	CEBPB	chr21:47611100-47611446	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr21:47608323-47608589	K562	blood:	n/a	n/a
13	CEBPB	chr21:47608387-47608644	IMR90	lung:	n/a	n/a
14	CEBPB	chr21:47611077-47611526	MCF-7	breast:	n/a	n/a
15	CEBPB	chr21:47611147-47611456	K562	blood:	n/a	n/a
16	CEBPZ	chr21:47608608-47608660	HepG2	liver:	n/a	n/a
17	CHD1	chr21:47609848-47609888	GM12878	blood:	n/a	n/a
18	CTCF	chr21:47608391-47608535	Hela-S3	cervix:	n/a	n/a
19	CTCF	chr21:47608400-47608550	HEK293	kidney:	n/a	n/a
20	CTCF	chr21:47608380-47608530	HMEC	breast:	n/a	n/a
21	CTCF	chr21:47608273-47608860	K562	blood:	n/a	n/a
22	CTCF	chr21:47608340-47608597	GM12878	blood:	n/a	n/a
23	CTCF	chr21:47608380-47608530	HepG2	liver:	n/a	n/a
24	CTCF	chr21:47608380-47608530	WERI-Rb-1	eye:	n/a	n/a
25	CTCF	chr21:47608400-47608550	MCF-7	breast:	n/a	n/a
26	CTCF	chr21:47608440-47608590	NB4	blood:	n/a	n/a
27	CTCF	chr21:47608352-47608580	K562	blood:	n/a	n/a
28	CTCF	chr21:47608345-47608669	K562	blood:	n/a	n/a
29	CUX1	chr21:47608115-47609329	K562	blood:	n/a	n/a
30	E2F4	chr21:47611213-47611399	MCF10A-Er-Src	breast:	n/a	n/a
31	EGR1	chr21:47611356-47611643	K562	blood:	n/a	n/a
32	EGR1	chr21:47608323-47608666	K562	blood:	n/a	n/a
33	EGR1	chr21:47608747-47609377	K562	blood:	n/a	n/a
34	EGR1	chr21:47608343-47608660	K562	blood:	n/a	n/a
35	EGR1	chr21:47611267-47611711	K562	blood:	n/a	chr21:47611343-47611353
36	EP300	chr21:47608190-47609219	K562	blood:	n/a	n/a
37	EP300	chr21:47608301-47608572	SK-N-SH_RA	brain:	n/a	n/a
38	EP300	chr21:47608316-47608617	K562	blood:	n/a	n/a
39	FOS	chr21:47608347-47608662	MCF10A-Er-Src	breast:	n/a	chr21:47608475-47608486
40	FOS	chr21:47608334-47608665	Hela-S3	cervix:	n/a	chr21:47608475-47608486
41	FOS	chr21:47611070-47611416	MCF10A-Er-Src	breast:	n/a	chr21:47611248-47611256 chr21:47611247-47611257 chr21:47611246-47611258 chr21:47611246-47611257
42	FOS	chr21:47608312-47608655	MCF10A-Er-Src	breast:	n/a	chr21:47608475-47608486
43	FOS	chr21:47608283-47608679	K562	blood:	n/a	chr21:47608475-47608486
44	FOS	chr21:47611070-47611402	MCF10A-Er-Src	breast:	n/a	chr21:47611248-47611256 chr21:47611247-47611257 chr21:47611246-47611258 chr21:47611246-47611257
45	FOS	chr21:47608346-47608670	MCF10A-Er-Src	breast:	n/a	chr21:47608475-47608486
46	FOS	chr21:47611061-47611428	MCF10A-Er-Src	breast:	n/a	chr21:47611248-47611256 chr21:47611247-47611257 chr21:47611246-47611258 chr21:47611246-47611257
47	FOS	chr21:47608224-47608777	HUVEC	blood vessel:	n/a	chr21:47608475-47608486
48	FOS	chr21:47609127-47609327	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr21:47611069-47611411	MCF10A-Er-Src	breast:	n/a	chr21:47611248-47611256 chr21:47611247-47611257 chr21:47611246-47611258 chr21:47611246-47611257
50	FOS	chr21:47611044-47611471	HUVEC	blood vessel:	n/a	chr21:47611248-47611256 chr21:47611247-47611257 chr21:47611246-47611258 chr21:47611246-47611257

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:47610096-47610146	BE2_C	brain:	n/a
2	chr21:47610096-47610146	AG04450	lung:	fetal
3	chr21:47610096-47610146	HEK293	kidney:	embryo
4	chr21:47610096-47610146	SAEC	small airway:	n/a
5	chr21:47610096-47610146	GM12891	blood:	n/a
6	chr21:47610096-47610146	PANC-1	pancreas:	n/a
7	chr21:47610096-47610146	HCF	heart:	n/a
8	chr21:47610096-47610146	NHDF-neo	bronchial:	n/a
9	chr21:47610096-47610146	PrEC	prostate:	n/a
10	chr21:47610096-47610146	HCM	heart:	n/a
11	chr21:47610096-47610146	AG09309	skin:	n/a
12	chr21:47610096-47610146	SKMC	muscle:	n/a
13	chr21:47610096-47610146	BJ	skin:	n/a
14	chr21:47610096-47610146	HRPEpiC	eye:	n/a
15	chr21:47610096-47610146	GM12878	blood:	n/a
16	chr21:47610096-47610146	HNPCEpiC	eye:	n/a
17	chr21:47610096-47610146	Jurkat	blood:	n/a
18	chr21:47610096-47610146	K562	blood:	n/a
19	chr21:47610096-47610146	HAEpiC	amniotic membrane:	n/a
20	chr21:47610096-47610146	GM06990	blood:	n/a
21	chr21:47610096-47610146	Caco-2	colon:	n/a
22	chr21:47610096-47610146	SK-N-MC	brain:	n/a
23	chr21:47610096-47610146	NT2-D1	testis:	n/a
24	chr21:47610096-47610146	GM19239	blood:	n/a
25	chr21:47610096-47610146	SK-N-SH_RA	brain:	n/a
26	chr21:47610096-47610146	NB4	blood:	n/a
27	chr21:47610096-47610146	HCPEpiC	choroid plexus:	n/a
28	chr21:47610096-47610146	SK-N-SH	brain:	n/a
29	chr21:47610096-47610146	HRE	kidney:	n/a
30	chr21:47610096-47610146	H1-hESC	embryonic stem cell:	embryo
31	chr21:47610096-47610146	MCF-7	breast:	n/a
32	chr21:47610096-47610146	AG09319	gingival:	n/a
33	chr21:47610096-47610146	GM12892	blood:	n/a
34	chr21:47610096-47610146	HL-60	blood:	n/a
35	chr21:47610096-47610146	NH-A	brain:	n/a
36	chr21:47610096-47610146	HEEpiC	esophagus:	n/a
37	chr21:47610096-47610146	Hela-S3	cervix:	n/a
38	chr21:47610096-47610146	CMK	blood:	n/a
39	chr21:47610096-47610146	Hepatocyte	liver:	n/a
40	chr21:47610096-47610146	T-47D	breast:	n/a
41	chr21:47610096-47610146	HIPEpiC	eye:	n/a
42	chr21:47610096-47610146	ovcar-3	ovarian:	n/a
43	chr21:47610096-47610146	HMEC	breast:	n/a
44	chr21:47610096-47610146	LNCaP	prostate:	n/a
45	chr21:47610096-47610146	AG04449	skin:	fetal
46	chr21:47610096-47610146	HUVEC	blood vessel:	n/a
47	chr21:47610096-47610146	A549	lung:	n/a
48	chr21:47610096-47610146	ProgFib	skin:	n/a
49	chr21:47610096-47610146	ECC-1	luminal epithelium:	n/a
50	chr21:47610096-47610146	HRCEpiC	kidney:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:47607532..47609411-chr21:47620514..47622375,2	K562	blood:
2	chr21:47608421..47610045-chr21:47610316..47614035,3	K562	blood:
3	chr21:47605676..47611866-chr21:47647121..47650700,5	K562	blood:
4	chr21:47611559..47613135-chr21:47649369..47651464,2	MCF-7	breast:
5	chr21:47603298..47606134-chr21:47609702..47612291,3	MCF-7	breast:
6	chr21:47608042..47610430-chr21:47629294..47631017,3	MCF-7	breast:
7	chr21:47609974..47612324-chr21:47641874..47644761,2	MCF-7	breast:
8	chr21:47572801..47575123-chr21:47608249..47610070,2	MCF-7	breast:
9	chr21:47606790..47609628-chr21:47614415..47615920,2	MCF-7	breast:
10	chr21:47571793..47574970-chr21:47606794..47610224,4	MCF-7	breast:
11	chr21:47606363..47609230-chr21:47646261..47649400,3	MCF-7	breast:
12	chr21:47601884..47606848-chr21:47606938..47611467,11	MCF-7	breast:
13	chr21:47609281..47613722-chr21:47615252..47618849,4	MCF-7	breast:
14	chr21:47607471..47609204-chr21:47739209..47740875,2	K562	blood:
15	chr21:47609774..47611316-chr21:47673784..47676392,2	MCF-7	breast:
16	chr21:47608276..47610056-chr21:47614112..47615724,2	K562	blood:
17	chr21:47610337..47611889-chr21:47614525..47616079,2	K562	blood:
18	chr21:47608474..47611132-chr21:47627898..47630715,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COL6A2-4	chr21:47608408-47608855	ENSG00000228404.1

No data

Variant related genes	Relation type
SPATC1L	TF binding region
SPATC1L	CpG island
ENSG00000160284	chromatin interactions
ENSG00000228404	chromatin interactions
ENSG00000160285	chromatin interactions
ENSG00000160298	chromatin interactions
ENSG00000215424	chromatin interactions
ENSG00000235878	chromatin interactions
ENSG00000239415	chromatin interactions

Extended variants
information (count: 159 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:159 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540483256	chr21:47608565-47608566	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
2	rs2968	chr21:47608580-47608581	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs116670456	chr21:47608625-47608626	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
4	rs530697328	chr21:47608693-47608694	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
5	rs76408279	chr21:47608710-47608711	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
6	rs185253995	chr21:47608743-47608744	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
7	rs376640756	chr21:47608758-47608759	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
8	rs201814314	chr21:47608792-47608793	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
9	rs190535596	chr21:47608820-47608821	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
10	rs529472955	chr21:47608845-47608846	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
11	rs147903820	chr21:47608849-47608850	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
12	rs56173768	chr21:47608877-47608878	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs558397449	chr21:47608914-47608915	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs566301215	chr21:47608941-47608942	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs576652132	chr21:47608949-47608950	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs182306824	chr21:47608967-47608968	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs555994002	chr21:47608972-47608973	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs374587643	chr21:47608996-47608997	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs541088205	chr21:47609012-47609013	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs528751084	chr21:47609019-47609020	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs573713761	chr21:47609061-47609062	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs559393019	chr21:47609088-47609089	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs577537211	chr21:47609092-47609093	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs544989357	chr21:47609145-47609146	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs563634768	chr21:47609185-47609186	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs530691412	chr21:47609188-47609189	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs548809051	chr21:47609207-47609208	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs187080789	chr21:47609241-47609242	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs529353746	chr21:47609244-47609245	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs113978064	chr21:47609246-47609247	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs115281881	chr21:47609258-47609259	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs557821610	chr21:47609266-47609267	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs531785388	chr21:47609267-47609268	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs143786157	chr21:47609329-47609330	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs552115427	chr21:47609331-47609332	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs148135994	chr21:47609373-47609374	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs570374941	chr21:47609374-47609375	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs114226873	chr21:47609397-47609398	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs556006445	chr21:47609448-47609449	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs79636523	chr21:47609476-47609477	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs75720076	chr21:47609477-47609478	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs567814928	chr21:47609486-47609487	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs141111301	chr21:47609495-47609496	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs188347703	chr21:47609507-47609508	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs9717	chr21:47609510-47609511	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs539110792	chr21:47609555-47609556	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs545016425	chr21:47609556-47609557	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs118184861	chr21:47609578-47609579	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs575532354	chr21:47609589-47609590	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs542471287	chr21:47609619-47609620	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	5 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:322 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:47604600-47609000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr21:47605000-47608600	Weak transcription	Gastric	stomach
3	chr21:47605000-47609200	Weak transcription	Lung	lung
4	chr21:47605000-47609200	Weak transcription	Spleen	Spleen
5	chr21:47605000-47609400	Weak transcription	Aorta	Aorta
6	chr21:47605000-47609400	Weak transcription	Esophagus	oesophagus
7	chr21:47605000-47610600	Weak transcription	Colon Smooth Muscle	Colon
8	chr21:47605000-47611600	Weak transcription	Small Intestine	intestine
9	chr21:47605000-47613600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr21:47605000-47613600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr21:47605000-47633200	Weak transcription	Stomach Mucosa	stomach
12	chr21:47605200-47609200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr21:47605200-47609400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr21:47605200-47609400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr21:47605200-47609400	Weak transcription	Colonic Mucosa	Colon
16	chr21:47605200-47610800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr21:47605200-47613200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr21:47605200-47646200	Weak transcription	Psoas Muscle	Psoas
19	chr21:47605400-47608600	Weak transcription	Fetal Intestine Small	intestine
20	chr21:47605400-47608800	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr21:47605400-47609200	Weak transcription	Primary T cells from cord blood	blood
22	chr21:47605400-47609400	Weak transcription	Duodenum Mucosa	Duodenum
23	chr21:47605400-47609400	Weak transcription	Right Ventricle	heart
24	chr21:47605400-47610200	Weak transcription	Fetal Intestine Large	intestine
25	chr21:47605400-47611000	Weak transcription	Rectal Smooth Muscle	rectum
26	chr21:47605400-47613400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr21:47605400-47613600	Weak transcription	Primary monocytes fromperipheralblood	blood
28	chr21:47605400-47625600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
29	chr21:47605400-47646200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
30	chr21:47605400-47646200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
31	chr21:47605600-47608600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr21:47605600-47609000	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr21:47605600-47609600	Weak transcription	Ovary	ovary
34	chr21:47605600-47610400	Weak transcription	Fetal Thymus	thymus
35	chr21:47605600-47610800	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr21:47605600-47610800	Weak transcription	Thymus	Thymus
37	chr21:47605600-47611200	Weak transcription	Fetal Lung	lung
38	chr21:47605600-47611600	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr21:47605600-47612000	Weak transcription	Monocytes-CD14+_RO01746	blood
40	chr21:47605600-47612600	Weak transcription	Primary hematopoietic stem cells	blood
41	chr21:47605600-47613400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr21:47605600-47613600	Weak transcription	Primary T helper cells fromperipheralblood	blood
43	chr21:47605800-47608600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr21:47605800-47608800	Weak transcription	GM12878-XiMat	blood
45	chr21:47605800-47610800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
46	chr21:47605800-47612400	Weak transcription	Primary B cells from cord blood	blood
47	chr21:47605800-47613600	Weak transcription	Primary B cells from peripheral blood	blood
48	chr21:47605800-47613600	Weak transcription	Primary T helper cells PMA-I stimulated	--
49	chr21:47605800-47621000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
50	chr21:47606000-47608800	Enhancers	Brain Inferior Temporal Lobe	brain

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