Variant report

Variant	esv3491903
Chromosome Location	chr21:47609024-47611872
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:137)
CpG islands
(count:62)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:137 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr21:47608341-47609112	K562	blood:	n/a	n/a
2	ATF3	chr21:47609133-47609351	K562	blood:	n/a	n/a
3	BHLHE40	chr21:47608321-47609421	K562	blood:	n/a	n/a
4	CEBPB	chr21:47611077-47611526	MCF-7	breast:	n/a	n/a
5	CEBPB	chr21:47611068-47611501	IMR90	lung:	n/a	n/a
6	CEBPB	chr21:47611120-47611390	A549	lung:	n/a	n/a
7	CEBPB	chr21:47611100-47611446	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr21:47611147-47611456	K562	blood:	n/a	n/a
9	CHD1	chr21:47609848-47609888	GM12878	blood:	n/a	n/a
10	CUX1	chr21:47608115-47609329	K562	blood:	n/a	n/a
11	E2F4	chr21:47611213-47611399	MCF10A-Er-Src	breast:	n/a	n/a
12	EGR1	chr21:47611267-47611711	K562	blood:	n/a	chr21:47611343-47611353
13	EGR1	chr21:47611356-47611643	K562	blood:	n/a	n/a
14	EGR1	chr21:47608747-47609377	K562	blood:	n/a	n/a
15	EP300	chr21:47608190-47609219	K562	blood:	n/a	n/a
16	FOS	chr21:47611069-47611411	MCF10A-Er-Src	breast:	n/a	chr21:47611248-47611256 chr21:47611247-47611257 chr21:47611246-47611258 chr21:47611246-47611257
17	FOS	chr21:47611061-47611428	MCF10A-Er-Src	breast:	n/a	chr21:47611248-47611256 chr21:47611247-47611257 chr21:47611246-47611258 chr21:47611246-47611257
18	FOS	chr21:47609127-47609327	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr21:47611070-47611402	MCF10A-Er-Src	breast:	n/a	chr21:47611248-47611256 chr21:47611247-47611257 chr21:47611246-47611258 chr21:47611246-47611257
20	FOS	chr21:47611070-47611416	MCF10A-Er-Src	breast:	n/a	chr21:47611248-47611256 chr21:47611247-47611257 chr21:47611246-47611258 chr21:47611246-47611257
21	FOS	chr21:47611044-47611471	HUVEC	blood vessel:	n/a	chr21:47611248-47611256 chr21:47611247-47611257 chr21:47611246-47611258 chr21:47611246-47611257
22	FOS	chr21:47608862-47609303	MCF10A-Er-Src	breast:	n/a	n/a
23	FOSL2	chr21:47611023-47611540	SK-N-SH	brain:	n/a	chr21:47611248-47611256 chr21:47611247-47611257 chr21:47611246-47611258
24	FOXP2	chr21:47611028-47611524	PFSK-1	brain:	n/a	n/a
25	GATA2	chr21:47608401-47609584	SH-SY5Y	brain:	n/a	n/a
26	GATA3	chr21:47608140-47609239	MCF-7	breast:	n/a	n/a
27	GATA3	chr21:47608846-47609091	SH-SY5Y	brain:	n/a	n/a
28	GATA3	chr21:47608060-47609757	MCF-7	breast:	n/a	n/a
29	GATA3	chr21:47608339-47609180	MCF-7	breast:	n/a	n/a
30	HMGN3	chr21:47609925-47610125	K562	blood:	n/a	n/a
31	JUN	chr21:47608105-47609273	K562	blood:	n/a	n/a
32	JUN	chr21:47608252-47609244	K562	blood:	n/a	n/a
33	JUN	chr21:47607675-47610104	K562	blood:	n/a	n/a
34	JUN	chr21:47608281-47609037	K562	blood:	n/a	n/a
35	JUND	chr21:47608127-47609553	SK-N-SH	brain:	n/a	chr21:47608475-47608486
36	JUND	chr21:47607968-47609364	K562	blood:	n/a	chr21:47608475-47608486
37	JUND	chr21:47609652-47609723	K562	blood:	n/a	n/a
38	MAX	chr21:47608984-47609453	SK-N-SH	brain:	n/a	chr21:47609251-47609261
39	MAX	chr21:47609030-47609443	K562	blood:	n/a	chr21:47609251-47609261
40	MAX	chr21:47608271-47610002	MCF-7	breast:	n/a	chr21:47609251-47609261
41	MAX	chr21:47609115-47609337	H1-hESC	embryonic stem cell:	n/a	chr21:47609251-47609261
42	MAX	chr21:47609062-47609494	SK-N-SH	brain:	n/a	chr21:47609251-47609261
43	MAX	chr21:47608888-47609796	Hela-S3	cervix:	n/a	chr21:47609251-47609261
44	MAX	chr21:47608809-47609681	K562	blood:	n/a	chr21:47609251-47609261
45	MAX	chr21:47608307-47609663	K562	blood:	n/a	chr21:47609251-47609261
46	MAX	chr21:47608835-47609929	MCF-7	breast:	n/a	chr21:47609251-47609261
47	MAX	chr21:47609062-47609442	NB4	blood:	n/a	chr21:47609251-47609261
48	MAX	chr21:47609074-47609412	HUVEC	blood vessel:	n/a	chr21:47609251-47609261
49	MAZ	chr21:47608289-47609143	K562	blood:	n/a	n/a
50	MXI1	chr21:47607576-47609895	SK-N-SH	brain:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:47610096-47610146	AG09309	skin:	n/a
2	chr21:47610096-47610146	AG09309	skin:	n/a
3	chr21:47610096-47610146	AoSMC	blood vessel:	n/a
4	chr21:47610096-47610146	HCF	heart:	n/a
5	chr21:47610096-47610146	SAEC	small airway:	n/a
6	chr21:47610096-47610146	PANC-1	pancreas:	n/a
7	chr21:47610096-47610146	HepG2	liver:	n/a
8	chr21:47610096-47610146	IMR90	lung:	fetal
9	chr21:47610096-47610146	ProgFib	skin:	n/a
10	chr21:47610096-47610146	NB4	blood:	n/a
11	chr21:47610096-47610146	SK-N-MC	brain:	n/a
12	chr21:47610096-47610146	RPTEC	kidney:	n/a
13	chr21:47610096-47610146	PrEC	prostate:	n/a
14	chr21:47610096-47610146	Hepatocyte	liver:	n/a
15	chr21:47610096-47610146	AG09319	gingival:	n/a
16	chr21:47610096-47610146	Caco-2	colon:	n/a
17	chr21:47610096-47610146	HRPEpiC	eye:	n/a
18	chr21:47610096-47610146	ovcar-3	ovarian:	n/a
19	chr21:47610096-47610146	A549	lung:	n/a
20	chr21:47610096-47610146	GM12878	blood:	n/a
21	chr21:47610096-47610146	HEEpiC	esophagus:	n/a
22	chr21:47610096-47610146	Hela-S3	cervix:	n/a
23	chr21:47610096-47610146	AG10803	skin:	n/a
24	chr21:47610096-47610146	SKMC	muscle:	n/a
25	chr21:47610096-47610146	GM06990	blood:	n/a
26	chr21:47610096-47610146	LNCaP	prostate:	n/a
27	chr21:47610096-47610146	HEK293	kidney:	embryo
28	chr21:47610096-47610146	HCPEpiC	choroid plexus:	n/a
29	chr21:47610096-47610146	GM12891	blood:	n/a
30	chr21:47610096-47610146	K562	blood:	n/a
31	chr21:47610096-47610146	AG04449	skin:	fetal
32	chr21:47610096-47610146	GM19239	blood:	n/a
33	chr21:47610096-47610146	HL-60	blood:	n/a
34	chr21:47610096-47610146	GM12892	blood:	n/a
35	chr21:47610096-47610146	T-47D	breast:	n/a
36	chr21:47610096-47610146	NHDF-neo	bronchial:	n/a
37	chr21:47610096-47610146	MCF-7	breast:	n/a
38	chr21:47610096-47610146	NT2-D1	testis:	n/a
39	chr21:47610096-47610146	HRCEpiC	kidney:	n/a
40	chr21:47610096-47610146	HCT-116	colon:	n/a
41	chr21:47610096-47610146	PFSK-1	brain:	n/a
42	chr21:47610096-47610146	HNPCEpiC	eye:	n/a
43	chr21:47610096-47610146	HUVEC	blood vessel:	n/a
44	chr21:47610096-47610146	HAEpiC	amniotic membrane:	n/a
45	chr21:47610096-47610146	AG04450	lung:	fetal
46	chr21:47610096-47610146	CMK	blood:	n/a
47	chr21:47610096-47610146	HPAEpiC	pulmonary alveolar:	n/a
48	chr21:47610096-47610146	Jurkat	blood:	n/a
49	chr21:47610096-47610146	U87	brain:	n/a
50	chr21:47610096-47610146	SK-N-SH_RA	brain:	n/a

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

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

No data

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

Extended variants
information (count: 133 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:133 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	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
25	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
26	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
27	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
28	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
29	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
30	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
31	rs560750345	chr21:47609654-47609655	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs79527568	chr21:47609655-47609656	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs914247	chr21:47609677-47609678	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
34	rs559827615	chr21:47609692-47609693	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs877746	chr21:47609731-47609732	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs551793213	chr21:47609814-47609815	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs569910734	chr21:47609830-47609831	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs138996335	chr21:47609847-47609848	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs549668423	chr21:47609861-47609862	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs567873744	chr21:47609918-47609919	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs180706255	chr21:47609922-47609923	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs553266758	chr21:47609923-47609924	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs571368251	chr21:47609948-47609949	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs117378205	chr21:47609974-47609975	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs556924268	chr21:47609980-47609981	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs150935428	chr21:47609989-47609990	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs575082042	chr21:47610008-47610009	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs542530542	chr21:47610011-47610012	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs554478433	chr21:47610017-47610018	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs572779568	chr21:47610056-47610057	Weak transcription Genic enhancers Strong transcription Enhancers 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:270 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:47605000-47609200	Weak transcription	Lung	lung
2	chr21:47605000-47609200	Weak transcription	Spleen	Spleen
3	chr21:47605000-47609400	Weak transcription	Aorta	Aorta
4	chr21:47605000-47609400	Weak transcription	Esophagus	oesophagus
5	chr21:47605000-47610600	Weak transcription	Colon Smooth Muscle	Colon
6	chr21:47605000-47611600	Weak transcription	Small Intestine	intestine
7	chr21:47605000-47613600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr21:47605000-47613600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr21:47605000-47633200	Weak transcription	Stomach Mucosa	stomach
10	chr21:47605200-47609200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr21:47605200-47609400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr21:47605200-47609400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr21:47605200-47609400	Weak transcription	Colonic Mucosa	Colon
14	chr21:47605200-47610800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr21:47605200-47613200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr21:47605200-47646200	Weak transcription	Psoas Muscle	Psoas
17	chr21:47605400-47609200	Weak transcription	Primary T cells from cord blood	blood
18	chr21:47605400-47609400	Weak transcription	Duodenum Mucosa	Duodenum
19	chr21:47605400-47609400	Weak transcription	Right Ventricle	heart
20	chr21:47605400-47610200	Weak transcription	Fetal Intestine Large	intestine
21	chr21:47605400-47611000	Weak transcription	Rectal Smooth Muscle	rectum
22	chr21:47605400-47613400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
23	chr21:47605400-47613600	Weak transcription	Primary monocytes fromperipheralblood	blood
24	chr21:47605400-47625600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
25	chr21:47605400-47646200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
26	chr21:47605400-47646200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
27	chr21:47605600-47609600	Weak transcription	Ovary	ovary
28	chr21:47605600-47610400	Weak transcription	Fetal Thymus	thymus
29	chr21:47605600-47610800	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr21:47605600-47610800	Weak transcription	Thymus	Thymus
31	chr21:47605600-47611200	Weak transcription	Fetal Lung	lung
32	chr21:47605600-47611600	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr21:47605600-47612000	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr21:47605600-47612600	Weak transcription	Primary hematopoietic stem cells	blood
35	chr21:47605600-47613400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr21:47605600-47613600	Weak transcription	Primary T helper cells fromperipheralblood	blood
37	chr21:47605800-47610800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr21:47605800-47612400	Weak transcription	Primary B cells from cord blood	blood
39	chr21:47605800-47613600	Weak transcription	Primary B cells from peripheral blood	blood
40	chr21:47605800-47613600	Weak transcription	Primary T helper cells PMA-I stimulated	--
41	chr21:47605800-47621000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
42	chr21:47606000-47611000	Weak transcription	Primary T cells fromperipheralblood	blood
43	chr21:47606000-47613600	Weak transcription	Primary neutrophils fromperipheralblood	blood
44	chr21:47606200-47611200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr21:47606200-47612400	Weak transcription	Fetal Brain Male	brain
46	chr21:47606600-47609600	Genic enhancers	K562	blood
47	chr21:47606600-47639800	Strong transcription	Fetal Brain Female	brain
48	chr21:47607200-47610800	Enhancers	Left Ventricle	heart
49	chr21:47607200-47611000	Enhancers	Right Atrium	heart
50	chr21:47607200-47611600	Genic enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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