Variant report

Variant	esv3406256
Chromosome Location	chr21:47608024-47612422
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:313)
CpG islands
(count:61)
Chromatin interactive
region (count:18)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:313 , 50 per page) page: 1 2 3 4 5 6 7

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	chr21:47608177-47608713	K562	blood:	n/a	n/a
5	ATF3	chr21:47608295-47608597	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	chr21:47608467-47608514	HepG2	liver:	n/a	n/a
9	CEBPB	chr21:47611068-47611501	IMR90	lung:	n/a	n/a
10	CEBPB	chr21:47611147-47611456	K562	blood:	n/a	n/a
11	CEBPB	chr21:47608387-47608644	IMR90	lung:	n/a	n/a
12	CEBPB	chr21:47608335-47608644	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr21:47611100-47611446	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr21:47611077-47611526	MCF-7	breast:	n/a	n/a
15	CEBPB	chr21:47611120-47611390	A549	lung:	n/a	n/a
16	CEBPB	chr21:47608323-47608589	K562	blood:	n/a	n/a
17	CEBPZ	chr21:47608608-47608660	HepG2	liver:	n/a	n/a
18	CHD1	chr21:47609848-47609888	GM12878	blood:	n/a	n/a
19	CHD2	chr21:47608354-47608507	K562	blood:	n/a	n/a
20	CTCF	chr21:47608300-47608450	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr21:47608352-47608580	K562	blood:	n/a	n/a
22	CTCF	chr21:47608280-47608430	RPTEC	kidney:	n/a	n/a
23	CTCF	chr21:47608273-47608860	K562	blood:	n/a	n/a
24	CTCF	chr21:47608340-47608490	Caco-2	colon:	n/a	n/a
25	CTCF	chr21:47608380-47608530	HMEC	breast:	n/a	n/a
26	CTCF	chr21:47608416-47608496	MCF-7	breast:	n/a	n/a
27	CTCF	chr21:47608380-47608530	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr21:47608440-47608590	NB4	blood:	n/a	n/a
29	CTCF	chr21:47608340-47608597	GM12878	blood:	n/a	n/a
30	CTCF	chr21:47608280-47608430	AG10803	skin:	n/a	n/a
31	CTCF	chr21:47608430-47608479	MCF-7	breast:	n/a	n/a
32	CTCF	chr21:47608380-47608530	HepG2	liver:	n/a	n/a
33	CTCF	chr21:47608408-47608508	MCF-7	breast:	n/a	n/a
34	CTCF	chr21:47608404-47608497	MCF-7	breast:	n/a	n/a
35	CTCF	chr21:47608432-47608488	MCF-7	breast:	n/a	n/a
36	CTCF	chr21:47608360-47608510	K562	blood:	n/a	n/a
37	CTCF	chr21:47608400-47608550	MCF-7	breast:	n/a	n/a
38	CTCF	chr21:47608300-47608450	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr21:47608320-47608470	BE2_C	brain:	n/a	n/a
40	CTCF	chr21:47608400-47608550	HEK293	kidney:	n/a	n/a
41	CTCF	chr21:47608381-47608506	K562	blood:	n/a	n/a
42	CTCF	chr21:47608391-47608535	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr21:47608345-47608669	K562	blood:	n/a	n/a
44	CTCFL	chr21:47608303-47608492	K562	blood:	n/a	n/a
45	CUX1	chr21:47608115-47609329	K562	blood:	n/a	n/a
46	E2F4	chr21:47611213-47611399	MCF10A-Er-Src	breast:	n/a	n/a
47	EGR1	chr21:47611356-47611643	K562	blood:	n/a	n/a
48	EGR1	chr21:47608747-47609377	K562	blood:	n/a	n/a
49	EGR1	chr21:47608323-47608666	K562	blood:	n/a	n/a
50	EGR1	chr21:47611267-47611711	K562	blood:	n/a	chr21:47611343-47611353

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:47610096-47610146	AG10803	skin:	n/a
2	chr21:47610096-47610146	HCM	heart:	n/a
3	chr21:47610096-47610146	HUVEC	blood vessel:	n/a
4	chr21:47610096-47610146	HepG2	liver:	n/a
5	chr21:47610096-47610146	GM19239	blood:	n/a
6	chr21:47610096-47610146	NH-A	brain:	n/a
7	chr21:47610096-47610146	HCPEpiC	choroid plexus:	n/a
8	chr21:47610096-47610146	HAEpiC	amniotic membrane:	n/a
9	chr21:47610096-47610146	HRCEpiC	kidney:	n/a
10	chr21:47610096-47610146	SKMC	muscle:	n/a
11	chr21:47610096-47610146	NHDF-neo	bronchial:	n/a
12	chr21:47610096-47610146	IMR90	lung:	fetal
13	chr21:47610096-47610146	ECC-1	luminal epithelium:	n/a
14	chr21:47610096-47610146	NHBE	bronchial:	n/a
15	chr21:47610096-47610146	AG09319	gingival:	n/a
16	chr21:47610096-47610146	Hela-S3	cervix:	n/a
17	chr21:47610096-47610146	AG09309	skin:	n/a
18	chr21:47610096-47610146	HNPCEpiC	eye:	n/a
19	chr21:47610096-47610146	PrEC	prostate:	n/a
20	chr21:47610096-47610146	HRE	kidney:	n/a
21	chr21:47610096-47610146	AG04449	skin:	fetal
22	chr21:47610096-47610146	HEK293	kidney:	embryo
23	chr21:47610096-47610146	MCF10A-Er-Src	breast:	n/a
24	chr21:47610096-47610146	SK-N-SH	brain:	n/a
25	chr21:47610096-47610146	AG04450	lung:	fetal
26	chr21:47610096-47610146	Hepatocyte	liver:	n/a
27	chr21:47610096-47610146	HIPEpiC	eye:	n/a
28	chr21:47610096-47610146	CMK	blood:	n/a
29	chr21:47610096-47610146	SK-N-SH_RA	brain:	n/a
30	chr21:47610096-47610146	A549	lung:	n/a
31	chr21:47610096-47610146	LNCaP	prostate:	n/a
32	chr21:47610096-47610146	Jurkat	blood:	n/a
33	chr21:47610096-47610146	SAEC	small airway:	n/a
34	chr21:47610096-47610146	RPTEC	kidney:	n/a
35	chr21:47610096-47610146	ProgFib	skin:	n/a
36	chr21:47610096-47610146	HRPEpiC	eye:	n/a
37	chr21:47610096-47610146	HMEC	breast:	n/a
38	chr21:47610096-47610146	BJ	skin:	n/a
39	chr21:47610096-47610146	H1-hESC	embryonic stem cell:	embryo
40	chr21:47610096-47610146	HL-60	blood:	n/a
41	chr21:47610096-47610146	HEEpiC	esophagus:	n/a
42	chr21:47610096-47610146	GM06990	blood:	n/a
43	chr21:47610096-47610146	HPAEpiC	pulmonary alveolar:	n/a
44	chr21:47610096-47610146	GM12892	blood:	n/a
45	chr21:47610096-47610146	HCT-116	colon:	n/a
46	chr21:47610096-47610146	GM12878	blood:	n/a
47	chr21:47610096-47610146	PFSK-1	brain:	n/a
48	chr21:47610096-47610146	MCF-7	breast:	n/a
49	chr21:47610096-47610146	BE2_C	brain:	n/a
50	chr21:47610096-47610146	K562	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr21:47572801..47575123-chr21:47608249..47610070,2	MCF-7	breast:
2	chr21:47609774..47611316-chr21:47673784..47676392,2	MCF-7	breast:
3	chr21:47608042..47610430-chr21:47629294..47631017,3	MCF-7	breast:
4	chr21:47571793..47574970-chr21:47606794..47610224,4	MCF-7	breast:
5	chr21:47608421..47610045-chr21:47610316..47614035,3	K562	blood:
6	chr21:47611559..47613135-chr21:47649369..47651464,2	MCF-7	breast:
7	chr21:47607532..47609411-chr21:47620514..47622375,2	K562	blood:
8	chr21:47610337..47611889-chr21:47614525..47616079,2	K562	blood:
9	chr21:47606363..47609230-chr21:47646261..47649400,3	MCF-7	breast:
10	chr21:47609974..47612324-chr21:47641874..47644761,2	MCF-7	breast:
11	chr21:47601884..47606848-chr21:47606938..47611467,11	MCF-7	breast:
12	chr21:47609281..47613722-chr21:47615252..47618849,4	MCF-7	breast:
13	chr21:47606790..47609628-chr21:47614415..47615920,2	MCF-7	breast:
14	chr21:47607471..47609204-chr21:47739209..47740875,2	K562	blood:
15	chr21:47608474..47611132-chr21:47627898..47630715,3	MCF-7	breast:
16	chr21:47608276..47610056-chr21:47614112..47615724,2	K562	blood:
17	chr21:47605676..47611866-chr21:47647121..47650700,5	K562	blood:
18	chr21:47603298..47606134-chr21:47609702..47612291,3	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
ENSG00000239415	chromatin interactions
ENSG00000235878	chromatin interactions
ENSG00000160298	chromatin interactions
ENSG00000160284	chromatin interactions
ENSG00000215424	chromatin interactions
ENSG00000160285	chromatin interactions
ENSG00000228404	chromatin interactions

Extended variants
information (count: 199 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:199 , 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	rs139219717	chr21:47608038-47608039	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs556592730	chr21:47608047-47608048	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs533789620	chr21:47608057-47608058	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs145285203	chr21:47608058-47608059	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs548776436	chr21:47608097-47608098	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs535488132	chr21:47608155-47608156	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs367852372	chr21:47608168-47608169	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs566092938	chr21:47608178-47608179	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs114033373	chr21:47608207-47608208	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs147634018	chr21:47608208-47608209	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs115226495	chr21:47608212-47608213	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs115723971	chr21:47608217-47608218	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs576554405	chr21:47608223-47608224	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs142351207	chr21:47608233-47608234	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs564098470	chr21:47608261-47608262	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs7283628	chr21:47608289-47608290	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs367863351	chr21:47608290-47608291	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs144580286	chr21:47608456-47608457	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
19	rs4505615	chr21:47608475-47608476	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
20	rs34614881	chr21:47608490-47608491	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
21	rs541075752	chr21:47608519-47608520	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
22	rs559382840	chr21:47608520-47608521	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
23	rs533086971	chr21:47608523-47608524	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
24	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
25	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
26	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
27	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
28	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
29	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
30	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
31	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
32	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
33	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
34	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
35	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
36	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
37	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
38	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
39	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
40	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
41	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
42	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
43	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
44	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
45	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
46	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
47	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
48	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
49	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
50	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

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:369 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:47604600-47609000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr21:47605000-47608400	Weak transcription	Pancreas	Pancrea
3	chr21:47605000-47608600	Weak transcription	Gastric	stomach
4	chr21:47605000-47609200	Weak transcription	Lung	lung
5	chr21:47605000-47609200	Weak transcription	Spleen	Spleen
6	chr21:47605000-47609400	Weak transcription	Aorta	Aorta
7	chr21:47605000-47609400	Weak transcription	Esophagus	oesophagus
8	chr21:47605000-47610600	Weak transcription	Colon Smooth Muscle	Colon
9	chr21:47605000-47611600	Weak transcription	Small Intestine	intestine
10	chr21:47605000-47613600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr21:47605000-47613600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr21:47605000-47633200	Weak transcription	Stomach Mucosa	stomach
13	chr21:47605200-47608200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr21:47605200-47608200	Weak transcription	HSMM	muscle
15	chr21:47605200-47608400	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr21:47605200-47608400	Weak transcription	Dnd41	blood
17	chr21:47605200-47608400	Weak transcription	Osteobl	bone
18	chr21:47605200-47609200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr21:47605200-47609400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr21:47605200-47609400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr21:47605200-47609400	Weak transcription	Colonic Mucosa	Colon
22	chr21:47605200-47610800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr21:47605200-47613200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr21:47605200-47646200	Weak transcription	Psoas Muscle	Psoas
25	chr21:47605400-47608200	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr21:47605400-47608200	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr21:47605400-47608200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr21:47605400-47608200	Weak transcription	Fetal Muscle Trunk	muscle
29	chr21:47605400-47608400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr21:47605400-47608400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr21:47605400-47608400	Weak transcription	Fetal Muscle Leg	muscle
32	chr21:47605400-47608600	Weak transcription	Fetal Intestine Small	intestine
33	chr21:47605400-47608800	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr21:47605400-47609200	Weak transcription	Primary T cells from cord blood	blood
35	chr21:47605400-47609400	Weak transcription	Duodenum Mucosa	Duodenum
36	chr21:47605400-47609400	Weak transcription	Right Ventricle	heart
37	chr21:47605400-47610200	Weak transcription	Fetal Intestine Large	intestine
38	chr21:47605400-47611000	Weak transcription	Rectal Smooth Muscle	rectum
39	chr21:47605400-47613400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr21:47605400-47613600	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr21:47605400-47625600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
42	chr21:47605400-47646200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
43	chr21:47605400-47646200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
44	chr21:47605600-47608200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr21:47605600-47608200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr21:47605600-47608600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr21:47605600-47609000	Weak transcription	Rectal Mucosa Donor 31	rectum
48	chr21:47605600-47609600	Weak transcription	Ovary	ovary
49	chr21:47605600-47610400	Weak transcription	Fetal Thymus	thymus
50	chr21:47605600-47610800	Weak transcription	Duodenum Smooth Muscle	Duodenum

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