Variant report

Variant	esv3322338
Chromosome Location	chr21:45526049-45528897
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:548)
CpG islands
(count:488)
Chromatin interactive
region (count:27)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:548 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:45527144-45527418	HepG2	liver:	n/a	n/a
2	ARID3A	chr21:45525257-45526502	K562	blood:	n/a	n/a
3	ARID3A	chr21:45527198-45527312	K562	blood:	n/a	n/a
4	ATF2	chr21:45526752-45527092	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr21:45527155-45527473	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr21:45527052-45527434	GM12878	blood:	n/a	n/a
7	ATF2	chr21:45526703-45527460	GM12878	blood:	n/a	n/a
8	BACH1	chr21:45528066-45528177	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr21:45527043-45527515	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr21:45526740-45527399	GM12878	blood:	n/a	chr21:45527219-45527232 chr21:45527254-45527267 chr21:45527199-45527208
11	BCL3	chr21:45526707-45527614	K562	blood:	n/a	chr21:45527219-45527232 chr21:45527254-45527267 chr21:45527199-45527208
12	BCL3	chr21:45526733-45527455	GM12878	blood:	n/a	chr21:45527219-45527232 chr21:45527254-45527267 chr21:45527199-45527208
13	BCL3	chr21:45527097-45527428	A549	lung:	n/a	chr21:45527219-45527232 chr21:45527254-45527267 chr21:45527199-45527208
14	BCLAF1	chr21:45526780-45527401	GM12878	blood:	n/a	chr21:45527219-45527232 chr21:45527254-45527267 chr21:45527199-45527208
15	BCLAF1	chr21:45526782-45527454	GM12878	blood:	n/a	chr21:45527219-45527232 chr21:45527254-45527267 chr21:45527199-45527208
16	BHLHE40	chr21:45527199-45527439	A549	lung:	n/a	n/a
17	BHLHE40	chr21:45526943-45527498	HepG2	liver:	n/a	n/a
18	BHLHE40	chr21:45526951-45527481	GM12878	blood:	n/a	n/a
19	BHLHE40	chr21:45526807-45527515	K562	blood:	n/a	n/a
20	BRCA1	chr21:45526965-45527333	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr21:45526595-45527399	K562	blood:	n/a	n/a
22	CCNT2	chr21:45526783-45527620	K562	blood:	n/a	n/a
23	CEBPD	chr21:45527066-45527407	HepG2	liver:	n/a	n/a
24	CHD1	chr21:45527279-45527444	GM12878	blood:	n/a	n/a
25	CHD2	chr21:45527277-45527312	HepG2	liver:	n/a	n/a
26	CHD2	chr21:45526792-45527401	Hela-S3	cervix:	n/a	chr21:45527090-45527100
27	CHD2	chr21:45526832-45527091	K562	blood:	n/a	n/a
28	CHD2	chr21:45527158-45527623	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr21:45526905-45527424	GM12878	blood:	n/a	chr21:45527090-45527100
30	CREB1	chr21:45526998-45527351	A549	lung:	n/a	n/a
31	CREB1	chr21:45526889-45527498	A549	lung:	n/a	n/a
32	CREB1	chr21:45526747-45527813	HepG2	liver:	n/a	n/a
33	CREB1	chr21:45526911-45527499	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr21:45526786-45527869	K562	blood:	n/a	n/a
35	CREB1	chr21:45526866-45527609	GM12878	blood:	n/a	n/a
36	CREB1	chr21:45526999-45527440	ECC-1	luminal epithelium:	n/a	n/a
37	CREB1	chr21:45526712-45527506	HepG2	liver:	n/a	n/a
38	CREB1	chr21:45527044-45527548	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr21:45526849-45527136	GM12878	blood:	n/a	n/a
40	CTCF	chr21:45527300-45527450	SK-N-SH_RA	brain:	n/a	chr21:45527390-45527403
41	CTCF	chr21:45527420-45527570	SAEC	small airway:	n/a	n/a
42	CTCF	chr21:45527420-45527570	K562	blood:	n/a	n/a
43	CTCF	chr21:45527300-45527450	WERI-Rb-1	eye:	n/a	chr21:45527390-45527403
44	CTCF	chr21:45527240-45527390	GM12864	blood:	n/a	n/a
45	CTCF	chr21:45527340-45527490	Hela-S3	cervix:	n/a	chr21:45527390-45527403
46	CTCF	chr21:45527362-45527422	GM13977	blood:	n/a	chr21:45527390-45527403
47	CTCF	chr21:45527096-45527156	GM19239	blood:	n/a	n/a
48	CTCF	chr21:45526906-45527013	Lung_OC	lung:	n/a	n/a
49	CTCF	chr21:45526860-45527010	AG04449	skin:	n/a	n/a
50	CTCF	chr21:45527480-45527630	HEK293	kidney:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:45526957-45527007	AG09319	gingival:	n/a
2	chr21:45526972-45527022	HPAEpiC	pulmonary alveolar:	n/a
3	chr21:45526459-45526509	HCF	heart:	n/a
4	chr21:45527029-45527079	NH-A	brain:	n/a
5	chr21:45527559-45527609	T-47D	breast:	n/a
6	chr21:45527559-45527609	HepG2	liver:	n/a
7	chr21:45527029-45527079	SK-N-SH_RA	brain:	n/a
8	chr21:45526459-45526509	HepG2	liver:	n/a
9	chr21:45526459-45526509	PFSK-1	brain:	n/a
10	chr21:45527029-45527079	BE2_C	brain:	n/a
11	chr21:45527559-45527609	HUVEC	blood vessel:	n/a
12	chr21:45527029-45527079	LNCaP	prostate:	n/a
13	chr21:45526957-45527007	HEEpiC	esophagus:	n/a
14	chr21:45528892-45528942	HUVEC	blood vessel:	n/a
15	chr21:45526459-45526509	Jurkat	blood:	n/a
16	chr21:45527350-45527400	H1-hESC	embryonic stem cell:	embryo
17	chr21:45526459-45526509	BE2_C	brain:	n/a
18	chr21:45526972-45527022	RPTEC	kidney:	n/a
19	chr21:45527350-45527400	ovcar-3	ovarian:	n/a
20	chr21:45526957-45527007	SAEC	small airway:	n/a
21	chr21:45526972-45527022	AG04450	lung:	fetal
22	chr21:45528892-45528942	HNPCEpiC	eye:	n/a
23	chr21:45527029-45527079	HIPEpiC	eye:	n/a
24	chr21:45528892-45528942	SK-N-MC	brain:	n/a
25	chr21:45526957-45527007	AG09309	skin:	n/a
26	chr21:45526961-45527011	HL-60	blood:	n/a
27	chr21:45527350-45527400	HMEC	breast:	n/a
28	chr21:45528892-45528942	NB4	blood:	n/a
29	chr21:45527350-45527400	SK-N-SH	brain:	n/a
30	chr21:45528892-45528942	HL-60	blood:	n/a
31	chr21:45526459-45526509	T-47D	breast:	n/a
32	chr21:45526972-45527022	HRCEpiC	kidney:	n/a
33	chr21:45527350-45527400	RPTEC	kidney:	n/a
34	chr21:45526459-45526509	HEEpiC	esophagus:	n/a
35	chr21:45526961-45527011	HUVEC	blood vessel:	n/a
36	chr21:45527029-45527079	AG09319	gingival:	n/a
37	chr21:45526961-45527011	SK-N-SH_RA	brain:	n/a
38	chr21:45527559-45527609	GM19239	blood:	n/a
39	chr21:45528892-45528942	LNCaP	prostate:	n/a
40	chr21:45526972-45527022	HIPEpiC	eye:	n/a
41	chr21:45526957-45527007	HepG2	liver:	n/a
42	chr21:45526459-45526509	MCF10A-Er-Src	breast:	n/a
43	chr21:45526459-45526509	HL-60	blood:	n/a
44	chr21:45526972-45527022	NHDF-neo	bronchial:	n/a
45	chr21:45528892-45528942	U87	brain:	n/a
46	chr21:45527029-45527079	BJ	skin:	n/a
47	chr21:45526972-45527022	GM12891	blood:	n/a
48	chr21:45527350-45527400	HL-60	blood:	n/a
49	chr21:45526972-45527022	PrEC	prostate:	n/a
50	chr21:45527350-45527400	A549	lung:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:45525933..45529754-chr21:45756924..45759975,4	MCF-7	breast:
2	chr21:45515403..45518351-chr21:45523507..45526490,2	K562	blood:
3	chr21:45430507..45434109-chr21:45525660..45529122,6	K562	blood:
4	chr21:45527693..45529600-chr21:45539778..45541804,2	MCF-7	breast:
5	chr21:45526020..45528445-chr21:46493573..46495387,2	K562	blood:
6	chr21:45430262..45433765-chr21:45524105..45528370,12	MCF-7	breast:
7	chr21:45228402..45230320-chr21:45526070..45527844,2	MCF-7	breast:
8	chr21:45446065..45448233-chr21:45527740..45530031,2	K562	blood:
9	chr21:45430220..45433985-chr21:45525454..45528690,3	MCF-7	breast:
10	chr21:45525708..45535025-chr21:45544493..45558414,30	MCF-7	breast:
11	chr21:45233457..45236060-chr21:45527747..45529523,2	MCF-7	breast:
12	chr21:45501440..45503025-chr21:45527582..45529145,2	MCF-7	breast:
13	chr21:45527099..45528898-chr21:45545746..45547620,2	MCF-7	breast:
14	chr21:45525373..45527219-chr21:45757637..45759650,2	K562	blood:
15	chr21:45525043..45527455-chr21:45658553..45661169,2	K562	blood:
16	chr21:45525797..45531105-chr21:45550576..45555096,10	MCF-7	breast:
17	chr21:45527359..45530919-chr21:45716038..45721178,5	K562	blood:
18	chr21:45432030..45433595-chr21:45528805..45531455,2	MCF-7	breast:
19	chr21:45528642..45531005-chr21:45719210..45722629,3	K562	blood:
20	chr21:45527479..45530084-chr21:45730033..45733150,3	K562	blood:
21	chr21:45502612..45504623-chr21:45528880..45531046,2	K562	blood:
22	chr21:45526873..45527551-chr6:26271493..26272199,2	Hela-S3	cervix:
23	chr21:45443004..45445894-chr21:45525431..45527091,3	K562	blood:
24	chr21:45429712..45433999-chr21:45522896..45529122,10	K562	blood:
25	chr21:45443004..45445894-chr21:45525520..45527091,2	K562	blood:
26	chr21:45514673..45516174-chr21:45524050..45526937,2	MCF-7	breast:
27	chr21:45444934..45447565-chr21:45527496..45530031,3	K562	blood:

No data

Variant related genes	Relation type
PWP2	TF binding region
PWP2	CpG island
ENSG00000241945	chromatin interactions
ENSG00000256018	chromatin interactions
ENSG00000232969	chromatin interactions
ENSG00000141959	chromatin interactions
ENSG00000160223	chromatin interactions
ENSG00000235374	chromatin interactions
ENSG00000197381	chromatin interactions
ENSG00000160218	chromatin interactions
ENSG00000160226	chromatin interactions
ENSG00000160221	chromatin interactions
ENSG00000215458	chromatin interactions

Extended variants
information (count: 120 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:120 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191074831	chr21:45526063-45526064	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
2	rs578178078	chr21:45526065-45526066	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
3	rs200847361	chr21:45526068-45526069	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
4	rs2516520	chr21:45526076-45526077	Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs182274478	chr21:45526091-45526092	Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
6	rs149375226	chr21:45526105-45526106	Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
7	rs199956097	chr21:45526114-45526115	Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
8	rs185507026	chr21:45526119-45526120	Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
9	rs11908887	chr21:45526152-45526153	Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs528606754	chr21:45526176-45526177	Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
11	rs547567200	chr21:45526191-45526192	Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
12	rs191099826	chr21:45526192-45526193	Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
13	rs576149702	chr21:45526214-45526215	Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
14	rs543272008	chr21:45526219-45526220	Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
15	rs183416708	chr21:45526262-45526263	Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
16	rs551416791	chr21:45526295-45526296	Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
17	rs561797942	chr21:45526299-45526300	Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
18	rs188060298	chr21:45526373-45526374	Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
19	rs144758616	chr21:45526400-45526401	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
20	rs148548163	chr21:45526430-45526431	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
21	rs529011254	chr21:45526456-45526457	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
22	rs77582160	chr21:45526509-45526510	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
23	rs375751836	chr21:45526568-45526569	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
24	rs66678358	chr21:45526571-45526572	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
25	rs543628506	chr21:45526574-45526575	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
26	rs563357229	chr21:45526596-45526597	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
27	rs377735224	chr21:45526620-45526621	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
28	rs532195884	chr21:45526666-45526667	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
29	rs193014270	chr21:45526739-45526740	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
30	rs541016583	chr21:45526759-45526760	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
31	rs553119144	chr21:45526805-45526806	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
32	rs578136112	chr21:45526857-45526858	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
33	rs541197082	chr21:45526870-45526871	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
34	rs545587857	chr21:45526882-45526883	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
35	rs557413298	chr21:45526883-45526884	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
36	rs575583194	chr21:45526908-45526909	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
37	rs543000595	chr21:45526919-45526920	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
38	rs534834965	chr21:45526932-45526933	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
39	rs561269257	chr21:45526984-45526985	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
40	rs528567690	chr21:45526991-45526992	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
41	rs540744841	chr21:45527036-45527037	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
42	rs71197878	chr21:45527045-45527046	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
43	rs398081635	chr21:45527048-45527049	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
44	rs397730432	chr21:45527049-45527050	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
45	rs559481786	chr21:45527072-45527073	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
46	rs533027939	chr21:45527085-45527086	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
47	rs551644505	chr21:45527105-45527106	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
48	rs569811306	chr21:45527110-45527111	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
49	rs72257518	chr21:45527113-45527114	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
50	rs71197879	chr21:45527118-45527119	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Down syndrome	17412756	CNVD
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Renal cell carcinoma	19461508	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
lymphocytic leukemia	21291569	CNVD
Melanoma	18172304	CNVD
Autism	22958593	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Wilms tumour	21544195	CNVD
Ewing''s sarcoma	17952124	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute myeloid leukemia	16864856	CNVD
Mental retardation	21031080	CNVD
Polymicrogyria	21031080	CNVD
periventricular nodular heterotopia	21031080	CNVD
Myelodysplastic syndrome	21606161	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Autism	18414403	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21858162	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17899364	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	20473283	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	18628472	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Ewing''s sarcoma	21437220	CNVD
Lung adenocarcinoma	17086460	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute myeloid leukemia	21358987	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	23341502	CNVD
Ovarian cancer	21720365	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	18496225	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 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
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	17142309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	18628472	CNVD
Leukemia	18628472	CNVD
small cell lung cancer	17426248	CNVD
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45473000-45526600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr21:45495600-45526800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr21:45514600-45526600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr21:45517400-45527600	Weak transcription	Fetal Brain Male	brain
5	chr21:45518600-45526600	Weak transcription	Fetal Kidney	kidney
6	chr21:45518800-45526400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr21:45519400-45526200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr21:45519400-45526200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr21:45520200-45527600	Weak transcription	Fetal Heart	heart
10	chr21:45520400-45526600	Weak transcription	HUVEC	blood vessel
11	chr21:45522400-45526800	Weak transcription	NH-A	brain
12	chr21:45522600-45526800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr21:45523000-45526800	Weak transcription	Stomach Mucosa	stomach
14	chr21:45523400-45526600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr21:45523400-45526600	Weak transcription	HMEC	breast
16	chr21:45523600-45526400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr21:45523600-45526400	Weak transcription	A549	lung
18	chr21:45523600-45526600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr21:45523600-45526600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr21:45523600-45526800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr21:45523800-45526400	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr21:45523800-45526400	Weak transcription	Brain Anterior Caudate	brain
23	chr21:45523800-45526400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr21:45523800-45526600	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr21:45523800-45526600	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr21:45523800-45526600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr21:45523800-45526600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr21:45523800-45526600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr21:45523800-45526600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr21:45523800-45526600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr21:45523800-45526600	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr21:45523800-45526600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr21:45523800-45526600	Weak transcription	Fetal Lung	lung
34	chr21:45523800-45526600	Weak transcription	Ovary	ovary
35	chr21:45523800-45526600	Weak transcription	HepG2	liver
36	chr21:45523800-45526600	Weak transcription	NHEK	skin
37	chr21:45523800-45526600	Weak transcription	NHLF	lung
38	chr21:45523800-45526800	Weak transcription	Aorta	Aorta
39	chr21:45523800-45526800	Weak transcription	Esophagus	oesophagus
40	chr21:45524000-45526400	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr21:45524000-45526400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr21:45524000-45526600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr21:45524000-45526600	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr21:45524000-45526600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr21:45524000-45526600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr21:45524000-45526600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr21:45524000-45526600	Weak transcription	Brain Angular Gyrus	brain
48	chr21:45524000-45526600	Weak transcription	Brain Cingulate Gyrus	brain
49	chr21:45524000-45526600	Weak transcription	Brain Hippocampus Middle	brain
50	chr21:45524000-45526600	Weak transcription	Brain Inferior Temporal Lobe	brain

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