Variant report

Variant	esv33771
Chromosome Location	chr21:45155220-45167253
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:391)
CpG islands
(count:183)
Chromatin interactive
region (count:31)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr21:45158438-45158813	K562	blood:	n/a	n/a
2	ATF3	chr21:45160710-45160988	A549	lung:	n/a	chr21:45160849-45160862
3	BACH1	chr21:45160396-45161112	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr21:45161393-45161618	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr21:45164297-45164791	GM12878	blood:	n/a	n/a
6	BCL3	chr21:45164262-45164666	GM12878	blood:	n/a	n/a
7	BCL3	chr21:45160274-45161086	A549	lung:	n/a	chr21:45160409-45160418
8	BCL3	chr21:45159769-45160260	A549	lung:	n/a	chr21:45159789-45159802
9	BHLHE40	chr21:45158061-45158395	HepG2	liver:	n/a	n/a
10	BHLHE40	chr21:45158311-45158664	K562	blood:	n/a	n/a
11	BHLHE40	chr21:45166168-45166321	K562	blood:	n/a	n/a
12	CBX3	chr21:45159315-45159743	K562	blood:	n/a	n/a
13	CBX3	chr21:45158262-45158880	K562	blood:	n/a	n/a
14	CCNT2	chr21:45156306-45156323	K562	blood:	n/a	n/a
15	CEBPB	chr21:45158312-45158814	K562	blood:	n/a	n/a
16	CEBPB	chr21:45156852-45156935	K562	blood:	n/a	n/a
17	CEBPB	chr21:45157993-45158303	HepG2	liver:	n/a	n/a
18	CEBPB	chr21:45165698-45165989	K562	blood:	n/a	n/a
19	CEBPB	chr21:45156847-45156939	A549	lung:	n/a	n/a
20	CEBPB	chr21:45165180-45165355	K562	blood:	n/a	n/a
21	CEBPB	chr21:45166217-45166362	K562	blood:	n/a	n/a
22	CEBPB	chr21:45156918-45156923	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr21:45156743-45157038	HepG2	liver:	n/a	n/a
24	CEBPD	chr21:45158300-45158858	K562	blood:	n/a	n/a
25	CREB1	chr21:45160660-45161034	H1-hESC	embryonic stem cell:	n/a	n/a
26	CREB1	chr21:45160649-45161059	A549	lung:	n/a	n/a
27	CTCF	chr21:45158237-45158340	HepG2	liver:	n/a	n/a
28	CTCF	chr21:45157260-45157410	HepG2	liver:	n/a	n/a
29	CTCF	chr21:45157290-45157306	MCF-7	breast:	n/a	n/a
30	CTCF	chr21:45161420-45161570	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr21:45157283-45157331	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr21:45157267-45157316	MCF-7	breast:	n/a	n/a
33	CTCF	chr21:45157140-45157290	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr21:45157180-45157330	RPTEC	kidney:	n/a	n/a
35	CTCF	chr21:45158160-45158310	HepG2	liver:	n/a	n/a
36	CTCF	chr21:45157340-45157490	HepG2	liver:	n/a	n/a
37	CTCF	chr21:45158180-45158330	HepG2	liver:	n/a	n/a
38	CTCF	chr21:45161360-45161510	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr21:45158631-45158670	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr21:45157100-45157250	GM12878	blood:	n/a	n/a
41	CTCF	chr21:45157260-45157410	A549	lung:	n/a	n/a
42	CTCF	chr21:45157300-45157450	Hela-S3	cervix:	n/a	n/a
43	CUX1	chr21:45158443-45158689	K562	blood:	n/a	n/a
44	CUX1	chr21:45166306-45166351	K562	blood:	n/a	n/a
45	E2F6	chr21:45158385-45158681	K562	blood:	n/a	n/a
46	E2F6	chr21:45158372-45158564	K562	blood:	n/a	n/a
47	E2F6	chr21:45158136-45158703	K562	blood:	n/a	n/a
48	EGR1	chr21:45161354-45161563	K562	blood:	n/a	n/a
49	EP300	chr21:45166185-45166325	K562	blood:	n/a	n/a
50	EP300	chr21:45158326-45158704	K562	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:45161359-45161409	SK-N-SH	brain:	n/a
2	chr21:45161415-45161465	SK-N-SH_RA	brain:	n/a
3	chr21:45161415-45161465	SAEC	small airway:	n/a
4	chr21:45161415-45161465	H1-hESC	embryonic stem cell:	embryo
5	chr21:45161415-45161465	Hepatocyte	liver:	n/a
6	chr21:45161359-45161409	HEEpiC	esophagus:	n/a
7	chr21:45163611-45163661	AoSMC	blood vessel:	n/a
8	chr21:45161415-45161465	GM19239	blood:	n/a
9	chr21:45163611-45163661	K562	blood:	n/a
10	chr21:45161415-45161465	GM06990	blood:	n/a
11	chr21:45161359-45161409	H1-hESC	embryonic stem cell:	embryo
12	chr21:45163611-45163661	ovcar-3	ovarian:	n/a
13	chr21:45161415-45161465	HUVEC	blood vessel:	n/a
14	chr21:45163611-45163661	HNPCEpiC	eye:	n/a
15	chr21:45161359-45161409	HCT-116	colon:	n/a
16	chr21:45161415-45161465	HPAEpiC	pulmonary alveolar:	n/a
17	chr21:45163611-45163661	SK-N-MC	brain:	n/a
18	chr21:45161359-45161409	ECC-1	luminal epithelium:	n/a
19	chr21:45163611-45163661	PANC-1	pancreas:	n/a
20	chr21:45163611-45163661	MCF10A-Er-Src	breast:	n/a
21	chr21:45161415-45161465	HepG2	liver:	n/a
22	chr21:45163611-45163661	HCM	heart:	n/a
23	chr21:45161359-45161409	HepG2	liver:	n/a
24	chr21:45161359-45161409	RPTEC	kidney:	n/a
25	chr21:45161415-45161465	Jurkat	blood:	n/a
26	chr21:45163611-45163661	GM12892	blood:	n/a
27	chr21:45163611-45163661	HCPEpiC	choroid plexus:	n/a
28	chr21:45163611-45163661	GM12878	blood:	n/a
29	chr21:45161359-45161409	PANC-1	pancreas:	n/a
30	chr21:45163611-45163661	GM12891	blood:	n/a
31	chr21:45161415-45161465	IMR90	lung:	fetal
32	chr21:45161415-45161465	AG04450	lung:	fetal
33	chr21:45161359-45161409	T-47D	breast:	n/a
34	chr21:45161359-45161409	SK-N-MC	brain:	n/a
35	chr21:45163611-45163661	Jurkat	blood:	n/a
36	chr21:45163611-45163661	AG09309	skin:	n/a
37	chr21:45163611-45163661	Hela-S3	cervix:	n/a
38	chr21:45161359-45161409	NB4	blood:	n/a
39	chr21:45161415-45161465	AG09309	skin:	n/a
40	chr21:45163611-45163661	HPAEpiC	pulmonary alveolar:	n/a
41	chr21:45163611-45163661	NHDF-neo	bronchial:	n/a
42	chr21:45161415-45161465	Caco-2	colon:	n/a
43	chr21:45163611-45163661	SK-N-SH_RA	brain:	n/a
44	chr21:45161415-45161465	AG04449	skin:	fetal
45	chr21:45161415-45161465	HNPCEpiC	eye:	n/a
46	chr21:45161415-45161465	RPTEC	kidney:	n/a
47	chr21:45161415-45161465	K562	blood:	n/a
48	chr21:45161359-45161409	SKMC	muscle:	n/a
49	chr21:45161359-45161409	LNCaP	prostate:	n/a
50	chr21:45163611-45163661	NT2-D1	testis:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:45163023..45165790-chr21:45170856..45174314,3	K562	blood:
2	chr21:45152139..45163298-chr21:45164540..45174522,16	K562	blood:
3	chr21:45162810..45165195-chr21:45176926..45179048,2	K562	blood:
4	chr21:45165588..45167444-chr21:45177367..45179445,2	MCF-7	breast:
5	chr21:45146930..45150669-chr21:45163613..45169103,5	K562	blood:
6	chr21:45152139..45163298-chr21:45164540..45174522,16	K562	blood:
7	chr21:45147353..45150091-chr21:45163613..45167274,4	K562	blood:
8	chr21:45151886..45156250-chr21:45192617..45197213,5	MCF-7	breast:
9	chr21:45158524..45162841-chr21:45165683..45171048,8	K562	blood:
10	chr21:45156014..45158647-chr21:45159074..45160757,2	K562	blood:
11	chr21:45156965..45158670-chr21:45174699..45176799,2	K562	blood:
12	chr21:45166127..45168190-chr21:45198985..45201869,2	K562	blood:
13	chr21:45137354..45140305-chr21:45163614..45165870,3	MCF-7	breast:
14	chr21:45165363..45167088-chr21:45194223..45196266,2	MCF-7	breast:
15	chr21:45162810..45165204-chr21:45175505..45178426,2	K562	blood:
16	chr21:45159502..45161246-chr21:45194764..45196763,2	MCF-7	breast:
17	chr21:45154001..45156611-chr21:45177637..45180387,2	K562	blood:
18	chr21:45158615..45161441-chr21:45207897..45210708,2	K562	blood:
19	chr21:44935059..44936997-chr21:45153609..45155904,2	MCF-7	breast:
20	chr21:45165894..45167884-chr21:45171722..45174273,2	K562	blood:
21	chr21:45164921..45166877-chr21:45166997..45169477,2	K562	blood:
22	chr21:45138749..45140625-chr21:45164594..45167451,2	MCF-7	breast:
23	chr21:45164290..45167394-chr21:45171722..45175273,3	K562	blood:
24	chr21:45156014..45158647-chr21:45159074..45160757,2	K562	blood:
25	chr21:45154933..45157513-chr21:45174243..45177077,2	MCF-7	breast:
26	chr21:45153763..45156767-chr21:45158365..45161211,5	MCF-7	breast:
27	chr21:45138760..45141316-chr21:45163664..45165255,2	K562	blood:
28	chr21:45156182..45158069-chr21:45230385..45232004,2	K562	blood:
29	chr21:45154618..45156575-chr21:45170589..45173066,2	K562	blood:
30	chr21:45159250..45162021-chr21:45208113..45211544,3	MCF-7	breast:
31	chr21:45156014..45158637-chr21:45159074..45161792,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PDXK	hsa-miR-193b-3p	chr21:45157285-45157305

Variant related genes	Relation type
PDXK	TF binding region
PDXK	CpG island
ENSG00000160214	chromatin interactions
ENSG00000160213	chromatin interactions
ENSG00000160209	chromatin interactions

Extended variants
information (count: 645 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:645 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558266850	chr21:45155223-45155224	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs113426459	chr21:45155249-45155250	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs372165456	chr21:45155403-45155404	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs574364831	chr21:45155428-45155429	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs73224934	chr21:45155494-45155495	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs560459598	chr21:45155518-45155519	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs527515767	chr21:45155538-45155539	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs562139451	chr21:45155541-45155542	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs369032074	chr21:45155583-45155584	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs58966243	chr21:45155625-45155626	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs564247728	chr21:45155627-45155628	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs140449047	chr21:45155726-45155727	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs371438127	chr21:45155727-45155728	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs550211459	chr21:45155756-45155757	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs568406494	chr21:45155765-45155766	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs529285810	chr21:45155784-45155785	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs547711910	chr21:45155788-45155789	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs114725586	chr21:45155816-45155817	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs150421845	chr21:45155829-45155830	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs557931743	chr21:45155867-45155868	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs9985073	chr21:45155876-45155877	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs138405989	chr21:45155899-45155900	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs143932193	chr21:45155905-45155906	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs147293492	chr21:45155916-45155917	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs192348761	chr21:45155935-45155936	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs369196760	chr21:45155944-45155945	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs553766572	chr21:45156100-45156101	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs572389633	chr21:45156132-45156133	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs546074648	chr21:45156197-45156198	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs564136932	chr21:45156198-45156199	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs555024034	chr21:45156217-45156218	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs373933585	chr21:45156231-45156232	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs139290917	chr21:45156253-45156254	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs114177111	chr21:45156291-45156292	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs562190402	chr21:45156297-45156298	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs529305093	chr21:45156313-45156314	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs79561603	chr21:45156330-45156331	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs149428017	chr21:45156366-45156367	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs144844600	chr21:45156420-45156421	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs377632841	chr21:45156427-45156428	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs570199966	chr21:45156433-45156434	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs79898513	chr21:45156443-45156444	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs184681689	chr21:45156487-45156488	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs34234452	chr21:45156511-45156512	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs77512963	chr21:45156528-45156529	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs568161484	chr21:45156579-45156580	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs189772783	chr21:45156626-45156627	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs559770028	chr21:45156644-45156645	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs572032521	chr21:45156653-45156654	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs7282274	chr21:45156674-45156675	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 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
Neuroblastoma	20406844	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
Breast cancer	21364760	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:613 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45146000-45163600	Weak transcription	Dnd41	blood
2	chr21:45149000-45194400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr21:45149400-45157600	Weak transcription	Aorta	Aorta
4	chr21:45149400-45175400	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr21:45149600-45157800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr21:45149600-45159400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr21:45149600-45163600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr21:45149600-45163600	Weak transcription	Rectal Smooth Muscle	rectum
9	chr21:45149600-45163800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr21:45149600-45164200	Weak transcription	Primary B cells from cord blood	blood
11	chr21:45149800-45157200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr21:45149800-45160200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr21:45149800-45164200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr21:45149800-45164400	Weak transcription	Fetal Kidney	kidney
15	chr21:45149800-45175200	Weak transcription	HUVEC	blood vessel
16	chr21:45149800-45188200	Weak transcription	Primary hematopoietic stem cells	blood
17	chr21:45150000-45158200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr21:45150000-45161600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr21:45150000-45163600	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr21:45150000-45173200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr21:45151000-45156400	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr21:45151200-45156400	Enhancers	Fetal Brain Male	brain
23	chr21:45151600-45155400	Enhancers	Stomach Mucosa	stomach
24	chr21:45151800-45155400	Enhancers	NH-A	brain
25	chr21:45152200-45160600	Genic enhancers	Fetal Intestine Large	intestine
26	chr21:45152200-45160600	Genic enhancers	Fetal Intestine Small	intestine
27	chr21:45152200-45183400	Strong transcription	Monocytes-CD14+_RO01746	blood
28	chr21:45152400-45155600	Enhancers	Brain Hippocampus Middle	brain
29	chr21:45152400-45156200	Enhancers	Brain Inferior Temporal Lobe	brain
30	chr21:45152400-45156600	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr21:45152400-45157800	Genic enhancers	HepG2	liver
32	chr21:45152400-45163800	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr21:45152400-45173200	Weak transcription	Psoas Muscle	Psoas
34	chr21:45152600-45156000	Enhancers	Fetal Thymus	thymus
35	chr21:45152800-45155600	Enhancers	Brain Germinal Matrix	brain
36	chr21:45153000-45157200	Enhancers	Brain Angular Gyrus	brain
37	chr21:45153200-45155600	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr21:45153200-45155800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr21:45153200-45156400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr21:45153200-45157200	Genic enhancers	Lung	lung
41	chr21:45153400-45155400	Enhancers	Placenta Amnion	Placenta Amnion
42	chr21:45153400-45155600	Genic enhancers	A549	lung
43	chr21:45153400-45158400	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr21:45153600-45155400	Enhancers	Osteobl	bone
45	chr21:45153600-45155600	Strong transcription	Spleen	Spleen
46	chr21:45153600-45156000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr21:45153600-45159400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr21:45153600-45163800	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr21:45154000-45158400	Strong transcription	Primary monocytes fromperipheralblood	blood
50	chr21:45154000-45159200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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