Variant report

Variant	esv1826549
Chromosome Location	chr21:45157128-45170285
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:422)
CpG islands
(count:184)
Chromatin interactive
region (count:33)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:422 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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	chr21:45161393-45161618	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr21:45160396-45161112	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr21:45164297-45164791	GM12878	blood:	n/a	n/a
6	BCL3	chr21:45169866-45170231	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	BCL3	chr21:45164262-45164666	GM12878	blood:	n/a	n/a
10	BHLHE40	chr21:45166168-45166321	K562	blood:	n/a	n/a
11	BHLHE40	chr21:45158311-45158664	K562	blood:	n/a	n/a
12	BHLHE40	chr21:45158061-45158395	HepG2	liver:	n/a	n/a
13	CBX3	chr21:45158262-45158880	K562	blood:	n/a	n/a
14	CBX3	chr21:45159315-45159743	K562	blood:	n/a	n/a
15	CEBPB	chr21:45166217-45166362	K562	blood:	n/a	n/a
16	CEBPB	chr21:45157993-45158303	HepG2	liver:	n/a	n/a
17	CEBPB	chr21:45165698-45165989	K562	blood:	n/a	n/a
18	CEBPB	chr21:45165180-45165355	K562	blood:	n/a	n/a
19	CEBPB	chr21:45158312-45158814	K562	blood:	n/a	n/a
20	CEBPD	chr21:45158300-45158858	K562	blood:	n/a	n/a
21	CREB1	chr21:45160649-45161059	A549	lung:	n/a	n/a
22	CREB1	chr21:45160660-45161034	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr21:45157283-45157331	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr21:45158631-45158670	Kidney_OC	kidney:	n/a	n/a
25	CTCF	chr21:45158180-45158330	HepG2	liver:	n/a	n/a
26	CTCF	chr21:45157290-45157306	MCF-7	breast:	n/a	n/a
27	CTCF	chr21:45161360-45161510	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr21:45169720-45169870	GM12878	blood:	n/a	chr21:45169768-45169781
29	CTCF	chr21:45157100-45157250	GM12878	blood:	n/a	n/a
30	CTCF	chr21:45169880-45170030	SAEC	small airway:	n/a	n/a
31	CTCF	chr21:45161420-45161570	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr21:45169713-45169808	GM19239	blood:	n/a	chr21:45169768-45169781
33	CTCF	chr21:45157300-45157450	Hela-S3	cervix:	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	chr21:45157260-45157410	A549	lung:	n/a	n/a
37	CTCF	chr21:45169729-45169858	GM12878	blood:	n/a	chr21:45169768-45169781
38	CTCF	chr21:45169732-45169803	GM19240	blood:	n/a	chr21:45169768-45169781
39	CTCF	chr21:45157267-45157316	MCF-7	breast:	n/a	n/a
40	CTCF	chr21:45157340-45157490	HepG2	liver:	n/a	n/a
41	CTCF	chr21:45169728-45169804	GM19238	blood:	n/a	chr21:45169768-45169781
42	CTCF	chr21:45169739-45169817	GM12891	blood:	n/a	chr21:45169768-45169781
43	CTCF	chr21:45157140-45157290	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr21:45169721-45169781	GM12892	blood:	n/a	chr21:45169768-45169781
45	CTCF	chr21:45158237-45158340	HepG2	liver:	n/a	n/a
46	CTCF	chr21:45157260-45157410	HepG2	liver:	n/a	n/a
47	CUX1	chr21:45166306-45166351	K562	blood:	n/a	n/a
48	CUX1	chr21:45158443-45158689	K562	blood:	n/a	n/a
49	E2F6	chr21:45158136-45158703	K562	blood:	n/a	n/a
50	E2F6	chr21:45158385-45158681	K562	blood:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:45161359-45161409	NB4	blood:	n/a
2	chr21:45161359-45161409	NB4	blood:	n/a
3	chr21:45161415-45161465	PANC-1	pancreas:	n/a
4	chr21:45161359-45161409	NHDF-neo	bronchial:	n/a
5	chr21:45161415-45161465	NT2-D1	testis:	n/a
6	chr21:45163611-45163661	SAEC	small airway:	n/a
7	chr21:45161359-45161409	AG10803	skin:	n/a
8	chr21:45161359-45161409	HCM	heart:	n/a
9	chr21:45163611-45163661	SK-N-SH_RA	brain:	n/a
10	chr21:45161415-45161465	ProgFib	skin:	n/a
11	chr21:45163611-45163661	H1-hESC	embryonic stem cell:	embryo
12	chr21:45161359-45161409	RPTEC	kidney:	n/a
13	chr21:45161359-45161409	GM12878	blood:	n/a
14	chr21:45161359-45161409	NT2-D1	testis:	n/a
15	chr21:45161415-45161465	K562	blood:	n/a
16	chr21:45161359-45161409	GM06990	blood:	n/a
17	chr21:45161359-45161409	BJ	skin:	n/a
18	chr21:45161415-45161465	ECC-1	luminal epithelium:	n/a
19	chr21:45161359-45161409	SAEC	small airway:	n/a
20	chr21:45163611-45163661	ECC-1	luminal epithelium:	n/a
21	chr21:45161415-45161465	HepG2	liver:	n/a
22	chr21:45163611-45163661	PANC-1	pancreas:	n/a
23	chr21:45161415-45161465	H1-hESC	embryonic stem cell:	embryo
24	chr21:45161359-45161409	HAEpiC	amniotic membrane:	n/a
25	chr21:45161415-45161465	HRCEpiC	kidney:	n/a
26	chr21:45161359-45161409	AG09309	skin:	n/a
27	chr21:45163611-45163661	BJ	skin:	n/a
28	chr21:45163611-45163661	HIPEpiC	eye:	n/a
29	chr21:45161415-45161465	Hepatocyte	liver:	n/a
30	chr21:45161415-45161465	HAEpiC	amniotic membrane:	n/a
31	chr21:45161415-45161465	HCT-116	colon:	n/a
32	chr21:45161415-45161465	HRE	kidney:	n/a
33	chr21:45163611-45163661	GM12892	blood:	n/a
34	chr21:45161359-45161409	HEEpiC	esophagus:	n/a
35	chr21:45161415-45161465	HEK293	kidney:	embryo
36	chr21:45163611-45163661	IMR90	lung:	fetal
37	chr21:45161359-45161409	PrEC	prostate:	n/a
38	chr21:45163611-45163661	HRPEpiC	eye:	n/a
39	chr21:45163611-45163661	MCF10A-Er-Src	breast:	n/a
40	chr21:45161359-45161409	BE2_C	brain:	n/a
41	chr21:45163611-45163661	GM19239	blood:	n/a
42	chr21:45161359-45161409	HNPCEpiC	eye:	n/a
43	chr21:45161415-45161465	SK-N-MC	brain:	n/a
44	chr21:45161359-45161409	HCT-116	colon:	n/a
45	chr21:45163611-45163661	HAEpiC	amniotic membrane:	n/a
46	chr21:45163611-45163661	HL-60	blood:	n/a
47	chr21:45161415-45161465	T-47D	breast:	n/a
48	chr21:45161359-45161409	ECC-1	luminal epithelium:	n/a
49	chr21:45161415-45161465	HCPEpiC	choroid plexus:	n/a
50	chr21:45161415-45161465	BJ	skin:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:45156014..45158647-chr21:45159074..45160757,2	K562	blood:
2	chr21:45166127..45168190-chr21:45198985..45201869,2	K562	blood:
3	chr21:45165894..45167884-chr21:45171722..45174273,2	K562	blood:
4	chr21:45156014..45158647-chr21:45159074..45160757,2	K562	blood:
5	chr21:45170139..45171974-chr21:45180747..45184494,3	K562	blood:
6	chr21:45152139..45163298-chr21:45164540..45174522,16	K562	blood:
7	chr21:45152139..45155102-chr21:45167592..45169327,2	K562	blood:
8	chr21:45167914..45170036-chr21:45175029..45177838,2	K562	blood:
9	chr21:45156965..45158670-chr21:45174699..45176799,2	K562	blood:
10	chr21:45162810..45165204-chr21:45175505..45178426,2	K562	blood:
11	chr21:45152139..45163298-chr21:45164540..45174522,16	K562	blood:
12	chr21:45146930..45150669-chr21:45163613..45169103,5	K562	blood:
13	chr21:45158615..45161441-chr21:45207897..45210708,2	K562	blood:
14	chr21:45156182..45158069-chr21:45230385..45232004,2	K562	blood:
15	chr21:45165298..45166880-chr21:45168417..45169952,2	MCF-7	breast:
16	chr21:45158524..45162841-chr21:45165683..45171048,8	K562	blood:
17	chr21:45138749..45140625-chr21:45164594..45167451,2	MCF-7	breast:
18	chr21:45164921..45166877-chr21:45166997..45169477,2	K562	blood:
19	chr21:45159502..45161246-chr21:45194764..45196763,2	MCF-7	breast:
20	chr21:45137354..45140305-chr21:45163614..45165870,3	MCF-7	breast:
21	chr21:45164290..45167394-chr21:45171722..45175273,3	K562	blood:
22	chr21:45163023..45165790-chr21:45170856..45174314,3	K562	blood:
23	chr21:45165588..45167444-chr21:45177367..45179445,2	MCF-7	breast:
24	chr21:45162810..45165195-chr21:45176926..45179048,2	K562	blood:
25	chr21:45147353..45150091-chr21:45163613..45167274,4	K562	blood:
26	chr21:45159250..45162021-chr21:45208113..45211544,3	MCF-7	breast:
27	chr21:45138760..45141316-chr21:45163664..45165255,2	K562	blood:
28	chr21:45168554..45170321-chr21:45172450..45175239,2	MCF-7	breast:
29	chr21:45156014..45158637-chr21:45159074..45161792,2	K562	blood:
30	chr21:45161547..45167086-chr21:45167365..45170424,6	MCF-7	breast:
31	chr21:45165363..45167088-chr21:45194223..45196266,2	MCF-7	breast:
32	chr21:45154933..45157513-chr21:45174243..45177077,2	MCF-7	breast:
33	chr21:33103919..33104588-chr21:45170107..45170783,2	Hela-S3	cervix:

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
ENSG00000156304	chromatin interactions
ENSG00000160213	chromatin interactions
ENSG00000160209	chromatin interactions
ENSG00000160214	chromatin interactions

Extended variants
information (count: 713 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:713 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73373294	chr21:45157128-45157129	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs374142798	chr21:45157159-45157160	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs573490340	chr21:45157164-45157165	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs115887388	chr21:45157168-45157169	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs189387115	chr21:45157171-45157172	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs577647093	chr21:45157177-45157178	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs545397104	chr21:45157190-45157191	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs563504965	chr21:45157201-45157202	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs531236318	chr21:45157221-45157222	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs113256378	chr21:45157222-45157223	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs376087472	chr21:45157233-45157234	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs370261846	chr21:45157243-45157244	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs371557326	chr21:45157249-45157250	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs374699059	chr21:45157266-45157267	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs528695971	chr21:45157273-45157274	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs547545321	chr21:45157288-45157289	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region miRNA target site	2 gene(s)	Overlapped CNVs	n/a
17	rs565765043	chr21:45157356-45157357	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs144058133	chr21:45157358-45157359	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs146483939	chr21:45157386-45157387	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs569505342	chr21:45157387-45157388	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs370869755	chr21:45157403-45157404	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs374254716	chr21:45157410-45157411	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs368058414	chr21:45157417-45157418	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs371479708	chr21:45157418-45157419	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs573527153	chr21:45157445-45157446	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs117050103	chr21:45157488-45157489	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs552712438	chr21:45157594-45157595	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs577734838	chr21:45157632-45157633	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs545123039	chr21:45157635-45157636	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs181840143	chr21:45157660-45157661	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs11702042	chr21:45157670-45157671	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs575541460	chr21:45157671-45157672	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs186494824	chr21:45157699-45157700	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs534817929	chr21:45157746-45157747	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs189298020	chr21:45157759-45157760	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs528732856	chr21:45157779-45157780	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs540844997	chr21:45157832-45157833	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs377089613	chr21:45157838-45157839	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs140836126	chr21:45157839-45157840	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs533051038	chr21:45157851-45157852	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs551151152	chr21:45157885-45157886	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs370403637	chr21:45157920-45157921	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs180872475	chr21:45157929-45157930	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs148070117	chr21:45157942-45157943	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs116696452	chr21:45157981-45157982	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs567236428	chr21:45158006-45158007	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs149733837	chr21:45158066-45158067	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs552750626	chr21:45158154-45158155	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs145650469	chr21:45158241-45158242	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
50	rs539165707	chr21:45158256-45158257	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

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:606 , 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	chr21:45152200-45160600	Genic enhancers	Fetal Intestine Large	intestine
22	chr21:45152200-45160600	Genic enhancers	Fetal Intestine Small	intestine
23	chr21:45152200-45183400	Strong transcription	Monocytes-CD14+_RO01746	blood
24	chr21:45152400-45157800	Genic enhancers	HepG2	liver
25	chr21:45152400-45163800	Weak transcription	Skeletal Muscle Female	skeletal muscle
26	chr21:45152400-45173200	Weak transcription	Psoas Muscle	Psoas
27	chr21:45153000-45157200	Enhancers	Brain Angular Gyrus	brain
28	chr21:45153200-45157200	Genic enhancers	Lung	lung
29	chr21:45153400-45158400	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr21:45153600-45159400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr21:45153600-45163800	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr21:45154000-45158400	Strong transcription	Primary monocytes fromperipheralblood	blood
33	chr21:45154000-45159200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr21:45154000-45167000	Weak transcription	Small Intestine	intestine
35	chr21:45154200-45157400	Enhancers	Brain Anterior Caudate	brain
36	chr21:45154200-45158200	Strong transcription	Placenta	Placenta
37	chr21:45154200-45163400	Weak transcription	Colon Smooth Muscle	Colon
38	chr21:45154200-45163800	Weak transcription	NHDF-Ad	bronchial
39	chr21:45154400-45158400	Strong transcription	Stomach Smooth Muscle	stomach
40	chr21:45154400-45160400	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr21:45154400-45160600	Strong transcription	Fetal Stomach	stomach
42	chr21:45154400-45184200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr21:45154600-45164200	Weak transcription	Brain Substantia Nigra	brain
44	chr21:45154800-45157800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
45	chr21:45154800-45158600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr21:45154800-45164200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
47	chr21:45154800-45174600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
48	chr21:45155000-45157200	Weak transcription	K562	blood
49	chr21:45155000-45157600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr21:45155000-45157800	Strong transcription	Colonic Mucosa	Colon

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