Variant report

Variant	esv3424921
Chromosome Location	chr21:47604361-47605179
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:356)
CpG islands
(count:306)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:356 , 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	ARID3A	chr21:47603955-47605670	K562	blood:	n/a	n/a
2	ATF1	chr21:47604322-47605322	K562	blood:	n/a	n/a
3	BACH1	chr21:47604648-47604803	K562	blood:	n/a	n/a
4	BACH1	chr21:47604533-47605159	H1-hESC	embryonic stem cell:	n/a	chr21:47604969-47604983
5	BATF	chr21:47604305-47604771	GM12878	blood:	n/a	n/a
6	BATF	chr21:47604311-47604581	GM12878	blood:	n/a	n/a
7	BCL11A	chr21:47604284-47604707	GM12878	blood:	n/a	n/a
8	BCL11A	chr21:47604296-47604778	GM12878	blood:	n/a	n/a
9	BHLHE40	chr21:47604531-47604866	GM12878	blood:	n/a	n/a
10	BHLHE40	chr21:47603834-47605107	K562	blood:	n/a	n/a
11	BRCA1	chr21:47604610-47604804	HepG2	liver:	n/a	n/a
12	BRCA1	chr21:47604428-47604792	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr21:47604617-47604806	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr21:47604496-47604500	GM12878	blood:	n/a	n/a
15	CBX3	chr21:47603261-47605256	K562	blood:	n/a	n/a
16	CCNT2	chr21:47603783-47605058	K562	blood:	n/a	n/a
17	CEBPB	chr21:47604664-47604999	H1-hESC	embryonic stem cell:	n/a	chr21:47604860-47604871
18	CEBPB	chr21:47604594-47605069	MCF-7	breast:	n/a	chr21:47604860-47604871
19	CEBPB	chr21:47604151-47605207	K562	blood:	n/a	chr21:47604860-47604871
20	CEBPB	chr21:47604611-47605154	K562	blood:	n/a	chr21:47604860-47604871
21	CEBPB	chr21:47604600-47605061	Hela-S3	cervix:	n/a	chr21:47604860-47604871
22	CEBPB	chr21:47604671-47605051	IMR90	lung:	n/a	chr21:47604860-47604871
23	CEBPB	chr21:47604639-47604980	K562	blood:	n/a	chr21:47604860-47604871
24	CEBPB	chr21:47604625-47605036	HepG2	liver:	n/a	chr21:47604860-47604871
25	CEBPZ	chr21:47604298-47604856	HepG2	liver:	n/a	n/a
26	CHD1	chr21:47604847-47605030	GM12878	blood:	n/a	n/a
27	CHD1	chr21:47604719-47604919	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr21:47603938-47605049	GM12878	blood:	n/a	n/a
29	CHD2	chr21:47604302-47605034	Hela-S3	cervix:	n/a	n/a
30	CHD2	chr21:47603959-47605020	K562	blood:	n/a	n/a
31	CHD2	chr21:47604138-47604903	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr21:47604350-47604863	HepG2	liver:	n/a	n/a
33	CREB1	chr21:47604524-47605208	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr21:47604132-47605133	GM12878	blood:	n/a	n/a
35	CREB1	chr21:47604538-47605161	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr21:47604195-47604926	K562	blood:	n/a	n/a
37	CTCF	chr21:47604431-47604693	GM10248	blood:	n/a	n/a
38	CTCF	chr21:47604577-47604585	Pancreas_OC	pancreas:	n/a	n/a
39	CTCF	chr21:47604514-47604616	GM10266	blood:	n/a	n/a
40	CTCF	chr21:47604372-47604613	LNCaP	prostate:	n/a	n/a
41	CTCF	chr21:47605149-47605174	K562	blood:	n/a	n/a
42	CTCF	chr21:47604403-47604632	GM13977	blood:	n/a	n/a
43	CTCF	chr21:47604359-47604575	Pancreas_OC	pancreas:	n/a	n/a
44	CTCF	chr21:47604506-47604514	GM12878	blood:	n/a	n/a
45	CTCF	chr21:47604920-47605070	HBMEC	blood vessel:	n/a	n/a
46	CTCF	chr21:47604386-47604693	Lung_OC	lung:	n/a	n/a
47	CTCF	chr21:47604800-47604950	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr21:47604165-47604743	K562	blood:	n/a	n/a
49	CTCF	chr21:47604660-47604810	HepG2	liver:	n/a	n/a
50	CTCF	chr21:47604416-47604656	Spleen_OC	spleen:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:47604986-47605036	AoSMC	blood vessel:	n/a
2	chr21:47604986-47605036	AoSMC	blood vessel:	n/a
3	chr21:47604986-47605036	HIPEpiC	eye:	n/a
4	chr21:47604361-47604411	HEK293	kidney:	embryo
5	chr21:47604986-47605036	HEK293	kidney:	embryo
6	chr21:47605174-47605224	HRE	kidney:	n/a
7	chr21:47604986-47605036	NB4	blood:	n/a
8	chr21:47605072-47605122	HAEpiC	amniotic membrane:	n/a
9	chr21:47604654-47604704	Jurkat	blood:	n/a
10	chr21:47604654-47604704	SKMC	muscle:	n/a
11	chr21:47604361-47604411	NB4	blood:	n/a
12	chr21:47604986-47605036	HEEpiC	esophagus:	n/a
13	chr21:47605072-47605122	GM06990	blood:	n/a
14	chr21:47605174-47605224	HIPEpiC	eye:	n/a
15	chr21:47605072-47605122	GM19239	blood:	n/a
16	chr21:47605072-47605122	HEK293	kidney:	embryo
17	chr21:47605072-47605122	AG09309	skin:	n/a
18	chr21:47604986-47605036	HL-60	blood:	n/a
19	chr21:47604986-47605036	NHBE	bronchial:	n/a
20	chr21:47604361-47604411	HL-60	blood:	n/a
21	chr21:47604986-47605036	NHDF-neo	bronchial:	n/a
22	chr21:47605072-47605122	GM12878	blood:	n/a
23	chr21:47604361-47604411	GM06990	blood:	n/a
24	chr21:47605174-47605224	HMEC	breast:	n/a
25	chr21:47604361-47604411	HCT-116	colon:	n/a
26	chr21:47604654-47604704	GM06990	blood:	n/a
27	chr21:47604361-47604411	HNPCEpiC	eye:	n/a
28	chr21:47605174-47605224	AG09319	gingival:	n/a
29	chr21:47604654-47604704	SAEC	small airway:	n/a
30	chr21:47605072-47605122	SAEC	small airway:	n/a
31	chr21:47605174-47605224	AG09309	skin:	n/a
32	chr21:47604986-47605036	HMEC	breast:	n/a
33	chr21:47604986-47605036	GM19239	blood:	n/a
34	chr21:47604986-47605036	NT2-D1	testis:	n/a
35	chr21:47604654-47604704	GM19239	blood:	n/a
36	chr21:47604986-47605036	HAEpiC	amniotic membrane:	n/a
37	chr21:47604361-47604411	HIPEpiC	eye:	n/a
38	chr21:47604361-47604411	NT2-D1	testis:	n/a
39	chr21:47604986-47605036	SK-N-SH_RA	brain:	n/a
40	chr21:47604361-47604411	HCM	heart:	n/a
41	chr21:47604986-47605036	HUVEC	blood vessel:	n/a
42	chr21:47605174-47605224	HPAEpiC	pulmonary alveolar:	n/a
43	chr21:47605072-47605122	AG04450	lung:	fetal
44	chr21:47604654-47604704	HCM	heart:	n/a
45	chr21:47604986-47605036	HPAEpiC	pulmonary alveolar:	n/a
46	chr21:47604654-47604704	NT2-D1	testis:	n/a
47	chr21:47604361-47604411	CMK	blood:	n/a
48	chr21:47604986-47605036	PrEC	prostate:	n/a
49	chr21:47604654-47604704	HUVEC	blood vessel:	n/a
50	chr21:47604986-47605036	HNPCEpiC	eye:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:47602595..47605401-chr21:47649000..47651929,3	K562	blood:
2	chr21:47602847..47606841-chr21:47742668..47745795,6	K562	blood:
3	chr21:47601827..47605045-chr21:47646095..47649627,4	MCF-7	breast:
4	chr21:47604083..47605836-chr21:47704849..47706499,2	K562	blood:
5	chr21:47603167..47605215-chr21:47743246..47745709,3	K562	blood:
6	chr21:47563716..47566123-chr21:47602803..47604796,2	K562	blood:
7	chr21:47563633..47565565-chr21:47603562..47606281,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COL6A2-4	chr21:47604993-47605101	ENSG00000228404.1

No data

Variant related genes	Relation type
SPATC1L	TF binding region
ENSG00000228404	TF binding region
SPATC1L	CpG island
ENSG00000228404	CpG island
ENSG00000160298	chromatin interactions
ENSG00000160299	chromatin interactions
ENSG00000215424	chromatin interactions
ENSG00000182362	chromatin interactions
ENSG00000160282	chromatin interactions
ENSG00000160294	chromatin interactions
ENSG00000160285	chromatin interactions

Extended variants
information (count: 48 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:48 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116170889	chr21:47604361-47604362	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs191606610	chr21:47604366-47604367	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs386819420	chr21:47604367-47604368	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs539485219	chr21:47604370-47604371	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs75391115	chr21:47604409-47604410	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
6	rs201645858	chr21:47604425-47604426	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
7	rs4364096	chr21:47604428-47604429	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
8	rs5018174	chr21:47604462-47604463	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
9	rs5844256	chr21:47604471-47604472	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
10	rs113549626	chr21:47604478-47604479	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
11	rs111719391	chr21:47604493-47604494	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
12	rs28484834	chr21:47604515-47604516	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
13	rs534728915	chr21:47604523-47604524	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs370465078	chr21:47604524-47604525	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs111687470	chr21:47604531-47604532	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs11701027	chr21:47604546-47604547	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs8132184	chr21:47604568-47604569	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs8132189	chr21:47604572-47604573	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs111431193	chr21:47604584-47604585	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs112641293	chr21:47604587-47604588	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs28563898	chr21:47604593-47604594	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs28450755	chr21:47604614-47604615	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs28413004	chr21:47604621-47604622	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs62215190	chr21:47604625-47604626	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	mRNA abundance
25	rs375245575	chr21:47604628-47604629	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs573428282	chr21:47604640-47604641	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs28625916	chr21:47604643-47604644	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs8132340	chr21:47604677-47604678	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	mRNA abundance
29	rs557710503	chr21:47604679-47604680	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs8132341	chr21:47604681-47604682	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	mRNA abundance
31	rs62215192	chr21:47604684-47604685	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs368547237	chr21:47604696-47604697	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs116442826	chr21:47604708-47604709	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	mRNA abundance
34	rs555692674	chr21:47604716-47604717	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
35	rs574130977	chr21:47604717-47604718	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
36	rs138439440	chr21:47604720-47604721	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
37	rs184422578	chr21:47604807-47604808	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
38	rs79179983	chr21:47604816-47604817	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
39	rs78897629	chr21:47604837-47604838	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
40	rs570702985	chr21:47604910-47604911	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
41	rs115910837	chr21:47604940-47604941	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
42	rs530751986	chr21:47604955-47604956	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
43	rs374616538	chr21:47604960-47604961	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
44	rs12482343	chr21:47604967-47604968	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs143910187	chr21:47605069-47605070	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
46	rs146842277	chr21:47605110-47605111	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs565867130	chr21:47605120-47605121	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs139221873	chr21:47605175-47605176	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 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:201 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:47602800-47605600	Active TSS	Brain Angular Gyrus	brain
2	chr21:47603000-47605200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr21:47603000-47605200	Active TSS	iPS-20b Cell Line	embryonic stem cell
4	chr21:47603000-47605400	Active TSS	iPS-18 Cell Line	embryonic stem cell
5	chr21:47603200-47605000	Active TSS	HUES64 Cell Line	embryonic stem cell
6	chr21:47603200-47605200	Active TSS	iPS-15b Cell Line	embryonic stem cell
7	chr21:47603200-47605200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr21:47603200-47605200	Active TSS	Brain Germinal Matrix	brain
9	chr21:47603200-47605200	Active TSS	Hela-S3	cervix
10	chr21:47603200-47605200	Active TSS	HSMM	muscle
11	chr21:47603200-47605400	Active TSS	Rectal Smooth Muscle	rectum
12	chr21:47603400-47605200	Active TSS	H9 Cell Line	embryonic stem cell
13	chr21:47603400-47605200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr21:47603400-47605200	Active TSS	HUES6 Cell Line	embryonic stem cell
15	chr21:47603400-47605400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr21:47603400-47605400	Active TSS	Brain Cingulate Gyrus	brain
17	chr21:47603400-47605600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr21:47603400-47605600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
19	chr21:47603400-47605600	Active TSS	K562	blood
20	chr21:47603600-47605200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr21:47603600-47605200	Active TSS	Fetal Adrenal Gland	Adrenal Gland
22	chr21:47603800-47604400	Flanking Active TSS	Primary B cells from cord blood	blood
23	chr21:47603800-47604400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
24	chr21:47603800-47604400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr21:47603800-47604400	Flanking Active TSS	Colonic Mucosa	Colon
26	chr21:47603800-47604400	Flanking Active TSS	Lung	lung
27	chr21:47603800-47604600	Active TSS	Left Ventricle	heart
28	chr21:47603800-47604600	Transcr. at gene 5' and 3'	Right Atrium	heart
29	chr21:47603800-47604800	Active TSS	Esophagus	oesophagus
30	chr21:47603800-47604800	Active TSS	HUVEC	blood vessel
31	chr21:47603800-47604800	Bivalent/Poised TSS	NHEK	skin
32	chr21:47603800-47605000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr21:47603800-47605000	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
34	chr21:47603800-47605000	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
35	chr21:47603800-47605000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
36	chr21:47603800-47605000	Active TSS	Colon Smooth Muscle	Colon
37	chr21:47603800-47605000	Flanking Active TSS	Placenta	Placenta
38	chr21:47603800-47605200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr21:47603800-47605200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr21:47603800-47605200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr21:47603800-47605200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
42	chr21:47603800-47605200	Active TSS	Fetal Intestine Small	intestine
43	chr21:47603800-47605200	Active TSS	NH-A	brain
44	chr21:47603800-47605200	Active TSS	Osteobl	bone
45	chr21:47603800-47605400	Active TSS	ES-I3 Cell Line	embryonic stem cell
46	chr21:47603800-47605400	Active TSS	H1 Cell Line	embryonic stem cell
47	chr21:47603800-47605400	Active TSS	HUES48 Cell Line	embryonic stem cell
48	chr21:47603800-47605400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr21:47603800-47605400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
50	chr21:47603800-47605400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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