Variant report

Variant	nsv1062730
Chromosome Location	chr21:14594223-15341527
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1656)
CpG islands
(count:3907)
Chromatin interactive
region (count:1)
LncRNA
region (count:68)
Mature miRNA
region (count: 3)
miRNA target
sites (count:0)

(count:1656 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:15295624-15295648	K562	blood:	n/a	n/a
2	ATF1	chr21:15091414-15091630	K562	blood:	n/a	n/a
3	ATF1	chr21:15249426-15249616	K562	blood:	n/a	n/a
4	BATF	chr21:15315150-15315618	GM12878	blood:	n/a	n/a
5	BATF	chr21:15063813-15064156	GM12878	blood:	n/a	chr21:15064016-15064027
6	BATF	chr21:15134301-15134500	GM12878	blood:	n/a	n/a
7	BATF	chr21:15315223-15315545	GM12878	blood:	n/a	n/a
8	BATF	chr21:15295169-15295585	GM12878	blood:	n/a	chr21:15295405-15295416
9	BATF	chr21:15319369-15319639	GM12878	blood:	n/a	n/a
10	BATF	chr21:15293789-15294119	GM12878	blood:	n/a	chr21:15293876-15293886
11	BATF	chr21:15319344-15319735	GM12878	blood:	n/a	n/a
12	BATF	chr21:15302414-15302611	GM12878	blood:	n/a	chr21:15302548-15302559
13	BATF	chr21:15321908-15322326	GM12878	blood:	n/a	chr21:15322062-15322070
14	BATF	chr21:15293789-15294118	GM12878	blood:	n/a	chr21:15293876-15293886
15	BATF	chr21:15321950-15322323	GM12878	blood:	n/a	chr21:15322062-15322070
16	BATF	chr21:15112499-15112702	GM12878	blood:	n/a	n/a
17	BATF	chr21:15315664-15315881	GM12878	blood:	n/a	n/a
18	BATF	chr21:15341379-15341645	GM12878	blood:	n/a	chr21:15341542-15341553
19	BATF	chr21:15340450-15340827	GM12878	blood:	n/a	n/a
20	BATF	chr21:15340388-15340909	GM12878	blood:	n/a	n/a
21	BATF	chr21:15295228-15295568	GM12878	blood:	n/a	chr21:15295405-15295416
22	BATF	chr21:14607219-14607387	GM12878	blood:	n/a	chr21:14607350-14607360
23	BCL11A	chr21:15340406-15340552	GM12878	blood:	n/a	chr21:15340521-15340530
24	BCL11A	chr21:15321900-15322332	GM12878	blood:	n/a	n/a
25	BCL11A	chr21:15319397-15319586	GM12878	blood:	n/a	n/a
26	BCL11A	chr21:15322021-15322201	GM12878	blood:	n/a	n/a
27	BCL11A	chr21:15063819-15064217	GM12878	blood:	n/a	n/a
28	BCL11A	chr21:15315283-15315608	GM12878	blood:	n/a	n/a
29	BCL11A	chr21:15293842-15294225	GM12878	blood:	n/a	n/a
30	BCL11A	chr21:15328745-15328928	GM12878	blood:	n/a	n/a
31	BCL11A	chr21:15223481-15223715	GM12878	blood:	n/a	n/a
32	BCL11A	chr21:15340450-15340836	GM12878	blood:	n/a	chr21:15340521-15340530 chr21:15340574-15340583
33	BCL11A	chr21:15319352-15319733	GM12878	blood:	n/a	n/a
34	BCL11A	chr21:15315306-15315658	GM12878	blood:	n/a	chr21:15315610-15315619
35	BCL11A	chr21:15063984-15064146	GM12878	blood:	n/a	n/a
36	BHLHE40	chr21:15069019-15069264	K562	blood:	n/a	n/a
37	BHLHE40	chr21:15145416-15145487	K562	blood:	n/a	chr21:15145432-15145441
38	BHLHE40	chr21:15095840-15095940	K562	blood:	n/a	chr21:15095898-15095914
39	BHLHE40	chr21:15295613-15295821	K562	blood:	n/a	n/a
40	CBX3	chr21:15091400-15091687	K562	blood:	n/a	n/a
41	CCNT2	chr21:15295624-15295806	K562	blood:	n/a	n/a
42	CEBPB	chr21:14748544-14748767	A549	lung:	n/a	chr21:14748653-14748664
43	CEBPB	chr21:15294348-15294556	IMR90	lung:	n/a	n/a
44	CEBPB	chr21:14748547-14748799	IMR90	lung:	n/a	chr21:14748653-14748664
45	CEBPB	chr21:15186322-15186471	HepG2	liver:	n/a	chr21:15186346-15186357
46	CEBPB	chr21:15020516-15020778	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr21:15168793-15168892	A549	lung:	n/a	n/a
48	CEBPB	chr21:15020469-15020779	K562	blood:	n/a	n/a
49	CEBPB	chr21:15277523-15277853	IMR90	lung:	n/a	chr21:15277673-15277684
50	CEBPB	chr21:15277580-15277731	HepG2	liver:	n/a	chr21:15277673-15277684

(count:3907 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:15215654-15215704	HPAEpiC	pulmonary alveolar:	n/a
2	chr21:15077096-15077146	HRPEpiC	eye:	n/a
3	chr21:15068553-15068603	NH-A	brain:	n/a
4	chr21:15215654-15215704	HPAEpiC	pulmonary alveolar:	n/a
5	chr21:15077096-15077146	HRPEpiC	eye:	n/a
6	chr21:15068553-15068603	NH-A	brain:	n/a
7	chr21:15199826-15199876	H1-hESC	embryonic stem cell:	embryo
8	chr21:15309724-15309774	AG09309	skin:	n/a
9	chr21:15194427-15194477	HCM	heart:	n/a
10	chr21:15112617-15112667	SKMC	muscle:	n/a
11	chr21:15135145-15135195	A549	lung:	n/a
12	chr21:15092941-15092991	HCT-116	colon:	n/a
13	chr21:15112617-15112667	BJ	skin:	n/a
14	chr21:15077096-15077146	ECC-1	luminal epithelium:	n/a
15	chr21:15200106-15200156	MCF10A-Er-Src	breast:	n/a
16	chr21:15095903-15095953	HCF	heart:	n/a
17	chr21:15307662-15307712	HEEpiC	esophagus:	n/a
18	chr21:15052411-15052461	Caco-2	colon:	n/a
19	chr21:15053472-15053522	SK-N-SH	brain:	n/a
20	chr21:15112617-15112667	HCPEpiC	choroid plexus:	n/a
21	chr21:14982363-14982413	HAEpiC	amniotic membrane:	n/a
22	chr21:15135043-15135093	NT2-D1	testis:	n/a
23	chr21:15147467-15147517	SKMC	muscle:	n/a
24	chr21:15147467-15147517	PFSK-1	brain:	n/a
25	chr21:15309846-15309896	RPTEC	kidney:	n/a
26	chr21:15220709-15220759	GM06990	blood:	n/a
27	chr21:14982350-14982400	ovcar-3	ovarian:	n/a
28	chr21:15096010-15096060	HRCEpiC	kidney:	n/a
29	chr21:15135145-15135195	ECC-1	luminal epithelium:	n/a
30	chr21:15138802-15138852	LNCaP	prostate:	n/a
31	chr21:15038314-15038364	GM12878	blood:	n/a
32	chr21:15092941-15092991	HEK293	kidney:	embryo
33	chr21:15069190-15069240	Jurkat	blood:	n/a
34	chr21:15200106-15200156	HL-60	blood:	n/a
35	chr21:15134491-15134541	GM12892	blood:	n/a
36	chr21:15095903-15095953	AoSMC	blood vessel:	n/a
37	chr21:14981404-14981454	HCPEpiC	choroid plexus:	n/a
38	chr21:15096426-15096476	SK-N-SH_RA	brain:	n/a
39	chr21:15215654-15215704	HNPCEpiC	eye:	n/a
40	chr21:15038629-15038679	U87	brain:	n/a
41	chr21:15038699-15038749	MCF-7	breast:	n/a
42	chr21:15095607-15095657	SK-N-MC	brain:	n/a
43	chr21:15036394-15036444	Hela-S3	cervix:	n/a
44	chr21:14982363-14982413	AG09309	skin:	n/a
45	chr21:15135580-15135630	HL-60	blood:	n/a
46	chr21:15096010-15096060	HPAEpiC	pulmonary alveolar:	n/a
47	chr21:15134738-15134788	HEEpiC	esophagus:	n/a
48	chr21:15309634-15309684	RPTEC	kidney:	n/a
49	chr21:15039424-15039474	RPTEC	kidney:	n/a
50	chr21:15309724-15309774	Hepatocyte	liver:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr18:14629664..14632607-chr21:14899242..14900976,2	MCF-7	breast:

(count:68 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BAGE4-7	chr21:14807106-14807331	expReg_chr21_145_-
2	lnc-LIPI-9	chr21:15119715-15119817	l_2168_chr21:15116917-15119815_placenta
3	lnc-POTED-1	chr21:14918354-14918444	NR_110544
4	lnc-BAGE4-10	chr21:15024549-15026514	NONHSAT081113
5	lnc-BAGE4-12	chr21:15047515-15047653	NONHSAT081117
6	lnc-POTED-1	chr21:14919301-14919449	NR_110544
7	lnc-LIPI-7	chr21:15218334-15218462	NONHSAT081124
8	lnc-POTED-6	chr21:15055902-15056343	NONHSAT081118
9	lnc-POTED-1	chr21:14930638-14930781	NR_110544
10	lnc-POTED-8	chr21:15211439-15211730	NONHSAT081121
11	lnc-LIPI-7	chr21:15215454-15215753	NONHSAT081124
12	lnc-POTED-1	chr21:14928714-14928832	NR_110544
13	lnc-BAGE4-12	chr21:15041937-15042566	NONHSAT081116
14	lnc-BAGE4-4	chr21:14789321-14789544	expReg_chr21_131_-
15	lnc-LIPI-7	chr21:15216343-15216456	NONHSAT081124
16	lnc-LIPI-7	chr21:15217426-15217595	NONHSAT081125
17	lnc-LIPI-7	chr21:15217326-15217595	NONHSAT081124
18	lnc-POTED-1	chr21:14928714-14928832	ENSG00000228159
19	lnc-POTED-11	chr21:15268407-15268509	NONHSAT081129
20	lnc-POTED-9	chr21:15212726-15212964	NONHSAT081122
21	lnc-POTED-2	chr21:15143886-15144061	XLOC_013860
22	lnc-POTED-7	chr21:14848692-14849584	NONHSAT081105
23	lnc-LIPI-4	chr21:15313136-15313299	NONHSAT081131
24	lnc-BAGE4-10	chr21:15023866-15023904	NONHSAT081113
25	lnc-POTED-1	chr21:14918354-14918444	ENSG00000228159
26	lnc-BAGE4-6	chr21:14792037-14792496	expReg_chr21_135_-
27	lnc-POTED-5	chr21:15035025-15035149	NONHSAT081114
28	lnc-LIPI-4	chr21:15313136-15313299	NONHSAT081132
29	lnc-POTED-12	chr21:14687514-14687778	l_2166_chr21:14677648-14687775_brain
30	lnc-LIPI-4	chr21:15310267-15310388	NONHSAT081131
31	lnc-POTED-2	chr21:15142253-15142534	XLOC_013860
32	lnc-BAGE4-3	chr21:14787066-14787369	expReg_chr21_126_-
33	lnc-LIPI-7	chr21:15218334-15218713	NONHSAT081125
34	lnc-LIPI-4	chr21:15323553-15323581	NONHSAT081131
35	lnc-LIPI-4	chr21:15311567-15311749	NONHSAT081131
36	lnc-LIPI-7	chr21:15216343-15216385	NONHSAT147184
37	lnc-LIPI-7	chr21:15219080-15219270	NONHSAT081124
38	lnc-BAGE4-5	chr21:14789550-14789761	expReg_chr21_132_-
39	lnc-BAGE4-13	chr21:15056956-15057423	expReg_chr21_194_-
40	lnc-POTED-11	chr21:15265662-15265761	NONHSAT081129
41	lnc-LIPI-4	chr21:15323388-15323460	NONHSAT081132
42	lnc-LIPI-4	chr21:15323553-15323581	NONHSAT081132
43	lnc-POTED-5	chr21:15048216-15048672	NONHSAT081114
44	lnc-LIPI-4	chr21:15335061-15335106	NONHSAT081132
45	lnc-LIPI-4	chr21:15335061-15335192	NONHSAT081133
46	lnc-LIPI-4	chr21:15311695-15311749	NONHSAT081132
47	lnc-LIPI-7	chr21:15220411-15220685	NONHSAT081124
48	lnc-LIPI-4	chr21:15323553-15323581	NONHSAT081133
49	lnc-BAGE4-12	chr21:15041937-15042566	NONHSAT081117
50	lnc-LIPI-4	chr21:15317360-15317464	NONHSAT081132

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3118	chr21:15017105-15017127	MIMAT0014980_5
hsa-miR-8069	chr21:15096563-15096585	MIMAT0030996
hsa-miR-3156-5p	chr21:14778752-14778773	MIMAT0015030_2

No data

Variant related genes	Relation type
VN1R8P	TF binding region
OR4K11P	TF binding region
FEM1AP1	TF binding region
ENSG00000269011	TF binding region
TERF1P1	TF binding region
ANKRD30BP1	TF binding region
RNU6-954P	TF binding region
ZNF114P1	TF binding region
RNU6-286P	TF binding region
MIR3156-3	TF binding region
ENSG00000224922	TF binding region
SNX18P13	TF binding region
FAM207CP	TF binding region
ENSG00000228159	TF binding region
GXYLT1P2	TF binding region
FGF7P2	TF binding region
CXADRP1	TF binding region
RHOT1P2	TF binding region
GRAMD4P1	TF binding region
ENSG00000256715	TF binding region
POTED	TF binding region
CNN2P7	TF binding region
MIR3118-5	TF binding region
GTF2IP2	TF binding region
CYP4F29P	TF binding region
ANKRD20A11P	TF binding region
OR4K12P	TF binding region
SNX19P1	TF binding region
VN1R8P	CpG island
OR4K11P	CpG island
FEM1AP1	CpG island
ENSG00000269011	CpG island
TERF1P1	CpG island
ANKRD30BP1	CpG island
RNU6-954P	CpG island
ZNF114P1	CpG island
RNU6-286P	CpG island
MIR3156-3	CpG island
ENSG00000224922	CpG island
SNX18P13	CpG island
FAM207CP	CpG island
ENSG00000228159	CpG island
GXYLT1P2	CpG island
FGF7P2	CpG island
CXADRP1	CpG island
RHOT1P2	CpG island
GRAMD4P1	CpG island
ENSG00000256715	CpG island
POTED	CpG island
CNN2P7	CpG island
MIR3118-5	CpG island
GTF2IP2	CpG island
CYP4F29P	CpG island
ANKRD20A11P	CpG island
OR4K12P	CpG island
SNX19P1	CpG island

Extended variants
information (count: 9970 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:9970 , 50 per page) page: 1 2 3 4 5 6 7 ... 200

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142211526	chr21:14619600-14619601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs113971599	chr21:14619616-14619617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs141460135	chr21:14619650-14619651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs184749096	chr21:14619666-14619667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs2997012	chr21:14619682-14619683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs2997013	chr21:14619696-14619697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs543406096	chr21:14619697-14619698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs146970651	chr21:14619767-14619768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs201232074	chr21:14619783-14619784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs202154830	chr21:14619837-14619838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs545571809	chr21:14619871-14619872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs2334427	chr21:14619876-14619877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs528655743	chr21:14619880-14619881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs548508032	chr21:14619883-14619884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs374289918	chr21:14619890-14619891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs568383164	chr21:14619895-14619896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs200381343	chr21:14619920-14619921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs530837093	chr21:14619935-14619936	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs550516159	chr21:14619961-14619962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs532816383	chr21:14620000-14620001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs2997014	chr21:14620026-14620027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs150232205	chr21:14620043-14620044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs2259468	chr21:14620054-14620055	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs565892189	chr21:14620059-14620060	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs559337326	chr21:14620075-14620076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs534795007	chr21:14620104-14620105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs528051472	chr21:14620140-14620141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs374908395	chr21:14620165-14620166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs574755775	chr21:14620201-14620202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs552388077	chr21:14620216-14620217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs369683207	chr21:14620224-14620225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs537045264	chr21:14620240-14620241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs373112936	chr21:14620276-14620277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs144688074	chr21:14620278-14620279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs576761000	chr21:14620279-14620280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs545912476	chr21:14620318-14620319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs559168018	chr21:14620320-14620321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs573119240	chr21:14620348-14620349	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs2259427	chr21:14620359-14620360	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs112689261	chr21:14667211-14667212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs192535622	chr21:14667227-14667228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs560316770	chr21:14667233-14667234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs7275943	chr21:14667238-14667239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs142040374	chr21:14667240-14667241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs562798966	chr21:14667242-14667243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs145899499	chr21:14667254-14667255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs551435107	chr21:14667270-14667271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs528259434	chr21:14667296-14667297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs568604593	chr21:14667367-14667368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs184922724	chr21:14667414-14667415	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
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
Sudden cardiac death	19188705	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21509527	CNVD
T-cell lymphomas	19863542	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
Myelofibrosis	22110671	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Metanephric adenoma	20802469	CNVD
Neuroblastoma	18923191	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Cancer	20164919	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	20409316	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute myeloid leukemia	21251322	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
abnormal development	18461090	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	21785460	CNVD
Melanoma	17363583	CNVD
Multiple myeloma	17550852	CNVD
Alzheimer''s disease	18923514	CNVD
Alzheimer''s disease	20877625	CNVD
Follicular lymphoma	20505157	CNVD
Alzheimer''s disease	21956041	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Melanoma	18172304	CNVD
Autism	22958593	CNVD
Schizophrenia	22958593	CNVD

Chromatin state (count:239 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:14619600-14620400	Enhancers	Brain Hippocampus Middle	brain
2	chr21:14667200-14668400	Enhancers	Brain Hippocampus Middle	brain
3	chr21:14676000-14676200	Enhancers	Liver	Liver
4	chr21:14676000-14676800	Enhancers	Brain Anterior Caudate	brain
5	chr21:14676200-14676800	Weak transcription	Liver	Liver
6	chr21:14676800-14677600	Enhancers	Liver	Liver
7	chr21:14677600-14682400	Weak transcription	Liver	Liver
8	chr21:14682400-14682800	Enhancers	Liver	Liver
9	chr21:14733400-14733800	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr21:14740600-14741200	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr21:14742800-14743200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr21:14742800-14743800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
13	chr21:14743000-14743800	ZNF genes & repeats	Adipose Nuclei	Adipose
14	chr21:14743400-14743800	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
15	chr21:14751400-14752800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr21:14752200-14752600	Active TSS	Primary T cells from cord blood	blood
17	chr21:14794200-14795400	Enhancers	Dnd41	blood
18	chr21:14866000-14867000	Enhancers	Dnd41	blood
19	chr21:14867000-14869000	Weak transcription	Dnd41	blood
20	chr21:14869000-14872400	Enhancers	Dnd41	blood
21	chr21:14888000-14888200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr21:14900000-14900400	ZNF genes & repeats	Dnd41	blood
23	chr21:14900400-14901400	Weak transcription	Dnd41	blood
24	chr21:14901400-14904800	Enhancers	Dnd41	blood
25	chr21:14916600-14920000	Enhancers	Dnd41	blood
26	chr21:14917000-14917600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
27	chr21:14920000-14922800	Weak transcription	Dnd41	blood
28	chr21:14922800-14923600	Enhancers	Dnd41	blood
29	chr21:14924200-14924400	Enhancers	Dnd41	blood
30	chr21:14965200-14966200	Enhancers	Dnd41	blood
31	chr21:14983000-14983200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
32	chr21:15035600-15036200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr21:15056200-15058400	Enhancers	Liver	Liver
34	chr21:15058400-15060200	Weak transcription	Liver	Liver
35	chr21:15060200-15062000	Enhancers	Liver	Liver
36	chr21:15066000-15068800	Weak transcription	Right Atrium	heart
37	chr21:15067000-15070200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
38	chr21:15067600-15069600	Enhancers	Liver	Liver
39	chr21:15067600-15069600	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
40	chr21:15067800-15070200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
41	chr21:15068200-15069600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr21:15068200-15069600	ZNF genes & repeats	Spleen	Spleen
43	chr21:15068400-15069400	Active TSS	Pancreas	Pancrea
44	chr21:15068600-15068800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
45	chr21:15068600-15068800	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
46	chr21:15068600-15069800	Enhancers	Placenta	Placenta
47	chr21:15068800-15069000	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
48	chr21:15068800-15069000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
49	chr21:15068800-15069400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
50	chr21:15068800-15069400	Active TSS	Brain Anterior Caudate	brain

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