Variant report

Variant	esv2758529
Chromosome Location	chr21:14634532-15339752
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1608)
CpG islands
(count:3908)
Chromatin interactive
region (count:1)
LncRNA
region (count:68)
Mature miRNA
region (count: 3)
miRNA target
sites (count:0)

(count:1608 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

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	chr21:15321950-15322323	GM12878	blood:	n/a	chr21:15322062-15322070
5	BATF	chr21:15293789-15294119	GM12878	blood:	n/a	chr21:15293876-15293886
6	BATF	chr21:15315150-15315618	GM12878	blood:	n/a	n/a
7	BATF	chr21:15295169-15295585	GM12878	blood:	n/a	chr21:15295405-15295416
8	BATF	chr21:15315664-15315881	GM12878	blood:	n/a	n/a
9	BATF	chr21:15295228-15295568	GM12878	blood:	n/a	chr21:15295405-15295416
10	BATF	chr21:15302414-15302611	GM12878	blood:	n/a	chr21:15302548-15302559
11	BATF	chr21:15063813-15064156	GM12878	blood:	n/a	chr21:15064016-15064027
12	BATF	chr21:15134301-15134500	GM12878	blood:	n/a	n/a
13	BATF	chr21:15319369-15319639	GM12878	blood:	n/a	n/a
14	BATF	chr21:15315223-15315545	GM12878	blood:	n/a	n/a
15	BATF	chr21:15319344-15319735	GM12878	blood:	n/a	n/a
16	BATF	chr21:15112499-15112702	GM12878	blood:	n/a	n/a
17	BATF	chr21:15321908-15322326	GM12878	blood:	n/a	chr21:15322062-15322070
18	BATF	chr21:15293789-15294118	GM12878	blood:	n/a	chr21:15293876-15293886
19	BCL11A	chr21:15319352-15319733	GM12878	blood:	n/a	n/a
20	BCL11A	chr21:15063819-15064217	GM12878	blood:	n/a	n/a
21	BCL11A	chr21:15315306-15315658	GM12878	blood:	n/a	chr21:15315610-15315619
22	BCL11A	chr21:15315283-15315608	GM12878	blood:	n/a	n/a
23	BCL11A	chr21:15321900-15322332	GM12878	blood:	n/a	n/a
24	BCL11A	chr21:15223481-15223715	GM12878	blood:	n/a	n/a
25	BCL11A	chr21:15293842-15294225	GM12878	blood:	n/a	n/a
26	BCL11A	chr21:15322021-15322201	GM12878	blood:	n/a	n/a
27	BCL11A	chr21:15063984-15064146	GM12878	blood:	n/a	n/a
28	BCL11A	chr21:15319397-15319586	GM12878	blood:	n/a	n/a
29	BCL11A	chr21:15328745-15328928	GM12878	blood:	n/a	n/a
30	BHLHE40	chr21:15295613-15295821	K562	blood:	n/a	n/a
31	BHLHE40	chr21:15095840-15095940	K562	blood:	n/a	chr21:15095898-15095914
32	BHLHE40	chr21:15069019-15069264	K562	blood:	n/a	n/a
33	BHLHE40	chr21:15145416-15145487	K562	blood:	n/a	chr21:15145432-15145441
34	CBX3	chr21:15091400-15091687	K562	blood:	n/a	n/a
35	CCNT2	chr21:15295624-15295806	K562	blood:	n/a	n/a
36	CEBPB	chr21:15020460-15020823	A549	lung:	n/a	n/a
37	CEBPB	chr21:15020588-15020668	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr21:15020469-15020779	K562	blood:	n/a	n/a
39	CEBPB	chr21:15130594-15130794	HepG2	liver:	n/a	chr21:15130731-15130742
40	CEBPB	chr21:15277580-15277731	HepG2	liver:	n/a	chr21:15277673-15277684
41	CEBPB	chr21:14748547-14748799	IMR90	lung:	n/a	chr21:14748653-14748664
42	CEBPB	chr21:15186322-15186471	HepG2	liver:	n/a	chr21:15186346-15186357
43	CEBPB	chr21:14748544-14748767	A549	lung:	n/a	chr21:14748653-14748664
44	CEBPB	chr21:15277523-15277688	K562	blood:	n/a	chr21:15277673-15277684
45	CEBPB	chr21:15020516-15020778	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr21:15168793-15168892	A549	lung:	n/a	n/a
47	CEBPB	chr21:15186319-15186519	IMR90	lung:	n/a	chr21:15186346-15186357
48	CEBPB	chr21:15294348-15294556	IMR90	lung:	n/a	n/a
49	CEBPB	chr21:15158571-15158864	IMR90	lung:	n/a	n/a
50	CEBPB	chr21:15277523-15277853	IMR90	lung:	n/a	chr21:15277673-15277684

(count:3908 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:15052411-15052461	AG10803	skin:	n/a
2	chr21:15077096-15077146	AG04449	skin:	fetal
3	chr21:15038314-15038364	HRCEpiC	kidney:	n/a
4	chr21:15069190-15069240	Hepatocyte	liver:	n/a
5	chr21:15052411-15052461	AG10803	skin:	n/a
6	chr21:15077096-15077146	AG04449	skin:	fetal
7	chr21:15038314-15038364	HRCEpiC	kidney:	n/a
8	chr21:15069190-15069240	Hepatocyte	liver:	n/a
9	chr21:15197291-15197341	GM12891	blood:	n/a
10	chr21:15077774-15077824	GM19239	blood:	n/a
11	chr21:15077774-15077824	HIPEpiC	eye:	n/a
12	chr21:14982080-14982130	HCT-116	colon:	n/a
13	chr21:15148636-15148686	AoSMC	blood vessel:	n/a
14	chr21:15057058-15057108	K562	blood:	n/a
15	chr21:15309846-15309896	BE2_C	brain:	n/a
16	chr21:15071306-15071356	GM19239	blood:	n/a
17	chr21:15194427-15194477	PFSK-1	brain:	n/a
18	chr21:15038629-15038679	BE2_C	brain:	n/a
19	chr21:15221404-15221454	AG09309	skin:	n/a
20	chr21:15215654-15215704	AG04450	lung:	fetal
21	chr21:15077562-15077612	HCM	heart:	n/a
22	chr21:15038699-15038749	AG09319	gingival:	n/a
23	chr21:15309724-15309774	Caco-2	colon:	n/a
24	chr21:15194427-15194477	MCF-7	breast:	n/a
25	chr21:15052411-15052461	PrEC	prostate:	n/a
26	chr21:15221404-15221454	NH-A	brain:	n/a
27	chr21:15036394-15036444	PANC-1	pancreas:	n/a
28	chr21:15307662-15307712	NB4	blood:	n/a
29	chr21:15194427-15194477	AG04449	skin:	fetal
30	chr21:15066572-15066622	AG10803	skin:	n/a
31	chr21:14982350-14982400	SK-N-MC	brain:	n/a
32	chr21:15035944-15035994	ProgFib	skin:	n/a
33	chr21:15220709-15220759	NT2-D1	testis:	n/a
34	chr21:15134738-15134788	SK-N-SH_RA	brain:	n/a
35	chr21:15066572-15066622	AG09309	skin:	n/a
36	chr21:15035883-15035933	NHDF-neo	bronchial:	n/a
37	chr21:15135145-15135195	HRE	kidney:	n/a
38	chr21:15135145-15135195	MCF10A-Er-Src	breast:	n/a
39	chr21:15131938-15131988	CMK	blood:	n/a
40	chr21:15309724-15309774	NHBE	bronchial:	n/a
41	chr21:15200106-15200156	HIPEpiC	eye:	n/a
42	chr21:15096426-15096476	NHBE	bronchial:	n/a
43	chr21:14982779-14982829	GM19239	blood:	n/a
44	chr21:15038314-15038364	MCF10A-Er-Src	breast:	n/a
45	chr21:15069557-15069607	HCPEpiC	choroid plexus:	n/a
46	chr21:15078554-15078604	ProgFib	skin:	n/a
47	chr21:15135043-15135093	IMR90	lung:	fetal
48	chr21:15221404-15221454	K562	blood:	n/a
49	chr21:15096626-15096676	HL-60	blood:	n/a
50	chr21:15096010-15096060	K562	blood:	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-BAGE4-4	chr21:14789321-14789544	expReg_chr21_131_-
2	lnc-POTED-8	chr21:15211439-15211730	NONHSAT081121
3	lnc-POTED-1	chr21:14930638-14930781	NR_110544
4	lnc-BAGE4-3	chr21:14787066-14787369	expReg_chr21_126_-
5	lnc-LIPI-7	chr21:15215457-15215753	NONHSAT147184
6	lnc-LIPI-7	chr21:15218334-15218713	NONHSAT081125
7	lnc-LIPI-4	chr21:15323388-15323460	NONHSAT081133
8	lnc-BAGE4-10	chr21:15023866-15023904	NONHSAT081113
9	lnc-LIPI-4	chr21:15313136-15313299	NONHSAT081131
10	lnc-LIPI-4	chr21:15323388-15323460	NONHSAT081132
11	lnc-BAGE4-7	chr21:14807106-14807331	expReg_chr21_145_-
12	lnc-LIPI-7	chr21:15220411-15220685	NONHSAT081124
13	lnc-POTED-7	chr21:14848692-14849584	NONHSAT081105
14	lnc-BAGE4-6	chr21:14792037-14792496	expReg_chr21_135_-
15	lnc-POTED-1	chr21:14930638-14930782	ENSG00000228159
16	lnc-POTED-5	chr21:15048216-15048672	NONHSAT081114
17	lnc-LIPI-4	chr21:15335061-15335192	NONHSAT081133
18	lnc-POTED-1	chr21:14919301-14919449	ENSG00000228159
19	lnc-POTED-1	chr21:14928714-14928832	ENSG00000228159
20	lnc-POTED-6	chr21:15057030-15057282	NONHSAT081118
21	lnc-BAGE4-12	chr21:15047992-15048057	NONHSAT081116
22	lnc-POTED-5	chr21:15035025-15035149	NONHSAT081114
23	lnc-LIPI-7	chr21:15216343-15216456	NONHSAT081124
24	lnc-LIPI-7	chr21:15219080-15219270	NONHSAT081124
25	lnc-BAGE4-2	chr21:14783236-14783504	expReg_chr21_122_-
26	lnc-BAGE4-10	chr21:15024549-15026514	NONHSAT081113
27	lnc-BAGE4-12	chr21:15041937-15042566	NONHSAT081116
28	lnc-LIPI-7	chr21:15215454-15215753	NONHSAT081124
29	lnc-LIPI-4	chr21:15323553-15323581	NONHSAT081133
30	lnc-LIPI-9	chr21:15119715-15119817	l_2168_chr21:15116917-15119815_placenta
31	lnc-LIPI-7	chr21:15217326-15217595	NONHSAT081124
32	lnc-BAGE4-12	chr21:15045054-15045100	NONHSAT081117
33	lnc-LIPI-4	chr21:15313136-15313299	NONHSAT081132
34	lnc-POTED-6	chr21:15055902-15056343	NONHSAT081118
35	lnc-LIPI-4	chr21:15339702-15339757	NONHSAT081133
36	lnc-BAGE4-12	chr21:15041937-15042566	NONHSAT081117
37	lnc-POTED-1	chr21:14928714-14928832	NR_110544
38	lnc-BAGE4-12	chr21:15045054-15045100	NONHSAT081116
39	lnc-LIPI-4	chr21:15311695-15311749	NONHSAT081132
40	lnc-POTED-1	chr21:14918354-14918444	ENSG00000228159
41	lnc-BAGE4-13	chr21:15056956-15057423	expReg_chr21_194_-
42	lnc-POTED-11	chr21:15268407-15268509	NONHSAT081129
43	lnc-POTED-11	chr21:15265662-15265761	NONHSAT081129
44	lnc-LIPI-9	chr21:15116918-15118607	l_2168_chr21:15116917-15119815_placenta
45	lnc-LIPI-4	chr21:15317360-15317464	NONHSAT081132
46	lnc-POTED-9	chr21:15240747-15241288	NONHSAT081122
47	lnc-LIPI-4	chr21:15310267-15310388	NONHSAT081131
48	lnc-LIPI-7	chr21:15218334-15218462	NONHSAT081124
49	lnc-POTED-2	chr21:15143886-15144061	XLOC_013860
50	lnc-LIPI-4	chr21:15335061-15335106	NONHSAT081132

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

No data

Variant related genes	Relation type
OR4K11P	TF binding region
ENSG00000269011	TF binding region
RNU6-286P	TF binding region
MIR3156-3	TF binding region
SNX18P13	TF binding region
FAM207CP	TF binding region
MIR3118-5	TF binding region
GTF2IP2	TF binding region
SNX19P1	TF binding region
VN1R8P	TF binding region
FEM1AP1	TF binding region
TERF1P1	TF binding region
ANKRD30BP1	TF binding region
ZNF114P1	TF binding region
ENSG00000224922	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
CYP4F29P	TF binding region
ANKRD20A11P	TF binding region
OR4K12P	TF binding region
OR4K11P	CpG island
ENSG00000269011	CpG island
RNU6-286P	CpG island
MIR3156-3	CpG island
SNX18P13	CpG island
FAM207CP	CpG island
MIR3118-5	CpG island
GTF2IP2	CpG island
SNX19P1	CpG island
VN1R8P	CpG island
FEM1AP1	CpG island
TERF1P1	CpG island
ANKRD30BP1	CpG island
ZNF114P1	CpG island
ENSG00000224922	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
CYP4F29P	CpG island
ANKRD20A11P	CpG island
OR4K12P	CpG island

Extended variants
information (count: 9844 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:9844 , 50 per page) page: 1 2 3 4 5 6 7 ... 197

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112689261	chr21:14667211-14667212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs192535622	chr21:14667227-14667228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs560316770	chr21:14667233-14667234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs7275943	chr21:14667238-14667239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs142040374	chr21:14667240-14667241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs562798966	chr21:14667242-14667243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs145899499	chr21:14667254-14667255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs551435107	chr21:14667270-14667271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs528259434	chr21:14667296-14667297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs568604593	chr21:14667367-14667368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs184922724	chr21:14667414-14667415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs2742184	chr21:14667425-14667426	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs189856090	chr21:14667432-14667433	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs62213461	chr21:14667454-14667455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs568220327	chr21:14667462-14667463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs536479801	chr21:14667506-14667507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs141135098	chr21:14667533-14667534	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs73153643	chr21:14667571-14667572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs73326606	chr21:14667598-14667599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs111857469	chr21:14667621-14667622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs570057067	chr21:14667632-14667633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs538908584	chr21:14667657-14667658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs182070239	chr21:14667658-14667659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs572323990	chr21:14667666-14667667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs116787324	chr21:14667709-14667710	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs554800346	chr21:14667716-14667717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs2989124	chr21:14667717-14667718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs75708911	chr21:14667722-14667723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs184440994	chr21:14667748-14667749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs536673699	chr21:14667763-14667764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs2989125	chr21:14667764-14667765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs77081384	chr21:14667770-14667771	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs562662893	chr21:14667858-14667859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs35618584	chr21:14667872-14667873	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs189269491	chr21:14667883-14667884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs2989126	chr21:14667887-14667888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs182017743	chr21:14667926-14667927	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs533653892	chr21:14667945-14667946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs77364652	chr21:14667948-14667949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs149547264	chr21:14667949-14667950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs369048679	chr21:14667958-14667959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs527255280	chr21:14667960-14667961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs369269436	chr21:14668000-14668001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs373557446	chr21:14668010-14668011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs76806407	chr21:14668036-14668037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs77328757	chr21:14668050-14668051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs560868644	chr21:14668067-14668068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs200749331	chr21:14668081-14668082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs529732388	chr21:14668089-14668090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs139637804	chr21:14668126-14668127	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
abnormal development	18461090	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	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:233 , 50 per page) page: 1 2 3 4 5

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

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