Variant report

Variant	nsv587803
Chromosome Location	chr21:45941000-45989488
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:377)
CpG islands
(count:857)
Chromatin interactive
region (count:31)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:377 , 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	chr21:45989043-45989370	K562	blood:	n/a	n/a
2	BACH1	chr21:45952715-45952726	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr21:45984861-45985442	GM12878	blood:	n/a	n/a
4	BATF	chr21:45984834-45985416	GM12878	blood:	n/a	n/a
5	BCL11A	chr21:45985180-45985430	GM12878	blood:	n/a	n/a
6	BCL3	chr21:45942765-45943027	GM12878	blood:	n/a	n/a
7	BCL3	chr21:45942675-45945280	GM12878	blood:	n/a	n/a
8	BCL3	chr21:45943030-45945278	GM12878	blood:	n/a	n/a
9	BHLHE40	chr21:45988860-45989389	K562	blood:	n/a	chr21:45988914-45988930
10	BHLHE40	chr21:45972745-45972757	K562	blood:	n/a	n/a
11	BHLHE40	chr21:45951118-45951409	K562	blood:	n/a	n/a
12	BRCA1	chr21:45942781-45942970	H1-hESC	embryonic stem cell:	n/a	n/a
13	BRCA1	chr21:45943609-45943919	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr21:45943217-45945247	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chr21:45944295-45944536	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr21:45962629-45963075	HCT-116	colon:	n/a	n/a
17	CBX3	chr21:45989069-45989379	K562	blood:	n/a	n/a
18	CBX3	chr21:45989101-45989409	K562	blood:	n/a	n/a
19	CEBPB	chr21:45945464-45945734	HepG2	liver:	n/a	n/a
20	CEBPB	chr21:45945969-45946339	HepG2	liver:	n/a	chr21:45946142-45946153
21	CEBPB	chr21:45946080-45946204	HepG2	liver:	n/a	chr21:45946142-45946153
22	CEBPB	chr21:45945965-45946326	HepG2	liver:	n/a	chr21:45946142-45946153
23	CEBPB	chr21:45973008-45973256	K562	blood:	n/a	chr21:45973116-45973127
24	CEBPB	chr21:45973047-45973275	HepG2	liver:	n/a	chr21:45973116-45973127
25	CEBPB	chr21:45973059-45973245	IMR90	lung:	n/a	chr21:45973116-45973127
26	CEBPD	chr21:45946046-45946255	HepG2	liver:	n/a	n/a
27	CHD2	chr21:45942650-45942684	HepG2	liver:	n/a	n/a
28	CHD2	chr21:45968793-45969352	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr21:45947404-45947445	K562	blood:	n/a	n/a
30	CREB1	chr21:45989022-45989466	K562	blood:	n/a	n/a
31	CREB1	chr21:45985166-45985492	GM12878	blood:	n/a	n/a
32	CTCF	chr21:45971072-45971114	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr21:45969751-45969812	MCF-7	breast:	n/a	n/a
34	CTCF	chr21:45969685-45969866	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr21:45971073-45971142	MCF-7	breast:	n/a	n/a
36	CTCF	chr21:45959480-45959529	NHEK	skin:	n/a	n/a
37	CTCF	chr21:45970791-45970938	NHEK	skin:	n/a	n/a
38	CTCF	chr21:45942908-45942938	GM20000	blood:	n/a	n/a
39	CTCF	chr21:45970860-45971010	SAEC	small airway:	n/a	n/a
40	CTCF	chr21:45969751-45969808	MCF-7	breast:	n/a	n/a
41	CTCF	chr21:45942500-45942650	MCF-7	breast:	n/a	n/a
42	CTCF	chr21:45942580-45942730	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr21:45959691-45959802	MCF-7	breast:	n/a	n/a
44	CTCF	chr21:45970861-45970908	GM19239	blood:	n/a	n/a
45	CTCF	chr21:45974144-45974166	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr21:45942540-45942690	MCF-7	breast:	n/a	n/a
47	CTCF	chr21:45959674-45959830	MCF-7	breast:	n/a	n/a
48	CTCF	chr21:45942553-45942691	MCF-7	breast:	n/a	n/a
49	CTCF	chr21:45942540-45942690	HepG2	liver:	n/a	n/a
50	CTCF	chr21:45971126-45971138	H1-hESC	embryonic stem cell:	n/a	n/a

(count:857 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:45979129-45979179	Hepatocyte	liver:	n/a
2	chr21:45979129-45979179	SK-N-MC	brain:	n/a
3	chr21:45979335-45979385	PANC-1	pancreas:	n/a
4	chr21:45979129-45979179	Hepatocyte	liver:	n/a
5	chr21:45979129-45979179	SK-N-MC	brain:	n/a
6	chr21:45979335-45979385	PANC-1	pancreas:	n/a
7	chr21:45971503-45971553	SAEC	small airway:	n/a
8	chr21:45972595-45972645	HCM	heart:	n/a
9	chr21:45971840-45971890	NHBE	bronchial:	n/a
10	chr21:45959142-45959192	HPAEpiC	pulmonary alveolar:	n/a
11	chr21:45972595-45972645	GM12878	blood:	n/a
12	chr21:45978747-45978797	BJ	skin:	n/a
13	chr21:45979335-45979385	HRE	kidney:	n/a
14	chr21:45961033-45961083	HCF	heart:	n/a
15	chr21:45960839-45960889	NT2-D1	testis:	n/a
16	chr21:45961033-45961083	HPAEpiC	pulmonary alveolar:	n/a
17	chr21:45978747-45978797	SAEC	small airway:	n/a
18	chr21:45960718-45960768	HUVEC	blood vessel:	n/a
19	chr21:45960718-45960768	MCF-7	breast:	n/a
20	chr21:45960839-45960889	Hepatocyte	liver:	n/a
21	chr21:45971503-45971553	CMK	blood:	n/a
22	chr21:45970330-45970380	HRPEpiC	eye:	n/a
23	chr21:45961033-45961083	Hela-S3	cervix:	n/a
24	chr21:45971503-45971553	HMEC	breast:	n/a
25	chr21:45961033-45961083	BE2_C	brain:	n/a
26	chr21:45970330-45970380	HCT-116	colon:	n/a
27	chr21:45979335-45979385	U87	brain:	n/a
28	chr21:45971840-45971890	PFSK-1	brain:	n/a
29	chr21:45977931-45977981	GM06990	blood:	n/a
30	chr21:45971840-45971890	AG09319	gingival:	n/a
31	chr21:45961033-45961083	AoSMC	blood vessel:	n/a
32	chr21:45960718-45960768	HRE	kidney:	n/a
33	chr21:45970330-45970380	HUVEC	blood vessel:	n/a
34	chr21:45960839-45960889	ProgFib	skin:	n/a
35	chr21:45979129-45979179	HCPEpiC	choroid plexus:	n/a
36	chr21:45978747-45978797	HepG2	liver:	n/a
37	chr21:45977931-45977981	HCPEpiC	choroid plexus:	n/a
38	chr21:45977931-45977981	Hela-S3	cervix:	n/a
39	chr21:45979129-45979179	HIPEpiC	eye:	n/a
40	chr21:45977931-45977981	ProgFib	skin:	n/a
41	chr21:45979335-45979385	IMR90	lung:	fetal
42	chr21:45961033-45961083	PFSK-1	brain:	n/a
43	chr21:45971850-45971900	SK-N-MC	brain:	n/a
44	chr21:45961033-45961083	A549	lung:	n/a
45	chr21:45960839-45960889	NH-A	brain:	n/a
46	chr21:45961033-45961083	NT2-D1	testis:	n/a
47	chr21:45960839-45960889	HUVEC	blood vessel:	n/a
48	chr21:45979620-45979670	SAEC	small airway:	n/a
49	chr21:45971503-45971553	ECC-1	luminal epithelium:	n/a
50	chr21:45978747-45978797	CMK	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr21:45963294..45964863-chr21:45968365..45969952,2	K562	blood:
2	chr21:45945365..45947938-chr21:45948297..45950745,2	K562	blood:
3	chr21:45945365..45947938-chr21:45948297..45950745,2	K562	blood:
4	chr21:45971316..45974046-chr21:45988116..45989981,2	MCF-7	breast:
5	chr21:45951755..45954984-chr21:45956330..45959030,3	MCF-7	breast:
6	chr21:45938263..45941219-chr21:46154705..46156912,2	K562	blood:
7	chr21:45936789..45940760-chr21:45945261..45949345,4	MCF-7	breast:
8	chr21:45944491..45947405-chr21:45954899..45956852,2	MCF-7	breast:
9	chr21:45963294..45964863-chr21:45968365..45969952,2	K562	blood:
10	chr21:45967694..45969320-chr21:45970824..45973124,2	K562	blood:
11	chr21:45944491..45947405-chr21:45954899..45956852,2	MCF-7	breast:
12	chr21:45952988..45954991-chr21:45956975..45959014,2	K562	blood:
13	chr21:45930910..45932830-chr21:45939919..45941918,2	MCF-7	breast:
14	chr21:45967572..45969194-chr21:45971624..45974010,2	K562	blood:
15	chr21:45987563..45989403-chr21:45990992..45992920,2	MCF-7	breast:
16	chr21:45951755..45954984-chr21:45956330..45959030,3	MCF-7	breast:
17	chr21:45947897..45950026-chr21:45993818..45996487,2	MCF-7	breast:
18	chr21:45942736..45946181-chr21:45947917..45949794,3	MCF-7	breast:
19	chr21:45932884..45935779-chr21:45942132..45943799,3	MCF-7	breast:
20	chr21:45987378..45989214-chr21:45998869..46000795,2	MCF-7	breast:
21	chr21:45954426..45956966-chr21:45958968..45961627,3	K562	blood:
22	chr21:45966428..45969422-chr21:45970172..45971926,2	MCF-7	breast:
23	chr21:45967572..45969194-chr21:45971624..45974010,2	K562	blood:
24	chr21:45952988..45954991-chr21:45956975..45959014,2	K562	blood:
25	chr21:45945120..45947803-chr21:45949245..45951145,3	K562	blood:
26	chr21:45957672..45960215-chr21:45961471..45964190,2	K562	blood:
27	chr21:45942736..45946181-chr21:45947917..45949794,3	MCF-7	breast:
28	chr21:45979063..45980801-chr21:45987415..45990235,2	MCF-7	breast:
29	chr21:45945120..45947803-chr21:45949245..45951145,3	K562	blood:
30	chr21:45938586..45940636-chr21:45942811..45945629,2	K562	blood:
31	chr21:45979063..45980801-chr21:45987415..45990235,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KRTAP10-2-1	chr21:45970318-45970557	NONHSAT082867
2	lnc-KRTAP10-1-1	chr21:45958781-45959193	NONHSAT082866
3	lnc-KRTAP10-2-1	chr21:45971264-45971388	NONHSAT082868
4	lnc-KRTAP10-2-1	chr21:45971263-45971388	NONHSAT082867
5	lnc-KRTAP10-2-1	chr21:45970319-45970557	NONHSAT082868

No data

Variant related genes	Relation type
KRTAP10-3	TF binding region
KRTAP10-2	TF binding region
KRTAP10-4	TF binding region
KRTAP10-1	TF binding region
KRTAP10-3	CpG island
KRTAP10-2	CpG island
KRTAP10-4	CpG island
KRTAP10-1	CpG island
ENSG00000241123	chromatin interactions
ENSG00000182912	chromatin interactions
ENSG00000215455	chromatin interactions
ENSG00000205445	chromatin interactions

Extended variants
information (count: 2507 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:2507 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587640232	chr21:45941051-45941052	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs587717294	chr21:45941110-45941111	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs587771213	chr21:45941111-45941112	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs587670700	chr21:45941124-45941125	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs587725746	chr21:45941130-45941131	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs587604666	chr21:45941134-45941135	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150704730	chr21:45941139-45941140	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs587714647	chr21:45941140-45941141	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs375174415	chr21:45941200-45941201	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs587607141	chr21:45941232-45941233	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs118126179	chr21:45941237-45941238	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs587747182	chr21:45941261-45941262	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs233229	chr21:45941286-45941287	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs587677635	chr21:45941309-45941310	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112115762	chr21:45941313-45941314	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs139022132	chr21:45941337-45941338	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs1976474	chr21:45941370-45941371	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs369672316	chr21:45941383-45941384	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs587681042	chr21:45941392-45941393	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs1976473	chr21:45941393-45941394	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs587611441	chr21:45941395-45941396	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs1976472	chr21:45941415-45941416	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs587771113	chr21:45941418-45941419	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs144993040	chr21:45941455-45941456	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs587673887	chr21:45941456-45941457	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs587703027	chr21:45941467-45941468	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs587713340	chr21:45941470-45941471	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs587756544	chr21:45941507-45941508	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs587656754	chr21:45941539-45941540	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs587709618	chr21:45941548-45941549	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs369744158	chr21:45941550-45941551	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112559156	chr21:45941556-45941557	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs28406087	chr21:45941581-45941582	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs587722721	chr21:45941591-45941592	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371018564	chr21:45941608-45941609	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs587601591	chr21:45941610-45941611	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs113920038	chr21:45941615-45941616	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs587675650	chr21:45941624-45941625	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs587708923	chr21:45941626-45941627	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs587603043	chr21:45941645-45941646	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373822584	chr21:45941725-45941726	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs587662546	chr21:45941742-45941743	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs587736431	chr21:45941743-45941744	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs374860475	chr21:45941744-45941745	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs376943948	chr21:45941746-45941747	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs370167540	chr21:45941753-45941754	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs199557392	chr21:45941754-45941755	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs587748100	chr21:45941756-45941757	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs117034581	chr21:45941761-45941762	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs151318000	chr21:45941766-45941767	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
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
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
small cell lung cancer	17426248	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:287 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45916800-45951600	Weak transcription	Right Atrium	heart
2	chr21:45939400-45941600	Bivalent Enhancer	Placenta	Placenta
3	chr21:45939800-45941600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr21:45940000-45941200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr21:45940800-45942800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr21:45941000-45942000	Enhancers	Fetal Muscle Trunk	muscle
7	chr21:45941200-45941400	ZNF genes & repeats	Spleen	Spleen
8	chr21:45941800-45946600	Weak transcription	Spleen	Spleen
9	chr21:45942000-45942800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
10	chr21:45942200-45942800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr21:45943600-45945200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
12	chr21:45944800-45945000	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
13	chr21:45944800-45946400	Enhancers	HepG2	liver
14	chr21:45945200-45946400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr21:45946400-45946800	Bivalent Enhancer	HepG2	liver
16	chr21:45946600-45947000	ZNF genes & repeats	Spleen	Spleen
17	chr21:45947800-45948200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr21:45948200-45949000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr21:45949000-45949200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr21:45950600-45951600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr21:45951000-45953600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
22	chr21:45951200-45953200	Enhancers	Fetal Muscle Leg	muscle
23	chr21:45951600-45952400	Strong transcription	Right Atrium	heart
24	chr21:45951600-45952800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr21:45951600-45953000	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr21:45951800-45952400	Enhancers	HMEC	breast
27	chr21:45952000-45952200	Bivalent Enhancer	HSMM	muscle
28	chr21:45952400-45969600	Weak transcription	Right Atrium	heart
29	chr21:45952800-45953200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr21:45953000-45954000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr21:45953000-45954400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr21:45953200-45953800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr21:45953600-45953800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr21:45953800-45954600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr21:45953800-45960000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr21:45954400-45954800	Enhancers	Primary neutrophils fromperipheralblood	blood
37	chr21:45954400-45956200	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr21:45954600-45954800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr21:45954800-45955400	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
40	chr21:45955800-45960000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr21:45956200-45959400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr21:45957600-45958000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr21:45959400-45960400	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr21:45959400-45960600	Enhancers	Primary neutrophils fromperipheralblood	blood
45	chr21:45960000-45960200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
46	chr21:45960000-45960400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr21:45960000-45960600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr21:45960200-45960600	Enhancers	H1 Cell Line	embryonic stem cell
49	chr21:45960400-45964600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr21:45960600-45961600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood

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