Variant report

Variant	nsv1061940
Chromosome Location	chr21:47317456-47343364
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:343)
CpG islands
(count:733)
Chromatin interactive
region (count:56)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:343 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:47343277-47343282	HepG2	liver:	n/a	n/a
2	CEBPB	chr21:47337545-47337774	A549	lung:	n/a	chr21:47337632-47337643 chr21:47337634-47337643 chr21:47337634-47337645
3	CEBPB	chr21:47337481-47337802	IMR90	lung:	n/a	chr21:47337632-47337643 chr21:47337634-47337643 chr21:47337634-47337645
4	CEBPB	chr21:47343103-47343371	IMR90	lung:	n/a	n/a
5	CEBPB	chr21:47337363-47337796	MCF-7	breast:	n/a	chr21:47337632-47337643 chr21:47337634-47337643 chr21:47337634-47337645
6	CEBPB	chr21:47337515-47337786	HepG2	liver:	n/a	chr21:47337632-47337643 chr21:47337634-47337643 chr21:47337634-47337645
7	CHD1	chr21:47342483-47343479	IMR90	lung:	n/a	n/a
8	CHD2	chr21:47343132-47343376	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr21:47342020-47342170	HCT-116	colon:	n/a	n/a
10	CTCF	chr21:47339080-47339230	HEK293	kidney:	n/a	n/a
11	CTCF	chr21:47343160-47343310	RPTEC	kidney:	n/a	chr21:47343282-47343290
12	CTCF	chr21:47343180-47343330	GM12870	blood:	n/a	chr21:47343282-47343290
13	CTCF	chr21:47343240-47343390	GM12872	blood:	n/a	chr21:47343282-47343290
14	CTCF	chr21:47343144-47343472	NHEK	skin:	n/a	chr21:47343282-47343290
15	CTCF	chr21:47342800-47342950	HepG2	liver:	n/a	n/a
16	CTCF	chr21:47343152-47343405	GM12892	blood:	n/a	chr21:47343282-47343290
17	CTCF	chr21:47343220-47343370	Hela-S3	cervix:	n/a	chr21:47343282-47343290
18	CTCF	chr21:47342045-47342105	MCF-7	breast:	n/a	n/a
19	CTCF	chr21:47343160-47343490	MCF-7	breast:	n/a	chr21:47343282-47343290
20	CTCF	chr21:47342977-47343621	HCT-116	colon:	n/a	chr21:47343282-47343290
21	CTCF	chr21:47343070-47343540	IMR90	lung:	n/a	chr21:47343282-47343290
22	CTCF	chr21:47339120-47339270	WERI-Rb-1	eye:	n/a	n/a
23	CTCF	chr21:47341908-47342127	HepG2	liver:	n/a	n/a
24	CTCF	chr21:47343200-47343350	K562	blood:	n/a	chr21:47343282-47343290
25	CTCF	chr21:47343148-47343481	LNCaP	prostate:	n/a	chr21:47343282-47343290
26	CTCF	chr21:47343180-47343330	WI-38	lung:	n/a	chr21:47343282-47343290
27	CTCF	chr21:47343200-47343350	HCT-116	colon:	n/a	chr21:47343282-47343290
28	CTCF	chr21:47342900-47343050	HPF	lung:	n/a	n/a
29	CTCF	chr21:47343180-47343330	NHDF-neo	bronchial:	n/a	chr21:47343282-47343290
30	CTCF	chr21:47343110-47343428	K562	blood:	n/a	chr21:47343282-47343290
31	CTCF	chr21:47343160-47343310	HA-sp	spinal cord:	n/a	chr21:47343282-47343290
32	CTCF	chr21:47342900-47343050	GM12869	blood:	n/a	n/a
33	CTCF	chr21:47343220-47343370	HEK293	kidney:	n/a	chr21:47343282-47343290
34	CTCF	chr21:47341996-47342150	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr21:47342640-47342790	HRPEpiC	eye:	n/a	n/a
36	CTCF	chr21:47343223-47343359	GM10266	blood:	n/a	chr21:47343282-47343290
37	CTCF	chr21:47343103-47343495	K562	blood:	n/a	chr21:47343282-47343290
38	CTCF	chr21:47343156-47343421	Lung_OC	lung:	n/a	chr21:47343282-47343290
39	CTCF	chr21:47343200-47343350	BE2_C	brain:	n/a	chr21:47343282-47343290
40	CTCF	chr21:47343156-47343444	ProgFib	skin:	n/a	chr21:47343282-47343290
41	CTCF	chr21:47342040-47342190	HMEC	breast:	n/a	n/a
42	CTCF	chr21:47343240-47343390	HVMF	connective:	n/a	chr21:47343282-47343290
43	CTCF	chr21:47342248-47342304	LNCaP	prostate:	n/a	n/a
44	CTCF	chr21:47342036-47342102	MCF-7	breast:	n/a	n/a
45	CTCF	chr21:47342971-47343640	MCF-7	breast:	n/a	chr21:47343282-47343290
46	CTCF	chr21:47343220-47343370	GM06990	blood:	n/a	chr21:47343282-47343290
47	CTCF	chr21:47343160-47343310	HFF-Myc	foreskin:	n/a	chr21:47343282-47343290
48	CTCF	chr21:47341965-47342157	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr21:47343200-47343350	SK-N-SH_RA	brain:	n/a	chr21:47343282-47343290
50	CTCF	chr21:47343099-47343443	T-47D	breast:	n/a	chr21:47343282-47343290

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:47334448-47334498	BJ	skin:	n/a
2	chr21:47334448-47334498	BJ	skin:	n/a
3	chr21:47335691-47335741	K562	blood:	n/a
4	chr21:47319304-47319354	HCF	heart:	n/a
5	chr21:47335691-47335741	ECC-1	luminal epithelium:	n/a
6	chr21:47334057-47334107	AG10803	skin:	n/a
7	chr21:47333731-47333781	AG09319	gingival:	n/a
8	chr21:47319304-47319354	PFSK-1	brain:	n/a
9	chr21:47334174-47334224	HNPCEpiC	eye:	n/a
10	chr21:47322452-47322502	PANC-1	pancreas:	n/a
11	chr21:47334057-47334107	SKMC	muscle:	n/a
12	chr21:47334057-47334107	GM19239	blood:	n/a
13	chr21:47334057-47334107	PFSK-1	brain:	n/a
14	chr21:47319304-47319354	NHBE	bronchial:	n/a
15	chr21:47342677-47342727	HIPEpiC	eye:	n/a
16	chr21:47322452-47322502	GM12892	blood:	n/a
17	chr21:47340130-47340180	HMEC	breast:	n/a
18	chr21:47337825-47337875	PrEC	prostate:	n/a
19	chr21:47340130-47340180	HAEpiC	amniotic membrane:	n/a
20	chr21:47330914-47330964	HCM	heart:	n/a
21	chr21:47335691-47335741	MCF10A-Er-Src	breast:	n/a
22	chr21:47337825-47337875	PFSK-1	brain:	n/a
23	chr21:47334174-47334224	HEK293	kidney:	embryo
24	chr21:47342677-47342727	HCF	heart:	n/a
25	chr21:47342677-47342727	SK-N-SH	brain:	n/a
26	chr21:47340130-47340180	GM12892	blood:	n/a
27	chr21:47322452-47322502	PFSK-1	brain:	n/a
28	chr21:47334448-47334498	SK-N-SH_RA	brain:	n/a
29	chr21:47319304-47319354	HMEC	breast:	n/a
30	chr21:47334057-47334107	U87	brain:	n/a
31	chr21:47318899-47318949	BJ	skin:	n/a
32	chr21:47342677-47342727	AG04450	lung:	fetal
33	chr21:47333731-47333781	Jurkat	blood:	n/a
34	chr21:47334057-47334107	AG04450	lung:	fetal
35	chr21:47340130-47340180	GM06990	blood:	n/a
36	chr21:47322452-47322502	HNPCEpiC	eye:	n/a
37	chr21:47319304-47319354	AG10803	skin:	n/a
38	chr21:47340130-47340180	SAEC	small airway:	n/a
39	chr21:47322452-47322502	BJ	skin:	n/a
40	chr21:47330914-47330964	HCT-116	colon:	n/a
41	chr21:47333731-47333781	U87	brain:	n/a
42	chr21:47322452-47322502	U87	brain:	n/a
43	chr21:47340130-47340180	AG09319	gingival:	n/a
44	chr21:47342677-47342727	SK-N-SH_RA	brain:	n/a
45	chr21:47334448-47334498	AG09319	gingival:	n/a
46	chr21:47340130-47340180	AG04449	skin:	fetal
47	chr21:47319304-47319354	HEEpiC	esophagus:	n/a
48	chr21:47342677-47342727	AG10803	skin:	n/a
49	chr21:47333731-47333781	HUVEC	blood vessel:	n/a
50	chr21:47334057-47334107	IMR90	lung:	fetal

(count:56 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr21:47188474..47189148-chr21:47343010..47343629,2	MCF-7	breast:
2	chr21:47253579..47256281-chr21:47326370..47329354,2	K562	blood:
3	chr21:47319454..47322116-chr21:47334445..47336417,2	MCF-7	breast:
4	chr21:47308842..47311490-chr21:47321844..47323697,2	MCF-7	breast:
5	chr21:47287743..47288527-chr21:47334754..47335348,2	MCF-7	breast:
6	chr21:47326278..47326802-chr21:47335871..47336440,2	MCF-7	breast:
7	chr21:47338168..47340965-chr21:47341072..47342617,2	K562	blood:
8	chr21:47342692..47343850-chr21:47390349..47391235,3	MCF-7	breast:
9	chr21:47324736..47327193-chr21:47327348..47329802,3	K562	blood:
10	chr21:47288031..47288840-chr21:47325915..47326785,5	MCF-7	breast:
11	chr21:46960597..46962517-chr21:47334850..47337245,2	MCF-7	breast:
12	chr21:47322615..47325568-chr21:47331282..47333525,2	K562	blood:
13	chr21:47325937..47326745-chr21:47335899..47336761,2	MCF-7	breast:
14	chr21:47240324..47241096-chr21:47342788..47343697,3	MCF-7	breast:
15	chr21:47300090..47300627-chr21:47342032..47342538,2	MCF-7	breast:
16	chr21:47336284..47339176-chr3:128004670..128006634,2	MCF-7	breast:
17	chr21:47325287..47328224-chr21:47334114..47336660,2	MCF-7	breast:
18	chr21:47299971..47300594-chr21:47342907..47343695,3	MCF-7	breast:
19	chr21:47336465..47338261-chr21:47339874..47342406,2	K562	blood:
20	chr21:47242790..47243479-chr21:47342941..47343666,2	MCF-7	breast:
21	chr21:47300119..47302715-chr21:47341992..47344397,3	MCF-7	breast:
22	chr21:47311846..47315136-chr21:47319001..47321928,3	K562	blood:
23	chr21:47290546..47292380-chr21:47322273..47324632,2	MCF-7	breast:
24	chr21:47335161..47336863-chr21:47355343..47357271,2	MCF-7	breast:
25	chr21:46976073..46976581-chr21:47342782..47343760,2	MCF-7	breast:
26	chr21:47172572..47175558-chr21:47335784..47338015,2	MCF-7	breast:
27	chr21:47322615..47325568-chr21:47331282..47333525,2	K562	blood:
28	chr21:47312796..47315650-chr21:47325639..47328184,2	MCF-7	breast:
29	chr21:47267694..47268408-chr21:47342147..47343416,5	MCF-7	breast:
30	chr21:47329285..47331470-chr21:47342066..47344987,2	MCF-7	breast:
31	chr21:47329095..47331174-chr21:47334966..47337510,2	MCF-7	breast:
32	chr21:47318888..47321827-chr21:47328391..47331106,3	MCF-7	breast:
33	chr21:47286434..47288542-chr21:47340592..47343360,3	MCF-7	breast:
34	chr21:47338875..47340965-chr21:47341117..47343595,2	K562	blood:
35	chr21:47300028..47300909-chr21:47342650..47343811,5	MCF-7	breast:
36	chr21:47338875..47340965-chr21:47341117..47343595,2	K562	blood:
37	chr21:47328644..47331016-chr21:47340908..47343121,3	MCF-7	breast:
38	chr21:47326278..47326802-chr21:47335871..47336440,2	MCF-7	breast:
39	chr21:47267610..47268453-chr21:47342093..47343648,5	MCF-7	breast:
40	chr21:47326297..47326825-chr21:47620902..47621507,2	MCF-7	breast:
41	chr21:46805769..46807395-chr21:47337287..47339395,2	MCF-7	breast:
42	chr21:47329095..47331174-chr21:47334966..47337510,2	MCF-7	breast:
43	chr21:47286639..47289783-chr21:47334819..47337166,3	MCF-7	breast:
44	chr21:47312057..47314177-chr21:47322993..47325323,2	MCF-7	breast:
45	chr21:47338168..47340965-chr21:47341072..47342617,2	K562	blood:
46	chr21:47328644..47331016-chr21:47340908..47343121,3	MCF-7	breast:
47	chr21:47325287..47328224-chr21:47334114..47336660,2	MCF-7	breast:
48	chr21:47324736..47327193-chr21:47327348..47329802,3	K562	blood:
49	chr21:47325937..47326745-chr21:47335899..47336761,2	MCF-7	breast:
50	chr21:47336465..47338261-chr21:47339874..47342406,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FTCD-6	chr21:47318001-47318626	NONHSAT082999
2	lnc-FTCD-6	chr21:47318759-47318789	NONHSAT082999

No data

Variant related genes	Relation type
PCBP3	TF binding region
PCBP3	CpG island
ENSG00000183570	chromatin interactions
ENSG00000173638	chromatin interactions

Extended variants
information (count: 1403 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:1403 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112364447	chr21:47317457-47317458	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs556223104	chr21:47317490-47317491	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs149350663	chr21:47317515-47317516	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs542150077	chr21:47317532-47317533	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs146293101	chr21:47317535-47317536	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs572211076	chr21:47317549-47317550	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs540343437	chr21:47317598-47317599	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs540594498	chr21:47317665-47317666	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs532501976	chr21:47317684-47317685	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs544176474	chr21:47317703-47317704	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs142886968	chr21:47317704-47317705	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs530319697	chr21:47317712-47317713	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs113167383	chr21:47317765-47317766	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs78136848	chr21:47317768-47317769	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs560303322	chr21:47317813-47317814	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs183858736	chr21:47317871-47317872	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs186816099	chr21:47317873-47317874	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs532612495	chr21:47317874-47317875	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs6518259	chr21:47317886-47317887	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs191274950	chr21:47317888-47317889	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs34156106	chr21:47317913-47317914	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs556188225	chr21:47317920-47317921	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs73907907	chr21:47317921-47317922	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs570101636	chr21:47317936-47317937	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs535343619	chr21:47317948-47317949	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs554058078	chr21:47317956-47317957	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs552457573	chr21:47317958-47317959	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs545961095	chr21:47317971-47317972	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs557557023	chr21:47317990-47317991	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs62211959	chr21:47318039-47318040	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	mRNA abundance
31	rs148782929	chr21:47318053-47318054	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs184239777	chr21:47318070-47318071	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs530109282	chr21:47318084-47318085	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs542128718	chr21:47318096-47318097	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs73907908	chr21:47318110-47318111	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs528004798	chr21:47318127-47318128	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs565884287	chr21:47318128-47318129	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs552736293	chr21:47318144-47318145	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs564711630	chr21:47318157-47318158	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs531396443	chr21:47318163-47318164	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs62213760	chr21:47318185-47318186	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs115098013	chr21:47318186-47318187	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs535451183	chr21:47318222-47318223	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs9980645	chr21:47318224-47318225	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs111908728	chr21:47318233-47318234	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	mRNA abundance
46	rs370793293	chr21:47318248-47318249	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs111646496	chr21:47318259-47318260	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs9980523	chr21:47318266-47318267	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs13050086	chr21:47318273-47318274	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs141111584	chr21:47318274-47318275	Weak transcription Strong transcription	TF binding region lncRNA	1 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:328 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:47308000-47343000	Weak transcription	Right Atrium	heart
2	chr21:47313200-47335600	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr21:47313400-47321000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr21:47313800-47321600	Weak transcription	Primary T cells from cord blood	blood
5	chr21:47314400-47330200	Weak transcription	Brain Hippocampus Middle	brain
6	chr21:47314600-47324600	Weak transcription	Rectal Smooth Muscle	rectum
7	chr21:47314600-47327400	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr21:47314600-47330200	Weak transcription	Brain Cingulate Gyrus	brain
9	chr21:47315000-47330200	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr21:47315200-47323400	Weak transcription	HSMMtube	muscle
11	chr21:47315200-47330200	Weak transcription	Adipose Nuclei	Adipose
12	chr21:47315800-47319600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr21:47316200-47322600	Weak transcription	Fetal Thymus	thymus
14	chr21:47316200-47326600	Strong transcription	Thymus	Thymus
15	chr21:47316600-47317600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr21:47317200-47318000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr21:47317200-47318000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr21:47317400-47317800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr21:47317400-47317800	Genic enhancers	Spleen	Spleen
20	chr21:47317600-47322400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr21:47317800-47318600	Strong transcription	Spleen	Spleen
22	chr21:47317800-47322400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr21:47318000-47318800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr21:47318000-47320000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr21:47318600-47321000	Weak transcription	Spleen	Spleen
26	chr21:47318800-47319600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
27	chr21:47318800-47321200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr21:47319200-47319600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr21:47319200-47321000	Enhancers	Fetal Muscle Leg	muscle
30	chr21:47319600-47319800	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr21:47319800-47320400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
32	chr21:47319800-47320800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr21:47319800-47321400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr21:47320000-47320200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr21:47320200-47320400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr21:47320200-47320400	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr21:47320200-47320400	Bivalent Enhancer	Fetal Stomach	stomach
38	chr21:47320200-47320800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr21:47320200-47330200	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr21:47320400-47320800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr21:47320800-47321400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
42	chr21:47320800-47321600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr21:47320800-47326000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr21:47321000-47321200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr21:47321000-47321200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr21:47321000-47321200	Enhancers	Fetal Stomach	stomach
47	chr21:47321000-47321800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr21:47321000-47323200	Strong transcription	Spleen	Spleen
49	chr21:47321200-47321400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr21:47321200-47321400	Bivalent Enhancer	Fetal Muscle Trunk	muscle

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