Variant report

Variant	nsv1056101
Chromosome Location	chr21:48028997-48074364
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:771)
CpG islands
(count:1162)
Chromatin interactive
region (count:90)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:771 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr21:48054800-48055606	GM12878	blood:	n/a	n/a
2	ATF2	chr21:48028361-48029224	GM12878	blood:	n/a	n/a
3	ATF3	chr21:48055226-48055739	K562	blood:	n/a	chr21:48055237-48055245 chr21:48055268-48055277
4	ATF3	chr21:48055269-48055747	A549	lung:	n/a	n/a
5	ATF3	chr21:48055257-48055907	A549	lung:	n/a	chr21:48055268-48055277
6	ATF3	chr21:48054937-48055231	K562	blood:	n/a	n/a
7	ATF3	chr21:48055269-48055855	K562	blood:	n/a	n/a
8	BATF	chr21:48058236-48058618	GM12878	blood:	n/a	n/a
9	BATF	chr21:48028436-48029053	GM12878	blood:	n/a	n/a
10	BATF	chr21:48058299-48058586	GM12878	blood:	n/a	n/a
11	BCL11A	chr21:48058286-48058514	GM12878	blood:	n/a	n/a
12	BCL11A	chr21:48058312-48058550	GM12878	blood:	n/a	n/a
13	BCLAF1	chr21:48054738-48055175	GM12878	blood:	n/a	n/a
14	BCLAF1	chr21:48028466-48029094	GM12878	blood:	n/a	n/a
15	CBX3	chr21:48054356-48056106	K562	blood:	n/a	n/a
16	CEBPB	chr21:48058257-48058541	K562	blood:	n/a	n/a
17	CEBPB	chr21:48064981-48065204	K562	blood:	n/a	n/a
18	CEBPB	chr21:48047791-48047968	K562	blood:	n/a	n/a
19	CEBPB	chr21:48047658-48048067	K562	blood:	n/a	n/a
20	CEBPD	chr21:48054859-48055913	K562	blood:	n/a	n/a
21	CEBPD	chr21:48055110-48055815	HepG2	liver:	n/a	n/a
22	CREB1	chr21:48054806-48056067	H1-hESC	embryonic stem cell:	n/a	n/a
23	CREB1	chr21:48054821-48056265	HepG2	liver:	n/a	n/a
24	CREB1	chr21:48054788-48056180	GM12878	blood:	n/a	n/a
25	CREB1	chr21:48054844-48055240	ECC-1	luminal epithelium:	n/a	n/a
26	CREB1	chr21:48054804-48055837	H1-hESC	embryonic stem cell:	n/a	n/a
27	CREB1	chr21:48054848-48056254	K562	blood:	n/a	n/a
28	CREB1	chr21:48054940-48056118	A549	lung:	n/a	n/a
29	CREB1	chr21:48054978-48055140	A549	lung:	n/a	n/a
30	CREB1	chr21:48054800-48055327	ECC-1	luminal epithelium:	n/a	n/a
31	CTCF	chr21:48059760-48059910	AG09319	gingival:	n/a	n/a
32	CTCF	chr21:48063380-48063530	HEK293	kidney:	n/a	n/a
33	CTCF	chr21:48059652-48060177	HCT-116	colon:	n/a	n/a
34	CTCF	chr21:48059820-48059970	MCF-7	breast:	n/a	n/a
35	CTCF	chr21:48059800-48059950	WI-38	lung:	n/a	n/a
36	CTCF	chr21:48055008-48055208	A549	lung:	n/a	chr21:48055091-48055107
37	CTCF	chr21:48055700-48055850	GM12865	blood:	n/a	n/a
38	CTCF	chr21:48059800-48059950	AoAF	blood vessel:	n/a	n/a
39	CTCF	chr21:48054973-48055206	MCF-7	breast:	n/a	chr21:48055091-48055107
40	CTCF	chr21:48059775-48059943	K562	blood:	n/a	n/a
41	CTCF	chr21:48059740-48059890	HepG2	liver:	n/a	n/a
42	CTCF	chr21:48065080-48065230	GM12873	blood:	n/a	n/a
43	CTCF	chr21:48054940-48055090	GM12865	blood:	n/a	n/a
44	CTCF	chr21:48055040-48055190	GM12864	blood:	n/a	chr21:48055091-48055107
45	CTCF	chr21:48054980-48055130	NHDF-neo	bronchial:	n/a	chr21:48055091-48055107
46	CTCF	chr21:48055321-48055396	MCF-7	breast:	n/a	n/a
47	CTCF	chr21:48065092-48065116	GM19239	blood:	n/a	n/a
48	CTCF	chr21:48054960-48055110	GM12874	blood:	n/a	chr21:48055091-48055107
49	CTCF	chr21:48059760-48059910	GM12872	blood:	n/a	n/a
50	CTCF	chr21:48055021-48055172	K562	blood:	n/a	chr21:48055091-48055107

(count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:48055715-48055765	HRPEpiC	eye:	n/a
2	chr21:48054897-48054947	AG04450	lung:	fetal
3	chr21:48055519-48055569	CMK	blood:	n/a
4	chr21:48055715-48055765	HRPEpiC	eye:	n/a
5	chr21:48054897-48054947	AG04450	lung:	fetal
6	chr21:48055519-48055569	CMK	blood:	n/a
7	chr21:48056967-48057017	GM12892	blood:	n/a
8	chr21:48072745-48072795	PrEC	prostate:	n/a
9	chr21:48054897-48054947	HNPCEpiC	eye:	n/a
10	chr21:48054897-48054947	HRCEpiC	kidney:	n/a
11	chr21:48068748-48068798	AG09309	skin:	n/a
12	chr21:48055338-48055388	AG04449	skin:	fetal
13	chr21:48055715-48055765	SKMC	muscle:	n/a
14	chr21:48055715-48055765	SK-N-MC	brain:	n/a
15	chr21:48054897-48054947	NHDF-neo	bronchial:	n/a
16	chr21:48055366-48055416	ProgFib	skin:	n/a
17	chr21:48055629-48055679	A549	lung:	n/a
18	chr21:48068748-48068798	PrEC	prostate:	n/a
19	chr21:48055893-48055943	SKMC	muscle:	n/a
20	chr21:48055366-48055416	Jurkat	blood:	n/a
21	chr21:48052757-48052807	AG09319	gingival:	n/a
22	chr21:48055629-48055679	HCT-116	colon:	n/a
23	chr21:48055715-48055765	ECC-1	luminal epithelium:	n/a
24	chr21:48055366-48055416	HUVEC	blood vessel:	n/a
25	chr21:48056967-48057017	HPAEpiC	pulmonary alveolar:	n/a
26	chr21:48069229-48069279	MCF-7	breast:	n/a
27	chr21:48055715-48055765	GM12891	blood:	n/a
28	chr21:48068452-48068502	ProgFib	skin:	n/a
29	chr21:48055629-48055679	HMEC	breast:	n/a
30	chr21:48054563-48054613	T-47D	breast:	n/a
31	chr21:48068748-48068798	NB4	blood:	n/a
32	chr21:48055715-48055765	Caco-2	colon:	n/a
33	chr21:48056967-48057017	SKMC	muscle:	n/a
34	chr21:48054897-48054947	K562	blood:	n/a
35	chr21:48055629-48055679	H1-hESC	embryonic stem cell:	embryo
36	chr21:48068452-48068502	SKMC	muscle:	n/a
37	chr21:48055629-48055679	AG04449	skin:	fetal
38	chr21:48055893-48055943	NB4	blood:	n/a
39	chr21:48069229-48069279	U87	brain:	n/a
40	chr21:48056967-48057017	NH-A	brain:	n/a
41	chr21:48055224-48055274	PANC-1	pancreas:	n/a
42	chr21:48068748-48068798	Jurkat	blood:	n/a
43	chr21:48055631-48055681	SK-N-MC	brain:	n/a
44	chr21:48069229-48069279	SK-N-MC	brain:	n/a
45	chr21:48068585-48068635	HMEC	breast:	n/a
46	chr21:48072745-48072795	AG09309	skin:	n/a
47	chr21:48052757-48052807	PANC-1	pancreas:	n/a
48	chr21:48055893-48055943	RPTEC	kidney:	n/a
49	chr21:48055224-48055274	GM19239	blood:	n/a
50	chr21:48055631-48055681	AoSMC	blood vessel:	n/a

(count:90 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr21:48059291..48062346-chr21:48062349..48064586,4	MCF-7	breast:
2	chr21:48027694..48030453-chr21:48039157..48041006,2	MCF-7	breast:
3	chr21:48068008..48071695-chr21:48072637..48076225,4	MCF-7	breast:
4	chr21:48054963..48055735-chr3:50329204..50329933,2	NB4	blood:
5	chr21:48021540..48023901-chr21:48055495..48057109,2	MCF-7	breast:
6	chr21:48066242..48069643-chr21:48070010..48074183,7	K562	blood:
7	chr14:75745044..75745708-chr21:48055135..48055722,2	Hela-S3	cervix:
8	chr21:48055126..48055735-chr3:196359119..196359988,2	NB4	blood:
9	chr21:47979038..47981600-chr21:48055778..48057959,2	MCF-7	breast:
10	chr21:48025522..48028149-chr21:48060514..48063166,2	MCF-7	breast:
11	chr21:48063366..48065608-chr21:48072817..48075580,2	MCF-7	breast:
12	chr21:47742343..47745058-chr21:48054003..48056846,3	K562	blood:
13	chr21:47741705..47745829-chr21:48053977..48057908,5	MCF-7	breast:
14	chr21:48055080..48055596-chr4:39046312..39046846,2	Hela-S3	cervix:
15	chr21:48054316..48057026-chr21:48067023..48068538,2	K562	blood:
16	chr21:48028979..48030812-chr21:48051870..48054019,2	K562	blood:
17	chr21:48070689..48072483-chr21:48074893..48076580,2	K562	blood:
18	chr21:48055128..48057107-chr21:48067363..48069357,2	MCF-7	breast:
19	chr21:48024544..48027148-chr21:48052838..48054939,2	K562	blood:
20	chr21:48005218..48007630-chr21:48055834..48057649,2	K562	blood:
21	chr21:48062111..48065887-chr21:48068207..48070347,4	K562	blood:
22	chr21:48069459..48071150-chr21:48080115..48082921,2	MCF-7	breast:
23	chr21:47877118..47880921-chr21:48053345..48058142,9	K562	blood:
24	chr21:48065668..48068253-chr21:48070018..48072007,3	MCF-7	breast:
25	chr21:48066242..48069643-chr21:48070010..48074183,7	K562	blood:
26	chr17:80250394..80251099-chr21:48055154..48055814,2	Hela-S3	cervix:
27	chr21:48044480..48047952-chr21:48055875..48058667,3	MCF-7	breast:
28	chr21:48016422..48019126-chr21:48030129..48032645,2	K562	blood:
29	chr21:48044131..48047004-chr21:48048003..48050751,2	MCF-7	breast:
30	chr21:48061876..48063858-chr21:48067311..48068866,2	K562	blood:
31	chr21:47875258..47880014-chr21:48054452..48058643,10	K562	blood:
32	chr21:48042730..48044237-chr21:48044461..48046707,2	K562	blood:
33	chr1:36396247..36397104-chr21:48055435..48056034,2	HCT-116	colon:
34	chr21:47647612..47649806-chr21:48055027..48056571,2	K562	blood:
35	chr21:48054348..48057362-chr21:48062068..48064635,4	K562	blood:
36	chr12:133287222..133287841-chr21:48055027..48055792,2	NB4	blood:
37	chr21:48066570..48068825-chr21:48072683..48075681,2	K562	blood:
38	chr17:25620789..25621556-chr21:48054884..48055505,2	Hela-S3	cervix:
39	chr21:48023339..48026982-chr21:48053855..48056881,6	MCF-7	breast:
40	chr21:48043562..48050060-chr21:48053506..48056859,7	MCF-7	breast:
41	chr21:47972251..47974231-chr21:48053496..48055796,2	K562	blood:
42	chr13:48877615..48878228-chr21:48055384..48056111,2	Hela-S3	cervix:
43	chr21:48055000..48055796-chr9:132251161..132252102,2	Hela-S3	cervix:
44	chr21:48044480..48047952-chr21:48055875..48058667,3	MCF-7	breast:
45	chr15:55790459..55791055-chr21:48054984..48055756,2	HCT-116	colon:
46	chr21:48054348..48057362-chr21:48062068..48064635,4	K562	blood:
47	chr16:81069280..81069978-chr21:48054904..48055633,2	Hela-S3	cervix:
48	chr21:48028979..48030812-chr21:48051870..48054019,2	K562	blood:
49	chr21:48061876..48063858-chr21:48067311..48068866,2	K562	blood:
50	chr21:48059228..48062672-chr21:48065959..48068776,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-S100B-1	chr21:48073470-48073934	NONHSAT083076
2	lnc-DIP2A-5	chr21:48055527-48055675	NONHSAT083074

No data

Variant related genes	Relation type
DSTNP1	TF binding region
PRMT2	TF binding region
S100B	TF binding region
DSTNP1	CpG island
PRMT2	CpG island
S100B	CpG island
ENSG00000160310	chromatin interactions
ENSG00000233224	chromatin interactions
ENSG00000265692	chromatin interactions
ENSG00000126070	chromatin interactions
ENSG00000160294	chromatin interactions
ENSG00000160299	chromatin interactions
ENSG00000129657	chromatin interactions
ENSG00000118873	chromatin interactions
ENSG00000214706	chromatin interactions
ENSG00000256061	chromatin interactions
ENSG00000160305	chromatin interactions
ENSG00000170345	chromatin interactions
ENSG00000204054	chromatin interactions
ENSG00000232065	chromatin interactions
ENSG00000105699	chromatin interactions
ENSG00000230982	chromatin interactions
ENSG00000196352	chromatin interactions
ENSG00000164330	chromatin interactions
ENSG00000182362	chromatin interactions
ENSG00000197153	chromatin interactions
ENSG00000202239	chromatin interactions
ENSG00000123358	chromatin interactions
ENSG00000160307	chromatin interactions
ENSG00000160285	chromatin interactions
ENSG00000263583	chromatin interactions
ENSG00000272283	chromatin interactions
ENSG00000247077	chromatin interactions
ENSG00000231473	chromatin interactions
ENSG00000166454	chromatin interactions
ENSG00000261771	chromatin interactions
ENSG00000160298	chromatin interactions
ENSG00000109790	chromatin interactions
ENSG00000139687	chromatin interactions
ENSG00000215424	chromatin interactions
ENSG00000260213	chromatin interactions
ENSG00000109046	chromatin interactions

Extended variants
information (count: 1826 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:1826 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558416497	chr21:48029016-48029017	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs115266927	chr21:48029038-48029039	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs545286668	chr21:48029054-48029055	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs563611366	chr21:48029105-48029106	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs73381515	chr21:48029135-48029136	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs201007567	chr21:48029175-48029176	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs397723858	chr21:48029177-48029178	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs115536587	chr21:48029192-48029193	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs79229123	chr21:48029227-48029228	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs199909269	chr21:48029258-48029259	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs200978175	chr21:48029259-48029260	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs528510547	chr21:48029286-48029287	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs149816889	chr21:48029400-48029401	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs565246968	chr21:48029455-48029456	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs8133385	chr21:48029460-48029461	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs550526807	chr21:48029581-48029582	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs543181412	chr21:48029622-48029623	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs569100706	chr21:48029628-48029629	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs73152893	chr21:48029696-48029697	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs9979500	chr21:48029698-48029699	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs566472742	chr21:48029731-48029732	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs533561029	chr21:48029736-48029737	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs558584918	chr21:48029785-48029786	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs144840411	chr21:48029819-48029820	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs140145099	chr21:48029831-48029832	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs536795743	chr21:48029896-48029897	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs185470231	chr21:48029906-48029907	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs575472537	chr21:48029977-48029978	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs36029844	chr21:48030044-48030045	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs542909492	chr21:48030116-48030117	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs554844352	chr21:48030126-48030127	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs117423218	chr21:48030184-48030185	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs540284578	chr21:48030215-48030216	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs144246603	chr21:48030228-48030229	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs147771234	chr21:48030229-48030230	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs141260865	chr21:48030251-48030252	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs562665283	chr21:48030346-48030347	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs529965166	chr21:48030356-48030357	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs75979247	chr21:48030396-48030397	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs376305972	chr21:48030398-48030399	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs545172832	chr21:48030412-48030413	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs145117654	chr21:48030431-48030432	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs368785358	chr21:48030432-48030433	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs9982863	chr21:48030465-48030466	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs11702240	chr21:48030487-48030488	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs189896174	chr21:48030498-48030499	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs150948537	chr21:48030502-48030503	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs559234600	chr21:48030506-48030507	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs140841674	chr21:48030515-48030516	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs11702243	chr21:48030537-48030538	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	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:1709 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:48025800-48054800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr21:48026600-48029400	Enhancers	Primary T cells from cord blood	blood
3	chr21:48026600-48030400	Weak transcription	Thymus	Thymus
4	chr21:48026600-48040000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr21:48026800-48040000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr21:48027200-48029600	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr21:48027600-48030000	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr21:48027600-48030400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr21:48027600-48030800	Flanking Active TSS	GM12878-XiMat	blood
10	chr21:48027800-48029600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr21:48028000-48030400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
12	chr21:48028400-48030200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr21:48028800-48029000	Enhancers	Primary B cells from peripheral blood	blood
14	chr21:48029600-48031000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
15	chr21:48029800-48030200	Bivalent Enhancer	HepG2	liver
16	chr21:48030000-48031000	Enhancers	Primary T cells fromperipheralblood	blood
17	chr21:48030000-48031000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr21:48030200-48030400	Flanking Active TSS	HepG2	liver
19	chr21:48030200-48030600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
20	chr21:48030200-48030600	Enhancers	Osteobl	bone
21	chr21:48030400-48030800	ZNF genes & repeats	Primary T killer memory cells from peripheral blood	blood
22	chr21:48030400-48031000	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
23	chr21:48030400-48031000	ZNF genes & repeats	Thymus	Thymus
24	chr21:48030400-48031000	Enhancers	HepG2	liver
25	chr21:48030800-48031000	Active TSS	GM12878-XiMat	blood
26	chr21:48030800-48039000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
27	chr21:48031000-48036200	Weak transcription	Thymus	Thymus
28	chr21:48031000-48039800	Weak transcription	HepG2	liver
29	chr21:48031000-48040000	Weak transcription	Primary T cells fromperipheralblood	blood
30	chr21:48031000-48040000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
31	chr21:48034600-48039000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr21:48036000-48037400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
33	chr21:48036000-48037600	Enhancers	Primary T cells from cord blood	blood
34	chr21:48036000-48037600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
35	chr21:48036400-48041000	Weak transcription	Thymus	Thymus
36	chr21:48037000-48037600	Enhancers	Fetal Heart	heart
37	chr21:48037200-48037400	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr21:48037200-48046800	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr21:48037400-48037600	Enhancers	Primary T helper cells PMA-I stimulated	--
40	chr21:48037400-48038600	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr21:48037400-48040000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr21:48037600-48038800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr21:48037600-48039000	Weak transcription	Primary T cells from cord blood	blood
44	chr21:48037600-48039000	Weak transcription	Primary T helper cells PMA-I stimulated	--
45	chr21:48038400-48041400	Weak transcription	Right Atrium	heart
46	chr21:48038600-48038800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
47	chr21:48038600-48038800	Enhancers	Brain Angular Gyrus	brain
48	chr21:48038600-48039600	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr21:48038600-48043400	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr21:48038800-48039600	Enhancers	Primary B cells from cord blood	blood

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