Variant report

Variant	nsv482564
Chromosome Location	chr10:52276564-52447589
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5684)
CpG islands
(count:2444)
Chromatin interactive
region (count:305)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:5684 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:52366335-52366645	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:52316432-52316925	K562	blood:	n/a	n/a
3	ARID3A	chr10:52336811-52338299	K562	blood:	n/a	n/a
4	ARID3A	chr10:52408594-52408636	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:52300691-52300891	K562	blood:	n/a	n/a
6	ARID3A	chr10:52360148-52360181	K562	blood:	n/a	n/a
7	ARID3A	chr10:52303304-52303406	K562	blood:	n/a	n/a
8	ARID3A	chr10:52305526-52305980	K562	blood:	n/a	n/a
9	ARID3A	chr10:52342572-52343135	K562	blood:	n/a	n/a
10	ARID3A	chr10:52339275-52340080	K562	blood:	n/a	n/a
11	ARID3A	chr10:52334069-52334485	K562	blood:	n/a	n/a
12	ARID3A	chr10:52325695-52326213	HepG2	liver:	n/a	n/a
13	ARID3A	chr10:52346350-52346636	K562	blood:	n/a	n/a
14	ARID3A	chr10:52384792-52385529	HepG2	liver:	n/a	n/a
15	ARID3A	chr10:52286076-52286244	K562	blood:	n/a	n/a
16	ARID3A	chr10:52304610-52304987	K562	blood:	n/a	n/a
17	ARID3A	chr10:52384212-52384454	K562	blood:	n/a	n/a
18	ARID3A	chr10:52309577-52310528	K562	blood:	n/a	n/a
19	ARID3A	chr10:52345577-52345762	K562	blood:	n/a	n/a
20	ARID3A	chr10:52312667-52312883	HepG2	liver:	n/a	n/a
21	ARID3A	chr10:52364871-52365512	HepG2	liver:	n/a	n/a
22	ARID3A	chr10:52334786-52335470	K562	blood:	n/a	n/a
23	ARID3A	chr10:52314639-52315474	K562	blood:	n/a	n/a
24	ARID3A	chr10:52365066-52365394	K562	blood:	n/a	n/a
25	ARID3A	chr10:52324760-52325414	K562	blood:	n/a	chr10:52324873-52324889 chr10:52324872-52324888
26	ARID3A	chr10:52312526-52313074	K562	blood:	n/a	n/a
27	ARID3A	chr10:52317499-52317727	K562	blood:	n/a	n/a
28	ARID3A	chr10:52336324-52336374	K562	blood:	n/a	n/a
29	ARID3A	chr10:52352624-52352893	K562	blood:	n/a	n/a
30	ARID3A	chr10:52384155-52384554	HepG2	liver:	n/a	n/a
31	ARID3A	chr10:52298940-52299140	K562	blood:	n/a	n/a
32	ARID3A	chr10:52331690-52332242	HepG2	liver:	n/a	n/a
33	ARID3A	chr10:52298911-52299383	HepG2	liver:	n/a	n/a
34	ARID3A	chr10:52369546-52369716	K562	blood:	n/a	n/a
35	ARID3A	chr10:52381808-52382344	K562	blood:	n/a	n/a
36	ARID3A	chr10:52287228-52287629	K562	blood:	n/a	n/a
37	ARID3A	chr10:52384890-52385350	K562	blood:	n/a	n/a
38	ATF1	chr10:52309927-52310489	K562	blood:	n/a	n/a
39	ATF1	chr10:52342536-52343457	K562	blood:	n/a	n/a
40	ATF1	chr10:52305607-52306012	K562	blood:	n/a	n/a
41	ATF1	chr10:52325038-52325828	K562	blood:	n/a	n/a
42	ATF1	chr10:52287195-52287626	K562	blood:	n/a	n/a
43	ATF1	chr10:52384112-52385291	K562	blood:	n/a	n/a
44	ATF1	chr10:52393942-52393968	K562	blood:	n/a	n/a
45	ATF1	chr10:52335441-52335481	K562	blood:	n/a	n/a
46	ATF1	chr10:52337408-52337934	K562	blood:	n/a	n/a
47	ATF1	chr10:52312597-52312900	K562	blood:	n/a	n/a
48	ATF1	chr10:52366344-52366675	K562	blood:	n/a	n/a
49	ATF1	chr10:52420013-52420185	K562	blood:	n/a	n/a
50	ATF1	chr10:52314659-52315372	K562	blood:	n/a	n/a

(count:2444 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:52390973-52391023	HL-60	blood:	n/a
2	chr10:52350890-52350940	NH-A	brain:	n/a
3	chr10:52434778-52434828	AG10803	skin:	n/a
4	chr10:52383849-52383899	HAEpiC	amniotic membrane:	n/a
5	chr10:52390973-52391023	HL-60	blood:	n/a
6	chr10:52350890-52350940	NH-A	brain:	n/a
7	chr10:52434778-52434828	AG10803	skin:	n/a
8	chr10:52383849-52383899	HAEpiC	amniotic membrane:	n/a
9	chr10:52382517-52382567	HRE	kidney:	n/a
10	chr10:52434552-52434602	HPAEpiC	pulmonary alveolar:	n/a
11	chr10:52324046-52324096	NB4	blood:	n/a
12	chr10:52384903-52384953	AG10803	skin:	n/a
13	chr10:52383929-52383979	HEEpiC	esophagus:	n/a
14	chr10:52363132-52363182	GM12892	blood:	n/a
15	chr10:52324046-52324096	SK-N-MC	brain:	n/a
16	chr10:52363132-52363182	LNCaP	prostate:	n/a
17	chr10:52433577-52433627	SK-N-SH	brain:	n/a
18	chr10:52434552-52434602	H1-hESC	embryonic stem cell:	embryo
19	chr10:52390957-52391007	NHBE	bronchial:	n/a
20	chr10:52363132-52363182	HIPEpiC	eye:	n/a
21	chr10:52313502-52313552	SK-N-MC	brain:	n/a
22	chr10:52336353-52336403	NB4	blood:	n/a
23	chr10:52373147-52373197	GM12892	blood:	n/a
24	chr10:52350890-52350940	AG10803	skin:	n/a
25	chr10:52383933-52383983	K562	blood:	n/a
26	chr10:52382136-52382186	ProgFib	skin:	n/a
27	chr10:52361663-52361713	Jurkat	blood:	n/a
28	chr10:52336353-52336403	HCPEpiC	choroid plexus:	n/a
29	chr10:52385225-52385275	HCM	heart:	n/a
30	chr10:52419357-52419407	HAEpiC	amniotic membrane:	n/a
31	chr10:52384065-52384115	GM12891	blood:	n/a
32	chr10:52383877-52383927	GM12891	blood:	n/a
33	chr10:52434552-52434602	GM06990	blood:	n/a
34	chr10:52383853-52383903	PFSK-1	brain:	n/a
35	chr10:52350890-52350940	HRE	kidney:	n/a
36	chr10:52434778-52434828	Caco-2	colon:	n/a
37	chr10:52431183-52431233	SK-N-SH	brain:	n/a
38	chr10:52383929-52383979	GM12878	blood:	n/a
39	chr10:52379467-52379517	ProgFib	skin:	n/a
40	chr10:52383853-52383903	HIPEpiC	eye:	n/a
41	chr10:52420019-52420069	LNCaP	prostate:	n/a
42	chr10:52384903-52384953	ECC-1	luminal epithelium:	n/a
43	chr10:52390957-52391007	AG09309	skin:	n/a
44	chr10:52383683-52383733	SK-N-SH	brain:	n/a
45	chr10:52366029-52366079	HEEpiC	esophagus:	n/a
46	chr10:52390973-52391023	PrEC	prostate:	n/a
47	chr10:52436125-52436175	AG10803	skin:	n/a
48	chr10:52436125-52436175	SKMC	muscle:	n/a
49	chr10:52390973-52391023	HAEpiC	amniotic membrane:	n/a
50	chr10:52434778-52434828	HRE	kidney:	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Distal block	Cell Line	Cell type
1	chr10:52293246..52296190-chr10:52300383..52302951,2	K562	blood:
2	chr10:52321488..52322151-chr10:52374019..52374674,2	MCF-7	breast:
3	chr10:52321239..52322152-chr10:52412979..52413544,2	MCF-7	breast:
4	chr10:52311229..52315083-chr10:52335257..52337670,4	K562	blood:
5	chr10:52364376..52366700-chr10:52391837..52394497,2	K562	blood:
6	chr10:52309255..52311683-chr10:52321787..52323365,2	K562	blood:
7	chr10:52359260..52360848-chr10:52387112..52388927,2	K562	blood:
8	chr10:52293246..52296190-chr10:52300383..52302951,2	K562	blood:
9	chr10:52291845..52294288-chr10:52302987..52304879,2	K562	blood:
10	chr10:52383477..52384291-chr15:65588151..65588664,2	HCT-116	colon:
11	chr10:52388132..52389633-chr10:52392535..52394699,2	MCF-7	breast:
12	chr10:52367316..52369194-chr10:52370537..52372396,2	MCF-7	breast:
13	chr10:52383358..52384122-chr6:159421120..159421666,2	Hela-S3	cervix:
14	chr10:52356810..52366659-chr10:52378806..52385975,25	MCF-7	breast:
15	chr10:52359176..52361319-chr10:52370214..52372763,2	K562	blood:
16	chr10:52287492..52289090-chr10:52346967..52349226,2	K562	blood:
17	chr10:52361922..52364870-chr10:52374462..52376104,2	MCF-7	breast:
18	chr10:52355890..52357907-chr10:52372209..52373860,2	K562	blood:
19	chr10:52287244..52289297-chr10:52294304..52296791,2	K562	blood:
20	chr10:52291946..52294684-chr10:52298483..52300716,2	K562	blood:
21	chr10:52394806..52397022-chr10:52398491..52400637,2	K562	blood:
22	chr10:52367499..52369355-chr10:52371590..52373670,2	MCF-7	breast:
23	chr10:52308481..52311283-chr10:52312051..52314747,2	MCF-7	breast:
24	chr10:52342671..52345197-chr10:52362617..52364673,2	MCF-7	breast:
25	chr10:52319465..52323601-chr10:52381894..52385353,11	MCF-7	breast:
26	chr10:52352876..52355415-chr10:52360770..52364645,3	K562	blood:
27	chr10:52321608..52322162-chr10:52374026..52374665,2	K562	blood:
28	chr10:52345136..52347979-chr10:52349121..52350897,2	MCF-7	breast:
29	chr10:52385910..52390098-chr10:52396807..52399699,3	MCF-7	breast:
30	chr10:52288714..52291350-chr10:52382116..52385010,2	K562	blood:
31	chr10:52383783..52384592-chr11:82866965..82867887,2	Hela-S3	cervix:
32	chr10:52291946..52294684-chr10:52298483..52300716,2	K562	blood:
33	chr10:52176158..52178831-chr10:52279498..52281000,2	MCF-7	breast:
34	chr10:52303071..52304706-chr10:52310411..52312427,2	K562	blood:
35	chr10:52315813..52318278-chr10:52376288..52379260,2	K562	blood:
36	chr10:52273248..52274821-chr10:52291297..52292939,2	MCF-7	breast:
37	chr10:52363840..52365627-chr10:52371839..52373893,2	K562	blood:
38	chr10:52346124..52348507-chr10:52350618..52352666,3	K562	blood:
39	chr10:52359953..52362709-chr10:52369369..52373300,4	MCF-7	breast:
40	chr10:52382192..52390666-chr10:52409582..52414601,12	MCF-7	breast:
41	chr10:52321910..52324715-chr10:52371827..52374232,3	K562	blood:
42	chr10:52311750..52313842-chr10:52375196..52377045,2	K562	blood:
43	chr10:52318973..52324648-chr10:52334040..52339164,5	K562	blood:
44	chr10:52324915..52329170-chr10:52335171..52340296,4	K562	blood:
45	chr10:52356810..52366659-chr10:52378806..52385975,25	MCF-7	breast:
46	chr10:52337504..52339571-chr10:52355930..52358209,2	K562	blood:
47	chr10:52285750..52287890-chr10:52311522..52314222,2	MCF-7	breast:
48	chr10:52340909..52343314-chr10:52378678..52381107,3	K562	blood:
49	chr10:52385385..52386943-chr10:52417956..52419960,2	MCF-7	breast:
50	chr10:52338640..52342298-chr10:52355605..52360278,4	MCF-7	breast:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASAH2B-2	chr10:52384723-52384951	ENSG00000226200.2
2	lnc-ASAH2B-2	chr10:52388791-52388938	ENSG00000226200.2
3	lnc-ASAH2B-2	chr10:52386783-52387546	NONHSAT013389
4	lnc-ASAH2B-2	chr10:52388791-52389019	NONHSAT013389
5	lnc-ASAH2B-2	chr10:52386410-52386565	ENSG00000226200.2
6	lnc-A1CF-2	chr10:52348409-52348560	ENSG00000226561.1
7	lnc-ASAH2B-2	chr10:52388910-52388938	ENSG00000226200.1
8	lnc-ASAH2B-2	chr10:52389337-52391396	ENSG00000226200.1
9	lnc-ASAH2B-2	chr10:52389337-52401211	ENSG00000226200.2
10	lnc-ASAH2B-2	chr10:52388791-52388938	ENSG00000226200.2
11	lnc-ASAH2B-2	chr10:52384711-52384951	ENSG00000226200.2
12	lnc-ASAH2B-2	chr10:52389337-52389732	ENSG00000226200.2
13	lnc-ASAH2B-2	chr10:52386430-52386565	ENSG00000226200.2
14	lnc-ASAH2B-2	chr10:52383739-52386623	NONHSAT013388
15	lnc-A1CF-2	chr10:52349302-52349592	ENSG00000226561.1

No data

Variant related genes	Relation type
SGMS1	TF binding region
RMRPP4	TF binding region
NUTM2HP	TF binding region
ENSG00000231588	TF binding region
ENSG00000226200	TF binding region
ENSG00000231345	TF binding region
ENSG00000230036	TF binding region
RNU7-107P	TF binding region
SGMS1	CpG island
RMRPP4	CpG island
NUTM2HP	CpG island
ENSG00000231588	CpG island
ENSG00000226200	CpG island
ENSG00000231345	CpG island
ENSG00000230036	CpG island
RNU7-107P	CpG island
ENSG00000198964	chromatin interactions
ENSG00000079459	chromatin interactions
ENSG00000205791	chromatin interactions
ENSG00000258704	chromatin interactions
ENSG00000269700	chromatin interactions
ENSG00000255046	chromatin interactions
ENSG00000238523	chromatin interactions
ENSG00000135723	chromatin interactions
ENSG00000101150	chromatin interactions
ENSG00000100883	chromatin interactions
ENSG00000224886	chromatin interactions
ENSG00000231588	chromatin interactions
ENSG00000171161	chromatin interactions
ENSG00000226200	chromatin interactions
ENSG00000225303	chromatin interactions
ENSG00000204147	chromatin interactions
ENSG00000130363	chromatin interactions
ENSG00000043143	chromatin interactions
ENSG00000199568	chromatin interactions
ENSG00000165714	chromatin interactions
ENSG00000231345	chromatin interactions
ENSG00000251950	chromatin interactions
ENSG00000230036	chromatin interactions

Extended variants
information (count: 6518 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:6518 , 50 per page) page: 1 2 3 4 5 6 7 ... 131

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571195646	chr10:52276611-52276612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs368336427	chr10:52276642-52276643	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs543672585	chr10:52276720-52276721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs540114238	chr10:52276751-52276752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs552246566	chr10:52276752-52276753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs182756900	chr10:52276847-52276848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs563375060	chr10:52276862-52276863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs537550964	chr10:52276923-52276924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs3011774	chr10:52277018-52277019	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs186987864	chr10:52277080-52277081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs534028915	chr10:52277168-52277169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs3011775	chr10:52277178-52277179	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs192725299	chr10:52277227-52277228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs142911100	chr10:52277279-52277280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs78701501	chr10:52277399-52277400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs4935727	chr10:52277400-52277401	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs541981144	chr10:52277444-52277445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs562176327	chr10:52277489-52277490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs527768238	chr10:52277578-52277579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs547996803	chr10:52277589-52277590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs564664764	chr10:52277594-52277595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs533706878	chr10:52277595-52277596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs550454566	chr10:52277599-52277600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs34928652	chr10:52277608-52277609	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs548367485	chr10:52277633-52277634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs537817097	chr10:52277659-52277660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs144428121	chr10:52277684-52277685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs568177773	chr10:52277692-52277693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs527940095	chr10:52277709-52277710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs540616422	chr10:52277743-52277744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs117172392	chr10:52277776-52277777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs530842765	chr10:52277853-52277854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs147982609	chr10:52277866-52277867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs376365062	chr10:52277874-52277875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs184509173	chr10:52278058-52278059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs11594062	chr10:52278066-52278067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs141661105	chr10:52278115-52278116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs187853390	chr10:52278131-52278132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs4935728	chr10:52278185-52278186	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs555453712	chr10:52278196-52278197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572546556	chr10:52278207-52278208	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs2983346	chr10:52278279-52278280	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs373996410	chr10:52278292-52278293	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs193124914	chr10:52278300-52278301	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs533515998	chr10:52278309-52278310	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs184636933	chr10:52278313-52278314	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs188990649	chr10:52278315-52278316	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs376654282	chr10:52278324-52278325	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529541926	chr10:52278345-52278346	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369195203	chr10:52278346-52278347	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ollier disease	21235737	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:4701 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:52262200-52287200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr10:52266800-52282400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr10:52267000-52282400	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr10:52267600-52277800	Enhancers	Brain Anterior Caudate	brain
5	chr10:52268200-52282400	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr10:52268200-52282600	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr10:52268400-52282200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr10:52268800-52278800	Weak transcription	Primary B cells from cord blood	blood
9	chr10:52270000-52282400	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr10:52270000-52282800	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr10:52270200-52282600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr10:52271200-52283000	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr10:52271600-52276800	Weak transcription	Fetal Lung	lung
14	chr10:52271600-52277400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr10:52271600-52300600	Weak transcription	Aorta	Aorta
16	chr10:52271800-52280800	Weak transcription	Primary monocytes fromperipheralblood	blood
17	chr10:52272200-52281000	Weak transcription	Fetal Intestine Large	intestine
18	chr10:52272400-52280000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr10:52272400-52280400	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr10:52272400-52284600	Weak transcription	Stomach Smooth Muscle	stomach
21	chr10:52272600-52302800	Weak transcription	Fetal Stomach	stomach
22	chr10:52272800-52279000	Weak transcription	Fetal Intestine Small	intestine
23	chr10:52272800-52281200	Weak transcription	Ovary	ovary
24	chr10:52272800-52281400	Weak transcription	Placenta	Placenta
25	chr10:52272800-52281600	Weak transcription	HepG2	liver
26	chr10:52272800-52288200	Weak transcription	HSMMtube	muscle
27	chr10:52273200-52278200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr10:52273200-52278600	Weak transcription	Primary hematopoietic stem cells	blood
29	chr10:52273200-52279000	Weak transcription	Lung	lung
30	chr10:52273200-52281000	Weak transcription	Fetal Muscle Trunk	muscle
31	chr10:52273200-52281600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr10:52273200-52282600	Weak transcription	Right Ventricle	heart
33	chr10:52273200-52285800	Weak transcription	K562	blood
34	chr10:52273200-52287200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr10:52273200-52287400	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr10:52273200-52288400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr10:52273400-52278400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr10:52273400-52279000	Weak transcription	Primary B cells from peripheral blood	blood
39	chr10:52273400-52279200	Weak transcription	Primary T cells fromperipheralblood	blood
40	chr10:52273400-52281000	Weak transcription	Fetal Muscle Leg	muscle
41	chr10:52273400-52281000	Weak transcription	Rectal Mucosa Donor 29	rectum
42	chr10:52273400-52281000	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr10:52273400-52282600	Weak transcription	Thymus	Thymus
44	chr10:52273400-52282800	Weak transcription	Spleen	Spleen
45	chr10:52273400-52283800	Weak transcription	Fetal Thymus	thymus
46	chr10:52273400-52286000	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr10:52273400-52287000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
48	chr10:52273400-52287200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
49	chr10:52273600-52286800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
50	chr10:52273600-52287400	Weak transcription	GM12878-XiMat	blood

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