Variant report

Variant	nsv871155
Chromosome Location	chr1:10858746-10998509
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1634)
CpG islands
(count:2075)
Chromatin interactive
region (count:218)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1634 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:10970150-10970166	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:10908411-10908591	HepG2	liver:	n/a	n/a
3	ATF1	chr1:10892500-10892630	K562	blood:	n/a	n/a
4	ATF1	chr1:10987025-10987052	K562	blood:	n/a	n/a
5	ATF3	chr1:10927199-10927525	K562	blood:	n/a	chr1:10927395-10927403
6	BACH1	chr1:10968551-10968571	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr1:10961489-10961737	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr1:10899649-10899712	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr1:10927179-10927591	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr1:10895531-10896453	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr1:10992136-10992425	GM12878	blood:	n/a	n/a
12	BATF	chr1:10992168-10992557	GM12878	blood:	n/a	n/a
13	BATF	chr1:10982326-10982673	GM12878	blood:	n/a	n/a
14	BATF	chr1:10982397-10982690	GM12878	blood:	n/a	n/a
15	BCL3	chr1:10871791-10872058	GM12878	blood:	n/a	n/a
16	BHLHE40	chr1:10937918-10938263	K562	blood:	n/a	chr1:10938096-10938105 chr1:10938095-10938104 chr1:10938093-10938106 chr1:10938089-10938110 chr1:10938094-10938103 chr1:10938095-10938104
17	BHLHE40	chr1:10997374-10997818	HepG2	liver:	n/a	chr1:10997650-10997666 chr1:10997658-10997674 chr1:10997661-10997677
18	BHLHE40	chr1:10992234-10992550	GM12878	blood:	n/a	n/a
19	BHLHE40	chr1:10997406-10997799	HepG2	liver:	n/a	chr1:10997650-10997666 chr1:10997658-10997674 chr1:10997661-10997677
20	BHLHE40	chr1:10927192-10927695	GM12878	blood:	n/a	chr1:10927415-10927431
21	BHLHE40	chr1:10937968-10938240	HepG2	liver:	n/a	chr1:10938096-10938105 chr1:10938095-10938104 chr1:10938093-10938106 chr1:10938089-10938110 chr1:10938094-10938103 chr1:10938095-10938104
22	BHLHE40	chr1:10997309-10997934	HepG2	liver:	n/a	chr1:10997650-10997666 chr1:10997658-10997674 chr1:10997661-10997677
23	BHLHE40	chr1:10961359-10961694	K562	blood:	n/a	chr1:10961520-10961529 chr1:10961520-10961529 chr1:10961514-10961535 chr1:10961521-10961530 chr1:10961519-10961528 chr1:10961518-10961531
24	BHLHE40	chr1:10961130-10961769	HepG2	liver:	n/a	chr1:10961520-10961529 chr1:10961520-10961529 chr1:10961514-10961535 chr1:10961521-10961530 chr1:10961519-10961528 chr1:10961518-10961531
25	BHLHE40	chr1:10927333-10927581	A549	lung:	n/a	chr1:10927415-10927431
26	BHLHE40	chr1:10927247-10927596	HepG2	liver:	n/a	chr1:10927415-10927431
27	BHLHE40	chr1:10927240-10927629	K562	blood:	n/a	chr1:10927415-10927431
28	BHLHE40	chr1:10930634-10930964	K562	blood:	n/a	n/a
29	BRCA1	chr1:10961773-10961917	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr1:10893936-10894419	H1-hESC	embryonic stem cell:	n/a	n/a
31	BRCA1	chr1:10895940-10896274	H1-hESC	embryonic stem cell:	n/a	n/a
32	BRCA1	chr1:10960317-10961304	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr1:10970675-10970798	HepG2	liver:	n/a	n/a
34	CBX3	chr1:10995794-10996117	K562	blood:	n/a	n/a
35	CBX3	chr1:10988617-10989159	K562	blood:	n/a	n/a
36	CBX3	chr1:10995877-10996179	K562	blood:	n/a	n/a
37	CBX3	chr1:10988712-10989044	K562	blood:	n/a	n/a
38	CBX3	chr1:10969712-10970070	K562	blood:	n/a	n/a
39	CBX3	chr1:10969742-10970096	K562	blood:	n/a	n/a
40	CCNT2	chr1:10927211-10927491	K562	blood:	n/a	n/a
41	CCNT2	chr1:10895926-10896187	K562	blood:	n/a	chr1:10896161-10896170
42	CEBPB	chr1:10900367-10900646	HepG2	liver:	n/a	chr1:10900546-10900559 chr1:10900490-10900501
43	CEBPB	chr1:10984450-10984509	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr1:10965287-10965487	HepG2	liver:	n/a	chr1:10965356-10965369
45	CEBPB	chr1:10984391-10984410	HepG2	liver:	n/a	n/a
46	CEBPB	chr1:10984373-10984395	IMR90	lung:	n/a	n/a
47	CEBPB	chr1:10871939-10872009	HepG2	liver:	n/a	chr1:10871985-10871996
48	CEBPB	chr1:10959901-10961228	MCF-7	breast:	n/a	chr1:10960233-10960244
49	CEBPB	chr1:10891037-10891376	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr1:10956633-10956722	HepG2	liver:	n/a	n/a

(count:2075 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:10896004-10896054	HAEpiC	amniotic membrane:	n/a
2	chr1:10896004-10896054	HAEpiC	amniotic membrane:	n/a
3	chr1:10927110-10927160	K562	blood:	n/a
4	chr1:10977926-10977976	GM12891	blood:	n/a
5	chr1:10896343-10896393	NHDF-neo	bronchial:	n/a
6	chr1:10874315-10874365	AoSMC	blood vessel:	n/a
7	chr1:10927403-10927453	NT2-D1	testis:	n/a
8	chr1:10891531-10891581	SK-N-SH_RA	brain:	n/a
9	chr1:10898189-10898239	GM19239	blood:	n/a
10	chr1:10895978-10896028	HCM	heart:	n/a
11	chr1:10961257-10961307	Hela-S3	cervix:	n/a
12	chr1:10969475-10969525	NH-A	brain:	n/a
13	chr1:10927403-10927453	A549	lung:	n/a
14	chr1:10977175-10977225	PANC-1	pancreas:	n/a
15	chr1:10888566-10888616	SK-N-SH	brain:	n/a
16	chr1:10917391-10917441	T-47D	breast:	n/a
17	chr1:10949192-10949242	LNCaP	prostate:	n/a
18	chr1:10969475-10969525	AG09309	skin:	n/a
19	chr1:10969475-10969525	HCM	heart:	n/a
20	chr1:10961257-10961307	U87	brain:	n/a
21	chr1:10891531-10891581	AoSMC	blood vessel:	n/a
22	chr1:10887875-10887925	MCF-7	breast:	n/a
23	chr1:10917391-10917441	ovcar-3	ovarian:	n/a
24	chr1:10927190-10927240	HRCEpiC	kidney:	n/a
25	chr1:10896343-10896393	GM12878	blood:	n/a
26	chr1:10895978-10896028	ProgFib	skin:	n/a
27	chr1:10961257-10961307	NT2-D1	testis:	n/a
28	chr1:10961257-10961307	HCPEpiC	choroid plexus:	n/a
29	chr1:10992454-10992504	HCT-116	colon:	n/a
30	chr1:10895517-10895567	NHBE	bronchial:	n/a
31	chr1:10887875-10887925	HUVEC	blood vessel:	n/a
32	chr1:10969475-10969525	SK-N-SH_RA	brain:	n/a
33	chr1:10992454-10992504	CMK	blood:	n/a
34	chr1:10924583-10924633	SKMC	muscle:	n/a
35	chr1:10992454-10992504	NT2-D1	testis:	n/a
36	chr1:10949192-10949242	HEK293	kidney:	embryo
37	chr1:10874315-10874365	A549	lung:	n/a
38	chr1:10898189-10898239	GM12878	blood:	n/a
39	chr1:10917451-10917501	Hepatocyte	liver:	n/a
40	chr1:10874315-10874365	HIPEpiC	eye:	n/a
41	chr1:10874315-10874365	ovcar-3	ovarian:	n/a
42	chr1:10961257-10961307	T-47D	breast:	n/a
43	chr1:10948457-10948507	AG04449	skin:	fetal
44	chr1:10896343-10896393	Hepatocyte	liver:	n/a
45	chr1:10970165-10970215	CMK	blood:	n/a
46	chr1:10896004-10896054	HUVEC	blood vessel:	n/a
47	chr1:10970165-10970215	HL-60	blood:	n/a
48	chr1:10997656-10997706	HIPEpiC	eye:	n/a
49	chr1:10898189-10898239	NHBE	bronchial:	n/a
50	chr1:10927403-10927453	MCF-7	breast:	n/a

(count:218 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr1:10849936..10852121-chr1:10862598..10865069,2	MCF-7	breast:
2	chr1:10951222..10953605-chr1:10998920..11000923,2	MCF-7	breast:
3	chr1:10994902..10997347-chr1:10999182..11001524,2	K562	blood:
4	chr1:10868041..10870911-chr1:10873576..10876593,3	K562	blood:
5	chr1:10872620..10874163-chr1:10875602..10877210,2	MCF-7	breast:
6	chr1:10855453..10857266-chr1:10883652..10886481,2	MCF-7	breast:
7	chr1:10919663..10923359-chr1:10925488..10928766,3	MCF-7	breast:
8	chr1:10892514..10895346-chr1:10924391..10927017,2	K562	blood:
9	chr1:10531686..10533815-chr1:10976786..10978412,2	MCF-7	breast:
10	chr1:10959252..10961751-chr1:10965337..10967392,2	K562	blood:
11	chr1:10880964..10882557-chr1:10895736..10897488,2	MCF-7	breast:
12	chr1:10950581..10952602-chr1:10959181..10961794,2	MCF-7	breast:
13	chr1:10908264..10910893-chr1:10918893..10922550,4	K562	blood:
14	chr1:10956858..10959439-chr1:10960861..10964225,4	MCF-7	breast:
15	chr1:10876866..10879184-chr1:10889466..10891905,3	K562	blood:
16	chr1:10859862..10862247-chr1:10862997..10864599,2	MCF-7	breast:
17	chr1:10955839..10958166-chr1:10962257..10965296,3	K562	blood:
18	chr1:10888572..10890725-chr1:10893676..10896099,3	K562	blood:
19	chr1:10834395..10836864-chr1:10924588..10926735,2	MCF-7	breast:
20	chr1:10947591..10949660-chr1:10955110..10956674,2	MCF-7	breast:
21	chr1:10926420..10929831-chr1:10932404..10934606,3	K562	blood:
22	chr1:10954410..10954912-chr15:76195676..76196245,2	Hela-S3	cervix:
23	chr1:10998249..11000521-chr1:11002224..11004304,2	K562	blood:
24	chr1:10974523..10977256-chr1:10996364..10997924,2	K562	blood:
25	chr1:10837835..10840476-chr1:10895758..10897278,2	MCF-7	breast:
26	chr1:10862515..10864185-chr1:10869932..10871983,2	MCF-7	breast:
27	chr1:10752376..10753024-chr1:10896001..10896596,2	MCF-7	breast:
28	chr1:10562142..10564951-chr1:10926770..10929049,2	K562	blood:
29	chr1:10936767..10939013-chr1:10968628..10971231,2	MCF-7	breast:
30	chr1:10868648..10871546-chr1:10878409..10880098,2	K562	blood:
31	chr1:10959209..10961578-chr1:10962035..10963966,2	MCF-7	breast:
32	chr1:10958477..10963134-chr1:10964033..10968980,6	MCF-7	breast:
33	chr1:10955198..10958166-chr1:10961207..10963906,3	K562	blood:
34	chr1:10876492..10878024-chr1:10879047..10880771,2	K562	blood:
35	chr1:10941792..10943849-chr1:10948665..10951435,2	K562	blood:
36	chr1:10958837..10960829-chr1:10964871..10966508,2	MCF-7	breast:
37	chr1:10576160..10578872-chr1:10926632..10929593,2	MCF-7	breast:
38	chr1:10872620..10874163-chr1:10875602..10877210,2	MCF-7	breast:
39	chr1:10918685..10920467-chr1:10928857..10931525,2	K562	blood:
40	chr1:10868718..10870802-chr1:10872433..10874614,2	MCF-7	breast:
41	chr1:10945438..10948042-chr1:10952167..10953701,2	K562	blood:
42	chr1:10752227..10753991-chr1:10926922..10928500,5	MCF-7	breast:
43	chr1:10966478..10970705-chr1:10971102..10976299,6	K562	blood:
44	chr1:10914701..10916708-chr1:10923191..10926876,3	MCF-7	breast:
45	chr1:10952544..10954110-chr1:10956474..10958853,2	MCF-7	breast:
46	chr1:10945438..10947067-chr1:10950984..10953667,2	K562	blood:
47	chr1:10957794..10962323-chr1:11069387..11074013,5	MCF-7	breast:
48	chr1:10926420..10929831-chr1:10932404..10934606,3	K562	blood:
49	chr1:10895615..10898736-chr1:10923813..10928307,5	K562	blood:
50	chr1:10568670..10571119-chr1:10926842..10928478,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CASZ1-3	chr1:10888161-10888435	uc_10_-
2	lnc-TARDBP-9	chr1:10925409-10925611	NONHSAT000869
3	lnc-TARDBP-8	chr1:10955818-10956055	NONHSAT000870
4	lnc-TARDBP-10	chr1:10888161-10888435	uc_10_+

No data

Variant related genes	Relation type
CASZ1	TF binding region
HSPE1P24	TF binding region
CASZ1	CpG island
HSPE1P24	CpG island
ENSG00000271989	chromatin interactions
ENSG00000142655	chromatin interactions
ENSG00000175279	chromatin interactions
ENSG00000116337	chromatin interactions
ENSG00000167196	chromatin interactions
ENSG00000225158	chromatin interactions
ENSG00000160049	chromatin interactions
ENSG00000130940	chromatin interactions
ENSG00000251503	chromatin interactions
ENSG00000243267	chromatin interactions
ENSG00000175262	chromatin interactions
ENSG00000120948	chromatin interactions

Extended variants
information (count: 5787 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:5787 , 50 per page) page: 1 2 3 4 5 6 7 ... 116

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs718047	chr1:10858746-10858747	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs144354998	chr1:10858759-10858760	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs527513432	chr1:10858783-10858784	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs576959043	chr1:10858816-10858817	Bivalent Enhancer Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs561191056	chr1:10858828-10858829	Bivalent Enhancer Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs372186472	chr1:10858869-10858870	Bivalent Enhancer Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs183603323	chr1:10858883-10858884	Bivalent Enhancer Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs537841144	chr1:10858914-10858915	Bivalent Enhancer Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs376825111	chr1:10858945-10858946	Bivalent Enhancer Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs549771604	chr1:10858968-10858969	Bivalent Enhancer Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs148635014	chr1:10858987-10858988	Bivalent Enhancer Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs76235396	chr1:10858995-10858996	Bivalent Enhancer Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs186038811	chr1:10859061-10859062	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs547551089	chr1:10859110-10859111	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs369021487	chr1:10859163-10859164	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs566943462	chr1:10859164-10859165	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs534450209	chr1:10859217-10859218	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs371669943	chr1:10859253-10859254	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs541878338	chr1:10859259-10859260	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs549312908	chr1:10859267-10859268	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs142136990	chr1:10859318-10859319	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs376698904	chr1:10859352-10859353	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs538163611	chr1:10859356-10859357	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs556107417	chr1:10859402-10859403	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs374815552	chr1:10859422-10859423	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs538729334	chr1:10859439-10859440	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs11121628	chr1:10859478-10859479	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs572453035	chr1:10859510-10859511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs1152728	chr1:10859513-10859514	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs12410929	chr1:10859525-10859526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
31	rs150705796	chr1:10859564-10859565	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs545777039	chr1:10859585-10859586	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs543768811	chr1:10859611-10859612	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs564859083	chr1:10859651-10859652	Bivalent Enhancer Weak transcription Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs114827876	chr1:10859669-10859670	Bivalent Enhancer Weak transcription Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs547510492	chr1:10859685-10859686	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs550579248	chr1:10859716-10859717	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs74652971	chr1:10859746-10859747	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs549519859	chr1:10859747-10859748	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs567781839	chr1:10859773-10859774	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs538125687	chr1:10859822-10859823	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs550092733	chr1:10859835-10859836	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs190360812	chr1:10859843-10859844	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs74052511	chr1:10859929-10859930	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs553891062	chr1:10859964-10859965	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs572471616	chr1:10860018-10860019	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs536371678	chr1:10860073-10860074	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs114494000	chr1:10860126-10860127	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs576340306	chr1:10860131-10860132	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs35994373	chr1:10860201-10860202	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	22429812	CNVD
Epilepsy	22118685	CNVD
Schizophrenia	22118685	CNVD
Ovarian cancer	21720365	CNVD
Developmental delay	19490664	CNVD
Ewing''s sarcoma	21437220	CNVD
Prader-willi syndrome	18797701	CNVD
periventricular nodular heterotopia	20648244	CNVD
1p36 deletion syndrome	22283845	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
Neuroblastoma	18923524	CNVD
Retinoblastoma	22278416	CNVD
Mental retardation	20152051	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Astrocytoma	17934521	CNVD
Glioblastoma	20031968	CNVD
Acute myeloid leukemia	18000384	CNVD
Glioblastoma multiforme	16951158	CNVD
Neuroblastoma	18574593	CNVD
Glioblastoma multiforme	17369134	CNVD
Autism	18414403	CNVD
Breast cancer	17001317	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Myoepithelioma	18604193	CNVD
Wilms tumour	19047088	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Neuroblastoma	18923191	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21138945	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian neoplasms	16753589	CNVD
Neuroblastoma	19287153	CNVD
Hepatocellular carcinoma	18929564	CNVD
Melanoma	17363583	CNVD
renal disease	17924346	CNVD
Uveal melanoma	20484589	CNVD
Multiple myeloma	16616336	CNVD
Glioblastoma multiforme	22286061	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	20808228	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2091 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:10857000-10859800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr1:10857000-10859800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:10857000-10873600	Weak transcription	Gastric	stomach
4	chr1:10857000-10882600	Weak transcription	Right Atrium	heart
5	chr1:10857200-10859800	Weak transcription	Fetal Intestine Large	intestine
6	chr1:10857200-10860400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr1:10857600-10860000	Weak transcription	Fetal Heart	heart
8	chr1:10857600-10860600	Weak transcription	Stomach Mucosa	stomach
9	chr1:10857800-10859200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr1:10858000-10858800	Enhancers	H9 Cell Line	embryonic stem cell
11	chr1:10858800-10859000	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
12	chr1:10859000-10859200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
13	chr1:10859200-10859400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr1:10859200-10859400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
15	chr1:10859200-10860200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr1:10859400-10859800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr1:10859600-10860000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
18	chr1:10859600-10860400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
19	chr1:10859800-10860000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr1:10859800-10860000	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr1:10859800-10860200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
22	chr1:10859800-10860200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
23	chr1:10859800-10860200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
24	chr1:10859800-10860200	Enhancers	Fetal Intestine Large	intestine
25	chr1:10859800-10860200	Bivalent Enhancer	Fetal Muscle Leg	muscle
26	chr1:10859800-10860400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr1:10859800-10860400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr1:10859800-10860400	Bivalent Enhancer	Duodenum Mucosa	Duodenum
29	chr1:10860000-10860200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
30	chr1:10860000-10860200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
31	chr1:10860000-10860200	Enhancers	Fetal Intestine Small	intestine
32	chr1:10860000-10860400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr1:10860000-10860600	Enhancers	Fetal Heart	heart
34	chr1:10860000-10863000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr1:10860200-10862800	Weak transcription	Fetal Intestine Large	intestine
36	chr1:10860200-10863200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr1:10860400-10863000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr1:10860400-10863200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr1:10860400-10864000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr1:10860400-10864000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr1:10860600-10861200	Enhancers	Stomach Mucosa	stomach
42	chr1:10860600-10862800	Weak transcription	Fetal Heart	heart
43	chr1:10861200-10863000	Weak transcription	Stomach Mucosa	stomach
44	chr1:10862800-10863000	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr1:10862800-10863000	Enhancers	HMEC	breast
46	chr1:10862800-10863200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr1:10862800-10863600	Enhancers	Fetal Heart	heart
48	chr1:10862800-10864600	Enhancers	Fetal Intestine Large	intestine
49	chr1:10863000-10863200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
50	chr1:10863000-10863200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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