Variant report

Variant	nsv1035850
Chromosome Location	chr12:38207030-38912512
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4552)
CpG islands
(count:3483)
Chromatin interactive
region (count:47)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4552 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:38778647-38778789	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:38493896-38494086	K562	blood:	n/a	n/a
3	ARID3A	chr12:38710113-38710696	HepG2	liver:	n/a	chr12:38710204-38710220 chr12:38710205-38710221
4	ARID3A	chr12:38482212-38482642	K562	blood:	n/a	n/a
5	ARID3A	chr12:38710301-38710555	K562	blood:	n/a	n/a
6	ARID3A	chr12:38543626-38543997	K562	blood:	n/a	n/a
7	ARID3A	chr12:38722185-38722490	HepG2	liver:	n/a	n/a
8	ARID3A	chr12:38518229-38518929	HepG2	liver:	n/a	n/a
9	ARID3A	chr12:38448696-38448896	HepG2	liver:	n/a	n/a
10	ARID3A	chr12:38722213-38722403	K562	blood:	n/a	n/a
11	ARID3A	chr12:38448701-38449068	K562	blood:	n/a	n/a
12	ARID3A	chr12:38532537-38532888	HepG2	liver:	n/a	n/a
13	ARID3A	chr12:38248444-38248820	HepG2	liver:	n/a	n/a
14	ATF1	chr12:38592349-38592545	K562	blood:	n/a	n/a
15	ATF1	chr12:38235844-38236214	K562	blood:	n/a	n/a
16	ATF1	chr12:38258619-38258986	K562	blood:	n/a	n/a
17	ATF1	chr12:38248442-38248819	K562	blood:	n/a	n/a
18	ATF1	chr12:38710296-38710661	K562	blood:	n/a	n/a
19	ATF1	chr12:38562455-38562511	K562	blood:	n/a	n/a
20	ATF1	chr12:38449777-38450205	K562	blood:	n/a	n/a
21	ATF1	chr12:38580930-38581004	K562	blood:	n/a	n/a
22	ATF1	chr12:38457173-38457374	K562	blood:	n/a	n/a
23	ATF2	chr12:38710293-38710713	GM12878	blood:	n/a	n/a
24	ATF2	chr12:38744101-38745067	GM12878	blood:	n/a	n/a
25	ATF2	chr12:38744225-38745089	GM12878	blood:	n/a	n/a
26	ATF2	chr12:38710159-38710775	GM12878	blood:	n/a	n/a
27	ATF3	chr12:38518161-38518657	A549	lung:	n/a	n/a
28	ATF3	chr12:38450770-38451371	A549	lung:	n/a	n/a
29	ATF3	chr12:38248534-38248701	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF3	chr12:38710223-38710780	A549	lung:	n/a	n/a
31	ATF3	chr12:38248441-38248721	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF3	chr12:38710219-38710780	A549	lung:	n/a	n/a
33	BACH1	chr12:38722036-38722207	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr12:38535652-38536024	K562	blood:	n/a	n/a
35	BACH1	chr12:38444623-38444996	K562	blood:	n/a	n/a
36	BACH1	chr12:38493592-38493998	K562	blood:	n/a	n/a
37	BACH1	chr12:38445410-38445790	K562	blood:	n/a	n/a
38	BACH1	chr12:38501131-38501616	K562	blood:	n/a	n/a
39	BACH1	chr12:38778825-38779049	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr12:38541011-38541384	K562	blood:	n/a	n/a
41	BACH1	chr12:38534226-38534319	K562	blood:	n/a	n/a
42	BACH1	chr12:38483362-38483596	K562	blood:	n/a	n/a
43	BACH1	chr12:38446968-38447169	K562	blood:	n/a	n/a
44	BACH1	chr12:38361554-38361929	K562	blood:	n/a	n/a
45	BACH1	chr12:38448694-38449069	K562	blood:	n/a	n/a
46	BACH1	chr12:38543625-38544007	K562	blood:	n/a	n/a
47	BACH1	chr12:38536600-38536974	K562	blood:	n/a	n/a
48	BATF	chr12:38341722-38341883	GM12878	blood:	n/a	n/a
49	BATF	chr12:38786453-38786734	GM12878	blood:	n/a	chr12:38786626-38786637
50	BATF	chr12:38710371-38710641	GM12878	blood:	n/a	n/a

(count:3483 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:38529156-38529206	MCF-7	breast:	n/a
2	chr12:38447636-38447686	HCPEpiC	choroid plexus:	n/a
3	chr12:38532713-38532763	NH-A	brain:	n/a
4	chr12:38547397-38547447	HCM	heart:	n/a
5	chr12:38449206-38449256	HL-60	blood:	n/a
6	chr12:38551782-38551832	ovcar-3	ovarian:	n/a
7	chr12:38529156-38529206	MCF-7	breast:	n/a
8	chr12:38447636-38447686	HCPEpiC	choroid plexus:	n/a
9	chr12:38532713-38532763	NH-A	brain:	n/a
10	chr12:38547397-38547447	HCM	heart:	n/a
11	chr12:38449206-38449256	HL-60	blood:	n/a
12	chr12:38551782-38551832	ovcar-3	ovarian:	n/a
13	chr12:38710604-38710654	HUVEC	blood vessel:	n/a
14	chr12:38595863-38595913	GM12892	blood:	n/a
15	chr12:38493714-38493764	NHDF-neo	bronchial:	n/a
16	chr12:38555558-38555608	HRE	kidney:	n/a
17	chr12:38710604-38710654	HRCEpiC	kidney:	n/a
18	chr12:38710491-38710541	SK-N-MC	brain:	n/a
19	chr12:38535710-38535760	HL-60	blood:	n/a
20	chr12:38448956-38449006	NHBE	bronchial:	n/a
21	chr12:38558124-38558174	GM19239	blood:	n/a
22	chr12:38724551-38724601	AG09309	skin:	n/a
23	chr12:38545214-38545264	AG04449	skin:	fetal
24	chr12:38556969-38557019	MCF-7	breast:	n/a
25	chr12:38710424-38710474	NH-A	brain:	n/a
26	chr12:38546326-38546376	U87	brain:	n/a
27	chr12:38531077-38531127	HepG2	liver:	n/a
28	chr12:38552636-38552686	HRE	kidney:	n/a
29	chr12:38447948-38447998	A549	lung:	n/a
30	chr12:38710452-38710502	ovcar-3	ovarian:	n/a
31	chr12:38551782-38551832	HCT-116	colon:	n/a
32	chr12:38710452-38710502	PrEC	prostate:	n/a
33	chr12:38447948-38447998	HRCEpiC	kidney:	n/a
34	chr12:38548782-38548832	HEEpiC	esophagus:	n/a
35	chr12:38710154-38710204	AG10803	skin:	n/a
36	chr12:38551782-38551832	ProgFib	skin:	n/a
37	chr12:38806793-38806843	PFSK-1	brain:	n/a
38	chr12:38557350-38557400	AG09319	gingival:	n/a
39	chr12:38556969-38557019	ovcar-3	ovarian:	n/a
40	chr12:38555256-38555306	HPAEpiC	pulmonary alveolar:	n/a
41	chr12:38710452-38710502	HNPCEpiC	eye:	n/a
42	chr12:38595404-38595454	SK-N-SH	brain:	n/a
43	chr12:38447636-38447686	HAEpiC	amniotic membrane:	n/a
44	chr12:38544936-38544986	HL-60	blood:	n/a
45	chr12:38447229-38447279	CMK	blood:	n/a
46	chr12:38531077-38531127	GM12878	blood:	n/a
47	chr12:38595601-38595651	SK-N-SH	brain:	n/a
48	chr12:38595404-38595454	BJ	skin:	n/a
49	chr12:38447636-38447686	HCM	heart:	n/a
50	chr12:38557350-38557400	T-47D	breast:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:38778961..38781578-chr12:38784417..38786236,2	MCF-7	breast:
2	chr12:38778961..38781578-chr12:38784417..38786236,2	MCF-7	breast:
3	chr12:38721916..38722780-chr12:39497511..39498068,2	MCF-7	breast:
4	chr12:38535401..38535902-chr2:133016817..133017415,2	MCF-7	breast:
5	chr12:38444870..38446430-chr16:33959034..33960923,3	MCF-7	breast:
6	chr12:38542302..38543806-chr20:26188737..26191492,2	K562	blood:
7	chr12:38843134..38845389-chr12:38847279..38849955,2	MCF-7	breast:
8	chr12:38764399..38764899-chr18:71815043..71815544,2	Hela-S3	cervix:
9	chr12:38637847..38640659-chr12:38643822..38646474,2	K562	blood:
10	chr12:38845594..38847956-chr12:38851662..38853438,2	K562	blood:
11	chr12:38722084..38722866-chr12:39667246..39667987,2	MCF-7	breast:
12	chr12:38444870..38446396-chr2:133021688..133023192,2	K562	blood:
13	chr12:38536304..38537296-chr14:88237622..88238153,2	K562	blood:
14	chr12:38845594..38847956-chr12:38851662..38853438,2	K562	blood:
15	chr12:38876753..38877648-chr6:116268599..116269448,2	MCF-7	breast:
16	chr12:38837698..38839402-chr12:38841166..38843830,2	K562	blood:
17	chr1:156185732..156186437-chr12:38543803..38544322,4	MCF-7	breast:
18	chr12:38721798..38722714-chr12:39305427..39306254,2	MCF-7	breast:
19	chr12:34241238..34243550-chr12:38853316..38855678,2	MCF-7	breast:
20	chr12:38444829..38445449-chr2:133022690..133023552,2	MCF-7	breast:
21	chr12:38447143..38447662-chr2:133026232..133026787,2	MCF-7	breast:
22	chr1:156185862..156186566-chr12:38543820..38544329,3	MCF-7	breast:
23	chr12:38843134..38845389-chr12:38847279..38849955,2	MCF-7	breast:
24	chr12:38532267..38533149-chr12:38709875..38710612,2	K562	blood:
25	chr12:38444806..38446368-chr16:33959419..33960990,2	MCF-7	breast:
26	chr1:186105531..186106141-chr12:38883322..38883955,2	MCF-7	breast:
27	chr12:38464739..38465619-chr4:45719335..45720093,2	MCF-7	breast:
28	chr1:156184764..156186317-chr12:38543820..38545325,2	K562	blood:
29	chr1:156185761..156186730-chr12:38543308..38544330,7	MCF-7	breast:
30	chr12:34405769..34407368-chr12:38464924..38466718,2	K562	blood:
31	chr12:38542306..38543824-chr20:26188496..26191492,2	K562	blood:
32	chr12:38536776..38537298-chr14:88237597..88238190,6	MCF-7	breast:
33	chr12:38637847..38640659-chr12:38643822..38646474,2	K562	blood:
34	chr12:38444887..38445591-chr16:33959228..33959997,3	MCF-7	breast:
35	chr1:156185820..156186795-chr12:38543314..38544329,6	MCF-7	breast:
36	chr12:38837698..38839402-chr12:38841166..38843830,2	K562	blood:
37	chr12:38450015..38451840-chr2:133028967..133030976,3	MCF-7	breast:
38	chr1:156184890..156186421-chr12:38543820..38545329,2	MCF-7	breast:
39	chr12:38543803..38545320-chr21:9824316..9826615,2	K562	blood:
40	chr12:38543320..38543832-chr21:9825931..9826770,2	K562	blood:
41	chr12:38532230..38532845-chr12:38709831..38710738,3	MCF-7	breast:
42	chr12:38542325..38545309-chr16:33964713..33967583,2	K562	blood:
43	chr12:38444306..38445077-chr21:37485779..37486279,2	MCF-7	breast:
44	chr12:34175001..34175865-chr12:38710413..38711151,3	HCT-116	colon:
45	chr12:38676913..38678502-chr12:38709612..38711993,2	MCF-7	breast:
46	chr12:38444597..38445444-chr16:33958723..33959994,4	MCF-7	breast:
47	chr12:38532568..38533113-chr12:39666750..39667387,2	K562	blood:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CPNE8-5	chr12:38837923-38838124	l_629_chr12:38821325-38838592_lung
2	lnc-CPNE8-7	chr12:38472331-38472801	NONHSAT027673
3	lnc-ALG10B-6	chr12:38449724-38450322	NONHSAT027672
4	lnc-ALG10B-3	chr12:38836308-38836412	NONHSAT027682
5	lnc-CPNE8-5	chr12:38821326-38822703	l_629_chr12:38821325-38838592_lung
6	lnc-ALG10B-4	chr12:38517498-38517593	NONHSAT027675
7	lnc-ALG10B-6	chr12:38451526-38451849	NONHSAT027672
8	lnc-CPNE8-6	chr12:38599188-38599814	NONHSAT027678
9	lnc-ALG10B-3	chr12:38847317-38847776	NONHSAT027683
10	lnc-CPNE8-5	chr12:38824250-38824373	l_629_chr12:38821325-38838592_lung
11	lnc-CPNE8-8	chr12:38447469-38447570	NONHSAT027671
12	lnc-CPNE8-5	chr12:38832098-38832212	l_629_chr12:38821325-38838592_lung
13	lnc-ALG10B-3	chr12:38846321-38846419	NONHSAT027683
14	lnc-CPNE8-8	chr12:38450354-38450755	NONHSAT027671
15	lnc-ALG10B-4	chr12:38520814-38520995	NONHSAT027675
16	lnc-CPNE8-5	chr12:38838505-38838592	l_629_chr12:38821325-38838592_lung
17	lnc-ALG10B-3	chr12:38847317-38847681	NONHSAT027682

No data

Variant related genes	Relation type
RNA5SP359	TF binding region
ENSG00000257173	TF binding region
TUBB8P5	TF binding region
ALG10B	TF binding region
ENSG00000253016	TF binding region
ENSG00000257292	TF binding region
ENSG00000258278	TF binding region
ENSG00000266333	TF binding region
ENSG00000258360	TF binding region
RNA5SP358	TF binding region
ENSG00000256878	TF binding region
RNA5SP359	CpG island
ENSG00000257173	CpG island
TUBB8P5	CpG island
ALG10B	CpG island
ENSG00000253016	CpG island
ENSG00000257292	CpG island
ENSG00000258278	CpG island
ENSG00000266333	CpG island
ENSG00000258360	CpG island
RNA5SP358	CpG island
ENSG00000256878	CpG island
ENSG00000264462	chromatin interactions
ENSG00000200434	chromatin interactions
ENSG00000175548	chromatin interactions
ENSG00000227195	chromatin interactions
ENSG00000264063	chromatin interactions
ENSG00000141665	chromatin interactions
ENSG00000139133	chromatin interactions

Extended variants
information (count: 31085 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:31085 , 50 per page) page: 1 2 3 4 5 6 7 ... 622

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551098697	chr12:38207030-38207031	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs570992226	chr12:38207039-38207040	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs533567918	chr12:38207041-38207042	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs370350214	chr12:38207049-38207050	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs553372387	chr12:38207063-38207064	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs573265766	chr12:38207082-38207083	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs374619600	chr12:38207121-38207122	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs536555279	chr12:38207127-38207128	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs186652712	chr12:38207128-38207129	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs191498330	chr12:38207138-38207139	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs544867329	chr12:38207142-38207143	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs534423235	chr12:38207155-38207156	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs578129219	chr12:38207170-38207171	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs372939947	chr12:38207212-38207213	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs540704375	chr12:38207227-38207228	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs555678910	chr12:38207234-38207235	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs181710780	chr12:38207266-38207267	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs186417189	chr12:38207285-38207286	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs376579965	chr12:38207298-38207299	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs544539382	chr12:38207305-38207306	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs61621942	chr12:38207306-38207307	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs111918852	chr12:38207308-38207309	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs191223773	chr12:38207363-38207364	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs199919994	chr12:38207381-38207382	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs562905968	chr12:38207383-38207384	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs183391418	chr12:38207385-38207386	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs145982431	chr12:38207386-38207387	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs567256086	chr12:38207417-38207418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs545115980	chr12:38207430-38207431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs556462137	chr12:38207441-38207442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs11495648	chr12:38207450-38207451	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs187469907	chr12:38207451-38207452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs558810236	chr12:38207457-38207458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs201810382	chr12:38207505-38207506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs112859905	chr12:38207513-38207514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201122707	chr12:38207517-38207518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs397849884	chr12:38207518-38207519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs78490406	chr12:38207520-38207521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs809739	chr12:38207525-38207526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs11179245	chr12:38207586-38207587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs554264571	chr12:38207642-38207643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs55962590	chr12:38207672-38207673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs372468290	chr12:38207673-38207674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs12423082	chr12:38207683-38207684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs561721743	chr12:38207692-38207693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs563222473	chr12:38207704-38207705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs529195982	chr12:38207713-38207714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs28507968	chr12:38207717-38207718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs377004850	chr12:38207746-38207747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs55745285	chr12:38207768-38207769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	20858243	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	21272361	CNVD
Autism	20531469	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1772 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:38206400-38207400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
2	chr12:38207400-38209800	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr12:38209800-38213200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
4	chr12:38209800-38215800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr12:38210000-38210600	ZNF genes & repeats	Adipose Nuclei	Adipose
6	chr12:38210000-38210800	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
7	chr12:38210200-38210600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
8	chr12:38210200-38210600	ZNF genes & repeats	Primary T killer memory cells from peripheral blood	blood
9	chr12:38216400-38216800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
10	chr12:38219600-38224600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
11	chr12:38228800-38229800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr12:38229200-38231400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
13	chr12:38230400-38238400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
14	chr12:38230400-38240600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr12:38231600-38232000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr12:38232000-38232200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr12:38233000-38243400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
18	chr12:38234200-38234600	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr12:38234400-38234600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr12:38234400-38234600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr12:38234400-38234600	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
22	chr12:38234400-38234600	ZNF genes & repeats	NH-A	brain
23	chr12:38234400-38234800	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr12:38234400-38234800	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
25	chr12:38234400-38234800	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
26	chr12:38234400-38234800	ZNF genes & repeats	Brain Hippocampus Middle	brain
27	chr12:38234400-38237800	ZNF genes & repeats	Liver	Liver
28	chr12:38234600-38235800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr12:38234800-38235800	Weak transcription	NH-A	brain
30	chr12:38235800-38236000	Enhancers	NH-A	brain
31	chr12:38235800-38236200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr12:38238800-38242400	ZNF genes & repeats	Liver	Liver
33	chr12:38242200-38249000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr12:38242600-38243400	ZNF genes & repeats	Adipose Nuclei	Adipose
35	chr12:38242800-38243400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr12:38246600-38248400	Weak transcription	Right Atrium	heart
37	chr12:38247800-38249000	ZNF genes & repeats	Liver	Liver
38	chr12:38247800-38249000	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
39	chr12:38247800-38250000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
40	chr12:38248000-38249000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
41	chr12:38248200-38248400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr12:38248200-38248400	Enhancers	Aorta	Aorta
43	chr12:38248200-38248400	Enhancers	Thymus	Thymus
44	chr12:38248200-38248800	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr12:38248200-38248800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
46	chr12:38248200-38248800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
47	chr12:38248200-38248800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr12:38248200-38248800	ZNF genes & repeats	Primary B cells from peripheral blood	blood
49	chr12:38248200-38248800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr12:38248200-38248800	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet

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