Variant report

Variant	nsv430724
Chromosome Location	chr2:37546820-37628704
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1871)
CpG islands
(count:1772)
Chromatin interactive
region (count:56)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1871 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:37552193-37552391	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:37561527-37561617	K562	blood:	n/a	n/a
3	ARID3A	chr2:37623091-37623410	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:37577106-37577517	HepG2	liver:	n/a	n/a
5	ATF1	chr2:37617624-37617917	K562	blood:	n/a	n/a
6	ATF1	chr2:37570916-37571082	K562	blood:	n/a	n/a
7	ATF2	chr2:37617085-37618190	GM12878	blood:	n/a	n/a
8	ATF2	chr2:37616992-37618390	GM12878	blood:	n/a	n/a
9	ATF2	chr2:37621361-37621836	GM12878	blood:	n/a	n/a
10	ATF2	chr2:37623009-37623320	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr2:37603422-37604696	GM12878	blood:	n/a	n/a
12	ATF2	chr2:37621331-37621814	GM12878	blood:	n/a	n/a
13	ATF2	chr2:37603327-37604723	GM12878	blood:	n/a	n/a
14	ATF3	chr2:37617663-37617929	K562	blood:	n/a	n/a
15	ATF3	chr2:37551727-37551962	K562	blood:	n/a	n/a
16	BACH1	chr2:37552372-37552375	K562	blood:	n/a	n/a
17	BACH1	chr2:37552113-37552380	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr2:37621461-37621765	GM12878	blood:	n/a	n/a
19	BATF	chr2:37592807-37593161	GM12878	blood:	n/a	n/a
20	BATF	chr2:37617246-37617989	GM12878	blood:	n/a	chr2:37617763-37617773 chr2:37617334-37617342
21	BATF	chr2:37604330-37604599	GM12878	blood:	n/a	n/a
22	BATF	chr2:37617114-37617996	GM12878	blood:	n/a	chr2:37617763-37617773 chr2:37617334-37617342
23	BATF	chr2:37592776-37593211	GM12878	blood:	n/a	n/a
24	BATF	chr2:37603476-37603965	GM12878	blood:	n/a	n/a
25	BATF	chr2:37603441-37604240	GM12878	blood:	n/a	chr2:37604023-37604032
26	BATF	chr2:37604273-37604670	GM12878	blood:	n/a	n/a
27	BCL11A	chr2:37604289-37604638	GM12878	blood:	n/a	n/a
28	BCL11A	chr2:37592868-37593224	GM12878	blood:	n/a	n/a
29	BCL11A	chr2:37621405-37621851	GM12878	blood:	n/a	n/a
30	BCL11A	chr2:37603523-37603907	GM12878	blood:	n/a	n/a
31	BCL11A	chr2:37617472-37617907	GM12878	blood:	n/a	chr2:37617802-37617811
32	BCL11A	chr2:37621405-37621768	GM12878	blood:	n/a	n/a
33	BCL11A	chr2:37604323-37604703	GM12878	blood:	n/a	n/a
34	BCL11A	chr2:37603413-37604222	GM12878	blood:	n/a	n/a
35	BCL11A	chr2:37617216-37617990	GM12878	blood:	n/a	chr2:37617802-37617811
36	BCL3	chr2:37617425-37617947	GM12878	blood:	n/a	chr2:37617802-37617811
37	BCL3	chr2:37603443-37603924	GM12878	blood:	n/a	n/a
38	BCL3	chr2:37551713-37552769	A549	lung:	n/a	chr2:37551761-37551774 chr2:37551765-37551774 chr2:37551768-37551777 chr2:37551759-37551768 chr2:37551760-37551773 chr2:37551763-37551776 chr2:37552068-37552081 chr2:37551762-37551771 chr2:37552069-37552078 chr2:37552050-37552063 chr2:37552030-37552038 chr2:37551722-37551731
39	BCLAF1	chr2:37603223-37603999	GM12878	blood:	n/a	n/a
40	BCLAF1	chr2:37617031-37618079	GM12878	blood:	n/a	chr2:37617802-37617811 chr2:37618048-37618057
41	BCLAF1	chr2:37550883-37551637	GM12878	blood:	n/a	chr2:37551555-37551564 chr2:37551550-37551563
42	BCLAF1	chr2:37603342-37604211	GM12878	blood:	n/a	n/a
43	BCLAF1	chr2:37621387-37621856	GM12878	blood:	n/a	n/a
44	BCLAF1	chr2:37617152-37618156	GM12878	blood:	n/a	chr2:37617802-37617811 chr2:37618048-37618057
45	BHLHE40	chr2:37604242-37604717	GM12878	blood:	n/a	n/a
46	BHLHE40	chr2:37617667-37617903	K562	blood:	n/a	n/a
47	BHLHE40	chr2:37554752-37554772	K562	blood:	n/a	n/a
48	BHLHE40	chr2:37617243-37617956	GM12878	blood:	n/a	n/a
49	BHLHE40	chr2:37598879-37599090	GM12878	blood:	n/a	n/a
50	BHLHE40	chr2:37621480-37621803	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:37571732-37571782	ovcar-3	ovarian:	n/a
2	chr2:37549315-37549365	Hela-S3	cervix:	n/a
3	chr2:37570604-37570654	ProgFib	skin:	n/a
4	chr2:37571732-37571782	ovcar-3	ovarian:	n/a
5	chr2:37549315-37549365	Hela-S3	cervix:	n/a
6	chr2:37570604-37570654	ProgFib	skin:	n/a
7	chr2:37571687-37571737	IMR90	lung:	fetal
8	chr2:37551081-37551131	PFSK-1	brain:	n/a
9	chr2:37551360-37551410	GM19239	blood:	n/a
10	chr2:37617601-37617651	ProgFib	skin:	n/a
11	chr2:37604081-37604131	AG04450	lung:	fetal
12	chr2:37553621-37553671	HEK293	kidney:	embryo
13	chr2:37553621-37553671	HEEpiC	esophagus:	n/a
14	chr2:37553621-37553671	HepG2	liver:	n/a
15	chr2:37604081-37604131	HIPEpiC	eye:	n/a
16	chr2:37594523-37594573	HEK293	kidney:	embryo
17	chr2:37571901-37571951	HCPEpiC	choroid plexus:	n/a
18	chr2:37571732-37571782	HUVEC	blood vessel:	n/a
19	chr2:37617601-37617651	NHDF-neo	bronchial:	n/a
20	chr2:37572102-37572152	Hela-S3	cervix:	n/a
21	chr2:37551081-37551131	Hela-S3	cervix:	n/a
22	chr2:37571677-37571727	K562	blood:	n/a
23	chr2:37617601-37617651	Jurkat	blood:	n/a
24	chr2:37571901-37571951	SK-N-MC	brain:	n/a
25	chr2:37551891-37551941	NH-A	brain:	n/a
26	chr2:37576821-37576871	LNCaP	prostate:	n/a
27	chr2:37570604-37570654	RPTEC	kidney:	n/a
28	chr2:37553621-37553671	Jurkat	blood:	n/a
29	chr2:37571178-37571228	CMK	blood:	n/a
30	chr2:37571687-37571737	HRCEpiC	kidney:	n/a
31	chr2:37571901-37571951	Hepatocyte	liver:	n/a
32	chr2:37572102-37572152	LNCaP	prostate:	n/a
33	chr2:37551081-37551131	HUVEC	blood vessel:	n/a
34	chr2:37600397-37600447	NT2-D1	testis:	n/a
35	chr2:37551024-37551074	AG04449	skin:	fetal
36	chr2:37554747-37554797	HCM	heart:	n/a
37	chr2:37571677-37571727	PrEC	prostate:	n/a
38	chr2:37551360-37551410	HEEpiC	esophagus:	n/a
39	chr2:37572102-37572152	AoSMC	blood vessel:	n/a
40	chr2:37572289-37572339	H1-hESC	embryonic stem cell:	embryo
41	chr2:37553621-37553671	AG10803	skin:	n/a
42	chr2:37572396-37572446	Hela-S3	cervix:	n/a
43	chr2:37551024-37551074	RPTEC	kidney:	n/a
44	chr2:37571687-37571737	ovcar-3	ovarian:	n/a
45	chr2:37594523-37594573	IMR90	lung:	fetal
46	chr2:37554747-37554797	SK-N-SH	brain:	n/a
47	chr2:37551108-37551158	T-47D	breast:	n/a
48	chr2:37571178-37571228	GM19239	blood:	n/a
49	chr2:37571178-37571228	Hepatocyte	liver:	n/a
50	chr2:37570604-37570654	HCF	heart:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:37540781..37542934-chr2:37546496..37548956,2	MCF-7	breast:
2	chr2:37545726..37548175-chr2:37554305..37557162,2	K562	blood:
3	chr2:37569671..37572468-chr2:37617600..37620463,2	MCF-7	breast:
4	chr2:37586244..37588961-chr2:37590934..37592508,2	K562	blood:
5	chr2:37445368..37447696-chr2:37615687..37618666,2	MCF-7	breast:
6	chr2:37584645..37586167-chr2:37590835..37592610,2	K562	blood:
7	chr2:37618498..37621396-chr2:37621786..37624740,2	K562	blood:
8	chr2:37616988..37619309-chr2:37620004..37622156,2	MCF-7	breast:
9	chr2:37622836..37623806-chr2:38104284..38105511,3	MCF-7	breast:
10	chr2:37586244..37588961-chr2:37590934..37592508,2	K562	blood:
11	chr2:37618498..37621396-chr2:37621786..37624740,2	K562	blood:
12	chr2:37541321..37543959-chr2:37558220..37560701,2	K562	blood:
13	chr2:37574642..37576209-chr2:37580099..37581679,2	K562	blood:
14	chr2:37553880..37556117-chr2:37565295..37568146,2	K562	blood:
15	chr2:37533235..37535380-chr2:37546761..37548910,2	MCF-7	breast:
16	chr2:37551825..37554292-chr2:37578586..37580717,2	K562	blood:
17	chr2:37585150..37587898-chr2:37588394..37591715,3	MCF-7	breast:
18	chr2:37533634..37536747-chr2:37545712..37547706,3	K562	blood:
19	chr2:37587482..37589041-chr2:37594550..37596941,2	K562	blood:
20	chr2:37622702..37623753-chr2:38104472..38105305,4	MCF-7	breast:
21	chr2:37617148..37619096-chr2:37640287..37642419,2	K562	blood:
22	chr2:37574642..37576209-chr2:37580099..37581679,2	K562	blood:
23	chr2:37466663..37469374-chr2:37548966..37550827,2	K562	blood:
24	chr2:37569565..37571229-chr2:37584533..37586394,2	K562	blood:
25	chr2:37453426..37455818-chr2:37549364..37551378,2	K562	blood:
26	chr2:37558808..37561496-chr2:37570984..37573398,2	MCF-7	breast:
27	chr2:37582825..37585072-chr2:37588211..37589764,2	MCF-7	breast:
28	chr2:37573383..37576359-chr2:37576591..37578098,2	K562	blood:
29	chr2:37622799..37624882-chr2:38117428..38119710,2	MCF-7	breast:
30	chr2:37573509..37575748-chr2:37602573..37605323,2	MCF-7	breast:
31	chr2:37551896..37552745-chr7:108166541..108167176,2	Hela-S3	cervix:
32	chr2:37616988..37619309-chr2:37620004..37622156,2	MCF-7	breast:
33	chr2:37579913..37583058-chr2:37585203..37589963,5	K562	blood:
34	chr2:37591915..37594227-chr2:37596693..37599097,2	MCF-7	breast:
35	chr2:37595963..37598255-chr2:37600328..37602598,2	MCF-7	breast:
36	chr17:3626527..3627417-chr2:37551455..37552202,2	NB4	blood:
37	chr2:37571184..37574506-chr2:37575236..37577117,3	MCF-7	breast:
38	chr2:37622662..37623680-chr2:38059375..38060179,5	K562	blood:
39	chr2:37622738..37623684-chr2:38059106..38060344,5	MCF-7	breast:
40	chr2:37582825..37585072-chr2:37588211..37589764,2	MCF-7	breast:
41	chr2:37549953..37551637-chr2:37554820..37556399,2	K562	blood:
42	chr2:37591915..37594227-chr2:37596693..37599097,2	MCF-7	breast:
43	chr2:37622806..37623442-chr2:38058313..38059174,2	K562	blood:
44	chr2:37553880..37556117-chr2:37565295..37568146,2	K562	blood:
45	chr2:37558808..37561496-chr2:37570984..37573398,2	MCF-7	breast:
46	chr2:37622553..37623459-chr2:38036724..38037237,2	MCF-7	breast:
47	chr2:37543073..37544935-chr2:37554432..37557348,2	K562	blood:
48	chr2:37595963..37598255-chr2:37600328..37602598,2	MCF-7	breast:
49	chr2:37595306..37596907-chr2:37600073..37601957,2	K562	blood:
50	chr2:37545726..37548175-chr2:37554305..37557162,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-QPCT-1	chr2:37553620-37553813	NONHSAT070118
2	lnc-QPCT-1	chr2:37553620-37553924	XLOC_001428
3	lnc-QPCT-1	chr2:37553620-37553940	XLOC_001428
4	lnc-QPCT-1	chr2:37552100-37552665	NONHSAT070118
5	lnc-QPCT-1	chr2:37552483-37552665	XLOC_001428
6	lnc-QPCT-1	chr2:37552203-37552259	XLOC_001428

No data

Variant related genes	Relation type
ENSG00000232028	TF binding region
RNU6-939P	TF binding region
QPCT	TF binding region
PRKD3	TF binding region
ENSG00000232028	CpG island
RNU6-939P	CpG island
QPCT	CpG island
PRKD3	CpG island
ENSG00000135241	chromatin interactions
ENSG00000232028	chromatin interactions
ENSG00000207364	chromatin interactions
ENSG00000177602	chromatin interactions
ENSG00000003509	chromatin interactions
ENSG00000115828	chromatin interactions
ENSG00000083457	chromatin interactions
ENSG00000115825	chromatin interactions

Extended variants
information (count: 3673 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:3673 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1158219	chr2:37546820-37546821	Weak transcription Enhancers Strong transcription Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs184009324	chr2:37546822-37546823	Weak transcription Enhancers Strong transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs543561143	chr2:37546829-37546830	Weak transcription Enhancers Strong transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs201035916	chr2:37546831-37546832	Weak transcription Enhancers Strong transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs1158218	chr2:37546845-37546846	Weak transcription Enhancers Strong transcription Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs540279666	chr2:37546846-37546847	Weak transcription Enhancers Strong transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs201486384	chr2:37546900-37546901	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs3050519	chr2:37546912-37546913	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs565323637	chr2:37546940-37546941	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs552474497	chr2:37546956-37546957	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs553224928	chr2:37546963-37546964	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs373179283	chr2:37546996-37546997	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs544330113	chr2:37547005-37547006	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs574592564	chr2:37547009-37547010	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs188644392	chr2:37547038-37547039	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs530631865	chr2:37547051-37547052	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs548736450	chr2:37547052-37547053	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs547003052	chr2:37547080-37547081	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs567450012	chr2:37547110-37547111	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs528345491	chr2:37547118-37547119	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs147185904	chr2:37547243-37547244	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs74863107	chr2:37547249-37547250	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs142889954	chr2:37547324-37547325	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs151056511	chr2:37547357-37547358	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs548645194	chr2:37547378-37547379	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs568944483	chr2:37547444-37547445	Weak transcription Strong transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs181062189	chr2:37547456-37547457	Weak transcription Strong transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs185222113	chr2:37547459-37547460	Weak transcription Strong transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs140960215	chr2:37547478-37547479	Weak transcription Strong transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs570761706	chr2:37547489-37547490	Weak transcription Strong transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs6722364	chr2:37547493-37547494	Weak transcription Strong transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs76421211	chr2:37547535-37547536	Weak transcription Strong transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs115751764	chr2:37547564-37547565	Weak transcription Strong transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs67189294	chr2:37547567-37547568	Weak transcription Strong transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs542565373	chr2:37547581-37547582	Weak transcription Strong transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs59526850	chr2:37547592-37547593	Weak transcription Strong transcription Active TSS Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs36104363	chr2:37547611-37547612	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs192072068	chr2:37547616-37547617	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs537250266	chr2:37547636-37547637	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs574543624	chr2:37547638-37547639	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs542464343	chr2:37547645-37547646	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs561176363	chr2:37547668-37547669	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs528268912	chr2:37547678-37547679	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs140691732	chr2:37547745-37547746	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs565161780	chr2:37547794-37547795	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs552776740	chr2:37547795-37547796	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs532161257	chr2:37547834-37547835	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs35157620	chr2:37547845-37547846	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs111435632	chr2:37547855-37547856	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs28710795	chr2:37547857-37547858	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:57)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD

Chromatin state (count:2213 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37484600-37550400	Weak transcription	Right Ventricle	heart
2	chr2:37509000-37550800	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr2:37511000-37550800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr2:37519000-37549400	Weak transcription	HSMM	muscle
5	chr2:37520200-37549600	Weak transcription	Fetal Muscle Leg	muscle
6	chr2:37520400-37549600	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr2:37520400-37550400	Weak transcription	Fetal Muscle Trunk	muscle
8	chr2:37530400-37548400	Weak transcription	K562	blood
9	chr2:37530600-37548200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr2:37530600-37550400	Weak transcription	Thymus	Thymus
11	chr2:37530800-37548600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr2:37530800-37549600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr2:37531000-37548600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr2:37533200-37550400	Weak transcription	Fetal Intestine Large	intestine
15	chr2:37533800-37549400	Weak transcription	Fetal Intestine Small	intestine
16	chr2:37534000-37550400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr2:37534400-37550400	Weak transcription	Lung	lung
18	chr2:37534400-37550600	Weak transcription	Left Ventricle	heart
19	chr2:37534600-37548400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr2:37534800-37548400	Weak transcription	A549	lung
21	chr2:37534800-37548800	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr2:37535000-37548400	Weak transcription	Duodenum Mucosa	Duodenum
23	chr2:37535000-37548600	Weak transcription	HUVEC	blood vessel
24	chr2:37535000-37549400	Weak transcription	Hela-S3	cervix
25	chr2:37535400-37548600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
26	chr2:37537000-37550400	Weak transcription	HSMMtube	muscle
27	chr2:37538400-37549600	Weak transcription	Psoas Muscle	Psoas
28	chr2:37538600-37548600	Weak transcription	Liver	Liver
29	chr2:37539000-37548400	Weak transcription	Primary hematopoietic stem cells	blood
30	chr2:37539800-37548600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
31	chr2:37539800-37548800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
32	chr2:37540600-37547400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr2:37540600-37548600	Weak transcription	Brain Hippocampus Middle	brain
34	chr2:37542000-37550400	Weak transcription	Colonic Mucosa	Colon
35	chr2:37542400-37548400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr2:37542400-37550800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr2:37542800-37548400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
38	chr2:37542800-37548400	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr2:37542800-37549600	Weak transcription	Stomach Smooth Muscle	stomach
40	chr2:37542800-37550800	Weak transcription	Gastric	stomach
41	chr2:37543000-37550400	Weak transcription	Primary T cells fromperipheralblood	blood
42	chr2:37543400-37548400	Enhancers	Colon Smooth Muscle	Colon
43	chr2:37543600-37548400	Weak transcription	Spleen	Spleen
44	chr2:37543600-37548400	Weak transcription	HepG2	liver
45	chr2:37543600-37548600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr2:37543600-37548800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr2:37543600-37548800	Weak transcription	Small Intestine	intestine
48	chr2:37543600-37549400	Weak transcription	Right Atrium	heart
49	chr2:37543600-37550400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr2:37543800-37548400	Weak transcription	Primary T cells from cord blood	blood

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