Variant report

Variant	nsv830265
Chromosome Location	chr5:37152221-37312233
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1107)
CpG islands
(count:1037)
Chromatin interactive
region (count:66)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1107 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:37187395-37187971	K562	blood:	n/a	n/a
2	ARID3A	chr5:37186654-37186894	K562	blood:	n/a	n/a
3	ARID3A	chr5:37249328-37249415	HepG2	liver:	n/a	n/a
4	ATF1	chr5:37212334-37212527	K562	blood:	n/a	n/a
5	ATF2	chr5:37249330-37249721	GM12878	blood:	n/a	n/a
6	ATF3	chr5:37272710-37273010	A549	lung:	n/a	n/a
7	ATF3	chr5:37199018-37199279	K562	blood:	n/a	n/a
8	BACH1	chr5:37305059-37305259	K562	blood:	n/a	n/a
9	BACH1	chr5:37249622-37249625	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr5:37226577-37226771	K562	blood:	n/a	n/a
11	BATF	chr5:37184885-37185136	GM12878	blood:	n/a	n/a
12	BCL11A	chr5:37197865-37198057	GM12878	blood:	n/a	n/a
13	BCL11A	chr5:37184880-37185082	GM12878	blood:	n/a	n/a
14	BCL3	chr5:37249087-37249607	A549	lung:	n/a	chr5:37249490-37249503 chr5:37249563-37249572
15	BCLAF1	chr5:37248901-37249584	GM12878	blood:	n/a	chr5:37249490-37249503 chr5:37249563-37249572
16	BHLHE40	chr5:37184866-37185356	GM12878	blood:	n/a	n/a
17	BHLHE40	chr5:37209321-37209328	K562	blood:	n/a	n/a
18	BHLHE40	chr5:37182444-37182640	GM12878	blood:	n/a	n/a
19	BHLHE40	chr5:37215222-37215328	GM12878	blood:	n/a	n/a
20	BRCA1	chr5:37272337-37273087	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr5:37248654-37249941	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr5:37174252-37174265	Hela-S3	cervix:	n/a	n/a
23	CBX3	chr5:37280036-37280373	K562	blood:	n/a	n/a
24	CBX3	chr5:37283321-37283700	K562	blood:	n/a	n/a
25	CBX3	chr5:37283319-37283770	K562	blood:	n/a	n/a
26	CBX3	chr5:37280051-37280337	K562	blood:	n/a	n/a
27	CEBPB	chr5:37225762-37225958	A549	lung:	n/a	n/a
28	CEBPB	chr5:37272622-37273009	ECC-1	luminal epithelium:	n/a	n/a
29	CEBPB	chr5:37198996-37199280	H1-hESC	embryonic stem cell:	n/a	chr5:37199149-37199160
30	CEBPB	chr5:37225787-37226067	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr5:37197783-37198047	IMR90	lung:	n/a	n/a
32	CEBPB	chr5:37272582-37273001	A549	lung:	n/a	n/a
33	CEBPB	chr5:37198988-37199323	IMR90	lung:	n/a	chr5:37199149-37199160
34	CEBPB	chr5:37310532-37310827	IMR90	lung:	n/a	chr5:37310662-37310673
35	CEBPB	chr5:37308914-37309247	Hela-S3	cervix:	n/a	chr5:37309062-37309073
36	CEBPB	chr5:37206917-37207168	K562	blood:	n/a	chr5:37207041-37207052 chr5:37207040-37207053
37	CEBPB	chr5:37225759-37225962	IMR90	lung:	n/a	n/a
38	CEBPB	chr5:37293342-37293474	A549	lung:	n/a	n/a
39	CEBPB	chr5:37272620-37272986	MCF-7	breast:	n/a	n/a
40	CEBPB	chr5:37180286-37180459	H1-hESC	embryonic stem cell:	n/a	chr5:37180403-37180414
41	CEBPB	chr5:37180266-37180438	HepG2	liver:	n/a	chr5:37180403-37180414
42	CEBPB	chr5:37308942-37309236	IMR90	lung:	n/a	chr5:37309062-37309073
43	CEBPB	chr5:37310517-37310821	HepG2	liver:	n/a	chr5:37310662-37310673
44	CEBPB	chr5:37206853-37207237	Hela-S3	cervix:	n/a	chr5:37207041-37207052 chr5:37207040-37207053
45	CEBPB	chr5:37308976-37309284	MCF-7	breast:	n/a	chr5:37309062-37309073
46	CEBPB	chr5:37225778-37226022	K562	blood:	n/a	n/a
47	CEBPB	chr5:37206894-37207221	HepG2	liver:	n/a	chr5:37207041-37207052 chr5:37207040-37207053
48	CEBPB	chr5:37308935-37309219	HepG2	liver:	n/a	chr5:37309062-37309073
49	CEBPB	chr5:37308935-37309170	K562	blood:	n/a	chr5:37309062-37309073
50	CEBPB	chr5:37206881-37207206	IMR90	lung:	n/a	chr5:37207041-37207052 chr5:37207040-37207053

(count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:37249567-37249617	GM12892	blood:	n/a
2	chr5:37209268-37209318	HNPCEpiC	eye:	n/a
3	chr5:37212448-37212498	MCF-7	breast:	n/a
4	chr5:37207622-37207672	HepG2	liver:	n/a
5	chr5:37209332-37209382	H1-hESC	embryonic stem cell:	embryo
6	chr5:37209268-37209318	RPTEC	kidney:	n/a
7	chr5:37209440-37209490	BE2_C	brain:	n/a
8	chr5:37249909-37249959	HAEpiC	amniotic membrane:	n/a
9	chr5:37209332-37209382	PrEC	prostate:	n/a
10	chr5:37207622-37207672	HUVEC	blood vessel:	n/a
11	chr5:37209440-37209490	LNCaP	prostate:	n/a
12	chr5:37209268-37209318	PANC-1	pancreas:	n/a
13	chr5:37211096-37211146	AG10803	skin:	n/a
14	chr5:37208976-37209026	HEK293	kidney:	embryo
15	chr5:37248984-37249034	AG09319	gingival:	n/a
16	chr5:37212448-37212498	LNCaP	prostate:	n/a
17	chr5:37248984-37249034	AG04449	skin:	fetal
18	chr5:37249405-37249455	HCF	heart:	n/a
19	chr5:37251010-37251060	HEEpiC	esophagus:	n/a
20	chr5:37249405-37249455	HMEC	breast:	n/a
21	chr5:37249567-37249617	MCF-7	breast:	n/a
22	chr5:37249567-37249617	HAEpiC	amniotic membrane:	n/a
23	chr5:37209268-37209318	NHBE	bronchial:	n/a
24	chr5:37209182-37209232	NHBE	bronchial:	n/a
25	chr5:37250092-37250142	NHBE	bronchial:	n/a
26	chr5:37251010-37251060	HCF	heart:	n/a
27	chr5:37251010-37251060	A549	lung:	n/a
28	chr5:37248984-37249034	HEK293	kidney:	embryo
29	chr5:37248984-37249034	ProgFib	skin:	n/a
30	chr5:37207622-37207672	PANC-1	pancreas:	n/a
31	chr5:37209440-37209490	ECC-1	luminal epithelium:	n/a
32	chr5:37249223-37249273	IMR90	lung:	fetal
33	chr5:37248984-37249034	AG04450	lung:	fetal
34	chr5:37209182-37209232	ovcar-3	ovarian:	n/a
35	chr5:37249909-37249959	GM12892	blood:	n/a
36	chr5:37206515-37206565	HRE	kidney:	n/a
37	chr5:37248894-37248944	GM12892	blood:	n/a
38	chr5:37212448-37212498	AG09309	skin:	n/a
39	chr5:37209268-37209318	SK-N-SH	brain:	n/a
40	chr5:37209268-37209318	AG04450	lung:	fetal
41	chr5:37209268-37209318	Jurkat	blood:	n/a
42	chr5:37250092-37250142	AG04450	lung:	fetal
43	chr5:37208976-37209026	SAEC	small airway:	n/a
44	chr5:37249909-37249959	ovcar-3	ovarian:	n/a
45	chr5:37211096-37211146	AG09319	gingival:	n/a
46	chr5:37249405-37249455	Caco-2	colon:	n/a
47	chr5:37206515-37206565	AG04450	lung:	fetal
48	chr5:37249405-37249455	ovcar-3	ovarian:	n/a
49	chr5:37209440-37209490	PFSK-1	brain:	n/a
50	chr5:37209332-37209382	ProgFib	skin:	n/a

(count:66 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:95867838..95868385-chr5:37249139..37249647,2	Hela-S3	cervix:
2	chr5:37161788..37164617-chr5:37168284..37171187,2	K562	blood:
3	chr5:37219467..37221366-chr5:37223359..37224948,2	K562	blood:
4	chr5:37242850..37244799-chr5:37268818..37270992,2	MCF-7	breast:
5	chr5:37189588..37191318-chr5:37194423..37196397,2	K562	blood:
6	chr5:37239505..37242479-chr5:37244689..37246213,2	MCF-7	breast:
7	chr5:37231083..37232617-chr5:37243518..37245919,2	K562	blood:
8	chr5:37244319..37247437-chr5:37248031..37251100,3	MCF-7	breast:
9	chr5:37225065..37226567-chr5:37275200..37277689,2	K562	blood:
10	chr5:37196006..37197813-chr5:37198667..37201494,2	K562	blood:
11	chr5:37207387..37209456-chr5:37214290..37217220,2	K562	blood:
12	chr19:55918635..55919160-chr5:37249246..37250155,2	Hela-S3	cervix:
13	chr5:37296733..37298868-chr5:37344772..37346341,2	K562	blood:
14	chr5:37270941..37273083-chr5:37281934..37283634,2	MCF-7	breast:
15	chr5:37247385..37249387-chr5:37291319..37293555,2	MCF-7	breast:
16	chr5:37300122..37302180-chr5:37303244..37306127,2	K562	blood:
17	chr5:37308340..37310527-chr5:37313095..37315302,2	K562	blood:
18	chr5:37247385..37249387-chr5:37291319..37293555,2	MCF-7	breast:
19	chr5:37239505..37242479-chr5:37244689..37246213,2	MCF-7	breast:
20	chr5:37161560..37164016-chr5:37164106..37165808,2	MCF-7	breast:
21	chr12:54388997..54389960-chr5:37248812..37249668,2	Hela-S3	cervix:
22	chr12:27397103..27397782-chr5:37248907..37249410,2	Hela-S3	cervix:
23	chr19:10612852..10613551-chr5:37248973..37249815,2	NB4	blood:
24	chr19:10222166..10222747-chr5:37249630..37250278,2	NB4	blood:
25	chr5:37288508..37291349-chr5:37291892..37294572,2	K562	blood:
26	chr5:37217019..37219861-chr5:37224561..37226290,2	MCF-7	breast:
27	chr5:37178213..37179782-chr5:37187972..37190398,2	K562	blood:
28	chr5:37161788..37164617-chr5:37168284..37171187,2	K562	blood:
29	chr5:37229744..37231254-chr5:37247811..37249701,2	MCF-7	breast:
30	chr5:37248986..37251639-chr5:37261227..37263594,2	MCF-7	breast:
31	chr16:2517911..2518776-chr5:37248952..37249746,2	Hela-S3	cervix:
32	chr5:37230434..37232617-chr5:37243518..37246467,2	K562	blood:
33	chr5:37231083..37232617-chr5:37243518..37245919,2	K562	blood:
34	chr11:67888391..67888933-chr5:37248964..37249645,2	Hela-S3	cervix:
35	chr5:37219467..37221366-chr5:37223359..37224948,2	K562	blood:
36	chr5:37248443..37250196-chr5:37254645..37256658,2	MCF-7	breast:
37	chr5:37197567..37199786-chr5:37206533..37208192,2	MCF-7	breast:
38	chr5:37270941..37273083-chr5:37281934..37283634,2	MCF-7	breast:
39	chr5:37198464..37201243-chr5:37207521..37209489,3	MCF-7	breast:
40	chr5:37242850..37244799-chr5:37268818..37270992,2	MCF-7	breast:
41	chr11:75110443..75111008-chr5:37248561..37249187,2	Hela-S3	cervix:
42	chr5:37197697..37200304-chr5:37369735..37371837,2	MCF-7	breast:
43	chr5:37219759..37221366-chr5:37222603..37224859,2	K562	blood:
44	chr5:37208938..37209800-chrX:13752746..13753402,2	Hela-S3	cervix:
45	chr5:37249278..37249862-chr6:27805404..27806202,2	Hela-S3	cervix:
46	chr5:37178213..37179782-chr5:37187972..37190398,2	K562	blood:
47	chr19:11450158..11450732-chr5:37248969..37249920,2	Hela-S3	cervix:
48	chr3:52016674..52017877-chr5:37249098..37249636,3	Hela-S3	cervix:
49	chr5:37230434..37232617-chr5:37243518..37246467,2	K562	blood:
50	chr5:37248573..37251161-chr5:37251715..37254222,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUP155-4	chr5:37157770-37157916	NONHSAT101054
2	lnc-NUP155-3	chr5:37176011-37176201	NONHSAT101055
3	lnc-NUP155-3	chr5:37169634-37169663	NONHSAT101055
4	lnc-WDR70-5	chr5:37248948-37249323	NONHSAT101057
5	lnc-WDR70-5	chr5:37250499-37250654	NONHSAT101058
6	lnc-NUP155-4	chr5:37158326-37158447	NONHSAT101054
7	lnc-NUP155-4	chr5:37162567-37162756	NONHSAT101054
8	lnc-WDR70-5	chr5:37249174-37249323	NONHSAT101058
9	lnc-NUP155-3	chr5:37173857-37174049	NONHSAT101055
10	lnc-NUP155-1	chr5:37286551-37287079	NONHSAT101059
11	lnc-WDR70-5	chr5:37254685-37254730	NONHSAT101057
12	lnc-NUP155-2	chr5:37246277-37246581	NONHSAT101056
13	lnc-NUP155-3	chr5:37170143-37170433	NONHSAT101055

No data

Variant related genes	Relation type
C5orf42	TF binding region
OFD1P17	TF binding region
RN7SL37P	TF binding region
ENSG00000270558	TF binding region
NUP155	TF binding region
C5orf42	CpG island
OFD1P17	CpG island
RN7SL37P	CpG island
ENSG00000270558	CpG island
NUP155	CpG island
ENSG00000197603	chromatin interactions
ENSG00000184348	chromatin interactions
ENSG00000180806	chromatin interactions
ENSG00000259895	chromatin interactions
ENSG00000149273	chromatin interactions
ENSG00000243989	chromatin interactions
ENSG00000046651	chromatin interactions
ENSG00000242493	chromatin interactions
ENSG00000228212	chromatin interactions
ENSG00000114779	chromatin interactions
ENSG00000110721	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000211455	chromatin interactions
ENSG00000250133	chromatin interactions
ENSG00000108106	chromatin interactions
ENSG00000113569	chromatin interactions
ENSG00000105514	chromatin interactions
ENSG00000244165	chromatin interactions
ENSG00000214770	chromatin interactions
ENSG00000111142	chromatin interactions
ENSG00000196459	chromatin interactions
ENSG00000079999	chromatin interactions

Extended variants
information (count: 5819 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:5819 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561982323	chr5:37152243-37152244	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs569022357	chr5:37152245-37152246	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs531348835	chr5:37152285-37152286	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs78166663	chr5:37152288-37152289	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs192325564	chr5:37152330-37152331	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs566511700	chr5:37152355-37152356	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs534118799	chr5:37152375-37152376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs552142765	chr5:37152376-37152377	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs143864559	chr5:37152429-37152430	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs376959581	chr5:37152440-37152441	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs138540793	chr5:37152456-37152457	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs184708425	chr5:37152472-37152473	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs143056030	chr5:37152478-37152479	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs550628023	chr5:37152484-37152485	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs376710865	chr5:37152490-37152491	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs78888706	chr5:37152497-37152498	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs114606840	chr5:37152531-37152532	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs189875706	chr5:37152579-37152580	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs56769263	chr5:37152597-37152598	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs566223711	chr5:37152656-37152657	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs10068501	chr5:37152734-37152735	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs564665843	chr5:37152745-37152746	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs527773757	chr5:37152817-37152818	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs576804510	chr5:37152865-37152866	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs544252174	chr5:37152867-37152868	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs562449661	chr5:37152920-37152921	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs140185344	chr5:37152955-37152956	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs548276403	chr5:37152977-37152978	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs560302010	chr5:37152994-37152995	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs148304320	chr5:37153052-37153053	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs527457137	chr5:37153088-37153089	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs193169860	chr5:37153221-37153222	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564967725	chr5:37153256-37153257	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs552342192	chr5:37153277-37153278	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570704773	chr5:37153357-37153358	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs537726955	chr5:37153372-37153373	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs549798550	chr5:37153389-37153390	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs568079670	chr5:37153393-37153394	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs146707677	chr5:37153417-37153418	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs545924313	chr5:37153423-37153424	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs185301630	chr5:37153522-37153523	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs553933881	chr5:37153528-37153529	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs572491714	chr5:37153529-37153530	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs564114917	chr5:37153639-37153640	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs113402646	chr5:37153658-37153659	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs114254915	chr5:37153663-37153664	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs73750938	chr5:37153714-37153715	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs544092729	chr5:37153722-37153723	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs60942985	chr5:37153728-37153729	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs189754732	chr5:37153791-37153792	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Myofibroblastic sarcoma	19369631	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Lung cancer	19153074	CNVD
Cornelia de Lange syndrome	21085971	CNVD
Autism	21701786	CNVD
Cervical cancer	16585170	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Autism	22549408	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:3729 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:37082800-37169200	Weak transcription	Spleen	Spleen
2	chr5:37105800-37156200	Weak transcription	NHLF	lung
3	chr5:37112200-37198200	Weak transcription	Small Intestine	intestine
4	chr5:37113600-37222200	Weak transcription	Psoas Muscle	Psoas
5	chr5:37113800-37157000	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chr5:37114600-37165400	Weak transcription	HMEC	breast
7	chr5:37118600-37153600	Weak transcription	Pancreas	Pancrea
8	chr5:37122000-37156000	Weak transcription	Brain Substantia Nigra	brain
9	chr5:37133200-37169400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr5:37134200-37171200	Weak transcription	Colonic Mucosa	Colon
11	chr5:37136200-37197200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr5:37136800-37170000	Weak transcription	Esophagus	oesophagus
13	chr5:37137400-37174000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr5:37137600-37169000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr5:37138000-37156000	Weak transcription	Aorta	Aorta
16	chr5:37138000-37157000	Weak transcription	Colon Smooth Muscle	Colon
17	chr5:37138400-37155200	Weak transcription	Brain Angular Gyrus	brain
18	chr5:37138400-37156800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr5:37138400-37196800	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr5:37138600-37153400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr5:37138600-37179600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
22	chr5:37138800-37156800	Weak transcription	HUVEC	blood vessel
23	chr5:37143000-37153400	Weak transcription	Rectal Mucosa Donor 29	rectum
24	chr5:37143400-37189600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr5:37143600-37156000	Weak transcription	Primary B cells from peripheral blood	blood
26	chr5:37143600-37157200	Weak transcription	Monocytes-CD14+_RO01746	blood
27	chr5:37143800-37152800	Weak transcription	Duodenum Mucosa	Duodenum
28	chr5:37143800-37153400	Weak transcription	HepG2	liver
29	chr5:37143800-37169200	Weak transcription	Primary T helper cells PMA-I stimulated	--
30	chr5:37144000-37153200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr5:37144000-37154800	Weak transcription	Gastric	stomach
32	chr5:37144000-37156000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr5:37144200-37156400	Weak transcription	Fetal Brain Male	brain
34	chr5:37144400-37153400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr5:37144400-37153800	Weak transcription	Primary hematopoietic stem cells	blood
36	chr5:37144400-37156000	Weak transcription	Lung	lung
37	chr5:37144400-37171400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr5:37144800-37152400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr5:37145600-37158800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr5:37146400-37174000	Weak transcription	GM12878-XiMat	blood
41	chr5:37146800-37152400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr5:37147200-37158600	Strong transcription	Dnd41	blood
43	chr5:37147200-37200600	Strong transcription	HSMM	muscle
44	chr5:37147400-37158600	Strong transcription	Adipose Nuclei	Adipose
45	chr5:37147600-37158400	Strong transcription	Stomach Smooth Muscle	stomach
46	chr5:37147800-37157400	Strong transcription	Fetal Intestine Large	intestine
47	chr5:37147800-37158600	Strong transcription	Fetal Lung	lung
48	chr5:37148000-37153800	Strong transcription	Placenta	Placenta
49	chr5:37148000-37156800	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr5:37148000-37182000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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