Variant report

Variant	nsv877554
Chromosome Location	chr3:141735532-141781890
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:784)
CpG islands
(count:306)
Chromatin interactive
region (count:48)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:784 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:141747897-141748597	K562	blood:	n/a	n/a
2	ARID3A	chr3:141740016-141740343	K562	blood:	n/a	n/a
3	ARID3A	chr3:141764957-141766278	K562	blood:	n/a	n/a
4	ARID3A	chr3:141745272-141745595	K562	blood:	n/a	n/a
5	ARID3A	chr3:141741164-141741659	K562	blood:	n/a	n/a
6	ARID3A	chr3:141746444-141747694	K562	blood:	n/a	chr3:141747189-141747205 chr3:141747188-141747204
7	ARID3A	chr3:141735922-141736175	K562	blood:	n/a	n/a
8	ARID3A	chr3:141744250-141744556	K562	blood:	n/a	n/a
9	ATF1	chr3:141735776-141736084	K562	blood:	n/a	n/a
10	ATF1	chr3:141741219-141741530	K562	blood:	n/a	n/a
11	ATF1	chr3:141765160-141765905	K562	blood:	n/a	n/a
12	ATF2	chr3:141741158-141741597	GM12878	blood:	n/a	n/a
13	ATF2	chr3:141738599-141738995	GM12878	blood:	n/a	n/a
14	ATF3	chr3:141765113-141765513	K562	blood:	n/a	n/a
15	BACH1	chr3:141744283-141744373	K562	blood:	n/a	n/a
16	BATF	chr3:141738609-141738930	GM12878	blood:	n/a	chr3:141738775-141738786
17	BATF	chr3:141741262-141741489	GM12878	blood:	n/a	n/a
18	BATF	chr3:141738639-141738904	GM12878	blood:	n/a	chr3:141738775-141738786
19	BATF	chr3:141747857-141748258	GM12878	blood:	n/a	n/a
20	BCLAF1	chr3:141747250-141747705	GM12878	blood:	n/a	n/a
21	BHLHE40	chr3:141764829-141766005	K562	blood:	n/a	n/a
22	BHLHE40	chr3:141747846-141747861	K562	blood:	n/a	n/a
23	BHLHE40	chr3:141747331-141748152	GM12878	blood:	n/a	n/a
24	BHLHE40	chr3:141746686-141746878	K562	blood:	n/a	n/a
25	BHLHE40	chr3:141741289-141741610	K562	blood:	n/a	n/a
26	CBX3	chr3:141754371-141754865	K562	blood:	n/a	n/a
27	CBX3	chr3:141747898-141748286	K562	blood:	n/a	n/a
28	CBX3	chr3:141765122-141765498	K562	blood:	n/a	n/a
29	CBX3	chr3:141747257-141747778	HCT-116	colon:	n/a	n/a
30	CBX3	chr3:141746543-141746981	HCT-116	colon:	n/a	n/a
31	CBX3	chr3:141741159-141741668	K562	blood:	n/a	n/a
32	CBX3	chr3:141764881-141765958	K562	blood:	n/a	n/a
33	CCNT2	chr3:141748024-141748269	K562	blood:	n/a	n/a
34	CCNT2	chr3:141735791-141736203	K562	blood:	n/a	n/a
35	CCNT2	chr3:141765174-141766037	K562	blood:	n/a	chr3:141765396-141765416 chr3:141765789-141765809
36	CCNT2	chr3:141741211-141741629	K562	blood:	n/a	chr3:141741410-141741430
37	CEBPB	chr3:141753473-141753678	K562	blood:	n/a	n/a
38	CEBPB	chr3:141738780-141739134	Hela-S3	cervix:	n/a	chr3:141738950-141738963 chr3:141738932-141738943
39	CEBPB	chr3:141765167-141765981	K562	blood:	n/a	n/a
40	CEBPB	chr3:141764863-141766102	K562	blood:	n/a	n/a
41	CEBPB	chr3:141738846-141739042	A549	lung:	n/a	chr3:141738950-141738963 chr3:141738932-141738943
42	CEBPB	chr3:141738801-141739090	K562	blood:	n/a	chr3:141738950-141738963 chr3:141738932-141738943
43	CEBPB	chr3:141738808-141739134	IMR90	lung:	n/a	chr3:141738950-141738963 chr3:141738932-141738943
44	CEBPB	chr3:141741155-141741617	K562	blood:	n/a	n/a
45	CEBPB	chr3:141741296-141741599	K562	blood:	n/a	n/a
46	CEBPB	chr3:141738629-141739213	HCT-116	colon:	n/a	chr3:141738950-141738963 chr3:141738932-141738943
47	CEBPB	chr3:141765132-141765508	K562	blood:	n/a	n/a
48	CEBPD	chr3:141765044-141766325	K562	blood:	n/a	n/a
49	CEBPD	chr3:141765060-141766118	K562	blood:	n/a	n/a
50	CEBPD	chr3:141752114-141752428	K562	blood:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:141762780-141762830	SK-N-MC	brain:	n/a
2	chr3:141762780-141762830	SK-N-MC	brain:	n/a
3	chr3:141748862-141748912	NHDF-neo	bronchial:	n/a
4	chr3:141762828-141762878	GM19239	blood:	n/a
5	chr3:141762963-141763013	CMK	blood:	n/a
6	chr3:141762828-141762878	SKMC	muscle:	n/a
7	chr3:141762780-141762830	GM12878	blood:	n/a
8	chr3:141762963-141763013	HMEC	breast:	n/a
9	chr3:141762780-141762830	MCF10A-Er-Src	breast:	n/a
10	chr3:141764977-141765027	HEEpiC	esophagus:	n/a
11	chr3:141748862-141748912	HEEpiC	esophagus:	n/a
12	chr3:141764977-141765027	ECC-1	luminal epithelium:	n/a
13	chr3:141762828-141762878	HAEpiC	amniotic membrane:	n/a
14	chr3:141764977-141765027	HRE	kidney:	n/a
15	chr3:141748862-141748912	AG09309	skin:	n/a
16	chr3:141762963-141763013	HRPEpiC	eye:	n/a
17	chr3:141764977-141765027	HPAEpiC	pulmonary alveolar:	n/a
18	chr3:141764977-141765027	AG04450	lung:	fetal
19	chr3:141748862-141748912	Jurkat	blood:	n/a
20	chr3:141764977-141765027	H1-hESC	embryonic stem cell:	embryo
21	chr3:141762963-141763013	AG09309	skin:	n/a
22	chr3:141748862-141748912	HUVEC	blood vessel:	n/a
23	chr3:141762780-141762830	AG04449	skin:	fetal
24	chr3:141762828-141762878	HNPCEpiC	eye:	n/a
25	chr3:141748862-141748912	HPAEpiC	pulmonary alveolar:	n/a
26	chr3:141762963-141763013	ovcar-3	ovarian:	n/a
27	chr3:141762963-141763013	BJ	skin:	n/a
28	chr3:141762963-141763013	HEK293	kidney:	embryo
29	chr3:141762963-141763013	U87	brain:	n/a
30	chr3:141762963-141763013	A549	lung:	n/a
31	chr3:141748862-141748912	HCPEpiC	choroid plexus:	n/a
32	chr3:141764977-141765027	HL-60	blood:	n/a
33	chr3:141748862-141748912	RPTEC	kidney:	n/a
34	chr3:141762780-141762830	SK-N-SH_RA	brain:	n/a
35	chr3:141762828-141762878	HCT-116	colon:	n/a
36	chr3:141762828-141762878	AG04450	lung:	fetal
37	chr3:141762780-141762830	NB4	blood:	n/a
38	chr3:141762828-141762878	GM06990	blood:	n/a
39	chr3:141748862-141748912	SK-N-SH_RA	brain:	n/a
40	chr3:141762963-141763013	GM12892	blood:	n/a
41	chr3:141748862-141748912	HRCEpiC	kidney:	n/a
42	chr3:141762780-141762830	AoSMC	blood vessel:	n/a
43	chr3:141762963-141763013	LNCaP	prostate:	n/a
44	chr3:141762780-141762830	SAEC	small airway:	n/a
45	chr3:141762780-141762830	ECC-1	luminal epithelium:	n/a
46	chr3:141762828-141762878	ECC-1	luminal epithelium:	n/a
47	chr3:141762780-141762830	HL-60	blood:	n/a
48	chr3:141762828-141762878	U87	brain:	n/a
49	chr3:141748862-141748912	AG10803	skin:	n/a
50	chr3:141762780-141762830	HCM	heart:	n/a

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:141767270..141770576-chr3:141773885..141776587,3	K562	blood:
2	chr3:141743896..141745578-chr3:141745998..141747599,2	MCF-7	breast:
3	chr3:141752908..141754951-chr3:141758367..141761126,3	K562	blood:
4	chr3:141767270..141770576-chr3:141773885..141776587,3	K562	blood:
5	chr3:141743220..141745863-chr3:141763714..141765255,2	K562	blood:
6	chr3:141739963..141741863-chr3:141746607..141749166,2	MCF-7	breast:
7	chr1:202085934..202088826-chr3:141779136..141781977,2	K562	blood:
8	chr3:141732044..141735482-chr3:141738671..141741539,4	MCF-7	breast:
9	chr3:141736074..141738288-chr3:141741449..141743046,2	K562	blood:
10	chr3:141765382..141767176-chr3:141772359..141774549,2	K562	blood:
11	chr3:141765860..141768702-chr3:141834792..141837643,2	K562	blood:
12	chr3:141772397..141774089-chr3:141777472..141780381,2	K562	blood:
13	chr3:141740917..141741877-chr3:141764906..141765846,2	K562	blood:
14	chr3:141746178..141749439-chr3:141764015..141767847,4	K562	blood:
15	chr3:141742047..141744583-chr3:141758221..141760066,2	K562	blood:
16	chr3:141724450..141726280-chr3:141745104..141746996,2	K562	blood:
17	chr3:141740917..141741877-chr3:141764906..141765846,2	K562	blood:
18	chr3:141743469..141745043-chr3:141753876..141755747,2	K562	blood:
19	chr3:141750870..141754798-chr3:141761535..141764566,4	K562	blood:
20	chr3:141739542..141742444-chr3:142003603..142005533,2	K562	blood:
21	chr3:141734018..141736974-chr3:141746098..141749383,3	K562	blood:
22	chr3:141747854..141750364-chr3:141771803..141774496,2	MCF-7	breast:
23	chr3:141740878..141741732-chr3:141899625..141900228,2	MCF-7	breast:
24	chr3:141746024..141748965-chr3:160116774..160118286,2	K562	blood:
25	chr3:141738796..141742970-chr3:141745258..141748964,7	K562	blood:
26	chr3:141765382..141767176-chr3:141772359..141774549,2	K562	blood:
27	chr3:141726584..141729404-chr3:141730969..141736139,5	K562	blood:
28	chr3:141746170..141748544-chr3:141765557..141767704,2	K562	blood:
29	chr3:141736074..141738288-chr3:141741449..141743046,2	K562	blood:
30	chr3:141740842..141741377-chr3:141998535..141999516,2	K562	blood:
31	chr3:141751486..141755736-chr3:141759507..141766558,8	K562	blood:
32	chr3:141745791..141750569-chr3:141753730..141757585,7	K562	blood:
33	chr3:141596118..141597741-chr3:141743168..141745555,2	K562	blood:
34	chr3:141743469..141745043-chr3:141753876..141755747,2	K562	blood:
35	chr3:141772328..141774089-chr3:141777712..141780381,2	K562	blood:
36	chr3:141746397..141747918-chr3:142295641..142297892,2	K562	blood:
37	chr3:141752908..141754951-chr3:141758367..141761126,3	K562	blood:
38	chr3:141748723..141752115-chr3:141753472..141758138,4	MCF-7	breast:
39	chr3:141748723..141752115-chr3:141753472..141758138,4	MCF-7	breast:
40	chr3:141772397..141774089-chr3:141777472..141780381,2	K562	blood:
41	chr3:141742047..141744583-chr3:141758221..141760066,2	K562	blood:
42	chr3:141776813..141779383-chr3:141780587..141782430,2	K562	blood:
43	chr3:141726568..141728875-chr3:141730614..141735743,6	K562	blood:
44	chr3:141772328..141774089-chr3:141777712..141780381,2	K562	blood:
45	chr3:141776813..141779383-chr3:141780587..141782430,2	K562	blood:
46	chr3:141733456..141735928-chr3:141995928..141997484,2	K562	blood:
47	chr3:141743220..141745863-chr3:141763714..141765255,2	K562	blood:
48	chr3:141151754..141154048-chr3:141748045..141749745,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000233597	TF binding region
TFDP2	TF binding region
ENSG00000233597	CpG island
TFDP2	CpG island
ENSG00000113810	chromatin interactions
ENSG00000233597	chromatin interactions
ENSG00000069849	chromatin interactions
ENSG00000068885	chromatin interactions
ENSG00000114126	chromatin interactions
ENSG00000175054	chromatin interactions

Extended variants
information (count: 1672 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:1672 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4683659	chr3:141735532-141735533	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs115984918	chr3:141735547-141735548	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs58625168	chr3:141735557-141735558	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs184699324	chr3:141735581-141735582	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs546086678	chr3:141735593-141735594	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs564395045	chr3:141735598-141735599	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs541410183	chr3:141735617-141735618	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs543476552	chr3:141735638-141735639	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs374040217	chr3:141735717-141735718	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs187879614	chr3:141735749-141735750	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs72990257	chr3:141735776-141735777	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs74553121	chr3:141735781-141735782	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs138273362	chr3:141735817-141735818	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs370568343	chr3:141735938-141735939	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs551628888	chr3:141736012-141736013	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs149629701	chr3:141736023-141736024	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs537040534	chr3:141736063-141736064	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs549407244	chr3:141736183-141736184	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs367589341	chr3:141736232-141736233	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs34280182	chr3:141736258-141736259	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs543684662	chr3:141736275-141736276	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs535076831	chr3:141736281-141736282	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs115765690	chr3:141736283-141736284	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs192176237	chr3:141736292-141736293	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs184950964	chr3:141736311-141736312	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs558068049	chr3:141736316-141736317	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs576444801	chr3:141736328-141736329	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs74460355	chr3:141736364-141736365	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs372799992	chr3:141736390-141736391	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs10535313	chr3:141736391-141736392	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs397874224	chr3:141736411-141736412	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs35106983	chr3:141736412-141736413	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs563338452	chr3:141736478-141736479	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs4683660	chr3:141736479-141736480	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs369878541	chr3:141736484-141736485	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs573150016	chr3:141736499-141736500	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs573563481	chr3:141736545-141736546	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs372951330	chr3:141736615-141736616	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs375789698	chr3:141736628-141736629	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs541084558	chr3:141736672-141736673	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs72990258	chr3:141736719-141736720	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs189455036	chr3:141736772-141736773	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs374321449	chr3:141736780-141736781	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs551601159	chr3:141736823-141736824	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs111884170	chr3:141736847-141736848	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs565732153	chr3:141736870-141736871	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs139062669	chr3:141736874-141736875	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs549421108	chr3:141736893-141736894	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs181180151	chr3:141736897-141736898	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs184666011	chr3:141736942-141736943	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
abnormal development	18461090	CNVD
Cancer	21129771	CNVD
Ovarian cancer	23621864	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:887 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:141629000-141739200	Weak transcription	Psoas Muscle	Psoas
2	chr3:141671800-141735600	Weak transcription	Aorta	Aorta
3	chr3:141677800-141739000	Weak transcription	Left Ventricle	heart
4	chr3:141678800-141745600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr3:141682800-141739000	Weak transcription	Pancreas	Pancrea
6	chr3:141682800-141745800	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr3:141682800-141746200	Weak transcription	Primary B cells from peripheral blood	blood
8	chr3:141683800-141746600	Weak transcription	Lung	lung
9	chr3:141698600-141738800	Weak transcription	HSMM	muscle
10	chr3:141706400-141746200	Weak transcription	Fetal Lung	lung
11	chr3:141708600-141745200	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr3:141716000-141738600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr3:141716000-141745600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr3:141719600-141738600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr3:141719600-141738600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr3:141719600-141739000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr3:141720200-141738000	Weak transcription	Fetal Intestine Large	intestine
18	chr3:141720200-141746600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr3:141720400-141737400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr3:141720400-141742600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr3:141721600-141739000	Weak transcription	Fetal Muscle Leg	muscle
22	chr3:141722600-141735600	Weak transcription	Thymus	Thymus
23	chr3:141722600-141745400	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr3:141723400-141745400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr3:141723400-141745400	Weak transcription	Fetal Kidney	kidney
26	chr3:141723600-141738400	Weak transcription	Primary B cells from cord blood	blood
27	chr3:141724400-141738600	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr3:141724400-141741200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr3:141724400-141745000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr3:141724600-141738400	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr3:141724600-141738400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr3:141728200-141746200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr3:141729400-141736600	Weak transcription	Fetal Intestine Small	intestine
34	chr3:141731400-141735600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
35	chr3:141731400-141738200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr3:141731400-141745400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr3:141731800-141735600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr3:141733200-141746200	Weak transcription	Adipose Nuclei	Adipose
39	chr3:141733400-141738200	Weak transcription	Primary hematopoietic stem cells	blood
40	chr3:141733400-141745800	Weak transcription	Fetal Stomach	stomach
41	chr3:141733400-141746600	Weak transcription	Colon Smooth Muscle	Colon
42	chr3:141733600-141747200	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr3:141733800-141736000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr3:141734000-141745400	Weak transcription	Stomach Smooth Muscle	stomach
45	chr3:141734200-141745400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr3:141734600-141735600	Weak transcription	Fetal Thymus	thymus
47	chr3:141734600-141735600	Weak transcription	Dnd41	blood
48	chr3:141734600-141735600	Weak transcription	K562	blood
49	chr3:141734600-141736200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr3:141734600-141746200	Weak transcription	NH-A	brain

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