Variant report

Variant	esv3447663
Chromosome Location	chr3:138096329-138273034
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2017)
CpG islands
(count:2258)
Chromatin interactive
region (count:79)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2017 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:138161304-138161671	K562	blood:	n/a	n/a
2	ARID3A	chr3:138198251-138198297	K562	blood:	n/a	n/a
3	ARID3A	chr3:138129663-138129710	K562	blood:	n/a	n/a
4	ARID3A	chr3:138119682-138119990	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:138117981-138118405	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:138161260-138161463	HepG2	liver:	n/a	n/a
7	ATF1	chr3:138161267-138161641	K562	blood:	n/a	n/a
8	ATF2	chr3:138232341-138232746	GM12878	blood:	n/a	n/a
9	ATF3	chr3:138109014-138109666	HCT-116	colon:	n/a	n/a
10	ATF3	chr3:138109096-138109544	A549	lung:	n/a	n/a
11	BACH1	chr3:138129506-138129569	K562	blood:	n/a	n/a
12	BACH1	chr3:138153468-138153646	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr3:138153892-138154114	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr3:138127504-138128011	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr3:138232250-138232641	GM12878	blood:	n/a	n/a
16	BATF	chr3:138232282-138232701	GM12878	blood:	n/a	n/a
17	BATF	chr3:138107966-138108138	GM12878	blood:	n/a	n/a
18	BCL11A	chr3:138232380-138232593	GM12878	blood:	n/a	n/a
19	BCL11A	chr3:138232300-138232602	GM12878	blood:	n/a	n/a
20	BCLAF1	chr3:138232232-138232651	GM12878	blood:	n/a	n/a
21	BHLHE40	chr3:138153202-138153422	HepG2	liver:	n/a	n/a
22	BHLHE40	chr3:138174985-138175101	K562	blood:	n/a	n/a
23	BHLHE40	chr3:138153048-138153470	HepG2	liver:	n/a	n/a
24	BHLHE40	chr3:138118625-138118951	HepG2	liver:	n/a	n/a
25	BHLHE40	chr3:138129486-138129880	K562	blood:	n/a	n/a
26	BHLHE40	chr3:138131603-138131866	K562	blood:	n/a	n/a
27	BHLHE40	chr3:138161357-138161658	K562	blood:	n/a	n/a
28	BHLHE40	chr3:138118065-138118395	HepG2	liver:	n/a	n/a
29	BHLHE40	chr3:138152952-138153745	HepG2	liver:	n/a	n/a
30	BHLHE40	chr3:138136381-138136766	HepG2	liver:	n/a	n/a
31	BHLHE40	chr3:138117959-138119029	HepG2	liver:	n/a	n/a
32	BHLHE40	chr3:138102722-138102828	K562	blood:	n/a	n/a
33	BHLHE40	chr3:138198379-138198526	K562	blood:	n/a	n/a
34	BRCA1	chr3:138109188-138109450	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr3:138226822-138227373	Hela-S3	cervix:	n/a	chr3:138226971-138226978
36	BRCA1	chr3:138136412-138136698	H1-hESC	embryonic stem cell:	n/a	n/a
37	BRCA1	chr3:138136385-138136736	Hela-S3	cervix:	n/a	n/a
38	CBX3	chr3:138264516-138264738	K562	blood:	n/a	n/a
39	CBX3	chr3:138264471-138264803	K562	blood:	n/a	n/a
40	CBX3	chr3:138136382-138136707	K562	blood:	n/a	n/a
41	CBX3	chr3:138108940-138109663	HCT-116	colon:	n/a	n/a
42	CBX3	chr3:138129493-138129788	K562	blood:	n/a	n/a
43	CBX3	chr3:138205231-138205782	K562	blood:	n/a	n/a
44	CBX3	chr3:138104995-138105351	HCT-116	colon:	n/a	n/a
45	CCNT2	chr3:138148699-138148899	K562	blood:	n/a	n/a
46	CCNT2	chr3:138161413-138161817	K562	blood:	n/a	n/a
47	CEBPB	chr3:138159387-138159772	MCF-7	breast:	n/a	chr3:138159591-138159602 chr3:138159590-138159603 chr3:138159590-138159603 chr3:138159590-138159601
48	CEBPB	chr3:138100795-138101202	HepG2	liver:	n/a	chr3:138100987-138101000 chr3:138100988-138100999 chr3:138100987-138100998
49	CEBPB	chr3:138100836-138101136	K562	blood:	n/a	chr3:138100987-138101000 chr3:138100988-138100999 chr3:138100987-138100998
50	CEBPB	chr3:138214478-138214739	A549	lung:	n/a	n/a

(count:2258 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:138167430-138167480	HPAEpiC	pulmonary alveolar:	n/a
2	chr3:138167430-138167480	HPAEpiC	pulmonary alveolar:	n/a
3	chr3:138170766-138170816	NT2-D1	testis:	n/a
4	chr3:138170705-138170755	MCF-7	breast:	n/a
5	chr3:138136952-138137002	ECC-1	luminal epithelium:	n/a
6	chr3:138153381-138153431	AG04450	lung:	fetal
7	chr3:138231780-138231830	NT2-D1	testis:	n/a
8	chr3:138172124-138172174	NT2-D1	testis:	n/a
9	chr3:138153168-138153218	PrEC	prostate:	n/a
10	chr3:138153763-138153813	HCF	heart:	n/a
11	chr3:138231780-138231830	HCPEpiC	choroid plexus:	n/a
12	chr3:138169728-138169778	Hepatocyte	liver:	n/a
13	chr3:138196760-138196810	HCPEpiC	choroid plexus:	n/a
14	chr3:138153372-138153422	ProgFib	skin:	n/a
15	chr3:138196760-138196810	NB4	blood:	n/a
16	chr3:138152837-138152887	H1-hESC	embryonic stem cell:	embryo
17	chr3:138174025-138174075	Caco-2	colon:	n/a
18	chr3:138153357-138153407	HUVEC	blood vessel:	n/a
19	chr3:138153168-138153218	Caco-2	colon:	n/a
20	chr3:138153168-138153218	ECC-1	luminal epithelium:	n/a
21	chr3:138115973-138116023	GM12891	blood:	n/a
22	chr3:138101310-138101360	HPAEpiC	pulmonary alveolar:	n/a
23	chr3:138153278-138153328	HPAEpiC	pulmonary alveolar:	n/a
24	chr3:138160066-138160116	NHDF-neo	bronchial:	n/a
25	chr3:138213002-138213052	SK-N-MC	brain:	n/a
26	chr3:138167430-138167480	U87	brain:	n/a
27	chr3:138170705-138170755	ProgFib	skin:	n/a
28	chr3:138160066-138160116	Hepatocyte	liver:	n/a
29	chr3:138128339-138128389	AG04449	skin:	fetal
30	chr3:138101415-138101465	NHBE	bronchial:	n/a
31	chr3:138153372-138153422	K562	blood:	n/a
32	chr3:138169728-138169778	BJ	skin:	n/a
33	chr3:138136952-138137002	PFSK-1	brain:	n/a
34	chr3:138152902-138152952	NHBE	bronchial:	n/a
35	chr3:138150379-138150429	T-47D	breast:	n/a
36	chr3:138157982-138158032	T-47D	breast:	n/a
37	chr3:138153357-138153407	HRE	kidney:	n/a
38	chr3:138172124-138172174	HPAEpiC	pulmonary alveolar:	n/a
39	chr3:138153763-138153813	GM19239	blood:	n/a
40	chr3:138160066-138160116	AG09319	gingival:	n/a
41	chr3:138121287-138121337	HAEpiC	amniotic membrane:	n/a
42	chr3:138154754-138154804	NT2-D1	testis:	n/a
43	chr3:138153372-138153422	LNCaP	prostate:	n/a
44	chr3:138213002-138213052	HepG2	liver:	n/a
45	chr3:138153381-138153431	HUVEC	blood vessel:	n/a
46	chr3:138153278-138153328	HepG2	liver:	n/a
47	chr3:138153372-138153422	ECC-1	luminal epithelium:	n/a
48	chr3:138136952-138137002	A549	lung:	n/a
49	chr3:138154620-138154670	GM06990	blood:	n/a
50	chr3:138154620-138154670	PFSK-1	brain:	n/a

(count:79 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:138066927..138067654-chr3:138136135..138137134,2	MCF-7	breast:
2	chr3:138173174..138174919-chr3:138181076..138182864,2	MCF-7	breast:
3	chr3:138108137..138110673-chr3:138113889..138116211,2	K562	blood:
4	chr3:138051070..138051808-chr3:138136099..138136657,2	MCF-7	breast:
5	chr3:138051022..138051610-chr3:138144950..138145530,2	MCF-7	breast:
6	chr3:138153677..138156615-chr3:138182530..138184739,2	MCF-7	breast:
7	chr3:138197115..138197897-chr3:138634489..138635059,2	MCF-7	breast:
8	chr3:138150985..138152959-chr3:138153482..138156074,2	MCF-7	breast:
9	chr1:109618765..109621666-chr3:138122913..138124560,2	MCF-7	breast:
10	chr3:138194164..138195969-chr3:138327251..138329519,2	MCF-7	breast:
11	chr3:138169355..138171117-chr3:138172389..138174530,2	MCF-7	breast:
12	chr3:138093996..138096598-chr4:123678799..123680914,2	MCF-7	breast:
13	chr3:138136460..138136987-chr3:138144957..138145493,2	MCF-7	breast:
14	chr3:138112677..138114319-chr3:138192057..138194447,2	MCF-7	breast:
15	chr3:138151622..138154032-chr3:138155099..138156633,2	K562	blood:
16	chr3:138099681..138102999-chr3:138104936..138107535,3	MCF-7	breast:
17	chr3:138113362..138114985-chr3:138120209..138122090,2	K562	blood:
18	chr3:138186886..138189284-chr3:138191772..138193552,2	K562	blood:
19	chr3:138153677..138156615-chr3:138182530..138184739,2	MCF-7	breast:
20	chr3:138108024..138110952-chr3:138113271..138115084,3	MCF-7	breast:
21	chr3:138148704..138150264-chr3:138152661..138154776,2	MCF-7	breast:
22	chr3:138147884..138150331-chr3:138154238..138156616,2	K562	blood:
23	chr3:138136837..138138757-chr3:138141028..138143594,2	K562	blood:
24	chr3:138130760..138133096-chr3:138134779..138137650,2	MCF-7	breast:
25	chr3:138228056..138229897-chr3:138230355..138233975,3	K562	blood:
26	chr3:138065940..138068792-chr3:138150528..138153476,2	K562	blood:
27	chr3:138079655..138082250-chr3:138142327..138144870,2	K562	blood:
28	chr20:3451237..3451899-chr3:138226141..138226668,2	MCF-7	breast:
29	chr3:138136384..138136956-chr3:139280690..139281277,2	K562	blood:
30	chr3:138112862..138116319-chr3:138116763..138120380,3	MCF-7	breast:
31	chr3:138112036..138114862-chr3:138120590..138122113,2	K562	blood:
32	chr3:138135853..138136964-chr3:138178372..138179276,3	MCF-7	breast:
33	chr3:138150985..138152959-chr3:138153482..138156074,2	MCF-7	breast:
34	chr3:138050301..138052204-chr3:138116487..138117341,9	MCF-7	breast:
35	chr3:138136460..138136987-chr3:138144957..138145493,2	MCF-7	breast:
36	chr3:138049031..138051913-chr3:138117150..138118923,2	MCF-7	breast:
37	chr3:138152067..138153775-chr3:138169983..138172416,2	MCF-7	breast:
38	chr3:138228056..138229897-chr3:138230355..138233975,3	K562	blood:
39	chr3:138186020..138187574-chr3:138189253..138191029,2	K562	blood:
40	chr3:138113362..138114985-chr3:138120209..138122090,2	K562	blood:
41	chr3:138130760..138133096-chr3:138134779..138137650,2	MCF-7	breast:
42	chr3:138169355..138171117-chr3:138172389..138174530,2	MCF-7	breast:
43	chr3:138173174..138174919-chr3:138181076..138182864,2	MCF-7	breast:
44	chr3:138185730..138189738-chr3:138190908..138194397,4	MCF-7	breast:
45	chr3:138222687..138224341-chr3:138230011..138232185,2	MCF-7	breast:
46	chr3:138136439..138137007-chr3:138313354..138314017,2	MCF-7	breast:
47	chr3:138094416..138096515-chr3:138105748..138108016,2	MCF-7	breast:
48	chr3:138136047..138137057-chr3:138178340..138179089,3	MCF-7	breast:
49	chr3:138089900..138093622-chr3:138093776..138096723,3	MCF-7	breast:
50	chr3:138143800..138147354-chr3:138150796..138153111,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ESYT3-3	chr3:138217403-138218541	ucscGeneNc_uc003erl_1

No data

Variant related genes	Relation type
ESYT3	TF binding region
CEP70	TF binding region
MRAS	TF binding region
ESYT3	CpG island
CEP70	CpG island
MRAS	CpG island
ENSG00000158234	chromatin interactions
ENSG00000158220	chromatin interactions
ENSG00000088812	chromatin interactions
ENSG00000114107	chromatin interactions
ENSG00000158186	chromatin interactions
ENSG00000114098	chromatin interactions

Extended variants
information (count: 6672 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:6672 , 50 per page) page: 1 2 3 4 5 6 7 ... 134

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547377711	chr3:138096366-138096367	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs552907569	chr3:138096442-138096443	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs566050563	chr3:138096480-138096481	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs181522419	chr3:138096499-138096500	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs548321198	chr3:138096506-138096507	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs566883542	chr3:138096507-138096508	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs4678417	chr3:138096512-138096513	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs150565242	chr3:138096513-138096514	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs79065223	chr3:138096583-138096584	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs369009000	chr3:138096602-138096603	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs187054910	chr3:138096622-138096623	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs539323536	chr3:138096670-138096671	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs552867630	chr3:138096706-138096707	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs573086127	chr3:138096718-138096719	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs139498304	chr3:138096756-138096757	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs541784319	chr3:138096889-138096890	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs555114946	chr3:138096890-138096891	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs149277649	chr3:138096986-138096987	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs191796927	chr3:138097025-138097026	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs563824568	chr3:138097040-138097041	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs183402251	chr3:138097153-138097154	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs546484871	chr3:138097180-138097181	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs142851159	chr3:138097236-138097237	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs559975626	chr3:138097279-138097280	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs6790121	chr3:138097304-138097305	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs253662	chr3:138097313-138097314	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs561948664	chr3:138097317-138097318	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs530869509	chr3:138097335-138097336	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs550684846	chr3:138097353-138097354	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs570280152	chr3:138097363-138097364	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs144431493	chr3:138097364-138097365	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs544656624	chr3:138097367-138097368	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs546414742	chr3:138097408-138097409	Genic enhancers Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
34	rs375861665	chr3:138097416-138097417	Genic enhancers Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
35	rs139132575	chr3:138097478-138097479	Genic enhancers Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
36	rs557551107	chr3:138097501-138097502	Genic enhancers Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
37	rs188049454	chr3:138097502-138097503	Genic enhancers Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
38	rs577369951	chr3:138097525-138097526	Genic enhancers Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
39	rs368572263	chr3:138097526-138097527	Genic enhancers Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
40	rs1678443	chr3:138097534-138097535	Genic enhancers Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
41	rs1679147	chr3:138097537-138097538	Genic enhancers Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs1678442	chr3:138097547-138097548	Genic enhancers Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs1720823	chr3:138097551-138097552	Genic enhancers Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs143893994	chr3:138097560-138097561	Genic enhancers Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
45	rs146891736	chr3:138097587-138097588	Genic enhancers Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
46	rs542163946	chr3:138097613-138097614	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
47	rs560004537	chr3:138097623-138097624	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
48	rs189832316	chr3:138097720-138097721	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
49	rs35441432	chr3:138097734-138097735	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
50	rs182384958	chr3:138097744-138097745	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
Cancer	21129771	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
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	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
Intracranial aneurysm	16715129	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
Developmental delay	21147756	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Gastric cancer	22014070	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:3208 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:138070000-138096600	Weak transcription	Fetal Brain Male	brain
2	chr3:138071200-138096600	Weak transcription	Aorta	Aorta
3	chr3:138076000-138108200	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr3:138078600-138100600	Weak transcription	NH-A	brain
5	chr3:138080200-138096400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr3:138081600-138108200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr3:138083000-138100400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr3:138083200-138100600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr3:138085200-138100000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr3:138086200-138100400	Weak transcription	HepG2	liver
11	chr3:138086800-138100600	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr3:138087200-138097000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr3:138087200-138100000	Weak transcription	Pancreas	Pancrea
14	chr3:138087200-138100600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr3:138087400-138097000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr3:138089200-138100000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr3:138089200-138100800	Weak transcription	Fetal Lung	lung
18	chr3:138089400-138100000	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr3:138089400-138100000	Weak transcription	Brain Angular Gyrus	brain
20	chr3:138089400-138102400	Weak transcription	Spleen	Spleen
21	chr3:138089600-138097600	Weak transcription	Brain Substantia Nigra	brain
22	chr3:138089600-138100200	Weak transcription	Lung	lung
23	chr3:138090400-138119400	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr3:138091000-138098000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr3:138091200-138096400	Weak transcription	Brain Anterior Caudate	brain
26	chr3:138091200-138100400	Weak transcription	Monocytes-CD14+_RO01746	blood
27	chr3:138091400-138096600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr3:138091400-138100800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr3:138091600-138098600	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr3:138091800-138098000	Strong transcription	HSMM	muscle
31	chr3:138092000-138096400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
32	chr3:138092200-138096800	Weak transcription	Brain Cingulate Gyrus	brain
33	chr3:138093400-138097600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr3:138093600-138100400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr3:138093800-138100000	Weak transcription	Colon Smooth Muscle	Colon
36	chr3:138093800-138100400	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr3:138094000-138097000	Weak transcription	Brain Hippocampus Middle	brain
38	chr3:138094000-138104800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr3:138094200-138096800	Weak transcription	Osteobl	bone
40	chr3:138094400-138097200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr3:138094400-138100200	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr3:138094600-138097400	Enhancers	Skeletal Muscle Female	skeletal muscle
43	chr3:138094600-138099000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr3:138094600-138100600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr3:138094800-138100200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr3:138095000-138096600	Enhancers	Skeletal Muscle Male	skeletal muscle
47	chr3:138095000-138098000	Strong transcription	Fetal Muscle Leg	muscle
48	chr3:138095200-138097600	Strong transcription	Brain Germinal Matrix	brain
49	chr3:138095400-138096600	Weak transcription	Stomach Smooth Muscle	stomach
50	chr3:138095400-138097400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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