Variant report

Variant	esv2757013
Chromosome Location	chr3:141756541-142094631
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3640)
CpG islands
(count:1770)
Chromatin interactive
region (count:185)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

(count:3640 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:141845072-141845387	K562	blood:	n/a	n/a
2	ARID3A	chr3:142037995-142038366	K562	blood:	n/a	n/a
3	ARID3A	chr3:142004029-142004406	K562	blood:	n/a	n/a
4	ARID3A	chr3:142034796-142035079	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:141868086-141868286	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:141818967-141818988	K562	blood:	n/a	n/a
7	ARID3A	chr3:141944333-141944542	K562	blood:	n/a	n/a
8	ARID3A	chr3:142085359-142085586	K562	blood:	n/a	n/a
9	ARID3A	chr3:141941528-141942036	K562	blood:	n/a	n/a
10	ARID3A	chr3:141868710-141868857	HepG2	liver:	n/a	n/a
11	ARID3A	chr3:141764957-141766278	K562	blood:	n/a	n/a
12	ARID3A	chr3:141944275-141944587	HepG2	liver:	n/a	n/a
13	ARID3A	chr3:141807405-141807560	HepG2	liver:	n/a	n/a
14	ARID3A	chr3:141845145-141845331	HepG2	liver:	n/a	n/a
15	ARID3A	chr3:142085451-142085580	HepG2	liver:	n/a	n/a
16	ARID3A	chr3:142082266-142082975	HepG2	liver:	n/a	n/a
17	ARID3A	chr3:142034735-142035065	K562	blood:	n/a	n/a
18	ARID3A	chr3:141848736-141848803	HepG2	liver:	n/a	n/a
19	ATF1	chr3:141817873-141818134	K562	blood:	n/a	n/a
20	ATF1	chr3:142038012-142038223	K562	blood:	n/a	n/a
21	ATF1	chr3:141994868-141995043	K562	blood:	n/a	n/a
22	ATF1	chr3:142034743-142035113	K562	blood:	n/a	n/a
23	ATF1	chr3:141765160-141765905	K562	blood:	n/a	n/a
24	ATF1	chr3:142026474-142026530	K562	blood:	n/a	n/a
25	ATF1	chr3:141944202-141944637	K562	blood:	n/a	n/a
26	ATF1	chr3:142004039-142004362	K562	blood:	n/a	n/a
27	ATF2	chr3:141944124-141944603	GM12878	blood:	n/a	n/a
28	ATF2	chr3:141944313-141944572	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF3	chr3:141944306-141944624	K562	blood:	n/a	chr3:141944456-141944466
30	ATF3	chr3:141765113-141765513	K562	blood:	n/a	n/a
31	ATF3	chr3:141817875-141818204	K562	blood:	n/a	n/a
32	ATF3	chr3:142034698-142035057	K562	blood:	n/a	n/a
33	BACH1	chr3:141867733-141868966	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr3:141944121-141944594	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr3:141988570-141988640	K562	blood:	n/a	n/a
36	BACH1	chr3:142037995-142038332	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr3:141909646-141909689	K562	blood:	n/a	n/a
38	BACH1	chr3:142037969-142038499	K562	blood:	n/a	n/a
39	BATF	chr3:141975772-141975937	GM12878	blood:	n/a	n/a
40	BATF	chr3:142074556-142074897	GM12878	blood:	n/a	n/a
41	BCLAF1	chr3:141944193-141944635	GM12878	blood:	n/a	n/a
42	BCLAF1	chr3:141998835-141999218	GM12878	blood:	n/a	n/a
43	BCLAF1	chr3:141998774-141999206	GM12878	blood:	n/a	n/a
44	BHLHE40	chr3:141868133-141868604	GM12878	blood:	n/a	n/a
45	BHLHE40	chr3:142066400-142066735	K562	blood:	n/a	n/a
46	BHLHE40	chr3:141998901-141999171	GM12878	blood:	n/a	n/a
47	BHLHE40	chr3:141998848-141999153	K562	blood:	n/a	n/a
48	BHLHE40	chr3:141998833-141999090	HepG2	liver:	n/a	n/a
49	BHLHE40	chr3:141944084-141944604	HepG2	liver:	n/a	n/a
50	BHLHE40	chr3:141764829-141766005	K562	blood:	n/a	n/a

(count:1770 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:141764977-141765027	NH-A	brain:	n/a
2	chr3:141764977-141765027	NH-A	brain:	n/a
3	chr3:141944620-141944670	ProgFib	skin:	n/a
4	chr3:141944300-141944350	AG09309	skin:	n/a
5	chr3:141943895-141943945	ECC-1	luminal epithelium:	n/a
6	chr3:141871386-141871436	HRE	kidney:	n/a
7	chr3:141944516-141944566	Hela-S3	cervix:	n/a
8	chr3:141868612-141868662	ECC-1	luminal epithelium:	n/a
9	chr3:141941279-141941329	GM06990	blood:	n/a
10	chr3:141943895-141943945	HEK293	kidney:	embryo
11	chr3:141762780-141762830	SKMC	muscle:	n/a
12	chr3:141867994-141868044	HUVEC	blood vessel:	n/a
13	chr3:141941279-141941329	NH-A	brain:	n/a
14	chr3:141762780-141762830	PFSK-1	brain:	n/a
15	chr3:141944344-141944394	HIPEpiC	eye:	n/a
16	chr3:141941279-141941329	HL-60	blood:	n/a
17	chr3:141877942-141877992	MCF10A-Er-Src	breast:	n/a
18	chr3:141871386-141871436	SK-N-SH	brain:	n/a
19	chr3:141941279-141941329	AG04450	lung:	fetal
20	chr3:141945703-141945753	HCT-116	colon:	n/a
21	chr3:141928789-141928839	AG09319	gingival:	n/a
22	chr3:141868409-141868459	Hepatocyte	liver:	n/a
23	chr3:141791518-141791568	T-47D	breast:	n/a
24	chr3:141928789-141928839	GM12892	blood:	n/a
25	chr3:141762828-141762878	HRPEpiC	eye:	n/a
26	chr3:141762963-141763013	NT2-D1	testis:	n/a
27	chr3:141944519-141944569	SK-N-SH	brain:	n/a
28	chr3:141945703-141945753	ovcar-3	ovarian:	n/a
29	chr3:141877942-141877992	GM12892	blood:	n/a
30	chr3:141944077-141944127	GM06990	blood:	n/a
31	chr3:141945703-141945753	HIPEpiC	eye:	n/a
32	chr3:141762963-141763013	Caco-2	colon:	n/a
33	chr3:141944344-141944394	NB4	blood:	n/a
34	chr3:141762828-141762878	GM06990	blood:	n/a
35	chr3:141877942-141877992	ECC-1	luminal epithelium:	n/a
36	chr3:141928789-141928839	MCF10A-Er-Src	breast:	n/a
37	chr3:141944318-141944368	GM12891	blood:	n/a
38	chr3:141928789-141928839	GM12891	blood:	n/a
39	chr3:141868409-141868459	GM12892	blood:	n/a
40	chr3:141945790-141945840	BJ	skin:	n/a
41	chr3:141944620-141944670	K562	blood:	n/a
42	chr3:141944519-141944569	HCM	heart:	n/a
43	chr3:141928789-141928839	U87	brain:	n/a
44	chr3:141868409-141868459	HEEpiC	esophagus:	n/a
45	chr3:141868409-141868459	ECC-1	luminal epithelium:	n/a
46	chr3:141945703-141945753	RPTEC	kidney:	n/a
47	chr3:141877942-141877992	GM12891	blood:	n/a
48	chr3:142027066-142027116	NH-A	brain:	n/a
49	chr3:141928789-141928839	ovcar-3	ovarian:	n/a
50	chr3:141868612-141868662	SK-N-SH_RA	brain:	n/a

(count:185 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr3:141940509..141943565-chr3:141944038..141945660,4	MCF-7	breast:
2	chr3:141883292..141885881-chr3:141942350..141944457,2	K562	blood:
3	chr3:141884381..141887042-chr3:141942350..141944309,2	K562	blood:
4	chr3:141844721..141845463-chr3:141945183..141945790,2	MCF-7	breast:
5	chr3:141942352..141946050-chr3:141946407..141950976,4	MCF-7	breast:
6	chr3:141835499..141837454-chr3:141839665..141841997,2	K562	blood:
7	chr3:141939241..141942550-chr3:141942923..141945578,4	MCF-7	breast:
8	chr3:141942905..141947103-chr3:141949028..141953369,8	MCF-7	breast:
9	chr3:141944137..141946098-chr3:141949464..141952210,3	K562	blood:
10	chr3:142026133..142029209-chr3:142034990..142037893,3	MCF-7	breast:
11	chr3:141681241..141682037-chr3:141894141..141895360,3	MCF-7	breast:
12	chr3:141929745..141931253-chr3:141941462..141943511,2	MCF-7	breast:
13	chr3:142025469..142027957-chr3:142037548..142040461,2	K562	blood:
14	chr3:141898603..141901511-chr3:141942977..141947111,4	MCF-7	breast:
15	chr3:142026133..142029209-chr3:142034990..142037893,3	MCF-7	breast:
16	chr3:141681127..141682067-chr3:141998956..141999598,2	MCF-7	breast:
17	chr3:141986894..141989145-chr3:141996424..141998046,2	K562	blood:
18	chr3:141845395..141847742-chr3:141867833..141869425,2	MCF-7	breast:
19	chr3:141874750..141877739-chr3:141886968..141889204,2	K562	blood:
20	chr3:141776813..141779383-chr3:141780587..141782430,2	K562	blood:
21	chr3:141739542..141742444-chr3:142003603..142005533,2	K562	blood:
22	chr3:142077588..142080075-chr3:142081701..142083765,2	K562	blood:
23	chr3:141823415..141824933-chr3:141840146..141843021,2	MCF-7	breast:
24	chr3:141944534..141946087-chr3:141987477..141990045,2	MCF-7	breast:
25	chr3:142077588..142080075-chr3:142081701..142083765,2	K562	blood:
26	chr3:141765382..141767176-chr3:141772359..141774549,2	K562	blood:
27	chr3:141872069..141873758-chr3:141878365..141880269,2	MCF-7	breast:
28	chr3:141889851..141891624-chr3:141894627..141896590,2	K562	blood:
29	chr3:142061779..142063304-chr3:142065930..142068810,2	K562	blood:
30	chr3:141914914..141916949-chr3:141917367..141920269,2	K562	blood:
31	chr3:141801212..141802755-chr3:141819835..141821788,2	K562	blood:
32	chr3:142071094..142074933-chr3:142076608..142079513,3	MCF-7	breast:
33	chr3:141924115..141926296-chr3:141927657..141929893,2	K562	blood:
34	chr3:141983516..141986399-chr3:141987635..141990028,2	MCF-7	breast:
35	chr3:141866172..141869567-chr3:141870149..141874954,7	MCF-7	breast:
36	chr3:141745328..141748975-chr3:142003993..142005586,3	K562	blood:
37	chr13:28032235..28033740-chr3:141906874..141908394,2	MCF-7	breast:
38	chr3:142085151..142088133-chr3:142116626..142119405,2	MCF-7	breast:
39	chr3:141816604..141818646-chr3:141821637..141823768,2	K562	blood:
40	chr3:142047932..142050372-chr3:142051605..142055072,3	K562	blood:
41	chr3:141939985..141942934-chr3:141962121..141964269,2	K562	blood:
42	chr3:141983516..141986399-chr3:141987635..141990028,2	MCF-7	breast:
43	chr3:141747548..141749276-chr3:141782334..141784054,2	MCF-7	breast:
44	chr3:141862592..141866605-chr3:141869452..141871962,3	MCF-7	breast:
45	chr3:141918846..141920526-chr3:141922656..141925151,2	K562	blood:
46	chr3:142034226..142036473-chr3:142044742..142046537,2	K562	blood:
47	chr3:141816249..141818254-chr3:141826549..141828683,2	MCF-7	breast:
48	chr3:141866047..141867912-chr3:141873721..141875434,2	K562	blood:
49	chr1:45284275..45285951-chr3:141939370..141941710,2	K562	blood:
50	chr3:141932221..141937955-chr3:141938851..141945696,9	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TFDP2-7	chr3:141876369-141880820	ENSG00000272565.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	XRN1	hsa-let-7b-5p	chr3:142030132-142030126
2	XRN1	hsa-miR-10a-5p	chr3:142029592-142029585
3	GK5	hsa-miR-340-5p	chr3:141878164-141878157
4	GK5	hsa-miR-124-3p	chr3:141883855-141883849
5	XRN1	hsa-miR-10a-5p	chr3:142029586-142029608
6	XRN1	hsa-miR-335-5p	chr3:142025482-142025506

Variant related genes	Relation type
ENSG00000233597	TF binding region
TFDP2	TF binding region
GK5	TF binding region
XRN1	TF binding region
RNU6-425P	TF binding region
ENSG00000272565	TF binding region
ENSG00000233597	CpG island
TFDP2	CpG island
GK5	CpG island
XRN1	CpG island
RNU6-425P	CpG island
ENSG00000272565	CpG island
ENSG00000114126	chromatin interactions
ENSG00000141526	chromatin interactions
ENSG00000125968	chromatin interactions
ENSG00000228878	chromatin interactions
ENSG00000253806	chromatin interactions
ENSG00000175066	chromatin interactions
ENSG00000160183	chromatin interactions
ENSG00000114125	chromatin interactions
ENSG00000162636	chromatin interactions
ENSG00000206604	chromatin interactions
ENSG00000199753	chromatin interactions
ENSG00000175054	chromatin interactions
ENSG00000114127	chromatin interactions
ENSG00000266402	chromatin interactions
ENSG00000202444	chromatin interactions
ENSG00000130193	chromatin interactions
ENSG00000272565	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000113387	chromatin interactions
ENSG00000122545	chromatin interactions

Extended variants
information (count: 11272 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:11272 , 50 per page) page: 1 2 3 4 5 6 7 ... 226

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1543064	chr3:141756541-141756542	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs181455344	chr3:141756593-141756594	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs549089743	chr3:141756595-141756596	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs562471576	chr3:141756601-141756602	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs373835669	chr3:141756609-141756610	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs529774727	chr3:141756652-141756653	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs562838290	chr3:141756659-141756660	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs367976511	chr3:141756663-141756664	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs541962519	chr3:141756731-141756732	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs560708560	chr3:141756760-141756761	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs372182324	chr3:141756804-141756805	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs542035135	chr3:141756833-141756834	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs552824881	chr3:141756839-141756840	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs571102861	chr3:141756852-141756853	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs6778085	chr3:141756869-141756870	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs549722426	chr3:141756894-141756895	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs374264154	chr3:141756936-141756937	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs568128531	chr3:141756953-141756954	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs370785031	chr3:141756957-141756958	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs535526220	chr3:141756993-141756994	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs553999189	chr3:141757010-141757011	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs555612911	chr3:141757064-141757065	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs9863685	chr3:141757097-141757098	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs533790831	chr3:141757098-141757099	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs558813664	chr3:141757204-141757205	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs577019934	chr3:141757210-141757211	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs141351250	chr3:141757223-141757224	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs80275819	chr3:141757225-141757226	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs77322751	chr3:141757229-141757230	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs13078440	chr3:141757249-141757250	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs138712760	chr3:141757266-141757267	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs372207255	chr3:141757280-141757281	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs556161784	chr3:141757384-141757385	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs142772431	chr3:141757402-141757403	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs184692808	chr3:141757446-141757447	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs560030839	chr3:141757547-141757548	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs190013683	chr3:141757555-141757556	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs546033390	chr3:141757569-141757570	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs181644044	chr3:141757571-141757572	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs575292486	chr3:141757574-141757575	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs186501283	chr3:141757575-141757576	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs191136959	chr3:141757751-141757752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568089868	chr3:141757792-141757793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529285140	chr3:141757851-141757852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547863873	chr3:141757866-141757867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566089913	chr3:141757886-141757887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs369165201	chr3:141757897-141757898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs539928132	chr3:141757899-141757900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs144544812	chr3:141757918-141757919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs575511184	chr3:141757969-141757970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:5829 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:141747600-141762600	Weak transcription	Fetal Muscle Leg	muscle
2	chr3:141747600-141762800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr3:141747600-141773000	Weak transcription	Duodenum Mucosa	Duodenum
4	chr3:141747600-141780400	Weak transcription	Left Ventricle	heart
5	chr3:141748800-141758400	Weak transcription	Thymus	Thymus
6	chr3:141751200-141765000	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr3:141751400-141759600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr3:141751400-141764400	Weak transcription	Primary hematopoietic stem cells	blood
9	chr3:141752400-141759800	Weak transcription	Dnd41	blood
10	chr3:141753600-141768400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr3:141755200-141771400	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr3:141755800-141758400	Weak transcription	Fetal Thymus	thymus
13	chr3:141756200-141756600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr3:141756200-141756800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr3:141756200-141762600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr3:141756400-141758400	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr3:141756400-141758400	Weak transcription	K562	blood
18	chr3:141756600-141759600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr3:141756800-141759600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr3:141757800-141762600	Weak transcription	Aorta	Aorta
21	chr3:141758200-141758400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr3:141758200-141758400	Enhancers	Fetal Muscle Trunk	muscle
23	chr3:141758200-141758600	Enhancers	A549	lung
24	chr3:141758200-141758800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr3:141758200-141758800	Enhancers	Esophagus	oesophagus
26	chr3:141758200-141758800	Enhancers	Fetal Intestine Large	intestine
27	chr3:141758200-141758800	Enhancers	Ovary	ovary
28	chr3:141758200-141758800	Enhancers	Pancreas	Pancrea
29	chr3:141758400-141758600	Enhancers	Right Ventricle	heart
30	chr3:141758400-141758800	Genic enhancers	Fetal Thymus	thymus
31	chr3:141758400-141758800	Enhancers	Sigmoid Colon	Sigmoid Colon
32	chr3:141758400-141758800	Genic enhancers	Thymus	Thymus
33	chr3:141758400-141760400	Enhancers	K562	blood
34	chr3:141758400-141762600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr3:141758400-141777400	Weak transcription	Fetal Muscle Trunk	muscle
36	chr3:141758800-141762200	Weak transcription	Thymus	Thymus
37	chr3:141758800-141762400	Weak transcription	Fetal Intestine Large	intestine
38	chr3:141758800-141762400	Weak transcription	Fetal Thymus	thymus
39	chr3:141758800-141762600	Weak transcription	Pancreas	Pancrea
40	chr3:141758800-141762600	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr3:141758800-141768800	Weak transcription	Esophagus	oesophagus
42	chr3:141758800-141775800	Weak transcription	Ovary	ovary
43	chr3:141759200-141760400	Enhancers	Fetal Intestine Small	intestine
44	chr3:141759600-141760200	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr3:141759600-141760400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr3:141759600-141760600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr3:141759600-141760800	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr3:141759800-141760000	Enhancers	Duodenum Smooth Muscle	Duodenum
49	chr3:141759800-141760400	Enhancers	Dnd41	blood
50	chr3:141760000-141770000	Weak transcription	Duodenum Smooth Muscle	Duodenum

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