Variant report

Variant	nsv1011883
Chromosome Location	chr3:141824744-142070290
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3097)
CpG islands
(count:1404)
Chromatin interactive
region (count:148)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

(count:3097 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

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	chr3:142034796-142035079	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:142037995-142038366	K562	blood:	n/a	n/a
4	ARID3A	chr3:142004029-142004406	K562	blood:	n/a	n/a
5	ARID3A	chr3:141845145-141845331	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:142034735-142035065	K562	blood:	n/a	n/a
7	ARID3A	chr3:141941528-141942036	K562	blood:	n/a	n/a
8	ARID3A	chr3:141868710-141868857	HepG2	liver:	n/a	n/a
9	ARID3A	chr3:141868086-141868286	HepG2	liver:	n/a	n/a
10	ARID3A	chr3:141848736-141848803	HepG2	liver:	n/a	n/a
11	ARID3A	chr3:141944275-141944587	HepG2	liver:	n/a	n/a
12	ARID3A	chr3:141944333-141944542	K562	blood:	n/a	n/a
13	ATF1	chr3:142004039-142004362	K562	blood:	n/a	n/a
14	ATF1	chr3:142026474-142026530	K562	blood:	n/a	n/a
15	ATF1	chr3:141994868-141995043	K562	blood:	n/a	n/a
16	ATF1	chr3:142034743-142035113	K562	blood:	n/a	n/a
17	ATF1	chr3:141944202-141944637	K562	blood:	n/a	n/a
18	ATF1	chr3:142038012-142038223	K562	blood:	n/a	n/a
19	ATF2	chr3:141944124-141944603	GM12878	blood:	n/a	n/a
20	ATF2	chr3:141944313-141944572	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF3	chr3:141944306-141944624	K562	blood:	n/a	chr3:141944456-141944466
22	ATF3	chr3:142034698-142035057	K562	blood:	n/a	n/a
23	BACH1	chr3:141909646-141909689	K562	blood:	n/a	n/a
24	BACH1	chr3:141944121-141944594	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr3:141867733-141868966	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr3:142037969-142038499	K562	blood:	n/a	n/a
27	BACH1	chr3:142037995-142038332	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr3:141988570-141988640	K562	blood:	n/a	n/a
29	BATF	chr3:141975772-141975937	GM12878	blood:	n/a	n/a
30	BCLAF1	chr3:141998774-141999206	GM12878	blood:	n/a	n/a
31	BCLAF1	chr3:141998835-141999218	GM12878	blood:	n/a	n/a
32	BCLAF1	chr3:141944193-141944635	GM12878	blood:	n/a	n/a
33	BHLHE40	chr3:141943947-141944618	K562	blood:	n/a	chr3:141944033-141944049
34	BHLHE40	chr3:141998901-141999171	GM12878	blood:	n/a	n/a
35	BHLHE40	chr3:141944084-141944604	HepG2	liver:	n/a	n/a
36	BHLHE40	chr3:141867704-141868571	HepG2	liver:	n/a	n/a
37	BHLHE40	chr3:141998833-141999090	HepG2	liver:	n/a	n/a
38	BHLHE40	chr3:142066400-142066735	K562	blood:	n/a	n/a
39	BHLHE40	chr3:141998848-141999153	K562	blood:	n/a	n/a
40	BHLHE40	chr3:141868133-141868604	GM12878	blood:	n/a	n/a
41	BHLHE40	chr3:141944144-141944582	GM12878	blood:	n/a	n/a
42	BRCA1	chr3:141933218-141933348	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr3:141944283-141944600	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr3:141994588-141995155	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr3:141867873-141868061	HepG2	liver:	n/a	n/a
46	CBX3	chr3:141972002-141972303	K562	blood:	n/a	n/a
47	CBX3	chr3:141951267-141951575	K562	blood:	n/a	n/a
48	CBX3	chr3:142003802-142004433	K562	blood:	n/a	n/a
49	CBX3	chr3:141868168-141868537	K562	blood:	n/a	n/a
50	CBX3	chr3:142003887-142004274	K562	blood:	n/a	n/a

(count:1404 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:141944620-141944670	NT2-D1	testis:	n/a
2	chr3:141944620-141944670	NT2-D1	testis:	n/a
3	chr3:141868409-141868459	PrEC	prostate:	n/a
4	chr3:141944516-141944566	AG10803	skin:	n/a
5	chr3:141868409-141868459	HL-60	blood:	n/a
6	chr3:141944516-141944566	IMR90	lung:	fetal
7	chr3:141943895-141943945	RPTEC	kidney:	n/a
8	chr3:141944620-141944670	U87	brain:	n/a
9	chr3:141868612-141868662	NHBE	bronchial:	n/a
10	chr3:141867994-141868044	PFSK-1	brain:	n/a
11	chr3:141944620-141944670	SK-N-SH_RA	brain:	n/a
12	chr3:141928789-141928839	HepG2	liver:	n/a
13	chr3:141941279-141941329	AoSMC	blood vessel:	n/a
14	chr3:141877942-141877992	HRPEpiC	eye:	n/a
15	chr3:141944318-141944368	ProgFib	skin:	n/a
16	chr3:141995701-141995751	AG04449	skin:	fetal
17	chr3:141945703-141945753	NH-A	brain:	n/a
18	chr3:141868409-141868459	HCF	heart:	n/a
19	chr3:142027066-142027116	NHDF-neo	bronchial:	n/a
20	chr3:141944519-141944569	A549	lung:	n/a
21	chr3:141888226-141888276	SK-N-MC	brain:	n/a
22	chr3:141868409-141868459	SAEC	small airway:	n/a
23	chr3:141928789-141928839	Caco-2	colon:	n/a
24	chr3:141871386-141871436	H1-hESC	embryonic stem cell:	embryo
25	chr3:141877942-141877992	HRCEpiC	kidney:	n/a
26	chr3:141944620-141944670	ovcar-3	ovarian:	n/a
27	chr3:141944300-141944350	GM12891	blood:	n/a
28	chr3:141945703-141945753	CMK	blood:	n/a
29	chr3:141941279-141941329	GM12891	blood:	n/a
30	chr3:141944620-141944670	AG04449	skin:	fetal
31	chr3:141944519-141944569	BE2_C	brain:	n/a
32	chr3:142027066-142027116	GM12891	blood:	n/a
33	chr3:141868612-141868662	ovcar-3	ovarian:	n/a
34	chr3:141928789-141928839	HUVEC	blood vessel:	n/a
35	chr3:141945703-141945753	PrEC	prostate:	n/a
36	chr3:141941279-141941329	HMEC	breast:	n/a
37	chr3:141944519-141944569	AG10803	skin:	n/a
38	chr3:141944519-141944569	LNCaP	prostate:	n/a
39	chr3:141944620-141944670	HCM	heart:	n/a
40	chr3:141944077-141944127	SAEC	small airway:	n/a
41	chr3:141944077-141944127	HepG2	liver:	n/a
42	chr3:141868459-141868509	AG09319	gingival:	n/a
43	chr3:141877942-141877992	HIPEpiC	eye:	n/a
44	chr3:141868612-141868662	LNCaP	prostate:	n/a
45	chr3:141944516-141944566	GM12892	blood:	n/a
46	chr3:141867994-141868044	T-47D	breast:	n/a
47	chr3:141941279-141941329	HL-60	blood:	n/a
48	chr3:141928789-141928839	PANC-1	pancreas:	n/a
49	chr3:141995701-141995751	GM06990	blood:	n/a
50	chr3:141945790-141945840	MCF-7	breast:	n/a

(count:148 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr3:141869138..141873341-chr3:141874948..141878227,4	MCF-7	breast:
2	chr3:141919625..141921887-chr3:141933849..141936243,2	K562	blood:
3	chr3:141862592..141866605-chr3:141869452..141871962,3	MCF-7	breast:
4	chr3:141873069..141875142-chr3:141877650..141879337,2	K562	blood:
5	chr3:141899683..141900200-chr3:141998508..141999054,2	K562	blood:
6	chr3:141681241..141682037-chr3:141894141..141895360,3	MCF-7	breast:
7	chr3:141881359..141883204-chr3:141942762..141944894,2	K562	blood:
8	chr3:141918846..141920526-chr3:141922656..141925151,2	K562	blood:
9	chr3:141746412..141748907-chr3:141928677..141931000,3	K562	blood:
10	chr3:142066835..142068380-chr3:142068524..142070586,2	K562	blood:
11	chr3:141942352..141946050-chr3:141946407..141950976,4	MCF-7	breast:
12	chr3:141866424..141868170-chr3:141875148..141877149,2	MCF-7	breast:
13	chr3:141929745..141931253-chr3:141941462..141943511,2	MCF-7	breast:
14	chr17:80184285..80186683-chr3:141942385..141945027,2	MCF-7	breast:
15	chr3:141941642..141944817-chr3:141944838..141947150,3	K562	blood:
16	chr3:142034226..142036473-chr3:142044742..142046537,2	K562	blood:
17	chr3:141944430..141944948-chr7:35839962..35840580,2	Hela-S3	cervix:
18	chr3:141916087..141917951-chr3:141939342..141941586,2	K562	blood:
19	chr3:141983516..141986399-chr3:141987635..141990028,2	MCF-7	breast:
20	chr3:141823415..141824933-chr3:141840146..141843021,2	MCF-7	breast:
21	chr3:142028519..142033203-chr3:142033786..142039324,7	K562	blood:
22	chr3:142028519..142031113-chr3:142035238..142036947,2	K562	blood:
23	chr3:142031696..142033287-chr3:142037661..142039925,2	MCF-7	breast:
24	chr19:13958223..13958787-chr3:141867467..141868136,2	Hela-S3	cervix:
25	chr3:142028519..142033203-chr3:142033786..142039324,7	K562	blood:
26	chr3:141939241..141942550-chr3:141942923..141945578,4	MCF-7	breast:
27	chr3:141681127..141682067-chr3:141998956..141999598,2	MCF-7	breast:
28	chr3:142047932..142050372-chr3:142051605..142055072,3	K562	blood:
29	chr3:141916087..141917951-chr3:141939342..141941586,2	K562	blood:
30	chr3:141939985..141942934-chr3:141962121..141964269,2	K562	blood:
31	chr3:141889851..141891624-chr3:141894627..141896590,2	K562	blood:
32	chr3:141899184..141899896-chr3:141998534..141999076,2	MCF-7	breast:
33	chr3:141918309..141919900-chr3:141924207..141926926,2	MCF-7	breast:
34	chr3:141898603..141901511-chr3:141942977..141947111,4	MCF-7	breast:
35	chr3:141888192..141890414-chr3:141943053..141945967,2	MCF-7	breast:
36	chr3:141919674..141922479-chr3:141924056..141926779,2	MCF-7	breast:
37	chr3:141681160..141682062-chr3:141998578..141999511,3	K562	blood:
38	chr3:141739542..141742444-chr3:142003603..142005533,2	K562	blood:
39	chr3:141872069..141873758-chr3:141878365..141880269,2	MCF-7	breast:
40	chr3:141845245..141847377-chr3:141943504..141945242,2	MCF-7	breast:
41	chr3:141927414..141929752-chr3:141932597..141934385,2	MCF-7	breast:
42	chr3:141816249..141818254-chr3:141826549..141828683,2	MCF-7	breast:
43	chr3:141929745..141931253-chr3:141941462..141943511,2	MCF-7	breast:
44	chr3:141880531..141882859-chr3:141943394..141945714,2	K562	blood:
45	chr3:142025469..142027957-chr3:142037548..142040461,2	K562	blood:
46	chr3:141866047..141867912-chr3:141873721..141875434,2	K562	blood:
47	chr3:142042619..142044340-chr3:142047762..142050315,2	K562	blood:
48	chr3:142061779..142063304-chr3:142065930..142068810,2	K562	blood:
49	chr3:141845395..141847742-chr3:141867833..141869425,2	MCF-7	breast:
50	chr3:141939985..141942934-chr3:141962121..141964269,2	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	chr3:142029586-142029608
3	GK5	hsa-miR-124-3p	chr3:141883855-141883849
4	XRN1	hsa-miR-10a-5p	chr3:142029592-142029585
5	GK5	hsa-miR-340-5p	chr3:141878164-141878157
6	XRN1	hsa-miR-335-5p	chr3:142025482-142025506

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

Extended variants
information (count: 7917 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:7917 , 50 per page) page: 1 2 3 4 5 6 7 ... 159

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs77900739	chr3:141824751-141824752	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs369078635	chr3:141824770-141824771	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs182369812	chr3:141824781-141824782	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs59971687	chr3:141824806-141824807	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs375685603	chr3:141824811-141824812	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs538054698	chr3:141824812-141824813	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs199676854	chr3:141824818-141824819	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs9857917	chr3:141824845-141824846	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs528647013	chr3:141824862-141824863	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs565614590	chr3:141824882-141824883	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs79309321	chr3:141824924-141824925	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs78910541	chr3:141824934-141824935	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs63019860	chr3:141824955-141824956	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs377441210	chr3:141824956-141824957	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs59797691	chr3:141824958-141824959	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs76026833	chr3:141824969-141824970	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs56008466	chr3:141825119-141825120	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs532557568	chr3:141825173-141825174	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs55881752	chr3:141825313-141825314	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs569339294	chr3:141825324-141825325	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs112687984	chr3:141825332-141825333	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs140651765	chr3:141825402-141825403	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs570543714	chr3:141825411-141825412	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs567494586	chr3:141825532-141825533	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs116576198	chr3:141825547-141825548	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs375795358	chr3:141825548-141825549	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs6773343	chr3:141825598-141825599	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs189258740	chr3:141825617-141825618	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538631039	chr3:141825658-141825659	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs181302549	chr3:141825674-141825675	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs375268538	chr3:141825695-141825696	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575169219	chr3:141825734-141825735	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs145830696	chr3:141825791-141825792	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs138471530	chr3:141825834-141825835	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs573123203	chr3:141825944-141825945	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs540396615	chr3:141825991-141825992	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs552285521	chr3:141825992-141825993	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs565249643	chr3:141826042-141826043	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs185323128	chr3:141826092-141826093	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs551255796	chr3:141826097-141826098	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs566017351	chr3:141826119-141826120	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562775870	chr3:141826179-141826180	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs141475604	chr3:141826219-141826220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs548719080	chr3:141826221-141826222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs370100611	chr3:141826231-141826232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs566934004	chr3:141826262-141826263	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs534820728	chr3:141826300-141826301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs374114326	chr3:141826310-141826311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs77876121	chr3:141826370-141826371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs571415183	chr3:141826420-141826421	Weak transcription Enhancers	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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21364760	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	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:4560 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:141764000-141825600	Weak transcription	Primary T cells from cord blood	blood
2	chr3:141795400-141835800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr3:141818200-141830600	Weak transcription	Fetal Intestine Small	intestine
4	chr3:141818200-141835800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr3:141819200-141827000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr3:141821200-141827000	Weak transcription	Thymus	Thymus
7	chr3:141822200-141825400	Weak transcription	Fetal Thymus	thymus
8	chr3:141823600-141825400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr3:141823600-141832000	Enhancers	Dnd41	blood
10	chr3:141823800-141825800	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr3:141824000-141826000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr3:141824800-141826000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr3:141825000-141825800	Enhancers	NHDF-Ad	bronchial
14	chr3:141825400-141825800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr3:141825400-141826000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr3:141825400-141826200	Enhancers	Fetal Brain Male	brain
17	chr3:141825400-141827000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr3:141825400-141831000	Enhancers	Fetal Thymus	thymus
19	chr3:141825600-141825800	Enhancers	Primary T cells from cord blood	blood
20	chr3:141825600-141825800	Enhancers	Duodenum Smooth Muscle	Duodenum
21	chr3:141825600-141826000	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr3:141825800-141826200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr3:141826200-141827000	Weak transcription	Fetal Brain Male	brain
24	chr3:141826800-141827200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr3:141826800-141832400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr3:141827000-141827200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr3:141827000-141827200	Enhancers	Fetal Brain Male	brain
28	chr3:141827000-141827800	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr3:141827000-141827800	Enhancers	GM12878-XiMat	blood
30	chr3:141827000-141828600	Enhancers	Thymus	Thymus
31	chr3:141827800-141828000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr3:141827800-141834600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr3:141828200-141830800	Enhancers	Placenta	Placenta
34	chr3:141828600-141829000	Genic enhancers	Thymus	Thymus
35	chr3:141828800-141829600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr3:141829000-141835200	Weak transcription	Thymus	Thymus
37	chr3:141830400-141830800	Enhancers	HepG2	liver
38	chr3:141830600-141831000	ZNF genes & repeats	Fetal Intestine Small	intestine
39	chr3:141830800-141832200	Weak transcription	Placenta	Placenta
40	chr3:141830800-141835400	Weak transcription	HepG2	liver
41	chr3:141831000-141831600	Weak transcription	Fetal Thymus	thymus
42	chr3:141831200-141832200	Weak transcription	Fetal Intestine Small	intestine
43	chr3:141831600-141833000	ZNF genes & repeats	Fetal Thymus	thymus
44	chr3:141832000-141834800	Weak transcription	Dnd41	blood
45	chr3:141832200-141832800	Enhancers	Placenta	Placenta
46	chr3:141832200-141833000	Strong transcription	Fetal Intestine Small	intestine
47	chr3:141832800-141835000	Weak transcription	Placenta	Placenta
48	chr3:141833000-141834800	Weak transcription	Fetal Thymus	thymus
49	chr3:141833000-141837800	Weak transcription	Fetal Intestine Small	intestine
50	chr3:141834200-141836400	Enhancers	Primary neutrophils fromperipheralblood	blood

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