Variant report

Variant	nsv591912
Chromosome Location	chr3:141812759-142071932
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3157)
CpG islands
(count:1403)
Chromatin interactive
region (count:153)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

(count:3157 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:141944333-141944542	K562	blood:	n/a	n/a
2	ARID3A	chr3:142034796-142035079	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:141818967-141818988	K562	blood:	n/a	n/a
4	ARID3A	chr3:142037995-142038366	K562	blood:	n/a	n/a
5	ARID3A	chr3:141845072-141845387	K562	blood:	n/a	n/a
6	ARID3A	chr3:141868086-141868286	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:142034735-142035065	K562	blood:	n/a	n/a
8	ARID3A	chr3:141941528-141942036	K562	blood:	n/a	n/a
9	ARID3A	chr3:142004029-142004406	K562	blood:	n/a	n/a
10	ARID3A	chr3:141845145-141845331	HepG2	liver:	n/a	n/a
11	ARID3A	chr3:141868710-141868857	HepG2	liver:	n/a	n/a
12	ARID3A	chr3:141848736-141848803	HepG2	liver:	n/a	n/a
13	ARID3A	chr3:141944275-141944587	HepG2	liver:	n/a	n/a
14	ATF1	chr3:142034743-142035113	K562	blood:	n/a	n/a
15	ATF1	chr3:142038012-142038223	K562	blood:	n/a	n/a
16	ATF1	chr3:141817873-141818134	K562	blood:	n/a	n/a
17	ATF1	chr3:141944202-141944637	K562	blood:	n/a	n/a
18	ATF1	chr3:142026474-142026530	K562	blood:	n/a	n/a
19	ATF1	chr3:142004039-142004362	K562	blood:	n/a	n/a
20	ATF1	chr3:141994868-141995043	K562	blood:	n/a	n/a
21	ATF2	chr3:141944124-141944603	GM12878	blood:	n/a	n/a
22	ATF2	chr3:141944313-141944572	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF3	chr3:141817875-141818204	K562	blood:	n/a	n/a
24	ATF3	chr3:141944306-141944624	K562	blood:	n/a	chr3:141944456-141944466
25	ATF3	chr3:142034698-142035057	K562	blood:	n/a	n/a
26	BACH1	chr3:141988570-141988640	K562	blood:	n/a	n/a
27	BACH1	chr3:141867733-141868966	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr3:142037995-142038332	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr3:141944121-141944594	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr3:141909646-141909689	K562	blood:	n/a	n/a
31	BACH1	chr3:142037969-142038499	K562	blood:	n/a	n/a
32	BATF	chr3:141975772-141975937	GM12878	blood:	n/a	n/a
33	BCLAF1	chr3:141998774-141999206	GM12878	blood:	n/a	n/a
34	BCLAF1	chr3:141998835-141999218	GM12878	blood:	n/a	n/a
35	BCLAF1	chr3:141944193-141944635	GM12878	blood:	n/a	n/a
36	BHLHE40	chr3:141867704-141868571	HepG2	liver:	n/a	n/a
37	BHLHE40	chr3:141943947-141944618	K562	blood:	n/a	chr3:141944033-141944049
38	BHLHE40	chr3:141998833-141999090	HepG2	liver:	n/a	n/a
39	BHLHE40	chr3:141944144-141944582	GM12878	blood:	n/a	n/a
40	BHLHE40	chr3:141998848-141999153	K562	blood:	n/a	n/a
41	BHLHE40	chr3:141944084-141944604	HepG2	liver:	n/a	n/a
42	BHLHE40	chr3:141817872-141818159	K562	blood:	n/a	n/a
43	BHLHE40	chr3:141868133-141868604	GM12878	blood:	n/a	n/a
44	BHLHE40	chr3:141998901-141999171	GM12878	blood:	n/a	n/a
45	BHLHE40	chr3:142066400-142066735	K562	blood:	n/a	n/a
46	BRCA1	chr3:141933218-141933348	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr3:141867873-141868061	HepG2	liver:	n/a	n/a
48	BRCA1	chr3:141944283-141944600	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr3:141994588-141995155	Hela-S3	cervix:	n/a	n/a
50	CBX3	chr3:141974109-141974466	K562	blood:	n/a	n/a

(count:1403 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:141995701-141995751	HepG2	liver:	n/a
2	chr3:141868459-141868509	HCT-116	colon:	n/a
3	chr3:141945703-141945753	GM19239	blood:	n/a
4	chr3:141944318-141944368	HCM	heart:	n/a
5	chr3:141944318-141944368	LNCaP	prostate:	n/a
6	chr3:141868409-141868459	HAEpiC	amniotic membrane:	n/a
7	chr3:141944077-141944127	Caco-2	colon:	n/a
8	chr3:141868409-141868459	MCF10A-Er-Src	breast:	n/a
9	chr3:141868459-141868509	AG10803	skin:	n/a
10	chr3:141888226-141888276	MCF-7	breast:	n/a
11	chr3:141945703-141945753	PFSK-1	brain:	n/a
12	chr3:141868409-141868459	T-47D	breast:	n/a
13	chr3:141868409-141868459	AG09309	skin:	n/a
14	chr3:141943895-141943945	ProgFib	skin:	n/a
15	chr3:141944620-141944670	A549	lung:	n/a
16	chr3:141944519-141944569	H1-hESC	embryonic stem cell:	embryo
17	chr3:141941279-141941329	HMEC	breast:	n/a
18	chr3:142027066-142027116	MCF-7	breast:	n/a
19	chr3:141944516-141944566	HepG2	liver:	n/a
20	chr3:141868997-141869047	RPTEC	kidney:	n/a
21	chr3:141871386-141871436	LNCaP	prostate:	n/a
22	chr3:141995701-141995751	K562	blood:	n/a
23	chr3:141868997-141869047	HUVEC	blood vessel:	n/a
24	chr3:141888226-141888276	U87	brain:	n/a
25	chr3:141944077-141944127	SKMC	muscle:	n/a
26	chr3:142027066-142027116	PANC-1	pancreas:	n/a
27	chr3:141928789-141928839	HRPEpiC	eye:	n/a
28	chr3:141995701-141995751	HEK293	kidney:	embryo
29	chr3:141941279-141941329	GM12891	blood:	n/a
30	chr3:141944300-141944350	GM12891	blood:	n/a
31	chr3:141944077-141944127	HEEpiC	esophagus:	n/a
32	chr3:141943895-141943945	HAEpiC	amniotic membrane:	n/a
33	chr3:141945790-141945840	HCF	heart:	n/a
34	chr3:142027066-142027116	PrEC	prostate:	n/a
35	chr3:141928789-141928839	K562	blood:	n/a
36	chr3:141944519-141944569	PFSK-1	brain:	n/a
37	chr3:141943895-141943945	SK-N-MC	brain:	n/a
38	chr3:141888226-141888276	NB4	blood:	n/a
39	chr3:141944620-141944670	HEEpiC	esophagus:	n/a
40	chr3:141888226-141888276	HPAEpiC	pulmonary alveolar:	n/a
41	chr3:141943895-141943945	AoSMC	blood vessel:	n/a
42	chr3:141943895-141943945	GM12891	blood:	n/a
43	chr3:141945703-141945753	ProgFib	skin:	n/a
44	chr3:141871386-141871436	HMEC	breast:	n/a
45	chr3:141944318-141944368	SAEC	small airway:	n/a
46	chr3:141868612-141868662	HIPEpiC	eye:	n/a
47	chr3:141944620-141944670	AG04450	lung:	fetal
48	chr3:141943895-141943945	Caco-2	colon:	n/a
49	chr3:141867862-141867912	GM06990	blood:	n/a
50	chr3:141888226-141888276	H1-hESC	embryonic stem cell:	embryo

(count:153 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr3:142061779..142063304-chr3:142065930..142068810,2	K562	blood:
2	chr3:141941960..141945693-chr3:142033521..142037066,3	K562	blood:
3	chr20:30192660..30193363-chr3:141943889..141944590,2	Hela-S3	cervix:
4	chr3:142031696..142033287-chr3:142037661..142039925,2	MCF-7	breast:
5	chr3:141986894..141989145-chr3:141996424..141998046,2	K562	blood:
6	chr3:141899683..141900200-chr3:141998508..141999054,2	K562	blood:
7	chr13:28032235..28033740-chr3:141906874..141908394,2	MCF-7	breast:
8	chr3:141823415..141824933-chr3:141840146..141843021,2	MCF-7	breast:
9	chr3:141874750..141877739-chr3:141886968..141889204,2	K562	blood:
10	chr3:141733456..141735928-chr3:141995928..141997484,2	K562	blood:
11	chr3:141866471..141869350-chr3:141942355..141944493,2	K562	blood:
12	chr3:141916087..141917951-chr3:141939342..141941586,2	K562	blood:
13	chr3:141863639..141867822-chr3:141868615..141873401,6	K562	blood:
14	chr3:142064702..142067188-chr3:142070699..142072268,2	K562	blood:
15	chr3:141456676..141459122-chr3:141866884..141869547,2	MCF-7	breast:
16	chr3:141873069..141875142-chr3:141877650..141879337,2	K562	blood:
17	chr3:141914914..141916949-chr3:141917367..141920269,2	K562	blood:
18	chr3:141928249..141931424-chr3:141932973..141936618,4	K562	blood:
19	chr3:141998539..142000204-chr3:142002540..142004917,2	K562	blood:
20	chr3:142028519..142033203-chr3:142033786..142039324,7	K562	blood:
21	chr3:141918898..141921887-chr3:141933656..141936243,2	K562	blood:
22	chr3:141873069..141875142-chr3:141877650..141879337,2	K562	blood:
23	chr3:142064702..142067188-chr3:142070699..142072268,2	K562	blood:
24	chr3:142061779..142063304-chr3:142065930..142068810,2	K562	blood:
25	chr3:142026133..142029209-chr3:142034990..142037893,3	MCF-7	breast:
26	chr3:142028519..142031113-chr3:142035238..142036947,2	K562	blood:
27	chr3:141681127..141682067-chr3:141998956..141999598,2	MCF-7	breast:
28	chr3:141872069..141873758-chr3:141878365..141880269,2	MCF-7	breast:
29	chr17:80184285..80186683-chr3:141942385..141945027,2	MCF-7	breast:
30	chr3:141943937..141944882-chr5:32585069..32586043,2	Hela-S3	cervix:
31	chr3:141872069..141873758-chr3:141878365..141880269,2	MCF-7	breast:
32	chr3:141919674..141922479-chr3:141924056..141926779,2	MCF-7	breast:
33	chr3:141869138..141873341-chr3:141874948..141878227,4	MCF-7	breast:
34	chr3:142028519..142031113-chr3:142035238..142036947,2	K562	blood:
35	chr3:141866820..141869360-chr3:141877733..141879741,3	MCF-7	breast:
36	chr3:141816249..141818254-chr3:141826549..141828683,2	MCF-7	breast:
37	chr3:142066835..142068380-chr3:142068524..142070586,2	K562	blood:
38	chr3:141944032..141945017-chr8:143808717..143809376,2	Hela-S3	cervix:
39	chr3:141998539..142000204-chr3:142002540..142004917,2	K562	blood:
40	chr3:141866047..141867912-chr3:141873721..141875434,2	K562	blood:
41	chr3:141819750..141822560-chr3:141822824..141825264,3	MCF-7	breast:
42	chr3:141939985..141942934-chr3:141962121..141964269,2	K562	blood:
43	chr3:141888823..141891624-chr3:141893774..141896590,3	K562	blood:
44	chr3:141844885..141845509-chr3:141998474..141999186,2	MCF-7	breast:
45	chr3:141831489..141833335-chr3:141922195..141926170,3	K562	blood:
46	chr3:141831489..141833335-chr3:141922195..141926170,3	K562	blood:
47	chr3:141844721..141845463-chr3:141945183..141945790,2	MCF-7	breast:
48	chr3:141942352..141946050-chr3:141946407..141950976,4	MCF-7	breast:
49	chr3:142042619..142044340-chr3:142047762..142050315,2	K562	blood:
50	chr3:141930773..141933744-chr3:141940549..141942064,2	MCF-7	breast:

(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-miR-10a-5p	chr3:142029592-142029585
2	GK5	hsa-miR-124-3p	chr3:141883855-141883849
3	XRN1	hsa-miR-10a-5p	chr3:142029586-142029608
4	XRN1	hsa-miR-335-5p	chr3:142025482-142025506
5	GK5	hsa-miR-340-5p	chr3:141878164-141878157
6	XRN1	hsa-let-7b-5p	chr3:142030132-142030126

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
ENSG00000130193	chromatin interactions
ENSG00000122545	chromatin interactions
ENSG00000199753	chromatin interactions
ENSG00000114127	chromatin interactions
ENSG00000114126	chromatin interactions
ENSG00000253806	chromatin interactions
ENSG00000202444	chromatin interactions
ENSG00000162636	chromatin interactions
ENSG00000125968	chromatin interactions
ENSG00000141526	chromatin interactions
ENSG00000113387	chromatin interactions
ENSG00000206604	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000160183	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000228878	chromatin interactions
ENSG00000175066	chromatin interactions
ENSG00000272565	chromatin interactions
ENSG00000175054	chromatin interactions
ENSG00000114125	chromatin interactions
ENSG00000266402	chromatin interactions

Extended variants
information (count: 8382 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:8382 , 50 per page) page: 1 2 3 4 5 6 7 ... 168

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9877817	chr3:141812759-141812760	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs145076086	chr3:141812796-141812797	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs533889166	chr3:141812851-141812852	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs558419064	chr3:141812965-141812966	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs576463303	chr3:141812966-141812967	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs537424341	chr3:141812990-141812991	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs78108506	chr3:141813022-141813023	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs149121902	chr3:141813030-141813031	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs7652258	chr3:141813050-141813051	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs116104255	chr3:141813083-141813084	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs531502555	chr3:141813098-141813099	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs564756587	chr3:141813134-141813135	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs374593035	chr3:141813147-141813148	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs34185822	chr3:141813158-141813159	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs398062867	chr3:141813163-141813164	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs371370872	chr3:141813164-141813165	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs7640665	chr3:141813172-141813173	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs550172965	chr3:141813191-141813192	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs562179201	chr3:141813196-141813197	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs529328713	chr3:141813228-141813229	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs192840260	chr3:141813233-141813234	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs377675669	chr3:141813238-141813239	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs566590154	chr3:141813337-141813338	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs147877018	chr3:141813349-141813350	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs202155278	chr3:141813376-141813377	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs570384225	chr3:141813396-141813397	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs141604932	chr3:141813452-141813453	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs555697140	chr3:141813484-141813485	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs568153294	chr3:141813513-141813514	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs185786788	chr3:141813518-141813519	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs553823401	chr3:141813550-141813551	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs376427558	chr3:141813651-141813652	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs527333522	chr3:141813668-141813669	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs114700481	chr3:141813674-141813675	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs547361061	chr3:141813708-141813709	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs576776272	chr3:141813743-141813744	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs566958169	chr3:141813747-141813748	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs543847700	chr3:141813752-141813753	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs562111489	chr3:141813764-141813765	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs529278861	chr3:141813767-141813768	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs563783791	chr3:141813803-141813804	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs541199996	chr3:141813821-141813822	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs62284561	chr3:141813822-141813823	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs149977736	chr3:141813831-141813832	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs373480120	chr3:141813839-141813840	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs147068471	chr3:141813902-141813903	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs551916891	chr3:141813983-141813984	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs148121694	chr3:141814003-141814004	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs141938718	chr3:141814089-141814090	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs565185330	chr3:141814091-141814092	Weak transcription Genic enhancers 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:4665 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:141761800-141819600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr3:141763000-141820000	Weak transcription	Pancreas	Pancrea
3	chr3:141763000-141824200	Weak transcription	Aorta	Aorta
4	chr3:141764000-141825600	Weak transcription	Primary T cells from cord blood	blood
5	chr3:141765000-141818800	Weak transcription	Primary B cells from cord blood	blood
6	chr3:141795400-141835800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr3:141797200-141813000	Weak transcription	Fetal Stomach	stomach
8	chr3:141797600-141819600	Weak transcription	Fetal Muscle Leg	muscle
9	chr3:141797600-141823600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr3:141799600-141814600	Weak transcription	Primary hematopoietic stem cells	blood
11	chr3:141803600-141814200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr3:141804000-141819200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr3:141804000-141820800	Weak transcription	Left Ventricle	heart
14	chr3:141806200-141818600	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr3:141807000-141817600	Weak transcription	Fetal Intestine Large	intestine
16	chr3:141807200-141817800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr3:141809000-141814200	Genic enhancers	Fetal Thymus	thymus
18	chr3:141809600-141814400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr3:141810800-141816200	Weak transcription	Thymus	Thymus
20	chr3:141811400-141816200	Weak transcription	Fetal Intestine Small	intestine
21	chr3:141811600-141817400	Enhancers	Dnd41	blood
22	chr3:141814200-141814600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr3:141814200-141815400	Weak transcription	Fetal Thymus	thymus
24	chr3:141814400-141816200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr3:141814400-141816400	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr3:141814600-141815000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr3:141814600-141815200	Enhancers	Primary hematopoietic stem cells	blood
28	chr3:141815000-141815800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr3:141815200-141815600	Weak transcription	Primary hematopoietic stem cells	blood
30	chr3:141815400-141821000	Genic enhancers	Fetal Thymus	thymus
31	chr3:141815600-141815800	Enhancers	Primary hematopoietic stem cells	blood
32	chr3:141815800-141817400	Weak transcription	Primary hematopoietic stem cells	blood
33	chr3:141815800-141817400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr3:141816200-141816400	Enhancers	Fetal Stomach	stomach
35	chr3:141816200-141816400	Strong transcription	Thymus	Thymus
36	chr3:141816200-141816800	Strong transcription	Fetal Intestine Small	intestine
37	chr3:141816200-141817400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr3:141816400-141816600	Genic enhancers	Thymus	Thymus
39	chr3:141816400-141817400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr3:141816600-141817200	Strong transcription	Thymus	Thymus
41	chr3:141816800-141817600	Weak transcription	Fetal Intestine Small	intestine
42	chr3:141817200-141817800	Genic enhancers	Thymus	Thymus
43	chr3:141817400-141817800	Enhancers	Primary hematopoietic stem cells	blood
44	chr3:141817400-141818200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr3:141817400-141818200	Flanking Active TSS	Dnd41	blood
46	chr3:141817400-141819200	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr3:141817400-141819200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr3:141817400-141819200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr3:141817400-141819800	Enhancers	K562	blood
50	chr3:141817600-141818200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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