Variant report

Variant	nsv1002123
Chromosome Location	chr3:141789746-141956778
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2339)
CpG islands
(count:1348)
Chromatin interactive
region (count:112)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:2339 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:141807405-141807560	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:141845145-141845331	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:141868710-141868857	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:141944333-141944542	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	chr3:141818967-141818988	K562	blood:	n/a	n/a
8	ARID3A	chr3:141848736-141848803	HepG2	liver:	n/a	n/a
9	ARID3A	chr3:141941528-141942036	K562	blood:	n/a	n/a
10	ARID3A	chr3:141944275-141944587	HepG2	liver:	n/a	n/a
11	ATF1	chr3:141944202-141944637	K562	blood:	n/a	n/a
12	ATF1	chr3:141817873-141818134	K562	blood:	n/a	n/a
13	ATF2	chr3:141944313-141944572	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr3:141944124-141944603	GM12878	blood:	n/a	n/a
15	ATF3	chr3:141944306-141944624	K562	blood:	n/a	chr3:141944456-141944466
16	ATF3	chr3:141817875-141818204	K562	blood:	n/a	n/a
17	BACH1	chr3:141909646-141909689	K562	blood:	n/a	n/a
18	BACH1	chr3:141867733-141868966	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr3:141944121-141944594	H1-hESC	embryonic stem cell:	n/a	n/a
20	BCLAF1	chr3:141944193-141944635	GM12878	blood:	n/a	n/a
21	BHLHE40	chr3:141944084-141944604	HepG2	liver:	n/a	n/a
22	BHLHE40	chr3:141817872-141818159	K562	blood:	n/a	n/a
23	BHLHE40	chr3:141867704-141868571	HepG2	liver:	n/a	n/a
24	BHLHE40	chr3:141868133-141868604	GM12878	blood:	n/a	n/a
25	BHLHE40	chr3:141943947-141944618	K562	blood:	n/a	chr3:141944033-141944049
26	BHLHE40	chr3:141944144-141944582	GM12878	blood:	n/a	n/a
27	BRCA1	chr3:141944283-141944600	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr3:141867873-141868061	HepG2	liver:	n/a	n/a
29	BRCA1	chr3:141933218-141933348	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr3:141868168-141868537	K562	blood:	n/a	n/a
31	CBX3	chr3:141951133-141951609	K562	blood:	n/a	n/a
32	CBX3	chr3:141951267-141951575	K562	blood:	n/a	n/a
33	CBX3	chr3:141943716-141945024	K562	blood:	n/a	n/a
34	CBX3	chr3:141844975-141845430	HCT-116	colon:	n/a	n/a
35	CCNT2	chr3:141867966-141868502	K562	blood:	n/a	chr3:141868472-141868481
36	CCNT2	chr3:141941669-141942029	K562	blood:	n/a	n/a
37	CCNT2	chr3:141943795-141944658	K562	blood:	n/a	n/a
38	CEBPB	chr3:141919031-141919175	HepG2	liver:	n/a	chr3:141919066-141919077
39	CEBPB	chr3:141837837-141838036	Hela-S3	cervix:	n/a	chr3:141837953-141837964
40	CEBPB	chr3:141941709-141942046	K562	blood:	n/a	chr3:141941830-141941843
41	CEBPB	chr3:141943324-141943690	K562	blood:	n/a	n/a
42	CEBPB	chr3:141807174-141807753	HCT-116	colon:	n/a	chr3:141807508-141807519
43	CEBPB	chr3:141944201-141944594	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr3:141807384-141807749	MCF-7	breast:	n/a	chr3:141807508-141807519
45	CEBPB	chr3:141817852-141818182	K562	blood:	n/a	n/a
46	CEBPB	chr3:141807322-141807697	HepG2	liver:	n/a	chr3:141807508-141807519
47	CEBPB	chr3:141807358-141807699	HepG2	liver:	n/a	chr3:141807508-141807519
48	CEBPB	chr3:141807355-141807687	H1-hESC	embryonic stem cell:	n/a	chr3:141807508-141807519
49	CEBPB	chr3:141807231-141807683	ECC-1	luminal epithelium:	n/a	chr3:141807508-141807519
50	CEBPB	chr3:141807355-141807717	A549	lung:	n/a	chr3:141807508-141807519

(count:1348 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:141944620-141944670	HL-60	blood:	n/a
2	chr3:141944620-141944670	PFSK-1	brain:	n/a
3	chr3:141871386-141871436	HCT-116	colon:	n/a
4	chr3:141868409-141868459	K562	blood:	n/a
5	chr3:141928789-141928839	HIPEpiC	eye:	n/a
6	chr3:141941279-141941329	HCF	heart:	n/a
7	chr3:141944620-141944670	HL-60	blood:	n/a
8	chr3:141944620-141944670	PFSK-1	brain:	n/a
9	chr3:141871386-141871436	HCT-116	colon:	n/a
10	chr3:141868409-141868459	K562	blood:	n/a
11	chr3:141928789-141928839	HIPEpiC	eye:	n/a
12	chr3:141941279-141941329	HCF	heart:	n/a
13	chr3:141868997-141869047	NT2-D1	testis:	n/a
14	chr3:141945703-141945753	MCF-7	breast:	n/a
15	chr3:141871386-141871436	IMR90	lung:	fetal
16	chr3:141877942-141877992	T-47D	breast:	n/a
17	chr3:141928789-141928839	T-47D	breast:	n/a
18	chr3:141944077-141944127	SAEC	small airway:	n/a
19	chr3:141944300-141944350	GM19239	blood:	n/a
20	chr3:141868459-141868509	ProgFib	skin:	n/a
21	chr3:141877942-141877992	LNCaP	prostate:	n/a
22	chr3:141941279-141941329	HPAEpiC	pulmonary alveolar:	n/a
23	chr3:141888226-141888276	GM12891	blood:	n/a
24	chr3:141868409-141868459	LNCaP	prostate:	n/a
25	chr3:141868409-141868459	IMR90	lung:	fetal
26	chr3:141868409-141868459	HRE	kidney:	n/a
27	chr3:141791518-141791568	MCF10A-Er-Src	breast:	n/a
28	chr3:141888226-141888276	HPAEpiC	pulmonary alveolar:	n/a
29	chr3:141867994-141868044	HNPCEpiC	eye:	n/a
30	chr3:141868612-141868662	HMEC	breast:	n/a
31	chr3:141944519-141944569	H1-hESC	embryonic stem cell:	embryo
32	chr3:141867862-141867912	A549	lung:	n/a
33	chr3:141945790-141945840	NB4	blood:	n/a
34	chr3:141867994-141868044	HCT-116	colon:	n/a
35	chr3:141945790-141945840	HIPEpiC	eye:	n/a
36	chr3:141928789-141928839	Caco-2	colon:	n/a
37	chr3:141944344-141944394	HCM	heart:	n/a
38	chr3:141867994-141868044	HEK293	kidney:	embryo
39	chr3:141928789-141928839	GM12892	blood:	n/a
40	chr3:141945790-141945840	AG04449	skin:	fetal
41	chr3:141867994-141868044	AG04450	lung:	fetal
42	chr3:141867862-141867912	AG04450	lung:	fetal
43	chr3:141944620-141944670	SKMC	muscle:	n/a
44	chr3:141944318-141944368	T-47D	breast:	n/a
45	chr3:141944344-141944394	SKMC	muscle:	n/a
46	chr3:141868997-141869047	HCM	heart:	n/a
47	chr3:141868459-141868509	U87	brain:	n/a
48	chr3:141944077-141944127	HEEpiC	esophagus:	n/a
49	chr3:141944300-141944350	Hepatocyte	liver:	n/a
50	chr3:141945703-141945753	HepG2	liver:	n/a

(count:112 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr17:62222919..62223709-chr3:141944062..141944934,2	HCT-116	colon:
2	chr3:141845395..141847742-chr3:141867833..141869425,2	MCF-7	breast:
3	chr3:141866820..141869360-chr3:141877733..141879741,3	MCF-7	breast:
4	chr3:141874750..141877739-chr3:141886968..141889204,2	K562	blood:
5	chr3:141942352..141946050-chr3:141946407..141950976,4	MCF-7	breast:
6	chr3:141921447..141923041-chr3:141938532..141940338,2	K562	blood:
7	chr3:141740878..141741732-chr3:141899625..141900228,2	MCF-7	breast:
8	chr3:141456676..141459122-chr3:141866884..141869547,2	MCF-7	breast:
9	chr3:141869138..141873341-chr3:141874948..141878227,4	MCF-7	breast:
10	chr3:141930773..141933744-chr3:141940549..141942064,2	MCF-7	breast:
11	chr3:141681155..141682217-chr3:141870930..141871455,3	MCF-7	breast:
12	chr3:141888823..141891624-chr3:141893774..141896590,3	K562	blood:
13	chr3:141918309..141919900-chr3:141924207..141926926,2	MCF-7	breast:
14	chr3:23982130..23982921-chr3:141945206..141945893,2	MCF-7	breast:
15	chr3:141880531..141882859-chr3:141943394..141945714,2	K562	blood:
16	chr3:141939241..141942550-chr3:141942923..141945578,4	MCF-7	breast:
17	chr3:141919674..141922479-chr3:141924056..141926779,2	MCF-7	breast:
18	chr3:141924115..141926296-chr3:141927657..141929893,2	K562	blood:
19	chr20:30192660..30193363-chr3:141943889..141944590,2	Hela-S3	cervix:
20	chr3:141866047..141867912-chr3:141873721..141875434,2	K562	blood:
21	chr3:141888192..141890414-chr3:141943053..141945967,2	MCF-7	breast:
22	chr3:141862592..141866605-chr3:141869452..141871962,3	MCF-7	breast:
23	chr3:141823415..141824933-chr3:141840146..141843021,2	MCF-7	breast:
24	chr21:43815752..43816528-chr3:141944124..141945000,2	Hela-S3	cervix:
25	chr1:45284275..45285951-chr3:141939370..141941710,2	K562	blood:
26	chr3:141866047..141867912-chr3:141873721..141875434,2	K562	blood:
27	chr3:141872069..141873758-chr3:141878365..141880269,2	MCF-7	breast:
28	chr3:141816249..141818254-chr3:141826549..141828683,2	MCF-7	breast:
29	chr3:141874750..141877739-chr3:141886968..141889204,2	K562	blood:
30	chr3:141816604..141818646-chr3:141821637..141823768,2	K562	blood:
31	chr3:141928249..141931424-chr3:141932973..141936618,4	K562	blood:
32	chr3:141869138..141873341-chr3:141874948..141878227,4	MCF-7	breast:
33	chr3:141866276..141868412-chr3:141942932..141945800,2	MCF-7	breast:
34	chr3:141866951..141869794-chr3:141871330..141873613,3	MCF-7	breast:
35	chr3:141866172..141869567-chr3:141870149..141874954,7	MCF-7	breast:
36	chr3:141898603..141901511-chr3:141942977..141947111,4	MCF-7	breast:
37	chr3:141929745..141931253-chr3:141941462..141943511,2	MCF-7	breast:
38	chr3:141920036..141922248-chr3:141942825..141944826,2	K562	blood:
39	chr3:141919625..141921887-chr3:141933849..141936243,2	K562	blood:
40	chr3:141930773..141933744-chr3:141940549..141942064,2	MCF-7	breast:
41	chr3:141940937..141945863-chr3:141947298..141949257,5	K562	blood:
42	chr3:141831489..141833335-chr3:141922195..141926170,3	K562	blood:
43	chr3:141921447..141923041-chr3:141938532..141940338,2	K562	blood:
44	chr3:141924115..141926296-chr3:141927657..141929893,2	K562	blood:
45	chr3:141835499..141837454-chr3:141839665..141841997,2	K562	blood:
46	chr3:141944534..141946087-chr3:141987477..141990045,2	MCF-7	breast:
47	chr3:141789085..141790599-chr3:141791414..141793692,2	MCF-7	breast:
48	chr3:141866424..141868170-chr3:141875148..141877149,2	MCF-7	breast:
49	chr3:141932221..141937955-chr3:141938851..141945696,9	K562	blood:
50	chr17:80184285..80186683-chr3:141942385..141945027,2	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:2 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	GK5	hsa-miR-340-5p	chr3:141878164-141878157
2	GK5	hsa-miR-124-3p	chr3:141883855-141883849

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

Extended variants
information (count: 5858 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:5858 , 50 per page) page: 1 2 3 4 5 6 7 ... 118

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530113576	chr3:141789754-141789755	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs369118016	chr3:141789782-141789783	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs534035042	chr3:141789867-141789868	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs549182322	chr3:141789881-141789882	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs554202844	chr3:141789883-141789884	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs560884797	chr3:141789894-141789895	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs185497275	chr3:141789895-141789896	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs148511456	chr3:141789897-141789898	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs571561085	chr3:141789904-141789905	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs538675374	chr3:141789962-141789963	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs112791197	chr3:141790003-141790004	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs576736522	chr3:141790004-141790005	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs544531343	chr3:141790092-141790093	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs550576194	chr3:141790101-141790102	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs568957957	chr3:141790144-141790145	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551790539	chr3:141790153-141790154	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189203596	chr3:141790154-141790155	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs375392258	chr3:141790279-141790280	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs555156585	chr3:141790300-141790301	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs573310759	chr3:141790315-141790316	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs180745224	chr3:141790388-141790389	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs573970494	chr3:141790433-141790434	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs184998616	chr3:141790488-141790489	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs188683834	chr3:141790536-141790537	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs376666880	chr3:141790554-141790555	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs562513900	chr3:141790585-141790586	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs574891430	chr3:141790628-141790629	Weak transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs371272305	chr3:141790664-141790665	Weak transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs146570109	chr3:141790697-141790698	Weak transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs561137683	chr3:141790749-141790750	Weak transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs181166438	chr3:141790780-141790781	Weak transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs540418558	chr3:141790798-141790799	Weak transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs78273107	chr3:141790799-141790800	Weak transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs532422109	chr3:141790848-141790849	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs550613822	chr3:141790856-141790857	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs542983451	chr3:141790869-141790870	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs568721498	chr3:141790920-141790921	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs558436121	chr3:141790971-141790972	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs143797043	chr3:141791030-141791031	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs186981282	chr3:141791056-141791057	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs577923436	chr3:141791060-141791061	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs558703444	chr3:141791086-141791087	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570829976	chr3:141791115-141791116	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs538115425	chr3:141791311-141791312	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs77092046	chr3:141791362-141791363	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191653039	chr3:141791381-141791382	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs4683419	chr3:141791408-141791409	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs554013205	chr3:141791490-141791491	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs572483720	chr3:141791519-141791520	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540456271	chr3:141791550-141791551	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

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

Chromatin state (count:3230 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:141760600-141800800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr3:141761000-141807800	Weak transcription	Fetal Lung	lung
3	chr3:141761800-141819600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr3:141763000-141820000	Weak transcription	Pancreas	Pancrea
5	chr3:141763000-141824200	Weak transcription	Aorta	Aorta
6	chr3:141764000-141825600	Weak transcription	Primary T cells from cord blood	blood
7	chr3:141765000-141818800	Weak transcription	Primary B cells from cord blood	blood
8	chr3:141767000-141798000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr3:141767600-141807200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr3:141769600-141790200	Strong transcription	Fetal Thymus	thymus
11	chr3:141770400-141795800	Weak transcription	Fetal Stomach	stomach
12	chr3:141774400-141798800	Weak transcription	Primary hematopoietic stem cells	blood
13	chr3:141776000-141805400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr3:141776400-141795800	Weak transcription	Ovary	ovary
15	chr3:141780600-141791400	Weak transcription	Thymus	Thymus
16	chr3:141780600-141796400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr3:141780800-141796400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr3:141781800-141790400	Weak transcription	Dnd41	blood
19	chr3:141783000-141795800	Weak transcription	Psoas Muscle	Psoas
20	chr3:141783800-141790600	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr3:141784000-141796000	Weak transcription	Lung	lung
22	chr3:141784600-141796000	Weak transcription	Fetal Muscle Leg	muscle
23	chr3:141785000-141790000	Weak transcription	Small Intestine	intestine
24	chr3:141785200-141796600	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr3:141785600-141791800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr3:141785800-141791200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr3:141785800-141791400	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr3:141785800-141791600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr3:141785800-141796200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr3:141786600-141792400	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr3:141789200-141792200	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr3:141789400-141789800	Weak transcription	Fetal Intestine Small	intestine
33	chr3:141789600-141805000	Weak transcription	HepG2	liver
34	chr3:141789800-141790000	Enhancers	Colonic Mucosa	Colon
35	chr3:141789800-141790200	Enhancers	Duodenum Mucosa	Duodenum
36	chr3:141789800-141792200	Enhancers	Fetal Intestine Small	intestine
37	chr3:141790000-141790200	Enhancers	Sigmoid Colon	Sigmoid Colon
38	chr3:141790000-141791000	Enhancers	Small Intestine	intestine
39	chr3:141790000-141792200	Enhancers	Fetal Intestine Large	intestine
40	chr3:141790000-141795800	Weak transcription	Colonic Mucosa	Colon
41	chr3:141790200-141790600	Weak transcription	Duodenum Mucosa	Duodenum
42	chr3:141790200-141790800	Genic enhancers	Fetal Thymus	thymus
43	chr3:141790200-141796000	Weak transcription	Sigmoid Colon	Sigmoid Colon
44	chr3:141790400-141791600	Enhancers	Dnd41	blood
45	chr3:141790400-141801600	Weak transcription	Brain Anterior Caudate	brain
46	chr3:141790600-141790800	Active TSS	Rectal Mucosa Donor 29	rectum
47	chr3:141790600-141792600	Enhancers	Duodenum Mucosa	Duodenum
48	chr3:141790800-141791000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
49	chr3:141790800-141792400	Strong transcription	Fetal Thymus	thymus
50	chr3:141791000-141791200	Weak transcription	Small Intestine	intestine

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