Variant report

Variant	nsv593211
Chromosome Location	chr4:716248-725867
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:193)
CpG islands
(count:1406)
Chromatin interactive
region (count:20)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:193 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:720284-720486	K562	blood:	n/a	n/a
2	BCL3	chr4:716760-717113	GM12878	blood:	n/a	n/a
3	BCL3	chr4:716688-717009	GM12878	blood:	n/a	n/a
4	BCL3	chr4:716063-716428	GM12878	blood:	n/a	n/a
5	BHLHE40	chr4:720362-720430	K562	blood:	n/a	n/a
6	BHLHE40	chr4:720673-720891	K562	blood:	n/a	n/a
7	CBX3	chr4:725085-726034	K562	blood:	n/a	n/a
8	CCNT2	chr4:725207-725407	K562	blood:	n/a	n/a
9	CCNT2	chr4:724844-724857	K562	blood:	n/a	n/a
10	CCNT2	chr4:719994-720430	K562	blood:	n/a	n/a
11	CEBPB	chr4:721475-721624	K562	blood:	n/a	n/a
12	CEBPB	chr4:720302-720668	K562	blood:	n/a	n/a
13	CEBPB	chr4:720295-720684	IMR90	lung:	n/a	n/a
14	CEBPD	chr4:725545-726059	K562	blood:	n/a	n/a
15	CHD2	chr4:725067-725083	K562	blood:	n/a	n/a
16	CTCF	chr4:720424-720587	K562	blood:	n/a	n/a
17	CTCF	chr4:718080-718230	HepG2	liver:	n/a	n/a
18	CTCF	chr4:719760-719910	AG10803	skin:	n/a	chr4:719846-719859 chr4:719833-719851
19	CTCF	chr4:718100-718250	HepG2	liver:	n/a	chr4:718218-718231
20	CTCF	chr4:716661-716711	Spleen_OC	spleen:	n/a	n/a
21	CTCF	chr4:722134-722286	GM19239	blood:	n/a	n/a
22	CTCF	chr4:719720-719870	AG10803	skin:	n/a	chr4:719846-719859 chr4:719833-719851
23	CTCF	chr4:719016-719035	Lung_OC	lung:	n/a	n/a
24	CTCF	chr4:718070-718260	HepG2	liver:	n/a	chr4:718218-718231
25	CUX1	chr4:720258-720439	K562	blood:	n/a	n/a
26	EGR1	chr4:719104-719426	H1-hESC	embryonic stem cell:	n/a	n/a
27	EGR1	chr4:725738-726092	K562	blood:	n/a	n/a
28	EGR1	chr4:725155-725505	K562	blood:	n/a	n/a
29	EGR1	chr4:725751-726098	K562	blood:	n/a	n/a
30	EGR1	chr4:725181-725413	K562	blood:	n/a	n/a
31	ELF1	chr4:723585-723975	GM12878	blood:	n/a	n/a
32	ELF1	chr4:724272-724583	GM12878	blood:	n/a	chr4:724375-724384
33	EP300	chr4:720190-720688	K562	blood:	n/a	chr4:720485-720499
34	FOXA1	chr4:718108-718388	HepG2	liver:	n/a	chr4:718280-718292
35	FOXA1	chr4:718062-718383	HepG2	liver:	n/a	chr4:718280-718292
36	GABPA	chr4:725263-726093	Hela-S3	cervix:	n/a	n/a
37	GABPA	chr4:716524-716766	GM12878	blood:	n/a	n/a
38	GABPA	chr4:725499-725737	Hela-S3	cervix:	n/a	n/a
39	GATA2	chr4:720187-720648	HUVEC	blood vessel:	n/a	chr4:720338-720348 chr4:720321-720330 chr4:720316-720330
40	HCFC1	chr4:720162-720420	K562	blood:	n/a	n/a
41	HDAC2	chr4:725732-725900	K562	blood:	n/a	n/a
42	HDAC2	chr4:720053-720275	K562	blood:	n/a	n/a
43	HDAC2	chr4:725160-725371	K562	blood:	n/a	n/a
44	HMGN3	chr4:724858-725278	K562	blood:	n/a	n/a
45	HMGN3	chr4:719787-720303	K562	blood:	n/a	n/a
46	HNF4A	chr4:718121-718391	HepG2	liver:	n/a	chr4:718264-718279 chr4:718264-718279 chr4:718264-718279 chr4:718264-718279 chr4:718264-718279
47	HNF4A	chr4:718092-718313	HepG2	liver:	n/a	chr4:718264-718279 chr4:718264-718279 chr4:718264-718279 chr4:718264-718279 chr4:718264-718279
48	IRF1	chr4:720265-720539	K562	blood:	n/a	chr4:720353-720367 chr4:720355-720368 chr4:720354-720374 chr4:720509-720520
49	IRF1	chr4:725773-726147	K562	blood:	n/a	n/a
50	IRF1	chr4:725114-725548	K562	blood:	n/a	n/a

(count:1406 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:719614-719664	BJ	skin:	n/a
2	chr4:720144-720194	AG09309	skin:	n/a
3	chr4:722207-722257	ovcar-3	ovarian:	n/a
4	chr4:719614-719664	BJ	skin:	n/a
5	chr4:720144-720194	AG09309	skin:	n/a
6	chr4:722207-722257	ovcar-3	ovarian:	n/a
7	chr4:721918-721968	AoSMC	blood vessel:	n/a
8	chr4:719011-719061	HCM	heart:	n/a
9	chr4:720218-720268	NHDF-neo	bronchial:	n/a
10	chr4:721972-722022	K562	blood:	n/a
11	chr4:716657-716707	LNCaP	prostate:	n/a
12	chr4:721918-721968	GM19239	blood:	n/a
13	chr4:719614-719664	Hela-S3	cervix:	n/a
14	chr4:719069-719119	Caco-2	colon:	n/a
15	chr4:721944-721994	BJ	skin:	n/a
16	chr4:719908-719958	RPTEC	kidney:	n/a
17	chr4:721972-722022	GM12878	blood:	n/a
18	chr4:720870-720920	LNCaP	prostate:	n/a
19	chr4:725336-725386	SAEC	small airway:	n/a
20	chr4:719614-719664	SAEC	small airway:	n/a
21	chr4:719614-719664	LNCaP	prostate:	n/a
22	chr4:716657-716707	AG04449	skin:	fetal
23	chr4:719011-719061	Hela-S3	cervix:	n/a
24	chr4:722207-722257	SKMC	muscle:	n/a
25	chr4:717040-717090	H1-hESC	embryonic stem cell:	embryo
26	chr4:722598-722648	HMEC	breast:	n/a
27	chr4:722282-722332	BJ	skin:	n/a
28	chr4:721918-721968	HRCEpiC	kidney:	n/a
29	chr4:720870-720920	ProgFib	skin:	n/a
30	chr4:725336-725386	T-47D	breast:	n/a
31	chr4:722598-722648	NB4	blood:	n/a
32	chr4:719908-719958	AoSMC	blood vessel:	n/a
33	chr4:725095-725145	HNPCEpiC	eye:	n/a
34	chr4:722207-722257	LNCaP	prostate:	n/a
35	chr4:722598-722648	SAEC	small airway:	n/a
36	chr4:719614-719664	U87	brain:	n/a
37	chr4:720809-720859	HCM	heart:	n/a
38	chr4:719069-719119	LNCaP	prostate:	n/a
39	chr4:722598-722648	GM19239	blood:	n/a
40	chr4:716657-716707	NH-A	brain:	n/a
41	chr4:716282-716332	HRPEpiC	eye:	n/a
42	chr4:720870-720920	AG04450	lung:	fetal
43	chr4:720809-720859	ovcar-3	ovarian:	n/a
44	chr4:721972-722022	AG09319	gingival:	n/a
45	chr4:716883-716933	HRCEpiC	kidney:	n/a
46	chr4:720809-720859	NHDF-neo	bronchial:	n/a
47	chr4:720809-720859	GM19239	blood:	n/a
48	chr4:717040-717090	PrEC	prostate:	n/a
49	chr4:725095-725145	NHDF-neo	bronchial:	n/a
50	chr4:719011-719061	HRCEpiC	kidney:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:701224..703407-chr4:720806..724106,3	K562	blood:
2	chr4:698948..701157-chr4:719763..722418,3	K562	blood:
3	chr4:725258..728014-chr4:756169..758632,2	MCF-7	breast:
4	chr4:718846..721970-chr4:722068..726476,6	K562	blood:
5	chr4:718839..721866-chr4:723337..725230,5	K562	blood:
6	chr4:718846..721970-chr4:722068..726476,6	K562	blood:
7	chr4:676118..678375-chr4:722491..724316,2	K562	blood:
8	chr4:707339..709378-chr4:720320..722157,2	MCF-7	breast:
9	chr4:715145..716657-chr4:716815..719761,2	MCF-7	breast:
10	chr4:723040..724822-chr4:760521..763494,2	K562	blood:
11	chr4:715797..718296-chr4:723930..726819,3	K562	blood:
12	chr4:713177..716700-chr4:718880..722359,3	MCF-7	breast:
13	chr4:675536..678279-chr4:719522..721602,2	K562	blood:
14	chr4:682540..684982-chr4:715450..717204,2	K562	blood:
15	chr4:685168..687948-chr4:720872..722966,2	K562	blood:
16	chr4:699453..701203-chr4:715716..717348,2	K562	blood:
17	chr4:715797..718296-chr4:723930..726819,3	K562	blood:
18	chr4:673516..676298-chr4:715248..717225,2	K562	blood:
19	chr4:680791..682732-chr4:718975..721351,2	K562	blood:
20	chr4:718839..721866-chr4:723337..725230,5	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MFSD7-1	chr4:717418-717823	NONHSAT094606
2	lnc-MFSD7-1	chr4:717418-717823	ENSG00000248416.1

No data

Variant related genes	Relation type
ENSG00000248416	TF binding region
PCGF3	TF binding region
ENSG00000248416	CpG island
PCGF3	CpG island
ENSG00000215375	chromatin interactions
ENSG00000169026	chromatin interactions
ENSG00000248416	chromatin interactions
ENSG00000185619	chromatin interactions

Extended variants
information (count: 534 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:534 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10452329	chr4:716248-716249	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs544091785	chr4:716263-716264	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs556231883	chr4:716264-716265	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs368376168	chr4:716272-716273	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs541421924	chr4:716286-716287	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs545717888	chr4:716292-716293	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs560112314	chr4:716299-716300	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs527355241	chr4:716302-716303	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs545940132	chr4:716306-716307	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs148811166	chr4:716314-716315	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs565459914	chr4:716315-716316	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs532792814	chr4:716325-716326	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs111979588	chr4:716327-716328	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	mRNA abundance
14	rs562993517	chr4:716379-716380	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs184794562	chr4:716380-716381	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs530430331	chr4:716381-716382	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs548254501	chr4:716387-716388	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs113162348	chr4:716392-716393	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs377210969	chr4:716399-716400	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs112681541	chr4:716400-716401	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs35232439	chr4:716421-716422	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs566880222	chr4:716428-716429	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs113600723	chr4:716454-716455	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs75901702	chr4:716463-716464	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs71602712	chr4:716484-716485	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs189522450	chr4:716487-716488	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs181631788	chr4:716496-716497	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs11732211	chr4:716497-716498	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs76971990	chr4:716521-716522	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	mRNA abundance
30	rs71604311	chr4:716522-716523	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs112145468	chr4:716525-716526	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	mRNA abundance
32	rs76625706	chr4:716530-716531	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	mRNA abundance
33	rs148348677	chr4:716545-716546	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	mRNA abundance
34	rs34667027	chr4:716577-716578	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs537602833	chr4:716606-716607	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs533030899	chr4:716607-716608	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs34077423	chr4:716609-716610	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs556335338	chr4:716637-716638	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs113017606	chr4:716641-716642	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs112398200	chr4:716673-716674	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs113371534	chr4:716702-716703	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs574612783	chr4:716704-716705	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs551276842	chr4:716733-716734	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs111656031	chr4:716734-716735	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs59071858	chr4:716737-716738	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs59397878	chr4:716747-716748	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs113358958	chr4:716750-716751	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs61649182	chr4:716751-716752	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs117983871	chr4:716755-716756	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs61268702	chr4:716764-716765	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17142309	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD
Type 2 diabetes	21754918	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:626 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:701200-724400	Weak transcription	Aorta	Aorta
2	chr4:701400-724400	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr4:701400-724800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr4:701600-716800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr4:702200-754800	Weak transcription	Hela-S3	cervix
6	chr4:702400-720000	Weak transcription	Brain Substantia Nigra	brain
7	chr4:702400-720200	Weak transcription	NH-A	brain
8	chr4:702600-716800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr4:702600-724400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr4:702800-726600	Weak transcription	Primary B cells from cord blood	blood
11	chr4:703000-716600	Weak transcription	Fetal Lung	lung
12	chr4:703400-717800	Weak transcription	Rectal Smooth Muscle	rectum
13	chr4:703400-724800	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr4:703400-726800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr4:703600-727200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr4:703800-724400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr4:704000-724400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr4:704400-721200	Weak transcription	Small Intestine	intestine
19	chr4:704400-721400	Weak transcription	A549	lung
20	chr4:704600-727600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr4:704800-724600	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr4:705000-724400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr4:708200-736400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
24	chr4:708600-716600	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr4:708600-719400	Weak transcription	Osteobl	bone
26	chr4:708800-717800	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr4:709200-724400	Weak transcription	Primary T cells fromperipheralblood	blood
28	chr4:709200-726200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
29	chr4:709200-726200	Weak transcription	Primary T helper cells PMA-I stimulated	--
30	chr4:710600-717400	Strong transcription	Fetal Intestine Small	intestine
31	chr4:711200-718400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr4:711200-718800	ZNF genes & repeats	Fetal Stomach	stomach
33	chr4:711800-724400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr4:713000-718200	ZNF genes & repeats	Brain Germinal Matrix	brain
35	chr4:713200-717200	Genic enhancers	Spleen	Spleen
36	chr4:713200-718000	Strong transcription	Dnd41	blood
37	chr4:713200-719400	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr4:713400-717400	Genic enhancers	Fetal Muscle Trunk	muscle
39	chr4:713400-717600	Strong transcription	H9 Cell Line	embryonic stem cell
40	chr4:713400-718600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
41	chr4:713400-727600	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr4:713600-717800	Strong transcription	Primary neutrophils fromperipheralblood	blood
43	chr4:713800-718200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr4:714000-717400	Genic enhancers	Gastric	stomach
45	chr4:714000-717800	Genic enhancers	Pancreas	Pancrea
46	chr4:714000-718000	Strong transcription	Monocytes-CD14+_RO01746	blood
47	chr4:714200-726200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr4:714400-717200	Strong transcription	Primary T cells from cord blood	blood
49	chr4:714600-716400	ZNF genes & repeats	Thymus	Thymus
50	chr4:714600-717200	Genic enhancers	Placenta	Placenta

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