Variant report

Variant	esv3440400
Chromosome Location	chr4:1301202-1303700
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:244)
CpG islands
(count:244)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:1303206-1303459	HepG2	liver:	n/a	n/a
2	ATF3	chr4:1303046-1303311	K562	blood:	n/a	n/a
3	ATF3	chr4:1303028-1303373	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr4:1302974-1303356	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr4:1303015-1303285	GM12878	blood:	n/a	n/a
6	BACH1	chr4:1303047-1303600	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr4:1302989-1303306	HepG2	liver:	n/a	chr4:1303183-1303192 chr4:1303184-1303193 chr4:1303274-1303290 chr4:1303184-1303193
8	BHLHE40	chr4:1302984-1303394	K562	blood:	n/a	chr4:1303183-1303192 chr4:1303184-1303193 chr4:1303274-1303290 chr4:1303184-1303193
9	BHLHE40	chr4:1303007-1303288	HepG2	liver:	n/a	chr4:1303183-1303192 chr4:1303184-1303193 chr4:1303184-1303193
10	BHLHE40	chr4:1302904-1303380	GM12878	blood:	n/a	chr4:1303183-1303192 chr4:1303184-1303193 chr4:1303274-1303290 chr4:1303184-1303193
11	BHLHE40	chr4:1302742-1303785	HepG2	liver:	n/a	chr4:1303183-1303192 chr4:1303184-1303193 chr4:1303274-1303290 chr4:1303184-1303193
12	CCNT2	chr4:1302319-1302370	K562	blood:	n/a	n/a
13	CEBPB	chr4:1303076-1303323	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPD	chr4:1303025-1303480	HepG2	liver:	n/a	n/a
15	CHD2	chr4:1303127-1303408	GM12878	blood:	n/a	n/a
16	CHD2	chr4:1303131-1303459	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr4:1303431-1303631	HepG2	liver:	n/a	n/a
18	CTCF	chr4:1303240-1303390	SK-N-SH_RA	brain:	n/a	n/a
19	CTCF	chr4:1303200-1303350	BJ	skin:	n/a	n/a
20	CTCF	chr4:1303180-1303330	AG09319	gingival:	n/a	n/a
21	CTCF	chr4:1303160-1303310	AG04449	skin:	n/a	n/a
22	CTCF	chr4:1303257-1303286	GM19238	blood:	n/a	n/a
23	CTCF	chr4:1303253-1303327	GM12891	blood:	n/a	n/a
24	CTCF	chr4:1301633-1301660	HepG2	liver:	n/a	n/a
25	CTCF	chr4:1301544-1301721	HepG2	liver:	n/a	n/a
26	CTCF	chr4:1303160-1303310	HUVEC	blood vessel:	n/a	n/a
27	CTCF	chr4:1303100-1303250	GM12873	blood:	n/a	n/a
28	CTCF	chr4:1303306-1303313	Lung_OC	lung:	n/a	n/a
29	CTCF	chr4:1303180-1303330	HPF	lung:	n/a	n/a
30	CTCF	chr4:1303200-1303350	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr4:1303220-1303370	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr4:1303580-1303730	AG04449	skin:	n/a	n/a
33	CTCF	chr4:1303260-1303410	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr4:1303100-1303250	HVMF	connective:	n/a	n/a
35	CTCF	chr4:1301520-1301670	HepG2	liver:	n/a	n/a
36	CTCF	chr4:1303170-1303336	Spleen_OC	spleen:	n/a	n/a
37	CTCF	chr4:1303294-1303318	GM19238	blood:	n/a	n/a
38	CTCF	chr4:1303257-1303452	IMR90	lung:	n/a	n/a
39	CTCF	chr4:1303220-1303370	AG04449	skin:	n/a	n/a
40	CTCF	chr4:1302840-1302990	AoAF	blood vessel:	n/a	n/a
41	CTCF	chr4:1303065-1303103	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr4:1303160-1303310	BJ	skin:	n/a	n/a
43	CTCF	chr4:1303020-1303170	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr4:1301635-1301695	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr4:1303580-1303730	HCPEpiC	choroid plexus:	n/a	n/a
46	E2F6	chr4:1303065-1303301	K562	blood:	n/a	n/a
47	EGR1	chr4:1303038-1303525	K562	blood:	n/a	chr4:1303403-1303414 chr4:1303403-1303414 chr4:1303511-1303521
48	EGR1	chr4:1303080-1303617	H1-hESC	embryonic stem cell:	n/a	chr4:1303403-1303414 chr4:1303403-1303414 chr4:1303511-1303521
49	EGR1	chr4:1303136-1303461	GM12878	blood:	n/a	chr4:1303403-1303414 chr4:1303403-1303414
50	EGR1	chr4:1303017-1303525	K562	blood:	n/a	chr4:1303403-1303414 chr4:1303403-1303414 chr4:1303511-1303521

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:1303317-1303367	HCF	heart:	n/a
2	chr4:1303491-1303541	SK-N-MC	brain:	n/a
3	chr4:1302456-1302506	AoSMC	blood vessel:	n/a
4	chr4:1302456-1302506	AG10803	skin:	n/a
5	chr4:1303317-1303367	RPTEC	kidney:	n/a
6	chr4:1303317-1303367	MCF10A-Er-Src	breast:	n/a
7	chr4:1302456-1302506	GM19239	blood:	n/a
8	chr4:1302456-1302506	RPTEC	kidney:	n/a
9	chr4:1303317-1303367	AG04449	skin:	fetal
10	chr4:1303491-1303541	A549	lung:	n/a
11	chr4:1302238-1302288	ovcar-3	ovarian:	n/a
12	chr4:1303491-1303541	HIPEpiC	eye:	n/a
13	chr4:1302238-1302288	Hela-S3	cervix:	n/a
14	chr4:1303491-1303541	HNPCEpiC	eye:	n/a
15	chr4:1303317-1303367	HPAEpiC	pulmonary alveolar:	n/a
16	chr4:1303491-1303541	MCF10A-Er-Src	breast:	n/a
17	chr4:1303491-1303541	GM12892	blood:	n/a
18	chr4:1303491-1303541	GM12878	blood:	n/a
19	chr4:1302238-1302288	H1-hESC	embryonic stem cell:	embryo
20	chr4:1303491-1303541	HCT-116	colon:	n/a
21	chr4:1303317-1303367	PFSK-1	brain:	n/a
22	chr4:1303317-1303367	LNCaP	prostate:	n/a
23	chr4:1302238-1302288	IMR90	lung:	fetal
24	chr4:1302456-1302506	HCPEpiC	choroid plexus:	n/a
25	chr4:1303317-1303367	AG10803	skin:	n/a
26	chr4:1302238-1302288	SK-N-SH_RA	brain:	n/a
27	chr4:1303317-1303367	ProgFib	skin:	n/a
28	chr4:1302456-1302506	ECC-1	luminal epithelium:	n/a
29	chr4:1302456-1302506	HRCEpiC	kidney:	n/a
30	chr4:1303317-1303367	HEK293	kidney:	embryo
31	chr4:1302456-1302506	HCF	heart:	n/a
32	chr4:1302456-1302506	AG04450	lung:	fetal
33	chr4:1303317-1303367	NT2-D1	testis:	n/a
34	chr4:1302238-1302288	HCPEpiC	choroid plexus:	n/a
35	chr4:1303491-1303541	H1-hESC	embryonic stem cell:	embryo
36	chr4:1303317-1303367	HMEC	breast:	n/a
37	chr4:1302238-1302288	SK-N-SH	brain:	n/a
38	chr4:1302238-1302288	HRCEpiC	kidney:	n/a
39	chr4:1303491-1303541	AG04449	skin:	fetal
40	chr4:1303491-1303541	HUVEC	blood vessel:	n/a
41	chr4:1302238-1302288	HUVEC	blood vessel:	n/a
42	chr4:1303317-1303367	Caco-2	colon:	n/a
43	chr4:1302456-1302506	MCF10A-Er-Src	breast:	n/a
44	chr4:1303317-1303367	GM12878	blood:	n/a
45	chr4:1302456-1302506	HCM	heart:	n/a
46	chr4:1302456-1302506	NB4	blood:	n/a
47	chr4:1302238-1302288	SAEC	small airway:	n/a
48	chr4:1302238-1302288	GM12878	blood:	n/a
49	chr4:1302238-1302288	PFSK-1	brain:	n/a
50	chr4:1302238-1302288	SKMC	muscle:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:1297989..1299587-chr4:1301090..1302609,2	K562	blood:
2	chr4:1299735..1301885-chr4:1304010..1308406,3	MCF-7	breast:
3	chr4:1232098..1233809-chr4:1299016..1301525,2	K562	blood:
4	chr4:1300397..1304694-chr4:1319400..1323043,4	K562	blood:
5	chr4:1300577..1302839-chr4:1339852..1342318,2	K562	blood:
6	chr4:1251988..1254188-chr4:1300555..1302807,2	K562	blood:
7	chr4:1300397..1302576-chr4:1320741..1323043,2	K562	blood:
8	chr4:1296042..1298860-chr4:1300283..1302360,3	K562	blood:

No data

Variant related genes	Relation type
MAEA	TF binding region
MAEA	CpG island
ENSG00000090316	chromatin interactions
ENSG00000163945	chromatin interactions

Extended variants
information (count: 115 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:115 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567392781	chr4:1301205-1301206	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs561300942	chr4:1301210-1301211	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs76030159	chr4:1301219-1301220	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs143829939	chr4:1301257-1301258	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs571033133	chr4:1301260-1301261	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs188995484	chr4:1301313-1301314	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs375692535	chr4:1301316-1301317	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs180959007	chr4:1301321-1301322	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs576651877	chr4:1301341-1301342	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs148174165	chr4:1301356-1301357	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs556033888	chr4:1301474-1301475	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs574102861	chr4:1301497-1301498	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs558923064	chr4:1301498-1301499	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs4974597	chr4:1301519-1301520	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs559849841	chr4:1301535-1301536	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs533497729	chr4:1301536-1301537	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs577224305	chr4:1301551-1301552	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs544691344	chr4:1301552-1301553	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs141088798	chr4:1301598-1301599	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs58058346	chr4:1301603-1301604	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs376403774	chr4:1301604-1301605	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs533150281	chr4:1301616-1301617	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs150255231	chr4:1301629-1301630	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs56240712	chr4:1301642-1301643	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs528245686	chr4:1301690-1301691	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs546406472	chr4:1301720-1301721	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs138960574	chr4:1301756-1301757	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs538373960	chr4:1301845-1301846	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs556913844	chr4:1301864-1301865	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs568719234	chr4:1301879-1301880	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs139614405	chr4:1301899-1301900	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs142041289	chr4:1301916-1301917	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs146321335	chr4:1301930-1301931	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs138233397	chr4:1302026-1302027	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs566573919	chr4:1302064-1302065	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs142736984	chr4:1302077-1302078	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs558322164	chr4:1302089-1302090	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs78721048	chr4:1302098-1302099	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs555412833	chr4:1302111-1302112	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs116720018	chr4:1302135-1302136	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs186188691	chr4:1302163-1302164	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs563816713	chr4:1302209-1302210	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs575506330	chr4:1302247-1302248	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs543032427	chr4:1302249-1302250	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs144223144	chr4:1302268-1302269	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs190989450	chr4:1302291-1302292	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs148491196	chr4:1302292-1302293	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs114375111	chr4:1302304-1302305	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs182867490	chr4:1302310-1302311	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs550357333	chr4:1302313-1302314	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Breast cancer	20932292	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Type 2 diabetes	21754918	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:487 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:1285200-1303400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:1285400-1302400	Weak transcription	Fetal Kidney	kidney
3	chr4:1285800-1302200	Weak transcription	NHDF-Ad	bronchial
4	chr4:1286200-1302400	Weak transcription	Fetal Brain Male	brain
5	chr4:1289400-1302200	Weak transcription	Fetal Heart	heart
6	chr4:1290000-1302400	Strong transcription	Fetal Stomach	stomach
7	chr4:1290400-1302200	Weak transcription	Right Atrium	heart
8	chr4:1290800-1302600	Weak transcription	Colon Smooth Muscle	Colon
9	chr4:1292000-1302200	Weak transcription	Fetal Lung	lung
10	chr4:1292000-1302600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr4:1292000-1302600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr4:1292000-1303400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr4:1292600-1302200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr4:1293200-1312000	Weak transcription	Hela-S3	cervix
15	chr4:1293600-1301800	Weak transcription	Brain Anterior Caudate	brain
16	chr4:1293800-1302200	Weak transcription	Brain Cingulate Gyrus	brain
17	chr4:1293800-1303400	Weak transcription	Aorta	Aorta
18	chr4:1294200-1302000	Weak transcription	Osteobl	bone
19	chr4:1294400-1301800	Weak transcription	Rectal Smooth Muscle	rectum
20	chr4:1294400-1302200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr4:1294400-1302600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr4:1294800-1302000	Weak transcription	Brain Angular Gyrus	brain
23	chr4:1294800-1302200	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr4:1294800-1302200	Weak transcription	Brain Substantia Nigra	brain
25	chr4:1295000-1301400	Weak transcription	NHLF	lung
26	chr4:1295000-1302000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr4:1295000-1302400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr4:1295000-1302600	Weak transcription	Duodenum Smooth Muscle	Duodenum
29	chr4:1295200-1301800	Weak transcription	Left Ventricle	heart
30	chr4:1295200-1302000	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr4:1295200-1302600	Weak transcription	Brain Germinal Matrix	brain
32	chr4:1295200-1303400	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr4:1295200-1303400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr4:1295400-1302800	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr4:1295400-1302800	Weak transcription	NH-A	brain
36	chr4:1295600-1302000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr4:1295600-1302000	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr4:1295600-1302200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr4:1295800-1301800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr4:1295800-1302600	Weak transcription	HSMMtube	muscle
41	chr4:1296000-1301800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr4:1296000-1302000	Weak transcription	Skeletal Muscle Male	skeletal muscle
43	chr4:1296000-1302600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr4:1296000-1302600	Weak transcription	HUVEC	blood vessel
45	chr4:1296200-1302400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr4:1296200-1302800	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr4:1296400-1302400	Weak transcription	Primary monocytes fromperipheralblood	blood
48	chr4:1296400-1302400	Weak transcription	Primary B cells from cord blood	blood
49	chr4:1296400-1302400	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr4:1296600-1302200	Strong transcription	Thymus	Thymus

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