Variant report

Variant	esv3409588
Chromosome Location	chr4:652502-655300
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:54)
CpG islands
(count:428)
Chromatin interactive
region (count:6)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:54 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:652831-653271	HepG2	liver:	n/a	n/a
2	BHLHE40	chr4:652747-653269	HepG2	liver:	n/a	n/a
3	CEBPZ	chr4:652988-653024	HepG2	liver:	n/a	n/a
4	CHD2	chr4:652751-652986	HepG2	liver:	n/a	n/a
5	CTCF	chr4:653260-653410	HepG2	liver:	n/a	n/a
6	CTCF	chr4:653300-653450	HepG2	liver:	n/a	n/a
7	EP300	chr4:652790-653234	HepG2	liver:	n/a	n/a
8	EP300	chr4:652811-653280	HepG2	liver:	n/a	n/a
9	EP300	chr4:653681-653803	HepG2	liver:	n/a	n/a
10	FOXA1	chr4:652691-653262	HepG2	liver:	n/a	n/a
11	FOXA1	chr4:652671-653343	HepG2	liver:	n/a	n/a
12	FOXA1	chr4:652659-653376	HepG2	liver:	n/a	n/a
13	FOXA1	chr4:652740-653259	HepG2	liver:	n/a	n/a
14	FOXA2	chr4:652511-653380	HepG2	liver:	n/a	n/a
15	FOXA2	chr4:652853-653231	HepG2	liver:	n/a	n/a
16	HNF4A	chr4:652893-653264	HepG2	liver:	n/a	n/a
17	JUND	chr4:652890-653227	HepG2	liver:	n/a	n/a
18	JUND	chr4:652814-653201	HepG2	liver:	n/a	n/a
19	MAX	chr4:652437-653567	HepG2	liver:	n/a	chr4:653422-653432 chr4:653369-653379 chr4:652843-652852 chr4:653434-653444 chr4:653412-653422
20	MAX	chr4:653180-653624	NB4	blood:	n/a	chr4:653422-653432 chr4:653369-653379 chr4:653434-653444 chr4:653412-653422
21	MAX	chr4:652724-653576	HepG2	liver:	n/a	chr4:653422-653432 chr4:653369-653379 chr4:652843-652852 chr4:653434-653444 chr4:653412-653422
22	MAX	chr4:653155-653698	HUVEC	blood vessel:	n/a	chr4:653422-653432 chr4:653369-653379 chr4:653434-653444 chr4:653412-653422
23	MAX	chr4:653155-653512	A549	lung:	n/a	chr4:653422-653432 chr4:653369-653379 chr4:653434-653444 chr4:653412-653422
24	MAX	chr4:653136-653620	H1-hESC	embryonic stem cell:	n/a	chr4:653422-653432 chr4:653369-653379 chr4:653434-653444 chr4:653412-653422
25	MXI1	chr4:652723-653579	HepG2	liver:	n/a	n/a
26	MYBL2	chr4:652653-653326	HepG2	liver:	n/a	n/a
27	MYC	chr4:652989-653050	HepG2	liver:	n/a	n/a
28	MYC	chr4:652923-652987	HepG2	liver:	n/a	n/a
29	MYC	chr4:652883-652921	HepG2	liver:	n/a	n/a
30	NFIC	chr4:652755-653269	HepG2	liver:	n/a	n/a
31	NR2C2	chr4:653286-653799	GM12878	blood:	n/a	n/a
32	NR2F2	chr4:651086-652523	MCF-7	breast:	n/a	n/a
33	POLR2A	chr4:652768-652813	H1-hESC	embryonic stem cell:	n/a	n/a
34	POLR2A	chr4:653558-655042	K562	blood:	n/a	n/a
35	POLR2A	chr4:653238-653511	GM12878	blood:	n/a	n/a
36	POLR2A	chr4:653134-653501	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr4:653707-653902	GM12878	blood:	n/a	n/a
38	POLR2A	chr4:653308-653419	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr4:652589-652650	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr4:653442-653561	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr4:653142-653544	GM12878	blood:	n/a	n/a
42	POLR2A	chr4:653247-653414	Gliobla	brain:	n/a	n/a
43	POLR2A	chr4:653127-653856	Raji	blood:	n/a	n/a
44	RCOR1	chr4:652802-653424	HepG2	liver:	n/a	n/a
45	RCOR1	chr4:653851-653893	HepG2	liver:	n/a	n/a
46	REST	chr4:652772-653251	HepG2	liver:	n/a	n/a
47	RFX5	chr4:653004-653157	HepG2	liver:	n/a	n/a
48	RXRA	chr4:651081-652578	HepG2	liver:	n/a	chr4:652317-652333
49	RXRA	chr4:652778-653192	HepG2	liver:	n/a	n/a
50	SP1	chr4:653170-653297	HepG2	liver:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:652823-652873	HRCEpiC	kidney:	n/a
2	chr4:652823-652873	HRCEpiC	kidney:	n/a
3	chr4:652907-652957	AG04449	skin:	fetal
4	chr4:652907-652957	Caco-2	colon:	n/a
5	chr4:652702-652752	HepG2	liver:	n/a
6	chr4:653615-653665	NT2-D1	testis:	n/a
7	chr4:652751-652801	HCF	heart:	n/a
8	chr4:652702-652752	Caco-2	colon:	n/a
9	chr4:652891-652941	NHBE	bronchial:	n/a
10	chr4:652527-652577	HEEpiC	esophagus:	n/a
11	chr4:652907-652957	GM12891	blood:	n/a
12	chr4:652891-652941	A549	lung:	n/a
13	chr4:652907-652957	SK-N-MC	brain:	n/a
14	chr4:652907-652957	NB4	blood:	n/a
15	chr4:652823-652873	Hepatocyte	liver:	n/a
16	chr4:652751-652801	AoSMC	blood vessel:	n/a
17	chr4:652891-652941	HCF	heart:	n/a
18	chr4:653615-653665	K562	blood:	n/a
19	chr4:652527-652577	HepG2	liver:	n/a
20	chr4:652527-652577	U87	brain:	n/a
21	chr4:652823-652873	AG09309	skin:	n/a
22	chr4:652907-652957	NT2-D1	testis:	n/a
23	chr4:652751-652801	NB4	blood:	n/a
24	chr4:652702-652752	ProgFib	skin:	n/a
25	chr4:652891-652941	NHDF-neo	bronchial:	n/a
26	chr4:652751-652801	ECC-1	luminal epithelium:	n/a
27	chr4:653615-653665	SK-N-SH	brain:	n/a
28	chr4:652527-652577	AG10803	skin:	n/a
29	chr4:652907-652957	ovcar-3	ovarian:	n/a
30	chr4:652907-652957	HEK293	kidney:	embryo
31	chr4:652751-652801	BJ	skin:	n/a
32	chr4:652751-652801	T-47D	breast:	n/a
33	chr4:652702-652752	SK-N-SH	brain:	n/a
34	chr4:652907-652957	NHDF-neo	bronchial:	n/a
35	chr4:652751-652801	GM19239	blood:	n/a
36	chr4:652751-652801	NHDF-neo	bronchial:	n/a
37	chr4:652751-652801	NHBE	bronchial:	n/a
38	chr4:653615-653665	GM06990	blood:	n/a
39	chr4:652891-652941	HEK293	kidney:	embryo
40	chr4:652907-652957	HIPEpiC	eye:	n/a
41	chr4:652527-652577	K562	blood:	n/a
42	chr4:652907-652957	HPAEpiC	pulmonary alveolar:	n/a
43	chr4:652527-652577	HCF	heart:	n/a
44	chr4:652907-652957	BJ	skin:	n/a
45	chr4:652823-652873	IMR90	lung:	fetal
46	chr4:652527-652577	HRPEpiC	eye:	n/a
47	chr4:653615-653665	BE2_C	brain:	n/a
48	chr4:652891-652941	PrEC	prostate:	n/a
49	chr4:652907-652957	AG09319	gingival:	n/a
50	chr4:652702-652752	HRPEpiC	eye:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:116512208..116512892-chr4:653530..654530,4	MCF-7	breast:
2	chr4:613849..616261-chr4:650426..653017,2	K562	blood:
3	chr4:649938..652851-chr4:653641..657433,6	K562	blood:
4	chr4:647827..650169-chr4:651801..653823,2	K562	blood:
5	chr4:646849..649113-chr4:654761..657491,3	K562	blood:
6	chr4:641525..644066-chr4:652058..654958,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATP5I-5	chr4:654998-655734	ENSG00000272927.1

No data

Variant related genes	Relation type
ENSG00000242686	TF binding region
PDE6B	TF binding region
ENSG00000242686	CpG island
PDE6B	CpG island
ENSG00000133256	chromatin interactions
ENSG00000272927	chromatin interactions
ENSG00000242686	chromatin interactions

Extended variants
information (count: 188 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:188 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537670102	chr4:652542-652543	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs557082487	chr4:652551-652552	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs556081812	chr4:652581-652582	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs190159296	chr4:652592-652593	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs376122906	chr4:652621-652622	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs535338968	chr4:652672-652673	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs112576560	chr4:652675-652676	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs370749360	chr4:652681-652682	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs373370425	chr4:652701-652702	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs377511027	chr4:652702-652703	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs370704907	chr4:652716-652717	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs200081409	chr4:652723-652724	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs182071364	chr4:652751-652752	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs140203507	chr4:652752-652753	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs143908642	chr4:652753-652754	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs150865214	chr4:652758-652759	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs375032863	chr4:652759-652760	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs200018423	chr4:652780-652781	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs200443661	chr4:652785-652786	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs202073030	chr4:652788-652789	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs139369984	chr4:652798-652799	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs140243735	chr4:652824-652825	Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs74464382	chr4:652826-652827	Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs116283697	chr4:652847-652848	Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs374791828	chr4:652848-652849	Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs10023609	chr4:652883-652884	Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs143432621	chr4:652907-652908	Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs550381905	chr4:652908-652909	Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs200778950	chr4:652916-652917	Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs377022744	chr4:652917-652918	Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs116168600	chr4:652926-652927	Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs564380241	chr4:652938-652939	Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs529831658	chr4:652941-652942	Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs549551630	chr4:653013-653014	Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs201652169	chr4:653041-653042	Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs567867534	chr4:653058-653059	Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs151118046	chr4:653066-653067	Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs553675872	chr4:653071-653072	Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs552221029	chr4:653102-653103	Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs571526081	chr4:653108-653109	Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs141074641	chr4:653116-653117	Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs562701734	chr4:653150-653151	Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs371204898	chr4:653188-653189	Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs557091964	chr4:653215-653216	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs575663077	chr4:653216-653217	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs533264545	chr4:653227-653228	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs115085351	chr4:653255-653256	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs368904134	chr4:653271-653272	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs554304759	chr4:653275-653276	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs540220222	chr4:653277-653278	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Pancreatic cancer	17952125	CNVD
Type 2 diabetes	21754918	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:631400-657000	Weak transcription	Right Atrium	heart
2	chr4:641800-657000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr4:642200-652800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr4:642400-654600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr4:642800-657000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr4:643000-657000	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr4:645800-656800	Weak transcription	Gastric	stomach
8	chr4:648400-657000	Weak transcription	Right Ventricle	heart
9	chr4:648800-653400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr4:649000-652800	Weak transcription	Brain Germinal Matrix	brain
11	chr4:649200-652800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr4:649200-653000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr4:649800-653200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr4:649800-655600	Weak transcription	Thymus	Thymus
15	chr4:650000-653200	Weak transcription	Fetal Brain Female	brain
16	chr4:650000-654000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr4:650000-654200	Enhancers	HepG2	liver
18	chr4:650200-652800	Weak transcription	Brain Substantia Nigra	brain
19	chr4:650600-652600	Weak transcription	Brain Anterior Caudate	brain
20	chr4:650600-652800	Weak transcription	Brain Angular Gyrus	brain
21	chr4:650800-652800	Weak transcription	Primary T cells from cord blood	blood
22	chr4:650800-656000	Weak transcription	Brain Cingulate Gyrus	brain
23	chr4:651000-652800	Weak transcription	Brain Hippocampus Middle	brain
24	chr4:651000-653200	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr4:651000-653600	Weak transcription	Fetal Brain Male	brain
26	chr4:651200-653200	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr4:651200-654400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr4:651400-653000	Enhancers	Lung	lung
29	chr4:651400-653200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr4:651400-653200	Weak transcription	Dnd41	blood
31	chr4:651400-653400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr4:651400-656400	Weak transcription	Pancreas	Pancrea
33	chr4:651600-653200	Weak transcription	Fetal Intestine Small	intestine
34	chr4:651600-657000	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr4:651600-657200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
36	chr4:651800-653200	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr4:651800-656800	Weak transcription	Primary B cells from cord blood	blood
38	chr4:652000-653600	Weak transcription	Fetal Stomach	stomach
39	chr4:652000-656800	Weak transcription	Fetal Lung	lung
40	chr4:652200-654000	Genic enhancers	Spleen	Spleen
41	chr4:652400-655200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr4:652400-656800	Weak transcription	Primary hematopoietic stem cells	blood
43	chr4:652600-654000	Strong transcription	Brain Anterior Caudate	brain
44	chr4:652600-656800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr4:652600-656800	Weak transcription	Fetal Thymus	thymus
46	chr4:652800-653600	Strong transcription	Primary T cells from cord blood	blood
47	chr4:652800-653600	Strong transcription	Brain Angular Gyrus	brain
48	chr4:652800-653600	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
49	chr4:652800-653800	Strong transcription	Brain Hippocampus Middle	brain
50	chr4:652800-654000	Strong transcription	iPS-15b Cell Line	embryonic stem cell

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