Variant report

Variant	nsv593637
Chromosome Location	chr4:8353829-8390646
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:343)
CpG islands
(count:2810)
Chromatin interactive
region (count:29)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:343 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:8359490-8359857	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF3	chr4:8386862-8387196	K562	blood:	n/a	n/a
3	ATF3	chr4:8386997-8387136	GM12878	blood:	n/a	n/a
4	BACH1	chr4:8359436-8359516	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr4:8385904-8386155	GM12878	blood:	n/a	n/a
6	BATF	chr4:8385984-8386148	GM12878	blood:	n/a	n/a
7	BCL3	chr4:8383586-8383809	GM12878	blood:	n/a	n/a
8	BCL3	chr4:8374921-8375373	GM12878	blood:	n/a	n/a
9	BCL3	chr4:8374852-8375403	GM12878	blood:	n/a	n/a
10	BHLHE40	chr4:8385991-8386223	GM12878	blood:	n/a	chr4:8386188-8386204
11	BHLHE40	chr4:8376765-8376915	K562	blood:	n/a	n/a
12	BHLHE40	chr4:8386960-8387164	GM12878	blood:	n/a	n/a
13	BHLHE40	chr4:8369879-8369917	K562	blood:	n/a	n/a
14	BHLHE40	chr4:8372628-8373087	K562	blood:	n/a	chr4:8372836-8372845 chr4:8372836-8372845
15	BHLHE40	chr4:8354399-8354611	K562	blood:	n/a	chr4:8354498-8354507 chr4:8354496-8354512
16	BHLHE40	chr4:8373374-8373615	K562	blood:	n/a	n/a
17	BHLHE40	chr4:8387010-8387297	HepG2	liver:	n/a	n/a
18	BHLHE40	chr4:8386788-8387307	K562	blood:	n/a	n/a
19	CEBPB	chr4:8389645-8389845	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr4:8353775-8353986	HepG2	liver:	n/a	n/a
21	CHD1	chr4:8359330-8359337	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr4:8359488-8360184	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr4:8383735-8383929	HepG2	liver:	n/a	n/a
24	CHD2	chr4:8377263-8377280	K562	blood:	n/a	n/a
25	CREB1	chr4:8386784-8387246	H1-hESC	embryonic stem cell:	n/a	n/a
26	CREB1	chr4:8386815-8387389	K562	blood:	n/a	n/a
27	CREB1	chr4:8386769-8387369	GM12878	blood:	n/a	n/a
28	CREB1	chr4:8386771-8387294	K562	blood:	n/a	n/a
29	CREB1	chr4:8386778-8387347	GM12878	blood:	n/a	n/a
30	CREB1	chr4:8386774-8387339	H1-hESC	embryonic stem cell:	n/a	n/a
31	CREB1	chr4:8386798-8387339	HepG2	liver:	n/a	n/a
32	CREB1	chr4:8386843-8387302	HepG2	liver:	n/a	n/a
33	CTCF	chr4:8377220-8377370	WERI-Rb-1	eye:	n/a	chr4:8377223-8377241 chr4:8377226-8377239 chr4:8377226-8377235
34	CTCF	chr4:8377126-8377354	H1-hESC	embryonic stem cell:	n/a	chr4:8377223-8377241 chr4:8377226-8377239 chr4:8377226-8377235
35	CTCF	chr4:8386780-8386930	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr4:8385640-8385790	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr4:8366700-8366850	GM12878	blood:	n/a	chr4:8366793-8366811 chr4:8366799-8366808
38	CTCF	chr4:8377160-8377310	HBMEC	blood vessel:	n/a	chr4:8377223-8377241 chr4:8377226-8377239 chr4:8377226-8377235
39	CTCF	chr4:8353880-8354030	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr4:8371880-8372030	Caco-2	colon:	n/a	n/a
41	CTCF	chr4:8385780-8385930	AG10803	skin:	n/a	n/a
42	CTCF	chr4:8378360-8378510	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr4:8377140-8377290	SK-N-SH_RA	brain:	n/a	chr4:8377223-8377241 chr4:8377226-8377239 chr4:8377226-8377235
44	CTCF	chr4:8377176-8377269	H1-hESC	embryonic stem cell:	n/a	chr4:8377223-8377241 chr4:8377226-8377239 chr4:8377226-8377235
45	CTCF	chr4:8383700-8383850	AG04449	skin:	n/a	n/a
46	CTCF	chr4:8368600-8368750	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr4:8383682-8383812	NHEK	skin:	n/a	n/a
48	CTCF	chr4:8383700-8383795	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr4:8377200-8377350	GM06990	blood:	n/a	chr4:8377223-8377241 chr4:8377226-8377239 chr4:8377226-8377235
50	CUX1	chr4:8356940-8357223	GM12878	blood:	n/a	n/a

(count:2810 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8390148-8390198	NHDF-neo	bronchial:	n/a
2	chr4:8372691-8372741	ovcar-3	ovarian:	n/a
3	chr4:8368575-8368625	HMEC	breast:	n/a
4	chr4:8386748-8386798	HEEpiC	esophagus:	n/a
5	chr4:8390148-8390198	NHDF-neo	bronchial:	n/a
6	chr4:8372691-8372741	ovcar-3	ovarian:	n/a
7	chr4:8368575-8368625	HMEC	breast:	n/a
8	chr4:8386748-8386798	HEEpiC	esophagus:	n/a
9	chr4:8386188-8386238	HEEpiC	esophagus:	n/a
10	chr4:8388438-8388488	MCF10A-Er-Src	breast:	n/a
11	chr4:8355043-8355093	MCF10A-Er-Src	breast:	n/a
12	chr4:8354138-8354188	AG09319	gingival:	n/a
13	chr4:8359247-8359297	T-47D	breast:	n/a
14	chr4:8390193-8390243	NH-A	brain:	n/a
15	chr4:8378176-8378226	AG09319	gingival:	n/a
16	chr4:8376764-8376814	SK-N-MC	brain:	n/a
17	chr4:8389770-8389820	K562	blood:	n/a
18	chr4:8359499-8359549	SK-N-MC	brain:	n/a
19	chr4:8386748-8386798	PrEC	prostate:	n/a
20	chr4:8372691-8372741	NT2-D1	testis:	n/a
21	chr4:8375240-8375290	HPAEpiC	pulmonary alveolar:	n/a
22	chr4:8368486-8368536	K562	blood:	n/a
23	chr4:8355043-8355093	GM12892	blood:	n/a
24	chr4:8368575-8368625	PFSK-1	brain:	n/a
25	chr4:8388670-8388720	HRE	kidney:	n/a
26	chr4:8359247-8359297	AG09309	skin:	n/a
27	chr4:8375240-8375290	PrEC	prostate:	n/a
28	chr4:8373516-8373566	HepG2	liver:	n/a
29	chr4:8390148-8390198	Hela-S3	cervix:	n/a
30	chr4:8374182-8374232	HRE	kidney:	n/a
31	chr4:8389808-8389858	NH-A	brain:	n/a
32	chr4:8368486-8368536	SAEC	small airway:	n/a
33	chr4:8386266-8386316	AG04450	lung:	fetal
34	chr4:8390244-8390294	SKMC	muscle:	n/a
35	chr4:8386266-8386316	NB4	blood:	n/a
36	chr4:8359269-8359319	HAEpiC	amniotic membrane:	n/a
37	chr4:8359269-8359319	HCPEpiC	choroid plexus:	n/a
38	chr4:8376908-8376958	ECC-1	luminal epithelium:	n/a
39	chr4:8388503-8388553	Jurkat	blood:	n/a
40	chr4:8373438-8373488	AG04449	skin:	fetal
41	chr4:8378947-8378997	HCM	heart:	n/a
42	chr4:8388438-8388488	HRCEpiC	kidney:	n/a
43	chr4:8359269-8359319	HCM	heart:	n/a
44	chr4:8374429-8374479	HEEpiC	esophagus:	n/a
45	chr4:8368486-8368536	GM12891	blood:	n/a
46	chr4:8388503-8388553	NHBE	bronchial:	n/a
47	chr4:8389770-8389820	GM06990	blood:	n/a
48	chr4:8376835-8376885	GM12892	blood:	n/a
49	chr4:8374182-8374232	Hepatocyte	liver:	n/a
50	chr4:8372758-8372808	GM12891	blood:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:8356734..8359057-chr4:8360589..8363448,2	K562	blood:
2	chr4:8308134..8310233-chr4:8366379..8367956,2	K562	blood:
3	chr4:8372807..8374828-chr4:8375470..8377502,2	K562	blood:
4	chr4:8356734..8359057-chr4:8360589..8363448,2	K562	blood:
5	chr4:8359754..8361327-chr4:8385821..8388152,2	MCF-7	breast:
6	chr4:8372002..8373720-chr4:8374604..8376742,2	MCF-7	breast:
7	chr4:8368733..8370902-chr4:8378657..8380163,2	MCF-7	breast:
8	chr4:8362353..8364168-chr4:8365634..8367261,2	K562	blood:
9	chr4:8358055..8360875-chr4:8366726..8369353,3	K562	blood:
10	chr4:8389242..8391252-chr4:8392488..8394168,2	MCF-7	breast:
11	chr4:8380856..8382490-chr4:8382492..8384875,2	MCF-7	breast:
12	chr4:8385149..8387717-chr4:8393140..8395716,2	K562	blood:
13	chr4:8362353..8364168-chr4:8365634..8367261,2	K562	blood:
14	chr4:8380860..8383722-chr4:8386573..8388850,2	K562	blood:
15	chr4:8366720..8368366-chr4:8370008..8372883,2	K562	blood:
16	chr4:8368733..8370902-chr4:8378657..8380163,2	MCF-7	breast:
17	chr4:8347622..8350029-chr4:8351308..8354631,3	MCF-7	breast:
18	chr4:8385799..8388766-chr4:8429513..8431932,2	K562	blood:
19	chr4:8385368..8387475-chr4:8389606..8391227,2	MCF-7	breast:
20	chr4:8380860..8383722-chr4:8386573..8388850,2	K562	blood:
21	chr4:8383597..8386239-chr4:8397040..8399494,2	K562	blood:
22	chr4:8348558..8350885-chr4:8366825..8368402,2	MCF-7	breast:
23	chr4:8385368..8387475-chr4:8389606..8391227,2	MCF-7	breast:
24	chr4:8356411..8359057-chr4:8360589..8362711,2	K562	blood:
25	chr4:8370118..8372500-chr4:8374648..8377546,2	K562	blood:
26	chr4:8356411..8359057-chr4:8360589..8362711,2	K562	blood:
27	chr4:8346988..8348504-chr4:8352358..8355226,2	K562	blood:
28	chr4:8380856..8382490-chr4:8382492..8384875,2	MCF-7	breast:
29	chr4:8366720..8368366-chr4:8370008..8372883,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ACOX3-5	chr4:8365860-8366475	NONHSAT095091
2	lnc-METTL19-5	chr4:8374584-8374779	l_2595_chr4:8372786-8374779_heart
3	lnc-HTRA3-4	chr4:8358049-8358702	NONHSAT095089
4	lnc-ACOX3-1	chr4:8356817-8359103	NONHSAT095088
5	lnc-METTL19-5	chr4:8376346-8376594	l_2595_chr4:8372786-8374779_heart
6	lnc-ACOX3-1	chr4:8356817-8360065	ENSG00000251615.3
7	lnc-ACOX3-5	chr4:8367183-8367485	NONHSAT095091
8	lnc-ACOX3-1	chr4:8357038-8359103	ENSG00000251615
9	lnc-METTL19-5	chr4:8372787-8373149	l_2595_chr4:8372786-8374779_heart
10	lnc-HTRA3-4	chr4:8358805-8360149	NONHSAT095089

No data

Variant related genes	Relation type
ENSG00000251615	TF binding region
ACOX3	TF binding region
RNA5SP152	TF binding region
ENSG00000251615	CpG island
ACOX3	CpG island
RNA5SP152	CpG island
ENSG00000087008	chromatin interactions
ENSG00000202054	chromatin interactions
ENSG00000251615	chromatin interactions

Extended variants
information (count: 1940 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1940 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1678272	chr4:8353829-8353830	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs560418285	chr4:8353876-8353877	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs142453495	chr4:8353905-8353906	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs547998837	chr4:8353937-8353938	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs566233183	chr4:8353943-8353944	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs34168098	chr4:8353947-8353948	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs151337595	chr4:8353953-8353954	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs369122703	chr4:8354003-8354004	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs73799141	chr4:8354015-8354016	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs559064983	chr4:8354016-8354017	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs73799142	chr4:8354060-8354061	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs545206205	chr4:8354076-8354077	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs192276951	chr4:8354138-8354139	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs1678273	chr4:8354149-8354150	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs577020786	chr4:8354193-8354194	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs561991665	chr4:8354239-8354240	Enhancers Bivalent Enhancer Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542862720	chr4:8354240-8354241	Enhancers Bivalent Enhancer Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs561038451	chr4:8354249-8354250	Enhancers Bivalent Enhancer Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs531175573	chr4:8354260-8354261	Enhancers Bivalent Enhancer Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs1720004	chr4:8354315-8354316	Enhancers Bivalent Enhancer Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs532111714	chr4:8354343-8354344	Enhancers Bivalent Enhancer Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs550982421	chr4:8354345-8354346	Enhancers Bivalent Enhancer Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs547670392	chr4:8354351-8354352	Enhancers Bivalent Enhancer Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs4696819	chr4:8354384-8354385	Enhancers Bivalent Enhancer Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs112809358	chr4:8354385-8354386	Enhancers Bivalent Enhancer Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs548828281	chr4:8354408-8354409	Enhancers Bivalent Enhancer Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs570381960	chr4:8354409-8354410	Enhancers Bivalent Enhancer Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs537419062	chr4:8354415-8354416	Enhancers Bivalent Enhancer Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs559023386	chr4:8354501-8354502	Enhancers Bivalent Enhancer Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs570950992	chr4:8354527-8354528	Enhancers Bivalent Enhancer Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs140716969	chr4:8354530-8354531	Enhancers Bivalent Enhancer Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs116697824	chr4:8354543-8354544	Enhancers Bivalent Enhancer Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs572166390	chr4:8354550-8354551	Enhancers Bivalent Enhancer Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs542474271	chr4:8354585-8354586	Enhancers Bivalent Enhancer Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs4696820	chr4:8354600-8354601	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs575959723	chr4:8354605-8354606	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs145751929	chr4:8354707-8354708	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs73085846	chr4:8354732-8354733	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs183950541	chr4:8354754-8354755	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs188680314	chr4:8354755-8354756	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs530284147	chr4:8354778-8354779	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs548524908	chr4:8354832-8354833	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs180758195	chr4:8354841-8354842	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs80134179	chr4:8354842-8354843	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs116617998	chr4:8354849-8354850	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs138427146	chr4:8354862-8354863	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs534719953	chr4:8354879-8354880	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs547039647	chr4:8354893-8354894	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs568484007	chr4:8354901-8354902	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs549558456	chr4:8354903-8354904	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Melanoma	20688739	CNVD
Wilms tumour	21544195	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
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1042 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8344600-8354000	Weak transcription	Left Ventricle	heart
2	chr4:8349000-8357600	Weak transcription	Fetal Heart	heart
3	chr4:8351400-8355400	Enhancers	Fetal Muscle Leg	muscle
4	chr4:8351400-8356400	Enhancers	Ovary	ovary
5	chr4:8351600-8354600	Enhancers	Spleen	Spleen
6	chr4:8351600-8355400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
7	chr4:8351600-8356000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
8	chr4:8351600-8362800	Enhancers	Placenta Amnion	Placenta Amnion
9	chr4:8351800-8354400	Enhancers	Adipose Nuclei	Adipose
10	chr4:8352200-8355600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr4:8352400-8354400	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr4:8352400-8355000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr4:8352400-8356200	Enhancers	Fetal Thymus	thymus
14	chr4:8352600-8354800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr4:8352600-8355000	Enhancers	Fetal Stomach	stomach
16	chr4:8352800-8354400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr4:8352800-8354400	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr4:8352800-8354400	Enhancers	Brain Cingulate Gyrus	brain
19	chr4:8352800-8355000	Enhancers	Skeletal Muscle Male	skeletal muscle
20	chr4:8352800-8355200	Enhancers	Fetal Lung	lung
21	chr4:8352800-8355400	Enhancers	HSMMtube	muscle
22	chr4:8353000-8354000	Enhancers	Primary T cells from cord blood	blood
23	chr4:8353000-8354000	Enhancers	Fetal Kidney	kidney
24	chr4:8353000-8354200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr4:8353000-8354600	Enhancers	Duodenum Smooth Muscle	Duodenum
26	chr4:8353000-8354600	Enhancers	Right Atrium	heart
27	chr4:8353000-8354800	Bivalent Enhancer	HepG2	liver
28	chr4:8353000-8355200	Bivalent Enhancer	Stomach Smooth Muscle	stomach
29	chr4:8353000-8356200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr4:8353000-8357400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr4:8353200-8354200	Enhancers	Thymus	Thymus
32	chr4:8353200-8354400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr4:8353200-8354400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr4:8353200-8354800	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr4:8353200-8355000	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr4:8353200-8355200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr4:8353200-8356600	Enhancers	Muscle Satellite Cultured Cells	--
38	chr4:8353400-8354200	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr4:8353400-8354200	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr4:8353400-8354400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr4:8353400-8354400	Enhancers	Brain Inferior Temporal Lobe	brain
42	chr4:8353400-8354400	Enhancers	Rectal Smooth Muscle	rectum
43	chr4:8353400-8354600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
44	chr4:8353400-8354800	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr4:8353400-8355000	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr4:8353400-8355400	Enhancers	HSMM	muscle
47	chr4:8353400-8366200	Weak transcription	Aorta	Aorta
48	chr4:8353600-8354000	Bivalent Enhancer	NHLF	lung
49	chr4:8353600-8354200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr4:8353600-8354200	Enhancers	Brain Substantia Nigra	brain

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