Variant report

Variant	esv3407904
Chromosome Location	chr7:4831051-4833599
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:361)
CpG islands
(count:367)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:361 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:4832282-4832726	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr7:4831795-4831907	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr7:4831699-4831994	K562	blood:	n/a	n/a
4	BHLHE40	chr7:4831700-4832012	GM12878	blood:	n/a	n/a
5	CBX3	chr7:4831686-4832003	K562	blood:	n/a	n/a
6	CCNT2	chr7:4831735-4832518	K562	blood:	n/a	n/a
7	CHD1	chr7:4831797-4831893	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD2	chr7:4832640-4832815	GM12878	blood:	n/a	n/a
9	CHD2	chr7:4831748-4832128	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD2	chr7:4831784-4831963	HepG2	liver:	n/a	n/a
11	CHD2	chr7:4831765-4831860	K562	blood:	n/a	n/a
12	CHD2	chr7:4832371-4832708	H1-hESC	embryonic stem cell:	n/a	n/a
13	CREB1	chr7:4831644-4832405	H1-hESC	embryonic stem cell:	n/a	n/a
14	CREB1	chr7:4831642-4832532	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr7:4831700-4831850	HRPEpiC	eye:	n/a	n/a
16	CTCF	chr7:4831780-4831930	HCT-116	colon:	n/a	n/a
17	CTCF	chr7:4831640-4831790	GM12873	blood:	n/a	n/a
18	CTCF	chr7:4831800-4831950	HRE	kidney:	n/a	n/a
19	CTCF	chr7:4831800-4831950	K562	blood:	n/a	n/a
20	CTCF	chr7:4831740-4831890	HMEC	breast:	n/a	n/a
21	CTCF	chr7:4831820-4831970	NHLF	lung:	n/a	n/a
22	CTCF	chr7:4831706-4832008	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr7:4831792-4831981	A549	lung:	n/a	n/a
24	CTCF	chr7:4831800-4831950	GM12871	blood:	n/a	n/a
25	CTCF	chr7:4831489-4831495	GM12891	blood:	n/a	n/a
26	CTCF	chr7:4831760-4831910	HPAF	blood vessel:	n/a	n/a
27	CTCF	chr7:4831780-4831930	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr7:4831800-4831950	AG09319	gingival:	n/a	n/a
29	CTCF	chr7:4831860-4832010	HCM	heart:	n/a	n/a
30	CTCF	chr7:4831500-4832025	GM12891	blood:	n/a	n/a
31	CTCF	chr7:4831780-4831930	Caco-2	colon:	n/a	n/a
32	CTCF	chr7:4831843-4831883	MCF-7	breast:	n/a	n/a
33	CTCF	chr7:4831800-4831950	HRPEpiC	eye:	n/a	n/a
34	CTCF	chr7:4831732-4831980	ProgFib	skin:	n/a	n/a
35	CTCF	chr7:4831709-4831710	Spleen_OC	spleen:	n/a	n/a
36	CTCF	chr7:4831780-4831930	RPTEC	kidney:	n/a	n/a
37	CTCF	chr7:4831840-4831990	HAc	cerebellar:	n/a	n/a
38	CTCF	chr7:4831820-4831970	AG10803	skin:	n/a	n/a
39	CTCF	chr7:4831800-4831950	HEK293	kidney:	n/a	n/a
40	CTCF	chr7:4831741-4831978	Fibrobl	skin:	n/a	n/a
41	CTCF	chr7:4831740-4831890	GM12875	blood:	n/a	n/a
42	CTCF	chr7:4831694-4831997	K562	blood:	n/a	n/a
43	CTCF	chr7:4831820-4831970	AG04449	skin:	n/a	n/a
44	CTCF	chr7:4831686-4832042	IMR90	lung:	n/a	n/a
45	CTCF	chr7:4831780-4831930	GM12873	blood:	n/a	n/a
46	CTCF	chr7:4831711-4832015	Spleen_OC	spleen:	n/a	n/a
47	CTCF	chr7:4831800-4831950	HA-sp	spinal cord:	n/a	n/a
48	CTCF	chr7:4831784-4831964	HepG2	liver:	n/a	n/a
49	CTCF	chr7:4831820-4831970	GM12864	blood:	n/a	n/a
50	CTCF	chr7:4832396-4832608	H1-hESC	embryonic stem cell:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:4832340-4832390	Hela-S3	cervix:	n/a
2	chr7:4832340-4832390	Hela-S3	cervix:	n/a
3	chr7:4832112-4832162	SK-N-SH_RA	brain:	n/a
4	chr7:4832174-4832224	NHDF-neo	bronchial:	n/a
5	chr7:4832112-4832162	ProgFib	skin:	n/a
6	chr7:4832535-4832585	SK-N-MC	brain:	n/a
7	chr7:4832174-4832224	GM12892	blood:	n/a
8	chr7:4832359-4832409	AG04449	skin:	fetal
9	chr7:4832112-4832162	AG09319	gingival:	n/a
10	chr7:4832112-4832162	U87	brain:	n/a
11	chr7:4832174-4832224	Caco-2	colon:	n/a
12	chr7:4832340-4832390	HRPEpiC	eye:	n/a
13	chr7:4831038-4831088	PANC-1	pancreas:	n/a
14	chr7:4832112-4832162	HIPEpiC	eye:	n/a
15	chr7:4832112-4832162	AG09309	skin:	n/a
16	chr7:4832112-4832162	PrEC	prostate:	n/a
17	chr7:4831038-4831088	HCM	heart:	n/a
18	chr7:4832112-4832162	A549	lung:	n/a
19	chr7:4832174-4832224	HAEpiC	amniotic membrane:	n/a
20	chr7:4831038-4831088	U87	brain:	n/a
21	chr7:4832359-4832409	SK-N-MC	brain:	n/a
22	chr7:4832359-4832409	HMEC	breast:	n/a
23	chr7:4831038-4831088	HPAEpiC	pulmonary alveolar:	n/a
24	chr7:4832112-4832162	T-47D	breast:	n/a
25	chr7:4832535-4832585	NT2-D1	testis:	n/a
26	chr7:4832112-4832162	CMK	blood:	n/a
27	chr7:4832535-4832585	LNCaP	prostate:	n/a
28	chr7:4832112-4832162	H1-hESC	embryonic stem cell:	embryo
29	chr7:4832535-4832585	HL-60	blood:	n/a
30	chr7:4831038-4831088	SK-N-MC	brain:	n/a
31	chr7:4832112-4832162	NB4	blood:	n/a
32	chr7:4832535-4832585	AG09309	skin:	n/a
33	chr7:4831038-4831088	MCF-7	breast:	n/a
34	chr7:4832174-4832224	HCPEpiC	choroid plexus:	n/a
35	chr7:4832112-4832162	LNCaP	prostate:	n/a
36	chr7:4831038-4831088	SK-N-SH	brain:	n/a
37	chr7:4832340-4832390	HL-60	blood:	n/a
38	chr7:4832340-4832390	AG04449	skin:	fetal
39	chr7:4832359-4832409	K562	blood:	n/a
40	chr7:4832174-4832224	PFSK-1	brain:	n/a
41	chr7:4832535-4832585	HCT-116	colon:	n/a
42	chr7:4832174-4832224	AG09319	gingival:	n/a
43	chr7:4831038-4831088	A549	lung:	n/a
44	chr7:4832359-4832409	HCF	heart:	n/a
45	chr7:4832174-4832224	AG09309	skin:	n/a
46	chr7:4832112-4832162	HCM	heart:	n/a
47	chr7:4832174-4832224	K562	blood:	n/a
48	chr7:4832535-4832585	Caco-2	colon:	n/a
49	chr7:4832359-4832409	PANC-1	pancreas:	n/a
50	chr7:4832112-4832162	AG10803	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:4830470..4833507-chr7:4836339..4839138,4	K562	blood:
2	chr7:4823905..4827107-chr7:4829333..4833521,4	MCF-7	breast:
3	chr7:4815280..4818251-chr7:4830682..4833750,3	MCF-7	breast:
4	chr7:4778391..4781100-chr7:4828582..4831115,2	K562	blood:
5	chr7:4831917..4833699-chr7:4922173..4923727,2	K562	blood:
6	chr7:4821235..4827640-chr7:4827846..4833141,11	K562	blood:

No data

Variant related genes	Relation type
MIR4656	TF binding region
MIR4656	CpG island
ENSG00000242802	chromatin interactions
ENSG00000157927	chromatin interactions
ENSG00000164916	chromatin interactions

Extended variants
information (count: 212 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:212 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12154545	chr7:4831061-4831062	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs73305393	chr7:4831084-4831085	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs546071452	chr7:4831089-4831090	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs577301873	chr7:4831105-4831106	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs144772761	chr7:4831106-4831107	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs112283999	chr7:4831108-4831109	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs575436631	chr7:4831115-4831116	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs576259662	chr7:4831135-4831136	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs544740791	chr7:4831137-4831138	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs113317994	chr7:4831154-4831155	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs139378554	chr7:4831157-4831158	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs183237366	chr7:4831163-4831164	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs540649048	chr7:4831164-4831165	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs186823399	chr7:4831166-4831167	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs191229687	chr7:4831171-4831172	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs570721516	chr7:4831172-4831173	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs551093436	chr7:4831174-4831175	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs150058274	chr7:4831190-4831191	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs530317142	chr7:4831198-4831199	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs550104638	chr7:4831204-4831205	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs548571464	chr7:4831205-4831206	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs368324617	chr7:4831207-4831208	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs373838070	chr7:4831210-4831211	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs73305394	chr7:4831221-4831222	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs534929490	chr7:4831228-4831229	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs535419745	chr7:4831245-4831246	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs570957705	chr7:4831257-4831258	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs12154621	chr7:4831266-4831267	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs12154622	chr7:4831292-4831293	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs140188885	chr7:4831315-4831316	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs377553602	chr7:4831363-4831364	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs575299983	chr7:4831389-4831390	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs12154696	chr7:4831394-4831395	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs554872454	chr7:4831402-4831403	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs573160974	chr7:4831403-4831404	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs560528325	chr7:4831418-4831419	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs200649898	chr7:4831429-4831430	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs149131747	chr7:4831448-4831449	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs577176341	chr7:4831456-4831457	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs544330793	chr7:4831461-4831462	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs563019050	chr7:4831497-4831498	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs143609133	chr7:4831499-4831500	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs548357776	chr7:4831500-4831501	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs114076345	chr7:4831547-4831548	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs527985598	chr7:4831548-4831549	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs146804830	chr7:4831553-4831554	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs370722002	chr7:4831566-4831567	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs538631490	chr7:4831577-4831578	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs550379429	chr7:4831579-4831580	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs568952005	chr7:4831592-4831593	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Glioblastoma multiforme	21525872	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:468 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:4816000-4832000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr7:4816200-4832000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr7:4816200-4834400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr7:4816600-4834800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr7:4816800-4834400	Weak transcription	K562	blood
6	chr7:4816800-4834800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
7	chr7:4817200-4832000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr7:4818000-4831600	Weak transcription	Stomach Mucosa	stomach
9	chr7:4818400-4831600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr7:4819600-4831400	Strong transcription	Primary T helper cells PMA-I stimulated	--
11	chr7:4819600-4831400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr7:4819600-4831600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr7:4819600-4831600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr7:4819600-4831600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr7:4819600-4831600	Strong transcription	Fetal Intestine Small	intestine
16	chr7:4819600-4831600	Strong transcription	Fetal Stomach	stomach
17	chr7:4819800-4831600	Strong transcription	Primary T helper cells fromperipheralblood	blood
18	chr7:4819800-4831800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr7:4819800-4832000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr7:4820200-4831200	Strong transcription	Stomach Smooth Muscle	stomach
21	chr7:4820200-4831400	Strong transcription	Primary monocytes fromperipheralblood	blood
22	chr7:4820200-4831400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr7:4820200-4831400	Strong transcription	Cortex derived primary cultured neurospheres	brain
24	chr7:4820200-4831400	Strong transcription	Fetal Thymus	thymus
25	chr7:4820200-4831400	Strong transcription	Monocytes-CD14+_RO01746	blood
26	chr7:4820200-4831600	Strong transcription	Primary B cells from peripheral blood	blood
27	chr7:4820200-4831600	Strong transcription	Primary T cells from cord blood	blood
28	chr7:4820200-4831600	Strong transcription	Thymus	Thymus
29	chr7:4820200-4832800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr7:4820200-4832800	Strong transcription	Dnd41	blood
31	chr7:4820400-4831200	Strong transcription	Fetal Muscle Trunk	muscle
32	chr7:4820400-4831200	Strong transcription	Left Ventricle	heart
33	chr7:4820400-4831400	Strong transcription	Primary neutrophils fromperipheralblood	blood
34	chr7:4820400-4831400	Strong transcription	Rectal Mucosa Donor 29	rectum
35	chr7:4820400-4831600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr7:4820400-4831600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr7:4820400-4831600	Strong transcription	Brain Germinal Matrix	brain
38	chr7:4820400-4831600	Strong transcription	Duodenum Mucosa	Duodenum
39	chr7:4820400-4831800	Strong transcription	Liver	Liver
40	chr7:4820400-4832000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr7:4820400-4832000	Strong transcription	NHLF	lung
42	chr7:4820400-4832200	Strong transcription	Placenta Amnion	Placenta Amnion
43	chr7:4820400-4832400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr7:4820400-4834400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr7:4820600-4831200	Strong transcription	HUES6 Cell Line	embryonic stem cell
46	chr7:4820600-4831200	Strong transcription	Ovary	ovary
47	chr7:4820600-4831400	Strong transcription	H1 Cell Line	embryonic stem cell
48	chr7:4820600-4831400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr7:4820600-4831400	Strong transcription	Brain Inferior Temporal Lobe	brain
50	chr7:4820600-4831400	Strong transcription	Esophagus	oesophagus

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