Variant report

Variant	esv3323761
Chromosome Location	chr7:5819451-5822299
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:722)
CpG islands
(count:733)
Chromatin interactive
region (count:11)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:722 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:5821215-5821617	K562	blood:	n/a	n/a
2	ARID3A	chr7:5821223-5821516	HepG2	liver:	n/a	n/a
3	ATF1	chr7:5821130-5821587	K562	blood:	n/a	n/a
4	ATF2	chr7:5821065-5821572	GM12878	blood:	n/a	n/a
5	ATF2	chr7:5821109-5821583	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr7:5821082-5821515	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr7:5821176-5821637	A549	lung:	n/a	n/a
8	ATF3	chr7:5821100-5821451	K562	blood:	n/a	n/a
9	ATF3	chr7:5821109-5821676	A549	lung:	n/a	n/a
10	BACH1	chr7:5821155-5821414	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL3	chr7:5821185-5821680	A549	lung:	n/a	chr7:5821285-5821298 chr7:5821316-5821324
12	BCL3	chr7:5821019-5821639	A549	lung:	n/a	chr7:5821285-5821298 chr7:5821316-5821324
13	BCLAF1	chr7:5821091-5821689	K562	blood:	n/a	chr7:5821285-5821298 chr7:5821316-5821324
14	BCLAF1	chr7:5821070-5821753	GM12878	blood:	n/a	chr7:5821285-5821298 chr7:5821316-5821324
15	BCLAF1	chr7:5821069-5821672	K562	blood:	n/a	chr7:5821285-5821298 chr7:5821316-5821324
16	BCLAF1	chr7:5821040-5821673	GM12878	blood:	n/a	chr7:5821285-5821298 chr7:5821316-5821324
17	BHLHE40	chr7:5821124-5821604	K562	blood:	n/a	chr7:5821155-5821171
18	BHLHE40	chr7:5821157-5821452	HepG2	liver:	n/a	n/a
19	BHLHE40	chr7:5821108-5821597	GM12878	blood:	n/a	chr7:5821155-5821171
20	BHLHE40	chr7:5820771-5820774	K562	blood:	n/a	n/a
21	BRCA1	chr7:5820533-5820584	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr7:5821222-5821465	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr7:5821213-5821484	HepG2	liver:	n/a	n/a
24	CBX3	chr7:5821041-5822095	K562	blood:	n/a	n/a
25	CBX3	chr7:5821114-5821700	K562	blood:	n/a	n/a
26	CBX3	chr7:5821023-5821768	HCT-116	colon:	n/a	n/a
27	CBX3	chr7:5820938-5821793	HCT-116	colon:	n/a	n/a
28	CCNT2	chr7:5820667-5821473	K562	blood:	n/a	n/a
29	CEBPB	chr7:5821228-5821484	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr7:5821144-5821543	K562	blood:	n/a	n/a
31	CEBPD	chr7:5821078-5821512	HepG2	liver:	n/a	n/a
32	CHD1	chr7:5821138-5821661	GM12878	blood:	n/a	chr7:5821300-5821310
33	CHD2	chr7:5820592-5820791	Hela-S3	cervix:	n/a	chr7:5820770-5820780
34	CHD2	chr7:5821246-5821441	HepG2	liver:	n/a	chr7:5821300-5821310
35	CHD2	chr7:5820661-5820826	K562	blood:	n/a	chr7:5820770-5820780
36	CHD2	chr7:5821008-5821519	Hela-S3	cervix:	n/a	chr7:5821300-5821310
37	CHD2	chr7:5821037-5821511	K562	blood:	n/a	chr7:5821300-5821310
38	CHD2	chr7:5820578-5820944	HepG2	liver:	n/a	chr7:5820770-5820780
39	CHD2	chr7:5821050-5821547	H1-hESC	embryonic stem cell:	n/a	chr7:5821300-5821310
40	CHD2	chr7:5821076-5821526	GM12878	blood:	n/a	chr7:5821300-5821310
41	CHD2	chr7:5820584-5820871	GM12878	blood:	n/a	chr7:5820770-5820780
42	CREB1	chr7:5821011-5821542	K562	blood:	n/a	n/a
43	CREB1	chr7:5821008-5821503	H1-hESC	embryonic stem cell:	n/a	n/a
44	CREB1	chr7:5821136-5821468	A549	lung:	n/a	n/a
45	CREB1	chr7:5820991-5821548	A549	lung:	n/a	n/a
46	CREB1	chr7:5820900-5821601	HepG2	liver:	n/a	n/a
47	CREB1	chr7:5820996-5821553	H1-hESC	embryonic stem cell:	n/a	n/a
48	CREB1	chr7:5820898-5821671	GM12878	blood:	n/a	n/a
49	CTBP2	chr7:5821208-5821521	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr7:5821300-5821450	NB4	blood:	n/a	chr7:5821317-5821335 chr7:5821318-5821334

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:5820542-5820592	GM06990	blood:	n/a
2	chr7:5820542-5820592	GM06990	blood:	n/a
3	chr7:5821294-5821344	NB4	blood:	n/a
4	chr7:5821307-5821357	RPTEC	kidney:	n/a
5	chr7:5821305-5821355	HCT-116	colon:	n/a
6	chr7:5820542-5820592	NHDF-neo	bronchial:	n/a
7	chr7:5821305-5821355	MCF-7	breast:	n/a
8	chr7:5821307-5821357	U87	brain:	n/a
9	chr7:5821294-5821344	HRCEpiC	kidney:	n/a
10	chr7:5821297-5821347	T-47D	breast:	n/a
11	chr7:5821307-5821357	NHBE	bronchial:	n/a
12	chr7:5820542-5820592	CMK	blood:	n/a
13	chr7:5822206-5822256	HEK293	kidney:	embryo
14	chr7:5820542-5820592	AG09309	skin:	n/a
15	chr7:5821297-5821347	GM12891	blood:	n/a
16	chr7:5821294-5821344	AG09309	skin:	n/a
17	chr7:5821500-5821550	GM12891	blood:	n/a
18	chr7:5821500-5821550	LNCaP	prostate:	n/a
19	chr7:5821596-5821646	GM12878	blood:	n/a
20	chr7:5820542-5820592	U87	brain:	n/a
21	chr7:5821099-5821149	HRCEpiC	kidney:	n/a
22	chr7:5822206-5822256	NT2-D1	testis:	n/a
23	chr7:5820542-5820592	IMR90	lung:	fetal
24	chr7:5821297-5821347	Caco-2	colon:	n/a
25	chr7:5821227-5821277	HUVEC	blood vessel:	n/a
26	chr7:5821227-5821277	HCM	heart:	n/a
27	chr7:5821227-5821277	AG04449	skin:	fetal
28	chr7:5821305-5821355	HCPEpiC	choroid plexus:	n/a
29	chr7:5821297-5821347	SAEC	small airway:	n/a
30	chr7:5821305-5821355	HNPCEpiC	eye:	n/a
31	chr7:5821313-5821363	HEK293	kidney:	embryo
32	chr7:5821099-5821149	HL-60	blood:	n/a
33	chr7:5821313-5821363	HPAEpiC	pulmonary alveolar:	n/a
34	chr7:5821313-5821363	ProgFib	skin:	n/a
35	chr7:5821297-5821347	AoSMC	blood vessel:	n/a
36	chr7:5821305-5821355	H1-hESC	embryonic stem cell:	embryo
37	chr7:5821297-5821347	HCM	heart:	n/a
38	chr7:5822206-5822256	HAEpiC	amniotic membrane:	n/a
39	chr7:5821294-5821344	ovcar-3	ovarian:	n/a
40	chr7:5821320-5821370	NT2-D1	testis:	n/a
41	chr7:5821099-5821149	A549	lung:	n/a
42	chr7:5821227-5821277	CMK	blood:	n/a
43	chr7:5821297-5821347	RPTEC	kidney:	n/a
44	chr7:5821313-5821363	RPTEC	kidney:	n/a
45	chr7:5821227-5821277	HPAEpiC	pulmonary alveolar:	n/a
46	chr7:5821320-5821370	HL-60	blood:	n/a
47	chr7:5821313-5821363	Hepatocyte	liver:	n/a
48	chr7:5822206-5822256	HCPEpiC	choroid plexus:	n/a
49	chr7:5821227-5821277	PFSK-1	brain:	n/a
50	chr7:5820542-5820592	ECC-1	luminal epithelium:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:5012695..5014428-chr7:5820890..5822170,10	MCF-7	breast:
2	chr7:5012944..5014466-chr7:5819776..5821589,2	MCF-7	breast:
3	chr7:5012931..5013720-chr7:5820910..5821674,3	MCF-7	breast:
4	chr7:5012983..5015694-chr7:5819277..5821133,2	K562	blood:
5	chr7:5012284..5014483-chr7:5819277..5821280,2	K562	blood:
6	chr7:5013311..5013911-chr7:5820908..5821412,3	HCT-116	colon:
7	chr6:74233083..74233652-chr7:5820678..5821633,2	Hela-S3	cervix:
8	chr7:5013249..5014674-chr7:5819932..5821408,8	Hela-S3	cervix:
9	chr7:5012217..5014206-chr7:5819722..5821650,2	MCF-7	breast:
10	chr7:5013565..5014445-chr7:5820432..5821785,4	K562	blood:
11	chr7:5798985..5801479-chr7:5819651..5822590,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RSPH10B-2	chr7:5819616-5819923	NONHSAT118935
2	lnc-RSPH10B-2	chr7:5819616-5819899	NONHSAT118936

No data

Variant related genes	Relation type
RNF216	TF binding region
RNF216	CpG island
ENSG00000229862	chromatin interactions
ENSG00000011275	chromatin interactions
ENSG00000196204	chromatin interactions
ENSG00000156508	chromatin interactions

Extended variants
information (count: 142 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:142 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568260364	chr7:5819451-5819452	Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs537837124	chr7:5819457-5819458	Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs79807001	chr7:5819459-5819460	Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs112640762	chr7:5819460-5819461	Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs34996643	chr7:5819475-5819476	Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs535265576	chr7:5819478-5819479	Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs192142288	chr7:5819494-5819495	Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs184114454	chr7:5819520-5819521	Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs188717925	chr7:5819521-5819522	Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs192218293	chr7:5819527-5819528	Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs576691905	chr7:5819556-5819557	Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs544076630	chr7:5819583-5819584	Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs73048736	chr7:5819591-5819592	Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs574181806	chr7:5819667-5819668	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
15	rs541187676	chr7:5819677-5819678	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
16	rs143447242	chr7:5819732-5819733	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
17	rs146453348	chr7:5819734-5819735	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
18	rs545425883	chr7:5819748-5819749	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
19	rs367553530	chr7:5819754-5819755	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
20	rs140947767	chr7:5819799-5819800	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
21	rs531173095	chr7:5819824-5819825	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
22	rs145782649	chr7:5819827-5819828	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
23	rs118004770	chr7:5819848-5819849	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
24	rs184324316	chr7:5819855-5819856	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
25	rs188717796	chr7:5819906-5819907	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
26	rs13239017	chr7:5819910-5819911	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs75742717	chr7:5819911-5819912	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
28	rs551832874	chr7:5819966-5819967	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs542310614	chr7:5819973-5819974	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs570056114	chr7:5819983-5819984	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs372724830	chr7:5820086-5820087	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs191732600	chr7:5820102-5820103	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs560049110	chr7:5820112-5820113	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs556035692	chr7:5820115-5820116	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs527472347	chr7:5820122-5820123	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs574241878	chr7:5820171-5820172	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs534935908	chr7:5820183-5820184	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs553131493	chr7:5820203-5820204	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs150262878	chr7:5820211-5820212	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs545510884	chr7:5820228-5820229	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs563994904	chr7:5820231-5820232	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs184570022	chr7:5820251-5820252	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs377166747	chr7:5820258-5820259	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs189551518	chr7:5820287-5820288	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs374713560	chr7:5820305-5820306	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs529198853	chr7:5820328-5820329	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs10247051	chr7:5820344-5820345	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs534197303	chr7:5820347-5820348	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs2008415	chr7:5820350-5820351	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs533124728	chr7:5820363-5820364	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	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
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
Pancreatic cancer	17952125	CNVD
Schizophrenia	21346763	CNVD
Acute myeloid leukemia	21251322	CNVD

Chromatin state (count:415 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5762000-5820400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr7:5784000-5819600	Weak transcription	Fetal Heart	heart
3	chr7:5790800-5820400	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr7:5792800-5820000	Weak transcription	Fetal Kidney	kidney
5	chr7:5792800-5820200	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr7:5792800-5820200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr7:5792800-5820200	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr7:5798800-5820400	Weak transcription	Esophagus	oesophagus
9	chr7:5799200-5819600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr7:5799200-5820200	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr7:5799600-5820200	Weak transcription	Thymus	Thymus
12	chr7:5800400-5819600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr7:5800600-5819600	Weak transcription	Liver	Liver
14	chr7:5807000-5820400	Weak transcription	Aorta	Aorta
15	chr7:5807400-5819600	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr7:5807400-5819600	Weak transcription	HSMMtube	muscle
17	chr7:5808200-5820400	Weak transcription	Gastric	stomach
18	chr7:5811400-5820200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
19	chr7:5813400-5820400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
20	chr7:5814400-5819600	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr7:5814600-5820400	Enhancers	Primary T helper naive cells from peripheral blood	blood
22	chr7:5815200-5819600	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr7:5815600-5819600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr7:5815800-5819600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr7:5815800-5819600	Weak transcription	Fetal Lung	lung
26	chr7:5816600-5819600	Genic enhancers	Dnd41	blood
27	chr7:5816800-5820200	Weak transcription	Fetal Intestine Small	intestine
28	chr7:5817000-5819800	Enhancers	Primary T helper cells fromperipheralblood	blood
29	chr7:5817200-5819600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr7:5817200-5819600	Enhancers	Primary T killer memory cells from peripheral blood	blood
31	chr7:5817200-5819600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr7:5817200-5819800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr7:5817200-5820000	Weak transcription	Fetal Thymus	thymus
34	chr7:5817200-5820200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
35	chr7:5817200-5820200	Weak transcription	Lung	lung
36	chr7:5817200-5820400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr7:5817400-5819600	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr7:5817400-5819600	Weak transcription	NHDF-Ad	bronchial
39	chr7:5817600-5819600	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr7:5817600-5819600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr7:5817600-5819600	Weak transcription	HSMM	muscle
42	chr7:5817600-5819800	Weak transcription	Fetal Brain Female	brain
43	chr7:5817800-5819600	Weak transcription	Pancreatic Islets	Pancreatic Islet
44	chr7:5817800-5819600	Weak transcription	K562	blood
45	chr7:5817800-5820200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr7:5817800-5820200	Weak transcription	Fetal Intestine Large	intestine
47	chr7:5818000-5819600	Weak transcription	A549	lung
48	chr7:5818000-5820200	Weak transcription	Psoas Muscle	Psoas
49	chr7:5818000-5820400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr7:5818200-5819600	Weak transcription	HMEC	breast

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