Variant report

Variant	esv1817740
Chromosome Location	chr7:5427128-5436368
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:376)
CpG islands
(count:429)
Chromatin interactive
region (count:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:376 , 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	ATF3	chr7:5436136-5436417	A549	lung:	n/a	n/a
2	BCL3	chr7:5436021-5437558	A549	lung:	n/a	chr7:5437106-5437119
3	BCLAF1	chr7:5436079-5436511	GM12878	blood:	n/a	n/a
4	BRCA1	chr7:5436099-5437258	Hela-S3	cervix:	n/a	n/a
5	CCNT2	chr7:5428102-5428108	K562	blood:	n/a	n/a
6	CCNT2	chr7:5427875-5427877	K562	blood:	n/a	n/a
7	CEBPB	chr7:5436131-5437414	A549	lung:	n/a	n/a
8	CEBPB	chr7:5429206-5429215	HepG2	liver:	n/a	n/a
9	CEBPB	chr7:5436094-5437326	A549	lung:	n/a	n/a
10	CEBPB	chr7:5436016-5437595	HCT-116	colon:	n/a	n/a
11	CEBPB	chr7:5435868-5437471	HCT-116	colon:	n/a	n/a
12	CEBPB	chr7:5436059-5437535	Hela-S3	cervix:	n/a	n/a
13	CHD1	chr7:5436153-5437315	GM12878	blood:	n/a	n/a
14	CHD2	chr7:5434063-5434079	HepG2	liver:	n/a	n/a
15	CHD2	chr7:5436169-5437402	GM12878	blood:	n/a	n/a
16	CHD2	chr7:5436073-5436491	Hela-S3	cervix:	n/a	n/a
17	CTCF	chr7:5436180-5436330	HEEpiC	esophagus:	n/a	n/a
18	CTCF	chr7:5436220-5436370	GM12869	blood:	n/a	n/a
19	CTCF	chr7:5436160-5436310	GM12866	blood:	n/a	n/a
20	CTCF	chr7:5436320-5436470	HA-sp	spinal cord:	n/a	n/a
21	CTCF	chr7:5436180-5436330	A549	lung:	n/a	n/a
22	CTCF	chr7:5436220-5436370	K562	blood:	n/a	n/a
23	CTCF	chr7:5432192-5432249	LNCaP	prostate:	n/a	n/a
24	CTCF	chr7:5436140-5436290	GM12870	blood:	n/a	n/a
25	CTCF	chr7:5436123-5436467	K562	blood:	n/a	n/a
26	CTCF	chr7:5427607-5427700	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr7:5436180-5436330	HPAF	blood vessel:	n/a	n/a
28	CTCF	chr7:5436220-5436370	AG10803	skin:	n/a	n/a
29	CTCF	chr7:5436181-5436386	A549	lung:	n/a	n/a
30	CTCF	chr7:5436120-5436270	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr7:5436135-5436312	IMR90	lung:	n/a	n/a
32	CTCF	chr7:5436180-5436330	GM12870	blood:	n/a	n/a
33	CTCF	chr7:5436160-5436310	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr7:5436160-5436310	HepG2	liver:	n/a	n/a
35	CTCF	chr7:5436175-5436366	MCF-7	breast:	n/a	n/a
36	CTCF	chr7:5436236-5436320	HepG2	liver:	n/a	n/a
37	CTCF	chr7:5436200-5436350	GM12864	blood:	n/a	n/a
38	CTCF	chr7:5436200-5436350	MCF-7	breast:	n/a	n/a
39	CTCF	chr7:5436211-5436306	ProgFib	skin:	n/a	n/a
40	CTCF	chr7:5436200-5436350	NHEK	skin:	n/a	n/a
41	CTCF	chr7:5436139-5436405	GM19240	blood:	n/a	n/a
42	CTCF	chr7:5436186-5436326	GM20000	blood:	n/a	n/a
43	CTCF	chr7:5436205-5436316	Gliobla	brain:	n/a	n/a
44	CTCF	chr7:5436180-5436330	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr7:5436200-5436350	SAEC	small airway:	n/a	n/a
46	CTCF	chr7:5436160-5436310	GM12872	blood:	n/a	n/a
47	CTCF	chr7:5436220-5436370	NB4	blood:	n/a	n/a
48	CTCF	chr7:5436180-5436330	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr7:5436124-5436407	Spleen_OC	spleen:	n/a	n/a
50	CTCF	chr7:5436160-5436310	HCT-116	colon:	n/a	n/a

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:5432820-5432870	A549	lung:	n/a
2	chr7:5427647-5427697	HIPEpiC	eye:	n/a
3	chr7:5432820-5432870	A549	lung:	n/a
4	chr7:5427647-5427697	HIPEpiC	eye:	n/a
5	chr7:5428633-5428683	LNCaP	prostate:	n/a
6	chr7:5428633-5428683	HPAEpiC	pulmonary alveolar:	n/a
7	chr7:5432820-5432870	NB4	blood:	n/a
8	chr7:5428014-5428064	SK-N-SH	brain:	n/a
9	chr7:5428014-5428064	Caco-2	colon:	n/a
10	chr7:5428014-5428064	NHDF-neo	bronchial:	n/a
11	chr7:5432820-5432870	GM12892	blood:	n/a
12	chr7:5429036-5429086	AoSMC	blood vessel:	n/a
13	chr7:5428014-5428064	MCF-7	breast:	n/a
14	chr7:5427647-5427697	GM12891	blood:	n/a
15	chr7:5432820-5432870	MCF-7	breast:	n/a
16	chr7:5432820-5432870	LNCaP	prostate:	n/a
17	chr7:5432820-5432870	PrEC	prostate:	n/a
18	chr7:5427647-5427697	H1-hESC	embryonic stem cell:	embryo
19	chr7:5428014-5428064	ovcar-3	ovarian:	n/a
20	chr7:5427647-5427697	CMK	blood:	n/a
21	chr7:5429036-5429086	NHDF-neo	bronchial:	n/a
22	chr7:5428014-5428064	SAEC	small airway:	n/a
23	chr7:5429428-5429478	HEEpiC	esophagus:	n/a
24	chr7:5427647-5427697	HAEpiC	amniotic membrane:	n/a
25	chr7:5427244-5427294	AG10803	skin:	n/a
26	chr7:5429428-5429478	LNCaP	prostate:	n/a
27	chr7:5428014-5428064	GM12891	blood:	n/a
28	chr7:5427647-5427697	HL-60	blood:	n/a
29	chr7:5427647-5427697	HCM	heart:	n/a
30	chr7:5428633-5428683	BE2_C	brain:	n/a
31	chr7:5427244-5427294	SK-N-SH	brain:	n/a
32	chr7:5429036-5429086	NB4	blood:	n/a
33	chr7:5429428-5429478	Hepatocyte	liver:	n/a
34	chr7:5429428-5429478	HCF	heart:	n/a
35	chr7:5432820-5432870	AG04450	lung:	fetal
36	chr7:5429036-5429086	HAEpiC	amniotic membrane:	n/a
37	chr7:5428633-5428683	HL-60	blood:	n/a
38	chr7:5428633-5428683	NHDF-neo	bronchial:	n/a
39	chr7:5427244-5427294	HEK293	kidney:	embryo
40	chr7:5428633-5428683	T-47D	breast:	n/a
41	chr7:5428633-5428683	HepG2	liver:	n/a
42	chr7:5427244-5427294	SAEC	small airway:	n/a
43	chr7:5429428-5429478	U87	brain:	n/a
44	chr7:5427244-5427294	U87	brain:	n/a
45	chr7:5428014-5428064	AoSMC	blood vessel:	n/a
46	chr7:5432820-5432870	U87	brain:	n/a
47	chr7:5429428-5429478	HUVEC	blood vessel:	n/a
48	chr7:5427647-5427697	HEEpiC	esophagus:	n/a
49	chr7:5427244-5427294	HPAEpiC	pulmonary alveolar:	n/a
50	chr7:5432820-5432870	SAEC	small airway:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:5426046..5429721-chr7:5429735..5433041,4	K562	blood:
2	chr7:5436029..5436865-chr7:5526680..5528172,4	K562	blood:
3	chr7:5406257..5408361-chr7:5427751..5430730,2	MCF-7	breast:
4	chr7:5435723..5440617-chr7:5455325..5461617,9	MCF-7	breast:
5	chr7:5428152..5429787-chr7:5466437..5469145,2	K562	blood:
6	chr7:5430820..5432432-chr7:5432742..5434912,2	K562	blood:
7	chr12:46384589..46385168-chr7:5436336..5437128,2	Hela-S3	cervix:
8	chr7:5430820..5432432-chr7:5432742..5434912,2	K562	blood:
9	chr7:5431460..5434900-chr7:5435582..5438933,4	MCF-7	breast:
10	chr7:5434488..5436637-chr7:5491001..5493945,3	K562	blood:
11	chr7:5430729..5434402-chr7:5435453..5437686,4	MCF-7	breast:
12	chr7:5430729..5434402-chr7:5435453..5437686,4	MCF-7	breast:
13	chr17:56708702..56709252-chr7:5435813..5436725,2	Hela-S3	cervix:
14	chr7:5435151..5439105-chr7:5445783..5449135,4	MCF-7	breast:
15	chr7:5420732..5423186-chr7:5425259..5427446,2	MCF-7	breast:
16	chr7:5431460..5434900-chr7:5435582..5438933,4	MCF-7	breast:
17	chr7:5429619..5431536-chr7:5464762..5466326,2	K562	blood:
18	chr7:5427419..5438627-chr7:5461902..5471481,26	MCF-7	breast:
19	chr7:5435671..5437370-chr7:5467545..5469862,2	K562	blood:
20	chr19:4600828..4601348-chr7:5436257..5437101,2	Hela-S3	cervix:
21	chr17:1619851..1620486-chr7:5436343..5437291,2	Hela-S3	cervix:
22	chr11:61730705..61731619-chr7:5436353..5437212,2	Hela-S3	cervix:
23	chr7:5398782..5401965-chr7:5435057..5437553,3	MCF-7	breast:
24	chr7:5420682..5423339-chr7:5431916..5434654,3	MCF-7	breast:
25	chr7:5420460..5423379-chr7:5428515..5430331,2	MCF-7	breast:
26	chr7:5425693..5431327-chr7:5431953..5435253,6	MCF-7	breast:
27	chr7:5427166..5429954-chr7:5431918..5434543,3	MCF-7	breast:
28	chr16:28835202..28835881-chr7:5436294..5437225,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
TNRC18	TF binding region
TNRC18	CpG island
ENSG00000188365	chromatin interactions
ENSG00000168488	chromatin interactions
ENSG00000186594	chromatin interactions
ENSG00000273084	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000182095	chromatin interactions
ENSG00000272953	chromatin interactions
ENSG00000234432	chromatin interactions
ENSG00000241269	chromatin interactions
ENSG00000167716	chromatin interactions

Extended variants
information (count: 495 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:495 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4724662	chr7:5427128-5427129	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs533307336	chr7:5427140-5427141	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs536077848	chr7:5427154-5427155	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs75805608	chr7:5427157-5427158	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs140831524	chr7:5427162-5427163	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs181453125	chr7:5427164-5427165	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs558986345	chr7:5427180-5427181	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs577310468	chr7:5427181-5427182	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs144659432	chr7:5427194-5427195	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs563189315	chr7:5427198-5427199	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs530453801	chr7:5427199-5427200	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs186192120	chr7:5427212-5427213	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
13	rs189737435	chr7:5427218-5427219	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
14	rs138622792	chr7:5427234-5427235	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
15	rs546292252	chr7:5427242-5427243	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
16	rs142955805	chr7:5427256-5427257	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
17	rs531996838	chr7:5427284-5427285	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
18	rs369318587	chr7:5427291-5427292	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
19	rs373224154	chr7:5427315-5427316	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
20	rs199547131	chr7:5427316-5427317	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
21	rs575229236	chr7:5427322-5427323	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
22	rs376322304	chr7:5427326-5427327	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
23	rs556357679	chr7:5427369-5427370	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
24	rs548073889	chr7:5427370-5427371	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
25	rs369115613	chr7:5427374-5427375	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
26	rs533987269	chr7:5427424-5427425	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs559101274	chr7:5427446-5427447	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs182202446	chr7:5427452-5427453	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs538262900	chr7:5427467-5427468	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs556632015	chr7:5427476-5427477	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs377708142	chr7:5427490-5427491	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs575024819	chr7:5427498-5427499	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs34693947	chr7:5427517-5427518	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs200058817	chr7:5427524-5427525	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs560438016	chr7:5427536-5427537	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs375720457	chr7:5427558-5427559	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs539906957	chr7:5427575-5427576	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs200830047	chr7:5427582-5427583	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs553905586	chr7:5427628-5427629	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs4720623	chr7:5427652-5427653	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs201755816	chr7:5427673-5427674	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs372640414	chr7:5427706-5427707	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs374947108	chr7:5427713-5427714	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs4724663	chr7:5427720-5427721	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs374739594	chr7:5427760-5427761	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs529943064	chr7:5427855-5427856	Strong transcription Weak transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs561545797	chr7:5427857-5427858	Strong transcription Weak transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs367864160	chr7:5427858-5427859	Strong transcription Weak transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs370101496	chr7:5427883-5427884	Strong transcription Weak transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs374594397	chr7:5427884-5427885	Strong transcription Weak transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
Bladder cancer	21909424	CNVD
Glioblastoma multiforme	21525872	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
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:589 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5410200-5429200	Weak transcription	Primary B cells from cord blood	blood
2	chr7:5413600-5435000	Weak transcription	HSMM	muscle
3	chr7:5416800-5430400	Weak transcription	GM12878-XiMat	blood
4	chr7:5422600-5431800	Strong transcription	Primary neutrophils fromperipheralblood	blood
5	chr7:5423000-5431600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr7:5423000-5434000	Strong transcription	Fetal Thymus	thymus
7	chr7:5423200-5427400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr7:5423200-5428200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr7:5423200-5435200	Strong transcription	Fetal Intestine Large	intestine
10	chr7:5423200-5436400	Weak transcription	Right Atrium	heart
11	chr7:5423400-5436400	Strong transcription	Fetal Intestine Small	intestine
12	chr7:5423400-5436400	Weak transcription	Psoas Muscle	Psoas
13	chr7:5423600-5434800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr7:5423600-5443600	Weak transcription	Fetal Brain Male	brain
15	chr7:5424000-5434200	Strong transcription	Thymus	Thymus
16	chr7:5424000-5437600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr7:5424200-5428200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr7:5424400-5428000	Strong transcription	Duodenum Mucosa	Duodenum
19	chr7:5424400-5439200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr7:5424600-5427400	Strong transcription	Primary B cells from peripheral blood	blood
21	chr7:5424600-5428000	Strong transcription	Primary monocytes fromperipheralblood	blood
22	chr7:5424600-5434200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr7:5424800-5427200	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr7:5424800-5427400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr7:5424800-5432600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
26	chr7:5424800-5432600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
27	chr7:5424800-5432800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr7:5424800-5432800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr7:5424800-5433000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr7:5424800-5433600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr7:5424800-5433800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
32	chr7:5424800-5433800	Strong transcription	Lung	lung
33	chr7:5424800-5434000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr7:5424800-5434200	Strong transcription	Gastric	stomach
35	chr7:5424800-5434600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr7:5424800-5434600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr7:5424800-5435400	Strong transcription	Fetal Muscle Leg	muscle
38	chr7:5424800-5436200	Strong transcription	Fetal Stomach	stomach
39	chr7:5424800-5447000	Weak transcription	Fetal Heart	heart
40	chr7:5425400-5428200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr7:5425600-5427800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr7:5425800-5427200	Genic enhancers	Colon Smooth Muscle	Colon
43	chr7:5425800-5427800	Strong transcription	Rectal Mucosa Donor 29	rectum
44	chr7:5425800-5427800	Strong transcription	Osteobl	bone
45	chr7:5425800-5434000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr7:5425800-5434200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr7:5425800-5434200	Strong transcription	Adipose Nuclei	Adipose
48	chr7:5425800-5434200	Strong transcription	Dnd41	blood
49	chr7:5425800-5434400	Strong transcription	Fetal Brain Female	brain
50	chr7:5425800-5435000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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