Variant report

Variant	esv3326672
Chromosome Location	chr7:128169741-128173589
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr7:128170954-128171294	K562	blood:	n/a	chr7:128171025-128171034 chr7:128171193-128171202
2	BACH1	chr7:128170628-128170836	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr7:128172517-128172702	GM12878	blood:	n/a	chr7:128172675-128172684
4	BCL11A	chr7:128171434-128171723	GM12878	blood:	n/a	chr7:128171499-128171508
5	BCLAF1	chr7:128170974-128171325	GM12878	blood:	n/a	chr7:128171050-128171059 chr7:128171250-128171263 chr7:128171258-128171271 chr7:128171221-128171234 chr7:128171220-128171233 chr7:128171026-128171035
6	BHLHE40	chr7:128171119-128171252	GM12878	blood:	n/a	n/a
7	BHLHE40	chr7:128171081-128171307	HepG2	liver:	n/a	n/a
8	BHLHE40	chr7:128171068-128171268	K562	blood:	n/a	n/a
9	BRCA1	chr7:128171221-128171570	Hela-S3	cervix:	n/a	chr7:128171373-128171382
10	BRCA1	chr7:128171403-128171433	HepG2	liver:	n/a	n/a
11	BRCA1	chr7:128171245-128171439	GM12878	blood:	n/a	chr7:128171373-128171382
12	CBX3	chr7:128170946-128171580	K562	blood:	n/a	n/a
13	CCNT2	chr7:128170987-128171312	K562	blood:	n/a	n/a
14	CCNT2	chr7:128171512-128172123	K562	blood:	n/a	chr7:128171671-128171680
15	CEBPB	chr7:128172257-128172491	Hela-S3	cervix:	n/a	n/a
16	CEBPD	chr7:128171003-128171461	HepG2	liver:	n/a	n/a
17	CEBPD	chr7:128171033-128171313	HepG2	liver:	n/a	n/a
18	CEBPD	chr7:128171003-128171705	K562	blood:	n/a	n/a
19	CHD1	chr7:128170782-128171972	IMR90	lung:	n/a	chr7:128171373-128171382
20	CHD1	chr7:128171610-128171975	GM12878	blood:	n/a	n/a
21	CHD1	chr7:128171116-128171305	GM12878	blood:	n/a	n/a
22	CHD2	chr7:128172301-128172445	K562	blood:	n/a	n/a
23	CHD2	chr7:128171022-128171802	K562	blood:	n/a	chr7:128171373-128171382
24	CHD2	chr7:128170887-128171969	Hela-S3	cervix:	n/a	chr7:128171373-128171382
25	CHD2	chr7:128171162-128171625	H1-hESC	embryonic stem cell:	n/a	chr7:128171373-128171382
26	CHD2	chr7:128172254-128172487	Hela-S3	cervix:	n/a	n/a
27	CHD2	chr7:128171068-128171784	HepG2	liver:	n/a	chr7:128171373-128171382
28	CHD2	chr7:128171061-128171675	GM12878	blood:	n/a	chr7:128171373-128171382
29	CREB1	chr7:128170951-128171328	A549	lung:	n/a	n/a
30	CTCF	chr7:128170700-128170824	GM19238	blood:	n/a	n/a
31	CTCF	chr7:128171580-128171730	GM12865	blood:	n/a	chr7:128171592-128171605
32	CTCF	chr7:128170708-128170791	GM19240	blood:	n/a	n/a
33	CTCF	chr7:128170039-128170086	MCF-7	breast:	n/a	chr7:128170056-128170072
34	CTCF	chr7:128170711-128170823	GM12892	blood:	n/a	n/a
35	CTCF	chr7:128170733-128170929	K562	blood:	n/a	n/a
36	CTCF	chr7:128170706-128170831	GM19239	blood:	n/a	n/a
37	CTCF	chr7:128170794-128170840	GM10248	blood:	n/a	n/a
38	CUX1	chr7:128171426-128171485	K562	blood:	n/a	n/a
39	E2F4	chr7:128173196-128173359	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F6	chr7:128172349-128172506	K562	blood:	n/a	n/a
41	E2F6	chr7:128170828-128171350	K562	blood:	n/a	chr7:128171191-128171200 chr7:128171246-128171255 chr7:128171029-128171039 chr7:128171050-128171060
42	E2F6	chr7:128170914-128171313	K562	blood:	n/a	chr7:128171191-128171200 chr7:128171246-128171255 chr7:128171029-128171039 chr7:128171050-128171060
43	E2F6	chr7:128170656-128171664	K562	blood:	n/a	chr7:128171191-128171200 chr7:128171246-128171255 chr7:128171609-128171618 chr7:128171029-128171039 chr7:128171621-128171631 chr7:128171050-128171060
44	E2F6	chr7:128171464-128171911	K562	blood:	n/a	chr7:128171842-128171852 chr7:128171845-128171855 chr7:128171609-128171618 chr7:128171621-128171631 chr7:128171677-128171686 chr7:128171839-128171849
45	E2F6	chr7:128170577-128170728	K562	blood:	n/a	chr7:128170606-128170615
46	EBF1	chr7:128170943-128171302	GM12878	blood:	n/a	n/a
47	EBF1	chr7:128170473-128170802	GM12878	blood:	n/a	chr7:128170645-128170654 chr7:128170644-128170655
48	EBF1	chr7:128170337-128170732	GM12878	blood:	n/a	chr7:128170645-128170654 chr7:128170644-128170655
49	EBF1	chr7:128170249-128170861	GM12878	blood:	n/a	chr7:128170645-128170654 chr7:128170644-128170655
50	EGR1	chr7:128171563-128171893	K562	blood:	n/a	chr7:128171677-128171687 chr7:128171667-128171677 chr7:128171871-128171884 chr7:128171672-128171685

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:128170611-128170661	H1-hESC	embryonic stem cell:	embryo
2	chr7:128170611-128170661	H1-hESC	embryonic stem cell:	embryo
3	chr7:128171939-128171989	AG09309	skin:	n/a
4	chr7:128172447-128172497	NHBE	bronchial:	n/a
5	chr7:128172288-128172338	GM19239	blood:	n/a
6	chr7:128171939-128171989	SAEC	small airway:	n/a
7	chr7:128171939-128171989	NB4	blood:	n/a
8	chr7:128170824-128170874	MCF10A-Er-Src	breast:	n/a
9	chr7:128172447-128172497	MCF10A-Er-Src	breast:	n/a
10	chr7:128171378-128171428	HNPCEpiC	eye:	n/a
11	chr7:128171939-128171989	GM06990	blood:	n/a
12	chr7:128170824-128170874	IMR90	lung:	fetal
13	chr7:128172447-128172497	GM12892	blood:	n/a
14	chr7:128171939-128171989	SKMC	muscle:	n/a
15	chr7:128170611-128170661	Hela-S3	cervix:	n/a
16	chr7:128171939-128171989	H1-hESC	embryonic stem cell:	embryo
17	chr7:128170824-128170874	ProgFib	skin:	n/a
18	chr7:128170824-128170874	ovcar-3	ovarian:	n/a
19	chr7:128172288-128172338	ECC-1	luminal epithelium:	n/a
20	chr7:128171939-128171989	HMEC	breast:	n/a
21	chr7:128170611-128170661	IMR90	lung:	fetal
22	chr7:128171939-128171989	LNCaP	prostate:	n/a
23	chr7:128171378-128171428	HEEpiC	esophagus:	n/a
24	chr7:128170824-128170874	RPTEC	kidney:	n/a
25	chr7:128171939-128171989	GM12878	blood:	n/a
26	chr7:128170824-128170874	HPAEpiC	pulmonary alveolar:	n/a
27	chr7:128170824-128170874	HEK293	kidney:	embryo
28	chr7:128172288-128172338	GM12878	blood:	n/a
29	chr7:128171378-128171428	PANC-1	pancreas:	n/a
30	chr7:128171939-128171989	HRCEpiC	kidney:	n/a
31	chr7:128170824-128170874	SKMC	muscle:	n/a
32	chr7:128172288-128172338	MCF10A-Er-Src	breast:	n/a
33	chr7:128170611-128170661	NT2-D1	testis:	n/a
34	chr7:128170611-128170661	ProgFib	skin:	n/a
35	chr7:128170611-128170661	AG10803	skin:	n/a
36	chr7:128172447-128172497	HAEpiC	amniotic membrane:	n/a
37	chr7:128171378-128171428	HPAEpiC	pulmonary alveolar:	n/a
38	chr7:128170824-128170874	SK-N-SH	brain:	n/a
39	chr7:128171378-128171428	HRE	kidney:	n/a
40	chr7:128171939-128171989	AoSMC	blood vessel:	n/a
41	chr7:128171378-128171428	SK-N-MC	brain:	n/a
42	chr7:128170824-128170874	AG04449	skin:	fetal
43	chr7:128171939-128171989	GM12891	blood:	n/a
44	chr7:128170611-128170661	GM12892	blood:	n/a
45	chr7:128171939-128171989	NT2-D1	testis:	n/a
46	chr7:128170824-128170874	SK-N-SH_RA	brain:	n/a
47	chr7:128170824-128170874	LNCaP	prostate:	n/a
48	chr7:128171378-128171428	MCF-7	breast:	n/a
49	chr7:128171378-128171428	U87	brain:	n/a
50	chr7:128170824-128170874	HMEC	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:60555036..60556427-chr7:128170464..128171900,5	Hela-S3	cervix:
2	chr1:43423670..43424605-chr7:128170752..128171420,2	Hela-S3	cervix:
3	chr7:128116465..128119803-chr7:128169321..128173196,4	MCF-7	breast:
4	chr7:128171075..128171582-chr9:128003090..128003828,2	Hela-S3	cervix:
5	chr17:60555428..60556734-chr7:128170618..128172295,7	MCF-7	breast:
6	chr17:60555522..60557036-chr7:128169502..128171568,2	MCF-7	breast:
7	chr17:60555920..60556424-chr7:128170752..128171283,2	HCT-116	colon:
8	chr7:128116092..128118343-chr7:128171049..128172892,4	K562	blood:
9	chr15:66796944..66797841-chr7:128170664..128171300,2	Hela-S3	cervix:
10	chr7:128044227..128046158-chr7:128169736..128172586,2	K562	blood:
11	chr14:55878199..55878800-chr7:128170749..128171703,2	NB4	blood:
12	chr17:60554358..60557025-chr7:128169837..128172731,3	MCF-7	breast:
13	chr7:128094511..128096087-chr7:128168839..128171295,2	K562	blood:
14	chr7:128171099..128172769-chr7:128337309..128338976,2	K562	blood:
15	chr19:12903229..12903859-chr7:128170833..128171585,2	Hela-S3	cervix:
16	chr7:128154968..128157377-chr7:128169188..128171020,2	K562	blood:
17	chr17:7387516..7388176-chr7:128171392..128172005,2	Hela-S3	cervix:
18	chr7:128095000..128097525-chr7:128170265..128171989,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-METTL2B-1	chr7:128169669-128170972	XLOC_006240

Variant related genes	Relation type
ENSG00000273270	TF binding region
ENSG00000242588	TF binding region
ENSG00000273270	CpG island
ENSG00000242588	CpG island
ENSG00000174442	chromatin interactions
ENSG00000201041	chromatin interactions
ENSG00000181222	chromatin interactions
ENSG00000252866	chromatin interactions
ENSG00000095066	chromatin interactions
ENSG00000146872	chromatin interactions
ENSG00000174444	chromatin interactions
ENSG00000126775	chromatin interactions
ENSG00000240758	chromatin interactions
ENSG00000174282	chromatin interactions
ENSG00000117394	chromatin interactions
ENSG00000135245	chromatin interactions
ENSG00000044574	chromatin interactions
ENSG00000106348	chromatin interactions
ENSG00000273184	chromatin interactions
ENSG00000165055	chromatin interactions

Extended variants
information (count: 137 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:137 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146640077	chr7:128169815-128169816	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
2	rs3802004	chr7:128169884-128169885	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs187744622	chr7:128169923-128169924	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
4	rs571713683	chr7:128169930-128169931	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
5	rs372558764	chr7:128169938-128169939	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
6	rs376049850	chr7:128169946-128169947	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
7	rs3802003	chr7:128169979-128169980	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs565902737	chr7:128170005-128170006	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
9	rs568272925	chr7:128170007-128170008	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
10	rs536667802	chr7:128170021-128170022	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
11	rs2956675	chr7:128170058-128170059	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
12	rs3802002	chr7:128170089-128170090	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs574018278	chr7:128170091-128170092	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
14	rs544410684	chr7:128170093-128170094	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
15	rs556129589	chr7:128170095-128170096	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
16	rs2956676	chr7:128170114-128170115	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
17	rs2956677	chr7:128170148-128170149	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
18	rs545375624	chr7:128170162-128170163	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
19	rs577769467	chr7:128170186-128170187	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
20	rs148315229	chr7:128170213-128170214	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
21	rs560206362	chr7:128170251-128170252	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
22	rs192305156	chr7:128170299-128170300	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
23	rs62483276	chr7:128170327-128170328	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs140494146	chr7:128170328-128170329	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
25	rs531930492	chr7:128170372-128170373	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
26	rs183461551	chr7:128170385-128170386	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
27	rs371564126	chr7:128170413-128170414	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
28	rs150442355	chr7:128170415-128170416	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
29	rs532757336	chr7:128170441-128170442	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
30	rs539299003	chr7:128170461-128170462	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
31	rs557375148	chr7:128170476-128170477	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
32	rs188515744	chr7:128170477-128170478	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
33	rs192743239	chr7:128170479-128170480	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
34	rs560841833	chr7:128170602-128170603	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
35	rs536631344	chr7:128170670-128170671	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
36	rs6966353	chr7:128170748-128170749	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
37	rs548642471	chr7:128170758-128170759	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
38	rs369509306	chr7:128170785-128170786	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
39	rs188427377	chr7:128170834-128170835	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
40	rs538090178	chr7:128170875-128170876	Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
41	rs556429703	chr7:128170906-128170907	Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
42	rs577728735	chr7:128170913-128170914	Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
43	rs538845592	chr7:128170947-128170948	Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
44	rs553561797	chr7:128170954-128170955	Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a
45	rs571852807	chr7:128170996-128170997	Active TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
46	rs542216239	chr7:128171067-128171068	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
47	rs113790722	chr7:128171094-128171095	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	mRNA abundance
48	rs191398424	chr7:128171102-128171103	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
49	rs376392372	chr7:128171128-128171129	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
50	rs10242420	chr7:128171136-128171137	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Retinitis pigmentosa	17160897	CNVD
Colorblindness	17160897	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:506 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:128163600-128169800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr7:128163600-128169800	Weak transcription	Psoas Muscle	Psoas
3	chr7:128163600-128170400	Weak transcription	Lung	lung
4	chr7:128163800-128169800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr7:128163800-128169800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr7:128163800-128169800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr7:128163800-128169800	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr7:128163800-128169800	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr7:128163800-128169800	Weak transcription	Brain Anterior Caudate	brain
10	chr7:128163800-128169800	Weak transcription	Colon Smooth Muscle	Colon
11	chr7:128163800-128169800	Weak transcription	Fetal Stomach	stomach
12	chr7:128163800-128169800	Weak transcription	Left Ventricle	heart
13	chr7:128163800-128169800	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr7:128163800-128169800	Weak transcription	Small Intestine	intestine
15	chr7:128163800-128169800	Weak transcription	Dnd41	blood
16	chr7:128163800-128169800	Weak transcription	GM12878-XiMat	blood
17	chr7:128163800-128170000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr7:128163800-128170000	Weak transcription	Brain Substantia Nigra	brain
19	chr7:128163800-128170000	Weak transcription	Stomach Mucosa	stomach
20	chr7:128163800-128170000	Weak transcription	NH-A	brain
21	chr7:128163800-128170200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr7:128163800-128170200	Weak transcription	Fetal Thymus	thymus
23	chr7:128164000-128169800	Weak transcription	Adipose Nuclei	Adipose
24	chr7:128164000-128169800	Weak transcription	Rectal Mucosa Donor 29	rectum
25	chr7:128164000-128170200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr7:128164200-128169800	Weak transcription	Brain Cingulate Gyrus	brain
27	chr7:128164200-128169800	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr7:128164200-128169800	Weak transcription	Monocytes-CD14+_RO01746	blood
29	chr7:128164400-128169800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr7:128164400-128169800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr7:128164400-128169800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr7:128164400-128169800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr7:128164400-128169800	Weak transcription	Pancreas	Pancrea
34	chr7:128164400-128169800	Weak transcription	K562	blood
35	chr7:128164400-128170000	Weak transcription	Fetal Lung	lung
36	chr7:128164400-128170000	Weak transcription	Skeletal Muscle Female	skeletal muscle
37	chr7:128164400-128170000	Weak transcription	Hela-S3	cervix
38	chr7:128164400-128170200	Weak transcription	Colonic Mucosa	Colon
39	chr7:128164400-128170200	Weak transcription	Fetal Intestine Large	intestine
40	chr7:128164400-128170200	Weak transcription	Fetal Intestine Small	intestine
41	chr7:128164400-128170200	Weak transcription	Fetal Muscle Trunk	muscle
42	chr7:128164400-128170400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr7:128164800-128169800	Weak transcription	Rectal Mucosa Donor 31	rectum
44	chr7:128165000-128169800	Weak transcription	Spleen	Spleen
45	chr7:128166000-128169800	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr7:128166000-128169800	Weak transcription	Fetal Heart	heart
47	chr7:128166000-128169800	Weak transcription	Right Atrium	heart
48	chr7:128166200-128170000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr7:128166400-128169800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr7:128166600-128169800	Weak transcription	A549	lung

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