Variant report

Variant	nsv818980
Chromosome Location	chr13:76111280-76119506
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:674)
CpG islands
(count:793)
Chromatin interactive
region (count:16)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:674 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:76111988-76112275	K562	blood:	n/a	n/a
2	ARID3A	chr13:76111847-76112381	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:76119103-76119402	HepG2	liver:	n/a	n/a
4	ATF1	chr13:76115164-76115846	K562	blood:	n/a	n/a
5	ATF2	chr13:76111559-76112389	GM12878	blood:	n/a	n/a
6	ATF2	chr13:76112008-76112514	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr13:76111716-76112543	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr13:76112015-76112538	A549	lung:	n/a	n/a
9	BCLAF1	chr13:76111591-76112186	GM12878	blood:	n/a	n/a
10	BHLHE40	chr13:76111845-76112497	K562	blood:	n/a	n/a
11	BHLHE40	chr13:76111626-76112484	HepG2	liver:	n/a	n/a
12	BHLHE40	chr13:76111540-76112825	GM12878	blood:	n/a	n/a
13	BHLHE40	chr13:76111942-76112433	A549	lung:	n/a	n/a
14	BRCA1	chr13:76111647-76112440	HepG2	liver:	n/a	n/a
15	BRCA1	chr13:76111988-76112550	H1-hESC	embryonic stem cell:	n/a	n/a
16	BRCA1	chr13:76111576-76112481	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr13:76111808-76112292	GM12878	blood:	n/a	n/a
18	CCNT2	chr13:76111554-76112436	K562	blood:	n/a	n/a
19	CEBPB	chr13:76119032-76119423	HepG2	liver:	n/a	chr13:76119247-76119258 chr13:76119186-76119203
20	CEBPB	chr13:76119008-76119530	Hela-S3	cervix:	n/a	chr13:76119247-76119258 chr13:76119186-76119203
21	CEBPB	chr13:76119018-76119446	IMR90	lung:	n/a	chr13:76119247-76119258 chr13:76119186-76119203
22	CEBPB	chr13:76119116-76119316	A549	lung:	n/a	chr13:76119247-76119258 chr13:76119186-76119203
23	CEBPB	chr13:76117488-76117562	A549	lung:	n/a	n/a
24	CEBPD	chr13:76111665-76112069	HepG2	liver:	n/a	n/a
25	CHD1	chr13:76111504-76112506	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD1	chr13:76111515-76112632	GM12878	blood:	n/a	n/a
27	CHD1	chr13:76111165-76112724	IMR90	lung:	n/a	n/a
28	CHD2	chr13:76111725-76112523	GM12878	blood:	n/a	n/a
29	CHD2	chr13:76111594-76112513	Hela-S3	cervix:	n/a	n/a
30	CHD2	chr13:76111716-76112448	HepG2	liver:	n/a	n/a
31	CHD2	chr13:76111795-76112421	K562	blood:	n/a	n/a
32	CHD2	chr13:76111873-76112550	H1-hESC	embryonic stem cell:	n/a	n/a
33	CREB1	chr13:76111842-76112398	A549	lung:	n/a	n/a
34	CREB1	chr13:76111785-76112474	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTBP2	chr13:76111695-76112410	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr13:76111720-76111870	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr13:76112080-76112230	HMEC	breast:	n/a	n/a
38	CTCF	chr13:76111840-76111990	HFF	foreskin:	n/a	n/a
39	CTCF	chr13:76111980-76112130	HCFaa	heart:	n/a	n/a
40	CTCF	chr13:76111960-76112110	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr13:76111920-76112070	SAEC	small airway:	n/a	n/a
42	CTCF	chr13:76111960-76112110	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr13:76111940-76112090	HCM	heart:	n/a	n/a
44	CTCF	chr13:76111880-76112030	GM12873	blood:	n/a	n/a
45	CTCF	chr13:76111980-76112130	NHDF-neo	bronchial:	n/a	n/a
46	CTCF	chr13:76111900-76112050	HMF	breast:	n/a	n/a
47	CTCF	chr13:76111700-76111850	GM12866	blood:	n/a	n/a
48	CTCF	chr13:76111997-76112046	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr13:76111980-76112130	AG09309	skin:	n/a	n/a
50	CTCF	chr13:76111940-76112090	NHLF	lung:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:76112030-76112080	Caco-2	colon:	n/a
2	chr13:76115526-76115576	HNPCEpiC	eye:	n/a
3	chr13:76112039-76112089	AG04449	skin:	fetal
4	chr13:76112274-76112324	HEEpiC	esophagus:	n/a
5	chr13:76112980-76113030	U87	brain:	n/a
6	chr13:76111785-76111835	H1-hESC	embryonic stem cell:	embryo
7	chr13:76112274-76112324	NH-A	brain:	n/a
8	chr13:76111751-76111801	HCT-116	colon:	n/a
9	chr13:76111980-76112030	IMR90	lung:	fetal
10	chr13:76112232-76112282	GM06990	blood:	n/a
11	chr13:76112030-76112080	A549	lung:	n/a
12	chr13:76112980-76113030	ECC-1	luminal epithelium:	n/a
13	chr13:76112187-76112237	HCPEpiC	choroid plexus:	n/a
14	chr13:76112973-76113023	HRCEpiC	kidney:	n/a
15	chr13:76111980-76112030	Hela-S3	cervix:	n/a
16	chr13:76112232-76112282	HUVEC	blood vessel:	n/a
17	chr13:76111918-76111968	HCPEpiC	choroid plexus:	n/a
18	chr13:76112187-76112237	Hepatocyte	liver:	n/a
19	chr13:76112980-76113030	PFSK-1	brain:	n/a
20	chr13:76112187-76112237	ovcar-3	ovarian:	n/a
21	chr13:76111980-76112030	GM12891	blood:	n/a
22	chr13:76112973-76113023	NT2-D1	testis:	n/a
23	chr13:76112039-76112089	HCF	heart:	n/a
24	chr13:76112274-76112324	Hela-S3	cervix:	n/a
25	chr13:76111918-76111968	PrEC	prostate:	n/a
26	chr13:76111785-76111835	HepG2	liver:	n/a
27	chr13:76112030-76112080	BE2_C	brain:	n/a
28	chr13:76111918-76111968	Caco-2	colon:	n/a
29	chr13:76112232-76112282	SK-N-SH	brain:	n/a
30	chr13:76111785-76111835	ECC-1	luminal epithelium:	n/a
31	chr13:76112030-76112080	ovcar-3	ovarian:	n/a
32	chr13:76112030-76112080	NH-A	brain:	n/a
33	chr13:76111980-76112030	GM06990	blood:	n/a
34	chr13:76111785-76111835	HRPEpiC	eye:	n/a
35	chr13:76112274-76112324	AG09309	skin:	n/a
36	chr13:76112232-76112282	AG04450	lung:	fetal
37	chr13:76115526-76115576	HRPEpiC	eye:	n/a
38	chr13:76112187-76112237	Hela-S3	cervix:	n/a
39	chr13:76113014-76113064	SAEC	small airway:	n/a
40	chr13:76115526-76115576	SKMC	muscle:	n/a
41	chr13:76112980-76113030	NHDF-neo	bronchial:	n/a
42	chr13:76111980-76112030	HRE	kidney:	n/a
43	chr13:76111918-76111968	U87	brain:	n/a
44	chr13:76115526-76115576	BJ	skin:	n/a
45	chr13:76111785-76111835	HCM	heart:	n/a
46	chr13:76111918-76111968	SK-N-SH	brain:	n/a
47	chr13:76113014-76113064	MCF-7	breast:	n/a
48	chr13:76112232-76112282	GM19239	blood:	n/a
49	chr13:76115526-76115576	HCT-116	colon:	n/a
50	chr13:76112232-76112282	HCM	heart:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:76111404..76112078-chr17:26989037..26989702,2	Hela-S3	cervix:
2	chr13:76111452..76114150-chr13:76122087..76125338,6	MCF-7	breast:
3	chr13:76101020..76103303-chr13:76108939..76111291,2	K562	blood:
4	chr11:65339613..65340413-chr13:76111532..76112034,2	NB4	blood:
5	chr13:76115839..76118347-chr13:76129572..76131579,2	K562	blood:
6	chr13:76055919..76057695-chr13:76110507..76112437,2	MCF-7	breast:
7	chr13:76109113..76111805-chr13:76112674..76114626,2	K562	blood:
8	chr13:76109717..76113590-chr13:76122029..76126081,5	MCF-7	breast:
9	chr13:76109687..76114004-chr13:76118514..76122227,3	K562	blood:
10	chr13:76055248..76057886-chr13:76110224..76112780,4	MCF-7	breast:
11	chr1:151253613..151254502-chr13:76111700..76112352,2	Hela-S3	cervix:
12	chr13:76111859..76112746-chr13:76123326..76123936,2	MCF-7	breast:
13	chr13:76111578..76112381-chrX:73511953..73512510,2	Hela-S3	cervix:
14	chr13:76102775..76109881-chr13:76110381..76113047,9	MCF-7	breast:
15	chr13:76109113..76111805-chr13:76112674..76114626,2	K562	blood:
16	chr13:76118168..76119687-chr13:76122527..76125250,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TBC1D4-2	chr13:76111635-76111811	NONHSAT034360

No data

Variant related genes	Relation type
COMMD6	TF binding region
ENSG00000261553	TF binding region
UCHL3	TF binding region
COMMD6	CpG island
ENSG00000261553	CpG island
UCHL3	CpG island
ENSG00000132581	chromatin interactions
ENSG00000230590	chromatin interactions
ENSG00000143373	chromatin interactions
ENSG00000188243	chromatin interactions
ENSG00000176973	chromatin interactions
ENSG00000109111	chromatin interactions
ENSG00000118939	chromatin interactions
ENSG00000261553	chromatin interactions
ENSG00000232671	chromatin interactions
ENSG00000136111	chromatin interactions

Extended variants
information (count: 356 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:356 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9573580	chr13:76111280-76111281	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs545765161	chr13:76111301-76111302	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs533707018	chr13:76111319-76111320	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs555540039	chr13:76111347-76111348	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs184704487	chr13:76111357-76111358	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs531535670	chr13:76111391-76111392	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs71433190	chr13:76111432-76111433	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs542296011	chr13:76111515-76111516	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs557520445	chr13:76111533-76111534	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs575708547	chr13:76111565-76111566	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs9600490	chr13:76111607-76111608	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs564729988	chr13:76111622-76111623	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs41286112	chr13:76111657-76111658	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
14	rs540444818	chr13:76111693-76111694	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
15	rs9600491	chr13:76111700-76111701	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
16	rs9543964	chr13:76111702-76111703	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs200497164	chr13:76111768-76111769	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
18	rs550239500	chr13:76111779-76111780	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
19	rs373284337	chr13:76111780-76111781	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
20	rs116744134	chr13:76111784-76111785	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
21	rs377543170	chr13:76111786-76111787	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
22	rs202041987	chr13:76111820-76111821	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
23	rs114316494	chr13:76111852-76111853	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
24	rs375005753	chr13:76111855-76111856	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
25	rs367689969	chr13:76111862-76111863	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
26	rs547445480	chr13:76111890-76111891	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
27	rs143172831	chr13:76111919-76111920	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
28	rs372073245	chr13:76111922-76111923	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
29	rs111633743	chr13:76111929-76111930	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
30	rs188582438	chr13:76111940-76111941	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
31	rs555410964	chr13:76111942-76111943	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
32	rs199894482	chr13:76111945-76111946	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
33	rs368420185	chr13:76111946-76111947	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
34	rs201671061	chr13:76111949-76111950	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
35	rs563289580	chr13:76111959-76111960	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
36	rs374256603	chr13:76111962-76111963	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
37	rs201230705	chr13:76111968-76111969	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
38	rs200274770	chr13:76111976-76111977	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
39	rs370887966	chr13:76111991-76111992	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
40	rs575817831	chr13:76112013-76112014	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
41	rs546173941	chr13:76112016-76112017	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
42	rs200147107	chr13:76112035-76112036	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
43	rs558207003	chr13:76112036-76112037	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
44	rs7335949	chr13:76112102-76112103	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs540904689	chr13:76112109-76112110	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs181341735	chr13:76112112-76112113	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs141249709	chr13:76112127-76112128	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs529485624	chr13:76112159-76112160	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs544440831	chr13:76112164-76112165	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs562201134	chr13:76112170-76112171	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21858162	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hirschsprung''s Disease	21712996	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Intracranial aneurysm	16715129	CNVD
Non-small cell lung cancer	19010865	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:358 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:76095800-76111400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr13:76096600-76111400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr13:76097000-76111600	Weak transcription	Spleen	Spleen
4	chr13:76098800-76111400	Weak transcription	Esophagus	oesophagus
5	chr13:76109200-76111400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr13:76109600-76111400	Weak transcription	Left Ventricle	heart
7	chr13:76109800-76111400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr13:76109800-76111400	Weak transcription	Gastric	stomach
9	chr13:76109800-76111400	Weak transcription	Lung	lung
10	chr13:76110000-76111400	Enhancers	Small Intestine	intestine
11	chr13:76110200-76111400	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr13:76110400-76111400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
13	chr13:76110400-76111400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
14	chr13:76110400-76111400	Flanking Active TSS	Osteobl	bone
15	chr13:76110400-76111600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr13:76110400-76112800	Active TSS	Rectal Mucosa Donor 29	rectum
17	chr13:76110600-76111400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr13:76110600-76111400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
19	chr13:76110600-76111400	Flanking Active TSS	Brain Anterior Caudate	brain
20	chr13:76110600-76111400	Flanking Active TSS	Brain Germinal Matrix	brain
21	chr13:76110600-76111400	Flanking Active TSS	Duodenum Mucosa	Duodenum
22	chr13:76110600-76111400	Enhancers	Pancreas	Pancrea
23	chr13:76110600-76111400	Flanking Active TSS	HepG2	liver
24	chr13:76110600-76111600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
25	chr13:76110600-76111800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
26	chr13:76110600-76111800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr13:76110600-76111800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr13:76110600-76112600	Active TSS	H9 Cell Line	embryonic stem cell
29	chr13:76110800-76111400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr13:76110800-76111400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr13:76110800-76111400	Flanking Active TSS	Brain Hippocampus Middle	brain
32	chr13:76110800-76111400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
33	chr13:76110800-76111400	Flanking Active TSS	Dnd41	blood
34	chr13:76110800-76111400	Flanking Active TSS	NHEK	skin
35	chr13:76110800-76111600	Flanking Active TSS	Primary T cells from cord blood	blood
36	chr13:76110800-76111600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
37	chr13:76110800-76111800	Flanking Active TSS	Primary B cells from cord blood	blood
38	chr13:76110800-76111800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
39	chr13:76110800-76112400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
40	chr13:76110800-76112400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr13:76110800-76112600	Active TSS	H1 Cell Line	embryonic stem cell
42	chr13:76110800-76112600	Active TSS	iPS-20b Cell Line	embryonic stem cell
43	chr13:76110800-76112600	Active TSS	Psoas Muscle	Psoas
44	chr13:76110800-76112600	Active TSS	NHDF-Ad	bronchial
45	chr13:76110800-76112800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr13:76110800-76112800	Active TSS	HUES48 Cell Line	embryonic stem cell
47	chr13:76110800-76112800	Active TSS	HUES64 Cell Line	embryonic stem cell
48	chr13:76110800-76112800	Active TSS	GM12878-XiMat	blood
49	chr13:76111000-76111400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
50	chr13:76111000-76111400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain

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