Variant report

Variant	esv2760289
Chromosome Location	chr13:76109536-76117768
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:666)
CpG islands
(count:856)
Chromatin interactive
region (count:18)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:666 , 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	ATF1	chr13:76115164-76115846	K562	blood:	n/a	n/a
4	ATF2	chr13:76111559-76112389	GM12878	blood:	n/a	n/a
5	ATF2	chr13:76112008-76112514	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr13:76111716-76112543	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr13:76112015-76112538	A549	lung:	n/a	n/a
8	BCLAF1	chr13:76111591-76112186	GM12878	blood:	n/a	n/a
9	BHLHE40	chr13:76111942-76112433	A549	lung:	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	BRCA1	chr13:76111808-76112292	GM12878	blood:	n/a	n/a
14	BRCA1	chr13:76111988-76112550	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chr13:76111647-76112440	HepG2	liver:	n/a	n/a
16	BRCA1	chr13:76111576-76112481	Hela-S3	cervix:	n/a	n/a
17	CCNT2	chr13:76111554-76112436	K562	blood:	n/a	n/a
18	CEBPB	chr13:76117488-76117562	A549	lung:	n/a	n/a
19	CEBPD	chr13:76111665-76112069	HepG2	liver:	n/a	n/a
20	CHD1	chr13:76111504-76112506	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD1	chr13:76111515-76112632	GM12878	blood:	n/a	n/a
22	CHD1	chr13:76111165-76112724	IMR90	lung:	n/a	n/a
23	CHD2	chr13:76111594-76112513	Hela-S3	cervix:	n/a	n/a
24	CHD2	chr13:76111795-76112421	K562	blood:	n/a	n/a
25	CHD2	chr13:76111725-76112523	GM12878	blood:	n/a	n/a
26	CHD2	chr13:76111873-76112550	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr13:76111716-76112448	HepG2	liver:	n/a	n/a
28	CREB1	chr13:76111842-76112398	A549	lung:	n/a	n/a
29	CREB1	chr13:76111785-76112474	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTBP2	chr13:76111695-76112410	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr13:76111960-76112110	HUVEC	blood vessel:	n/a	n/a
32	CTCF	chr13:76111880-76112030	GM12873	blood:	n/a	n/a
33	CTCF	chr13:76111940-76112090	GM12866	blood:	n/a	n/a
34	CTCF	chr13:76111940-76112090	NHLF	lung:	n/a	n/a
35	CTCF	chr13:76111920-76112070	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr13:76111940-76112090	HFF-Myc	foreskin:	n/a	n/a
37	CTCF	chr13:76111840-76111990	HepG2	liver:	n/a	n/a
38	CTCF	chr13:76111960-76112110	AG04450	lung:	n/a	n/a
39	CTCF	chr13:76111960-76112110	HPF	lung:	n/a	n/a
40	CTCF	chr13:76111920-76112070	SAEC	small airway:	n/a	n/a
41	CTCF	chr13:76111960-76112110	RPTEC	kidney:	n/a	n/a
42	CTCF	chr13:76111980-76112130	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr13:76111880-76112030	GM12865	blood:	n/a	n/a
44	CTCF	chr13:76112240-76112390	AG04449	skin:	n/a	n/a
45	CTCF	chr13:76111860-76112010	GM12878	blood:	n/a	n/a
46	CTCF	chr13:76111804-76112257	GM12878	blood:	n/a	n/a
47	CTCF	chr13:76111940-76112090	AG04450	lung:	n/a	n/a
48	CTCF	chr13:76112080-76112230	HMEC	breast:	n/a	n/a
49	CTCF	chr13:76111971-76112033	GM19239	blood:	n/a	n/a
50	CTCF	chr13:76111900-76112050	HPAF	blood vessel:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:76112030-76112080	SK-N-MC	brain:	n/a
2	chr13:76112030-76112080	SK-N-SH	brain:	n/a
3	chr13:76112030-76112080	SK-N-MC	brain:	n/a
4	chr13:76112030-76112080	SK-N-SH	brain:	n/a
5	chr13:76112274-76112324	SK-N-SH_RA	brain:	n/a
6	chr13:76112973-76113023	NHBE	bronchial:	n/a
7	chr13:76111918-76111968	NHDF-neo	bronchial:	n/a
8	chr13:76112274-76112324	HAEpiC	amniotic membrane:	n/a
9	chr13:76112232-76112282	Hepatocyte	liver:	n/a
10	chr13:76111980-76112030	GM12878	blood:	n/a
11	chr13:76113014-76113064	ProgFib	skin:	n/a
12	chr13:76112232-76112282	GM12892	blood:	n/a
13	chr13:76112039-76112089	HNPCEpiC	eye:	n/a
14	chr13:76112039-76112089	Caco-2	colon:	n/a
15	chr13:76111107-76111157	PANC-1	pancreas:	n/a
16	chr13:76113014-76113064	BJ	skin:	n/a
17	chr13:76111918-76111968	HNPCEpiC	eye:	n/a
18	chr13:76111751-76111801	NB4	blood:	n/a
19	chr13:76112980-76113030	HCM	heart:	n/a
20	chr13:76111980-76112030	NHBE	bronchial:	n/a
21	chr13:76112030-76112080	HEEpiC	esophagus:	n/a
22	chr13:76111918-76111968	MCF10A-Er-Src	breast:	n/a
23	chr13:76112232-76112282	AG10803	skin:	n/a
24	chr13:76111107-76111157	T-47D	breast:	n/a
25	chr13:76112232-76112282	GM12891	blood:	n/a
26	chr13:76112030-76112080	MCF-7	breast:	n/a
27	chr13:76112274-76112324	HRPEpiC	eye:	n/a
28	chr13:76111785-76111835	Caco-2	colon:	n/a
29	chr13:76111918-76111968	HCT-116	colon:	n/a
30	chr13:76112039-76112089	HRE	kidney:	n/a
31	chr13:76111980-76112030	NT2-D1	testis:	n/a
32	chr13:76111918-76111968	HAEpiC	amniotic membrane:	n/a
33	chr13:76112274-76112324	NHDF-neo	bronchial:	n/a
34	chr13:76112973-76113023	CMK	blood:	n/a
35	chr13:76112980-76113030	HRPEpiC	eye:	n/a
36	chr13:76113014-76113064	AG04450	lung:	fetal
37	chr13:76112274-76112324	SAEC	small airway:	n/a
38	chr13:76112030-76112080	NHBE	bronchial:	n/a
39	chr13:76112232-76112282	AG09319	gingival:	n/a
40	chr13:76112187-76112237	GM12891	blood:	n/a
41	chr13:76112030-76112080	H1-hESC	embryonic stem cell:	embryo
42	chr13:76112232-76112282	HCPEpiC	choroid plexus:	n/a
43	chr13:76112232-76112282	GM19239	blood:	n/a
44	chr13:76112980-76113030	AG09309	skin:	n/a
45	chr13:76113014-76113064	GM19239	blood:	n/a
46	chr13:76112187-76112237	Caco-2	colon:	n/a
47	chr13:76111918-76111968	GM19239	blood:	n/a
48	chr13:76111918-76111968	HCPEpiC	choroid plexus:	n/a
49	chr13:76112232-76112282	ovcar-3	ovarian:	n/a
50	chr13:76112274-76112324	HCF	heart:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:76101122..76104303-chr13:76108576..76110569,3	K562	blood:
2	chr13:76055248..76057886-chr13:76110224..76112780,4	MCF-7	breast:
3	chr13:76102775..76109881-chr13:76110381..76113047,9	MCF-7	breast:
4	chr13:76107791..76110428-chr13:76144234..76145882,2	K562	blood:
5	chr13:76111404..76112078-chr17:26989037..26989702,2	Hela-S3	cervix:
6	chr13:76101020..76103303-chr13:76108939..76111291,2	K562	blood:
7	chr13:76111452..76114150-chr13:76122087..76125338,6	MCF-7	breast:
8	chr13:76111859..76112746-chr13:76123326..76123936,2	MCF-7	breast:
9	chr13:76109113..76111805-chr13:76112674..76114626,2	K562	blood:
10	chr11:65339613..65340413-chr13:76111532..76112034,2	NB4	blood:
11	chr13:76109717..76113590-chr13:76122029..76126081,5	MCF-7	breast:
12	chr13:76055919..76057695-chr13:76110507..76112437,2	MCF-7	breast:
13	chr1:151253613..151254502-chr13:76111700..76112352,2	Hela-S3	cervix:
14	chr13:76111578..76112381-chrX:73511953..73512510,2	Hela-S3	cervix:
15	chr13:76115839..76118347-chr13:76129572..76131579,2	K562	blood:
16	chr13:76102775..76109881-chr13:76110381..76113047,9	MCF-7	breast:
17	chr13:76109113..76111805-chr13:76112674..76114626,2	K562	blood:
18	chr13:76106394..76109955-chr13:76110419..76113939,6	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
COMMD6	CpG island
ENSG00000143373	chromatin interactions
ENSG00000109111	chromatin interactions
ENSG00000118939	chromatin interactions
ENSG00000232671	chromatin interactions
ENSG00000132581	chromatin interactions
ENSG00000261553	chromatin interactions
ENSG00000230590	chromatin interactions
ENSG00000176973	chromatin interactions
ENSG00000188243	chromatin interactions
ENSG00000136111	chromatin interactions

Extended variants
information (count: 346 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:346 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7985488	chr13:76109536-76109537	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs190218707	chr13:76109558-76109559	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs552811575	chr13:76109589-76109590	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs570608255	chr13:76109591-76109592	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs570536431	chr13:76109611-76109612	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs534725295	chr13:76109612-76109613	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs553069463	chr13:76109613-76109614	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs574332786	chr13:76109697-76109698	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs535480483	chr13:76109755-76109756	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs537607915	chr13:76109766-76109767	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs577121626	chr13:76109789-76109790	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs375025266	chr13:76109804-76109805	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs575183661	chr13:76109815-76109816	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs6562905	chr13:76109836-76109837	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs563961357	chr13:76109932-76109933	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs576892679	chr13:76109933-76109934	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs182767865	chr13:76109958-76109959	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs559822159	chr13:76110003-76110004	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs568115429	chr13:76110024-76110025	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs534221177	chr13:76110028-76110029	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs187649166	chr13:76110202-76110203	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs137957924	chr13:76110215-76110216	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs115613540	chr13:76110306-76110307	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs535452395	chr13:76110338-76110339	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs553793366	chr13:76110349-76110350	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs193224549	chr13:76110364-76110365	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs571044859	chr13:76110378-76110379	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs535264567	chr13:76110382-76110383	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs572697572	chr13:76110383-76110384	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs568188264	chr13:76110396-76110397	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs535067283	chr13:76110470-76110471	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs142435984	chr13:76110473-76110474	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs143909466	chr13:76110492-76110493	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs9543963	chr13:76110543-76110544	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs185564613	chr13:76110598-76110599	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs148191541	chr13:76110601-76110602	Genic enhancers Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs56084319	chr13:76110679-76110680	Genic enhancers Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs141129963	chr13:76110761-76110762	Genic enhancers Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs115863432	chr13:76110765-76110766	Genic enhancers Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs116259533	chr13:76110766-76110767	Genic enhancers Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs563690567	chr13:76110770-76110771	Genic enhancers Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs150799117	chr13:76110780-76110781	Genic enhancers Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs187378524	chr13:76110901-76110902	Genic enhancers Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs139738020	chr13:76110902-76110903	Genic enhancers Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs528669692	chr13:76110980-76110981	Genic enhancers Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs117641217	chr13:76111025-76111026	Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs568018680	chr13:76111068-76111069	Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs145252203	chr13:76111072-76111073	Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs550271871	chr13:76111166-76111167	Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs559675648	chr13:76111168-76111169	Flanking Active TSS Active TSS Weak transcription Enhancers	Chromatin interactive region	4 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:627 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:76095800-76111400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr13:76096600-76110400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr13:76096600-76111400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr13:76097000-76111000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr13:76097000-76111600	Weak transcription	Spleen	Spleen
6	chr13:76097800-76110400	Weak transcription	Brain Angular Gyrus	brain
7	chr13:76097800-76110600	Weak transcription	Fetal Brain Male	brain
8	chr13:76097800-76110600	Weak transcription	Fetal Kidney	kidney
9	chr13:76097800-76110600	Weak transcription	Psoas Muscle	Psoas
10	chr13:76097800-76111200	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr13:76098000-76110400	Weak transcription	A549	lung
12	chr13:76098000-76110400	Weak transcription	HUVEC	blood vessel
13	chr13:76098000-76110600	Weak transcription	Brain Anterior Caudate	brain
14	chr13:76098000-76110600	Weak transcription	Rectal Smooth Muscle	rectum
15	chr13:76098000-76111200	Weak transcription	Aorta	Aorta
16	chr13:76098200-76109600	Weak transcription	Brain Germinal Matrix	brain
17	chr13:76098200-76110400	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr13:76098400-76110200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr13:76098600-76111000	Weak transcription	Colonic Mucosa	Colon
20	chr13:76098800-76110400	Weak transcription	Brain Cingulate Gyrus	brain
21	chr13:76098800-76111400	Weak transcription	Esophagus	oesophagus
22	chr13:76099400-76110400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr13:76099600-76110200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr13:76099600-76111000	Weak transcription	K562	blood
25	chr13:76100000-76110600	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr13:76100000-76111200	Weak transcription	Ovary	ovary
27	chr13:76100200-76110400	Weak transcription	Brain Substantia Nigra	brain
28	chr13:76100200-76110600	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr13:76100400-76110600	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr13:76100800-76110000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr13:76100800-76110600	Weak transcription	Right Ventricle	heart
32	chr13:76102200-76110400	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr13:76103600-76111000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr13:76104000-76110600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr13:76104400-76110400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr13:76105000-76110600	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr13:76105000-76111200	Weak transcription	Stomach Mucosa	stomach
38	chr13:76105200-76110600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
39	chr13:76105200-76110600	Weak transcription	NHDF-Ad	bronchial
40	chr13:76105400-76110400	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr13:76105600-76110400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr13:76106000-76110000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr13:76106000-76110000	Weak transcription	Small Intestine	intestine
44	chr13:76106000-76110400	Strong transcription	HUES64 Cell Line	embryonic stem cell
45	chr13:76106200-76109800	Strong transcription	Fetal Lung	lung
46	chr13:76106200-76110000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr13:76106200-76110200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr13:76106200-76110400	Weak transcription	Primary neutrophils fromperipheralblood	blood
49	chr13:76106200-76110600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
50	chr13:76106200-76110600	Strong transcription	Fetal Thymus	thymus

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