Variant report

Variant	esv3410885
Chromosome Location	chr9:86236957-86239705
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:474)
CpG islands
(count:245)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:474 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:86238855-86239052	K562	blood:	n/a	n/a
2	BCLAF1	chr9:86237789-86238553	GM12878	blood:	n/a	chr9:86237988-86238001 chr9:86238011-86238020 chr9:86238184-86238193 chr9:86238181-86238190
3	BCLAF1	chr9:86237581-86238703	GM12878	blood:	n/a	chr9:86237988-86238001 chr9:86238011-86238020 chr9:86238184-86238193 chr9:86238181-86238190
4	BHLHE40	chr9:86238529-86238730	K562	blood:	n/a	n/a
5	BHLHE40	chr9:86237852-86238126	K562	blood:	n/a	chr9:86237988-86238004
6	CCNT2	chr9:86237895-86238638	K562	blood:	n/a	n/a
7	CEBPB	chr9:86238767-86239165	K562	blood:	n/a	n/a
8	CEBPB	chr9:86237766-86238283	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr9:86237819-86237963	HepG2	liver:	n/a	n/a
10	CEBPB	chr9:86238262-86238454	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr9:86237789-86237994	A549	lung:	n/a	n/a
12	CEBPD	chr9:86237597-86238227	HepG2	liver:	n/a	n/a
13	CHD1	chr9:86237495-86239059	GM12878	blood:	n/a	n/a
14	CHD1	chr9:86238062-86238251	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr9:86238464-86238909	HepG2	liver:	n/a	n/a
16	CHD2	chr9:86238930-86238931	GM12878	blood:	n/a	n/a
17	CHD2	chr9:86237489-86238150	GM12878	blood:	n/a	n/a
18	CHD2	chr9:86238403-86238581	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr9:86237936-86237937	K562	blood:	n/a	n/a
20	CHD2	chr9:86238471-86238690	K562	blood:	n/a	n/a
21	CHD2	chr9:86237779-86238893	Hela-S3	cervix:	n/a	n/a
22	CHD2	chr9:86238024-86238216	HepG2	liver:	n/a	n/a
23	CREB1	chr9:86237841-86238422	H1-hESC	embryonic stem cell:	n/a	n/a
24	CREB1	chr9:86237843-86238338	K562	blood:	n/a	n/a
25	CREB1	chr9:86237669-86238222	A549	lung:	n/a	n/a
26	CREB1	chr9:86237874-86238256	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTBP2	chr9:86237678-86238518	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr9:86238480-86238630	GM12872	blood:	n/a	n/a
29	CTCF	chr9:86237660-86237810	HepG2	liver:	n/a	n/a
30	CTCF	chr9:86237717-86237831	GM10266	blood:	n/a	n/a
31	CTCF	chr9:86237732-86237998	GM12878	blood:	n/a	n/a
32	CTCF	chr9:86238466-86238561	GM19238	blood:	n/a	n/a
33	CTCF	chr9:86237660-86237810	AG10803	skin:	n/a	n/a
34	CTCF	chr9:86238468-86238567	MCF-7	breast:	n/a	n/a
35	CTCF	chr9:86238440-86238590	GM12874	blood:	n/a	n/a
36	CTCF	chr9:86237720-86237870	HMEC	breast:	n/a	n/a
37	CTCF	chr9:86238520-86238670	HRE	kidney:	n/a	n/a
38	CTCF	chr9:86238420-86238570	GM12875	blood:	n/a	n/a
39	CTCF	chr9:86238480-86238630	AG04449	skin:	n/a	n/a
40	CTCF	chr9:86238420-86238570	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr9:86238469-86238509	GM19239	blood:	n/a	n/a
42	CTCF	chr9:86238875-86238940	K562	blood:	n/a	n/a
43	CTCF	chr9:86238080-86238230	GM12864	blood:	n/a	chr9:86238143-86238156
44	CTCF	chr9:86238475-86238575	GM12891	blood:	n/a	n/a
45	CTCF	chr9:86238360-86238510	GM12866	blood:	n/a	n/a
46	CTCF	chr9:86237460-86237610	AG04449	skin:	n/a	n/a
47	CTCF	chr9:86238554-86238557	GM19240	blood:	n/a	n/a
48	CTCF	chr9:86238300-86238450	GM12865	blood:	n/a	n/a
49	CTCF	chr9:86237700-86237850	GM12865	blood:	n/a	n/a
50	CTCF	chr9:86238420-86238570	AG04449	skin:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:86238119-86238169	HCF	heart:	n/a
2	chr9:86238119-86238169	HCF	heart:	n/a
3	chr9:86238119-86238169	HRE	kidney:	n/a
4	chr9:86237793-86237843	AG04449	skin:	fetal
5	chr9:86238535-86238585	BJ	skin:	n/a
6	chr9:86237793-86237843	HL-60	blood:	n/a
7	chr9:86238119-86238169	HAEpiC	amniotic membrane:	n/a
8	chr9:86238535-86238585	Caco-2	colon:	n/a
9	chr9:86237590-86237640	AG09309	skin:	n/a
10	chr9:86237590-86237640	PrEC	prostate:	n/a
11	chr9:86237590-86237640	RPTEC	kidney:	n/a
12	chr9:86238119-86238169	H1-hESC	embryonic stem cell:	embryo
13	chr9:86237590-86237640	HIPEpiC	eye:	n/a
14	chr9:86237793-86237843	HNPCEpiC	eye:	n/a
15	chr9:86238535-86238585	HAEpiC	amniotic membrane:	n/a
16	chr9:86238119-86238169	HEK293	kidney:	embryo
17	chr9:86237793-86237843	IMR90	lung:	fetal
18	chr9:86237590-86237640	HMEC	breast:	n/a
19	chr9:86238119-86238169	A549	lung:	n/a
20	chr9:86238535-86238585	Hepatocyte	liver:	n/a
21	chr9:86238535-86238585	SAEC	small airway:	n/a
22	chr9:86237590-86237640	MCF-7	breast:	n/a
23	chr9:86238119-86238169	PANC-1	pancreas:	n/a
24	chr9:86238535-86238585	PANC-1	pancreas:	n/a
25	chr9:86238535-86238585	HNPCEpiC	eye:	n/a
26	chr9:86237590-86237640	GM06990	blood:	n/a
27	chr9:86238119-86238169	GM12891	blood:	n/a
28	chr9:86237590-86237640	HCPEpiC	choroid plexus:	n/a
29	chr9:86237793-86237843	T-47D	breast:	n/a
30	chr9:86237793-86237843	SK-N-MC	brain:	n/a
31	chr9:86238535-86238585	HCM	heart:	n/a
32	chr9:86237590-86237640	ECC-1	luminal epithelium:	n/a
33	chr9:86237793-86237843	SKMC	muscle:	n/a
34	chr9:86237590-86237640	K562	blood:	n/a
35	chr9:86237793-86237843	HUVEC	blood vessel:	n/a
36	chr9:86237793-86237843	GM06990	blood:	n/a
37	chr9:86238119-86238169	NT2-D1	testis:	n/a
38	chr9:86238535-86238585	Hela-S3	cervix:	n/a
39	chr9:86237793-86237843	AG09309	skin:	n/a
40	chr9:86238535-86238585	Jurkat	blood:	n/a
41	chr9:86238535-86238585	AG09319	gingival:	n/a
42	chr9:86238535-86238585	MCF10A-Er-Src	breast:	n/a
43	chr9:86237590-86237640	SK-N-SH_RA	brain:	n/a
44	chr9:86237590-86237640	SK-N-MC	brain:	n/a
45	chr9:86238119-86238169	HCM	heart:	n/a
46	chr9:86238535-86238585	AoSMC	blood vessel:	n/a
47	chr9:86238119-86238169	HPAEpiC	pulmonary alveolar:	n/a
48	chr9:86238535-86238585	H1-hESC	embryonic stem cell:	embryo
49	chr9:86237793-86237843	PrEC	prostate:	n/a
50	chr9:86237590-86237640	BJ	skin:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:151712214..151713783-chr9:86237532..86239422,2	MCF-7	breast:
2	chr9:86236280..86241962-chr9:86320992..86325340,9	MCF-7	breast:
3	chr9:86237033..86239481-chr9:86571525..86573399,2	MCF-7	breast:
4	chr9:86235893..86237501-chr9:86238448..86240518,2	MCF-7	breast:
5	chr9:86234634..86237562-chr9:86262513..86264120,2	MCF-7	breast:
6	chr9:86238599..86242233-chr9:86242446..86245459,4	K562	blood:
7	chr9:86236616..86242493-chr9:86533666..86537484,7	MCF-7	breast:
8	chr6:75994626..75995177-chr9:86238029..86238568,2	Hela-S3	cervix:
9	chr9:86235893..86237501-chr9:86238448..86240518,2	MCF-7	breast:
10	chr9:86236918..86239524-chr9:86322198..86323756,2	K562	blood:
11	chr16:73080234..73082394-chr9:86236447..86238062,2	MCF-7	breast:
12	chr9:86153786..86156686-chr9:86238312..86239923,2	MCF-7	breast:
13	chr9:86237271..86239294-chr9:86534482..86537409,3	MCF-7	breast:
14	chr9:86237285..86238795-chr9:86535469..86537545,2	K562	blood:

No data

Variant related genes	Relation type
IDNK	TF binding region
IDNK	CpG island
ENSG00000165118	chromatin interactions
ENSG00000140836	chromatin interactions
ENSG00000112697	chromatin interactions
ENSG00000135018	chromatin interactions
ENSG00000165115	chromatin interactions
ENSG00000225793	chromatin interactions
ENSG00000254473	chromatin interactions
ENSG00000181472	chromatin interactions

Extended variants
information (count: 86 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:86 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553306245	chr9:86237008-86237009	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs559227987	chr9:86237009-86237010	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs533037184	chr9:86237032-86237033	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs566668427	chr9:86237046-86237047	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs182294265	chr9:86237056-86237057	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs557792387	chr9:86237110-86237111	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs146646742	chr9:86237132-86237133	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs376091674	chr9:86237137-86237138	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs186705308	chr9:86237174-86237175	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs550078247	chr9:86237189-86237190	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs10118651	chr9:86237198-86237199	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs535485406	chr9:86237216-86237217	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs143419603	chr9:86237237-86237238	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs566083924	chr9:86237240-86237241	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs539910173	chr9:86237306-86237307	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs554745230	chr9:86237359-86237360	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs557698594	chr9:86237405-86237406	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs576328445	chr9:86237411-86237412	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs574848554	chr9:86237444-86237445	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs537165975	chr9:86237621-86237622	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs189604588	chr9:86237635-86237636	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs147983356	chr9:86237687-86237688	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs573977228	chr9:86237703-86237704	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs111705935	chr9:86237730-86237731	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs540456906	chr9:86237837-86237838	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs72138468	chr9:86237896-86237897	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs34621288	chr9:86237903-86237904	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs560110573	chr9:86237917-86237918	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs148724222	chr9:86237951-86237952	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs367733214	chr9:86238025-86238026	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs563011090	chr9:86238041-86238042	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs116949863	chr9:86238047-86238048	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs543564853	chr9:86238053-86238054	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs562092273	chr9:86238067-86238068	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs529584491	chr9:86238084-86238085	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs2811903	chr9:86238086-86238087	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs566045982	chr9:86238097-86238098	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs533148684	chr9:86238124-86238125	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs369212033	chr9:86238160-86238161	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs570114655	chr9:86238216-86238217	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs537287042	chr9:86238239-86238240	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs76971639	chr9:86238251-86238252	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs377764359	chr9:86238256-86238257	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs150119668	chr9:86238271-86238272	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs373239324	chr9:86238329-86238330	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs377312150	chr9:86238352-86238353	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs138804746	chr9:86238432-86238433	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs552964194	chr9:86238460-86238461	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs577582029	chr9:86238615-86238616	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs544639350	chr9:86238660-86238661	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Urothelial cell carcinoma	18451213	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Renal cell carcinoma	18765545	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD

Chromatin state (count:569 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:86216200-86237400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:86235600-86237400	Enhancers	Fetal Intestine Large	intestine
3	chr9:86235600-86237400	Enhancers	Fetal Intestine Small	intestine
4	chr9:86235600-86237400	Enhancers	Fetal Thymus	thymus
5	chr9:86235800-86237400	Enhancers	Thymus	Thymus
6	chr9:86236200-86237200	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr9:86236200-86237200	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr9:86236200-86237200	Weak transcription	Primary B cells from peripheral blood	blood
9	chr9:86236200-86237200	Weak transcription	Primary hematopoietic stem cells	blood
10	chr9:86236200-86237200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr9:86236200-86237200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr9:86236200-86237200	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr9:86236200-86237200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr9:86236200-86237200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr9:86236200-86237200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr9:86236200-86237200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr9:86236200-86237200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr9:86236200-86237200	Weak transcription	GM12878-XiMat	blood
19	chr9:86236200-86237200	Weak transcription	Monocytes-CD14+_RO01746	blood
20	chr9:86236200-86237200	Weak transcription	Osteobl	bone
21	chr9:86236200-86237400	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr9:86236200-86237400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr9:86236200-86237400	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr9:86236200-86237400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr9:86236200-86237400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr9:86236200-86237400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr9:86236200-86237400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr9:86236200-86237400	Weak transcription	Primary monocytes fromperipheralblood	blood
29	chr9:86236200-86237400	Weak transcription	Primary T cells from cord blood	blood
30	chr9:86236200-86237400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr9:86236200-86237400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr9:86236200-86237400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr9:86236200-86237400	Weak transcription	Adipose Nuclei	Adipose
34	chr9:86236200-86237400	Weak transcription	Brain Anterior Caudate	brain
35	chr9:86236200-86237400	Weak transcription	Brain Cingulate Gyrus	brain
36	chr9:86236200-86237400	Weak transcription	Colonic Mucosa	Colon
37	chr9:86236200-86237400	Weak transcription	Esophagus	oesophagus
38	chr9:86236200-86237400	Weak transcription	Fetal Heart	heart
39	chr9:86236200-86237400	Weak transcription	Left Ventricle	heart
40	chr9:86236200-86237400	Weak transcription	Pancreas	Pancrea
41	chr9:86236200-86237400	Weak transcription	Rectal Smooth Muscle	rectum
42	chr9:86236200-86237400	Weak transcription	Right Atrium	heart
43	chr9:86236200-86237400	Weak transcription	Skeletal Muscle Male	skeletal muscle
44	chr9:86236200-86237400	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr9:86236200-86237400	Enhancers	Stomach Mucosa	stomach
46	chr9:86236200-86237400	Weak transcription	Spleen	Spleen
47	chr9:86236200-86237400	Weak transcription	K562	blood
48	chr9:86236200-86237400	Weak transcription	NHLF	lung
49	chr9:86236200-86237600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr9:86236200-86237600	Weak transcription	Cortex derived primary cultured neurospheres	brain

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