Variant report

Variant	nsv892061
Chromosome Location	chr9:2229694-2262889
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:780)
CpG islands
(count:366)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:780 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:2241873-2242174	K562	blood:	n/a	n/a
2	ARID3A	chr9:2241752-2242185	HepG2	liver:	n/a	n/a
3	ATF2	chr9:2241813-2242242	GM12878	blood:	n/a	n/a
4	ATF2	chr9:2241499-2242598	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr9:2241795-2242260	GM12878	blood:	n/a	n/a
6	ATF2	chr9:2229291-2229713	GM12878	blood:	n/a	n/a
7	ATF2	chr9:2241526-2242216	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr9:2229314-2229763	GM12878	blood:	n/a	n/a
9	ATF3	chr9:2241780-2242300	A549	lung:	n/a	n/a
10	BACH1	chr9:2241631-2242354	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr9:2230017-2230285	GM12878	blood:	n/a	chr9:2230183-2230193 chr9:2230182-2230193
12	BCL11A	chr9:2241903-2242115	GM12878	blood:	n/a	n/a
13	BCL3	chr9:2241755-2242399	A549	lung:	n/a	n/a
14	BCL3	chr9:2241690-2242337	A549	lung:	n/a	n/a
15	BCLAF1	chr9:2241766-2242280	GM12878	blood:	n/a	n/a
16	BCLAF1	chr9:2241790-2242233	GM12878	blood:	n/a	n/a
17	BCLAF1	chr9:2229240-2229763	GM12878	blood:	n/a	chr9:2229561-2229570
18	BHLHE40	chr9:2241822-2242611	HepG2	liver:	n/a	n/a
19	BHLHE40	chr9:2241630-2242313	K562	blood:	n/a	n/a
20	BHLHE40	chr9:2241927-2242471	GM12878	blood:	n/a	n/a
21	BRCA1	chr9:2241818-2242305	H1-hESC	embryonic stem cell:	n/a	n/a
22	BRCA1	chr9:2242326-2242348	GM12878	blood:	n/a	n/a
23	CBX3	chr9:2260466-2261875	HCT-116	colon:	n/a	n/a
24	CBX3	chr9:2241820-2242161	K562	blood:	n/a	n/a
25	CBX3	chr9:2241713-2242381	HCT-116	colon:	n/a	n/a
26	CBX3	chr9:2241725-2242505	HCT-116	colon:	n/a	n/a
27	CBX3	chr9:2260461-2261583	HCT-116	colon:	n/a	n/a
28	CCNT2	chr9:2241616-2242096	K562	blood:	n/a	n/a
29	CEBPB	chr9:2260562-2261566	HCT-116	colon:	n/a	n/a
30	CEBPB	chr9:2244301-2244558	HepG2	liver:	n/a	chr9:2244415-2244426
31	CEBPB	chr9:2241906-2242117	GM12878	blood:	n/a	n/a
32	CEBPB	chr9:2241419-2242557	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr9:2244293-2244527	A549	lung:	n/a	chr9:2244415-2244426
34	CEBPB	chr9:2241880-2242260	A549	lung:	n/a	n/a
35	CEBPB	chr9:2241958-2242358	IMR90	lung:	n/a	n/a
36	CEBPB	chr9:2244398-2244576	H1-hESC	embryonic stem cell:	n/a	chr9:2244415-2244426
37	CEBPD	chr9:2241904-2242154	HepG2	liver:	n/a	n/a
38	CHD1	chr9:2241257-2241480	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD1	chr9:2241921-2242230	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr9:2241862-2242283	HepG2	liver:	n/a	n/a
41	CHD2	chr9:2241878-2242214	GM12878	blood:	n/a	n/a
42	CHD2	chr9:2241286-2242724	H1-hESC	embryonic stem cell:	n/a	chr9:2241605-2241612
43	CREB1	chr9:2241813-2242284	A549	lung:	n/a	n/a
44	CREB1	chr9:2241910-2242146	A549	lung:	n/a	n/a
45	CREB1	chr9:2241484-2242307	H1-hESC	embryonic stem cell:	n/a	n/a
46	CREB1	chr9:2241445-2242826	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTBP2	chr9:2241450-2242887	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr9:2241602-2242164	K562	blood:	n/a	chr9:2241689-2241698
49	CTCF	chr9:2241640-2241790	HRPEpiC	eye:	n/a	chr9:2241689-2241698
50	CTCF	chr9:2241620-2241770	HA-sp	spinal cord:	n/a	chr9:2241689-2241698

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:2234921-2234971	HNPCEpiC	eye:	n/a
2	chr9:2241892-2241942	AG09319	gingival:	n/a
3	chr9:2241688-2241738	SAEC	small airway:	n/a
4	chr9:2241688-2241738	ovcar-3	ovarian:	n/a
5	chr9:2241256-2241306	AG09319	gingival:	n/a
6	chr9:2241688-2241738	A549	lung:	n/a
7	chr9:2239671-2239721	HAEpiC	amniotic membrane:	n/a
8	chr9:2241892-2241942	HAEpiC	amniotic membrane:	n/a
9	chr9:2241256-2241306	NH-A	brain:	n/a
10	chr9:2242468-2242518	NT2-D1	testis:	n/a
11	chr9:2241688-2241738	HIPEpiC	eye:	n/a
12	chr9:2241688-2241738	HCT-116	colon:	n/a
13	chr9:2241688-2241738	PANC-1	pancreas:	n/a
14	chr9:2239671-2239721	CMK	blood:	n/a
15	chr9:2241256-2241306	ProgFib	skin:	n/a
16	chr9:2241892-2241942	NH-A	brain:	n/a
17	chr9:2241688-2241738	AG10803	skin:	n/a
18	chr9:2234921-2234971	HCPEpiC	choroid plexus:	n/a
19	chr9:2241688-2241738	AG09309	skin:	n/a
20	chr9:2241688-2241738	T-47D	breast:	n/a
21	chr9:2242468-2242518	HRCEpiC	kidney:	n/a
22	chr9:2241688-2241738	GM06990	blood:	n/a
23	chr9:2234921-2234971	HUVEC	blood vessel:	n/a
24	chr9:2239671-2239721	BE2_C	brain:	n/a
25	chr9:2242468-2242518	HEK293	kidney:	embryo
26	chr9:2241256-2241306	U87	brain:	n/a
27	chr9:2242468-2242518	PANC-1	pancreas:	n/a
28	chr9:2242468-2242518	HRE	kidney:	n/a
29	chr9:2241892-2241942	GM12892	blood:	n/a
30	chr9:2234921-2234971	AoSMC	blood vessel:	n/a
31	chr9:2241892-2241942	HUVEC	blood vessel:	n/a
32	chr9:2241256-2241306	SK-N-MC	brain:	n/a
33	chr9:2242468-2242518	ECC-1	luminal epithelium:	n/a
34	chr9:2239671-2239721	MCF-7	breast:	n/a
35	chr9:2242468-2242518	BJ	skin:	n/a
36	chr9:2241892-2241942	Caco-2	colon:	n/a
37	chr9:2234921-2234971	Hela-S3	cervix:	n/a
38	chr9:2242468-2242518	AG04450	lung:	fetal
39	chr9:2239671-2239721	HCPEpiC	choroid plexus:	n/a
40	chr9:2241892-2241942	AG04450	lung:	fetal
41	chr9:2242468-2242518	AG09309	skin:	n/a
42	chr9:2241892-2241942	NHDF-neo	bronchial:	n/a
43	chr9:2242468-2242518	AG10803	skin:	n/a
44	chr9:2241892-2241942	SAEC	small airway:	n/a
45	chr9:2241688-2241738	HUVEC	blood vessel:	n/a
46	chr9:2234921-2234971	HRCEpiC	kidney:	n/a
47	chr9:2239671-2239721	NB4	blood:	n/a
48	chr9:2241688-2241738	NH-A	brain:	n/a
49	chr9:2242468-2242518	HAEpiC	amniotic membrane:	n/a
50	chr9:2242468-2242518	GM12892	blood:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:2255030..2255773-chr9:2600478..2601011,2	MCF-7	breast:
2	chr9:2229879..2232148-chr9:2238435..2240178,2	K562	blood:
3	chr9:2257367..2260216-chr9:2810940..2813820,2	MCF-7	breast:
4	chr9:2229879..2232148-chr9:2238435..2240178,2	K562	blood:
5	chr9:2016060..2018467-chr9:2241276..2243249,2	K562	blood:
6	chr9:2242145..2244162-chr9:2246197..2248614,2	MCF-7	breast:
7	chr9:2232135..2233681-chr9:2242107..2243678,2	MCF-7	breast:
8	chr9:2217416..2220117-chr9:2231617..2233140,2	MCF-7	breast:
9	chr9:2256748..2259220-chr9:2292192..2293911,2	MCF-7	breast:
10	chr9:2229721..2232093-chr9:2241469..2243158,2	MCF-7	breast:
11	chr9:2231807..2233920-chr9:2241447..2243691,2	MCF-7	breast:
12	chr9:2243537..2246838-chr9:2247520..2250621,4	MCF-7	breast:
13	chr9:2231807..2233920-chr9:2241447..2243691,2	MCF-7	breast:
14	chr9:2243537..2246838-chr9:2247520..2250621,4	MCF-7	breast:
15	chr9:2240721..2243292-chr9:2621569..2623384,2	MCF-7	breast:
16	chr9:2229721..2232093-chr9:2241469..2243158,2	MCF-7	breast:
17	chr9:2242145..2244162-chr9:2246197..2248614,2	MCF-7	breast:
18	chr9:2232135..2233681-chr9:2242107..2243678,2	MCF-7	breast:
19	chr9:2226247..2228750-chr9:2234155..2236078,2	MCF-7	breast:
20	chr9:2244966..2246945-chr9:2263682..2266605,2	MCF-7	breast:

No data

Variant related genes	Relation type
RN7SL592P	TF binding region
RN7SL592P	CpG island
ENSG00000147852	chromatin interactions
ENSG00000236404	chromatin interactions
ENSG00000080503	chromatin interactions

Extended variants
information (count: 1892 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:1892 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4741655	chr9:2229694-2229695	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs10965292	chr9:2229703-2229704	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs148382223	chr9:2229757-2229758	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs533200885	chr9:2229761-2229762	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs540619537	chr9:2229765-2229766	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs528766924	chr9:2229766-2229767	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs373216111	chr9:2229783-2229784	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs528330293	chr9:2229807-2229808	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs377218745	chr9:2229811-2229812	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs183392701	chr9:2229826-2229827	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs369240621	chr9:2229849-2229850	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs567886301	chr9:2229864-2229865	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs530644857	chr9:2229896-2229897	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs550436822	chr9:2229945-2229946	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs570503488	chr9:2229964-2229965	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs74823122	chr9:2230000-2230001	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs1324209	chr9:2230003-2230004	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs186614247	chr9:2230046-2230047	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs10965294	chr9:2230049-2230050	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs371006831	chr9:2230053-2230054	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs373566861	chr9:2230063-2230064	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs556014425	chr9:2230064-2230065	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs575784188	chr9:2230068-2230069	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs72614070	chr9:2230072-2230073	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs558016269	chr9:2230143-2230144	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs578042855	chr9:2230149-2230150	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs540242704	chr9:2230157-2230158	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs117005202	chr9:2230161-2230162	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs117398631	chr9:2230166-2230167	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs541685553	chr9:2230182-2230183	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs537470866	chr9:2230190-2230191	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs377203982	chr9:2230214-2230215	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs189883650	chr9:2230231-2230232	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs554112394	chr9:2230306-2230307	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs13285858	chr9:2230334-2230335	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs570491943	chr9:2230360-2230361	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs533826381	chr9:2230391-2230392	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs115757523	chr9:2230397-2230398	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs566444319	chr9:2230421-2230422	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs373083302	chr9:2230437-2230438	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs182518303	chr9:2230440-2230441	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs141496369	chr9:2230458-2230459	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs553983496	chr9:2230474-2230475	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs538096950	chr9:2230475-2230476	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs558290638	chr9:2230477-2230478	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs578035827	chr9:2230483-2230484	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs534001992	chr9:2230543-2230544	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs553765393	chr9:2230560-2230561	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs576952218	chr9:2230570-2230571	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs146366866	chr9:2230600-2230601	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Gastric cancer	16715143	CNVD
Glioblastoma multiforme	22286061	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Disorders of sex development	21048976	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	21373258	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:869 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:2223600-2240800	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr9:2227400-2234400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr9:2227800-2230200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr9:2227800-2231400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr9:2227800-2231600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr9:2227800-2231600	Weak transcription	Ovary	ovary
7	chr9:2227800-2234400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr9:2228000-2229800	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr9:2228000-2231000	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr9:2228000-2231200	Weak transcription	Osteobl	bone
11	chr9:2228000-2231400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr9:2228000-2234600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr9:2228200-2229800	Enhancers	HMEC	breast
14	chr9:2228200-2230400	Enhancers	Primary B cells from peripheral blood	blood
15	chr9:2228400-2229800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr9:2228400-2229800	Enhancers	HepG2	liver
17	chr9:2228400-2230000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr9:2228400-2230000	Enhancers	Primary hematopoietic stem cells	blood
19	chr9:2228400-2230000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr9:2228400-2230000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
21	chr9:2228400-2230200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr9:2228400-2230200	Enhancers	Stomach Mucosa	stomach
23	chr9:2228800-2230400	Enhancers	Placenta Amnion	Placenta Amnion
24	chr9:2228800-2234200	Weak transcription	NHEK	skin
25	chr9:2229000-2230800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr9:2229200-2229800	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr9:2229200-2229800	Enhancers	HSMMtube	muscle
28	chr9:2229200-2230000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr9:2229200-2230200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr9:2229200-2230200	Enhancers	Fetal Heart	heart
31	chr9:2229200-2230400	Flanking Active TSS	GM12878-XiMat	blood
32	chr9:2229200-2230800	Weak transcription	Spleen	Spleen
33	chr9:2229400-2229800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr9:2229400-2230000	Weak transcription	Right Ventricle	heart
35	chr9:2229400-2230200	Enhancers	Primary neutrophils fromperipheralblood	blood
36	chr9:2229400-2231000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr9:2229400-2234400	Weak transcription	Placenta	Placenta
38	chr9:2229600-2229800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr9:2229600-2230000	Weak transcription	Right Atrium	heart
40	chr9:2229600-2230200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr9:2229600-2230200	Enhancers	Primary B cells from cord blood	blood
42	chr9:2229600-2230800	Weak transcription	Fetal Muscle Leg	muscle
43	chr9:2229800-2230000	Enhancers	Duodenum Mucosa	Duodenum
44	chr9:2229800-2230800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
45	chr9:2229800-2231600	Weak transcription	HSMM	muscle
46	chr9:2229800-2231600	Weak transcription	HSMMtube	muscle
47	chr9:2229800-2233800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr9:2229800-2234200	Weak transcription	HMEC	breast
49	chr9:2230000-2230200	Enhancers	Right Atrium	heart
50	chr9:2230000-2230200	Enhancers	Right Ventricle	heart

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