Variant report

Variant	nsv894143
Chromosome Location	chr9:136874066-136906752
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:927)
CpG islands
(count:915)
Chromatin interactive
region (count:45)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:927 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:136890416-136890552	K562	blood:	n/a	n/a
2	ARID3A	chr9:136889805-136890105	K562	blood:	n/a	n/a
3	ARID3A	chr9:136876031-136876182	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:136890361-136890664	HepG2	liver:	n/a	n/a
5	ATF2	chr9:136890271-136890720	GM12878	blood:	n/a	n/a
6	ATF2	chr9:136890042-136890385	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr9:136890447-136890733	K562	blood:	n/a	chr9:136890464-136890473
8	ATF3	chr9:136890308-136890719	A549	lung:	n/a	chr9:136890464-136890473
9	ATF3	chr9:136885323-136885812	HCT-116	colon:	n/a	n/a
10	ATF3	chr9:136890380-136890723	A549	lung:	n/a	chr9:136890464-136890473
11	BCL11A	chr9:136879082-136879526	GM12878	blood:	n/a	n/a
12	BCL11A	chr9:136879263-136879437	GM12878	blood:	n/a	n/a
13	BCL3	chr9:136885430-136885587	GM12878	blood:	n/a	n/a
14	BCLAF1	chr9:136890309-136890720	GM12878	blood:	n/a	n/a
15	BHLHE40	chr9:136890947-136891211	GM12878	blood:	n/a	n/a
16	BHLHE40	chr9:136890357-136891137	K562	blood:	n/a	n/a
17	BHLHE40	chr9:136890128-136890704	GM12878	blood:	n/a	n/a
18	BRCA1	chr9:136889902-136890644	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr9:136879187-136879552	K562	blood:	n/a	n/a
20	CBX3	chr9:136879192-136879515	K562	blood:	n/a	n/a
21	CBX3	chr9:136890207-136890673	K562	blood:	n/a	n/a
22	CCNT2	chr9:136890317-136890723	K562	blood:	n/a	n/a
23	CCNT2	chr9:136894475-136894494	K562	blood:	n/a	n/a
24	CEBPB	chr9:136895005-136895272	HepG2	liver:	n/a	chr9:136895110-136895121
25	CEBPB	chr9:136885485-136885560	K562	blood:	n/a	chr9:136885519-136885530
26	CEBPB	chr9:136895034-136895244	Hela-S3	cervix:	n/a	chr9:136895110-136895121
27	CEBPB	chr9:136885363-136885707	IMR90	lung:	n/a	chr9:136885519-136885530
28	CEBPB	chr9:136886770-136886790	K562	blood:	n/a	n/a
29	CEBPB	chr9:136893926-136893986	HepG2	liver:	n/a	n/a
30	CEBPB	chr9:136885365-136885672	HepG2	liver:	n/a	chr9:136885519-136885530
31	CEBPB	chr9:136895074-136895254	K562	blood:	n/a	chr9:136895110-136895121
32	CEBPB	chr9:136885358-136885685	Hela-S3	cervix:	n/a	chr9:136885519-136885530
33	CEBPB	chr9:136885427-136885670	MCF-7	breast:	n/a	chr9:136885519-136885530
34	CEBPB	chr9:136895034-136895259	IMR90	lung:	n/a	chr9:136895110-136895121
35	CEBPB	chr9:136890374-136890636	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr9:136885367-136885880	HCT-116	colon:	n/a	chr9:136885519-136885530
37	CEBPB	chr9:136899189-136899274	HepG2	liver:	n/a	n/a
38	CEBPB	chr9:136899119-136899301	A549	lung:	n/a	n/a
39	CEBPB	chr9:136885378-136885732	HCT-116	colon:	n/a	chr9:136885519-136885530
40	CEBPD	chr9:136890072-136890740	HepG2	liver:	n/a	n/a
41	CEBPD	chr9:136890298-136890625	HepG2	liver:	n/a	n/a
42	CHD1	chr9:136890836-136891106	GM12878	blood:	n/a	n/a
43	CHD2	chr9:136890890-136891207	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr9:136889926-136890675	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr9:136890124-136890658	K562	blood:	n/a	n/a
46	CHD2	chr9:136890152-136890646	HepG2	liver:	n/a	n/a
47	CHD2	chr9:136889986-136890724	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr9:136889973-136890692	GM12878	blood:	n/a	n/a
49	CREB1	chr9:136890081-136890863	K562	blood:	n/a	n/a
50	CREB1	chr9:136890071-136890755	H1-hESC	embryonic stem cell:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:136876905-136876955	SK-N-SH	brain:	n/a
2	chr9:136876366-136876416	GM12891	blood:	n/a
3	chr9:136891212-136891262	SK-N-MC	brain:	n/a
4	chr9:136891620-136891670	HPAEpiC	pulmonary alveolar:	n/a
5	chr9:136897185-136897235	SAEC	small airway:	n/a
6	chr9:136890948-136890998	HRPEpiC	eye:	n/a
7	chr9:136891212-136891262	HIPEpiC	eye:	n/a
8	chr9:136891620-136891670	BE2_C	brain:	n/a
9	chr9:136890014-136890064	PrEC	prostate:	n/a
10	chr9:136890014-136890064	Caco-2	colon:	n/a
11	chr9:136879298-136879348	H1-hESC	embryonic stem cell:	embryo
12	chr9:136879298-136879348	A549	lung:	n/a
13	chr9:136891620-136891670	GM06990	blood:	n/a
14	chr9:136877010-136877060	ECC-1	luminal epithelium:	n/a
15	chr9:136891620-136891670	AG09309	skin:	n/a
16	chr9:136876905-136876955	HCF	heart:	n/a
17	chr9:136891620-136891670	NB4	blood:	n/a
18	chr9:136890948-136890998	IMR90	lung:	fetal
19	chr9:136897185-136897235	SK-N-MC	brain:	n/a
20	chr9:136889061-136889111	HCPEpiC	choroid plexus:	n/a
21	chr9:136882828-136882878	PANC-1	pancreas:	n/a
22	chr9:136890948-136890998	AG04449	skin:	fetal
23	chr9:136889061-136889111	HAEpiC	amniotic membrane:	n/a
24	chr9:136876366-136876416	Hepatocyte	liver:	n/a
25	chr9:136879298-136879348	Hela-S3	cervix:	n/a
26	chr9:136882828-136882878	NH-A	brain:	n/a
27	chr9:136890948-136890998	Caco-2	colon:	n/a
28	chr9:136891620-136891670	GM12891	blood:	n/a
29	chr9:136876366-136876416	Hela-S3	cervix:	n/a
30	chr9:136876905-136876955	HL-60	blood:	n/a
31	chr9:136877010-136877060	Hepatocyte	liver:	n/a
32	chr9:136876905-136876955	ECC-1	luminal epithelium:	n/a
33	chr9:136882828-136882878	AoSMC	blood vessel:	n/a
34	chr9:136879746-136879796	HCF	heart:	n/a
35	chr9:136879746-136879796	AG09319	gingival:	n/a
36	chr9:136889061-136889111	Hela-S3	cervix:	n/a
37	chr9:136891212-136891262	A549	lung:	n/a
38	chr9:136897185-136897235	HCF	heart:	n/a
39	chr9:136879746-136879796	U87	brain:	n/a
40	chr9:136890014-136890064	HRE	kidney:	n/a
41	chr9:136898139-136898189	SAEC	small airway:	n/a
42	chr9:136877010-136877060	GM12892	blood:	n/a
43	chr9:136877010-136877060	HEEpiC	esophagus:	n/a
44	chr9:136889061-136889111	HEK293	kidney:	embryo
45	chr9:136890014-136890064	HEEpiC	esophagus:	n/a
46	chr9:136882828-136882878	AG10803	skin:	n/a
47	chr9:136876366-136876416	NHBE	bronchial:	n/a
48	chr9:136876366-136876416	PANC-1	pancreas:	n/a
49	chr9:136876366-136876416	ECC-1	luminal epithelium:	n/a
50	chr9:136897185-136897235	IMR90	lung:	fetal

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:136904204..136906541-chr9:136912804..136914805,2	MCF-7	breast:
2	chr9:136856335..136860882-chr9:136888369..136892368,8	MCF-7	breast:
3	chr9:136894584..136896138-chr9:136898590..136900782,2	MCF-7	breast:
4	chr9:136866726..136869330-chr9:136873056..136875890,3	MCF-7	breast:
5	chr9:136894545..136896842-chr9:136932305..136933888,2	K562	blood:
6	chr9:136905256..136906897-chr9:136914538..136916500,2	K562	blood:
7	chr9:136890645..136892420-chr9:136892471..136894163,2	K562	blood:
8	chr9:136890470..136892525-chr9:136914394..136917333,2	K562	blood:
9	chr9:136890645..136892420-chr9:136892471..136894163,2	K562	blood:
10	chr9:136888954..136894255-chr9:136931474..136935040,9	K562	blood:
11	chr9:136890090..136893385-chr9:136896775..136900887,5	MCF-7	breast:
12	chr9:136895614..136897554-chr9:136931662..136933717,2	MCF-7	breast:
13	chr9:136857193..136859735-chr9:136888278..136891342,4	MCF-7	breast:
14	chr9:136894979..136900303-chr9:136903239..136907725,5	K562	blood:
15	chr9:136896455..136899327-chr9:136905044..136906848,2	MCF-7	breast:
16	chr9:136904571..136907466-chr9:136931191..136933515,2	MCF-7	breast:
17	chr9:136896455..136899327-chr9:136905044..136906848,2	MCF-7	breast:
18	chr9:136873407..136875793-chr9:136883186..136885281,2	MCF-7	breast:
19	chr9:136890629..136892958-chr9:136894290..136896400,3	K562	blood:
20	chr9:136889377..136892336-chr9:136904315..136908613,4	MCF-7	breast:
21	chr9:136904281..136909955-chr9:136916883..136922324,6	MCF-7	breast:
22	chr9:136888792..136891646-chr9:137000403..137003499,3	MCF-7	breast:
23	chr9:136889586..136891747-chr9:136893297..136895999,4	MCF-7	breast:
24	chr9:136895812..136897521-chr9:136897928..136899960,3	MCF-7	breast:
25	chr9:136895551..136897428-chr9:136900118..136902185,2	MCF-7	breast:
26	chr9:136888457..136893834-chr9:136930854..136936517,11	MCF-7	breast:
27	chr9:136889327..136891768-chr9:136933108..136935436,5	MCF-7	breast:
28	chr9:136891192..136895857-chr9:136919376..136921931,6	MCF-7	breast:
29	chr9:136898945..136901283-chr9:136905250..136907083,2	K562	blood:
30	chr9:136895812..136897521-chr9:136897928..136899960,3	MCF-7	breast:
31	chr9:136900423..136902351-chr9:136931412..136933439,2	K562	blood:
32	chr9:136889586..136891747-chr9:136893297..136895999,4	MCF-7	breast:
33	chr9:136889870..136892902-chr9:136892951..136894891,4	MCF-7	breast:
34	chr9:136894584..136896138-chr9:136898590..136900782,2	MCF-7	breast:
35	chr9:136889824..136891845-chr9:137000522..137002324,2	K562	blood:
36	chr9:136904109..136906442-chr9:136930032..136931682,2	K562	blood:
37	chr9:136888985..136892489-chr9:136929943..136933995,5	K562	blood:
38	chr9:136889381..136892384-chr9:136898086..136899845,3	K562	blood:
39	chr9:136873407..136875793-chr9:136883186..136885281,2	MCF-7	breast:
40	chr9:136903179..136904744-chr9:136926419..136927992,2	MCF-7	breast:
41	chr9:136894029..136896298-chr9:136914063..136916323,3	MCF-7	breast:
42	chr9:136890636..136894416-chr9:136894536..136898108,4	K562	blood:
43	chr9:136889377..136892336-chr9:136904315..136908613,4	MCF-7	breast:
44	chr9:136889870..136892902-chr9:136892951..136894891,4	MCF-7	breast:
45	chr9:136895551..136897428-chr9:136900118..136902185,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VAV2-1	chr9:136895487-136897308	NONHSAT135365
2	lnc-WDR5-3	chr9:136890608-136890658	ENSG00000235106
3	lnc-WDR5-3	chr9:136891330-136891671	NONHSAT135349
4	lnc-WDR5-3	chr9:136890967-136891212	ENSG00000235106
5	lnc-WDR5-3	chr9:136896903-136897282	NONHSAT135363
6	lnc-WDR5-3	chr9:136890967-136891212	NONHSAT135349
7	lnc-WDR5-3	chr9:136893948-136894637	ENSG00000235106
8	lnc-WDR5-3	chr9:136894161-136894237	ENSG00000235106.4
9	lnc-WDR5-3	chr9:136891330-136891671	ENSG00000235106
10	lnc-WDR5-3	chr9:136892273-136892384	ENSG00000235106
11	lnc-WDR5-3	chr9:136894083-136894237	NONHSAT135363
12	lnc-WDR5-3	chr9:136899634-136899788	ENSG00000235106.4
13	lnc-WDR5-3	chr9:136893948-136894376	ENSG00000235106
14	lnc-WDR5-3	chr9:136893893-136895581	ENSG00000235106.4
15	lnc-WDR5-3	chr9:136893948-136895445	NONHSAT135349
16	lnc-WDR5-3	chr9:136890561-136890658	NONHSAT135349

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	BRD3	hsa-miR-192-5p	chr9:136898561-136898555
2	BRD3	hsa-miR-192-5p	chr9:136898555-136898575
3	BRD3	hsa-miR-141-3p	chr9:136898594-136898587
4	BRD3	hsa-miR-141-3p	chr9:136898588-136898606

Variant related genes	Relation type
LINC00094	TF binding region
LINC00094	CpG island
ENSG00000235138	chromatin interactions
ENSG00000169925	chromatin interactions
ENSG00000196363	chromatin interactions
ENSG00000235106	chromatin interactions
ENSG00000273249	chromatin interactions
ENSG00000160293	chromatin interactions
CSE1L	miRNA target sites
OTUD1	miRNA target sites
CCND2	miRNA target sites
MRPL19	miRNA target sites
PRKAA1	miRNA target sites
TH1L	miRNA target sites

Extended variants
information (count: 1747 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1747 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17664384	chr9:136874066-136874067	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs554949573	chr9:136874067-136874068	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs553586376	chr9:136874092-136874093	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs565825058	chr9:136874134-136874135	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs539245247	chr9:136874141-136874142	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs557979156	chr9:136874143-136874144	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs464930	chr9:136874158-136874159	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs565969778	chr9:136874187-136874188	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs556561248	chr9:136874205-136874206	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs565969996	chr9:136874273-136874274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs574889999	chr9:136874284-136874285	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs79314038	chr9:136874285-136874286	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs534222950	chr9:136874294-136874295	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs55912976	chr9:136874338-136874339	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs55829426	chr9:136874341-136874342	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs371928781	chr9:136874352-136874353	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs181526056	chr9:136874368-136874369	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs7037625	chr9:136874378-136874379	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs187566967	chr9:136874403-136874404	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs567670346	chr9:136874433-136874434	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs116276469	chr9:136874521-136874522	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547408049	chr9:136874550-136874551	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs565631715	chr9:136874585-136874586	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs140937525	chr9:136874608-136874609	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs557967654	chr9:136874609-136874610	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs199789173	chr9:136874613-136874614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs541847630	chr9:136874614-136874615	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs150193054	chr9:136874619-136874620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs555710058	chr9:136874626-136874627	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs571993917	chr9:136874670-136874671	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574026449	chr9:136874714-136874715	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs138849231	chr9:136874749-136874750	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs554166112	chr9:136874754-136874755	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs572435163	chr9:136874765-136874766	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs546297586	chr9:136874802-136874803	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs10993890	chr9:136874855-136874856	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs373679192	chr9:136874858-136874859	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs374639573	chr9:136874878-136874879	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs377601445	chr9:136874885-136874886	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs201727459	chr9:136874889-136874890	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs199920162	chr9:136874890-136874891	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs537707567	chr9:136874891-136874892	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs398087608	chr9:136874900-136874901	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs398012536	chr9:136874901-136874902	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs527537682	chr9:136874913-136874914	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs190729989	chr9:136874914-136874915	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs529636916	chr9:136874915-136874916	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541344716	chr9:136874991-136874992	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547055659	chr9:136875055-136875056	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs559333566	chr9:136875101-136875102	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Oral squamous cell carcinoma	17134496	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
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	18632612	CNVD
Cardiac fibroma	18329553	CNVD
Lung cancer	19147751	CNVD
Melanoma	18172304	CNVD
Cervical cancer	16585170	CNVD
Ependymoma	19289631	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Cervical cancer	17311676	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Chordoma	18071362	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Kleefstra Syndrome	21538692	CNVD
Disorders of sex development	22290220	CNVD
Cancer	21183584	CNVD
Chronic myelomonocytic leukemia	16760666	CNVD
Abnormal phenotypes	18644119	CNVD
Ovarian cancer	21720365	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Sudden cardiac death	19188705	CNVD
Myoepithelioma	18604193	CNVD
Tuberous sclerosis	19566914	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21364760	CNVD
Cancer	20581869	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Hepatocellular carcinoma	22174799	CNVD
Bladder cancer	21909424	CNVD
Cancer	17160897	CNVD
Ependymoma	20639864	CNVD
Breast cancer	20932292	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Idiopathic chronic pancreatitis	21572526	CNVD
Kleefstra syndrome	22670141	CNVD
Schizophrenia	22241247	CNVD
9q deletion syndrome	16826528	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Non-small cell lung cancer	21829676	CNVD
Non-syndromic sensorineural hearing loss	19293338	CNVD
Neurodevelopmental disorder	22521361	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:1029 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:136859600-136875400	Weak transcription	Spleen	Spleen
2	chr9:136871800-136877000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr9:136872000-136876800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr9:136872800-136875200	Weak transcription	HSMMtube	muscle
5	chr9:136873000-136876800	Enhancers	Fetal Muscle Trunk	muscle
6	chr9:136874000-136874200	Bivalent Enhancer	Fetal Muscle Leg	muscle
7	chr9:136874200-136876800	Enhancers	Fetal Muscle Leg	muscle
8	chr9:136874400-136874600	Enhancers	HepG2	liver
9	chr9:136874800-136875200	Weak transcription	HepG2	liver
10	chr9:136875200-136875800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
11	chr9:136875200-136875800	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
12	chr9:136875200-136875800	Enhancers	HepG2	liver
13	chr9:136875200-136876000	Enhancers	Placenta	Placenta
14	chr9:136875200-136876000	Enhancers	Psoas Muscle	Psoas
15	chr9:136875200-136876200	Enhancers	HSMMtube	muscle
16	chr9:136875200-136876400	Enhancers	Liver	Liver
17	chr9:136875400-136876200	Enhancers	Brain Hippocampus Middle	brain
18	chr9:136875400-136876200	Enhancers	Spleen	Spleen
19	chr9:136875400-136876400	Enhancers	Lung	lung
20	chr9:136875600-136876200	Enhancers	Fetal Brain Male	brain
21	chr9:136875600-136876400	Enhancers	Pancreas	Pancrea
22	chr9:136875600-136876800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
23	chr9:136875800-136876000	Enhancers	Brain Inferior Temporal Lobe	brain
24	chr9:136875800-136876000	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
25	chr9:136875800-136876200	Enhancers	Brain Anterior Caudate	brain
26	chr9:136875800-136876200	Enhancers	Brain Substantia Nigra	brain
27	chr9:136875800-136876200	Enhancers	Duodenum Mucosa	Duodenum
28	chr9:136875800-136876200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr9:136875800-136876200	Enhancers	Right Ventricle	heart
30	chr9:136875800-136876200	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
31	chr9:136875800-136876200	Flanking Active TSS	HepG2	liver
32	chr9:136875800-136876200	Enhancers	HUVEC	blood vessel
33	chr9:136875800-136876400	Enhancers	Fetal Heart	heart
34	chr9:136875800-136876600	Enhancers	Stomach Mucosa	stomach
35	chr9:136876000-136876200	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
36	chr9:136876000-136876200	Enhancers	Right Atrium	heart
37	chr9:136876000-136876200	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
38	chr9:136876200-136876400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
39	chr9:136876200-136876800	Enhancers	HepG2	liver
40	chr9:136876200-136889800	Weak transcription	Right Atrium	heart
41	chr9:136876600-136876800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr9:136876600-136876800	Enhancers	Brain Inferior Temporal Lobe	brain
43	chr9:136879800-136880000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
44	chr9:136879800-136880200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr9:136880600-136885600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr9:136884600-136889400	Weak transcription	Fetal Muscle Leg	muscle
47	chr9:136885600-136885800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr9:136885800-136890000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr9:136889200-136889600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr9:136889400-136889600	Enhancers	iPS-15b Cell Line	embryonic stem cell

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