Variant report

Variant	nsv893570
Chromosome Location	chr9:93973938-94148084
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1597)
CpG islands
(count:549)
Chromatin interactive
region (count:159)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:1597 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:93974406-93974698	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:93996841-93997111	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:93973638-93974128	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:94008233-94008558	K562	blood:	n/a	n/a
5	ARID3A	chr9:94124059-94124074	HepG2	liver:	n/a	n/a
6	ATF1	chr9:94036501-94036819	K562	blood:	n/a	n/a
7	ATF2	chr9:94121297-94121788	GM12878	blood:	n/a	n/a
8	ATF2	chr9:94069451-94069865	GM12878	blood:	n/a	n/a
9	ATF2	chr9:94069503-94069923	GM12878	blood:	n/a	n/a
10	ATF3	chr9:94123991-94124282	K562	blood:	n/a	n/a
11	ATF3	chr9:94065145-94065338	K562	blood:	n/a	n/a
12	ATF3	chr9:94065007-94065685	HCT-116	colon:	n/a	n/a
13	ATF3	chr9:94036490-94036743	K562	blood:	n/a	n/a
14	ATF3	chr9:94036527-94036842	HCT-116	colon:	n/a	n/a
15	ATF3	chr9:94064997-94065567	HCT-116	colon:	n/a	n/a
16	BACH1	chr9:94123201-94123687	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr9:94111309-94111601	GM12878	blood:	n/a	n/a
18	BATF	chr9:94007655-94007942	GM12878	blood:	n/a	n/a
19	BATF	chr9:94140852-94141093	GM12878	blood:	n/a	chr9:94140995-94141006
20	BATF	chr9:94121345-94121739	GM12878	blood:	n/a	n/a
21	BATF	chr9:94070468-94070787	GM12878	blood:	n/a	n/a
22	BATF	chr9:94121305-94121753	GM12878	blood:	n/a	n/a
23	BATF	chr9:94007628-94008011	GM12878	blood:	n/a	n/a
24	BCL11A	chr9:93979682-93979925	H1-hESC	embryonic stem cell:	n/a	n/a
25	BCL11A	chr9:94121346-94121644	GM12878	blood:	n/a	n/a
26	BCL11A	chr9:94069636-94069881	GM12878	blood:	n/a	n/a
27	BCLAF1	chr9:94069547-94069957	GM12878	blood:	n/a	n/a
28	BCLAF1	chr9:94123940-94124273	GM12878	blood:	n/a	n/a
29	BCLAF1	chr9:94121271-94121750	GM12878	blood:	n/a	n/a
30	BHLHE40	chr9:94123128-94123306	K562	blood:	n/a	n/a
31	BHLHE40	chr9:94121411-94121680	GM12878	blood:	n/a	n/a
32	BHLHE40	chr9:93974176-93974195	GM12878	blood:	n/a	n/a
33	BHLHE40	chr9:94124042-94124520	GM12878	blood:	n/a	n/a
34	BHLHE40	chr9:94036291-94036639	GM12878	blood:	n/a	n/a
35	BHLHE40	chr9:94122895-94123198	GM12878	blood:	n/a	n/a
36	BHLHE40	chr9:94123742-94124241	K562	blood:	n/a	chr9:94123866-94123882
37	BRCA1	chr9:94124004-94124080	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr9:94123210-94123211	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr9:94124345-94124688	Hela-S3	cervix:	n/a	n/a
40	CBX3	chr9:94065028-94065740	HCT-116	colon:	n/a	n/a
41	CBX3	chr9:94127053-94127384	K562	blood:	n/a	n/a
42	CBX3	chr9:94075029-94075779	HCT-116	colon:	n/a	n/a
43	CBX3	chr9:94064964-94065678	HCT-116	colon:	n/a	n/a
44	CBX3	chr9:94063379-94064081	HCT-116	colon:	n/a	n/a
45	CBX3	chr9:94126860-94127446	K562	blood:	n/a	n/a
46	CBX3	chr9:94075051-94075773	HCT-116	colon:	n/a	n/a
47	CCNT2	chr9:94015880-94016051	K562	blood:	n/a	n/a
48	CCNT2	chr9:94123397-94124410	K562	blood:	n/a	n/a
49	CEBPB	chr9:94064924-94065774	HCT-116	colon:	n/a	chr9:94065253-94065264
50	CEBPB	chr9:94075168-94075580	ECC-1	luminal epithelium:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:94123704-94123754	SK-N-SH_RA	brain:	n/a
2	chr9:94124362-94124412	Jurkat	blood:	n/a
3	chr9:93983210-93983260	HNPCEpiC	eye:	n/a
4	chr9:94124044-94124094	ProgFib	skin:	n/a
5	chr9:94124060-94124110	AG04450	lung:	fetal
6	chr9:94123659-94123709	ovcar-3	ovarian:	n/a
7	chr9:94123704-94123754	SAEC	small airway:	n/a
8	chr9:94123704-94123754	ovcar-3	ovarian:	n/a
9	chr9:94124044-94124094	HRCEpiC	kidney:	n/a
10	chr9:94060853-94060903	HCPEpiC	choroid plexus:	n/a
11	chr9:94124746-94124796	GM12878	blood:	n/a
12	chr9:94123659-94123709	PFSK-1	brain:	n/a
13	chr9:94124060-94124110	GM06990	blood:	n/a
14	chr9:94124746-94124796	ProgFib	skin:	n/a
15	chr9:94124655-94124705	HPAEpiC	pulmonary alveolar:	n/a
16	chr9:94060853-94060903	Hela-S3	cervix:	n/a
17	chr9:93983210-93983260	HIPEpiC	eye:	n/a
18	chr9:94124044-94124094	GM12892	blood:	n/a
19	chr9:94123659-94123709	U87	brain:	n/a
20	chr9:94124044-94124094	HCT-116	colon:	n/a
21	chr9:94124362-94124412	SKMC	muscle:	n/a
22	chr9:94124060-94124110	HCT-116	colon:	n/a
23	chr9:94123704-94123754	AG09319	gingival:	n/a
24	chr9:94123659-94123709	ProgFib	skin:	n/a
25	chr9:94124362-94124412	RPTEC	kidney:	n/a
26	chr9:94124060-94124110	HRCEpiC	kidney:	n/a
27	chr9:94124044-94124094	HRPEpiC	eye:	n/a
28	chr9:94124044-94124094	SK-N-SH_RA	brain:	n/a
29	chr9:94124655-94124705	GM06990	blood:	n/a
30	chr9:94124746-94124796	MCF-7	breast:	n/a
31	chr9:94124655-94124705	H1-hESC	embryonic stem cell:	embryo
32	chr9:94124060-94124110	BE2_C	brain:	n/a
33	chr9:94124655-94124705	BJ	skin:	n/a
34	chr9:94123704-94123754	AG10803	skin:	n/a
35	chr9:94124044-94124094	AG10803	skin:	n/a
36	chr9:94124655-94124705	HL-60	blood:	n/a
37	chr9:94124655-94124705	GM19239	blood:	n/a
38	chr9:93983210-93983260	HUVEC	blood vessel:	n/a
39	chr9:94123659-94123709	MCF-7	breast:	n/a
40	chr9:94124362-94124412	AG09309	skin:	n/a
41	chr9:94060853-94060903	HepG2	liver:	n/a
42	chr9:94124362-94124412	HNPCEpiC	eye:	n/a
43	chr9:94060853-94060903	HUVEC	blood vessel:	n/a
44	chr9:94124746-94124796	SK-N-SH_RA	brain:	n/a
45	chr9:94123704-94123754	HCF	heart:	n/a
46	chr9:94124746-94124796	GM19239	blood:	n/a
47	chr9:94124362-94124412	MCF-7	breast:	n/a
48	chr9:94124655-94124705	ovcar-3	ovarian:	n/a
49	chr9:94124655-94124705	ECC-1	luminal epithelium:	n/a
50	chr9:94060853-94060903	HAEpiC	amniotic membrane:	n/a

(count:159 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr9:94112745..94114937-chr9:94118041..94119870,2	MCF-7	breast:
2	chr9:94123933..94127271-chr9:94127797..94131157,4	K562	blood:
3	chr9:94099451..94101101-chr9:94108763..94110540,2	MCF-7	breast:
4	chr9:94010552..94013353-chr9:94014239..94017543,3	K562	blood:
5	chr9:94104145..94106983-chr9:94120665..94122259,2	K562	blood:
6	chr9:93959750..93961882-chr9:94121877..94124140,2	K562	blood:
7	chr9:93953759..93956492-chr9:93979934..93981745,2	K562	blood:
8	chr9:94112282..94113941-chr9:94121360..94122984,2	K562	blood:
9	chr9:94077918..94080792-chr9:94096846..94099494,2	MCF-7	breast:
10	chr9:94083958..94089590-chr9:94090031..94094657,6	K562	blood:
11	chr9:94001722..94003904-chr9:94005920..94007942,2	K562	blood:
12	chr9:94043137..94044689-chr9:94050291..94052171,2	MCF-7	breast:
13	chr9:94122694..94125118-chr9:94127022..94132461,6	MCF-7	breast:
14	chr9:94122021..94124488-chr9:94184872..94187456,5	MCF-7	breast:
15	chr9:94103649..94105719-chr9:94123863..94125427,2	MCF-7	breast:
16	chr9:94117423..94119022-chr9:94128192..94130184,2	MCF-7	breast:
17	chr9:94115075..94117611-chr9:94184527..94186673,2	MCF-7	breast:
18	chr9:94093775..94096685-chr9:94097839..94101388,3	MCF-7	breast:
19	chr9:94108222..94110620-chr9:94122202..94123731,2	MCF-7	breast:
20	chr9:93969893..93972438-chr9:93978667..93980846,2	K562	blood:
21	chr9:94112282..94113941-chr9:94121360..94122984,2	K562	blood:
22	chr9:94145262..94147906-chr9:94148347..94150501,2	MCF-7	breast:
23	chr9:94063221..94065813-chr9:94122626..94124840,2	MCF-7	breast:
24	chr9:94118243..94121111-chr9:94121420..94123747,2	MCF-7	breast:
25	chr9:94112112..94113944-chr9:94115686..94118252,2	MCF-7	breast:
26	chr9:94114946..94116593-chr9:94118141..94120132,2	K562	blood:
27	chr9:94103117..94103617-chr9:94188208..94188917,2	MCF-7	breast:
28	chr9:93723955..93726511-chr9:94076092..94077713,2	MCF-7	breast:
29	chr9:94103409..94105645-chr9:94120684..94122259,2	K562	blood:
30	chr9:93852040..93852708-chr9:93997819..93998576,2	MCF-7	breast:
31	chr9:94016834..94019698-chr9:94185976..94188010,2	K562	blood:
32	chr9:94040815..94043088-chr9:94045185..94047903,2	MCF-7	breast:
33	chr9:94093775..94096685-chr9:94097839..94101388,3	MCF-7	breast:
34	chr9:94124603..94127271-chr9:94129657..94131975,2	K562	blood:
35	chr9:94068643..94071374-chr9:94072196..94073935,2	K562	blood:
36	chr9:94096260..94098366-chr9:94101881..94104584,2	MCF-7	breast:
37	chr9:94127807..94131251-chr9:94131803..94134824,3	K562	blood:
38	chr16:66583326..66584035-chr9:94123309..94124144,2	NB4	blood:
39	chr9:94097644..94101149-chr9:94101391..94105187,4	K562	blood:
40	chr9:94066213..94070359-chr9:94073999..94077137,3	MCF-7	breast:
41	chr9:93972883..93975853-chr9:93985098..93987013,2	K562	blood:
42	chr9:94075638..94079433-chr9:94082125..94086172,6	MCF-7	breast:
43	chr9:94120989..94122585-chr9:94173872..94176280,2	K562	blood:
44	chr18:5296256..5296760-chr9:94124226..94125038,2	Hela-S3	cervix:
45	chr9:94098360..94101047-chr9:94184402..94186027,2	MCF-7	breast:
46	chr9:94083711..94086738-chr9:94095670..94099237,3	K562	blood:
47	chr9:94079615..94081294-chr9:94087767..94090304,2	K562	blood:
48	chr9:94104145..94106983-chr9:94120665..94122259,2	K562	blood:
49	chr9:94096260..94098366-chr9:94101881..94104584,2	MCF-7	breast:
50	chr9:94068643..94070163-chr9:94072196..94073834,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NFIL3-3	chr9:94035854-94039649	NONHSAT133133

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	AUH	hsa-miR-9-5p	chr9:93976242-93976263
2	AUH	hsa-miR-9-5p	chr9:93976532-93976526
3	AUH	hsa-miR-9-5p	chr9:93976223-93976246
4	AUH	hsa-miR-9-5p	chr9:93976526-93976548

Variant related genes	Relation type
AUH	TF binding region
ENSG00000273381	TF binding region
AUH	CpG island
ENSG00000273381	CpG island
ENSG00000165030	chromatin interactions
ENSG00000196456	chromatin interactions
ENSG00000166548	chromatin interactions
ENSG00000233081	chromatin interactions
ENSG00000074266	chromatin interactions
ENSG00000088448	chromatin interactions
ENSG00000214022	chromatin interactions
ENSG00000148090	chromatin interactions

Extended variants
information (count: 6148 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:6148 , 50 per page) page: 1 2 3 4 5 6 7 ... 123

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16907283	chr9:93973938-93973939	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs567294028	chr9:93973980-93973981	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs578015257	chr9:93974012-93974013	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs200967905	chr9:93974033-93974034	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs138943466	chr9:93974068-93974069	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs374737645	chr9:93974072-93974073	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs74362134	chr9:93974083-93974084	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs184042175	chr9:93974113-93974114	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs76473946	chr9:93974130-93974131	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs538454481	chr9:93974209-93974210	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs553975580	chr9:93974271-93974272	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs573835285	chr9:93974274-93974275	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs572209515	chr9:93974287-93974288	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs148324050	chr9:93974294-93974295	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs188623031	chr9:93974303-93974304	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs576040673	chr9:93974345-93974346	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs562202046	chr9:93974348-93974349	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs542756445	chr9:93974387-93974388	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs10991830	chr9:93974413-93974414	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs143956382	chr9:93974435-93974436	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs200605573	chr9:93974437-93974438	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs75069666	chr9:93974477-93974478	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs142078749	chr9:93974494-93974495	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs76953673	chr9:93974510-93974511	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs572095513	chr9:93974541-93974542	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs192165894	chr9:93974542-93974543	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs773507	chr9:93974553-93974554	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs531312568	chr9:93974558-93974559	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs118125222	chr9:93974599-93974600	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs535650417	chr9:93974647-93974648	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs561089088	chr9:93974665-93974666	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs549495351	chr9:93974698-93974699	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs571247309	chr9:93974713-93974714	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs145986266	chr9:93974753-93974754	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs374702579	chr9:93974821-93974822	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs184004348	chr9:93974841-93974842	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs565557949	chr9:93974855-93974856	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs572171629	chr9:93974902-93974903	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs536104009	chr9:93974921-93974922	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs149359544	chr9:93974944-93974945	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs56687646	chr9:93974945-93974946	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs368067958	chr9:93974965-93974966	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs554427038	chr9:93974966-93974967	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs575957660	chr9:93975022-93975023	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs139919745	chr9:93975033-93975034	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs187230463	chr9:93975049-93975050	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs577226709	chr9:93975068-93975069	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs541517426	chr9:93975086-93975087	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs191310758	chr9:93975120-93975121	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs531510068	chr9:93975175-93975176	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Mental retardation	21693067	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:3633 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:93961200-93975600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr9:93969600-93974200	Enhancers	Pancreas	Pancrea
3	chr9:93969800-93976400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr9:93970200-93979200	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr9:93970200-93984000	Weak transcription	K562	blood
6	chr9:93970400-93976400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr9:93970400-94005400	Weak transcription	Aorta	Aorta
8	chr9:93970600-93976600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr9:93970800-93974400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr9:93970800-93974800	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr9:93970800-93974800	Weak transcription	Fetal Muscle Leg	muscle
12	chr9:93970800-93975400	Weak transcription	Brain Cingulate Gyrus	brain
13	chr9:93970800-93976200	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr9:93970800-93980800	Weak transcription	NHDF-Ad	bronchial
15	chr9:93970800-93981400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr9:93970800-93983600	Weak transcription	Brain Substantia Nigra	brain
17	chr9:93970800-93983800	Weak transcription	Brain Angular Gyrus	brain
18	chr9:93970800-93984200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr9:93970800-93985200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr9:93971000-93974400	Weak transcription	Rectal Smooth Muscle	rectum
21	chr9:93971000-93974400	Enhancers	HepG2	liver
22	chr9:93971000-93974400	Weak transcription	Osteobl	bone
23	chr9:93971000-93974800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr9:93971000-93975400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr9:93971000-93979800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr9:93971000-93980800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr9:93971000-93981000	Weak transcription	Primary T helper cells fromperipheralblood	blood
28	chr9:93971000-93983200	Weak transcription	Colon Smooth Muscle	Colon
29	chr9:93971000-93984200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr9:93971000-94007800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr9:93971200-93974200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr9:93971200-93974400	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr9:93971200-93979800	Weak transcription	Primary T cells from cord blood	blood
34	chr9:93971200-93980800	Weak transcription	Stomach Smooth Muscle	stomach
35	chr9:93971200-93981200	Weak transcription	Thymus	Thymus
36	chr9:93971200-93982400	Weak transcription	Brain Hippocampus Middle	brain
37	chr9:93971200-93983800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
38	chr9:93971400-93974000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
39	chr9:93971400-93974200	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr9:93971400-93974400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr9:93971400-93975200	Weak transcription	Left Ventricle	heart
42	chr9:93971400-93979600	Weak transcription	Fetal Muscle Trunk	muscle
43	chr9:93971400-93979800	Weak transcription	Fetal Thymus	thymus
44	chr9:93971400-93980800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr9:93971400-93981200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr9:93971400-93981200	Weak transcription	Esophagus	oesophagus
47	chr9:93971400-93981200	Weak transcription	Lung	lung
48	chr9:93971400-93982400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr9:93971400-93982400	Weak transcription	Right Ventricle	heart
50	chr9:93971400-93982800	Weak transcription	Duodenum Smooth Muscle	Duodenum

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