Variant report

Variant	nsv530946
Chromosome Location	chr9:94633154-94715023
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1697)
CpG islands
(count:1160)
Chromatin interactive
region (count:107)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1697 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:94649685-94650080	K562	blood:	n/a	n/a
2	ARID3A	chr9:94646446-94646721	K562	blood:	n/a	n/a
3	ARID3A	chr9:94668381-94668483	K562	blood:	n/a	n/a
4	ARID3A	chr9:94712529-94712598	K562	blood:	n/a	n/a
5	ARID3A	chr9:94661238-94661538	K562	blood:	n/a	n/a
6	ARID3A	chr9:94663083-94663283	K562	blood:	n/a	chr9:94663149-94663165 chr9:94663150-94663166
7	ARID3A	chr9:94710383-94710964	K562	blood:	n/a	n/a
8	ARID3A	chr9:94662177-94662643	K562	blood:	n/a	n/a
9	ARID3A	chr9:94670329-94671087	K562	blood:	n/a	n/a
10	ARID3A	chr9:94669671-94669968	K562	blood:	n/a	n/a
11	ARID3A	chr9:94706132-94706682	K562	blood:	n/a	n/a
12	ARID3A	chr9:94663527-94663801	K562	blood:	n/a	n/a
13	ARID3A	chr9:94707375-94708666	K562	blood:	n/a	n/a
14	ARID3A	chr9:94664900-94665337	K562	blood:	n/a	n/a
15	ATF1	chr9:94669508-94669943	K562	blood:	n/a	n/a
16	ATF1	chr9:94706177-94706583	K562	blood:	n/a	n/a
17	ATF1	chr9:94665913-94666217	K562	blood:	n/a	n/a
18	ATF1	chr9:94707597-94708122	K562	blood:	n/a	n/a
19	ATF1	chr9:94663416-94663914	K562	blood:	n/a	n/a
20	ATF3	chr9:94706209-94706598	K562	blood:	n/a	n/a
21	ATF3	chr9:94670322-94670548	K562	blood:	n/a	n/a
22	BACH1	chr9:94670882-94671058	K562	blood:	n/a	n/a
23	BACH1	chr9:94646446-94646569	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr9:94711162-94711495	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr9:94648939-94649366	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr9:94662386-94662471	K562	blood:	n/a	n/a
27	BACH1	chr9:94712501-94712871	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr9:94690261-94690487	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr9:94659139-94659187	K562	blood:	n/a	n/a
30	BHLHE40	chr9:94663363-94663365	K562	blood:	n/a	n/a
31	BHLHE40	chr9:94649808-94650019	K562	blood:	n/a	n/a
32	BHLHE40	chr9:94707056-94708939	K562	blood:	n/a	n/a
33	BHLHE40	chr9:94661119-94661634	K562	blood:	n/a	n/a
34	BHLHE40	chr9:94711063-94711373	K562	blood:	n/a	chr9:94711166-94711182
35	BHLHE40	chr9:94668250-94668772	K562	blood:	n/a	n/a
36	BHLHE40	chr9:94710423-94710707	K562	blood:	n/a	n/a
37	BHLHE40	chr9:94667180-94667284	K562	blood:	n/a	n/a
38	BHLHE40	chr9:94661982-94663104	K562	blood:	n/a	n/a
39	BHLHE40	chr9:94670309-94670622	K562	blood:	n/a	n/a
40	BHLHE40	chr9:94712258-94712984	K562	blood:	n/a	chr9:94712633-94712649 chr9:94712636-94712652
41	BHLHE40	chr9:94659172-94659458	K562	blood:	n/a	n/a
42	BRCA1	chr9:94665784-94665807	Hela-S3	cervix:	n/a	n/a
43	CBX3	chr9:94666973-94667947	K562	blood:	n/a	n/a
44	CBX3	chr9:94668243-94668654	K562	blood:	n/a	n/a
45	CBX3	chr9:94661852-94663269	K562	blood:	n/a	n/a
46	CBX3	chr9:94692599-94693285	K562	blood:	n/a	n/a
47	CBX3	chr9:94692453-94693363	K562	blood:	n/a	n/a
48	CBX3	chr9:94692522-94693285	HCT-116	colon:	n/a	n/a
49	CBX3	chr9:94714154-94714684	K562	blood:	n/a	n/a
50	CBX3	chr9:94710994-94711464	K562	blood:	n/a	n/a

(count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:94648674-94648724	GM12892	blood:	n/a
2	chr9:94648674-94648724	GM12892	blood:	n/a
3	chr9:94712122-94712172	SK-N-MC	brain:	n/a
4	chr9:94666754-94666804	NT2-D1	testis:	n/a
5	chr9:94711818-94711868	Jurkat	blood:	n/a
6	chr9:94710679-94710729	HNPCEpiC	eye:	n/a
7	chr9:94712472-94712522	AG09319	gingival:	n/a
8	chr9:94666754-94666804	HRE	kidney:	n/a
9	chr9:94647670-94647720	PFSK-1	brain:	n/a
10	chr9:94711214-94711264	HCPEpiC	choroid plexus:	n/a
11	chr9:94710679-94710729	HRPEpiC	eye:	n/a
12	chr9:94712780-94712830	NB4	blood:	n/a
13	chr9:94662566-94662616	GM06990	blood:	n/a
14	chr9:94659196-94659246	HRE	kidney:	n/a
15	chr9:94710679-94710729	MCF-7	breast:	n/a
16	chr9:94662199-94662249	A549	lung:	n/a
17	chr9:94662566-94662616	Caco-2	colon:	n/a
18	chr9:94647670-94647720	ProgFib	skin:	n/a
19	chr9:94711214-94711264	Hela-S3	cervix:	n/a
20	chr9:94659196-94659246	HAEpiC	amniotic membrane:	n/a
21	chr9:94666754-94666804	H1-hESC	embryonic stem cell:	embryo
22	chr9:94710553-94710603	HepG2	liver:	n/a
23	chr9:94712472-94712522	HRPEpiC	eye:	n/a
24	chr9:94659196-94659246	AG04449	skin:	fetal
25	chr9:94711818-94711868	LNCaP	prostate:	n/a
26	chr9:94648732-94648782	HAEpiC	amniotic membrane:	n/a
27	chr9:94710679-94710729	HUVEC	blood vessel:	n/a
28	chr9:94712122-94712172	HUVEC	blood vessel:	n/a
29	chr9:94662199-94662249	NH-A	brain:	n/a
30	chr9:94648674-94648724	HEEpiC	esophagus:	n/a
31	chr9:94712780-94712830	GM19239	blood:	n/a
32	chr9:94711214-94711264	HEEpiC	esophagus:	n/a
33	chr9:94662199-94662249	HepG2	liver:	n/a
34	chr9:94652849-94652899	AG09319	gingival:	n/a
35	chr9:94710553-94710603	HNPCEpiC	eye:	n/a
36	chr9:94712472-94712522	SKMC	muscle:	n/a
37	chr9:94666754-94666804	GM12878	blood:	n/a
38	chr9:94710679-94710729	ovcar-3	ovarian:	n/a
39	chr9:94659196-94659246	LNCaP	prostate:	n/a
40	chr9:94648732-94648782	HEK293	kidney:	embryo
41	chr9:94662566-94662616	GM12891	blood:	n/a
42	chr9:94712122-94712172	MCF-7	breast:	n/a
43	chr9:94712472-94712522	HL-60	blood:	n/a
44	chr9:94646100-94646150	HCF	heart:	n/a
45	chr9:94712909-94712959	SAEC	small airway:	n/a
46	chr9:94661334-94661384	LNCaP	prostate:	n/a
47	chr9:94659196-94659246	Jurkat	blood:	n/a
48	chr9:94710553-94710603	LNCaP	prostate:	n/a
49	chr9:94711818-94711868	H1-hESC	embryonic stem cell:	embryo
50	chr9:94666754-94666804	AG04450	lung:	fetal

(count:107 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr9:94646595..94649139-chr9:94708273..94710120,2	K562	blood:
2	chr9:94537694..94538378-chr9:94712239..94713033,2	K562	blood:
3	chr9:94657831..94659746-chr9:94710124..94712631,2	K562	blood:
4	chr9:94661900..94664292-chr9:94705248..94709269,4	K562	blood:
5	chr9:94513749..94516669-chr9:94667565..94670057,2	K562	blood:
6	chr9:94643211..94646019-chr9:94657149..94659875,2	K562	blood:
7	chr9:94634801..94638279-chr9:94639316..94642885,4	K562	blood:
8	chr9:94633023..94637402-chr9:94642921..94647325,4	MCF-7	breast:
9	chr9:94702364..94705189-chr9:94709744..94712716,4	K562	blood:
10	chr9:94676427..94678807-chr9:94685179..94687567,2	K562	blood:
11	chr9:94696439..94698046-chr9:94704884..94707640,2	K562	blood:
12	chr9:94631828..94632674-chr9:94658603..94659404,2	K562	blood:
13	chr9:94664745..94669992-chr9:94681267..94685780,5	K562	blood:
14	chr9:94533336..94534896-chr9:94707634..94709527,2	MCF-7	breast:
15	chr9:94667534..94670775-chr9:94707582..94710553,5	K562	blood:
16	chr9:94650894..94652826-chr9:94665751..94669153,3	K562	blood:
17	chr9:94659650..94662569-chr9:94690819..94692460,2	K562	blood:
18	chr9:94636703..94639887-chr9:94643001..94646217,3	K562	blood:
19	chr9:94650853..94651554-chr9:94712434..94713072,2	MCF-7	breast:
20	chr9:94667170..94669992-chr9:94682219..94685194,2	K562	blood:
21	chr9:94689308..94690973-chr9:94691805..94694661,2	K562	blood:
22	chr9:94697432..94700387-chr9:94709013..94711926,3	MCF-7	breast:
23	chr9:94663383..94666047-chr9:94676965..94679095,2	K562	blood:
24	chr9:94654512..94657434-chr9:94657669..94659838,4	K562	blood:
25	chr9:94661900..94664292-chr9:94705248..94709269,4	K562	blood:
26	chr9:94631930..94633777-chr9:94645726..94647722,2	K562	blood:
27	chr9:94641817..94643317-chr9:94650910..94653000,2	K562	blood:
28	chr9:94661029..94661939-chr9:94710741..94711644,2	K562	blood:
29	chr9:94537481..94538450-chr9:94712230..94712819,2	MCF-7	breast:
30	chr9:94666595..94672238-chr9:94672403..94678372,8	K562	blood:
31	chr9:94667321..94670775-chr9:94706336..94711619,7	K562	blood:
32	chr9:94537471..94538153-chr9:94694764..94695511,3	MCF-7	breast:
33	chr9:94680096..94683212-chr9:94691490..94694919,3	K562	blood:
34	chr9:94706737..94709425-chr9:94709648..94712474,2	MCF-7	breast:
35	chr9:94679676..94683212-chr9:94692527..94694919,4	K562	blood:
36	chr9:94658826..94661180-chr9:94661410..94663593,2	K562	blood:
37	chr9:94653069..94655970-chr9:94661069..94663824,3	K562	blood:
38	chr9:94645315..94647676-chr9:94666839..94670309,3	K562	blood:
39	chr3:179280666..179282550-chr9:94696148..94698847,2	MCF-7	breast:
40	chr9:94689308..94690973-chr9:94691805..94694661,2	K562	blood:
41	chr9:94667170..94669992-chr9:94682219..94685194,2	K562	blood:
42	chr9:94656937..94658928-chr9:94660784..94663442,2	MCF-7	breast:
43	chr9:94658826..94661180-chr9:94661410..94663593,2	K562	blood:
44	chr9:94647061..94649202-chr9:94659654..94661828,2	MCF-7	breast:
45	chr9:94650894..94652826-chr9:94665751..94669153,3	K562	blood:
46	chr9:94626760..94629171-chr9:94633039..94635717,3	K562	blood:
47	chr9:94714221..94717070-chr9:94719717..94722305,2	K562	blood:
48	chr9:94676298..94678105-chr9:94680028..94681662,2	MCF-7	breast:
49	chr9:94659650..94662569-chr9:94690819..94692460,2	K562	blood:
50	chr9:94634167..94636496-chr9:94639519..94641175,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPTLC1-6	chr9:94712149-94712188	NONHSAT133144
2	lnc-SPTLC1-6	chr9:94685950-94686210	NONHSAT133145
3	lnc-SPTLC1-6	chr9:94710889-94710997	NONHSAT133145
4	lnc-SPTLC1-6	chr9:94685935-94686210	NONHSAT133144

No data

Variant related genes	Relation type
ROR2	TF binding region
ROR2	CpG island
ENSG00000136518	chromatin interactions
ENSG00000169071	chromatin interactions

Extended variants
information (count: 3362 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:3362 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1534529	chr9:94633156-94633157	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs551590091	chr9:94633166-94633167	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs545144479	chr9:94633187-94633188	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs142717396	chr9:94633234-94633235	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs527634040	chr9:94633280-94633281	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs187881744	chr9:94633333-94633334	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs191827459	chr9:94633346-94633347	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs544274613	chr9:94633358-94633359	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs556247877	chr9:94633361-94633362	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs1881387	chr9:94633406-94633407	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs538736361	chr9:94633439-94633440	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs144259392	chr9:94633484-94633485	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs11793320	chr9:94633498-94633499	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs148741369	chr9:94633536-94633537	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs554846545	chr9:94633580-94633581	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs142369076	chr9:94633621-94633622	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs151279911	chr9:94633652-94633653	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs562328600	chr9:94633687-94633688	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs183430899	chr9:94633700-94633701	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs187362692	chr9:94633792-94633793	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs76986920	chr9:94633793-94633794	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs114742394	chr9:94633798-94633799	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs549168679	chr9:94633810-94633811	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs78254105	chr9:94633830-94633831	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs139551481	chr9:94633845-94633846	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs12002460	chr9:94633912-94633913	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs192223252	chr9:94633917-94633918	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs144419436	chr9:94634021-94634022	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs529974863	chr9:94634066-94634067	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs547493132	chr9:94634093-94634094	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs376230802	chr9:94634098-94634099	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs536471191	chr9:94634099-94634100	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs554709271	chr9:94634113-94634114	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs573963824	chr9:94634121-94634122	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs569909653	chr9:94634123-94634124	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs537325219	chr9:94634124-94634125	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs556173547	chr9:94634130-94634131	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs566217248	chr9:94634165-94634166	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs544982605	chr9:94634166-94634167	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs147837729	chr9:94634199-94634200	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs558742581	chr9:94634229-94634230	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs572135100	chr9:94634236-94634237	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs183940817	chr9:94634245-94634246	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs141486064	chr9:94634253-94634254	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs7874281	chr9:94634254-94634255	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs187833190	chr9:94634302-94634303	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs565145860	chr9:94634328-94634329	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs146928143	chr9:94634335-94634336	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550660928	chr9:94634374-94634375	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547360435	chr9:94634382-94634383	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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	21364760	CNVD
overgrowth syndrome	16570072	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2147 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:94621400-94638000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr9:94623200-94634000	Weak transcription	Fetal Intestine Small	intestine
3	chr9:94626600-94636200	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr9:94627000-94635000	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr9:94627000-94650800	Weak transcription	Gastric	stomach
6	chr9:94627200-94648600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr9:94627600-94647400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr9:94628000-94635400	Weak transcription	Fetal Heart	heart
9	chr9:94629800-94633800	Weak transcription	Fetal Stomach	stomach
10	chr9:94630200-94634600	Weak transcription	Rectal Smooth Muscle	rectum
11	chr9:94630200-94636200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr9:94630200-94636400	Weak transcription	Ovary	ovary
13	chr9:94630400-94633400	Weak transcription	Fetal Lung	lung
14	chr9:94630400-94641400	Weak transcription	K562	blood
15	chr9:94631200-94639400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr9:94632200-94633800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr9:94632400-94633400	Enhancers	Stomach Smooth Muscle	stomach
18	chr9:94632600-94634000	Enhancers	Fetal Muscle Leg	muscle
19	chr9:94632800-94633800	Weak transcription	Right Atrium	heart
20	chr9:94632800-94641000	Enhancers	Colon Smooth Muscle	Colon
21	chr9:94633000-94644600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr9:94633400-94634000	Enhancers	Fetal Lung	lung
23	chr9:94633400-94634200	Weak transcription	Stomach Smooth Muscle	stomach
24	chr9:94633800-94634000	Enhancers	Right Atrium	heart
25	chr9:94633800-94634200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr9:94633800-94635200	Strong transcription	Fetal Stomach	stomach
27	chr9:94634000-94634200	ZNF genes & repeats	Fetal Intestine Small	intestine
28	chr9:94634000-94635000	Weak transcription	Fetal Muscle Leg	muscle
29	chr9:94634000-94636000	Weak transcription	Right Atrium	heart
30	chr9:94634000-94637600	Weak transcription	Fetal Lung	lung
31	chr9:94634200-94634400	Strong transcription	Fetal Intestine Small	intestine
32	chr9:94634200-94634600	Enhancers	Stomach Smooth Muscle	stomach
33	chr9:94634200-94635000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr9:94634400-94637600	Weak transcription	Fetal Intestine Small	intestine
35	chr9:94634600-94635000	Flanking Active TSS	Stomach Smooth Muscle	stomach
36	chr9:94634600-94638200	Enhancers	Rectal Smooth Muscle	rectum
37	chr9:94635000-94636000	Enhancers	Stomach Smooth Muscle	stomach
38	chr9:94635000-94636200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr9:94635000-94636600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr9:94635000-94637200	Enhancers	Fetal Muscle Trunk	muscle
41	chr9:94635000-94637400	Enhancers	Fetal Muscle Leg	muscle
42	chr9:94635200-94636000	Weak transcription	Fetal Stomach	stomach
43	chr9:94635400-94636600	Enhancers	Fetal Heart	heart
44	chr9:94635400-94637000	Enhancers	Fetal Thymus	thymus
45	chr9:94635600-94635800	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chr9:94635800-94636600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr9:94635800-94636600	Enhancers	Left Ventricle	heart
48	chr9:94636000-94636400	Flanking Active TSS	Stomach Smooth Muscle	stomach
49	chr9:94636000-94636600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr9:94636000-94636600	Enhancers	Right Atrium	heart

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