Variant report

Variant	nsv893698
Chromosome Location	chr9:109998563-110052660
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2293)
CpG islands
(count:610)
Chromatin interactive
region (count:84)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2293 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:110031821-110032643	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:110013867-110014737	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:110046237-110046508	K562	blood:	n/a	n/a
4	ARID3A	chr9:110045052-110045347	K562	blood:	n/a	n/a
5	ARID3A	chr9:110001859-110002073	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:110046153-110047491	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:110011416-110012008	HepG2	liver:	n/a	n/a
8	ARID3A	chr9:110047714-110048670	HepG2	liver:	n/a	chr9:110048184-110048200
9	ARID3A	chr9:110036414-110036656	K562	blood:	n/a	n/a
10	ARID3A	chr9:110037185-110037511	HepG2	liver:	n/a	n/a
11	ARID3A	chr9:110045009-110045810	HepG2	liver:	n/a	chr9:110045434-110045449
12	ARID3A	chr9:110036725-110036781	HepG2	liver:	n/a	n/a
13	ARID3A	chr9:110047220-110047304	K562	blood:	n/a	n/a
14	ARID3A	chr9:110005888-110006603	HepG2	liver:	n/a	n/a
15	ARID3A	chr9:110009304-110009379	HepG2	liver:	n/a	n/a
16	ATF1	chr9:110036408-110036778	K562	blood:	n/a	n/a
17	ATF1	chr9:110014292-110014556	K562	blood:	n/a	n/a
18	ATF2	chr9:110046031-110046621	GM12878	blood:	n/a	n/a
19	ATF2	chr9:110045098-110045623	GM12878	blood:	n/a	n/a
20	ATF2	chr9:110044852-110045763	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr9:110022652-110023216	GM12878	blood:	n/a	n/a
22	ATF2	chr9:110022562-110023254	GM12878	blood:	n/a	n/a
23	ATF2	chr9:110006037-110006456	GM12878	blood:	n/a	n/a
24	ATF2	chr9:110045037-110045781	GM12878	blood:	n/a	n/a
25	ATF2	chr9:110045165-110045650	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF2	chr9:110046251-110046681	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr9:110046053-110046739	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF3	chr9:110005775-110006598	HCT-116	colon:	n/a	n/a
29	ATF3	chr9:110045348-110045766	A549	lung:	n/a	chr9:110045426-110045435 chr9:110045456-110045465
30	ATF3	chr9:110045122-110045585	K562	blood:	n/a	chr9:110045426-110045435 chr9:110045456-110045465
31	ATF3	chr9:110045136-110045322	K562	blood:	n/a	n/a
32	ATF3	chr9:110005747-110006559	HCT-116	colon:	n/a	n/a
33	ATF3	chr9:110006171-110006425	K562	blood:	n/a	n/a
34	ATF3	chr9:110045250-110045774	A549	lung:	n/a	chr9:110045426-110045435 chr9:110045456-110045465
35	ATF3	chr9:110037191-110037492	A549	lung:	n/a	n/a
36	BACH1	chr9:110045136-110046659	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr9:110045491-110045738	K562	blood:	n/a	n/a
38	BATF	chr9:110006087-110006418	GM12878	blood:	n/a	chr9:110006287-110006297 chr9:110006269-110006280 chr9:110006270-110006280
39	BATF	chr9:110037246-110037568	GM12878	blood:	n/a	chr9:110037421-110037432
40	BATF	chr9:110000174-110000452	GM12878	blood:	n/a	chr9:110000295-110000306
41	BATF	chr9:110045436-110045708	GM12878	blood:	n/a	n/a
42	BATF	chr9:110000192-110000478	GM12878	blood:	n/a	chr9:110000295-110000306
43	BATF	chr9:110022689-110023117	GM12878	blood:	n/a	n/a
44	BCL11A	chr9:110045398-110045733	GM12878	blood:	n/a	n/a
45	BCL11A	chr9:110022680-110023129	GM12878	blood:	n/a	chr9:110022891-110022900
46	BCL11A	chr9:110022683-110023135	GM12878	blood:	n/a	chr9:110022891-110022900
47	BCL11A	chr9:110046128-110046407	GM12878	blood:	n/a	n/a
48	BCL3	chr9:110022678-110023080	GM12878	blood:	n/a	chr9:110022891-110022900
49	BCL3	chr9:110045275-110045838	A549	lung:	n/a	n/a
50	BCL3	chr9:110045901-110046482	A549	lung:	n/a	chr9:110046044-110046057 chr9:110046065-110046074 chr9:110046054-110046067

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:110045363-110045413	HCPEpiC	choroid plexus:	n/a
2	chr9:110045363-110045413	HRE	kidney:	n/a
3	chr9:110045363-110045413	A549	lung:	n/a
4	chr9:110045982-110046032	PFSK-1	brain:	n/a
5	chr9:110045363-110045413	HL-60	blood:	n/a
6	chr9:110045982-110046032	HIPEpiC	eye:	n/a
7	chr9:110045295-110045345	ECC-1	luminal epithelium:	n/a
8	chr9:110044887-110044937	GM19239	blood:	n/a
9	chr9:110045129-110045179	SK-N-MC	brain:	n/a
10	chr9:110045901-110045951	GM12878	blood:	n/a
11	chr9:110045904-110045954	HRE	kidney:	n/a
12	chr9:110045901-110045951	AG10803	skin:	n/a
13	chr9:110045363-110045413	GM12891	blood:	n/a
14	chr9:110044887-110044937	HRCEpiC	kidney:	n/a
15	chr9:110044887-110044937	RPTEC	kidney:	n/a
16	chr9:110046671-110046721	SK-N-SH_RA	brain:	n/a
17	chr9:110046671-110046721	HIPEpiC	eye:	n/a
18	chr9:110045982-110046032	AG04450	lung:	fetal
19	chr9:110045295-110045345	HCM	heart:	n/a
20	chr9:110045904-110045954	HAEpiC	amniotic membrane:	n/a
21	chr9:110045363-110045413	AoSMC	blood vessel:	n/a
22	chr9:110044872-110044922	NT2-D1	testis:	n/a
23	chr9:110045363-110045413	GM19239	blood:	n/a
24	chr9:110045982-110046032	SKMC	muscle:	n/a
25	chr9:110045901-110045951	HCPEpiC	choroid plexus:	n/a
26	chr9:110045295-110045345	AG04450	lung:	fetal
27	chr9:110045295-110045345	GM19239	blood:	n/a
28	chr9:110046671-110046721	HUVEC	blood vessel:	n/a
29	chr9:110046671-110046721	HCPEpiC	choroid plexus:	n/a
30	chr9:110045982-110046032	AG04449	skin:	fetal
31	chr9:110045295-110045345	HCPEpiC	choroid plexus:	n/a
32	chr9:110045363-110045413	HRCEpiC	kidney:	n/a
33	chr9:110045129-110045179	GM12878	blood:	n/a
34	chr9:110044887-110044937	PANC-1	pancreas:	n/a
35	chr9:110045363-110045413	NT2-D1	testis:	n/a
36	chr9:110045363-110045413	AG04449	skin:	fetal
37	chr9:110045901-110045951	AoSMC	blood vessel:	n/a
38	chr9:110045901-110045951	IMR90	lung:	fetal
39	chr9:110044872-110044922	HepG2	liver:	n/a
40	chr9:110045295-110045345	AG09319	gingival:	n/a
41	chr9:110045129-110045179	MCF10A-Er-Src	breast:	n/a
42	chr9:110044872-110044922	HCF	heart:	n/a
43	chr9:110045129-110045179	SK-N-SH	brain:	n/a
44	chr9:110046224-110046274	HCF	heart:	n/a
45	chr9:110045901-110045951	NHDF-neo	bronchial:	n/a
46	chr9:110045904-110045954	U87	brain:	n/a
47	chr9:110044872-110044922	HUVEC	blood vessel:	n/a
48	chr9:110045901-110045951	HCT-116	colon:	n/a
49	chr9:110045363-110045413	ovcar-3	ovarian:	n/a
50	chr9:110046224-110046274	CMK	blood:	n/a

(count:84 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:110045113..110046713-chr9:110046851..110048527,3	MCF-7	breast:
2	chr9:110004582..110011651-chr9:110041707..110048879,25	MCF-7	breast:
3	chr9:110050921..110052628-chr9:110056459..110059114,2	MCF-7	breast:
4	chr9:110022591..110024814-chr9:110044876..110048033,4	MCF-7	breast:
5	chr9:110001935..110002443-chr9:110184199..110185147,2	MCF-7	breast:
6	chr9:110012891..110014822-chr9:110023736..110026167,2	MCF-7	breast:
7	chr9:109997045..109999849-chr9:110000685..110002475,2	K562	blood:
8	chr9:110007276..110009572-chr9:110012956..110014515,2	K562	blood:
9	chr9:110017405..110019153-chr9:110019371..110020959,2	MCF-7	breast:
10	chr9:110022283..110024488-chr9:110040936..110043082,2	MCF-7	breast:
11	chr9:110030231..110032782-chr9:110035060..110038842,3	MCF-7	breast:
12	chr9:110049581..110051989-chr9:110070046..110072937,2	MCF-7	breast:
13	chr9:110013982..110015486-chr9:110023325..110025849,2	K562	blood:
14	chr9:110006509..110008886-chr9:110028591..110031057,2	MCF-7	breast:
15	chr6:27860628..27861288-chr9:110045415..110046393,2	Hela-S3	cervix:
16	chr9:110044689..110046322-chr9:110067933..110070602,2	MCF-7	breast:
17	chr9:110007873..110010290-chr9:110031092..110033178,2	K562	blood:
18	chr9:110036136..110039453-chr9:110043491..110047008,5	MCF-7	breast:
19	chr17:56738323..56740813-chr9:110045478..110047129,2	MCF-7	breast:
20	chr9:110021549..110024530-chr9:110031690..110034147,2	MCF-7	breast:
21	chr9:109893618..109894481-chr9:110005806..110006859,6	MCF-7	breast:
22	chr12:54673289..54673950-chr9:110045597..110046480,2	Hela-S3	cervix:
23	chr9:110001502..110002534-chr9:110103139..110104123,8	MCF-7	breast:
24	chr9:110015966..110018595-chr9:110020108..110022273,3	MCF-7	breast:
25	chr9:110004629..110007184-chr9:110036620..110038464,2	MCF-7	breast:
26	chr9:109972512..109975127-chr9:110005713..110007836,2	MCF-7	breast:
27	chr9:110038034..110040721-chr9:110051893..110053905,2	MCF-7	breast:
28	chr9:110021549..110024530-chr9:110031690..110034147,2	MCF-7	breast:
29	chr9:110034708..110043058-chr9:110043083..110050663,16	MCF-7	breast:
30	chr9:110022816..110024667-chr9:110034684..110036365,2	MCF-7	breast:
31	chr9:110021032..110023010-chr9:110046369..110047881,2	MCF-7	breast:
32	chr9:109997045..109999849-chr9:110000685..110002475,2	K562	blood:
33	chr9:110001230..110003494-chr9:110052662..110055320,2	MCF-7	breast:
34	chr9:110030757..110033354-chr9:110044206..110047003,3	MCF-7	breast:
35	chr9:110009341..110011173-chr9:110013824..110016663,3	MCF-7	breast:
36	chr9:110007992..110013194-chr9:110021107..110025881,5	MCF-7	breast:
37	chr9:110004629..110007184-chr9:110036620..110038464,2	MCF-7	breast:
38	chr13:28674529..28675157-chr9:110045318..110046072,2	NB4	blood:
39	chr9:110011669..110017049-chr9:110043880..110047775,8	MCF-7	breast:
40	chr9:109998399..110000270-chr9:110004881..110006442,2	MCF-7	breast:
41	chr9:110014211..110018622-chr9:110040932..110043716,4	MCF-7	breast:
42	chr9:110000595..110013733-chr9:110042800..110048700,27	MCF-7	breast:
43	chr9:110000462..110002471-chr9:110023885..110026019,2	MCF-7	breast:
44	chr9:110045521..110048079-chr9:110251760..110253947,2	MCF-7	breast:
45	chr9:109996343..109999220-chr9:109999435..110002268,3	MCF-7	breast:
46	chr9:109999870..110001713-chr9:110004205..110007979,4	K562	blood:
47	chr9:109996343..109999220-chr9:109999435..110002268,3	MCF-7	breast:
48	chr9:110007992..110013194-chr9:110021107..110025881,5	MCF-7	breast:
49	chr9:110038034..110040721-chr9:110051893..110053905,2	MCF-7	breast:
50	chr9:110021248..110023658-chr9:110046181..110048340,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAD23B-3	chr9:110017675-110017878	XLOC_007504

No data

Variant related genes	Relation type
RAD23B	TF binding region
RAD23B	CpG island
ENSG00000233224	chromatin interactions
ENSG00000197153	chromatin interactions
ENSG00000165983	chromatin interactions
ENSG00000094916	chromatin interactions
ENSG00000266826	chromatin interactions
ENSG00000196331	chromatin interactions
ENSG00000119318	chromatin interactions
ENSG00000122025	chromatin interactions
ENSG00000029993	chromatin interactions
ENSG00000136826	chromatin interactions
MRPS34	miRNA target sites

Extended variants
information (count: 1940 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1940 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2808363	chr9:109998563-109998564	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs534046100	chr9:109998585-109998586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs2680218	chr9:109998648-109998649	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs568989765	chr9:109998662-109998663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs34553883	chr9:109998718-109998719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs183086200	chr9:109998769-109998770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs557318771	chr9:109998849-109998850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs62567692	chr9:109998883-109998884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs187737425	chr9:109998888-109998889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs542772761	chr9:109998910-109998911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs560935669	chr9:109998932-109998933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs528138452	chr9:109998936-109998937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs571605810	chr9:109998947-109998948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs138969222	chr9:109999013-109999014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs142900798	chr9:109999042-109999043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs59581003	chr9:109999059-109999060	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs192701156	chr9:109999072-109999073	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs2680219	chr9:109999115-109999116	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs530344567	chr9:109999203-109999204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs548725578	chr9:109999242-109999243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs183564270	chr9:109999321-109999322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs62567693	chr9:109999336-109999337	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs368662040	chr9:109999352-109999353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs113255350	chr9:109999356-109999357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs59128243	chr9:109999437-109999438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570845327	chr9:109999452-109999453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs62567694	chr9:109999468-109999469	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs2808364	chr9:109999502-109999503	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs575454898	chr9:109999504-109999505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs542560815	chr9:109999594-109999595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs534501281	chr9:109999712-109999713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs531291984	chr9:109999811-109999812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572991941	chr9:109999813-109999814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs139762746	chr9:109999815-109999816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs539922577	chr9:109999818-109999819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs573625817	chr9:109999820-109999821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs532100228	chr9:109999829-109999830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs1519051	chr9:109999831-109999832	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs139157478	chr9:109999866-109999867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs551400301	chr9:109999964-109999965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs371852460	chr9:109999985-109999986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs12378819	chr9:110000031-110000032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs149788535	chr9:110000032-110000033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs1519052	chr9:110000036-110000037	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs35362250	chr9:110000115-110000116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs527924576	chr9:110000123-110000124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs144749577	chr9:110000131-110000132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs574159912	chr9:110000148-110000149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs117974330	chr9:110000161-110000162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs113919928	chr9:110000163-110000164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
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
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Fukuyama congenital muscular dystrophy	21572526	CNVD
Testicular germ cell tumor	18059402	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1700 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:109997400-109999200	Enhancers	Liver	Liver
2	chr9:109998200-109998600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr9:109998200-109998600	Enhancers	Fetal Intestine Small	intestine
4	chr9:109998600-110006800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr9:109999200-110008600	Weak transcription	Liver	Liver
6	chr9:110000000-110000400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr9:110000000-110000600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr9:110000000-110000600	Enhancers	NHDF-Ad	bronchial
9	chr9:110000400-110000600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr9:110000400-110001800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr9:110000600-110001400	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr9:110000600-110002000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr9:110000600-110003200	Weak transcription	NHDF-Ad	bronchial
14	chr9:110000600-110003400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr9:110000800-110002200	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr9:110000800-110003600	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr9:110001000-110001200	Enhancers	H9 Cell Line	embryonic stem cell
18	chr9:110001000-110001200	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr9:110001200-110001800	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr9:110001200-110002000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr9:110001400-110001800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr9:110001400-110002200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr9:110001400-110002400	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr9:110001400-110002400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr9:110001600-110002400	Enhancers	HepG2	liver
26	chr9:110001800-110002000	Enhancers	H1 Cell Line	embryonic stem cell
27	chr9:110001800-110002000	Enhancers	H9 Cell Line	embryonic stem cell
28	chr9:110001800-110002200	Enhancers	Fetal Kidney	kidney
29	chr9:110001800-110002400	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr9:110001800-110002400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr9:110001800-110002400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr9:110001800-110006000	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr9:110002000-110002200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr9:110002000-110002400	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr9:110002000-110002400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr9:110002000-110005000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr9:110002000-110010000	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr9:110002000-110011400	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr9:110002200-110002400	Enhancers	Muscle Satellite Cultured Cells	--
40	chr9:110002200-110002800	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr9:110002200-110003200	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr9:110002200-110003400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr9:110002200-110003400	Weak transcription	Fetal Kidney	kidney
44	chr9:110002400-110003200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr9:110002400-110003400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr9:110002400-110003800	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr9:110002400-110005000	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr9:110002400-110005600	Weak transcription	HepG2	liver
49	chr9:110002400-110006000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr9:110002400-110006000	Weak transcription	Muscle Satellite Cultured Cells	--

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