Variant report

Variant	nsv892060
Chromosome Location	chr9:2218129-2261944
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1020)
CpG islands
(count:368)
Chromatin interactive
region (count:25)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1020 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:2241752-2242185	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:2241873-2242174	K562	blood:	n/a	n/a
3	ATF2	chr9:2241526-2242216	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr9:2229291-2229713	GM12878	blood:	n/a	n/a
5	ATF2	chr9:2241499-2242598	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr9:2241813-2242242	GM12878	blood:	n/a	n/a
7	ATF2	chr9:2241795-2242260	GM12878	blood:	n/a	n/a
8	ATF2	chr9:2229314-2229763	GM12878	blood:	n/a	n/a
9	ATF3	chr9:2241780-2242300	A549	lung:	n/a	n/a
10	BACH1	chr9:2241631-2242354	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr9:2230017-2230285	GM12878	blood:	n/a	chr9:2230183-2230193 chr9:2230182-2230193
12	BCL11A	chr9:2241903-2242115	GM12878	blood:	n/a	n/a
13	BCL3	chr9:2241690-2242337	A549	lung:	n/a	n/a
14	BCL3	chr9:2241755-2242399	A549	lung:	n/a	n/a
15	BCLAF1	chr9:2241790-2242233	GM12878	blood:	n/a	n/a
16	BCLAF1	chr9:2229240-2229763	GM12878	blood:	n/a	chr9:2229561-2229570
17	BCLAF1	chr9:2241766-2242280	GM12878	blood:	n/a	n/a
18	BHLHE40	chr9:2241927-2242471	GM12878	blood:	n/a	n/a
19	BHLHE40	chr9:2241822-2242611	HepG2	liver:	n/a	n/a
20	BHLHE40	chr9:2241630-2242313	K562	blood:	n/a	n/a
21	BRCA1	chr9:2242326-2242348	GM12878	blood:	n/a	n/a
22	BRCA1	chr9:2241818-2242305	H1-hESC	embryonic stem cell:	n/a	n/a
23	CBX3	chr9:2241820-2242161	K562	blood:	n/a	n/a
24	CBX3	chr9:2241713-2242381	HCT-116	colon:	n/a	n/a
25	CBX3	chr9:2241725-2242505	HCT-116	colon:	n/a	n/a
26	CBX3	chr9:2260466-2261875	HCT-116	colon:	n/a	n/a
27	CBX3	chr9:2260461-2261583	HCT-116	colon:	n/a	n/a
28	CCNT2	chr9:2241616-2242096	K562	blood:	n/a	n/a
29	CEBPB	chr9:2227505-2227839	H1-hESC	embryonic stem cell:	n/a	chr9:2227644-2227655
30	CEBPB	chr9:2241958-2242358	IMR90	lung:	n/a	n/a
31	CEBPB	chr9:2228100-2228461	ECC-1	luminal epithelium:	n/a	n/a
32	CEBPB	chr9:2227480-2227815	MCF-7	breast:	n/a	chr9:2227644-2227655
33	CEBPB	chr9:2228159-2228502	A549	lung:	n/a	n/a
34	CEBPB	chr9:2227489-2227810	K562	blood:	n/a	chr9:2227644-2227655
35	CEBPB	chr9:2241906-2242117	GM12878	blood:	n/a	n/a
36	CEBPB	chr9:2228170-2228469	A549	lung:	n/a	n/a
37	CEBPB	chr9:2228196-2228506	IMR90	lung:	n/a	n/a
38	CEBPB	chr9:2227487-2227843	HepG2	liver:	n/a	chr9:2227644-2227655
39	CEBPB	chr9:2227460-2227833	IMR90	lung:	n/a	chr9:2227644-2227655
40	CEBPB	chr9:2260562-2261566	HCT-116	colon:	n/a	n/a
41	CEBPB	chr9:2228058-2228601	A549	lung:	n/a	n/a
42	CEBPB	chr9:2244293-2244527	A549	lung:	n/a	chr9:2244415-2244426
43	CEBPB	chr9:2241419-2242557	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr9:2244398-2244576	H1-hESC	embryonic stem cell:	n/a	chr9:2244415-2244426
45	CEBPB	chr9:2241880-2242260	A549	lung:	n/a	n/a
46	CEBPB	chr9:2228058-2228629	HCT-116	colon:	n/a	n/a
47	CEBPB	chr9:2244301-2244558	HepG2	liver:	n/a	chr9:2244415-2244426
48	CEBPB	chr9:2227485-2227803	Hela-S3	cervix:	n/a	chr9:2227644-2227655
49	CEBPB	chr9:2228177-2228478	ECC-1	luminal epithelium:	n/a	n/a
50	CEBPB	chr9:2228094-2228527	H1-hESC	embryonic stem cell:	n/a	n/a

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:2241688-2241738	ECC-1	luminal epithelium:	n/a
2	chr9:2239671-2239721	HRCEpiC	kidney:	n/a
3	chr9:2241688-2241738	ECC-1	luminal epithelium:	n/a
4	chr9:2239671-2239721	HRCEpiC	kidney:	n/a
5	chr9:2239671-2239721	BE2_C	brain:	n/a
6	chr9:2241256-2241306	PANC-1	pancreas:	n/a
7	chr9:2242468-2242518	SK-N-SH_RA	brain:	n/a
8	chr9:2234921-2234971	HRCEpiC	kidney:	n/a
9	chr9:2241892-2241942	HUVEC	blood vessel:	n/a
10	chr9:2234921-2234971	PANC-1	pancreas:	n/a
11	chr9:2242468-2242518	HCPEpiC	choroid plexus:	n/a
12	chr9:2241892-2241942	HEK293	kidney:	embryo
13	chr9:2241892-2241942	AoSMC	blood vessel:	n/a
14	chr9:2241892-2241942	NH-A	brain:	n/a
15	chr9:2239671-2239721	HRPEpiC	eye:	n/a
16	chr9:2242468-2242518	HNPCEpiC	eye:	n/a
17	chr9:2241688-2241738	HAEpiC	amniotic membrane:	n/a
18	chr9:2241892-2241942	PrEC	prostate:	n/a
19	chr9:2239671-2239721	IMR90	lung:	fetal
20	chr9:2241688-2241738	HL-60	blood:	n/a
21	chr9:2242468-2242518	AG04449	skin:	fetal
22	chr9:2234921-2234971	Hepatocyte	liver:	n/a
23	chr9:2241892-2241942	H1-hESC	embryonic stem cell:	embryo
24	chr9:2241892-2241942	K562	blood:	n/a
25	chr9:2234921-2234971	AG09319	gingival:	n/a
26	chr9:2241688-2241738	LNCaP	prostate:	n/a
27	chr9:2242468-2242518	Jurkat	blood:	n/a
28	chr9:2241256-2241306	IMR90	lung:	fetal
29	chr9:2239671-2239721	NHBE	bronchial:	n/a
30	chr9:2234921-2234971	HRPEpiC	eye:	n/a
31	chr9:2239671-2239721	NT2-D1	testis:	n/a
32	chr9:2241688-2241738	HCF	heart:	n/a
33	chr9:2241256-2241306	LNCaP	prostate:	n/a
34	chr9:2241688-2241738	GM12891	blood:	n/a
35	chr9:2239671-2239721	HCT-116	colon:	n/a
36	chr9:2234921-2234971	HCF	heart:	n/a
37	chr9:2242468-2242518	PrEC	prostate:	n/a
38	chr9:2241892-2241942	BE2_C	brain:	n/a
39	chr9:2241688-2241738	PFSK-1	brain:	n/a
40	chr9:2241256-2241306	HEK293	kidney:	embryo
41	chr9:2239671-2239721	HCF	heart:	n/a
42	chr9:2241256-2241306	HCPEpiC	choroid plexus:	n/a
43	chr9:2242468-2242518	T-47D	breast:	n/a
44	chr9:2241256-2241306	HRCEpiC	kidney:	n/a
45	chr9:2239671-2239721	HCM	heart:	n/a
46	chr9:2239671-2239721	AG10803	skin:	n/a
47	chr9:2242468-2242518	GM12878	blood:	n/a
48	chr9:2242468-2242518	HIPEpiC	eye:	n/a
49	chr9:2242468-2242518	RPTEC	kidney:	n/a
50	chr9:2241892-2241942	HRPEpiC	eye:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:2228114..2228719-chr9:2625246..2626097,2	MCF-7	breast:
2	chr9:2229879..2232148-chr9:2238435..2240178,2	K562	blood:
3	chr9:2226247..2228750-chr9:2234155..2236078,2	MCF-7	breast:
4	chr9:2255030..2255773-chr9:2600478..2601011,2	MCF-7	breast:
5	chr9:2231807..2233920-chr9:2241447..2243691,2	MCF-7	breast:
6	chr9:2242145..2244162-chr9:2246197..2248614,2	MCF-7	breast:
7	chr9:2229721..2232093-chr9:2241469..2243158,2	MCF-7	breast:
8	chr9:2256748..2259220-chr9:2292192..2293911,2	MCF-7	breast:
9	chr9:2244966..2246945-chr9:2263682..2266605,2	MCF-7	breast:
10	chr9:2217416..2220117-chr9:2231617..2233140,2	MCF-7	breast:
11	chr9:2016060..2018467-chr9:2241276..2243249,2	K562	blood:
12	chr9:2257367..2260216-chr9:2810940..2813820,2	MCF-7	breast:
13	chr9:2231807..2233920-chr9:2241447..2243691,2	MCF-7	breast:
14	chr9:2243537..2246838-chr9:2247520..2250621,4	MCF-7	breast:
15	chr9:2240721..2243292-chr9:2621569..2623384,2	MCF-7	breast:
16	chr9:2232135..2233681-chr9:2242107..2243678,2	MCF-7	breast:
17	chr9:2216988..2218532-chr9:2223642..2225471,2	MCF-7	breast:
18	chr9:2216988..2218532-chr9:2223642..2225471,2	MCF-7	breast:
19	chr9:2242145..2244162-chr9:2246197..2248614,2	MCF-7	breast:
20	chr9:2243537..2246838-chr9:2247520..2250621,4	MCF-7	breast:
21	chr9:2226247..2228750-chr9:2234155..2236078,2	MCF-7	breast:
22	chr9:2217416..2220117-chr9:2231617..2233140,2	MCF-7	breast:
23	chr9:2229879..2232148-chr9:2238435..2240178,2	K562	blood:
24	chr9:2229721..2232093-chr9:2241469..2243158,2	MCF-7	breast:
25	chr9:2232135..2233681-chr9:2242107..2243678,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIAA0020-6	chr9:2228963-2229241	NONHSAT129990

No data

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

Extended variants
information (count: 2539 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:2539 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17455320	chr9:2218129-2218130	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs531691372	chr9:2218136-2218137	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs551476170	chr9:2218147-2218148	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs10115148	chr9:2218152-2218153	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs191834474	chr9:2218158-2218159	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs370355991	chr9:2218159-2218160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs558939747	chr9:2218165-2218166	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs566302820	chr9:2218166-2218167	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs535201402	chr9:2218193-2218194	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs16938040	chr9:2218209-2218210	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs575236437	chr9:2218222-2218223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs377587578	chr9:2218284-2218285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs147072894	chr9:2218338-2218339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs183469572	chr9:2218374-2218375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs72614069	chr9:2218423-2218424	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs10811655	chr9:2218425-2218426	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs73641015	chr9:2218497-2218498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs529444939	chr9:2218499-2218500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs548583602	chr9:2218507-2218508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs140952966	chr9:2218557-2218558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs75020510	chr9:2218661-2218662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs187242468	chr9:2218715-2218716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs114615806	chr9:2218728-2218729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551391256	chr9:2218734-2218735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs190970679	chr9:2218752-2218753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs571271523	chr9:2218766-2218767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs533077835	chr9:2218770-2218771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs546443267	chr9:2218778-2218779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs370940963	chr9:2218793-2218794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs535677856	chr9:2218832-2218833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs76194272	chr9:2218839-2218840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs564308437	chr9:2218852-2218853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs13294554	chr9:2218854-2218855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs545915048	chr9:2218885-2218886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs563165523	chr9:2218900-2218901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531896655	chr9:2218901-2218902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs186601370	chr9:2218910-2218911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs577686741	chr9:2218928-2218929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs534502720	chr9:2218934-2218935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs138096927	chr9:2218964-2218965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs368809670	chr9:2218969-2218970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs543252447	chr9:2218987-2218988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs562919815	chr9:2218989-2218990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs371509278	chr9:2218990-2218991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570914585	chr9:2219003-2219004	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576495421	chr9:2219036-2219037	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545070800	chr9:2219124-2219125	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs373668545	chr9:2219137-2219138	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs564938803	chr9:2219173-2219174	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs527639259	chr9:2219190-2219191	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

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

Chromatin state (count:899 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:2191600-2221200	Weak transcription	Gastric	stomach
2	chr9:2210600-2219000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr9:2217000-2218200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr9:2217600-2219400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr9:2219000-2219400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr9:2219400-2223000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr9:2221200-2223000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr9:2223000-2223200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr9:2223000-2223600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
10	chr9:2223000-2224600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr9:2223200-2228400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr9:2223600-2240800	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr9:2224600-2229400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr9:2225600-2228400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr9:2226800-2227800	Enhancers	Ovary	ovary
16	chr9:2226800-2229000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr9:2227000-2228000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr9:2227000-2228000	Enhancers	Osteobl	bone
19	chr9:2227200-2227400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr9:2227200-2227800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr9:2227200-2227800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr9:2227200-2227800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr9:2227200-2227800	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr9:2227200-2228000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr9:2227200-2229200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr9:2227400-2234400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr9:2227600-2227800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr9:2227600-2227800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr9:2227600-2229400	Enhancers	Pancreas	Pancrea
30	chr9:2227800-2229400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr9:2227800-2230200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr9:2227800-2231400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr9:2227800-2231600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr9:2227800-2231600	Weak transcription	Ovary	ovary
35	chr9:2227800-2234400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr9:2228000-2228400	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr9:2228000-2229000	Enhancers	Primary neutrophils fromperipheralblood	blood
38	chr9:2228000-2229800	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr9:2228000-2231000	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr9:2228000-2231200	Weak transcription	Osteobl	bone
41	chr9:2228000-2231400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr9:2228000-2234600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr9:2228200-2229200	Enhancers	Primary B cells from cord blood	blood
44	chr9:2228200-2229200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr9:2228200-2229400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
46	chr9:2228200-2229600	Enhancers	Right Atrium	heart
47	chr9:2228200-2229800	Enhancers	HMEC	breast
48	chr9:2228200-2230400	Enhancers	Primary B cells from peripheral blood	blood
49	chr9:2228400-2229200	Enhancers	Fetal Thymus	thymus
50	chr9:2228400-2229200	Enhancers	Spleen	Spleen

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