Variant report

Variant	nsv524381
Chromosome Location	chr9:15165032-15202417
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:69)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:69 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr9:15180159-15180457	GM12878	blood:	n/a	n/a
2	CEBPB	chr9:15180457-15180756	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr9:15186752-15186814	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTCF	chr9:15165620-15165770	A549	lung:	n/a	n/a
5	CTCF	chr9:15183935-15183943	ProgFib	skin:	n/a	n/a
6	CTCF	chr9:15178485-15178562	MCF-7	breast:	n/a	n/a
7	CTCF	chr9:15189563-15189731	HUVEC	blood vessel:	n/a	n/a
8	CTCF	chr9:15178460-15178610	GM12866	blood:	n/a	n/a
9	CTCF	chr9:15178479-15178547	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr9:15165660-15165810	HEK293	kidney:	n/a	n/a
11	CTCF	chr9:15201419-15201453	Fibrobl	skin:	n/a	n/a
12	CTCF	chr9:15165760-15165910	GM12873	blood:	n/a	n/a
13	CTCF	chr9:15173620-15173770	Caco-2	colon:	n/a	n/a
14	E2F4	chr9:15188664-15188863	MCF10A-Er-Src	breast:	n/a	n/a
15	E2F4	chr9:15200116-15200316	MCF10A-Er-Src	breast:	n/a	n/a
16	EBF1	chr9:15180068-15180482	GM12878	blood:	n/a	chr9:15180418-15180427 chr9:15180220-15180231
17	EP300	chr9:15182707-15183092	SK-N-SH_RA	brain:	n/a	n/a
18	EP300	chr9:15182004-15182350	SK-N-SH_RA	brain:	n/a	n/a
19	EP300	chr9:15182736-15183852	SK-N-SH	brain:	n/a	chr9:15183546-15183559 chr9:15183464-15183478 chr9:15183465-15183479 chr9:15183463-15183477
20	EP300	chr9:15181638-15182622	SK-N-SH	brain:	n/a	n/a
21	EP300	chr9:15182064-15182331	SK-N-SH_RA	brain:	n/a	n/a
22	FAM48A	chr9:15184842-15185004	GM12878	blood:	n/a	n/a
23	FOS	chr9:15193293-15193541	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr9:15193309-15193604	MCF10A-Er-Src	breast:	n/a	n/a
25	GATA2	chr9:15187586-15187819	SH-SY5Y	brain:	n/a	n/a
26	GATA3	chr9:15183180-15183541	SH-SY5Y	brain:	n/a	n/a
27	GATA3	chr9:15187628-15187723	SH-SY5Y	brain:	n/a	n/a
28	GATA3	chr9:15184386-15184479	SH-SY5Y	brain:	n/a	n/a
29	GATA3	chr9:15186038-15186171	SH-SY5Y	brain:	n/a	n/a
30	IRF3	chr9:15174918-15174923	GM12878	blood:	n/a	n/a
31	MAFF	chr9:15179838-15180038	HepG2	liver:	n/a	n/a
32	MAFF	chr9:15191694-15191859	HepG2	liver:	n/a	chr9:15191777-15191795
33	MAFF	chr9:15181962-15182276	HepG2	liver:	n/a	chr9:15182095-15182113
34	MAFK	chr9:15181943-15182280	HepG2	liver:	n/a	n/a
35	MAFK	chr9:15181946-15182260	HepG2	liver:	n/a	n/a
36	MAFK	chr9:15179850-15180125	HepG2	liver:	n/a	n/a
37	MAFK	chr9:15191633-15191910	HepG2	liver:	n/a	chr9:15191779-15191794
38	MAFK	chr9:15181922-15182279	IMR90	lung:	n/a	n/a
39	MAFK	chr9:15191636-15191923	HepG2	liver:	n/a	chr9:15191779-15191794
40	MAFK	chr9:15179851-15180137	HepG2	liver:	n/a	n/a
41	MEF2A	chr9:15180031-15180437	GM12878	blood:	n/a	chr9:15180234-15180250 chr9:15180230-15180251 chr9:15180235-15180249
42	MXI1	chr9:15182667-15183507	SK-N-SH	brain:	n/a	n/a
43	MXI1	chr9:15197869-15197886	GM12878	blood:	n/a	n/a
44	POLR2A	chr9:15189179-15189183	MCF10A-Er-Src	breast:	n/a	n/a
45	POLR2A	chr9:15186859-15186903	GM12878	blood:	n/a	n/a
46	POLR2A	chr9:15181790-15182598	H1-neurons	neurons:	n/a	n/a
47	POLR2A	chr9:15181810-15182437	H1-neurons	neurons:	n/a	n/a
48	POLR2A	chr9:15194251-15194283	MCF10A-Er-Src	breast:	n/a	n/a
49	POLR2A	chr9:15166477-15166643	MCF10A-Er-Src	breast:	n/a	n/a
50	POLR2A	chr9:15192956-15193072	A549	lung:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:15183958-15184008	AG09319	gingival:	n/a
2	chr9:15183958-15184008	HMEC	breast:	n/a
3	chr9:15183958-15184008	MCF10A-Er-Src	breast:	n/a
4	chr9:15183958-15184008	HRPEpiC	eye:	n/a
5	chr9:15183958-15184008	HL-60	blood:	n/a
6	chr9:15183958-15184008	HCPEpiC	choroid plexus:	n/a
7	chr9:15183958-15184008	GM12878	blood:	n/a
8	chr9:15183958-15184008	HPAEpiC	pulmonary alveolar:	n/a
9	chr9:15183958-15184008	HRE	kidney:	n/a
10	chr9:15183958-15184008	HAEpiC	amniotic membrane:	n/a
11	chr9:15183958-15184008	SAEC	small airway:	n/a
12	chr9:15183958-15184008	ECC-1	luminal epithelium:	n/a
13	chr9:15183958-15184008	ovcar-3	ovarian:	n/a
14	chr9:15183958-15184008	ProgFib	skin:	n/a
15	chr9:15183958-15184008	HEK293	kidney:	embryo
16	chr9:15183958-15184008	GM12892	blood:	n/a
17	chr9:15183958-15184008	GM12891	blood:	n/a
18	chr9:15183958-15184008	HCT-116	colon:	n/a
19	chr9:15183958-15184008	HCM	heart:	n/a
20	chr9:15183958-15184008	AG04449	skin:	fetal
21	chr9:15183958-15184008	PFSK-1	brain:	n/a
22	chr9:15183958-15184008	SK-N-SH_RA	brain:	n/a
23	chr9:15183958-15184008	NB4	blood:	n/a
24	chr9:15183958-15184008	HEEpiC	esophagus:	n/a
25	chr9:15183958-15184008	NT2-D1	testis:	n/a
26	chr9:15183958-15184008	PrEC	prostate:	n/a
27	chr9:15183958-15184008	AG09309	skin:	n/a
28	chr9:15183958-15184008	GM19239	blood:	n/a
29	chr9:15183958-15184008	SK-N-SH	brain:	n/a
30	chr9:15183958-15184008	HNPCEpiC	eye:	n/a
31	chr9:15183958-15184008	Hela-S3	cervix:	n/a
32	chr9:15183958-15184008	AG04450	lung:	fetal
33	chr9:15183958-15184008	Hepatocyte	liver:	n/a
34	chr9:15183958-15184008	A549	lung:	n/a
35	chr9:15183958-15184008	RPTEC	kidney:	n/a
36	chr9:15183958-15184008	BJ	skin:	n/a
37	chr9:15183958-15184008	AG10803	skin:	n/a
38	chr9:15183958-15184008	HUVEC	blood vessel:	n/a
39	chr9:15183958-15184008	IMR90	lung:	fetal
40	chr9:15183958-15184008	Jurkat	blood:	n/a
41	chr9:15183958-15184008	HCF	heart:	n/a
42	chr9:15183958-15184008	LNCaP	prostate:	n/a
43	chr9:15183958-15184008	NHBE	bronchial:	n/a
44	chr9:15183958-15184008	H1-hESC	embryonic stem cell:	embryo
45	chr9:15183958-15184008	HepG2	liver:	n/a
46	chr9:15183958-15184008	SKMC	muscle:	n/a
47	chr9:15183958-15184008	GM06990	blood:	n/a
48	chr9:15183958-15184008	Caco-2	colon:	n/a
49	chr9:15183958-15184008	SK-N-MC	brain:	n/a
50	chr9:15183958-15184008	NH-A	brain:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:94585854..94588550-chr9:15169410..15171976,2	K562	blood:
2	chr9:15163944..15166887-chr9:15170115..15173415,3	K562	blood:
3	chr9:15178556..15180974-chr9:15188192..15191171,2	MCF-7	breast:
4	chr9:15163944..15166887-chr9:15170115..15173415,3	K562	blood:
5	chr9:15178556..15180974-chr9:15188192..15191171,2	MCF-7	breast:
6	chr3:179614969..179615837-chr9:15168720..15169434,2	MCF-7	breast:
7	chr9:15180910..15183220-chr9:15227592..15229851,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TTC39B-1	chr9:15163622-15166031	NONHSAT130260

No data

Variant related genes	Relation type
TTC39B	TF binding region
TTC39B	CpG island

Extended variants
information (count: 1795 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1795 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7026350	chr9:15165032-15165033	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs369708769	chr9:15165042-15165043	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs576432169	chr9:15165063-15165064	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs182994935	chr9:15165071-15165072	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs2800582	chr9:15165075-15165076	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs528548455	chr9:15165083-15165084	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs373824067	chr9:15165120-15165121	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs567398130	chr9:15165137-15165138	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs147271536	chr9:15165142-15165143	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs140688699	chr9:15165143-15165144	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs139589458	chr9:15165147-15165148	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs149707864	chr9:15165157-15165158	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs556908101	chr9:15165167-15165168	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs201022852	chr9:15165168-15165169	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs188532739	chr9:15165188-15165189	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs536102922	chr9:15165202-15165203	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs34002515	chr9:15165204-15165205	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs192751597	chr9:15165219-15165220	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs542637624	chr9:15165227-15165228	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs201573778	chr9:15165243-15165244	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs184705844	chr9:15165280-15165281	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs148473952	chr9:15165321-15165322	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs543525332	chr9:15165329-15165330	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs187636407	chr9:15165386-15165387	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs10961903	chr9:15165399-15165400	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs146431974	chr9:15165406-15165407	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs191587235	chr9:15165437-15165438	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs530396159	chr9:15165452-15165453	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs549035496	chr9:15165503-15165504	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs183771588	chr9:15165519-15165520	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs560072367	chr9:15165605-15165606	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs537948123	chr9:15165611-15165612	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs367975201	chr9:15165623-15165624	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs571310603	chr9:15165627-15165628	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs538500903	chr9:15165644-15165645	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs117321985	chr9:15165665-15165666	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs1830727	chr9:15165736-15165737	Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs542477541	chr9:15165769-15165770	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs541183295	chr9:15165771-15165772	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs554566523	chr9:15165773-15165774	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs576313896	chr9:15165815-15165816	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs189580945	chr9:15165847-15165848	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs140800465	chr9:15165857-15165858	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs548663967	chr9:15165860-15165861	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs115284728	chr9:15165865-15165866	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs932711	chr9:15165877-15165878	Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs559973165	chr9:15165901-15165902	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs181884347	chr9:15165917-15165918	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs702198	chr9:15165935-15165936	Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs560946951	chr9:15165948-15165949	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	19835627	CNVD
early-passage human iPS cells	21368824	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:679 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15155600-15181400	Weak transcription	Rectal Smooth Muscle	rectum
2	chr9:15156200-15185400	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr9:15156400-15171200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr9:15156600-15194200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr9:15156800-15169000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr9:15156800-15170200	Weak transcription	Esophagus	oesophagus
7	chr9:15156800-15170800	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr9:15156800-15173800	Weak transcription	Stomach Smooth Muscle	stomach
9	chr9:15156800-15175600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr9:15156800-15181600	Weak transcription	Fetal Muscle Leg	muscle
11	chr9:15156800-15190400	Weak transcription	Brain Anterior Caudate	brain
12	chr9:15156800-15211800	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr9:15158600-15168000	Weak transcription	Liver	Liver
14	chr9:15158800-15168000	Weak transcription	Aorta	Aorta
15	chr9:15159000-15166600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr9:15159000-15170800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr9:15159000-15177000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr9:15159000-15211200	Weak transcription	HMEC	breast
19	chr9:15159200-15168000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr9:15159200-15169000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr9:15159200-15205800	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr9:15161000-15169000	Weak transcription	Fetal Intestine Large	intestine
23	chr9:15161200-15181400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr9:15161800-15165800	Weak transcription	Primary T cells from cord blood	blood
25	chr9:15162000-15170200	Weak transcription	Ovary	ovary
26	chr9:15162000-15181600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr9:15162000-15183800	Weak transcription	Fetal Intestine Small	intestine
28	chr9:15162800-15168000	Weak transcription	Fetal Brain Female	brain
29	chr9:15162800-15193000	Weak transcription	Spleen	Spleen
30	chr9:15163000-15168000	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr9:15163000-15175200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr9:15163000-15233000	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr9:15163200-15176000	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr9:15163200-15185400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr9:15163200-15186800	Weak transcription	Fetal Kidney	kidney
36	chr9:15163400-15165200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr9:15163400-15179000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr9:15163400-15181400	Weak transcription	Fetal Stomach	stomach
39	chr9:15163800-15185200	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr9:15164000-15170600	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr9:15164200-15169000	Weak transcription	Rectal Mucosa Donor 29	rectum
42	chr9:15164200-15170400	Weak transcription	Primary hematopoietic stem cells	blood
43	chr9:15164400-15178400	Weak transcription	Fetal Brain Male	brain
44	chr9:15164600-15172200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
45	chr9:15164800-15168000	Weak transcription	Primary T helper cells PMA-I stimulated	--
46	chr9:15164800-15169200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr9:15164800-15169200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr9:15164800-15170600	Weak transcription	HepG2	liver
49	chr9:15165000-15170400	Weak transcription	Stomach Mucosa	stomach
50	chr9:15165200-15176600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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