Variant report

Variant	nsv892652
Chromosome Location	chr9:16843128-16958312
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr9:16870940-16871146	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr9:16934628-16934951	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr9:16870063-16870262	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr9:16934659-16934853	K562	blood:	n/a	n/a
5	BCL3	chr9:16921833-16922234	A549	lung:	n/a	chr9:16922220-16922229
6	BRCA1	chr9:16870026-16870092	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr9:16865182-16865443	IMR90	lung:	n/a	n/a
8	CEBPB	chr9:16901687-16902029	IMR90	lung:	n/a	chr9:16901848-16901859
9	CEBPB	chr9:16870607-16870634	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr9:16885265-16885574	Hela-S3	cervix:	n/a	chr9:16885528-16885541
11	CEBPB	chr9:16873187-16873697	Hela-S3	cervix:	n/a	chr9:16873434-16873445
12	CEBPB	chr9:16868084-16868399	H1-hESC	embryonic stem cell:	n/a	chr9:16868232-16868241 chr9:16868232-16868243 chr9:16868230-16868241
13	CEBPB	chr9:16939818-16939821	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr9:16868060-16868408	A549	lung:	n/a	chr9:16868232-16868241 chr9:16868232-16868243 chr9:16868230-16868241
15	CEBPB	chr9:16868064-16868414	HepG2	liver:	n/a	chr9:16868232-16868241 chr9:16868232-16868243 chr9:16868230-16868241
16	CEBPB	chr9:16884994-16885796	IMR90	lung:	n/a	chr9:16885528-16885541
17	CEBPB	chr9:16850629-16850828	H1-hESC	embryonic stem cell:	n/a	chr9:16850746-16850757
18	CEBPB	chr9:16901728-16901993	A549	lung:	n/a	chr9:16901848-16901859
19	CEBPB	chr9:16927604-16927635	HepG2	liver:	n/a	n/a
20	CEBPB	chr9:16901588-16902121	A549	lung:	n/a	chr9:16901848-16901859
21	CEBPB	chr9:16850699-16850775	Hela-S3	cervix:	n/a	chr9:16850746-16850757
22	CEBPB	chr9:16923221-16923363	IMR90	lung:	n/a	n/a
23	CEBPB	chr9:16868041-16868355	ECC-1	luminal epithelium:	n/a	chr9:16868232-16868241 chr9:16868232-16868243 chr9:16868230-16868241
24	CEBPB	chr9:16850597-16850910	IMR90	lung:	n/a	chr9:16850746-16850757
25	CEBPB	chr9:16867953-16868427	IMR90	lung:	n/a	chr9:16868232-16868241 chr9:16868232-16868243 chr9:16868230-16868241
26	CEBPB	chr9:16850575-16850932	HepG2	liver:	n/a	chr9:16850746-16850757
27	CEBPB	chr9:16850582-16850900	A549	lung:	n/a	chr9:16850746-16850757
28	CEBPB	chr9:16901689-16902044	Hela-S3	cervix:	n/a	chr9:16901848-16901859
29	CEBPB	chr9:16849320-16849487	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr9:16880221-16880332	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr9:16873229-16873384	A549	lung:	n/a	n/a
32	CEBPB	chr9:16868029-16868431	Hela-S3	cervix:	n/a	chr9:16868232-16868241 chr9:16868232-16868243 chr9:16868230-16868241
33	CEBPB	chr9:16868049-16868429	ECC-1	luminal epithelium:	n/a	chr9:16868232-16868241 chr9:16868232-16868243 chr9:16868230-16868241
34	CEBPB	chr9:16848154-16848536	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr9:16867927-16868542	A549	lung:	n/a	chr9:16868232-16868241 chr9:16868232-16868243 chr9:16868230-16868241
36	CEBPB	chr9:16868014-16868463	A549	lung:	n/a	chr9:16868232-16868241 chr9:16868232-16868243 chr9:16868230-16868241
37	CEBPB	chr9:16868073-16868432	MCF-7	breast:	n/a	chr9:16868232-16868241 chr9:16868232-16868243 chr9:16868230-16868241
38	CEBPB	chr9:16873182-16873748	IMR90	lung:	n/a	chr9:16873434-16873445
39	CHD1	chr9:16869619-16870710	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD1	chr9:16871612-16872256	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD1	chr9:16871061-16871345	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr9:16921955-16922155	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr9:16870873-16871230	H1-hESC	embryonic stem cell:	n/a	chr9:16871004-16871014
44	CHD2	chr9:16871622-16871908	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr9:16870578-16870957	A549	lung:	n/a	n/a
46	CTBP2	chr9:16869579-16870832	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr9:16922080-16922230	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr9:16870631-16870745	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr9:16870616-16870783	A549	lung:	n/a	n/a
50	CTCF	chr9:16866780-16866930	AG09319	gingival:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:16875612-16875662	GM06990	blood:	n/a
2	chr9:16875612-16875662	GM06990	blood:	n/a
3	chr9:16872192-16872242	HPAEpiC	pulmonary alveolar:	n/a
4	chr9:16871185-16871235	ProgFib	skin:	n/a
5	chr9:16871106-16871156	T-47D	breast:	n/a
6	chr9:16870464-16870514	K562	blood:	n/a
7	chr9:16868891-16868941	T-47D	breast:	n/a
8	chr9:16870464-16870514	PFSK-1	brain:	n/a
9	chr9:16872192-16872242	Hela-S3	cervix:	n/a
10	chr9:16871185-16871235	SK-N-MC	brain:	n/a
11	chr9:16870091-16870141	SK-N-MC	brain:	n/a
12	chr9:16871185-16871235	AG04450	lung:	fetal
13	chr9:16871185-16871235	Hela-S3	cervix:	n/a
14	chr9:16868891-16868941	GM12891	blood:	n/a
15	chr9:16870464-16870514	HepG2	liver:	n/a
16	chr9:16870091-16870141	ECC-1	luminal epithelium:	n/a
17	chr9:16870091-16870141	HUVEC	blood vessel:	n/a
18	chr9:16870091-16870141	AG09319	gingival:	n/a
19	chr9:16870464-16870514	HCPEpiC	choroid plexus:	n/a
20	chr9:16868891-16868941	Hepatocyte	liver:	n/a
21	chr9:16870464-16870514	SK-N-MC	brain:	n/a
22	chr9:16870464-16870514	T-47D	breast:	n/a
23	chr9:16864746-16864796	HAEpiC	amniotic membrane:	n/a
24	chr9:16870464-16870514	MCF10A-Er-Src	breast:	n/a
25	chr9:16868891-16868941	SKMC	muscle:	n/a
26	chr9:16871106-16871156	NT2-D1	testis:	n/a
27	chr9:16871185-16871235	AoSMC	blood vessel:	n/a
28	chr9:16868891-16868941	AoSMC	blood vessel:	n/a
29	chr9:16870893-16870943	HEK293	kidney:	embryo
30	chr9:16870289-16870339	HCPEpiC	choroid plexus:	n/a
31	chr9:16868891-16868941	SK-N-SH	brain:	n/a
32	chr9:16870464-16870514	HCT-116	colon:	n/a
33	chr9:16870289-16870339	HCF	heart:	n/a
34	chr9:16875612-16875662	HRCEpiC	kidney:	n/a
35	chr9:16864746-16864796	AoSMC	blood vessel:	n/a
36	chr9:16864746-16864796	ovcar-3	ovarian:	n/a
37	chr9:16870464-16870514	Hela-S3	cervix:	n/a
38	chr9:16870091-16870141	HRE	kidney:	n/a
39	chr9:16864746-16864796	SKMC	muscle:	n/a
40	chr9:16871106-16871156	GM06990	blood:	n/a
41	chr9:16864746-16864796	MCF-7	breast:	n/a
42	chr9:16870091-16870141	A549	lung:	n/a
43	chr9:16864746-16864796	GM06990	blood:	n/a
44	chr9:16864746-16864796	SK-N-SH	brain:	n/a
45	chr9:16870893-16870943	HRCEpiC	kidney:	n/a
46	chr9:16875612-16875662	HEK293	kidney:	embryo
47	chr9:16864746-16864796	SAEC	small airway:	n/a
48	chr9:16872192-16872242	GM06990	blood:	n/a
49	chr9:16875612-16875662	PFSK-1	brain:	n/a
50	chr9:16870893-16870943	LNCaP	prostate:	n/a

Variant related genes	Relation type
BNC2	TF binding region
BNC2	CpG island

Extended variants
information (count: 4927 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:4927 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10810644	chr9:16843128-16843129	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs76267904	chr9:16843132-16843133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs10962634	chr9:16843134-16843135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs368988622	chr9:16843155-16843156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs144859992	chr9:16843214-16843215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs566589564	chr9:16843237-16843238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs538668488	chr9:16843238-16843239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs148555272	chr9:16843262-16843263	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs546751646	chr9:16843275-16843276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs115111380	chr9:16843279-16843280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs374822504	chr9:16843307-16843308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs112076753	chr9:16843342-16843343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs10756817	chr9:16843384-16843385	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs551036061	chr9:16843386-16843387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs141960084	chr9:16843421-16843422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs539815393	chr9:16843425-16843426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs74884666	chr9:16843460-16843461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs570718318	chr9:16843462-16843463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534917422	chr9:16843490-16843491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs372257276	chr9:16843532-16843533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs553175383	chr9:16843549-16843550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs375759895	chr9:16843596-16843597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574699644	chr9:16843601-16843602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs369854023	chr9:16843612-16843613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs535325893	chr9:16843618-16843619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs556996259	chr9:16843624-16843625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs569091274	chr9:16843638-16843639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575294017	chr9:16843645-16843646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574783943	chr9:16843666-16843667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs545777385	chr9:16843699-16843700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201212048	chr9:16843723-16843724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs563750428	chr9:16843726-16843727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs573157835	chr9:16843750-16843751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs10962635	chr9:16843773-16843774	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs560276497	chr9:16843781-16843782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs562076013	chr9:16843783-16843784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs140832640	chr9:16843803-16843804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs144578796	chr9:16843870-16843871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147877531	chr9:16843907-16843908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs533275735	chr9:16843911-16843912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs187787700	chr9:16843934-16843935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs191094634	chr9:16843952-16843953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs139278601	chr9:16843955-16843956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs183606407	chr9:16843960-16843961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs955138	chr9:16843999-16844000	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs535637162	chr9:16844030-16844031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs149955217	chr9:16844031-16844032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs575260729	chr9:16844034-16844035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs377344980	chr9:16844070-16844071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs145128885	chr9:16844075-16844076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
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
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	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
Breast cancer	21611746	CNVD
Pancreatic cancer	21811587	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1016 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:16829200-16852800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:16829800-16864200	Weak transcription	NH-A	brain
3	chr9:16831000-16859600	Weak transcription	HSMM	muscle
4	chr9:16831200-16852600	Weak transcription	Fetal Lung	lung
5	chr9:16831200-16863400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr9:16831200-16864400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr9:16833800-16863800	Weak transcription	NHLF	lung
8	chr9:16834600-16852600	Weak transcription	Fetal Stomach	stomach
9	chr9:16835200-16848400	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr9:16836200-16864400	Weak transcription	NHDF-Ad	bronchial
11	chr9:16838800-16852000	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr9:16839200-16846400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr9:16840400-16852000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr9:16840600-16849400	Weak transcription	Ovary	ovary
15	chr9:16841000-16848200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr9:16842200-16852000	Weak transcription	Colon Smooth Muscle	Colon
17	chr9:16842600-16843200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr9:16843000-16853200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr9:16843200-16843400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr9:16843400-16850600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr9:16844800-16845200	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr9:16845200-16849600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr9:16846000-16851200	Weak transcription	Fetal Muscle Leg	muscle
24	chr9:16846400-16846600	Enhancers	H1 Cell Line	embryonic stem cell
25	chr9:16846400-16846600	Enhancers	H9 Cell Line	embryonic stem cell
26	chr9:16846400-16846600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr9:16846400-16846600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr9:16846400-16846600	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr9:16846600-16848200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr9:16846600-16852000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr9:16846600-16852800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr9:16847000-16848200	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr9:16848000-16849400	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr9:16848200-16848600	Enhancers	H1 Cell Line	embryonic stem cell
35	chr9:16848200-16848600	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr9:16848200-16848600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr9:16848200-16848600	Enhancers	Fetal Kidney	kidney
38	chr9:16848200-16849000	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr9:16848400-16848800	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr9:16848400-16852800	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr9:16848600-16852000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr9:16848600-16852600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr9:16848600-16852800	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr9:16848800-16852400	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr9:16849000-16852600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr9:16849400-16849800	Enhancers	Ovary	ovary
47	chr9:16849400-16852400	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr9:16849600-16849800	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr9:16849800-16850200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr9:16849800-16850600	Weak transcription	Ovary	ovary

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