Variant report

Variant	nsv892636
Chromosome Location	chr9:15794858-15876507
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	ARID3A	chr9:15873620-15873926	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:15824460-15824492	HepG2	liver:	n/a	n/a
3	BHLHE40	chr9:15837128-15837398	GM12878	blood:	n/a	n/a
4	CEBPB	chr9:15831451-15831723	Hela-S3	cervix:	n/a	chr9:15831596-15831609
5	CEBPB	chr9:15875974-15876186	A549	lung:	n/a	n/a
6	CEBPB	chr9:15825568-15825724	HepG2	liver:	n/a	chr9:15825609-15825620
7	CEBPB	chr9:15825520-15825732	IMR90	lung:	n/a	chr9:15825609-15825620
8	CEBPB	chr9:15817338-15817562	A549	lung:	n/a	n/a
9	CEBPB	chr9:15803709-15804025	IMR90	lung:	n/a	chr9:15803862-15803873
10	CEBPB	chr9:15850052-15850257	A549	lung:	n/a	chr9:15850110-15850122
11	CEBPB	chr9:15856572-15856992	IMR90	lung:	n/a	n/a
12	CEBPB	chr9:15845846-15845992	A549	lung:	n/a	chr9:15845914-15845927 chr9:15845914-15845925 chr9:15845916-15845925
13	CEBPB	chr9:15845792-15846013	HepG2	liver:	n/a	chr9:15845914-15845927 chr9:15845914-15845925 chr9:15845916-15845925
14	CEBPB	chr9:15863418-15863420	A549	lung:	n/a	n/a
15	CEBPB	chr9:15817342-15817541	IMR90	lung:	n/a	n/a
16	CEBPB	chr9:15845785-15846037	MCF-7	breast:	n/a	chr9:15845914-15845927 chr9:15845914-15845925 chr9:15845916-15845925
17	CEBPB	chr9:15845758-15846062	IMR90	lung:	n/a	chr9:15845914-15845927 chr9:15845914-15845925 chr9:15845916-15845925
18	CEBPB	chr9:15831422-15831741	ECC-1	luminal epithelium:	n/a	chr9:15831596-15831609
19	CEBPB	chr9:15803721-15803998	HepG2	liver:	n/a	chr9:15803862-15803873
20	CEBPB	chr9:15803787-15803977	A549	lung:	n/a	chr9:15803862-15803873
21	CEBPB	chr9:15831522-15831716	A549	lung:	n/a	chr9:15831596-15831609
22	CTCF	chr9:15839500-15839650	HMF	breast:	n/a	n/a
23	CTCF	chr9:15837220-15837370	Hela-S3	cervix:	n/a	chr9:15837266-15837274 chr9:15837261-15837279 chr9:15837262-15837278 chr9:15837263-15837284
24	CTCF	chr9:15837164-15837341	ProgFib	skin:	n/a	chr9:15837266-15837274 chr9:15837261-15837279 chr9:15837262-15837278 chr9:15837263-15837284
25	CTCF	chr9:15873760-15873910	HMEC	breast:	n/a	n/a
26	CTCF	chr9:15837140-15837290	HCM	heart:	n/a	chr9:15837266-15837274 chr9:15837261-15837279 chr9:15837262-15837278 chr9:15837263-15837284
27	CTCF	chr9:15824397-15824590	Gliobla	brain:	n/a	chr9:15824497-15824515 chr9:15824499-15824512
28	CTCF	chr9:15873591-15873942	K562	blood:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
29	CTCF	chr9:15837160-15837310	AoAF	blood vessel:	n/a	chr9:15837266-15837274 chr9:15837261-15837279 chr9:15837262-15837278 chr9:15837263-15837284
30	CTCF	chr9:15837200-15837350	AG09319	gingival:	n/a	chr9:15837266-15837274 chr9:15837261-15837279 chr9:15837262-15837278 chr9:15837263-15837284
31	CTCF	chr9:15839500-15839650	RPTEC	kidney:	n/a	n/a
32	CTCF	chr9:15873680-15873830	HEK293	kidney:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
33	CTCF	chr9:15873700-15873850	Caco-2	colon:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
34	CTCF	chr9:15873700-15873850	GM12875	blood:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
35	CTCF	chr9:15837120-15837270	WI-38	lung:	n/a	n/a
36	CTCF	chr9:15824460-15824610	AG09319	gingival:	n/a	chr9:15824497-15824515 chr9:15824499-15824512
37	CTCF	chr9:15837020-15837402	A549	lung:	n/a	chr9:15837266-15837274 chr9:15837261-15837279 chr9:15837262-15837278 chr9:15837263-15837284
38	CTCF	chr9:15837180-15837330	RPTEC	kidney:	n/a	chr9:15837266-15837274 chr9:15837261-15837279 chr9:15837262-15837278 chr9:15837263-15837284
39	CTCF	chr9:15837168-15837358	GM13976	blood:	n/a	chr9:15837266-15837274 chr9:15837261-15837279 chr9:15837262-15837278 chr9:15837263-15837284
40	CTCF	chr9:15873688-15873884	A549	lung:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
41	CTCF	chr9:15824368-15824613	H1-hESC	embryonic stem cell:	n/a	chr9:15824497-15824515 chr9:15824499-15824512
42	CTCF	chr9:15837180-15837330	HPAF	blood vessel:	n/a	chr9:15837266-15837274 chr9:15837261-15837279 chr9:15837262-15837278 chr9:15837263-15837284
43	CTCF	chr9:15873571-15873980	GM12878	blood:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
44	CTCF	chr9:15837186-15837310	Fibrobl	skin:	n/a	chr9:15837266-15837274 chr9:15837261-15837279 chr9:15837262-15837278 chr9:15837263-15837284
45	CTCF	chr9:15873600-15873750	A549	lung:	n/a	n/a
46	CTCF	chr9:15873585-15873983	IMR90	lung:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
47	CTCF	chr9:15824402-15824574	HepG2	liver:	n/a	chr9:15824497-15824515 chr9:15824499-15824512
48	CTCF	chr9:15824320-15824470	RPTEC	kidney:	n/a	n/a
49	CTCF	chr9:15873653-15873884	GM10266	blood:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
50	CTCF	chr9:15852080-15852230	HPAF	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:15810627-15810677	HMEC	breast:	n/a
2	chr9:15810627-15810677	PANC-1	pancreas:	n/a
3	chr9:15810627-15810677	HUVEC	blood vessel:	n/a
4	chr9:15810627-15810677	ovcar-3	ovarian:	n/a
5	chr9:15810627-15810677	T-47D	breast:	n/a
6	chr9:15810627-15810677	PFSK-1	brain:	n/a
7	chr9:15810627-15810677	BJ	skin:	n/a
8	chr9:15810627-15810677	AG10803	skin:	n/a
9	chr9:15810627-15810677	AG09319	gingival:	n/a
10	chr9:15810627-15810677	HCM	heart:	n/a
11	chr9:15810627-15810677	SK-N-SH	brain:	n/a
12	chr9:15810627-15810677	Hepatocyte	liver:	n/a
13	chr9:15810627-15810677	H1-hESC	embryonic stem cell:	embryo
14	chr9:15810627-15810677	NHDF-neo	bronchial:	n/a
15	chr9:15810627-15810677	HRPEpiC	eye:	n/a
16	chr9:15810627-15810677	HPAEpiC	pulmonary alveolar:	n/a
17	chr9:15810627-15810677	NH-A	brain:	n/a
18	chr9:15810627-15810677	NHBE	bronchial:	n/a
19	chr9:15810627-15810677	AG09309	skin:	n/a
20	chr9:15810627-15810677	HAEpiC	amniotic membrane:	n/a
21	chr9:15810627-15810677	K562	blood:	n/a
22	chr9:15810627-15810677	HepG2	liver:	n/a
23	chr9:15810627-15810677	SK-N-SH_RA	brain:	n/a
24	chr9:15810627-15810677	HRCEpiC	kidney:	n/a
25	chr9:15810627-15810677	GM12891	blood:	n/a
26	chr9:15810627-15810677	AG04449	skin:	fetal
27	chr9:15810627-15810677	U87	brain:	n/a
28	chr9:15810627-15810677	GM12892	blood:	n/a
29	chr9:15810627-15810677	HL-60	blood:	n/a
30	chr9:15810627-15810677	GM06990	blood:	n/a
31	chr9:15810627-15810677	HRE	kidney:	n/a
32	chr9:15810627-15810677	HCPEpiC	choroid plexus:	n/a
33	chr9:15810627-15810677	NT2-D1	testis:	n/a
34	chr9:15810627-15810677	HEK293	kidney:	embryo
35	chr9:15810627-15810677	HEEpiC	esophagus:	n/a
36	chr9:15810627-15810677	IMR90	lung:	fetal
37	chr9:15810627-15810677	LNCaP	prostate:	n/a
38	chr9:15810627-15810677	AG04450	lung:	fetal
39	chr9:15810627-15810677	Hela-S3	cervix:	n/a
40	chr9:15810627-15810677	Caco-2	colon:	n/a
41	chr9:15810627-15810677	GM12878	blood:	n/a
42	chr9:15810627-15810677	BE2_C	brain:	n/a
43	chr9:15810627-15810677	SKMC	muscle:	n/a
44	chr9:15810627-15810677	ProgFib	skin:	n/a
45	chr9:15810627-15810677	MCF-7	breast:	n/a
46	chr9:15810627-15810677	SK-N-MC	brain:	n/a
47	chr9:15810627-15810677	PrEC	prostate:	n/a
48	chr9:15810627-15810677	A549	lung:	n/a
49	chr9:15810627-15810677	SAEC	small airway:	n/a
50	chr9:15810627-15810677	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:15873671..15874276-chr9:16131035..16131676,2	MCF-7	breast:
2	chr9:15873337..15874253-chr9:16131080..16131915,3	MCF-7	breast:
3	chr9:15836820..15837651-chr9:16133566..16134324,2	MCF-7	breast:
4	chr9:15876069..15878996-chr9:15881161..15882668,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNAPC3-1	chr9:15874539-15874661	NONHSAT130279
2	lnc-C9orf92-3	chr9:15864309-15864521	uc_251_-
3	lnc-SNAPC3-5	chr9:15864309-15864521	uc_251_+

Variant related genes	Relation type
CCDC171	TF binding region
CCDC171	CpG island

Extended variants
information (count: 3875 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:3875 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6474973	chr9:15794858-15794859	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs6474974	chr9:15794897-15794898	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs537662207	chr9:15794925-15794926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs555983355	chr9:15794955-15794956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs79614735	chr9:15794964-15794965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs545512027	chr9:15794967-15794968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs368487875	chr9:15794968-15794969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs533814302	chr9:15794979-15794980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs372371704	chr9:15794997-15794998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560368598	chr9:15795027-15795028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs572420254	chr9:15795028-15795029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs547059513	chr9:15795043-15795044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs567190475	chr9:15795104-15795105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs182275218	chr9:15795144-15795145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs538930846	chr9:15795155-15795156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs375762697	chr9:15795192-15795193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs561569151	chr9:15795256-15795257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs186817647	chr9:15795258-15795259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs550486248	chr9:15795268-15795269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565520488	chr9:15795271-15795272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs115723301	chr9:15795314-15795315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs551485186	chr9:15795315-15795316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs191664700	chr9:15795330-15795331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs183010429	chr9:15795340-15795341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs370690516	chr9:15795349-15795350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs548531793	chr9:15795392-15795393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs199530565	chr9:15795437-15795438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566915280	chr9:15795445-15795446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537798158	chr9:15795448-15795449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575388333	chr9:15795470-15795471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs60655538	chr9:15795519-15795520	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs7860528	chr9:15795532-15795533	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs554684657	chr9:15795569-15795570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs538421857	chr9:15795586-15795587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554264337	chr9:15795601-15795602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs7860755	chr9:15795602-15795603	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs543051955	chr9:15795623-15795624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs376956961	chr9:15795637-15795638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs7846970	chr9:15795646-15795647	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs141846890	chr9:15795672-15795673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs559151614	chr9:15795676-15795677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs143673524	chr9:15795738-15795739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs186995743	chr9:15795749-15795750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs189870441	chr9:15795751-15795752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs527427494	chr9:15795770-15795771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs148080417	chr9:15795797-15795798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs79611697	chr9:15795833-15795834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531192315	chr9:15795835-15795836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs182141398	chr9:15795861-15795862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs7860992	chr9:15795865-15795866	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:133 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15777000-15810600	Weak transcription	Pancreas	Pancrea
2	chr9:15783600-15802000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr9:15785000-15808600	Weak transcription	Aorta	Aorta
4	chr9:15787200-15796800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr9:15787200-15799600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr9:15790200-15800000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr9:15799600-15799800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
8	chr9:15801400-15803000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr9:15802200-15802600	ZNF genes & repeats	Primary hematopoietic stem cells	blood
10	chr9:15803400-15804000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr9:15804200-15804400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr9:15805600-15812600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr9:15807600-15809600	ZNF genes & repeats	Primary hematopoietic stem cells	blood
14	chr9:15807800-15810600	Weak transcription	Ovary	ovary
15	chr9:15808000-15810600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr9:15808600-15809800	Strong transcription	Aorta	Aorta
17	chr9:15808800-15810000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr9:15809800-15810600	Weak transcription	Aorta	Aorta
19	chr9:15810600-15811000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr9:15810600-15811000	ZNF genes & repeats	Aorta	Aorta
21	chr9:15810600-15811000	ZNF genes & repeats	Ovary	ovary
22	chr9:15810600-15811200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
23	chr9:15810600-15811200	ZNF genes & repeats	Pancreas	Pancrea
24	chr9:15810800-15811000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr9:15810800-15811000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr9:15810800-15811200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
27	chr9:15811000-15811600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr9:15811200-15815000	Weak transcription	Primary hematopoietic stem cells	blood
29	chr9:15811200-15816000	Weak transcription	Pancreas	Pancrea
30	chr9:15812000-15813400	Weak transcription	Psoas Muscle	Psoas
31	chr9:15814800-15815400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr9:15814800-15831200	Weak transcription	Psoas Muscle	Psoas
33	chr9:15815000-15815200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
34	chr9:15815000-15815200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr9:15815000-15815400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr9:15816400-15818400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr9:15816800-15817200	Weak transcription	Thymus	Thymus
38	chr9:15817000-15817400	ZNF genes & repeats	Stomach Smooth Muscle	stomach
39	chr9:15817200-15817600	ZNF genes & repeats	Thymus	Thymus
40	chr9:15824400-15825200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr9:15825200-15826600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr9:15826400-15827000	Enhancers	Brain Cingulate Gyrus	brain
43	chr9:15826400-15827000	Enhancers	Brain Hippocampus Middle	brain
44	chr9:15826600-15827000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr9:15827000-15834600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr9:15828200-15828800	Enhancers	Muscle Satellite Cultured Cells	--
47	chr9:15830200-15857200	Weak transcription	Primary hematopoietic stem cells	blood
48	chr9:15834600-15835000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr9:15834600-15835000	Enhancers	Fetal Lung	lung
50	chr9:15834600-15835200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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