Variant report

Variant	nsv933345
Chromosome Location	chr9:14695436-14750474
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:178)
CpG islands
(count:244)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:178 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr9:14722568-14723014	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr9:14722642-14723053	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr9:14722811-14722999	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr9:14710917-14711211	IMR90	lung:	n/a	n/a
5	CEBPB	chr9:14720785-14721085	A549	lung:	n/a	chr9:14720966-14720983
6	CREB1	chr9:14741415-14741701	GM12878	blood:	n/a	n/a
7	CTCF	chr9:14742360-14742510	BE2_C	brain:	n/a	n/a
8	CTCF	chr9:14742140-14742290	BE2_C	brain:	n/a	n/a
9	CTCF	chr9:14746280-14746430	GM12875	blood:	n/a	n/a
10	CTCF	chr9:14708792-14708853	LNCaP	prostate:	n/a	n/a
11	CTCF	chr9:14739140-14739290	GM12878	blood:	n/a	n/a
12	CTCF	chr9:14747313-14747353	Fibrobl	skin:	n/a	n/a
13	CTCF	chr9:14742160-14742310	BE2_C	brain:	n/a	n/a
14	CTCF	chr9:14714859-14714893	Fibrobl	skin:	n/a	n/a
15	E2F4	chr9:14710918-14711411	MCF10A-Er-Src	breast:	n/a	n/a
16	E2F4	chr9:14749811-14749898	MCF10A-Er-Src	breast:	n/a	n/a
17	EP300	chr9:14722544-14723149	H1-hESC	embryonic stem cell:	n/a	chr9:14722744-14722753 chr9:14722809-14722819
18	FOS	chr9:14747156-14747453	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr9:14710907-14711249	MCF10A-Er-Src	breast:	n/a	chr9:14711083-14711094
20	FOS	chr9:14747099-14747500	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr9:14746615-14747547	HUVEC	blood vessel:	n/a	chr9:14746832-14746839 chr9:14746829-14746840 chr9:14746831-14746839
22	FOS	chr9:14747100-14747500	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr9:14710908-14711247	MCF10A-Er-Src	breast:	n/a	chr9:14711083-14711094
24	FOS	chr9:14747157-14747449	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr9:14713528-14713631	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr9:14710945-14711205	HUVEC	blood vessel:	n/a	chr9:14711083-14711094
27	FOS	chr9:14710905-14711244	MCF10A-Er-Src	breast:	n/a	chr9:14711083-14711094
28	FOS	chr9:14710883-14711251	MCF10A-Er-Src	breast:	n/a	chr9:14711083-14711094
29	FOSL2	chr9:14731700-14732024	HepG2	liver:	n/a	n/a
30	FOSL2	chr9:14727977-14728315	HepG2	liver:	n/a	n/a
31	FOSL2	chr9:14731055-14731610	HepG2	liver:	n/a	n/a
32	GATA2	chr9:14746171-14747513	HUVEC	blood vessel:	n/a	n/a
33	GATA3	chr9:14710716-14711302	SK-N-SH	brain:	n/a	n/a
34	GATA3	chr9:14710941-14710959	SH-SY5Y	brain:	n/a	n/a
35	GATA3	chr9:14710692-14711189	SK-N-SH	brain:	n/a	n/a
36	GTF2F1	chr9:14722869-14723065	H1-hESC	embryonic stem cell:	n/a	n/a
37	HDAC2	chr9:14722605-14723076	H1-hESC	embryonic stem cell:	n/a	n/a
38	JUN	chr9:14722746-14723114	H1-hESC	embryonic stem cell:	n/a	n/a
39	JUN	chr9:14746650-14747436	HUVEC	blood vessel:	n/a	chr9:14746832-14746839 chr9:14746831-14746839
40	JUND	chr9:14722698-14723115	H1-hESC	embryonic stem cell:	n/a	n/a
41	JUND	chr9:14722734-14723038	H1-hESC	embryonic stem cell:	n/a	n/a
42	KAP1	chr9:14706589-14707033	HEK293	kidney:	n/a	n/a
43	KAP1	chr9:14705016-14705455	K562	blood:	n/a	n/a
44	MAFF	chr9:14733144-14733510	HepG2	liver:	n/a	chr9:14733322-14733340
45	MAFF	chr9:14706060-14706228	HepG2	liver:	n/a	chr9:14706149-14706167
46	MAFF	chr9:14713227-14713698	HepG2	liver:	n/a	n/a
47	MAFF	chr9:14733156-14733505	K562	blood:	n/a	chr9:14733322-14733340
48	MAFF	chr9:14748127-14748293	HepG2	liver:	n/a	chr9:14748177-14748195
49	MAFF	chr9:14737934-14738174	HepG2	liver:	n/a	n/a
50	MAFF	chr9:14713278-14713496	K562	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:14720244-14720294	AG10803	skin:	n/a
2	chr9:14720244-14720294	ECC-1	luminal epithelium:	n/a
3	chr9:14723496-14723546	HRCEpiC	kidney:	n/a
4	chr9:14723496-14723546	NB4	blood:	n/a
5	chr9:14722864-14722914	SK-N-SH_RA	brain:	n/a
6	chr9:14723496-14723546	GM12892	blood:	n/a
7	chr9:14722864-14722914	HNPCEpiC	eye:	n/a
8	chr9:14723496-14723546	ProgFib	skin:	n/a
9	chr9:14722864-14722914	HAEpiC	amniotic membrane:	n/a
10	chr9:14722864-14722914	AG09319	gingival:	n/a
11	chr9:14723496-14723546	HCPEpiC	choroid plexus:	n/a
12	chr9:14722864-14722914	T-47D	breast:	n/a
13	chr9:14749903-14749953	AoSMC	blood vessel:	n/a
14	chr9:14723496-14723546	SAEC	small airway:	n/a
15	chr9:14723496-14723546	HepG2	liver:	n/a
16	chr9:14723496-14723546	HNPCEpiC	eye:	n/a
17	chr9:14749903-14749953	HRPEpiC	eye:	n/a
18	chr9:14722864-14722914	K562	blood:	n/a
19	chr9:14723496-14723546	HEK293	kidney:	embryo
20	chr9:14749903-14749953	GM06990	blood:	n/a
21	chr9:14720244-14720294	SKMC	muscle:	n/a
22	chr9:14722864-14722914	SK-N-SH	brain:	n/a
23	chr9:14720244-14720294	GM12892	blood:	n/a
24	chr9:14749903-14749953	K562	blood:	n/a
25	chr9:14720244-14720294	BE2_C	brain:	n/a
26	chr9:14722864-14722914	BE2_C	brain:	n/a
27	chr9:14720244-14720294	ovcar-3	ovarian:	n/a
28	chr9:14749903-14749953	NHBE	bronchial:	n/a
29	chr9:14722864-14722914	MCF10A-Er-Src	breast:	n/a
30	chr9:14722864-14722914	GM19239	blood:	n/a
31	chr9:14722864-14722914	HepG2	liver:	n/a
32	chr9:14749903-14749953	IMR90	lung:	fetal
33	chr9:14723496-14723546	Caco-2	colon:	n/a
34	chr9:14720244-14720294	NB4	blood:	n/a
35	chr9:14720244-14720294	HNPCEpiC	eye:	n/a
36	chr9:14720244-14720294	GM06990	blood:	n/a
37	chr9:14722864-14722914	H1-hESC	embryonic stem cell:	embryo
38	chr9:14749903-14749953	Hepatocyte	liver:	n/a
39	chr9:14720244-14720294	MCF10A-Er-Src	breast:	n/a
40	chr9:14749903-14749953	U87	brain:	n/a
41	chr9:14749903-14749953	MCF-7	breast:	n/a
42	chr9:14723496-14723546	AoSMC	blood vessel:	n/a
43	chr9:14722864-14722914	NHDF-neo	bronchial:	n/a
44	chr9:14723496-14723546	SK-N-MC	brain:	n/a
45	chr9:14720244-14720294	ProgFib	skin:	n/a
46	chr9:14723496-14723546	HUVEC	blood vessel:	n/a
47	chr9:14723496-14723546	NHDF-neo	bronchial:	n/a
48	chr9:14749903-14749953	AG09319	gingival:	n/a
49	chr9:14723496-14723546	HRPEpiC	eye:	n/a
50	chr9:14749903-14749953	HIPEpiC	eye:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:14693520..14695525-chr9:14717829..14719510,2	MCF-7	breast:
2	chr21:20745898..20746419-chr9:14747590..14748110,2	MCF-7	breast:
3	chr9:14723716..14725255-chr9:14725943..14728400,2	K562	blood:
4	chr9:14691736..14693392-chr9:14716118..14717957,2	MCF-7	breast:
5	chr9:14685829..14688724-chr9:14693473..14695940,2	K562	blood:
6	chr9:14690708..14693231-chr9:14713433..14715842,2	MCF-7	breast:
7	chr9:14691643..14693414-chr9:14700745..14703153,2	K562	blood:
8	chr9:14700452..14703179-chr9:14705217..14707235,2	MCF-7	breast:
9	chr9:14692215..14694584-chr9:14703998..14706013,2	MCF-7	breast:
10	chr9:14677358..14679032-chr9:14729314..14731148,2	MCF-7	breast:
11	chr9:14723716..14725255-chr9:14725943..14728400,2	K562	blood:
12	chr9:14693520..14695525-chr9:14717829..14719510,2	MCF-7	breast:
13	chr9:14700452..14703179-chr9:14705217..14707235,2	MCF-7	breast:

No data

Variant related genes	Relation type
ZDHHC21	TF binding region
CER1	TF binding region
ZDHHC21	CpG island
CER1	CpG island
ENSG00000175893	chromatin interactions

Extended variants
information (count: 2578 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:2578 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138340223	chr9:14695444-14695445	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs189414249	chr9:14695446-14695447	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs575587308	chr9:14695476-14695477	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs149631856	chr9:14695510-14695511	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs144239164	chr9:14695545-14695546	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs181455574	chr9:14695550-14695551	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs72704969	chr9:14695553-14695554	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs185851704	chr9:14695560-14695561	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532116811	chr9:14695573-14695574	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs545873567	chr9:14695639-14695640	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs7862474	chr9:14695641-14695642	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs531315085	chr9:14695648-14695649	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550896429	chr9:14695661-14695662	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567635648	chr9:14695692-14695693	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs577192414	chr9:14695697-14695698	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs188401431	chr9:14695722-14695723	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs567015446	chr9:14695731-14695732	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs116960782	chr9:14695748-14695749	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs181888991	chr9:14695764-14695765	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs143826347	chr9:14695772-14695773	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs550826347	chr9:14695875-14695876	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs13300667	chr9:14695880-14695881	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs79583625	chr9:14695888-14695889	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554972806	chr9:14695998-14695999	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs75139546	chr9:14696054-14696055	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs77899772	chr9:14696071-14696072	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs553723916	chr9:14696109-14696110	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs73644823	chr9:14696114-14696115	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs545608334	chr9:14696117-14696118	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs148704922	chr9:14696153-14696154	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs531275203	chr9:14696185-14696186	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs541447314	chr9:14696197-14696198	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs369644227	chr9:14696210-14696211	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs138506222	chr9:14696221-14696222	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs112127826	chr9:14696257-14696258	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs62539801	chr9:14696312-14696313	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs5896644	chr9:14696316-14696317	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs373398542	chr9:14696317-14696318	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs34431144	chr9:14696333-14696334	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs112479899	chr9:14696340-14696341	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs78607970	chr9:14696343-14696344	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs3081699	chr9:14696344-14696345	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546882226	chr9:14696350-14696351	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs13285074	chr9:14696352-14696353	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs567002518	chr9:14696354-14696355	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs60434302	chr9:14696359-14696360	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs73644824	chr9:14696360-14696361	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552428574	chr9:14696383-14696384	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569353000	chr9:14696405-14696406	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538293386	chr9:14696440-14696441	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
early-passage human iPS cells	21368824	CNVD
Glioblastoma multiforme	18628472	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	21811587	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:340 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14694000-14695800	Weak transcription	Psoas Muscle	Psoas
2	chr9:14694000-14704400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr9:14694000-14719400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr9:14695000-14701400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr9:14696000-14696200	Enhancers	Psoas Muscle	Psoas
6	chr9:14696800-14697000	Enhancers	Spleen	Spleen
7	chr9:14701000-14710200	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr9:14701400-14701600	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr9:14701600-14702400	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr9:14701800-14702200	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr9:14702200-14702600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
12	chr9:14702400-14704000	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr9:14703200-14706000	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr9:14704000-14704400	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr9:14704400-14704600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr9:14704400-14705200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr9:14704600-14704800	ZNF genes & repeats	Right Atrium	heart
18	chr9:14704600-14705000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr9:14704800-14719400	Weak transcription	Right Atrium	heart
20	chr9:14705200-14705800	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr9:14705800-14707000	ZNF genes & repeats	Primary B cells from peripheral blood	blood
22	chr9:14705800-14708400	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr9:14706000-14706600	Strong transcription	HUES64 Cell Line	embryonic stem cell
24	chr9:14706200-14706400	Enhancers	GM12878-XiMat	blood
25	chr9:14706200-14707400	Enhancers	Primary B cells from cord blood	blood
26	chr9:14706400-14706600	Flanking Active TSS	GM12878-XiMat	blood
27	chr9:14706600-14707400	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr9:14706600-14707400	ZNF genes & repeats	GM12878-XiMat	blood
29	chr9:14707400-14707800	Strong transcription	HUES64 Cell Line	embryonic stem cell
30	chr9:14707800-14708800	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr9:14708400-14709200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr9:14708800-14710000	Strong transcription	HUES64 Cell Line	embryonic stem cell
33	chr9:14709200-14712600	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr9:14710000-14715000	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr9:14710200-14710600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
36	chr9:14710400-14713600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr9:14710600-14717400	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr9:14710800-14712000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr9:14710800-14714000	Enhancers	NHEK	skin
40	chr9:14711000-14711600	Enhancers	Muscle Satellite Cultured Cells	--
41	chr9:14711200-14711600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr9:14711200-14712000	Enhancers	HMEC	breast
43	chr9:14712000-14713000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr9:14712000-14713400	Weak transcription	HMEC	breast
45	chr9:14712600-14713600	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr9:14712600-14714200	Enhancers	Placenta	Placenta
47	chr9:14713000-14714000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr9:14713400-14714000	Bivalent Enhancer	Primary B cells from peripheral blood	blood
49	chr9:14713400-14714000	Enhancers	HMEC	breast
50	chr9:14713600-14715200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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