Variant report

Variant	nsv1020552
Chromosome Location	chr9:43726990-44273229
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2441)
CpG islands
(count:671)
Chromatin interactive
region (count:1)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2441 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:44118677-44118886	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:44108136-44108696	HepG2	liver:	n/a	n/a
3	ATF1	chr9:43939526-43939892	K562	blood:	n/a	n/a
4	ATF3	chr9:43939586-43939712	K562	blood:	n/a	n/a
5	BACH1	chr9:44227257-44227630	K562	blood:	n/a	n/a
6	BACH1	chr9:44227184-44227631	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr9:43875906-43876190	GM12878	blood:	n/a	n/a
8	BATF	chr9:44030553-44030791	GM12878	blood:	n/a	n/a
9	BATF	chr9:44063096-44063309	GM12878	blood:	n/a	n/a
10	BATF	chr9:44108319-44108733	GM12878	blood:	n/a	chr9:44108541-44108552
11	BATF	chr9:44086306-44086516	GM12878	blood:	n/a	n/a
12	BATF	chr9:44070573-44070887	GM12878	blood:	n/a	n/a
13	BATF	chr9:44088928-44089261	GM12878	blood:	n/a	chr9:44088983-44088991
14	BATF	chr9:43925013-43925176	GM12878	blood:	n/a	n/a
15	BATF	chr9:44125333-44125599	GM12878	blood:	n/a	n/a
16	BATF	chr9:44243686-44243967	GM12878	blood:	n/a	n/a
17	BATF	chr9:44110679-44110958	GM12878	blood:	n/a	n/a
18	BATF	chr9:44245139-44246113	GM12878	blood:	n/a	n/a
19	BATF	chr9:44108035-44108219	GM12878	blood:	n/a	n/a
20	BATF	chr9:44030517-44030875	GM12878	blood:	n/a	n/a
21	BATF	chr9:44245375-44245745	GM12878	blood:	n/a	n/a
22	BATF	chr9:44072527-44072766	GM12878	blood:	n/a	chr9:44072668-44072679
23	BATF	chr9:44124043-44124400	GM12878	blood:	n/a	n/a
24	BATF	chr9:44118541-44118761	GM12878	blood:	n/a	n/a
25	BATF	chr9:44054788-44055026	GM12878	blood:	n/a	n/a
26	BATF	chr9:44088871-44089267	GM12878	blood:	n/a	chr9:44088983-44088991
27	BATF	chr9:44095589-44095794	GM12878	blood:	n/a	n/a
28	BATF	chr9:44076866-44077089	GM12878	blood:	n/a	n/a
29	BATF	chr9:44086267-44086535	GM12878	blood:	n/a	n/a
30	BATF	chr9:44082194-44082452	GM12878	blood:	n/a	n/a
31	BATF	chr9:44212521-44212907	GM12878	blood:	n/a	chr9:44212712-44212723
32	BATF	chr9:44070553-44070898	GM12878	blood:	n/a	n/a
33	BATF	chr9:44124132-44124352	GM12878	blood:	n/a	n/a
34	BATF	chr9:44105673-44105873	GM12878	blood:	n/a	n/a
35	BATF	chr9:44030085-44030326	GM12878	blood:	n/a	n/a
36	BATF	chr9:44212515-44212942	GM12878	blood:	n/a	chr9:44212712-44212723
37	BATF	chr9:44145517-44145676	GM12878	blood:	n/a	n/a
38	BATF	chr9:44065378-44065708	GM12878	blood:	n/a	n/a
39	BATF	chr9:44107334-44107970	GM12878	blood:	n/a	n/a
40	BATF	chr9:44108339-44108646	GM12878	blood:	n/a	chr9:44108541-44108552
41	BATF	chr9:43837850-43838056	GM12878	blood:	n/a	n/a
42	BATF	chr9:44072537-44072807	GM12878	blood:	n/a	chr9:44072668-44072679
43	BATF	chr9:43844088-43844411	GM12878	blood:	n/a	n/a
44	BATF	chr9:44176537-44176725	GM12878	blood:	n/a	n/a
45	BATF	chr9:44012526-44012769	GM12878	blood:	n/a	n/a
46	BATF	chr9:44133305-44133513	GM12878	blood:	n/a	chr9:44133433-44133441
47	BATF	chr9:44108799-44108996	GM12878	blood:	n/a	n/a
48	BATF	chr9:44265544-44265770	GM12878	blood:	n/a	n/a
49	BATF	chr9:44065395-44065684	GM12878	blood:	n/a	n/a
50	BATF	chr9:44107144-44107983	GM12878	blood:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:44119823-44119873	Hela-S3	cervix:	n/a
2	chr9:44120147-44120197	HIPEpiC	eye:	n/a
3	chr9:44118014-44118064	Jurkat	blood:	n/a
4	chr9:43915234-43915284	MCF-7	breast:	n/a
5	chr9:44118915-44118965	NHBE	bronchial:	n/a
6	chr9:44120147-44120197	U87	brain:	n/a
7	chr9:44119413-44119463	SK-N-SH	brain:	n/a
8	chr9:44227210-44227260	PANC-1	pancreas:	n/a
9	chr9:44227339-44227389	Jurkat	blood:	n/a
10	chr9:44119823-44119873	PANC-1	pancreas:	n/a
11	chr9:44120147-44120197	HRE	kidney:	n/a
12	chr9:43860027-43860077	PANC-1	pancreas:	n/a
13	chr9:44118236-44118286	HEK293	kidney:	embryo
14	chr9:44118236-44118286	AG09319	gingival:	n/a
15	chr9:44119413-44119463	HEK293	kidney:	embryo
16	chr9:44120147-44120197	LNCaP	prostate:	n/a
17	chr9:44120147-44120197	HEEpiC	esophagus:	n/a
18	chr9:44120147-44120197	HPAEpiC	pulmonary alveolar:	n/a
19	chr9:44120147-44120197	HAEpiC	amniotic membrane:	n/a
20	chr9:43915234-43915284	SK-N-MC	brain:	n/a
21	chr9:44119823-44119873	ECC-1	luminal epithelium:	n/a
22	chr9:44120147-44120197	AG04450	lung:	fetal
23	chr9:44118236-44118286	PrEC	prostate:	n/a
24	chr9:44227210-44227260	H1-hESC	embryonic stem cell:	embryo
25	chr9:43860965-43861015	GM12878	blood:	n/a
26	chr9:44120147-44120197	K562	blood:	n/a
27	chr9:44118236-44118286	T-47D	breast:	n/a
28	chr9:44118014-44118064	BE2_C	brain:	n/a
29	chr9:44119413-44119463	GM12891	blood:	n/a
30	chr9:44227339-44227389	T-47D	breast:	n/a
31	chr9:44120147-44120197	HEK293	kidney:	embryo
32	chr9:44227339-44227389	NT2-D1	testis:	n/a
33	chr9:44119823-44119873	Caco-2	colon:	n/a
34	chr9:43915234-43915284	HAEpiC	amniotic membrane:	n/a
35	chr9:44119823-44119873	SAEC	small airway:	n/a
36	chr9:44119823-44119873	HCF	heart:	n/a
37	chr9:43860027-43860077	U87	brain:	n/a
38	chr9:44227339-44227389	HRCEpiC	kidney:	n/a
39	chr9:44118014-44118064	IMR90	lung:	fetal
40	chr9:43860027-43860077	HRPEpiC	eye:	n/a
41	chr9:43915234-43915284	A549	lung:	n/a
42	chr9:43915234-43915284	Jurkat	blood:	n/a
43	chr9:44118915-44118965	GM12892	blood:	n/a
44	chr9:44118915-44118965	AG09319	gingival:	n/a
45	chr9:44118236-44118286	IMR90	lung:	fetal
46	chr9:44119413-44119463	AG09319	gingival:	n/a
47	chr9:44120147-44120197	NH-A	brain:	n/a
48	chr9:44119413-44119463	HCPEpiC	choroid plexus:	n/a
49	chr9:44119413-44119463	SAEC	small airway:	n/a
50	chr9:44120147-44120197	GM19239	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:107699957..107700478-chr9:44227430..44227950,2	MCF-7	breast:

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-160N1.10.1-8	chr9:43822729-43822779	NONHSAT131364
2	lnc-RP11-160N1.10.1-8	chr9:43828157-43828221	NONHSAT131364
3	lnc-FAM75A6-6	chr9:43830636-43831108	NONHSAT131365
4	lnc-FAM75A6-6	chr9:43833702-43835037	NONHSAT131365
5	lnc-FAM75A6-3	chr9:44256580-44256817	ENSG00000233424.2
6	lnc-CNTNAP3B-3	chr9:44011053-44011839	NONHSAT131369
7	lnc-FAM75A6-2	chr9:44182692-44183417	XLOC_007697
8	lnc-FAM75A6-8	chr9:44075932-44076173	NONHSAT131372
9	lnc-RP11-160N1.10.1-8	chr9:43822613-43822699	NONHSAT131364
10	lnc-FAM75A6-3	chr9:44256189-44256817	ENSG00000233424
11	lnc-FAM75A6-1	chr9:44136621-44137011	XLOC_007696
12	lnc-FAM75A6-3	chr9:44260052-44260139	ENSG00000233424
13	lnc-RP11-160N1.10.1-8	chr9:43853497-43853563	NONHSAT131364
14	lnc-FAM75A6-3	chr9:44260422-44263319	ENSG00000233424
15	lnc-FAM75A6-3	chr9:44260422-44263319	ENSG00000233424.2
16	lnc-FAM75A6-2	chr9:44181550-44181732	XLOC_007697
17	lnc-FAM75A6-5	chr9:43802781-43803039	NONHSAT131363
18	lnc-RP11-160N1.10.1-8	chr9:43861003-43861206	NONHSAT131364
19	lnc-FAM75A6-7	chr9:44046989-44047817	NONHSAT131371
20	lnc-RP11-160N1.10.1-8	chr9:43844144-43844200	NONHSAT131364
21	lnc-RP11-160N1.10.1-8	chr9:43875989-43876034	NONHSAT131364
22	lnc-FAM75A6-1	chr9:44144869-44145101	XLOC_007696
23	lnc-FAM75A6-3	chr9:44260052-44260139	ENSG00000233424.2

No data

Variant related genes	Relation type
ENSG00000204818	TF binding region
ENSG00000237207	TF binding region
ENSG00000229079	TF binding region
MEP1AP4	TF binding region
CYP4F60P	TF binding region
ENSG00000170165	TF binding region
ENSG00000233424	TF binding region
ENSG00000270909	TF binding region
SNX18P5	TF binding region
ANKRD20A7P	TF binding region
RNU6-599P	TF binding region
CNN2P4	TF binding region
RN7SL343P	TF binding region
CNTNAP3B	TF binding region
ENSG00000204818	CpG island
ENSG00000237207	CpG island
ENSG00000229079	CpG island
MEP1AP4	CpG island
CYP4F60P	CpG island
ENSG00000170165	CpG island
ENSG00000233424	CpG island
ENSG00000270909	CpG island
SNX18P5	CpG island
ANKRD20A7P	CpG island
RNU6-599P	CpG island
CNN2P4	CpG island
RN7SL343P	CpG island
CNTNAP3B	CpG island
ZBTB39	miRNA target sites

Extended variants
information (count: 7251 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:7251 , 50 per page) page: 1 2 3 4 5 6 7 ... 146

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562694746	chr9:43733612-43733613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs62558912	chr9:43733688-43733689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs201390720	chr9:43733723-43733724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs386361255	chr9:43733724-43733725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs180729239	chr9:43733741-43733742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs374902375	chr9:43733756-43733757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs185515236	chr9:43733798-43733799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs62558913	chr9:43733828-43733829	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs142561253	chr9:43733843-43733844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs368105205	chr9:43733854-43733855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs560763173	chr9:43733878-43733879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs527863411	chr9:43733891-43733892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs372345599	chr9:43733901-43733902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs543208052	chr9:43733906-43733907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs189931962	chr9:43733929-43733930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs140819023	chr9:43733942-43733943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs111364654	chr9:43733943-43733944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs145915180	chr9:43733974-43733975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs117224854	chr9:43733976-43733977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs568750983	chr9:43733983-43733984	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs183852593	chr9:43733994-43733995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs368491209	chr9:43734005-43734006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs372342711	chr9:43734013-43734014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs545538450	chr9:43734034-43734035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs28638036	chr9:43734092-43734093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs188346644	chr9:43734118-43734119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs574932639	chr9:43734141-43734142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs533755112	chr9:43734151-43734152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs28542093	chr9:43734193-43734194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs138716216	chr9:43734195-43734196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs537911604	chr9:43734197-43734198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs534907339	chr9:43742404-43742405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs201090838	chr9:43742412-43742413	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs3864736	chr9:43742443-43742444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs553252978	chr9:43742480-43742481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs574665081	chr9:43742494-43742495	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs542379077	chr9:43742496-43742497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs369288309	chr9:43742514-43742515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs563823160	chr9:43742546-43742547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs575600411	chr9:43742547-43742548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs546185878	chr9:43742584-43742585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs369422693	chr9:43742599-43742600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs528805129	chr9:43742618-43742619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs546866228	chr9:43742664-43742665	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs561977982	chr9:43742732-43742733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs529461695	chr9:43742751-43742752	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs201175157	chr9:43742797-43742798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs550867077	chr9:43742831-43742832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs569736705	chr9:43742850-43742851	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs536711674	chr9:43742873-43742874	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
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
Oral squamous cell carcinoma	17134496	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Oral cancer	21386901	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Sezary syndrome	18413736	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	21346763	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Lung adenocarcinoma	17086460	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Lung cancer	17086460	CNVD
Rhabdomyosarcoma	16790082	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20967226	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:416 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:43733600-43734000	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr9:43733600-43734200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr9:43733800-43734000	Enhancers	Lung	lung
4	chr9:43742400-43743200	Enhancers	HUVEC	blood vessel
5	chr9:43783400-43783800	Active TSS	Breast Myoepithelial Primary Cells	Breast
6	chr9:43795400-43795800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr9:43795400-43795800	Enhancers	HUVEC	blood vessel
8	chr9:43795600-43795800	Enhancers	NH-A	brain
9	chr9:43795600-43796000	Enhancers	HMEC	breast
10	chr9:43823600-43828400	Weak transcription	A549	lung
11	chr9:43824200-43828600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr9:43827800-43850400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr9:43838400-43863800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr9:43844400-43856400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr9:43845200-43863600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr9:43845600-43856400	Weak transcription	HUVEC	blood vessel
17	chr9:43858400-43863600	Weak transcription	Adipose Nuclei	Adipose
18	chr9:44057200-44070600	Weak transcription	Liver	Liver
19	chr9:44070200-44070600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr9:44070600-44070800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr9:44070600-44070800	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
22	chr9:44070600-44070800	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
23	chr9:44070600-44070800	ZNF genes & repeats	Primary T cells from cord blood	blood
24	chr9:44070600-44070800	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
25	chr9:44070600-44070800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
26	chr9:44070600-44070800	ZNF genes & repeats	Primary T helper 17 cells PMA-I stimulated	--
27	chr9:44070600-44070800	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
28	chr9:44070600-44070800	Flanking Bivalent TSS/Enh	Primary T killer naive cells fromperipheralblood	blood
29	chr9:44070600-44070800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr9:44070600-44070800	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
31	chr9:44070600-44070800	Enhancers	Adipose Nuclei	Adipose
32	chr9:44070600-44070800	Bivalent Enhancer	Aorta	Aorta
33	chr9:44070600-44070800	Active TSS	Brain Anterior Caudate	brain
34	chr9:44070600-44070800	ZNF genes & repeats	Colonic Mucosa	Colon
35	chr9:44070600-44070800	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
36	chr9:44070600-44070800	Enhancers	Right Ventricle	heart
37	chr9:44070600-44071000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
38	chr9:44070600-44071000	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
39	chr9:44070600-44071000	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr9:44070600-44071000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr9:44070600-44071000	Flanking Bivalent TSS/Enh	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr9:44070600-44071000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr9:44070600-44071000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
44	chr9:44070600-44071000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
45	chr9:44070600-44071000	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
46	chr9:44070600-44071000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
47	chr9:44070600-44071000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
48	chr9:44070600-44071000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr9:44070600-44071000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr9:44070600-44071000	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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