Variant report

Variant	nsv831639
Chromosome Location	chr9:84501548-84651151
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:387)
CpG islands
(count:489)
Chromatin interactive
region (count:13)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:387 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:84527237-84527267	HepG2	liver:	n/a	n/a
2	BATF	chr9:84607607-84607942	GM12878	blood:	n/a	n/a
3	BATF	chr9:84532243-84532605	GM12878	blood:	n/a	chr9:84532461-84532472
4	BHLHE40	chr9:84594278-84594368	GM12878	blood:	n/a	n/a
5	CBX3	chr9:84635988-84636628	HCT-116	colon:	n/a	n/a
6	CEBPB	chr9:84636158-84636446	IMR90	lung:	n/a	n/a
7	CEBPB	chr9:84505062-84505311	MCF-7	breast:	n/a	chr9:84505234-84505245
8	CEBPB	chr9:84646397-84646830	IMR90	lung:	n/a	n/a
9	CEBPB	chr9:84505024-84505447	A549	lung:	n/a	chr9:84505234-84505245
10	CEBPB	chr9:84579449-84579744	HepG2	liver:	n/a	chr9:84579615-84579626
11	CEBPB	chr9:84646533-84646685	A549	lung:	n/a	n/a
12	CEBPB	chr9:84505086-84505376	IMR90	lung:	n/a	chr9:84505234-84505245
13	CEBPB	chr9:84579303-84579751	H1-hESC	embryonic stem cell:	n/a	chr9:84579615-84579626
14	CEBPB	chr9:84505076-84505382	A549	lung:	n/a	chr9:84505234-84505245
15	CEBPB	chr9:84529493-84529693	HepG2	liver:	n/a	chr9:84529585-84529596
16	CEBPB	chr9:84529518-84529680	IMR90	lung:	n/a	chr9:84529585-84529596
17	CEBPB	chr9:84579228-84579766	IMR90	lung:	n/a	chr9:84579615-84579626
18	CEBPB	chr9:84505979-84506079	A549	lung:	n/a	n/a
19	CEBPB	chr9:84521545-84522088	IMR90	lung:	n/a	n/a
20	CEBPB	chr9:84505108-84505351	HepG2	liver:	n/a	chr9:84505234-84505245
21	CEBPB	chr9:84646291-84646831	MCF-7	breast:	n/a	n/a
22	CEBPB	chr9:84530997-84531232	IMR90	lung:	n/a	n/a
23	CHD2	chr9:84594382-84594421	GM12878	blood:	n/a	n/a
24	CTCF	chr9:84609180-84609330	GM12866	blood:	n/a	n/a
25	CTCF	chr9:84607665-84607706	GM20000	blood:	n/a	n/a
26	CTCF	chr9:84591420-84591570	A549	lung:	n/a	n/a
27	CTCF	chr9:84533150-84533206	GM13976	blood:	n/a	n/a
28	CTCF	chr9:84510020-84510170	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr9:84568180-84568330	HFF-Myc	foreskin:	n/a	n/a
30	CTCF	chr9:84585000-84585150	HMEC	breast:	n/a	n/a
31	CTCF	chr9:84529710-84529755	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr9:84563982-84564047	LNCaP	prostate:	n/a	n/a
33	CTCF	chr9:84636200-84636350	AG04449	skin:	n/a	n/a
34	CTCF	chr9:84508971-84509014	ProgFib	skin:	n/a	n/a
35	CTCF	chr9:84591398-84591546	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr9:84606818-84606896	LNCaP	prostate:	n/a	n/a
37	CTCF	chr9:84646740-84646890	AG09319	gingival:	n/a	chr9:84646759-84646780 chr9:84646775-84646783 chr9:84646760-84646773 chr9:84646757-84646775
38	CTCF	chr9:84585076-84585102	Spleen_OC	spleen:	n/a	n/a
39	CTCF	chr9:84603726-84603788	LNCaP	prostate:	n/a	n/a
40	CTCF	chr9:84535739-84535829	Spleen_OC	spleen:	n/a	n/a
41	CTCF	chr9:84608997-84609047	Lung_OC	lung:	n/a	n/a
42	CTCF	chr9:84529698-84529751	GM10266	blood:	n/a	n/a
43	CTCF	chr9:84554429-84554466	LNCaP	prostate:	n/a	n/a
44	CTCF	chr9:84586780-84586930	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr9:84591366-84591578	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr9:84585180-84585330	HEEpiC	esophagus:	n/a	n/a
47	CTCF	chr9:84585060-84585210	AG04450	lung:	n/a	n/a
48	CTCF	chr9:84582860-84583010	HEK293	kidney:	n/a	n/a
49	CTCF	chr9:84550703-84550791	LNCaP	prostate:	n/a	n/a
50	CTCF	chr9:84584980-84585130	HEEpiC	esophagus:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:84532813-84532863	SK-N-MC	brain:	n/a
2	chr9:84532813-84532863	SK-N-MC	brain:	n/a
3	chr9:84527546-84527596	HIPEpiC	eye:	n/a
4	chr9:84532813-84532863	AG10803	skin:	n/a
5	chr9:84646696-84646746	HRE	kidney:	n/a
6	chr9:84606739-84606789	LNCaP	prostate:	n/a
7	chr9:84527546-84527596	PANC-1	pancreas:	n/a
8	chr9:84528281-84528331	BE2_C	brain:	n/a
9	chr9:84532813-84532863	PrEC	prostate:	n/a
10	chr9:84527546-84527596	NT2-D1	testis:	n/a
11	chr9:84604383-84604433	HRPEpiC	eye:	n/a
12	chr9:84604383-84604433	HEK293	kidney:	embryo
13	chr9:84532813-84532863	SK-N-SH	brain:	n/a
14	chr9:84606739-84606789	Jurkat	blood:	n/a
15	chr9:84606739-84606789	HEEpiC	esophagus:	n/a
16	chr9:84603063-84603113	GM12878	blood:	n/a
17	chr9:84603063-84603113	LNCaP	prostate:	n/a
18	chr9:84528281-84528331	HCT-116	colon:	n/a
19	chr9:84528281-84528331	HepG2	liver:	n/a
20	chr9:84646696-84646746	HIPEpiC	eye:	n/a
21	chr9:84606739-84606789	PrEC	prostate:	n/a
22	chr9:84603063-84603113	HMEC	breast:	n/a
23	chr9:84527546-84527596	HepG2	liver:	n/a
24	chr9:84528281-84528331	SAEC	small airway:	n/a
25	chr9:84603063-84603113	Caco-2	colon:	n/a
26	chr9:84532813-84532863	AG04449	skin:	fetal
27	chr9:84532813-84532863	Hela-S3	cervix:	n/a
28	chr9:84603063-84603113	HUVEC	blood vessel:	n/a
29	chr9:84606739-84606789	AG09319	gingival:	n/a
30	chr9:84604383-84604433	HepG2	liver:	n/a
31	chr9:84646696-84646746	AoSMC	blood vessel:	n/a
32	chr9:84604383-84604433	A549	lung:	n/a
33	chr9:84646696-84646746	ovcar-3	ovarian:	n/a
34	chr9:84603063-84603113	HRCEpiC	kidney:	n/a
35	chr9:84528281-84528331	K562	blood:	n/a
36	chr9:84606739-84606789	GM12891	blood:	n/a
37	chr9:84527546-84527596	SK-N-MC	brain:	n/a
38	chr9:84646696-84646746	HNPCEpiC	eye:	n/a
39	chr9:84532813-84532863	Hepatocyte	liver:	n/a
40	chr9:84609982-84610032	HRPEpiC	eye:	n/a
41	chr9:84532813-84532863	SK-N-SH_RA	brain:	n/a
42	chr9:84609982-84610032	NHBE	bronchial:	n/a
43	chr9:84606739-84606789	U87	brain:	n/a
44	chr9:84528281-84528331	GM06990	blood:	n/a
45	chr9:84609982-84610032	AG10803	skin:	n/a
46	chr9:84527546-84527596	HNPCEpiC	eye:	n/a
47	chr9:84646696-84646746	SKMC	muscle:	n/a
48	chr9:84606739-84606789	MCF10A-Er-Src	breast:	n/a
49	chr9:84528281-84528331	H1-hESC	embryonic stem cell:	embryo
50	chr9:84603063-84603113	Hepatocyte	liver:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr9:84511424..84513572-chr9:84514305..84516417,2	MCF-7	breast:
2	chr9:84581823..84583506-chr9:84588522..84590887,2	MCF-7	breast:
3	chr9:84511424..84513572-chr9:84514305..84516417,2	MCF-7	breast:
4	chr9:84503918..84506226-chr9:84512695..84515365,2	MCF-7	breast:
5	chr9:84642456..84644101-chr9:84644555..84646122,2	MCF-7	breast:
6	chr9:84581823..84583506-chr9:84588522..84590887,2	MCF-7	breast:
7	chr9:84642456..84644101-chr9:84644555..84646122,2	MCF-7	breast:
8	chr9:84582181..84584645-chr9:84585725..84588134,2	MCF-7	breast:
9	chr15:56997213..56998082-chr9:84571851..84572510,2	Hela-S3	cervix:
10	chr9:84579954..84582797-chr9:84592231..84595041,2	MCF-7	breast:
11	chr9:84579954..84582797-chr9:84592231..84595041,2	MCF-7	breast:
12	chr9:84608627..84610536-chr9:84691532..84693199,2	MCF-7	breast:
13	chr9:84503918..84506226-chr9:84512695..84515365,2	MCF-7	breast:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM75B-1	chr9:84588997-84589162	ENSG00000267559.1
2	lnc-FAM75D1-5	chr9:84528352-84528572	NR_026851
3	lnc-FAM75D1-5	chr9:84530307-84534842	NR_026851
4	lnc-FAM75B-1	chr9:84588856-84589162	ENSG00000267559.1
5	lnc-FAM75B-1	chr9:84545141-84546309	ENSG00000267559.1
6	lnc-C9orf103-9	chr9:84603703-84603919	NONHSAT132690
7	lnc-FAM75B-1	chr9:84561353-84561401	ENSG00000267559.1
8	lnc-FAM75D1-5	chr9:84529963-84530023	NR_026851
9	lnc-FAM75B-1	chr9:84591523-84592004	ENSG00000267559.1
10	lnc-FAM75B-1	chr9:84582451-84582603	ENSG00000267559.1
11	lnc-C9orf103-9	chr9:84604693-84605063	NONHSAT132690
12	lnc-FAM75B-1	chr9:84561305-84561401	ENSG00000267559.1
13	lnc-FAM75B-1	chr9:84582451-84582603	ENSG00000267559.1
14	lnc-FAM75D1-5	chr9:84529316-84529361	NR_026851
15	lnc-FAM75B-1	chr9:84591523-84591721	ENSG00000267559.1

No data

Variant related genes	Relation type
ENSG00000200969	TF binding region
SPATA31D5P	TF binding region
ENSG00000267559	TF binding region
SPATA31D4	TF binding region
SPATA31D2P	TF binding region
SPATA31D1	TF binding region
SPATA31D3	TF binding region
ENSG00000230846	TF binding region
ENSG00000200969	CpG island
SPATA31D5P	CpG island
ENSG00000267559	CpG island
SPATA31D4	CpG island
SPATA31D2P	CpG island
SPATA31D1	CpG island
SPATA31D3	CpG island
ENSG00000230846	CpG island
ENSG00000237770	chromatin interactions

Extended variants
information (count: 2147 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:2147 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114209814	chr9:84501553-84501554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs147842066	chr9:84501560-84501561	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs577310644	chr9:84501602-84501603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs539906389	chr9:84501630-84501631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs141464400	chr9:84501646-84501647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs147313688	chr9:84501654-84501655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs143618804	chr9:84501659-84501660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs151032863	chr9:84501668-84501669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs569917329	chr9:84501701-84501702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs373487705	chr9:84501743-84501744	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs533319132	chr9:84501823-84501824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs551671277	chr9:84501841-84501842	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs569996391	chr9:84501843-84501844	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs530450856	chr9:84501897-84501898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs369950465	chr9:84501934-84501935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs548959303	chr9:84502008-84502009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs376528778	chr9:84502028-84502029	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs182886123	chr9:84502029-84502030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs552766184	chr9:84502033-84502034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs571483551	chr9:84502047-84502048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs538821464	chr9:84502073-84502074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs573500698	chr9:84502089-84502090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs557320719	chr9:84502121-84502122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs575610258	chr9:84502144-84502145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140959155	chr9:84502192-84502193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs73478214	chr9:84502234-84502235	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs573906269	chr9:84502250-84502251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs541533411	chr9:84502256-84502257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs559384469	chr9:84502265-84502266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs533379778	chr9:84502298-84502299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs545175045	chr9:84502300-84502301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs374201393	chr9:84502301-84502302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs74305078	chr9:84502325-84502326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs549369883	chr9:84502374-84502375	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs567276484	chr9:84502380-84502381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs528041443	chr9:84502441-84502442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs544384527	chr9:84502457-84502458	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs138867630	chr9:84502474-84502475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs111453433	chr9:84502490-84502491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs538885709	chr9:84502506-84502507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs557187517	chr9:84502511-84502512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs142101648	chr9:84502573-84502574	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs189211433	chr9:84505200-84505201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs181584806	chr9:84505205-84505206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs566948071	chr9:84505264-84505265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs534439594	chr9:84505265-84505266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs369577274	chr9:84505282-84505283	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs552792891	chr9:84505312-84505313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs539801218	chr9:84505316-84505317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs200573861	chr9:84505329-84505330	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Urothelial cell carcinoma	18451213	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Renal cell carcinoma	18765545	CNVD
Astrocytoma	22246337	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Epilepsy	20502679	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Medulloblastoma	21163964	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:84500200-84501600	Enhancers	Brain Cingulate Gyrus	brain
2	chr9:84500200-84501800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr9:84500400-84501600	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr9:84500400-84501800	Enhancers	Brain Germinal Matrix	brain
5	chr9:84500400-84502600	Enhancers	Fetal Brain Male	brain
6	chr9:84501200-84501600	Enhancers	Fetal Muscle Leg	muscle
7	chr9:84501200-84501800	Enhancers	Fetal Lung	lung
8	chr9:84501400-84501600	Enhancers	Brain Inferior Temporal Lobe	brain
9	chr9:84501400-84501800	Enhancers	Fetal Brain Female	brain
10	chr9:84505200-84505400	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr9:84505400-84507200	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr9:84507200-84507400	Enhancers	Rectal Mucosa Donor 31	rectum
13	chr9:84507400-84508400	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr9:84508400-84508600	Enhancers	Rectal Mucosa Donor 31	rectum
15	chr9:84508600-84509400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr9:84513600-84513800	Enhancers	Aorta	Aorta
17	chr9:84513600-84514400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr9:84513800-84514000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr9:84514000-84515000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr9:84514600-84515600	Enhancers	Fetal Lung	lung
21	chr9:84515000-84515800	Enhancers	H9 Cell Line	embryonic stem cell
22	chr9:84515000-84516000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr9:84515400-84515800	Enhancers	Aorta	Aorta
24	chr9:84515400-84516000	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr9:84515600-84519600	Weak transcription	Fetal Lung	lung
26	chr9:84516000-84517400	Enhancers	Stomach Smooth Muscle	stomach
27	chr9:84516600-84518000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr9:84517000-84517800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr9:84517200-84518000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr9:84517400-84517800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr9:84517400-84517800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr9:84517400-84518000	Enhancers	NHEK	skin
33	chr9:84517600-84518000	Enhancers	HMEC	breast
34	chr9:84517600-84518000	Enhancers	NHDF-Ad	bronchial
35	chr9:84517800-84521200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr9:84518000-84521400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr9:84519600-84520000	Enhancers	Fetal Lung	lung
38	chr9:84521200-84522200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr9:84521400-84521800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr9:84521400-84521800	Enhancers	NH-A	brain
41	chr9:84521400-84521800	Enhancers	Osteobl	bone
42	chr9:84521400-84522000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr9:84521400-84522400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr9:84526400-84526600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr9:84526600-84527000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr9:84526600-84527800	Enhancers	Liver	Liver
47	chr9:84530400-84531000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr9:84530400-84531200	Enhancers	HSMMtube	muscle
49	chr9:84570200-84571000	ZNF genes & repeats	Brain Hippocampus Middle	brain
50	chr9:84579000-84580000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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