Variant report

Variant	esv1798245
Chromosome Location	chr9:96098930-96120432
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:160)
CpG islands
(count:183)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:160 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr9:96108635-96109071	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr9:96120037-96120249	GM12878	blood:	n/a	n/a
3	BHLHE40	chr9:96102416-96102622	HepG2	liver:	n/a	n/a
4	BRCA1	chr9:96108654-96108656	H1-hESC	embryonic stem cell:	n/a	n/a
5	CBX3	chr9:96100770-96100997	K562	blood:	n/a	n/a
6	CBX3	chr9:96100741-96101106	K562	blood:	n/a	n/a
7	CEBPB	chr9:96115822-96116022	HepG2	liver:	n/a	chr9:96115900-96115911 chr9:96115901-96115910
8	CEBPB	chr9:96109315-96109647	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr9:96115771-96115977	H1-hESC	embryonic stem cell:	n/a	chr9:96115900-96115911 chr9:96115901-96115910
10	CEBPB	chr9:96105793-96105794	A549	lung:	n/a	n/a
11	CHD2	chr9:96108248-96108795	H1-hESC	embryonic stem cell:	n/a	chr9:96108730-96108740
12	CREB1	chr9:96119859-96120341	GM12878	blood:	n/a	n/a
13	CREB1	chr9:96119877-96120303	GM12878	blood:	n/a	n/a
14	CTBP2	chr9:96107924-96109053	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr9:96108740-96108890	HCPEpiC	choroid plexus:	n/a	n/a
16	CTCF	chr9:96120123-96120137	GM19239	blood:	n/a	n/a
17	CTCF	chr9:96120096-96120167	GM12892	blood:	n/a	n/a
18	CTCF	chr9:96098900-96099050	HCT-116	colon:	n/a	n/a
19	CTCF	chr9:96108020-96108170	HepG2	liver:	n/a	n/a
20	CTCF	chr9:96108600-96108750	HCM	heart:	n/a	n/a
21	CTCF	chr9:96108680-96108830	SK-N-SH_RA	brain:	n/a	n/a
22	CTCF	chr9:96120022-96120210	GM12878	blood:	n/a	n/a
23	CTCF	chr9:96108100-96108350	HCFaa	heart:	n/a	n/a
24	CTCF	chr9:96120138-96120148	GM13977	blood:	n/a	n/a
25	CTCF	chr9:96108078-96108166	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr9:96099200-96099350	HEK293	kidney:	n/a	n/a
27	CTCF	chr9:96114155-96114247	Lung_OC	lung:	n/a	n/a
28	CTCF	chr9:96099200-96099350	HepG2	liver:	n/a	n/a
29	CTCF	chr9:96107963-96108224	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr9:96099197-96099311	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr9:96103585-96103625	Lung_OC	lung:	n/a	n/a
32	CTCF	chr9:96107951-96108152	K562	blood:	n/a	n/a
33	CTCF	chr9:96120060-96120210	GM12871	blood:	n/a	n/a
34	CTCF	chr9:96101755-96101844	Pancreas_OC	pancreas:	n/a	n/a
35	CTCF	chr9:96107950-96108187	K562	blood:	n/a	n/a
36	CTCF	chr9:96099320-96099470	HCT-116	colon:	n/a	chr9:96099439-96099448
37	CTCF	chr9:96099180-96099330	HepG2	liver:	n/a	n/a
38	CTCF	chr9:96108807-96108840	Pancreas_OC	pancreas:	n/a	n/a
39	CTCF	chr9:96099180-96099330	HEK293	kidney:	n/a	n/a
40	CTCF	chr9:96108660-96108810	AG09319	gingival:	n/a	n/a
41	CTCF	chr9:96108800-96108950	HRE	kidney:	n/a	n/a
42	CTCF	chr9:96108720-96108870	SK-N-SH_RA	brain:	n/a	n/a
43	E2F6	chr9:96108269-96109198	H1-hESC	embryonic stem cell:	n/a	chr9:96108619-96108628 chr9:96108696-96108708
44	E2F6	chr9:96107898-96109269	H1-hESC	embryonic stem cell:	n/a	chr9:96108619-96108628 chr9:96108056-96108068 chr9:96108696-96108708
45	EP300	chr9:96120071-96120167	GM12878	blood:	n/a	n/a
46	FOS	chr9:96116802-96117153	MCF10A-Er-Src	breast:	n/a	chr9:96116957-96116966
47	FOS	chr9:96116801-96117144	MCF10A-Er-Src	breast:	n/a	chr9:96116957-96116966
48	FOS	chr9:96116830-96117137	MCF10A-Er-Src	breast:	n/a	chr9:96116957-96116966
49	FOSL1	chr9:96116663-96117254	HCT-116	colon:	n/a	chr9:96116957-96116966
50	FOXA2	chr9:96114505-96114863	A549	lung:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:96108467-96108517	ECC-1	luminal epithelium:	n/a
2	chr9:96108319-96108369	AG09319	gingival:	n/a
3	chr9:96106281-96106331	Caco-2	colon:	n/a
4	chr9:96108319-96108369	RPTEC	kidney:	n/a
5	chr9:96108467-96108517	K562	blood:	n/a
6	chr9:96108467-96108517	HCPEpiC	choroid plexus:	n/a
7	chr9:96108467-96108517	HCF	heart:	n/a
8	chr9:96108467-96108517	NHDF-neo	bronchial:	n/a
9	chr9:96108319-96108369	NHBE	bronchial:	n/a
10	chr9:96108319-96108369	HCF	heart:	n/a
11	chr9:96108319-96108369	HepG2	liver:	n/a
12	chr9:96106281-96106331	MCF10A-Er-Src	breast:	n/a
13	chr9:96106281-96106331	HMEC	breast:	n/a
14	chr9:96108319-96108369	NT2-D1	testis:	n/a
15	chr9:96106281-96106331	AG10803	skin:	n/a
16	chr9:96108319-96108369	AoSMC	blood vessel:	n/a
17	chr9:96108467-96108517	GM12892	blood:	n/a
18	chr9:96108467-96108517	A549	lung:	n/a
19	chr9:96108467-96108517	HRCEpiC	kidney:	n/a
20	chr9:96108319-96108369	Caco-2	colon:	n/a
21	chr9:96108319-96108369	ECC-1	luminal epithelium:	n/a
22	chr9:96106281-96106331	HEK293	kidney:	embryo
23	chr9:96106281-96106331	HCPEpiC	choroid plexus:	n/a
24	chr9:96108467-96108517	Jurkat	blood:	n/a
25	chr9:96106281-96106331	GM12892	blood:	n/a
26	chr9:96108467-96108517	MCF-7	breast:	n/a
27	chr9:96108467-96108517	HCT-116	colon:	n/a
28	chr9:96106281-96106331	ProgFib	skin:	n/a
29	chr9:96106281-96106331	SK-N-SH_RA	brain:	n/a
30	chr9:96108467-96108517	Hepatocyte	liver:	n/a
31	chr9:96108319-96108369	SK-N-MC	brain:	n/a
32	chr9:96108467-96108517	ProgFib	skin:	n/a
33	chr9:96106281-96106331	HRCEpiC	kidney:	n/a
34	chr9:96108467-96108517	HPAEpiC	pulmonary alveolar:	n/a
35	chr9:96108467-96108517	GM12878	blood:	n/a
36	chr9:96108467-96108517	HIPEpiC	eye:	n/a
37	chr9:96108467-96108517	CMK	blood:	n/a
38	chr9:96106281-96106331	HIPEpiC	eye:	n/a
39	chr9:96106281-96106331	LNCaP	prostate:	n/a
40	chr9:96106281-96106331	HepG2	liver:	n/a
41	chr9:96106281-96106331	CMK	blood:	n/a
42	chr9:96108319-96108369	ovcar-3	ovarian:	n/a
43	chr9:96106281-96106331	HCM	heart:	n/a
44	chr9:96108319-96108369	IMR90	lung:	fetal
45	chr9:96106281-96106331	HRPEpiC	eye:	n/a
46	chr9:96108319-96108369	MCF10A-Er-Src	breast:	n/a
47	chr9:96106281-96106331	GM12891	blood:	n/a
48	chr9:96108467-96108517	NHBE	bronchial:	n/a
49	chr9:96106281-96106331	AG04450	lung:	fetal
50	chr9:96108319-96108369	HCM	heart:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:96102610..96104810-chr9:96126925..96128745,2	MCF-7	breast:
2	chr9:96102234..96103753-chr9:96106109..96107624,2	K562	blood:
3	chr9:96102234..96103753-chr9:96106109..96107624,2	K562	blood:
4	chr9:96093481..96095896-chr9:96100994..96102832,2	MCF-7	breast:
5	chr9:96102856..96105406-chr9:96141051..96143168,2	MCF-7	breast:

No data

Variant related genes	Relation type
C9orf129	TF binding region
C9orf129	CpG island

Extended variants
information (count: 947 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:947 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16909069	chr9:96098930-96098931	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs73514552	chr9:96098990-96098991	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs77098571	chr9:96098994-96098995	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs554683725	chr9:96099001-96099002	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs2841676	chr9:96099009-96099010	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs543433503	chr9:96099027-96099028	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs375016777	chr9:96099044-96099045	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs183724956	chr9:96099049-96099050	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577407474	chr9:96099068-96099069	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs545234689	chr9:96099113-96099114	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs143415484	chr9:96099171-96099172	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs188548285	chr9:96099187-96099188	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs549330259	chr9:96099199-96099200	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs193118505	chr9:96099201-96099202	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs112747136	chr9:96099202-96099203	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs140461808	chr9:96099204-96099205	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs571326352	chr9:96099240-96099241	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs538298007	chr9:96099272-96099273	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs76388776	chr9:96099277-96099278	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs182771937	chr9:96099316-96099317	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs117871551	chr9:96099319-96099320	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs546365815	chr9:96099324-96099325	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs150399352	chr9:96099330-96099331	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs116347124	chr9:96099370-96099371	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs2927572	chr9:96099377-96099378	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs368878500	chr9:96099381-96099382	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs371766324	chr9:96099444-96099445	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs577419358	chr9:96099451-96099452	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs143899609	chr9:96099455-96099456	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs187096928	chr9:96099476-96099477	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs34590502	chr9:96099482-96099483	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs572297039	chr9:96099493-96099494	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542453954	chr9:96099503-96099504	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs114601919	chr9:96099514-96099515	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs531464733	chr9:96099628-96099629	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs550417254	chr9:96099638-96099639	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs543406489	chr9:96099654-96099655	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs138074917	chr9:96099701-96099702	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs532090536	chr9:96099702-96099703	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs34676681	chr9:96099717-96099718	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs191485192	chr9:96099784-96099785	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs565417701	chr9:96099816-96099817	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs530279508	chr9:96099895-96099896	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs79698310	chr9:96099937-96099938	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs35378355	chr9:96099983-96099984	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs568823349	chr9:96100003-96100004	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs143618082	chr9:96100012-96100013	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs537300104	chr9:96100032-96100033	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs568100019	chr9:96100059-96100060	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs558933245	chr9:96100063-96100064	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Mental retardation	21693067	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Microcephaly	18830227	CNVD
overgrowth syndrome	16570072	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:510 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96068400-96100400	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr9:96081000-96100600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr9:96083200-96100400	Weak transcription	Fetal Stomach	stomach
4	chr9:96089200-96099400	Weak transcription	Fetal Brain Female	brain
5	chr9:96094000-96099800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr9:96094400-96099000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr9:96095000-96100000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr9:96095200-96099800	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr9:96096400-96099000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr9:96096400-96099000	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr9:96096400-96099000	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr9:96097200-96100200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr9:96097800-96099000	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr9:96098600-96108000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr9:96098800-96099200	Enhancers	Skeletal Muscle Female	skeletal muscle
16	chr9:96098800-96099400	Enhancers	Skeletal Muscle Male	skeletal muscle
17	chr9:96098800-96105000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
18	chr9:96099000-96099200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr9:96099000-96099400	Strong transcription	H1 Cell Line	embryonic stem cell
20	chr9:96099000-96099400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
21	chr9:96099000-96099400	Enhancers	Fetal Heart	heart
22	chr9:96099000-96099400	Enhancers	Psoas Muscle	Psoas
23	chr9:96099000-96102800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
24	chr9:96099000-96103400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
25	chr9:96099400-96100200	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr9:96099800-96100000	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
27	chr9:96099800-96102600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
28	chr9:96100000-96103000	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
29	chr9:96100200-96100400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr9:96100200-96102800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
31	chr9:96100400-96100600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr9:96100600-96101200	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr9:96100600-96101200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
34	chr9:96101200-96102000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr9:96101400-96107200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr9:96101800-96102800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
37	chr9:96101800-96103200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr9:96102000-96102200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
39	chr9:96102000-96102200	Flanking Bivalent TSS/Enh	HepG2	liver
40	chr9:96102000-96102800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr9:96102200-96102600	Bivalent Enhancer	HepG2	liver
42	chr9:96102200-96102800	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
43	chr9:96102200-96103200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr9:96102400-96102600	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr9:96102400-96102800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr9:96102400-96102800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
47	chr9:96102400-96102800	ZNF genes & repeats	Fetal Brain Male	brain
48	chr9:96102400-96102800	Enhancers	Gastric	stomach
49	chr9:96102600-96106000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr9:96102600-96107600	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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