Variant report

Variant	nsv892091
Chromosome Location	chr9:3459635-3508284
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:817)
CpG islands
(count:0)
Chromatin interactive
region (count:42)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:817 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:3507381-3509202	K562	blood:	n/a	n/a
2	ATF2	chr9:3475292-3476102	GM12878	blood:	n/a	n/a
3	ATF2	chr9:3479428-3480436	GM12878	blood:	n/a	n/a
4	ATF2	chr9:3479370-3480333	GM12878	blood:	n/a	n/a
5	ATF2	chr9:3475443-3476039	GM12878	blood:	n/a	n/a
6	ATF2	chr9:3478340-3478822	GM12878	blood:	n/a	n/a
7	ATF2	chr9:3478178-3478876	GM12878	blood:	n/a	n/a
8	ATF3	chr9:3475317-3475567	HepG2	liver:	n/a	n/a
9	ATF3	chr9:3475231-3475643	K562	blood:	n/a	n/a
10	ATF3	chr9:3475331-3475578	K562	blood:	n/a	n/a
11	BATF	chr9:3475628-3476049	GM12878	blood:	n/a	n/a
12	BATF	chr9:3479480-3479762	GM12878	blood:	n/a	n/a
13	BATF	chr9:3475282-3475581	GM12878	blood:	n/a	chr9:3475427-3475438
14	BATF	chr9:3475305-3475599	GM12878	blood:	n/a	chr9:3475427-3475438
15	BATF	chr9:3480020-3480395	GM12878	blood:	n/a	n/a
16	BCL11A	chr9:3475655-3476069	GM12878	blood:	n/a	n/a
17	BCL11A	chr9:3475688-3476026	GM12878	blood:	n/a	n/a
18	BCL11A	chr9:3479574-3480056	GM12878	blood:	n/a	chr9:3479921-3479930
19	BCL3	chr9:3475614-3476073	GM12878	blood:	n/a	n/a
20	BCLAF1	chr9:3479414-3480223	GM12878	blood:	n/a	chr9:3479921-3479930
21	BCLAF1	chr9:3478308-3479065	GM12878	blood:	n/a	n/a
22	BCLAF1	chr9:3475372-3476053	GM12878	blood:	n/a	n/a
23	BCLAF1	chr9:3475517-3476108	GM12878	blood:	n/a	n/a
24	BCLAF1	chr9:3467518-3468055	GM12878	blood:	n/a	chr9:3467803-3467812
25	BCLAF1	chr9:3473349-3473785	GM12878	blood:	n/a	n/a
26	BHLHE40	chr9:3475319-3475706	K562	blood:	n/a	n/a
27	BHLHE40	chr9:3475328-3476086	GM12878	blood:	n/a	n/a
28	BHLHE40	chr9:3475349-3475581	HepG2	liver:	n/a	n/a
29	BHLHE40	chr9:3467628-3467956	GM12878	blood:	n/a	n/a
30	CBX3	chr9:3475298-3475599	K562	blood:	n/a	n/a
31	CBX3	chr9:3477770-3478100	K562	blood:	n/a	n/a
32	CCNT2	chr9:3507800-3508014	K562	blood:	n/a	n/a
33	CEBPB	chr9:3467468-3468111	GM12878	blood:	n/a	n/a
34	CEBPB	chr9:3507551-3508188	K562	blood:	n/a	n/a
35	CEBPB	chr9:3464201-3464484	IMR90	lung:	n/a	n/a
36	CEBPB	chr9:3507443-3507897	A549	lung:	n/a	n/a
37	CEBPB	chr9:3464214-3464434	K562	blood:	n/a	n/a
38	CEBPB	chr9:3466283-3466577	IMR90	lung:	n/a	n/a
39	CEBPB	chr9:3475235-3476196	GM12878	blood:	n/a	n/a
40	CEBPB	chr9:3507691-3508016	K562	blood:	n/a	n/a
41	CEBPB	chr9:3502452-3503130	A549	lung:	n/a	chr9:3502457-3502470 chr9:3502459-3502470
42	CEBPB	chr9:3466338-3466511	A549	lung:	n/a	n/a
43	CHD1	chr9:3477640-3477760	GM12878	blood:	n/a	n/a
44	CHD2	chr9:3475646-3476022	GM12878	blood:	n/a	n/a
45	CHD2	chr9:3467608-3468058	GM12878	blood:	n/a	n/a
46	CREB1	chr9:3479525-3480334	GM12878	blood:	n/a	n/a
47	CTCF	chr9:3467630-3467917	GM10266	blood:	n/a	chr9:3467769-3467790 chr9:3467767-3467785
48	CTCF	chr9:3467700-3467850	HRE	kidney:	n/a	chr9:3467769-3467790 chr9:3467767-3467785
49	CTCF	chr9:3467660-3467810	HVMF	connective:	n/a	chr9:3467769-3467790 chr9:3467767-3467785
50	CTCF	chr9:3475869-3476050	GM19240	blood:	n/a	n/a

No data

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:3474527..3477268-chr9:3526312..3529776,3	K562	blood:
2	chr9:3479015..3481934-chr9:3484671..3486572,2	K562	blood:
3	chr9:3460990..3463630-chr9:3491395..3493289,2	K562	blood:
4	chr9:3488422..3492745-chr9:3526119..3529756,3	K562	blood:
5	chr9:3505495..3510523-chr9:3529335..3535947,8	K562	blood:
6	chr9:3472148..3476426-chr9:3525120..3528323,5	MCF-7	breast:
7	chr9:3462529..3469298-chr9:3525044..3529022,8	MCF-7	breast:
8	chr9:3470655..3472991-chr9:3531327..3534236,2	K562	blood:
9	chr9:3477335..3480982-chr9:3525320..3527937,6	MCF-7	breast:
10	chr9:3465058..3467363-chr9:3472646..3474184,2	K562	blood:
11	chr9:3461663..3464190-chr9:3509726..3512985,3	K562	blood:
12	chr9:3467888..3469865-chr9:4296792..4299430,2	MCF-7	breast:
13	chr9:3465058..3467363-chr9:3472646..3474184,2	K562	blood:
14	chr9:3498806..3500362-chr9:3527236..3529774,2	K562	blood:
15	chr9:3491268..3494910-chr9:3525417..3527620,3	MCF-7	breast:
16	chr9:3462690..3464398-chr9:3511341..3512985,2	K562	blood:
17	chr9:3479015..3481934-chr9:3484671..3486572,2	K562	blood:
18	chr9:3486226..3487734-chr9:3489487..3491455,2	K562	blood:
19	chr9:3500140..3503117-chr9:3505256..3509401,4	K562	blood:
20	chr9:3501077..3503324-chr9:3523015..3525744,2	MCF-7	breast:
21	chr9:3497780..3499700-chr9:3524560..3526876,2	K562	blood:
22	chr9:3493140..3494788-chr9:3496837..3499206,2	K562	blood:
23	chr9:3478739..3481374-chr9:3498869..3500820,2	MCF-7	breast:
24	chr9:3478739..3481374-chr9:3498869..3500820,2	MCF-7	breast:
25	chr9:3460990..3463630-chr9:3491395..3493289,2	K562	blood:
26	chr9:3474241..3476726-chr9:3530164..3531864,2	K562	blood:
27	chr9:3466442..3469407-chr9:3524530..3526691,2	K562	blood:
28	chr9:3505863..3515695-chr9:3520675..3529318,33	K562	blood:
29	chr9:3493140..3494788-chr9:3496837..3499206,2	K562	blood:
30	chr9:3498254..3500362-chr9:3527205..3528736,2	K562	blood:
31	chr9:3489743..3491847-chr9:3522486..3524735,2	K562	blood:
32	chr9:3500140..3503117-chr9:3505256..3509401,4	K562	blood:
33	chr9:3486226..3487734-chr9:3489487..3491455,2	K562	blood:
34	chr9:3478923..3481537-chr9:3524337..3526099,2	K562	blood:
35	chr9:3481303..3484512-chr9:3524609..3529415,5	MCF-7	breast:
36	chr9:3489811..3492188-chr9:3524629..3527115,2	MCF-7	breast:
37	chr9:3495106..3497016-chr9:3524367..3527205,3	MCF-7	breast:
38	chr9:3507570..3510389-chr9:4297452..4299363,2	MCF-7	breast:
39	chr9:3474071..3478012-chr9:3525066..3526947,3	K562	blood:
40	chr9:3472046..3474328-chr9:3525232..3527655,2	K562	blood:
41	chr9:3495458..3497256-chr9:3517334..3519565,2	K562	blood:
42	chr9:3467327..3468207-chr9:3521230..3521983,2	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNV2-7	chr9:3469874-3471237	ucscGeneNc_uc003zhu_2
2	lnc-KCNV2-8	chr9:3479874-3481237	NONHSAT130020

No data

Variant related genes	Relation type
RFX3	TF binding region
ENSG00000203286	TF binding region
ENSG00000107249	chromatin interactions
ENSG00000080298	chromatin interactions
ENSG00000232104	chromatin interactions
ENSG00000228322	chromatin interactions

Extended variants
information (count: 2146 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:2146 , 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	rs7859887	chr9:3459635-3459636	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs530707893	chr9:3459647-3459648	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs544008166	chr9:3459688-3459689	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs555026162	chr9:3459696-3459697	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs75848206	chr9:3459734-3459735	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs574951323	chr9:3459761-3459762	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs185551761	chr9:3459818-3459819	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs375115175	chr9:3459827-3459828	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs566024494	chr9:3459849-3459850	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs138689988	chr9:3459918-3459919	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs143310570	chr9:3459925-3459926	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568775360	chr9:3459954-3459955	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188194890	chr9:3459959-3459960	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs537694924	chr9:3459969-3459970	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs147523499	chr9:3459975-3459976	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs552872421	chr9:3459979-3459980	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs571024585	chr9:3459986-3459987	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs368863374	chr9:3460018-3460019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs201092650	chr9:3460079-3460080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs6476451	chr9:3460092-3460093	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs139415580	chr9:3460114-3460115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs541853561	chr9:3460132-3460133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs149605654	chr9:3460154-3460155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs115507324	chr9:3460176-3460177	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs544968503	chr9:3460201-3460202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs112615593	chr9:3460242-3460243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs191109195	chr9:3460260-3460261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs183621419	chr9:3460267-3460268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs559844941	chr9:3460299-3460300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs75375733	chr9:3460303-3460304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs548567546	chr9:3460305-3460306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs34647706	chr9:3460309-3460310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs562035346	chr9:3460339-3460340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs531248010	chr9:3460344-3460345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs79092445	chr9:3460413-3460414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs571140062	chr9:3460430-3460431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs7047337	chr9:3460433-3460434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs181246296	chr9:3460468-3460469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs566574182	chr9:3460573-3460574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs565137979	chr9:3460600-3460601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs138550729	chr9:3460603-3460604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs535155694	chr9:3460616-3460617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs529896687	chr9:3460624-3460625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs34706848	chr9:3460634-3460635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs555360856	chr9:3460656-3460657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs574857992	chr9:3460658-3460659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs78742712	chr9:3460663-3460664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs144348768	chr9:3460673-3460674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557657397	chr9:3460788-3460789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs7028681	chr9:3460790-3460791	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Gastric cancer	16715143	CNVD
Glioblastoma multiforme	22286061	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Disorders of sex development	21048976	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	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
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	21373258	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Autism	20808228	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD

Chromatin state (count:827 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:3432400-3467800	Weak transcription	GM12878-XiMat	blood
2	chr9:3432600-3460600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr9:3435000-3473200	Weak transcription	Primary T cells from cord blood	blood
4	chr9:3438400-3472800	Weak transcription	Primary B cells from cord blood	blood
5	chr9:3447400-3478800	Weak transcription	Aorta	Aorta
6	chr9:3448000-3475800	Weak transcription	Fetal Intestine Small	intestine
7	chr9:3452200-3464200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr9:3455000-3483000	Weak transcription	Fetal Thymus	thymus
9	chr9:3456000-3460000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr9:3456200-3467600	Weak transcription	Ovary	ovary
11	chr9:3456200-3473200	Weak transcription	Primary hematopoietic stem cells	blood
12	chr9:3458000-3467800	Weak transcription	A549	lung
13	chr9:3458600-3459800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr9:3458800-3460000	Enhancers	Fetal Brain Male	brain
15	chr9:3458800-3460200	Enhancers	Dnd41	blood
16	chr9:3459200-3460200	Weak transcription	Fetal Brain Female	brain
17	chr9:3459400-3461400	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr9:3459400-3467600	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr9:3459400-3467600	Weak transcription	Brain Anterior Caudate	brain
20	chr9:3459400-3467800	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr9:3459600-3472800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr9:3459800-3467400	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr9:3459800-3467800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr9:3460000-3460800	Weak transcription	Fetal Brain Male	brain
25	chr9:3460000-3462000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr9:3460200-3460400	Enhancers	Fetal Brain Female	brain
27	chr9:3460800-3461000	Enhancers	Fetal Brain Male	brain
28	chr9:3461000-3467600	Weak transcription	Fetal Brain Male	brain
29	chr9:3461400-3461600	Enhancers	Pancreatic Islets	Pancreatic Islet
30	chr9:3461600-3461800	Enhancers	HUVEC	blood vessel
31	chr9:3461800-3471000	Weak transcription	HUVEC	blood vessel
32	chr9:3462000-3462600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr9:3462000-3467800	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr9:3462600-3463200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr9:3463400-3467800	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr9:3463600-3467600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
37	chr9:3463800-3464600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr9:3463800-3464800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr9:3464000-3464600	Enhancers	NHDF-Ad	bronchial
40	chr9:3464000-3467800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
41	chr9:3464200-3464400	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr9:3464400-3467200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr9:3464600-3464800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr9:3464600-3467800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr9:3464600-3467800	Weak transcription	NHDF-Ad	bronchial
46	chr9:3464800-3467600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr9:3464800-3467800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr9:3467200-3470200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr9:3467400-3469000	Enhancers	Brain Germinal Matrix	brain
50	chr9:3467400-3469200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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