Variant report

Variant	nsv893182
Chromosome Location	chr9:43504854-43734193
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr9:43686226-43686817	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr9:43653838-43653993	GM12878	blood:	n/a	n/a
3	BATF	chr9:43529040-43529422	GM12878	blood:	n/a	n/a
4	BATF	chr9:43714519-43714714	GM12878	blood:	n/a	n/a
5	BHLHE40	chr9:43505744-43505995	A549	lung:	n/a	n/a
6	CEBPB	chr9:43686226-43687047	A549	lung:	n/a	chr9:43686435-43686447
7	CTCF	chr9:43677983-43678051	A549	lung:	n/a	n/a
8	CTCF	chr9:43658088-43658108	GM20000	blood:	n/a	n/a
9	CTCF	chr9:43583060-43583210	HCT-116	colon:	n/a	n/a
10	CTCF	chr9:43685291-43685364	Gliobla	brain:	n/a	n/a
11	CTCF	chr9:43712695-43712735	GM13976	blood:	n/a	n/a
12	CTCF	chr9:43653836-43653969	LNCaP	prostate:	n/a	chr9:43653906-43653927 chr9:43653907-43653920 chr9:43653904-43653922 chr9:43653905-43653921 chr9:43653909-43653919
13	CTCF	chr9:43720802-43720888	GM20000	blood:	n/a	n/a
14	CTCF	chr9:43643268-43643348	GM10266	blood:	n/a	n/a
15	CTCF	chr9:43693140-43693290	HCFaa	heart:	n/a	n/a
16	CTCF	chr9:43686540-43686690	A549	lung:	n/a	n/a
17	CTCF	chr9:43733843-43733904	Medullo	brain:	n/a	n/a
18	CTCF	chr9:43589736-43589840	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr9:43653876-43653935	Pancreas_OC	pancreas:	n/a	chr9:43653906-43653927 chr9:43653907-43653920 chr9:43653904-43653922 chr9:43653905-43653921 chr9:43653909-43653919
20	CTCF	chr9:43653760-43653910	AG09319	gingival:	n/a	n/a
21	CTCF	chr9:43653760-43653910	HPAF	blood vessel:	n/a	n/a
22	CTCF	chr9:43685268-43685368	A549	lung:	n/a	n/a
23	CTCF	chr9:43684574-43684965	A549	lung:	n/a	chr9:43684809-43684822 chr9:43684811-43684819
24	CTCF	chr9:43686520-43686670	HPAF	blood vessel:	n/a	n/a
25	CTCF	chr9:43653760-43653910	SAEC	small airway:	n/a	n/a
26	CTCF	chr9:43728237-43728253	LNCaP	prostate:	n/a	n/a
27	CTCF	chr9:43692974-43693224	A549	lung:	n/a	n/a
28	CTCF	chr9:43704998-43705104	GM13976	blood:	n/a	n/a
29	CTCF	chr9:43692982-43693182	K562	blood:	n/a	n/a
30	CTCF	chr9:43686653-43687033	A549	lung:	n/a	chr9:43686883-43686904 chr9:43686882-43686898
31	CTCF	chr9:43653760-43653910	HCFaa	heart:	n/a	n/a
32	CTCF	chr9:43653780-43653930	GM12867	blood:	n/a	chr9:43653906-43653927 chr9:43653907-43653920 chr9:43653904-43653922 chr9:43653905-43653921 chr9:43653909-43653919
33	CTCF	chr9:43693108-43693224	Kidney_OC	kidney:	n/a	n/a
34	CTCF	chr9:43653772-43654018	Gliobla	brain:	n/a	chr9:43653906-43653927 chr9:43653907-43653920 chr9:43653904-43653922 chr9:43653905-43653921 chr9:43653909-43653919
35	CTCF	chr9:43653780-43653930	HMEC	breast:	n/a	chr9:43653906-43653927 chr9:43653907-43653920 chr9:43653904-43653922 chr9:43653905-43653921 chr9:43653909-43653919
36	CTCF	chr9:43673780-43673843	LNCaP	prostate:	n/a	n/a
37	CTCF	chr9:43641026-43641132	Kidney_OC	kidney:	n/a	n/a
38	CTCF	chr9:43653807-43654024	A549	lung:	n/a	chr9:43653906-43653927 chr9:43653907-43653920 chr9:43653904-43653922 chr9:43653905-43653921 chr9:43653909-43653919
39	CTCF	chr9:43730117-43730226	Lung_OC	lung:	n/a	n/a
40	CTCF	chr9:43693100-43693250	NHEK	skin:	n/a	n/a
41	CTCF	chr9:43686740-43686890	A549	lung:	n/a	n/a
42	CTCF	chr9:43693074-43693102	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr9:43533558-43533635	MCF-7	breast:	n/a	n/a
44	CTCF	chr9:43732082-43732116	Kidney_OC	kidney:	n/a	n/a
45	CTCF	chr9:43684920-43685070	AoAF	blood vessel:	n/a	n/a
46	CTCF	chr9:43721666-43721688	Spleen_OC	spleen:	n/a	n/a
47	CTCF	chr9:43594301-43594313	NHEK	skin:	n/a	n/a
48	CTCF	chr9:43653760-43653910	GM12873	blood:	n/a	n/a
49	CTCF	chr9:43686808-43686957	HUVEC	blood vessel:	n/a	chr9:43686883-43686904 chr9:43686882-43686898
50	CTCF	chr9:43533432-43533702	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:43525320-43525370	GM12878	blood:	n/a
2	chr9:43525948-43525998	HPAEpiC	pulmonary alveolar:	n/a
3	chr9:43525948-43525998	SK-N-MC	brain:	n/a
4	chr9:43525320-43525370	MCF-7	breast:	n/a
5	chr9:43525320-43525370	CMK	blood:	n/a
6	chr9:43525320-43525370	NH-A	brain:	n/a
7	chr9:43631161-43631211	PANC-1	pancreas:	n/a
8	chr9:43631161-43631211	HCT-116	colon:	n/a
9	chr9:43525320-43525370	HEEpiC	esophagus:	n/a
10	chr9:43631161-43631211	PrEC	prostate:	n/a
11	chr9:43525948-43525998	AG10803	skin:	n/a
12	chr9:43631161-43631211	ECC-1	luminal epithelium:	n/a
13	chr9:43525948-43525998	HAEpiC	amniotic membrane:	n/a
14	chr9:43631161-43631211	U87	brain:	n/a
15	chr9:43631161-43631211	HL-60	blood:	n/a
16	chr9:43525948-43525998	HL-60	blood:	n/a
17	chr9:43525948-43525998	HUVEC	blood vessel:	n/a
18	chr9:43525320-43525370	AG04450	lung:	fetal
19	chr9:43631161-43631211	K562	blood:	n/a
20	chr9:43631161-43631211	HepG2	liver:	n/a
21	chr9:43631161-43631211	HCPEpiC	choroid plexus:	n/a
22	chr9:43631161-43631211	SK-N-SH	brain:	n/a
23	chr9:43525948-43525998	Caco-2	colon:	n/a
24	chr9:43631161-43631211	HCM	heart:	n/a
25	chr9:43525948-43525998	SKMC	muscle:	n/a
26	chr9:43631161-43631211	ProgFib	skin:	n/a
27	chr9:43525948-43525998	NT2-D1	testis:	n/a
28	chr9:43525320-43525370	Hepatocyte	liver:	n/a
29	chr9:43525320-43525370	AoSMC	blood vessel:	n/a
30	chr9:43525320-43525370	T-47D	breast:	n/a
31	chr9:43525948-43525998	HepG2	liver:	n/a
32	chr9:43525948-43525998	IMR90	lung:	fetal
33	chr9:43631161-43631211	NT2-D1	testis:	n/a
34	chr9:43525320-43525370	BE2_C	brain:	n/a
35	chr9:43525948-43525998	MCF-7	breast:	n/a
36	chr9:43631161-43631211	Caco-2	colon:	n/a
37	chr9:43525320-43525370	Hela-S3	cervix:	n/a
38	chr9:43525948-43525998	HNPCEpiC	eye:	n/a
39	chr9:43525320-43525370	K562	blood:	n/a
40	chr9:43631161-43631211	HEK293	kidney:	embryo
41	chr9:43525320-43525370	GM12892	blood:	n/a
42	chr9:43525320-43525370	HCPEpiC	choroid plexus:	n/a
43	chr9:43525948-43525998	PANC-1	pancreas:	n/a
44	chr9:43631161-43631211	ovcar-3	ovarian:	n/a
45	chr9:43525320-43525370	HMEC	breast:	n/a
46	chr9:43525948-43525998	Jurkat	blood:	n/a
47	chr9:43525948-43525998	NHBE	bronchial:	n/a
48	chr9:43631161-43631211	SAEC	small airway:	n/a
49	chr9:43525320-43525370	HRPEpiC	eye:	n/a
50	chr9:43525948-43525998	AG09319	gingival:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANKRD20A3-13	chr9:43629020-43629117	NONHSAT131362
2	lnc-ANKRD20A3-13	chr9:43628634-43628694	NONHSAT131362
3	lnc-ANKRD20A3-13	chr9:43627769-43628378	NONHSAT131362
4	lnc-CNTNAP3B-2	chr9:43617727-43618056	NONHSAT131361

Variant related genes	Relation type
ENSG00000239986	TF binding region
SPATA31A6	TF binding region
CNTNAP3B	TF binding region
ENSG00000239986	CpG island
SPATA31A6	CpG island
CNTNAP3B	CpG island

Extended variants
information (count: 1538 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1538 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7046296	chr9:43504854-43504855	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs76083425	chr9:43504857-43504858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs139635618	chr9:43504865-43504866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs143632613	chr9:43504877-43504878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs528942087	chr9:43504894-43504895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs376660648	chr9:43504904-43504905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs550190727	chr9:43504920-43504921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs118184004	chr9:43504969-43504970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs542087906	chr9:43504978-43504979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs34510391	chr9:43504979-43504980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs397716411	chr9:43504995-43504996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs539391166	chr9:43505023-43505024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs147208280	chr9:43505041-43505042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs183970921	chr9:43505048-43505049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534295040	chr9:43505089-43505090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs374571819	chr9:43505125-43505126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs113074188	chr9:43505134-43505135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs117209599	chr9:43505152-43505153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs549821108	chr9:43505244-43505245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs142792861	chr9:43505270-43505271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs371840014	chr9:43505278-43505279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs117309235	chr9:43505303-43505304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs188524325	chr9:43505304-43505305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs569866943	chr9:43505320-43505321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs578062032	chr9:43505368-43505369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs545724174	chr9:43505374-43505375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560595189	chr9:43505405-43505406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs193071592	chr9:43505408-43505409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs185066444	chr9:43505414-43505415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs542887810	chr9:43505437-43505438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs548513805	chr9:43505456-43505457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs537559836	chr9:43505479-43505480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs561511465	chr9:43505480-43505481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs151043723	chr9:43505486-43505487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs550254161	chr9:43505487-43505488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs139759098	chr9:43505525-43505526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs75326764	chr9:43505546-43505547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs551673898	chr9:43505554-43505555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs116752908	chr9:43505582-43505583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs149788831	chr9:43505588-43505589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs146822690	chr9:43505598-43505599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs541054249	chr9:43505606-43505607	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs112293036	chr9:43505627-43505628	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs140637734	chr9:43505631-43505632	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs556654580	chr9:43505645-43505646	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs144407205	chr9:43505653-43505654	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs146635526	chr9:43505677-43505678	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs7847919	chr9:43505687-43505688	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs117644646	chr9:43505739-43505740	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs116536608	chr9:43505788-43505789	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
Colorectal cancer	16272173	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
Breast cancer	20409316	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	15273396	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
Breast cancer	22522925	CNVD
Lung cancer	17086460	CNVD
Rhabdomyosarcoma	16790082	CNVD

Chromatin state (count:187 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:43491200-43505400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr9:43491200-43505800	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr9:43505400-43505600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr9:43505400-43506000	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr9:43505400-43506400	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr9:43505400-43507000	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr9:43505600-43506000	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr9:43505600-43506000	Genic enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr9:43505600-43506200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr9:43505600-43507000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr9:43505800-43506000	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr9:43505800-43506200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr9:43506000-43506200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr9:43506000-43506800	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr9:43506000-43506800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr9:43506200-43506800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr9:43506400-43506800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr9:43506800-43507000	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr9:43506800-43507200	Active TSS	iPS-18 Cell Line	embryonic stem cell
20	chr9:43506800-43507400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr9:43506800-43507400	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr9:43507000-43507400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
23	chr9:43507000-43507400	Active TSS	iPS-20b Cell Line	embryonic stem cell
24	chr9:43507000-43508400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr9:43507200-43507400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
26	chr9:43507400-43507600	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr9:43507400-43508200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr9:43507400-43508200	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr9:43507600-43508000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr9:43507600-43508000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr9:43508000-43508800	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr9:43508200-43508600	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr9:43508200-43508800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr9:43508400-43508600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr9:43508600-43508800	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr9:43508800-43509800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr9:43509800-43510000	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr9:43581000-43583400	Active TSS	A549	lung
39	chr9:43581200-43581600	Enhancers	HUVEC	blood vessel
40	chr9:43581200-43582200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr9:43581600-43582800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr9:43582200-43582600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr9:43582400-43582800	Enhancers	Fetal Brain Male	brain
44	chr9:43582600-43583000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr9:43588400-43589000	Enhancers	HUVEC	blood vessel
46	chr9:43589000-43590200	Weak transcription	HUVEC	blood vessel
47	chr9:43590200-43590800	Enhancers	HUVEC	blood vessel
48	chr9:43590800-43593800	Weak transcription	HUVEC	blood vessel
49	chr9:43593800-43595000	Enhancers	HUVEC	blood vessel
50	chr9:43594200-43594600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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