Variant report

Variant	nsv893206
Chromosome Location	chr9:43592096-43790296
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	chr9:43714519-43714714	GM12878	blood:	n/a	n/a
3	BATF	chr9:43653838-43653993	GM12878	blood:	n/a	n/a
4	CEBPB	chr9:43686226-43687047	A549	lung:	n/a	chr9:43686435-43686447
5	CEBPB	chr9:43772398-43772773	A549	lung:	n/a	n/a
6	CTCF	chr9:43744871-43744936	GM13977	blood:	n/a	n/a
7	CTCF	chr9:43653760-43653910	AG09319	gingival:	n/a	n/a
8	CTCF	chr9:43653760-43653910	AG04449	skin:	n/a	n/a
9	CTCF	chr9:43628927-43629150	K562	blood:	n/a	n/a
10	CTCF	chr9:43653760-43653910	HEK293	kidney:	n/a	n/a
11	CTCF	chr9:43653780-43653930	HMEC	breast:	n/a	chr9:43653906-43653927 chr9:43653907-43653920 chr9:43653904-43653922 chr9:43653905-43653921 chr9:43653909-43653919
12	CTCF	chr9:43653760-43653910	HA-sp	spinal cord:	n/a	n/a
13	CTCF	chr9:43756001-43756039	GM10266	blood:	n/a	n/a
14	CTCF	chr9:43685330-43685353	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr9:43709666-43709770	Kidney_OC	kidney:	n/a	n/a
16	CTCF	chr9:43755894-43755968	Kidney_OC	kidney:	n/a	n/a
17	CTCF	chr9:43686500-43686650	HMEC	breast:	n/a	n/a
18	CTCF	chr9:43653873-43653928	Hela-S3	cervix:	n/a	chr9:43653906-43653927 chr9:43653907-43653920 chr9:43653904-43653922 chr9:43653905-43653921 chr9:43653909-43653919
19	CTCF	chr9:43641026-43641132	Kidney_OC	kidney:	n/a	n/a
20	CTCF	chr9:43693140-43693290	HCFaa	heart:	n/a	n/a
21	CTCF	chr9:43679020-43679170	HCT-116	colon:	n/a	n/a
22	CTCF	chr9:43713052-43713091	Kidney_OC	kidney:	n/a	n/a
23	CTCF	chr9:43789914-43790084	NHEK	skin:	n/a	n/a
24	CTCF	chr9:43653813-43653942	GM10248	blood:	n/a	chr9:43653906-43653927 chr9:43653907-43653920 chr9:43653904-43653922 chr9:43653905-43653921 chr9:43653909-43653919
25	CTCF	chr9:43713474-43713597	Kidney_OC	kidney:	n/a	n/a
26	CTCF	chr9:43686552-43686605	Fibrobl	skin:	n/a	n/a
27	CTCF	chr9:43684736-43684912	Spleen_OC	spleen:	n/a	chr9:43684809-43684822 chr9:43684811-43684819
28	CTCF	chr9:43746860-43746888	Kidney_OC	kidney:	n/a	n/a
29	CTCF	chr9:43728263-43728274	LNCaP	prostate:	n/a	n/a
30	CTCF	chr9:43684800-43684950	HRE	kidney:	n/a	chr9:43684809-43684822 chr9:43684811-43684819
31	CTCF	chr9:43686840-43686990	HMEC	breast:	n/a	chr9:43686883-43686904 chr9:43686882-43686898
32	CTCF	chr9:43686774-43687098	HCT-116	colon:	n/a	chr9:43686883-43686904 chr9:43686882-43686898
33	CTCF	chr9:43653760-43653910	HMEC	breast:	n/a	n/a
34	CTCF	chr9:43653760-43653910	HCFaa	heart:	n/a	n/a
35	CTCF	chr9:43693036-43693250	LNCaP	prostate:	n/a	n/a
36	CTCF	chr9:43653836-43653969	LNCaP	prostate:	n/a	chr9:43653906-43653927 chr9:43653907-43653920 chr9:43653904-43653922 chr9:43653905-43653921 chr9:43653909-43653919
37	CTCF	chr9:43653898-43653939	GM12892	blood:	n/a	chr9:43653906-43653927 chr9:43653907-43653920 chr9:43653904-43653922 chr9:43653905-43653921 chr9:43653909-43653919
38	CTCF	chr9:43684574-43684965	A549	lung:	n/a	chr9:43684809-43684822 chr9:43684811-43684819
39	CTCF	chr9:43604568-43604635	GM13977	blood:	n/a	n/a
40	CTCF	chr9:43677983-43678051	A549	lung:	n/a	n/a
41	CTCF	chr9:43653760-43653910	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr9:43684713-43685132	K562	blood:	n/a	chr9:43684809-43684822 chr9:43684811-43684819
43	CTCF	chr9:43653760-43653910	HepG2	liver:	n/a	n/a
44	CTCF	chr9:43748784-43748862	GM13976	blood:	n/a	n/a
45	CTCF	chr9:43686460-43686610	RPTEC	kidney:	n/a	n/a
46	CTCF	chr9:43789934-43790054	A549	lung:	n/a	n/a
47	CTCF	chr9:43653760-43653910	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr9:43693074-43693102	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr9:43693063-43693259	K562	blood:	n/a	n/a
50	CTCF	chr9:43653832-43653982	K562	blood:	n/a	chr9:43653906-43653927 chr9:43653907-43653920 chr9:43653904-43653922 chr9:43653905-43653921 chr9:43653909-43653919

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:43631161-43631211	RPTEC	kidney:	n/a
2	chr9:43631161-43631211	RPTEC	kidney:	n/a
3	chr9:43631161-43631211	SK-N-MC	brain:	n/a
4	chr9:43631161-43631211	PANC-1	pancreas:	n/a
5	chr9:43631161-43631211	GM12892	blood:	n/a
6	chr9:43631161-43631211	GM19239	blood:	n/a
7	chr9:43631161-43631211	AG04450	lung:	fetal
8	chr9:43631161-43631211	AG09309	skin:	n/a
9	chr9:43631161-43631211	AG10803	skin:	n/a
10	chr9:43631161-43631211	H1-hESC	embryonic stem cell:	embryo
11	chr9:43631161-43631211	NHDF-neo	bronchial:	n/a
12	chr9:43631161-43631211	HAEpiC	amniotic membrane:	n/a
13	chr9:43631161-43631211	HCT-116	colon:	n/a
14	chr9:43631161-43631211	ovcar-3	ovarian:	n/a
15	chr9:43631161-43631211	HL-60	blood:	n/a
16	chr9:43631161-43631211	Jurkat	blood:	n/a
17	chr9:43631161-43631211	HCF	heart:	n/a
18	chr9:43631161-43631211	PrEC	prostate:	n/a
19	chr9:43631161-43631211	GM12891	blood:	n/a
20	chr9:43631161-43631211	HRPEpiC	eye:	n/a
21	chr9:43631161-43631211	A549	lung:	n/a
22	chr9:43631161-43631211	NHBE	bronchial:	n/a
23	chr9:43631161-43631211	Caco-2	colon:	n/a
24	chr9:43631161-43631211	SK-N-SH_RA	brain:	n/a
25	chr9:43631161-43631211	HCPEpiC	choroid plexus:	n/a
26	chr9:43631161-43631211	SAEC	small airway:	n/a
27	chr9:43631161-43631211	HCM	heart:	n/a
28	chr9:43631161-43631211	PFSK-1	brain:	n/a
29	chr9:43631161-43631211	NT2-D1	testis:	n/a
30	chr9:43631161-43631211	HIPEpiC	eye:	n/a
31	chr9:43631161-43631211	HEEpiC	esophagus:	n/a
32	chr9:43631161-43631211	K562	blood:	n/a
33	chr9:43631161-43631211	HEK293	kidney:	embryo
34	chr9:43631161-43631211	HepG2	liver:	n/a
35	chr9:43631161-43631211	U87	brain:	n/a
36	chr9:43631161-43631211	IMR90	lung:	fetal
37	chr9:43631161-43631211	BJ	skin:	n/a
38	chr9:43631161-43631211	AoSMC	blood vessel:	n/a
39	chr9:43631161-43631211	HPAEpiC	pulmonary alveolar:	n/a
40	chr9:43631161-43631211	MCF10A-Er-Src	breast:	n/a
41	chr9:43631161-43631211	AG04449	skin:	fetal
42	chr9:43631161-43631211	Hepatocyte	liver:	n/a
43	chr9:43631161-43631211	ProgFib	skin:	n/a
44	chr9:43631161-43631211	SK-N-SH	brain:	n/a
45	chr9:43631161-43631211	NH-A	brain:	n/a
46	chr9:43631161-43631211	HRE	kidney:	n/a
47	chr9:43631161-43631211	MCF-7	breast:	n/a
48	chr9:43631161-43631211	HRCEpiC	kidney:	n/a
49	chr9:43631161-43631211	AG09319	gingival:	n/a
50	chr9:43631161-43631211	LNCaP	prostate:	n/a

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

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: 1079 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1079 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1531141	chr9:43592096-43592097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs117206127	chr9:43592103-43592104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs371385882	chr9:43592112-43592113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs112535305	chr9:43592298-43592299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565024665	chr9:43592302-43592303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs532252357	chr9:43592323-43592324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs534061864	chr9:43592326-43592327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs111361655	chr9:43592353-43592354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs573739081	chr9:43592373-43592374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs537848282	chr9:43592401-43592402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs140791796	chr9:43592404-43592405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs3122024	chr9:43592411-43592412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs577878979	chr9:43592420-43592421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs188407181	chr9:43592433-43592434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs547477826	chr9:43592436-43592437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs191514006	chr9:43592442-43592443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs560450325	chr9:43592446-43592447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs572575631	chr9:43592482-43592483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs539985980	chr9:43592484-43592485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs561755985	chr9:43592489-43592490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs56852433	chr9:43592492-43592493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs550547658	chr9:43592511-43592512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562780466	chr9:43592522-43592523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs533044370	chr9:43592527-43592528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs58946836	chr9:43592531-43592532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs551632028	chr9:43592532-43592533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs12000485	chr9:43592552-43592553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs533982975	chr9:43592574-43592575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs60239577	chr9:43592643-43592644	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs549114060	chr9:43592651-43592652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs183668681	chr9:43592672-43592673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs537860739	chr9:43592682-43592683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188718919	chr9:43592688-43592689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs578210613	chr9:43592705-43592706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181111301	chr9:43592718-43592719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527956503	chr9:43592720-43592721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs572591246	chr9:43592726-43592727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543201227	chr9:43592741-43592742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs555504345	chr9:43592758-43592759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573737388	chr9:43592825-43592826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs3882715	chr9:43592831-43592832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs187155455	chr9:43592834-43592835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs532926103	chr9:43592855-43592856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529635928	chr9:43592874-43592875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs370265006	chr9:43592927-43592928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs527499967	chr9:43592934-43592935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548728818	chr9:43592935-43592936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189944491	chr9:43592936-43592937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs531663753	chr9:43592942-43592943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549684976	chr9:43592958-43592959	Weak transcription	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
Lung cancer	17086460	CNVD
Rhabdomyosarcoma	16790082	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:142 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:43590800-43593800	Weak transcription	HUVEC	blood vessel
2	chr9:43593800-43595000	Enhancers	HUVEC	blood vessel
3	chr9:43594200-43594600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr9:43594200-43595000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr9:43609400-43609800	Enhancers	HUVEC	blood vessel
6	chr9:43684200-43685200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr9:43684200-43685200	Active TSS	HUES64 Cell Line	embryonic stem cell
8	chr9:43684200-43685200	Active TSS	iPS-18 Cell Line	embryonic stem cell
9	chr9:43684200-43685200	Active TSS	iPS-20b Cell Line	embryonic stem cell
10	chr9:43684200-43685200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr9:43684200-43685200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr9:43684200-43685200	Active TSS	Fetal Brain Female	brain
13	chr9:43684200-43686200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr9:43684200-43686400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr9:43684200-43687000	Active TSS	Right Ventricle	heart
16	chr9:43684200-43687000	Active TSS	A549	lung
17	chr9:43684200-43687200	Active TSS	Breast Myoepithelial Primary Cells	Breast
18	chr9:43684400-43685200	Active TSS	HUES48 Cell Line	embryonic stem cell
19	chr9:43684400-43685200	Active TSS	iPS-15b Cell Line	embryonic stem cell
20	chr9:43684800-43685000	Active TSS	Colonic Mucosa	Colon
21	chr9:43684800-43685200	Active TSS	H1 Cell Line	embryonic stem cell
22	chr9:43684800-43685200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr9:43684800-43685200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr9:43684800-43685200	Active TSS	HUES6 Cell Line	embryonic stem cell
25	chr9:43684800-43685200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
26	chr9:43684800-43685200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr9:43684800-43685200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr9:43684800-43685200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr9:43684800-43685200	Active TSS	Adipose Nuclei	Adipose
30	chr9:43684800-43685200	Active TSS	Duodenum Smooth Muscle	Duodenum
31	chr9:43684800-43685200	Active TSS	Psoas Muscle	Psoas
32	chr9:43684800-43685200	Active TSS	Osteobl	bone
33	chr9:43684800-43686400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr9:43684800-43686800	Active TSS	Cortex derived primary cultured neurospheres	brain
35	chr9:43684800-43687000	Active TSS	Stomach Smooth Muscle	stomach
36	chr9:43684800-43687200	Active TSS	HMEC	breast
37	chr9:43684800-43687200	Active TSS	HUVEC	blood vessel
38	chr9:43685000-43685200	Bivalent/Poised TSS	Colonic Mucosa	Colon
39	chr9:43685200-43686000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr9:43685200-43686000	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr9:43685200-43686000	Weak transcription	Fetal Brain Female	brain
42	chr9:43685200-43686200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr9:43685200-43686200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr9:43685200-43686200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr9:43685200-43686200	Weak transcription	Adipose Nuclei	Adipose
46	chr9:43685200-43686200	Weak transcription	Psoas Muscle	Psoas
47	chr9:43685200-43686400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr9:43685800-43686200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr9:43685800-43687000	Active TSS	NH-A	brain
50	chr9:43685800-43687200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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