Variant report

Variant	nsv829881
Chromosome Location	chr4:22084704-22254679
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	ARID3A	chr4:22239692-22240117	HepG2	liver:	n/a	n/a
2	BATF	chr4:22176374-22176536	GM12878	blood:	n/a	n/a
3	BATF	chr4:22117037-22117289	GM12878	blood:	n/a	chr4:22117167-22117178
4	BHLHE40	chr4:22238995-22239000	GM12878	blood:	n/a	n/a
5	BRCA1	chr4:22206447-22206466	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr4:22086644-22086933	IMR90	lung:	n/a	chr4:22086780-22086797 chr4:22086757-22086770
7	CEBPB	chr4:22091217-22091388	A549	lung:	n/a	chr4:22091369-22091380
8	CEBPB	chr4:22091256-22091515	IMR90	lung:	n/a	chr4:22091369-22091380
9	CEBPB	chr4:22240531-22240641	HepG2	liver:	n/a	n/a
10	CEBPB	chr4:22091251-22091497	HepG2	liver:	n/a	chr4:22091369-22091380
11	CEBPB	chr4:22137438-22137500	HepG2	liver:	n/a	n/a
12	CEBPB	chr4:22183725-22184025	ECC-1	luminal epithelium:	n/a	chr4:22183891-22183904 chr4:22183893-22183904
13	CEBPB	chr4:22203386-22203529	A549	lung:	n/a	n/a
14	CEBPB	chr4:22086670-22086925	A549	lung:	n/a	chr4:22086780-22086797 chr4:22086757-22086770
15	CEBPB	chr4:22204052-22204260	IMR90	lung:	n/a	n/a
16	CEBPB	chr4:22086625-22086937	HepG2	liver:	n/a	chr4:22086780-22086797 chr4:22086757-22086770
17	CEBPB	chr4:22203404-22203506	HepG2	liver:	n/a	n/a
18	CHD2	chr4:22131276-22131322	GM12878	blood:	n/a	n/a
19	CTCF	chr4:22131200-22131350	GM12870	blood:	n/a	chr4:22131265-22131283 chr4:22131267-22131288
20	CTCF	chr4:22131160-22131310	HFF-Myc	foreskin:	n/a	chr4:22131265-22131283 chr4:22131267-22131288
21	CTCF	chr4:22131200-22131350	HRPEpiC	eye:	n/a	chr4:22131265-22131283 chr4:22131267-22131288
22	CTCF	chr4:22238733-22239113	H1-hESC	embryonic stem cell:	n/a	chr4:22238973-22238991
23	CTCF	chr4:22238900-22239050	HRE	kidney:	n/a	chr4:22238973-22238991
24	CTCF	chr4:22131197-22131341	GM13977	blood:	n/a	chr4:22131265-22131283 chr4:22131267-22131288
25	CTCF	chr4:22238900-22239050	HMEC	breast:	n/a	chr4:22238973-22238991
26	CTCF	chr4:22240500-22240650	HepG2	liver:	n/a	n/a
27	CTCF	chr4:22238856-22239068	MCF-7	breast:	n/a	chr4:22238973-22238991
28	CTCF	chr4:22240506-22240645	LNCaP	prostate:	n/a	n/a
29	CTCF	chr4:22238920-22239070	GM12867	blood:	n/a	chr4:22238973-22238991
30	CTCF	chr4:22131145-22131397	MCF-7	breast:	n/a	chr4:22131265-22131283 chr4:22131267-22131288
31	CTCF	chr4:22131200-22131350	AoAF	blood vessel:	n/a	chr4:22131265-22131283 chr4:22131267-22131288
32	CTCF	chr4:22093040-22093190	AG09319	gingival:	n/a	n/a
33	CTCF	chr4:22088012-22088098	GM10266	blood:	n/a	n/a
34	CTCF	chr4:22239720-22239870	RPTEC	kidney:	n/a	n/a
35	CTCF	chr4:22239740-22239890	GM12874	blood:	n/a	n/a
36	CTCF	chr4:22238829-22239130	Gliobla	brain:	n/a	chr4:22238973-22238991
37	CTCF	chr4:22131160-22131310	NHDF-neo	bronchial:	n/a	chr4:22131265-22131283 chr4:22131267-22131288
38	CTCF	chr4:22238900-22239050	AG09319	gingival:	n/a	chr4:22238973-22238991
39	CTCF	chr4:22131140-22131290	GM06990	blood:	n/a	chr4:22131265-22131283 chr4:22131267-22131288
40	CTCF	chr4:22172020-22172170	HPAF	blood vessel:	n/a	chr4:22172134-22172155
41	CTCF	chr4:22131180-22131330	GM12864	blood:	n/a	chr4:22131265-22131283 chr4:22131267-22131288
42	CTCF	chr4:22131120-22131428	Gliobla	brain:	n/a	chr4:22131265-22131283 chr4:22131267-22131288
43	CTCF	chr4:22131180-22131330	HUVEC	blood vessel:	n/a	chr4:22131265-22131283 chr4:22131267-22131288
44	CTCF	chr4:22238920-22239070	HMF	breast:	n/a	chr4:22238973-22238991
45	CTCF	chr4:22238840-22238990	HVMF	connective:	n/a	n/a
46	CTCF	chr4:22131180-22131330	HCM	heart:	n/a	chr4:22131265-22131283 chr4:22131267-22131288
47	CTCF	chr4:22131200-22131350	GM12875	blood:	n/a	chr4:22131265-22131283 chr4:22131267-22131288
48	CTCF	chr4:22131200-22131350	HEK293	kidney:	n/a	chr4:22131265-22131283 chr4:22131267-22131288
49	CTCF	chr4:22240491-22240671	HepG2	liver:	n/a	n/a
50	CTCF	chr4:22240476-22240654	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:22148230-22148280	AG04449	skin:	fetal
2	chr4:22148230-22148280	AG04449	skin:	fetal
3	chr4:22148354-22148404	A549	lung:	n/a
4	chr4:22148354-22148404	GM06990	blood:	n/a
5	chr4:22239907-22239957	SKMC	muscle:	n/a
6	chr4:22148230-22148280	HMEC	breast:	n/a
7	chr4:22148354-22148404	Jurkat	blood:	n/a
8	chr4:22148354-22148404	GM12891	blood:	n/a
9	chr4:22239907-22239957	AG09319	gingival:	n/a
10	chr4:22148230-22148280	T-47D	breast:	n/a
11	chr4:22148230-22148280	HL-60	blood:	n/a
12	chr4:22148230-22148280	HCM	heart:	n/a
13	chr4:22148354-22148404	HIPEpiC	eye:	n/a
14	chr4:22148230-22148280	A549	lung:	n/a
15	chr4:22148354-22148404	HRE	kidney:	n/a
16	chr4:22148354-22148404	AG09319	gingival:	n/a
17	chr4:22148354-22148404	ProgFib	skin:	n/a
18	chr4:22148230-22148280	GM12878	blood:	n/a
19	chr4:22148354-22148404	SAEC	small airway:	n/a
20	chr4:22239907-22239957	ovcar-3	ovarian:	n/a
21	chr4:22239907-22239957	HAEpiC	amniotic membrane:	n/a
22	chr4:22239907-22239957	AG04450	lung:	fetal
23	chr4:22239907-22239957	SK-N-MC	brain:	n/a
24	chr4:22148230-22148280	AG09319	gingival:	n/a
25	chr4:22239907-22239957	HCT-116	colon:	n/a
26	chr4:22148230-22148280	K562	blood:	n/a
27	chr4:22239907-22239957	HUVEC	blood vessel:	n/a
28	chr4:22148230-22148280	GM06990	blood:	n/a
29	chr4:22239907-22239957	Hepatocyte	liver:	n/a
30	chr4:22148230-22148280	HIPEpiC	eye:	n/a
31	chr4:22148230-22148280	BE2_C	brain:	n/a
32	chr4:22148354-22148404	SKMC	muscle:	n/a
33	chr4:22148354-22148404	RPTEC	kidney:	n/a
34	chr4:22239907-22239957	HRPEpiC	eye:	n/a
35	chr4:22148230-22148280	AG04450	lung:	fetal
36	chr4:22239907-22239957	HEEpiC	esophagus:	n/a
37	chr4:22148354-22148404	HUVEC	blood vessel:	n/a
38	chr4:22148354-22148404	SK-N-SH	brain:	n/a
39	chr4:22148354-22148404	NH-A	brain:	n/a
40	chr4:22148354-22148404	ovcar-3	ovarian:	n/a
41	chr4:22148230-22148280	NH-A	brain:	n/a
42	chr4:22148230-22148280	GM19239	blood:	n/a
43	chr4:22148230-22148280	PANC-1	pancreas:	n/a
44	chr4:22148230-22148280	PFSK-1	brain:	n/a
45	chr4:22148354-22148404	K562	blood:	n/a
46	chr4:22148230-22148280	LNCaP	prostate:	n/a
47	chr4:22239907-22239957	AG10803	skin:	n/a
48	chr4:22148230-22148280	MCF10A-Er-Src	breast:	n/a
49	chr4:22148354-22148404	Caco-2	colon:	n/a
50	chr4:22148230-22148280	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:22238564..22239075-chr4:22358901..22359564,2	MCF-7	breast:
2	chr4:22045762..22048489-chr4:22082694..22085288,2	MCF-7	breast:
3	chr4:22219857..22222824-chr4:22225422..22227720,2	K562	blood:
4	chr4:22219857..22222824-chr4:22225422..22227720,2	K562	blood:
5	chr4:22130852..22132108-chr4:22390561..22391530,5	MCF-7	breast:
6	chr4:21791838..21792739-chr4:22130763..22131377,2	MCF-7	breast:
7	chr4:22131171..22132005-chr4:22358195..22359539,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PACRGL-5	chr4:22103115-22103259	ENSG00000250039.2
2	lnc-PACRGL-5	chr4:22103117-22103253	ENSG00000250039.3

Variant related genes	Relation type
RNU6-420P	TF binding region
RNU6-420P	CpG island

Extended variants
information (count: 2601 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2601 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13150165	chr4:22087242-22087243	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs530682052	chr4:22087359-22087360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs73803721	chr4:22087366-22087367	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs13123835	chr4:22087470-22087471	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs563980355	chr4:22087477-22087478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs114772153	chr4:22087522-22087523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs150040327	chr4:22087547-22087548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs189930591	chr4:22087598-22087599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs186200024	chr4:22091837-22091838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs376971840	chr4:22091843-22091844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs149668677	chr4:22091854-22091855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs552592077	chr4:22091884-22091885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs112148620	chr4:22092022-22092023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs117670263	chr4:22092026-22092027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs549794400	chr4:22092047-22092048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs568401500	chr4:22092067-22092068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs115533798	chr4:22092099-22092100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs368290199	chr4:22092126-22092127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs551403824	chr4:22092139-22092140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs111657553	chr4:22092146-22092147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs191174228	chr4:22092153-22092154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs2875013	chr4:22092178-22092179	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs183433257	chr4:22092179-22092180	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs142585635	chr4:22092233-22092234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs117051793	chr4:22092254-22092255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs561699455	chr4:22092276-22092277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs117358685	chr4:22092324-22092325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs371857076	chr4:22092339-22092340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs374813692	chr4:22092344-22092345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs186377307	chr4:22092383-22092384	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs571294259	chr4:22092387-22092388	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs533105911	chr4:22092411-22092412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs527809760	chr4:22092422-22092423	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs190451037	chr4:22092430-22092431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs373355769	chr4:22092438-22092439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs34780697	chr4:22092439-22092440	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs531728494	chr4:22092495-22092496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs549757303	chr4:22092504-22092505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs568164871	chr4:22092522-22092523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs529254449	chr4:22092544-22092545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs547645277	chr4:22092576-22092577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs528733415	chr4:22092583-22092584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs13135950	chr4:22092586-22092587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs183108620	chr4:22092617-22092618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs539995161	chr4:22092625-22092626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs558095872	chr4:22092639-22092640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs569716426	chr4:22092646-22092647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs71608904	chr4:22092654-22092655	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs374005381	chr4:22092674-22092675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs13113611	chr4:22092677-22092678	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Olfactory neuroblastoma	18408657	CNVD
Burkitt''s lymphoma	20823134	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Cancer	22183965	CNVD
Gastric cancer	16891809	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:22087200-22087600	Enhancers	HSMMtube	muscle
2	chr4:22091800-22093400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr4:22092400-22093000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr4:22092600-22093000	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr4:22092600-22093000	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr4:22092600-22093000	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr4:22092600-22095000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr4:22093000-22094400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr4:22093000-22094800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr4:22093200-22094200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr4:22093600-22093800	Enhancers	Osteobl	bone
12	chr4:22093600-22094400	Enhancers	Adipose Nuclei	Adipose
13	chr4:22099000-22101800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr4:22101000-22102200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr4:22101000-22103200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr4:22101200-22101800	Enhancers	HMEC	breast
17	chr4:22101200-22101800	Enhancers	NH-A	brain
18	chr4:22101200-22102200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr4:22101400-22102000	Enhancers	Osteobl	bone
20	chr4:22103000-22103200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr4:22110800-22111200	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
22	chr4:22116200-22116400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr4:22123800-22124400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr4:22124000-22124600	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr4:22131000-22131400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr4:22131000-22131600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr4:22131400-22131600	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr4:22131600-22132400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr4:22132400-22133600	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr4:22134000-22134600	Enhancers	Fetal Brain Male	brain
31	chr4:22169000-22172400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr4:22171600-22172800	Enhancers	HMEC	breast
33	chr4:22171600-22172800	Enhancers	HSMM	muscle
34	chr4:22171600-22173200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr4:22171800-22172800	Enhancers	Muscle Satellite Cultured Cells	--
36	chr4:22171800-22172800	Enhancers	NH-A	brain
37	chr4:22171800-22173000	Enhancers	Osteobl	bone
38	chr4:22172000-22172600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr4:22172000-22172600	Enhancers	NHEK	skin
40	chr4:22172000-22172800	Enhancers	HSMMtube	muscle
41	chr4:22172200-22172600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr4:22172200-22172600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr4:22172200-22172800	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr4:22172400-22172800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr4:22172800-22180400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr4:22179800-22180600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr4:22180200-22181200	Enhancers	NH-A	brain
48	chr4:22180400-22180600	Enhancers	Muscle Satellite Cultured Cells	--
49	chr4:22180400-22181000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr4:22180400-22181000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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