Variant report

Variant	esv3528527
Chromosome Location	chr20:25988952-26027050
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:354)
CpG islands
(count:305)
Chromatin interactive
region (count:0)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:354 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:25989422-25989527	HepG2	liver:	n/a	n/a
2	ATF2	chr20:25990276-25990617	GM12878	blood:	n/a	n/a
3	BATF	chr20:25991390-25991666	GM12878	blood:	n/a	n/a
4	BCL11A	chr20:26010805-26011025	GM12878	blood:	n/a	n/a
5	BCL11A	chr20:25990610-25990918	GM12878	blood:	n/a	n/a
6	BRCA1	chr20:25990237-25990584	HepG2	liver:	n/a	chr20:25990394-25990403
7	BRCA1	chr20:25990208-25990605	Hela-S3	cervix:	n/a	chr20:25990394-25990403
8	BRCA1	chr20:25990247-25990579	GM12878	blood:	n/a	chr20:25990394-25990403
9	CEBPB	chr20:25990281-25990629	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr20:25989272-25989628	IMR90	lung:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
11	CEBPB	chr20:25989327-25989510	HepG2	liver:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
12	CEBPB	chr20:25989264-25989635	K562	blood:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
13	CEBPB	chr20:25989351-25989594	K562	blood:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
14	CEBPB	chr20:25988927-25989639	A549	lung:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
15	CEBPB	chr20:25988753-25989639	HepG2	liver:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
16	CEBPB	chr20:25988884-25989639	Hela-S3	cervix:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
17	CEBPB	chr20:25989323-25989598	H1-hESC	embryonic stem cell:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
18	CEBPB	chr20:25989230-25989660	K562	blood:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
19	CEBPB	chr20:25989347-25989484	HepG2	liver:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
20	CEBPD	chr20:25990293-25990725	HepG2	liver:	n/a	n/a
21	CHD1	chr20:25990580-25990581	GM12878	blood:	n/a	n/a
22	CHD2	chr20:25990214-25990586	K562	blood:	n/a	chr20:25990394-25990403
23	CHD2	chr20:25990208-25990784	GM12878	blood:	n/a	chr20:25990394-25990403
24	CHD2	chr20:25990200-25990660	HepG2	liver:	n/a	chr20:25990394-25990403
25	CHD2	chr20:25990204-25990773	Hela-S3	cervix:	n/a	chr20:25990394-25990403
26	CTCF	chr20:26022800-26022867	Fibrobl	skin:	n/a	n/a
27	CTCF	chr20:25991586-25991706	Spleen_OC	spleen:	n/a	n/a
28	CTCF	chr20:26022742-26022934	MCF-7	breast:	n/a	n/a
29	CTCF	chr20:25993777-25993844	GM13976	blood:	n/a	n/a
30	CTCF	chr20:26022832-26022906	Medullo	brain:	n/a	n/a
31	CTCF	chr20:26022781-26022894	A549	lung:	n/a	n/a
32	CTCF	chr20:25990000-25990060	LNCaP	prostate:	n/a	n/a
33	CTCF	chr20:26014302-26014317	GM13977	blood:	n/a	n/a
34	CTCF	chr20:25990600-25990750	GM12867	blood:	n/a	n/a
35	CTCF	chr20:26022756-26022904	MCF-7	breast:	n/a	n/a
36	CTCF	chr20:25999107-25999194	GM20000	blood:	n/a	n/a
37	CTCF	chr20:26022771-26022938	LNCaP	prostate:	n/a	n/a
38	CTCF	chr20:26022765-26022887	HepG2	liver:	n/a	n/a
39	CTCF	chr20:26022744-26022916	MCF-7	breast:	n/a	n/a
40	CTCF	chr20:26014290-26014299	GM13977	blood:	n/a	n/a
41	CTCF	chr20:26009738-26009859	GM20000	blood:	n/a	n/a
42	CTCF	chr20:25998384-25998452	LNCaP	prostate:	n/a	n/a
43	CTCF	chr20:26022754-26022923	MCF-7	breast:	n/a	n/a
44	CTCF	chr20:26022764-26022924	MCF-7	breast:	n/a	n/a
45	CTCF	chr20:26005438-26005533	GM10248	blood:	n/a	n/a
46	CTCF	chr20:26022795-26022875	ProgFib	skin:	n/a	n/a
47	CTCF	chr20:25990360-25990510	HepG2	liver:	n/a	n/a
48	CTCF	chr20:26022775-26022911	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr20:26006053-26006100	GM10248	blood:	n/a	n/a
50	CTCF	chr20:26022791-26022793	ProgFib	skin:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:25990680-25990730	H1-hESC	embryonic stem cell:	embryo
2	chr20:25991114-25991164	AG09319	gingival:	n/a
3	chr20:25989775-25989825	Jurkat	blood:	n/a
4	chr20:25989775-25989825	ProgFib	skin:	n/a
5	chr20:25989032-25989082	CMK	blood:	n/a
6	chr20:25989775-25989825	HRCEpiC	kidney:	n/a
7	chr20:25989674-25989724	AG04449	skin:	fetal
8	chr20:25989775-25989825	PrEC	prostate:	n/a
9	chr20:25989674-25989724	SK-N-SH	brain:	n/a
10	chr20:25991114-25991164	Hepatocyte	liver:	n/a
11	chr20:25990680-25990730	MCF-7	breast:	n/a
12	chr20:25991114-25991164	Caco-2	colon:	n/a
13	chr20:25990680-25990730	PANC-1	pancreas:	n/a
14	chr20:25991114-25991164	HCF	heart:	n/a
15	chr20:25989775-25989825	SKMC	muscle:	n/a
16	chr20:25991114-25991164	GM12892	blood:	n/a
17	chr20:25991114-25991164	HCPEpiC	choroid plexus:	n/a
18	chr20:25989032-25989082	PFSK-1	brain:	n/a
19	chr20:25989032-25989082	HRPEpiC	eye:	n/a
20	chr20:25989775-25989825	AG09309	skin:	n/a
21	chr20:25989775-25989825	AG04449	skin:	fetal
22	chr20:25990680-25990730	HAEpiC	amniotic membrane:	n/a
23	chr20:25989032-25989082	K562	blood:	n/a
24	chr20:25990680-25990730	U87	brain:	n/a
25	chr20:25989775-25989825	NH-A	brain:	n/a
26	chr20:25990680-25990730	Hela-S3	cervix:	n/a
27	chr20:25991114-25991164	NHBE	bronchial:	n/a
28	chr20:25991114-25991164	MCF-7	breast:	n/a
29	chr20:25989032-25989082	RPTEC	kidney:	n/a
30	chr20:25990680-25990730	MCF10A-Er-Src	breast:	n/a
31	chr20:25991114-25991164	GM12878	blood:	n/a
32	chr20:25991114-25991164	ECC-1	luminal epithelium:	n/a
33	chr20:25989032-25989082	NB4	blood:	n/a
34	chr20:25989775-25989825	ECC-1	luminal epithelium:	n/a
35	chr20:25989775-25989825	HL-60	blood:	n/a
36	chr20:25989032-25989082	HCPEpiC	choroid plexus:	n/a
37	chr20:25989674-25989724	T-47D	breast:	n/a
38	chr20:25989032-25989082	SK-N-SH_RA	brain:	n/a
39	chr20:25989674-25989724	AG04450	lung:	fetal
40	chr20:25991114-25991164	NT2-D1	testis:	n/a
41	chr20:25989674-25989724	SK-N-MC	brain:	n/a
42	chr20:25989775-25989825	HNPCEpiC	eye:	n/a
43	chr20:25989032-25989082	HRE	kidney:	n/a
44	chr20:25991114-25991164	T-47D	breast:	n/a
45	chr20:25991114-25991164	SK-N-SH_RA	brain:	n/a
46	chr20:25989775-25989825	H1-hESC	embryonic stem cell:	embryo
47	chr20:25989674-25989724	HEK293	kidney:	embryo
48	chr20:25990680-25990730	HEK293	kidney:	embryo
49	chr20:25989674-25989724	IMR90	lung:	fetal
50	chr20:25990680-25990730	SKMC	muscle:	n/a

No data

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM182B-3	chr20:25990891-25991167	XLOC_013712
2	lnc-FAM182A-6	chr20:26000465-26000560	NONHSAT147161
3	lnc-FAM182A-6	chr20:26011530-26013121	ucscGeneNc_uc010gdq_1
4	lnc-FAM182A-6	chr20:26009800-26010026	ucscGeneNc_uc010gdq_1
5	lnc-FAM182A-6	chr20:26001272-26001320	NONHSAT147161
6	lnc-FAM182A-6	chr20:25999712-25999838	NONHSAT147161
7	lnc-FAM182A-6	chr20:25999468-25999548	NONHSAT147161
8	lnc-FAM182A-6	chr20:26002406-26002505	ucscGeneNc_uc010gdq_1
9	lnc-FAM182A-6	chr20:25997553-25997840	ucscGeneNc_uc010gdq_1
10	lnc-FAM182A-6	chr20:25990334-25991091	NONHSAT079206
11	lnc-FAM182B-3	chr20:25989427-25989691	XLOC_013712

No data

Variant related genes	Relation type
ENSG00000231081	TF binding region
ENSG00000204556	TF binding region
ENSG00000231081	CpG island
ENSG00000204556	CpG island
MUC17	miRNA target sites
LIMCH1	miRNA target sites

Extended variants
information (count: 104 )
Associated
traits (count: 47 )

Variant overlapped rSNPs/rCNVs (count:104 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560077679	chr20:25988972-25988973	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs6107130	chr20:25988984-25988985	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs552248095	chr20:25988987-25988988	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs146267871	chr20:25988990-25988991	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs530972251	chr20:25989021-25989022	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs183023632	chr20:25989092-25989093	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567592543	chr20:25989114-25989115	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs187354065	chr20:25989135-25989136	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs546714147	chr20:25989141-25989142	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs6107131	chr20:25989152-25989153	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs538796705	chr20:25989193-25989194	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs559051824	chr20:25989237-25989238	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs569076019	chr20:25989263-25989264	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs138166506	chr20:25989287-25989288	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs571232120	chr20:25989305-25989306	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs76013671	chr20:25989308-25989309	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs376396420	chr20:25989329-25989330	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs141729689	chr20:25989429-25989430	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs574818192	chr20:25989475-25989476	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs540496075	chr20:25989495-25989496	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs192809519	chr20:25989498-25989499	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs576764781	chr20:25989551-25989552	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs533300737	chr20:25989589-25989590	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs66769568	chr20:25989600-25989601	Active TSS Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs6084040	chr20:25989665-25989666	Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
26	rs375639731	chr20:25989702-25989703	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs531031373	chr20:25989728-25989729	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs73353672	chr20:25989767-25989768	Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs139726857	chr20:25989789-25989790	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs527444506	chr20:25989875-25989876	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs530356445	chr20:25989876-25989877	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs6084041	chr20:25989898-25989899	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs78217349	chr20:25989942-25989943	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs547262097	chr20:25989975-25989976	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs112172757	chr20:25989994-25989995	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs6051087	chr20:25990002-25990003	Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs552725751	chr20:25990009-25990010	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs569335923	chr20:25990027-25990028	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs184920846	chr20:25990063-25990064	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs201206145	chr20:25990088-25990089	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs114795197	chr20:25990123-25990124	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs554829549	chr20:25990228-25990229	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs112887778	chr20:25990230-25990231	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs533884986	chr20:25990241-25990242	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs553996296	chr20:25990259-25990260	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs576769064	chr20:25990269-25990270	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs189459021	chr20:25990307-25990308	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs192772436	chr20:25990346-25990347	Active TSS Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs575767480	chr20:25990356-25990357	Active TSS Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs8182807	chr20:25990385-25990386	Active TSS Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:47)

Disease	PMID	Source
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Bladder cancer	21909424	CNVD
Esophageal cancer	21851588	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD

Chromatin state (count:169 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:25985600-25989600	Weak transcription	HepG2	liver
2	chr20:25988800-25990200	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr20:25989200-25990200	Enhancers	Placenta	Placenta
4	chr20:25989600-25990400	Active TSS	HepG2	liver
5	chr20:25989600-25991600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr20:25989800-25990000	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr20:25989800-25990000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr20:25989800-25990000	Enhancers	Duodenum Smooth Muscle	Duodenum
9	chr20:25989800-25990000	Enhancers	Fetal Brain Female	brain
10	chr20:25989800-25990000	Enhancers	Fetal Lung	lung
11	chr20:25989800-25990000	Enhancers	Hela-S3	cervix
12	chr20:25989800-25990200	Enhancers	NHDF-Ad	bronchial
13	chr20:25989800-25990400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr20:25989800-25990400	Enhancers	Sigmoid Colon	Sigmoid Colon
15	chr20:25989800-25990400	Enhancers	Spleen	Spleen
16	chr20:25989800-25990600	Active TSS	Skeletal Muscle Female	skeletal muscle
17	chr20:25989800-25991600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr20:25989800-25991600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr20:25989800-25991600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr20:25989800-25991600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr20:25989800-25991600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr20:25989800-25991600	Active TSS	Brain Cingulate Gyrus	brain
23	chr20:25989800-25991600	Active TSS	A549	lung
24	chr20:25990000-25990200	Enhancers	Primary neutrophils fromperipheralblood	blood
25	chr20:25990000-25990600	Active TSS	Fetal Lung	lung
26	chr20:25990000-25990600	Active TSS	Skeletal Muscle Male	skeletal muscle
27	chr20:25990000-25990800	Active TSS	Adipose Nuclei	Adipose
28	chr20:25990000-25990800	Active TSS	Fetal Thymus	thymus
29	chr20:25990000-25991000	Active TSS	Fetal Muscle Leg	muscle
30	chr20:25990000-25991000	Active TSS	Fetal Stomach	stomach
31	chr20:25990000-25991000	Active TSS	Rectal Smooth Muscle	rectum
32	chr20:25990000-25991400	Active TSS	Primary hematopoietic stem cells short term culture	blood
33	chr20:25990000-25991400	Active TSS	Cortex derived primary cultured neurospheres	brain
34	chr20:25990000-25991400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr20:25990000-25991400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr20:25990000-25991400	Active TSS	Duodenum Smooth Muscle	Duodenum
37	chr20:25990000-25991400	Active TSS	Fetal Brain Female	brain
38	chr20:25990000-25991400	Active TSS	Fetal Kidney	kidney
39	chr20:25990000-25991400	Active TSS	Pancreatic Islets	Pancreatic Islet
40	chr20:25990000-25991400	Active TSS	Psoas Muscle	Psoas
41	chr20:25990000-25991400	Active TSS	Right Atrium	heart
42	chr20:25990000-25991600	Active TSS	HUES48 Cell Line	embryonic stem cell
43	chr20:25990000-25991600	Active TSS	HUES64 Cell Line	embryonic stem cell
44	chr20:25990000-25991600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr20:25990000-25991600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr20:25990000-25991600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr20:25990000-25991600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr20:25990000-25991600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr20:25990000-25991600	Active TSS	Muscle Satellite Cultured Cells	--
50	chr20:25990000-25991600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain

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