Variant report

Variant	esv2759368
Chromosome Location	chr5:106491726-106551811
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	CBX3	chr5:106506231-106506793	HCT-116	colon:	n/a	n/a
2	CEBPB	chr5:106521516-106521822	HepG2	liver:	n/a	n/a
3	CEBPB	chr5:106536248-106536250	A549	lung:	n/a	n/a
4	CEBPB	chr5:106531529-106531741	HepG2	liver:	n/a	n/a
5	CEBPB	chr5:106531570-106531610	A549	lung:	n/a	n/a
6	CHD2	chr5:106517883-106517892	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr5:106493626-106493650	ProgFib	skin:	n/a	n/a
8	CTCF	chr5:106493830-106493879	GM20000	blood:	n/a	n/a
9	CTCF	chr5:106493703-106493705	Medullo	brain:	n/a	n/a
10	CTCF	chr5:106530677-106530761	GM20000	blood:	n/a	n/a
11	CTCF	chr5:106535580-106535730	NHDF-neo	bronchial:	n/a	n/a
12	CTCF	chr5:106493619-106493625	ProgFib	skin:	n/a	n/a
13	CTCF	chr5:106493700-106493850	HRPEpiC	eye:	n/a	n/a
14	CTCF	chr5:106493680-106493830	WERI-Rb-1	eye:	n/a	n/a
15	CTCF	chr5:106493706-106493807	Medullo	brain:	n/a	n/a
16	CUX1	chr5:106539164-106539309	GM12878	blood:	n/a	n/a
17	E2F4	chr5:106511801-106512104	MCF10A-Er-Src	breast:	n/a	n/a
18	E2F4	chr5:106514550-106514625	MCF10A-Er-Src	breast:	n/a	n/a
19	EP300	chr5:106551356-106551626	SK-N-SH_RA	brain:	n/a	chr5:106551422-106551431 chr5:106551497-106551506
20	EP300	chr5:106548748-106549068	SK-N-SH_RA	brain:	n/a	n/a
21	EP300	chr5:106548776-106549084	SK-N-SH_RA	brain:	n/a	n/a
22	EP300	chr5:106548094-106550089	SK-N-SH	brain:	n/a	n/a
23	FOS	chr5:106519757-106519971	MCF10A-Er-Src	breast:	n/a	chr5:106519858-106519867 chr5:106519859-106519866 chr5:106519858-106519866 chr5:106519856-106519867
24	FOS	chr5:106519689-106520070	HUVEC	blood vessel:	n/a	chr5:106519858-106519867 chr5:106519859-106519866 chr5:106519858-106519866 chr5:106519856-106519867
25	FOS	chr5:106540805-106540957	MCF10A-Er-Src	breast:	n/a	chr5:106540855-106540864 chr5:106540855-106540862 chr5:106540853-106540865 chr5:106540854-106540864 chr5:106540854-106540864
26	FOS	chr5:106551224-106551676	HUVEC	blood vessel:	n/a	n/a
27	FOS	chr5:106519849-106520049	MCF10A-Er-Src	breast:	n/a	chr5:106519858-106519867 chr5:106519859-106519866 chr5:106519858-106519866 chr5:106519856-106519867
28	FOXP2	chr5:106532188-106532606	SK-N-MC	brain:	n/a	n/a
29	FOXP2	chr5:106531666-106531957	SK-N-MC	brain:	n/a	n/a
30	GATA2	chr5:106548739-106549067	SH-SY5Y	brain:	n/a	chr5:106548812-106548828 chr5:106548812-106548828
31	GATA3	chr5:106548622-106548991	SH-SY5Y	brain:	n/a	chr5:106548812-106548828 chr5:106548812-106548828
32	GATA3	chr5:106532264-106532439	SH-SY5Y	brain:	n/a	chr5:106532329-106532336 chr5:106532329-106532336 chr5:106532322-106532343 chr5:106532329-106532336 chr5:106532325-106532341
33	GATA3	chr5:106540741-106540938	SH-SY5Y	brain:	n/a	chr5:106540856-106540865
34	JUND	chr5:106531568-106531787	HepG2	liver:	n/a	n/a
35	KAP1	chr5:106510607-106510813	K562	blood:	n/a	n/a
36	KAP1	chr5:106505998-106506857	HEK293	kidney:	n/a	n/a
37	KAP1	chr5:106506297-106506647	K562	blood:	n/a	n/a
38	MAFF	chr5:106501015-106501384	HepG2	liver:	n/a	chr5:106501187-106501205
39	MAFF	chr5:106544602-106544853	K562	blood:	n/a	chr5:106544762-106544780
40	MAFF	chr5:106544592-106544947	HepG2	liver:	n/a	chr5:106544762-106544780
41	MAFF	chr5:106501027-106501334	K562	blood:	n/a	chr5:106501187-106501205
42	MAFK	chr5:106544589-106544943	IMR90	lung:	n/a	chr5:106544765-106544774 chr5:106544758-106544778 chr5:106544759-106544776 chr5:106544763-106544778 chr5:106544766-106544780 chr5:106544763-106544779
43	MAFK	chr5:106501020-106501377	HepG2	liver:	n/a	chr5:106501189-106501204
44	MAFK	chr5:106535338-106535513	HepG2	liver:	n/a	n/a
45	MAFK	chr5:106501077-106501351	H1-hESC	embryonic stem cell:	n/a	chr5:106501189-106501204
46	MAFK	chr5:106501017-106501399	HepG2	liver:	n/a	chr5:106501189-106501204
47	MAFK	chr5:106501004-106501380	IMR90	lung:	n/a	chr5:106501189-106501204
48	MAFK	chr5:106544624-106544901	H1-hESC	embryonic stem cell:	n/a	chr5:106544765-106544774 chr5:106544758-106544778 chr5:106544759-106544776 chr5:106544763-106544778 chr5:106544766-106544780 chr5:106544763-106544779
49	MAFK	chr5:106545664-106545885	HepG2	liver:	n/a	n/a
50	MAFK	chr5:106548250-106548361	HepG2	liver:	n/a	chr5:106548327-106548343

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:106530218-106530268	Hepatocyte	liver:	n/a
2	chr5:106530218-106530268	Hepatocyte	liver:	n/a
3	chr5:106530218-106530268	HIPEpiC	eye:	n/a
4	chr5:106530218-106530268	GM06990	blood:	n/a
5	chr5:106530218-106530268	K562	blood:	n/a
6	chr5:106530218-106530268	HCT-116	colon:	n/a
7	chr5:106530218-106530268	HRE	kidney:	n/a
8	chr5:106530218-106530268	BJ	skin:	n/a
9	chr5:106530218-106530268	MCF10A-Er-Src	breast:	n/a
10	chr5:106530218-106530268	BE2_C	brain:	n/a
11	chr5:106530218-106530268	T-47D	breast:	n/a
12	chr5:106530218-106530268	Caco-2	colon:	n/a
13	chr5:106530218-106530268	AG04449	skin:	fetal
14	chr5:106530218-106530268	NB4	blood:	n/a
15	chr5:106530218-106530268	IMR90	lung:	fetal
16	chr5:106530218-106530268	H1-hESC	embryonic stem cell:	embryo
17	chr5:106530218-106530268	HCM	heart:	n/a
18	chr5:106530218-106530268	AG09319	gingival:	n/a
19	chr5:106530218-106530268	GM19239	blood:	n/a
20	chr5:106530218-106530268	PANC-1	pancreas:	n/a
21	chr5:106530218-106530268	SK-N-SH_RA	brain:	n/a
22	chr5:106530218-106530268	HCPEpiC	choroid plexus:	n/a
23	chr5:106530218-106530268	HRCEpiC	kidney:	n/a
24	chr5:106530218-106530268	HMEC	breast:	n/a
25	chr5:106530218-106530268	HL-60	blood:	n/a
26	chr5:106530218-106530268	NHDF-neo	bronchial:	n/a
27	chr5:106530218-106530268	AG04450	lung:	fetal
28	chr5:106530218-106530268	HUVEC	blood vessel:	n/a
29	chr5:106530218-106530268	RPTEC	kidney:	n/a
30	chr5:106530218-106530268	HEK293	kidney:	embryo
31	chr5:106530218-106530268	AG09309	skin:	n/a
32	chr5:106530218-106530268	SAEC	small airway:	n/a
33	chr5:106530218-106530268	HNPCEpiC	eye:	n/a
34	chr5:106530218-106530268	GM12892	blood:	n/a
35	chr5:106530218-106530268	PFSK-1	brain:	n/a
36	chr5:106530218-106530268	A549	lung:	n/a
37	chr5:106530218-106530268	AoSMC	blood vessel:	n/a
38	chr5:106530218-106530268	PrEC	prostate:	n/a
39	chr5:106530218-106530268	SK-N-SH	brain:	n/a
40	chr5:106530218-106530268	NT2-D1	testis:	n/a
41	chr5:106530218-106530268	ProgFib	skin:	n/a
42	chr5:106530218-106530268	SK-N-MC	brain:	n/a
43	chr5:106530218-106530268	HepG2	liver:	n/a
44	chr5:106530218-106530268	ovcar-3	ovarian:	n/a
45	chr5:106530218-106530268	SKMC	muscle:	n/a
46	chr5:106530218-106530268	HRPEpiC	eye:	n/a
47	chr5:106530218-106530268	NHBE	bronchial:	n/a
48	chr5:106530218-106530268	GM12891	blood:	n/a
49	chr5:106530218-106530268	U87	brain:	n/a
50	chr5:106530218-106530268	HAEpiC	amniotic membrane:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:106525438..106528218-chr5:106529605..106532112,2	MCF-7	breast:
2	chr5:105620861..105623100-chr5:106539185..106542118,2	MCF-7	breast:

Variant related genes	Relation type
PSMC1P5	TF binding region
PSMC1P5	CpG island
ENSG00000250273	chromatin interactions

Extended variants
information (count: 724 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:724 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138151116	chr5:106493206-106493207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs543744558	chr5:106493210-106493211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs377451111	chr5:106493236-106493237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs564040686	chr5:106493239-106493240	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs529581833	chr5:106493260-106493261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs115346418	chr5:106493290-106493291	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs115589986	chr5:106493327-106493328	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs528130487	chr5:106493341-106493342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs10043242	chr5:106493350-106493351	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs149126656	chr5:106493353-106493354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs184013382	chr5:106493361-106493362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs527393040	chr5:106493399-106493400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs80059122	chr5:106493402-106493403	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs536161850	chr5:106493429-106493430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs553083688	chr5:106493461-106493462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs573120128	chr5:106493465-106493466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs535114512	chr5:106493468-106493469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs558319471	chr5:106493513-106493514	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs189820015	chr5:106493536-106493537	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs78751427	chr5:106493555-106493556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs55689542	chr5:106493635-106493636	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs563551582	chr5:106493637-106493638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs574237077	chr5:106493658-106493659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs542957268	chr5:106493671-106493672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs559519045	chr5:106493678-106493679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs528692926	chr5:106493727-106493728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs551037452	chr5:106493736-106493737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs181870728	chr5:106493756-106493757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs530532826	chr5:106493822-106493823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs185213241	chr5:106493927-106493928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs115954094	chr5:106493931-106493932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs536542951	chr5:106493957-106493958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs546617936	chr5:106493973-106493974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs190490410	chr5:106494012-106494013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs567354471	chr5:106494045-106494046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs112653560	chr5:106494050-106494051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs558809993	chr5:106494051-106494052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs538084953	chr5:106494057-106494058	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs181787481	chr5:106494058-106494059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs557278566	chr5:106494059-106494060	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs573998791	chr5:106494076-106494077	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs116346665	chr5:106494154-106494155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs376309483	chr5:106494165-106494166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs573220795	chr5:106494188-106494189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs17159517	chr5:106502647-106502648	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs568438993	chr5:106502657-106502658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs569351621	chr5:106502658-106502659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs59911789	chr5:106502690-106502691	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs536479671	chr5:106502706-106502707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs75929154	chr5:106502719-106502720	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	21509527	CNVD
Breast cancer	16608533	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	16773561	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:106493200-106494000	Enhancers	Fetal Muscle Trunk	muscle
2	chr5:106493400-106493800	Enhancers	Fetal Muscle Leg	muscle
3	chr5:106493400-106494000	Enhancers	Placenta	Placenta
4	chr5:106493400-106494200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr5:106502600-106503200	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr5:106502800-106503400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr5:106503400-106504200	Enhancers	Fetal Brain Female	brain
8	chr5:106503400-106505000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr5:106504600-106505200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr5:106504800-106505200	Enhancers	Fetal Heart	heart
11	chr5:106505000-106505400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr5:106505200-106507000	Weak transcription	Fetal Heart	heart
13	chr5:106510000-106510400	Enhancers	Esophagus	oesophagus
14	chr5:106528200-106528600	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr5:106528200-106528800	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr5:106528800-106531200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr5:106529400-106529600	Bivalent/Poised TSS	Liver	Liver
18	chr5:106530200-106530400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr5:106532000-106533000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr5:106534400-106534800	Enhancers	Muscle Satellite Cultured Cells	--
21	chr5:106538800-106539200	Enhancers	Fetal Brain Male	brain
22	chr5:106539000-106539400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr5:106539000-106539400	Active TSS	NHDF-Ad	bronchial
24	chr5:106539000-106539600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr5:106539000-106539600	Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr5:106539000-106539800	Enhancers	GM12878-XiMat	blood
27	chr5:106540200-106540400	Enhancers	Skeletal Muscle Female	skeletal muscle
28	chr5:106547000-106547800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr5:106547200-106547800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr5:106547400-106547800	Enhancers	Brain Germinal Matrix	brain
31	chr5:106547800-106553200	Weak transcription	Brain Germinal Matrix	brain
32	chr5:106548800-106549000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr5:106548800-106549000	Enhancers	Aorta	Aorta
34	chr5:106548800-106549200	Enhancers	Left Ventricle	heart
35	chr5:106548800-106550400	Enhancers	Fetal Heart	heart
36	chr5:106549000-106549200	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr5:106549000-106549200	Enhancers	Right Ventricle	heart
38	chr5:106549200-106551400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr5:106549200-106551600	Weak transcription	Right Ventricle	heart
40	chr5:106549200-106552000	Weak transcription	Left Ventricle	heart
41	chr5:106549200-106552400	Weak transcription	Aorta	Aorta
42	chr5:106550200-106552000	Enhancers	HUVEC	blood vessel
43	chr5:106550400-106551400	Weak transcription	Fetal Heart	heart
44	chr5:106551000-106551800	Enhancers	Muscle Satellite Cultured Cells	--
45	chr5:106551000-106554600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr5:106551000-106555000	Enhancers	NHEK	skin
47	chr5:106551200-106554200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr5:106551200-106555200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr5:106551400-106551600	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr5:106551400-106551600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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