Variant report

Variant	esv2757925
Chromosome Location	chr4:22011581-22230718
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	chr4:22064885-22065182	HepG2	liver:	n/a	n/a
2	ATF2	chr4:22073321-22073749	GM12878	blood:	n/a	n/a
3	BATF	chr4:22176374-22176536	GM12878	blood:	n/a	n/a
4	BATF	chr4:22117037-22117289	GM12878	blood:	n/a	chr4:22117167-22117178
5	BATF	chr4:22073466-22073678	GM12878	blood:	n/a	chr4:22073609-22073620
6	BATF	chr4:22073447-22073794	GM12878	blood:	n/a	chr4:22073609-22073620
7	BHLHE40	chr4:22073483-22073611	GM12878	blood:	n/a	n/a
8	BRCA1	chr4:22206447-22206466	H1-hESC	embryonic stem cell:	n/a	n/a
9	CCNT2	chr4:22044425-22044625	K562	blood:	n/a	n/a
10	CEBPB	chr4:22033002-22033226	A549	lung:	n/a	chr4:22033085-22033098 chr4:22033086-22033097
11	CEBPB	chr4:22022669-22023046	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr4:22032931-22033260	HepG2	liver:	n/a	chr4:22033085-22033098 chr4:22033086-22033097
13	CEBPB	chr4:22086625-22086937	HepG2	liver:	n/a	chr4:22086780-22086797 chr4:22086757-22086770
14	CEBPB	chr4:22056386-22056428	HepG2	liver:	n/a	chr4:22056412-22056423
15	CEBPB	chr4:22203404-22203506	HepG2	liver:	n/a	n/a
16	CEBPB	chr4:22091217-22091388	A549	lung:	n/a	chr4:22091369-22091380
17	CEBPB	chr4:22032052-22032304	HepG2	liver:	n/a	chr4:22032167-22032178
18	CEBPB	chr4:22065237-22065571	HepG2	liver:	n/a	n/a
19	CEBPB	chr4:22183725-22184025	ECC-1	luminal epithelium:	n/a	chr4:22183891-22183904 chr4:22183893-22183904
20	CEBPB	chr4:22032010-22032340	H1-hESC	embryonic stem cell:	n/a	chr4:22032167-22032178
21	CEBPB	chr4:22086644-22086933	IMR90	lung:	n/a	chr4:22086780-22086797 chr4:22086757-22086770
22	CEBPB	chr4:22021270-22021749	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr4:22091251-22091497	HepG2	liver:	n/a	chr4:22091369-22091380
24	CEBPB	chr4:22086670-22086925	A549	lung:	n/a	chr4:22086780-22086797 chr4:22086757-22086770
25	CEBPB	chr4:22203386-22203529	A549	lung:	n/a	n/a
26	CEBPB	chr4:22091256-22091515	IMR90	lung:	n/a	chr4:22091369-22091380
27	CEBPB	chr4:22137438-22137500	HepG2	liver:	n/a	n/a
28	CEBPB	chr4:22032080-22032306	MCF-7	breast:	n/a	chr4:22032167-22032178
29	CEBPB	chr4:22032936-22033221	IMR90	lung:	n/a	chr4:22033085-22033098 chr4:22033086-22033097
30	CEBPB	chr4:22204052-22204260	IMR90	lung:	n/a	n/a
31	CEBPB	chr4:22032080-22032306	A549	lung:	n/a	chr4:22032167-22032178
32	CHD2	chr4:22131276-22131322	GM12878	blood:	n/a	n/a
33	CTCF	chr4:22131159-22131348	MCF-7	breast:	n/a	chr4:22131265-22131283 chr4:22131267-22131288
34	CTCF	chr4:22131200-22131350	SAEC	small airway:	n/a	chr4:22131265-22131283 chr4:22131267-22131288
35	CTCF	chr4:22131200-22131350	GM12872	blood:	n/a	chr4:22131265-22131283 chr4:22131267-22131288
36	CTCF	chr4:22131160-22131310	HVMF	connective:	n/a	chr4:22131265-22131283 chr4:22131267-22131288
37	CTCF	chr4:22123836-22123880	GM19239	blood:	n/a	n/a
38	CTCF	chr4:22131126-22131397	LNCaP	prostate:	n/a	chr4:22131265-22131283 chr4:22131267-22131288
39	CTCF	chr4:22131160-22131310	HFF-Myc	foreskin:	n/a	chr4:22131265-22131283 chr4:22131267-22131288
40	CTCF	chr4:22131160-22131310	SK-N-SH_RA	brain:	n/a	chr4:22131265-22131283 chr4:22131267-22131288
41	CTCF	chr4:22131110-22131403	HCT-116	colon:	n/a	chr4:22131265-22131283 chr4:22131267-22131288
42	CTCF	chr4:22131180-22131330	GM12868	blood:	n/a	chr4:22131265-22131283 chr4:22131267-22131288
43	CTCF	chr4:22131180-22131330	AG09319	gingival:	n/a	chr4:22131265-22131283 chr4:22131267-22131288
44	CTCF	chr4:22039793-22039889	Spleen_OC	spleen:	n/a	n/a
45	CTCF	chr4:22131140-22131290	GM12868	blood:	n/a	chr4:22131265-22131283 chr4:22131267-22131288
46	CTCF	chr4:22131142-22131344	SK-N-SH_RA	brain:	n/a	chr4:22131265-22131283 chr4:22131267-22131288
47	CTCF	chr4:22131240-22131390	AG04450	lung:	n/a	chr4:22131265-22131283 chr4:22131267-22131288
48	CTCF	chr4:22074651-22074711	ProgFib	skin:	n/a	n/a
49	CTCF	chr4:22131200-22131350	GM12869	blood:	n/a	chr4:22131265-22131283 chr4:22131267-22131288
50	CTCF	chr4:22131200-22131350	GM12870	blood:	n/a	chr4:22131265-22131283 chr4:22131267-22131288

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:22031559-22031609	GM06990	blood:	n/a
2	chr4:22031559-22031609	HIPEpiC	eye:	n/a
3	chr4:22148354-22148404	NHDF-neo	bronchial:	n/a
4	chr4:22031559-22031609	LNCaP	prostate:	n/a
5	chr4:22148230-22148280	GM19239	blood:	n/a
6	chr4:22148230-22148280	BJ	skin:	n/a
7	chr4:22148354-22148404	Jurkat	blood:	n/a
8	chr4:22148354-22148404	NB4	blood:	n/a
9	chr4:22148230-22148280	HMEC	breast:	n/a
10	chr4:22031559-22031609	MCF-7	breast:	n/a
11	chr4:22031559-22031609	NT2-D1	testis:	n/a
12	chr4:22148230-22148280	Jurkat	blood:	n/a
13	chr4:22031559-22031609	HRPEpiC	eye:	n/a
14	chr4:22031559-22031609	HAEpiC	amniotic membrane:	n/a
15	chr4:22148354-22148404	ECC-1	luminal epithelium:	n/a
16	chr4:22148354-22148404	BE2_C	brain:	n/a
17	chr4:22148354-22148404	Caco-2	colon:	n/a
18	chr4:22148230-22148280	AG09309	skin:	n/a
19	chr4:22031559-22031609	AoSMC	blood vessel:	n/a
20	chr4:22148230-22148280	RPTEC	kidney:	n/a
21	chr4:22148354-22148404	HEK293	kidney:	embryo
22	chr4:22148230-22148280	T-47D	breast:	n/a
23	chr4:22031559-22031609	SK-N-SH_RA	brain:	n/a
24	chr4:22148354-22148404	SK-N-MC	brain:	n/a
25	chr4:22148354-22148404	AG09319	gingival:	n/a
26	chr4:22148230-22148280	MCF10A-Er-Src	breast:	n/a
27	chr4:22031559-22031609	GM12891	blood:	n/a
28	chr4:22031559-22031609	HCT-116	colon:	n/a
29	chr4:22031559-22031609	GM12878	blood:	n/a
30	chr4:22148230-22148280	HCM	heart:	n/a
31	chr4:22148230-22148280	U87	brain:	n/a
32	chr4:22148230-22148280	PFSK-1	brain:	n/a
33	chr4:22031559-22031609	AG04449	skin:	fetal
34	chr4:22031559-22031609	PFSK-1	brain:	n/a
35	chr4:22031559-22031609	NHDF-neo	bronchial:	n/a
36	chr4:22031559-22031609	ovcar-3	ovarian:	n/a
37	chr4:22031559-22031609	U87	brain:	n/a
38	chr4:22148354-22148404	LNCaP	prostate:	n/a
39	chr4:22148354-22148404	CMK	blood:	n/a
40	chr4:22148230-22148280	GM06990	blood:	n/a
41	chr4:22031559-22031609	AG09319	gingival:	n/a
42	chr4:22148230-22148280	MCF-7	breast:	n/a
43	chr4:22148354-22148404	AoSMC	blood vessel:	n/a
44	chr4:22031559-22031609	SAEC	small airway:	n/a
45	chr4:22148354-22148404	PFSK-1	brain:	n/a
46	chr4:22148230-22148280	PANC-1	pancreas:	n/a
47	chr4:22148230-22148280	AoSMC	blood vessel:	n/a
48	chr4:22148230-22148280	HRE	kidney:	n/a
49	chr4:22148354-22148404	T-47D	breast:	n/a
50	chr4:22031559-22031609	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:22219857..22222824-chr4:22225422..22227720,2	K562	blood:
2	chr4:22045762..22048489-chr4:22082694..22085288,2	MCF-7	breast:
3	chr4:22028111..22029824-chr4:22035660..22037244,2	MCF-7	breast:
4	chr4:22131171..22132005-chr4:22358195..22359539,3	MCF-7	breast:
5	chr4:22028111..22029824-chr4:22035660..22037244,2	MCF-7	breast:
6	chr4:22022641..22025613-chr4:22031377..22033219,2	K562	blood:
7	chr4:22130852..22132108-chr4:22390561..22391530,5	MCF-7	breast:
8	chr4:21791838..21792739-chr4:22130763..22131377,2	MCF-7	breast:
9	chr4:22045762..22048489-chr4:22082694..22085288,2	MCF-7	breast:
10	chr4:21790635..21791482-chr4:22083518..22084264,2	MCF-7	breast:
11	chr4:22219857..22222824-chr4:22225422..22227720,2	K562	blood:
12	chr4:22022641..22025613-chr4:22031377..22033219,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PACRGL-5	chr4:22103117-22103253	ENSG00000250039.3
2	lnc-PACRGL-5	chr4:22060696-22060983	ENSG00000250039.2
3	lnc-PACRGL-5	chr4:22060707-22060983	ENSG00000250039.3
4	lnc-PACRGL-5	chr4:22103115-22103259	ENSG00000250039.2

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

Extended variants
information (count: 3214 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:3214 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190892974	chr4:22015419-22015420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs78020422	chr4:22015420-22015421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs572285251	chr4:22015427-22015428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs182067036	chr4:22015428-22015429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs575872110	chr4:22015474-22015475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs550355496	chr4:22015522-22015523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs542987799	chr4:22015538-22015539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs536425041	chr4:22015540-22015541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs188020089	chr4:22015550-22015551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs73102666	chr4:22015618-22015619	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs576220851	chr4:22015627-22015628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs192694874	chr4:22015714-22015715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs564599917	chr4:22015720-22015721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs112674056	chr4:22015785-22015786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs73102668	chr4:22015795-22015796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs188313893	chr4:22015832-22015833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs369726526	chr4:22015864-22015865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs193040990	chr4:22015904-22015905	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs150691735	chr4:22015915-22015916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs371072364	chr4:22015938-22015939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs114757410	chr4:22015979-22015980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs533926552	chr4:22016012-22016013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs139134812	chr4:22016038-22016039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs184621664	chr4:22016102-22016103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs538786423	chr4:22016135-22016136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs557308763	chr4:22016140-22016141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs1513574	chr4:22016141-22016142	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs143979631	chr4:22016201-22016202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs13144713	chr4:22016223-22016224	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs146462291	chr4:22016243-22016244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs540419495	chr4:22016278-22016279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs13117670	chr4:22016295-22016296	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs576504277	chr4:22016302-22016303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs546020954	chr4:22016319-22016320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs373971614	chr4:22016326-22016327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs544008904	chr4:22016337-22016338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs562616486	chr4:22016340-22016341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs529628165	chr4:22016372-22016373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs548169672	chr4:22016376-22016377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs189282858	chr4:22016382-22016383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs34151417	chr4:22016414-22016415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs192553452	chr4:22016423-22016424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs183753526	chr4:22016459-22016460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs68147450	chr4:22016461-22016462	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs548864986	chr4:22016494-22016495	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs545490656	chr4:22016508-22016509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs189652167	chr4:22016510-22016511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs532777667	chr4:22022618-22022619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs184110734	chr4:22022641-22022642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs561172158	chr4:22022660-22022661	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:225 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:22015400-22016600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr4:22015600-22016600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr4:22015800-22016600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr4:22022600-22023400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr4:22025200-22025600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr4:22028600-22028800	Enhancers	H9 Cell Line	embryonic stem cell
7	chr4:22028800-22029000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
8	chr4:22031000-22032000	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr4:22031000-22032200	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr4:22031200-22032400	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr4:22031600-22031800	Active TSS	iPS-20b Cell Line	embryonic stem cell
12	chr4:22031600-22032000	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr4:22031600-22032200	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr4:22031800-22032000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
15	chr4:22031800-22032200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr4:22045200-22046000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr4:22046200-22047400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr4:22059800-22066400	Weak transcription	Pancreas	Pancrea
19	chr4:22060800-22062200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr4:22062200-22063200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr4:22063200-22066400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr4:22066400-22066600	ZNF genes & repeats	Pancreas	Pancrea
23	chr4:22066400-22073200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr4:22073200-22073800	Enhancers	NHEK	skin
25	chr4:22073200-22074200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr4:22073200-22074400	Enhancers	HMEC	breast
27	chr4:22073400-22074200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr4:22073400-22074400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr4:22074400-22077800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr4:22077800-22078400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr4:22078400-22078800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr4:22078800-22079400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr4:22087200-22087600	Enhancers	HSMMtube	muscle
34	chr4:22091800-22093400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr4:22092400-22093000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr4:22092600-22093000	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr4:22092600-22093000	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr4:22092600-22093000	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr4:22092600-22095000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr4:22093000-22094400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr4:22093000-22094800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr4:22093200-22094200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr4:22093600-22093800	Enhancers	Osteobl	bone
44	chr4:22093600-22094400	Enhancers	Adipose Nuclei	Adipose
45	chr4:22099000-22101800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr4:22101000-22102200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr4:22101000-22103200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr4:22101200-22101800	Enhancers	HMEC	breast
49	chr4:22101200-22101800	Enhancers	NH-A	brain
50	chr4:22101200-22102200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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