Variant report

Variant	nsv428756
Chromosome Location	chr4:22239826-22406106
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	chr4:22339323-22339686	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:22239692-22240117	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:22350171-22350215	HepG2	liver:	n/a	n/a
4	BATF	chr4:22340569-22340828	GM12878	blood:	n/a	n/a
5	BATF	chr4:22340630-22340895	GM12878	blood:	n/a	n/a
6	BCL11A	chr4:22340639-22340830	GM12878	blood:	n/a	n/a
7	BCL11A	chr4:22340625-22340881	GM12878	blood:	n/a	n/a
8	BHLHE40	chr4:22390851-22391189	GM12878	blood:	n/a	n/a
9	BRCA1	chr4:22390959-22391165	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr4:22314504-22314794	IMR90	lung:	n/a	chr4:22314672-22314683
11	CEBPB	chr4:22335955-22336149	A549	lung:	n/a	chr4:22336030-22336041 chr4:22335991-22336002
12	CEBPB	chr4:22284305-22284648	HepG2	liver:	n/a	chr4:22284476-22284487
13	CEBPB	chr4:22385141-22385383	HepG2	liver:	n/a	chr4:22385294-22385305
14	CEBPB	chr4:22339317-22339689	HepG2	liver:	n/a	n/a
15	CEBPB	chr4:22284321-22284665	IMR90	lung:	n/a	chr4:22284476-22284487
16	CEBPB	chr4:22387249-22387794	HCT-116	colon:	n/a	n/a
17	CEBPB	chr4:22391209-22391400	H1-hESC	embryonic stem cell:	n/a	chr4:22391362-22391374
18	CEBPB	chr4:22284358-22284611	A549	lung:	n/a	chr4:22284476-22284487
19	CEBPB	chr4:22284423-22284523	H1-hESC	embryonic stem cell:	n/a	chr4:22284476-22284487
20	CEBPB	chr4:22240531-22240641	HepG2	liver:	n/a	n/a
21	CEBPB	chr4:22335841-22336189	HepG2	liver:	n/a	chr4:22336030-22336041 chr4:22335991-22336002
22	CEBPB	chr4:22314532-22314837	HepG2	liver:	n/a	chr4:22314672-22314683
23	CEBPB	chr4:22350158-22350485	IMR90	lung:	n/a	n/a
24	CEBPB	chr4:22284472-22284512	K562	blood:	n/a	chr4:22284476-22284487
25	CTCF	chr4:22391000-22391150	HCPEpiC	choroid plexus:	n/a	chr4:22391053-22391071 chr4:22391055-22391068 chr4:22391054-22391070 chr4:22391048-22391069
26	CTCF	chr4:22240475-22240676	Gliobla	brain:	n/a	n/a
27	CTCF	chr4:22240476-22240670	MCF-7	breast:	n/a	n/a
28	CTCF	chr4:22338607-22338671	MCF-7	breast:	n/a	n/a
29	CTCF	chr4:22391267-22391413	GM19238	blood:	n/a	n/a
30	CTCF	chr4:22338608-22338657	LNCaP	prostate:	n/a	n/a
31	CTCF	chr4:22240486-22240673	MCF-7	breast:	n/a	n/a
32	CTCF	chr4:22358980-22359130	HA-sp	spinal cord:	n/a	n/a
33	CTCF	chr4:22358900-22359174	Gliobla	brain:	n/a	n/a
34	CTCF	chr4:22338460-22338610	HCT-116	colon:	n/a	n/a
35	CTCF	chr4:22390980-22391130	HRE	kidney:	n/a	chr4:22391053-22391071 chr4:22391055-22391068 chr4:22391054-22391070 chr4:22391048-22391069
36	CTCF	chr4:22358960-22359110	SAEC	small airway:	n/a	n/a
37	CTCF	chr4:22359020-22359170	A549	lung:	n/a	n/a
38	CTCF	chr4:22390953-22391200	Hela-S3	cervix:	n/a	chr4:22391053-22391071 chr4:22391055-22391068 chr4:22391054-22391070 chr4:22391048-22391069
39	CTCF	chr4:22240486-22240676	MCF-7	breast:	n/a	n/a
40	CTCF	chr4:22390960-22391110	GM12874	blood:	n/a	chr4:22391053-22391071 chr4:22391055-22391068 chr4:22391054-22391070 chr4:22391048-22391069
41	CTCF	chr4:22390965-22391188	ProgFib	skin:	n/a	chr4:22391053-22391071 chr4:22391055-22391068 chr4:22391054-22391070 chr4:22391048-22391069
42	CTCF	chr4:22390965-22391232	K562	blood:	n/a	chr4:22391053-22391071 chr4:22391055-22391068 chr4:22391054-22391070 chr4:22391048-22391069
43	CTCF	chr4:22358850-22359172	MCF-7	breast:	n/a	n/a
44	CTCF	chr4:22390980-22391130	MCF-7	breast:	n/a	chr4:22391053-22391071 chr4:22391055-22391068 chr4:22391054-22391070 chr4:22391048-22391069
45	CTCF	chr4:22390980-22391130	SAEC	small airway:	n/a	chr4:22391053-22391071 chr4:22391055-22391068 chr4:22391054-22391070 chr4:22391048-22391069
46	CTCF	chr4:22390918-22391223	Spleen_OC	spleen:	n/a	chr4:22391053-22391071 chr4:22391055-22391068 chr4:22391054-22391070 chr4:22391048-22391069
47	CTCF	chr4:22240540-22240690	A549	lung:	n/a	n/a
48	CTCF	chr4:22358960-22359110	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr4:22390978-22391169	Fibrobl	skin:	n/a	chr4:22391053-22391071 chr4:22391055-22391068 chr4:22391054-22391070 chr4:22391048-22391069
50	CTCF	chr4:22240500-22240650	BJ	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:22390126-22390176	GM06990	blood:	n/a
2	chr4:22390012-22390062	BE2_C	brain:	n/a
3	chr4:22389706-22389756	GM19239	blood:	n/a
4	chr4:22389934-22389984	GM19239	blood:	n/a
5	chr4:22239907-22239957	HNPCEpiC	eye:	n/a
6	chr4:22390126-22390176	SK-N-SH_RA	brain:	n/a
7	chr4:22390012-22390062	NHDF-neo	bronchial:	n/a
8	chr4:22390012-22390062	SK-N-SH_RA	brain:	n/a
9	chr4:22390126-22390176	AG10803	skin:	n/a
10	chr4:22390126-22390176	AG09319	gingival:	n/a
11	chr4:22239907-22239957	MCF-7	breast:	n/a
12	chr4:22392700-22392750	HUVEC	blood vessel:	n/a
13	chr4:22390012-22390062	ovcar-3	ovarian:	n/a
14	chr4:22392700-22392750	HL-60	blood:	n/a
15	chr4:22389706-22389756	PrEC	prostate:	n/a
16	chr4:22390012-22390062	SK-N-SH	brain:	n/a
17	chr4:22389746-22389796	HAEpiC	amniotic membrane:	n/a
18	chr4:22390012-22390062	HCPEpiC	choroid plexus:	n/a
19	chr4:22392700-22392750	SK-N-SH	brain:	n/a
20	chr4:22390012-22390062	HRE	kidney:	n/a
21	chr4:22392700-22392750	GM06990	blood:	n/a
22	chr4:22392700-22392750	NH-A	brain:	n/a
23	chr4:22389934-22389984	NH-A	brain:	n/a
24	chr4:22389746-22389796	K562	blood:	n/a
25	chr4:22389934-22389984	SAEC	small airway:	n/a
26	chr4:22392700-22392750	PFSK-1	brain:	n/a
27	chr4:22389706-22389756	NB4	blood:	n/a
28	chr4:22390012-22390062	MCF-7	breast:	n/a
29	chr4:22239907-22239957	AG09319	gingival:	n/a
30	chr4:22389934-22389984	ProgFib	skin:	n/a
31	chr4:22390126-22390176	MCF-7	breast:	n/a
32	chr4:22390012-22390062	RPTEC	kidney:	n/a
33	chr4:22389934-22389984	AG09319	gingival:	n/a
34	chr4:22390126-22390176	HEEpiC	esophagus:	n/a
35	chr4:22390012-22390062	HAEpiC	amniotic membrane:	n/a
36	chr4:22389934-22389984	AG04449	skin:	fetal
37	chr4:22390012-22390062	HCM	heart:	n/a
38	chr4:22390012-22390062	SKMC	muscle:	n/a
39	chr4:22392700-22392750	HRPEpiC	eye:	n/a
40	chr4:22389746-22389796	ProgFib	skin:	n/a
41	chr4:22389746-22389796	NH-A	brain:	n/a
42	chr4:22239907-22239957	SAEC	small airway:	n/a
43	chr4:22389934-22389984	Hepatocyte	liver:	n/a
44	chr4:22389934-22389984	PANC-1	pancreas:	n/a
45	chr4:22390126-22390176	HCPEpiC	choroid plexus:	n/a
46	chr4:22390012-22390062	Hepatocyte	liver:	n/a
47	chr4:22389706-22389756	Caco-2	colon:	n/a
48	chr4:22392700-22392750	ECC-1	luminal epithelium:	n/a
49	chr4:22390012-22390062	NHBE	bronchial:	n/a
50	chr4:22239907-22239957	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:22131171..22132005-chr4:22358195..22359539,3	MCF-7	breast:
2	chr4:22391010..22391614-chr4:22608701..22609240,2	MCF-7	breast:
3	chr4:22238564..22239075-chr4:22358901..22359564,2	MCF-7	breast:
4	chr4:22306671..22307308-chr4:127827877..127828727,2	MCF-7	breast:
5	chr4:22287110..22290036-chr4:22291416..22294469,3	K562	blood:
6	chr4:22130852..22132108-chr4:22390561..22391530,5	MCF-7	breast:
7	chr4:22386027..22387843-chr4:22392194..22394951,2	MCF-7	breast:
8	chr4:21790239..21792742-chr4:22389960..22391772,13	MCF-7	breast:
9	chr4:21790330..21793132-chr4:22390550..22391689,10	MCF-7	breast:
10	chr4:22386027..22387843-chr4:22392194..22394951,2	MCF-7	breast:
11	chr4:22287110..22290036-chr4:22291416..22294469,3	K562	blood:
12	chr4:21769756..21770575-chr4:22358426..22359045,2	MCF-7	breast:
13	chr14:26600846..26601469-chr4:22299814..22300678,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR125-3	chr4:22328990-22329512	NONHSAT095753
2	lnc-PACRGL-5	chr4:22330939-22331953	ENSG00000250039.2
3	lnc-GPR125-1	chr4:22348356-22348426	XLOC_003904
4	lnc-PACRGL-8	chr4:22368195-22368761	NONHSAT095756
5	lnc-GPR125-3	chr4:22341203-22341289	NONHSAT095753
6	lnc-GPR125-3	chr4:22331480-22331627	NONHSAT095753
7	lnc-GPR125-1	chr4:22346156-22346187	XLOC_003904
8	lnc-GPR125-3	chr4:22336664-22336790	NONHSAT095753
9	lnc-PACRGL-5	chr4:22330939-22331953	ENSG00000250039.3
10	lnc-GPR125-1	chr4:22346780-22346968	XLOC_003904

Variant related genes	Relation type
GPR125	TF binding region
ENSG00000238383	TF binding region
GPR125	CpG island
ENSG00000238383	CpG island
ENSG00000251516	chromatin interactions

Extended variants
information (count: 4005 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:4005 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577194678	chr4:22239858-22239859	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs372104669	chr4:22239883-22239884	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs544275103	chr4:22239886-22239887	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs71608913	chr4:22239907-22239908	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs563234577	chr4:22239908-22239909	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs185381248	chr4:22239913-22239914	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs542464993	chr4:22239927-22239928	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs560637886	chr4:22239938-22239939	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs527875696	chr4:22239941-22239942	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs552329650	chr4:22239950-22239951	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs60980377	chr4:22239955-22239956	Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs190034118	chr4:22239994-22239995	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs529477834	chr4:22240013-22240014	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs181698761	chr4:22240046-22240047	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs377152119	chr4:22240107-22240108	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs549142654	chr4:22240150-22240151	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs535336705	chr4:22240168-22240169	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs186818769	chr4:22240172-22240173	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs11933715	chr4:22240249-22240250	Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs142480966	chr4:22240271-22240272	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs73107814	chr4:22240338-22240339	Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs551760636	chr4:22240365-22240366	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs558671437	chr4:22240377-22240378	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs115113396	chr4:22240383-22240384	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs138040102	chr4:22240393-22240394	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs377082286	chr4:22240394-22240395	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs114712354	chr4:22240414-22240415	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs556258147	chr4:22240456-22240457	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs541783626	chr4:22240469-22240470	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs4466029	chr4:22240473-22240474	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs567748593	chr4:22240516-22240517	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs191669800	chr4:22240539-22240540	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs560747998	chr4:22240575-22240576	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs183910808	chr4:22240598-22240599	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs186538595	chr4:22240625-22240626	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs114691264	chr4:22240680-22240681	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs4697276	chr4:22240695-22240696	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs146504213	chr4:22240744-22240745	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs561491195	chr4:22240753-22240754	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs73243023	chr4:22240871-22240872	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs547316225	chr4:22240904-22240905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs189759452	chr4:22240922-22240923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs4697003	chr4:22240923-22240924	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs556389689	chr4:22240928-22240929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs570925891	chr4:22240955-22240956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs537920499	chr4:22240962-22240963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs141714310	chr4:22240974-22240975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs558026849	chr4:22240975-22240976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs78189497	chr4:22240976-22240977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs112126630	chr4:22240990-22240991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
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
Wilms tumour	21544195	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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:696 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:22238800-22240000	Active TSS	Rectal Mucosa Donor 31	rectum
2	chr4:22238800-22240400	Enhancers	Brain Hippocampus Middle	brain
3	chr4:22239000-22240200	Active TSS	Duodenum Mucosa	Duodenum
4	chr4:22239000-22240200	Active TSS	Fetal Intestine Small	intestine
5	chr4:22239000-22240400	Active TSS	Colonic Mucosa	Colon
6	chr4:22239000-22240800	Active TSS	Rectal Mucosa Donor 29	rectum
7	chr4:22239200-22240000	Active TSS	Primary T cells fromperipheralblood	blood
8	chr4:22239200-22240000	Active TSS	Pancreatic Islets	Pancreatic Islet
9	chr4:22239200-22240200	Active TSS	Primary hematopoietic stem cells	blood
10	chr4:22239200-22240200	Active TSS	Ovary	ovary
11	chr4:22239200-22240200	Active TSS	Stomach Mucosa	stomach
12	chr4:22239400-22240000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr4:22239400-22240000	Active TSS	Primary B cells from peripheral blood	blood
14	chr4:22239400-22240200	Active TSS	Duodenum Smooth Muscle	Duodenum
15	chr4:22239400-22240200	Active TSS	Fetal Intestine Large	intestine
16	chr4:22239400-22240200	Enhancers	HepG2	liver
17	chr4:22239400-22240600	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr4:22239600-22240000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr4:22239600-22240000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr4:22239600-22240000	Enhancers	Brain Angular Gyrus	brain
21	chr4:22239600-22240200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr4:22239600-22240200	Active TSS	Rectal Smooth Muscle	rectum
23	chr4:22239600-22240200	Active TSS	Osteobl	bone
24	chr4:22239600-22240400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr4:22239600-22240400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr4:22239600-22240400	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr4:22239600-22240400	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr4:22239600-22240400	Flanking Active TSS	Liver	Liver
29	chr4:22239600-22240400	Active TSS	Brain Anterior Caudate	brain
30	chr4:22239600-22240400	Enhancers	Brain Germinal Matrix	brain
31	chr4:22239600-22240600	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr4:22239600-22240600	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr4:22239800-22240000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr4:22239800-22240000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr4:22239800-22240000	Enhancers	Brain Cingulate Gyrus	brain
36	chr4:22239800-22240400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr4:22239800-22240400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr4:22239800-22240600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr4:22240000-22240200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr4:22240000-22240400	Enhancers	Pancreatic Islets	Pancreatic Islet
41	chr4:22240000-22240600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
42	chr4:22240200-22240400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr4:22240200-22240400	Flanking Active TSS	Fetal Intestine Large	intestine
44	chr4:22240200-22240400	Flanking Active TSS	Fetal Intestine Small	intestine
45	chr4:22240200-22240400	Enhancers	Ovary	ovary
46	chr4:22240200-22240400	Flanking Active TSS	Stomach Mucosa	stomach
47	chr4:22240200-22240600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
48	chr4:22240200-22240600	Flanking Active TSS	Duodenum Mucosa	Duodenum
49	chr4:22240200-22240600	Flanking Active TSS	HepG2	liver
50	chr4:22240400-22240800	Enhancers	Liver	Liver

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