Variant report

Variant	nsv881405
Chromosome Location	chr4:167193885-167628013
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1608)
CpG islands
(count:122)
Chromatin interactive
region (count:27)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1608 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:167245551-167245839	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:167323220-167323249	HepG2	liver:	n/a	n/a
3	ATF2	chr4:167402837-167403336	GM12878	blood:	n/a	n/a
4	ATF2	chr4:167583032-167584075	GM12878	blood:	n/a	n/a
5	ATF2	chr4:167402894-167403312	GM12878	blood:	n/a	n/a
6	ATF2	chr4:167583070-167584155	GM12878	blood:	n/a	n/a
7	ATF2	chr4:167422943-167423479	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr4:167423063-167423487	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr4:167423072-167423419	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:167308058-167308258	H1-hESC	embryonic stem cell:	n/a	chr4:167308080-167308094
11	BACH1	chr4:167489118-167489236	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr4:167423095-167423380	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr4:167448712-167449039	GM12878	blood:	n/a	n/a
14	BATF	chr4:167546532-167546732	GM12878	blood:	n/a	n/a
15	BATF	chr4:167307660-167308129	GM12878	blood:	n/a	chr4:167308080-167308090 chr4:167307751-167307761
16	BATF	chr4:167402811-167403225	GM12878	blood:	n/a	chr4:167402976-167402987
17	BATF	chr4:167583206-167583784	GM12878	blood:	n/a	n/a
18	BATF	chr4:167402235-167402454	GM12878	blood:	n/a	n/a
19	BATF	chr4:167583263-167584030	GM12878	blood:	n/a	n/a
20	BATF	chr4:167402867-167403200	GM12878	blood:	n/a	chr4:167402976-167402987
21	BCL11A	chr4:167501286-167501687	GM12878	blood:	n/a	n/a
22	BCL11A	chr4:167583341-167583941	GM12878	blood:	n/a	n/a
23	BCL11A	chr4:167448647-167448992	GM12878	blood:	n/a	n/a
24	BCL11A	chr4:167307669-167308219	GM12878	blood:	n/a	chr4:167307753-167307762 chr4:167308082-167308091 chr4:167307863-167307872 chr4:167307754-167307763 chr4:167308083-167308092
25	BCL11A	chr4:167583205-167584043	GM12878	blood:	n/a	n/a
26	BCL11A	chr4:167448711-167449006	GM12878	blood:	n/a	n/a
27	BCL11A	chr4:167402857-167403289	GM12878	blood:	n/a	n/a
28	BCL3	chr4:167307872-167308181	GM12878	blood:	n/a	chr4:167308082-167308091 chr4:167308083-167308092
29	BCL3	chr4:167583224-167583883	GM12878	blood:	n/a	n/a
30	BCLAF1	chr4:167583198-167584150	GM12878	blood:	n/a	n/a
31	BCLAF1	chr4:167583324-167584100	GM12878	blood:	n/a	n/a
32	BHLHE40	chr4:167579687-167580153	GM12878	blood:	n/a	n/a
33	BHLHE40	chr4:167284487-167284669	GM12878	blood:	n/a	n/a
34	BHLHE40	chr4:167402945-167403257	GM12878	blood:	n/a	n/a
35	BHLHE40	chr4:167583209-167584151	GM12878	blood:	n/a	n/a
36	BHLHE40	chr4:167421014-167421210	GM12878	blood:	n/a	n/a
37	BHLHE40	chr4:167501050-167501864	HepG2	liver:	n/a	n/a
38	BRCA1	chr4:167423134-167423289	H1-hESC	embryonic stem cell:	n/a	n/a
39	BRCA1	chr4:167557398-167557434	GM12878	blood:	n/a	n/a
40	BRCA1	chr4:167515545-167515688	HepG2	liver:	n/a	n/a
41	CBX3	chr4:167245426-167245902	HCT-116	colon:	n/a	n/a
42	CBX3	chr4:167298713-167299125	HCT-116	colon:	n/a	n/a
43	CBX3	chr4:167515547-167515801	HCT-116	colon:	n/a	n/a
44	CEBPB	chr4:167259757-167260005	HepG2	liver:	n/a	chr4:167259925-167259936
45	CEBPB	chr4:167550162-167550463	HepG2	liver:	n/a	chr4:167550309-167550318 chr4:167550307-167550318
46	CEBPB	chr4:167241438-167241800	IMR90	lung:	n/a	chr4:167241615-167241626
47	CEBPB	chr4:167201970-167202208	MCF-7	breast:	n/a	chr4:167202074-167202087
48	CEBPB	chr4:167241483-167241745	K562	blood:	n/a	chr4:167241615-167241626
49	CEBPB	chr4:167196005-167196311	K562	blood:	n/a	chr4:167196127-167196138 chr4:167196045-167196056 chr4:167196125-167196142 chr4:167196126-167196139
50	CEBPB	chr4:167423114-167423505	MCF-7	breast:	n/a	chr4:167423248-167423259

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:167448796-167448846	SK-N-MC	brain:	n/a
2	chr4:167384733-167384783	NHBE	bronchial:	n/a
3	chr4:167448796-167448846	HepG2	liver:	n/a
4	chr4:167448796-167448846	HUVEC	blood vessel:	n/a
5	chr4:167448796-167448846	NHBE	bronchial:	n/a
6	chr4:167448796-167448846	AG09309	skin:	n/a
7	chr4:167384733-167384783	T-47D	breast:	n/a
8	chr4:167384733-167384783	GM06990	blood:	n/a
9	chr4:167448796-167448846	PANC-1	pancreas:	n/a
10	chr4:167448796-167448846	SK-N-SH	brain:	n/a
11	chr4:167384733-167384783	HMEC	breast:	n/a
12	chr4:167384733-167384783	HCM	heart:	n/a
13	chr4:167384733-167384783	HAEpiC	amniotic membrane:	n/a
14	chr4:167384733-167384783	HRE	kidney:	n/a
15	chr4:167448796-167448846	AG04450	lung:	fetal
16	chr4:167448796-167448846	K562	blood:	n/a
17	chr4:167384733-167384783	MCF-7	breast:	n/a
18	chr4:167384733-167384783	Caco-2	colon:	n/a
19	chr4:167448796-167448846	Hepatocyte	liver:	n/a
20	chr4:167448796-167448846	MCF-7	breast:	n/a
21	chr4:167384733-167384783	PFSK-1	brain:	n/a
22	chr4:167448796-167448846	HEK293	kidney:	embryo
23	chr4:167384733-167384783	GM12891	blood:	n/a
24	chr4:167448796-167448846	AG09319	gingival:	n/a
25	chr4:167448796-167448846	Hela-S3	cervix:	n/a
26	chr4:167384733-167384783	GM12892	blood:	n/a
27	chr4:167384733-167384783	SKMC	muscle:	n/a
28	chr4:167448796-167448846	RPTEC	kidney:	n/a
29	chr4:167384733-167384783	GM19239	blood:	n/a
30	chr4:167448796-167448846	HCM	heart:	n/a
31	chr4:167384733-167384783	AoSMC	blood vessel:	n/a
32	chr4:167384733-167384783	ProgFib	skin:	n/a
33	chr4:167448796-167448846	U87	brain:	n/a
34	chr4:167384733-167384783	SK-N-MC	brain:	n/a
35	chr4:167384733-167384783	CMK	blood:	n/a
36	chr4:167448796-167448846	ovcar-3	ovarian:	n/a
37	chr4:167448796-167448846	HNPCEpiC	eye:	n/a
38	chr4:167448796-167448846	NB4	blood:	n/a
39	chr4:167384733-167384783	HCF	heart:	n/a
40	chr4:167448796-167448846	GM06990	blood:	n/a
41	chr4:167448796-167448846	HEEpiC	esophagus:	n/a
42	chr4:167448796-167448846	H1-hESC	embryonic stem cell:	embryo
43	chr4:167448796-167448846	HIPEpiC	eye:	n/a
44	chr4:167384733-167384783	HPAEpiC	pulmonary alveolar:	n/a
45	chr4:167384733-167384783	IMR90	lung:	fetal
46	chr4:167384733-167384783	NT2-D1	testis:	n/a
47	chr4:167384733-167384783	HRCEpiC	kidney:	n/a
48	chr4:167384733-167384783	HCT-116	colon:	n/a
49	chr4:167384733-167384783	HepG2	liver:	n/a
50	chr4:167448796-167448846	CMK	blood:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:167244994..167245863-chr4:167515216..167516030,3	MCF-7	breast:
2	chr4:167423153..167423656-chr4:167515182..167515903,2	MCF-7	breast:
3	chr4:167090069..167090971-chr4:167515205..167515895,2	MCF-7	breast:
4	chr4:167552287..167553829-chr4:167557638..167559725,2	K562	blood:
5	chr4:167332041..167334748-chr4:167341372..167343978,2	K562	blood:
6	chr4:167407304..167409099-chr4:167497184..167500129,2	K562	blood:
7	chr4:167407304..167409099-chr4:167497184..167500129,2	K562	blood:
8	chr4:167332041..167334748-chr4:167341372..167343978,2	K562	blood:
9	chr4:167086761..167087587-chr4:167515275..167516081,4	MCF-7	breast:
10	chr4:167524991..167527331-chr4:167531005..167532808,2	K562	blood:
11	chr4:167484390..167486125-chr4:167489099..167491015,2	MCF-7	breast:
12	chr4:167239410..167241651-chr4:167242890..167245668,2	K562	blood:
13	chr4:167055604..167058496-chr4:167332499..167335064,2	K562	blood:
14	chr4:167423153..167423656-chr4:167515182..167515903,2	MCF-7	breast:
15	chr4:167546008..167548762-chr4:167550829..167552670,2	K562	blood:
16	chr4:167239410..167241651-chr4:167242890..167245668,2	K562	blood:
17	chr4:167524991..167527331-chr4:167531005..167532808,2	K562	blood:
18	chr4:167484390..167486125-chr4:167489099..167491015,2	MCF-7	breast:
19	chr4:167245228..167246184-chr4:167515396..167516066,3	MCF-7	breast:
20	chr4:167546008..167548762-chr4:167550829..167552670,2	K562	blood:
21	chr4:167616122..167618390-chr4:167618848..167621322,2	MCF-7	breast:
22	chr4:167245228..167246184-chr4:167515396..167516066,3	MCF-7	breast:
23	chr4:167616122..167618390-chr4:167618848..167621322,2	MCF-7	breast:
24	chr4:167349986..167352184-chr4:167352810..167354578,2	K562	blood:
25	chr4:167552287..167553829-chr4:167557638..167559725,2	K562	blood:
26	chr4:167244994..167245863-chr4:167515216..167516030,3	MCF-7	breast:
27	chr4:167349986..167352184-chr4:167352810..167354578,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPOCK3-5	chr4:167236991-167240148	predAs_chen_BG208718_1

No data

Variant related genes	Relation type
ENSG00000249675	TF binding region
ENSG00000206711	TF binding region
ENSG00000249675	CpG island
ENSG00000206711	CpG island

Extended variants
information (count: 8464 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:8464 , 50 per page) page: 1 2 3 4 5 6 7 ... 170

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs382617	chr4:167198238-167198239	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs144425494	chr4:167198264-167198265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs572341870	chr4:167198330-167198331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs543144766	chr4:167198332-167198333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs561204395	chr4:167198335-167198336	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs529109616	chr4:167198341-167198342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs182439398	chr4:167198352-167198353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs544061817	chr4:167198395-167198396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs410691	chr4:167198429-167198430	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs74530010	chr4:167198444-167198445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs10024954	chr4:167198461-167198462	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs421201	chr4:167198487-167198488	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs527270538	chr4:167198491-167198492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs549082089	chr4:167198496-167198497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs567315652	chr4:167198532-167198533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs454256	chr4:167198580-167198581	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs502270	chr4:167198601-167198602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs538447025	chr4:167198621-167198622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs563957211	chr4:167198622-167198623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs556744876	chr4:167198631-167198632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs571869650	chr4:167198634-167198635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs77240753	chr4:167198642-167198643	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs79704206	chr4:167198655-167198656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs377656273	chr4:167198681-167198682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs139793459	chr4:167198718-167198719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs564252973	chr4:167198730-167198731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs542628543	chr4:167198760-167198761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs1870531	chr4:167198762-167198763	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs188053710	chr4:167198776-167198777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs543507542	chr4:167198781-167198782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs562382766	chr4:167198785-167198786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs142678817	chr4:167198797-167198798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs532943545	chr4:167198808-167198809	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs376488106	chr4:167198816-167198817	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs560157298	chr4:167198828-167198829	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527294416	chr4:167198882-167198883	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530375948	chr4:167198957-167198958	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs72432253	chr4:167198969-167198970	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs531271112	chr4:167198970-167198971	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548658175	chr4:167198977-167198978	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs199596874	chr4:167198981-167198982	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs563253256	chr4:167198982-167198983	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs538856565	chr4:167198983-167198984	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs528865642	chr4:167198984-167198985	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs6830174	chr4:167198990-167198991	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs377688891	chr4:167199010-167199011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548589514	chr4:167199017-167199018	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs79123576	chr4:167199060-167199061	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs75118318	chr4:167199061-167199062	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs1663605	chr4:167199111-167199112	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Glioblastoma multiforme	22286061	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	16774939	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Myelofibrosis	22110671	CNVD
intellectual deficit	22127048	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Epilepsy	21635232	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Chronic lymphocytic leukemia	21215367	CNVD

Chromatin state (count:457 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:167198200-167198800	Enhancers	Osteobl	bone
2	chr4:167198200-167199400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr4:167198400-167198800	Enhancers	Muscle Satellite Cultured Cells	--
4	chr4:167198400-167199600	Enhancers	NH-A	brain
5	chr4:167198800-167199200	Weak transcription	Osteobl	bone
6	chr4:167199200-167199600	Enhancers	Osteobl	bone
7	chr4:167213000-167213400	Enhancers	HUVEC	blood vessel
8	chr4:167213400-167213800	Weak transcription	HUVEC	blood vessel
9	chr4:167213800-167215000	Enhancers	HUVEC	blood vessel
10	chr4:167214400-167214800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr4:167214400-167214800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr4:167214400-167215000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr4:167214400-167215000	Enhancers	Muscle Satellite Cultured Cells	--
14	chr4:167222000-167222400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr4:167222200-167222400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr4:167222200-167222400	Enhancers	NH-A	brain
17	chr4:167222400-167222800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr4:167222400-167223000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr4:167222600-167223000	Enhancers	Osteobl	bone
20	chr4:167222800-167223000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr4:167223000-167223200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr4:167223000-167223200	Enhancers	NH-A	brain
23	chr4:167226600-167230000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr4:167229000-167231200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr4:167229200-167230400	Enhancers	NHEK	skin
26	chr4:167229400-167231000	Enhancers	HMEC	breast
27	chr4:167229600-167230600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr4:167229800-167230000	Enhancers	Pancreatic Islets	Pancreatic Islet
29	chr4:167230000-167230800	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr4:167230000-167231200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr4:167230800-167231000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr4:167230800-167231000	Enhancers	Osteobl	bone
33	chr4:167230800-167231600	Enhancers	Pancreatic Islets	Pancreatic Islet
34	chr4:167231000-167231200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr4:167231000-167232600	Weak transcription	HMEC	breast
36	chr4:167231000-167232600	Weak transcription	Osteobl	bone
37	chr4:167231200-167232400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr4:167231200-167233000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr4:167231400-167232400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr4:167231600-167240600	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr4:167232400-167233400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr4:167232400-167233800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr4:167232600-167233200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
44	chr4:167232600-167233200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr4:167232600-167233200	Enhancers	Osteobl	bone
46	chr4:167232600-167233400	Enhancers	HMEC	breast
47	chr4:167233000-167233200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr4:167233000-167233200	Enhancers	Aorta	Aorta
49	chr4:167233000-167233600	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr4:167233000-167233600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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