Variant report

Variant	esv1807459
Chromosome Location	chr4:70070178-70254884
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:881)
CpG islands
(count:122)
Chromatin interactive
region (count:7)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:881 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:70105523-70105754	K562	blood:	n/a	n/a
2	ARID3A	chr4:70210667-70210694	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:70254846-70255212	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:70105540-70105900	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:70106482-70106878	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:70080605-70080753	HepG2	liver:	n/a	n/a
7	ATF1	chr4:70105493-70105808	K562	blood:	n/a	n/a
8	ATF1	chr4:70175307-70175700	K562	blood:	n/a	n/a
9	ATF1	chr4:70087666-70087866	K562	blood:	n/a	n/a
10	ATF1	chr4:70187845-70188142	K562	blood:	n/a	n/a
11	BACH1	chr4:70097393-70097475	K562	blood:	n/a	n/a
12	BCL3	chr4:70080358-70080837	A549	lung:	n/a	n/a
13	BHLHE40	chr4:70209675-70209715	K562	blood:	n/a	n/a
14	BHLHE40	chr4:70105574-70105707	K562	blood:	n/a	n/a
15	BHLHE40	chr4:70087582-70087589	K562	blood:	n/a	n/a
16	CBX3	chr4:70175213-70175493	K562	blood:	n/a	n/a
17	CCNT2	chr4:70105530-70105702	K562	blood:	n/a	n/a
18	CEBPB	chr4:70211562-70211766	HepG2	liver:	n/a	chr4:70211703-70211714
19	CEBPB	chr4:70077881-70078188	HepG2	liver:	n/a	chr4:70078030-70078041 chr4:70078032-70078043
20	CEBPB	chr4:70105462-70105782	K562	blood:	n/a	n/a
21	CEBPB	chr4:70226229-70226403	HepG2	liver:	n/a	chr4:70226280-70226289 chr4:70226280-70226291
22	CEBPB	chr4:70148592-70148690	A549	lung:	n/a	chr4:70148623-70148634
23	CEBPB	chr4:70209480-70209728	K562	blood:	n/a	n/a
24	CEBPB	chr4:70106514-70106708	HepG2	liver:	n/a	n/a
25	CEBPB	chr4:70107648-70107863	HepG2	liver:	n/a	chr4:70107721-70107732 chr4:70107722-70107733
26	CEBPB	chr4:70077980-70078075	K562	blood:	n/a	chr4:70078030-70078041 chr4:70078032-70078043
27	CEBPB	chr4:70080509-70080873	A549	lung:	n/a	n/a
28	CEBPB	chr4:70148603-70148719	H1-hESC	embryonic stem cell:	n/a	chr4:70148623-70148634
29	CEBPB	chr4:70118972-70119263	HepG2	liver:	n/a	chr4:70119163-70119176
30	CEBPB	chr4:70221057-70221267	HepG2	liver:	n/a	n/a
31	CEBPB	chr4:70105548-70105721	K562	blood:	n/a	n/a
32	CEBPB	chr4:70148545-70148642	K562	blood:	n/a	chr4:70148623-70148634
33	CEBPB	chr4:70077864-70078215	IMR90	lung:	n/a	chr4:70078030-70078041 chr4:70078032-70078043
34	CEBPB	chr4:70107631-70107834	A549	lung:	n/a	chr4:70107721-70107732 chr4:70107722-70107733
35	CEBPD	chr4:70105414-70105831	K562	blood:	n/a	n/a
36	CTCF	chr4:70189135-70189278	K562	blood:	n/a	n/a
37	CTCF	chr4:70183780-70183930	GM12872	blood:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
38	CTCF	chr4:70187137-70187165	MCF-7	breast:	n/a	n/a
39	CTCF	chr4:70183711-70183929	Spleen_OC	spleen:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
40	CTCF	chr4:70183692-70183938	LNCaP	prostate:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
41	CTCF	chr4:70209564-70209651	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr4:70183740-70183890	HMF	breast:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
43	CTCF	chr4:70214160-70214310	GM06990	blood:	n/a	n/a
44	CTCF	chr4:70155388-70155482	Kidney_OC	kidney:	n/a	n/a
45	CTCF	chr4:70183656-70183893	ECC-1	luminal epithelium:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
46	CTCF	chr4:70189180-70189330	GM12869	blood:	n/a	n/a
47	CTCF	chr4:70097033-70097046	GM13977	blood:	n/a	n/a
48	CTCF	chr4:70134460-70134610	HepG2	liver:	n/a	n/a
49	CTCF	chr4:70201360-70201510	HA-sp	spinal cord:	n/a	n/a
50	CTCF	chr4:70189218-70189227	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:70080453-70080503	U87	brain:	n/a
2	chr4:70155747-70155797	Caco-2	colon:	n/a
3	chr4:70155747-70155797	SAEC	small airway:	n/a
4	chr4:70080453-70080503	HPAEpiC	pulmonary alveolar:	n/a
5	chr4:70080453-70080503	HUVEC	blood vessel:	n/a
6	chr4:70080453-70080503	T-47D	breast:	n/a
7	chr4:70155747-70155797	HRCEpiC	kidney:	n/a
8	chr4:70155747-70155797	HEEpiC	esophagus:	n/a
9	chr4:70080453-70080503	AG10803	skin:	n/a
10	chr4:70155747-70155797	RPTEC	kidney:	n/a
11	chr4:70155747-70155797	NHBE	bronchial:	n/a
12	chr4:70155747-70155797	H1-hESC	embryonic stem cell:	embryo
13	chr4:70080453-70080503	IMR90	lung:	fetal
14	chr4:70155747-70155797	HAEpiC	amniotic membrane:	n/a
15	chr4:70080453-70080503	LNCaP	prostate:	n/a
16	chr4:70155747-70155797	BJ	skin:	n/a
17	chr4:70155747-70155797	SK-N-SH	brain:	n/a
18	chr4:70155747-70155797	HRE	kidney:	n/a
19	chr4:70080453-70080503	SKMC	muscle:	n/a
20	chr4:70155747-70155797	CMK	blood:	n/a
21	chr4:70080453-70080503	AG09319	gingival:	n/a
22	chr4:70155747-70155797	HepG2	liver:	n/a
23	chr4:70080453-70080503	PrEC	prostate:	n/a
24	chr4:70080453-70080503	ECC-1	luminal epithelium:	n/a
25	chr4:70155747-70155797	NHDF-neo	bronchial:	n/a
26	chr4:70155747-70155797	HL-60	blood:	n/a
27	chr4:70080453-70080503	Jurkat	blood:	n/a
28	chr4:70080453-70080503	NH-A	brain:	n/a
29	chr4:70080453-70080503	Hepatocyte	liver:	n/a
30	chr4:70080453-70080503	GM12878	blood:	n/a
31	chr4:70080453-70080503	NB4	blood:	n/a
32	chr4:70080453-70080503	GM12891	blood:	n/a
33	chr4:70155747-70155797	GM19239	blood:	n/a
34	chr4:70080453-70080503	HIPEpiC	eye:	n/a
35	chr4:70080453-70080503	AG09309	skin:	n/a
36	chr4:70155747-70155797	HCF	heart:	n/a
37	chr4:70155747-70155797	HMEC	breast:	n/a
38	chr4:70155747-70155797	SK-N-SH_RA	brain:	n/a
39	chr4:70155747-70155797	GM12892	blood:	n/a
40	chr4:70155747-70155797	AG10803	skin:	n/a
41	chr4:70080453-70080503	SK-N-MC	brain:	n/a
42	chr4:70080453-70080503	CMK	blood:	n/a
43	chr4:70155747-70155797	AoSMC	blood vessel:	n/a
44	chr4:70080453-70080503	Caco-2	colon:	n/a
45	chr4:70155747-70155797	IMR90	lung:	fetal
46	chr4:70155747-70155797	Hela-S3	cervix:	n/a
47	chr4:70155747-70155797	U87	brain:	n/a
48	chr4:70080453-70080503	GM12892	blood:	n/a
49	chr4:70155747-70155797	AG04449	skin:	fetal
50	chr4:70080453-70080503	SK-N-SH_RA	brain:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:70183340..70184245-chr4:70482427..70483057,3	MCF-7	breast:
2	chr4:70183605..70184238-chr4:70482598..70483352,3	MCF-7	breast:
3	chr20:45932378..45933054-chr4:70163468..70164237,2	MCF-7	breast:
4	chr4:69673177..69674687-chr4:70085938..70087696,2	MCF-7	breast:
5	chr4:69789542..69791043-chr4:70152702..70154403,2	MCF-7	breast:
6	chr4:70188461..70190645-chr4:70191525..70193153,2	K562	blood:
7	chr4:70188461..70190645-chr4:70191525..70193153,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2B28-1	chr4:70076784-70076865	ENSG00000250696.1
2	lnc-UGT2B28-1	chr4:70080191-70080193	ENSG00000250696.1
3	lnc-UGT2B28-1	chr4:70076784-70076865	ENSG00000250696.1
4	lnc-UGT2B28-1	chr4:70080191-70082484	ENSG00000250696.1
5	lnc-UGT2B28-4	chr4:70253298-70254025	NONHSAT096763

No data

Variant related genes	Relation type
ENSG00000268209	TF binding region
ENSG00000268803	TF binding region
ENSG00000249763	TF binding region
UGT2B28	TF binding region
ENSG00000251691	TF binding region
ENSG00000215110	TF binding region
UGT2B11	TF binding region
ENSG00000250612	TF binding region
ENSG00000268209	CpG island
ENSG00000268803	CpG island
ENSG00000249763	CpG island
UGT2B28	CpG island
ENSG00000251691	CpG island
ENSG00000215110	CpG island
UGT2B11	CpG island
ENSG00000250612	CpG island
ENSG00000198277	chromatin interactions

Extended variants
information (count: 2544 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:2544 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138194120	chr4:70070186-70070187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs143674057	chr4:70070196-70070197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs546179431	chr4:70070206-70070207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs375046767	chr4:70070214-70070215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs140410140	chr4:70070215-70070216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs185382950	chr4:70070226-70070227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs142097172	chr4:70070251-70070252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs150725238	chr4:70070255-70070256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs144151608	chr4:70070259-70070260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs113129893	chr4:70070287-70070288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530884474	chr4:70070288-70070289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs551085437	chr4:70070303-70070304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs377330008	chr4:70070320-70070321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs570747517	chr4:70070346-70070347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs541118778	chr4:70070348-70070349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs539868084	chr4:70070364-70070365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs144106768	chr4:70070366-70070367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs146890806	chr4:70070367-70070368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs535275140	chr4:70070466-70070467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs532937546	chr4:70070474-70070475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs535617103	chr4:70070515-70070516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs555581449	chr4:70070541-70070542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs569068453	chr4:70070564-70070565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs538520505	chr4:70071643-70071644	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs558214533	chr4:70071653-70071654	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs112131036	chr4:70071658-70071659	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs578183741	chr4:70071665-70071666	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs536505387	chr4:70071668-70071669	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs72639753	chr4:70071685-70071686	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs554275120	chr4:70071705-70071706	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs534672122	chr4:70073217-70073218	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs141328462	chr4:70073226-70073227	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs568479418	chr4:70073254-70073255	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs542934413	chr4:70073279-70073280	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs186316764	chr4:70073283-70073284	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs191617022	chr4:70073335-70073336	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs372806110	chr4:70073364-70073365	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs183343222	chr4:70073384-70073385	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs553068830	chr4:70073390-70073391	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs572994622	chr4:70073463-70073464	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs541972900	chr4:70073471-70073472	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs561510905	chr4:70073499-70073500	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs572775308	chr4:70073515-70073516	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs544808904	chr4:70073516-70073517	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs564700849	chr4:70073517-70073518	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs564018408	chr4:70073521-70073522	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs137951617	chr4:70073534-70073535	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs546010615	chr4:70073546-70073547	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs377412806	chr4:70073558-70073559	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs186833120	chr4:70073562-70073563	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Multiple myeloma	16616336	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
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Graft versus host disease	20877625	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Osteoporosis	20877625	CNVD
Osteoporosis	19737800	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Glioblastoma multiforme	21138945	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioblastoma multiforme	21510904	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Oral cancer	21386901	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:70067800-70070600	Weak transcription	Liver	Liver
2	chr4:70076400-70076600	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr4:70076800-70077800	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr4:70077800-70078200	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr4:70080400-70080800	Enhancers	HepG2	liver
6	chr4:70080600-70081200	Enhancers	Rectal Smooth Muscle	rectum
7	chr4:70080800-70081200	Enhancers	A549	lung
8	chr4:70085800-70086000	Enhancers	Fetal Intestine Large	intestine
9	chr4:70086000-70086400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr4:70086000-70087000	Weak transcription	Fetal Intestine Large	intestine
11	chr4:70086400-70087400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr4:70087000-70087600	Enhancers	Fetal Intestine Large	intestine
13	chr4:70087200-70088600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr4:70087400-70087600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr4:70088600-70090200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr4:70090200-70091000	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr4:70090400-70090600	Enhancers	HepG2	liver
18	chr4:70090600-70091000	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr4:70090600-70091000	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr4:70090600-70091000	Enhancers	Fetal Stomach	stomach
21	chr4:70104600-70106600	Enhancers	Fetal Intestine Large	intestine
22	chr4:70105000-70106600	Enhancers	Fetal Intestine Small	intestine
23	chr4:70105000-70106600	Enhancers	HepG2	liver
24	chr4:70105200-70106000	Enhancers	Rectal Mucosa Donor 29	rectum
25	chr4:70105200-70106400	Enhancers	Duodenum Mucosa	Duodenum
26	chr4:70105200-70106400	Enhancers	Rectal Mucosa Donor 31	rectum
27	chr4:70105200-70106600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr4:70105200-70106800	Enhancers	Stomach Mucosa	stomach
29	chr4:70105400-70105800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr4:70105400-70106200	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr4:70106200-70106600	Enhancers	Small Intestine	intestine
32	chr4:70106600-70108400	Weak transcription	HepG2	liver
33	chr4:70108400-70108800	Enhancers	HepG2	liver
34	chr4:70111600-70112000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr4:70112000-70113400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr4:70113400-70114000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr4:70132400-70133000	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr4:70132400-70133200	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr4:70132800-70133200	Enhancers	H9 Cell Line	embryonic stem cell
40	chr4:70135200-70135600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr4:70174000-70176000	Enhancers	Stomach Mucosa	stomach
42	chr4:70174200-70175000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr4:70174400-70174600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr4:70174400-70176400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr4:70174600-70175400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr4:70174600-70175400	Enhancers	HepG2	liver
47	chr4:70174600-70176200	Enhancers	Fetal Intestine Large	intestine
48	chr4:70174600-70176200	Enhancers	Fetal Intestine Small	intestine
49	chr4:70174800-70175200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr4:70174800-70176600	Enhancers	Primary hematopoietic stem cells short term culture	blood

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