Variant report

Variant	nsv879403
Chromosome Location	chr4:70081901-70234419
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:742)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:742 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:70105540-70105900	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:70210667-70210694	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:70106482-70106878	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:70105523-70105754	K562	blood:	n/a	n/a
5	ATF1	chr4:70087666-70087866	K562	blood:	n/a	n/a
6	ATF1	chr4:70105493-70105808	K562	blood:	n/a	n/a
7	ATF1	chr4:70175307-70175700	K562	blood:	n/a	n/a
8	ATF1	chr4:70187845-70188142	K562	blood:	n/a	n/a
9	BACH1	chr4:70097393-70097475	K562	blood:	n/a	n/a
10	BHLHE40	chr4:70209675-70209715	K562	blood:	n/a	n/a
11	BHLHE40	chr4:70087582-70087589	K562	blood:	n/a	n/a
12	BHLHE40	chr4:70105574-70105707	K562	blood:	n/a	n/a
13	CBX3	chr4:70175213-70175493	K562	blood:	n/a	n/a
14	CCNT2	chr4:70105530-70105702	K562	blood:	n/a	n/a
15	CEBPB	chr4:70221057-70221267	HepG2	liver:	n/a	n/a
16	CEBPB	chr4:70148545-70148642	K562	blood:	n/a	chr4:70148623-70148634
17	CEBPB	chr4:70211562-70211766	HepG2	liver:	n/a	chr4:70211703-70211714
18	CEBPB	chr4:70105462-70105782	K562	blood:	n/a	n/a
19	CEBPB	chr4:70118972-70119263	HepG2	liver:	n/a	chr4:70119163-70119176
20	CEBPB	chr4:70209480-70209728	K562	blood:	n/a	n/a
21	CEBPB	chr4:70148603-70148719	H1-hESC	embryonic stem cell:	n/a	chr4:70148623-70148634
22	CEBPB	chr4:70107648-70107863	HepG2	liver:	n/a	chr4:70107721-70107732 chr4:70107722-70107733
23	CEBPB	chr4:70226229-70226403	HepG2	liver:	n/a	chr4:70226280-70226289 chr4:70226280-70226291
24	CEBPB	chr4:70105548-70105721	K562	blood:	n/a	n/a
25	CEBPB	chr4:70106514-70106708	HepG2	liver:	n/a	n/a
26	CEBPB	chr4:70107631-70107834	A549	lung:	n/a	chr4:70107721-70107732 chr4:70107722-70107733
27	CEBPB	chr4:70148592-70148690	A549	lung:	n/a	chr4:70148623-70148634
28	CEBPD	chr4:70105414-70105831	K562	blood:	n/a	n/a
29	CTCF	chr4:70201300-70201450	A549	lung:	n/a	n/a
30	CTCF	chr4:70183800-70183950	MCF-7	breast:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
31	CTCF	chr4:70201300-70201450	HEK293	kidney:	n/a	n/a
32	CTCF	chr4:70183600-70183750	RPTEC	kidney:	n/a	n/a
33	CTCF	chr4:70183680-70183891	Hela-S3	cervix:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
34	CTCF	chr4:70183580-70183730	HAc	cerebellar:	n/a	n/a
35	CTCF	chr4:70201200-70201450	Caco-2	colon:	n/a	n/a
36	CTCF	chr4:70105505-70105507	LNCaP	prostate:	n/a	n/a
37	CTCF	chr4:70183600-70183750	HAc	cerebellar:	n/a	n/a
38	CTCF	chr4:70201380-70201530	HAc	cerebellar:	n/a	n/a
39	CTCF	chr4:70134415-70134604	MCF-7	breast:	n/a	n/a
40	CTCF	chr4:70134460-70134610	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr4:70183700-70183850	AoAF	blood vessel:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
42	CTCF	chr4:70201300-70201450	HCM	heart:	n/a	n/a
43	CTCF	chr4:70201323-70201448	HepG2	liver:	n/a	n/a
44	CTCF	chr4:70201260-70201410	HMEC	breast:	n/a	n/a
45	CTCF	chr4:70183740-70183890	GM12872	blood:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
46	CTCF	chr4:70201360-70201510	SAEC	small airway:	n/a	n/a
47	CTCF	chr4:70183720-70183870	GM12870	blood:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
48	CTCF	chr4:70183674-70183923	HepG2	liver:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
49	CTCF	chr4:70134405-70134621	MCF-7	breast:	n/a	n/a
50	CTCF	chr4:70183720-70183870	GM06990	blood:	n/a	chr4:70183815-70183833 chr4:70183817-70183838

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:70155747-70155797	AG09309	skin:	n/a
2	chr4:70155747-70155797	ECC-1	luminal epithelium:	n/a
3	chr4:70155747-70155797	U87	brain:	n/a
4	chr4:70155747-70155797	HCF	heart:	n/a
5	chr4:70155747-70155797	GM12878	blood:	n/a
6	chr4:70155747-70155797	T-47D	breast:	n/a
7	chr4:70155747-70155797	SK-N-MC	brain:	n/a
8	chr4:70155747-70155797	AG04449	skin:	fetal
9	chr4:70155747-70155797	HIPEpiC	eye:	n/a
10	chr4:70155747-70155797	NH-A	brain:	n/a
11	chr4:70155747-70155797	HPAEpiC	pulmonary alveolar:	n/a
12	chr4:70155747-70155797	HAEpiC	amniotic membrane:	n/a
13	chr4:70155747-70155797	GM06990	blood:	n/a
14	chr4:70155747-70155797	HL-60	blood:	n/a
15	chr4:70155747-70155797	NHBE	bronchial:	n/a
16	chr4:70155747-70155797	AG10803	skin:	n/a
17	chr4:70155747-70155797	GM12892	blood:	n/a
18	chr4:70155747-70155797	BE2_C	brain:	n/a
19	chr4:70155747-70155797	NHDF-neo	bronchial:	n/a
20	chr4:70155747-70155797	PFSK-1	brain:	n/a
21	chr4:70155747-70155797	HEEpiC	esophagus:	n/a
22	chr4:70155747-70155797	H1-hESC	embryonic stem cell:	embryo
23	chr4:70155747-70155797	HepG2	liver:	n/a
24	chr4:70155747-70155797	ProgFib	skin:	n/a
25	chr4:70155747-70155797	CMK	blood:	n/a
26	chr4:70155747-70155797	PrEC	prostate:	n/a
27	chr4:70155747-70155797	HEK293	kidney:	embryo
28	chr4:70155747-70155797	Jurkat	blood:	n/a
29	chr4:70155747-70155797	NB4	blood:	n/a
30	chr4:70155747-70155797	SKMC	muscle:	n/a
31	chr4:70155747-70155797	HUVEC	blood vessel:	n/a
32	chr4:70155747-70155797	GM19239	blood:	n/a
33	chr4:70155747-70155797	NT2-D1	testis:	n/a
34	chr4:70155747-70155797	HCPEpiC	choroid plexus:	n/a
35	chr4:70155747-70155797	HRCEpiC	kidney:	n/a
36	chr4:70155747-70155797	HCM	heart:	n/a
37	chr4:70155747-70155797	BJ	skin:	n/a
38	chr4:70155747-70155797	MCF-7	breast:	n/a
39	chr4:70155747-70155797	SK-N-SH_RA	brain:	n/a
40	chr4:70155747-70155797	AoSMC	blood vessel:	n/a
41	chr4:70155747-70155797	HRPEpiC	eye:	n/a
42	chr4:70155747-70155797	ovcar-3	ovarian:	n/a
43	chr4:70155747-70155797	AG04450	lung:	fetal
44	chr4:70155747-70155797	A549	lung:	n/a
45	chr4:70155747-70155797	SAEC	small airway:	n/a
46	chr4:70155747-70155797	HCT-116	colon:	n/a
47	chr4:70155747-70155797	MCF10A-Er-Src	breast:	n/a
48	chr4:70155747-70155797	LNCaP	prostate:	n/a
49	chr4:70155747-70155797	HNPCEpiC	eye:	n/a
50	chr4:70155747-70155797	RPTEC	kidney:	n/a

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

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2B28-1	chr4:70080191-70082484	ENSG00000250696.1

No data

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

Extended variants
information (count: 2163 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:2163 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9996390	chr4:70081901-70081902	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs531278526	chr4:70081922-70081923	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs528483779	chr4:70081979-70081980	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs76494747	chr4:70082027-70082028	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs183845980	chr4:70082101-70082102	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs561660794	chr4:70082110-70082111	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs142968884	chr4:70082111-70082112	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs530856868	chr4:70082115-70082116	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs550782625	chr4:70082130-70082131	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs570598377	chr4:70082189-70082190	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs12500268	chr4:70082266-70082267	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs546381095	chr4:70082290-70082291	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs566422666	chr4:70082340-70082341	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs547693385	chr4:70082345-70082346	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs535098534	chr4:70082388-70082389	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs111709532	chr4:70082421-70082422	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs554815665	chr4:70082448-70082449	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs539665441	chr4:70082932-70082933	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs4296739	chr4:70082935-70082936	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs77785653	chr4:70082966-70082967	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs557194359	chr4:70085804-70085805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs577294800	chr4:70085853-70085854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs189509686	chr4:70085856-70085857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs559825517	chr4:70085870-70085871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs528392650	chr4:70085872-70085873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs542146565	chr4:70085873-70085874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs34091436	chr4:70085882-70085883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs561823235	chr4:70085894-70085895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs530635423	chr4:70085904-70085905	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs550623529	chr4:70085972-70085973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs112229182	chr4:70085981-70085982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs398083177	chr4:70085983-70085984	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs397689210	chr4:70085984-70085985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs113893279	chr4:70085985-70085986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs181171534	chr4:70085998-70085999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs148408097	chr4:70086042-70086043	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs186574017	chr4:70086058-70086059	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546370962	chr4:70086086-70086087	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546180932	chr4:70086089-70086090	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs566179884	chr4:70086108-70086109	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs534941754	chr4:70086116-70086117	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554854442	chr4:70086126-70086127	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs77331739	chr4:70086148-70086149	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs537223675	chr4:70086159-70086160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571540324	chr4:70086186-70086187	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs58371816	chr4:70086216-70086217	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539985376	chr4:70086221-70086222	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs553356653	chr4:70086225-70086226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs190348200	chr4:70086230-70086231	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs573281884	chr4:70086237-70086238	Enhancers Weak transcription	n/a	n/a	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:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:70085800-70086000	Enhancers	Fetal Intestine Large	intestine
2	chr4:70086000-70086400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr4:70086000-70087000	Weak transcription	Fetal Intestine Large	intestine
4	chr4:70086400-70087400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr4:70087000-70087600	Enhancers	Fetal Intestine Large	intestine
6	chr4:70087200-70088600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr4:70087400-70087600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr4:70088600-70090200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr4:70090200-70091000	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr4:70090400-70090600	Enhancers	HepG2	liver
11	chr4:70090600-70091000	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr4:70090600-70091000	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr4:70090600-70091000	Enhancers	Fetal Stomach	stomach
14	chr4:70104600-70106600	Enhancers	Fetal Intestine Large	intestine
15	chr4:70105000-70106600	Enhancers	Fetal Intestine Small	intestine
16	chr4:70105000-70106600	Enhancers	HepG2	liver
17	chr4:70105200-70106000	Enhancers	Rectal Mucosa Donor 29	rectum
18	chr4:70105200-70106400	Enhancers	Duodenum Mucosa	Duodenum
19	chr4:70105200-70106400	Enhancers	Rectal Mucosa Donor 31	rectum
20	chr4:70105200-70106600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr4:70105200-70106800	Enhancers	Stomach Mucosa	stomach
22	chr4:70105400-70105800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr4:70105400-70106200	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr4:70106200-70106600	Enhancers	Small Intestine	intestine
25	chr4:70106600-70108400	Weak transcription	HepG2	liver
26	chr4:70108400-70108800	Enhancers	HepG2	liver
27	chr4:70111600-70112000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr4:70112000-70113400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr4:70113400-70114000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr4:70132400-70133000	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr4:70132400-70133200	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr4:70132800-70133200	Enhancers	H9 Cell Line	embryonic stem cell
33	chr4:70135200-70135600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr4:70174000-70176000	Enhancers	Stomach Mucosa	stomach
35	chr4:70174200-70175000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr4:70174400-70174600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr4:70174400-70176400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr4:70174600-70175400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr4:70174600-70175400	Enhancers	HepG2	liver
40	chr4:70174600-70176200	Enhancers	Fetal Intestine Large	intestine
41	chr4:70174600-70176200	Enhancers	Fetal Intestine Small	intestine
42	chr4:70174800-70175200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr4:70174800-70176600	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr4:70175000-70175800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr4:70175000-70176000	Enhancers	Rectal Mucosa Donor 31	rectum
46	chr4:70175800-70176800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr4:70176000-70181400	Weak transcription	Stomach Mucosa	stomach
48	chr4:70176600-70178600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
49	chr4:70176800-70183400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr4:70178600-70178800	Enhancers	Primary hematopoietic stem cells short term culture	blood

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