Variant report

Variant	esv3393902
Chromosome Location	chr4:57935600-57939401
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:36)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:36 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr4:57937527-57937867	HepG2	liver:	n/a	chr4:57937683-57937694 chr4:57937652-57937663
2	CEBPB	chr4:57937614-57937765	K562	blood:	n/a	chr4:57937683-57937694 chr4:57937652-57937663
3	CEBPB	chr4:57937468-57937931	IMR90	lung:	n/a	chr4:57937683-57937694 chr4:57937652-57937663
4	CEBPB	chr4:57937501-57937856	A549	lung:	n/a	chr4:57937683-57937694 chr4:57937652-57937663
5	CEBPB	chr4:57937491-57937863	Hela-S3	cervix:	n/a	chr4:57937683-57937694 chr4:57937652-57937663
6	CEBPB	chr4:57937405-57937922	A549	lung:	n/a	chr4:57937683-57937694 chr4:57937652-57937663
7	CTCF	chr4:57938820-57938970	A549	lung:	n/a	chr4:57938823-57938832
8	CTCF	chr4:57938740-57938890	BE2_C	brain:	n/a	chr4:57938823-57938832
9	CTCF	chr4:57938620-57938770	A549	lung:	n/a	n/a
10	FOS	chr4:57936650-57936959	MCF10A-Er-Src	breast:	n/a	n/a
11	FOS	chr4:57936678-57936873	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr4:57937559-57937752	MCF10A-Er-Src	breast:	n/a	n/a
13	FOS	chr4:57936673-57936961	MCF10A-Er-Src	breast:	n/a	n/a
14	FOS	chr4:57937519-57937805	MCF10A-Er-Src	breast:	n/a	n/a
15	FOS	chr4:57936741-57936843	MCF10A-Er-Src	breast:	n/a	n/a
16	FOS	chr4:57937485-57937821	MCF10A-Er-Src	breast:	n/a	n/a
17	KAP1	chr4:57935678-57936233	HEK293	kidney:	n/a	n/a
18	KAP1	chr4:57935678-57936104	U2OS	brain:	n/a	n/a
19	KAP1	chr4:57936665-57937892	HEK293	kidney:	n/a	n/a
20	MAX	chr4:57937482-57937939	NB4	blood:	n/a	n/a
21	MXI1	chr4:57937141-57938110	IMR90	lung:	n/a	n/a
22	MYC	chr4:57937541-57937811	MCF10A-Er-Src	breast:	n/a	n/a
23	MYC	chr4:57937559-57937796	MCF10A-Er-Src	breast:	n/a	n/a
24	MYC	chr4:57937535-57937913	NB4	blood:	n/a	n/a
25	POLR2A	chr4:57937770-57937823	MCF10A-Er-Src	breast:	n/a	n/a
26	POLR2A	chr4:57936859-57936875	HUVEC	blood vessel:	n/a	n/a
27	POLR2A	chr4:57937402-57937860	U87	brain:	n/a	n/a
28	POLR2A	chr4:57936902-57936920	HUVEC	blood vessel:	n/a	n/a
29	POLR2A	chr4:57936944-57936962	HUVEC	blood vessel:	n/a	n/a
30	POLR2A	chr4:57936579-57937416	HUVEC	blood vessel:	n/a	n/a
31	POLR2A	chr4:57935662-57935856	HUVEC	blood vessel:	n/a	n/a
32	POLR2A	chr4:57937741-57937784	HUVEC	blood vessel:	n/a	n/a
33	POLR2A	chr4:57938543-57938700	HUVEC	blood vessel:	n/a	n/a
34	RCOR1	chr4:57937081-57938149	IMR90	lung:	n/a	n/a
35	SETDB1	chr4:57935714-57935972	U2OS	brain:	n/a	n/a
36	STAT3	chr4:57937566-57937764	MCF10A-Er-Src	breast:	n/a	chr4:57937716-57937727

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:57937220-57937270	NB4	blood:	n/a
2	chr4:57937220-57937270	A549	lung:	n/a
3	chr4:57937220-57937270	LNCaP	prostate:	n/a
4	chr4:57937220-57937270	HPAEpiC	pulmonary alveolar:	n/a
5	chr4:57937220-57937270	HNPCEpiC	eye:	n/a
6	chr4:57937220-57937270	GM12891	blood:	n/a
7	chr4:57937220-57937270	HCM	heart:	n/a
8	chr4:57937220-57937270	GM12878	blood:	n/a
9	chr4:57937220-57937270	PFSK-1	brain:	n/a
10	chr4:57937220-57937270	HAEpiC	amniotic membrane:	n/a
11	chr4:57937220-57937270	HRE	kidney:	n/a
12	chr4:57937220-57937270	AoSMC	blood vessel:	n/a
13	chr4:57937220-57937270	PANC-1	pancreas:	n/a
14	chr4:57937220-57937270	PrEC	prostate:	n/a
15	chr4:57937220-57937270	BJ	skin:	n/a
16	chr4:57937220-57937270	BE2_C	brain:	n/a
17	chr4:57937220-57937270	Hela-S3	cervix:	n/a
18	chr4:57937220-57937270	HCF	heart:	n/a
19	chr4:57937220-57937270	HIPEpiC	eye:	n/a
20	chr4:57937220-57937270	NH-A	brain:	n/a
21	chr4:57937220-57937270	ECC-1	luminal epithelium:	n/a
22	chr4:57937220-57937270	HEK293	kidney:	embryo
23	chr4:57937220-57937270	GM06990	blood:	n/a
24	chr4:57937220-57937270	SKMC	muscle:	n/a
25	chr4:57937220-57937270	H1-hESC	embryonic stem cell:	embryo
26	chr4:57937220-57937270	SK-N-SH_RA	brain:	n/a
27	chr4:57937220-57937270	HCT-116	colon:	n/a
28	chr4:57937220-57937270	HMEC	breast:	n/a
29	chr4:57937220-57937270	Jurkat	blood:	n/a
30	chr4:57937220-57937270	Hepatocyte	liver:	n/a
31	chr4:57937220-57937270	HL-60	blood:	n/a
32	chr4:57937220-57937270	ovcar-3	ovarian:	n/a
33	chr4:57937220-57937270	MCF-7	breast:	n/a
34	chr4:57937220-57937270	K562	blood:	n/a
35	chr4:57937220-57937270	AG04450	lung:	fetal
36	chr4:57937220-57937270	T-47D	breast:	n/a
37	chr4:57937220-57937270	NT2-D1	testis:	n/a
38	chr4:57937220-57937270	AG04449	skin:	fetal
39	chr4:57937220-57937270	HepG2	liver:	n/a
40	chr4:57937220-57937270	HRCEpiC	kidney:	n/a
41	chr4:57937220-57937270	SK-N-SH	brain:	n/a
42	chr4:57937220-57937270	U87	brain:	n/a
43	chr4:57937220-57937270	NHBE	bronchial:	n/a
44	chr4:57937220-57937270	AG10803	skin:	n/a
45	chr4:57937220-57937270	MCF10A-Er-Src	breast:	n/a
46	chr4:57937220-57937270	GM19239	blood:	n/a
47	chr4:57937220-57937270	SAEC	small airway:	n/a
48	chr4:57937220-57937270	HEEpiC	esophagus:	n/a
49	chr4:57937220-57937270	IMR90	lung:	fetal
50	chr4:57937220-57937270	HRPEpiC	eye:	n/a

No data

Variant related genes	Relation type
UBE2CP3	TF binding region
IGFBP7	TF binding region
UBE2CP3	CpG island
IGFBP7	CpG island

Extended variants
information (count: 170 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:170 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143088143	chr4:57935619-57935620	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs547432257	chr4:57935630-57935631	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs558066046	chr4:57935723-57935724	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs73242635	chr4:57935733-57935734	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs1064798	chr4:57935845-57935846	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs372340101	chr4:57935878-57935879	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs17087484	chr4:57935905-57935906	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs148186488	chr4:57935907-57935908	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs183583559	chr4:57935924-57935925	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs539043353	chr4:57935932-57935933	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs555264535	chr4:57935971-57935972	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs572353822	chr4:57935975-57935976	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs6857597	chr4:57935976-57935977	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs7697699	chr4:57935977-57935978	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs62308265	chr4:57935985-57935986	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs543564649	chr4:57936007-57936008	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs141139557	chr4:57936015-57936016	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs35672134	chr4:57936043-57936044	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs572095937	chr4:57936057-57936058	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs573638967	chr4:57936065-57936066	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs188186048	chr4:57936093-57936094	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs190440237	chr4:57936120-57936121	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs534293821	chr4:57936176-57936177	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs3986230	chr4:57936188-57936189	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs547643161	chr4:57936203-57936204	Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs564153594	chr4:57936220-57936221	Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs3849657	chr4:57936227-57936228	Weak transcription Enhancers Genic enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs542389149	chr4:57936255-57936256	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs561703038	chr4:57936301-57936302	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs549740670	chr4:57936306-57936307	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs570176612	chr4:57936310-57936311	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs540829341	chr4:57936324-57936325	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs370833196	chr4:57936342-57936343	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs549166136	chr4:57936372-57936373	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs3849658	chr4:57936421-57936422	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs534932372	chr4:57936426-57936427	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs73818302	chr4:57936473-57936474	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs558056101	chr4:57936563-57936564	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs552253071	chr4:57936620-57936621	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs577982761	chr4:57936636-57936637	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs10516161	chr4:57936735-57936736	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs556673567	chr4:57936753-57936754	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs573725407	chr4:57936803-57936804	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs529510653	chr4:57936823-57936824	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs150728307	chr4:57936824-57936825	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs1718843	chr4:57936829-57936830	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs36027930	chr4:57936836-57936837	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs541346087	chr4:57936912-57936913	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs10516162	chr4:57936920-57936921	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs182276401	chr4:57936928-57936929	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:88)

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	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	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
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	19435819	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
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
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian neoplasms	16753589	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Glioblastoma	17504929	CNVD
Glioblastoma	16823502	CNVD
Melanoma	16908931	CNVD
Glioblastoma	20031968	CNVD
Medulloblastoma	19270706	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Olfactory neuroblastoma	18408657	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Rhabdomyosarcoma	16790082	CNVD
Gastrointestinal stromal cancer	17438095	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	22183965	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:222 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:57899600-57942200	Weak transcription	Primary hematopoietic stem cells	blood
2	chr4:57918600-57936800	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr4:57923800-57937200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr4:57927000-57937400	Weak transcription	Small Intestine	intestine
5	chr4:57929600-57944400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr4:57930800-57937400	Weak transcription	Fetal Kidney	kidney
7	chr4:57931200-57936000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
8	chr4:57931200-57936600	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr4:57931200-57937000	Weak transcription	Brain Cingulate Gyrus	brain
10	chr4:57931600-57940600	Weak transcription	Hela-S3	cervix
11	chr4:57931800-57938800	Weak transcription	Pancreas	Pancrea
12	chr4:57932000-57935800	Strong transcription	NHEK	skin
13	chr4:57932400-57935800	Genic enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr4:57932400-57936000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr4:57932400-57936800	Weak transcription	Brain Hippocampus Middle	brain
16	chr4:57932400-57945600	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr4:57932400-57947600	Genic enhancers	Osteobl	bone
18	chr4:57932600-57936000	Enhancers	A549	lung
19	chr4:57932600-57936600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr4:57932600-57936800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr4:57932600-57936800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr4:57932600-57937200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr4:57932600-57937200	Weak transcription	Adipose Nuclei	Adipose
24	chr4:57932600-57937200	Weak transcription	Fetal Intestine Large	intestine
25	chr4:57932600-57937600	Weak transcription	Stomach Smooth Muscle	stomach
26	chr4:57932600-57944000	Weak transcription	Fetal Stomach	stomach
27	chr4:57932800-57936600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr4:57934200-57935600	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr4:57934200-57935600	Genic enhancers	HSMMtube	muscle
30	chr4:57934200-57935800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr4:57934200-57935800	Enhancers	Fetal Heart	heart
32	chr4:57934200-57936200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr4:57934200-57936200	Weak transcription	Primary monocytes fromperipheralblood	blood
34	chr4:57934200-57936200	Enhancers	Left Ventricle	heart
35	chr4:57934400-57936200	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr4:57934400-57951600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr4:57934600-57935600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
38	chr4:57934600-57935600	Enhancers	Skeletal Muscle Female	skeletal muscle
39	chr4:57934600-57935600	Enhancers	HSMM	muscle
40	chr4:57934600-57935600	Enhancers	NHLF	lung
41	chr4:57934600-57935800	Enhancers	Muscle Satellite Cultured Cells	--
42	chr4:57934600-57935800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
43	chr4:57934600-57935800	Enhancers	Right Atrium	heart
44	chr4:57934600-57936000	Weak transcription	HMEC	breast
45	chr4:57934600-57948200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr4:57934800-57935800	Enhancers	HUVEC	blood vessel
47	chr4:57935000-57935800	Enhancers	Psoas Muscle	Psoas
48	chr4:57935000-57935800	Enhancers	Right Ventricle	heart
49	chr4:57935000-57936800	Weak transcription	Fetal Lung	lung
50	chr4:57935200-57935600	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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