Variant report

Variant	esv2759370
Chromosome Location	chr5:114697260-114737583
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	ATF1	chr5:114711661-114711875	K562	blood:	n/a	n/a
2	ATF2	chr5:114715221-114716055	GM12878	blood:	n/a	n/a
3	ATF2	chr5:114715251-114715709	GM12878	blood:	n/a	n/a
4	BACH1	chr5:114720717-114720907	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr5:114718054-114718318	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr5:114705486-114705858	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr5:114715269-114716018	GM12878	blood:	n/a	n/a
8	BATF	chr5:114702031-114702260	GM12878	blood:	n/a	n/a
9	BATF	chr5:114715290-114715606	GM12878	blood:	n/a	n/a
10	BCL11A	chr5:114715278-114715702	GM12878	blood:	n/a	n/a
11	BCL3	chr5:114715272-114715629	GM12878	blood:	n/a	n/a
12	BCLAF1	chr5:114715256-114715970	GM12878	blood:	n/a	n/a
13	BHLHE40	chr5:114715349-114716125	GM12878	blood:	n/a	chr5:114715801-114715817
14	BHLHE40	chr5:114711549-114711968	GM12878	blood:	n/a	n/a
15	BHLHE40	chr5:114709857-114709938	K562	blood:	n/a	n/a
16	BHLHE40	chr5:114702074-114702308	K562	blood:	n/a	n/a
17	BRCA1	chr5:114711556-114712073	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr5:114707911-114708168	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr5:114701905-114702485	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr5:114715124-114716346	HCT-116	colon:	n/a	n/a
21	CBX3	chr5:114715155-114716230	HCT-116	colon:	n/a	n/a
22	CEBPB	chr5:114711619-114711939	IMR90	lung:	n/a	n/a
23	CEBPB	chr5:114701826-114702381	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr5:114715214-114716197	HCT-116	colon:	n/a	n/a
25	CEBPB	chr5:114713241-114713724	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr5:114718694-114719074	A549	lung:	n/a	chr5:114718881-114718892 chr5:114718880-114718891 chr5:114718880-114718893 chr5:114718882-114718891 chr5:114718880-114718893
27	CEBPB	chr5:114718747-114719023	H1-hESC	embryonic stem cell:	n/a	chr5:114718881-114718892 chr5:114718880-114718891 chr5:114718880-114718893 chr5:114718882-114718891 chr5:114718880-114718893
28	CEBPB	chr5:114734352-114734795	IMR90	lung:	n/a	n/a
29	CEBPB	chr5:114718663-114719063	Hela-S3	cervix:	n/a	chr5:114718881-114718892 chr5:114718880-114718891 chr5:114718880-114718893 chr5:114718882-114718891 chr5:114718880-114718893
30	CEBPB	chr5:114718768-114718990	K562	blood:	n/a	chr5:114718881-114718892 chr5:114718880-114718891 chr5:114718880-114718893 chr5:114718882-114718891 chr5:114718880-114718893
31	CEBPB	chr5:114707627-114708240	ECC-1	luminal epithelium:	n/a	n/a
32	CEBPB	chr5:114718695-114719034	MCF-7	breast:	n/a	chr5:114718881-114718892 chr5:114718880-114718891 chr5:114718880-114718893 chr5:114718882-114718891 chr5:114718880-114718893
33	CEBPB	chr5:114718706-114719075	HepG2	liver:	n/a	chr5:114718881-114718892 chr5:114718880-114718891 chr5:114718880-114718893 chr5:114718882-114718891 chr5:114718880-114718893
34	CEBPB	chr5:114707779-114708294	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr5:114718708-114719083	K562	blood:	n/a	chr5:114718881-114718892 chr5:114718880-114718891 chr5:114718880-114718893 chr5:114718882-114718891 chr5:114718880-114718893
36	CEBPB	chr5:114711559-114711883	HepG2	liver:	n/a	n/a
37	CEBPB	chr5:114734428-114734730	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr5:114718712-114719084	ECC-1	luminal epithelium:	n/a	chr5:114718881-114718892 chr5:114718880-114718891 chr5:114718880-114718893 chr5:114718882-114718891 chr5:114718880-114718893
39	CEBPB	chr5:114728292-114728655	IMR90	lung:	n/a	n/a
40	CEBPB	chr5:114728365-114728517	K562	blood:	n/a	n/a
41	CEBPB	chr5:114711455-114712247	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr5:114718696-114719073	IMR90	lung:	n/a	chr5:114718881-114718892 chr5:114718880-114718891 chr5:114718880-114718893 chr5:114718882-114718891 chr5:114718880-114718893
43	CEBPB	chr5:114713220-114713712	IMR90	lung:	n/a	n/a
44	CEBPB	chr5:114707638-114708298	ECC-1	luminal epithelium:	n/a	n/a
45	CHD2	chr5:114711628-114712050	GM12878	blood:	n/a	n/a
46	CHD2	chr5:114701819-114702367	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr5:114711608-114712001	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr5:114725553-114725855	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr5:114715173-114715777	GM12878	blood:	n/a	n/a
50	CREB1	chr5:114711610-114711958	GM12878	blood:	n/a	chr5:114711765-114711778

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:114713211-114713261	SK-N-SH	brain:	n/a
2	chr5:114713211-114713261	SK-N-MC	brain:	n/a
3	chr5:114713211-114713261	AG09319	gingival:	n/a
4	chr5:114701205-114701255	SKMC	muscle:	n/a
5	chr5:114701205-114701255	HPAEpiC	pulmonary alveolar:	n/a
6	chr5:114701205-114701255	AG04449	skin:	fetal
7	chr5:114701205-114701255	HUVEC	blood vessel:	n/a
8	chr5:114701205-114701255	MCF-7	breast:	n/a
9	chr5:114713211-114713261	HRE	kidney:	n/a
10	chr5:114701205-114701255	PFSK-1	brain:	n/a
11	chr5:114701205-114701255	SK-N-SH	brain:	n/a
12	chr5:114701205-114701255	HepG2	liver:	n/a
13	chr5:114701205-114701255	AG04450	lung:	fetal
14	chr5:114701205-114701255	AG09319	gingival:	n/a
15	chr5:114713211-114713261	Jurkat	blood:	n/a
16	chr5:114713211-114713261	K562	blood:	n/a
17	chr5:114713211-114713261	BJ	skin:	n/a
18	chr5:114713211-114713261	NB4	blood:	n/a
19	chr5:114701205-114701255	BE2_C	brain:	n/a
20	chr5:114701205-114701255	IMR90	lung:	fetal
21	chr5:114713211-114713261	PFSK-1	brain:	n/a
22	chr5:114713211-114713261	MCF-7	breast:	n/a
23	chr5:114713211-114713261	HL-60	blood:	n/a
24	chr5:114701205-114701255	HRPEpiC	eye:	n/a
25	chr5:114713211-114713261	ovcar-3	ovarian:	n/a
26	chr5:114713211-114713261	HCM	heart:	n/a
27	chr5:114713211-114713261	BE2_C	brain:	n/a
28	chr5:114713211-114713261	AG04450	lung:	fetal
29	chr5:114701205-114701255	U87	brain:	n/a
30	chr5:114713211-114713261	HCT-116	colon:	n/a
31	chr5:114701205-114701255	GM12878	blood:	n/a
32	chr5:114701205-114701255	AG10803	skin:	n/a
33	chr5:114701205-114701255	T-47D	breast:	n/a
34	chr5:114701205-114701255	Caco-2	colon:	n/a
35	chr5:114701205-114701255	HCF	heart:	n/a
36	chr5:114713211-114713261	SKMC	muscle:	n/a
37	chr5:114713211-114713261	IMR90	lung:	fetal
38	chr5:114701205-114701255	HEK293	kidney:	embryo
39	chr5:114701205-114701255	HCM	heart:	n/a
40	chr5:114713211-114713261	A549	lung:	n/a
41	chr5:114713211-114713261	HCF	heart:	n/a
42	chr5:114701205-114701255	Jurkat	blood:	n/a
43	chr5:114713211-114713261	Hepatocyte	liver:	n/a
44	chr5:114713211-114713261	HRPEpiC	eye:	n/a
45	chr5:114713211-114713261	ECC-1	luminal epithelium:	n/a
46	chr5:114713211-114713261	HCPEpiC	choroid plexus:	n/a
47	chr5:114713211-114713261	SK-N-SH_RA	brain:	n/a
48	chr5:114701205-114701255	CMK	blood:	n/a
49	chr5:114713211-114713261	AG10803	skin:	n/a
50	chr5:114701205-114701255	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:114700131..114702425-chr5:114706517..114709440,2	MCF-7	breast:
2	chr5:114712822..114713353-chr5:114921928..114922705,2	MCF-7	breast:
3	chr5:114717884..114719836-chr5:114879578..114881305,2	MCF-7	breast:
4	chr5:114684315..114686804-chr5:114699761..114703151,3	MCF-7	breast:
5	chr5:114700686..114702330-chr5:114878580..114880982,2	MCF-7	breast:
6	chr5:114700131..114702425-chr5:114706517..114709440,2	MCF-7	breast:
7	chr5:114701068..114703742-chr5:114706747..114709542,2	MCF-7	breast:
8	chr5:114725594..114727819-chr5:114879941..114881957,2	MCF-7	breast:
9	chr5:114713804..114715548-chr5:114724717..114726881,2	MCF-7	breast:
10	chr5:114708411..114710984-chr5:114878847..114880354,2	MCF-7	breast:
11	chr5:114630803..114632408-chr5:114701382..114703629,2	MCF-7	breast:
12	chr5:114713336..114714974-chr5:114920219..114921988,2	MCF-7	breast:
13	chr5:114702805..114704848-chr5:114889870..114892622,2	K562	blood:
14	chr5:114645624..114646196-chr5:114709538..114710375,2	MCF-7	breast:
15	chr5:114709493..114710351-chr5:114909755..114910754,3	MCF-7	breast:
16	chr5:114712072..114714398-chr5:114878860..114881275,2	MCF-7	breast:
17	chr5:114713804..114715548-chr5:114724717..114726881,2	MCF-7	breast:
18	chr5:114701068..114703742-chr5:114706747..114709542,2	MCF-7	breast:
19	chr5:114711869..114714907-chr5:114878578..114880723,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000249026	TF binding region
AK3P4	TF binding region
ENSG00000249026	CpG island
AK3P4	CpG island
ENSG00000145780	chromatin interactions
ENSG00000164221	chromatin interactions

Extended variants
information (count: 1929 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1929 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2964557	chr5:114697260-114697261	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs367807610	chr5:114697350-114697351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs191572284	chr5:114697356-114697357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs571359635	chr5:114697384-114697385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs554252003	chr5:114697388-114697389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs368374964	chr5:114697392-114697393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs574133877	chr5:114697396-114697397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs543137485	chr5:114697398-114697399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs563113171	chr5:114697441-114697442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs183479934	chr5:114697444-114697445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs545744150	chr5:114697463-114697464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs372728741	chr5:114697500-114697501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs375752454	chr5:114697530-114697531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs370401409	chr5:114697532-114697533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs546233785	chr5:114697542-114697543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs560091679	chr5:114697545-114697546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs374065314	chr5:114697560-114697561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528996178	chr5:114697614-114697615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs553869517	chr5:114697638-114697639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs35573706	chr5:114697660-114697661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548653113	chr5:114697664-114697665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568743215	chr5:114697765-114697766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs537625441	chr5:114697802-114697803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551671894	chr5:114697861-114697862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs560648492	chr5:114697886-114697887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs116471505	chr5:114697904-114697905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs367692768	chr5:114697905-114697906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs534198575	chr5:114697957-114697958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs144923623	chr5:114697967-114697968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs138666445	chr5:114698018-114698019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs17137659	chr5:114698051-114698052	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs188420204	chr5:114698077-114698078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576731535	chr5:114698082-114698083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs192413983	chr5:114698113-114698114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs183479071	chr5:114698117-114698118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186721472	chr5:114698121-114698122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541702468	chr5:114698122-114698123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs191551387	chr5:114698174-114698175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528837721	chr5:114698176-114698177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548693655	chr5:114698217-114698218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs562213261	chr5:114698238-114698239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs375870860	chr5:114698253-114698254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs184700377	chr5:114698258-114698259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551243131	chr5:114698264-114698265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571414825	chr5:114698266-114698267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs190022660	chr5:114698270-114698271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547651956	chr5:114698290-114698291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs567691631	chr5:114698291-114698292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs536619638	chr5:114698317-114698318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547280562	chr5:114698323-114698324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Sezary syndrome	18413736	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:578 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:114690800-114701400	Weak transcription	Hela-S3	cervix
2	chr5:114695400-114697400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr5:114696400-114701400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr5:114696400-114701400	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr5:114696400-114701400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr5:114696400-114701400	Weak transcription	NH-A	brain
7	chr5:114696400-114701400	Weak transcription	NHLF	lung
8	chr5:114696400-114701600	Weak transcription	Osteobl	bone
9	chr5:114696400-114701800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr5:114696600-114701400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr5:114696600-114701400	Weak transcription	HSMMtube	muscle
12	chr5:114696600-114701600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr5:114696600-114701600	Weak transcription	A549	lung
14	chr5:114696600-114701800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr5:114696800-114702000	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr5:114696800-114704200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr5:114698800-114699600	Weak transcription	Gastric	stomach
18	chr5:114699200-114700400	Enhancers	Skeletal Muscle Male	skeletal muscle
19	chr5:114699400-114699800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr5:114699400-114700200	Enhancers	Pancreas	Pancrea
21	chr5:114699600-114699800	Enhancers	Brain Anterior Caudate	brain
22	chr5:114699600-114699800	Enhancers	Gastric	stomach
23	chr5:114699600-114699800	Enhancers	Left Ventricle	heart
24	chr5:114699600-114700000	Enhancers	Fetal Muscle Trunk	muscle
25	chr5:114699600-114700000	Enhancers	Psoas Muscle	Psoas
26	chr5:114699600-114700200	Enhancers	Skeletal Muscle Female	skeletal muscle
27	chr5:114699600-114702600	Enhancers	Fetal Muscle Leg	muscle
28	chr5:114699800-114701400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr5:114699800-114701400	Weak transcription	Right Ventricle	heart
30	chr5:114699800-114706600	Weak transcription	Gastric	stomach
31	chr5:114700000-114700600	Enhancers	NHDF-Ad	bronchial
32	chr5:114700000-114701400	Weak transcription	Psoas Muscle	Psoas
33	chr5:114700000-114703000	Enhancers	HUVEC	blood vessel
34	chr5:114700000-114704200	Weak transcription	Fetal Muscle Trunk	muscle
35	chr5:114700200-114701400	Weak transcription	Skeletal Muscle Female	skeletal muscle
36	chr5:114700200-114715800	Weak transcription	Pancreas	Pancrea
37	chr5:114700400-114701200	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr5:114700600-114701000	Weak transcription	NHDF-Ad	bronchial
39	chr5:114701000-114703000	Enhancers	NHDF-Ad	bronchial
40	chr5:114701200-114703000	Enhancers	Skeletal Muscle Male	skeletal muscle
41	chr5:114701400-114701800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr5:114701400-114701800	Enhancers	HSMMtube	muscle
43	chr5:114701400-114702000	Enhancers	Placenta	Placenta
44	chr5:114701400-114702000	Enhancers	Psoas Muscle	Psoas
45	chr5:114701400-114702000	Enhancers	Right Ventricle	heart
46	chr5:114701400-114702200	Enhancers	Left Ventricle	heart
47	chr5:114701400-114702200	Enhancers	Placenta Amnion	Placenta Amnion
48	chr5:114701400-114702200	Enhancers	NHLF	lung
49	chr5:114701400-114702400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr5:114701400-114702400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin

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