Variant report

Variant	esv2752056
Chromosome Location	chr5:106422649-106563101
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:531)
CpG islands
(count:183)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:531 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr5:106485049-106485238	GM12878	blood:	n/a	n/a
2	BCL11A	chr5:106484967-106485226	GM12878	blood:	n/a	n/a
3	BCL11A	chr5:106484974-106485223	GM12878	blood:	n/a	n/a
4	BHLHE40	chr5:106483675-106483684	GM12878	blood:	n/a	n/a
5	BRCA1	chr5:106440589-106440633	GM12878	blood:	n/a	n/a
6	CBX3	chr5:106476217-106476688	HCT-116	colon:	n/a	n/a
7	CBX3	chr5:106506231-106506793	HCT-116	colon:	n/a	n/a
8	CEBPB	chr5:106436098-106436334	A549	lung:	n/a	chr5:106436244-106436255
9	CEBPB	chr5:106553359-106553826	MCF-7	breast:	n/a	chr5:106553578-106553591
10	CEBPB	chr5:106554529-106554950	A549	lung:	n/a	chr5:106554937-106554950
11	CEBPB	chr5:106453242-106453333	A549	lung:	n/a	n/a
12	CEBPB	chr5:106436093-106436418	HepG2	liver:	n/a	chr5:106436244-106436255
13	CEBPB	chr5:106553239-106553882	HCT-116	colon:	n/a	chr5:106553578-106553591
14	CEBPB	chr5:106463626-106464087	HepG2	liver:	n/a	chr5:106463966-106463975 chr5:106463964-106463975 chr5:106463754-106463765
15	CEBPB	chr5:106436097-106436414	IMR90	lung:	n/a	chr5:106436244-106436255
16	CEBPB	chr5:106431815-106431940	H1-hESC	embryonic stem cell:	n/a	chr5:106431849-106431860
17	CEBPB	chr5:106431750-106431932	A549	lung:	n/a	chr5:106431849-106431860
18	CEBPB	chr5:106428418-106428625	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr5:106554588-106555075	Hela-S3	cervix:	n/a	chr5:106554937-106554950
20	CEBPB	chr5:106431711-106431917	HepG2	liver:	n/a	chr5:106431849-106431860
21	CEBPB	chr5:106521516-106521822	HepG2	liver:	n/a	n/a
22	CEBPB	chr5:106531529-106531741	HepG2	liver:	n/a	n/a
23	CEBPB	chr5:106531570-106531610	A549	lung:	n/a	n/a
24	CEBPB	chr5:106536248-106536250	A549	lung:	n/a	n/a
25	CEBPB	chr5:106553331-106553810	MCF-7	breast:	n/a	chr5:106553578-106553591
26	CHD2	chr5:106517883-106517892	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr5:106440445-106440667	GM19238	blood:	n/a	n/a
28	CTCF	chr5:106440449-106440637	GM13977	blood:	n/a	n/a
29	CTCF	chr5:106440560-106440710	GM12878	blood:	n/a	n/a
30	CTCF	chr5:106440438-106440661	MCF-7	breast:	n/a	n/a
31	CTCF	chr5:106440511-106440516	ProgFib	skin:	n/a	n/a
32	CTCF	chr5:106440460-106440610	HA-sp	spinal cord:	n/a	n/a
33	CTCF	chr5:106440480-106440630	HPAF	blood vessel:	n/a	n/a
34	CTCF	chr5:106440500-106440650	NHEK	skin:	n/a	n/a
35	CTCF	chr5:106440438-106440666	LNCaP	prostate:	n/a	n/a
36	CTCF	chr5:106440460-106440610	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr5:106440480-106440630	AG09309	skin:	n/a	n/a
38	CTCF	chr5:106440460-106440610	BE2_C	brain:	n/a	n/a
39	CTCF	chr5:106440520-106440670	GM12870	blood:	n/a	n/a
40	CTCF	chr5:106466922-106467052	HUVEC	blood vessel:	n/a	chr5:106466973-106466991
41	CTCF	chr5:106440520-106440670	HMF	breast:	n/a	n/a
42	CTCF	chr5:106440480-106440630	GM12865	blood:	n/a	n/a
43	CTCF	chr5:106466940-106467090	MCF-7	breast:	n/a	chr5:106466973-106466991
44	CTCF	chr5:106440440-106440590	GM12874	blood:	n/a	n/a
45	CTCF	chr5:106440520-106440670	Caco-2	colon:	n/a	n/a
46	CTCF	chr5:106466945-106467043	MCF-7	breast:	n/a	chr5:106466973-106466991
47	CTCF	chr5:106440476-106440635	HepG2	liver:	n/a	n/a
48	CTCF	chr5:106440463-106440649	GM19240	blood:	n/a	n/a
49	CTCF	chr5:106493680-106493830	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr5:106440526-106440623	GM12891	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:106434764-106434814	HCF	heart:	n/a
2	chr5:106453699-106453749	HRCEpiC	kidney:	n/a
3	chr5:106453699-106453749	SK-N-SH_RA	brain:	n/a
4	chr5:106530218-106530268	HRCEpiC	kidney:	n/a
5	chr5:106434764-106434814	AG09319	gingival:	n/a
6	chr5:106434764-106434814	HPAEpiC	pulmonary alveolar:	n/a
7	chr5:106453699-106453749	PrEC	prostate:	n/a
8	chr5:106434764-106434814	NHDF-neo	bronchial:	n/a
9	chr5:106530218-106530268	PFSK-1	brain:	n/a
10	chr5:106530218-106530268	ProgFib	skin:	n/a
11	chr5:106530218-106530268	Hepatocyte	liver:	n/a
12	chr5:106453699-106453749	NHBE	bronchial:	n/a
13	chr5:106434764-106434814	HAEpiC	amniotic membrane:	n/a
14	chr5:106453699-106453749	HCPEpiC	choroid plexus:	n/a
15	chr5:106434764-106434814	SAEC	small airway:	n/a
16	chr5:106453699-106453749	PFSK-1	brain:	n/a
17	chr5:106530218-106530268	U87	brain:	n/a
18	chr5:106453699-106453749	GM12878	blood:	n/a
19	chr5:106530218-106530268	HAEpiC	amniotic membrane:	n/a
20	chr5:106530218-106530268	NHBE	bronchial:	n/a
21	chr5:106530218-106530268	Caco-2	colon:	n/a
22	chr5:106530218-106530268	NT2-D1	testis:	n/a
23	chr5:106453699-106453749	ECC-1	luminal epithelium:	n/a
24	chr5:106530218-106530268	NHDF-neo	bronchial:	n/a
25	chr5:106434764-106434814	MCF-7	breast:	n/a
26	chr5:106434764-106434814	GM12878	blood:	n/a
27	chr5:106453699-106453749	NB4	blood:	n/a
28	chr5:106434764-106434814	HIPEpiC	eye:	n/a
29	chr5:106434764-106434814	ovcar-3	ovarian:	n/a
30	chr5:106434764-106434814	BJ	skin:	n/a
31	chr5:106434764-106434814	CMK	blood:	n/a
32	chr5:106530218-106530268	ovcar-3	ovarian:	n/a
33	chr5:106530218-106530268	PrEC	prostate:	n/a
34	chr5:106453699-106453749	HEEpiC	esophagus:	n/a
35	chr5:106453699-106453749	SAEC	small airway:	n/a
36	chr5:106453699-106453749	NH-A	brain:	n/a
37	chr5:106453699-106453749	U87	brain:	n/a
38	chr5:106453699-106453749	A549	lung:	n/a
39	chr5:106434764-106434814	SKMC	muscle:	n/a
40	chr5:106530218-106530268	RPTEC	kidney:	n/a
41	chr5:106530218-106530268	AG09319	gingival:	n/a
42	chr5:106530218-106530268	HCPEpiC	choroid plexus:	n/a
43	chr5:106434764-106434814	SK-N-MC	brain:	n/a
44	chr5:106434764-106434814	GM19239	blood:	n/a
45	chr5:106434764-106434814	AG09309	skin:	n/a
46	chr5:106530218-106530268	HMEC	breast:	n/a
47	chr5:106530218-106530268	HRE	kidney:	n/a
48	chr5:106453699-106453749	BE2_C	brain:	n/a
49	chr5:106434764-106434814	ECC-1	luminal epithelium:	n/a
50	chr5:106434764-106434814	Hepatocyte	liver:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:106473556..106475980-chr5:106486188..106488146,2	K562	blood:
2	chr5:106440118..106440828-chr5:106583731..106584326,2	MCF-7	breast:
3	chr5:106473556..106475980-chr5:106486188..106488146,2	K562	blood:
4	chr11:1775027..1777258-chr5:106478451..106479952,2	MCF-7	breast:
5	chr5:106440457..106441006-chr5:107009040..107009721,2	MCF-7	breast:
6	chr5:105620861..105623100-chr5:106539185..106542118,2	MCF-7	breast:
7	chr5:106438990..106441364-chr5:107007772..107009984,2	MCF-7	breast:
8	chr5:106389025..106391862-chr5:106427124..106429120,2	MCF-7	breast:
9	chr5:106525438..106528218-chr5:106529605..106532112,2	MCF-7	breast:

No data

Variant related genes	Relation type
PSMC1P5	TF binding region
PSMC1P5	CpG island
ENSG00000250273	chromatin interactions
ENSG00000117984	chromatin interactions

Extended variants
information (count: 3224 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:3224 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76935052	chr5:106423608-106423609	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs560754219	chr5:106423646-106423647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs532899415	chr5:106423728-106423729	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs552490600	chr5:106423746-106423747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs532869435	chr5:106423788-106423789	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs185418007	chr5:106423822-106423823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs572553692	chr5:106423875-106423876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs531267044	chr5:106423897-106423898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs188319180	chr5:106423907-106423908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs114525701	chr5:106423918-106423919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs11959317	chr5:106424010-106424011	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs180682203	chr5:106424031-106424032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs553385003	chr5:106424035-106424036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs553252445	chr5:106424075-106424076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs76480140	chr5:106424083-106424084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs539352211	chr5:106424161-106424162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs531911514	chr5:106424169-106424170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs115967761	chr5:106424175-106424176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs564922428	chr5:106424196-106424197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs115640898	chr5:106424206-106424207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs183760768	chr5:106424211-106424212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs374295255	chr5:106424226-106424227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs544352757	chr5:106424335-106424336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs144701575	chr5:106424346-106424347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs575022291	chr5:106424347-106424348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs547456118	chr5:106424374-106424375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs75537825	chr5:106424378-106424379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs560520543	chr5:106424389-106424390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs532804913	chr5:106424403-106424404	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs147883080	chr5:106424418-106424419	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs188826290	chr5:106424449-106424450	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs531953936	chr5:106424516-106424517	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181212501	chr5:106424521-106424522	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs567799286	chr5:106424544-106424545	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs527423747	chr5:106424553-106424554	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs200740949	chr5:106424558-106424559	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs566550068	chr5:106424587-106424588	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs527437356	chr5:106424639-106424640	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs573389630	chr5:106424658-106424659	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs570123465	chr5:106424660-106424661	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs539321912	chr5:106424667-106424668	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556443820	chr5:106424672-106424673	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs141512149	chr5:106424717-106424718	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569561951	chr5:106424796-106424797	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs535624463	chr5:106424806-106424807	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs143188682	chr5:106424885-106424886	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs148259877	chr5:106424986-106424987	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs140390385	chr5:106424987-106424988	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs551762207	chr5:106424992-106424993	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs79305999	chr5:106425077-106425078	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	21509527	CNVD
Breast cancer	16608533	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	16773561	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:311 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:106423600-106425200	Enhancers	Skeletal Muscle Male	skeletal muscle
2	chr5:106423800-106430000	Weak transcription	Aorta	Aorta
3	chr5:106424200-106425200	Enhancers	Skeletal Muscle Female	skeletal muscle
4	chr5:106424400-106425000	Enhancers	Muscle Satellite Cultured Cells	--
5	chr5:106424400-106426400	Enhancers	HSMMtube	muscle
6	chr5:106425000-106425200	Enhancers	HSMM	muscle
7	chr5:106425000-106426200	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr5:106425200-106426200	Weak transcription	HSMM	muscle
9	chr5:106425200-106426400	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr5:106426000-106426600	Enhancers	Fetal Lung	lung
11	chr5:106426000-106426600	Enhancers	Rectal Smooth Muscle	rectum
12	chr5:106426200-106426600	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr5:106426200-106426600	Enhancers	Muscle Satellite Cultured Cells	--
14	chr5:106426200-106426600	Enhancers	HSMM	muscle
15	chr5:106426400-106426600	Enhancers	Skeletal Muscle Female	skeletal muscle
16	chr5:106428400-106428800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr5:106430000-106430600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr5:106430000-106430600	ZNF genes & repeats	Aorta	Aorta
19	chr5:106430600-106438800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr5:106430600-106438800	Weak transcription	Aorta	Aorta
21	chr5:106434200-106434400	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr5:106434200-106435400	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr5:106434200-106435400	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr5:106434400-106435000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
25	chr5:106434400-106435000	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr5:106434400-106435000	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr5:106434400-106435000	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr5:106434400-106435000	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr5:106435000-106440200	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr5:106435000-106440200	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr5:106435000-106440200	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr5:106435000-106440200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr5:106435400-106440200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr5:106436000-106436600	Enhancers	A549	lung
35	chr5:106436600-106440200	Weak transcription	A549	lung
36	chr5:106438800-106439000	Enhancers	Pancreas	Pancrea
37	chr5:106438800-106439200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr5:106438800-106439200	ZNF genes & repeats	Aorta	Aorta
39	chr5:106439200-106440000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr5:106439200-106444000	Weak transcription	Aorta	Aorta
41	chr5:106440000-106440200	Enhancers	Psoas Muscle	Psoas
42	chr5:106440000-106440400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr5:106440000-106440400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr5:106440000-106440600	Enhancers	H9 Cell Line	embryonic stem cell
45	chr5:106440200-106440600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr5:106440200-106440600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr5:106440200-106440600	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr5:106440200-106440600	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr5:106440200-106440600	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr5:106440200-106440600	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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