Variant report

Variant	nsv964844
Chromosome Location	chr5:37080836-37107123
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:106)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:106 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:37093963-37094296	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:37086569-37086924	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:37090579-37090786	HepG2	liver:	n/a	n/a
4	CCNT2	chr5:37086862-37086915	K562	blood:	n/a	n/a
5	CEBPB	chr5:37087000-37087299	HepG2	liver:	n/a	n/a
6	CEBPB	chr5:37086955-37087263	IMR90	lung:	n/a	n/a
7	CEBPB	chr5:37098897-37099006	A549	lung:	n/a	n/a
8	CTCF	chr5:37085412-37085474	GM10266	blood:	n/a	n/a
9	CTCF	chr5:37090560-37090615	GM10248	blood:	n/a	n/a
10	CTCF	chr5:37103520-37103670	NB4	blood:	n/a	n/a
11	CTCF	chr5:37088849-37088883	GM13976	blood:	n/a	n/a
12	EP300	chr5:37087061-37087156	HepG2	liver:	n/a	n/a
13	FOS	chr5:37087048-37087145	MCF10A-Er-Src	breast:	n/a	n/a
14	FOS	chr5:37087064-37087140	MCF10A-Er-Src	breast:	n/a	n/a
15	FOXA1	chr5:37081086-37081522	HepG2	liver:	n/a	n/a
16	FOXA1	chr5:37093765-37094342	HepG2	liver:	n/a	n/a
17	FOXA1	chr5:37093789-37094365	HepG2	liver:	n/a	n/a
18	FOXA1	chr5:37090396-37090930	HepG2	liver:	n/a	n/a
19	FOXA1	chr5:37090279-37091004	HepG2	liver:	n/a	n/a
20	FOXA1	chr5:37093903-37094288	HepG2	liver:	n/a	n/a
21	FOXA1	chr5:37081154-37081605	HepG2	liver:	n/a	n/a
22	FOXA1	chr5:37086490-37087055	HepG2	liver:	n/a	n/a
23	FOXA1	chr5:37090443-37090927	HepG2	liver:	n/a	n/a
24	FOXA1	chr5:37086529-37086916	HepG2	liver:	n/a	n/a
25	FOXA1	chr5:37081088-37081490	HepG2	liver:	n/a	n/a
26	FOXA1	chr5:37086436-37086967	HepG2	liver:	n/a	n/a
27	FOXA1	chr5:37086490-37087083	HepG2	liver:	n/a	n/a
28	FOXA1	chr5:37093911-37094273	HepG2	liver:	n/a	n/a
29	FOXA1	chr5:37090461-37090965	HepG2	liver:	n/a	n/a
30	FOXA2	chr5:37090391-37090838	HepG2	liver:	n/a	n/a
31	FOXA2	chr5:37086462-37086967	HepG2	liver:	n/a	n/a
32	FOXA2	chr5:37093914-37094282	HepG2	liver:	n/a	n/a
33	FOXA2	chr5:37086274-37087057	HepG2	liver:	n/a	n/a
34	GATA2	chr5:37082882-37083482	HUVEC	blood vessel:	n/a	chr5:37083273-37083287
35	GATA2	chr5:37083034-37083480	SH-SY5Y	brain:	n/a	chr5:37083273-37083287
36	GATA3	chr5:37083097-37083335	T-47D	breast:	n/a	n/a
37	GATA3	chr5:37090230-37090871	MCF-7	breast:	n/a	chr5:37090665-37090673
38	GATA3	chr5:37083061-37083405	MCF-7	breast:	n/a	n/a
39	GATA3	chr5:37083079-37083348	T-47D	breast:	n/a	n/a
40	GTF2F1	chr5:37099251-37099254	Hela-S3	cervix:	n/a	n/a
41	HDAC2	chr5:37086609-37086895	HepG2	liver:	n/a	n/a
42	HDAC2	chr5:37090501-37090783	HepG2	liver:	n/a	n/a
43	HDAC2	chr5:37090466-37090763	HepG2	liver:	n/a	n/a
44	HNF4G	chr5:37086558-37086903	HepG2	liver:	n/a	n/a
45	HNF4G	chr5:37086608-37086890	HepG2	liver:	n/a	n/a
46	JUND	chr5:37094021-37094202	HepG2	liver:	n/a	n/a
47	JUND	chr5:37086641-37086806	HepG2	liver:	n/a	n/a
48	JUND	chr5:37090461-37090661	HepG2	liver:	n/a	n/a
49	KAP1	chr5:37086669-37087289	HEK293	kidney:	n/a	n/a
50	KAP1	chr5:37090371-37090826	U2OS	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:37107062-37107112	HEK293	kidney:	embryo
2	chr5:37107062-37107112	AG10803	skin:	n/a
3	chr5:37107062-37107112	NHBE	bronchial:	n/a
4	chr5:37107062-37107112	HPAEpiC	pulmonary alveolar:	n/a
5	chr5:37107062-37107112	HCT-116	colon:	n/a
6	chr5:37107062-37107112	NH-A	brain:	n/a
7	chr5:37107062-37107112	HNPCEpiC	eye:	n/a
8	chr5:37107062-37107112	ovcar-3	ovarian:	n/a
9	chr5:37107062-37107112	A549	lung:	n/a
10	chr5:37107062-37107112	GM12891	blood:	n/a
11	chr5:37107062-37107112	H1-hESC	embryonic stem cell:	embryo
12	chr5:37107062-37107112	PrEC	prostate:	n/a
13	chr5:37107062-37107112	BE2_C	brain:	n/a
14	chr5:37107062-37107112	GM12878	blood:	n/a
15	chr5:37107062-37107112	U87	brain:	n/a
16	chr5:37107062-37107112	HAEpiC	amniotic membrane:	n/a
17	chr5:37107062-37107112	HCPEpiC	choroid plexus:	n/a
18	chr5:37107062-37107112	GM12892	blood:	n/a
19	chr5:37107062-37107112	HIPEpiC	eye:	n/a
20	chr5:37107062-37107112	GM19239	blood:	n/a
21	chr5:37107062-37107112	T-47D	breast:	n/a
22	chr5:37107062-37107112	SK-N-SH	brain:	n/a
23	chr5:37107062-37107112	Caco-2	colon:	n/a
24	chr5:37107062-37107112	CMK	blood:	n/a
25	chr5:37107062-37107112	AG09319	gingival:	n/a
26	chr5:37107062-37107112	HCM	heart:	n/a
27	chr5:37107062-37107112	K562	blood:	n/a
28	chr5:37107062-37107112	Hela-S3	cervix:	n/a
29	chr5:37107062-37107112	Jurkat	blood:	n/a
30	chr5:37107062-37107112	NT2-D1	testis:	n/a
31	chr5:37107062-37107112	AG09309	skin:	n/a
32	chr5:37107062-37107112	Hepatocyte	liver:	n/a
33	chr5:37107062-37107112	AG04449	skin:	fetal
34	chr5:37107062-37107112	HCF	heart:	n/a
35	chr5:37107062-37107112	AG04450	lung:	fetal
36	chr5:37107062-37107112	NB4	blood:	n/a
37	chr5:37107062-37107112	AoSMC	blood vessel:	n/a
38	chr5:37107062-37107112	LNCaP	prostate:	n/a
39	chr5:37107062-37107112	SK-N-SH_RA	brain:	n/a
40	chr5:37107062-37107112	HRE	kidney:	n/a
41	chr5:37107062-37107112	GM06990	blood:	n/a
42	chr5:37107062-37107112	SKMC	muscle:	n/a
43	chr5:37107062-37107112	PFSK-1	brain:	n/a
44	chr5:37107062-37107112	HUVEC	blood vessel:	n/a
45	chr5:37107062-37107112	RPTEC	kidney:	n/a
46	chr5:37107062-37107112	HRPEpiC	eye:	n/a
47	chr5:37107062-37107112	SAEC	small airway:	n/a
48	chr5:37107062-37107112	HMEC	breast:	n/a
49	chr5:37107062-37107112	HRCEpiC	kidney:	n/a
50	chr5:37107062-37107112	ProgFib	skin:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:37089091..37091586-chr5:37092682..37094967,2	K562	blood:
2	chr5:37080220..37082600-chr5:37085134..37087206,2	K562	blood:
3	chr5:37074333..37077289-chr5:37078175..37080893,2	K562	blood:
4	chr5:37089091..37091586-chr5:37092682..37094967,2	K562	blood:

No data

Variant related genes	Relation type
RPS4XP6	TF binding region
RPS4XP6	CpG island
ENSG00000244073	chromatin interactions

Extended variants
information (count: 862 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:862 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375695577	chr5:37080848-37080849	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs572391696	chr5:37080852-37080853	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs141293050	chr5:37080870-37080871	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs558192627	chr5:37080875-37080876	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs576456932	chr5:37080935-37080936	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs145081275	chr5:37080937-37080938	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs191774306	chr5:37081005-37081006	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs367828468	chr5:37081208-37081209	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs574029203	chr5:37081229-37081230	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs371686486	chr5:37081248-37081249	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs184938917	chr5:37081305-37081306	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs138802063	chr5:37081333-37081334	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs189270793	chr5:37081375-37081376	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs180952719	chr5:37081402-37081403	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs187240748	chr5:37081415-37081416	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs138779156	chr5:37081444-37081445	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs141986314	chr5:37081457-37081458	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs549493992	chr5:37081465-37081466	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs550442626	chr5:37081507-37081508	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs13156205	chr5:37081511-37081512	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs568173564	chr5:37081512-37081513	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs535171111	chr5:37081529-37081530	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs189258346	chr5:37081549-37081550	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs181964930	chr5:37081554-37081555	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs185847350	chr5:37081571-37081572	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs190648832	chr5:37081690-37081691	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs300046	chr5:37081705-37081706	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs549352406	chr5:37081723-37081724	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs201172660	chr5:37081733-37081734	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs183088396	chr5:37081863-37081864	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs386687270	chr5:37081880-37081881	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs13176880	chr5:37081882-37081883	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs541128141	chr5:37081899-37081900	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs144687343	chr5:37081911-37081912	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs577864900	chr5:37081964-37081965	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs186371977	chr5:37081965-37081966	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs530054486	chr5:37082015-37082016	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs545185502	chr5:37082016-37082017	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs190930358	chr5:37082042-37082043	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs549926122	chr5:37082076-37082077	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs182640554	chr5:37082100-37082101	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs543424909	chr5:37082126-37082127	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs561491464	chr5:37082149-37082150	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs528993270	chr5:37082153-37082154	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs368610604	chr5:37082172-37082173	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs537666727	chr5:37082176-37082177	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs201551165	chr5:37082196-37082197	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs148053603	chr5:37082243-37082244	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs570101902	chr5:37082249-37082250	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs565776927	chr5:37082280-37082281	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Myofibroblastic sarcoma	19369631	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	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
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Lung cancer	19153074	CNVD
Breast cancer	21364760	CNVD
Cornelia de Lange syndrome	21085971	CNVD
Autism	21701786	CNVD
Cervical cancer	16585170	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:560 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:36949600-37086800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr5:37058600-37090000	Weak transcription	Right Ventricle	heart
3	chr5:37061200-37096800	Weak transcription	Psoas Muscle	Psoas
4	chr5:37061200-37103400	Weak transcription	Fetal Kidney	kidney
5	chr5:37064200-37105000	Weak transcription	Fetal Brain Male	brain
6	chr5:37064600-37104000	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr5:37064800-37086800	Weak transcription	Pancreas	Pancrea
8	chr5:37064800-37087000	Weak transcription	Colonic Mucosa	Colon
9	chr5:37064800-37093600	Weak transcription	Brain Germinal Matrix	brain
10	chr5:37065000-37083000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr5:37065000-37083000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr5:37065000-37084400	Weak transcription	Fetal Intestine Small	intestine
13	chr5:37065000-37086800	Weak transcription	Lung	lung
14	chr5:37065000-37087000	Weak transcription	Esophagus	oesophagus
15	chr5:37065000-37092600	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr5:37065000-37092600	Weak transcription	Small Intestine	intestine
17	chr5:37065000-37097400	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr5:37065000-37099400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr5:37065000-37107600	Weak transcription	Rectal Smooth Muscle	rectum
20	chr5:37065200-37090800	Weak transcription	Primary T cells from cord blood	blood
21	chr5:37065200-37103400	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr5:37065600-37085000	Weak transcription	Duodenum Mucosa	Duodenum
23	chr5:37065600-37086600	Weak transcription	Fetal Intestine Large	intestine
24	chr5:37065600-37089400	Weak transcription	Primary T cells fromperipheralblood	blood
25	chr5:37065600-37102400	Weak transcription	Placenta	Placenta
26	chr5:37065800-37087000	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr5:37066000-37086400	Weak transcription	Primary T helper cells PMA-I stimulated	--
28	chr5:37066200-37085800	Weak transcription	Primary B cells from cord blood	blood
29	chr5:37067000-37087000	Weak transcription	Colon Smooth Muscle	Colon
30	chr5:37067000-37111400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chr5:37072400-37086600	Weak transcription	NHLF	lung
32	chr5:37072600-37097400	Weak transcription	Brain Angular Gyrus	brain
33	chr5:37072600-37103600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr5:37072800-37090200	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr5:37072800-37090800	Weak transcription	Brain Anterior Caudate	brain
36	chr5:37073200-37085200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr5:37073200-37094200	Weak transcription	Brain Substantia Nigra	brain
38	chr5:37073400-37085600	Weak transcription	NH-A	brain
39	chr5:37073400-37103600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr5:37073600-37081600	Weak transcription	HUVEC	blood vessel
41	chr5:37077000-37082200	Strong transcription	Fetal Muscle Leg	muscle
42	chr5:37078000-37081400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr5:37078200-37081000	Strong transcription	Adipose Nuclei	Adipose
44	chr5:37078200-37081200	Strong transcription	Dnd41	blood
45	chr5:37078200-37082200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr5:37078800-37086600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr5:37078800-37086800	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr5:37078800-37086800	Weak transcription	Osteobl	bone
49	chr5:37078800-37097600	Weak transcription	Primary hematopoietic stem cells	blood
50	chr5:37078800-37105000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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