Variant report

Variant	nsv968905
Chromosome Location	chr5:37378041-37390033
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:646)
CpG islands
(count:793)
Chromatin interactive
region (count:8)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:646 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:37379206-37379473	K562	blood:	n/a	n/a
2	ATF1	chr5:37379197-37379483	K562	blood:	n/a	n/a
3	ATF2	chr5:37379058-37379502	GM12878	blood:	n/a	n/a
4	ATF2	chr5:37379198-37379480	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr5:37379100-37379507	A549	lung:	n/a	n/a
6	ATF3	chr5:37379108-37379491	K562	blood:	n/a	n/a
7	ATF3	chr5:37379172-37379508	A549	lung:	n/a	n/a
8	BATF	chr5:37379223-37379461	GM12878	blood:	n/a	n/a
9	BCL3	chr5:37379056-37379575	A549	lung:	n/a	n/a
10	BCL3	chr5:37379009-37379598	A549	lung:	n/a	n/a
11	BCLAF1	chr5:37379111-37379567	GM12878	blood:	n/a	n/a
12	BCLAF1	chr5:37379066-37379572	K562	blood:	n/a	n/a
13	BCLAF1	chr5:37379017-37379502	K562	blood:	n/a	n/a
14	BCLAF1	chr5:37379021-37379585	GM12878	blood:	n/a	n/a
15	BHLHE40	chr5:37379191-37379467	K562	blood:	n/a	n/a
16	BHLHE40	chr5:37379174-37379470	GM12878	blood:	n/a	n/a
17	BRCA1	chr5:37379222-37379473	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr5:37378896-37379572	K562	blood:	n/a	n/a
19	CBX3	chr5:37379023-37379535	HCT-116	colon:	n/a	n/a
20	CBX3	chr5:37379094-37379529	K562	blood:	n/a	n/a
21	CCNT2	chr5:37379217-37379472	K562	blood:	n/a	n/a
22	CEBPB	chr5:37379055-37379320	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr5:37379090-37379578	GM12878	blood:	n/a	n/a
24	CEBPB	chr5:37379136-37379389	K562	blood:	n/a	n/a
25	CEBPB	chr5:37379003-37379483	K562	blood:	n/a	n/a
26	CEBPB	chr5:37379060-37379576	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr5:37379133-37379425	HepG2	liver:	n/a	n/a
28	CEBPD	chr5:37379165-37379668	K562	blood:	n/a	n/a
29	CEBPD	chr5:37379209-37379537	HepG2	liver:	n/a	n/a
30	CHD1	chr5:37379221-37379370	GM12878	blood:	n/a	n/a
31	CHD1	chr5:37379228-37379547	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr5:37379219-37379466	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr5:37379182-37379491	GM12878	blood:	n/a	n/a
34	CHD2	chr5:37379124-37379543	Hela-S3	cervix:	n/a	n/a
35	CHD2	chr5:37379286-37379436	K562	blood:	n/a	n/a
36	CREB1	chr5:37379183-37379504	HepG2	liver:	n/a	n/a
37	CREB1	chr5:37379201-37379474	A549	lung:	n/a	n/a
38	CREB1	chr5:37379112-37379598	A549	lung:	n/a	n/a
39	CREB1	chr5:37379040-37379463	GM12878	blood:	n/a	n/a
40	CREB1	chr5:37379148-37379401	K562	blood:	n/a	n/a
41	CREB1	chr5:37379176-37379387	GM12878	blood:	n/a	n/a
42	CTCF	chr5:37379240-37379390	GM12878	blood:	n/a	n/a
43	CTCF	chr5:37378700-37378850	GM12867	blood:	n/a	n/a
44	CTCF	chr5:37379220-37379370	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr5:37379169-37379437	MCF-7	breast:	n/a	n/a
46	CTCF	chr5:37379200-37379350	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr5:37379200-37379350	GM12868	blood:	n/a	n/a
48	CTCF	chr5:37379240-37379390	HRE	kidney:	n/a	n/a
49	CTCF	chr5:37379220-37379370	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr5:37379158-37379468	Lung_OC	lung:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:37379396-37379446	PrEC	prostate:	n/a
2	chr5:37382801-37382851	Hela-S3	cervix:	n/a
3	chr5:37379267-37379317	HepG2	liver:	n/a
4	chr5:37382801-37382851	GM12878	blood:	n/a
5	chr5:37379822-37379872	K562	blood:	n/a
6	chr5:37379269-37379319	GM12878	blood:	n/a
7	chr5:37379396-37379446	HEEpiC	esophagus:	n/a
8	chr5:37382801-37382851	AG04450	lung:	fetal
9	chr5:37379272-37379322	HRE	kidney:	n/a
10	chr5:37379396-37379446	BJ	skin:	n/a
11	chr5:37378050-37378100	NHBE	bronchial:	n/a
12	chr5:37379374-37379424	Hepatocyte	liver:	n/a
13	chr5:37379374-37379424	H1-hESC	embryonic stem cell:	embryo
14	chr5:37379272-37379322	Hepatocyte	liver:	n/a
15	chr5:37379269-37379319	HCM	heart:	n/a
16	chr5:37379822-37379872	IMR90	lung:	fetal
17	chr5:37379358-37379408	Hepatocyte	liver:	n/a
18	chr5:37378272-37378322	Caco-2	colon:	n/a
19	chr5:37378272-37378322	Jurkat	blood:	n/a
20	chr5:37379272-37379322	PrEC	prostate:	n/a
21	chr5:37379272-37379322	HCF	heart:	n/a
22	chr5:37379822-37379872	BE2_C	brain:	n/a
23	chr5:37379374-37379424	GM06990	blood:	n/a
24	chr5:37379822-37379872	MCF10A-Er-Src	breast:	n/a
25	chr5:37378050-37378100	HEEpiC	esophagus:	n/a
26	chr5:37378050-37378100	Jurkat	blood:	n/a
27	chr5:37382801-37382851	Jurkat	blood:	n/a
28	chr5:37379396-37379446	HIPEpiC	eye:	n/a
29	chr5:37379269-37379319	HL-60	blood:	n/a
30	chr5:37378229-37378279	NH-A	brain:	n/a
31	chr5:37379267-37379317	HL-60	blood:	n/a
32	chr5:37378272-37378322	NHBE	bronchial:	n/a
33	chr5:37379374-37379424	GM12892	blood:	n/a
34	chr5:37378272-37378322	HCM	heart:	n/a
35	chr5:37378272-37378322	PrEC	prostate:	n/a
36	chr5:37379822-37379872	NHBE	bronchial:	n/a
37	chr5:37379267-37379317	ovcar-3	ovarian:	n/a
38	chr5:37379358-37379408	HL-60	blood:	n/a
39	chr5:37382801-37382851	HMEC	breast:	n/a
40	chr5:37379396-37379446	SK-N-MC	brain:	n/a
41	chr5:37379461-37379511	PrEC	prostate:	n/a
42	chr5:37382801-37382851	MCF10A-Er-Src	breast:	n/a
43	chr5:37379461-37379511	SK-N-MC	brain:	n/a
44	chr5:37378272-37378322	HepG2	liver:	n/a
45	chr5:37379396-37379446	NHBE	bronchial:	n/a
46	chr5:37379272-37379322	SK-N-MC	brain:	n/a
47	chr5:37379358-37379408	NT2-D1	testis:	n/a
48	chr5:37378050-37378100	PANC-1	pancreas:	n/a
49	chr5:37379822-37379872	HNPCEpiC	eye:	n/a
50	chr5:37379374-37379424	HCT-116	colon:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:37370037..37373489-chr5:37377973..37381470,5	K562	blood:
2	chr5:37369760..37372730-chr5:37375256..37380889,7	MCF-7	breast:
3	chr1:117601635..117602147-chr5:37379314..37380058,2	Hela-S3	cervix:
4	chr5:37379216..37379885-chr6:58287233..58287739,2	Hela-S3	cervix:
5	chr5:37389025..37391631-chr5:37392336..37394905,2	K562	blood:
6	chr5:37369538..37373129-chr5:37377393..37380859,4	MCF-7	breast:
7	chr5:21459174..21459727-chr5:37379374..37379881,2	Hela-S3	cervix:
8	chr5:37378209..37381818-chr5:37388003..37389859,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NIPBL-7	chr5:37381704-37381911	NONHSAT101065
2	lnc-WDR70-4	chr5:37377986-37378073	NONHSAT101062
3	lnc-NIPBL-7	chr5:37379404-37379494	NONHSAT101065
4	lnc-NIPBL-7	chr5:37379591-37379656	NONHSAT101065

No data

Variant related genes	Relation type
WDR70	TF binding region
WDR70	CpG island
ENSG00000082068	chromatin interactions
ENSG00000113569	chromatin interactions
ENSG00000236137	chromatin interactions
ENSG00000215190	chromatin interactions
ENSG00000183666	chromatin interactions

Extended variants
information (count: 462 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:462 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550457850	chr5:37378079-37378080	Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs59775401	chr5:37378083-37378084	Weak transcription	CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs367731379	chr5:37378098-37378099	Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs559247802	chr5:37378137-37378138	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs529740548	chr5:37378146-37378147	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs61154857	chr5:37378156-37378157	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs566442324	chr5:37378177-37378178	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs533897391	chr5:37378203-37378204	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs551523823	chr5:37378215-37378216	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs571379612	chr5:37378296-37378297	Weak transcription Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs570671820	chr5:37378423-37378424	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs534077258	chr5:37378458-37378459	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs35923123	chr5:37378468-37378469	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs556470429	chr5:37378567-37378568	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs574626886	chr5:37378582-37378583	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs185184067	chr5:37378588-37378589	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs553893076	chr5:37378622-37378623	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs547415235	chr5:37378632-37378633	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs146798511	chr5:37378634-37378635	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs35624435	chr5:37378735-37378736	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs545893787	chr5:37378790-37378791	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs188411345	chr5:37378872-37378873	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs373970781	chr5:37378894-37378895	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs536207578	chr5:37378919-37378920	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs543651280	chr5:37378935-37378936	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs191769862	chr5:37378937-37378938	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs529575857	chr5:37378942-37378943	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs184089980	chr5:37378959-37378960	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs28661178	chr5:37379023-37379024	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs371715003	chr5:37379029-37379030	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs113004732	chr5:37379033-37379034	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs371994267	chr5:37379064-37379065	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs217836	chr5:37379087-37379088	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs34599131	chr5:37379098-37379099	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs36096798	chr5:37379123-37379124	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs35727443	chr5:37379190-37379191	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs73749028	chr5:37379216-37379217	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs538075266	chr5:37379223-37379224	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs188085649	chr5:37379273-37379274	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs568209919	chr5:37379290-37379291	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs535404319	chr5:37379301-37379302	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs553601530	chr5:37379347-37379348	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs572116034	chr5:37379375-37379376	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs539437986	chr5:37379382-37379383	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs199839331	chr5:37379385-37379386	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs576106388	chr5:37379401-37379402	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs558310846	chr5:37379416-37379417	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
48	rs543864820	chr5:37379419-37379420	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
49	rs200819438	chr5:37379430-37379431	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
50	rs374806437	chr5:37379459-37379460	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
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	21364760	CNVD
Schizophrenia	23813976	CNVD
Schizophrenia	21346763	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:506 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:37372200-37378800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr5:37372600-37379000	Weak transcription	HepG2	liver
3	chr5:37376200-37379000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr5:37376400-37379000	Weak transcription	K562	blood
5	chr5:37378200-37378400	Enhancers	Dnd41	blood
6	chr5:37378400-37378800	Flanking Active TSS	Dnd41	blood
7	chr5:37378600-37378800	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr5:37378600-37378800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr5:37378600-37380200	Active TSS	Stomach Smooth Muscle	stomach
10	chr5:37378800-37379000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr5:37378800-37379000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
12	chr5:37378800-37379200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr5:37378800-37379800	Active TSS	Primary neutrophils fromperipheralblood	blood
14	chr5:37378800-37379800	Active TSS	Primary hematopoietic stem cells	blood
15	chr5:37378800-37379800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr5:37378800-37379800	Active TSS	Duodenum Mucosa	Duodenum
17	chr5:37378800-37379800	Active TSS	Monocytes-CD14+_RO01746	blood
18	chr5:37378800-37380000	Active TSS	iPS-15b Cell Line	embryonic stem cell
19	chr5:37378800-37380000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr5:37378800-37380000	Active TSS	Colon Smooth Muscle	Colon
21	chr5:37378800-37380000	Active TSS	Fetal Adrenal Gland	Adrenal Gland
22	chr5:37378800-37380000	Active TSS	Thymus	Thymus
23	chr5:37378800-37380000	Active TSS	Dnd41	blood
24	chr5:37378800-37380000	Active TSS	Hela-S3	cervix
25	chr5:37378800-37380000	Active TSS	Osteobl	bone
26	chr5:37378800-37380200	Active TSS	Breast Myoepithelial Primary Cells	Breast
27	chr5:37378800-37380200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr5:37378800-37380200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr5:37378800-37380200	Active TSS	Fetal Intestine Large	intestine
30	chr5:37378800-37380200	Active TSS	Skeletal Muscle Male	skeletal muscle
31	chr5:37378800-37380200	Active TSS	GM12878-XiMat	blood
32	chr5:37378800-37380200	Active TSS	HSMM	muscle
33	chr5:37379000-37379200	Flanking Active TSS	Primary B cells from peripheral blood	blood
34	chr5:37379000-37379200	Flanking Active TSS	Fetal Stomach	stomach
35	chr5:37379000-37379200	Flanking Active TSS	Fetal Thymus	thymus
36	chr5:37379000-37379400	Flanking Active TSS	Primary B cells from cord blood	blood
37	chr5:37379000-37379400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
38	chr5:37379000-37379400	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
39	chr5:37379000-37379400	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
40	chr5:37379000-37379400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr5:37379000-37379400	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
42	chr5:37379000-37379600	Active TSS	Primary T helper cells fromperipheralblood	blood
43	chr5:37379000-37379800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
44	chr5:37379000-37379800	Active TSS	Primary monocytes fromperipheralblood	blood
45	chr5:37379000-37379800	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
46	chr5:37379000-37379800	Active TSS	Primary T killer memory cells from peripheral blood	blood
47	chr5:37379000-37379800	Active TSS	Adipose Nuclei	Adipose
48	chr5:37379000-37379800	Active TSS	Left Ventricle	heart
49	chr5:37379000-37379800	Active TSS	Rectal Mucosa Donor 29	rectum
50	chr5:37379000-37379800	Active TSS	Rectal Mucosa Donor 31	rectum

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