Variant report

Variant	nsv882145
Chromosome Location	chr5:70316072-70498086
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:843)
CpG islands
(count:122)
Chromatin interactive
region (count:0)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:843 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr5:70473436-70473649	GM12878	blood:	n/a	n/a
2	BATF	chr5:70473270-70473572	GM12878	blood:	n/a	n/a
3	BATF	chr5:70363439-70363749	GM12878	blood:	n/a	n/a
4	BATF	chr5:70362170-70362374	GM12878	blood:	n/a	n/a
5	BATF	chr5:70405611-70405957	GM12878	blood:	n/a	n/a
6	BATF	chr5:70456649-70456978	GM12878	blood:	n/a	n/a
7	BATF	chr5:70363039-70363251	GM12878	blood:	n/a	n/a
8	BATF	chr5:70362121-70362600	GM12878	blood:	n/a	n/a
9	BATF	chr5:70456678-70456913	GM12878	blood:	n/a	n/a
10	BATF	chr5:70363259-70363809	GM12878	blood:	n/a	n/a
11	BCL11A	chr5:70363265-70363860	GM12878	blood:	n/a	chr5:70363563-70363572
12	BCL11A	chr5:70363241-70363801	GM12878	blood:	n/a	chr5:70363563-70363572
13	BCL11A	chr5:70405618-70405863	GM12878	blood:	n/a	n/a
14	BCL11A	chr5:70456746-70456985	GM12878	blood:	n/a	n/a
15	BCL11A	chr5:70493340-70493531	GM12878	blood:	n/a	n/a
16	BCL11A	chr5:70362110-70362487	GM12878	blood:	n/a	n/a
17	BCL11A	chr5:70466178-70466577	GM12878	blood:	n/a	n/a
18	BCL11A	chr5:70321346-70321632	GM12878	blood:	n/a	n/a
19	BCL11A	chr5:70497555-70497741	GM12878	blood:	n/a	n/a
20	BCL11A	chr5:70466234-70466446	GM12878	blood:	n/a	n/a
21	BCL11A	chr5:70456762-70456944	GM12878	blood:	n/a	n/a
22	BCL11A	chr5:70467406-70467579	GM12878	blood:	n/a	n/a
23	BCL11A	chr5:70321231-70321752	GM12878	blood:	n/a	n/a
24	BCL11A	chr5:70491903-70492088	GM12878	blood:	n/a	n/a
25	BHLHE40	chr5:70476360-70476599	HepG2	liver:	n/a	n/a
26	BHLHE40	chr5:70495349-70495582	HepG2	liver:	n/a	n/a
27	BHLHE40	chr5:70363384-70363696	HepG2	liver:	n/a	chr5:70363608-70363624 chr5:70363624-70363640
28	BHLHE40	chr5:70435263-70435547	HepG2	liver:	n/a	n/a
29	BHLHE40	chr5:70467222-70467633	HepG2	liver:	n/a	n/a
30	BHLHE40	chr5:70473739-70473978	HepG2	liver:	n/a	n/a
31	CBX3	chr5:70362704-70364093	K562	blood:	n/a	n/a
32	CBX3	chr5:70363327-70363979	K562	blood:	n/a	n/a
33	CEBPB	chr5:70362066-70362404	K562	blood:	n/a	n/a
34	CEBPB	chr5:70362104-70362275	K562	blood:	n/a	n/a
35	CEBPB	chr5:70362898-70363936	GM12878	blood:	n/a	n/a
36	CEBPB	chr5:70393343-70393363	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPD	chr5:70363322-70363798	K562	blood:	n/a	n/a
38	CTCF	chr5:70325992-70326059	Kidney_OC	kidney:	n/a	n/a
39	CTCF	chr5:70343924-70344029	GM13976	blood:	n/a	n/a
40	CTCF	chr5:70363567-70363714	GM19239	blood:	n/a	n/a
41	CTCF	chr5:70363581-70363713	NHEK	skin:	n/a	n/a
42	CTCF	chr5:70380705-70380760	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr5:70363597-70363702	A549	lung:	n/a	n/a
44	CTCF	chr5:70363584-70363712	MCF-7	breast:	n/a	n/a
45	CTCF	chr5:70363468-70363740	GM13977	blood:	n/a	n/a
46	CTCF	chr5:70363628-70363698	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr5:70363357-70363771	Spleen_OC	spleen:	n/a	n/a
48	CTCF	chr5:70366045-70366103	GM10248	blood:	n/a	n/a
49	CTCF	chr5:70363334-70363784	A549	lung:	n/a	n/a
50	CTCF	chr5:70424036-70424400	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:70372505-70372555	RPTEC	kidney:	n/a
2	chr5:70372505-70372555	PFSK-1	brain:	n/a
3	chr5:70372505-70372555	HRCEpiC	kidney:	n/a
4	chr5:70372505-70372555	SK-N-MC	brain:	n/a
5	chr5:70320693-70320743	HCPEpiC	choroid plexus:	n/a
6	chr5:70320693-70320743	SKMC	muscle:	n/a
7	chr5:70320693-70320743	HPAEpiC	pulmonary alveolar:	n/a
8	chr5:70372505-70372555	SK-N-SH	brain:	n/a
9	chr5:70320693-70320743	HRCEpiC	kidney:	n/a
10	chr5:70320693-70320743	ProgFib	skin:	n/a
11	chr5:70320693-70320743	U87	brain:	n/a
12	chr5:70372505-70372555	H1-hESC	embryonic stem cell:	embryo
13	chr5:70320693-70320743	BJ	skin:	n/a
14	chr5:70372505-70372555	Hela-S3	cervix:	n/a
15	chr5:70372505-70372555	HAEpiC	amniotic membrane:	n/a
16	chr5:70320693-70320743	AG09319	gingival:	n/a
17	chr5:70372505-70372555	MCF10A-Er-Src	breast:	n/a
18	chr5:70372505-70372555	GM12891	blood:	n/a
19	chr5:70320693-70320743	HepG2	liver:	n/a
20	chr5:70372505-70372555	CMK	blood:	n/a
21	chr5:70372505-70372555	BE2_C	brain:	n/a
22	chr5:70320693-70320743	NT2-D1	testis:	n/a
23	chr5:70320693-70320743	HL-60	blood:	n/a
24	chr5:70372505-70372555	HCF	heart:	n/a
25	chr5:70372505-70372555	NT2-D1	testis:	n/a
26	chr5:70320693-70320743	Caco-2	colon:	n/a
27	chr5:70372505-70372555	HCT-116	colon:	n/a
28	chr5:70320693-70320743	GM12892	blood:	n/a
29	chr5:70372505-70372555	NHBE	bronchial:	n/a
30	chr5:70372505-70372555	HRE	kidney:	n/a
31	chr5:70372505-70372555	GM06990	blood:	n/a
32	chr5:70320693-70320743	GM12891	blood:	n/a
33	chr5:70372505-70372555	AG04450	lung:	fetal
34	chr5:70320693-70320743	BE2_C	brain:	n/a
35	chr5:70320693-70320743	NH-A	brain:	n/a
36	chr5:70372505-70372555	HUVEC	blood vessel:	n/a
37	chr5:70320693-70320743	RPTEC	kidney:	n/a
38	chr5:70320693-70320743	MCF10A-Er-Src	breast:	n/a
39	chr5:70320693-70320743	HEEpiC	esophagus:	n/a
40	chr5:70372505-70372555	SAEC	small airway:	n/a
41	chr5:70372505-70372555	T-47D	breast:	n/a
42	chr5:70372505-70372555	HCPEpiC	choroid plexus:	n/a
43	chr5:70320693-70320743	PANC-1	pancreas:	n/a
44	chr5:70372505-70372555	AG04449	skin:	fetal
45	chr5:70372505-70372555	GM12878	blood:	n/a
46	chr5:70320693-70320743	SAEC	small airway:	n/a
47	chr5:70320693-70320743	Hepatocyte	liver:	n/a
48	chr5:70372505-70372555	HMEC	breast:	n/a
49	chr5:70320693-70320743	GM19239	blood:	n/a
50	chr5:70372505-70372555	HCM	heart:	n/a

No data

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GTF2H2-7	chr5:70493473-70493614	NONHSAT102003
2	lnc-GTF2H2-1	chr5:70329997-70330227	ENSG00000254353
3	lnc-GTF2H2-7	chr5:70493473-70493608	NONHSAT102005
4	lnc-SMN1-3	chr5:70485544-70485865	NONHSAT102004
5	lnc-SMN1-2	chr5:70378669-70379081	NONHSAT101998
6	lnc-GTF2H2-7	chr5:70435716-70435861	NONHSAT102003
7	lnc-NAIP-1	chr5:70360952-70361049	NONHSAT101997
8	lnc-GTF2H2-1	chr5:70328995-70329470	ENSG00000254353
9	lnc-GTF2H2-7	chr5:70438472-70438586	NONHSAT102003
10	lnc-NAIP-1	chr5:70363123-70363465	NONHSAT101997
11	lnc-GTF2H2-7	chr5:70492974-70493188	NONHSAT102005
12	lnc-NAIP-1	chr5:70358579-70358623	NONHSAT101997

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	GTF2H2	hsa-miR-30a-5p	chr5:70331287-70331308

Variant related genes	Relation type
ENSG00000230847	TF binding region
CDH12P4	TF binding region
ENSG00000251634	TF binding region
NAIP	TF binding region
GTF2H2	TF binding region
ENSG00000254353	TF binding region
ENSG00000238451	TF binding region
GUSBP9	TF binding region
ENSG00000230847	CpG island
CDH12P4	CpG island
ENSG00000251634	CpG island
NAIP	CpG island
GTF2H2	CpG island
ENSG00000254353	CpG island
ENSG00000238451	CpG island
GUSBP9	CpG island

Extended variants
information (count: 551 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs62372685	chr5:70321111-70321112	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs555654194	chr5:70321168-70321169	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs184690763	chr5:70321191-70321192	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs188548110	chr5:70321269-70321270	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs181354082	chr5:70321276-70321277	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs574108948	chr5:70321288-70321289	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs201942662	chr5:70321434-70321435	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs541152519	chr5:70321453-70321454	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs577339246	chr5:70321515-70321516	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs199933642	chr5:70321552-70321553	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs553376014	chr5:70321594-70321595	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs201104195	chr5:70324913-70324914	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs558643763	chr5:70325097-70325098	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs143303610	chr5:70325174-70325175	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs541090441	chr5:70325249-70325250	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs374033236	chr5:70325400-70325401	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs543628351	chr5:70325472-70325473	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs146659404	chr5:70327776-70327777	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs182047991	chr5:70327783-70327784	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183796632	chr5:70329087-70329088	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs565733032	chr5:70329154-70329155	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs74915773	chr5:70329173-70329174	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs71241375	chr5:70329226-70329227	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs112400707	chr5:70329229-70329230	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs370450878	chr5:70329240-70329241	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs551361490	chr5:70329366-70329367	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs2436201	chr5:70330095-70330096	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs567751184	chr5:70330200-70330201	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs569655905	chr5:70335142-70335143	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs531279950	chr5:70335176-70335177	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs139408340	chr5:70340864-70340865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs7713504	chr5:70340990-70340991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs201660879	chr5:70341290-70341291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562434037	chr5:70341309-70341310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201224974	chr5:70341525-70341526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs556552850	chr5:70341539-70341540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs545116584	chr5:70341563-70341564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs563321384	chr5:70341667-70341668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530430548	chr5:70341722-70341723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548926275	chr5:70341730-70341731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs193116223	chr5:70341748-70341749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs528758754	chr5:70341796-70341797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546823061	chr5:70341830-70341831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs199510530	chr5:70341962-70341963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571498024	chr5:70342156-70342157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs373421426	chr5:70342222-70342223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs200479018	chr5:70342378-70342379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538793335	chr5:70342405-70342406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550663326	chr5:70342420-70342421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs569294168	chr5:70342478-70342479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:117)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
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
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ovarian cancer	21781307	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	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
Hepatocellular carcinoma	16750200	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
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
abnormal development	18461090	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21045282	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelodysplastic syndrome	18663149	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Sezary syndrome	18413736	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21990379	CNVD
Hirschsprung''s Disease	21712996	CNVD
Apoptosis	19488400	CNVD
Breast cancer	22048815	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Acute monocytic leukemia	16498392	CNVD
Colorectal cancer	20459617	CNVD
Gastric adenocarcinoma	19115996	CNVD
Spinal muscular atrophy	17160897	CNVD
Spinal muscular atrophy	17668391	CNVD
Spinal muscular atrophy	17668395	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pseudo-TORCH syndrome	20727516	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Obesity	21131291	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Autism	22549408	CNVD
Disease	19212409	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Recurrent pregnancy loss	19789632	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:70325000-70325400	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr5:70325000-70325400	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr5:70325200-70325600	Enhancers	Monocytes-CD14+_RO01746	blood
4	chr5:70325400-70327600	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr5:70325400-70327800	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr5:70325400-70327800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr5:70327600-70328000	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr5:70327800-70328000	Enhancers	Primary neutrophils fromperipheralblood	blood
9	chr5:70340200-70351400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr5:70340600-70350600	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr5:70340600-70350600	Weak transcription	Fetal Stomach	stomach
12	chr5:70340800-70350000	Weak transcription	Primary B cells from peripheral blood	blood
13	chr5:70346400-70352000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr5:70346600-70352600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr5:70347600-70352600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr5:70347800-70350800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr5:70348200-70352600	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr5:70348200-70376200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr5:70348400-70350000	Weak transcription	Primary T cells fromperipheralblood	blood
20	chr5:70348400-70350000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr5:70348400-70350800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr5:70348400-70350800	Weak transcription	Monocytes-CD14+_RO01746	blood
23	chr5:70348400-70352600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr5:70348400-70352600	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr5:70348400-70352600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr5:70348400-70354800	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr5:70348600-70351000	Weak transcription	Primary neutrophils fromperipheralblood	blood
28	chr5:70348600-70355600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr5:70348600-70355800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr5:70348600-70360400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr5:70349400-70351800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr5:70349400-70351800	Weak transcription	HMEC	breast
33	chr5:70350000-70350200	Enhancers	Fetal Intestine Small	intestine
34	chr5:70350000-70351400	Strong transcription	Primary B cells from peripheral blood	blood
35	chr5:70350000-70351400	Strong transcription	Primary T cells fromperipheralblood	blood
36	chr5:70350000-70351400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr5:70350200-70352000	Weak transcription	Fetal Intestine Small	intestine
38	chr5:70350600-70351400	Strong transcription	HUES64 Cell Line	embryonic stem cell
39	chr5:70350800-70351000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr5:70351000-70352800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr5:70351400-70353000	Weak transcription	Primary B cells from peripheral blood	blood
42	chr5:70351400-70353000	Weak transcription	Primary T cells fromperipheralblood	blood
43	chr5:70351400-70353000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr5:70351400-70356000	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr5:70392600-70395000	Weak transcription	Lung	lung
46	chr5:70392600-70395800	Weak transcription	Fetal Muscle Trunk	muscle
47	chr5:70393400-70393800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr5:70393400-70393800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr5:70393400-70400600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr5:70393600-70393800	Enhancers	HUES48 Cell Line	embryonic stem cell

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