Variant report

Variant	nsv917254
Chromosome Location	chr5:70247769-70587019
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2747)
CpG islands
(count:244)
Chromatin interactive
region (count:0)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:2747 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:70586985-70587016	HepG2	liver:	n/a	n/a
2	BATF	chr5:70541641-70542422	GM12878	blood:	n/a	n/a
3	BATF	chr5:70535000-70535215	GM12878	blood:	n/a	n/a
4	BATF	chr5:70523358-70523643	GM12878	blood:	n/a	n/a
5	BATF	chr5:70586369-70587093	GM12878	blood:	n/a	n/a
6	BATF	chr5:70555205-70555418	GM12878	blood:	n/a	n/a
7	BATF	chr5:70585691-70586274	GM12878	blood:	n/a	n/a
8	BATF	chr5:70473270-70473572	GM12878	blood:	n/a	n/a
9	BATF	chr5:70473436-70473649	GM12878	blood:	n/a	n/a
10	BATF	chr5:70575508-70575709	GM12878	blood:	n/a	chr5:70575634-70575644 chr5:70575633-70575644
11	BATF	chr5:70541131-70541377	GM12878	blood:	n/a	n/a
12	BATF	chr5:70456649-70456978	GM12878	blood:	n/a	n/a
13	BATF	chr5:70575518-70575716	GM12878	blood:	n/a	chr5:70575634-70575644 chr5:70575633-70575644
14	BATF	chr5:70581822-70582238	GM12878	blood:	n/a	n/a
15	BATF	chr5:70362121-70362600	GM12878	blood:	n/a	n/a
16	BATF	chr5:70585008-70585657	GM12878	blood:	n/a	n/a
17	BATF	chr5:70541636-70542413	GM12878	blood:	n/a	n/a
18	BATF	chr5:70544001-70544158	GM12878	blood:	n/a	n/a
19	BATF	chr5:70543154-70543357	GM12878	blood:	n/a	n/a
20	BATF	chr5:70558118-70558400	GM12878	blood:	n/a	n/a
21	BATF	chr5:70558516-70558791	GM12878	blood:	n/a	chr5:70558607-70558616
22	BATF	chr5:70538662-70539061	GM12878	blood:	n/a	n/a
23	BATF	chr5:70363039-70363251	GM12878	blood:	n/a	n/a
24	BATF	chr5:70578359-70578809	GM12878	blood:	n/a	n/a
25	BATF	chr5:70580375-70580726	GM12878	blood:	n/a	n/a
26	BATF	chr5:70545061-70545287	GM12878	blood:	n/a	n/a
27	BATF	chr5:70362170-70362374	GM12878	blood:	n/a	n/a
28	BATF	chr5:70558503-70558784	GM12878	blood:	n/a	chr5:70558607-70558616
29	BATF	chr5:70572459-70572639	GM12878	blood:	n/a	n/a
30	BATF	chr5:70574041-70574264	GM12878	blood:	n/a	n/a
31	BATF	chr5:70583052-70583325	GM12878	blood:	n/a	n/a
32	BATF	chr5:70584431-70584744	GM12878	blood:	n/a	n/a
33	BATF	chr5:70580342-70580785	GM12878	blood:	n/a	n/a
34	BATF	chr5:70539589-70539933	GM12878	blood:	n/a	n/a
35	BATF	chr5:70578302-70579195	GM12878	blood:	n/a	n/a
36	BATF	chr5:70536594-70536821	GM12878	blood:	n/a	n/a
37	BATF	chr5:70557168-70557369	GM12878	blood:	n/a	n/a
38	BATF	chr5:70505255-70505621	GM12878	blood:	n/a	n/a
39	BATF	chr5:70557586-70557801	GM12878	blood:	n/a	n/a
40	BATF	chr5:70363259-70363809	GM12878	blood:	n/a	n/a
41	BATF	chr5:70523279-70523646	GM12878	blood:	n/a	n/a
42	BATF	chr5:70557634-70557835	GM12878	blood:	n/a	n/a
43	BATF	chr5:70585975-70586260	GM12878	blood:	n/a	n/a
44	BATF	chr5:70583794-70584001	GM12878	blood:	n/a	n/a
45	BATF	chr5:70552069-70552305	GM12878	blood:	n/a	n/a
46	BATF	chr5:70582281-70582533	GM12878	blood:	n/a	n/a
47	BATF	chr5:70405611-70405957	GM12878	blood:	n/a	n/a
48	BATF	chr5:70586371-70586849	GM12878	blood:	n/a	n/a
49	BATF	chr5:70280725-70281071	GM12878	blood:	n/a	n/a
50	BATF	chr5:70505333-70505618	GM12878	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:70372505-70372555	SAEC	small airway:	n/a
2	chr5:70372505-70372555	BJ	skin:	n/a
3	chr5:70309843-70309893	AG09319	gingival:	n/a
4	chr5:70320693-70320743	HEEpiC	esophagus:	n/a
5	chr5:70308497-70308547	HCPEpiC	choroid plexus:	n/a
6	chr5:70320693-70320743	H1-hESC	embryonic stem cell:	embryo
7	chr5:70309843-70309893	HPAEpiC	pulmonary alveolar:	n/a
8	chr5:70372505-70372555	HCF	heart:	n/a
9	chr5:70309843-70309893	U87	brain:	n/a
10	chr5:70309843-70309893	HCM	heart:	n/a
11	chr5:70320693-70320743	RPTEC	kidney:	n/a
12	chr5:70308497-70308547	NHDF-neo	bronchial:	n/a
13	chr5:70372505-70372555	HCT-116	colon:	n/a
14	chr5:70320693-70320743	ECC-1	luminal epithelium:	n/a
15	chr5:70308497-70308547	HRCEpiC	kidney:	n/a
16	chr5:70309843-70309893	HepG2	liver:	n/a
17	chr5:70320693-70320743	NHDF-neo	bronchial:	n/a
18	chr5:70372505-70372555	SK-N-SH	brain:	n/a
19	chr5:70309843-70309893	HAEpiC	amniotic membrane:	n/a
20	chr5:70309843-70309893	SK-N-MC	brain:	n/a
21	chr5:70308497-70308547	NHBE	bronchial:	n/a
22	chr5:70308497-70308547	SAEC	small airway:	n/a
23	chr5:70320693-70320743	HCF	heart:	n/a
24	chr5:70372505-70372555	SK-N-SH_RA	brain:	n/a
25	chr5:70309843-70309893	PrEC	prostate:	n/a
26	chr5:70309843-70309893	PFSK-1	brain:	n/a
27	chr5:70320693-70320743	SAEC	small airway:	n/a
28	chr5:70320693-70320743	BJ	skin:	n/a
29	chr5:70308497-70308547	SK-N-SH_RA	brain:	n/a
30	chr5:70309843-70309893	NHBE	bronchial:	n/a
31	chr5:70372505-70372555	HEK293	kidney:	embryo
32	chr5:70308497-70308547	PANC-1	pancreas:	n/a
33	chr5:70372505-70372555	GM06990	blood:	n/a
34	chr5:70372505-70372555	HCPEpiC	choroid plexus:	n/a
35	chr5:70320693-70320743	PFSK-1	brain:	n/a
36	chr5:70308497-70308547	H1-hESC	embryonic stem cell:	embryo
37	chr5:70372505-70372555	HL-60	blood:	n/a
38	chr5:70309843-70309893	A549	lung:	n/a
39	chr5:70308497-70308547	PrEC	prostate:	n/a
40	chr5:70372505-70372555	PrEC	prostate:	n/a
41	chr5:70320693-70320743	ProgFib	skin:	n/a
42	chr5:70372505-70372555	SKMC	muscle:	n/a
43	chr5:70320693-70320743	HCPEpiC	choroid plexus:	n/a
44	chr5:70309843-70309893	MCF-7	breast:	n/a
45	chr5:70309843-70309893	IMR90	lung:	fetal
46	chr5:70372505-70372555	AoSMC	blood vessel:	n/a
47	chr5:70372505-70372555	HRPEpiC	eye:	n/a
48	chr5:70320693-70320743	A549	lung:	n/a
49	chr5:70309843-70309893	GM12878	blood:	n/a
50	chr5:70309843-70309893	AG04450	lung:	fetal

No data

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GTF2H2-7	chr5:70438472-70438586	NONHSAT102003
2	lnc-GTF2H2-1	chr5:70328995-70329470	ENSG00000254353
3	lnc-GTF2H2-1	chr5:70329997-70330227	ENSG00000254353
4	lnc-SMN1-3	chr5:70485544-70485865	NONHSAT102004
5	lnc-GTF2H2-6	chr5:70529887-70530059	NONHSAT102010
6	lnc-NAIP-1	chr5:70358579-70358623	NONHSAT101997
7	lnc-GTF2H2-6	chr5:70528927-70529141	NONHSAT102010
8	lnc-GTF2H2-7	chr5:70435716-70435861	NONHSAT102003
9	lnc-GTF2H2-7	chr5:70493473-70493614	NONHSAT102003
10	lnc-BDP1-5	chr5:70504655-70505021	NONHSAT102007
11	lnc-SMN1-2	chr5:70378669-70379081	NONHSAT101998
12	lnc-NAIP-1	chr5:70360952-70361049	NONHSAT101997
13	lnc-GTF2H2-5	chr5:70525720-70525924	NONHSAT102009
14	lnc-GTF2H2-7	chr5:70492974-70493188	NONHSAT102005
15	lnc-NAIP-1	chr5:70363123-70363465	NONHSAT101997
16	lnc-GTF2H2-7	chr5:70493473-70493608	NONHSAT102005

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	GTF2H2	hsa-miR-30a-5p	chr5:70331287-70331308
2	SMN2	hsa-miR-132-3p	chr5:70248617-70248638
3	SMN2	hsa-miR-186-5p	chr5:70248811-70248834
4	SMN2	hsa-miR-30a-5p	chr5:70248784-70248805

Variant related genes	Relation type
ENSG00000251634	TF binding region
NAIP	TF binding region
ENSG00000238451	TF binding region
ENSG00000254276	TF binding region
ENSG00000230847	TF binding region
ENSG00000254133	TF binding region
CDH12P4	TF binding region
GTF2H2	TF binding region
ENSG00000254353	TF binding region
ENSG00000235558	TF binding region
GUSBP9	TF binding region
ENSG00000251634	CpG island
NAIP	CpG island
ENSG00000238451	CpG island
ENSG00000254276	CpG island
ENSG00000230847	CpG island
ENSG00000254133	CpG island
CDH12P4	CpG island
GTF2H2	CpG island
ENSG00000254353	CpG island
ENSG00000235558	CpG island
GUSBP9	CpG island

Extended variants
information (count: 1039 )
Associated
traits (count: 127 )

Variant overlapped rSNPs/rCNVs (count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76163360	chr5:70247769-70247770	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs368899583	chr5:70247797-70247798	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs187925143	chr5:70247798-70247799	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs577891293	chr5:70247841-70247842	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs544954304	chr5:70247853-70247854	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs143838139	chr5:70247901-70247902	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs530720159	chr5:70247934-70247935	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs200563560	chr5:70247937-70247938	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs542796385	chr5:70247944-70247945	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs560975018	chr5:70247945-70247946	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs528159367	chr5:70247946-70247947	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs546594138	chr5:70248020-70248021	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs571132285	chr5:70248032-70248033	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs147714462	chr5:70248060-70248061	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs199757161	chr5:70248108-70248109	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs368877148	chr5:70248109-70248110	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs550983818	chr5:70248162-70248163	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs577919667	chr5:70248165-70248166	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs569157372	chr5:70248236-70248237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536454213	chr5:70248250-70248251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs554705316	chr5:70248292-70248293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566640154	chr5:70248337-70248338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs200800214	chr5:70248472-70248473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2457869	chr5:70249068-70249069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558939374	chr5:70249079-70249080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs76540811	chr5:70249102-70249103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577154106	chr5:70249107-70249108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs138733257	chr5:70249110-70249111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs563483368	chr5:70250537-70250538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs542397933	chr5:70250553-70250554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200261532	chr5:70250640-70250641	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575569227	chr5:70250667-70250668	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542859628	chr5:70250675-70250676	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs76649276	chr5:70250730-70250731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs561033887	chr5:70250767-70250768	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs530911542	chr5:70250857-70250858	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs367802698	chr5:70250881-70250882	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs528215527	chr5:70250899-70250900	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs539933002	chr5:70250907-70250908	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564933582	chr5:70251061-70251062	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs62372678	chr5:70251118-70251119	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs532010301	chr5:70251254-70251255	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550505462	chr5:70251484-70251485	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs137941972	chr5:70251499-70251500	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs569221554	chr5:70251561-70251562	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530298016	chr5:70252528-70252529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs212203	chr5:70252538-70252539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs548396854	chr5:70252613-70252614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs111517196	chr5:70252750-70252751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs531459148	chr5:70253131-70253132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:127)

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
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	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
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
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
Mental retardation	20877625	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Spinal muscular atrophy	17647030	CNVD
Spinal muscular atrophy	20937953	CNVD
Spinal muscular atrophy	20442745	CNVD
Spinal muscular atrophy	21227393	CNVD
Autism	21865298	CNVD
Breast cancer	22522925	CNVD
Autism	22549408	CNVD
Disease	19212409	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Recurrent pregnancy loss	19789632	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:176 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:70238000-70257800	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr5:70239000-70252400	Weak transcription	Liver	Liver
3	chr5:70239400-70252000	Weak transcription	Primary T helper cells PMA-I stimulated	--
4	chr5:70244400-70253000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr5:70244600-70250800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr5:70244800-70256200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr5:70245000-70253000	Weak transcription	Fetal Intestine Small	intestine
8	chr5:70245000-70257600	Weak transcription	Fetal Stomach	stomach
9	chr5:70245200-70250600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr5:70245200-70250800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr5:70245200-70258200	Weak transcription	Fetal Thymus	thymus
12	chr5:70245400-70252600	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr5:70246400-70252400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr5:70246400-70252800	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr5:70246400-70256000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr5:70246400-70258200	Weak transcription	Primary T helper cells fromperipheralblood	blood
17	chr5:70246600-70252800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr5:70247000-70259600	Weak transcription	Fetal Muscle Leg	muscle
19	chr5:70247600-70248200	Strong transcription	HUES64 Cell Line	embryonic stem cell
20	chr5:70247600-70250800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr5:70247600-70253000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr5:70247800-70248200	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr5:70247800-70248200	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr5:70248200-70251600	Weak transcription	Monocytes-CD14+_RO01746	blood
25	chr5:70248200-70256800	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr5:70248600-70251000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr5:70248600-70251400	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr5:70248600-70251400	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr5:70248600-70251400	Weak transcription	Thymus	Thymus
30	chr5:70249000-70250800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr5:70249200-70258200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr5:70249200-70266400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr5:70249400-70257600	Weak transcription	Dnd41	blood
34	chr5:70249600-70257800	Weak transcription	Stomach Smooth Muscle	stomach
35	chr5:70249800-70252200	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr5:70249800-70252200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
37	chr5:70249800-70252200	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr5:70249800-70252200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr5:70250600-70251600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr5:70250800-70251000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr5:70250800-70251000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr5:70250800-70251200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr5:70250800-70251200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr5:70251000-70251200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr5:70251000-70251600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr5:70251200-70251600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr5:70251200-70257800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr5:70251600-70256600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr5:70256600-70256800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr5:70273600-70276000	Weak transcription	Primary monocytes fromperipheralblood	blood

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