Variant report

Variant	nsv1031941
Chromosome Location	chr5:70654060-70710447
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:207)
CpG islands
(count:183)
Chromatin interactive
region (count:0)
LncRNA
region (count:38)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:207 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:70680601-70681425	K562	blood:	n/a	n/a
2	ARID3A	chr5:70684142-70684593	K562	blood:	n/a	n/a
3	ATF1	chr5:70681067-70681385	K562	blood:	n/a	n/a
4	ATF1	chr5:70684123-70684476	K562	blood:	n/a	n/a
5	ATF3	chr5:70684188-70684378	K562	blood:	n/a	n/a
6	ATF3	chr5:70684044-70684532	K562	blood:	n/a	n/a
7	ATF3	chr5:70681028-70681425	K562	blood:	n/a	n/a
8	BHLHE40	chr5:70684143-70684361	K562	blood:	n/a	n/a
9	BHLHE40	chr5:70681145-70681372	K562	blood:	n/a	n/a
10	CBX3	chr5:70681091-70681532	K562	blood:	n/a	n/a
11	CCNT2	chr5:70681162-70681370	K562	blood:	n/a	n/a
12	CEBPB	chr5:70681020-70681421	K562	blood:	n/a	n/a
13	CEBPB	chr5:70684002-70684402	K562	blood:	n/a	chr5:70684074-70684085
14	CEBPB	chr5:70681033-70681389	K562	blood:	n/a	n/a
15	CEBPB	chr5:70680044-70680325	K562	blood:	n/a	chr5:70680207-70680218
16	CEBPB	chr5:70683968-70684224	IMR90	lung:	n/a	chr5:70684074-70684085 chr5:70683969-70683982
17	CEBPB	chr5:70705347-70705398	K562	blood:	n/a	n/a
18	CEBPB	chr5:70683919-70684546	K562	blood:	n/a	chr5:70684074-70684085 chr5:70683969-70683982
19	CEBPB	chr5:70656741-70656969	K562	blood:	n/a	chr5:70656854-70656867 chr5:70656926-70656937 chr5:70656854-70656865 chr5:70656854-70656867
20	CEBPB	chr5:70684029-70684323	Hela-S3	cervix:	n/a	chr5:70684074-70684085
21	CEBPB	chr5:70681065-70681367	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr5:70683952-70684467	K562	blood:	n/a	chr5:70684074-70684085 chr5:70683969-70683982
23	CEBPB	chr5:70680937-70681529	K562	blood:	n/a	n/a
24	CEBPB	chr5:70680010-70680377	K562	blood:	n/a	chr5:70680207-70680218
25	CEBPB	chr5:70680058-70680274	HepG2	liver:	n/a	chr5:70680207-70680218
26	CEBPB	chr5:70684020-70684344	A549	lung:	n/a	chr5:70684074-70684085
27	CEBPB	chr5:70680047-70680298	Hela-S3	cervix:	n/a	chr5:70680207-70680218
28	CEBPB	chr5:70683982-70684232	HepG2	liver:	n/a	chr5:70684074-70684085
29	CEBPD	chr5:70680467-70681533	K562	blood:	n/a	n/a
30	CEBPD	chr5:70683932-70684625	K562	blood:	n/a	n/a
31	CEBPD	chr5:70681041-70681482	K562	blood:	n/a	n/a
32	CTCF	chr5:70691275-70691350	GM13977	blood:	n/a	n/a
33	CTCF	chr5:70665016-70665045	GM13976	blood:	n/a	n/a
34	CTCF	chr5:70670066-70670106	MCF-7	breast:	n/a	n/a
35	CTCF	chr5:70673755-70673833	Medullo	brain:	n/a	n/a
36	CTCF	chr5:70681792-70681882	Spleen_OC	spleen:	n/a	n/a
37	CTCF	chr5:70675168-70675250	GM13976	blood:	n/a	n/a
38	CTCF	chr5:70658941-70658981	Medullo	brain:	n/a	n/a
39	CTCF	chr5:70659007-70659110	Medullo	brain:	n/a	n/a
40	CTCF	chr5:70698400-70698442	GM20000	blood:	n/a	n/a
41	CUX1	chr5:70680746-70680750	K562	blood:	n/a	n/a
42	CUX1	chr5:70681070-70681353	K562	blood:	n/a	n/a
43	CUX1	chr5:70684147-70684467	K562	blood:	n/a	n/a
44	EP300	chr5:70681163-70681368	K562	blood:	n/a	n/a
45	EP300	chr5:70684107-70684506	K562	blood:	n/a	n/a
46	EP300	chr5:70680560-70681533	K562	blood:	n/a	n/a
47	FOSL1	chr5:70681098-70681339	K562	blood:	n/a	n/a
48	FOXP2	chr5:70668703-70669005	SK-N-MC	brain:	n/a	n/a
49	GABPA	chr5:70681034-70681427	K562	blood:	n/a	n/a
50	GABPA	chr5:70684184-70684373	K562	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	chr5:70670374-70670424	HRPEpiC	eye:	n/a
2	chr5:70671179-70671229	MCF-7	breast:	n/a
3	chr5:70671764-70671814	AG04449	skin:	fetal
4	chr5:70671179-70671229	HNPCEpiC	eye:	n/a
5	chr5:70670374-70670424	GM12878	blood:	n/a
6	chr5:70671179-70671229	HepG2	liver:	n/a
7	chr5:70671179-70671229	LNCaP	prostate:	n/a
8	chr5:70671764-70671814	ECC-1	luminal epithelium:	n/a
9	chr5:70671179-70671229	SKMC	muscle:	n/a
10	chr5:70671764-70671814	CMK	blood:	n/a
11	chr5:70671764-70671814	HAEpiC	amniotic membrane:	n/a
12	chr5:70671764-70671814	Hela-S3	cervix:	n/a
13	chr5:70670374-70670424	AG09319	gingival:	n/a
14	chr5:70670374-70670424	HUVEC	blood vessel:	n/a
15	chr5:70671764-70671814	MCF10A-Er-Src	breast:	n/a
16	chr5:70671764-70671814	H1-hESC	embryonic stem cell:	embryo
17	chr5:70671764-70671814	SKMC	muscle:	n/a
18	chr5:70671179-70671229	SK-N-SH	brain:	n/a
19	chr5:70671179-70671229	A549	lung:	n/a
20	chr5:70671764-70671814	ProgFib	skin:	n/a
21	chr5:70671764-70671814	PrEC	prostate:	n/a
22	chr5:70671764-70671814	AG09319	gingival:	n/a
23	chr5:70671764-70671814	NB4	blood:	n/a
24	chr5:70671764-70671814	HCPEpiC	choroid plexus:	n/a
25	chr5:70670374-70670424	H1-hESC	embryonic stem cell:	embryo
26	chr5:70670374-70670424	PANC-1	pancreas:	n/a
27	chr5:70671179-70671229	HCM	heart:	n/a
28	chr5:70670374-70670424	HMEC	breast:	n/a
29	chr5:70670374-70670424	CMK	blood:	n/a
30	chr5:70670374-70670424	AG04450	lung:	fetal
31	chr5:70670374-70670424	AG09309	skin:	n/a
32	chr5:70671179-70671229	IMR90	lung:	fetal
33	chr5:70671179-70671229	HMEC	breast:	n/a
34	chr5:70670374-70670424	HRCEpiC	kidney:	n/a
35	chr5:70671179-70671229	AG10803	skin:	n/a
36	chr5:70671179-70671229	AG09319	gingival:	n/a
37	chr5:70670374-70670424	ovcar-3	ovarian:	n/a
38	chr5:70671179-70671229	HRE	kidney:	n/a
39	chr5:70671179-70671229	HAEpiC	amniotic membrane:	n/a
40	chr5:70670374-70670424	Hepatocyte	liver:	n/a
41	chr5:70670374-70670424	ProgFib	skin:	n/a
42	chr5:70671179-70671229	Hepatocyte	liver:	n/a
43	chr5:70671179-70671229	BJ	skin:	n/a
44	chr5:70670374-70670424	HL-60	blood:	n/a
45	chr5:70671179-70671229	HL-60	blood:	n/a
46	chr5:70671764-70671814	Caco-2	colon:	n/a
47	chr5:70670374-70670424	Hela-S3	cervix:	n/a
48	chr5:70671179-70671229	MCF10A-Er-Src	breast:	n/a
49	chr5:70671179-70671229	GM06990	blood:	n/a
50	chr5:70671764-70671814	BJ	skin:	n/a

No data

(count:38 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GTF2H2-2	chr5:70670666-70670725	ENSG00000253985
2	lnc-BDP1-3	chr5:70707870-70709163	NONHSAT102021
3	lnc-BDP1-4	chr5:70681643-70681819	NONHSAT102017
4	lnc-BDP1-4	chr5:70674302-70674445	NONHSAT102014
5	lnc-BDP1-4	chr5:70673331-70673407	NONHSAT102019
6	lnc-BDP1-4	chr5:70672114-70673407	NONHSAT102018
7	lnc-BDP1-3	chr5:70709089-70709163	NONHSAT102022
8	lnc-BDP1-4	chr5:70674302-70674445	NONHSAT102017
9	lnc-BDP1-4	chr5:70671612-70671843	NONHSAT102015
10	lnc-BDP1-4	chr5:70681643-70681819	NONHSAT102014
11	lnc-BDP1-4	chr5:70681643-70681819	NONHSAT102015
12	lnc-BDP1-4	chr5:70671612-70671843	NONHSAT102016
13	lnc-GTF2H2-9	chr5:70683438-70685506	ucscGeneNc_uc010iyu_1
14	lnc-BDP1-3	chr5:70707369-70707599	NONHSAT102021
15	lnc-BDP1-4	chr5:70681123-70681215	NONHSAT102015
16	lnc-GTF2H2-2	chr5:70668503-70668856	ENSG00000253985
17	lnc-BDP1-4	chr5:70681643-70681820	NONHSAT102016
18	lnc-BDP1-4	chr5:70674302-70674445	NONHSAT102015
19	lnc-BDP1-4	chr5:70681123-70681260	NONHSAT102016
20	lnc-BDP1-4	chr5:70681368-70681621	NONHSAT102018
21	lnc-GTF2H2-2	chr5:70670423-70670509	ENSG00000253985
22	lnc-BDP1-4	chr5:70681157-70681260	NONHSAT102014
23	lnc-BDP1-4	chr5:70673333-70673407	NONHSAT102017
24	lnc-BDP1-3	chr5:70709089-70709163	NONHSAT102025
25	lnc-BDP1-3	chr5:70707369-70707599	NONHSAT102025
26	lnc-BDP1-4	chr5:70681123-70681260	NONHSAT102018
27	lnc-BDP1-3	chr5:70707369-70707599	NONHSAT102022
28	lnc-BDP1-3	chr5:70707870-70709163	NONHSAT102023
29	lnc-BDP1-3	chr5:70709089-70709163	NONHSAT102024
30	lnc-BDP1-4	chr5:70671612-70671843	NONHSAT102017
31	lnc-BDP1-4	chr5:70674302-70675060	NONHSAT102019
32	lnc-BDP1-3	chr5:70707369-70707599	NONHSAT102023
33	lnc-BDP1-4	chr5:70673333-70673407	NONHSAT102014
34	lnc-BDP1-3	chr5:70707369-70707599	NONHSAT102024
35	lnc-BDP1-4	chr5:70671612-70671843	NONHSAT102014
36	lnc-BDP1-4	chr5:70671613-70671843	NONHSAT102018
37	lnc-BDP1-4	chr5:70673333-70673407	NONHSAT102015
38	lnc-BDP1-4	chr5:70672114-70673407	NONHSAT102016

No data

Variant related genes	Relation type
ENSG00000253985	TF binding region
ENSG00000265132	TF binding region
PMCHL2	TF binding region
ENSG00000253985	CpG island
ENSG00000265132	CpG island
PMCHL2	CpG island

Extended variants
information (count: 968 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:968 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551264439	chr5:70663248-70663249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs568711469	chr5:70663320-70663321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs536240589	chr5:70663328-70663329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs547916433	chr5:70663419-70663420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs566554905	chr5:70663494-70663495	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs533899559	chr5:70663513-70663514	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs558754760	chr5:70663551-70663552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs532389145	chr5:70663556-70663557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs570678126	chr5:70663570-70663571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs537710639	chr5:70663601-70663602	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs187041462	chr5:70663669-70663670	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs141996099	chr5:70663683-70663684	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs192955029	chr5:70663719-70663720	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs372431249	chr5:70663739-70663740	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200931420	chr5:70663780-70663781	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs562436594	chr5:70663870-70663871	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs554578577	chr5:70663917-70663918	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs572979350	chr5:70663925-70663926	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs540345069	chr5:70663985-70663986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565096719	chr5:70664226-70664227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs532742451	chr5:70664427-70664428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs544525028	chr5:70664429-70664430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs550792831	chr5:70664446-70664447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs563185836	chr5:70664453-70664454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs148319299	chr5:70664503-70664504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs376634147	chr5:70664555-70664556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs530358845	chr5:70664645-70664646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs10057058	chr5:70664663-70664664	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
29	rs566494322	chr5:70664689-70664690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs562606858	chr5:70664698-70664699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs529715760	chr5:70664699-70664700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs527350728	chr5:70664744-70664745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs148186959	chr5:70664745-70664746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs570615854	chr5:70664859-70664860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs184119681	chr5:70664892-70664893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs7712480	chr5:70664918-70664919	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
37	rs556127157	chr5:70665023-70665024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs189489122	chr5:70665043-70665044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs535412135	chr5:70665100-70665101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs376882458	chr5:70665109-70665110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182051673	chr5:70665271-70665272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184858804	chr5:70665342-70665343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs572910357	chr5:70665394-70665395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540281907	chr5:70665408-70665409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558622519	chr5:70665416-70665417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs577306587	chr5:70665428-70665429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs115216147	chr5:70665526-70665527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs562966518	chr5:70665560-70665561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs59966095	chr5:70665606-70665607	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs542552287	chr5:70665623-70665624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

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
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
Pancreatic ductal adenocarcinoma	19077451	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:101 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:70663200-70663600	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr5:70663400-70664600	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr5:70663600-70664000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr5:70664000-70664600	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr5:70664200-70664600	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr5:70664600-70669200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr5:70667400-70667600	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr5:70667600-70668600	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr5:70668400-70670200	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr5:70668600-70669200	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr5:70669200-70669800	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr5:70680000-70681000	Enhancers	K562	blood
13	chr5:70680200-70680600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr5:70680600-70680800	Enhancers	Fetal Lung	lung
15	chr5:70680600-70681600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr5:70681000-70682000	Weak transcription	K562	blood
17	chr5:70682000-70682400	Enhancers	K562	blood
18	chr5:70682200-70682400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr5:70682400-70684000	Weak transcription	K562	blood
20	chr5:70683800-70684400	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr5:70684000-70684600	Enhancers	K562	blood
22	chr5:70684200-70684600	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr5:70686000-70686200	Enhancers	Pancreatic Islets	Pancreatic Islet
24	chr5:70686000-70686400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr5:70686000-70686400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr5:70686200-70687000	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr5:70686400-70688200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr5:70687000-70687200	Enhancers	Pancreatic Islets	Pancreatic Islet
29	chr5:70687200-70687600	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr5:70687600-70688400	Active TSS	Pancreatic Islets	Pancreatic Islet
31	chr5:70688200-70688600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr5:70693600-70693800	Enhancers	H1 Cell Line	embryonic stem cell
33	chr5:70693600-70694400	Active TSS	Brain Anterior Caudate	brain
34	chr5:70693600-70694600	Active TSS	Brain Inferior Temporal Lobe	brain
35	chr5:70693600-70694800	Active TSS	Pancreatic Islets	Pancreatic Islet
36	chr5:70693800-70694400	Active TSS	Brain Cingulate Gyrus	brain
37	chr5:70693800-70694400	Active TSS	Brain Substantia Nigra	brain
38	chr5:70693800-70694600	Active TSS	Brain Angular Gyrus	brain
39	chr5:70694200-70694400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr5:70694400-70694600	Enhancers	H1 Cell Line	embryonic stem cell
41	chr5:70694400-70694600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr5:70694400-70694600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr5:70694400-70694600	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr5:70694400-70694600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr5:70694400-70694600	Flanking Active TSS	Brain Anterior Caudate	brain
46	chr5:70694400-70694600	Flanking Active TSS	Brain Cingulate Gyrus	brain
47	chr5:70694400-70694600	Flanking Active TSS	Brain Substantia Nigra	brain
48	chr5:70694400-70694600	Active TSS	Fetal Brain Male	brain
49	chr5:70694400-70694800	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr5:70694400-70694800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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