Variant report

Variant	nsv1029145
Chromosome Location	chr5:57905821-58141221
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:912)
CpG islands
(count:244)
Chromatin interactive
region (count:31)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:912 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:58034173-58034665	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:58057374-58057701	HepG2	liver:	n/a	n/a
3	ATF2	chr5:58090684-58091046	GM12878	blood:	n/a	n/a
4	ATF2	chr5:58013442-58013904	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr5:58096289-58096534	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr5:57983542-57983702	H1-hESC	embryonic stem cell:	n/a	chr5:57983613-57983627
7	BACH1	chr5:58013386-58013817	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr5:58115092-58115266	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr5:58017951-58018378	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr5:58029295-58029345	K562	blood:	n/a	n/a
11	BATF	chr5:58071564-58071928	GM12878	blood:	n/a	n/a
12	BATF	chr5:58055568-58055929	GM12878	blood:	n/a	chr5:58055673-58055683
13	BATF	chr5:58071624-58071944	GM12878	blood:	n/a	n/a
14	BATF	chr5:58081934-58082186	GM12878	blood:	n/a	chr5:58082060-58082071
15	BATF	chr5:58055514-58055951	GM12878	blood:	n/a	chr5:58055673-58055683
16	BCL11A	chr5:58055536-58055881	GM12878	blood:	n/a	chr5:58055675-58055684 chr5:58055676-58055685
17	BCL11A	chr5:58012637-58012872	GM12878	blood:	n/a	n/a
18	BCL3	chr5:58047064-58047342	GM12878	blood:	n/a	n/a
19	BCL3	chr5:58090770-58091027	GM12878	blood:	n/a	n/a
20	BCL3	chr5:58047096-58047373	GM12878	blood:	n/a	n/a
21	BHLHE40	chr5:58090220-58090373	GM12878	blood:	n/a	n/a
22	BHLHE40	chr5:57977856-57978047	GM12878	blood:	n/a	n/a
23	BHLHE40	chr5:58012650-58012921	GM12878	blood:	n/a	n/a
24	BRCA1	chr5:58126912-58126937	GM12878	blood:	n/a	n/a
25	CEBPB	chr5:58043427-58043489	Hela-S3	cervix:	n/a	chr5:58043466-58043475 chr5:58043464-58043477 chr5:58043466-58043475 chr5:58043466-58043477 chr5:58043464-58043477 chr5:58043466-58043475 chr5:58043464-58043475 chr5:58043466-58043475
26	CEBPB	chr5:58109690-58110047	HepG2	liver:	n/a	chr5:58109865-58109878
27	CEBPB	chr5:58005664-58005888	A549	lung:	n/a	n/a
28	CEBPB	chr5:58138665-58139156	A549	lung:	n/a	n/a
29	CEBPB	chr5:58031615-58032039	HepG2	liver:	n/a	chr5:58031989-58032000 chr5:58031761-58031769 chr5:58031745-58031758
30	CEBPB	chr5:57977264-57977326	H1-hESC	embryonic stem cell:	n/a	chr5:57977312-57977323 chr5:57977311-57977324
31	CEBPB	chr5:58109704-58110030	IMR90	lung:	n/a	chr5:58109865-58109878
32	CEBPB	chr5:58109689-58110030	MCF-7	breast:	n/a	chr5:58109865-58109878
33	CEBPB	chr5:57985048-57985248	A549	lung:	n/a	chr5:57985129-57985140
34	CEBPB	chr5:57954859-57954925	IMR90	lung:	n/a	n/a
35	CEBPB	chr5:57977198-57977419	HepG2	liver:	n/a	chr5:57977312-57977323 chr5:57977311-57977324
36	CEBPB	chr5:58121369-58121571	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr5:57964600-57964818	IMR90	lung:	n/a	n/a
38	CEBPB	chr5:57954497-57954774	HepG2	liver:	n/a	chr5:57954631-57954642 chr5:57954594-57954605
39	CEBPB	chr5:58140698-58140863	A549	lung:	n/a	chr5:58140760-58140773 chr5:58140760-58140771
40	CEBPB	chr5:57969423-57969677	HepG2	liver:	n/a	chr5:57969576-57969587
41	CEBPB	chr5:58098318-58098522	HepG2	liver:	n/a	chr5:58098402-58098413 chr5:58098455-58098463
42	CEBPB	chr5:58140237-58140622	MCF-7	breast:	n/a	n/a
43	CEBPB	chr5:58122574-58122761	Hela-S3	cervix:	n/a	chr5:58122653-58122662 chr5:58122651-58122664 chr5:58122652-58122663
44	CEBPB	chr5:58098393-58098471	A549	lung:	n/a	chr5:58098402-58098413 chr5:58098455-58098463
45	CEBPB	chr5:58002457-58002657	HepG2	liver:	n/a	chr5:58002507-58002518
46	CEBPB	chr5:58109694-58110029	A549	lung:	n/a	chr5:58109865-58109878
47	CEBPB	chr5:58013491-58013836	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr5:57964544-57964862	HepG2	liver:	n/a	n/a
49	CEBPB	chr5:58109710-58109990	Hela-S3	cervix:	n/a	chr5:58109865-58109878
50	CEBPB	chr5:58096994-58097294	A549	lung:	n/a	chr5:58097157-58097168

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:58082727-58082777	HRE	kidney:	n/a
2	chr5:58082800-58082850	MCF-7	breast:	n/a
3	chr5:57925482-57925532	GM19239	blood:	n/a
4	chr5:58082800-58082850	HCPEpiC	choroid plexus:	n/a
5	chr5:58082800-58082850	A549	lung:	n/a
6	chr5:57925482-57925532	CMK	blood:	n/a
7	chr5:58096519-58096569	Caco-2	colon:	n/a
8	chr5:58082800-58082850	NB4	blood:	n/a
9	chr5:58096519-58096569	Hepatocyte	liver:	n/a
10	chr5:58096519-58096569	MCF-7	breast:	n/a
11	chr5:58096519-58096569	IMR90	lung:	fetal
12	chr5:58096519-58096569	HepG2	liver:	n/a
13	chr5:58082800-58082850	GM19239	blood:	n/a
14	chr5:58096519-58096569	HMEC	breast:	n/a
15	chr5:58082800-58082850	GM12878	blood:	n/a
16	chr5:58082800-58082850	HL-60	blood:	n/a
17	chr5:58096519-58096569	H1-hESC	embryonic stem cell:	embryo
18	chr5:58082800-58082850	AG04450	lung:	fetal
19	chr5:58082800-58082850	K562	blood:	n/a
20	chr5:58096519-58096569	HNPCEpiC	eye:	n/a
21	chr5:58082727-58082777	AG04450	lung:	fetal
22	chr5:58096519-58096569	HCPEpiC	choroid plexus:	n/a
23	chr5:58082727-58082777	Hepatocyte	liver:	n/a
24	chr5:57925482-57925532	AG10803	skin:	n/a
25	chr5:58096519-58096569	HEK293	kidney:	embryo
26	chr5:58082727-58082777	HEK293	kidney:	embryo
27	chr5:58096519-58096569	GM19239	blood:	n/a
28	chr5:58096519-58096569	CMK	blood:	n/a
29	chr5:58082727-58082777	NHBE	bronchial:	n/a
30	chr5:57925482-57925532	AoSMC	blood vessel:	n/a
31	chr5:58082727-58082777	Caco-2	colon:	n/a
32	chr5:57925482-57925532	Jurkat	blood:	n/a
33	chr5:58096519-58096569	SK-N-MC	brain:	n/a
34	chr5:58082800-58082850	HRPEpiC	eye:	n/a
35	chr5:58082800-58082850	HAEpiC	amniotic membrane:	n/a
36	chr5:58082800-58082850	BE2_C	brain:	n/a
37	chr5:57925482-57925532	ECC-1	luminal epithelium:	n/a
38	chr5:57925482-57925532	PANC-1	pancreas:	n/a
39	chr5:58082727-58082777	ECC-1	luminal epithelium:	n/a
40	chr5:57925482-57925532	GM12878	blood:	n/a
41	chr5:57925482-57925532	HUVEC	blood vessel:	n/a
42	chr5:58096519-58096569	HL-60	blood:	n/a
43	chr5:58096519-58096569	HRE	kidney:	n/a
44	chr5:58082727-58082777	HEEpiC	esophagus:	n/a
45	chr5:58082727-58082777	NH-A	brain:	n/a
46	chr5:58096519-58096569	U87	brain:	n/a
47	chr5:57925482-57925532	SAEC	small airway:	n/a
48	chr5:58082727-58082777	HCT-116	colon:	n/a
49	chr5:58082800-58082850	HepG2	liver:	n/a
50	chr5:58082800-58082850	SKMC	muscle:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:57920138..57921757-chr5:58071419..58073943,2	K562	blood:
2	chr5:57794206..57795033-chr5:58012774..58013560,4	MCF-7	breast:
3	chr5:58101554..58104220-chr5:58106207..58108235,2	K562	blood:
4	chr5:57932028..57933873-chr5:57935161..57938695,3	K562	blood:
5	chr5:57946400..57947922-chr5:58037144..58039712,2	K562	blood:
6	chr5:58001489..58004314-chr5:58005059..58006816,2	MCF-7	breast:
7	chr5:58065303..58068063-chr5:58070867..58073757,2	K562	blood:
8	chr5:58104982..58107927-chr5:58108105..58110860,2	K562	blood:
9	chr5:57946400..57947922-chr5:58037144..58039712,2	K562	blood:
10	chr14:54976700..54977279-chr5:58013417..58014233,2	MCF-7	breast:
11	chr5:57932028..57933873-chr5:57935161..57938695,3	K562	blood:
12	chr5:57920138..57921757-chr5:58071419..58073943,2	K562	blood:
13	chr5:57797123..57798291-chr5:58108900..58109754,3	MCF-7	breast:
14	chr5:58090787..58092872-chr5:58094144..58096762,2	K562	blood:
15	chr5:58075819..58077953-chr5:58081872..58085394,3	K562	blood:
16	chr5:58090787..58092872-chr5:58094144..58096762,2	K562	blood:
17	chr5:58022097..58023766-chr5:58024865..58027239,2	K562	blood:
18	chr5:58101554..58104220-chr5:58106207..58108235,2	K562	blood:
19	chr5:58060694..58062677-chr5:58063178..58064752,2	MCF-7	breast:
20	chr5:58065303..58068063-chr5:58070867..58073757,2	K562	blood:
21	chr5:58125945..58128696-chr5:58136309..58138886,2	MCF-7	breast:
22	chr5:57793931..57794799-chr5:58108780..58109770,6	MCF-7	breast:
23	chr15:50124105..50124982-chr5:57921872..57922373,2	MCF-7	breast:
24	chr5:58001489..58004314-chr5:58005059..58006816,2	MCF-7	breast:
25	chr5:58125945..58128696-chr5:58136309..58138886,2	MCF-7	breast:
26	chr5:58104982..58107927-chr5:58108105..58110860,2	K562	blood:
27	chr5:58060694..58062677-chr5:58063178..58064752,2	MCF-7	breast:
28	chr5:58022097..58023766-chr5:58024865..58027239,2	K562	blood:
29	chr5:57798012..57798630-chr5:58109216..58109808,2	MCF-7	breast:
30	chr5:57931843..57934379-chr5:57955747..57957509,2	K562	blood:
31	chr5:57931843..57934379-chr5:57955747..57957509,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GAPT-6	chr5:58119397-58119541	NONHSAT101620
2	lnc-CTD-2117L12.1.1-1	chr5:58037408-58037827	ENSG00000248475.1
3	lnc-CTD-2117L12.1.1-1	chr5:58112871-58112926	ENSG00000248475.1
4	lnc-CTD-2117L12.1.1-1	chr5:58080551-58080606	ENSG00000248475.1
5	lnc-CTD-2117L12.1.1-1	chr5:58111561-58111639	ENSG00000248475.1
6	lnc-CTD-2117L12.1.1-1	chr5:58110487-58110572	ENSG00000248475.1
7	lnc-GAPT-6	chr5:58118330-58119081	NONHSAT101620
8	lnc-CTD-2117L12.1.1-1	chr5:58037408-58037827	ENSG00000248475.1

No data

Variant related genes	Relation type
ENSG00000248475	TF binding region
RPL5P15	TF binding region
RAB3C	TF binding region
ENSG00000248475	CpG island
RPL5P15	CpG island
RAB3C	CpG island
ENSG00000100532	chromatin interactions
ENSG00000152932	chromatin interactions

Extended variants
information (count: 7371 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:7371 , 50 per page) page: 1 2 3 4 5 6 7 ... 148

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138613624	chr5:57911643-57911644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs571570632	chr5:57911665-57911666	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs114483786	chr5:57911675-57911676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs292969	chr5:57911704-57911705	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs561798215	chr5:57911705-57911706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs558199138	chr5:57911715-57911716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs529366061	chr5:57911732-57911733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs190029072	chr5:57911748-57911749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs192269899	chr5:57911778-57911779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs570142966	chr5:57911796-57911797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs71604753	chr5:57911812-57911813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs58004467	chr5:57911838-57911839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs292970	chr5:57911848-57911849	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs75982113	chr5:57911858-57911859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs555917437	chr5:57911902-57911903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs16877131	chr5:57911904-57911905	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs566650052	chr5:57911921-57911922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs527455176	chr5:57911947-57911948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs141132313	chr5:57911966-57911967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs568796952	chr5:57912031-57912032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs376609905	chr5:57912043-57912044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs74948611	chr5:57912050-57912051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs150724472	chr5:57912059-57912060	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs184504219	chr5:57912076-57912077	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs292971	chr5:57912077-57912078	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs540126303	chr5:57912101-57912102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs373422326	chr5:57912108-57912109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs75035995	chr5:57912152-57912153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs573493140	chr5:57912155-57912156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs78746112	chr5:57912619-57912620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs113312559	chr5:57912653-57912654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs549168828	chr5:57912654-57912655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs561092640	chr5:57912672-57912673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs531416804	chr5:57912677-57912678	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs549939343	chr5:57912678-57912679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs571324733	chr5:57912683-57912684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs544586046	chr5:57912693-57912694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs547387642	chr5:57912694-57912695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs139385620	chr5:57912717-57912718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs562974452	chr5:57912736-57912737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs73759508	chr5:57912763-57912764	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs374133685	chr5:57912774-57912775	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs181947600	chr5:57912820-57912821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs185738282	chr5:57912856-57912857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs537946891	chr5:57912868-57912869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs556335814	chr5:57912880-57912881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs200828027	chr5:57912883-57912884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs145229305	chr5:57912885-57912886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs578056563	chr5:57912890-57912891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs545039079	chr5:57912891-57912892	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

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
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
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
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Acute myeloid leukemia	20729466	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
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Cancer	20164920	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:809 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:57911600-57912200	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr5:57912600-57913400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr5:57912600-57913400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr5:57913000-57913600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr5:57913200-57913600	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr5:57913200-57914000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr5:57913400-57913800	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr5:57913400-57919200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr5:57913600-57919000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr5:57914000-57918200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr5:57917200-57919000	Weak transcription	Fetal Brain Male	brain
12	chr5:57917600-57918400	Enhancers	Ovary	ovary
13	chr5:57917800-57918200	Enhancers	Fetal Intestine Small	intestine
14	chr5:57917800-57918400	Enhancers	Fetal Stomach	stomach
15	chr5:57917800-57918400	Enhancers	Small Intestine	intestine
16	chr5:57917800-57919200	Enhancers	Stomach Mucosa	stomach
17	chr5:57918000-57919600	Enhancers	Left Ventricle	heart
18	chr5:57918000-57919800	Enhancers	Fetal Lung	lung
19	chr5:57918400-57918800	Weak transcription	Fetal Stomach	stomach
20	chr5:57918400-57918800	Weak transcription	Ovary	ovary
21	chr5:57918400-57924400	Weak transcription	Small Intestine	intestine
22	chr5:57918600-57919800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr5:57918800-57919800	Enhancers	Ovary	ovary
24	chr5:57918800-57920200	Enhancers	Fetal Stomach	stomach
25	chr5:57919000-57919200	Enhancers	Right Atrium	heart
26	chr5:57919000-57919400	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr5:57919000-57919400	Active TSS	Fetal Brain Male	brain
28	chr5:57919000-57919600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr5:57919000-57919800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr5:57919200-57919600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr5:57919200-57919600	Enhancers	Fetal Heart	heart
32	chr5:57919200-57919800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr5:57919200-57920000	Weak transcription	Right Atrium	heart
34	chr5:57919200-57924200	Weak transcription	Stomach Mucosa	stomach
35	chr5:57919400-57919600	Flanking Active TSS	Fetal Brain Male	brain
36	chr5:57919600-57920200	Enhancers	Fetal Brain Male	brain
37	chr5:57919600-57924200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr5:57919800-57924400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr5:57919800-57924400	Weak transcription	Fetal Lung	lung
40	chr5:57919800-57925000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr5:57920000-57920200	Enhancers	Right Atrium	heart
42	chr5:57920200-57924400	Weak transcription	Fetal Stomach	stomach
43	chr5:57920200-57924400	Weak transcription	Right Atrium	heart
44	chr5:57920600-57921000	Enhancers	Pancreatic Islets	Pancreatic Islet
45	chr5:57921000-57933000	Weak transcription	Pancreatic Islets	Pancreatic Islet
46	chr5:57922800-57923000	Enhancers	Rectal Mucosa Donor 31	rectum
47	chr5:57923200-57924200	Weak transcription	Rectal Mucosa Donor 31	rectum
48	chr5:57924000-57925400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr5:57924000-57925400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr5:57924200-57924400	Enhancers	Rectal Mucosa Donor 29	rectum

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