Variant report

Variant	nsv882690
Chromosome Location	chr5:107834247-107954485
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:798)
CpG islands
(count:550)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:798 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:107866895-107867642	K562	blood:	n/a	n/a
2	ARID3A	chr5:107884853-107885065	K562	blood:	n/a	n/a
3	ATF1	chr5:107953146-107953510	K562	blood:	n/a	n/a
4	ATF1	chr5:107857560-107858116	K562	blood:	n/a	n/a
5	ATF1	chr5:107845044-107845073	K562	blood:	n/a	n/a
6	ATF1	chr5:107884522-107885090	K562	blood:	n/a	n/a
7	ATF1	chr5:107867085-107867597	K562	blood:	n/a	n/a
8	ATF1	chr5:107865021-107865296	K562	blood:	n/a	n/a
9	ATF2	chr5:107856863-107858221	GM12878	blood:	n/a	n/a
10	ATF2	chr5:107856989-107857566	GM12878	blood:	n/a	n/a
11	ATF2	chr5:107858975-107859524	GM12878	blood:	n/a	n/a
12	ATF3	chr5:107867007-107867526	K562	blood:	n/a	n/a
13	BACH1	chr5:107867090-107867230	K562	blood:	n/a	n/a
14	BATF	chr5:107859072-107859403	GM12878	blood:	n/a	n/a
15	BATF	chr5:107840719-107841039	GM12878	blood:	n/a	n/a
16	BATF	chr5:107857019-107857349	GM12878	blood:	n/a	n/a
17	BATF	chr5:107859118-107859414	GM12878	blood:	n/a	n/a
18	BCL11A	chr5:107856971-107857412	GM12878	blood:	n/a	n/a
19	BCL11A	chr5:107857065-107857357	GM12878	blood:	n/a	n/a
20	BCL3	chr5:107857006-107857386	GM12878	blood:	n/a	n/a
21	BCL3	chr5:107857010-107857368	GM12878	blood:	n/a	n/a
22	BCLAF1	chr5:107856848-107857910	GM12878	blood:	n/a	n/a
23	BCLAF1	chr5:107859030-107859479	GM12878	blood:	n/a	chr5:107859366-107859375
24	BCLAF1	chr5:107856982-107857453	GM12878	blood:	n/a	n/a
25	BHLHE40	chr5:107856680-107857405	GM12878	blood:	n/a	n/a
26	BHLHE40	chr5:107892383-107892428	K562	blood:	n/a	n/a
27	BHLHE40	chr5:107893505-107893734	K562	blood:	n/a	n/a
28	BHLHE40	chr5:107859169-107859272	GM12878	blood:	n/a	n/a
29	BHLHE40	chr5:107867031-107867702	K562	blood:	n/a	n/a
30	BHLHE40	chr5:107884384-107884565	K562	blood:	n/a	n/a
31	BHLHE40	chr5:107884799-107885045	K562	blood:	n/a	n/a
32	CBX3	chr5:107910485-107910776	K562	blood:	n/a	n/a
33	CBX3	chr5:107866835-107867612	K562	blood:	n/a	n/a
34	CBX3	chr5:107866242-107867898	K562	blood:	n/a	n/a
35	CBX3	chr5:107884693-107885070	K562	blood:	n/a	n/a
36	CCNT2	chr5:107884750-107885058	K562	blood:	n/a	n/a
37	CCNT2	chr5:107867058-107867608	K562	blood:	n/a	n/a
38	CEBPB	chr5:107893360-107893725	IMR90	lung:	n/a	chr5:107893540-107893551
39	CEBPB	chr5:107918308-107918471	HepG2	liver:	n/a	n/a
40	CEBPB	chr5:107882769-107882978	IMR90	lung:	n/a	n/a
41	CEBPB	chr5:107893377-107893707	K562	blood:	n/a	chr5:107893540-107893551
42	CEBPB	chr5:107885367-107885551	A549	lung:	n/a	chr5:107885381-107885392
43	CEBPB	chr5:107866991-107867532	K562	blood:	n/a	n/a
44	CEBPB	chr5:107893418-107893669	Hela-S3	cervix:	n/a	chr5:107893540-107893551
45	CEBPB	chr5:107867009-107867572	K562	blood:	n/a	n/a
46	CEBPB	chr5:107896155-107896719	IMR90	lung:	n/a	n/a
47	CEBPB	chr5:107893371-107893734	K562	blood:	n/a	chr5:107893540-107893551
48	CEBPB	chr5:107861143-107861213	A549	lung:	n/a	chr5:107861152-107861163
49	CEBPB	chr5:107951631-107951782	K562	blood:	n/a	n/a
50	CEBPB	chr5:107950968-107951303	IMR90	lung:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:107929274-107929324	IMR90	lung:	fetal
2	chr5:107929274-107929324	IMR90	lung:	fetal
3	chr5:107929274-107929324	HCT-116	colon:	n/a
4	chr5:107890797-107890847	PFSK-1	brain:	n/a
5	chr5:107895657-107895707	SAEC	small airway:	n/a
6	chr5:107896573-107896623	T-47D	breast:	n/a
7	chr5:107899390-107899440	RPTEC	kidney:	n/a
8	chr5:107917716-107917766	Hepatocyte	liver:	n/a
9	chr5:107929300-107929350	GM12878	blood:	n/a
10	chr5:107917716-107917766	AG09319	gingival:	n/a
11	chr5:107895657-107895707	T-47D	breast:	n/a
12	chr5:107896573-107896623	GM12878	blood:	n/a
13	chr5:107917716-107917766	GM12892	blood:	n/a
14	chr5:107883502-107883552	HCM	heart:	n/a
15	chr5:107883502-107883552	PFSK-1	brain:	n/a
16	chr5:107917716-107917766	Jurkat	blood:	n/a
17	chr5:107896573-107896623	HMEC	breast:	n/a
18	chr5:107896573-107896623	HCPEpiC	choroid plexus:	n/a
19	chr5:107890797-107890847	HMEC	breast:	n/a
20	chr5:107899390-107899440	HMEC	breast:	n/a
21	chr5:107890797-107890847	HCT-116	colon:	n/a
22	chr5:107890797-107890847	SK-N-MC	brain:	n/a
23	chr5:107883502-107883552	Hepatocyte	liver:	n/a
24	chr5:107929300-107929350	SAEC	small airway:	n/a
25	chr5:107890797-107890847	NB4	blood:	n/a
26	chr5:107917716-107917766	HAEpiC	amniotic membrane:	n/a
27	chr5:107899390-107899440	HL-60	blood:	n/a
28	chr5:107874409-107874459	ECC-1	luminal epithelium:	n/a
29	chr5:107899390-107899440	GM12891	blood:	n/a
30	chr5:107874409-107874459	HPAEpiC	pulmonary alveolar:	n/a
31	chr5:107874409-107874459	IMR90	lung:	fetal
32	chr5:107890797-107890847	HAEpiC	amniotic membrane:	n/a
33	chr5:107929274-107929324	HepG2	liver:	n/a
34	chr5:107895657-107895707	Hela-S3	cervix:	n/a
35	chr5:107874409-107874459	AoSMC	blood vessel:	n/a
36	chr5:107874409-107874459	NB4	blood:	n/a
37	chr5:107899390-107899440	H1-hESC	embryonic stem cell:	embryo
38	chr5:107929274-107929324	CMK	blood:	n/a
39	chr5:107899390-107899440	HPAEpiC	pulmonary alveolar:	n/a
40	chr5:107890797-107890847	SK-N-SH_RA	brain:	n/a
41	chr5:107874409-107874459	HMEC	breast:	n/a
42	chr5:107929274-107929324	SK-N-SH	brain:	n/a
43	chr5:107899390-107899440	GM12878	blood:	n/a
44	chr5:107929274-107929324	NHDF-neo	bronchial:	n/a
45	chr5:107929274-107929324	GM12892	blood:	n/a
46	chr5:107929300-107929350	SK-N-MC	brain:	n/a
47	chr5:107874409-107874459	GM06990	blood:	n/a
48	chr5:107929274-107929324	Hepatocyte	liver:	n/a
49	chr5:107896573-107896623	HL-60	blood:	n/a
50	chr5:107929300-107929350	NHDF-neo	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:107836788..107838333-chr5:107838466..107840794,2	MCF-7	breast:
2	chr5:107884635..107886852-chr5:107895762..107899343,3	K562	blood:
3	chr5:107887157..107888973-chr5:107890068..107891576,2	MCF-7	breast:
4	chr5:107836788..107838333-chr5:107838466..107840794,2	MCF-7	breast:
5	chr5:107884635..107886852-chr5:107895762..107899343,3	K562	blood:
6	chr5:107857631..107858195-chr5:107977739..107978434,2	MCF-7	breast:
7	chr5:107843593..107846288-chr5:107847770..107850260,3	K562	blood:
8	chr5:107859256..107860913-chr5:108063920..108066391,2	K562	blood:
9	chr5:107938341..107940376-chr5:107941040..107943245,2	K562	blood:
10	chr5:107855833..107857545-chr5:109024014..109025642,2	MCF-7	breast:
11	chr5:107843593..107846288-chr5:107847770..107850260,3	K562	blood:
12	chr5:107884635..107887326-chr5:107896881..107899343,3	K562	blood:
13	chr5:107884635..107887326-chr5:107896881..107899343,3	K562	blood:
14	chr5:107938341..107940376-chr5:107941040..107943245,2	K562	blood:
15	chr5:107887157..107888973-chr5:107890068..107891576,2	MCF-7	breast:
16	chr5:107856773..107859561-chr5:108084375..108085888,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000244245	TF binding region
ENSG00000244245	CpG island
ENSG00000112893	chromatin interactions
ENSG00000272523	chromatin interactions
ENSG00000151422	chromatin interactions
ENSG00000271849	chromatin interactions

Extended variants
information (count: 4201 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:4201 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75934901	chr5:107836002-107836003	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs538255767	chr5:107836060-107836061	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs552108855	chr5:107836066-107836067	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs568873553	chr5:107836068-107836069	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs548769891	chr5:107836070-107836071	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs141948005	chr5:107836127-107836128	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs570276629	chr5:107836139-107836140	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs557615721	chr5:107836147-107836148	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs530985010	chr5:107836153-107836154	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs536985456	chr5:107836185-107836186	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs552707067	chr5:107836213-107836214	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs570971032	chr5:107836259-107836260	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs371920791	chr5:107836291-107836292	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs573436714	chr5:107836329-107836330	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs190845409	chr5:107836355-107836356	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs371601054	chr5:107836405-107836406	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs565250603	chr5:107836415-107836416	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs575357861	chr5:107836477-107836478	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs534698854	chr5:107836492-107836493	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs1304964	chr5:107836501-107836502	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs560785355	chr5:107836515-107836516	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs529832836	chr5:107836573-107836574	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs546725052	chr5:107836583-107836584	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs560193967	chr5:107836599-107836600	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs113460175	chr5:107839444-107839445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs556503687	chr5:107839448-107839449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs577953437	chr5:107839453-107839454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs573423421	chr5:107839484-107839485	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs540438585	chr5:107839521-107839522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs560441524	chr5:107839544-107839545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs17161364	chr5:107839586-107839587	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs190711925	chr5:107839626-107839627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs115543107	chr5:107839629-107839630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs574004328	chr5:107839682-107839683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs541565697	chr5:107839688-107839689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs564519512	chr5:107839794-107839795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs180745838	chr5:107839825-107839826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs17161366	chr5:107839840-107839841	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs186467149	chr5:107839882-107839883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs6893020	chr5:107839906-107839907	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs191248283	chr5:107839910-107839911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs182926704	chr5:107839952-107839953	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs528373141	chr5:107839954-107839955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs34472101	chr5:107839960-107839961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs551696256	chr5:107839966-107839967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs571095064	chr5:107839997-107839998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs536874704	chr5:107840005-107840006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs144562213	chr5:107840050-107840051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs556610492	chr5:107840070-107840071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs542574388	chr5:107840074-107840075	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
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
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	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
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
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	21509527	CNVD
Breast cancer	16608533	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	16773561	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:406 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:107836000-107836600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
2	chr5:107839400-107840200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr5:107843400-107844600	Enhancers	Fetal Heart	heart
4	chr5:107846200-107846600	Enhancers	H9 Cell Line	embryonic stem cell
5	chr5:107847800-107848000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr5:107848000-107853800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr5:107851000-107851400	Enhancers	Fetal Stomach	stomach
8	chr5:107851200-107851800	Enhancers	Adipose Nuclei	Adipose
9	chr5:107851200-107852000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr5:107851200-107852400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr5:107851400-107852000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr5:107851600-107852000	Enhancers	Duodenum Mucosa	Duodenum
13	chr5:107852000-107852400	Weak transcription	Duodenum Mucosa	Duodenum
14	chr5:107852000-107852600	Enhancers	Fetal Intestine Large	intestine
15	chr5:107852000-107854000	Enhancers	Fetal Intestine Small	intestine
16	chr5:107852400-107852600	Enhancers	Duodenum Mucosa	Duodenum
17	chr5:107852600-107853000	Weak transcription	Fetal Intestine Large	intestine
18	chr5:107852600-107856800	Weak transcription	Duodenum Mucosa	Duodenum
19	chr5:107852800-107853400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr5:107853000-107853200	Enhancers	Fetal Intestine Large	intestine
21	chr5:107853200-107854000	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr5:107853200-107859200	Weak transcription	Fetal Intestine Large	intestine
23	chr5:107853400-107853600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr5:107853400-107853800	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr5:107853400-107854000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr5:107853400-107857200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr5:107853800-107854400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr5:107853800-107856600	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr5:107854000-107856400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr5:107854000-107856600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr5:107854000-107857200	Weak transcription	Fetal Intestine Small	intestine
32	chr5:107855600-107856600	Enhancers	GM12878-XiMat	blood
33	chr5:107856200-107858200	Enhancers	Primary B cells from peripheral blood	blood
34	chr5:107856400-107858000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr5:107856600-107857000	Active TSS	Rectal Mucosa Donor 29	rectum
36	chr5:107856600-107857000	Flanking Active TSS	GM12878-XiMat	blood
37	chr5:107856600-107857400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr5:107856600-107857600	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr5:107856600-107857600	Enhancers	Primary hematopoietic stem cells	blood
40	chr5:107856600-107857600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr5:107856600-107858000	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr5:107856600-107858200	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr5:107856600-107858200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr5:107856800-107857200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr5:107856800-107857400	Enhancers	H1 Cell Line	embryonic stem cell
46	chr5:107856800-107857400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr5:107856800-107857600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
48	chr5:107856800-107857600	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr5:107856800-107857600	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr5:107856800-107858000	Enhancers	HUES64 Cell Line	embryonic stem cell

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