Variant report

Variant	nsv964892
Chromosome Location	chr5:70703111-70745996
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:268)
CpG islands
(count:183)
Chromatin interactive
region (count:1)
LncRNA
region (count:28)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:268 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr5:70743342-70743354	K562	blood:	n/a	n/a
2	CEBPB	chr5:70711583-70711773	HepG2	liver:	n/a	chr5:70711699-70711710
3	CEBPB	chr5:70743188-70743385	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr5:70711663-70711773	K562	blood:	n/a	chr5:70711699-70711710
5	CEBPB	chr5:70711655-70711828	Hela-S3	cervix:	n/a	chr5:70711699-70711710
6	CEBPB	chr5:70705347-70705398	K562	blood:	n/a	n/a
7	CEBPB	chr5:70711597-70711864	H1-hESC	embryonic stem cell:	n/a	chr5:70711699-70711710
8	CTCF	chr5:70718466-70718496	GM20000	blood:	n/a	n/a
9	CTCF	chr5:70743111-70743394	MCF-7	breast:	n/a	n/a
10	CTCF	chr5:70743100-70743250	NHDF-neo	bronchial:	n/a	n/a
11	CTCF	chr5:70743143-70743380	HepG2	liver:	n/a	n/a
12	CTCF	chr5:70743100-70743250	HMEC	breast:	n/a	n/a
13	CTCF	chr5:70743129-70743352	SK-N-SH_RA	brain:	n/a	n/a
14	CTCF	chr5:70743129-70743401	GM10266	blood:	n/a	n/a
15	CTCF	chr5:70743099-70743347	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr5:70743092-70743422	MCF-7	breast:	n/a	n/a
17	CTCF	chr5:70743200-70743350	HEK293	kidney:	n/a	n/a
18	CTCF	chr5:70743200-70743350	HPF	lung:	n/a	n/a
19	CTCF	chr5:70743100-70743250	GM12870	blood:	n/a	n/a
20	CTCF	chr5:70743200-70743350	AG09319	gingival:	n/a	n/a
21	CTCF	chr5:70743100-70743250	MCF-7	breast:	n/a	n/a
22	CTCF	chr5:70743148-70743391	GM13976	blood:	n/a	n/a
23	CTCF	chr5:70743100-70743250	BE2_C	brain:	n/a	n/a
24	CTCF	chr5:70743200-70743350	HPAF	blood vessel:	n/a	n/a
25	CTCF	chr5:70743100-70743250	NB4	blood:	n/a	n/a
26	CTCF	chr5:70743099-70743413	Medullo	brain:	n/a	n/a
27	CTCF	chr5:70743121-70743353	T-47D	breast:	n/a	n/a
28	CTCF	chr5:70743100-70743250	HCT-116	colon:	n/a	n/a
29	CTCF	chr5:70721390-70721478	GM13976	blood:	n/a	n/a
30	CTCF	chr5:70743120-70743270	HA-sp	spinal cord:	n/a	n/a
31	CTCF	chr5:70743100-70743250	GM12871	blood:	n/a	n/a
32	CTCF	chr5:70743200-70743350	K562	blood:	n/a	n/a
33	CTCF	chr5:70743200-70743350	HCPEpiC	choroid plexus:	n/a	n/a
34	CTCF	chr5:70743125-70743377	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr5:70743200-70743350	AG04450	lung:	n/a	n/a
36	CTCF	chr5:70743096-70743424	Gliobla	brain:	n/a	n/a
37	CTCF	chr5:70743122-70743385	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr5:70743131-70743392	LNCaP	prostate:	n/a	n/a
39	CTCF	chr5:70743120-70743397	K562	blood:	n/a	n/a
40	CTCF	chr5:70743100-70743250	HRPEpiC	eye:	n/a	n/a
41	CTCF	chr5:70743121-70743365	A549	lung:	n/a	n/a
42	CTCF	chr5:70743172-70743408	IMR90	lung:	n/a	n/a
43	CTCF	chr5:70743030-70743415	GM12878	blood:	n/a	n/a
44	CTCF	chr5:70743100-70743250	HVMF	connective:	n/a	n/a
45	CTCF	chr5:70743109-70743319	HCT-116	colon:	n/a	n/a
46	CTCF	chr5:70739681-70739747	ProgFib	skin:	n/a	n/a
47	CTCF	chr5:70715065-70715121	Medullo	brain:	n/a	n/a
48	CTCF	chr5:70743120-70743270	HCT-116	colon:	n/a	n/a
49	CTCF	chr5:70743088-70743400	Spleen_OC	spleen:	n/a	n/a
50	CTCF	chr5:70743200-70743350	HMEC	breast:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:70741802-70741852	Caco-2	colon:	n/a
2	chr5:70741802-70741852	T-47D	breast:	n/a
3	chr5:70742551-70742601	HNPCEpiC	eye:	n/a
4	chr5:70742893-70742943	HL-60	blood:	n/a
5	chr5:70742551-70742601	HRCEpiC	kidney:	n/a
6	chr5:70742551-70742601	K562	blood:	n/a
7	chr5:70742893-70742943	HCPEpiC	choroid plexus:	n/a
8	chr5:70741802-70741852	HIPEpiC	eye:	n/a
9	chr5:70741802-70741852	RPTEC	kidney:	n/a
10	chr5:70742551-70742601	H1-hESC	embryonic stem cell:	embryo
11	chr5:70742893-70742943	A549	lung:	n/a
12	chr5:70741802-70741852	NB4	blood:	n/a
13	chr5:70741802-70741852	PANC-1	pancreas:	n/a
14	chr5:70742551-70742601	T-47D	breast:	n/a
15	chr5:70742551-70742601	GM12892	blood:	n/a
16	chr5:70742551-70742601	HRPEpiC	eye:	n/a
17	chr5:70741802-70741852	GM06990	blood:	n/a
18	chr5:70742551-70742601	Hela-S3	cervix:	n/a
19	chr5:70742551-70742601	HCPEpiC	choroid plexus:	n/a
20	chr5:70742551-70742601	MCF10A-Er-Src	breast:	n/a
21	chr5:70741802-70741852	ProgFib	skin:	n/a
22	chr5:70742551-70742601	AG10803	skin:	n/a
23	chr5:70742893-70742943	MCF-7	breast:	n/a
24	chr5:70742893-70742943	Hela-S3	cervix:	n/a
25	chr5:70742551-70742601	HCM	heart:	n/a
26	chr5:70742551-70742601	Jurkat	blood:	n/a
27	chr5:70742893-70742943	HRPEpiC	eye:	n/a
28	chr5:70742893-70742943	ECC-1	luminal epithelium:	n/a
29	chr5:70741802-70741852	AG09309	skin:	n/a
30	chr5:70741802-70741852	HCPEpiC	choroid plexus:	n/a
31	chr5:70741802-70741852	K562	blood:	n/a
32	chr5:70742551-70742601	Hepatocyte	liver:	n/a
33	chr5:70742893-70742943	HMEC	breast:	n/a
34	chr5:70742551-70742601	HEK293	kidney:	embryo
35	chr5:70742893-70742943	GM06990	blood:	n/a
36	chr5:70741802-70741852	NHDF-neo	bronchial:	n/a
37	chr5:70741802-70741852	BJ	skin:	n/a
38	chr5:70742551-70742601	SK-N-SH_RA	brain:	n/a
39	chr5:70741802-70741852	AoSMC	blood vessel:	n/a
40	chr5:70741802-70741852	MCF-7	breast:	n/a
41	chr5:70742893-70742943	AG04450	lung:	fetal
42	chr5:70742551-70742601	NHDF-neo	bronchial:	n/a
43	chr5:70742551-70742601	NHBE	bronchial:	n/a
44	chr5:70741802-70741852	HEEpiC	esophagus:	n/a
45	chr5:70741802-70741852	PrEC	prostate:	n/a
46	chr5:70742893-70742943	ProgFib	skin:	n/a
47	chr5:70741802-70741852	HRPEpiC	eye:	n/a
48	chr5:70741802-70741852	SK-N-SH_RA	brain:	n/a
49	chr5:70741802-70741852	AG10803	skin:	n/a
50	chr5:70742893-70742943	GM19239	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:70742035..70743794-chr5:70750287..70752992,2	MCF-7	breast:

(count:28 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BDP1-3	chr5:70717124-70717292	NONHSAT102022
2	lnc-BDP1-3	chr5:70707369-70707599	NONHSAT102023
3	lnc-GTF2H2-3	chr5:70741472-70742169	ENSG00000250387
4	lnc-BDP1-3	chr5:70716917-70717016	NONHSAT102025
5	lnc-BDP1-3	chr5:70717124-70717292	NONHSAT102025
6	lnc-BDP1-3	chr5:70716879-70717016	NONHSAT102022
7	lnc-BDP1-3	chr5:70707369-70707599	NONHSAT102025
8	lnc-BDP1-3	chr5:70707369-70707599	NONHSAT102021
9	lnc-BDP1-1	chr5:70741443-70741499	XLOC_004418
10	lnc-BDP1-3	chr5:70709089-70709163	NONHSAT102025
11	lnc-BDP1-3	chr5:70707870-70709163	NONHSAT102023
12	lnc-BDP1-3	chr5:70717124-70717292	NONHSAT102024
13	lnc-BDP1-3	chr5:70717124-70717292	NONHSAT102023
14	lnc-BDP1-3	chr5:70716917-70717016	NONHSAT102024
15	lnc-BDP1-3	chr5:70716879-70717016	NONHSAT102023
16	lnc-GTF2H2-3	chr5:70741472-70741612	NONHSAT102012
17	lnc-BDP1-3	chr5:70710615-70710691	NONHSAT102024
18	lnc-BDP1-3	chr5:70707369-70707599	NONHSAT102022
19	lnc-GTF2H2-3	chr5:70741777-70742163	NONHSAT102012
20	lnc-BDP1-3	chr5:70709089-70709163	NONHSAT102024
21	lnc-BDP1-3	chr5:70717399-70717576	NONHSAT102021
22	lnc-GTF2H2-3	chr5:70741777-70742163	ENSG00000250387
23	lnc-BDP1-3	chr5:70707369-70707599	NONHSAT102024
24	lnc-BDP1-3	chr5:70709089-70709163	NONHSAT102022
25	lnc-BDP1-1	chr5:70741887-70742396	XLOC_004418
26	lnc-GTF2H2-3	chr5:70741472-70741612	ENSG00000250387
27	lnc-BDP1-3	chr5:70716879-70717016	NONHSAT102021
28	lnc-BDP1-3	chr5:70707870-70709163	NONHSAT102021

No data

Variant related genes	Relation type
ENSG00000249981	TF binding region
ENSG00000250387	TF binding region
ENSG00000249981	CpG island
ENSG00000250387	CpG island
ENSG00000145734	chromatin interactions
RAB5B	miRNA target sites

Extended variants
information (count: 788 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:788 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565053802	chr5:70703117-70703118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs542280664	chr5:70703124-70703125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs188873941	chr5:70703155-70703156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs543988536	chr5:70703423-70703424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs562562074	chr5:70703424-70703425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs546332347	chr5:70703443-70703444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs200669212	chr5:70703515-70703516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs564534515	chr5:70703533-70703534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs529660603	chr5:70703536-70703537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs376722640	chr5:70703579-70703580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs550204252	chr5:70703583-70703584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs562071660	chr5:70703586-70703587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs540652380	chr5:70703632-70703633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs528842017	chr5:70703633-70703634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs547002878	chr5:70703638-70703639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs565407547	chr5:70703654-70703655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs181418492	chr5:70703714-70703715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551509733	chr5:70703724-70703725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs569749660	chr5:70703774-70703775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs150749579	chr5:70703842-70703843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs555685535	chr5:70703856-70703857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562014132	chr5:70703899-70703900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs62372728	chr5:70703905-70703906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554211698	chr5:70703908-70703909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs10058316	chr5:70703986-70703987	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs545972055	chr5:70704015-70704016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564649388	chr5:70704050-70704051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs6453529	chr5:70704077-70704078	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
29	rs377312272	chr5:70704111-70704112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs546816976	chr5:70704119-70704120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs143909673	chr5:70704138-70704139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562008476	chr5:70704181-70704182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571767039	chr5:70704193-70704194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs539186309	chr5:70704209-70704210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs540575069	chr5:70704277-70704278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs558930295	chr5:70704288-70704289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs6881126	chr5:70704359-70704360	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs185948970	chr5:70704424-70704425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs569769338	chr5:70704442-70704443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189913681	chr5:70704468-70704469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569335005	chr5:70704573-70704574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs181398466	chr5:70704647-70704648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs201307904	chr5:70704766-70704767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs71668272	chr5:70704767-70704768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs199909403	chr5:70704768-70704769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576599579	chr5:70704781-70704782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185907234	chr5:70704844-70704845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554987518	chr5:70704871-70704872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534925961	chr5:70704877-70704878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191223309	chr5:70704884-70704885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD

Chromatin state (count:148 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:70699600-70707000	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr5:70702000-70706800	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr5:70702000-70717400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr5:70702400-70707200	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr5:70702400-70717600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr5:70706800-70707600	Active TSS	Pancreatic Islets	Pancreatic Islet
7	chr5:70707000-70707400	Active TSS	Brain Angular Gyrus	brain
8	chr5:70707000-70707400	Bivalent Enhancer	A549	lung
9	chr5:70707000-70707600	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr5:70707200-70707600	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr5:70707400-70714000	Weak transcription	Liver	Liver
12	chr5:70707600-70716000	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr5:70707600-70716400	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr5:70707800-70716400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr5:70713800-70714200	Enhancers	HepG2	liver
16	chr5:70714000-70714800	Enhancers	Liver	Liver
17	chr5:70714800-70717400	Weak transcription	Liver	Liver
18	chr5:70715600-70718000	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr5:70715800-70716000	Enhancers	H9 Cell Line	embryonic stem cell
20	chr5:70715800-70718000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr5:70715800-70718200	Enhancers	H1 Cell Line	embryonic stem cell
22	chr5:70716000-70717000	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr5:70716000-70718400	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr5:70716400-70716600	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr5:70716400-70718000	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr5:70716400-70718400	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr5:70716400-70718400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr5:70716600-70716800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
29	chr5:70716800-70717000	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr5:70716800-70718000	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr5:70717000-70717200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
32	chr5:70717000-70718200	Enhancers	H9 Cell Line	embryonic stem cell
33	chr5:70717200-70718200	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr5:70717400-70717600	Enhancers	Liver	Liver
35	chr5:70717400-70717800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr5:70717400-70718000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr5:70717600-70718600	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr5:70721400-70722000	Enhancers	Fetal Heart	heart
39	chr5:70728000-70728400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr5:70728000-70728600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr5:70736200-70738400	Enhancers	Liver	Liver
42	chr5:70736400-70736600	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr5:70736800-70737800	Enhancers	Primary neutrophils fromperipheralblood	blood
44	chr5:70737800-70741800	Weak transcription	Primary neutrophils fromperipheralblood	blood
45	chr5:70738400-70738800	Weak transcription	Liver	Liver
46	chr5:70738600-70738800	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr5:70738800-70739000	Enhancers	Liver	Liver
48	chr5:70738800-70742800	Active TSS	Pancreatic Islets	Pancreatic Islet
49	chr5:70739000-70739800	Weak transcription	Liver	Liver
50	chr5:70739400-70740000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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