Variant report

Variant	nsv882501
Chromosome Location	chr5:101291960-101341123
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:101338849-101338931	K562	blood:	n/a	n/a
2	BHLHE40	chr5:101313640-101313757	GM12878	blood:	n/a	n/a
3	CEBPB	chr5:101307299-101307533	HepG2	liver:	n/a	chr5:101307466-101307477
4	CEBPB	chr5:101336311-101336608	HepG2	liver:	n/a	chr5:101336472-101336483
5	CEBPB	chr5:101336317-101336589	A549	lung:	n/a	chr5:101336472-101336483
6	CEBPB	chr5:101323591-101323733	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr5:101331266-101331761	MCF-7	breast:	n/a	n/a
8	CEBPB	chr5:101310922-101310941	A549	lung:	n/a	n/a
9	CEBPB	chr5:101307371-101307487	A549	lung:	n/a	chr5:101307466-101307477
10	CTCF	chr5:101313560-101313710	AG04449	skin:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
11	CTCF	chr5:101313520-101313670	HA-sp	spinal cord:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
12	CTCF	chr5:101313540-101313690	HRE	kidney:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
13	CTCF	chr5:101313600-101313750	GM12870	blood:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
14	CTCF	chr5:101313540-101313690	GM12870	blood:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
15	CTCF	chr5:101313540-101313690	GM12874	blood:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
16	CTCF	chr5:101313540-101313690	BE2_C	brain:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
17	CTCF	chr5:101313540-101313690	HBMEC	blood vessel:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
18	CTCF	chr5:101313580-101313730	HRPEpiC	eye:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
19	CTCF	chr5:101313557-101313769	GM10248	blood:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
20	CTCF	chr5:101313540-101313690	GM12864	blood:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
21	CTCF	chr5:101313580-101313730	A549	lung:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
22	CTCF	chr5:101313540-101313690	AoAF	blood vessel:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
23	CTCF	chr5:101313540-101313690	WERI-Rb-1	eye:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
24	CTCF	chr5:101313437-101313851	HepG2	liver:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
25	CTCF	chr5:101313461-101313811	K562	blood:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
26	CTCF	chr5:101313600-101313750	GM06990	blood:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
27	CTCF	chr5:101313503-101313838	HUVEC	blood vessel:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
28	CTCF	chr5:101313496-101313732	ECC-1	luminal epithelium:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
29	CTCF	chr5:101313535-101313759	Pancreas_OC	pancreas:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
30	CTCF	chr5:101313560-101313710	HPF	lung:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
31	CTCF	chr5:101313552-101313752	Lung_OC	lung:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
32	CTCF	chr5:101313620-101313770	GM12875	blood:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
33	CTCF	chr5:101313560-101313710	AG09309	skin:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
34	CTCF	chr5:101313540-101313690	GM12866	blood:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
35	CTCF	chr5:101313541-101313753	HepG2	liver:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
36	CTCF	chr5:101313562-101313754	Spleen_OC	spleen:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
37	CTCF	chr5:101313585-101313758	GM10266	blood:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
38	CTCF	chr5:101313520-101313670	GM12871	blood:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
39	CTCF	chr5:101313531-101313748	K562	blood:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
40	CTCF	chr5:101313520-101313670	AG09309	skin:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
41	CTCF	chr5:101313580-101313730	HPAF	blood vessel:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
42	CTCF	chr5:101313540-101313690	AG04449	skin:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
43	CTCF	chr5:101313600-101313750	BJ	skin:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
44	CTCF	chr5:101313540-101313690	HCT-116	colon:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
45	CTCF	chr5:101313620-101313770	HL-60	blood:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
46	CTCF	chr5:101313560-101313710	HEEpiC	esophagus:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
47	CTCF	chr5:101313493-101313737	ECC-1	luminal epithelium:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652
48	CTCF	chr5:101313575-101313610	Fibrobl	skin:	n/a	n/a
49	CTCF	chr5:101313840-101313990	HepG2	liver:	n/a	n/a
50	CTCF	chr5:101313540-101313690	HUVEC	blood vessel:	n/a	chr5:101313639-101313647 chr5:101313629-101313650 chr5:101313636-101313649 chr5:101313635-101313651 chr5:101313634-101313652

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:101297137-101297187	NHBE	bronchial:	n/a
2	chr5:101297174-101297224	HRE	kidney:	n/a
3	chr5:101297137-101297187	Hela-S3	cervix:	n/a
4	chr5:101297174-101297224	BJ	skin:	n/a
5	chr5:101297174-101297224	K562	blood:	n/a
6	chr5:101297137-101297187	HRPEpiC	eye:	n/a
7	chr5:101297137-101297187	HepG2	liver:	n/a
8	chr5:101297137-101297187	HRE	kidney:	n/a
9	chr5:101297137-101297187	HL-60	blood:	n/a
10	chr5:101297137-101297187	AG10803	skin:	n/a
11	chr5:101297137-101297187	HEEpiC	esophagus:	n/a
12	chr5:101297137-101297187	BJ	skin:	n/a
13	chr5:101297137-101297187	Jurkat	blood:	n/a
14	chr5:101297174-101297224	IMR90	lung:	fetal
15	chr5:101297137-101297187	HCM	heart:	n/a
16	chr5:101297174-101297224	AG09319	gingival:	n/a
17	chr5:101297174-101297224	HCM	heart:	n/a
18	chr5:101297137-101297187	LNCaP	prostate:	n/a
19	chr5:101297174-101297224	NHDF-neo	bronchial:	n/a
20	chr5:101297174-101297224	ECC-1	luminal epithelium:	n/a
21	chr5:101297137-101297187	AG04450	lung:	fetal
22	chr5:101297137-101297187	AG04449	skin:	fetal
23	chr5:101297137-101297187	HAEpiC	amniotic membrane:	n/a
24	chr5:101297174-101297224	HRCEpiC	kidney:	n/a
25	chr5:101297137-101297187	CMK	blood:	n/a
26	chr5:101297174-101297224	AoSMC	blood vessel:	n/a
27	chr5:101297174-101297224	HUVEC	blood vessel:	n/a
28	chr5:101297174-101297224	HCF	heart:	n/a
29	chr5:101297137-101297187	HCT-116	colon:	n/a
30	chr5:101297137-101297187	ovcar-3	ovarian:	n/a
31	chr5:101297174-101297224	Caco-2	colon:	n/a
32	chr5:101297174-101297224	GM12878	blood:	n/a
33	chr5:101297137-101297187	MCF-7	breast:	n/a
34	chr5:101297137-101297187	HRCEpiC	kidney:	n/a
35	chr5:101297137-101297187	H1-hESC	embryonic stem cell:	embryo
36	chr5:101297137-101297187	PrEC	prostate:	n/a
37	chr5:101297174-101297224	HPAEpiC	pulmonary alveolar:	n/a
38	chr5:101297174-101297224	HEK293	kidney:	embryo
39	chr5:101297137-101297187	ProgFib	skin:	n/a
40	chr5:101297174-101297224	HIPEpiC	eye:	n/a
41	chr5:101297137-101297187	NH-A	brain:	n/a
42	chr5:101297174-101297224	LNCaP	prostate:	n/a
43	chr5:101297137-101297187	Caco-2	colon:	n/a
44	chr5:101297174-101297224	HAEpiC	amniotic membrane:	n/a
45	chr5:101297174-101297224	HMEC	breast:	n/a
46	chr5:101297137-101297187	PFSK-1	brain:	n/a
47	chr5:101297174-101297224	AG10803	skin:	n/a
48	chr5:101297174-101297224	BE2_C	brain:	n/a
49	chr5:101297174-101297224	HCT-116	colon:	n/a
50	chr5:101297137-101297187	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:101326987..101328842-chr5:101335717..101338180,2	MCF-7	breast:
2	chr5:101326987..101328842-chr5:101335717..101338180,2	MCF-7	breast:
3	chr5:101312840..101313801-chr5:101426237..101427126,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PAM-8	chr5:101312000-101312502	NONHSAT103019

Variant related genes	Relation type
ENSG00000249495	TF binding region
ENSG00000249495	CpG island

Extended variants
information (count: 674 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:674 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6870397	chr5:101291960-101291961	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs576575427	chr5:101291972-101291973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs537540312	chr5:101291983-101291984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs185131539	chr5:101291985-101291986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs555954491	chr5:101292022-101292023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs6874565	chr5:101292035-101292036	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs542828551	chr5:101292037-101292038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs544927008	chr5:101292059-101292060	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs543855584	chr5:101292117-101292118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs145586743	chr5:101292120-101292121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs573562689	chr5:101292143-101292144	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs148875573	chr5:101292144-101292145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs565277011	chr5:101292273-101292274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs532507426	chr5:101292312-101292313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs374980926	chr5:101292313-101292314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs551056495	chr5:101292345-101292346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs189939635	chr5:101292349-101292350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs529285022	chr5:101300800-101300801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs6886984	chr5:101300824-101300825	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs368870282	chr5:101300891-101300892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs566091747	chr5:101300914-101300915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs539916267	chr5:101300917-101300918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs184376924	chr5:101300972-101300973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs562529150	chr5:101301010-101301011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs551535434	chr5:101301011-101301012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs569851369	chr5:101301012-101301013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs371298527	chr5:101301056-101301057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs537207411	chr5:101301084-101301085	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs189989161	chr5:101301102-101301103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs35435657	chr5:101301130-101301131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs34937259	chr5:101301142-101301143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs192851554	chr5:101301170-101301171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs144543429	chr5:101301191-101301192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs10688189	chr5:101301192-101301193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs67106500	chr5:101301193-101301194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs10655237	chr5:101301194-101301195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs184831484	chr5:101301221-101301222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs116281864	chr5:101301240-101301241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs552924313	chr5:101301267-101301268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs149871651	chr5:101301293-101301294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs545092095	chr5:101301301-101301302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs563209753	chr5:101301317-101301318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs115147193	chr5:101301359-101301360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs563511721	chr5:101301395-101301396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs899045	chr5:101301416-101301417	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs76372458	chr5:101301419-101301420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs78305184	chr5:101301429-101301430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs540899531	chr5:101301442-101301443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs144950405	chr5:101301470-101301471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs550805256	chr5:101301484-101301485	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
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
Merkel cell carcinoma	19020549	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
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	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
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	21509527	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:101289800-101292000	Weak transcription	Primary hematopoietic stem cells	blood
2	chr5:101291200-101292400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr5:101291400-101292200	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr5:101291400-101292200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr5:101291800-101292200	Enhancers	Fetal Stomach	stomach
6	chr5:101292000-101292400	Enhancers	Primary hematopoietic stem cells	blood
7	chr5:101300800-101303000	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr5:101302000-101302800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr5:101302200-101302600	Enhancers	Brain Germinal Matrix	brain
10	chr5:101302200-101302800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr5:101302400-101302800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr5:101303000-101305400	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr5:101305000-101306000	Enhancers	HepG2	liver
14	chr5:101305400-101305600	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr5:101305600-101306000	Enhancers	Liver	Liver
16	chr5:101305600-101306000	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr5:101305600-101306000	Enhancers	Fetal Lung	lung
18	chr5:101306400-101306800	Enhancers	Fetal Stomach	stomach
19	chr5:101313000-101313600	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr5:101313200-101313600	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr5:101313200-101313600	Enhancers	Brain Germinal Matrix	brain
22	chr5:101313200-101314000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr5:101315400-101316000	Enhancers	Stomach Mucosa	stomach
24	chr5:101316000-101317000	Weak transcription	Stomach Mucosa	stomach
25	chr5:101317000-101317200	Enhancers	Stomach Mucosa	stomach
26	chr5:101325600-101325800	Enhancers	Rectal Mucosa Donor 31	rectum
27	chr5:101325800-101329000	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr5:101329000-101331000	Enhancers	Rectal Mucosa Donor 31	rectum
29	chr5:101329800-101332800	Enhancers	Fetal Intestine Small	intestine
30	chr5:101330000-101331000	Enhancers	Fetal Intestine Large	intestine
31	chr5:101330800-101331000	Enhancers	Psoas Muscle	Psoas
32	chr5:101330800-101331200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr5:101330800-101331400	Enhancers	H9 Cell Line	embryonic stem cell
34	chr5:101330800-101331600	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr5:101330800-101333200	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr5:101331000-101331200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
37	chr5:101331000-101332600	Weak transcription	Psoas Muscle	Psoas
38	chr5:101331200-101331600	Active TSS	Rectal Mucosa Donor 31	rectum
39	chr5:101331200-101331800	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr5:101331400-101332200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr5:101331400-101332600	Enhancers	Placenta Amnion	Placenta Amnion
42	chr5:101331600-101331800	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr5:101332600-101332800	Active TSS	Psoas Muscle	Psoas

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