Variant report

Variant	nsv882248
Chromosome Location	chr5:82971921-83036792
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	ARID3A	chr5:83007859-83008155	K562	blood:	n/a	n/a
2	ARID3A	chr5:83007825-83008170	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:83022905-83023115	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:83014084-83014436	HepG2	liver:	n/a	chr5:83014365-83014381 chr5:83014366-83014382
5	BACH1	chr5:83017416-83018675	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr5:83018379-83018565	GM12878	blood:	n/a	n/a
7	BRCA1	chr5:83020954-83021027	HepG2	liver:	n/a	n/a
8	BRCA1	chr5:83018278-83018541	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr5:82992679-82992872	A549	lung:	n/a	n/a
10	CEBPB	chr5:82992757-82992827	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr5:83007837-83008146	A549	lung:	n/a	n/a
12	CEBPB	chr5:83007809-83008109	K562	blood:	n/a	n/a
13	CEBPB	chr5:83007823-83008164	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr5:83030881-83031038	H1-hESC	embryonic stem cell:	n/a	chr5:83030932-83030943
15	CEBPB	chr5:82987762-82987990	A549	lung:	n/a	chr5:82987878-82987889
16	CEBPB	chr5:82987732-82988040	HepG2	liver:	n/a	chr5:82987878-82987889
17	CEBPB	chr5:82987713-82988045	IMR90	lung:	n/a	chr5:82987878-82987889
18	CEBPB	chr5:82997795-82997977	K562	blood:	n/a	n/a
19	CEBPB	chr5:82987826-82987979	H1-hESC	embryonic stem cell:	n/a	chr5:82987878-82987889
20	CEBPB	chr5:83007823-83008145	HepG2	liver:	n/a	n/a
21	CEBPB	chr5:83018098-83018511	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr5:83030868-83031045	HepG2	liver:	n/a	chr5:83030932-83030943
23	CEBPB	chr5:83007868-83008136	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr5:83030863-83031037	A549	lung:	n/a	chr5:83030932-83030943
25	CEBPB	chr5:82997742-82998019	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr5:83007829-83008156	IMR90	lung:	n/a	n/a
27	CEBPB	chr5:83024909-83025052	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD1	chr5:83018207-83018289	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD1	chr5:83017793-83017979	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD1	chr5:83017263-83017390	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr5:83018014-83018449	H1-hESC	embryonic stem cell:	n/a	n/a
32	CREB1	chr5:83018136-83018460	A549	lung:	n/a	n/a
33	CTBP2	chr5:83016614-83018461	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr5:83007900-83008050	K562	blood:	n/a	chr5:83007998-83008016 chr5:83008000-83008021
35	CTCF	chr5:83018280-83018430	Caco-2	colon:	n/a	chr5:83018392-83018410 chr5:83018394-83018407
36	CTCF	chr5:83007900-83008050	GM12871	blood:	n/a	chr5:83007998-83008016 chr5:83008000-83008021
37	CTCF	chr5:83014120-83014270	HPF	lung:	n/a	chr5:83014206-83014222 chr5:83014205-83014223 chr5:83014209-83014216 chr5:83014207-83014228 chr5:83014208-83014221
38	CTCF	chr5:83014100-83014250	GM12869	blood:	n/a	chr5:83014206-83014222 chr5:83014205-83014223 chr5:83014209-83014216 chr5:83014207-83014228 chr5:83014208-83014221
39	CTCF	chr5:83014080-83014230	GM12870	blood:	n/a	chr5:83014206-83014222 chr5:83014205-83014223 chr5:83014209-83014216 chr5:83014207-83014228 chr5:83014208-83014221
40	CTCF	chr5:83007960-83008110	BE2_C	brain:	n/a	chr5:83007998-83008016 chr5:83008000-83008021
41	CTCF	chr5:83018220-83018370	GM12873	blood:	n/a	n/a
42	CTCF	chr5:83018300-83018450	GM12878	blood:	n/a	chr5:83018392-83018410 chr5:83018394-83018407
43	CTCF	chr5:83014100-83014250	HFF-Myc	foreskin:	n/a	chr5:83014206-83014222 chr5:83014205-83014223 chr5:83014209-83014216 chr5:83014207-83014228 chr5:83014208-83014221
44	CTCF	chr5:83013885-83014691	SK-N-SH	brain:	n/a	chr5:83014206-83014222 chr5:83014205-83014223 chr5:83014209-83014216 chr5:83014207-83014228 chr5:83014208-83014221
45	CTCF	chr5:83018240-83018390	GM12873	blood:	n/a	n/a
46	CTCF	chr5:83007580-83007730	HMEC	breast:	n/a	n/a
47	CTCF	chr5:83014058-83014376	Medullo	brain:	n/a	chr5:83014206-83014222 chr5:83014205-83014223 chr5:83014209-83014216 chr5:83014207-83014228 chr5:83014208-83014221
48	CTCF	chr5:83018134-83018585	T-47D	breast:	n/a	chr5:83018392-83018410 chr5:83018394-83018407
49	CTCF	chr5:83007900-83008050	WERI-Rb-1	eye:	n/a	chr5:83007998-83008016 chr5:83008000-83008021
50	CTCF	chr5:83014089-83014324	ProgFib	skin:	n/a	chr5:83014206-83014222 chr5:83014205-83014223 chr5:83014209-83014216 chr5:83014207-83014228 chr5:83014208-83014221

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:83016630-83016680	T-47D	breast:	n/a
2	chr5:83017184-83017234	AG09319	gingival:	n/a
3	chr5:83016630-83016680	T-47D	breast:	n/a
4	chr5:83017184-83017234	AG09319	gingival:	n/a
5	chr5:83017000-83017050	RPTEC	kidney:	n/a
6	chr5:83016630-83016680	PrEC	prostate:	n/a
7	chr5:83016717-83016767	NHDF-neo	bronchial:	n/a
8	chr5:83018280-83018330	NB4	blood:	n/a
9	chr5:83016717-83016767	SAEC	small airway:	n/a
10	chr5:83017644-83017694	RPTEC	kidney:	n/a
11	chr5:83017184-83017234	NT2-D1	testis:	n/a
12	chr5:83011366-83011416	AG09319	gingival:	n/a
13	chr5:83016630-83016680	GM12891	blood:	n/a
14	chr5:83011366-83011416	H1-hESC	embryonic stem cell:	embryo
15	chr5:83017553-83017603	A549	lung:	n/a
16	chr5:83021451-83021501	PANC-1	pancreas:	n/a
17	chr5:83017078-83017128	NHBE	bronchial:	n/a
18	chr5:83017921-83017971	GM12892	blood:	n/a
19	chr5:83016779-83016829	Caco-2	colon:	n/a
20	chr5:83016717-83016767	AG10803	skin:	n/a
21	chr5:83018422-83018472	T-47D	breast:	n/a
22	chr5:83021451-83021501	IMR90	lung:	fetal
23	chr5:83017009-83017059	GM12891	blood:	n/a
24	chr5:83017078-83017128	T-47D	breast:	n/a
25	chr5:83016717-83016767	Hepatocyte	liver:	n/a
26	chr5:83017000-83017050	T-47D	breast:	n/a
27	chr5:83018422-83018472	GM12892	blood:	n/a
28	chr5:83017009-83017059	ovcar-3	ovarian:	n/a
29	chr5:83017553-83017603	LNCaP	prostate:	n/a
30	chr5:83017078-83017128	AG10803	skin:	n/a
31	chr5:83017078-83017128	HRCEpiC	kidney:	n/a
32	chr5:83017921-83017971	HepG2	liver:	n/a
33	chr5:83017184-83017234	LNCaP	prostate:	n/a
34	chr5:83017000-83017050	AG09309	skin:	n/a
35	chr5:83021451-83021501	BE2_C	brain:	n/a
36	chr5:83017184-83017234	NH-A	brain:	n/a
37	chr5:83017644-83017694	NH-A	brain:	n/a
38	chr5:83017009-83017059	AG09309	skin:	n/a
39	chr5:83016717-83016767	ECC-1	luminal epithelium:	n/a
40	chr5:83017184-83017234	HMEC	breast:	n/a
41	chr5:83017009-83017059	HMEC	breast:	n/a
42	chr5:83017921-83017971	NHDF-neo	bronchial:	n/a
43	chr5:83017921-83017971	HRPEpiC	eye:	n/a
44	chr5:83021451-83021501	GM19239	blood:	n/a
45	chr5:83018357-83018407	AG04449	skin:	fetal
46	chr5:83017921-83017971	HPAEpiC	pulmonary alveolar:	n/a
47	chr5:83011366-83011416	NHBE	bronchial:	n/a
48	chr5:83017009-83017059	SK-N-SH	brain:	n/a
49	chr5:83017644-83017694	HRPEpiC	eye:	n/a
50	chr5:83017644-83017694	HCPEpiC	choroid plexus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:83016152..83018963-chr5:83026461..83028069,2	MCF-7	breast:
2	chr5:82990308..82992988-chr5:82995071..82997196,2	K562	blood:
3	chr5:83007855..83008473-chr5:86308448..86309317,2	K562	blood:
4	chr5:83014165..83014708-chr5:85974957..85975511,2	K562	blood:
5	chr5:82968270..82970854-chr5:82970907..82973750,2	MCF-7	breast:
6	chr15:53212411..53213163-chr5:82978820..82979601,2	MCF-7	breast:
7	chr5:83013777..83014670-chr5:86308556..86309476,3	K562	blood:
8	chr5:82990308..82992988-chr5:82995071..82997196,2	K562	blood:
9	chr5:83018122..83018815-chr5:84344759..84345464,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EDIL3-5	chr5:83016572-83017020	NONHSAT102526

Variant related genes	Relation type
HAPLN1	TF binding region
RNU6-620P	TF binding region
RN7SKP295	TF binding region
HAPLN1	CpG island
RNU6-620P	CpG island
RN7SKP295	CpG island
ENSG00000145681	chromatin interactions

Extended variants
information (count: 2474 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2474 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10514260	chr5:82971921-82971922	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs144158919	chr5:82971959-82971960	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs71605867	chr5:82971963-82971964	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs112622250	chr5:82971984-82971985	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs368676228	chr5:82971985-82971986	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs141180749	chr5:82971995-82971996	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs113186858	chr5:82972004-82972005	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs569130970	chr5:82972005-82972006	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs70975517	chr5:82972014-82972015	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs112764973	chr5:82972024-82972025	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs552053220	chr5:82972025-82972026	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs144987005	chr5:82972044-82972045	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs181599451	chr5:82972045-82972046	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs558209457	chr5:82972061-82972062	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs577941783	chr5:82972078-82972079	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs34176270	chr5:82972131-82972132	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs556153902	chr5:82972139-82972140	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs538360990	chr5:82972184-82972185	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs557157073	chr5:82972246-82972247	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs149086942	chr5:82972257-82972258	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs545735102	chr5:82972378-82972379	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs143058806	chr5:82972391-82972392	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs186836168	chr5:82972438-82972439	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs540259103	chr5:82972449-82972450	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs375365044	chr5:82972483-82972484	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs561424924	chr5:82972492-82972493	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs148231602	chr5:82972574-82972575	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs535437417	chr5:82972619-82972620	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs558699845	chr5:82972635-82972636	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs562695291	chr5:82972649-82972650	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs75595580	chr5:82972664-82972665	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs73133854	chr5:82972669-82972670	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs191220233	chr5:82972746-82972747	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs115456540	chr5:82972765-82972766	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs549327609	chr5:82972788-82972789	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs567677998	chr5:82972812-82972813	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs538299576	chr5:82972843-82972844	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs575350247	chr5:82972851-82972852	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs2909013	chr5:82972878-82972879	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs183068300	chr5:82972910-82972911	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs539662626	chr5:82972950-82972951	Strong transcription ZNF genes & repeats Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs187746778	chr5:82973056-82973057	Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs573119877	chr5:82973082-82973083	Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs17206110	chr5:82973084-82973085	Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs573346489	chr5:82973088-82973089	Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs6886123	chr5:82973102-82973103	Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs141124267	chr5:82973134-82973135	Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs543900077	chr5:82973162-82973163	Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs562282039	chr5:82973168-82973169	Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs146937608	chr5:82973175-82973176	Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

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	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Prostate cancer	21965145	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
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
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Esophageal adenocarcinoma	18519675	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
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Tetralogy of Fallot	22912587	CNVD
Basal cell lymphoma	17053054	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	19592390	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:632 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:82945000-82974800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr5:82970400-82972800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr5:82970600-82973000	Weak transcription	Osteobl	bone
4	chr5:82970600-82974000	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr5:82972800-82973400	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr5:82973000-82973400	ZNF genes & repeats	Osteobl	bone
7	chr5:82973400-82983200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr5:82973600-82973800	Weak transcription	Osteobl	bone
9	chr5:82974000-82975200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr5:82974800-82975400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr5:82975200-82976800	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr5:82975400-82975600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr5:82975600-82978000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr5:82976800-82980800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr5:82978000-82988200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr5:82978400-82980200	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr5:82978400-82980400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr5:82978600-82980400	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr5:82979000-82980000	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr5:82979000-82980200	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr5:82979000-82980400	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr5:82979200-82980000	Enhancers	H9 Cell Line	embryonic stem cell
23	chr5:82979200-82980200	Enhancers	H1 Cell Line	embryonic stem cell
24	chr5:82979200-82980200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr5:82979200-82980200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr5:82979200-82980200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr5:82979200-82980400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr5:82979200-82980400	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr5:82979400-82980000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
30	chr5:82979800-82980400	Enhancers	Fetal Intestine Small	intestine
31	chr5:82979800-82980600	Enhancers	Fetal Intestine Large	intestine
32	chr5:82980000-82983400	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr5:82980200-82981600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr5:82980200-82982200	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr5:82980200-82983600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr5:82980400-82984000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chr5:82980800-82987400	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr5:82981600-82982600	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr5:82982200-82982600	Enhancers	H1 Cell Line	embryonic stem cell
40	chr5:82982200-82984800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr5:82982200-82985200	Enhancers	Fetal Brain Female	brain
42	chr5:82982400-82982600	Enhancers	Brain Germinal Matrix	brain
43	chr5:82982400-82982600	Enhancers	Fetal Brain Male	brain
44	chr5:82982600-82983800	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr5:82982600-82983800	Weak transcription	Brain Germinal Matrix	brain
46	chr5:82982600-82984200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr5:82983000-82983200	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr5:82983000-82986000	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr5:82983200-82983800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr5:82983400-82984000	Enhancers	HUES48 Cell Line	embryonic stem cell

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