Variant report

Variant	nsv1022693
Chromosome Location	chr5:120026332-120132790
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:492)
CpG islands
(count:490)
Chromatin interactive
region (count:10)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:492 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr5:120031373-120031760	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr5:120030827-120031258	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr5:120042574-120042977	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr5:120033417-120033942	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr5:120032153-120033315	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr5:120042500-120043085	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr5:120026709-120027291	H1-hESC	embryonic stem cell:	n/a	n/a
8	BRCA1	chr5:120039223-120039493	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr5:120065904-120066245	IMR90	lung:	n/a	chr5:120066061-120066072
10	CEBPB	chr5:120103021-120103545	Hela-S3	cervix:	n/a	chr5:120103332-120103343 chr5:120103309-120103322
11	CEBPB	chr5:120124235-120124536	K562	blood:	n/a	n/a
12	CEBPB	chr5:120102910-120103783	IMR90	lung:	n/a	chr5:120103332-120103343 chr5:120103309-120103322
13	CEBPB	chr5:120065915-120066207	A549	lung:	n/a	chr5:120066061-120066072
14	CEBPB	chr5:120124187-120124543	K562	blood:	n/a	n/a
15	CEBPB	chr5:120054965-120055296	HepG2	liver:	n/a	chr5:120055099-120055108 chr5:120055097-120055108 chr5:120055099-120055110
16	CEBPB	chr5:120065902-120066254	K562	blood:	n/a	chr5:120066061-120066072
17	CEBPB	chr5:120102949-120103507	HepG2	liver:	n/a	chr5:120103332-120103343 chr5:120103309-120103322
18	CEBPB	chr5:120054977-120055190	A549	lung:	n/a	chr5:120055099-120055108 chr5:120055097-120055108 chr5:120055099-120055110
19	CEBPB	chr5:120124290-120124476	K562	blood:	n/a	n/a
20	CEBPB	chr5:120054932-120055285	IMR90	lung:	n/a	chr5:120055099-120055108 chr5:120055097-120055108 chr5:120055099-120055110
21	CEBPB	chr5:120106984-120107025	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr5:120032291-120032614	IMR90	lung:	n/a	chr5:120032468-120032481
23	CEBPB	chr5:120038927-120039237	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr5:120103071-120103392	K562	blood:	n/a	chr5:120103332-120103343 chr5:120103309-120103322
25	CEBPB	chr5:120039460-120039708	H1-hESC	embryonic stem cell:	n/a	chr5:120039507-120039520
26	CEBPB	chr5:120106872-120107188	IMR90	lung:	n/a	n/a
27	CEBPB	chr5:120065886-120066248	HepG2	liver:	n/a	chr5:120066061-120066072
28	CEBPB	chr5:120030269-120030469	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr5:120066038-120066233	H1-hESC	embryonic stem cell:	n/a	chr5:120066061-120066072
30	CEBPB	chr5:120103253-120103501	H1-hESC	embryonic stem cell:	n/a	chr5:120103332-120103343 chr5:120103309-120103322
31	CEBPB	chr5:120042643-120042971	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr5:120100946-120101290	IMR90	lung:	n/a	chr5:120101121-120101134
33	CEBPB	chr5:120052477-120052610	K562	blood:	n/a	n/a
34	CEBPB	chr5:120102971-120103502	A549	lung:	n/a	chr5:120103332-120103343 chr5:120103309-120103322
35	CEBPB	chr5:120052476-120052658	A549	lung:	n/a	n/a
36	CEBPB	chr5:120045408-120045601	A549	lung:	n/a	n/a
37	CHD1	chr5:120035597-120035939	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD1	chr5:120036490-120036609	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD1	chr5:120029006-120029026	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD1	chr5:120078612-120078614	GM12878	blood:	n/a	n/a
41	CHD1	chr5:120039143-120039613	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD1	chr5:120032133-120033294	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD1	chr5:120037261-120038640	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr5:120029029-120029308	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr5:120029548-120030096	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr5:120030736-120031572	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr5:120070900-120071050	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr5:120070980-120071130	HA-sp	spinal cord:	n/a	n/a
49	CTCF	chr5:120070720-120070870	HFF-Myc	foreskin:	n/a	n/a
50	CTCF	chr5:120070860-120071010	AG09319	gingival:	n/a	n/a

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:120081741-120081791	HCT-116	colon:	n/a
2	chr5:120115250-120115300	CMK	blood:	n/a
3	chr5:120081741-120081791	HCT-116	colon:	n/a
4	chr5:120115250-120115300	CMK	blood:	n/a
5	chr5:120069936-120069986	HRE	kidney:	n/a
6	chr5:120040283-120040333	SK-N-MC	brain:	n/a
7	chr5:120081741-120081791	H1-hESC	embryonic stem cell:	embryo
8	chr5:120081741-120081791	Jurkat	blood:	n/a
9	chr5:120115250-120115300	K562	blood:	n/a
10	chr5:120115250-120115300	AoSMC	blood vessel:	n/a
11	chr5:120038342-120038392	A549	lung:	n/a
12	chr5:120038247-120038297	NT2-D1	testis:	n/a
13	chr5:120040283-120040333	AG04450	lung:	fetal
14	chr5:120097654-120097704	HCF	heart:	n/a
15	chr5:120097654-120097704	HPAEpiC	pulmonary alveolar:	n/a
16	chr5:120026632-120026682	AG09319	gingival:	n/a
17	chr5:120097654-120097704	A549	lung:	n/a
18	chr5:120026632-120026682	HEEpiC	esophagus:	n/a
19	chr5:120081741-120081791	BE2_C	brain:	n/a
20	chr5:120115250-120115300	IMR90	lung:	fetal
21	chr5:120069936-120069986	HCF	heart:	n/a
22	chr5:120115250-120115300	ovcar-3	ovarian:	n/a
23	chr5:120097654-120097704	AG09319	gingival:	n/a
24	chr5:120038342-120038392	HCT-116	colon:	n/a
25	chr5:120097654-120097704	LNCaP	prostate:	n/a
26	chr5:120026632-120026682	HEK293	kidney:	embryo
27	chr5:120038247-120038297	BE2_C	brain:	n/a
28	chr5:120097654-120097704	HNPCEpiC	eye:	n/a
29	chr5:120115250-120115300	ProgFib	skin:	n/a
30	chr5:120038342-120038392	HCM	heart:	n/a
31	chr5:120038342-120038392	HRPEpiC	eye:	n/a
32	chr5:120081741-120081791	HEEpiC	esophagus:	n/a
33	chr5:120069936-120069986	GM12891	blood:	n/a
34	chr5:120040283-120040333	HAEpiC	amniotic membrane:	n/a
35	chr5:120081741-120081791	HMEC	breast:	n/a
36	chr5:120115250-120115300	SK-N-MC	brain:	n/a
37	chr5:120026632-120026682	ovcar-3	ovarian:	n/a
38	chr5:120038247-120038297	HL-60	blood:	n/a
39	chr5:120115250-120115300	HCPEpiC	choroid plexus:	n/a
40	chr5:120097654-120097704	ovcar-3	ovarian:	n/a
41	chr5:120097654-120097704	AG04450	lung:	fetal
42	chr5:120081741-120081791	CMK	blood:	n/a
43	chr5:120069936-120069986	HCPEpiC	choroid plexus:	n/a
44	chr5:120040283-120040333	T-47D	breast:	n/a
45	chr5:120038342-120038392	HEK293	kidney:	embryo
46	chr5:120040283-120040333	HRPEpiC	eye:	n/a
47	chr5:120081741-120081791	Caco-2	colon:	n/a
48	chr5:120038342-120038392	IMR90	lung:	fetal
49	chr5:120038342-120038392	GM12892	blood:	n/a
50	chr5:120097654-120097704	HMEC	breast:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:120040953..120043952-chr5:120045648..120047608,2	K562	blood:
2	chr5:120023459..120026241-chr5:120030447..120032911,2	K562	blood:
3	chr5:120072445..120075135-chr5:120093078..120094683,2	K562	blood:
4	chr5:119852123..119854010-chr5:120038446..120041236,2	K562	blood:
5	chr5:120020785..120023634-chr5:120024255..120028253,3	K562	blood:
6	chr5:120082635..120085459-chr5:120095219..120098019,2	K562	blood:
7	chr5:120076937..120079853-chr5:120080038..120082536,3	K562	blood:
8	chr5:120082635..120085459-chr5:120095219..120098019,2	K562	blood:
9	chr5:120072445..120075135-chr5:120093078..120094683,2	K562	blood:
10	chr5:120076937..120079853-chr5:120080038..120082536,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRR16-1	chr5:120115791-120115896	XLOC_004528
2	lnc-PRR16-1	chr5:120118132-120118267	XLOC_004528
3	lnc-PRR16-1	chr5:120125649-120126473	XLOC_004528
4	lnc-PRR16-1	chr5:120116913-120117106	XLOC_004528
5	lnc-PRR16-1	chr5:120116913-120117201	XLOC_004528
6	lnc-PRR16-1	chr5:120115735-120115896	XLOC_004528
7	lnc-PRR16-1	chr5:120109041-120109070	XLOC_004528
8	lnc-PRR16-1	chr5:120116913-120117201	XLOC_004528

No data

Variant related genes	Relation type
RNU4-69P	TF binding region
ENSG00000248927	TF binding region
RNU4-69P	CpG island
ENSG00000248927	CpG island
ENSG00000222609	chromatin interactions
PSIP1	miRNA target sites
UAP1	miRNA target sites

Extended variants
information (count: 3594 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:3594 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17502163	chr5:120026332-120026333	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs533645696	chr5:120026341-120026342	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530710444	chr5:120026343-120026344	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs552136027	chr5:120026350-120026351	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs112082962	chr5:120026361-120026362	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs562396254	chr5:120026363-120026364	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs200927783	chr5:120026389-120026390	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs188489344	chr5:120026390-120026391	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs114178241	chr5:120026408-120026409	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs10043860	chr5:120026412-120026413	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs553532019	chr5:120026443-120026444	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs114468398	chr5:120026459-120026460	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs530459343	chr5:120026472-120026473	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs150053606	chr5:120026478-120026479	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs576340799	chr5:120026535-120026536	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs192708500	chr5:120026544-120026545	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs543462355	chr5:120026563-120026564	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs11241561	chr5:120026585-120026586	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs574047447	chr5:120026641-120026642	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs541565478	chr5:120026763-120026764	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs377359744	chr5:120026795-120026796	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533580837	chr5:120026828-120026829	Enhancers Weak transcription Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs140697253	chr5:120026856-120026857	Enhancers Weak transcription Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs1868458	chr5:120026886-120026887	Enhancers Weak transcription Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs550844111	chr5:120026907-120026908	Enhancers Weak transcription Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs114363984	chr5:120026935-120026936	Enhancers Weak transcription Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs541860943	chr5:120026999-120027000	Enhancers Weak transcription Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549498411	chr5:120027024-120027025	Enhancers Weak transcription Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568078254	chr5:120027144-120027145	Enhancers Weak transcription Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs552243396	chr5:120027154-120027155	Enhancers Weak transcription Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs79491748	chr5:120027156-120027157	Enhancers Weak transcription Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs71586492	chr5:120027199-120027200	Enhancers Weak transcription Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs535186836	chr5:120027223-120027224	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs567401075	chr5:120027236-120027237	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs547108190	chr5:120027299-120027300	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565512371	chr5:120027324-120027325	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs1868459	chr5:120027347-120027348	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs184865738	chr5:120027351-120027352	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs535758376	chr5:120027358-120027359	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs377681138	chr5:120027362-120027363	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569843656	chr5:120027368-120027369	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs547342790	chr5:120027372-120027373	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs536555235	chr5:120027413-120027414	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs537398333	chr5:120027443-120027444	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs555453941	chr5:120027478-120027479	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187732429	chr5:120027531-120027532	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574013271	chr5:120027539-120027540	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs376964130	chr5:120027545-120027546	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs541502142	chr5:120027579-120027580	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs545719564	chr5:120027585-120027586	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
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
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
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:419 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:120020800-120026800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr5:120020800-120027200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr5:120020800-120033600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr5:120021000-120031800	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr5:120021200-120026400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr5:120021200-120026600	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr5:120021200-120026600	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr5:120021200-120031800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr5:120021200-120037600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr5:120021600-120028000	Strong transcription	HSMM	muscle
11	chr5:120021800-120031200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr5:120022400-120027600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr5:120022400-120027800	Weak transcription	Osteobl	bone
14	chr5:120022400-120028200	Weak transcription	Fetal Lung	lung
15	chr5:120022400-120029200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr5:120022400-120030400	Weak transcription	HSMMtube	muscle
17	chr5:120022800-120030800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr5:120023000-120030600	Weak transcription	NHDF-Ad	bronchial
19	chr5:120024800-120029000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr5:120025600-120026800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr5:120025800-120031400	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr5:120026000-120026400	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr5:120026400-120027000	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr5:120026400-120027200	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr5:120026400-120027400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr5:120026600-120027200	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr5:120026600-120028000	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr5:120026800-120027200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr5:120026800-120028000	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr5:120027200-120032200	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr5:120027200-120032200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr5:120027400-120028000	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr5:120027600-120027800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr5:120027600-120028000	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr5:120027800-120035600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr5:120028000-120028400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr5:120028000-120029000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr5:120028000-120031200	Weak transcription	HSMM	muscle
39	chr5:120028000-120031400	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr5:120028000-120032000	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr5:120028400-120028600	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr5:120028600-120031000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr5:120029000-120029400	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr5:120029400-120032200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr5:120031000-120032800	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr5:120031200-120031400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr5:120031200-120031400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr5:120031400-120032200	Strong transcription	HUES48 Cell Line	embryonic stem cell
49	chr5:120031400-120034800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr5:120031800-120032200	Strong transcription	iPS-20b Cell Line	embryonic stem cell

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