Variant report

Variant	nsv599602
Chromosome Location	chr5:119866504-120023393
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1089)
CpG islands
(count:244)
Chromatin interactive
region (count:37)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1089 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:119899838-119899993	K562	blood:	n/a	n/a
2	BACH1	chr5:120023318-120023332	K562	blood:	n/a	n/a
3	BACH1	chr5:119959300-119959328	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr5:119991637-119991644	K562	blood:	n/a	n/a
5	BRCA1	chr5:119940521-119941137	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr5:119974391-119974481	GM12878	blood:	n/a	n/a
7	CCNT2	chr5:119927724-119927859	K562	blood:	n/a	n/a
8	CCNT2	chr5:120010812-120011012	K562	blood:	n/a	n/a
9	CCNT2	chr5:119891204-119891275	K562	blood:	n/a	n/a
10	CCNT2	chr5:119868130-119868256	K562	blood:	n/a	n/a
11	CEBPB	chr5:119940627-119940974	IMR90	lung:	n/a	n/a
12	CEBPB	chr5:119955880-119956197	K562	blood:	n/a	chr5:119956004-119956015
13	CEBPB	chr5:119918081-119918135	HepG2	liver:	n/a	chr5:119918093-119918104
14	CEBPB	chr5:119940538-119941604	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr5:119908492-119908611	IMR90	lung:	n/a	n/a
16	CEBPB	chr5:119936395-119936681	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr5:119993776-119994043	HepG2	liver:	n/a	chr5:119993879-119993890
18	CEBPB	chr5:119937714-119938123	Hela-S3	cervix:	n/a	chr5:119937940-119937951
19	CEBPB	chr5:119937773-119938120	IMR90	lung:	n/a	chr5:119937940-119937951
20	CEBPB	chr5:119959643-119959893	Hela-S3	cervix:	n/a	chr5:119959754-119959765 chr5:119959754-119959767 chr5:119959754-119959767
21	CEBPB	chr5:119980295-119980384	HepG2	liver:	n/a	chr5:119980319-119980332 chr5:119980319-119980330
22	CEBPB	chr5:119935239-119935784	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr5:119937786-119938093	HepG2	liver:	n/a	chr5:119937940-119937951
24	CEBPB	chr5:119977083-119977356	IMR90	lung:	n/a	chr5:119977215-119977226
25	CEBPB	chr5:119977093-119977344	A549	lung:	n/a	chr5:119977215-119977226
26	CEBPB	chr5:119951673-119952096	IMR90	lung:	n/a	chr5:119951865-119951878
27	CEBPB	chr5:119984469-119984716	HepG2	liver:	n/a	n/a
28	CEBPB	chr5:119937761-119938116	K562	blood:	n/a	chr5:119937940-119937951
29	CEBPB	chr5:119981493-119981734	HepG2	liver:	n/a	chr5:119981633-119981644
30	CEBPB	chr5:119977079-119977372	H1-hESC	embryonic stem cell:	n/a	chr5:119977215-119977226
31	CEBPB	chr5:119984458-119984709	IMR90	lung:	n/a	n/a
32	CEBPB	chr5:119936349-119936589	HepG2	liver:	n/a	n/a
33	CEBPB	chr5:119951672-119952058	Hela-S3	cervix:	n/a	chr5:119951865-119951878
34	CEBPB	chr5:119945256-119945647	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr5:119937909-119937973	A549	lung:	n/a	chr5:119937940-119937951
36	CEBPB	chr5:119977083-119977287	K562	blood:	n/a	chr5:119977215-119977226
37	CEBPB	chr5:119977078-119977396	HepG2	liver:	n/a	chr5:119977215-119977226
38	CEBPB	chr5:119950210-119950705	IMR90	lung:	n/a	n/a
39	CEBPB	chr5:119959582-119960151	IMR90	lung:	n/a	chr5:119959754-119959765 chr5:119959754-119959767 chr5:119959754-119959767
40	CEBPB	chr5:119931729-119931789	A549	lung:	n/a	n/a
41	CEBPB	chr5:119935306-119935685	IMR90	lung:	n/a	n/a
42	CEBPB	chr5:119977038-119977401	Hela-S3	cervix:	n/a	chr5:119977215-119977226
43	CEBPB	chr5:119873912-119874713	IMR90	lung:	n/a	n/a
44	CEBPB	chr5:119955906-119956141	HepG2	liver:	n/a	chr5:119956004-119956015
45	CHD2	chr5:119940555-119940962	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr5:119868660-119868810	RPTEC	kidney:	n/a	n/a
47	CTCF	chr5:119991640-119991790	GM12864	blood:	n/a	chr5:119991711-119991729 chr5:119991714-119991723 chr5:119991714-119991727 chr5:119991713-119991734 chr5:119991712-119991728
48	CTCF	chr5:120020840-120020990	HMF	breast:	n/a	n/a
49	CTCF	chr5:119991640-119991790	AG04449	skin:	n/a	chr5:119991711-119991729 chr5:119991714-119991723 chr5:119991714-119991727 chr5:119991713-119991734 chr5:119991712-119991728
50	CTCF	chr5:120020860-120021010	AG09319	gingival:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:119942454-119942504	HRCEpiC	kidney:	n/a
2	chr5:119942454-119942504	AoSMC	blood vessel:	n/a
3	chr5:119952679-119952729	CMK	blood:	n/a
4	chr5:119942454-119942504	HCPEpiC	choroid plexus:	n/a
5	chr5:119951527-119951577	HNPCEpiC	eye:	n/a
6	chr5:119951527-119951577	HCPEpiC	choroid plexus:	n/a
7	chr5:120018164-120018214	HRPEpiC	eye:	n/a
8	chr5:119942454-119942504	GM19239	blood:	n/a
9	chr5:119951527-119951577	Hela-S3	cervix:	n/a
10	chr5:119942454-119942504	GM12892	blood:	n/a
11	chr5:119942454-119942504	CMK	blood:	n/a
12	chr5:120018164-120018214	Hepatocyte	liver:	n/a
13	chr5:119942454-119942504	Hepatocyte	liver:	n/a
14	chr5:120018164-120018214	AoSMC	blood vessel:	n/a
15	chr5:120018164-120018214	HepG2	liver:	n/a
16	chr5:119952679-119952729	AG09319	gingival:	n/a
17	chr5:120018164-120018214	SK-N-SH	brain:	n/a
18	chr5:119942454-119942504	GM06990	blood:	n/a
19	chr5:119951527-119951577	LNCaP	prostate:	n/a
20	chr5:119952679-119952729	HPAEpiC	pulmonary alveolar:	n/a
21	chr5:119951527-119951577	GM06990	blood:	n/a
22	chr5:119952679-119952729	HUVEC	blood vessel:	n/a
23	chr5:119951527-119951577	HCM	heart:	n/a
24	chr5:119952679-119952729	HEK293	kidney:	embryo
25	chr5:119942454-119942504	PrEC	prostate:	n/a
26	chr5:119951527-119951577	Caco-2	colon:	n/a
27	chr5:119951527-119951577	HRCEpiC	kidney:	n/a
28	chr5:119952679-119952729	T-47D	breast:	n/a
29	chr5:119942454-119942504	MCF10A-Er-Src	breast:	n/a
30	chr5:119951527-119951577	HEEpiC	esophagus:	n/a
31	chr5:119951527-119951577	AoSMC	blood vessel:	n/a
32	chr5:119942454-119942504	NB4	blood:	n/a
33	chr5:119952679-119952729	BE2_C	brain:	n/a
34	chr5:119942454-119942504	Jurkat	blood:	n/a
35	chr5:120018164-120018214	NHDF-neo	bronchial:	n/a
36	chr5:120018164-120018214	AG04449	skin:	fetal
37	chr5:119952679-119952729	MCF-7	breast:	n/a
38	chr5:120018164-120018214	HCPEpiC	choroid plexus:	n/a
39	chr5:119952679-119952729	HepG2	liver:	n/a
40	chr5:119951527-119951577	AG04450	lung:	fetal
41	chr5:119952679-119952729	U87	brain:	n/a
42	chr5:119951527-119951577	RPTEC	kidney:	n/a
43	chr5:120018164-120018214	HIPEpiC	eye:	n/a
44	chr5:119942454-119942504	Caco-2	colon:	n/a
45	chr5:120018164-120018214	BJ	skin:	n/a
46	chr5:119952679-119952729	HNPCEpiC	eye:	n/a
47	chr5:119942454-119942504	HUVEC	blood vessel:	n/a
48	chr5:119942454-119942504	U87	brain:	n/a
49	chr5:119951527-119951577	AG09309	skin:	n/a
50	chr5:120018164-120018214	H1-hESC	embryonic stem cell:	embryo

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:119926337..119929229-chr5:119929732..119932370,2	K562	blood:
2	chr5:119877678..119879721-chr5:119882058..119884163,2	K562	blood:
3	chr5:119906837..119908623-chr5:119910419..119912812,2	K562	blood:
4	chr5:119991257..119992549-chr5:121285272..121286241,6	MCF-7	breast:
5	chr5:119901221..119903356-chr5:119911285..119913616,2	K562	blood:
6	chr5:119926337..119929229-chr5:119929732..119932370,2	K562	blood:
7	chr5:119899537..119902283-chr5:119906756..119908959,2	K562	blood:
8	chr5:119858416..119860878-chr5:119871767..119873808,2	K562	blood:
9	chr5:119847102..119848643-chr5:119877942..119880653,2	K562	blood:
10	chr5:119980670..119983266-chr5:119989740..119991907,2	K562	blood:
11	chr5:119870688..119872446-chr5:119874411..119876714,2	K562	blood:
12	chr5:120020785..120023634-chr5:120024255..120028253,3	K562	blood:
13	chr5:119891736..119894093-chr5:119898854..119902222,3	K562	blood:
14	chr5:119990484..119993004-chr5:119995293..119997349,2	K562	blood:
15	chr5:119906837..119908623-chr5:119910419..119912812,2	K562	blood:
16	chr5:119866722..119869345-chr5:119872405..119873933,2	K562	blood:
17	chr5:119849515..119851535-chr5:119903167..119905944,2	K562	blood:
18	chr5:119980670..119983266-chr5:119989740..119991907,2	K562	blood:
19	chr5:120009986..120011754-chr5:120014103..120015876,2	K562	blood:
20	chr5:119886756..119889709-chr5:119891670..119893322,2	K562	blood:
21	chr5:119886756..119889709-chr5:119891670..119893322,2	K562	blood:
22	chr5:119991420..119991957-chr5:121285300..121286207,2	MCF-7	breast:
23	chr5:119877678..119879721-chr5:119882058..119884163,2	K562	blood:
24	chr5:119889111..119891337-chr5:119901156..119903856,2	K562	blood:
25	chr5:119899537..119902283-chr5:119906756..119908959,2	K562	blood:
26	chr5:119891736..119894093-chr5:119898854..119902222,3	K562	blood:
27	chr5:120009986..120011754-chr5:120014103..120015876,2	K562	blood:
28	chr5:119933357..119934903-chr5:119957823..119959697,2	K562	blood:
29	chr5:119991478..119992421-chr5:120138412..120139232,3	MCF-7	breast:
30	chr5:119991277..119991777-chr5:120137719..120138239,2	MCF-7	breast:
31	chr5:119875090..119877798-chr5:119880363..119881947,2	K562	blood:
32	chr5:119901221..119903356-chr5:119911285..119913616,2	K562	blood:
33	chr5:119870688..119872446-chr5:119874411..119876714,2	K562	blood:
34	chr5:119875090..119877798-chr5:119880363..119881947,2	K562	blood:
35	chr5:119990484..119993004-chr5:119995293..119997349,2	K562	blood:
36	chr5:119933357..119934903-chr5:119957823..119959697,2	K562	blood:
37	chr5:119889111..119891337-chr5:119901156..119903856,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LOX-9	chr5:119993772-119994066	NONHSAT103445

No data

Variant related genes	Relation type
ENSG00000270741	TF binding region
PRR16	TF binding region
ENSG00000270741	CpG island
PRR16	CpG island
ENSG00000184838	chromatin interactions

Extended variants
information (count: 6505 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:6505 , 50 per page) page: 1 2 3 4 5 6 7 ... 131

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4895161	chr5:119866504-119866505	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs559353015	chr5:119866506-119866507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs572819730	chr5:119866508-119866509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs2604160	chr5:119866531-119866532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs4895261	chr5:119866564-119866565	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs561497782	chr5:119866591-119866592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs150474668	chr5:119866608-119866609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs138334219	chr5:119866628-119866629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs544890017	chr5:119866629-119866630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs563828967	chr5:119866662-119866663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs371751232	chr5:119866689-119866690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs532454840	chr5:119866745-119866746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs553580993	chr5:119866754-119866755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs552580232	chr5:119866792-119866793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565731807	chr5:119866799-119866800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs192923878	chr5:119866811-119866812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs17425658	chr5:119866866-119866867	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs185144689	chr5:119866900-119866901	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs537270393	chr5:119866929-119866930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs202218546	chr5:119866933-119866934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs146421928	chr5:119866934-119866935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs189671206	chr5:119866969-119866970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs9327147	chr5:119866981-119866982	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs553052701	chr5:119867044-119867045	Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs531340724	chr5:119867062-119867063	Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs541782671	chr5:119867063-119867064	Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs12523269	chr5:119867065-119867066	Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs9327148	chr5:119867069-119867070	Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs575004315	chr5:119867129-119867130	Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs139135980	chr5:119867136-119867137	Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs534637952	chr5:119867162-119867163	Enhancers Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
32	rs1404300	chr5:119867182-119867183	Enhancers Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs1404299	chr5:119867187-119867188	Enhancers Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs559355763	chr5:119867226-119867227	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs143150312	chr5:119867287-119867288	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs537303187	chr5:119867349-119867350	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs75017769	chr5:119867360-119867361	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs369638228	chr5:119867361-119867362	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369965562	chr5:119867376-119867377	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs181522492	chr5:119867379-119867380	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550794648	chr5:119867408-119867409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs373110527	chr5:119867434-119867435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs570552560	chr5:119867463-119867464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs556435787	chr5:119867466-119867467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs539551835	chr5:119867472-119867473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs553091446	chr5:119867480-119867481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs566538719	chr5:119867488-119867489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs148443356	chr5:119867505-119867506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs555357145	chr5:119867590-119867591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs575088490	chr5:119867597-119867598	Weak transcription Enhancers	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
Prostate cancer	22341455	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:989 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:119839800-119879800	Weak transcription	Psoas Muscle	Psoas
2	chr5:119854000-119868800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr5:119864400-119867200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr5:119864600-119871400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr5:119864600-119874200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr5:119864600-119874400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr5:119865200-119867000	Weak transcription	NHDF-Ad	bronchial
8	chr5:119865400-119868600	Weak transcription	Osteobl	bone
9	chr5:119865400-119869600	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr5:119865800-119874000	Weak transcription	HSMM	muscle
11	chr5:119866200-119867400	Enhancers	Skeletal Muscle Male	skeletal muscle
12	chr5:119866400-119867200	Enhancers	Skeletal Muscle Female	skeletal muscle
13	chr5:119866400-119867200	Enhancers	HSMMtube	muscle
14	chr5:119866800-119867400	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr5:119867000-119867200	Flanking Bivalent TSS/Enh	Gastric	stomach
16	chr5:119867000-119867200	Enhancers	Left Ventricle	heart
17	chr5:119867000-119867400	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr5:119867000-119867400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr5:119867000-119867400	Enhancers	H1 Cell Line	embryonic stem cell
20	chr5:119867000-119867400	Enhancers	K562	blood
21	chr5:119867000-119867400	Enhancers	NHDF-Ad	bronchial
22	chr5:119867000-119869000	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr5:119867200-119867400	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr5:119867200-119867600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr5:119867200-119879800	Weak transcription	Left Ventricle	heart
26	chr5:119867400-119868600	Weak transcription	NHDF-Ad	bronchial
27	chr5:119867400-119868800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr5:119867400-119868800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr5:119867600-119867800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr5:119867600-119868800	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr5:119867800-119868800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr5:119868600-119869800	Enhancers	NHDF-Ad	bronchial
33	chr5:119868600-119869800	Enhancers	Osteobl	bone
34	chr5:119868800-119869200	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr5:119868800-119869200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr5:119868800-119869400	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr5:119868800-119869800	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr5:119868800-119870800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr5:119869000-119869800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr5:119869000-119874400	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr5:119869200-119869400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr5:119869200-119869600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr5:119869400-119869600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr5:119869400-119874200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr5:119869600-119869800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr5:119869600-119869800	Enhancers	Muscle Satellite Cultured Cells	--
47	chr5:119869600-119870000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr5:119869800-119871800	Weak transcription	Osteobl	bone
49	chr5:119869800-119873000	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr5:119869800-119873200	Weak transcription	NHDF-Ad	bronchial

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