Variant report

Variant	rs160709
Chromosome Location	chr5:43015214-43015215
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1)
CpG islands
(count:0)
Chromatin interactive
region (count:12)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr5:43015200-43015378	Hela-S3	cervix:	n/a	n/a

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:43015093..43022227-chr5:43063428..43069370,31	MCF-7	breast:
2	chr5:42912044..42912956-chr5:43015192..43016130,2	MCF-7	breast:
3	chr5:43014739..43026335-chr5:43034830..43045515,33	MCF-7	breast:
4	chr5:43014239..43016974-chr5:43061678..43063870,2	MCF-7	breast:
5	chr5:43013791..43017090-chr5:43037504..43040048,4	K562	blood:
6	chr5:43015196..43017902-chr5:43077071..43078758,2	K562	blood:
7	chr5:43013791..43016658-chr5:43037504..43040048,3	K562	blood:
8	chr5:43014339..43016528-chr5:43043270..43046214,3	K562	blood:
9	chr5:43014273..43017123-chr5:43048431..43050012,2	MCF-7	breast:
10	chr5:43014215..43016341-chr5:43018446..43020762,2	K562	blood:
11	chr5:43014475..43016471-chr5:43023730..43026437,2	K562	blood:
12	chr5:43014423..43017348-chr5:43018588..43021322,3	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C5orf39-1	chr5:43014838-43015252	ENSG00000177738
2	lnc-C5orf39-1	chr5:43013701-43015252	XLOC_004804
3	lnc-C5orf39-1	chr5:43014831-43015252	NR_104651
4	lnc-C5orf39-1	chr5:43014831-43015252	NR_104650

No data

Variant related genes	Relation type
ENSG00000251131	TF binding region
ENSG00000251131	Chromatin interaction
ENSG00000177721	Chromatin interaction
ENSG00000177738	Chromatin interaction
ENSG00000215068	Chromatin interaction
ENSG00000172262	Chromatin interaction

Extended variants
information (count: 110 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:97)

rs_ID	r²[population]
rs10064003	0.96[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap];0.84[YRI][hapmap];0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10522	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10941604	0.95[JPT][hapmap];0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10941605	0.81[CHB][hapmap];0.95[JPT][hapmap];0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11747435	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11747714	0.81[ASW][hapmap];0.87[CHD][hapmap];0.95[JPT][hapmap]
rs11748821	0.83[EUR][1000 genomes]
rs11958008	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12697439	0.92[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13169690	0.87[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13170208	0.94[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13171133	0.86[ASN][1000 genomes]
rs13178479	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13179934	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1542369	0.94[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.80[MEX][hapmap];0.80[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1574407	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs1618891	0.84[CHD][hapmap];0.90[JPT][hapmap]
rs1624415	0.84[CHD][hapmap];0.90[JPT][hapmap];0.80[YRI][hapmap]
rs178415	0.81[ASW][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.89[MKK][hapmap];0.84[YRI][hapmap]
rs186323	0.80[ASN][1000 genomes]
rs186324	0.83[CHB][hapmap];0.95[JPT][hapmap];0.92[YRI][hapmap];0.86[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs1902101	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2100473	1.00[CEU][hapmap];0.81[CHB][hapmap];0.95[JPT][hapmap];0.81[YRI][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2124069	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs222060	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2247280	0.89[AMR][1000 genomes]
rs2253450	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2329994	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2329995	0.92[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.92[TSI][hapmap];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2444779	0.88[YRI][hapmap]
rs2548334	0.87[ASW][hapmap];0.83[CHB][hapmap];0.87[CHD][hapmap];0.93[GIH][hapmap];0.95[JPT][hapmap];0.86[LWK][hapmap];1.00[MEX][hapmap];0.82[TSI][hapmap];0.92[YRI][hapmap];0.86[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs2548336	0.84[AFR][1000 genomes]
rs2548339	0.80[ASN][1000 genomes]
rs2548345	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2548349	0.88[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2548350	0.95[CEU][hapmap];0.87[CHB][hapmap];0.90[JPT][hapmap];0.84[YRI][hapmap];0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2548353	0.88[CEU][hapmap];0.95[JPT][hapmap];0.96[YRI][hapmap];0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2548356	0.88[CEU][hapmap];0.95[JPT][hapmap];0.92[YRI][hapmap];0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2548373	0.90[AMR][1000 genomes]
rs2603295	0.81[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs2603620	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2603634	0.90[AMR][1000 genomes]
rs2603636	0.81[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs2603644	0.95[JPT][hapmap];0.84[YRI][hapmap];0.85[AFR][1000 genomes]
rs2603656	0.83[CHB][hapmap];0.97[CHD][hapmap];0.95[JPT][hapmap];0.80[MEX][hapmap];0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2882295	0.95[JPT][hapmap];0.96[YRI][hapmap];0.86[AFR][1000 genomes]
rs2924817	0.87[AMR][1000 genomes]
rs309909	1.00[ASW][hapmap];0.96[CEU][hapmap];0.83[CHB][hapmap];0.92[CHD][hapmap];0.85[GIH][hapmap];0.95[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.86[TSI][hapmap];0.92[YRI][hapmap];0.92[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs309914	0.96[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs309921	0.85[AMR][1000 genomes]
rs309923	0.89[CHD][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap];0.84[MEX][hapmap];0.80[ASN][1000 genomes]
rs309924	0.81[CHB][hapmap];0.95[JPT][hapmap];0.87[YRI][hapmap];0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs309925	0.82[CHB][hapmap];0.95[JPT][hapmap];0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs309926	0.83[CHB][hapmap];0.95[JPT][hapmap];0.87[YRI][hapmap];0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs309927	0.83[CHB][hapmap];0.95[JPT][hapmap];0.82[YRI][hapmap];0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs309948	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs309950	0.87[ASW][hapmap];0.87[CHD][hapmap];0.95[JPT][hapmap];0.86[LWK][hapmap];0.92[YRI][hapmap];0.84[AFR][1000 genomes]
rs309951	0.83[ASN][1000 genomes]
rs316395	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs316396	0.86[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs316400	0.87[ASN][1000 genomes]
rs316402	0.81[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs316403	0.82[ASN][1000 genomes]
rs316404	0.81[ASW][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.88[MKK][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs316408	0.81[ASW][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];0.91[MKK][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs316413	1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.86[MKK][hapmap];0.96[YRI][hapmap]
rs316414	0.93[ASW][hapmap];0.88[CEU][hapmap];0.94[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];0.92[TSI][hapmap];0.92[YRI][hapmap];0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs316416	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs316419	0.98[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs316422	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3909456	0.89[CHD][hapmap];0.95[JPT][hapmap]
rs4033115	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4092293	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4092294	0.87[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.97[TSI][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4296812	0.92[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs512921	0.90[JPT][hapmap]
rs515970	0.83[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs543569	0.87[ASN][1000 genomes]
rs557076	0.84[CHD][hapmap];0.90[JPT][hapmap]
rs565761	0.85[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs567884	0.84[CHD][hapmap];0.90[JPT][hapmap]
rs613825	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs643307	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6451660	0.96[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6451661	0.96[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6451662	0.87[ASW][hapmap];0.92[CEU][hapmap];0.94[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.92[TSI][hapmap];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6875214	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6879130	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6892422	0.84[CHD][hapmap];0.90[JPT][hapmap]
rs724430	0.94[CHB][hapmap];0.95[JPT][hapmap];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs768441	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7715065	0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs782971	0.90[JPT][hapmap]
rs782978	0.84[CHD][hapmap];0.90[JPT][hapmap];0.84[YRI][hapmap]
rs782984	0.84[CHD][hapmap];0.90[JPT][hapmap]
rs903391	0.90[JPT][hapmap];0.82[YRI][hapmap]
rs9292862	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];0.92[MEX][hapmap];1.00[MKK][hapmap];0.94[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv993554	chr5:42720939-43251863	Bivalent/Poised TSS Strong transcription Active TSS Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	298 gene(s)	inside rSNPs	diseases
2	nsv462126	chr5:42728831-43237188	Active TSS Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	297 gene(s)	inside rSNPs	diseases
3	nsv597925	chr5:42728831-43237188	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	297 gene(s)	inside rSNPs	diseases
4	nsv1023741	chr5:42768215-43348145	Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	309 gene(s)	inside rSNPs	diseases
5	nsv537737	chr5:42768215-43348145	Genic enhancers Enhancers Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	309 gene(s)	inside rSNPs	diseases
6	nsv534185	chr5:42804840-43067088	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	165 gene(s)	inside rSNPs	diseases
7	nsv1029288	chr5:42928085-43047323	Flanking Bivalent TSS/Enh Active TSS Genic enhancers Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	120 gene(s)	inside rSNPs	diseases
8	nsv968169	chr5:42956713-43043472	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	116 gene(s)	inside rSNPs	diseases
9	nsv1024636	chr5:42959979-43295782	Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	283 gene(s)	inside rSNPs	diseases
10	nsv537739	chr5:42959979-43295782	Strong transcription Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	283 gene(s)	inside rSNPs	diseases
11	nsv880447	chr5:42967215-43030798	Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	97 gene(s)	inside rSNPs	diseases
12	nsv881640	chr5:42978644-43028221	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	94 gene(s)	inside rSNPs	diseases
13	nsv880415	chr5:42978644-43030798	Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	94 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs160709	LOC646887	cis	multi-tissue	Pritchard
rs160709	PPP2R2A	trans	parietal	SCAN
rs160709	LOC643977	cis	multi-tissue	Pritchard

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:43009000-43016200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr5:43009000-43016400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr5:43009000-43016600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr5:43009000-43017600	Weak transcription	Pancreas	Pancrea
5	chr5:43009400-43016600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr5:43010000-43017400	Weak transcription	Esophagus	oesophagus
7	chr5:43010400-43017000	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr5:43010400-43017400	Weak transcription	NHLF	lung
9	chr5:43010600-43016200	Weak transcription	Osteobl	bone
10	chr5:43010600-43017200	Weak transcription	HSMM	muscle
11	chr5:43010800-43016200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr5:43011000-43016200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr5:43011000-43016400	Weak transcription	Placenta	Placenta
14	chr5:43011000-43016400	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr5:43011000-43017600	Weak transcription	Gastric	stomach
16	chr5:43011000-43017600	Weak transcription	Lung	lung
17	chr5:43011200-43015600	Weak transcription	HUVEC	blood vessel
18	chr5:43011200-43016600	Weak transcription	NH-A	brain
19	chr5:43011200-43016800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr5:43011400-43015400	Weak transcription	Thymus	Thymus
21	chr5:43011400-43015600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr5:43011400-43016200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr5:43011400-43016400	Weak transcription	Spleen	Spleen
24	chr5:43011400-43017200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr5:43011400-43018200	Weak transcription	K562	blood
26	chr5:43011600-43015400	Weak transcription	Fetal Thymus	thymus
27	chr5:43011600-43015600	Weak transcription	Hela-S3	cervix
28	chr5:43011600-43016400	Weak transcription	Primary hematopoietic stem cells	blood
29	chr5:43011600-43016400	Weak transcription	NHDF-Ad	bronchial
30	chr5:43011800-43015400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr5:43011800-43015400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
32	chr5:43011800-43015400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr5:43011800-43016400	Weak transcription	Primary monocytes fromperipheralblood	blood
34	chr5:43011800-43016600	Weak transcription	Primary neutrophils fromperipheralblood	blood
35	chr5:43011800-43016600	Weak transcription	Monocytes-CD14+_RO01746	blood
36	chr5:43012000-43015400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr5:43012000-43016200	Weak transcription	Primary B cells from cord blood	blood
38	chr5:43012000-43016200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr5:43012400-43015400	Weak transcription	Primary B cells from peripheral blood	blood
40	chr5:43014000-43015400	Genic enhancers	Dnd41	blood
41	chr5:43014200-43015400	Enhancers	Primary T cells from cord blood	blood
42	chr5:43014200-43016800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
43	chr5:43014400-43015800	Enhancers	Primary T helper cells fromperipheralblood	blood
44	chr5:43014400-43016400	Enhancers	Primary T helper cells PMA-I stimulated	--
45	chr5:43014400-43016800	Enhancers	Primary T helper naive cells from peripheral blood	blood
46	chr5:43014600-43016800	Enhancers	Primary T cells fromperipheralblood	blood
47	chr5:43014800-43017000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr5:43015000-43015600	Enhancers	GM12878-XiMat	blood
49	chr5:43015000-43016200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr5:43015000-43016200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell

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