Variant report

Variant	rs6676749
Chromosome Location	chr1:45264545-45264546
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:6)
CpG islands
(count:0)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:6 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MAFF	chr1:45264381-45264635	K562	blood:	n/a	chr1:45264496-45264514
2	FOXA2	chr1:45264414-45264696	HepG2	liver:	n/a	n/a
3	MAFK	chr1:45264341-45264667	HepG2	liver:	n/a	chr1:45264497-45264512
4	MAFF	chr1:45264370-45264670	HepG2	liver:	n/a	chr1:45264496-45264514
5	MAFK	chr1:45264433-45264622	K562	blood:	n/a	chr1:45264497-45264512
6	MAFK	chr1:45264363-45264635	HepG2	liver:	n/a	chr1:45264497-45264512

No data

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:45264279..45267905-chr1:45476139..45480748,9	K562	blood:
2	chr1:45194731..45198369-chr1:45262951..45267593,8	MCF-7	breast:
3	chr1:45186012..45189065-chr1:45262922..45268915,8	MCF-7	breast:
4	chr1:45181918..45183928-chr1:45263993..45265560,2	MCF-7	breast:
5	chr1:45239518..45243020-chr1:45264375..45267077,6	MCF-7	breast:
6	chr1:45262923..45267744-chr1:45767225..45772183,8	K562	blood:
7	chr1:45194156..45199355-chr1:45264282..45268731,9	MCF-7	breast:
8	chr1:45264331..45265874-chr1:46048752..46050631,2	K562	blood:
9	chr1:45238319..45262026-chr1:45262351..45301953,358	K562	blood:
10	chr1:45239609..45242950-chr1:45264036..45267552,6	MCF-7	breast:
11	chr1:45264331..45266422-chr1:46049131..46050804,3	K562	blood:
12	chr1:45178001..45208867-chr1:45262751..45305400,520	K562	blood:
13	chr1:45264355..45267553-chr1:45476139..45481796,8	K562	blood:
14	chr1:45248852..45254229-chr1:45263166..45267959,10	MCF-7	breast:
15	chr1:45178748..45209946-chr1:45262890..45299284,515	K562	blood:

No data

Variant related genes	Relation type
PLK3	TF binding region
ENSG00000132780	Chromatin interaction
ENSG00000142959	Chromatin interaction
ENSG00000198520	Chromatin interaction
ENSG00000264294	Chromatin interaction
ENSG00000207421	Chromatin interaction
ENSG00000126107	Chromatin interaction
ENSG00000200169	Chromatin interaction
ENSG00000225721	Chromatin interaction
ENSG00000126088	Chromatin interaction
ENSG00000162415	Chromatin interaction
ENSG00000199377	Chromatin interaction
ENSG00000142945	Chromatin interaction
ENSG00000200913	Chromatin interaction
ENSG00000142937	Chromatin interaction
ENSG00000234093	Chromatin interaction
ENSG00000202031	Chromatin interaction

Extended variants
information (count: 107 )
Associated
traits (count: 10 )

rSNPs within LD-proxies of this variant (count:94)

rs_ID	r²[population]
rs10890313	0.93[CEU][hapmap]
rs11211025	0.92[CEU][hapmap]
rs11211026	0.93[CEU][hapmap];0.85[TSI][hapmap]
rs11211036	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11211038	0.81[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];1.00[LWK][hapmap];0.93[MEX][hapmap];0.87[MKK][hapmap];0.95[TSI][hapmap];0.86[YRI][hapmap];0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11211040	0.81[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.87[MKK][hapmap];0.95[TSI][hapmap];0.94[YRI][hapmap];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11211045	0.90[ASN][1000 genomes]
rs11211048	0.90[ASN][1000 genomes]
rs11211051	0.88[ASN][1000 genomes]
rs11211053	0.93[CEU][hapmap];0.90[CHB][hapmap];0.89[JPT][hapmap]
rs1140279	0.89[ASW][hapmap];0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.88[MEX][hapmap];0.82[MKK][hapmap];0.90[TSI][hapmap];0.81[YRI][hapmap];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11556200	0.85[CHD][hapmap]
rs11573542	0.89[ASN][1000 genomes]
rs11573557	0.87[ASN][1000 genomes]
rs11573559	0.87[ASN][1000 genomes]
rs11573562	1.00[CEU][hapmap];0.95[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];0.81[JPT][hapmap];0.87[MEX][hapmap];0.95[TSI][hapmap];0.87[ASN][1000 genomes]
rs11573592	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11578233	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11580010	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11580159	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11582718	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11584440	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];0.95[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11800505	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11801990	0.95[CHB][hapmap];0.85[JPT][hapmap];0.85[ASN][1000 genomes]
rs11803622	1.00[CEU][hapmap];0.95[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];0.84[JPT][hapmap];0.87[MEX][hapmap];0.90[TSI][hapmap];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11806832	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11809931	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12125367	0.85[CHD][hapmap]
rs12126318	0.82[CHD][hapmap]
rs12126557	0.84[CEU][hapmap]
rs12139143	1.00[CEU][hapmap];0.95[CHB][hapmap];0.89[CHD][hapmap];0.96[GIH][hapmap];0.89[JPT][hapmap];0.91[TSI][hapmap];0.87[ASN][1000 genomes]
rs12566610	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12569156	0.90[ASN][1000 genomes]
rs12723764	0.90[ASN][1000 genomes]
rs12729917	0.87[ASN][1000 genomes]
rs12732939	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12733586	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.89[ASN][1000 genomes]
rs12733796	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12735038	0.90[ASN][1000 genomes]
rs12735637	0.85[CHD][hapmap]
rs12735728	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12738360	0.90[ASN][1000 genomes]
rs12741443	0.94[ASN][1000 genomes]
rs12746270	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[TSI][hapmap];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12749130	0.85[CHD][hapmap]
rs16832227	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16832263	1.00[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];0.81[JPT][hapmap];0.94[MEX][hapmap];0.95[TSI][hapmap];0.87[ASN][1000 genomes]
rs16832265	0.90[ASN][1000 genomes]
rs17881698	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];0.91[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17883049	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.94[LWK][hapmap];0.94[MEX][hapmap];0.95[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17886118	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2295997	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];0.88[JPT][hapmap];0.94[MEX][hapmap];0.95[TSI][hapmap];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2295998	0.91[ASN][1000 genomes]
rs2295999	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs263989	0.85[CHD][hapmap]
rs264022	0.85[CHD][hapmap]
rs264025	0.85[CHD][hapmap]
rs34436945	0.87[ASN][1000 genomes]
rs34541568	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34639510	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34984079	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35343809	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35932693	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs35957134	0.90[ASN][1000 genomes]
rs364482	0.85[CHD][hapmap]
rs3795713	0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3795714	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3795719	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3820586	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[TSI][hapmap];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4342887	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap];0.95[TSI][hapmap];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4399199	0.85[CHD][hapmap]
rs57995027	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs59366549	0.90[ASN][1000 genomes]
rs59788723	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6429549	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6429550	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.90[ASN][1000 genomes]
rs6670449	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6689911	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[TSI][hapmap];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6692487	1.00[CEU][hapmap];0.94[CHB][hapmap];0.89[JPT][hapmap];0.90[ASN][1000 genomes]
rs6695350	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6697153	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6702415	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6703452	1.00[CEU][hapmap];0.95[CHB][hapmap];0.89[CHD][hapmap];0.96[GIH][hapmap];0.89[JPT][hapmap];0.91[TSI][hapmap];0.87[ASN][1000 genomes]
rs6704436	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs67408784	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs67742332	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7517439	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];1.00[GIH][hapmap];0.89[JPT][hapmap];0.91[TSI][hapmap];0.90[ASN][1000 genomes]
rs7517639	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.90[ASN][1000 genomes]
rs7527787	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7528461	0.90[ASN][1000 genomes]
rs7534487	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7536078	0.94[CHB][hapmap];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7539538	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7546285	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.89[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	nsv533037	chr1:44361728-45333408	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	469 gene(s)	inside rSNPs	diseases
2	nsv998476	chr1:45001278-45311757	Flanking Active TSS Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	426 gene(s)	inside rSNPs	diseases
3	nsv534941	chr1:45001278-45311757	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	426 gene(s)	inside rSNPs	diseases
4	nsv1014894	chr1:45139123-45397943	Flanking Active TSS Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	414 gene(s)	inside rSNPs	diseases
5	nsv529677	chr1:45179509-45748571	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	424 gene(s)	inside rSNPs	diseases
6	nsv1002026	chr1:45187594-45758048	Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	386 gene(s)	inside rSNPs	diseases
7	nsv461406	chr1:45218542-45293518	Strong transcription Flanking Active TSS Genic enhancers Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	127 gene(s)	inside rSNPs	diseases
8	nsv546145	chr1:45218542-45293518	Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	127 gene(s)	inside rSNPs	diseases
9	nsv870815	chr1:45233638-45318752	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	127 gene(s)	inside rSNPs	diseases
10	nsv546146	chr1:45258141-45318752	Genic enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	109 gene(s)	inside rSNPs	diseases
11	nsv871320	chr1:45259295-45274841	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	58 gene(s)	inside rSNPs	diseases
12	nsv870773	chr1:45259295-45287306	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	108 gene(s)	inside rSNPs	diseases
13	nsv870876	chr1:45264545-45273531	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	56 gene(s)	inside rSNPs	diseases

mRNA abundance (count:10)

SNP	Gene	Cis/trans	Tissue	Source
rs6676749	SNORD55	cis	cerebellum	SCAN
rs6676749	TIE1	cis	parietal	SCAN
rs6676749	SNORD55	cis	parietal	SCAN
rs6676749	UROD	cis	multi-tissue	Pritchard
rs6676749	BEST4	cis	lymphoblastoid	seeQTL
rs6676749	UROD	cis	Artery Tibial	GTEx
rs6676749	ZNF691	cis	cerebellum	SCAN
rs6676749	EIF2B3	cis	cerebellum	SCAN
rs6676749	UROD	cis	lung	GTEx
rs6676749	FOXJ3	cis	parietal	SCAN

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:45252400-45265200	Weak transcription	Right Atrium	heart
2	chr1:45252400-45265600	Weak transcription	Gastric	stomach
3	chr1:45256000-45264800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:45256000-45265200	Weak transcription	NHEK	skin
5	chr1:45257400-45264800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr1:45259200-45265400	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr1:45259200-45265600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr1:45259400-45264600	Weak transcription	Fetal Intestine Large	intestine
9	chr1:45259400-45264600	Weak transcription	Hela-S3	cervix
10	chr1:45259400-45265200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr1:45259400-45265200	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr1:45259400-45265400	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr1:45259600-45264600	Weak transcription	NH-A	brain
14	chr1:45259600-45264800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr1:45259600-45264800	Weak transcription	Esophagus	oesophagus
16	chr1:45259600-45265200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr1:45259600-45265200	Weak transcription	Osteobl	bone
18	chr1:45259800-45265200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr1:45261200-45265000	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr1:45262600-45264600	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr1:45262600-45265000	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr1:45262800-45264600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr1:45262800-45264800	Weak transcription	Placenta	Placenta
24	chr1:45264000-45265200	Enhancers	HepG2	liver
25	chr1:45264200-45264600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr1:45264200-45264600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr1:45264200-45264600	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr1:45264200-45264800	Enhancers	K562	blood
29	chr1:45264200-45265000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr1:45264200-45265000	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr1:45264200-45265200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr1:45264200-45265200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr1:45264200-45265200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr1:45264200-45265200	Enhancers	HMEC	breast
35	chr1:45264200-45265400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr1:45264200-45265600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr1:45264200-45265600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr1:45264400-45265200	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr1:45264400-45265200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr1:45264400-45265200	Enhancers	Skeletal Muscle Female	skeletal muscle
41	chr1:45264400-45265200	Enhancers	A549	lung
42	chr1:45264400-45265200	Enhancers	Dnd41	blood
43	chr1:45264400-45265400	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr1:45264400-45265400	Enhancers	Primary B cells from peripheral blood	blood
45	chr1:45264400-45265400	Enhancers	Liver	Liver

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