Variant report

Variant	rs7527788
Chromosome Location	chr1:152596414-152596415
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
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	ZNF274	chr1:152596357-152596896	NT2-D1	testis:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:152596413-152596463	HRCEpiC	kidney:	n/a
2	chr1:152596413-152596463	BE2_C	brain:	n/a
3	chr1:152596413-152596463	HCF	heart:	n/a
4	chr1:152596413-152596463	MCF-7	breast:	n/a
5	chr1:152596413-152596463	GM12878	blood:	n/a
6	chr1:152596413-152596463	GM12891	blood:	n/a
7	chr1:152596413-152596463	SKMC	muscle:	n/a
8	chr1:152596413-152596463	SK-N-MC	brain:	n/a
9	chr1:152596413-152596463	Hepatocyte	liver:	n/a
10	chr1:152596413-152596463	PFSK-1	brain:	n/a
11	chr1:152596413-152596463	HAEpiC	amniotic membrane:	n/a
12	chr1:152596413-152596463	HCPEpiC	choroid plexus:	n/a
13	chr1:152596413-152596463	H1-hESC	embryonic stem cell:	embryo
14	chr1:152596413-152596463	T-47D	breast:	n/a
15	chr1:152596413-152596463	HCT-116	colon:	n/a
16	chr1:152596413-152596463	BJ	skin:	n/a
17	chr1:152596413-152596463	AG09309	skin:	n/a
18	chr1:152596413-152596463	SK-N-SH	brain:	n/a
19	chr1:152596413-152596463	NT2-D1	testis:	n/a
20	chr1:152596413-152596463	HEEpiC	esophagus:	n/a
21	chr1:152596413-152596463	HRPEpiC	eye:	n/a
22	chr1:152596413-152596463	U87	brain:	n/a
23	chr1:152596413-152596463	AG09319	gingival:	n/a
24	chr1:152596413-152596463	HMEC	breast:	n/a
25	chr1:152596413-152596463	SK-N-SH_RA	brain:	n/a
26	chr1:152596413-152596463	HCM	heart:	n/a
27	chr1:152596413-152596463	Caco-2	colon:	n/a
28	chr1:152596413-152596463	NHDF-neo	bronchial:	n/a
29	chr1:152596413-152596463	ProgFib	skin:	n/a
30	chr1:152596413-152596463	CMK	blood:	n/a
31	chr1:152596413-152596463	IMR90	lung:	fetal
32	chr1:152596413-152596463	GM12892	blood:	n/a
33	chr1:152596413-152596463	PANC-1	pancreas:	n/a
34	chr1:152596413-152596463	NB4	blood:	n/a
35	chr1:152596413-152596463	SAEC	small airway:	n/a
36	chr1:152596413-152596463	NHBE	bronchial:	n/a
37	chr1:152596413-152596463	K562	blood:	n/a
38	chr1:152596413-152596463	AG04449	skin:	fetal
39	chr1:152596413-152596463	HepG2	liver:	n/a
40	chr1:152596413-152596463	AG04450	lung:	fetal
41	chr1:152596413-152596463	LNCaP	prostate:	n/a
42	chr1:152596413-152596463	Hela-S3	cervix:	n/a
43	chr1:152596413-152596463	NH-A	brain:	n/a
44	chr1:152596413-152596463	ECC-1	luminal epithelium:	n/a
45	chr1:152596413-152596463	HL-60	blood:	n/a
46	chr1:152596413-152596463	HNPCEpiC	eye:	n/a
47	chr1:152596413-152596463	GM19239	blood:	n/a
48	chr1:152596413-152596463	GM06990	blood:	n/a
49	chr1:152596413-152596463	A549	lung:	n/a
50	chr1:152596413-152596463	ovcar-3	ovarian:	n/a

No data

Variant related genes	Relation type
LCE3A	TF binding region
LCE3A	CpG island

Extended variants
information (count: 121 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:101)

rs_ID	r²[population]
rs1011297	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10749673	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10788843	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10788844	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10888504	0.86[CHB][hapmap];0.97[CHD][hapmap]
rs10888505	0.86[CHB][hapmap];0.97[CHD][hapmap]
rs10888506	0.86[ASN][1000 genomes]
rs10888507	0.86[CHB][hapmap];0.97[CHD][hapmap];0.86[ASN][1000 genomes]
rs11205045	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11205046	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11205047	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11205048	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11205049	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11205050	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11205060	0.86[CHB][hapmap];0.97[CHD][hapmap]
rs11205061	0.86[CHB][hapmap];0.97[CHD][hapmap];0.86[ASN][1000 genomes]
rs11205062	0.97[CHD][hapmap];0.85[ASN][1000 genomes]
rs11205072	0.85[ASN][1000 genomes]
rs11205073	1.00[CEU][hapmap];0.90[CHB][hapmap];0.94[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.91[TSI][hapmap];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11205078	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11205080	0.90[ASW][hapmap]
rs11205083	0.88[CEU][hapmap];0.90[JPT][hapmap]
rs11580546	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11581621	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11582021	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11587218	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12032251	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12041270	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12043198	0.85[ASN][1000 genomes]
rs12071335	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12074783	0.83[ASN][1000 genomes]
rs12081753	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12081793	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12239432	0.87[ASN][1000 genomes]
rs12239456	0.87[ASN][1000 genomes]
rs12564254	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12564476	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12566080	0.87[ASN][1000 genomes]
rs12728742	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12745646	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12752346	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1325508	0.87[ASN][1000 genomes]
rs1332497	0.94[CHD][hapmap]
rs1359515	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];0.95[TSI][hapmap];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1359516	0.87[ASN][1000 genomes]
rs1412542	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap]
rs1474168	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1474169	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1575753	0.87[ASN][1000 genomes]
rs1581802	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.95[TSI][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1581804	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.98[TSI][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1853805	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1886732	0.85[ASN][1000 genomes]
rs1888966	0.85[ASN][1000 genomes]
rs1925661	0.94[CHD][hapmap];0.85[ASN][1000 genomes]
rs1925663	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1930126	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3904413	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap]
rs3904414	0.82[ASN][1000 genomes]
rs3904415	0.83[ASN][1000 genomes]
rs3908717	0.83[ASN][1000 genomes]
rs4287181	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];0.91[TSI][hapmap];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4320779	0.90[CHB][hapmap];0.97[CHD][hapmap];0.85[ASN][1000 genomes]
rs4353096	0.87[ASN][1000 genomes]
rs4540662	0.87[ASN][1000 genomes]
rs4845317	1.00[CEU][hapmap];0.90[CHB][hapmap];0.92[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.91[TSI][hapmap];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4845445	0.86[EUR][1000 genomes]
rs4845456	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4845457	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs512208	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs55644922	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55687384	0.87[ASN][1000 genomes]
rs59349974	0.84[ASN][1000 genomes]
rs59540569	0.87[ASN][1000 genomes]
rs59633986	0.87[ASN][1000 genomes]
rs59863780	0.87[ASN][1000 genomes]
rs60208884	0.87[ASN][1000 genomes]
rs60350222	0.87[ASN][1000 genomes]
rs60861680	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61813877	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6660162	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6662989	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6671975	0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6687570	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6687574	1.00[CEU][hapmap];0.88[TSI][hapmap];0.94[EUR][1000 genomes]
rs6687682	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6702474	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73009167	0.85[ASN][1000 genomes]
rs7540520	0.85[EUR][1000 genomes]
rs908929	0.86[CHB][hapmap];0.97[CHD][hapmap]
rs925976	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs925977	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs942826	0.86[CHB][hapmap];1.00[CHD][hapmap];0.87[ASN][1000 genomes]
rs942827	0.87[ASN][1000 genomes]
rs960752	0.81[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];0.97[TSI][hapmap];0.83[YRI][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs989831	0.87[ASN][1000 genomes]
rs989832	0.87[ASN][1000 genomes]
rs989833	0.87[ASN][1000 genomes]
rs989834	0.86[CHB][hapmap];1.00[CHD][hapmap];0.87[ASN][1000 genomes]
rs9970033	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9970657	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2750810	chr1:152453669-152660927	Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	esv1827111	chr1:152472839-152690073	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	esv1830764	chr1:152472839-152690073	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	esv2757755	chr1:152472839-152898153	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
5	esv2758970	chr1:152472839-152898153	ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
6	nsv547878	chr1:152530510-152597948	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
7	nsv2888	chr1:152532137-152620444	Flanking Active TSS Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv68	chr1:152549956-152608472	Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
9	esv33483	chr1:152550269-152775526	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
10	nsv872447	chr1:152551276-152643160	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
11	nsv535168	chr1:152555074-152617494	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	esv2764248	chr1:152555527-152597371	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
13	nsv547891	chr1:152556085-152770446	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
14	nsv872448	chr1:152561408-152643160	Weak transcription Bivalent/Poised TSS Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
15	nsv469873	chr1:152563260-152713616	ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
16	nsv482518	chr1:152563260-152713616	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
17	nsv535169	chr1:152572876-152600388	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
18	nsv1001647	chr1:152572876-152678509	Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
19	nsv427786	chr1:152572990-152898153	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
20	nsv872449	chr1:152583678-152643160	Weak transcription Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs7527788	SMCP	cis	cerebellum	SCAN
rs7527788	NUP210L	cis	parietal	SCAN
rs7527788	VPS45	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:152595200-152596600	Enhancers	Monocytes-CD14+_RO01746	blood
2	chr1:152595600-152596800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr1:152596000-152596600	Enhancers	Muscle Satellite Cultured Cells	--
4	chr1:152596000-152596800	Enhancers	Fetal Muscle Trunk	muscle
5	chr1:152596200-152596800	Enhancers	Fetal Muscle Leg	muscle
6	chr1:152596200-152597000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr1:152596400-152596800	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr1:152596400-152597000	Enhancers	HSMM	muscle
9	chr1:152596400-152597200	Weak transcription	Pancreas	Pancrea
10	chr1:152596400-152599400	Weak transcription	Adipose Nuclei	Adipose

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