Variant report

Variant	rs6727929
Chromosome Location	chr2:48795109-48795110
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:48795067-48795117	AoSMC	blood vessel:	n/a
2	chr2:48795067-48795117	PrEC	prostate:	n/a
3	chr2:48795067-48795117	LNCaP	prostate:	n/a
4	chr2:48795067-48795117	HCT-116	colon:	n/a
5	chr2:48795067-48795117	GM19239	blood:	n/a
6	chr2:48795067-48795117	A549	lung:	n/a
7	chr2:48795067-48795117	SK-N-SH_RA	brain:	n/a
8	chr2:48795067-48795117	NT2-D1	testis:	n/a
9	chr2:48795067-48795117	HPAEpiC	pulmonary alveolar:	n/a
10	chr2:48795067-48795117	HIPEpiC	eye:	n/a
11	chr2:48795067-48795117	HCM	heart:	n/a
12	chr2:48795067-48795117	MCF-7	breast:	n/a
13	chr2:48795067-48795117	HL-60	blood:	n/a
14	chr2:48795067-48795117	GM12878	blood:	n/a
15	chr2:48795067-48795117	SK-N-MC	brain:	n/a
16	chr2:48795067-48795117	HNPCEpiC	eye:	n/a
17	chr2:48795067-48795117	U87	brain:	n/a
18	chr2:48795067-48795117	HepG2	liver:	n/a
19	chr2:48795067-48795117	HRCEpiC	kidney:	n/a
20	chr2:48795067-48795117	Hepatocyte	liver:	n/a
21	chr2:48795067-48795117	HMEC	breast:	n/a
22	chr2:48795067-48795117	SK-N-SH	brain:	n/a
23	chr2:48795067-48795117	CMK	blood:	n/a
24	chr2:48795067-48795117	GM06990	blood:	n/a
25	chr2:48795067-48795117	AG09319	gingival:	n/a
26	chr2:48795067-48795117	BJ	skin:	n/a
27	chr2:48795067-48795117	NHBE	bronchial:	n/a
28	chr2:48795067-48795117	GM12891	blood:	n/a
29	chr2:48795067-48795117	HRE	kidney:	n/a
30	chr2:48795067-48795117	Jurkat	blood:	n/a
31	chr2:48795067-48795117	HRPEpiC	eye:	n/a
32	chr2:48795067-48795117	Caco-2	colon:	n/a
33	chr2:48795067-48795117	HEK293	kidney:	embryo
34	chr2:48795067-48795117	ovcar-3	ovarian:	n/a
35	chr2:48795067-48795117	PFSK-1	brain:	n/a
36	chr2:48795067-48795117	Hela-S3	cervix:	n/a
37	chr2:48795067-48795117	T-47D	breast:	n/a
38	chr2:48795067-48795117	RPTEC	kidney:	n/a
39	chr2:48795067-48795117	NB4	blood:	n/a
40	chr2:48795067-48795117	IMR90	lung:	fetal
41	chr2:48795067-48795117	AG04449	skin:	fetal
42	chr2:48795067-48795117	SAEC	small airway:	n/a
43	chr2:48795067-48795117	BE2_C	brain:	n/a
44	chr2:48795067-48795117	MCF10A-Er-Src	breast:	n/a
45	chr2:48795067-48795117	NHDF-neo	bronchial:	n/a
46	chr2:48795067-48795117	NH-A	brain:	n/a
47	chr2:48795067-48795117	HAEpiC	amniotic membrane:	n/a
48	chr2:48795067-48795117	ECC-1	luminal epithelium:	n/a
49	chr2:48795067-48795117	H1-hESC	embryonic stem cell:	embryo
50	chr2:48795067-48795117	HCF	heart:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:48788958..48790786-chr2:48792304..48795204,2	K562	blood:

No data

Variant related genes	Relation type
STON1-GTF2A1L	CpG island

Extended variants
information (count: 82 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs10495953	0.92[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.96[YRI][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11676150	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11678306	0.85[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.96[YRI][hapmap];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11680574	0.85[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.96[YRI][hapmap];0.84[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs11681276	0.85[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.96[YRI][hapmap];0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11681426	0.81[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.96[YRI][hapmap];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11681868	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11683611	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11693429	0.89[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11693559	0.85[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.96[YRI][hapmap];0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11693691	0.85[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap];0.96[YRI][hapmap];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12475789	0.97[ASN][1000 genomes]
rs12990079	1.00[CHB][hapmap];0.95[JPT][hapmap];0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12992755	0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12992870	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12999304	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13010692	0.84[YRI][hapmap];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13011288	1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];0.99[ASN][1000 genomes]
rs13014112	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13016899	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13025488	0.80[ASW][hapmap];0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[LWK][hapmap];0.95[MEX][hapmap];0.87[TSI][hapmap];0.96[YRI][hapmap];0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13027618	0.81[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.96[YRI][hapmap];0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13030948	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13031184	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13034063	0.81[AMR][1000 genomes]
rs13034951	0.81[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.96[YRI][hapmap];0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17037412	1.00[CHB][hapmap]
rs17039250	0.85[CEU][hapmap];0.82[CHB][hapmap];0.91[JPT][hapmap];0.96[YRI][hapmap];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1996970	1.00[CHB][hapmap];0.95[JPT][hapmap];0.99[ASN][1000 genomes]
rs2103112	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2177489	0.96[CEU][hapmap];0.87[CHB][hapmap];0.86[JPT][hapmap];0.96[YRI][hapmap];0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2293270	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2293271	0.83[ASN][1000 genomes]
rs2293272	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2293274	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2349098	0.94[ASW][hapmap];0.89[CEU][hapmap];0.87[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];0.95[JPT][hapmap];1.00[LWK][hapmap];0.95[MEX][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2882084	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3749142	1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];0.92[YRI][hapmap];0.99[ASN][1000 genomes]
rs3749144	0.85[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.96[YRI][hapmap];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3749145	0.88[ASW][hapmap];0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];0.95[MEX][hapmap];0.90[TSI][hapmap];0.96[YRI][hapmap];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3792234	0.87[CHB][hapmap];1.00[CHD][hapmap];0.91[JPT][hapmap];0.92[YRI][hapmap];0.91[ASN][1000 genomes]
rs3792235	0.82[ASW][hapmap];0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.80[GIH][hapmap];0.95[JPT][hapmap];0.83[LWK][hapmap];0.95[MEX][hapmap];0.90[MKK][hapmap];0.90[TSI][hapmap];0.96[YRI][hapmap];0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3792236	0.88[ASW][hapmap];0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];0.90[MEX][hapmap];0.90[TSI][hapmap];0.87[YRI][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3792237	0.85[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.96[YRI][hapmap];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3792238	0.91[CHB][hapmap];0.91[JPT][hapmap];0.95[ASN][1000 genomes]
rs3828340	0.88[ASW][hapmap];0.92[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.90[TSI][hapmap];0.96[YRI][hapmap];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4566410	0.85[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.96[YRI][hapmap];0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55641971	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs55700200	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs55858189	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56111874	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62135230	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62135231	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62135232	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62135233	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62135236	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6545048	0.92[ASN][1000 genomes]
rs66888174	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6709043	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6710565	0.95[CHB][hapmap];0.90[JPT][hapmap];0.96[ASN][1000 genomes]
rs6712592	0.85[CEU][hapmap];0.87[CHB][hapmap];0.95[JPT][hapmap];0.96[YRI][hapmap];0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6712724	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6716291	1.00[CHB][hapmap];0.95[JPT][hapmap];0.88[YRI][hapmap];0.97[ASN][1000 genomes]
rs6722556	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6729860	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6732365	0.88[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.92[TSI][hapmap];0.81[YRI][hapmap];0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6737732	0.80[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs6741341	0.92[CEU][hapmap];0.87[CHB][hapmap];0.95[JPT][hapmap];0.96[YRI][hapmap];0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6741677	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6742725	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6757847	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6761796	0.99[ASN][1000 genomes]
rs940389	0.89[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005954	chr2:48692696-48905723	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv535682	chr2:48692696-48905723	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv833981	chr2:48705444-48878179	ZNF genes & repeats Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1007491	chr2:48752185-48796441	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv535683	chr2:48752185-48796441	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv581776	chr2:48763382-48913019	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv1000419	chr2:48766957-48795327	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv1010494	chr2:48767055-49027310	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
9	nsv1002793	chr2:48771220-49466550	ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	11 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs6727929	STON1	cis	Esophagus Muscularis	GTEx
rs6727929	STON1-GTF2A1L	cis	lung	GTEx
rs6727929	FOXN2	cis	parietal	SCAN
rs6727929	STON1-GTF2A1L	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:48759000-48827600	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr2:48767200-48807800	Weak transcription	Aorta	Aorta
3	chr2:48773000-48808800	Weak transcription	Right Ventricle	heart
4	chr2:48777200-48807800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr2:48779400-48800200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr2:48787800-48802200	Weak transcription	Esophagus	oesophagus
7	chr2:48788200-48795200	Weak transcription	Right Atrium	heart
8	chr2:48788200-48798200	Weak transcription	Lung	lung
9	chr2:48788400-48799400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr2:48788400-48804600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr2:48788600-48812000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr2:48790000-48800000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr2:48793000-48795600	Enhancers	Colon Smooth Muscle	Colon
14	chr2:48793200-48796000	Enhancers	Fetal Lung	lung
15	chr2:48793600-48795400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr2:48793600-48795600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr2:48793600-48795600	Enhancers	Fetal Stomach	stomach
18	chr2:48793600-48796200	Enhancers	Fetal Kidney	kidney
19	chr2:48793600-48796200	Enhancers	Placenta	Placenta
20	chr2:48793800-48795200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr2:48793800-48795400	Enhancers	Brain Hippocampus Middle	brain
22	chr2:48793800-48795600	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr2:48793800-48795600	Enhancers	Fetal Heart	heart
24	chr2:48793800-48795800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr2:48793800-48795800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr2:48793800-48796000	Enhancers	Adipose Nuclei	Adipose
27	chr2:48793800-48796000	Enhancers	Fetal Muscle Leg	muscle
28	chr2:48793800-48796000	Enhancers	Rectal Smooth Muscle	rectum
29	chr2:48794000-48795200	Enhancers	Brain Inferior Temporal Lobe	brain
30	chr2:48794000-48795400	Enhancers	Duodenum Smooth Muscle	Duodenum
31	chr2:48794000-48796000	Enhancers	Brain Substantia Nigra	brain
32	chr2:48794000-48807800	Weak transcription	Psoas Muscle	Psoas
33	chr2:48794200-48807800	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr2:48794400-48795600	Enhancers	Osteobl	bone
35	chr2:48794400-48796200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr2:48794400-48799600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr2:48794400-48807800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr2:48794400-48812000	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr2:48794400-48827200	Weak transcription	NHDF-Ad	bronchial
40	chr2:48794600-48795200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr2:48794600-48796400	Enhancers	Placenta Amnion	Placenta Amnion
42	chr2:48794600-48811200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr2:48794800-48795400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr2:48794800-48795600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr2:48794800-48796200	Enhancers	Ovary	ovary
46	chr2:48794800-48798200	Weak transcription	Fetal Muscle Trunk	muscle
47	chr2:48795000-48795400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr2:48795000-48795400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr2:48795000-48795600	Enhancers	HSMMtube	muscle
50	chr2:48795000-48796200	Genic enhancers	Stomach Smooth Muscle	stomach

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