Variant report

Variant	rs2005892
Chromosome Location	chr2:39586264-39586265
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:39569119..39570627-chr2:39583431..39586281,2	K562	blood:

Extended variants
information (count: 129 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:109)

rs_ID	r²[population]
rs10153665	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.97[GIH][hapmap];0.81[JPT][hapmap];0.89[MEX][hapmap];0.87[TSI][hapmap];0.94[EUR][1000 genomes]
rs10170424	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10170604	0.89[AFR][1000 genomes]
rs10170617	0.87[EUR][1000 genomes]
rs10172736	1.00[CEU][hapmap];0.81[GIH][hapmap];0.90[EUR][1000 genomes]
rs10173556	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10174268	0.86[CHB][hapmap]
rs10175038	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10175333	0.88[YRI][hapmap];0.84[AFR][1000 genomes]
rs10181650	0.85[AFR][1000 genomes]
rs10190069	0.87[AFR][1000 genomes];0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10195629	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1035232	0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10865149	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10865150	1.00[ASW][hapmap];0.82[CEU][hapmap];1.00[CHB][hapmap];0.90[GIH][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];0.94[YRI][hapmap];0.89[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs10865152	0.99[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11124668	0.81[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs11124673	0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11124676	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11124677	0.93[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs11124679	0.92[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11124681	0.81[AFR][1000 genomes]
rs1125839	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11688728	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1211996	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12622941	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12712636	0.84[EUR][1000 genomes]
rs12712641	0.89[AFR][1000 genomes]
rs13005378	1.00[CHB][hapmap]
rs13028561	0.85[AFR][1000 genomes]
rs1468902	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1474424	0.91[ASW][hapmap];0.95[LWK][hapmap];0.98[MKK][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs1477164	0.93[YRI][hapmap];0.87[AFR][1000 genomes]
rs1548170	0.86[CHB][hapmap]
rs17023372	0.86[CHB][hapmap]
rs17023837	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1861735	0.88[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs1922827	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2056654	0.84[AFR][1000 genomes]
rs2111382	0.90[YRI][hapmap];0.86[AFR][1000 genomes]
rs2178760	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2178762	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2193422	0.99[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2373527	0.86[CHB][hapmap]
rs2373534	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2373535	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2373536	0.88[YRI][hapmap];0.85[AFR][1000 genomes]
rs2542008	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2665157	0.91[ASW][hapmap];0.89[YRI][hapmap]
rs2708222	0.86[CHB][hapmap]
rs2708223	0.86[CHB][hapmap]
rs2888594	0.92[EUR][1000 genomes]
rs2888598	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3755177	0.94[EUR][1000 genomes]
rs3755178	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3770663	0.80[MEX][hapmap]
rs3770670	0.88[AFR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3770675	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3770678	0.86[AFR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4670285	0.89[MEX][hapmap]
rs4670918	0.86[CHB][hapmap]
rs4670934	1.00[ASW][hapmap];0.95[LWK][hapmap];0.95[MKK][hapmap];0.94[YRI][hapmap];0.84[AFR][1000 genomes]
rs4670935	0.88[YRI][hapmap];0.84[AFR][1000 genomes]
rs4670936	0.89[YRI][hapmap];0.82[AFR][1000 genomes]
rs6419603	0.87[AFR][1000 genomes]
rs6544210	0.82[CHB][hapmap]
rs6544213	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6544220	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6544222	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6544223	1.00[ASW][hapmap];0.95[LWK][hapmap];0.98[MKK][hapmap];0.94[YRI][hapmap];0.87[AFR][1000 genomes]
rs6544224	0.82[CEU][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6544228	0.84[AFR][1000 genomes]
rs6706711	0.86[CHB][hapmap]
rs6710989	0.91[ASW][hapmap];0.81[MKK][hapmap];0.89[YRI][hapmap]
rs6712274	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6712921	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6718134	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6724393	0.85[AFR][1000 genomes]
rs6725938	0.88[AFR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6730902	0.84[AFR][1000 genomes]
rs6732611	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6736700	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6741019	0.85[AFR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6741312	0.89[YRI][hapmap]
rs6742170	0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6743041	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6753323	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6756183	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.92[YRI][hapmap];0.88[AFR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6759495	0.84[AFR][1000 genomes]
rs6760382	0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7562981	0.86[CHB][hapmap]
rs7563941	0.83[ASN][1000 genomes]
rs7566123	0.86[CHB][hapmap]
rs7568561	0.86[AMR][1000 genomes]
rs7569834	0.91[ASW][hapmap];0.86[CHB][hapmap]
rs7574250	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7575216	0.91[ASW][hapmap];0.86[CHB][hapmap]
rs7578136	0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7579414	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7582160	1.00[ASW][hapmap];0.90[LWK][hapmap];0.95[MKK][hapmap];0.94[YRI][hapmap];0.87[AFR][1000 genomes]
rs7595041	0.85[AFR][1000 genomes]
rs759589	0.92[EUR][1000 genomes]
rs7600014	0.83[ASW][hapmap];1.00[CEU][hapmap];0.97[GIH][hapmap];0.94[EUR][1000 genomes]
rs7600046	0.85[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs7601700	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[GIH][hapmap];1.00[LWK][hapmap];0.98[MKK][hapmap];0.94[YRI][hapmap];0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7603337	0.92[EUR][1000 genomes]
rs7603392	0.88[YRI][hapmap];0.84[AFR][1000 genomes]
rs7604047	0.91[AFR][1000 genomes];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7608153	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[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	nsv1010874	chr2:39255376-39604535	Strong transcription Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
2	nsv535649	chr2:39255376-39604535	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
3	nsv531346	chr2:39263225-39606367	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
4	nsv533348	chr2:39264345-39596169	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
5	nsv1014520	chr2:39270598-39596299	Enhancers Active TSS Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
6	nsv535650	chr2:39270598-39596299	Enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
7	nsv1009379	chr2:39271472-39604535	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
8	nsv581494	chr2:39277851-39626388	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
9	nsv533456	chr2:39281834-39596298	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
10	esv1832414	chr2:39385155-39588797	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
11	esv1827292	chr2:39385155-39675339	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription 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	21 gene(s)	inside rSNPs	diseases
12	esv1812828	chr2:39396457-39675339	Flanking Active TSS Strong transcription Active TSS Enhancers Weak transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
13	nsv833847	chr2:39410762-39604640	ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
14	nsv533445	chr2:39412970-39605266	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
15	esv1830024	chr2:39440552-39588797	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
16	nsv873887	chr2:39468676-39601889	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
17	nsv997934	chr2:39473548-39751029	Enhancers Strong transcription ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
18	esv1809158	chr2:39474679-39588797	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
19	esv1828851	chr2:39508121-39588797	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
20	esv1806203	chr2:39570427-39588797	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:84 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:39539000-39586400	Weak transcription	Pancreas	Pancrea
2	chr2:39541000-39586400	Weak transcription	Lung	lung
3	chr2:39554600-39586400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr2:39557000-39586800	Weak transcription	Aorta	Aorta
5	chr2:39558800-39586600	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr2:39559000-39586400	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr2:39562400-39586600	Weak transcription	NHLF	lung
8	chr2:39572200-39597600	Weak transcription	Osteobl	bone
9	chr2:39574200-39586400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr2:39575600-39586400	Weak transcription	Gastric	stomach
11	chr2:39579200-39586400	Weak transcription	Fetal Thymus	thymus
12	chr2:39579200-39587600	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr2:39580400-39586600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr2:39582400-39586400	Weak transcription	Fetal Intestine Large	intestine
15	chr2:39582600-39586400	Weak transcription	Left Ventricle	heart
16	chr2:39582800-39586400	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr2:39582800-39587200	Weak transcription	Stomach Smooth Muscle	stomach
18	chr2:39583000-39586600	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr2:39583000-39587000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr2:39583200-39586400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr2:39583400-39586400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr2:39584200-39588400	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr2:39584400-39586400	Weak transcription	Ovary	ovary
24	chr2:39584400-39598400	Weak transcription	Colon Smooth Muscle	Colon
25	chr2:39584400-39604600	Weak transcription	Right Ventricle	heart
26	chr2:39584600-39586400	Weak transcription	HSMMtube	muscle
27	chr2:39584800-39586400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr2:39584800-39586400	Weak transcription	Brain Anterior Caudate	brain
29	chr2:39584800-39586600	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr2:39584800-39591600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr2:39585000-39586400	Weak transcription	Brain Angular Gyrus	brain
32	chr2:39585000-39588400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
33	chr2:39585000-39591400	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr2:39585200-39586400	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr2:39585200-39590600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
36	chr2:39585200-39590600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
37	chr2:39585200-39591400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
38	chr2:39585400-39586400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr2:39585400-39586400	Weak transcription	HSMM	muscle
40	chr2:39585400-39586600	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr2:39585400-39587200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr2:39585400-39588400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr2:39585400-39590200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
44	chr2:39585600-39587400	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
45	chr2:39585600-39588000	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
46	chr2:39585600-39588400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
47	chr2:39585600-39588400	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr2:39585600-39591600	Weak transcription	Fetal Heart	heart
49	chr2:39585800-39586400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr2:39585800-39586800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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