Variant report

Variant	rs7557281
Chromosome Location	chr2:113034820-113034821
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:21)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:113033844..113035666-chr2:113048299..113050198,2	K562	blood:
2	chr2:113033406..113035209-chr2:113052659..113055582,2	K562	blood:
3	chr2:113032909..113035758-chr2:113089627..113091636,2	K562	blood:
4	chr2:113031252..113036924-chr2:113235926..113242226,12	K562	blood:
5	chr2:113031538..113036695-chr2:113297613..113301921,6	K562	blood:
6	chr2:113031437..113035560-chr2:113235674..113241590,9	K562	blood:
7	chr2:113008666..113014085-chr2:113030385..113035561,7	MCF-7	breast:
8	chr2:113032266..113035570-chr2:113088065..113092560,6	MCF-7	breast:
9	chr2:113033771..113036191-chr2:113057480..113059266,2	K562	blood:
10	chr2:113033709..113035506-chr2:113052735..113055582,2	K562	blood:
11	chr2:112813166..112815786-chr2:113032980..113035642,2	MCF-7	breast:
12	chr2:113033733..113035486-chr2:113341389..113343978,2	K562	blood:
13	chr2:112811397..112814190-chr2:113032583..113035282,3	K562	blood:
14	chr2:113031869..113034952-chr2:113341167..113343629,3	MCF-7	breast:
15	chr2:112639923..112643380-chr2:113032282..113036126,7	K562	blood:
16	chr2:113010163..113016150-chr2:113027955..113035093,25	K562	blood:
17	chr2:112639923..112643257-chr2:113032585..113036126,5	K562	blood:
18	chr2:113033498..113035486-chr2:113341389..113343143,2	K562	blood:
19	chr2:113009256..113015419-chr2:113031181..113035814,11	MCF-7	breast:
20	chr2:113032895..113034868-chr2:113298043..113301369,3	K562	blood:
21	chr2:113006375..113009126-chr2:113033246..113034837,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000125630	Chromatin interaction
ENSG00000125611	Chromatin interaction
ENSG00000248341	Chromatin interaction
ENSG00000153107	Chromatin interaction
ENSG00000144161	Chromatin interaction
ENSG00000114999	Chromatin interaction
ENSG00000153214	Chromatin interaction

Extended variants
information (count: 95 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs10167090	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10167748	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10169159	0.95[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs10175234	0.98[ASN][1000 genomes]
rs10177573	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10183121	0.94[CHB][hapmap];0.88[JPT][hapmap];0.81[YRI][hapmap];0.85[ASN][1000 genomes]
rs10191002	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];0.96[MEX][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10203843	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10205038	1.00[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs10211300	0.93[CHB][hapmap];0.94[JPT][hapmap]
rs10439391	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10864903	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11123132	0.94[CHB][hapmap]
rs11123136	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11674953	1.00[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs11688418	0.95[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs11689487	0.92[ASN][1000 genomes]
rs11691431	1.00[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs11691794	0.93[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs11896500	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11902928	0.83[EUR][1000 genomes]
rs11903741	1.00[ASW][hapmap];0.96[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[TSI][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11904424	0.92[ASW][hapmap];0.87[CEU][hapmap];0.98[GIH][hapmap];1.00[TSI][hapmap];0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12464478	0.82[AFR][1000 genomes]
rs12711737	0.86[ASN][1000 genomes]
rs12711738	0.91[ASW][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];1.00[JPT][hapmap];0.87[LWK][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs12711739	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs13387611	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];0.96[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs34471791	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs34623958	0.95[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs4258804	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4299347	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs4332934	0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4352239	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4392265	0.97[ASN][1000 genomes]
rs4399734	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4430968	1.00[ASW][hapmap];0.96[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[TSI][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4446076	0.97[ASN][1000 genomes]
rs4450606	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4450607	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4456711	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4507112	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4522611	1.00[ASW][hapmap];0.96[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[TSI][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4525706	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4539797	0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4542853	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs4578863	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs4622729	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4849056	0.85[ASN][1000 genomes]
rs4849057	0.86[ASN][1000 genomes]
rs58337061	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6542045	0.91[ASW][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.96[LWK][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs6542048	0.88[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs6542050	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6542051	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6542052	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6542053	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6706874	0.87[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs6708164	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6716010	0.95[ASN][1000 genomes]
rs6733138	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6744364	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6745942	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6751146	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6758110	1.00[ASW][hapmap];0.96[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[TSI][hapmap];1.00[YRI][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6761599	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs71414636	0.88[ASN][1000 genomes]
rs72831684	0.97[ASN][1000 genomes]
rs7557862	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7564052	0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7569894	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7571435	1.00[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs7579561	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7591439	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];0.96[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7598168	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7599041	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7600338	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7601200	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs7601888	0.95[ASN][1000 genomes]
rs8179708	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv874863	chr2:112591224-113157344	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
2	nsv874864	chr2:112617280-113104142	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
3	nsv874865	chr2:112623098-113049274	Enhancers Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
4	esv3422414	chr2:112883450-113200285	Strong transcription Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
5	nsv582703	chr2:112920219-113100014	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
6	nsv874867	chr2:112930064-113038409	Flanking Active TSS Enhancers Strong transcription Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
7	esv1805614	chr2:112949713-113048705	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
8	nsv949573	chr2:112986955-113320975	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
9	nsv874868	chr2:113021811-113076095	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
10	nsv874869	chr2:113021811-113089267	Flanking Active TSS Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
11	nsv874870	chr2:113021811-113097699	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
12	nsv874871	chr2:113021811-113217630	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
13	nsv874872	chr2:113027569-113070889	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
14	nsv874873	chr2:113027569-113083367	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription 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	33 gene(s)	inside rSNPs	diseases
15	nsv874874	chr2:113027569-113089267	Active TSS Strong transcription Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs7557281	POLR1B	cis	parietal	SCAN
rs7557281	ZC3H6	cis	multi-tissue	Pritchard

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:113032000-113035200	Active TSS	iPS-20b Cell Line	embryonic stem cell
2	chr2:113032200-113035000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr2:113032400-113035000	Active TSS	GM12878-XiMat	blood
4	chr2:113032600-113035000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr2:113034200-113035000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr2:113034200-113035200	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
7	chr2:113034200-113035600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr2:113034200-113058200	Weak transcription	Ovary	ovary
9	chr2:113034400-113035000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
10	chr2:113034400-113035000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr2:113034400-113035000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr2:113034400-113035000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr2:113034400-113035000	Enhancers	Fetal Intestine Small	intestine
14	chr2:113034400-113035000	Enhancers	Fetal Kidney	kidney
15	chr2:113034400-113035200	Enhancers	Duodenum Smooth Muscle	Duodenum
16	chr2:113034400-113035400	Weak transcription	Primary T cells fromperipheralblood	blood
17	chr2:113034400-113035400	Weak transcription	Fetal Thymus	thymus
18	chr2:113034400-113035400	Weak transcription	Thymus	Thymus
19	chr2:113034400-113035600	Enhancers	Primary B cells from cord blood	blood
20	chr2:113034400-113035600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr2:113034400-113035800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
22	chr2:113034400-113035800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
23	chr2:113034400-113036600	Enhancers	Primary T killer memory cells from peripheral blood	blood
24	chr2:113034400-113047800	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr2:113034400-113051400	Weak transcription	Skeletal Muscle Female	skeletal muscle
26	chr2:113034400-113097000	Weak transcription	Psoas Muscle	Psoas
27	chr2:113034600-113035000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr2:113034600-113035000	Enhancers	Rectal Mucosa Donor 29	rectum
29	chr2:113034600-113035000	Flanking Active TSS	K562	blood
30	chr2:113034600-113035200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr2:113034600-113035400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
32	chr2:113034600-113035400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr2:113034600-113035400	Weak transcription	Brain Anterior Caudate	brain
34	chr2:113034600-113035600	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr2:113034600-113035600	Enhancers	Brain Hippocampus Middle	brain
36	chr2:113034600-113035600	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr2:113034600-113035600	Enhancers	NHDF-Ad	bronchial
38	chr2:113034600-113035800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr2:113034600-113035800	Enhancers	Primary T cells from cord blood	blood
40	chr2:113034600-113035800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
41	chr2:113034600-113035800	Enhancers	Dnd41	blood
42	chr2:113034600-113036000	Enhancers	Adipose Nuclei	Adipose
43	chr2:113034600-113037400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr2:113034600-113039600	Weak transcription	Fetal Heart	heart
45	chr2:113034800-113035000	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr2:113034800-113035000	Flanking Active TSS	Liver	Liver
47	chr2:113034800-113035000	Enhancers	Fetal Brain Female	brain
48	chr2:113034800-113035000	Enhancers	Fetal Lung	lung
49	chr2:113034800-113035200	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr2:113034800-113035200	Enhancers	Primary T helper cells PMA-I stimulated	--

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