Variant report

Variant	rs12624242
Chromosome Location	chr2:39508121-39508122
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:39506271..39508619-chr2:39510238..39511844,2	K562	blood:

Variant related genes	Relation type
ENSG00000252473	Chromatin interaction

Extended variants
information (count: 114 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:91)

rs_ID	r²[population]
rs1012689	0.90[ASN][1000 genomes]
rs10166473	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs10168941	0.84[AMR][1000 genomes]
rs10169329	0.92[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs10175094	0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10179936	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs10185961	0.83[JPT][hapmap];0.84[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10193636	0.81[AFR][1000 genomes]
rs10193807	0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10196447	0.81[YRI][hapmap]
rs10199948	0.84[YRI][hapmap]
rs10865148	0.83[ASW][hapmap];0.93[CHD][hapmap];0.87[GIH][hapmap];0.83[JPT][hapmap];0.85[MKK][hapmap];0.81[YRI][hapmap];0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11124667	0.81[ASN][1000 genomes]
rs11124669	0.81[AFR][1000 genomes]
rs11124670	0.81[AFR][1000 genomes]
rs11124671	0.81[JPT][hapmap];0.94[YRI][hapmap];0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11124672	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs11124674	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11124675	0.95[YRI][hapmap];0.94[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs11124678	0.87[AFR][1000 genomes]
rs11124680	0.81[JPT][hapmap]
rs11677383	0.81[YRI][hapmap];0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11688033	0.93[AFR][1000 genomes];0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11688352	0.81[ASN][1000 genomes]
rs11695072	0.88[CHD][hapmap];0.82[JPT][hapmap]
rs12151392	0.83[JPT][hapmap];0.94[YRI][hapmap];0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12162306	0.84[AFR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12617901	0.85[CHB][hapmap];0.84[CHD][hapmap]
rs12618944	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12712633	0.82[GIH][hapmap]
rs12712634	1.00[ASW][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];0.83[JPT][hapmap];0.85[LWK][hapmap];0.90[YRI][hapmap];0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12712640	0.92[ASW][hapmap];0.93[CHD][hapmap];0.83[JPT][hapmap];0.87[LWK][hapmap];0.90[MKK][hapmap];0.88[ASN][1000 genomes]
rs12997072	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13002095	0.82[EUR][1000 genomes]
rs13015356	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13405577	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1861733	0.81[JPT][hapmap];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1861734	0.93[CHD][hapmap];0.95[GIH][hapmap];0.81[JPT][hapmap];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2024514	0.97[CHD][hapmap];0.97[GIH][hapmap];0.83[JPT][hapmap];0.89[MKK][hapmap];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2058863	0.87[AFR][1000 genomes]
rs2302749	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2373528	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2888593	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3755171	1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3755172	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3755176	0.83[JPT][hapmap];0.95[YRI][hapmap];0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3770662	0.82[JPT][hapmap]
rs3770663	0.85[LWK][hapmap];0.81[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs3770664	0.85[CHB][hapmap];0.89[CHD][hapmap];0.87[LWK][hapmap];0.80[YRI][hapmap];0.83[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs3770668	0.81[AMR][1000 genomes]
rs3770671	0.92[ASW][hapmap];0.93[CHD][hapmap];0.95[GIH][hapmap];0.87[LWK][hapmap];0.85[MKK][hapmap];0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3770672	0.85[CEU][hapmap];0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3770673	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3770674	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4488638	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4670938	0.85[MKK][hapmap]
rs62138511	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6544214	0.93[CHD][hapmap];0.95[GIH][hapmap];0.88[JPT][hapmap];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6544215	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6544216	0.92[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6709424	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6714566	0.85[CEU][hapmap];0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6719469	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6720537	0.83[MKK][hapmap]
rs6720951	0.85[MKK][hapmap]
rs6725790	0.91[AMR][1000 genomes]
rs6753014	0.95[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6758596	0.86[MKK][hapmap]
rs7340455	0.88[JPT][hapmap];0.80[YRI][hapmap];0.81[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7559752	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs7559756	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs7561630	0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7569037	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7569492	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7573923	0.81[YRI][hapmap];0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7581692	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7582848	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7594145	0.87[ASN][1000 genomes]
rs7595469	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7596222	1.00[ASW][hapmap];0.82[LWK][hapmap];0.90[YRI][hapmap]
rs7597300	0.95[AFR][1000 genomes];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7598583	0.87[CHD][hapmap]
rs7600636	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs7605427	0.91[AFR][1000 genomes]
rs7605939	0.88[MKK][hapmap]
rs7608958	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9037	0.84[ASW][hapmap];0.93[CHD][hapmap];0.95[GIH][hapmap];0.82[JPT][hapmap];0.90[MKK][hapmap];0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9309036	1.00[ASW][hapmap];0.97[GIH][hapmap];0.90[LWK][hapmap];0.93[MKK][hapmap];0.89[YRI][hapmap];0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9309037	0.82[JPT][hapmap];0.89[YRI][hapmap];0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9309038	0.89[AFR][1000 genomes]
rs9309039	0.95[YRI][hapmap];0.85[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv873885	chr2:39200198-39573521	Enhancers Strong transcription Weak transcription Flanking Active TSS 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 miRNA target site	36 gene(s)	inside rSNPs	diseases
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	nsv581493	chr2:39277851-39547575	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	nsv2693	chr2:39468641-39513800	Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
19	nsv873886	chr2:39468676-39573521	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
20	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
21	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
22	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
23	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

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs12624242	SOS1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:39473400-39517400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr2:39476600-39527600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr2:39478600-39543400	Weak transcription	Stomach Mucosa	stomach
4	chr2:39479000-39521200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr2:39481000-39580200	Weak transcription	NHEK	skin
6	chr2:39484400-39516400	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr2:39487600-39513200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr2:39493600-39523800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr2:39493600-39565800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr2:39493800-39509800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr2:39493800-39516600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
12	chr2:39493800-39525000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr2:39494000-39525600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr2:39494000-39553000	Weak transcription	GM12878-XiMat	blood
15	chr2:39495600-39510400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr2:39495600-39523200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr2:39496400-39521200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr2:39496600-39515000	Weak transcription	Primary neutrophils fromperipheralblood	blood
19	chr2:39496600-39520400	Strong transcription	Placenta	Placenta
20	chr2:39497000-39510800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr2:39497000-39516600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr2:39497200-39516000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr2:39503400-39511200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr2:39504000-39511400	Weak transcription	Primary B cells from cord blood	blood
25	chr2:39504400-39521400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr2:39504600-39510200	Weak transcription	A549	lung
27	chr2:39504600-39512200	Weak transcription	NHLF	lung
28	chr2:39504600-39513000	Weak transcription	Colonic Mucosa	Colon
29	chr2:39504600-39513200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr2:39504600-39513200	Weak transcription	Fetal Brain Female	brain
31	chr2:39504600-39513200	Weak transcription	Gastric	stomach
32	chr2:39504600-39513200	Weak transcription	Pancreas	Pancrea
33	chr2:39504600-39515000	Weak transcription	Brain Cingulate Gyrus	brain
34	chr2:39504600-39523600	Weak transcription	Brain Substantia Nigra	brain
35	chr2:39504600-39540000	Weak transcription	Right Ventricle	heart
36	chr2:39504600-39562000	Weak transcription	Psoas Muscle	Psoas
37	chr2:39504800-39509600	Weak transcription	Fetal Heart	heart
38	chr2:39504800-39510000	Weak transcription	Primary T helper cells PMA-I stimulated	--
39	chr2:39504800-39510200	Weak transcription	Colon Smooth Muscle	Colon
40	chr2:39504800-39511400	Weak transcription	Primary T helper cells fromperipheralblood	blood
41	chr2:39504800-39512400	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr2:39504800-39512800	Weak transcription	HUVEC	blood vessel
43	chr2:39504800-39513200	Weak transcription	Brain Anterior Caudate	brain
44	chr2:39504800-39513200	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr2:39504800-39513200	Weak transcription	HMEC	breast
46	chr2:39504800-39518400	Weak transcription	Esophagus	oesophagus
47	chr2:39504800-39518800	Weak transcription	Rectal Smooth Muscle	rectum
48	chr2:39504800-39521800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr2:39504800-39527800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr2:39504800-39538400	Weak transcription	Small Intestine	intestine

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