Variant report

Variant	rs2073497
Chromosome Location	chr3:50367867-50367868
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:21)
CpG islands
(count:0)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr3:50366610-50368422	HL-60	blood:	n/a	n/a
2	POLR2A	chr3:50366819-50368507	NB4	blood:	n/a	n/a
3	POLR2A	chr3:50366725-50368630	Hela-S3	cervix:	n/a	n/a
4	POLR2A	chr3:50367180-50368258	K562	blood:	n/a	n/a
5	POLR2A	chr3:50367845-50368054	GM12878	blood:	n/a	n/a
6	POLR2A	chr3:50367253-50368151	K562	blood:	n/a	n/a
7	POLR2A	chr3:50366597-50368418	HL-60	blood:	n/a	n/a
8	POLR2A	chr3:50367779-50368100	MCF-7	breast:	n/a	n/a
9	POLR2A	chr3:50366872-50368367	Hela-S3	cervix:	n/a	n/a
10	POLR2A	chr3:50367857-50367876	HUVEC	blood vessel:	n/a	n/a
11	POLR2A	chr3:50367208-50368458	GM12892	blood:	n/a	n/a
12	POLR2A	chr3:50364925-50368510	HepG2	liver:	n/a	n/a
13	POLR2A	chr3:50367195-50368469	GM12878	blood:	n/a	n/a
14	POLR2A	chr3:50367174-50368018	PFSK-1	brain:	n/a	n/a
15	POLR2A	chr3:50367260-50368052	GM12892	blood:	n/a	n/a
16	POLR2A	chr3:50367727-50368011	GM12878	blood:	n/a	n/a
17	POLR2A	chr3:50367260-50368449	K562	blood:	n/a	n/a
18	POLR2A	chr3:50366596-50367988	GM12892	blood:	n/a	n/a
19	POLR2A	chr3:50365500-50370094	K562	blood:	n/a	n/a
20	POLR2A	chr3:50364560-50368458	K562	blood:	n/a	n/a
21	POLR2A	chr3:50367683-50368864	K562	blood:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:50306730..50308956-chr3:50367443..50369203,2	MCF-7	breast:
2	chr3:50327690..50333528-chr3:50363706..50369146,7	MCF-7	breast:

No data

Variant related genes	Relation type
TUSC2	TF binding region
ENSG00000012171	Chromatin interaction
ENSG00000186792	Chromatin interaction
ENSG00000214706	Chromatin interaction

Extended variants
information (count: 113 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:92)

rs_ID	r²[population]
rs11130248	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12054052	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12054403	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12485286	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12485390	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12485909	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12487392	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12488235	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12488302	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12490809	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12490837	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12492683	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12492880	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12493693	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12494414	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12495261	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12496815	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12497018	0.89[ASN][1000 genomes]
rs12498048	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12721544	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2006199	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2071203	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2071204	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2071205	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2071801	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2071804	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2072053	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2072054	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2073500	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2229647	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2233476	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2236940	0.85[ASN][1000 genomes]
rs2236941	0.84[ASN][1000 genomes]
rs2236943	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2236944	0.87[ASN][1000 genomes]
rs2236946	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2236949	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2236986	0.81[AMR][1000 genomes]
rs2269430	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2269432	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2269568	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2269569	0.87[ASN][1000 genomes]
rs2282750	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2285043	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2285044	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2298953	0.85[ASN][1000 genomes]
rs2298954	0.85[ASN][1000 genomes]
rs3213621	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35455589	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35587949	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3774736	0.82[EUR][1000 genomes]
rs3774739	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs3774741	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs3774748	0.82[AMR][1000 genomes]
rs3774752	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs3774753	0.97[ASN][1000 genomes]
rs3774754	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3774755	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4141407	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4688679	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4688682	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4688683	0.82[EUR][1000 genomes]
rs4688721	0.82[AMR][1000 genomes]
rs4688724	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4688725	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4688728	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4688732	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4688733	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4688734	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4688736	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4688738	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4688741	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4688742	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4688743	0.81[AMR][1000 genomes]
rs4688744	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4688746	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4688747	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs57944420	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57978992	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs58137261	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs58181992	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs58191283	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs58648044	0.85[ASN][1000 genomes]
rs60276643	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72932959	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72932987	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7645537	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9311449	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9681992	0.93[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs9830408	0.86[ASN][1000 genomes]
rs9882618	1.00[EUR][1000 genomes]
rs9883222	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv523662	chr3:50144951-50584999	Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
2	nsv876769	chr3:50155468-50408398	Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
3	esv1821728	chr3:50156142-50657253	Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
4	esv1793751	chr3:50157364-50476363	Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
5	esv1828162	chr3:50157364-50506151	Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
6	nsv470561	chr3:50158774-50584999	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	99 gene(s)	inside rSNPs	diseases
7	nsv876770	chr3:50158774-50609624	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
8	nsv1001993	chr3:50187646-50640808	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
9	esv2757870	chr3:50198478-50371377	Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
10	esv2759148	chr3:50198478-50371377	Enhancers Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
11	nsv834692	chr3:50198485-50393464	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
12	nsv590254	chr3:50243510-50388607	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
13	nsv460531	chr3:50247824-50436827	Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
14	nsv590255	chr3:50247824-50436827	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
15	nsv876772	chr3:50255305-50436827	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
16	nsv590257	chr3:50302830-50393640	Genic enhancers Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
17	nsv590256	chr3:50302830-50420554	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
18	nsv876774	chr3:50302830-50436827	Enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
19	nsv876773	chr3:50302830-50480131	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
20	nsv834693	chr3:50302830-50507964	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
21	nsv876775	chr3:50324672-50504896	Flanking Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:50366000-50374000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr3:50366200-50368400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr3:50366200-50370600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr3:50366200-50370800	Strong transcription	HSMM	muscle
5	chr3:50366200-50371200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr3:50366400-50369600	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr3:50366400-50369600	Strong transcription	Skeletal Muscle Male	skeletal muscle
8	chr3:50366400-50370600	Weak transcription	Fetal Heart	heart
9	chr3:50366400-50370600	Weak transcription	Right Atrium	heart
10	chr3:50366400-50371200	Strong transcription	Fetal Stomach	stomach
11	chr3:50366600-50369600	Strong transcription	Fetal Muscle Trunk	muscle
12	chr3:50366600-50370600	Strong transcription	Fetal Intestine Small	intestine
13	chr3:50366600-50370800	Strong transcription	Fetal Thymus	thymus
14	chr3:50366600-50371800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr3:50366800-50368000	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr3:50366800-50369000	Strong transcription	Placenta Amnion	Placenta Amnion
17	chr3:50366800-50369400	Strong transcription	Primary T cells fromperipheralblood	blood
18	chr3:50366800-50369400	Strong transcription	Left Ventricle	heart
19	chr3:50366800-50369600	Strong transcription	H9 Cell Line	embryonic stem cell
20	chr3:50366800-50369600	Strong transcription	Primary hematopoietic stem cells	blood
21	chr3:50366800-50369600	Strong transcription	Aorta	Aorta
22	chr3:50366800-50369600	Strong transcription	Liver	Liver
23	chr3:50366800-50369600	Strong transcription	Brain Cingulate Gyrus	brain
24	chr3:50366800-50369600	Strong transcription	Pancreas	Pancrea
25	chr3:50366800-50369600	Strong transcription	NH-A	brain
26	chr3:50366800-50369800	Strong transcription	H1 Cell Line	embryonic stem cell
27	chr3:50366800-50369800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr3:50366800-50369800	Strong transcription	HUES48 Cell Line	embryonic stem cell
29	chr3:50366800-50369800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr3:50366800-50369800	Strong transcription	Primary monocytes fromperipheralblood	blood
31	chr3:50366800-50369800	Strong transcription	Muscle Satellite Cultured Cells	--
32	chr3:50366800-50369800	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr3:50366800-50369800	Strong transcription	Colon Smooth Muscle	Colon
34	chr3:50366800-50369800	Strong transcription	Fetal Brain Female	brain
35	chr3:50366800-50369800	Strong transcription	Rectal Mucosa Donor 29	rectum
36	chr3:50366800-50369800	Strong transcription	Skeletal Muscle Female	skeletal muscle
37	chr3:50366800-50370000	Strong transcription	HUES64 Cell Line	embryonic stem cell
38	chr3:50366800-50370000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr3:50366800-50370000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr3:50366800-50370000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr3:50366800-50370000	Strong transcription	Adipose Nuclei	Adipose
42	chr3:50366800-50370000	Strong transcription	Esophagus	oesophagus
43	chr3:50366800-50370200	Strong transcription	Primary T helper cells fromperipheralblood	blood
44	chr3:50366800-50370200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
45	chr3:50366800-50370200	Strong transcription	Fetal Intestine Large	intestine
46	chr3:50366800-50370200	Strong transcription	Rectal Mucosa Donor 31	rectum
47	chr3:50366800-50370400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr3:50366800-50370400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr3:50366800-50370600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr3:50366800-50370600	Strong transcription	Breast Myoepithelial Primary Cells	Breast

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