Variant report

Variant	rs2911428
Chromosome Location	chr16:82203274-82203275
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr16:82200674-82204569	MCF10A-Er-Src	breast:	n/a	n/a
2	CHD1	chr16:82203241-82203743	H1-hESC	embryonic stem cell:	n/a	n/a
3	POLR2A	chr16:82202498-82204512	MCF10A-Er-Src	breast:	n/a	n/a
4	FOXA1	chr16:82203247-82203826	HepG2	liver:	n/a	n/a
5	MYBL2	chr16:82203236-82204417	HepG2	liver:	n/a	n/a
6	MXI1	chr16:82203256-82204560	IMR90	lung:	n/a	chr16:82204198-82204207
7	POLR2A	chr16:82203176-82204191	HepG2	liver:	n/a	n/a
8	MXI1	chr16:82203145-82204612	SK-N-SH	brain:	n/a	chr16:82204198-82204207
9	POLR2A	chr16:82203270-82204316	K562	blood:	n/a	n/a
10	EP300	chr16:82203161-82203311	K562	blood:	n/a	n/a
11	MAX	chr16:82203272-82204558	A549	lung:	n/a	chr16:82203651-82203661 chr16:82204199-82204209 chr16:82204200-82204209 chr16:82204197-82204212 chr16:82203837-82203846 chr16:82204201-82204208

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:82171180..82173441-chr16:82201395..82203780,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000261029	TF binding region
ENSG00000261235	Chromatin interaction

Extended variants
information (count: 118 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:104)

rs_ID	r²[population]
rs10514531	1.00[CEU][hapmap];0.94[CHB][hapmap];0.90[JPT][hapmap];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10514533	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10514534	0.86[EUR][1000 genomes]
rs1056629	1.00[CEU][hapmap];0.88[CHB][hapmap];0.85[CHD][hapmap];0.97[GIH][hapmap];0.89[JPT][hapmap];0.86[MEX][hapmap];0.86[TSI][hapmap];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1056654	1.00[CEU][hapmap];0.94[CHB][hapmap];0.90[CHD][hapmap];0.97[GIH][hapmap];0.95[JPT][hapmap];0.86[MEX][hapmap];0.86[TSI][hapmap];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1056690	1.00[CEU][hapmap];0.94[CHB][hapmap];0.90[CHD][hapmap];0.97[GIH][hapmap];0.95[JPT][hapmap];0.87[MEX][hapmap];0.86[TSI][hapmap];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11150443	1.00[CEU][hapmap];0.97[GIH][hapmap];0.86[TSI][hapmap];0.86[EUR][1000 genomes]
rs11150444	0.86[EUR][1000 genomes]
rs11150445	0.86[EUR][1000 genomes]
rs11641082	0.92[EUR][1000 genomes]
rs11641178	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11642247	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11642251	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11643324	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.97[GIH][hapmap];0.95[JPT][hapmap];0.87[MEX][hapmap];0.86[TSI][hapmap];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11643724	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11644183	0.86[EUR][1000 genomes]
rs11645604	0.94[CHB][hapmap];0.90[JPT][hapmap];0.89[ASN][1000 genomes]
rs11645618	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11645924	0.95[ASN][1000 genomes]
rs11646480	1.00[CEU][hapmap];0.89[CHB][hapmap];0.92[EUR][1000 genomes]
rs11647519	0.86[EUR][1000 genomes]
rs11647563	1.00[CEU][hapmap];0.83[CHB][hapmap];0.97[GIH][hapmap];0.91[TSI][hapmap];0.92[EUR][1000 genomes]
rs11647691	1.00[CEU][hapmap];0.82[CHB][hapmap];0.92[EUR][1000 genomes]
rs11647928	0.86[EUR][1000 genomes]
rs11649427	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12444846	1.00[CEU][hapmap];0.94[GIH][hapmap];0.85[TSI][hapmap];0.86[EUR][1000 genomes]
rs12445764	1.00[CEU][hapmap];0.88[CHB][hapmap];0.92[EUR][1000 genomes]
rs12446030	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12446104	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12447225	1.00[CEU][hapmap];0.88[CHB][hapmap];0.92[EUR][1000 genomes]
rs12447597	1.00[CEU][hapmap];0.82[CHB][hapmap];0.92[EUR][1000 genomes]
rs12447673	0.92[EUR][1000 genomes]
rs12447876	0.92[EUR][1000 genomes]
rs12447913	0.92[EUR][1000 genomes]
rs12448665	0.86[EUR][1000 genomes]
rs12448672	1.00[CEU][hapmap];0.94[CHB][hapmap];0.90[CHD][hapmap];0.97[GIH][hapmap];0.95[JPT][hapmap];0.87[MEX][hapmap];0.86[TSI][hapmap];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12448785	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12597638	0.91[CEU][hapmap]
rs12599196	0.91[CEU][hapmap]
rs12931886	0.91[CEU][hapmap]
rs13330853	1.00[CEU][hapmap];0.97[GIH][hapmap];0.86[TSI][hapmap]
rs13333365	0.85[EUR][1000 genomes]
rs1424153	0.81[EUR][1000 genomes]
rs16956483	1.00[CEU][hapmap];0.97[GIH][hapmap];0.86[TSI][hapmap];0.86[EUR][1000 genomes]
rs16956524	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs16956527	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs16956533	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs16956547	0.91[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs16956550	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs16956555	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16956556	1.00[CEU][hapmap];0.94[CHB][hapmap];0.90[JPT][hapmap];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs16956565	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16956572	1.00[CEU][hapmap];0.94[CHB][hapmap];0.90[JPT][hapmap];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs16956576	1.00[CEU][hapmap];0.94[CHB][hapmap];0.97[CHD][hapmap];0.97[GIH][hapmap];0.95[JPT][hapmap];0.82[MEX][hapmap];0.91[TSI][hapmap];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17804513	0.86[EUR][1000 genomes]
rs17804602	0.86[EUR][1000 genomes]
rs1862821	0.82[CEU][hapmap]
rs2081256	1.00[CEU][hapmap];0.97[GIH][hapmap];0.86[TSI][hapmap];0.86[EUR][1000 genomes]
rs2081257	1.00[CEU][hapmap];0.94[GIH][hapmap];0.85[EUR][1000 genomes]
rs2081258	0.86[EUR][1000 genomes]
rs2098749	1.00[CEU][hapmap];0.97[GIH][hapmap];0.86[TSI][hapmap];0.85[EUR][1000 genomes]
rs2098750	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs2303268	1.00[CEU][hapmap];0.94[CHB][hapmap];0.90[CHD][hapmap];0.97[GIH][hapmap];0.90[JPT][hapmap];0.86[MEX][hapmap];0.91[TSI][hapmap];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34652971	0.81[EUR][1000 genomes]
rs35328670	0.85[EUR][1000 genomes]
rs3751863	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3751865	0.91[CEU][hapmap];0.94[CHB][hapmap];0.90[CHD][hapmap];0.97[GIH][hapmap];0.95[JPT][hapmap];0.87[MEX][hapmap];0.86[TSI][hapmap];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3794704	0.95[ASN][1000 genomes]
rs3794705	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3829542	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.97[GIH][hapmap];0.95[JPT][hapmap];0.87[MEX][hapmap];0.91[TSI][hapmap];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3829552	0.82[CEU][hapmap];0.95[TSI][hapmap];0.92[EUR][1000 genomes]
rs4243231	0.82[CEU][hapmap];0.91[EUR][1000 genomes]
rs4530129	1.00[CEU][hapmap];0.97[GIH][hapmap];0.86[TSI][hapmap];0.86[EUR][1000 genomes]
rs4569272	0.82[CEU][hapmap];0.91[EUR][1000 genomes]
rs4888206	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4888207	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4889463	0.83[EUR][1000 genomes]
rs4889468	0.85[EUR][1000 genomes]
rs4889475	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4889478	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4889480	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61366082	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs61702998	0.81[EUR][1000 genomes]
rs7186965	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs7187080	0.91[CEU][hapmap]
rs7193463	0.91[CEU][hapmap]
rs7193586	0.85[EUR][1000 genomes]
rs7195778	0.91[CEU][hapmap]
rs7202019	0.94[CHB][hapmap];0.95[CHD][hapmap];0.90[JPT][hapmap];0.95[ASN][1000 genomes]
rs72487977	0.92[EUR][1000 genomes]
rs7404586	0.81[EUR][1000 genomes]
rs7405214	0.89[EUR][1000 genomes]
rs7498125	0.91[CEU][hapmap]
rs7501253	0.91[CEU][hapmap]
rs9635584	0.86[EUR][1000 genomes]
rs9635585	0.86[EUR][1000 genomes]
rs9922715	0.85[EUR][1000 genomes]
rs9929117	0.91[CEU][hapmap]
rs9929380	0.91[CEU][hapmap]
rs9936872	0.91[CEU][hapmap]
rs9937667	0.85[EUR][1000 genomes]
rs9940821	0.85[EUR][1000 genomes]
rs9940865	0.85[EUR][1000 genomes]
rs9941179	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532598	chr16:82034475-82738733	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
2	nsv532599	chr16:82074439-82926863	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
3	nsv573367	chr16:82140561-83040846	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
4	nsv457579	chr16:82150293-82216622	Strong transcription Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS 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	13 gene(s)	inside rSNPs	diseases
5	nsv573368	chr16:82150293-82216622	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	nsv525467	chr16:82154619-82223485	Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
7	nsv1061064	chr16:82165314-82213799	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
8	nsv1056381	chr16:82165314-82215388	Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
9	nsv1062687	chr16:82165516-82213799	Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
10	nsv518129	chr16:82188173-82228076	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
11	nsv833302	chr16:82188351-82363863	Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
12	esv1844598	chr16:82195234-82429790	Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
13	esv1847414	chr16:82195234-82429790	Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
14	nsv532600	chr16:82197554-82314289	Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs2911428	MPHOSPH6	cis	lymphoblastoid	seeQTL
rs2911428	MPHOSPH6	cis	Artery Tibial	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:82196400-82203400	Weak transcription	Aorta	Aorta
2	chr16:82196400-82203400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr16:82202200-82203400	Enhancers	Sigmoid Colon	Sigmoid Colon
4	chr16:82202200-82204400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr16:82202400-82203400	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr16:82202400-82203400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr16:82202400-82203400	Enhancers	Spleen	Spleen
8	chr16:82202400-82203600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr16:82202400-82204000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr16:82202400-82204000	Active TSS	HUES48 Cell Line	embryonic stem cell
11	chr16:82202400-82204000	Active TSS	HUES64 Cell Line	embryonic stem cell
12	chr16:82202400-82204400	Active TSS	iPS-20b Cell Line	embryonic stem cell
13	chr16:82202400-82204400	Active TSS	HSMM	muscle
14	chr16:82202600-82203400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr16:82202600-82203400	Flanking Active TSS	Fetal Lung	lung
16	chr16:82202600-82203600	Flanking Active TSS	Adipose Nuclei	Adipose
17	chr16:82202600-82203600	Flanking Active TSS	Liver	Liver
18	chr16:82202600-82203600	Enhancers	Fetal Heart	heart
19	chr16:82202600-82204200	Active TSS	HUES6 Cell Line	embryonic stem cell
20	chr16:82202600-82204200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr16:82202600-82204200	Active TSS	A549	lung
22	chr16:82202600-82204600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr16:82202600-82204600	Active TSS	HSMMtube	muscle
24	chr16:82202600-82205000	Active TSS	Fetal Brain Female	brain
25	chr16:82202800-82203400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr16:82202800-82203400	Flanking Active TSS	Brain Hippocampus Middle	brain
27	chr16:82202800-82203600	Flanking Active TSS	Primary B cells from cord blood	blood
28	chr16:82202800-82203600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
29	chr16:82202800-82203600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr16:82202800-82203600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
31	chr16:82202800-82204000	Active TSS	ES-I3 Cell Line	embryonic stem cell
32	chr16:82202800-82204000	Active TSS	H1 Cell Line	embryonic stem cell
33	chr16:82202800-82204000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
34	chr16:82202800-82204000	Active TSS	Fetal Intestine Large	intestine
35	chr16:82202800-82204200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr16:82202800-82204600	Active TSS	H9 Cell Line	embryonic stem cell
37	chr16:82202800-82204600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr16:82202800-82204600	Active TSS	Pancreatic Islets	Pancreatic Islet
39	chr16:82202800-82204600	Active TSS	Psoas Muscle	Psoas
40	chr16:82203000-82203400	Flanking Active TSS	Primary hematopoietic stem cells	blood
41	chr16:82203000-82203400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
42	chr16:82203000-82203400	Active TSS	HepG2	liver
43	chr16:82203000-82203600	Active TSS	Right Atrium	heart
44	chr16:82203000-82204000	Active TSS	iPS-18 Cell Line	embryonic stem cell
45	chr16:82203000-82204000	Active TSS	Colonic Mucosa	Colon
46	chr16:82203000-82204000	Active TSS	Fetal Thymus	thymus
47	chr16:82203000-82204000	Active TSS	Gastric	stomach
48	chr16:82203000-82204000	Active TSS	Pancreas	Pancrea
49	chr16:82203000-82204000	Active TSS	HMEC	breast
50	chr16:82203000-82204200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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