Variant report

Variant	rs4888253
Chromosome Location	chr16:74583146-74583147
allele	C/T
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	CEBPB	chr16:74583056-74583350	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:74582009..74584400-chr16:74603645..74605956,2	K562	blood:

Variant related genes	Relation type
ENSG00000240861	TF binding region

Extended variants
information (count: 135 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:124)

rs_ID	r²[population]
rs1019572	0.80[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap]
rs1019573	0.83[CEU][hapmap];1.00[JPT][hapmap]
rs10468356	0.84[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs10500587	0.92[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap]
rs11149722	0.84[CEU][hapmap];0.82[CHB][hapmap];0.85[CHD][hapmap];1.00[JPT][hapmap];0.86[TSI][hapmap]
rs11639812	0.92[CEU][hapmap];0.82[CHB][hapmap];0.80[CHD][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap]
rs11644298	0.82[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap]
rs11648868	0.95[CHD][hapmap];1.00[JPT][hapmap]
rs12325017	0.80[CEU][hapmap];0.82[CHB][hapmap];0.84[CHD][hapmap];1.00[JPT][hapmap];0.86[TSI][hapmap]
rs12445991	0.82[CHB][hapmap];0.92[JPT][hapmap];0.80[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs12446054	0.85[CHD][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap]
rs12448026	0.84[CEU][hapmap];0.91[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];0.92[JPT][hapmap];0.91[MEX][hapmap];0.81[TSI][hapmap];0.89[ASN][1000 genomes]
rs12598701	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap]
rs12598791	0.84[MKK][hapmap]
rs13339156	0.81[EUR][1000 genomes]
rs13339161	0.88[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs13359	0.96[CEU][hapmap];0.82[CHB][hapmap];0.85[CHD][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap]
rs1469140	0.88[ASW][hapmap];0.84[CEU][hapmap];0.91[CHB][hapmap];0.86[CHD][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];0.93[MKK][hapmap];0.88[TSI][hapmap];1.00[YRI][hapmap]
rs1820262	0.96[CEU][hapmap];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2098754	0.82[CHB][hapmap];0.86[CHD][hapmap];1.00[JPT][hapmap]
rs2288053	0.85[CHD][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap]
rs2303275	0.80[CHD][hapmap];1.00[JPT][hapmap]
rs2303278	0.92[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap]
rs2303281	0.88[ASW][hapmap];0.80[CEU][hapmap];0.91[CHB][hapmap];0.86[CHD][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];0.81[MEX][hapmap];0.94[MKK][hapmap];0.88[TSI][hapmap];1.00[YRI][hapmap]
rs2550824	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs3785312	0.92[CEU][hapmap];1.00[JPT][hapmap]
rs3826239	0.80[CEU][hapmap];1.00[JPT][hapmap];0.88[TSI][hapmap]
rs3851729	0.92[JPT][hapmap]
rs3923201	0.96[ASN][1000 genomes]
rs4072222	0.92[CHB][hapmap];0.92[JPT][hapmap]
rs4072450	0.96[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap]
rs4243108	0.96[CEU][hapmap];1.00[CHB][hapmap];0.85[CHD][hapmap];0.91[GIH][hapmap];0.84[JPT][hapmap];0.91[MEX][hapmap];0.87[TSI][hapmap]
rs4438331	0.82[CHB][hapmap];0.84[CHD][hapmap];0.92[JPT][hapmap]
rs4564599	0.80[ASN][1000 genomes]
rs4600490	0.82[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[JPT][hapmap];0.89[LWK][hapmap];0.95[YRI][hapmap];0.84[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs4887772	0.88[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];1.00[MEX][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs4887776	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[CHD][hapmap];0.97[GIH][hapmap];0.92[JPT][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.81[EUR][1000 genomes]
rs4887777	0.92[CEU][hapmap];0.92[CHB][hapmap];0.84[CHD][hapmap];0.97[GIH][hapmap];0.92[JPT][hapmap];0.85[MEX][hapmap];0.95[TSI][hapmap]
rs4887779	0.92[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];0.97[GIH][hapmap];0.92[JPT][hapmap];0.91[MEX][hapmap];0.95[TSI][hapmap];0.80[ASN][1000 genomes]
rs4888238	0.82[ASW][hapmap];0.84[CEU][hapmap];0.82[CHB][hapmap];0.85[CHD][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];0.91[MKK][hapmap];0.86[TSI][hapmap];0.86[YRI][hapmap]
rs4888240	0.80[CHD][hapmap];0.92[JPT][hapmap];0.86[MEX][hapmap]
rs4888242	0.82[ASW][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.88[LWK][hapmap];0.93[MKK][hapmap];0.86[TSI][hapmap];0.91[YRI][hapmap]
rs4888256	0.84[CEU][hapmap];0.91[CHB][hapmap];0.90[CHD][hapmap];0.85[GIH][hapmap];0.84[JPT][hapmap];0.86[MEX][hapmap];0.81[TSI][hapmap]
rs4888258	0.81[EUR][1000 genomes]
rs4888262	0.92[JPT][hapmap]
rs4888265	0.85[JPT][hapmap]
rs4888266	0.96[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap]
rs4888267	0.90[JPT][hapmap]
rs4888274	0.92[JPT][hapmap]
rs55960814	0.88[ASN][1000 genomes]
rs62054177	0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs6564117	0.92[CEU][hapmap];0.92[CHB][hapmap];0.80[CHD][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];0.95[MEX][hapmap];0.94[MKK][hapmap];0.95[TSI][hapmap];0.91[YRI][hapmap]
rs6564141	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6564142	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6564145	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6564146	0.80[ASN][1000 genomes]
rs6564147	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6564149	0.80[ASN][1000 genomes]
rs6564152	0.81[ASN][1000 genomes]
rs6564153	0.81[ASN][1000 genomes]
rs6564154	0.80[CEU][hapmap];0.91[CHB][hapmap];0.85[CHD][hapmap];0.82[GIH][hapmap];0.92[JPT][hapmap];0.82[MEX][hapmap]
rs6564157	0.82[CHB][hapmap]
rs67414268	0.88[ASN][1000 genomes]
rs71392603	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7184754	0.80[ASN][1000 genomes]
rs7185026	0.84[CEU][hapmap];0.91[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.81[TSI][hapmap];0.94[ASN][1000 genomes]
rs7185722	0.81[ASN][1000 genomes]
rs7189123	0.82[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap]
rs7191665	0.92[JPT][hapmap]
rs7193583	0.92[CEU][hapmap];0.80[ASN][1000 genomes]
rs7193959	0.92[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.80[ASN][1000 genomes]
rs7194143	0.82[CHB][hapmap];0.84[CHD][hapmap];0.92[JPT][hapmap]
rs7194687	0.80[ASN][1000 genomes]
rs7201105	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7201320	0.86[JPT][hapmap]
rs7203452	0.84[CEU][hapmap];0.91[CHB][hapmap];1.00[CHD][hapmap];0.87[GIH][hapmap];0.84[JPT][hapmap];0.85[MEX][hapmap];0.81[TSI][hapmap];0.92[ASN][1000 genomes]
rs7204382	0.90[CHB][hapmap];0.80[CHD][hapmap];0.82[GIH][hapmap];0.81[MEX][hapmap]
rs7204804	0.91[CHB][hapmap];0.85[CHD][hapmap];0.85[GIH][hapmap];0.92[JPT][hapmap];0.82[MEX][hapmap];0.81[ASN][1000 genomes]
rs7205258	0.96[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];0.97[GIH][hapmap];0.92[JPT][hapmap];0.91[MEX][hapmap];0.93[TSI][hapmap]
rs7205813	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7342732	0.96[CEU][hapmap];1.00[CHB][hapmap];0.85[CHD][hapmap];0.91[GIH][hapmap];0.92[JPT][hapmap];0.91[MEX][hapmap];0.90[TSI][hapmap]
rs7359390	0.86[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs7978	0.92[JPT][hapmap]
rs8045848	0.82[CHB][hapmap];0.95[CHD][hapmap];0.84[JPT][hapmap]
rs8046158	0.84[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs8047243	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs8048239	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8049138	0.92[ASN][1000 genomes]
rs8050624	0.96[CEU][hapmap];1.00[CHB][hapmap];0.85[CHD][hapmap];0.94[GIH][hapmap];0.92[JPT][hapmap];0.91[MEX][hapmap];0.93[TSI][hapmap]
rs8050668	0.94[ASN][1000 genomes]
rs8050850	0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8051990	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8052389	0.84[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs8052923	0.96[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap]
rs8053084	0.80[ASN][1000 genomes]
rs8053369	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8055380	0.86[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs8055784	0.80[CEU][hapmap];0.91[CHB][hapmap];0.85[CHD][hapmap];0.82[GIH][hapmap];0.92[JPT][hapmap];0.82[MEX][hapmap]
rs8055803	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs8056718	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs8058133	0.92[JPT][hapmap]
rs8058256	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs8058437	0.84[ASN][1000 genomes]
rs8058692	0.84[CEU][hapmap];0.91[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];0.92[JPT][hapmap];0.86[MEX][hapmap];0.81[TSI][hapmap];0.95[ASN][1000 genomes]
rs8058922	0.80[CEU][hapmap];0.91[CHB][hapmap];0.85[CHD][hapmap];0.82[GIH][hapmap];0.84[JPT][hapmap];0.82[MEX][hapmap]
rs8059869	0.92[JPT][hapmap];0.81[MEX][hapmap]
rs8062404	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs8062783	0.86[JPT][hapmap]
rs918782	0.84[CEU][hapmap];0.91[CHB][hapmap];0.86[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap]
rs9888950	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9888968	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9888976	0.96[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap];0.87[YRI][hapmap];0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9923145	0.92[JPT][hapmap]
rs9923616	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs9923644	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9927073	0.80[CEU][hapmap];0.91[CHB][hapmap];0.84[CHD][hapmap];0.85[GIH][hapmap];0.92[JPT][hapmap];0.82[MEX][hapmap]
rs9929483	0.80[CEU][hapmap];0.91[CHB][hapmap];0.85[CHD][hapmap];0.82[GIH][hapmap];0.92[JPT][hapmap];0.82[MEX][hapmap]
rs9929933	0.84[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs9930003	0.96[ASN][1000 genomes]
rs9931225	0.92[CHB][hapmap];0.92[JPT][hapmap]
rs9932831	0.81[CHB][hapmap];0.84[CHD][hapmap];0.92[JPT][hapmap]
rs9936239	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9938833	0.91[CHB][hapmap];0.85[CHD][hapmap];0.82[GIH][hapmap];0.92[JPT][hapmap];0.82[MEX][hapmap]
rs9938859	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948443	chr16:73994997-74627711	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv916687	chr16:74241238-74896721	Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	102 gene(s)	inside rSNPs	diseases
3	esv2758431	chr16:74334780-74587185	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	esv2758656	chr16:74334780-74587185	Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
5	nsv833278	chr16:74415944-74584123	Weak transcription Active TSS Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv949374	chr16:74466960-75172358	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
7	nsv1060629	chr16:74483574-74660669	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
8	nsv1062517	chr16:74483574-74710623	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
9	nsv833279	chr16:74490746-74663073	Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
10	nsv1061095	chr16:74519718-75407020	Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	123 gene(s)	inside rSNPs	diseases
11	nsv906905	chr16:74527618-74679244	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS 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 miRNA target site	19 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs4888253	MLKL	Cis_1M	lymphoblastoid	RTeQTL
rs4888253	RFWD3	cis	Skin Sun Exposed Lower leg	GTEx
rs4888253	RFWD3	cis	Esophagus Mucosa	GTEx
rs4888253	RFWD3	cis	Thyroid	GTEx
rs4888253	RFWD3	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:74537600-74604800	Weak transcription	Thymus	Thymus
2	chr16:74542800-74590400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr16:74556400-74595600	Weak transcription	NH-A	brain
4	chr16:74559200-74594000	Weak transcription	Ovary	ovary
5	chr16:74559400-74591200	Weak transcription	Primary T cells from cord blood	blood
6	chr16:74563200-74598000	Weak transcription	Fetal Intestine Small	intestine
7	chr16:74563200-74622400	Weak transcription	Fetal Stomach	stomach
8	chr16:74565000-74597000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr16:74565600-74597000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr16:74578400-74591200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr16:74578600-74587600	Weak transcription	HUVEC	blood vessel
12	chr16:74578600-74589800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr16:74578600-74597400	Weak transcription	Pancreas	Pancrea
14	chr16:74579200-74597200	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr16:74580200-74591400	Weak transcription	HepG2	liver
16	chr16:74580200-74593400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr16:74580400-74591200	Weak transcription	Primary T cells fromperipheralblood	blood
18	chr16:74580600-74591200	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr16:74581800-74583200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
20	chr16:74581800-74590400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr16:74582000-74584200	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr16:74582400-74584800	Weak transcription	Fetal Brain Male	brain
23	chr16:74582600-74595000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr16:74582800-74591200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr16:74582800-74594800	Weak transcription	Left Ventricle	heart
26	chr16:74582800-74595000	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr16:74583000-74595600	Weak transcription	Hela-S3	cervix
28	chr16:74583000-74617200	Weak transcription	Fetal Muscle Leg	muscle

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