Variant report

Variant	rs12716768
Chromosome Location	chr16:74556486-74556487
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:74556016..74558934-chr16:74697504..74700485,2	K562	blood:

Variant related genes	Relation type
ENSG00000168411	Chromatin interaction

Extended variants
information (count: 125 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:111)

rs_ID	r²[population]
rs1019572	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs1019573	0.82[CEU][hapmap];1.00[JPT][hapmap]
rs10500587	0.92[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
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];0.86[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.95[TSI][hapmap]
rs11640021	0.88[ASN][1000 genomes]
rs11641958	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11644298	0.82[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs11648786	0.89[ASN][1000 genomes]
rs11648868	0.85[CHD][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs12325017	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]
rs12446054	0.85[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap]
rs12446095	0.89[ASN][1000 genomes]
rs12446217	0.81[ASN][1000 genomes]
rs12448026	0.84[CEU][hapmap];0.91[CHB][hapmap];0.89[CHD][hapmap];0.85[GIH][hapmap];0.92[JPT][hapmap];0.82[MEX][hapmap];0.81[TSI][hapmap]
rs12449071	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs12449125	0.80[ASN][1000 genomes]
rs12598701	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12598791	0.85[MKK][hapmap]
rs12927939	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12930645	0.86[ASN][1000 genomes]
rs13339161	0.82[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap];0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13339456	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13359	0.96[CEU][hapmap];0.82[CHB][hapmap];0.85[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.95[TSI][hapmap]
rs13380609	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1469140	0.82[ASW][hapmap];0.84[CEU][hapmap];0.91[CHB][hapmap];0.86[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];0.94[MKK][hapmap];0.88[TSI][hapmap];0.95[YRI][hapmap];0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs17672539	0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs1820262	0.96[CEU][hapmap]
rs1971071	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1985611	0.80[ASN][1000 genomes]
rs2098754	0.82[CHB][hapmap];0.86[CHD][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs2288053	0.85[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap]
rs2303275	0.80[CHD][hapmap];1.00[JPT][hapmap]
rs2303278	0.91[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap]
rs2303281	0.82[ASW][hapmap];0.91[CHB][hapmap];0.86[CHD][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];0.96[MKK][hapmap];0.88[TSI][hapmap];0.95[YRI][hapmap];0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs2549063	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2549559	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2550816	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2868035	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28762730	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3096409	0.89[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs3785312	0.92[CEU][hapmap];1.00[JPT][hapmap]
rs3826239	1.00[JPT][hapmap];0.88[TSI][hapmap]
rs3851729	0.92[JPT][hapmap]
rs3865164	0.84[AMR][1000 genomes]
rs3960602	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3973385	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[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];0.85[GIH][hapmap];0.84[JPT][hapmap];0.82[MEX][hapmap];0.87[TSI][hapmap]
rs4404098	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4438331	0.82[CHB][hapmap];0.84[CHD][hapmap];0.92[JPT][hapmap]
rs4600490	1.00[CHB][hapmap];0.89[CHD][hapmap];0.84[JPT][hapmap];0.88[LWK][hapmap];1.00[YRI][hapmap]
rs4887772	0.82[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.91[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap];0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4887776	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[CHD][hapmap];0.91[GIH][hapmap];0.92[JPT][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap]
rs4887777	0.92[CEU][hapmap];0.92[CHB][hapmap];0.84[CHD][hapmap];0.91[GIH][hapmap];0.92[JPT][hapmap];0.95[TSI][hapmap]
rs4887779	0.92[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];0.91[GIH][hapmap];0.92[JPT][hapmap];0.82[MEX][hapmap];0.95[TSI][hapmap]
rs4888238	0.84[CEU][hapmap];0.82[CHB][hapmap];0.85[CHD][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];0.93[MKK][hapmap];0.86[TSI][hapmap];0.82[YRI][hapmap]
rs4888240	0.80[CHD][hapmap];0.83[GIH][hapmap];0.92[JPT][hapmap]
rs4888242	0.82[CHB][hapmap];1.00[JPT][hapmap];0.88[LWK][hapmap];0.94[MKK][hapmap];0.85[TSI][hapmap];0.86[YRI][hapmap];0.80[ASN][1000 genomes]
rs4888253	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];0.91[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap]
rs4888256	0.84[CEU][hapmap];0.91[CHB][hapmap];0.90[CHD][hapmap];0.84[JPT][hapmap];0.81[TSI][hapmap]
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]
rs6564117	0.92[CEU][hapmap];0.92[CHB][hapmap];0.80[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.85[LWK][hapmap];0.86[MEX][hapmap];0.96[MKK][hapmap];0.95[TSI][hapmap];0.87[YRI][hapmap]
rs6564154	0.91[CHB][hapmap];0.85[CHD][hapmap];0.92[JPT][hapmap]
rs6564157	0.82[CHB][hapmap]
rs7185026	0.84[CEU][hapmap];0.91[CHB][hapmap];0.89[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.81[TSI][hapmap]
rs7188050	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7188197	0.89[ASN][1000 genomes]
rs7189123	0.92[CEU][hapmap];1.00[CHB][hapmap];0.84[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.91[MEX][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];0.91[YRI][hapmap];0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7190577	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7191665	0.92[JPT][hapmap]
rs7193583	0.92[CEU][hapmap]
rs7193959	0.92[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap]
rs7194143	0.82[CHB][hapmap];0.84[CHD][hapmap];0.92[JPT][hapmap]
rs7195020	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7195196	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7195198	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7201320	0.86[JPT][hapmap]
rs7203452	0.84[CEU][hapmap];0.91[CHB][hapmap];0.89[CHD][hapmap];0.82[GIH][hapmap];0.84[JPT][hapmap];0.81[TSI][hapmap]
rs7204382	0.90[CHB][hapmap];0.80[CHD][hapmap]
rs7204804	0.91[CHB][hapmap];0.85[CHD][hapmap];0.92[JPT][hapmap]
rs7205258	0.96[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];0.91[GIH][hapmap];0.92[JPT][hapmap];0.82[MEX][hapmap];0.93[TSI][hapmap]
rs7342732	0.96[CEU][hapmap];1.00[CHB][hapmap];0.85[CHD][hapmap];0.85[GIH][hapmap];0.92[JPT][hapmap];0.82[MEX][hapmap];0.90[TSI][hapmap]
rs7978	0.92[JPT][hapmap]
rs8045653	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8045848	0.82[CHB][hapmap];0.95[CHD][hapmap];0.84[JPT][hapmap]
rs8050624	0.96[CEU][hapmap];1.00[CHB][hapmap];0.85[CHD][hapmap];0.88[GIH][hapmap];0.92[JPT][hapmap];0.82[MEX][hapmap];0.93[TSI][hapmap]
rs8052923	0.96[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap]
rs8053599	0.89[ASN][1000 genomes]
rs8055784	0.91[CHB][hapmap];0.85[CHD][hapmap];0.92[JPT][hapmap]
rs8058133	0.92[JPT][hapmap]
rs8058692	0.84[CEU][hapmap];0.91[CHB][hapmap];0.89[CHD][hapmap];0.86[GIH][hapmap];0.92[JPT][hapmap];0.81[TSI][hapmap]
rs8058922	0.91[CHB][hapmap];0.85[CHD][hapmap];0.84[JPT][hapmap]
rs8059869	0.92[JPT][hapmap]
rs8062783	0.86[JPT][hapmap]
rs918782	0.84[CEU][hapmap];0.91[CHB][hapmap];0.86[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs9888755	0.82[AFR][1000 genomes]
rs9888976	0.96[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap];0.83[YRI][hapmap]
rs9923145	0.92[JPT][hapmap]
rs9923616	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.80[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9927073	0.91[CHB][hapmap];0.84[CHD][hapmap];0.92[JPT][hapmap]
rs9929483	0.91[CHB][hapmap];0.85[CHD][hapmap];0.92[JPT][hapmap]
rs9931225	0.92[CHB][hapmap];0.92[JPT][hapmap]
rs9932831	0.81[CHB][hapmap];0.84[CHD][hapmap];0.92[JPT][hapmap]
rs9938833	0.91[CHB][hapmap];0.85[CHD][hapmap];0.92[JPT][hapmap]

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	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	nsv1065964	chr16:74088091-74575604	Active TSS Flanking Active TSS Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer 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	34 gene(s)	inside rSNPs	diseases
3	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
4	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
5	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
6	nsv428806	chr16:74394226-74580125	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
7	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
8	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
9	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
10	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
11	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
12	nsv978169	chr16:74507776-74560104	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
13	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
14	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
rs12716768	RFWD3	cis	Esophagus Mucosa	GTEx
rs12716768	RFWD3	cis	Thyroid	GTEx
rs12716768	RFWD3	cis	multi-tissue	Pritchard
rs12716768	MLKL	cis	multi-tissue	Pritchard
rs12716768	RFWD3	cis	Skin Sun Exposed Lower leg	GTEx

Chromatin state (count:104 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:74525200-74565200	Weak transcription	Fetal Brain Male	brain
2	chr16:74525400-74561000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr16:74525400-74572200	Weak transcription	HUVEC	blood vessel
4	chr16:74530800-74558600	Weak transcription	Fetal Lung	lung
5	chr16:74535800-74557800	Weak transcription	Primary hematopoietic stem cells	blood
6	chr16:74536000-74558600	Weak transcription	Dnd41	blood
7	chr16:74536000-74563800	Weak transcription	Fetal Kidney	kidney
8	chr16:74537400-74567000	Weak transcription	Colon Smooth Muscle	Colon
9	chr16:74537600-74559200	Weak transcription	Stomach Smooth Muscle	stomach
10	chr16:74537600-74565200	Weak transcription	Colonic Mucosa	Colon
11	chr16:74537600-74568600	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr16:74537600-74579800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr16:74537600-74604800	Weak transcription	Thymus	Thymus
14	chr16:74537800-74568800	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr16:74538000-74567000	Weak transcription	HMEC	breast
16	chr16:74538200-74560600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr16:74538600-74557200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr16:74538600-74558400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr16:74538600-74558800	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr16:74538800-74566000	Weak transcription	NHEK	skin
21	chr16:74539000-74558000	Weak transcription	Duodenum Mucosa	Duodenum
22	chr16:74539000-74564000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr16:74539200-74558200	Weak transcription	GM12878-XiMat	blood
24	chr16:74539200-74562400	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr16:74539200-74578200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr16:74539200-74581600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr16:74539800-74557800	Weak transcription	Fetal Intestine Small	intestine
28	chr16:74539800-74565200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr16:74540000-74579800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr16:74540800-74566400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr16:74541000-74558600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
32	chr16:74541200-74558200	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr16:74541600-74558600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr16:74542600-74557800	Weak transcription	Primary monocytes fromperipheralblood	blood
35	chr16:74542600-74557800	Weak transcription	Fetal Muscle Trunk	muscle
36	chr16:74542600-74558000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr16:74542600-74558400	Weak transcription	Primary B cells from cord blood	blood
38	chr16:74542600-74567400	Weak transcription	Primary B cells from peripheral blood	blood
39	chr16:74542600-74574800	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr16:74542800-74557800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr16:74542800-74557800	Weak transcription	Fetal Intestine Large	intestine
42	chr16:74542800-74558000	Weak transcription	Fetal Thymus	thymus
43	chr16:74542800-74558200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
44	chr16:74542800-74558200	Weak transcription	Liver	Liver
45	chr16:74542800-74566800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr16:74542800-74590400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
47	chr16:74543000-74557000	Weak transcription	Monocytes-CD14+_RO01746	blood
48	chr16:74543000-74558000	Weak transcription	HepG2	liver
49	chr16:74543000-74558400	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr16:74543000-74558400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood

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