Variant report

Variant	rs1469140
Chromosome Location	chr16:74520295-74520296
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr16:74519695..74521614-chr16:74523670..74527438,3	MCF-7	breast:
2	chr16:74518172..74521190-chr16:74639634..74642594,6	MCF-7	breast:
3	chr16:74519662..74521671-chr16:74634535..74637468,2	MCF-7	breast:
4	chr16:74514035..74516362-chr16:74518414..74521351,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000090863	Chromatin interaction

Extended variants
information (count: 119 )
Associated
traits (count: 4 )

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

rs_ID	r²[population]
rs1019572	0.96[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1019573	0.91[CEU][hapmap];1.00[JPT][hapmap]
rs10500587	0.84[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs11149722	0.92[CEU][hapmap];0.91[CHB][hapmap];0.90[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.97[TSI][hapmap]
rs11639812	0.84[CEU][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];0.88[TSI][hapmap];0.85[ASN][1000 genomes]
rs11640021	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11640632	0.82[ASN][1000 genomes]
rs11641958	0.93[ASN][1000 genomes]
rs11643293	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11644298	0.95[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs11648786	0.81[ASN][1000 genomes]
rs11648868	0.81[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs12325017	0.96[CEU][hapmap];0.91[CHB][hapmap];0.95[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12445991	0.92[JPT][hapmap]
rs12446054	0.81[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap]
rs12446095	0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12447531	0.87[ASN][1000 genomes]
rs12448026	0.81[CHB][hapmap];0.86[CHD][hapmap];0.92[JPT][hapmap]
rs12449071	0.98[ASN][1000 genomes]
rs12449125	0.88[ASN][1000 genomes]
rs12598701	0.91[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.87[AFR][1000 genomes];0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12598791	0.85[MKK][hapmap]
rs12716768	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12927939	0.92[ASN][1000 genomes]
rs12930645	0.89[ASN][1000 genomes]
rs13339161	1.00[ASW][hapmap];0.84[CEU][hapmap];0.91[CHB][hapmap];0.95[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];0.88[TSI][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs13339456	0.82[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs13359	0.81[CEU][hapmap];0.91[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap];0.88[TSI][hapmap]
rs13380609	0.91[ASN][1000 genomes]
rs17672539	0.96[ASN][1000 genomes]
rs1985611	0.88[ASN][1000 genomes]
rs2098754	0.84[CEU][hapmap];0.90[CHB][hapmap];1.00[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];0.81[TSI][hapmap];0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2288053	0.81[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap]
rs2303275	0.95[CHD][hapmap];1.00[JPT][hapmap]
rs2303278	0.84[CEU][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs2303281	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];0.99[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2549063	0.81[AMR][1000 genomes]
rs2549559	0.88[ASN][1000 genomes]
rs2550816	0.86[ASN][1000 genomes]
rs28762730	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs3096409	0.85[ASN][1000 genomes]
rs3785312	0.84[CEU][hapmap];0.81[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs3826239	0.96[CEU][hapmap];0.81[CHB][hapmap];0.91[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3851729	0.92[JPT][hapmap]
rs3960602	0.83[ASN][1000 genomes]
rs3973385	0.86[ASN][1000 genomes]
rs4072222	0.83[CHB][hapmap];0.92[JPT][hapmap]
rs4072450	0.81[CEU][hapmap];0.91[CHB][hapmap];0.84[JPT][hapmap]
rs4243108	0.81[CEU][hapmap];0.91[CHB][hapmap];0.81[CHD][hapmap];0.84[JPT][hapmap]
rs4438331	0.81[CHD][hapmap];0.92[JPT][hapmap]
rs4600490	0.91[CHB][hapmap];0.86[CHD][hapmap];0.84[JPT][hapmap];0.85[LWK][hapmap];0.95[YRI][hapmap]
rs4887772	1.00[ASW][hapmap];0.84[CEU][hapmap];0.91[CHB][hapmap];0.95[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];0.99[MKK][hapmap];0.88[TSI][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4887776	0.84[CEU][hapmap];0.91[CHB][hapmap];0.81[CHD][hapmap];0.92[JPT][hapmap];0.88[TSI][hapmap]
rs4887777	0.83[CHB][hapmap];0.81[CHD][hapmap];0.92[JPT][hapmap];0.84[TSI][hapmap]
rs4887779	0.84[CEU][hapmap];0.91[CHB][hapmap];0.86[CHD][hapmap];0.92[JPT][hapmap];0.84[TSI][hapmap]
rs4888238	0.94[ASW][hapmap];0.92[CEU][hapmap];0.91[CHB][hapmap];0.90[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];1.00[MEX][hapmap];0.99[MKK][hapmap];0.97[TSI][hapmap];0.86[YRI][hapmap]
rs4888240	0.81[CHB][hapmap];0.86[CHD][hapmap];0.92[JPT][hapmap]
rs4888242	0.94[ASW][hapmap];0.92[CEU][hapmap];0.91[CHB][hapmap];0.95[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];0.97[MKK][hapmap];0.97[TSI][hapmap];0.91[YRI][hapmap];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4888253	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]
rs4888256	0.81[CHB][hapmap];0.86[CHD][hapmap];0.84[JPT][hapmap]
rs4888262	0.92[JPT][hapmap]
rs4888265	0.85[JPT][hapmap]
rs4888266	0.81[CEU][hapmap];0.91[CHB][hapmap];0.92[JPT][hapmap]
rs4888267	0.90[JPT][hapmap]
rs4888274	0.92[JPT][hapmap]
rs6564117	0.82[ASW][hapmap];0.84[CEU][hapmap];0.83[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.88[LWK][hapmap];0.82[MEX][hapmap];0.96[MKK][hapmap];0.88[TSI][hapmap];0.91[YRI][hapmap];0.86[ASN][1000 genomes]
rs6564154	0.81[CHB][hapmap];0.81[CHD][hapmap];0.92[JPT][hapmap]
rs7185026	0.81[CHB][hapmap];0.86[CHD][hapmap];1.00[JPT][hapmap]
rs7188050	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs7188197	0.86[ASN][1000 genomes]
rs7189123	0.94[ASW][hapmap];0.91[CHB][hapmap];0.90[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];0.97[MKK][hapmap];0.88[TSI][hapmap];0.95[YRI][hapmap];0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7190577	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7191665	0.92[JPT][hapmap]
rs7193959	0.91[CHB][hapmap];0.92[JPT][hapmap]
rs7194143	0.81[CHD][hapmap];0.92[JPT][hapmap]
rs7195020	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs7195196	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs7195198	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs7201320	0.86[JPT][hapmap]
rs7203452	0.81[CHB][hapmap];0.85[CHD][hapmap];0.84[JPT][hapmap]
rs7204804	0.81[CHB][hapmap];0.81[CHD][hapmap];0.92[JPT][hapmap]
rs7205258	0.81[CEU][hapmap];0.91[CHB][hapmap];0.86[CHD][hapmap];0.92[JPT][hapmap];0.82[TSI][hapmap]
rs7342732	0.81[CEU][hapmap];0.91[CHB][hapmap];0.81[CHD][hapmap];0.92[JPT][hapmap]
rs7978	0.92[JPT][hapmap]
rs8045653	0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs8045848	0.90[CHD][hapmap];0.84[JPT][hapmap]
rs8050624	0.81[CEU][hapmap];0.91[CHB][hapmap];0.81[CHD][hapmap];0.92[JPT][hapmap];0.80[TSI][hapmap]
rs8052923	0.81[CEU][hapmap];0.91[CHB][hapmap];0.92[JPT][hapmap]
rs8053599	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8055784	0.81[CHB][hapmap];0.81[CHD][hapmap];0.92[JPT][hapmap]
rs8058133	0.92[JPT][hapmap]
rs8058692	0.81[CHB][hapmap];0.86[CHD][hapmap];0.92[JPT][hapmap]
rs8058922	0.81[CHB][hapmap];0.81[CHD][hapmap];0.84[JPT][hapmap]
rs8059869	0.92[JPT][hapmap]
rs8062783	0.86[JPT][hapmap]
rs918782	0.81[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs9888976	0.91[CHB][hapmap];0.84[JPT][hapmap];0.87[YRI][hapmap]
rs9923145	0.92[JPT][hapmap]
rs9923616	0.91[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9927073	0.81[CHB][hapmap];0.81[CHD][hapmap];0.92[JPT][hapmap]
rs9929483	0.81[CHB][hapmap];0.81[CHD][hapmap];0.92[JPT][hapmap]
rs9931225	0.83[CHB][hapmap];0.92[JPT][hapmap]
rs9932831	0.81[CHD][hapmap];0.92[JPT][hapmap]
rs9938833	0.81[CHB][hapmap];0.81[CHD][hapmap];0.92[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:15 , 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	nsv1066212	chr16:74068470-74527133	Weak transcription Active TSS Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv542954	chr16:74068470-74527133	Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs1469140	RFWD3	cis	Skin Sun Exposed Lower leg	GTEx
rs1469140	RFWD3	Cis_1M	lymphoblastoid	RTeQTL
rs1469140	RFWD3	cis	Esophagus Mucosa	GTEx
rs1469140	MLKL	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:74480400-74530800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr16:74480400-74530800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr16:74480400-74531800	Strong transcription	Primary T helper cells fromperipheralblood	blood
4	chr16:74480600-74530600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr16:74480800-74530600	Strong transcription	Primary neutrophils fromperipheralblood	blood
6	chr16:74480800-74530800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr16:74483000-74530600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
8	chr16:74483000-74530800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr16:74483200-74520400	Strong transcription	HUES64 Cell Line	embryonic stem cell
10	chr16:74483800-74530600	Strong transcription	Liver	Liver
11	chr16:74484400-74532200	Strong transcription	Monocytes-CD14+_RO01746	blood
12	chr16:74485000-74530800	Strong transcription	Primary monocytes fromperipheralblood	blood
13	chr16:74485600-74542600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr16:74488800-74530600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr16:74489200-74531000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr16:74498800-74544400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr16:74499200-74539200	Strong transcription	Primary B cells from peripheral blood	blood
18	chr16:74501400-74530800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
19	chr16:74501400-74531000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr16:74502000-74530600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr16:74503800-74537200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr16:74504000-74523600	Weak transcription	Small Intestine	intestine
23	chr16:74507000-74535400	Weak transcription	Psoas Muscle	Psoas
24	chr16:74508600-74544000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr16:74511400-74524000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr16:74511600-74523400	Weak transcription	Gastric	stomach
27	chr16:74512600-74524600	Weak transcription	Brain Angular Gyrus	brain
28	chr16:74513400-74533800	Strong transcription	HepG2	liver
29	chr16:74513800-74523400	Weak transcription	Esophagus	oesophagus
30	chr16:74513800-74523600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr16:74513800-74524600	Weak transcription	Colonic Mucosa	Colon
32	chr16:74513800-74524800	Weak transcription	NHLF	lung
33	chr16:74514000-74523400	Weak transcription	Brain Hippocampus Middle	brain
34	chr16:74514200-74529400	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr16:74514400-74521200	Weak transcription	Muscle Satellite Cultured Cells	--
36	chr16:74514400-74524800	Weak transcription	Colon Smooth Muscle	Colon
37	chr16:74514400-74526800	Weak transcription	Fetal Heart	heart
38	chr16:74514400-74529000	Strong transcription	Fetal Muscle Leg	muscle
39	chr16:74514600-74521200	Weak transcription	NHDF-Ad	bronchial
40	chr16:74514800-74524800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr16:74515200-74530800	Strong transcription	Fetal Thymus	thymus
42	chr16:74515200-74535400	Weak transcription	Stomach Mucosa	stomach
43	chr16:74515400-74531000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr16:74515600-74530200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr16:74516000-74522800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr16:74516000-74525400	Strong transcription	Primary B cells from cord blood	blood
47	chr16:74516000-74530400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr16:74516200-74520400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr16:74516200-74520400	Strong transcription	GM12878-XiMat	blood
50	chr16:74516600-74520400	Strong transcription	Dnd41	blood

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