Variant report

Variant	rs4468203
Chromosome Location	chr1:46113272-46113273
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:19)
CpG islands
(count:0)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:19 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr1:46112851-46113652	H1-hESC	embryonic stem cell:	n/a	n/a
2	SPI1	chr1:46113018-46113605	HL-60	blood:	n/a	n/a
3	POLR2A	chr1:46112950-46113994	K562	blood:	n/a	n/a
4	POLR2A	chr1:46113080-46113911	HepG2	liver:	n/a	n/a
5	POLR2A	chr1:46112852-46113533	GM12878	blood:	n/a	n/a
6	POLR2A	chr1:46113216-46113571	H1-hESC	embryonic stem cell:	n/a	n/a
7	POLR2A	chr1:46113253-46113563	H1-neurons	neurons:	n/a	n/a
8	POLR2A	chr1:46112979-46113754	GM12892	blood:	n/a	n/a
9	POLR2A	chr1:46113220-46113593	HepG2	liver:	n/a	n/a
10	POLR2A	chr1:46113205-46114408	K562	blood:	n/a	n/a
11	POLR2A	chr1:46112712-46113929	K562	blood:	n/a	n/a
12	POLR2A	chr1:46113007-46113422	A549	lung:	n/a	n/a
13	POLR2A	chr1:46113050-46113695	GM12892	blood:	n/a	n/a
14	POLR2A	chr1:46113098-46113843	H1-hESC	embryonic stem cell:	n/a	n/a
15	SPI1	chr1:46113154-46113540	HL-60	blood:	n/a	n/a
16	POLR2A	chr1:46112885-46113771	GM12878	blood:	n/a	n/a
17	POLR2A	chr1:46112914-46113770	K562	blood:	n/a	n/a
18	POLR2A	chr1:46113180-46113853	GM12891	blood:	n/a	n/a
19	POLR2A	chr1:46113138-46113594	GM12891	blood:	n/a	n/a

No data

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:46048335..46051372-chr1:46110517..46113642,3	K562	blood:
2	chr1:46106624..46108539-chr1:46111914..46115684,3	K562	blood:
3	chr1:46112781..46115036-chr1:46118827..46120883,2	K562	blood:
4	chr1:46112537..46114281-chr1:46118229..46120327,2	K562	blood:
5	chr1:46098172..46100532-chr1:46111333..46113412,2	K562	blood:

No data

Variant related genes	Relation type
RPS15AP10	TF binding region
ENSG00000132780	Chromatin interaction
ENSG00000159592	Chromatin interaction

Extended variants
information (count: 175 )
Associated
traits (count: 18 )

rSNPs within LD-proxies of this variant (count:169)

rs_ID	r²[population]
rs10157795	0.87[ASN][1000 genomes]
rs10430105	0.84[CHB][hapmap]
rs10430123	0.89[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs10430124	0.89[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs10749856	0.90[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs10789467	0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs10789468	0.96[ASN][1000 genomes]
rs10789470	0.94[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs10890333	0.94[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs10890334	0.85[CHB][hapmap]
rs10890335	0.85[CHB][hapmap]
rs10890336	0.94[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs10890337	0.96[ASN][1000 genomes]
rs10890341	0.85[CHB][hapmap]
rs10890343	0.96[ASN][1000 genomes]
rs10890344	0.93[ASN][1000 genomes]
rs10890346	0.84[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs11211151	0.97[ASN][1000 genomes]
rs11211157	0.94[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs11211158	0.96[ASN][1000 genomes]
rs11211159	0.96[ASN][1000 genomes]
rs11211160	0.81[CHB][hapmap]
rs11211163	0.94[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs11211165	0.96[ASN][1000 genomes]
rs11211166	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs11211174	0.88[ASN][1000 genomes]
rs11211175	0.88[ASN][1000 genomes]
rs11211176	0.90[ASN][1000 genomes]
rs11211178	0.84[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs11211179	0.87[ASN][1000 genomes]
rs11211181	0.84[CHB][hapmap];0.94[JPT][hapmap];0.86[ASN][1000 genomes]
rs11211199	0.83[YRI][hapmap]
rs1135812	0.85[CHB][hapmap]
rs11587650	0.86[EUR][1000 genomes]
rs12022673	0.82[ASN][1000 genomes]
rs12023439	0.80[CHB][hapmap]
rs12025621	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12031182	0.88[ASN][1000 genomes]
rs12037459	0.94[CHB][hapmap]
rs12037803	0.96[ASN][1000 genomes]
rs12043945	0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs12045096	0.97[ASN][1000 genomes]
rs12049027	0.94[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs12069121	0.83[ASN][1000 genomes]
rs12091503	0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs12404197	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1250	0.94[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs12564201	0.88[ASN][1000 genomes]
rs1541131	0.93[ASN][1000 genomes]
rs1547924	0.94[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1547925	0.84[CHB][hapmap]
rs2050376	0.94[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs2088102	0.88[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap]
rs2230657	0.95[CEU][hapmap];0.95[CHB][hapmap];0.94[JPT][hapmap];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2230658	0.94[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs2230659	0.94[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs2253862	0.84[CHB][hapmap]
rs2275085	0.94[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs2275086	0.84[CHB][hapmap]
rs28361459	0.91[ASN][1000 genomes]
rs28378621	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs28406914	0.88[ASN][1000 genomes]
rs28432365	0.88[ASN][1000 genomes]
rs28438704	0.93[ASN][1000 genomes]
rs28442079	0.93[ASN][1000 genomes]
rs28456069	0.81[ASN][1000 genomes]
rs28474773	0.88[ASN][1000 genomes]
rs28490344	0.88[ASN][1000 genomes]
rs28495425	0.88[ASN][1000 genomes]
rs28498557	0.86[ASN][1000 genomes]
rs28501477	0.88[ASN][1000 genomes]
rs28528139	0.90[ASN][1000 genomes]
rs28564319	0.88[ASN][1000 genomes]
rs28617418	0.82[ASN][1000 genomes]
rs28635845	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28641748	0.88[ASN][1000 genomes]
rs28647556	0.90[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs28683093	0.83[ASN][1000 genomes]
rs28789495	0.88[ASN][1000 genomes]
rs28817701	0.82[CHB][hapmap];0.94[JPT][hapmap];0.88[ASN][1000 genomes]
rs28844317	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2934857	0.90[CEU][hapmap];1.00[CHB][hapmap];0.83[JPT][hapmap]
rs2934859	0.94[JPT][hapmap]
rs2991972	0.94[JPT][hapmap]
rs2991975	0.86[CEU][hapmap];0.94[JPT][hapmap]
rs2991977	0.84[ASN][1000 genomes]
rs2991981	0.84[ASN][1000 genomes]
rs2991985	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2991986	0.94[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs2991987	0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs2991988	0.84[CHB][hapmap]
rs2991989	0.85[CHB][hapmap]
rs2993263	0.94[JPT][hapmap]
rs3013594	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3013595	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3013596	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3013597	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3014210	0.94[CHB][hapmap];0.89[JPT][hapmap];0.85[ASN][1000 genomes]
rs3014212	0.84[ASN][1000 genomes]
rs3014216	0.90[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];1.00[YRI][hapmap]
rs3014218	0.85[CEU][hapmap];0.89[CHB][hapmap];0.89[JPT][hapmap];0.96[YRI][hapmap]
rs3014235	0.85[CHB][hapmap]
rs3014236	0.93[ASN][1000 genomes]
rs3014238	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3014239	0.94[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs3014242	0.94[CHB][hapmap];0.89[JPT][hapmap]
rs3014243	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3014245	0.84[CHB][hapmap]
rs3014247	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3014251	0.90[ASN][1000 genomes]
rs34895634	0.87[ASN][1000 genomes]
rs3811435	0.96[ASN][1000 genomes]
rs3811436	0.84[CHB][hapmap];0.81[ASN][1000 genomes]
rs3935296	0.88[ASN][1000 genomes]
rs4274104	0.95[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4330955	0.87[ASN][1000 genomes]
rs4353138	0.92[EUR][1000 genomes]
rs4391704	0.90[CEU][hapmap];0.94[CHB][hapmap];0.84[JPT][hapmap];0.94[EUR][1000 genomes]
rs4423054	0.88[ASN][1000 genomes]
rs4431884	0.89[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs4439382	0.84[CHB][hapmap]
rs4559551	0.89[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs4564187	0.90[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs4607935	0.89[CHB][hapmap];0.81[ASN][1000 genomes]
rs4609469	0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs4626927	0.85[CEU][hapmap];0.82[JPT][hapmap]
rs4660312	0.84[CEU][hapmap];0.88[CHB][hapmap];0.88[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4660314	0.87[ASN][1000 genomes]
rs4660879	0.91[ASN][1000 genomes]
rs4660882	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4660883	0.84[CHB][hapmap];0.94[JPT][hapmap];0.86[ASN][1000 genomes]
rs4660885	0.81[CEU][hapmap]
rs499600	0.81[CHB][hapmap]
rs5021934	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs512026	0.89[JPT][hapmap]
rs518216	0.94[CHB][hapmap];0.89[JPT][hapmap]
rs518365	0.83[JPT][hapmap]
rs56177313	0.87[ASN][1000 genomes]
rs56255771	0.87[ASN][1000 genomes]
rs59916372	0.87[ASN][1000 genomes]
rs61784796	0.94[ASN][1000 genomes]
rs61784800	0.90[ASN][1000 genomes]
rs61784803	0.88[ASN][1000 genomes]
rs61784824	0.81[ASN][1000 genomes]
rs61784833	0.86[ASN][1000 genomes]
rs622798	0.94[JPT][hapmap]
rs6429574	0.96[ASN][1000 genomes]
rs6429575	0.96[ASN][1000 genomes]
rs6429576	0.95[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6656279	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6658700	0.84[CHB][hapmap]
rs6665808	0.94[ASN][1000 genomes]
rs6671802	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6686944	0.92[ASN][1000 genomes]
rs6690926	0.96[ASN][1000 genomes]
rs6694889	0.85[CHB][hapmap]
rs6697821	0.89[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs6699418	0.94[ASN][1000 genomes]
rs6703748	0.81[CHB][hapmap]
rs6703960	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72688483	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7519900	0.87[ASN][1000 genomes]
rs7520123	0.87[ASN][1000 genomes]
rs7545118	0.82[ASN][1000 genomes]
rs7547414	0.83[ASN][1000 genomes]
rs8179296	0.96[ASN][1000 genomes]
rs8179402	0.96[ASN][1000 genomes]
rs9429172	0.82[CHB][hapmap]
rs9793568	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529631	chr1:45905936-46335246	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	207 gene(s)	inside rSNPs	diseases
2	nsv932680	chr1:45935520-46686477	Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	232 gene(s)	inside rSNPs	diseases
3	nsv868828	chr1:45953923-46686477	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	232 gene(s)	inside rSNPs	diseases
4	nsv871928	chr1:46024701-46609736	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer 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
5	nsv1011587	chr1:46051672-46244492	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
6	nsv1014128	chr1:46097670-46394540	Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases

mRNA abundance (count:18)

SNP	Gene	Cis/trans	Tissue	Source
rs4468203	CCDC163P	cis	Nerve Tibial	GTEx
rs4468203	MAST2	cis	Artery Aorta	GTEx
rs4468203	CCDC163P	cis	Thyroid	GTEx
rs4468203	CCDC163P	cis	Muscle Skeletal	GTEx
rs4468203	CCDC163P	cis	Skin Sun Exposed Lower leg	GTEx
rs4468203	CCDC163P	cis	Whole Blood	GTEx
rs4468203	CCDC163P	cis	Stomach	GTEx
rs4468203	CCDC163P	cis	lung	GTEx
rs4468203	GPBP1L1	cis	Whole Blood	GTEx
rs4468203	IPP	Cis_1M	lymphoblastoid	RTeQTL
rs4468203	LOC126661	Cis_1M	lymphoblastoid	RTeQTL
rs4468203	CCDC163P	cis	Artery Tibial	GTEx
rs4468203	CCDC163P	cis	Heart Left Ventricle	GTEx
rs4468203	MAST2	cis	Artery Tibial	GTEx
rs4468203	Hs.396207	cis	multi-tissue	Pritchard
rs4468203	CCDC163P	cis	Esophagus Mucosa	GTEx
rs4468203	CCDC163P	cis	Adipose Subcutaneous	GTEx
rs4468203	CCDC163P	cis	Esophagus Muscularis	GTEx

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:46053200-46127400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr1:46087600-46129200	Strong transcription	Fetal Thymus	thymus
3	chr1:46088600-46127400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:46088800-46113400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr1:46089600-46126400	Strong transcription	Primary T cells from cord blood	blood
6	chr1:46089800-46127000	Strong transcription	HUES6 Cell Line	embryonic stem cell
7	chr1:46091000-46126400	Strong transcription	Fetal Muscle Trunk	muscle
8	chr1:46091200-46120400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr1:46091200-46120800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr1:46091200-46127000	Strong transcription	HUES48 Cell Line	embryonic stem cell
11	chr1:46091200-46127000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
12	chr1:46091200-46127200	Strong transcription	HUES64 Cell Line	embryonic stem cell
13	chr1:46091200-46128200	Strong transcription	Dnd41	blood
14	chr1:46091400-46127000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr1:46091400-46127000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
16	chr1:46091400-46127000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr1:46092800-46120200	Strong transcription	HSMM	muscle
18	chr1:46093200-46127000	Strong transcription	K562	blood
19	chr1:46097200-46126800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr1:46098400-46133400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr1:46099400-46115800	Weak transcription	Fetal Brain Male	brain
22	chr1:46100200-46135600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr1:46104000-46114600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr1:46105400-46116800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr1:46106200-46140000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
26	chr1:46106400-46120200	Weak transcription	Psoas Muscle	Psoas
27	chr1:46106600-46114000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
28	chr1:46106800-46116800	Weak transcription	Esophagus	oesophagus
29	chr1:46107000-46115600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr1:46107000-46116200	Weak transcription	NH-A	brain
31	chr1:46107200-46113400	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr1:46107200-46114200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
33	chr1:46107400-46115600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr1:46107800-46116800	Weak transcription	Aorta	Aorta
35	chr1:46108000-46116000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr1:46108200-46113400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr1:46108200-46113400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
38	chr1:46108200-46113400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
39	chr1:46108200-46114000	Weak transcription	HMEC	breast
40	chr1:46108200-46114600	Weak transcription	Colon Smooth Muscle	Colon
41	chr1:46108200-46116600	Weak transcription	Gastric	stomach
42	chr1:46108200-46116600	Weak transcription	Ovary	ovary
43	chr1:46108200-46116600	Weak transcription	Spleen	Spleen
44	chr1:46108600-46116800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
45	chr1:46108800-46116600	Weak transcription	Colonic Mucosa	Colon
46	chr1:46109000-46115800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
47	chr1:46109200-46115800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr1:46109400-46115400	Weak transcription	Fetal Kidney	kidney
49	chr1:46109600-46114600	Weak transcription	Fetal Brain Female	brain
50	chr1:46110600-46120200	Weak transcription	Pancreatic Islets	Pancreatic Islet

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