Variant report

Variant	rs1766200
Chromosome Location	chr6:106741463-106741464
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 112 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:97)

rs_ID	r²[population]
rs10484575	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11754416	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11756379	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11756420	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11759048	0.87[ASW][hapmap];1.00[CEU][hapmap];0.85[CHD][hapmap];0.97[GIH][hapmap];0.82[JPT][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.94[TSI][hapmap];0.95[YRI][hapmap];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11760170	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11961415	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1623780	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1624009	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1624701	0.87[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1626224	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1626503	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1627312	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17488854	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs17513225	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1766192	0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1766196	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1766199	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1766205	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1766208	0.81[GIH][hapmap]
rs1769962	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1769963	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs1769964	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1769968	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1769970	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1769971	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1769972	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1769974	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1769975	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1769978	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1769981	0.87[CEU][hapmap];1.00[CHB][hapmap];0.85[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1832408	0.85[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2743560	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2743562	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2743563	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2743564	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2757132	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2757133	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2763210	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2763211	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2763212	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];0.94[MKK][hapmap];0.94[TSI][hapmap];0.95[YRI][hapmap];0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2763214	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2763215	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2763216	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2763217	0.96[ASN][1000 genomes]
rs2763218	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2763221	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2787521	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2787525	0.87[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2787527	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2787528	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2787529	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2787530	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2787531	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2787535	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2787536	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2787538	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2787539	0.96[ASN][1000 genomes]
rs2787540	0.87[CEU][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2787543	0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2787544	0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2787545	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2787546	0.96[ASN][1000 genomes]
rs2787547	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2787548	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2787549	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2787551	0.96[ASN][1000 genomes]
rs2787552	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2787553	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2791114	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2791116	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2853338	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2853340	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3827647	0.96[ASN][1000 genomes]
rs41292420	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4310087	0.96[ASN][1000 genomes]
rs4607457	0.89[ASN][1000 genomes]
rs543465	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs577707	0.96[ASN][1000 genomes]
rs595875	0.96[ASN][1000 genomes]
rs626664	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs676099	0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs687709	0.96[ASN][1000 genomes]
rs6920944	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[MKK][hapmap];0.95[YRI][hapmap];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6930834	0.87[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73520690	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73522606	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73522607	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73522610	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73522612	0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73522614	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73522619	0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73522625	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73522642	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73522648	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs796707	0.87[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.94[TSI][hapmap];0.95[YRI][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs960323	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]

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	nsv932155	chr6:106281728-107030467	Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	nsv1025900	chr6:106529777-106898421	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
3	nsv1018270	chr6:106531658-106908606	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
4	nsv538399	chr6:106531658-106908606	Flanking Active TSS Active TSS Enhancers Strong transcription Genic enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
5	nsv1035110	chr6:106557281-106802212	Enhancers Strong transcription ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
6	nsv538400	chr6:106557281-106802212	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
7	nsv1022855	chr6:106570926-106802072	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
8	nsv538401	chr6:106570926-106802072	Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
9	nsv532047	chr6:106591482-107143252	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
10	nsv1025963	chr6:106593639-106848778	Strong transcription Bivalent Enhancer Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
11	nsv1020047	chr6:106597828-106912047	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
12	nsv970664	chr6:106635267-106887670	Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
13	nsv1030367	chr6:106667748-106802072	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
14	nsv538403	chr6:106667748-106802072	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
15	nsv870375	chr6:106696090-107047892	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1766200	GPR6	cis	parietal	SCAN

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:106699200-106767400	Weak transcription	Stomach Mucosa	stomach
2	chr6:106711600-106762800	Weak transcription	Pancreas	Pancrea
3	chr6:106711600-106762800	Weak transcription	Right Ventricle	heart
4	chr6:106713600-106747800	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr6:106717400-106741800	Weak transcription	Colonic Mucosa	Colon
6	chr6:106718000-106771600	Weak transcription	Fetal Brain Female	brain
7	chr6:106720600-106760400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr6:106723000-106771800	Weak transcription	Rectal Smooth Muscle	rectum
9	chr6:106727400-106742000	Weak transcription	Brain Anterior Caudate	brain
10	chr6:106727400-106762200	Weak transcription	Ovary	ovary
11	chr6:106727600-106760800	Weak transcription	Brain Hippocampus Middle	brain
12	chr6:106731600-106745600	Weak transcription	Fetal Intestine Small	intestine
13	chr6:106734800-106762800	Weak transcription	Gastric	stomach
14	chr6:106734800-106771800	Weak transcription	Esophagus	oesophagus
15	chr6:106735200-106773000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr6:106735400-106742400	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr6:106738200-106761400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr6:106738600-106741800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr6:106739600-106760600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr6:106739800-106762800	Weak transcription	Lung	lung
21	chr6:106740000-106742000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr6:106740000-106742000	Weak transcription	Fetal Brain Male	brain
23	chr6:106740000-106742400	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr6:106740000-106752800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr6:106740000-106756600	Weak transcription	Hela-S3	cervix
26	chr6:106740000-106757000	Weak transcription	Fetal Heart	heart
27	chr6:106740000-106760000	Weak transcription	Fetal Kidney	kidney
28	chr6:106740000-106771400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr6:106740000-106773000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr6:106740200-106741600	Strong transcription	K562	blood
31	chr6:106740200-106742200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr6:106740200-106742200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr6:106740200-106742200	Strong transcription	Primary monocytes fromperipheralblood	blood
34	chr6:106740200-106742200	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr6:106740200-106742600	Weak transcription	Stomach Smooth Muscle	stomach
36	chr6:106740200-106743600	Weak transcription	HSMMtube	muscle
37	chr6:106740200-106744600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
38	chr6:106740200-106744800	Weak transcription	Fetal Muscle Trunk	muscle
39	chr6:106740200-106744800	Weak transcription	NHDF-Ad	bronchial
40	chr6:106740200-106747600	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr6:106740200-106751200	Weak transcription	Colon Smooth Muscle	Colon
42	chr6:106740200-106755800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr6:106740200-106757000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr6:106740200-106757800	Weak transcription	Aorta	Aorta
45	chr6:106740200-106759000	Weak transcription	Adipose Nuclei	Adipose
46	chr6:106740200-106759000	Weak transcription	NHLF	lung
47	chr6:106740200-106760800	Weak transcription	Sigmoid Colon	Sigmoid Colon
48	chr6:106740200-106761000	Weak transcription	H1 Cell Line	embryonic stem cell
49	chr6:106740200-106761400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr6:106740200-106761600	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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