Variant report

Variant	rs1358883
Chromosome Location	chr6:167467433-167467434
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:167150380..167152971-chr6:167466714..167468496,2	K562	blood:

Extended variants
information (count: 136 )
Associated
traits (count: 8 )

rSNPs within LD-proxies of this variant (count:120)

rs_ID	r²[population]
rs10484530	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10484531	0.81[AMR][1000 genomes]
rs10946204	0.83[GIH][hapmap]
rs10946205	0.85[CEU][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10946207	0.85[CEU][hapmap];0.87[EUR][1000 genomes]
rs10946208	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12178491	0.83[EUR][1000 genomes]
rs12193698	0.80[EUR][1000 genomes]
rs12203510	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12208359	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12209395	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12213683	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12523712	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12526548	1.00[ASW][hapmap];0.85[CEU][hapmap];0.95[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];0.85[JPT][hapmap];0.98[MKK][hapmap];0.86[TSI][hapmap];0.95[YRI][hapmap];0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12527827	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12528323	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12528689	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12529238	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12529876	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12529959	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13195812	0.96[YRI][hapmap];0.88[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs13199692	0.81[AMR][1000 genomes]
rs13204839	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13208636	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13210649	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13213249	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1322077	0.83[AMR][1000 genomes]
rs1358882	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1407315	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17524252	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17615336	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1810644	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1810645	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1894603	1.00[ASW][hapmap];0.85[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];0.91[MEX][hapmap];0.98[MKK][hapmap];0.87[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2001114	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2001115	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2017338	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2038580	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2181058	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2181059	0.95[AFR][1000 genomes];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2236313	0.80[CHD][hapmap];0.80[JPT][hapmap]
rs2237273	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2237274	0.83[JPT][hapmap];0.90[YRI][hapmap]
rs2237276	0.96[YRI][hapmap];0.88[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs2237277	0.84[CEU][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2239823	0.80[EUR][1000 genomes]
rs2239826	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2239827	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2282860	1.00[ASW][hapmap];0.85[CEU][hapmap];0.91[GIH][hapmap];0.97[LWK][hapmap];0.98[MKK][hapmap];0.87[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2282861	1.00[ASW][hapmap];0.85[CEU][hapmap];0.91[GIH][hapmap];0.97[LWK][hapmap];0.84[MEX][hapmap];0.98[MKK][hapmap];0.87[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2285147	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2285148	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2301436	1.00[ASW][hapmap];0.85[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];0.92[MEX][hapmap];0.98[MKK][hapmap];0.87[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs239933	0.83[AMR][1000 genomes]
rs35171809	0.87[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs377232	0.95[YRI][hapmap]
rs408087	0.87[YRI][hapmap]
rs4710175	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4710176	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62436765	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6456143	0.85[AMR][1000 genomes]
rs6456146	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs6456149	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6456150	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6456151	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6456152	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6456153	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6456154	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6900701	0.95[YRI][hapmap];0.87[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs6902119	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6904946	0.84[GIH][hapmap];0.87[MEX][hapmap];0.87[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs6909180	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6909475	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6909502	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6918286	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6920858	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6921588	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6923582	0.96[YRI][hapmap];0.87[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs6925969	0.84[EUR][1000 genomes]
rs6929466	0.84[AMR][1000 genomes]
rs6932740	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6934043	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6936261	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6941355	0.87[EUR][1000 genomes]
rs720325	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7742305	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7748224	0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7749278	1.00[ASW][hapmap];0.85[CEU][hapmap];0.91[GIH][hapmap];0.94[LWK][hapmap];0.84[MEX][hapmap];0.98[MKK][hapmap];0.87[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7760495	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7761977	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7762156	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7766242	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs911632	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs916331	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9295384	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9295385	0.93[ASW][hapmap];0.84[GIH][hapmap];0.83[LWK][hapmap];0.87[MEX][hapmap];0.96[YRI][hapmap];0.88[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs9457249	0.80[CEU][hapmap];0.83[JPT][hapmap];0.82[AMR][1000 genomes]
rs9457251	0.82[AMR][1000 genomes]
rs9457252	0.84[GIH][hapmap];0.83[MEX][hapmap]
rs9457257	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9457258	0.95[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs9457260	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9457261	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9457268	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9457270	0.84[EUR][1000 genomes]
rs9459835	0.85[CEU][hapmap];0.82[AMR][1000 genomes]
rs9459836	0.83[GIH][hapmap]
rs9459839	0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9459840	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs9459841	0.91[YRI][hapmap];0.85[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs9459842	0.89[AFR][1000 genomes];0.85[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9459845	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9459846	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9459853	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9459854	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9459855	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9459862	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9459871	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9459872	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9459874	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019381	chr6:167090236-167558598	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
2	nsv538541	chr6:167090236-167558598	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
3	nsv948634	chr6:167200671-167838993	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
4	nsv482507	chr6:167282376-167474915	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking 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	11 gene(s)	inside rSNPs	diseases
5	nsv532074	chr6:167320656-167781977	Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
6	nsv1031039	chr6:167324021-167741439	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	21 gene(s)	inside rSNPs	diseases
7	nsv538543	chr6:167324021-167741439	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	21 gene(s)	inside rSNPs	diseases
8	nsv1026972	chr6:167335031-167671042	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	19 gene(s)	inside rSNPs	diseases
9	nsv464140	chr6:167426681-167492552	Active TSS Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
10	nsv886943	chr6:167440244-167502638	Strong transcription Flanking Active TSS Genic enhancers Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	esv2752099	chr6:167448181-167579102	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
12	nsv519550	chr6:167450609-167473685	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
13	esv1841903	chr6:167459596-167489090	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
14	esv1824563	chr6:167461501-167489090	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
15	esv1837292	chr6:167461501-167489090	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
16	esv1840181	chr6:167461562-167489090	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

mRNA abundance (count:8)

SNP	Gene	Cis/trans	Tissue	Source
rs1358883	CCR6	cis	multi-tissue	Pritchard
rs1358883	TCTE3	cis	parietal	SCAN
rs1358883	RNASET2	cis	Esophagus Mucosa	GTEx
rs1358883	AL133458.1	cis	Whole Blood	GTEx
rs1358883	CCR6	cis	parietal	SCAN
rs1358883	RNASET2	cis	Whole Blood	GTEx
rs1358883	RNASET2	cis	cerebellum	SCAN
rs1358883	CCR6	cis	cerebellum	SCAN

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167441400-167473400	Weak transcription	Psoas Muscle	Psoas
2	chr6:167449000-167467800	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr6:167449000-167470400	Weak transcription	Brain Anterior Caudate	brain
4	chr6:167451600-167468400	Weak transcription	Esophagus	oesophagus
5	chr6:167455000-167470600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr6:167455200-167467600	Weak transcription	Liver	Liver
7	chr6:167456200-167468400	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr6:167456200-167470800	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr6:167456600-167473200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr6:167458400-167471200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr6:167458600-167469000	Weak transcription	Fetal Stomach	stomach
12	chr6:167460400-167469800	Weak transcription	Gastric	stomach
13	chr6:167460800-167467800	Weak transcription	Fetal Intestine Small	intestine
14	chr6:167460800-167468800	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr6:167461400-167468400	Weak transcription	Thymus	Thymus
16	chr6:167461800-167467600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr6:167461800-167468800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr6:167461800-167470000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr6:167462000-167468600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr6:167462000-167469800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr6:167464200-167469000	Weak transcription	Primary B cells from cord blood	blood
22	chr6:167464200-167469400	Weak transcription	Primary B cells from peripheral blood	blood
23	chr6:167465000-167469600	Weak transcription	GM12878-XiMat	blood
24	chr6:167466000-167470800	Enhancers	Primary T helper cells fromperipheralblood	blood
25	chr6:167466000-167472000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
26	chr6:167466000-167472000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
27	chr6:167466200-167471000	Enhancers	Primary T cells from cord blood	blood
28	chr6:167466400-167471000	Enhancers	Primary T cells fromperipheralblood	blood
29	chr6:167466400-167471000	Enhancers	Primary T helper cells PMA-I stimulated	--
30	chr6:167466400-167471000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
31	chr6:167466600-167470600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr6:167467000-167467600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
33	chr6:167467000-167468200	Enhancers	Left Ventricle	heart
34	chr6:167467000-167470600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr6:167467000-167470800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr6:167467000-167471000	Enhancers	Primary hematopoietic stem cells	blood
37	chr6:167467200-167467600	Enhancers	Right Ventricle	heart
38	chr6:167467200-167467600	Enhancers	NHEK	skin
39	chr6:167467200-167467800	Enhancers	HMEC	breast
40	chr6:167467400-167467600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr6:167467400-167467600	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr6:167467400-167467600	Enhancers	Ovary	ovary

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