Variant report

Variant	rs933257
Chromosome Location	chr6:118822566-118822567
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLN-1	chr6:118822536-118824996	NR_002730

Extended variants
information (count: 123 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:96)

rs_ID	r²[population]
rs1016095	0.81[CHB][hapmap];0.84[JPT][hapmap];0.85[ASN][1000 genomes]
rs10457334	0.80[ASN][1000 genomes]
rs10457344	0.81[CHB][hapmap];0.84[CHD][hapmap];0.84[JPT][hapmap]
rs10484287	0.81[CHB][hapmap];0.84[JPT][hapmap];0.85[ASN][1000 genomes]
rs1051429	0.81[CHB][hapmap];0.84[JPT][hapmap];0.80[ASN][1000 genomes]
rs11153754	0.85[ASN][1000 genomes]
rs11153761	0.85[CHB][hapmap]
rs11754973	0.85[ASN][1000 genomes]
rs11756983	0.85[ASN][1000 genomes]
rs12153938	0.80[ASN][1000 genomes]
rs12196194	0.83[ASN][1000 genomes]
rs12204456	0.81[CHB][hapmap];0.84[CHD][hapmap];0.90[GIH][hapmap];0.84[JPT][hapmap];0.85[ASN][1000 genomes]
rs12526557	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12530169	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];0.96[MEX][hapmap];1.00[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];0.98[ASN][1000 genomes]
rs1344249	0.80[ASN][1000 genomes]
rs1547326	0.81[CHB][hapmap];0.84[JPT][hapmap];0.85[ASN][1000 genomes]
rs17080423	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1891712	0.88[GIH][hapmap]
rs1936059	1.00[ASW][hapmap];0.95[CEU][hapmap];0.95[CHB][hapmap];0.90[CHD][hapmap];0.97[GIH][hapmap];0.95[JPT][hapmap];0.91[LWK][hapmap];0.96[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2157569	0.85[ASN][1000 genomes]
rs2181513	0.81[CHB][hapmap];0.84[CHD][hapmap];0.84[JPT][hapmap]
rs2187945	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2213858	0.82[ASN][1000 genomes]
rs2356178	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2356182	0.80[ASN][1000 genomes]
rs2356184	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2356493	0.82[ASN][1000 genomes]
rs2356502	0.81[CHB][hapmap];0.84[CHD][hapmap];0.90[GIH][hapmap];0.84[JPT][hapmap]
rs25421	0.81[CHB][hapmap];0.84[JPT][hapmap];0.82[ASN][1000 genomes]
rs25423	0.81[CHB][hapmap];0.84[CHD][hapmap];0.90[GIH][hapmap];0.84[JPT][hapmap];0.80[MEX][hapmap];0.81[TSI][hapmap];0.82[ASN][1000 genomes]
rs3734382	0.81[CHB][hapmap];0.84[CHD][hapmap];0.90[GIH][hapmap];0.84[JPT][hapmap];0.80[ASN][1000 genomes]
rs4027728	0.81[CHB][hapmap];0.84[CHD][hapmap];0.90[GIH][hapmap];0.84[JPT][hapmap]
rs422312	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.96[TSI][hapmap];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4412243	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4502975	0.85[CHB][hapmap];0.83[JPT][hapmap];0.81[ASN][1000 genomes]
rs482910	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs485416	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs492562	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4946343	0.94[ASN][1000 genomes]
rs4946349	0.81[CHB][hapmap];0.84[CHD][hapmap];0.90[GIH][hapmap];0.84[JPT][hapmap]
rs516212	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs516463	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs541442	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs55868726	0.80[ASN][1000 genomes]
rs6569022	0.81[CHB][hapmap];0.84[JPT][hapmap]
rs6569023	0.93[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6911599	1.00[YRI][hapmap]
rs6919887	0.81[CHB][hapmap];0.81[CHD][hapmap];0.90[GIH][hapmap];0.80[ASN][1000 genomes]
rs6929390	0.81[CHB][hapmap];0.84[JPT][hapmap];0.82[ASN][1000 genomes]
rs763255	0.81[CHB][hapmap];0.84[CHD][hapmap];0.84[JPT][hapmap]
rs7740922	0.81[CHB][hapmap];0.84[JPT][hapmap];0.85[ASN][1000 genomes]
rs7741644	0.84[JPT][hapmap];0.85[ASN][1000 genomes]
rs7742696	0.94[ASN][1000 genomes]
rs7749208	0.81[CHB][hapmap];0.82[JPT][hapmap];0.82[ASN][1000 genomes]
rs7749694	0.84[JPT][hapmap];0.85[ASN][1000 genomes]
rs7754293	0.81[CHB][hapmap];0.84[JPT][hapmap]
rs7757337	0.81[CHB][hapmap];0.84[JPT][hapmap];0.85[ASN][1000 genomes]
rs7757407	0.81[CHB][hapmap];0.84[CHD][hapmap];0.84[JPT][hapmap]
rs7759088	0.81[CHB][hapmap];0.84[JPT][hapmap]
rs7761717	0.85[ASN][1000 genomes]
rs7761996	0.82[ASN][1000 genomes]
rs7762990	0.84[CHB][hapmap]
rs9372506	0.85[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9374733	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9374735	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9374736	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9387586	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9387596	0.83[CEU][hapmap];1.00[YRI][hapmap]
rs9401073	1.00[ASW][hapmap];0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9401081	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9481807	0.80[ASN][1000 genomes]
rs9481815	0.80[CHB][hapmap];0.84[JPT][hapmap];0.82[ASN][1000 genomes]
rs9481819	0.84[JPT][hapmap];0.85[ASN][1000 genomes]
rs9481840	0.81[CHB][hapmap];0.84[JPT][hapmap]
rs9489401	0.80[ASN][1000 genomes]
rs9489403	0.84[CHB][hapmap];0.83[JPT][hapmap];0.80[ASN][1000 genomes]
rs9489406	0.82[ASN][1000 genomes]
rs9489414	0.81[CHB][hapmap];0.89[JPT][hapmap];0.82[ASN][1000 genomes]
rs9489417	0.83[ASN][1000 genomes]
rs9489419	0.81[CHB][hapmap];0.84[JPT][hapmap];0.85[ASN][1000 genomes]
rs9489420	0.84[JPT][hapmap];0.85[ASN][1000 genomes]
rs9489421	0.83[ASN][1000 genomes]
rs9489424	0.81[CHB][hapmap];0.84[CHD][hapmap];0.90[GIH][hapmap];0.84[JPT][hapmap];0.85[ASN][1000 genomes]
rs9489425	0.85[ASN][1000 genomes]
rs9489432	0.81[CHB][hapmap];0.84[JPT][hapmap];0.82[ASN][1000 genomes]
rs9489437	0.81[CHB][hapmap];0.84[CHD][hapmap];0.84[JPT][hapmap];0.80[ASN][1000 genomes]
rs9489438	0.81[CHB][hapmap];0.84[JPT][hapmap];0.80[ASN][1000 genomes]
rs9489439	0.81[CHB][hapmap];0.84[JPT][hapmap];0.80[ASN][1000 genomes]
rs9489446	0.84[JPT][hapmap]
rs9489448	0.81[CHB][hapmap];0.84[JPT][hapmap]
rs9489449	0.81[CHB][hapmap];0.84[JPT][hapmap]
rs9489456	0.81[CHB][hapmap];0.84[CHD][hapmap];0.84[JPT][hapmap]
rs9489461	0.81[CHB][hapmap];0.84[JPT][hapmap]
rs9489478	0.81[CHB][hapmap];0.84[JPT][hapmap]
rs9489487	0.88[GIH][hapmap]
rs9689896	0.81[CHB][hapmap];0.84[CHD][hapmap];0.84[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:27 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532051	chr6:118551027-119044197	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1020463	chr6:118593028-119146363	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats 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	10 gene(s)	inside rSNPs	diseases
3	nsv1025403	chr6:118635123-119122551	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv1025456	chr6:118669672-119058789	Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
5	nsv1027444	chr6:118687556-119121660	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
6	nsv538428	chr6:118687556-119121660	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
7	nsv949321	chr6:118692304-119137658	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
8	nsv432958	chr6:118692307-119010307	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
9	nsv604555	chr6:118695049-118856822	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
10	nsv1034448	chr6:118698169-119016383	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
11	nsv1025097	chr6:118699752-119058789	Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers 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	9 gene(s)	inside rSNPs	diseases
12	nsv1020586	chr6:118711098-118900012	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
13	nsv532052	chr6:118711850-119057295	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers 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	9 gene(s)	inside rSNPs	diseases
14	nsv432959	chr6:118716318-119010307	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
15	nsv604556	chr6:118722589-119065365	Active TSS Strong transcription Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
16	nsv432960	chr6:118723307-118826307	Strong transcription ZNF genes & repeats Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
17	nsv525179	chr6:118726243-118876092	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
18	nsv1019357	chr6:118731468-118860705	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
19	nsv464027	chr6:118768150-118856822	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	n/a
20	nsv604557	chr6:118768150-118856822	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	n/a
21	nsv464029	chr6:118768150-118861263	ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	n/a
22	nsv604558	chr6:118768150-118861263	Weak transcription Genic enhancers ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	n/a
23	nsv949416	chr6:118772508-119033063	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
24	nsv948980	chr6:118772508-119137658	Genic enhancers Flanking Active TSS Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
25	nsv604559	chr6:118786486-119113317	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers 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	9 gene(s)	inside rSNPs	diseases
26	nsv1022865	chr6:118786586-119058789	ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
27	nsv1020405	chr6:118786586-119241006	ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs933257	C6orf60	cis	normal skin	skin_eQTL
rs933257	SSXP10	cis	Artery Tibial	GTEx
rs933257	RFX6	cis	cerebellum	SCAN

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:118784600-118827600	Weak transcription	Esophagus	oesophagus
2	chr6:118791000-118846000	Weak transcription	Gastric	stomach
3	chr6:118807400-118842600	Weak transcription	NHLF	lung
4	chr6:118809200-118825200	Weak transcription	Lung	lung
5	chr6:118810000-118845800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr6:118810800-118825200	Weak transcription	HSMMtube	muscle
7	chr6:118810800-118825400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr6:118810800-118827400	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr6:118810800-118827400	Weak transcription	Small Intestine	intestine
10	chr6:118810800-118827600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr6:118810800-118827800	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr6:118811000-118828000	Weak transcription	Spleen	Spleen
13	chr6:118811400-118825800	Weak transcription	Ovary	ovary
14	chr6:118811400-118835800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr6:118811800-118823600	Weak transcription	K562	blood
16	chr6:118811800-118828600	Weak transcription	GM12878-XiMat	blood
17	chr6:118812000-118823400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr6:118812400-118845800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
19	chr6:118813200-118834400	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr6:118813200-118842800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
21	chr6:118814000-118833400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr6:118814600-118833200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr6:118814600-118844400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr6:118814600-118846200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
25	chr6:118815200-118826800	Strong transcription	Primary T cells from cord blood	blood
26	chr6:118815800-118831400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr6:118816000-118833200	Weak transcription	Aorta	Aorta
28	chr6:118816000-118843400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr6:118817200-118825200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr6:118817200-118825400	Weak transcription	Liver	Liver
31	chr6:118817200-118827400	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr6:118817200-118827600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr6:118817200-118833400	Weak transcription	Adipose Nuclei	Adipose
34	chr6:118817200-118842400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr6:118817400-118823000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr6:118817400-118823200	Weak transcription	HSMM	muscle
37	chr6:118817400-118823400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
38	chr6:118817400-118823400	Weak transcription	Osteobl	bone
39	chr6:118817400-118823600	Weak transcription	Primary T helper cells fromperipheralblood	blood
40	chr6:118817400-118823800	Weak transcription	NH-A	brain
41	chr6:118817400-118825600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr6:118817400-118845800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr6:118817400-118845800	Weak transcription	Pancreas	Pancrea
44	chr6:118817400-118845800	Weak transcription	HMEC	breast
45	chr6:118817400-118847200	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr6:118817600-118846600	Weak transcription	HUVEC	blood vessel
47	chr6:118818200-118823800	Weak transcription	Cortex derived primary cultured neurospheres	brain
48	chr6:118818400-118825800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr6:118819800-118827400	Weak transcription	Psoas Muscle	Psoas
50	chr6:118821000-118824200	ZNF genes & repeats	Primary hematopoietic stem cells	blood

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