Variant report

Variant	rs3132461
Chromosome Location	chr6:31480668-31480669
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:31478866..31481420-chr6:31494881..31496533,2	MCF-7	breast:
2	chr6:31477608..31482305-chr6:31507294..31511382,6	MCF-7	breast:
3	chr6:31479655..31481792-chr6:31482247..31485242,2	K562	blood:
4	chr6:31480216..31481923-chr6:31482906..31485478,2	K562	blood:
5	chr6:31479768..31481286-chr6:31482878..31485599,2	MCF-7	breast:
6	chr6:31472617..31475122-chr6:31479324..31482046,2	K562	blood:

Variant related genes	Relation type
ENSG00000265236	Chromatin interaction
ENSG00000204511	Chromatin interaction
ENSG00000256851	Chromatin interaction
ENSG00000234006	Chromatin interaction
ENSG00000225499	Chromatin interaction
ENSG00000198563	Chromatin interaction
ENSG00000204516	Chromatin interaction

Extended variants
information (count: 92 )
Associated
traits (count: 24 )

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs1129640	0.86[EUR][1000 genomes]
rs2286713	0.93[ASN][1000 genomes]
rs2516393	0.86[EUR][1000 genomes]
rs2516394	0.86[EUR][1000 genomes]
rs2523502	0.83[EUR][1000 genomes]
rs2523508	0.83[EUR][1000 genomes]
rs2523510	0.86[EUR][1000 genomes]
rs2523511	0.86[EUR][1000 genomes]
rs2855805	0.83[ASN][1000 genomes]
rs3093948	0.81[EUR][1000 genomes]
rs3093950	0.86[EUR][1000 genomes]
rs3093953	0.93[ASN][1000 genomes]
rs3093954	0.93[ASN][1000 genomes]
rs3093955	0.89[ASN][1000 genomes]
rs3093976	0.85[EUR][1000 genomes]
rs3093977	0.87[EUR][1000 genomes]
rs3093978	0.86[EUR][1000 genomes]
rs3093979	0.86[EUR][1000 genomes]
rs3093980	0.86[EUR][1000 genomes]
rs3093981	0.86[EUR][1000 genomes]
rs3093982	0.87[EUR][1000 genomes]
rs3093983	0.86[EUR][1000 genomes]
rs3093984	0.86[EUR][1000 genomes]
rs3093985	0.85[EUR][1000 genomes]
rs3093986	0.86[EUR][1000 genomes]
rs3093990	0.81[EUR][1000 genomes]
rs3093995	0.86[EUR][1000 genomes]
rs3094001	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3094002	0.89[ASN][1000 genomes]
rs3094003	0.89[ASN][1000 genomes]
rs3095230	0.89[ASN][1000 genomes]
rs3095231	0.89[ASN][1000 genomes]
rs3095232	0.89[ASN][1000 genomes]
rs3095234	0.89[ASN][1000 genomes]
rs3095235	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3115536	0.83[EUR][1000 genomes]
rs3115537	0.85[EUR][1000 genomes]
rs3130054	0.86[EUR][1000 genomes]
rs3130056	0.86[EUR][1000 genomes]
rs3130057	0.86[EUR][1000 genomes]
rs3130058	0.86[EUR][1000 genomes]
rs3130638	0.81[EUR][1000 genomes]
rs3130925	0.89[ASN][1000 genomes]
rs3130927	0.89[ASN][1000 genomes]
rs3131628	0.86[EUR][1000 genomes]
rs3131629	0.85[EUR][1000 genomes]
rs3131633	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3132458	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3132463	0.95[ASN][1000 genomes]
rs3132464	0.91[ASN][1000 genomes]
rs3132465	0.95[ASN][1000 genomes]
rs3134891	0.95[ASN][1000 genomes]
rs3134892	0.82[ASN][1000 genomes]
rs3134894	0.95[ASN][1000 genomes]
rs3134895	0.95[ASN][1000 genomes]
rs3134897	0.89[ASN][1000 genomes]
rs3134899	0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:35 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1015372	chr6:30704734-31582152	Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
2	nsv538173	chr6:30704734-31582152	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
3	esv2758042	chr6:31028290-31497106	Weak transcription Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	101 gene(s)	inside rSNPs	diseases
4	esv2759414	chr6:31028290-31542308	Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	151 gene(s)	inside rSNPs	diseases
5	esv3381377	chr6:31192213-31498578	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	72 gene(s)	inside rSNPs	diseases
6	esv3340592	chr6:31192248-31498535	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	72 gene(s)	inside rSNPs	diseases
7	nsv1021052	chr6:31206639-31485736	Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
8	nsv1022451	chr6:31279535-31485736	Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
9	nsv601609	chr6:31280101-31799786	Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Genic enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	332 gene(s)	inside rSNPs	diseases
10	nsv601610	chr6:31280101-31960770	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	370 gene(s)	inside rSNPs	diseases
11	nsv601628	chr6:31280327-31990098	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
12	nsv601629	chr6:31280327-31996185	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
13	nsv601630	chr6:31280327-32011317	Genic enhancers Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	378 gene(s)	inside rSNPs	diseases
14	nsv601631	chr6:31280327-32017540	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	378 gene(s)	inside rSNPs	diseases
15	nsv1023939	chr6:31325961-32026747	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
16	nsv538188	chr6:31325961-32026747	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
17	nsv1018463	chr6:31337336-31525275	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	104 gene(s)	inside rSNPs	diseases
18	nsv538189	chr6:31337336-31525275	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	104 gene(s)	inside rSNPs	diseases
19	nsv432868	chr6:31338844-31721033	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	250 gene(s)	inside rSNPs	diseases
20	esv2752115	chr6:31352880-31498721	Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
21	esv2752118	chr6:31353329-31481321	Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
22	esv2757162	chr6:31353329-31542308	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	99 gene(s)	inside rSNPs	diseases
23	esv2752119	chr6:31359621-31498521	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
24	nsv1022499	chr6:31360095-31485174	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
25	nsv1018716	chr6:31362310-31481299	Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
26	nsv432874	chr6:31379821-31498521	Weak transcription Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
27	nsv1021747	chr6:31386219-31907266	Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	330 gene(s)	inside rSNPs	diseases
28	nsv432877	chr6:31412961-31528690	Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	88 gene(s)	inside rSNPs	diseases
29	nsv1018960	chr6:31446366-31481299	Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
30	nsv1025961	chr6:31448533-31497835	Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
31	nsv1021578	chr6:31448533-31498737	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
32	nsv884414	chr6:31458633-31498497	Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
33	nsv884415	chr6:31458633-31501413	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
34	nsv462869	chr6:31463963-31481105	Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Active TSS Strong transcription Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
35	nsv601940	chr6:31463963-31481105	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases

mRNA abundance (count:24)

SNP	Gene	Cis/trans	Tissue	Source
rs3132461	HLA-B	cis	Whole Blood	GTEx
rs3132461	HLA-C	cis	Artery Tibial	GTEx
rs3132461	HLA-C	cis	Muscle Skeletal	GTEx
rs3132461	XXbac-BPG248L24.12	cis	Esophagus Muscularis	GTEx
rs3132461	HLA-B	cis	Artery Tibial	GTEx
rs3132461	XXbac-BPG248L24.12	cis	Adipose Subcutaneous	GTEx
rs3132461	HLA-B	cis	Muscle Skeletal	GTEx
rs3132461	XXbac-BPG248L24.12	cis	Artery Tibial	GTEx
rs3132461	XXbac-BPG181B23.7	cis	Artery Tibial	GTEx
rs3132461	HLA-B	cis	Skin Sun Exposed Lower leg	GTEx
rs3132461	HLA-C	cis	Whole Blood	GTEx
rs3132461	HLA-C	cis	lung	GTEx
rs3132461	XXbac-BPG181B23.7	cis	Muscle Skeletal	GTEx
rs3132461	XXbac-BPG181B23.7	cis	Esophagus Muscularis	GTEx
rs3132461	XXbac-BPG248L24.12	cis	Nerve Tibial	GTEx
rs3132461	XXbac-BPG248L24.12	cis	Esophagus Mucosa	GTEx
rs3132461	XXbac-BPG248L24.12	cis	Skin Sun Exposed Lower leg	GTEx
rs3132461	XXbac-BPG248L24.12	cis	Muscle Skeletal	GTEx
rs3132461	XXbac-BPG181B23.7	cis	Adipose Subcutaneous	GTEx
rs3132461	XXbac-BPG248L24.12	cis	Thyroid	GTEx
rs3132461	XXbac-BPG248L24.12	cis	Whole Blood	GTEx
rs3132461	XXbac-BPG248L24.12	cis	lung	GTEx
rs3132461	XXbac-BPG248L24.12	cis	Heart Left Ventricle	GTEx
rs3132461	HLA-C	cis	Thyroid	GTEx

Chromatin state (count:76 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31466800-31481200	Weak transcription	NHDF-Ad	bronchial
2	chr6:31467200-31481200	Weak transcription	Liver	Liver
3	chr6:31467400-31506600	Weak transcription	Right Atrium	heart
4	chr6:31467600-31481000	Weak transcription	HSMM	muscle
5	chr6:31467600-31481400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr6:31468600-31481600	Weak transcription	Left Ventricle	heart
7	chr6:31474000-31481800	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr6:31475200-31480800	Weak transcription	Rectal Smooth Muscle	rectum
9	chr6:31475800-31481400	Weak transcription	Pancreas	Pancrea
10	chr6:31475800-31482800	Weak transcription	Right Ventricle	heart
11	chr6:31475800-31493600	Weak transcription	Gastric	stomach
12	chr6:31476000-31482200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr6:31476400-31482200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr6:31477000-31483400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr6:31478000-31481400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr6:31478000-31481600	Weak transcription	Aorta	Aorta
17	chr6:31478000-31482600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr6:31478000-31483400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr6:31478200-31480800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr6:31478200-31481000	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr6:31478200-31481000	Weak transcription	NH-A	brain
22	chr6:31478200-31481400	Weak transcription	Esophagus	oesophagus
23	chr6:31478200-31483800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr6:31478200-31485000	Weak transcription	K562	blood
25	chr6:31478200-31485600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr6:31478200-31486400	Weak transcription	HMEC	breast
27	chr6:31478200-31497200	Weak transcription	A549	lung
28	chr6:31478400-31480800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr6:31478400-31480800	Weak transcription	Osteobl	bone
30	chr6:31478400-31481000	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr6:31478400-31481000	Weak transcription	HUVEC	blood vessel
32	chr6:31478400-31482200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
33	chr6:31478400-31497200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr6:31478400-31497800	Weak transcription	Primary B cells from cord blood	blood
35	chr6:31478400-31498200	Weak transcription	Primary hematopoietic stem cells	blood
36	chr6:31478600-31480800	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr6:31478600-31484200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr6:31478600-31498200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
39	chr6:31479000-31481600	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr6:31479200-31480800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr6:31479200-31481200	Weak transcription	Hela-S3	cervix
42	chr6:31479200-31481400	Weak transcription	NHEK	skin
43	chr6:31479200-31483200	Weak transcription	Primary monocytes fromperipheralblood	blood
44	chr6:31479200-31497400	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr6:31479200-31497400	Weak transcription	Primary T cells from cord blood	blood
46	chr6:31479200-31497600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
47	chr6:31479400-31480800	Weak transcription	NHLF	lung
48	chr6:31479400-31481200	Weak transcription	Lung	lung
49	chr6:31479400-31481400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr6:31479400-31481400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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