Variant report

Variant	rs2523502
Chromosome Location	chr6:31513864-31513865
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5)
CpG islands
(count:0)
Chromatin interactive
region (count:31)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	RCOR1	chr6:31513595-31516462	IMR90	lung:	n/a	n/a
2	REST	chr6:31513683-31515927	H1-neurons	neurons:	n/a	chr6:31513993-31514011 chr6:31514391-31514404
3	SMC3	chr6:31513846-31516397	SK-N-SH	brain:	n/a	n/a
4	CTCF	chr6:31513813-31515560	SK-N-SH	brain:	n/a	n/a
5	MXI1	chr6:31513801-31517077	SK-N-SH	brain:	n/a	n/a

No data

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31512487..31517874-chr6:31628889..31634381,12	K562	blood:
2	chr6:31464396..31467286-chr6:31513352..31515783,2	MCF-7	breast:
3	chr6:31513172..31514702-chr6:31830028..31832398,2	MCF-7	breast:
4	chr6:31461866..31464235-chr6:31513189..31515982,2	K562	blood:
5	chr6:31507451..31516055-chr6:31617949..31624791,11	MCF-7	breast:
6	chr6:31511781..31517209-chr6:31545410..31553496,14	K562	blood:
7	chr6:31513227..31514963-chr6:31602419..31605642,3	K562	blood:
8	chr6:31513206..31515445-chr6:31647940..31649568,2	MCF-7	breast:
9	chr6:31513047..31514729-chr6:31802148..31804053,2	MCF-7	breast:
10	chr6:31513724..31516419-chr6:31731123..31734011,2	K562	blood:
11	chr6:31462227..31464927-chr6:31513555..31516059,3	MCF-7	breast:
12	chr6:31460255..31464524-chr6:31513189..31516444,5	K562	blood:
13	chr6:31512960..31516876-chr6:31549415..31551752,3	MCF-7	breast:
14	chr6:31512174..31516924-chr6:31632110..31634699,4	MCF-7	breast:
15	chr6:31512553..31516955-chr6:31618753..31622292,7	K562	blood:
16	chr6:31511934..31514047-chr6:31634162..31636336,2	MCF-7	breast:
17	chr6:31511829..31516829-chr6:31586761..31590434,8	MCF-7	breast:
18	chr6:31513113..31516557-chr6:31559255..31561759,3	K562	blood:
19	chr6:31513116..31516827-chr6:31558104..31561639,4	K562	blood:
20	chr6:31513053..31519210-chr6:31585987..31595406,29	K562	blood:
21	chr6:31513771..31519008-chr6:31582734..31585702,4	K562	blood:
22	chr6:31513726..31516111-chr6:31705969..31708009,2	MCF-7	breast:
23	chr6:31507406..31516955-chr6:31615847..31623354,26	K562	blood:
24	chr6:31513237..31516038-chr6:31696007..31697508,2	K562	blood:
25	chr6:31513245..31516542-chr6:31782394..31785632,3	MCF-7	breast:
26	chr6:31512646..31517552-chr6:31586243..31590655,20	K562	blood:
27	chr6:31513697..31516891-chr6:31590663..31594798,6	K562	blood:
28	chr6:31513816..31516540-chr6:31705988..31708603,3	K562	blood:
29	chr6:31513842..31516738-chr6:31801353..31804200,3	K562	blood:
30	chr6:31512487..31516692-chr6:31630820..31634965,11	K562	blood:
31	chr6:31513234..31515924-chr6:31582326..31585070,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NFKBIL1-8	chr6:31513762-31514096	NONHSAT108787

No data

Variant related genes	Relation type
NFKBIL1	TF binding region
DDX39B	TF binding region
SNORD84	TF binding region
ENSG00000201680	Chromatin interaction
ENSG00000204410	Chromatin interaction
ENSG00000235663	Chromatin interaction
ENSG00000204389	Chromatin interaction
ENSG00000204472	Chromatin interaction
ENSG00000204463	Chromatin interaction
ENSG00000204390	Chromatin interaction
ENSG00000227507	Chromatin interaction
ENSG00000263020	Chromatin interaction
ENSG00000201207	Chromatin interaction
ENSG00000200816	Chromatin interaction
ENSG00000204444	Chromatin interaction
ENSG00000204428	Chromatin interaction
ENSG00000204469	Chromatin interaction
ENSG00000204516	Chromatin interaction
ENSG00000204475	Chromatin interaction
ENSG00000204435	Chromatin interaction
ENSG00000204438	Chromatin interaction
ENSG00000213722	Chromatin interaction
ENSG00000204387	Chromatin interaction
ENSG00000255152	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000213719	Chromatin interaction
ENSG00000201823	Chromatin interaction
ENSG00000228727	Chromatin interaction

Extended variants
information (count: 57 )
Associated
traits (count: 18 )

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs1129640	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2516393	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2516394	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2523508	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2523510	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2523511	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3093948	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3093950	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3093976	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3093977	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3093978	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3093979	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3093980	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3093981	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3093982	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3093983	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3093984	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3093985	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3093986	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3093990	0.90[AFR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3093995	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3094001	0.84[EUR][1000 genomes]
rs3095235	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3115536	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3115537	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3130051	0.81[EUR][1000 genomes]
rs3130054	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3130056	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3130057	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3130058	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3130640	0.81[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs3131628	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3131629	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3131630	0.90[ASN][1000 genomes]
rs3131633	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3132458	0.83[EUR][1000 genomes]
rs3132461	0.83[EUR][1000 genomes]
rs9267485	0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 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	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	nsv830627	chr6:31496214-31659950	Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	182 gene(s)	inside rSNPs	diseases
19	nsv470809	chr6:31496915-31544189	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	76 gene(s)	inside rSNPs	diseases

mRNA abundance (count:18)

SNP	Gene	Cis/trans	Tissue	Source
rs2523502	XXbac-BPG248L24.12	cis	Heart Left Ventricle	GTEx
rs2523502	XXbac-BPG248L24.12	cis	Nerve Tibial	GTEx
rs2523502	HLA-B	cis	Skin Sun Exposed Lower leg	GTEx
rs2523502	HLA-B	cis	Artery Tibial	GTEx
rs2523502	XXbac-BPG248L24.12	cis	Adipose Subcutaneous	GTEx
rs2523502	XXbac-BPG248L24.12	cis	Esophagus Mucosa	GTEx
rs2523502	XXbac-BPG248L24.12	cis	Artery Tibial	GTEx
rs2523502	HLA-B	cis	Whole Blood	GTEx
rs2523502	HLA-C	cis	lung	GTEx
rs2523502	HLA-B	cis	Muscle Skeletal	GTEx
rs2523502	XXbac-BPG248L24.12	cis	Muscle Skeletal	GTEx
rs2523502	HLA-C	cis	Whole Blood	GTEx
rs2523502	HLA-C	cis	Artery Tibial	GTEx
rs2523502	XXbac-BPG248L24.12	cis	lung	GTEx
rs2523502	XXbac-BPG248L24.12	cis	Esophagus Muscularis	GTEx
rs2523502	XXbac-BPG248L24.12	cis	Whole Blood	GTEx
rs2523502	XXbac-BPG248L24.12	cis	Thyroid	GTEx
rs2523502	XXbac-BPG248L24.12	cis	Skin Sun Exposed Lower leg	GTEx

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31510600-31514200	Weak transcription	Aorta	Aorta
2	chr6:31510600-31514600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr6:31510600-31514600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr6:31510600-31515800	Weak transcription	Gastric	stomach
5	chr6:31510800-31514400	Weak transcription	Right Atrium	heart
6	chr6:31510800-31514600	Weak transcription	Small Intestine	intestine
7	chr6:31510800-31515400	Weak transcription	Lung	lung
8	chr6:31511000-31514000	Weak transcription	Primary T cells from cord blood	blood
9	chr6:31511000-31514000	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr6:31511000-31514000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr6:31511000-31514200	Weak transcription	Primary B cells from peripheral blood	blood
12	chr6:31511000-31514200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr6:31511000-31514200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr6:31511000-31514200	Weak transcription	Adipose Nuclei	Adipose
15	chr6:31511000-31514200	Weak transcription	Placenta	Placenta
16	chr6:31511000-31514200	Weak transcription	Thymus	Thymus
17	chr6:31511000-31514400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
18	chr6:31511000-31514400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr6:31511000-31514400	Weak transcription	Spleen	Spleen
20	chr6:31511000-31514600	Weak transcription	Right Ventricle	heart
21	chr6:31511200-31514000	Weak transcription	Primary neutrophils fromperipheralblood	blood
22	chr6:31511200-31514000	Weak transcription	Primary hematopoietic stem cells	blood
23	chr6:31511200-31514000	Weak transcription	Liver	Liver
24	chr6:31511200-31514000	Weak transcription	Fetal Intestine Small	intestine
25	chr6:31511200-31514000	Weak transcription	Rectal Smooth Muscle	rectum
26	chr6:31511200-31514000	Weak transcription	HSMMtube	muscle
27	chr6:31511200-31514200	Weak transcription	Primary monocytes fromperipheralblood	blood
28	chr6:31511200-31514200	Weak transcription	Primary B cells from cord blood	blood
29	chr6:31511200-31514200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
30	chr6:31511200-31514200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
31	chr6:31511200-31514200	Weak transcription	Primary T helper cells PMA-I stimulated	--
32	chr6:31511200-31514200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
33	chr6:31511200-31514200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
34	chr6:31511200-31514200	Weak transcription	Colonic Mucosa	Colon
35	chr6:31511200-31514200	Weak transcription	Stomach Mucosa	stomach
36	chr6:31511200-31514200	Weak transcription	Monocytes-CD14+_RO01746	blood
37	chr6:31511200-31514400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr6:31511200-31514400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr6:31511200-31514400	Weak transcription	HUVEC	blood vessel
40	chr6:31511200-31514600	Weak transcription	Pancreas	Pancrea
41	chr6:31511400-31514200	Weak transcription	Primary T helper cells fromperipheralblood	blood
42	chr6:31511400-31514200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
43	chr6:31511400-31514200	Weak transcription	Colon Smooth Muscle	Colon
44	chr6:31511400-31514200	Weak transcription	Duodenum Mucosa	Duodenum
45	chr6:31511400-31514200	Weak transcription	GM12878-XiMat	blood
46	chr6:31511400-31514200	Weak transcription	Hela-S3	cervix
47	chr6:31511600-31514600	Weak transcription	Psoas Muscle	Psoas
48	chr6:31511800-31514200	Weak transcription	K562	blood
49	chr6:31513000-31514000	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
50	chr6:31513200-31514200	Flanking Active TSS	Fetal Brain Female	brain

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