Variant report

Variant	rs1059307
Chromosome Location	chr6:86387888-86387889
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:244)
CpG islands
(count:0)
Chromatin interactive
region (count:29)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr6:86381750-86389506	Hela-S3	cervix:	n/a	n/a
2	POLR2A	chr6:86387789-86388569	HepG2	liver:	n/a	n/a
3	EP300	chr6:86387400-86389406	GM12878	blood:	n/a	chr6:86389040-86389056 chr6:86388650-86388666
4	MAX	chr6:86387777-86389283	K562	blood:	n/a	chr6:86389008-86389017 chr6:86389007-86389018
5	POLR2A	chr6:86386940-86389304	H1-hESC	embryonic stem cell:	n/a	n/a
6	YY1	chr6:86387718-86389273	ECC-1	luminal epithelium:	n/a	n/a
7	POLR2A	chr6:86381804-86389694	K562	blood:	n/a	n/a
8	REST	chr6:86387472-86389238	H1-neurons	neurons:	n/a	n/a
9	EP300	chr6:86387884-86389412	ECC-1	luminal epithelium:	n/a	chr6:86389040-86389056 chr6:86388650-86388666
10	EP300	chr6:86387826-86389443	GM12878	blood:	n/a	chr6:86389040-86389056 chr6:86388650-86388666
11	REST	chr6:86387810-86389625	HL-60	blood:	n/a	n/a
12	POLR2A	chr6:86387849-86389404	GM12878	blood:	n/a	n/a
13	SIN3AK20	chr6:86387722-86389205	K562	blood:	n/a	n/a
14	YY1	chr6:86387726-86389269	H1-hESC	embryonic stem cell:	n/a	n/a
15	POLR2A	chr6:86387658-86389341	K562	blood:	n/a	n/a
16	POLR2A	chr6:86387687-86389267	Hela-S3	cervix:	n/a	n/a
17	POLR2A	chr6:86387425-86389393	HL-60	blood:	n/a	n/a
18	HEY1	chr6:86386803-86389291	HepG2	liver:	n/a	n/a
19	RUNX3	chr6:86387800-86389346	GM12878	blood:	n/a	n/a
20	POLR2A	chr6:86386861-86389609	GM12892	blood:	n/a	n/a
21	RELA	chr6:86387490-86389647	GM15510	blood:	n/a	n/a
22	TBP	chr6:86386818-86389855	Hela-S3	cervix:	n/a	chr6:86388472-86388483
23	POLR2A	chr6:86381512-86389676	PFSK-1	brain:	n/a	n/a
24	MXI1	chr6:86386518-86390564	IMR90	lung:	n/a	n/a
25	ELK1	chr6:86387293-86389199	K562	blood:	n/a	n/a
26	HCFC1	chr6:86387002-86390095	Hela-S3	cervix:	n/a	n/a
27	MAX	chr6:86387813-86389683	HCT-116	colon:	n/a	chr6:86389008-86389017 chr6:86389007-86389018
28	TBP	chr6:86387832-86389319	H1-hESC	embryonic stem cell:	n/a	chr6:86388472-86388483
29	POLR2A	chr6:86387665-86389472	SK-N-MC	brain:	n/a	n/a
30	POLR2A	chr6:86387133-86388922	HepG2	liver:	n/a	n/a
31	POLR2A	chr6:86387858-86389282	GM12878	blood:	n/a	n/a
32	ATF2	chr6:86387753-86388914	H1-hESC	embryonic stem cell:	n/a	n/a
33	USF2	chr6:86387798-86389382	Hela-S3	cervix:	n/a	n/a
34	POLR2A	chr6:86381786-86389590	IMR90	lung:	n/a	n/a
35	TAF7	chr6:86384285-86389287	H1-hESC	embryonic stem cell:	n/a	n/a
36	RCOR1	chr6:86387835-86389629	K562	blood:	n/a	n/a
37	TBL1XR1	chr6:86386955-86389434	K562	blood:	n/a	n/a
38	MYC	chr6:86387783-86389633	A549	lung:	n/a	chr6:86389008-86389017 chr6:86389007-86389018
39	SIN3AK20	chr6:86387731-86389476	HCT-116	colon:	n/a	n/a
40	MYBL2	chr6:86387785-86389356	HepG2	liver:	n/a	n/a
41	BCLAF1	chr6:86387880-86389283	GM12878	blood:	n/a	chr6:86388918-86388931
42	YY1	chr6:86387706-86388853	SK-N-SH_RA	brain:	n/a	n/a
43	POLR2A	chr6:86387754-86389222	GM12878	blood:	n/a	n/a
44	FOXM1	chr6:86387609-86389349	GM12878	blood:	n/a	n/a
45	TAF1	chr6:86387776-86389166	K562	blood:	n/a	n/a
46	HCFC1	chr6:86387723-86389236	K562	blood:	n/a	n/a
47	POLR2A	chr6:86387851-86389260	HUVEC	blood vessel:	n/a	n/a
48	POLR2A	chr6:86387773-86389233	ECC-1	luminal epithelium:	n/a	n/a
49	MYBL2	chr6:86387868-86389351	HepG2	liver:	n/a	n/a
50	PML	chr6:86386714-86389546	GM12878	blood:	n/a	n/a

No data

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:86338689..86357756-chr6:86378394..86390434,115	MCF-7	breast:
2	chr6:86360455..86373602-chr6:86382637..86391992,19	MCF-7	breast:
3	chr6:86322647..86325206-chr6:86387381..86389770,2	MCF-7	breast:
4	chr6:86287818..86291892-chr6:86385672..86390313,6	MCF-7	breast:
5	chr6:86352417..86353203-chr6:86386848..86388878,6	MCF-7	breast:
6	chr17:73775484..73776235-chr6:86387856..86388540,2	Hela-S3	cervix:
7	chr6:85471670..85475300-chr6:86386961..86389961,4	K562	blood:
8	chr6:86323280..86334231-chr6:86380512..86390230,24	K562	blood:
9	chr6:86258616..86262862-chr6:86386972..86389770,3	K562	blood:
10	chr6:86302271..86307129-chr6:86385631..86390073,11	MCF-7	breast:
11	chr6:86353436..86354584-chr6:86387812..86388533,4	Hela-S3	cervix:
12	chr20:32890403..32890932-chr6:86387883..86389053,3	Hela-S3	cervix:
13	chr6:86386878..86389803-chr6:86445514..86448985,3	K562	blood:
14	chr10:38146274..38146953-chr6:86387888..86388601,2	Hela-S3	cervix:
15	chr6:86387690..86388567-chrX:47863298..47863848,2	Hela-S3	cervix:
16	chr6:86246106..86247862-chr6:86386298..86390203,3	K562	blood:
17	chr6:86246140..86247926-chr6:86387829..86390203,2	K562	blood:
18	chr19:39897973..39898580-chr6:86387847..86388601,2	Hela-S3	cervix:
19	chr14:64971394..64971969-chr6:86387618..86388524,2	Hela-S3	cervix:
20	chr6:86386962..86389714-chr6:87862273..87864563,2	MCF-7	breast:
21	chr6:86300286..86310605-chr6:86384413..86390498,39	K562	blood:
22	chr6:86277967..86280027-chr6:86387160..86389820,3	K562	blood:
23	chr6:86298349..86307534-chr6:86383938..86391964,31	K562	blood:
24	chr6:86258544..86261104-chr6:86387142..86389153,2	K562	blood:
25	chr6:86353346..86353951-chr6:86387391..86388065,2	MCF-7	breast:
26	chr6:86352199..86352987-chr6:86387888..86388697,2	NB4	blood:
27	chr12:53399949..53400478-chr6:86387665..86388469,2	Hela-S3	cervix:
28	chr6:86301325..86305014-chr6:86385299..86388840,4	MCF-7	breast:
29	chr14:90862079..90865060-chr6:86387137..86388839,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NT5E-3	chr6:86387854-86388112	NONHSAT113858

No data

Variant related genes	Relation type
SNHG5	TF binding region
ENSG00000147118	Chromatin interaction
ENSG00000135316	Chromatin interaction
ENSG00000128016	Chromatin interaction
ENSG00000188994	Chromatin interaction
ENSG00000089775	Chromatin interaction
ENSG00000236514	Chromatin interaction
ENSG00000063046	Chromatin interaction
ENSG00000171489	Chromatin interaction
ENSG00000112837	Chromatin interaction
ENSG00000198105	Chromatin interaction
ENSG00000271793	Chromatin interaction
ENSG00000236016	Chromatin interaction
ENSG00000126804	Chromatin interaction
ENSG00000198668	Chromatin interaction
ENSG00000101444	Chromatin interaction
ENSG00000132475	Chromatin interaction
ENSG00000135317	Chromatin interaction
ENSG00000220563	Chromatin interaction
ENSG00000198738	Chromatin interaction

Extended variants
information (count: 55 )
Associated
traits (count: 24 )

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs1173416	0.86[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs1173417	0.83[CHB][hapmap];0.82[CHD][hapmap]
rs1173418	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11752795	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12193777	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12203963	0.96[CEU][hapmap];0.82[CHB][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];0.86[EUR][1000 genomes]
rs12206573	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12212560	0.91[CEU][hapmap];0.81[MEX][hapmap]
rs2475792	0.91[CEU][hapmap];0.83[CHB][hapmap];0.82[CHD][hapmap];0.86[MEX][hapmap]
rs2758842	0.87[CEU][hapmap]
rs2758843	0.87[CEU][hapmap]
rs2758845	0.87[CEU][hapmap]
rs2758848	1.00[ASW][hapmap];0.96[CEU][hapmap];0.83[CHB][hapmap];0.81[CHD][hapmap];0.98[GIH][hapmap];0.85[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2758849	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2842600	0.96[CEU][hapmap];0.83[CHB][hapmap];0.83[CHD][hapmap];0.98[GIH][hapmap];0.85[JPT][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];0.93[TSI][hapmap];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2842603	0.83[CEU][hapmap]
rs2842605	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2842610	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2842611	0.96[CEU][hapmap];0.83[CHB][hapmap];0.81[CHD][hapmap];0.98[GIH][hapmap];0.85[JPT][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];0.93[TSI][hapmap];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2842614	0.87[CEU][hapmap]
rs2842615	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3087978	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34980280	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4296866	0.87[GIH][hapmap]
rs4348284	0.96[CEU][hapmap];0.85[JPT][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4431401	1.00[ASW][hapmap];0.96[CEU][hapmap];0.93[GIH][hapmap];0.85[JPT][hapmap];0.90[LWK][hapmap];0.91[MEX][hapmap];0.82[MKK][hapmap];0.84[TSI][hapmap];0.84[YRI][hapmap]
rs4640862	0.87[EUR][1000 genomes]
rs4707211	0.96[CEU][hapmap];0.83[CHB][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];0.87[EUR][1000 genomes]
rs4707212	0.87[EUR][1000 genomes]
rs6454472	0.91[CEU][hapmap];0.83[CHB][hapmap];0.81[CHD][hapmap];0.95[GIH][hapmap];0.85[JPT][hapmap];0.95[MEX][hapmap];0.93[TSI][hapmap];0.86[EUR][1000 genomes]
rs6909767	0.87[CEU][hapmap]
rs6935918	0.87[CEU][hapmap]
rs7742691	0.91[CEU][hapmap]
rs7766485	1.00[ASW][hapmap];0.91[CEU][hapmap];0.83[CHB][hapmap];0.81[CHD][hapmap];0.95[GIH][hapmap];0.85[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];0.80[AFR][1000 genomes];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs911927	0.87[CEU][hapmap]
rs9342045	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9344533	0.87[CEU][hapmap]
rs9344540	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9344542	0.91[CEU][hapmap];0.83[CHB][hapmap];0.82[CHD][hapmap];0.86[MEX][hapmap]
rs9353327	0.91[CEU][hapmap];0.83[CHB][hapmap];0.82[CHD][hapmap];0.86[MEX][hapmap]
rs9362232	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9444351	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9444352	0.96[CEU][hapmap];0.83[CHB][hapmap];0.81[CHD][hapmap];0.98[GIH][hapmap];0.85[JPT][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.83[YRI][hapmap];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9444354	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9450284	0.87[CEU][hapmap]
rs9450285	1.00[ASW][hapmap];0.96[CEU][hapmap];0.81[CHD][hapmap];0.98[GIH][hapmap];0.85[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.95[MKK][hapmap];0.91[TSI][hapmap];1.00[YRI][hapmap]
rs9450288	0.82[ASW][hapmap];0.83[CHB][hapmap];0.81[GIH][hapmap];0.81[JPT][hapmap];1.00[MEX][hapmap];0.84[TSI][hapmap]
rs9450292	0.86[EUR][1000 genomes]
rs9450302	0.87[CEU][hapmap]
rs9450311	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022445	chr6:85972678-86392968	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
2	nsv538349	chr6:85972678-86392968	Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats 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	136 gene(s)	inside rSNPs	diseases
3	nsv886334	chr6:86214507-86394403	Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Enhancers Active TSS 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	124 gene(s)	inside rSNPs	diseases
4	nsv1028293	chr6:86353958-86778912	Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	100 gene(s)	inside rSNPs	diseases
5	nsv538350	chr6:86353958-86778912	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	100 gene(s)	inside rSNPs	diseases

mRNA abundance (count:24)

SNP	Gene	Cis/trans	Tissue	Source
rs1059307	SNHG5	cis	multi-tissue	Pritchard
rs1059307	SNHG5	cis	lung	GTEx
rs1059307	SNHG5	cis	Skin Sun Exposed Lower leg	GTEx
rs1059307	C6orf160	cis	uninvolved skin	skin_eQTL
rs1059307	SNHG5	cis	Adipose Subcutaneous	GTEx
rs1059307	KIAA1009	cis	cerebellum	SCAN
rs1059307	SNHG5	cis	Artery Tibial	GTEx
rs1059307	C6orf160	cis	normal skin	skin_eQTL
rs1059307	SNHG5	cis	Esophagus Muscularis	GTEx
rs1059307	SNHG5	cis	Muscle Skeletal	GTEx
rs1059307	SNHG5,SNORD50A	cis	brain	BrainEAC
rs1059307	SNHG5	cis	Heart Left Ventricle	GTEx
rs1059307	SNHG5	cis	Nerve Tibial	GTEx
rs1059307	C6orf160	cis	lesional skin	skin_eQTL
rs1059307	SNHG5	cis	Stomach	GTEx
rs1059307	SNHG5	cis	Whole Blood	GTEx
rs1059307	SNHG5	cis	lymphoblastoid	seeQTL
rs1059307	SNHG5	cis	Artery Aorta	GTEx
rs1059307	SNHG5,SNORD50A	cis	inferior olivary nucleus	BrainEAC
rs1059307	C6orf160	cis	multi-tissue	Pritchard
rs1059307	SNHG5	cis	Esophagus Mucosa	GTEx
rs1059307	SNHG5	cis	Thyroid	GTEx
rs1059307	SNHG5,SNORD50A	cis	intralobular white matter	BrainEAC
rs1059307	SNORD50B	cis	parietal	SCAN

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:86384200-86388200	Transcr. at gene 5' and 3'	iPS-20b Cell Line	embryonic stem cell
2	chr6:86384400-86388000	Transcr. at gene 5' and 3'	HUES64 Cell Line	embryonic stem cell
3	chr6:86384600-86388000	Transcr. at gene 5' and 3'	iPS-18 Cell Line	embryonic stem cell
4	chr6:86384800-86388000	Transcr. at gene 5' and 3'	ES-I3 Cell Line	embryonic stem cell
5	chr6:86384800-86388000	Transcr. at gene 5' and 3'	NH-A	brain
6	chr6:86384800-86388200	Transcr. at gene 5' and 3'	Muscle Satellite Cultured Cells	--
7	chr6:86384800-86388200	Active TSS	Right Atrium	heart
8	chr6:86384800-86388400	Transcr. at gene 5' and 3'	HUES6 Cell Line	embryonic stem cell
9	chr6:86385000-86388000	Transcr. at gene 5' and 3'	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr6:86385000-86389400	Active TSS	Right Ventricle	heart
11	chr6:86385000-86390200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr6:86385000-86390400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr6:86385200-86388800	Active TSS	Skeletal Muscle Male	skeletal muscle
14	chr6:86385200-86389000	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
15	chr6:86385200-86389800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
16	chr6:86385200-86390000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr6:86385400-86388000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr6:86385400-86388000	Transcr. at gene 5' and 3'	HMEC	breast
19	chr6:86385400-86388000	Transcr. at gene 5' and 3'	NHEK	skin
20	chr6:86385400-86389400	Active TSS	Aorta	Aorta
21	chr6:86385400-86389400	Active TSS	Ovary	ovary
22	chr6:86385600-86388400	Flanking Active TSS	Primary hematopoietic stem cells	blood
23	chr6:86385800-86388800	Active TSS	Colonic Mucosa	Colon
24	chr6:86385800-86389000	Active TSS	Stomach Smooth Muscle	stomach
25	chr6:86385800-86389200	Active TSS	Colon Smooth Muscle	Colon
26	chr6:86385800-86389200	Active TSS	Left Ventricle	heart
27	chr6:86385800-86389200	Active TSS	Lung	lung
28	chr6:86385800-86389400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr6:86385800-86389400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr6:86386000-86388200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr6:86386000-86389000	Active TSS	Fetal Intestine Small	intestine
32	chr6:86386000-86389000	Active TSS	HSMMtube	muscle
33	chr6:86386000-86389200	Active TSS	Duodenum Smooth Muscle	Duodenum
34	chr6:86386000-86389200	Active TSS	Small Intestine	intestine
35	chr6:86386000-86389200	Active TSS	Stomach Mucosa	stomach
36	chr6:86386000-86389600	Active TSS	Psoas Muscle	Psoas
37	chr6:86386000-86390200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr6:86386200-86388000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
39	chr6:86386200-86389000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr6:86386200-86389000	Active TSS	Brain Inferior Temporal Lobe	brain
41	chr6:86386200-86389000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
42	chr6:86386200-86389000	Active TSS	Fetal Intestine Large	intestine
43	chr6:86386200-86389000	Active TSS	Fetal Stomach	stomach
44	chr6:86386200-86389200	Active TSS	Fetal Heart	heart
45	chr6:86386200-86389200	Active TSS	Thymus	Thymus
46	chr6:86386200-86389400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr6:86386200-86389400	Active TSS	Fetal Muscle Leg	muscle
48	chr6:86386200-86390600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr6:86386400-86388000	Active TSS	Brain Germinal Matrix	brain
50	chr6:86386400-86388800	Active TSS	Primary B cells from peripheral blood	blood

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