Variant report

Variant	rs6132822
Chromosome Location	chr20:25228695-25228696
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	NR3C1	chr20:25228655-25229025	A549	lung:	n/a	n/a
2	TAF1	chr20:25228515-25229573	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPD	chr20:25228294-25228991	HepG2	liver:	n/a	n/a
4	CCNT2	chr20:25227947-25229451	K562	blood:	n/a	chr20:25229398-25229407
5	POLR2A	chr20:25228363-25229167	H1-neurons	neurons:	n/a	n/a
6	POLR2A	chr20:25228405-25229705	H1-hESC	embryonic stem cell:	n/a	n/a
7	ELF1	chr20:25228667-25229124	MCF-7	breast:	n/a	chr20:25228839-25228852 chr20:25228799-25228808
8	TAF1	chr20:25228626-25228917	K562	blood:	n/a	n/a
9	ELF1	chr20:25228627-25229118	K562	blood:	n/a	chr20:25228839-25228852 chr20:25228799-25228808
10	TAF1	chr20:25228650-25229066	GM12892	blood:	n/a	n/a
11	MXI1	chr20:25227853-25229524	Hela-S3	cervix:	n/a	n/a
12	ZBTB7A	chr20:25228675-25229390	ECC-1	luminal epithelium:	n/a	n/a
13	MAX	chr20:25227734-25229632	MCF-7	breast:	n/a	chr20:25229402-25229412
14	TCF12	chr20:25228657-25228912	GM12878	blood:	n/a	n/a
15	POLR2A	chr20:25228638-25229104	GM12892	blood:	n/a	n/a
16	CTCF	chr20:25228695-25228781	GM12891	blood:	n/a	n/a
17	TBP	chr20:25228378-25229079	HepG2	liver:	n/a	n/a
18	POLR2A	chr20:25228668-25229025	GM12891	blood:	n/a	n/a
19	SP1	chr20:25228233-25229146	A549	lung:	n/a	chr20:25228404-25228418 chr20:25229068-25229077 chr20:25229067-25229079
20	FOXA2	chr20:25228656-25229120	A549	lung:	n/a	n/a
21	NR3C1	chr20:25228626-25229092	A549	lung:	n/a	n/a
22	TAF1	chr20:25228540-25229516	H1-hESC	embryonic stem cell:	n/a	n/a
23	EP300	chr20:25228200-25229685	ECC-1	luminal epithelium:	n/a	chr20:25228336-25228352 chr20:25228370-25228386 chr20:25229243-25229259
24	TAF1	chr20:25228641-25229020	GM12892	blood:	n/a	n/a
25	ELF1	chr20:25228637-25229116	HepG2	liver:	n/a	chr20:25228839-25228852 chr20:25228799-25228808
26	POLR2A	chr20:25228629-25229430	GM12878	blood:	n/a	n/a
27	ELK1	chr20:25228665-25228963	Hela-S3	cervix:	n/a	n/a
28	TAF1	chr20:25228648-25229169	GM12878	blood:	n/a	n/a
29	IRF1	chr20:25228403-25229151	K562	blood:	n/a	n/a
30	EGR1	chr20:25228668-25228878	GM12878	blood:	n/a	chr20:25228774-25228788 chr20:25228794-25228808
31	POLR2A	chr20:25228416-25228924	HepG2	liver:	n/a	n/a
32	ELF1	chr20:25228657-25229014	K562	blood:	n/a	chr20:25228839-25228852 chr20:25228799-25228808
33	POLR2A	chr20:25228655-25228956	U87	brain:	n/a	n/a
34	YY1	chr20:25228668-25228943	K562	blood:	n/a	chr20:25228799-25228808
35	POLR2A	chr20:25228648-25229121	Hela-S3	cervix:	n/a	n/a
36	POLR2A	chr20:25228520-25229171	HUVEC	blood vessel:	n/a	n/a
37	POLR2A	chr20:25228658-25229083	GM12878	blood:	n/a	n/a
38	PBX3	chr20:25228539-25229029	A549	lung:	n/a	n/a
39	POLR2A	chr20:25228120-25229114	GM12878	blood:	n/a	n/a
40	SIN3AK20	chr20:25228635-25229053	PFSK-1	brain:	n/a	n/a
41	PBX3	chr20:25228660-25229139	SK-N-SH	brain:	n/a	n/a
42	TAF1	chr20:25227722-25229193	A549	lung:	n/a	n/a
43	POLR2A	chr20:25228641-25228965	K562	blood:	n/a	n/a
44	POLR2A	chr20:25228359-25229276	GM12878	blood:	n/a	n/a
45	POLR2A	chr20:25227358-25229473	MCF-7	breast:	n/a	n/a
46	E2F6	chr20:25228628-25228954	K562	blood:	n/a	n/a
47	POLR2A	chr20:25228195-25229126	U87	brain:	n/a	n/a
48	UBTF	chr20:25227726-25229649	K562	blood:	n/a	n/a
49	ELF1	chr20:25228325-25229184	MCF-7	breast:	n/a	chr20:25228569-25228578 chr20:25228839-25228852 chr20:25228799-25228808
50	E2F6	chr20:25228662-25229199	A549	lung:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:25228557..25231308-chr20:25476839..25479017,2	MCF-7	breast:
2	chr20:25204037..25205721-chr20:25227160..25229400,2	K562	blood:
3	chr11:78285600..78286417-chr20:25228512..25229228,2	NB4	blood:
4	chr2:198364442..198365011-chr20:25228269..25228983,2	HCT-116	colon:
5	chr12:104531363..104532174-chr20:25228138..25229130,2	NB4	blood:
6	chr20:25057289..25058975-chr20:25226619..25228863,2	MCF-7	breast:
7	chr20:24971839..24974533-chr20:25228512..25230139,2	MCF-7	breast:
8	chr20:25204221..25206637-chr20:25227058..25229400,2	K562	blood:
9	chr20:25200007..25207026-chr20:25227086..25230373,11	MCF-7	breast:
10	chr20:25174902..25179249-chr20:25225017..25231959,9	MCF-7	breast:
11	chr20:25228549..25230437-chr20:25281061..25283760,2	MCF-7	breast:
12	chr20:25202506..25206898-chr20:25226343..25231297,7	MCF-7	breast:
13	chr20:24971946..24973582-chr20:25227704..25229248,2	MCF-7	breast:
14	chr12:53339776..53342666-chr20:25227973..25230849,2	MCF-7	breast:
15	chr17:80186667..80187466-chr20:25228580..25229101,2	HCT-116	colon:
16	chr20:25174010..25179528-chr20:25225802..25231331,13	MCF-7	breast:

Variant related genes	Relation type
PYGB	TF binding region
ENSG00000101004	Chromatin interaction
ENSG00000120837	Chromatin interaction
ENSG00000100997	Chromatin interaction
ENSG00000111057	Chromatin interaction
ENSG00000137513	Chromatin interaction
ENSG00000100987	Chromatin interaction
ENSG00000115541	Chromatin interaction
ENSG00000141526	Chromatin interaction
ENSG00000144381	Chromatin interaction
ENSG00000101474	Chromatin interaction
ENSG00000197586	Chromatin interaction

Extended variants
information (count: 61 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs1044573	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1118963	0.94[AFR][1000 genomes];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11699953	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1555330	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2260997	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2273473	0.84[EUR][1000 genomes]
rs2424698	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2474766	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2474769	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3746337	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4355182	0.80[EUR][1000 genomes]
rs4619688	0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6037062	0.88[ASN][1000 genomes]
rs6037069	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6050463	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6050464	0.86[EUR][1000 genomes]
rs6050481	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6050482	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6107015	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6107017	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6107019	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6115093	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs6115094	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6115099	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs6115100	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6115101	0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6115109	0.95[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6115118	0.90[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs6132819	0.88[AFR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6132820	0.94[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6132821	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6132824	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6132825	0.80[AMR][1000 genomes]
rs6138545	0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs6138546	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6138550	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6138553	0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6138554	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs6138555	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6138556	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7453	0.93[ASN][1000 genomes]
rs8115257	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8184820	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1062140	chr20:24807962-25304054	Strong transcription Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv544219	chr20:24807962-25304054	Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Active TSS Enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv1055341	chr20:24848416-25302271	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
4	nsv1063494	chr20:25067286-25468557	Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
5	nsv1063016	chr20:25067286-25475629	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
6	nsv1065101	chr20:25068046-25466542	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
7	nsv544220	chr20:25068046-25466542	Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
8	nsv531480	chr20:25070067-25472684	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
9	nsv585746	chr20:25071454-25470056	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
10	nsv1062742	chr20:25071454-25475629	Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
11	nsv949389	chr20:25071454-25506582	Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
12	nsv531481	chr20:25080583-25448944	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
13	nsv949479	chr20:25096494-25467359	Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS 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 target site	52 gene(s)	inside rSNPs	diseases
14	nsv1061109	chr20:25101715-25472685	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
15	nsv544221	chr20:25101715-25472685	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
16	nsv1066667	chr20:25133066-25238976	Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
17	nsv544222	chr20:25133066-25238976	Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
18	nsv828708	chr20:25223895-25231601	Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs6132822	ABHD12	Cis_1M	lymphoblastoid	RTeQTL
rs6132822	ABHD12	cis	multi-tissue	Pritchard
rs6132822	GINS1	Cis_1M	lymphoblastoid	RTeQTL
rs6132822	PYGB	cis	Whole Blood	GTEx
rs6132822	PYGB	cis	multi-tissue	Pritchard

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:25227600-25229600	Active TSS	Primary T killer memory cells from peripheral blood	blood
2	chr20:25227600-25229800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr20:25227600-25229800	Active TSS	Duodenum Smooth Muscle	Duodenum
4	chr20:25227600-25230000	Active TSS	Fetal Brain Female	brain
5	chr20:25227600-25230200	Active TSS	H9 Cell Line	embryonic stem cell
6	chr20:25227600-25231200	Active TSS	Sigmoid Colon	Sigmoid Colon
7	chr20:25227800-25228800	Weak transcription	Fetal Heart	heart
8	chr20:25227800-25229200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
9	chr20:25227800-25229600	Active TSS	Fetal Intestine Small	intestine
10	chr20:25227800-25229600	Active TSS	Fetal Kidney	kidney
11	chr20:25227800-25229800	Active TSS	Pancreatic Islets	Pancreatic Islet
12	chr20:25227800-25229800	Active TSS	Small Intestine	intestine
13	chr20:25227800-25230000	Active TSS	A549	lung
14	chr20:25227800-25230200	Flanking Active TSS	Primary hematopoietic stem cells	blood
15	chr20:25227800-25230800	Active TSS	ES-I3 Cell Line	embryonic stem cell
16	chr20:25227800-25230800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr20:25227800-25231000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr20:25227800-25231200	Active TSS	Left Ventricle	heart
19	chr20:25227800-25231600	Active TSS	Right Atrium	heart
20	chr20:25228000-25228800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr20:25228000-25229000	Active TSS	Gastric	stomach
22	chr20:25228000-25229200	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr20:25228000-25229400	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
24	chr20:25228000-25229400	Active TSS	Rectal Mucosa Donor 31	rectum
25	chr20:25228000-25229600	Active TSS	Hela-S3	cervix
26	chr20:25228000-25229800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr20:25228000-25229800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr20:25228000-25229800	Active TSS	Ovary	ovary
29	chr20:25228000-25230000	Active TSS	iPS-18 Cell Line	embryonic stem cell
30	chr20:25228000-25230000	Active TSS	Rectal Mucosa Donor 29	rectum
31	chr20:25228000-25230000	Active TSS	NHDF-Ad	bronchial
32	chr20:25228000-25230200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
33	chr20:25228000-25230200	Active TSS	Psoas Muscle	Psoas
34	chr20:25228000-25230200	Active TSS	Stomach Mucosa	stomach
35	chr20:25228000-25230600	Active TSS	NHEK	skin
36	chr20:25228000-25230800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr20:25228000-25230800	Active TSS	Aorta	Aorta
38	chr20:25228000-25230800	Active TSS	Rectal Smooth Muscle	rectum
39	chr20:25228000-25230800	Active TSS	HMEC	breast
40	chr20:25228000-25230800	Active TSS	HSMM	muscle
41	chr20:25228200-25229200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
42	chr20:25228200-25229200	Active TSS	Monocytes-CD14+_RO01746	blood
43	chr20:25228200-25229400	Active TSS	Primary T cells from cord blood	blood
44	chr20:25228200-25229400	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr20:25228200-25229400	Active TSS	Skeletal Muscle Male	skeletal muscle
46	chr20:25228200-25229400	Active TSS	Spleen	Spleen
47	chr20:25228200-25229400	Active TSS	K562	blood
48	chr20:25228200-25229600	Active TSS	HUES48 Cell Line	embryonic stem cell
49	chr20:25228200-25229600	Active TSS	Primary T helper naive cells from peripheral blood	blood
50	chr20:25228200-25229600	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--

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