Variant report

Variant	rs12902399
Chromosome Location	chr15:51058470-51058471
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:38)
CpG islands
(count:0)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:38 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr15:51057112-51058590	Hela-S3	cervix:	n/a	n/a
2	POLR2A	chr15:51057266-51058507	GM19193	blood:	n/a	n/a
3	ELF1	chr15:51056417-51058579	MCF-7	breast:	n/a	chr15:51057901-51057912 chr15:51057612-51057624 chr15:51057882-51057894
4	POLR2A	chr15:51057170-51058791	HepG2	liver:	n/a	n/a
5	MTA3	chr15:51057932-51058474	GM12878	blood:	n/a	n/a
6	PML	chr15:51057426-51058484	MCF-7	breast:	n/a	n/a
7	POLR2A	chr15:51057256-51058563	GM12892	blood:	n/a	n/a
8	POLR2A	chr15:51057102-51058480	Hela-S3	cervix:	n/a	n/a
9	POLR2A	chr15:51056505-51058634	GM12891	blood:	n/a	n/a
10	TCF12	chr15:51056791-51058603	A549	lung:	n/a	n/a
11	GABPA	chr15:51057349-51058472	SK-N-SH	brain:	n/a	n/a
12	POLR2A	chr15:51057188-51058515	PANC-1	pancreas:	n/a	n/a
13	POLR2A	chr15:51056366-51058477	PBDE	blood:	n/a	n/a
14	MAX	chr15:51057143-51058634	MCF-7	breast:	n/a	n/a
15	SIN3AK20	chr15:51056910-51058644	MCF-7	breast:	n/a	n/a
16	POLR2A	chr15:51056526-51058625	GM12878	blood:	n/a	n/a
17	MAX	chr15:51056881-51058539	MCF-7	breast:	n/a	n/a
18	POLR2A	chr15:51057059-51058605	GM12878	blood:	n/a	n/a
19	POLR2A	chr15:51056829-51058526	K562	blood:	n/a	n/a
20	POLR2A	chr15:51056967-51058472	U87	brain:	n/a	n/a
21	ELF1	chr15:51057273-51058539	MCF-7	breast:	n/a	chr15:51057901-51057912 chr15:51057612-51057624 chr15:51057882-51057894
22	POLR2A	chr15:51056277-51058480	GM12878	blood:	n/a	n/a
23	POLR2A	chr15:51056967-51058515	U87	brain:	n/a	n/a
24	POLR2A	chr15:51057231-51058617	K562	blood:	n/a	n/a
25	MTA3	chr15:51056611-51058661	GM12878	blood:	n/a	n/a
26	HCFC1	chr15:51056257-51058632	Hela-S3	cervix:	n/a	n/a
27	POLR2A	chr15:51056541-51058474	GM18951	blood:	n/a	n/a
28	POLR2A	chr15:51057206-51058512	HL-60	blood:	n/a	n/a
29	POLR2A	chr15:51057203-51058612	ProgFib	skin:	n/a	n/a
30	POLR2A	chr15:51056332-51058476	MCF10A-Er-Src	breast:	n/a	n/a
31	GABPA	chr15:51056772-51058757	MCF-7	breast:	n/a	n/a
32	SIN3AK20	chr15:51056837-51058502	MCF-7	breast:	n/a	n/a
33	ELF1	chr15:51057320-51058497	HCT-116	colon:	n/a	chr15:51057901-51057912 chr15:51057612-51057624 chr15:51057882-51057894
34	MXI1	chr15:51056198-51058626	SK-N-SH	brain:	n/a	n/a
35	POLR2A	chr15:51056699-51058526	GM12892	blood:	n/a	n/a
36	MAZ	chr15:51056581-51058556	IMR90	lung:	n/a	n/a
37	POLR2A	chr15:51056384-51058619	GM18505	blood:	n/a	n/a
38	POLR2A	chr15:51057300-51058507	H1-hESC	embryonic stem cell:	n/a	n/a

No data

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:51057644..51058522-chr18:61089470..61090340,2	NB4	blood:
2	chr15:51056442..51059084-chr15:51199726..51202707,2	MCF-7	breast:
3	chr15:51039062..51042009-chr15:51057876..51060168,3	MCF-7	breast:
4	chr15:50644661..50647207-chr15:51058214..51061180,2	MCF-7	breast:
5	chr15:51045886..51047999-chr15:51058293..51060374,2	K562	blood:
6	chr15:51056750..51061263-chr15:51087602..51092500,6	MCF-7	breast:
7	chr15:50976295..50981465-chr15:51052766..51059546,15	MCF-7	breast:
8	chr11:60926802..60929238-chr15:51056528..51059041,2	MCF-7	breast:
9	chr15:51057662..51059502-chr5:36875365..36877060,2	MCF-7	breast:
10	chr15:51057335..51059727-chr6:26020365..26022635,2	MCF-7	breast:
11	chr15:50977419..50980911-chr15:51055926..51058477,4	K562	blood:
12	chr15:51056515..51059362-chr15:51088829..51092887,6	MCF-7	breast:
13	chr15:50977319..50980700-chr15:51053372..51060901,7	MCF-7	breast:
14	chr15:51058134..51060047-chr15:51086816..51088508,2	MCF-7	breast:

No data

Variant related genes	Relation type
SPPL2A	TF binding region
ENSG00000164190	Chromatin interaction
ENSG00000092439	Chromatin interaction
ENSG00000241130	Chromatin interaction
ENSG00000138600	Chromatin interaction
ENSG00000198366	Chromatin interaction
ENSG00000196176	Chromatin interaction
ENSG00000119541	Chromatin interaction
ENSG00000081014	Chromatin interaction
ENSG00000243027	Chromatin interaction
ENSG00000167987	Chromatin interaction

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10519284	0.88[EUR][1000 genomes]
rs1052459	0.85[EUR][1000 genomes]
rs11858096	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12898588	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12899321	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12899943	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12900933	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12903573	0.84[EUR][1000 genomes]
rs12904353	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12904617	0.85[EUR][1000 genomes]
rs12904729	0.88[EUR][1000 genomes]
rs12905720	0.88[EUR][1000 genomes]
rs12908546	0.85[EUR][1000 genomes]
rs12910613	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12911654	0.88[EUR][1000 genomes]
rs12911753	0.83[EUR][1000 genomes]
rs12912192	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12912835	0.88[EUR][1000 genomes]
rs12912921	0.88[EUR][1000 genomes]
rs12913494	0.82[EUR][1000 genomes]
rs12913733	0.88[EUR][1000 genomes]
rs12914606	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12915606	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12917462	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28641162	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs34885055	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs35597009	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs71397503	0.85[EUR][1000 genomes]
rs71397504	0.85[EUR][1000 genomes]
rs71397507	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs71471514	0.80[AMR][1000 genomes]
rs71471515	0.80[AMR][1000 genomes]
rs7165492	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9920083	0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1053966	chr15:50715572-51133186	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
2	nsv542383	chr15:50715572-51133186	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
3	nsv1043805	chr15:50715572-51208891	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
4	nsv542384	chr15:50715572-51208891	Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
5	nsv1047443	chr15:50744781-51647023	Strong transcription Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
6	nsv1051990	chr15:50745814-51133186	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
7	nsv457134	chr15:50770868-51184583	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
8	nsv471242	chr15:50770868-51184583	Genic enhancers ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
9	nsv569396	chr15:50770868-51184583	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
10	nsv457135	chr15:50770868-51189707	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
11	nsv569397	chr15:50770868-51189707	Strong transcription Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
12	nsv1048621	chr15:50775451-51115535	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
13	nsv1047039	chr15:50782070-51187804	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats 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	54 gene(s)	inside rSNPs	diseases
14	nsv542385	chr15:50782070-51187804	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
15	nsv457136	chr15:50789125-51294995	Strong transcription ZNF genes & repeats Weak transcription Active TSS Enhancers Genic enhancers Flanking 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	66 gene(s)	inside rSNPs	diseases
16	nsv569398	chr15:50789125-51294995	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats 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	66 gene(s)	inside rSNPs	diseases
17	nsv1036081	chr15:50818569-51097229	Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
18	nsv1055112	chr15:50822035-51133186	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
19	nsv1042372	chr15:50846461-51208891	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
20	nsv542386	chr15:50846461-51208891	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
21	nsv569399	chr15:50874964-51562198	Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
22	nsv569400	chr15:50874964-51767265	ZNF genes & repeats Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
23	nsv904212	chr15:50979738-51132170	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
24	nsv904213	chr15:51011402-51119731	Strong transcription Weak transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
25	nsv1044320	chr15:51016364-51074061	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
26	nsv457137	chr15:51019117-51117524	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
27	nsv569402	chr15:51019117-51117524	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
28	nsv529339	chr15:51048579-51270372	Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Enhancers 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	43 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:93 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:51056000-51058600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr15:51056000-51058600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr15:51056200-51058600	Active TSS	Psoas Muscle	Psoas
4	chr15:51056400-51058600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr15:51056400-51058600	Active TSS	Fetal Brain Female	brain
6	chr15:51056600-51058600	Active TSS	HUES6 Cell Line	embryonic stem cell
7	chr15:51056600-51058600	Active TSS	Brain Angular Gyrus	brain
8	chr15:51056600-51058600	Active TSS	Fetal Stomach	stomach
9	chr15:51056600-51058600	Active TSS	Rectal Smooth Muscle	rectum
10	chr15:51056800-51058600	Active TSS	Duodenum Mucosa	Duodenum
11	chr15:51057000-51058600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr15:51057000-51058600	Active TSS	Brain Anterior Caudate	brain
13	chr15:51057000-51058600	Active TSS	Brain Substantia Nigra	brain
14	chr15:51057400-51058600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr15:51058000-51058600	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
16	chr15:51058000-51058600	Flanking Active TSS	Dnd41	blood
17	chr15:51058000-51058600	Flanking Active TSS	K562	blood
18	chr15:51058000-51059000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
19	chr15:51058000-51059000	Flanking Active TSS	Stomach Smooth Muscle	stomach
20	chr15:51058200-51058600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr15:51058200-51058600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
22	chr15:51058200-51058600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
23	chr15:51058200-51058600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
24	chr15:51058200-51058600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
25	chr15:51058200-51058600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr15:51058200-51058600	Flanking Active TSS	Adipose Nuclei	Adipose
27	chr15:51058200-51058600	Flanking Active TSS	Liver	Liver
28	chr15:51058200-51058600	Flanking Active TSS	Brain Germinal Matrix	brain
29	chr15:51058200-51058600	Flanking Active TSS	Fetal Muscle Trunk	muscle
30	chr15:51058200-51058600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
31	chr15:51058200-51058600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
32	chr15:51058200-51058600	Flanking Active TSS	Thymus	Thymus
33	chr15:51058200-51058600	Enhancers	Spleen	Spleen
34	chr15:51058200-51058600	Flanking Active TSS	Hela-S3	cervix
35	chr15:51058200-51058600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
36	chr15:51058200-51059000	Enhancers	Lung	lung
37	chr15:51058200-51059000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
38	chr15:51058400-51058600	Enhancers	Primary B cells from cord blood	blood
39	chr15:51058400-51058600	Enhancers	Primary B cells from peripheral blood	blood
40	chr15:51058400-51058600	Enhancers	Primary T cells from cord blood	blood
41	chr15:51058400-51058600	Active TSS	Primary hematopoietic stem cells	blood
42	chr15:51058400-51058600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
43	chr15:51058400-51058600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
44	chr15:51058400-51058600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr15:51058400-51058600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
46	chr15:51058400-51058600	Enhancers	Primary T killer memory cells from peripheral blood	blood
47	chr15:51058400-51058600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr15:51058400-51058600	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr15:51058400-51058600	Flanking Active TSS	Brain Hippocampus Middle	brain
50	chr15:51058400-51058600	Enhancers	Brain Inferior Temporal Lobe	brain

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