Variant report

Variant	rs11904110
Chromosome Location	chr2:98261802-98261803
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	MAX	chr2:98261488-98263007	A549	lung:	n/a	chr2:98262404-98262414
2	MAX	chr2:98261796-98262937	ECC-1	luminal epithelium:	n/a	chr2:98262404-98262414
3	SIN3AK20	chr2:98261557-98263138	MCF-7	breast:	n/a	n/a
4	PML	chr2:98261735-98262858	MCF-7	breast:	n/a	n/a
5	POLR2A	chr2:98261353-98263086	MCF10A-Er-Src	breast:	n/a	n/a
6	RCOR1	chr2:98261745-98262708	GM12878	blood:	n/a	n/a
7	POLR2A	chr2:98261643-98262759	K562	blood:	n/a	n/a
8	IRF1	chr2:98261721-98262750	K562	blood:	n/a	chr2:98262017-98262028 chr2:98262334-98262348 chr2:98261945-98261959
9	RUNX3	chr2:98261735-98262732	GM12878	blood:	n/a	n/a
10	POLR2A	chr2:98261758-98262934	HepG2	liver:	n/a	n/a
11	TBL1XR1	chr2:98261773-98262747	GM12878	blood:	n/a	n/a
12	MAX	chr2:98261600-98262815	NB4	blood:	n/a	chr2:98262404-98262414
13	POLR2A	chr2:98261715-98262942	GM12892	blood:	n/a	n/a
14	POLR2A	chr2:98261542-98263124	HL-60	blood:	n/a	n/a
15	YY1	chr2:98261732-98261980	SK-N-SH_RA	brain:	n/a	n/a
16	POLR2A	chr2:98261685-98263038	MCF10A-Er-Src	breast:	n/a	n/a
17	JUN	chr2:98261598-98262747	K562	blood:	n/a	n/a
18	EGR1	chr2:98261791-98262636	K562	blood:	n/a	chr2:98262421-98262435 chr2:98262400-98262414 chr2:98262396-98262418 chr2:98262401-98262411 chr2:98262420-98262433 chr2:98262073-98262086 chr2:98261990-98262004 chr2:98262401-98262414 chr2:98262481-98262494 chr2:98262068-98262090 chr2:98262402-98262413 chr2:98262419-98262434 chr2:98262401-98262414 chr2:98262421-98262432 chr2:98262398-98262412 chr2:98261950-98261963 chr2:98262339-98262352 chr2:98262401-98262414 chr2:98262402-98262411 chr2:98262401-98262414 chr2:98262400-98262415
19	KAP1	chr2:98261796-98262756	U2OS	brain:	n/a	n/a
20	POLR2A	chr2:98261628-98263070	PFSK-1	brain:	n/a	n/a
21	EGR1	chr2:98261669-98262952	HCT-116	colon:	n/a	chr2:98262421-98262435 chr2:98262400-98262414 chr2:98262396-98262418 chr2:98262401-98262411 chr2:98262420-98262433 chr2:98262073-98262086 chr2:98261990-98262004 chr2:98262401-98262414 chr2:98262481-98262494 chr2:98262068-98262090 chr2:98262402-98262413 chr2:98262419-98262434 chr2:98262401-98262414 chr2:98262421-98262432 chr2:98262398-98262412 chr2:98261950-98261963 chr2:98262339-98262352 chr2:98262401-98262414 chr2:98262402-98262411 chr2:98262401-98262414 chr2:98262400-98262415
22	POLR2A	chr2:98261549-98262845	HUVEC	blood vessel:	n/a	n/a
23	POLR2A	chr2:98261697-98262795	HCT-116	colon:	n/a	n/a
24	BHLHE40	chr2:98261746-98262777	GM12878	blood:	n/a	n/a
25	PML	chr2:98261697-98263035	GM12878	blood:	n/a	n/a
26	POLR2A	chr2:98261582-98262860	GM12891	blood:	n/a	n/a
27	REST	chr2:98261614-98263063	H1-neurons	neurons:	n/a	chr2:98261959-98261968 chr2:98261928-98261942
28	POLR2A	chr2:98261732-98262953	GM12878	blood:	n/a	n/a
29	POLR2A	chr2:98261593-98263085	K562	blood:	n/a	n/a
30	POLR2A	chr2:98261667-98263002	NB4	blood:	n/a	n/a
31	POLR2A	chr2:98261634-98262909	GM19099	blood:	n/a	n/a
32	POLR2A	chr2:98261644-98262831	U87	brain:	n/a	n/a
33	POLR2A	chr2:98261394-98263167	Raji	blood:	n/a	n/a
34	MAX	chr2:98261499-98262743	K562	blood:	n/a	chr2:98262404-98262414
35	MAX	chr2:98261765-98262865	MCF-7	breast:	n/a	chr2:98262404-98262414
36	TAF1	chr2:98261712-98262781	H1-hESC	embryonic stem cell:	n/a	n/a
37	GABPA	chr2:98261734-98263066	MCF-7	breast:	n/a	chr2:98262386-98262397 chr2:98262383-98262397 chr2:98262338-98262347 chr2:98262386-98262400
38	MXI1	chr2:98261729-98262924	HepG2	liver:	n/a	n/a
39	EGR1	chr2:98261786-98262768	MCF-7	breast:	n/a	chr2:98262421-98262435 chr2:98262400-98262414 chr2:98262396-98262418 chr2:98262401-98262411 chr2:98262420-98262433 chr2:98262073-98262086 chr2:98261990-98262004 chr2:98262401-98262414 chr2:98262481-98262494 chr2:98262068-98262090 chr2:98262402-98262413 chr2:98262419-98262434 chr2:98262401-98262414 chr2:98262421-98262432 chr2:98262398-98262412 chr2:98261950-98261963 chr2:98262339-98262352 chr2:98262401-98262414 chr2:98262402-98262411 chr2:98262401-98262414 chr2:98262400-98262415
40	POLR2A	chr2:98261359-98263035	K562	blood:	n/a	n/a
41	JUND	chr2:98261639-98262762	K562	blood:	n/a	n/a
42	POLR2A	chr2:98261496-98262938	HUVEC	blood vessel:	n/a	n/a
43	EGR1	chr2:98261758-98262721	ECC-1	luminal epithelium:	n/a	chr2:98262421-98262435 chr2:98262400-98262414 chr2:98262396-98262418 chr2:98262401-98262411 chr2:98262420-98262433 chr2:98262073-98262086 chr2:98261990-98262004 chr2:98262401-98262414 chr2:98262481-98262494 chr2:98262068-98262090 chr2:98262402-98262413 chr2:98262419-98262434 chr2:98262401-98262414 chr2:98262421-98262432 chr2:98262398-98262412 chr2:98261950-98261963 chr2:98262339-98262352 chr2:98262401-98262414 chr2:98262402-98262411 chr2:98262401-98262414 chr2:98262400-98262415
44	SIN3A	chr2:98261750-98262969	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr2:98261559-98263254	SK-N-MC	brain:	n/a	n/a
46	ELF1	chr2:98261766-98263024	GM12878	blood:	n/a	chr2:98261846-98261857 chr2:98262517-98262528 chr2:98262518-98262527 chr2:98262485-98262496 chr2:98262486-98262495
47	SPI1	chr2:98261578-98262060	HL-60	blood:	n/a	chr2:98261864-98261877
48	MAFK	chr2:98261635-98262631	K562	blood:	n/a	chr2:98261904-98261919
49	POLR2A	chr2:98261638-98262837	U87	brain:	n/a	n/a
50	TAF1	chr2:98261740-98262868	MCF-7	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:98261015..98264268-chr2:98289158..98291782,3	K562	blood:
2	chr2:98260499..98265219-chr2:98284794..98288071,4	MCF-7	breast:
3	chr2:98204043..98208769-chr2:98260858..98263741,4	MCF-7	breast:

Variant related genes	Relation type
COX5B	TF binding region
ENSG00000228486	Chromatin interaction
ENSG00000196912	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11886025	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11886239	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17022045	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17841861	1.00[CEU][hapmap]
rs3475	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55981050	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs59134572	0.92[ASN][1000 genomes]
rs6543021	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6745653	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[CHD][hapmap];1.00[GIH][hapmap];0.94[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];0.95[TSI][hapmap];0.89[YRI][hapmap];0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72951131	0.80[AMR][1000 genomes]
rs73959752	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73959753	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73959769	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73959786	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73959787	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757819	chr2:97571109-98336507	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	64 gene(s)	inside rSNPs	diseases
2	esv2759077	chr2:97571109-98336507	Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	64 gene(s)	inside rSNPs	diseases
3	nsv431402	chr2:97669032-98281634	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
4	nsv535831	chr2:97671335-98270990	Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
5	esv2752937	chr2:97708611-98269110	Genic enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
6	esv2756939	chr2:97708611-98274527	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
7	esv2763630	chr2:97731133-98279050	Strong transcription Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
8	nsv431413	chr2:97753585-98274527	Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
9	nsv522486	chr2:97768178-98265491	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
10	nsv869602	chr2:97820572-98263438	Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
11	nsv1005903	chr2:97872625-98264679	Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
12	nsv999118	chr2:97886322-98264679	Strong transcription Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
13	nsv1011958	chr2:97886322-98269110	Weak transcription Bivalent/Poised TSS Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
14	nsv1001249	chr2:97972600-98274527	Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
15	nsv1005846	chr2:97972600-98281634	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
16	nsv1010905	chr2:98013814-98269110	Weak transcription Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
17	nsv1003384	chr2:98013814-98270884	Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers 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	20 gene(s)	inside rSNPs	diseases
18	nsv1010167	chr2:98013814-98273619	Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
19	nsv999627	chr2:98013814-98274527	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS 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	20 gene(s)	inside rSNPs	diseases
20	nsv1009263	chr2:98013814-98281634	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers 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	33 gene(s)	inside rSNPs	diseases
21	esv1829350	chr2:98170405-98315611	Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
22	nsv531382	chr2:98250628-98457616	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:98261000-98262000	Enhancers	Spleen	Spleen
2	chr2:98261400-98262000	Flanking Active TSS	Brain Anterior Caudate	brain
3	chr2:98261400-98262000	Enhancers	Fetal Heart	heart
4	chr2:98261400-98262200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
5	chr2:98261400-98262200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr2:98261400-98262200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr2:98261400-98262200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr2:98261400-98262200	Flanking Active TSS	Adipose Nuclei	Adipose
9	chr2:98261400-98262200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
10	chr2:98261400-98262200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
11	chr2:98261400-98262200	Flanking Active TSS	Dnd41	blood
12	chr2:98261400-98262200	Flanking Active TSS	K562	blood
13	chr2:98261400-98262200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
14	chr2:98261400-98263200	Active TSS	Rectal Mucosa Donor 29	rectum
15	chr2:98261400-98263400	Active TSS	ES-I3 Cell Line	embryonic stem cell
16	chr2:98261400-98263400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr2:98261400-98263400	Active TSS	HUES48 Cell Line	embryonic stem cell
18	chr2:98261400-98263400	Active TSS	Breast Myoepithelial Primary Cells	Breast
19	chr2:98261400-98263400	Active TSS	Brain Angular Gyrus	brain
20	chr2:98261400-98263400	Active TSS	Fetal Brain Female	brain
21	chr2:98261400-98263400	Active TSS	Sigmoid Colon	Sigmoid Colon
22	chr2:98261400-98263600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
23	chr2:98261400-98263600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr2:98261400-98263800	Active TSS	Right Ventricle	heart
25	chr2:98261600-98262000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr2:98261600-98262000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr2:98261600-98262000	Flanking Active TSS	Primary T cells from cord blood	blood
28	chr2:98261600-98262000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
29	chr2:98261600-98262000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
30	chr2:98261600-98262000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr2:98261600-98262000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr2:98261600-98262000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr2:98261600-98262000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr2:98261600-98262000	Flanking Active TSS	Liver	Liver
35	chr2:98261600-98262000	Flanking Active TSS	Brain Hippocampus Middle	brain
36	chr2:98261600-98262000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
37	chr2:98261600-98262000	Flanking Active TSS	Duodenum Mucosa	Duodenum
38	chr2:98261600-98262000	Flanking Active TSS	Fetal Intestine Large	intestine
39	chr2:98261600-98262000	Flanking Active TSS	Fetal Intestine Small	intestine
40	chr2:98261600-98262000	Flanking Active TSS	Fetal Lung	lung
41	chr2:98261600-98262000	Flanking Active TSS	Rectal Smooth Muscle	rectum
42	chr2:98261600-98262000	Flanking Active TSS	A549	lung
43	chr2:98261600-98262200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr2:98261600-98262200	Flanking Active TSS	Primary B cells from peripheral blood	blood
45	chr2:98261600-98262200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
46	chr2:98261600-98262200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
47	chr2:98261600-98262200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
48	chr2:98261600-98262200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
49	chr2:98261600-98262200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
50	chr2:98261600-98262200	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood

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