Variant report

Variant	rs56872371
Chromosome Location	chr17:46663774-46663775
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:38)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
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	MAZ	chr17:46662285-46664134	IMR90	lung:	n/a	n/a
2	MTA3	chr17:46662378-46664216	GM12878	blood:	n/a	n/a
3	RUNX3	chr17:46663642-46663969	GM12878	blood:	n/a	n/a
4	CTCF	chr17:46663760-46663910	HMF	breast:	n/a	n/a
5	POLR2A	chr17:46663610-46663991	HCT-116	colon:	n/a	n/a
6	RAD21	chr17:46662302-46663990	HCT-116	colon:	n/a	chr17:46663448-46663458 chr17:46663122-46663136 chr17:46663448-46663460
7	POU2F2	chr17:46663661-46663997	GM12891	blood:	n/a	n/a
8	CTBP2	chr17:46662351-46663925	H1-hESC	embryonic stem cell:	n/a	n/a
9	POLR2A	chr17:46663567-46663867	HUVEC	blood vessel:	n/a	n/a
10	POLR2A	chr17:46662730-46664028	HUVEC	blood vessel:	n/a	n/a
11	ZNF263	chr17:46662541-46663982	HEK293-T-REx	kidney:	n/a	chr17:46663483-46663492
12	CHD1	chr17:46662335-46676284	IMR90	lung:	n/a	chr17:46662455-46662465 chr17:46670083-46670093 chr17:46669891-46669901
13	RUNX3	chr17:46663565-46664054	GM12878	blood:	n/a	n/a
14	SUZ12	chr17:46662649-46665098	NT2-D1	testis:	n/a	n/a
15	RCOR1	chr17:46663680-46663878	GM12878	blood:	n/a	n/a
16	EGR1	chr17:46663671-46663917	GM12878	blood:	n/a	chr17:46663799-46663813 chr17:46663775-46663788 chr17:46663778-46663792
17	FOSL2	chr17:46662359-46663909	A549	lung:	n/a	n/a
18	RELA	chr17:46662733-46663936	GM19099	blood:	n/a	n/a
19	MAX	chr17:46663736-46663914	GM12878	blood:	n/a	n/a
20	SIN3AK20	chr17:46662148-46664308	PANC-1	pancreas:	n/a	n/a
21	POLR2A	chr17:46663671-46663960	ECC-1	luminal epithelium:	n/a	n/a
22	POLR2A	chr17:46663617-46663979	HCT-116	colon:	n/a	n/a
23	SUZ12	chr17:46662105-46664500	H1-hESC	embryonic stem cell:	n/a	n/a
24	HMGN3	chr17:46663699-46663922	K562	blood:	n/a	n/a
25	POLR2A	chr17:46655911-46684927	PANC-1	pancreas:	n/a	n/a
26	POU2F2	chr17:46663642-46664055	GM12878	blood:	n/a	n/a
27	EGR1	chr17:46663701-46663898	K562	blood:	n/a	chr17:46663799-46663813 chr17:46663775-46663788 chr17:46663778-46663792
28	POLR2A	chr17:46663725-46663954	HUVEC	blood vessel:	n/a	n/a
29	EGR1	chr17:46663681-46663901	GM12878	blood:	n/a	chr17:46663799-46663813 chr17:46663775-46663788 chr17:46663778-46663792
30	CCNT2	chr17:46663763-46664002	K562	blood:	n/a	chr17:46663780-46663789
31	TCF12	chr17:46662035-46663784	A549	lung:	n/a	chr17:46662977-46662984
32	BHLHE40	chr17:46663750-46663860	GM12878	blood:	n/a	n/a
33	POLR2A	chr17:46662333-46663778	U87	brain:	n/a	n/a
34	EP300	chr17:46662697-46663974	GM12878	blood:	n/a	chr17:46663847-46663863 chr17:46663183-46663199 chr17:46663880-46663896 chr17:46663074-46663088 chr17:46663824-46663833
35	POLR2A	chr17:46663608-46663938	ECC-1	luminal epithelium:	n/a	n/a
36	POLR2A	chr17:46645331-46684907	PANC-1	pancreas:	n/a	n/a
37	MXI1	chr17:46663654-46663835	GM12878	blood:	n/a	n/a
38	MAZ	chr17:46663477-46664082	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:46663759-46663809	AG04450	lung:	fetal
2	chr17:46663759-46663809	AG10803	skin:	n/a
3	chr17:46663759-46663809	HCF	heart:	n/a
4	chr17:46663759-46663809	Caco-2	colon:	n/a
5	chr17:46663759-46663809	HNPCEpiC	eye:	n/a
6	chr17:46663759-46663809	HEEpiC	esophagus:	n/a
7	chr17:46663759-46663809	GM12892	blood:	n/a
8	chr17:46663759-46663809	PFSK-1	brain:	n/a
9	chr17:46663759-46663809	BJ	skin:	n/a
10	chr17:46663759-46663809	AG09319	gingival:	n/a
11	chr17:46663759-46663809	U87	brain:	n/a
12	chr17:46663759-46663809	HEK293	kidney:	embryo
13	chr17:46663759-46663809	GM12878	blood:	n/a
14	chr17:46663759-46663809	ovcar-3	ovarian:	n/a
15	chr17:46663759-46663809	A549	lung:	n/a
16	chr17:46663759-46663809	CMK	blood:	n/a
17	chr17:46663759-46663809	AoSMC	blood vessel:	n/a
18	chr17:46663759-46663809	HUVEC	blood vessel:	n/a
19	chr17:46663759-46663809	IMR90	lung:	fetal
20	chr17:46663759-46663809	HRE	kidney:	n/a
21	chr17:46663759-46663809	T-47D	breast:	n/a
22	chr17:46663759-46663809	NHDF-neo	bronchial:	n/a
23	chr17:46663759-46663809	GM12891	blood:	n/a
24	chr17:46663759-46663809	ProgFib	skin:	n/a
25	chr17:46663759-46663809	SAEC	small airway:	n/a
26	chr17:46663759-46663809	SK-N-MC	brain:	n/a
27	chr17:46663759-46663809	GM06990	blood:	n/a
28	chr17:46663759-46663809	MCF-7	breast:	n/a
29	chr17:46663759-46663809	NHBE	bronchial:	n/a
30	chr17:46663759-46663809	K562	blood:	n/a
31	chr17:46663759-46663809	SKMC	muscle:	n/a
32	chr17:46663759-46663809	H1-hESC	embryonic stem cell:	embryo
33	chr17:46663759-46663809	NH-A	brain:	n/a
34	chr17:46663759-46663809	MCF10A-Er-Src	breast:	n/a
35	chr17:46663759-46663809	HPAEpiC	pulmonary alveolar:	n/a
36	chr17:46663759-46663809	Jurkat	blood:	n/a
37	chr17:46663759-46663809	LNCaP	prostate:	n/a
38	chr17:46663759-46663809	HCM	heart:	n/a
39	chr17:46663759-46663809	SK-N-SH_RA	brain:	n/a
40	chr17:46663759-46663809	BE2_C	brain:	n/a
41	chr17:46663759-46663809	AG09309	skin:	n/a
42	chr17:46663759-46663809	NB4	blood:	n/a
43	chr17:46663759-46663809	Hepatocyte	liver:	n/a
44	chr17:46663759-46663809	GM19239	blood:	n/a
45	chr17:46663759-46663809	HL-60	blood:	n/a
46	chr17:46663759-46663809	ECC-1	luminal epithelium:	n/a
47	chr17:46663759-46663809	SK-N-SH	brain:	n/a
48	chr17:46663759-46663809	NT2-D1	testis:	n/a
49	chr17:46663759-46663809	PrEC	prostate:	n/a
50	chr17:46663759-46663809	AG04449	skin:	fetal

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:46589537..46591935-chr17:46661739..46663956,2	MCF-7	breast:
2	chr17:46639764..46641981-chr17:46663009..46664957,2	MCF-7	breast:
3	chr17:46572626..46574764-chr17:46662731..46664611,2	MCF-7	breast:
4	chr17:46660229..46663792-chr17:46665732..46668852,4	K562	blood:
5	chr17:46530850..46533321-chr17:46662351..46664282,2	K562	blood:
6	chr17:46569545..46570868-chr17:46662367..46663838,14	MCF-7	breast:
7	chr17:46663028..46666157-chr17:46668975..46671535,3	MCF-7	breast:

No data

Variant related genes	Relation type
HOXB-AS3	TF binding region
MIR10A	TF binding region
HOXB3	TF binding region
HOXB-AS3	CpG island
MIR10A	CpG island
HOXB3	CpG island
ENSG00000233101	Chromatin interaction
ENSG00000120093	Chromatin interaction
ENSG00000120075	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs12453445	1.00[AMR][1000 genomes]
rs4793882	1.00[AMR][1000 genomes]
rs4793883	1.00[AMR][1000 genomes]
rs58218522	1.00[AMR][1000 genomes]
rs61648156	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs71377361	1.00[AMR][1000 genomes]
rs73985849	1.00[AMR][1000 genomes]
rs73985851	1.00[AMR][1000 genomes]
rs73985874	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73985882	0.89[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833469	chr17:46491849-46709406	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	349 gene(s)	inside rSNPs	diseases
2	esv3420538	chr17:46504944-46861553	Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	369 gene(s)	inside rSNPs	diseases
3	nsv908577	chr17:46584900-46704536	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	343 gene(s)	inside rSNPs	diseases
4	nsv908578	chr17:46592413-46698710	Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	335 gene(s)	inside rSNPs	diseases
5	nsv908579	chr17:46592413-46727289	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	349 gene(s)	inside rSNPs	diseases
6	nsv532113	chr17:46598247-47588570	Genic enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	453 gene(s)	inside rSNPs	diseases
7	esv2758459	chr17:46602673-46836837	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	364 gene(s)	inside rSNPs	diseases
8	esv2758694	chr17:46602673-46836837	Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	364 gene(s)	inside rSNPs	diseases
9	nsv908580	chr17:46609103-46698710	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	335 gene(s)	inside rSNPs	diseases
10	nsv908581	chr17:46610646-46735520	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	349 gene(s)	inside rSNPs	diseases
11	nsv575480	chr17:46617019-46684929	Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	322 gene(s)	inside rSNPs	diseases
12	nsv908582	chr17:46617019-46698710	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
13	nsv908583	chr17:46617019-46704536	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	342 gene(s)	inside rSNPs	diseases
14	nsv833471	chr17:46617787-46783345	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	356 gene(s)	inside rSNPs	diseases
15	nsv908584	chr17:46618926-46735520	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	348 gene(s)	inside rSNPs	diseases
16	nsv457822	chr17:46620402-46698710	Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
17	nsv575481	chr17:46620402-46698710	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
18	nsv457823	chr17:46620402-46704536	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	342 gene(s)	inside rSNPs	diseases
19	nsv575482	chr17:46620402-46704536	Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	342 gene(s)	inside rSNPs	diseases
20	nsv457824	chr17:46625519-46693491	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	332 gene(s)	inside rSNPs	diseases
21	nsv575483	chr17:46625519-46693491	Flanking Active TSS Bivalent Enhancer Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	332 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:46658800-46665800	Transcr. at gene 5' and 3'	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr17:46661600-46667000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr17:46661800-46663800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr17:46661800-46664000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr17:46662000-46663800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
6	chr17:46662000-46664600	Active TSS	NHDF-Ad	bronchial
7	chr17:46662000-46665200	Active TSS	Colon Smooth Muscle	Colon
8	chr17:46662200-46664000	Active TSS	Fetal Kidney	kidney
9	chr17:46662200-46664000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
10	chr17:46662200-46664000	Active TSS	Right Atrium	heart
11	chr17:46662200-46664200	Active TSS	Rectal Smooth Muscle	rectum
12	chr17:46662400-46663800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr17:46662400-46663800	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
14	chr17:46662400-46663800	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
15	chr17:46662400-46663800	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
16	chr17:46662400-46663800	Active TSS	Psoas Muscle	Psoas
17	chr17:46662400-46664000	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
18	chr17:46662400-46664000	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
19	chr17:46662400-46664000	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr17:46662400-46664000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr17:46662400-46664000	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
22	chr17:46662400-46664000	Flanking Active TSS	Stomach Smooth Muscle	stomach
23	chr17:46662400-46664200	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
24	chr17:46662400-46664200	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
25	chr17:46662400-46664200	Flanking Bivalent TSS/Enh	Fetal Intestine Large	intestine
26	chr17:46662400-46664200	Flanking Active TSS	HUVEC	blood vessel
27	chr17:46662400-46665000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
28	chr17:46662400-46665000	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
29	chr17:46662400-46665600	Flanking Active TSS	Adipose Nuclei	Adipose
30	chr17:46662400-46668000	Flanking Active TSS	Primary hematopoietic stem cells	blood
31	chr17:46662600-46663800	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr17:46662600-46663800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr17:46662600-46664000	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
34	chr17:46662600-46664000	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
35	chr17:46662800-46663800	Flanking Bivalent TSS/Enh	Primary monocytes fromperipheralblood	blood
36	chr17:46662800-46663800	Flanking Bivalent TSS/Enh	Primary B cells from cord blood	blood
37	chr17:46662800-46664000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr17:46662800-46664000	Active TSS	Right Ventricle	heart
39	chr17:46663000-46663800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr17:46663000-46663800	Flanking Bivalent TSS/Enh	Primary T killer naive cells fromperipheralblood	blood
41	chr17:46663000-46663800	Flanking Bivalent TSS/Enh	Liver	Liver
42	chr17:46663000-46663800	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
43	chr17:46663000-46664000	Flanking Bivalent TSS/Enh	Primary T cells from cord blood	blood
44	chr17:46663000-46664000	Flanking Bivalent TSS/Enh	Primary mononuclear cells fromperipheralblood	Blood
45	chr17:46663200-46663800	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
46	chr17:46663200-46663800	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr17:46663200-46663800	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
48	chr17:46663200-46663800	Flanking Bivalent TSS/Enh	Primary T helper memory cells from peripheral blood 2	blood
49	chr17:46663200-46663800	Flanking Bivalent TSS/Enh	Primary T helper memory cells from peripheral blood 1	blood
50	chr17:46663200-46663800	Flanking Bivalent TSS/Enh	Primary Natural Killer cells fromperipheralblood	blood

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