Variant report

Variant	rs67128646
Chromosome Location	chr16:30672097-30672098
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:62)
CpG islands
(count:61)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:62 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr16:30671057-30673269	GM12878	blood:	n/a	n/a
2	POLR2A	chr16:30671780-30672558	GM12892	blood:	n/a	n/a
3	RELA	chr16:30671981-30672426	GM18951	blood:	n/a	n/a
4	RELA	chr16:30671084-30672399	GM15510	blood:	n/a	chr16:30671327-30671336 chr16:30671327-30671336
5	EBF1	chr16:30671174-30672351	GM12878	blood:	n/a	chr16:30671470-30671480 chr16:30671470-30671479 chr16:30671469-30671480
6	POLR2A	chr16:30668106-30672800	GM12892	blood:	n/a	n/a
7	STAT5A	chr16:30671955-30672372	GM12878	blood:	n/a	n/a
8	ATF2	chr16:30671633-30672435	GM12878	blood:	n/a	n/a
9	POLR2A	chr16:30671843-30672941	GM12891	blood:	n/a	n/a
10	YY1	chr16:30671942-30672374	GM12878	blood:	n/a	n/a
11	POLR2A	chr16:30672076-30672116	HUVEC	blood vessel:	n/a	n/a
12	POLR2A	chr16:30672091-30672142	Raji	blood:	n/a	n/a
13	POLR2A	chr16:30671116-30672496	GM12891	blood:	n/a	n/a
14	SP1	chr16:30671931-30672416	GM12878	blood:	n/a	n/a
15	POLR2A	chr16:30671721-30672532	GM12891	blood:	n/a	n/a
16	RELA	chr16:30671779-30672451	GM12878	blood:	n/a	n/a
17	ELF1	chr16:30671924-30672440	GM12878	blood:	n/a	n/a
18	POLR2A	chr16:30668198-30673294	GM12878	blood:	n/a	n/a
19	SPI1	chr16:30672030-30672250	GM12878	blood:	n/a	n/a
20	MTA3	chr16:30671719-30672794	GM12878	blood:	n/a	n/a
21	SPI1	chr16:30672015-30672302	GM12891	blood:	n/a	n/a
22	RELA	chr16:30671092-30672581	GM12891	blood:	n/a	chr16:30671327-30671336 chr16:30671327-30671336
23	RELA	chr16:30671793-30672413	GM10847	blood:	n/a	n/a
24	WRNIP1	chr16:30671897-30673073	GM12878	blood:	n/a	n/a
25	FOXM1	chr16:30671761-30672453	GM12878	blood:	n/a	n/a
26	PML	chr16:30671990-30672334	GM12878	blood:	n/a	n/a
27	NFIC	chr16:30671222-30672417	GM12878	blood:	n/a	n/a
28	POLR2A	chr16:30670859-30672818	GM12892	blood:	n/a	n/a
29	BCLAF1	chr16:30671930-30672532	GM12878	blood:	n/a	n/a
30	YY1	chr16:30671986-30672328	GM12878	blood:	n/a	n/a
31	RELA	chr16:30671148-30672680	GM19193	blood:	n/a	chr16:30671327-30671336 chr16:30671327-30671336
32	TAF1	chr16:30672008-30672244	GM12892	blood:	n/a	n/a
33	MAZ	chr16:30668538-30672392	IMR90	lung:	n/a	chr16:30670803-30670813 chr16:30670487-30670497 chr16:30669313-30669322
34	RCOR1	chr16:30671813-30672370	GM12878	blood:	n/a	n/a
35	TAF1	chr16:30671949-30672309	GM12878	blood:	n/a	n/a
36	RELA	chr16:30671857-30672448	GM19099	blood:	n/a	n/a
37	HCFC1	chr16:30668484-30672437	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr16:30672007-30672360	GM12878	blood:	n/a	n/a
39	POLR2A	chr16:30671969-30672820	GM12878	blood:	n/a	n/a
40	POLR2A	chr16:30671754-30672502	GM12891	blood:	n/a	n/a
41	RUNX3	chr16:30671577-30672456	GM12878	blood:	n/a	n/a
42	RELA	chr16:30671870-30672443	GM18505	blood:	n/a	n/a
43	NFIC	chr16:30671820-30672386	GM12878	blood:	n/a	n/a
44	PML	chr16:30670907-30672906	GM12878	blood:	n/a	n/a
45	POLR2A	chr16:30671801-30672306	GM12891	blood:	n/a	n/a
46	MXI1	chr16:30671917-30672380	GM12878	blood:	n/a	n/a
47	CHD1	chr16:30668947-30672210	GM12878	blood:	n/a	chr16:30670030-30670037 chr16:30670024-30670034
48	POLR2A	chr16:30671938-30672405	GM12892	blood:	n/a	n/a
49	EP300	chr16:30671807-30672336	GM12878	blood:	n/a	n/a
50	BHLHE40	chr16:30671852-30672346	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:30672051-30672101	LNCaP	prostate:	n/a
2	chr16:30672051-30672101	HCPEpiC	choroid plexus:	n/a
3	chr16:30672051-30672101	ECC-1	luminal epithelium:	n/a
4	chr16:30672051-30672101	NH-A	brain:	n/a
5	chr16:30672051-30672101	HPAEpiC	pulmonary alveolar:	n/a
6	chr16:30672051-30672101	NB4	blood:	n/a
7	chr16:30672051-30672101	HCF	heart:	n/a
8	chr16:30672051-30672101	Jurkat	blood:	n/a
9	chr16:30672051-30672101	HRE	kidney:	n/a
10	chr16:30672051-30672101	BJ	skin:	n/a
11	chr16:30672051-30672101	GM12891	blood:	n/a
12	chr16:30672051-30672101	AG04450	lung:	fetal
13	chr16:30672051-30672101	HUVEC	blood vessel:	n/a
14	chr16:30672051-30672101	SK-N-SH	brain:	n/a
15	chr16:30672051-30672101	GM12878	blood:	n/a
16	chr16:30672051-30672101	PANC-1	pancreas:	n/a
17	chr16:30672051-30672101	A549	lung:	n/a
18	chr16:30672051-30672101	Hepatocyte	liver:	n/a
19	chr16:30672051-30672101	IMR90	lung:	fetal
20	chr16:30672051-30672101	K562	blood:	n/a
21	chr16:30672051-30672101	HRCEpiC	kidney:	n/a
22	chr16:30672051-30672101	U87	brain:	n/a
23	chr16:30672051-30672101	HNPCEpiC	eye:	n/a
24	chr16:30672051-30672101	GM12892	blood:	n/a
25	chr16:30672051-30672101	AG04449	skin:	fetal
26	chr16:30672051-30672101	NHBE	bronchial:	n/a
27	chr16:30672051-30672101	ProgFib	skin:	n/a
28	chr16:30672051-30672101	HEEpiC	esophagus:	n/a
29	chr16:30672051-30672101	GM06990	blood:	n/a
30	chr16:30672051-30672101	H1-hESC	embryonic stem cell:	embryo
31	chr16:30672051-30672101	HAEpiC	amniotic membrane:	n/a
32	chr16:30672051-30672101	Hela-S3	cervix:	n/a
33	chr16:30672051-30672101	CMK	blood:	n/a
34	chr16:30672051-30672101	SK-N-SH_RA	brain:	n/a
35	chr16:30672051-30672101	AG09309	skin:	n/a
36	chr16:30672051-30672101	GM19239	blood:	n/a
37	chr16:30672051-30672101	Caco-2	colon:	n/a
38	chr16:30672051-30672101	NHDF-neo	bronchial:	n/a
39	chr16:30672051-30672101	HCT-116	colon:	n/a
40	chr16:30672051-30672101	HCM	heart:	n/a
41	chr16:30672051-30672101	SKMC	muscle:	n/a
42	chr16:30672051-30672101	HRPEpiC	eye:	n/a
43	chr16:30672051-30672101	MCF10A-Er-Src	breast:	n/a
44	chr16:30672051-30672101	HepG2	liver:	n/a
45	chr16:30672051-30672101	HL-60	blood:	n/a
46	chr16:30672051-30672101	PFSK-1	brain:	n/a
47	chr16:30672051-30672101	AoSMC	blood vessel:	n/a
48	chr16:30672051-30672101	NT2-D1	testis:	n/a
49	chr16:30672051-30672101	AG09319	gingival:	n/a
50	chr16:30672051-30672101	SAEC	small airway:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:30669436..30672389-chr17:73774530..73776217,2	MCF-7	breast:
2	chr16:30534881..30538738-chr16:30669014..30672874,5	MCF-7	breast:
3	chr16:30665738..30673826-chr16:30707321..30713630,33	K562	blood:
4	chr16:30581261..30583067-chr16:30670889..30672636,2	K562	blood:
5	chr16:30665347..30684079-chr16:30697204..30714344,66	MCF-7	breast:
6	chr16:30669272..30672997-chr16:30933501..30936286,4	MCF-7	breast:
7	chr16:30671278..30673717-chr16:30785023..30788710,4	MCF-7	breast:
8	chr16:30670863..30673913-chr16:30759873..30762559,3	MCF-7	breast:
9	chr16:30669616..30672714-chr16:30750078..30754286,5	MCF-7	breast:
10	chr16:30455687..30457449-chr16:30670431..30673736,3	MCF-7	breast:
11	chr16:30581724..30584025-chr16:30669136..30672320,3	MCF-7	breast:
12	chr16:30667507..30674392-chr16:30704170..30712522,40	MCF-7	breast:
13	chr16:30671487..30673418-chr16:30969039..30970586,2	K562	blood:
14	chr16:30667783..30674540-chr16:30707310..30714065,38	K562	blood:
15	chr16:30670901..30672764-chr20:45946982..45948705,2	MCF-7	breast:
16	chr16:30670913..30673780-chr16:30684113..30687198,4	MCF-7	breast:
17	chr16:30455343..30457757-chr16:30668968..30672214,3	MCF-7	breast:
18	chr16:30404931..30406633-chr16:30670446..30672250,2	MCF-7	breast:
19	chr16:30635973..30637940-chr16:30671557..30674235,2	MCF-7	breast:

No data

Variant related genes	Relation type
FBRS	TF binding region
FBRS	CpG island
ENSG00000132475	Chromatin interaction
ENSG00000179918	Chromatin interaction
ENSG00000261840	Chromatin interaction
ENSG00000180035	Chromatin interaction
ENSG00000239791	Chromatin interaction
ENSG00000101040	Chromatin interaction
ENSG00000080603	Chromatin interaction
ENSG00000099364	Chromatin interaction
ENSG00000260852	Chromatin interaction
ENSG00000169957	Chromatin interaction
ENSG00000103549	Chromatin interaction
ENSG00000267882	Chromatin interaction
ENSG00000099381	Chromatin interaction
ENSG00000222287	Chromatin interaction
ENSG00000229809	Chromatin interaction
ENSG00000261680	Chromatin interaction
ENSG00000260899	Chromatin interaction
ENSG00000156873	Chromatin interaction
ENSG00000252074	Chromatin interaction
ENSG00000180096	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs13338946	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2289442	0.80[EUR][1000 genomes]
rs35629860	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35969813	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3747481	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4616297	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs67456513	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7187359	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7197770	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7204278	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8048448	0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8051050	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8055315	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8055661	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8058578	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8058928	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs885107	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1062456	chr16:30442166-31253997	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	437 gene(s)	inside rSNPs	diseases
2	nsv542898	chr16:30442166-31253997	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	437 gene(s)	inside rSNPs	diseases
3	nsv905727	chr16:30564526-30689696	Active TSS Flanking Active TSS Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
4	nsv469724	chr16:30632445-30840263	Strong transcription Transcr. at gene 5' and 3' Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	143 gene(s)	inside rSNPs	diseases
5	nsv482704	chr16:30632445-30840263	Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	143 gene(s)	inside rSNPs	diseases
6	nsv833188	chr16:30632446-30840263	Active TSS Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	143 gene(s)	inside rSNPs	diseases
7	nsv1064134	chr16:30640293-31087327	Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	238 gene(s)	inside rSNPs	diseases
8	nsv905728	chr16:30642867-30928970	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	171 gene(s)	inside rSNPs	diseases
9	nsv905729	chr16:30642867-31247924	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	387 gene(s)	inside rSNPs	diseases
10	nsv905730	chr16:30667031-30681816	Genic enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
11	nsv905731	chr16:30667031-30685089	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
12	esv1825223	chr16:30669091-30971810	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
13	esv3506214	chr16:30670001-30672099	Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	46 gene(s)	inside rSNPs	diseases
14	esv3506215	chr16:30670001-30672099	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	46 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:30668600-30672800	Active TSS	Pancreatic Islets	Pancreatic Islet
2	chr16:30669000-30672200	Active TSS	Esophagus	oesophagus
3	chr16:30669000-30672200	Active TSS	Small Intestine	intestine
4	chr16:30669200-30672200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr16:30669200-30672200	Active TSS	GM12878-XiMat	blood
6	chr16:30669600-30672200	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
7	chr16:30669800-30672400	Active TSS	Ovary	ovary
8	chr16:30669800-30674000	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
9	chr16:30670800-30672600	Flanking Active TSS	Primary hematopoietic stem cells	blood
10	chr16:30671000-30672200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
11	chr16:30671000-30672200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
12	chr16:30671000-30672400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr16:30671000-30672400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr16:30671200-30672200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
15	chr16:30671200-30672200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
16	chr16:30671200-30672200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr16:30671200-30672400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr16:30671200-30672400	Flanking Active TSS	Adipose Nuclei	Adipose
19	chr16:30671200-30672400	Flanking Active TSS	Liver	Liver
20	chr16:30671200-30672400	Flanking Active TSS	Brain Germinal Matrix	brain
21	chr16:30671200-30672400	Transcr. at gene 5' and 3'	Fetal Lung	lung
22	chr16:30671200-30672400	Transcr. at gene 5' and 3'	Fetal Stomach	stomach
23	chr16:30671200-30672400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
24	chr16:30671200-30672400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
25	chr16:30671200-30672600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
26	chr16:30671200-30672600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
27	chr16:30671200-30672800	Transcr. at gene 5' and 3'	Rectal Mucosa Donor 31	rectum
28	chr16:30671200-30672800	Transcr. at gene 5' and 3'	Dnd41	blood
29	chr16:30671200-30673400	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
30	chr16:30671200-30673400	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
31	chr16:30671200-30674200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr16:30671400-30672200	Flanking Active TSS	Psoas Muscle	Psoas
33	chr16:30671400-30672400	Flanking Active TSS	Colonic Mucosa	Colon
34	chr16:30671400-30672600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr16:30671400-30672600	Flanking Active TSS	Duodenum Mucosa	Duodenum
36	chr16:30671400-30672800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
37	chr16:30671400-30672800	Transcr. at gene 5' and 3'	Skeletal Muscle Male	skeletal muscle
38	chr16:30671400-30673400	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
39	chr16:30671600-30672200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr16:30671600-30672200	Transcr. at gene 5' and 3'	Fetal Muscle Leg	muscle
41	chr16:30671600-30672200	Flanking Active TSS	Right Ventricle	heart
42	chr16:30671600-30672200	Flanking Active TSS	Spleen	Spleen
43	chr16:30671600-30672200	Flanking Active TSS	Osteobl	bone
44	chr16:30671600-30672600	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr16:30671600-30672600	Flanking Active TSS	Brain Substantia Nigra	brain
46	chr16:30671600-30672600	Flanking Active TSS	Colon Smooth Muscle	Colon
47	chr16:30671600-30672600	Flanking Active TSS	Hela-S3	cervix
48	chr16:30671600-30672800	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr16:30671600-30672800	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
50	chr16:30671600-30672800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood

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