Variant report

Variant	rs10982358
Chromosome Location	chr9:117416112-117416113
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:21)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:117416002..117416888-chr9:117423842..117425020,4	K562	blood:
2	chr9:117373715..117375270-chr9:117414882..117416697,2	K562	blood:
3	chr9:117270094..117270690-chr9:117415535..117416447,3	MCF-7	breast:
4	chr9:117266287..117267144-chr9:117415499..117416200,3	K562	blood:
5	chr9:117167847..117168465-chr9:117415767..117416282,2	MCF-7	breast:
6	chr9:117348713..117353392-chr9:117414408..117416676,6	MCF-7	breast:
7	chr9:117349947..117351922-chr9:117414743..117417101,2	MCF-7	breast:
8	chr9:117249626..117250546-chr9:117415527..117416432,3	MCF-7	breast:
9	chr9:117194841..117195813-chr9:117415726..117416281,2	K562	blood:
10	chr9:117249656..117250225-chr9:117415559..117416512,3	MCF-7	breast:
11	chr9:117354258..117355182-chr9:117415580..117416309,2	MCF-7	breast:
12	chr9:117101434..117102012-chr9:117415923..117416790,3	K562	blood:
13	chr9:117166499..117167106-chr9:117415943..117416523,2	K562	blood:
14	chr9:117300529..117301254-chr9:117415850..117416693,4	MCF-7	breast:
15	chr9:117372175..117375270-chr9:117412558..117416382,3	K562	blood:
16	chr9:117373194..117375222-chr9:117413423..117416291,4	MCF-7	breast:
17	chr9:117196796..117197719-chr9:117415530..117416633,5	MCF-7	breast:
18	chr9:117257498..117260270-chr9:117415668..117417413,2	K562	blood:
19	chr9:117415926..117417563-chr9:117422296..117424202,2	K562	blood:
20	chr9:117196733..117197724-chr9:117415399..117416903,8	K562	blood:
21	chr9:117249999..117250545-chr9:117415690..117416258,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000095397	Chromatin interaction
ENSG00000157693	Chromatin interaction
ENSG00000136888	Chromatin interaction
ENSG00000230054	Chromatin interaction

Extended variants
information (count: 79 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs1055110	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1058278	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1058280	0.87[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10759728	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.89[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10759729	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10817652	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10817653	0.96[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10817654	0.96[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10817656	0.96[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10817659	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10817660	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][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]
rs10817661	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10982343	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs10982344	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs10982345	0.87[CHB][hapmap];0.93[JPT][hapmap];0.89[ASN][1000 genomes]
rs10982346	0.89[ASN][1000 genomes]
rs10982347	0.89[ASN][1000 genomes]
rs10982351	0.93[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10982353	0.96[AFR][1000 genomes];0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10982354	0.96[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10982355	0.96[AFR][1000 genomes];0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10982361	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10982362	0.93[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs12004578	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12115252	0.88[YRI][hapmap]
rs12686294	0.84[ASN][1000 genomes]
rs16930445	0.93[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs1811141	0.84[ASN][1000 genomes]
rs1887784	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2183018	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2274598	0.93[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs34202085	0.93[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34376344	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3810935	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs4615654	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap]
rs56765969	0.84[ASN][1000 genomes]
rs59422754	0.84[ASN][1000 genomes]
rs59962384	0.89[ASN][1000 genomes]
rs60387901	0.85[ASN][1000 genomes]
rs62579685	0.93[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62579686	0.93[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62579731	0.96[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7027937	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7028121	0.93[JPT][hapmap];0.81[EUR][1000 genomes]
rs7041824	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7043739	0.84[CEU][hapmap]
rs752858	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][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]
rs756015	0.81[CHB][hapmap];0.93[JPT][hapmap];0.85[ASN][1000 genomes]
rs7855505	0.89[ASN][1000 genomes]
rs7857127	0.84[ASN][1000 genomes]
rs7857224	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7866902	0.93[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs7870135	0.85[ASN][1000 genomes]
rs9775036	0.82[ASN][1000 genomes]
rs9775041	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9775854	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051544	chr9:116944940-117443031	ZNF genes & repeats Genic enhancers Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
2	nsv540203	chr9:116944940-117443031	Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
3	nsv1048093	chr9:116945025-117456210	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
4	nsv1050991	chr9:116953739-117442999	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
5	nsv1046311	chr9:116953739-117447142	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
6	nsv1052877	chr9:116953739-117456210	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
7	nsv1039681	chr9:116953739-117457158	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
8	nsv1051987	chr9:116955841-117453668	Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
9	nsv1044374	chr9:116955841-117460150	Genic enhancers Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
10	nsv466534	chr9:116956268-117455810	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
11	nsv615234	chr9:116956268-117455810	Enhancers Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS 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	157 gene(s)	inside rSNPs	diseases
12	nsv1048817	chr9:116957958-117456210	Flanking Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
13	nsv615236	chr9:116958144-117455810	Strong transcription Genic enhancers Enhancers Weak transcription Flanking Active TSS 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 miRNA target site	157 gene(s)	inside rSNPs	diseases
14	nsv466535	chr9:116958144-117456175	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
15	nsv615237	chr9:116958144-117456175	Strong transcription Active TSS Genic enhancers Enhancers Weak transcription Bivalent/Poised TSS Flanking Active 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 miRNA target site	157 gene(s)	inside rSNPs	diseases
16	nsv615238	chr9:116958144-117458475	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats 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 miRNA target site	157 gene(s)	inside rSNPs	diseases
17	nsv430094	chr9:116958446-117456446	Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
18	nsv1053756	chr9:116975934-117443031	Enhancers Genic enhancers Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
19	nsv540204	chr9:116975934-117443031	Genic enhancers Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
20	nsv530951	chr9:117032675-117439804	Flanking Active TSS Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
21	nsv831694	chr9:117328640-117502785	Flanking Active TSS Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer 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	30 gene(s)	inside rSNPs	diseases
22	nsv893766	chr9:117385992-117516418	Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
23	nsv615249	chr9:117394595-117424855	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:117405800-117423800	Weak transcription	Fetal Intestine Small	intestine
2	chr9:117406800-117419600	Weak transcription	Pancreas	Pancrea
3	chr9:117407000-117418200	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr9:117407000-117423200	Weak transcription	Fetal Brain Female	brain
5	chr9:117407000-117423400	Weak transcription	Ovary	ovary
6	chr9:117407800-117420600	Weak transcription	Spleen	Spleen
7	chr9:117408200-117423000	Weak transcription	Brain Germinal Matrix	brain
8	chr9:117408400-117418600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr9:117408600-117420000	Weak transcription	Lung	lung
10	chr9:117408600-117420600	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr9:117410000-117418200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr9:117410200-117418200	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr9:117414200-117416200	Enhancers	Fetal Thymus	thymus
14	chr9:117414200-117416400	Enhancers	GM12878-XiMat	blood
15	chr9:117414400-117416400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
16	chr9:117414400-117416400	Enhancers	Primary T helper cells PMA-I stimulated	--
17	chr9:117414400-117416400	Enhancers	Primary T helper cells fromperipheralblood	blood
18	chr9:117414400-117416600	Enhancers	Primary B cells from peripheral blood	blood
19	chr9:117414600-117416200	Enhancers	Primary T cells fromperipheralblood	blood
20	chr9:117414600-117416200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
21	chr9:117414600-117416400	Enhancers	Primary T helper naive cells from peripheral blood	blood
22	chr9:117414600-117416400	Enhancers	Primary T killer memory cells from peripheral blood	blood
23	chr9:117414600-117416400	Enhancers	NHDF-Ad	bronchial
24	chr9:117414800-117416200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr9:117414800-117416200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr9:117415200-117416200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
27	chr9:117415600-117416200	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr9:117415600-117416200	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr9:117415600-117416200	Enhancers	Primary hematopoietic stem cells	blood
30	chr9:117415600-117416200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
31	chr9:117415600-117416200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr9:117415600-117416200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
33	chr9:117415600-117416200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr9:117415600-117416200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr9:117415600-117416200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr9:117415600-117416200	Enhancers	Adipose Nuclei	Adipose
37	chr9:117415600-117416200	Enhancers	Brain Hippocampus Middle	brain
38	chr9:117415600-117416200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
39	chr9:117415600-117416200	Enhancers	Brain Substantia Nigra	brain
40	chr9:117415600-117416200	Enhancers	Fetal Muscle Leg	muscle
41	chr9:117415600-117416200	Enhancers	Fetal Stomach	stomach
42	chr9:117415600-117416200	Enhancers	Hela-S3	cervix
43	chr9:117415600-117416400	Enhancers	Primary B cells from cord blood	blood
44	chr9:117415600-117416400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
45	chr9:117415600-117416400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr9:117415600-117416400	Enhancers	Brain Inferior Temporal Lobe	brain
47	chr9:117415600-117416400	Enhancers	Stomach Smooth Muscle	stomach
48	chr9:117415600-117416400	Enhancers	K562	blood
49	chr9:117415800-117416200	Enhancers	Liver	Liver
50	chr9:117415800-117416400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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