Variant report

Variant	rs1296023
Chromosome Location	chr8:11726817-11726818
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2)
CpG islands
(count:0)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ZNF384	chr8:11726797-11727404	K562	blood:	n/a	n/a
2	POLR2A	chr8:11720772-11734387	K562	blood:	n/a	n/a

No data

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:11625866..11628884-chr8:11724599..11727626,3	MCF-7	breast:
2	chr8:11706290..11708186-chr8:11724044..11726922,3	MCF-7	breast:
3	chr8:11659426..11661474-chr8:11724613..11726870,3	MCF-7	breast:
4	chr8:11710197..11714536-chr8:11724997..11727273,4	K562	blood:
5	chr8:11708512..11715317-chr8:11723234..11727095,9	MCF-7	breast:

No data

Variant related genes	Relation type
CTSB	TF binding region
ENSG00000164733	Chromatin interaction
ENSG00000154328	Chromatin interaction
ENSG00000255046	Chromatin interaction
ENSG00000079459	Chromatin interaction

Extended variants
information (count: 76 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs1293303	0.82[CHB][hapmap];0.88[CHD][hapmap]
rs1293306	0.86[CHB][hapmap]
rs1293309	0.89[CEU][hapmap];0.82[CHB][hapmap];0.91[JPT][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1293310	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1293311	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1293312	0.86[ASN][1000 genomes]
rs1296022	0.88[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs1297511	0.82[ASN][1000 genomes]
rs1299525	0.82[CHB][hapmap];0.86[CHD][hapmap];0.86[ASN][1000 genomes]
rs1619003	0.89[CEU][hapmap];0.86[CHB][hapmap];0.81[CHD][hapmap];0.82[GIH][hapmap];0.91[JPT][hapmap];0.89[TSI][hapmap];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1619200	0.89[CEU][hapmap];0.81[GIH][hapmap];0.91[JPT][hapmap];0.84[TSI][hapmap];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1620833	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1624088	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1630950	0.80[JPT][hapmap]
rs1692791	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1692803	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1692804	0.91[CHB][hapmap];0.81[CHD][hapmap];0.82[JPT][hapmap];0.90[ASN][1000 genomes]
rs1692807	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1692808	0.89[CEU][hapmap];0.82[CHB][hapmap];0.91[JPT][hapmap];0.89[TSI][hapmap];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1736117	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1736118	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1736119	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1736120	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1736121	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2250903	0.89[CEU][hapmap];0.86[CHB][hapmap];0.82[GIH][hapmap];0.91[JPT][hapmap];0.89[TSI][hapmap];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2472430	0.86[EUR][1000 genomes]
rs2645412	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2645415	0.86[CHB][hapmap];0.91[CHD][hapmap];0.91[MEX][hapmap];0.83[ASN][1000 genomes]
rs2740596	0.94[ASN][1000 genomes]
rs2740597	0.95[CHB][hapmap];0.93[CHD][hapmap];0.91[JPT][hapmap];0.92[ASN][1000 genomes]
rs2740600	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2740601	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2740602	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3104255	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3116070	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3116071	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6980952	0.82[CHD][hapmap]
rs7828791	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7844154	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs904016	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs904017	0.89[CEU][hapmap];0.86[CHB][hapmap];0.84[CHD][hapmap];0.87[JPT][hapmap];0.89[TSI][hapmap];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs966785	0.89[JPT][hapmap];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs966786	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs966787	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:32 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529399	chr8:10970091-11805960	Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
2	nsv1018978	chr8:11438267-11858466	Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv917963	chr8:11540723-11751798	Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
4	nsv1027378	chr8:11541739-11858466	Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
5	nsv1028229	chr8:11575762-11805961	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS 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 target site	23 gene(s)	inside rSNPs	diseases
6	nsv539475	chr8:11575762-11805961	Flanking Active TSS Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
7	nsv428514	chr8:11580381-11765706	Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
8	nsv1034014	chr8:11602337-11858466	Enhancers Active TSS Strong transcription Weak transcription Genic enhancers Flanking Active TSS 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	26 gene(s)	inside rSNPs	diseases
9	nsv890361	chr8:11625808-11755513	Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
10	nsv890362	chr8:11625808-11771089	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
11	nsv1034132	chr8:11657033-12198242	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
12	nsv890365	chr8:11666451-11735641	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
13	nsv890366	chr8:11666451-11900847	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
14	nsv1031158	chr8:11666558-11759064	Bivalent Enhancer Active TSS Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
15	nsv539477	chr8:11666558-11759064	Enhancers Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
16	nsv1018042	chr8:11667496-11882385	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
17	nsv890367	chr8:11668153-11793529	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
18	nsv890369	chr8:11671041-11840011	Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
19	nsv1016952	chr8:11679271-11849955	Flanking Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
20	nsv1029093	chr8:11679271-11858466	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
21	nsv539478	chr8:11679271-11858466	Bivalent/Poised TSS Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
22	nsv1017334	chr8:11688534-11732949	Enhancers Active TSS Genic enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
23	nsv539479	chr8:11688534-11732949	Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
24	nsv1019738	chr8:11696393-11732949	Flanking Active TSS Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
25	nsv539480	chr8:11696393-11732949	Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
26	nsv1031972	chr8:11696393-11805961	Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
27	nsv539481	chr8:11696393-11805961	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
28	esv34042	chr8:11698337-11726817	Genic enhancers Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
29	nsv610293	chr8:11698747-11929734	Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
30	nsv516685	chr8:11698747-12570199	Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	74 gene(s)	inside rSNPs	diseases
31	esv3409280	chr8:11724368-11727116	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
32	esv3375446	chr8:11724743-11727091	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs1296023	CTSB	cis	multi-tissue	Pritchard
rs1296023	CTSB	cis	cerebellum	SCAN
rs1296023	TDH	cis	cerebellum	SCAN

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11724000-11727400	Active TSS	Rectal Smooth Muscle	rectum
2	chr8:11724600-11727000	Active TSS	Duodenum Mucosa	Duodenum
3	chr8:11725600-11734600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr8:11726200-11731600	Weak transcription	Dnd41	blood
5	chr8:11726400-11727400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr8:11726400-11727400	Weak transcription	Adipose Nuclei	Adipose
7	chr8:11726400-11727600	Enhancers	Fetal Intestine Small	intestine
8	chr8:11726400-11729400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr8:11726400-11729600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr8:11726400-11729600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr8:11726400-11729600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr8:11726400-11729600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr8:11726400-11729600	Weak transcription	Brain Cingulate Gyrus	brain
14	chr8:11726400-11729600	Weak transcription	NHDF-Ad	bronchial
15	chr8:11726400-11729600	Weak transcription	Osteobl	bone
16	chr8:11726400-11729800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr8:11726400-11730200	Weak transcription	Fetal Muscle Leg	muscle
18	chr8:11726400-11731200	Weak transcription	HMEC	breast
19	chr8:11726400-11731200	Weak transcription	NHEK	skin
20	chr8:11726400-11731800	Weak transcription	Primary B cells from peripheral blood	blood
21	chr8:11726400-11731800	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr8:11726400-11731800	Weak transcription	GM12878-XiMat	blood
23	chr8:11726400-11731800	Weak transcription	NH-A	brain
24	chr8:11726400-11732000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr8:11726400-11732000	Weak transcription	HSMM	muscle
26	chr8:11726400-11732600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr8:11726400-11734600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr8:11726400-11734800	Weak transcription	Esophagus	oesophagus
29	chr8:11726400-11735200	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr8:11726400-11735200	Weak transcription	Right Ventricle	heart
31	chr8:11726600-11727400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr8:11726600-11727400	Enhancers	A549	lung
33	chr8:11726600-11729400	Weak transcription	Primary monocytes fromperipheralblood	blood
34	chr8:11726600-11729600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
35	chr8:11726600-11729600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr8:11726600-11729600	Weak transcription	Monocytes-CD14+_RO01746	blood
37	chr8:11726600-11729800	Weak transcription	Fetal Intestine Large	intestine
38	chr8:11726600-11731200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr8:11726600-11731800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr8:11726600-11731800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr8:11726600-11731800	Weak transcription	HUVEC	blood vessel
42	chr8:11726600-11732000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr8:11726600-11732000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr8:11726600-11732000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr8:11726600-11732000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr8:11726600-11734200	Weak transcription	Lung	lung
47	chr8:11726600-11736400	Weak transcription	Spleen	Spleen
48	chr8:11726800-11727200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr8:11726800-11727200	Active TSS	HepG2	liver
50	chr8:11726800-11727400	Enhancers	Placenta	Placenta

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