Variant report

Variant	rs9910165
Chromosome Location	chr17:60088707-60088708
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:60004882..60006474-chr17:60088691..60090538,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000108506	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs16945796	0.91[AFR][1000 genomes]
rs17400363	0.81[AFR][1000 genomes]
rs28435233	0.96[AFR][1000 genomes]
rs28442160	0.93[AFR][1000 genomes]
rs58707352	0.85[AFR][1000 genomes]
rs7214601	0.96[AFR][1000 genomes]
rs7219120	0.89[AFR][1000 genomes]
rs7225456	0.80[AFR][1000 genomes]
rs73991963	0.81[AFR][1000 genomes]
rs8076333	0.81[AFR][1000 genomes]
rs9747362	1.00[AFR][1000 genomes]
rs9889643	0.89[AFR][1000 genomes]
rs9892441	0.80[AFR][1000 genomes]
rs9893675	0.96[AFR][1000 genomes]
rs9904797	0.89[AFR][1000 genomes]
rs9905198	0.93[AFR][1000 genomes]
rs9905273	0.81[AFR][1000 genomes]
rs9907648	0.84[AFR][1000 genomes]
rs9909731	0.93[AFR][1000 genomes]
rs9912291	0.98[AFR][1000 genomes]
rs9915402	0.88[AFR][1000 genomes]
rs9916776	0.96[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3378293	chr17:59744117-60124899	ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	175 gene(s)	inside rSNPs	diseases
2	nsv916786	chr17:59890834-60103687	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	116 gene(s)	inside rSNPs	diseases
3	nsv1062816	chr17:60074670-60470465	Strong transcription Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
4	esv2753884	chr17:60077852-60190630	Strong transcription Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
5	esv2755037	chr17:60086508-60386211	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:60021200-60097000	Strong transcription	Dnd41	blood
2	chr17:60025400-60107600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr17:60033000-60128400	Weak transcription	Stomach Mucosa	stomach
4	chr17:60042800-60105200	Weak transcription	Psoas Muscle	Psoas
5	chr17:60048800-60097600	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr17:60050200-60100800	Weak transcription	Small Intestine	intestine
7	chr17:60060400-60090600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr17:60060400-60096200	Weak transcription	Fetal Brain Male	brain
9	chr17:60060400-60098800	Weak transcription	Gastric	stomach
10	chr17:60060400-60099800	Weak transcription	Aorta	Aorta
11	chr17:60061600-60099600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr17:60062400-60106800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr17:60069200-60107600	Weak transcription	Spleen	Spleen
14	chr17:60069600-60099000	Weak transcription	Colonic Mucosa	Colon
15	chr17:60072400-60100600	Weak transcription	Right Ventricle	heart
16	chr17:60074600-60123800	Weak transcription	Right Atrium	heart
17	chr17:60075000-60092800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr17:60075800-60114400	Strong transcription	Primary monocytes fromperipheralblood	blood
19	chr17:60077200-60136800	Strong transcription	Fetal Thymus	thymus
20	chr17:60077800-60099800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
21	chr17:60079800-60094000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr17:60080000-60093200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr17:60080000-60094000	Strong transcription	GM12878-XiMat	blood
24	chr17:60080200-60099000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr17:60081200-60093000	Strong transcription	Placenta	Placenta
26	chr17:60081400-60096400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr17:60081600-60090600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr17:60081800-60091600	Strong transcription	Primary neutrophils fromperipheralblood	blood
29	chr17:60081800-60093200	Strong transcription	Duodenum Mucosa	Duodenum
30	chr17:60081800-60111600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
31	chr17:60082000-60096200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr17:60082600-60093000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr17:60083400-60098800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr17:60083600-60096400	Weak transcription	Brain Germinal Matrix	brain
35	chr17:60084600-60099000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr17:60085200-60092800	Strong transcription	Fetal Lung	lung
37	chr17:60085600-60089200	Strong transcription	Primary T cells fromperipheralblood	blood
38	chr17:60085600-60089600	Strong transcription	Osteobl	bone
39	chr17:60085800-60088800	Strong transcription	Primary B cells from cord blood	blood
40	chr17:60085800-60088800	Strong transcription	HSMM	muscle
41	chr17:60085800-60089000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr17:60085800-60089200	Strong transcription	H1 Cell Line	embryonic stem cell
43	chr17:60085800-60089400	Strong transcription	Muscle Satellite Cultured Cells	--
44	chr17:60085800-60091000	Strong transcription	Primary T helper cells fromperipheralblood	blood
45	chr17:60085800-60092400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
46	chr17:60085800-60092800	Strong transcription	HUES6 Cell Line	embryonic stem cell
47	chr17:60085800-60093000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
48	chr17:60086000-60096600	Strong transcription	HepG2	liver
49	chr17:60086200-60089200	Strong transcription	Rectal Mucosa Donor 31	rectum
50	chr17:60086200-60092200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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