Variant report

Variant	rs569114226
Chromosome Location	chr17:45164712-45164713
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr17:45155821..45158287-chr17:45163734..45167832,3	K562	blood:
2	chr17:45163760..45166072-chr17:45166357..45168655,2	K562	blood:
3	chr17:45159211..45163683-chr17:45163741..45168313,5	K562	blood:
4	chr17:45156502..45159050-chr17:45162212..45165184,2	K562	blood:

Extended variants
information (count: 14 )
Associated
traits (count: 0)

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	esv3502492	chr17:44305975-45169159	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
2	esv3502493	chr17:44305975-45169159	Active TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
3	nsv833466	chr17:45020360-45204537	Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv1062983	chr17:45030095-45789543	Strong transcription Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
5	nsv833467	chr17:45063935-45252624	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer 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
6	nsv522797	chr17:45084279-45183152	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
7	esv3332795	chr17:45116212-45209297	Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers 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	13 gene(s)	inside rSNPs	diseases
8	esv3386521	chr17:45116232-45209267	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
9	esv21010	chr17:45125753-45177221	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
10	nsv1059766	chr17:45130765-45203468	Flanking Active TSS Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Genic enhancers 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	9 gene(s)	inside rSNPs	diseases
11	esv2760450	chr17:45130777-45225222	Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
12	nsv521632	chr17:45151549-45196190	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
13	nsv908563	chr17:45158537-45230311	ZNF genes & repeats Strong transcription Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
14	nsv962456	chr17:45163689-45212872	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45145000-45169800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr17:45145000-45169800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr17:45145000-45169800	Weak transcription	Fetal Lung	lung
4	chr17:45145000-45176400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr17:45145000-45176600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr17:45145000-45176800	Weak transcription	Lung	lung
7	chr17:45145200-45169200	Weak transcription	Primary B cells from cord blood	blood
8	chr17:45145200-45170200	Weak transcription	Brain Germinal Matrix	brain
9	chr17:45145200-45176600	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr17:45145400-45176000	Weak transcription	Primary T cells from cord blood	blood
11	chr17:45146400-45169800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr17:45146400-45170800	Weak transcription	Dnd41	blood
13	chr17:45148800-45175400	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr17:45149000-45168600	Weak transcription	Primary B cells from peripheral blood	blood
15	chr17:45149000-45170000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr17:45149000-45173800	Weak transcription	Primary T helper cells PMA-I stimulated	--
17	chr17:45149600-45175400	Weak transcription	Primary T cells fromperipheralblood	blood
18	chr17:45149600-45176800	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr17:45150200-45170000	Weak transcription	Ovary	ovary
20	chr17:45150200-45174600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr17:45150600-45167200	Weak transcription	Spleen	Spleen
22	chr17:45150600-45169800	Weak transcription	Fetal Muscle Leg	muscle
23	chr17:45150600-45170600	Weak transcription	HSMM	muscle
24	chr17:45150600-45176400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr17:45150600-45176800	Weak transcription	Left Ventricle	heart
26	chr17:45155000-45169800	Weak transcription	Fetal Brain Female	brain
27	chr17:45155600-45170200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr17:45155600-45170200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr17:45155600-45170200	Weak transcription	NHEK	skin
30	chr17:45155600-45173600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr17:45158200-45170600	Weak transcription	A549	lung
32	chr17:45158600-45169800	Weak transcription	Fetal Thymus	thymus
33	chr17:45158600-45175000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr17:45159200-45175600	Weak transcription	Monocytes-CD14+_RO01746	blood
35	chr17:45159600-45169800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr17:45159800-45169800	Weak transcription	Fetal Stomach	stomach
37	chr17:45159800-45170200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr17:45162600-45170000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr17:45162800-45164800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr17:45163200-45165200	Weak transcription	K562	blood
41	chr17:45163200-45170200	Weak transcription	Primary hematopoietic stem cells	blood
42	chr17:45163200-45176800	Weak transcription	Fetal Intestine Large	intestine
43	chr17:45163400-45170200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
44	chr17:45163800-45166400	Weak transcription	Fetal Intestine Small	intestine
45	chr17:45163800-45175000	Weak transcription	HepG2	liver
46	chr17:45164200-45168400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr17:45164200-45169800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr17:45164200-45170600	Weak transcription	Brain Cingulate Gyrus	brain
49	chr17:45164400-45164800	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr17:45164400-45165000	Enhancers	iPS-18 Cell Line	embryonic stem cell

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