Variant report

Variant	rs60117866
Chromosome Location	chr17:15862421-15862422
allele	A/G
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:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:15847630..15850213-chr17:15861016..15863900,2	K562	blood:
2	chr17:15861172..15863617-chr17:15879746..15882543,3	K562	blood:
3	chr17:15861872..15863395-chr17:15873905..15875556,2	K562	blood:
4	chr17:15848433..15851819-chr17:15861241..15867680,6	MCF-7	breast:
5	chr17:15861872..15864251-chr17:15873905..15876165,2	K562	blood:
6	chr17:15860784..15862668-chr17:15867479..15869134,2	MCF-7	breast:
7	chr17:15860952..15862454-chr17:15899696..15901427,2	K562	blood:
8	chr17:15856750..15859514-chr17:15860824..15862643,2	K562	blood:
9	chr17:15859179..15862826-chr17:15901862..15905162,4	MCF-7	breast:
10	chr17:15847638..15850175-chr17:15861024..15863509,3	MCF-7	breast:
11	chr17:15848713..15850591-chr17:15862400..15865313,2	K562	blood:
12	chr17:15855716..15858528-chr17:15860406..15862714,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000170425	Chromatin interaction
ENSG00000011295	Chromatin interaction
ENSG00000214941	Chromatin interaction

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs56785477	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58545409	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59445662	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59848501	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73276032	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73276033	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8069362	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv934185	chr17:15552960-16551197	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	190 gene(s)	inside rSNPs	diseases
2	nsv1062951	chr17:15561070-15890644	Weak transcription Strong transcription Active TSS ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv1066023	chr17:15607267-16053512	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
4	esv3330182	chr17:15652014-16569534	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	177 gene(s)	inside rSNPs	diseases
5	esv3446844	chr17:15654843-16572246	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS 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 miRNA target site	177 gene(s)	inside rSNPs	diseases
6	nsv1061222	chr17:15672934-15999778	ZNF genes & repeats Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
7	nsv907706	chr17:15731923-16056442	ZNF genes & repeats Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS 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	35 gene(s)	inside rSNPs	diseases
8	nsv1067555	chr17:15804228-16001117	Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Enhancers Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
9	nsv1063459	chr17:15804228-16543593	Weak transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
10	nsv907707	chr17:15846535-15950751	Strong transcription Weak transcription Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
11	nsv907709	chr17:15851196-15937487	Weak transcription Genic enhancers Strong transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS 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	28 gene(s)	inside rSNPs	diseases
12	nsv907708	chr17:15851196-15950751	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS 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	30 gene(s)	inside rSNPs	diseases
13	nsv1057493	chr17:15852125-15930718	Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
14	nsv543215	chr17:15852125-15930718	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS 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 miRNA target site	27 gene(s)	inside rSNPs	diseases
15	nsv907710	chr17:15854257-15950751	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
16	nsv960192	chr17:15856207-15867176	Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
17	nsv512478	chr17:15861087-15864603	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:15851200-15869600	Weak transcription	Gastric	stomach
2	chr17:15855800-15869800	Weak transcription	Fetal Intestine Small	intestine
3	chr17:15857200-15866600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr17:15858000-15868200	Weak transcription	Fetal Muscle Trunk	muscle
5	chr17:15859200-15864000	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr17:15859400-15862600	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr17:15859600-15863600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr17:15860000-15868400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr17:15860200-15862800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
10	chr17:15860600-15862800	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr17:15860600-15863600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr17:15860800-15862800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr17:15860800-15864200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr17:15860800-15868400	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr17:15861000-15862800	Enhancers	Placenta Amnion	Placenta Amnion
16	chr17:15861000-15863400	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr17:15861000-15863600	Enhancers	HMEC	breast
18	chr17:15861000-15868600	Weak transcription	Esophagus	oesophagus
19	chr17:15861200-15863400	Enhancers	Primary hematopoietic stem cells	blood
20	chr17:15861200-15863600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr17:15861200-15868400	Weak transcription	Thymus	Thymus
22	chr17:15861400-15863000	Enhancers	Rectal Mucosa Donor 29	rectum
23	chr17:15861400-15863200	Enhancers	HSMM	muscle
24	chr17:15861600-15862600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
25	chr17:15861600-15863200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
26	chr17:15861600-15863200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr17:15861800-15862600	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr17:15861800-15862600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr17:15861800-15862600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr17:15861800-15862600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr17:15861800-15862600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr17:15861800-15862600	Enhancers	Adipose Nuclei	Adipose
33	chr17:15861800-15862600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr17:15861800-15862600	Flanking Active TSS	GM12878-XiMat	blood
35	chr17:15861800-15862600	Flanking Active TSS	NHDF-Ad	bronchial
36	chr17:15861800-15862600	Flanking Active TSS	NHEK	skin
37	chr17:15861800-15862800	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr17:15861800-15862800	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr17:15861800-15862800	Flanking Active TSS	K562	blood
40	chr17:15861800-15862800	Enhancers	NHLF	lung
41	chr17:15861800-15863000	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr17:15861800-15863200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
43	chr17:15861800-15863400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr17:15861800-15863400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr17:15861800-15863400	Enhancers	Stomach Mucosa	stomach
46	chr17:15861800-15863400	Enhancers	HepG2	liver
47	chr17:15861800-15863600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr17:15862000-15862600	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr17:15862000-15862600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr17:15862000-15862600	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood

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