Variant report

Variant	rs17504267
Chromosome Location	chr8:118923798-118923799
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs17475395	1.00[AFR][1000 genomes]
rs17475471	1.00[AFR][1000 genomes]
rs17504246	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019636	chr8:118598433-118946091	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv539734	chr8:118598433-118946091	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv933516	chr8:118764605-119009093	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv1030459	chr8:118840179-119155835	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv831440	chr8:118871930-119052269	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv891411	chr8:118891896-118942698	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv1032355	chr8:118896733-119003223	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv465785	chr8:118901928-118970300	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv612046	chr8:118901928-118970300	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:118908800-118925800	Weak transcription	Duodenum Mucosa	Duodenum
2	chr8:118912000-118925800	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr8:118913400-118925600	Weak transcription	Colon Smooth Muscle	Colon
4	chr8:118916200-118925800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr8:118919000-118926800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr8:118919200-118933200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr8:118919800-118925800	Weak transcription	Small Intestine	intestine
8	chr8:118921200-118926400	Enhancers	NHDF-Ad	bronchial
9	chr8:118921200-118926600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr8:118921400-118923800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr8:118921400-118924600	Enhancers	HMEC	breast
12	chr8:118921600-118924000	Enhancers	NHEK	skin
13	chr8:118921600-118924200	Enhancers	NH-A	brain
14	chr8:118921600-118926400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr8:118921800-118924000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr8:118921800-118926400	Enhancers	NHLF	lung
17	chr8:118922000-118924000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr8:118922200-118923800	Enhancers	Fetal Muscle Leg	muscle
19	chr8:118922200-118923800	Enhancers	Right Ventricle	heart
20	chr8:118922200-118923800	Enhancers	HUVEC	blood vessel
21	chr8:118922200-118924000	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr8:118922200-118924000	Enhancers	Adipose Nuclei	Adipose
23	chr8:118922200-118924000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr8:118922200-118924000	Enhancers	Left Ventricle	heart
25	chr8:118922200-118924000	Enhancers	Ovary	ovary
26	chr8:118922400-118924000	Enhancers	Skeletal Muscle Male	skeletal muscle
27	chr8:118922400-118926400	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr8:118922600-118923800	Enhancers	Aorta	Aorta
29	chr8:118922600-118923800	Enhancers	HSMM	muscle
30	chr8:118922600-118924000	Enhancers	Lung	lung
31	chr8:118922600-118925000	Enhancers	Liver	Liver
32	chr8:118922800-118932800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr8:118922800-118934800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr8:118923000-118923800	Enhancers	Pancreas	Pancrea
35	chr8:118923000-118924000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr8:118923000-118924000	Enhancers	A549	lung
37	chr8:118923000-118926600	Enhancers	Muscle Satellite Cultured Cells	--
38	chr8:118923200-118924000	Enhancers	Gastric	stomach
39	chr8:118923200-118924200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr8:118923200-118925600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr8:118923200-118926400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr8:118923200-118926400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr8:118923200-118933000	Weak transcription	Stomach Smooth Muscle	stomach
44	chr8:118923400-118924800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr8:118923400-118925000	Weak transcription	Esophagus	oesophagus
46	chr8:118923400-118925400	Weak transcription	HSMMtube	muscle
47	chr8:118923600-118923800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr8:118923600-118923800	Enhancers	Fetal Stomach	stomach
49	chr8:118923600-118926800	Enhancers	Osteobl	bone

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