Variant report

Variant	rs17265357
Chromosome Location	chr1:61746225-61746226
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:61741419..61744047-chr1:61744125..61746996,2	K562	blood:
2	chr1:61744927..61747648-chr1:61751228..61753700,3	K562	blood:
3	chr1:61737789..61739540-chr1:61743962..61746875,2	K562	blood:
4	chr1:61744404..61747125-chr1:61759357..61761056,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs1336184	0.90[AMR][1000 genomes]
rs17265364	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17265370	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17311775	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv994970	chr1:61693951-62199657	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer 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	19 gene(s)	inside rSNPs	diseases
2	nsv1006142	chr1:61696142-62119763	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS 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 target site	6 gene(s)	inside rSNPs	diseases
3	nsv534980	chr1:61696142-62119763	Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Bivalent Enhancer 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	6 gene(s)	inside rSNPs	diseases
4	nsv916868	chr1:61700430-62119762	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Bivalent Enhancer 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	6 gene(s)	inside rSNPs	diseases
5	nsv1001052	chr1:61702011-62090670	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats 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	3 gene(s)	inside rSNPs	diseases
6	nsv817402	chr1:61703965-62119762	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats 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	6 gene(s)	inside rSNPs	diseases
7	nsv1010797	chr1:61703966-62125970	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers 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	6 gene(s)	inside rSNPs	diseases
8	nsv530494	chr1:61723918-62084045	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 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	chr1:61720800-61755800	Weak transcription	Fetal Intestine Small	intestine
2	chr1:61721000-61754400	Weak transcription	Pancreas	Pancrea
3	chr1:61725800-61750400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr1:61729600-61754400	Weak transcription	Lung	lung
5	chr1:61732800-61750000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr1:61737000-61750000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr1:61737200-61751600	Weak transcription	Hela-S3	cervix
8	chr1:61737400-61747600	Weak transcription	HepG2	liver
9	chr1:61737400-61750000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr1:61737400-61751800	Weak transcription	Esophagus	oesophagus
11	chr1:61737600-61750200	Weak transcription	NHEK	skin
12	chr1:61738000-61752600	Weak transcription	HUVEC	blood vessel
13	chr1:61740800-61748000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr1:61741000-61747600	Weak transcription	Liver	Liver
15	chr1:61742800-61747800	Weak transcription	A549	lung
16	chr1:61743000-61748000	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr1:61743200-61747600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr1:61743200-61747800	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr1:61743200-61748000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr1:61743200-61752600	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr1:61743400-61748200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr1:61743400-61748200	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr1:61743400-61749600	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr1:61743400-61754400	Weak transcription	Aorta	Aorta
25	chr1:61743400-61756400	Weak transcription	Right Ventricle	heart
26	chr1:61743600-61748000	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr1:61744600-61746400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr1:61744600-61748200	Weak transcription	Right Atrium	heart
29	chr1:61744600-61750000	Weak transcription	Fetal Stomach	stomach
30	chr1:61744600-61798600	Weak transcription	Fetal Muscle Trunk	muscle
31	chr1:61745000-61746400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr1:61745400-61746600	Enhancers	NHDF-Ad	bronchial
33	chr1:61745600-61746400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr1:61745600-61747000	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr1:61745600-61747200	Weak transcription	Psoas Muscle	Psoas
36	chr1:61745600-61747800	Weak transcription	Left Ventricle	heart
37	chr1:61745600-61747800	Weak transcription	Sigmoid Colon	Sigmoid Colon
38	chr1:61745600-61750000	Weak transcription	Fetal Muscle Leg	muscle
39	chr1:61745600-61750800	Weak transcription	Brain Germinal Matrix	brain
40	chr1:61745800-61749600	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr1:61745800-61750600	Weak transcription	Adipose Nuclei	Adipose
42	chr1:61746000-61748000	Weak transcription	Colon Smooth Muscle	Colon
43	chr1:61746000-61748000	Weak transcription	Fetal Brain Female	brain
44	chr1:61746000-61748200	Weak transcription	Brain Cingulate Gyrus	brain
45	chr1:61746000-61749600	Weak transcription	Brain Anterior Caudate	brain
46	chr1:61746000-61749800	Weak transcription	GM12878-XiMat	blood
47	chr1:61746000-61750800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr1:61746000-61751000	Weak transcription	Brain Hippocampus Middle	brain
49	chr1:61746000-61751400	Weak transcription	Brain Angular Gyrus	brain
50	chr1:61746000-61751600	Weak transcription	Brain Substantia Nigra	brain

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