Variant report

Variant	rs62561181
Chromosome Location	chr9:101754200-101754201
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:101744002..101749570-chr9:101754118..101758389,6	K562	blood:
2	chr9:101751401..101755112-chr9:101755767..101760642,5	MCF-7	breast:

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

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs12379516	1.00[ASN][1000 genomes]
rs2151617	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2184214	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35250850	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41283636	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41283638	1.00[ASN][1000 genomes]
rs55697146	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55771115	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55881088	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55980075	1.00[ASN][1000 genomes]
rs55996120	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56358572	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62561172	1.00[ASN][1000 genomes]
rs62561176	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62561177	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62561178	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62561179	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62561185	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62561243	0.85[EUR][1000 genomes]
rs62561248	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62561249	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62561250	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72739264	1.00[ASN][1000 genomes]
rs72739265	1.00[ASN][1000 genomes]
rs72739266	1.00[ASN][1000 genomes]
rs882727	1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv6635	chr9:101728257-101773253	Enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:101737800-101760800	Weak transcription	Gastric	stomach
2	chr9:101740400-101756800	Weak transcription	Ovary	ovary
3	chr9:101742800-101754200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr9:101746800-101754400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr9:101750200-101755200	Weak transcription	Brain Substantia Nigra	brain
6	chr9:101750400-101754400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr9:101751800-101755200	Strong transcription	Fetal Muscle Leg	muscle
8	chr9:101752000-101760800	Weak transcription	Brain Hippocampus Middle	brain
9	chr9:101752400-101755400	Weak transcription	Rectal Smooth Muscle	rectum
10	chr9:101752600-101754200	Weak transcription	Stomach Mucosa	stomach
11	chr9:101752600-101755200	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr9:101752600-101755800	Weak transcription	Colon Smooth Muscle	Colon
13	chr9:101752800-101755000	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr9:101752800-101755200	Weak transcription	Fetal Heart	heart
15	chr9:101752800-101755600	Weak transcription	A549	lung
16	chr9:101753000-101754400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr9:101753000-101754800	Strong transcription	Fetal Muscle Trunk	muscle
18	chr9:101753000-101755000	Strong transcription	Adipose Nuclei	Adipose
19	chr9:101753000-101755200	Weak transcription	HSMMtube	muscle
20	chr9:101753000-101755200	Weak transcription	NHDF-Ad	bronchial
21	chr9:101753000-101755400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr9:101753000-101755600	Weak transcription	Left Ventricle	heart
23	chr9:101753000-101756600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr9:101753000-101756600	Weak transcription	Right Atrium	heart
25	chr9:101753000-101756800	Weak transcription	Pancreas	Pancrea
26	chr9:101753000-101759800	Weak transcription	Hela-S3	cervix
27	chr9:101753200-101754800	Weak transcription	Right Ventricle	heart
28	chr9:101753200-101755200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr9:101753200-101755400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr9:101753200-101755400	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr9:101753400-101754400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr9:101753400-101754800	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr9:101753600-101754400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr9:101753600-101754400	Weak transcription	Spleen	Spleen
35	chr9:101753800-101754200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr9:101753800-101754400	Weak transcription	Fetal Stomach	stomach
37	chr9:101753800-101754600	Weak transcription	Stomach Smooth Muscle	stomach
38	chr9:101754000-101754400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr9:101754200-101755800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

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