Variant report

Variant	rs62557498
Chromosome Location	chr9:100186430-100186431
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:100184396..100186994-chr9:100352263..100355014,2	K562	blood:
2	chr9:100185198..100188170-chr9:100190845..100193697,2	MCF-7	breast:
3	chr9:100185616..100187642-chr9:100190384..100191951,2	MCF-7	breast:

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs11999505	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12001521	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12006001	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs16920147	0.95[ASN][1000 genomes]
rs16920171	0.95[ASN][1000 genomes]
rs16920387	0.90[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs16920392	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs16920394	0.84[ASN][1000 genomes]
rs16920403	0.84[ASN][1000 genomes]
rs16920407	0.84[ASN][1000 genomes]
rs16920414	0.84[ASN][1000 genomes]
rs16920418	0.84[ASN][1000 genomes]
rs35600334	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs58008468	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs59749998	0.86[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs59837265	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs60023110	0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs61418045	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs62557474	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs62557475	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs62557493	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs62557495	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs62557499	0.94[AFR][1000 genomes];0.80[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs62557500	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs62557501	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs62557502	0.83[AFR][1000 genomes]
rs62557510	0.81[AFR][1000 genomes];0.80[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs62557513	0.83[AFR][1000 genomes]
rs7044475	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7048438	0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs732688	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs732689	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7853578	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[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	nsv893609	chr9:100163998-100297592	Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:68 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:100175400-100190400	Weak transcription	Aorta	Aorta
2	chr9:100175400-100190800	Weak transcription	Left Ventricle	heart
3	chr9:100175400-100230800	Weak transcription	Psoas Muscle	Psoas
4	chr9:100175600-100189600	Weak transcription	Primary T cells from cord blood	blood
5	chr9:100175600-100191200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr9:100175600-100202600	Weak transcription	Fetal Muscle Leg	muscle
7	chr9:100175600-100245200	Weak transcription	Right Ventricle	heart
8	chr9:100176000-100191200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr9:100176200-100190400	Weak transcription	Spleen	Spleen
10	chr9:100176200-100194400	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr9:100176200-100203000	Weak transcription	Dnd41	blood
12	chr9:100176400-100192000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr9:100176600-100192600	Weak transcription	Fetal Brain Male	brain
14	chr9:100179600-100190400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr9:100179600-100190800	Weak transcription	Lung	lung
16	chr9:100179800-100190600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr9:100181000-100190400	Weak transcription	Primary B cells from cord blood	blood
18	chr9:100181200-100190400	Weak transcription	Monocytes-CD14+_RO01746	blood
19	chr9:100181200-100190800	Weak transcription	Primary neutrophils fromperipheralblood	blood
20	chr9:100181600-100191400	Weak transcription	Colonic Mucosa	Colon
21	chr9:100181800-100193800	Weak transcription	Brain Hippocampus Middle	brain
22	chr9:100182000-100188000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr9:100182000-100190800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
24	chr9:100182000-100190800	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr9:100182000-100190800	Weak transcription	Gastric	stomach
26	chr9:100182000-100190800	Weak transcription	Ovary	ovary
27	chr9:100182000-100191400	Weak transcription	Small Intestine	intestine
28	chr9:100182000-100199600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr9:100182000-100205200	Weak transcription	Esophagus	oesophagus
30	chr9:100182000-100215600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr9:100182000-100234200	Weak transcription	A549	lung
32	chr9:100182200-100186800	Weak transcription	Duodenum Mucosa	Duodenum
33	chr9:100182200-100186800	Weak transcription	Rectal Mucosa Donor 29	rectum
34	chr9:100182200-100187200	Weak transcription	Fetal Intestine Large	intestine
35	chr9:100182200-100187200	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr9:100182200-100187600	Weak transcription	Fetal Intestine Small	intestine
37	chr9:100182200-100189800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr9:100182200-100190200	Weak transcription	Primary monocytes fromperipheralblood	blood
39	chr9:100182200-100190400	Weak transcription	HMEC	breast
40	chr9:100182200-100190800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr9:100182200-100199400	Weak transcription	Pancreas	Pancrea
42	chr9:100182200-100202400	Weak transcription	NHLF	lung
43	chr9:100182200-100202800	Weak transcription	HSMMtube	muscle
44	chr9:100182200-100236000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr9:100182200-100263400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr9:100182400-100189800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr9:100182400-100190200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr9:100182400-100203800	Weak transcription	Muscle Satellite Cultured Cells	--
49	chr9:100182600-100190800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr9:100182600-100190800	Weak transcription	NHDF-Ad	bronchial

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