Variant report

Variant	rs7074115
Chromosome Location	chr10:93321472-93321473
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:93320690..93322917-chr10:93329298..93330979,2	K562	blood:
2	chr10:93315882..93318453-chr10:93320289..93322933,2	MCF-7	breast:
3	chr10:93320978..93323661-chr10:93390295..93392458,2	MCF-7	breast:

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10881918	0.81[ASN][1000 genomes]
rs10881919	0.81[ASN][1000 genomes]
rs10881923	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11186610	0.81[ASN][1000 genomes]
rs11186613	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12241797	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12246543	0.81[ASN][1000 genomes]
rs12255223	0.81[ASN][1000 genomes]
rs12256369	0.81[ASN][1000 genomes]
rs12256726	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12260905	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12263117	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12268133	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1411120	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1411121	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17106760	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2094710	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4933659	0.81[ASN][1000 genomes]
rs4933660	0.81[ASN][1000 genomes]
rs4933661	0.81[ASN][1000 genomes]
rs4933662	0.81[ASN][1000 genomes]
rs4933663	0.81[ASN][1000 genomes]
rs4933665	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4933666	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4933667	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4933668	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4933669	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56198147	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59997744	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7068979	0.81[ASN][1000 genomes]
rs716361	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72819249	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72819252	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7477129	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7895083	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7908831	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7910891	0.91[ASN][1000 genomes]
rs7911125	0.85[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs928118	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];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	esv19622	chr10:93305214-93361590	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:93314800-93321600	Enhancers	Stomach Mucosa	stomach
2	chr10:93315200-93322600	Weak transcription	Aorta	Aorta
3	chr10:93315200-93325600	Weak transcription	Gastric	stomach
4	chr10:93315200-93335600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr10:93315400-93323000	Weak transcription	Pancreas	Pancrea
6	chr10:93316600-93323200	Weak transcription	Colon Smooth Muscle	Colon
7	chr10:93317200-93322600	Weak transcription	Right Atrium	heart
8	chr10:93317200-93323000	Weak transcription	Left Ventricle	heart
9	chr10:93317200-93324000	Weak transcription	Fetal Muscle Leg	muscle
10	chr10:93318000-93323000	Weak transcription	Stomach Smooth Muscle	stomach
11	chr10:93318400-93322600	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr10:93318600-93322400	Weak transcription	Fetal Heart	heart
13	chr10:93319200-93322600	Weak transcription	Psoas Muscle	Psoas
14	chr10:93320000-93322600	Weak transcription	Liver	Liver
15	chr10:93320000-93322600	Weak transcription	Fetal Lung	lung
16	chr10:93320200-93321600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr10:93320400-93322600	Weak transcription	HepG2	liver
18	chr10:93320600-93321600	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr10:93320600-93321600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr10:93320600-93325800	Enhancers	Skeletal Muscle Female	skeletal muscle
21	chr10:93320800-93321600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr10:93321000-93321600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr10:93321000-93321600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr10:93321000-93321800	ZNF genes & repeats	Fetal Intestine Large	intestine
25	chr10:93321000-93321800	ZNF genes & repeats	Fetal Intestine Small	intestine
26	chr10:93321000-93321800	Enhancers	HSMMtube	muscle
27	chr10:93321200-93321600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr10:93321200-93321800	Enhancers	Fetal Muscle Trunk	muscle
29	chr10:93321200-93322000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr10:93321200-93322400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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