Variant report

Variant	rs10187420
Chromosome Location	chr2:96350826-96350827
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10167824	1.00[EUR][1000 genomes]
rs10172762	1.00[EUR][1000 genomes]
rs10176455	0.98[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10176771	0.98[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10198238	1.00[EUR][1000 genomes]
rs10205464	1.00[EUR][1000 genomes]
rs13389648	1.00[EUR][1000 genomes]
rs13390615	1.00[EUR][1000 genomes]
rs13402791	1.00[EUR][1000 genomes]
rs13410926	1.00[EUR][1000 genomes]
rs55845625	1.00[EUR][1000 genomes]
rs56225135	1.00[EUR][1000 genomes]
rs73957746	1.00[EUR][1000 genomes]
rs7565104	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3416818	chr2:96072529-96680708	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
2	nsv874660	chr2:96091132-96669134	Strong transcription Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
3	nsv516044	chr2:96150959-96683378	Weak transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
4	nsv998587	chr2:96170558-96378228	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv834301	chr2:96285762-96427246	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	esv18352	chr2:96291856-96391581	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv1002700	chr2:96296630-96422939	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv1003371	chr2:96326106-96684876	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
9	nsv874661	chr2:96334397-96459313	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv874662	chr2:96334397-96578621	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
11	nsv874663	chr2:96345518-96459313	Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:96348200-96352200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:96348800-96351400	Weak transcription	A549	lung
3	chr2:96349200-96351600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:96349200-96351800	Weak transcription	NH-A	brain
5	chr2:96349200-96352200	Weak transcription	Gastric	stomach
6	chr2:96349200-96352200	Weak transcription	Stomach Mucosa	stomach
7	chr2:96349200-96352400	Weak transcription	Lung	lung
8	chr2:96349200-96352400	Weak transcription	Pancreas	Pancrea
9	chr2:96349200-96353600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr2:96349400-96351000	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr2:96349400-96351200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr2:96349400-96351200	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr2:96349400-96351200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr2:96349400-96351200	Weak transcription	Fetal Lung	lung
15	chr2:96349400-96351200	Weak transcription	NHLF	lung
16	chr2:96349400-96351400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr2:96349400-96351400	Weak transcription	HSMM	muscle
18	chr2:96349400-96351400	Weak transcription	Osteobl	bone
19	chr2:96349400-96351800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr2:96349400-96351800	Weak transcription	NHEK	skin
21	chr2:96349400-96352000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr2:96349400-96352200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr2:96349400-96352200	Weak transcription	Adipose Nuclei	Adipose
24	chr2:96349400-96352200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr2:96349400-96352200	Weak transcription	HMEC	breast
26	chr2:96349400-96352400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr2:96349400-96352400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr2:96349400-96352400	Weak transcription	Fetal Muscle Leg	muscle
29	chr2:96349400-96352400	Weak transcription	HSMMtube	muscle
30	chr2:96349400-96352600	Weak transcription	Ovary	ovary
31	chr2:96349400-96353600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr2:96349400-96356400	Weak transcription	Spleen	Spleen
33	chr2:96350200-96351200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr2:96350400-96353400	Enhancers	Liver	Liver
35	chr2:96350400-96354400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr2:96350600-96351800	Enhancers	NHDF-Ad	bronchial

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