Variant report

Variant	rs2642307
Chromosome Location	chr10:27914001-27914002
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs2642305	0.82[EUR][1000 genomes]
rs2642306	0.82[EUR][1000 genomes]
rs2808291	0.81[EUR][1000 genomes]
rs2815505	0.81[EUR][1000 genomes]
rs2815508	0.81[EUR][1000 genomes]
rs903282	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv550241	chr10:27569521-28025771	Enhancers ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv1045257	chr10:27572440-27926946	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	nsv1053952	chr10:27659365-27915029	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
4	esv3368825	chr10:27864181-28043820	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
5	nsv894985	chr10:27869503-27957785	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv894986	chr10:27904646-27957785	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:27904400-27914600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr10:27910800-27923000	Weak transcription	Aorta	Aorta
3	chr10:27911000-27914200	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr10:27911000-27914200	Weak transcription	HSMM	muscle
5	chr10:27911000-27914200	Enhancers	NHDF-Ad	bronchial
6	chr10:27912000-27914200	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr10:27912400-27914200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr10:27912400-27915000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr10:27913200-27915000	Enhancers	Fetal Muscle Trunk	muscle
10	chr10:27913400-27914400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr10:27913600-27914200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
12	chr10:27913600-27914200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr10:27913600-27914200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr10:27913600-27914400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr10:27913600-27914600	Bivalent Enhancer	Fetal Muscle Leg	muscle
16	chr10:27913600-27915000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr10:27913600-27915200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr10:27913600-27917800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr10:27913800-27914200	Enhancers	Adipose Nuclei	Adipose
20	chr10:27913800-27914400	Active TSS	ES-I3 Cell Line	embryonic stem cell
21	chr10:27913800-27914400	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr10:27913800-27914600	Active TSS	H9 Cell Line	embryonic stem cell
23	chr10:27913800-27915000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr10:27913800-27915000	Enhancers	HSMMtube	muscle
25	chr10:27913800-27916000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr10:27914000-27914200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
27	chr10:27914000-27914400	Active TSS	HUES6 Cell Line	embryonic stem cell
28	chr10:27914000-27914400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
29	chr10:27914000-27914800	Active TSS	iPS-20b Cell Line	embryonic stem cell
30	chr10:27914000-27914800	Enhancers	Fetal Stomach	stomach
31	chr10:27914000-27914800	Enhancers	Osteobl	bone
32	chr10:27914000-27915000	Enhancers	H1 Cell Line	embryonic stem cell
33	chr10:27914000-27915000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr10:27914000-27915400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr10:27914000-27915400	Enhancers	Brain Germinal Matrix	brain

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