Variant report

Variant	rs4907282
Chromosome Location	chr2:96518022-96518023
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs2315417	0.81[AMR][1000 genomes]
rs2315421	0.81[AMR][1000 genomes]
rs4063021	0.81[AMR][1000 genomes]
rs6717101	0.80[AMR][1000 genomes]
rs6719831	0.80[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 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	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
5	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
6	nsv874664	chr2:96370571-96534132	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv874665	chr2:96370571-96596515	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv874666	chr2:96370571-96691125	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
9	nsv1004482	chr2:96408987-96596717	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Bivalent Enhancer	TF binding region CpG island lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv834303	chr2:96432935-96551704	ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	TF binding region CpG island lncRNA	5 gene(s)	inside rSNPs	diseases
11	nsv428054	chr2:96438238-96627125	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island lncRNA	7 gene(s)	inside rSNPs	diseases
12	nsv961832	chr2:96453677-96671971	Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
13	nsv874667	chr2:96465201-96596515	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region lncRNA	4 gene(s)	inside rSNPs	diseases
14	nsv874668	chr2:96465201-96600569	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region lncRNA	4 gene(s)	inside rSNPs	diseases
15	esv1826589	chr2:96468292-96583910	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region lncRNA	4 gene(s)	inside rSNPs	diseases
16	esv1826305	chr2:96468492-96583710	Strong transcription ZNF genes & repeats Enhancers Weak transcription Genic enhancers	TF binding region lncRNA	4 gene(s)	inside rSNPs	diseases
17	esv1848259	chr2:96477989-96583252	ZNF genes & repeats Strong transcription Enhancers Weak transcription Genic enhancers	TF binding region lncRNA	3 gene(s)	inside rSNPs	diseases
18	nsv834304	chr2:96493545-96667472	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
19	esv20639	chr2:96515590-96527840	Strong transcription ZNF genes & repeats Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
20	nsv821038	chr2:96515590-96527840	Strong transcription Weak transcription ZNF genes & repeats Enhancers	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs4907282	FAHD2CP	cis	lung	GTEx
rs4907282	FAHD2CP	cis	Adipose Subcutaneous	GTEx
rs4907282	ADRA2B	cis	Thyroid	GTEx
rs4907282	ASTL	cis	Esophagus Mucosa	GTEx
rs4907282	ADRA2B	cis	Nerve Tibial	GTEx

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:96495000-96523200	Weak transcription	Primary T helper cells PMA-I stimulated	--
2	chr2:96495000-96532800	Weak transcription	HSMM	muscle
3	chr2:96496600-96521200	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr2:96497400-96521200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr2:96500200-96522000	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr2:96500600-96553400	Weak transcription	Brain Anterior Caudate	brain
7	chr2:96500800-96521000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr2:96500800-96521600	Weak transcription	Aorta	Aorta
9	chr2:96501000-96519400	Weak transcription	Stomach Smooth Muscle	stomach
10	chr2:96501000-96526400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr2:96501600-96526400	Weak transcription	Gastric	stomach
12	chr2:96501800-96524200	Weak transcription	K562	blood
13	chr2:96502600-96523000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr2:96502600-96547800	Weak transcription	Fetal Thymus	thymus
15	chr2:96502600-96561400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr2:96502800-96521200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr2:96502800-96522200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr2:96502800-96524800	Weak transcription	Primary T cells fromperipheralblood	blood
19	chr2:96502800-96526400	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr2:96502800-96527400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr2:96502800-96533800	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr2:96502800-96535600	Weak transcription	Brain Germinal Matrix	brain
23	chr2:96502800-96548400	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr2:96502800-96548600	Weak transcription	Thymus	Thymus
25	chr2:96502800-96551400	Weak transcription	Brain Cingulate Gyrus	brain
26	chr2:96502800-96555200	Weak transcription	Ovary	ovary
27	chr2:96502800-96585000	Weak transcription	Left Ventricle	heart
28	chr2:96502800-96616600	Weak transcription	Fetal Stomach	stomach
29	chr2:96503000-96519800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr2:96503000-96521400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr2:96503000-96563600	Weak transcription	Brain Hippocampus Middle	brain
32	chr2:96503200-96544400	Weak transcription	Primary T cells from cord blood	blood
33	chr2:96503200-96548800	Weak transcription	Primary T helper cells fromperipheralblood	blood
34	chr2:96505200-96521000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr2:96506200-96549400	Weak transcription	Primary hematopoietic stem cells	blood
36	chr2:96506600-96562000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr2:96514000-96526400	Weak transcription	Psoas Muscle	Psoas
38	chr2:96515600-96518800	Strong transcription	Dnd41	blood
39	chr2:96516000-96534600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
40	chr2:96516200-96521200	Weak transcription	Fetal Brain Male	brain
41	chr2:96516200-96523800	Weak transcription	Duodenum Mucosa	Duodenum
42	chr2:96516200-96548400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr2:96516200-96549200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr2:96516400-96526400	Weak transcription	Fetal Muscle Leg	muscle
45	chr2:96516800-96548600	Weak transcription	Adipose Nuclei	Adipose
46	chr2:96516800-96553400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr2:96517400-96521200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr2:96517600-96523400	Weak transcription	Fetal Intestine Large	intestine
49	chr2:96517800-96521200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
50	chr2:96517800-96521200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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