Variant report

Variant	rs74099519
Chromosome Location	chr12:59256052-59256053
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs11520079	0.85[AFR][1000 genomes]
rs11520080	0.85[AFR][1000 genomes]
rs74099638	0.89[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758311	chr12:59022729-59323045	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
2	esv2759902	chr12:59022729-59323045	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
3	nsv1043385	chr12:59149582-59758952	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
4	nsv1067596	chr12:59167152-59764208	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
5	nsv492251	chr12:59167152-59764208	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
6	nsv1038273	chr12:59232371-59259628	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	esv3440532	chr12:59244734-59266539	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:59243000-59257600	Weak transcription	NH-A	brain
2	chr12:59243200-59263600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr12:59245200-59257400	Weak transcription	NHDF-Ad	bronchial
4	chr12:59245200-59260000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr12:59250400-59257800	Weak transcription	Gastric	stomach
6	chr12:59251000-59266400	Weak transcription	Esophagus	oesophagus
7	chr12:59251200-59257800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr12:59251200-59261800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr12:59251400-59261400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr12:59251600-59256800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr12:59251800-59257600	Weak transcription	HMEC	breast
12	chr12:59251800-59263400	Weak transcription	NHEK	skin
13	chr12:59252000-59257000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr12:59252200-59259800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr12:59253000-59270200	Weak transcription	Fetal Brain Male	brain
16	chr12:59253400-59257000	Enhancers	Fetal Intestine Small	intestine
17	chr12:59253400-59265400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr12:59254400-59260000	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr12:59254400-59261600	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr12:59254600-59262000	Weak transcription	Osteobl	bone
21	chr12:59254600-59268600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr12:59254800-59262200	Weak transcription	Stomach Mucosa	stomach
23	chr12:59254800-59266400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr12:59254800-59267000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr12:59255000-59265400	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr12:59255000-59267400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr12:59255200-59259800	Weak transcription	Fetal Stomach	stomach
28	chr12:59255200-59263400	Weak transcription	Duodenum Mucosa	Duodenum
29	chr12:59255400-59256200	Weak transcription	Fetal Intestine Large	intestine
30	chr12:59255400-59267000	Weak transcription	Pancreas	Pancrea
31	chr12:59255800-59257600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr12:59256000-59261400	Weak transcription	Sigmoid Colon	Sigmoid Colon

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