Variant report

Variant rs187905066
Chromosome Location chr1:113430088-113430089
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:113421400-113435200 Weak transcription Fetal Heart heart
2 chr1:113425000-113430200 Weak transcription Fetal Intestine Large intestine
3 chr1:113425200-113430400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
4 chr1:113425600-113430200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr1:113425600-113430400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr1:113425600-113430400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr1:113425600-113430400 Weak transcription Right Atrium heart
8 chr1:113425800-113430200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr1:113425800-113430200 Weak transcription Muscle Satellite Cultured Cells --
10 chr1:113425800-113430200 Weak transcription HSMM muscle
11 chr1:113425800-113430400 Weak transcription Sigmoid Colon Sigmoid Colon
12 chr1:113425800-113430400 Weak transcription HSMMtube muscle
13 chr1:113425800-113435200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr1:113426600-113430200 Weak transcription K562 blood
15 chr1:113429400-113430800 Enhancers Stomach Mucosa stomach
16 chr1:113429600-113430600 Enhancers Colonic Mucosa Colon
17 chr1:113430000-113430600 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
18 chr1:113430000-113430600 Flanking Active TSS Duodenum Mucosa Duodenum
19 chr1:113430000-113431200 Enhancers Fetal Intestine Small intestine
20 chr1:113430000-113431400 Enhancers Gastric stomach

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