Variant report

Variant rs12057832
Chromosome Location chr1:210243949-210243950
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:210223600-210245600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
2 chr1:210224400-210250000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr1:210242800-210245800 Weak transcription HUES48 Cell Line embryonic stem cell
4 chr1:210243200-210244400 Enhancers iPS-18 Cell Line embryonic stem cell
5 chr1:210243200-210244400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
6 chr1:210243200-210247000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr1:210243200-210247200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
8 chr1:210243600-210244000 Enhancers iPS-15b Cell Line embryonic stem cell
9 chr1:210243600-210244200 Enhancers Brain Anterior Caudate brain
10 chr1:210243800-210244200 Enhancers Brain Cingulate Gyrus brain
11 chr1:210243800-210244600 Enhancers Brain Germinal Matrix brain
12 chr1:210243800-210245600 Weak transcription HUES64 Cell Line embryonic stem cell

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