Variant report

Variant rs74126528
Chromosome Location chr1:171867288-171867289
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:171858400-171868200 Weak transcription Left Ventricle heart
2 chr1:171860600-171868200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr1:171862200-171868200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
4 chr1:171862200-171882600 Weak transcription Aorta Aorta
5 chr1:171865800-171868000 Enhancers Brain Hippocampus Middle brain
6 chr1:171865800-171868000 Enhancers Brain Inferior Temporal Lobe brain
7 chr1:171866000-171867400 Enhancers Brain Angular Gyrus brain
8 chr1:171866000-171868000 Enhancers Brain Anterior Caudate brain
9 chr1:171866200-171867400 Enhancers Brain Substantia Nigra brain
10 chr1:171866400-171868200 Weak transcription H9 Cell Line embryonic stem cell
11 chr1:171866400-171870800 Enhancers Fetal Brain Male brain
12 chr1:171866600-171868000 Enhancers Fetal Brain Female brain
13 chr1:171867200-171867400 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
14 chr1:171867200-171867400 Enhancers Brain Cingulate Gyrus brain
15 chr1:171867200-171867400 Enhancers Duodenum Smooth Muscle Duodenum
16 chr1:171867200-171868200 Enhancers Cortex derived primary cultured neurospheres brain
17 chr1:171867200-171868800 Enhancers Fetal Adrenal Gland Adrenal Gland
18 chr1:171867200-171870000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin

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