Variant report

Variant rs10911356
Chromosome Location chr1:172209747-172209748
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:172207000-172211200 Enhancers Cortex derived primary cultured neurospheres brain
2 chr1:172207400-172211400 Enhancers Fetal Stomach stomach
3 chr1:172207800-172212400 Weak transcription Fetal Brain Female brain
4 chr1:172208000-172209800 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
5 chr1:172208400-172210200 Enhancers Fetal Lung lung
6 chr1:172208400-172210800 Weak transcription Brain Angular Gyrus brain
7 chr1:172208400-172210800 Weak transcription Brain Hippocampus Middle brain
8 chr1:172208600-172209800 Enhancers Fetal Intestine Large intestine
9 chr1:172208600-172210000 Enhancers Rectal Smooth Muscle rectum
10 chr1:172208800-172227600 Weak transcription Brain Inferior Temporal Lobe brain
11 chr1:172209000-172209800 Enhancers Colon Smooth Muscle Colon
12 chr1:172209000-172209800 Enhancers Fetal Heart heart
13 chr1:172209000-172210200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
14 chr1:172209400-172214400 Weak transcription Pancreas Pancrea
15 chr1:172209400-172218400 Weak transcription Fetal Adrenal Gland Adrenal Gland
16 chr1:172209400-172220800 Weak transcription Right Ventricle heart
17 chr1:172209600-172210400 Weak transcription Brain Cingulate Gyrus brain
18 chr1:172209600-172210600 Weak transcription Fetal Muscle Leg muscle
19 chr1:172209600-172216200 Weak transcription Brain Substantia Nigra brain

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