Variant report

Variant rs10492245
Chromosome Location chr12:31171028-31171029
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:31147200-31185000 Weak transcription Right Atrium heart
2 chr12:31158400-31174600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr12:31161600-31176400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr12:31162800-31176200 Weak transcription Fetal Brain Female brain
5 chr12:31168600-31177000 Enhancers Fetal Thymus thymus
6 chr12:31169000-31175000 Weak transcription Fetal Stomach stomach
7 chr12:31169000-31185000 Weak transcription Right Ventricle heart
8 chr12:31169600-31171400 Enhancers Spleen Spleen
9 chr12:31169600-31173800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
10 chr12:31170600-31171400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr12:31170600-31171600 Enhancers Fetal Adrenal Gland Adrenal Gland
12 chr12:31170600-31172000 Enhancers Adipose Nuclei Adipose
13 chr12:31170600-31172000 Enhancers Fetal Muscle Leg muscle
14 chr12:31170600-31172200 Enhancers HUVEC blood vessel
15 chr12:31170800-31171200 Weak transcription Thymus Thymus
16 chr12:31170800-31171400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
17 chr12:31170800-31172000 Enhancers Lung lung
18 chr12:31171000-31171400 Enhancers Fetal Muscle Trunk muscle

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