Variant report

Variant rs9621096
Chromosome Location chr22:31180536-31180537
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:31140000-31185400 Weak transcription Fetal Brain Female brain
2 chr22:31168000-31185400 Weak transcription Brain Inferior Temporal Lobe brain
3 chr22:31172800-31189400 Weak transcription Fetal Heart heart
4 chr22:31173800-31181600 Weak transcription Spleen Spleen
5 chr22:31173800-31198200 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
6 chr22:31177600-31182800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr22:31177800-31185800 Weak transcription HSMMtube muscle
8 chr22:31178400-31180600 Enhancers A549 lung
9 chr22:31178800-31187600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
10 chr22:31179800-31181200 Enhancers Fetal Adrenal Gland Adrenal Gland
11 chr22:31179800-31181400 Enhancers Fetal Intestine Small intestine
12 chr22:31179800-31181800 Enhancers Fetal Intestine Large intestine
13 chr22:31180400-31181200 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived

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