Variant report

Variant rs140199278
Chromosome Location chr2:96773101-96773102
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:96769600-96773400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr2:96770600-96773400 Weak transcription Right Ventricle heart
3 chr2:96770600-96774000 Weak transcription Right Atrium heart
4 chr2:96770800-96773200 Weak transcription Left Ventricle heart
5 chr2:96770800-96773600 Weak transcription Fetal Heart heart
6 chr2:96771600-96773200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr2:96772000-96773200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
8 chr2:96772000-96774000 Weak transcription Spleen Spleen
9 chr2:96772000-96782200 Weak transcription Liver Liver
10 chr2:96772800-96773400 Enhancers Skeletal Muscle Male skeletal muscle
11 chr2:96772800-96774400 Enhancers Fetal Muscle Trunk muscle
12 chr2:96772800-96774800 Enhancers Duodenum Smooth Muscle Duodenum
13 chr2:96772800-96774800 Enhancers Fetal Muscle Leg muscle
14 chr2:96773000-96773600 Bivalent Enhancer H1 Derived Mesenchymal Stem Cells ES cell derived
15 chr2:96773000-96773800 Enhancers HepG2 liver
16 chr2:96773000-96775400 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived

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