Variant report

Variant rs34859030
Chromosome Location chr2:127705641-127705642
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:127701800-127706000 Enhancers Fetal Kidney kidney
2 chr2:127702800-127705800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr2:127704800-127705800 Enhancers H9 Cell Line embryonic stem cell
4 chr2:127704800-127706000 Enhancers HUES48 Cell Line embryonic stem cell
5 chr2:127704800-127706000 Enhancers iPS-18 Cell Line embryonic stem cell
6 chr2:127704800-127706200 Bivalent Enhancer H1 Cell Line embryonic stem cell
7 chr2:127704800-127706400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
8 chr2:127705000-127705800 Bivalent Enhancer iPS-20b Cell Line embryonic stem cell
9 chr2:127705000-127706200 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell
10 chr2:127705000-127706400 Weak transcription Fetal Muscle Leg muscle
11 chr2:127705400-127706600 Enhancers HUES6 Cell Line embryonic stem cell
12 chr2:127705600-127705800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
13 chr2:127705600-127705800 Enhancers Fetal Muscle Trunk muscle
14 chr2:127705600-127706200 Enhancers iPS DF 6.9 Cell Line embryonic stem cell

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