Variant report

Variant rs6656855
Chromosome Location chr1:210289728-210289729
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:210274200-210290600 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
2 chr1:210280000-210290600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr1:210283000-210298000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr1:210289200-210289800 Enhancers ES-I3 Cell Line embryonic stem cell
5 chr1:210289200-210290000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
6 chr1:210289400-210290000 Enhancers iPS-18 Cell Line embryonic stem cell
7 chr1:210289400-210291800 Enhancers HUES64 Cell Line embryonic stem cell
8 chr1:210289400-210291800 Enhancers iPS-15b Cell Line embryonic stem cell
9 chr1:210289600-210290000 Enhancers H9 Cell Line embryonic stem cell
10 chr1:210289600-210290400 Enhancers HUES6 Cell Line embryonic stem cell
11 chr1:210289600-210290600 Weak transcription iPS-20b Cell Line embryonic stem cell
12 chr1:210289600-210290600 Enhancers ES-UCSF4 Cell Line embryonic stem cell
13 chr1:210289600-210291000 Enhancers HUES48 Cell Line embryonic stem cell

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