Variant report

Variant rs4667226
Chromosome Location chr2:189295789-189295790
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:189285600-189318800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr2:189285800-189318200 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
3 chr2:189291600-189297400 Weak transcription ES-WA7 Cell Line embryonic stem cell
4 chr2:189291800-189297400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
5 chr2:189291800-189297600 Weak transcription iPS-18 Cell Line embryonic stem cell
6 chr2:189292000-189297600 Weak transcription ES-I3 Cell Line embryonic stem cell
7 chr2:189292400-189306200 Weak transcription H9 Cell Line embryonic stem cell
8 chr2:189292800-189297400 Weak transcription iPS-15b Cell Line embryonic stem cell
9 chr2:189292800-189298000 Weak transcription H1 Cell Line embryonic stem cell
10 chr2:189293600-189308800 Weak transcription HUVEC blood vessel
11 chr2:189294200-189297800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
12 chr2:189294200-189308000 Weak transcription Ovary ovary
13 chr2:189295200-189298800 Enhancers HUES64 Cell Line embryonic stem cell
14 chr2:189295600-189296000 Enhancers HUES48 Cell Line embryonic stem cell
15 chr2:189295600-189296000 Enhancers Stomach Mucosa stomach
16 chr2:189295600-189296200 Enhancers iPS-20b Cell Line embryonic stem cell
17 chr2:189295600-189304200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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