Variant report

Variant rs6680211
Chromosome Location chr1:46315007-46315008
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:46270200-46317000 Weak transcription Gastric stomach
2 chr1:46287400-46315600 Weak transcription Cortex derived primary cultured neurospheres brain
3 chr1:46288800-46315600 Weak transcription Primary T cells from cord blood blood
4 chr1:46296800-46315200 Weak transcription Primary hematopoietic stem cells blood
5 chr1:46298000-46316000 Weak transcription Dnd41 blood
6 chr1:46298400-46315200 Weak transcription Primary hematopoietic stem cells short term culture blood
7 chr1:46301000-46315600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr1:46307000-46316000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr1:46309600-46315400 Weak transcription Duodenum Mucosa Duodenum
10 chr1:46313000-46316800 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
11 chr1:46313200-46316600 Weak transcription Muscle Satellite Cultured Cells --
12 chr1:46313400-46315600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr1:46313400-46320400 Weak transcription NHLF lung
14 chr1:46313600-46320400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
15 chr1:46313800-46315600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
16 chr1:46314400-46315200 ZNF genes & repeats hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
17 chr1:46314400-46315600 Weak transcription H1 Cell Line embryonic stem cell
18 chr1:46314400-46316400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
19 chr1:46314400-46327400 Weak transcription K562 blood
20 chr1:46314600-46317000 Weak transcription iPS-18 Cell Line embryonic stem cell
21 chr1:46314800-46315800 ZNF genes & repeats Ganglion Eminence derived primary cultured neurospheres brain

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