Variant report

Variant rs7138661
Chromosome Location chr12:9001114-9001115
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:8982200-9022000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr12:8983400-9017600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr12:8987600-9004200 Weak transcription HUES6 Cell Line embryonic stem cell
4 chr12:8987600-9040000 Weak transcription H1 Cell Line embryonic stem cell
5 chr12:8987800-9002800 Weak transcription H9 Cell Line embryonic stem cell
6 chr12:8987800-9004800 Weak transcription HUES64 Cell Line embryonic stem cell
7 chr12:8987800-9012800 Weak transcription HUES48 Cell Line embryonic stem cell
8 chr12:8988200-9012800 Weak transcription ES-I3 Cell Line embryonic stem cell
9 chr12:8994800-9016600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr12:8996000-9007000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
11 chr12:8996000-9040000 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
12 chr12:8996200-9001200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr12:8997000-9001600 Strong transcription Esophagus oesophagus
14 chr12:8997600-9004200 Weak transcription Brain Anterior Caudate brain
15 chr12:8998000-9001200 Weak transcription Brain Substantia Nigra brain
16 chr12:8998000-9002200 Weak transcription Adipose Nuclei Adipose
17 chr12:8998000-9002200 Weak transcription K562 blood
18 chr12:8998800-9014600 Weak transcription Right Atrium heart
19 chr12:8999000-9016400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
20 chr12:9000400-9003400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
21 chr12:9000800-9012400 Weak transcription Placenta Amnion Placenta Amnion

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