Variant report

Variant rs6972218
Chromosome Location chr7:138426230-138426231
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:138400600-138439000 Weak transcription Right Atrium heart
2 chr7:138419800-138437400 Weak transcription H9 Cell Line embryonic stem cell
3 chr7:138423200-138438200 Weak transcription ES-WA7 Cell Line embryonic stem cell
4 chr7:138423600-138426400 Weak transcription Fetal Stomach stomach
5 chr7:138423600-138436800 Weak transcription Placenta Placenta
6 chr7:138424000-138431400 Weak transcription iPS-15b Cell Line embryonic stem cell
7 chr7:138424000-138435200 Weak transcription Dnd41 blood
8 chr7:138424200-138429800 Weak transcription Fetal Thymus thymus
9 chr7:138424200-138437200 Weak transcription ES-I3 Cell Line embryonic stem cell
10 chr7:138424400-138429800 Weak transcription Thymus Thymus
11 chr7:138425800-138426400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr7:138426000-138426400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr7:138426000-138426400 Enhancers Hela-S3 cervix
14 chr7:138426000-138426400 Enhancers HUVEC blood vessel
15 chr7:138426000-138426400 Enhancers Osteobl bone
16 chr7:138426000-138426600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
17 chr7:138426000-138426600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
18 chr7:138426000-138426800 Enhancers HSMMtube muscle
19 chr7:138426000-138426800 Enhancers NH-A brain
20 chr7:138426200-138426600 Enhancers NHDF-Ad bronchial
21 chr7:138426200-138435800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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