Variant report

Variant rs55691648
Chromosome Location chr15:83836050-83836051
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:83825800-83847200 Weak transcription Left Ventricle heart
2 chr15:83826000-83836200 Weak transcription Colon Smooth Muscle Colon
3 chr15:83830200-83838600 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
4 chr15:83832200-83865600 Weak transcription HSMM muscle
5 chr15:83834000-83860600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr15:83834200-83836400 Enhancers iPS-20b Cell Line embryonic stem cell
7 chr15:83834200-83839000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr15:83834200-83842200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
9 chr15:83834200-83846800 Weak transcription Osteobl bone
10 chr15:83835400-83836400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
11 chr15:83835800-83837400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
12 chr15:83835800-83838000 Enhancers HUES48 Cell Line embryonic stem cell
13 chr15:83836000-83836200 ZNF genes & repeats Right Atrium heart
14 chr15:83836000-83836800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
15 chr15:83836000-83836800 Weak transcription K562 blood
16 chr15:83836000-83840000 Weak transcription HUVEC blood vessel
17 chr15:83836000-83847400 Weak transcription HUES64 Cell Line embryonic stem cell
18 chr15:83836000-83870200 Weak transcription H9 Cell Line embryonic stem cell

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