Variant report

Variant rs10077934
Chromosome Location chr5:154470468-154470469
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:154462200-154474400 Weak transcription Right Ventricle heart
2 chr5:154464000-154472000 Enhancers Placenta Placenta
3 chr5:154464200-154472800 Enhancers Placenta Amnion Placenta Amnion
4 chr5:154467400-154470600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr5:154467400-154470600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr5:154467400-154470600 Weak transcription HMEC breast
7 chr5:154467400-154470600 Weak transcription HSMMtube muscle
8 chr5:154467400-154474800 Weak transcription Left Ventricle heart
9 chr5:154468200-154470600 Weak transcription Rectal Smooth Muscle rectum
10 chr5:154468400-154471400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr5:154468800-154470600 Weak transcription Colon Smooth Muscle Colon
12 chr5:154468800-154470600 Weak transcription Fetal Stomach stomach
13 chr5:154468800-154472000 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
14 chr5:154469200-154470800 Weak transcription Ovary ovary
15 chr5:154469600-154470600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
16 chr5:154469600-154470600 Weak transcription NHEK skin
17 chr5:154469600-154471600 Weak transcription HUVEC blood vessel
18 chr5:154469800-154470600 Weak transcription HSMM muscle
19 chr5:154470200-154472000 Enhancers Fetal Heart heart

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