Variant report

Variant rs59041016
Chromosome Location chr1:173465835-173465836
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:173448000-173477000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr1:173457200-173466200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr1:173457200-173466800 Weak transcription Gastric stomach
4 chr1:173457600-173466000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
5 chr1:173458600-173467200 Weak transcription HSMMtube muscle
6 chr1:173458600-173468400 Weak transcription Sigmoid Colon Sigmoid Colon
7 chr1:173458600-173475600 Weak transcription Fetal Kidney kidney
8 chr1:173458600-173476600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr1:173458800-173466200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr1:173458800-173470400 Weak transcription Ovary ovary
11 chr1:173459200-173466000 Weak transcription Adipose Nuclei Adipose
12 chr1:173459400-173474000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr1:173459400-173475400 Weak transcription Rectal Mucosa Donor 31 rectum
14 chr1:173459600-173470000 Weak transcription Skeletal Muscle Male skeletal muscle
15 chr1:173459800-173469200 Weak transcription Left Ventricle heart
16 chr1:173461800-173470200 Weak transcription Skeletal Muscle Female skeletal muscle
17 chr1:173464400-173466600 Enhancers Hela-S3 cervix
18 chr1:173465000-173466400 Enhancers K562 blood
19 chr1:173465400-173466400 Weak transcription Liver Liver

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