Variant report

Variant rs899168
Chromosome Location chr5:180074990-180074991
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:180066400-180075600 Enhancers Spleen Spleen
2 chr5:180071800-180075200 Bivalent Enhancer Fetal Muscle Trunk muscle
3 chr5:180072600-180075000 Enhancers Placenta Placenta
4 chr5:180072800-180075400 Bivalent Enhancer Skeletal Muscle Female skeletal muscle
5 chr5:180072800-180075600 Weak transcription Primary hematopoietic stem cells blood
6 chr5:180072800-180075600 Weak transcription Right Atrium heart
7 chr5:180073800-180075000 Bivalent Enhancer Adipose Nuclei Adipose
8 chr5:180073800-180075200 Bivalent Enhancer Skeletal Muscle Male skeletal muscle
9 chr5:180073800-180075600 Bivalent Enhancer Right Ventricle heart
10 chr5:180074200-180075400 Weak transcription HUVEC blood vessel
11 chr5:180074600-180075200 Weak transcription Lung lung
12 chr5:180074600-180075600 Bivalent/Poised TSS Fetal Adrenal Gland Adrenal Gland
13 chr5:180074800-180075000 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
14 chr5:180074800-180075200 Bivalent/Poised TSS Fetal Muscle Leg muscle

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