Variant report

Variant rs17684901
Chromosome Location chr8:2096448-2096449
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:2076000-2109600 Weak transcription Right Atrium heart
2 chr8:2076400-2097800 Strong transcription Skeletal Muscle Female skeletal muscle
3 chr8:2076600-2096800 Strong transcription Skeletal Muscle Male skeletal muscle
4 chr8:2080800-2096800 Strong transcription Left Ventricle heart
5 chr8:2086200-2096800 Weak transcription Spleen Spleen
6 chr8:2090200-2096600 Weak transcription Psoas Muscle Psoas
7 chr8:2093000-2096600 Weak transcription Fetal Muscle Trunk muscle
8 chr8:2093000-2103400 Weak transcription Pancreas Pancrea
9 chr8:2093000-2107200 Weak transcription Gastric stomach
10 chr8:2093200-2098400 Weak transcription Fetal Stomach stomach
11 chr8:2094000-2122400 Weak transcription Right Ventricle heart
12 chr8:2095400-2100800 Weak transcription Fetal Thymus thymus
13 chr8:2095400-2103200 Weak transcription Primary T helper naive cells fromperipheralblood blood
14 chr8:2095600-2097000 Enhancers Primary Natural Killer cells fromperipheralblood blood
15 chr8:2096200-2097000 Enhancers Primary T cells fromperipheralblood blood
16 chr8:2096200-2097600 Strong transcription Fetal Muscle Leg muscle
17 chr8:2096400-2096600 Bivalent Enhancer HSMMtube muscle
18 chr8:2096400-2096800 Enhancers HUES6 Cell Line embryonic stem cell
19 chr8:2096400-2097000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
20 chr8:2096400-2101600 Weak transcription Primary mononuclear cells fromperipheralblood Blood

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