Variant report

Variant rs2097594
Chromosome Location chr22:22947156-22947157
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:22943800-22951600 Weak transcription Fetal Muscle Trunk muscle
2 chr22:22945200-22950600 Weak transcription Fetal Muscle Leg muscle
3 chr22:22945600-22947400 ZNF genes & repeats Primary B cells from peripheral blood blood
4 chr22:22945600-22947600 Strong transcription Right Atrium heart
5 chr22:22946000-22948000 Enhancers Primary B cells from cord blood blood
6 chr22:22946200-22947600 Enhancers Spleen Spleen
7 chr22:22946600-22947200 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
8 chr22:22946800-22948000 Flanking Active TSS GM12878-XiMat blood
9 chr22:22947000-22947400 Bivalent Enhancer ES-I3 Cell Line embryonic stem cell
10 chr22:22947000-22947400 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
11 chr22:22947000-22947600 Bivalent Enhancer HUES48 Cell Line embryonic stem cell
12 chr22:22947000-22947600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
13 chr22:22947000-22947600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
14 chr22:22947000-22947600 Enhancers Fetal Adrenal Gland Adrenal Gland

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