Variant report
| Variant | rs1555389 |
|---|---|
| Chromosome Location | chr1:86936770-86936771 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:86933000-86937800 | Weak transcription | Primary hematopoietic stem cells short term culture | blood |
| 2 | chr1:86933000-86938000 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
| 3 | chr1:86933000-86942800 | Weak transcription | K562 | blood |
| 4 | chr1:86933200-86936800 | Weak transcription | Osteobl | bone |
| 5 | chr1:86934200-86938000 | Active TSS | Rectal Mucosa Donor 31 | rectum |
| 6 | chr1:86934600-86938200 | Active TSS | Fetal Intestine Large | intestine |
| 7 | chr1:86934600-86938800 | Active TSS | Rectal Mucosa Donor 29 | rectum |
| 8 | chr1:86935400-86942800 | Weak transcription | Rectal Smooth Muscle | rectum |
| 9 | chr1:86936000-86938000 | Enhancers | NHDF-Ad | bronchial |
| 10 | chr1:86936200-86937000 | Bivalent/Poised TSS | Duodenum Mucosa | Duodenum |
| 11 | chr1:86936200-86937200 | Enhancers | Fetal Heart | heart |
| 12 | chr1:86936200-86939400 | Weak transcription | Pancreatic Islets | Pancreatic Islet |
| 13 | chr1:86936400-86936800 | Bivalent/Poised TSS | Fetal Intestine Small | intestine |
| 14 | chr1:86936400-86937000 | Bivalent Enhancer | GM12878-XiMat | blood |
| 15 | chr1:86936600-86936800 | Enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |
| 16 | chr1:86936600-86937000 | Flanking Active TSS | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
| 17 | chr1:86936600-86937000 | Bivalent Enhancer | HUVEC | blood vessel |
| 18 | chr1:86936600-86938200 | Enhancers | Foreskin Fibroblast Primary Cells skin01 | Skin |
