Variant report

Variant rs1977262
Chromosome Location chr6:1853568-1853569
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:1829800-1856600 Weak transcription Primary T cells from cord blood blood
2 chr6:1833400-1856600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr6:1838200-1862200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr6:1842800-1872400 Weak transcription Gastric stomach
5 chr6:1845600-1861200 Weak transcription Aorta Aorta
6 chr6:1846400-1856800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr6:1848600-1856800 Weak transcription HepG2 liver
8 chr6:1850800-1853800 Weak transcription Cortex derived primary cultured neurospheres brain
9 chr6:1850800-1854000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
10 chr6:1850800-1856200 Weak transcription Primary B cells from peripheral blood blood
11 chr6:1851200-1856400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr6:1851200-1895600 Weak transcription Rectal Mucosa Donor 29 rectum
13 chr6:1851400-1856800 Weak transcription Fetal Intestine Small intestine
14 chr6:1851400-1861200 Weak transcription Colonic Mucosa Colon
15 chr6:1851400-1865000 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
16 chr6:1851400-1872200 Weak transcription Pancreas Pancrea
17 chr6:1851400-1909600 Weak transcription Rectal Mucosa Donor 31 rectum
18 chr6:1852400-1856400 Weak transcription Small Intestine intestine
19 chr6:1852600-1854000 Weak transcription Dnd41 blood

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