Variant report

Variant rs60125061
Chromosome Location chr2:10436742-10436743
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:10426200-10438000 Weak transcription ES-WA7 Cell Line embryonic stem cell
2 chr2:10426800-10437600 Weak transcription Spleen Spleen
3 chr2:10429600-10436800 Weak transcription Monocytes-CD14+_RO01746 blood
4 chr2:10434000-10437400 Weak transcription HMEC breast
5 chr2:10435200-10438200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr2:10435200-10438800 Enhancers Placenta Placenta
7 chr2:10435400-10438600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr2:10435600-10437800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr2:10435800-10437600 Weak transcription Sigmoid Colon Sigmoid Colon
10 chr2:10435800-10437800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr2:10435800-10441000 Weak transcription Stomach Mucosa stomach
12 chr2:10436000-10442000 Enhancers Primary monocytes fromperipheralblood blood
13 chr2:10436400-10437200 Enhancers HUES48 Cell Line embryonic stem cell
14 chr2:10436600-10436800 Enhancers iPS-20b Cell Line embryonic stem cell
15 chr2:10436600-10437000 Enhancers H1 Cell Line embryonic stem cell
16 chr2:10436600-10437200 Weak transcription K562 blood
17 chr2:10436600-10437600 Weak transcription NHEK skin
18 chr2:10436600-10437800 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
19 chr2:10436600-10438600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
20 chr2:10436600-10442200 Weak transcription Placenta Amnion Placenta Amnion

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