Variant report

Variant rs10209424
Chromosome Location chr2:189155182-189155183
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:189144000-189155400 Weak transcription Aorta Aorta
2 chr2:189144200-189156000 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
3 chr2:189145000-189155400 Weak transcription iPS-15b Cell Line embryonic stem cell
4 chr2:189150200-189155200 Weak transcription H1 Cell Line embryonic stem cell
5 chr2:189150800-189155200 Weak transcription Stomach Mucosa stomach
6 chr2:189151200-189155800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr2:189152000-189155400 Weak transcription HUES48 Cell Line embryonic stem cell
8 chr2:189152800-189155800 Weak transcription Placenta Placenta
9 chr2:189153000-189155600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
10 chr2:189154400-189155200 Enhancers HUES64 Cell Line embryonic stem cell
11 chr2:189154400-189155400 Enhancers K562 blood
12 chr2:189154400-189155800 Enhancers Colon Smooth Muscle Colon
13 chr2:189154600-189155200 Enhancers A549 lung
14 chr2:189154600-189155400 Enhancers iPS-18 Cell Line embryonic stem cell
15 chr2:189154600-189155800 Enhancers Ovary ovary
16 chr2:189154600-189156000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
17 chr2:189155000-189155200 Enhancers iPS-20b Cell Line embryonic stem cell
18 chr2:189155000-189155200 Enhancers HUVEC blood vessel

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