Variant report

Variant rs10872034
Chromosome Location chr6:109807239-109807240
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:109804400-109814200 Weak transcription Gastric stomach
2 chr6:109805000-109817000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr6:109805200-109809200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr6:109805400-109807400 Weak transcription Fetal Intestine Large intestine
5 chr6:109805400-109807800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
6 chr6:109805400-109808800 Weak transcription Fetal Adrenal Gland Adrenal Gland
7 chr6:109805400-109812000 Weak transcription H9 Cell Line embryonic stem cell
8 chr6:109805600-109807400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr6:109805600-109812400 Weak transcription Brain Angular Gyrus brain
10 chr6:109806000-109811400 Weak transcription Dnd41 blood
11 chr6:109806200-109812200 Weak transcription Primary hematopoietic stem cells blood
12 chr6:109806400-109807600 Enhancers Rectal Mucosa Donor 31 rectum
13 chr6:109806800-109812200 Weak transcription Fetal Muscle Leg muscle
14 chr6:109807000-109807400 Enhancers Placenta Placenta
15 chr6:109807200-109807400 Enhancers Stomach Mucosa stomach
16 chr6:109807200-109808000 Enhancers Hela-S3 cervix

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