Variant report

Variant rs55876140
Chromosome Location chr6:12350213-12350214
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:12343200-12351400 Weak transcription Colonic Mucosa Colon
2 chr6:12347800-12351400 Enhancers Fetal Intestine Small intestine
3 chr6:12347800-12352800 Enhancers Fetal Intestine Large intestine
4 chr6:12348000-12352000 Enhancers Stomach Mucosa stomach
5 chr6:12348600-12351400 Enhancers NHEK skin
6 chr6:12348800-12350400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr6:12349000-12351400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr6:12349000-12351600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr6:12349200-12350400 Flanking Active TSS A549 lung
10 chr6:12349400-12351400 Weak transcription Duodenum Mucosa Duodenum
11 chr6:12349400-12351400 Weak transcription Small Intestine intestine
12 chr6:12349400-12352000 Enhancers Rectal Mucosa Donor 31 rectum
13 chr6:12349600-12350400 Enhancers Rectal Mucosa Donor 29 rectum
14 chr6:12349800-12352000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr6:12349800-12354000 Weak transcription HUVEC blood vessel
16 chr6:12349800-12354000 Weak transcription Osteobl bone
17 chr6:12349800-12355000 Weak transcription Placenta Amnion Placenta Amnion
18 chr6:12350000-12353800 ZNF genes & repeats ES-I3 Cell Line embryonic stem cell
19 chr6:12350000-12355000 Weak transcription Sigmoid Colon Sigmoid Colon
20 chr6:12350200-12351200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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