Variant report

Variant rs1344249
Chromosome Location chr6:118778242-118778243
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:118774400-118808600 Weak transcription Placenta Amnion Placenta Amnion
2 chr6:118775000-118779600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr6:118775600-118784600 Weak transcription HSMM muscle
4 chr6:118776000-118792400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
5 chr6:118776200-118786000 Weak transcription Adipose Nuclei Adipose
6 chr6:118776600-118785800 Weak transcription Cortex derived primary cultured neurospheres brain
7 chr6:118776800-118808800 Weak transcription Fetal Stomach stomach
8 chr6:118777000-118780000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr6:118777400-118786400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
10 chr6:118777600-118790800 Weak transcription Pancreas Pancrea
11 chr6:118777800-118788000 Weak transcription HMEC breast
12 chr6:118777800-118791000 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
13 chr6:118778000-118784800 Weak transcription Osteobl bone
14 chr6:118778000-118785000 Weak transcription Primary T cells from cord blood blood
15 chr6:118778200-118778600 Flanking Active TSS Fetal Heart heart
16 chr6:118778200-118781400 Weak transcription Fetal Muscle Leg muscle
17 chr6:118778200-118786000 Weak transcription Fetal Muscle Trunk muscle

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