Variant report

Variant rs373282290
Chromosome Location chr6:29945756-29945757
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:29945000-29945800 Bivalent Enhancer Fetal Heart heart
2 chr6:29945000-29945800 Flanking Active TSS K562 blood
3 chr6:29945200-29945800 Enhancers Liver Liver
4 chr6:29945200-29948600 Weak transcription Small Intestine intestine
5 chr6:29945200-29948600 Weak transcription Spleen Spleen
6 chr6:29945400-29945800 Enhancers Breast Myoepithelial Primary Cells Breast
7 chr6:29945400-29945800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
8 chr6:29945400-29945800 Enhancers Fetal Intestine Small intestine
9 chr6:29945400-29945800 Enhancers Pancreatic Islets Pancreatic Islet
10 chr6:29945400-29945800 Enhancers A549 lung
11 chr6:29945400-29948800 Weak transcription Rectal Mucosa Donor 29 rectum
12 chr6:29945400-29950200 Weak transcription Right Atrium heart
13 chr6:29945600-29945800 Enhancers Skeletal Muscle Male skeletal muscle
14 chr6:29945600-29945800 Enhancers HepG2 liver
15 chr6:29945600-29948000 Weak transcription Colonic Mucosa Colon
16 chr6:29945600-29948600 Weak transcription Rectal Mucosa Donor 31 rectum
17 chr6:29945600-29948600 Weak transcription Stomach Mucosa stomach
18 chr6:29945600-29948800 Weak transcription Duodenum Mucosa Duodenum
19 chr6:29945600-29966400 Weak transcription Pancreas Pancrea

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