Variant report

Variant rs2814968
Chromosome Location chr6:34713138-34713139
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:23 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:34698000-34714000 Weak transcription Esophagus oesophagus
2 chr6:34708600-34713200 Weak transcription Liver Liver
3 chr6:34711200-34713200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr6:34711200-34713200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr6:34711400-34714600 Enhancers Placenta Placenta
6 chr6:34711600-34715400 Enhancers Fetal Intestine Large intestine
7 chr6:34712200-34714800 Enhancers Fetal Intestine Small intestine
8 chr6:34712400-34714400 Enhancers Placenta Amnion Placenta Amnion
9 chr6:34712600-34714200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr6:34712800-34713200 Enhancers Colonic Mucosa Colon
11 chr6:34712800-34713400 Enhancers A549 lung
12 chr6:34712800-34713400 Flanking Active TSS NHEK skin
13 chr6:34712800-34714400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr6:34712800-34714400 Flanking Active TSS HepG2 liver
15 chr6:34712800-34714600 Enhancers Rectal Mucosa Donor 31 rectum
16 chr6:34713000-34713200 Flanking Active TSS Duodenum Mucosa Duodenum
17 chr6:34713000-34713200 Flanking Active TSS Rectal Mucosa Donor 29 rectum
18 chr6:34713000-34713200 Flanking Active TSS Stomach Mucosa stomach
19 chr6:34713000-34713200 Enhancers Hela-S3 cervix
20 chr6:34713000-34713400 Flanking Active TSS K562 blood
21 chr6:34713000-34713400 Enhancers NH-A brain
22 chr6:34713000-34714000 Enhancers HMEC breast
23 chr6:34713000-34714200 Weak transcription Small Intestine intestine

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