Variant report

Variant rs56740066
Chromosome Location chr19:55697148-55697149
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:55691200-55718200 Weak transcription Right Atrium heart
2 chr19:55691600-55718200 Weak transcription Placenta Amnion Placenta Amnion
3 chr19:55691800-55717600 Strong transcription Fetal Intestine Small intestine
4 chr19:55692000-55697600 Weak transcription Hela-S3 cervix
5 chr19:55692000-55707800 Weak transcription K562 blood
6 chr19:55692200-55710000 Weak transcription Pancreas Pancrea
7 chr19:55692600-55701200 Strong transcription Fetal Adrenal Gland Adrenal Gland
8 chr19:55692600-55717000 Strong transcription Duodenum Mucosa Duodenum
9 chr19:55693000-55702800 Weak transcription Fetal Intestine Large intestine
10 chr19:55693800-55700200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
11 chr19:55694600-55702200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
12 chr19:55696400-55702600 Weak transcription Rectal Mucosa Donor 31 rectum
13 chr19:55696600-55697600 Strong transcription Stomach Mucosa stomach
14 chr19:55696600-55698200 Strong transcription Rectal Mucosa Donor 29 rectum
15 chr19:55696800-55697200 Active TSS iPS DF 19.11 Cell Line embryonic stem cell
16 chr19:55696800-55697400 Strong transcription Gastric stomach
17 chr19:55696800-55697800 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin
18 chr19:55696800-55698200 Strong transcription Spleen Spleen
19 chr19:55697000-55697200 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin02 Skin
20 chr19:55697000-55697600 Strong transcription HepG2 liver

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