Variant report

Variant rs9489719
Chromosome Location chr6:119780772-119780773
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:119776200-119789200 Weak transcription Fetal Heart heart
2 chr6:119777600-119784200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr6:119779800-119780800 ZNF genes & repeats Primary hematopoietic stem cells blood
4 chr6:119780000-119780800 Enhancers Gastric stomach
5 chr6:119780000-119781000 Enhancers Duodenum Mucosa Duodenum
6 chr6:119780000-119781000 Enhancers Small Intestine intestine
7 chr6:119780000-119781000 Enhancers Stomach Mucosa stomach
8 chr6:119780000-119781000 Flanking Active TSS GM12878-XiMat blood
9 chr6:119780000-119781400 Enhancers Sigmoid Colon Sigmoid Colon
10 chr6:119780000-119781800 Enhancers Rectal Mucosa Donor 31 rectum
11 chr6:119780000-119782000 Enhancers Primary B cells from peripheral blood blood
12 chr6:119780200-119781600 Enhancers Primary B cells from cord blood blood
13 chr6:119780400-119780800 Enhancers Fetal Intestine Large intestine
14 chr6:119780400-119780800 Flanking Active TSS Rectal Mucosa Donor 29 rectum
15 chr6:119780600-119780800 Enhancers Aorta Aorta
16 chr6:119780600-119781000 Enhancers Fetal Intestine Small intestine

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