Variant report

Variant rs13318969
Chromosome Location chr3:100348843-100348844
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:100343800-100352000 Weak transcription Fetal Intestine Large intestine
2 chr3:100347600-100349200 Weak transcription Small Intestine intestine
3 chr3:100347600-100350000 Enhancers HUVEC blood vessel
4 chr3:100347600-100350400 Enhancers K562 blood
5 chr3:100347800-100349800 Enhancers Primary hematopoietic stem cells short term culture blood
6 chr3:100348200-100349800 Enhancers NHEK skin
7 chr3:100348200-100352200 Weak transcription Primary neutrophils fromperipheralblood blood
8 chr3:100348400-100349200 Enhancers Duodenum Mucosa Duodenum
9 chr3:100348400-100349400 Enhancers Fetal Intestine Small intestine
10 chr3:100348400-100350600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr3:100348400-100350600 Enhancers HMEC breast
12 chr3:100348600-100349800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
13 chr3:100348600-100350200 Enhancers Hela-S3 cervix
14 chr3:100348600-100350400 Enhancers HUES64 Cell Line embryonic stem cell
15 chr3:100348600-100353400 Weak transcription Primary hematopoietic stem cells blood
16 chr3:100348600-100354200 Weak transcription Sigmoid Colon Sigmoid Colon
17 chr3:100348800-100349800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --

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