Variant report

Variant rs548230291
Chromosome Location chr6:11939496-11939497
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:11937800-11940200 Weak transcription Thymus Thymus
2 chr6:11937800-11940600 Enhancers iPS-18 Cell Line embryonic stem cell
3 chr6:11938600-11940200 Enhancers GM12878-XiMat blood
4 chr6:11938800-11939800 Enhancers Primary hematopoietic stem cells blood
5 chr6:11939000-11939600 Weak transcription iPS-20b Cell Line embryonic stem cell
6 chr6:11939000-11939600 Enhancers Fetal Intestine Small intestine
7 chr6:11939000-11939600 Enhancers HUVEC blood vessel
8 chr6:11939000-11939800 Enhancers Fetal Intestine Large intestine
9 chr6:11939000-11940000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
10 chr6:11939000-11940200 Weak transcription Fetal Kidney kidney
11 chr6:11939200-11940400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr6:11939200-11940600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
13 chr6:11939200-11940800 Enhancers K562 blood
14 chr6:11939200-11942800 Weak transcription Liver Liver
15 chr6:11939200-11943400 Weak transcription Breast Myoepithelial Primary Cells Breast
16 chr6:11939200-11943400 Weak transcription Duodenum Mucosa Duodenum
17 chr6:11939200-11943600 Weak transcription Pancreas Pancrea
18 chr6:11939400-11939800 Weak transcription Fetal Adrenal Gland Adrenal Gland

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