Variant report

Variant rs9481933
Chromosome Location chr6:119816240-119816241
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:119814600-119816600 Enhancers Pancreatic Islets Pancreatic Islet
2 chr6:119814600-119817200 Enhancers Stomach Mucosa stomach
3 chr6:119814800-119816800 Enhancers HepG2 liver
4 chr6:119815200-119817000 Enhancers Rectal Mucosa Donor 31 rectum
5 chr6:119815200-119817200 Enhancers Fetal Intestine Small intestine
6 chr6:119815200-119817200 Enhancers Pancreas Pancrea
7 chr6:119815200-119817200 Enhancers Small Intestine intestine
8 chr6:119815200-119817400 Enhancers Fetal Adrenal Gland Adrenal Gland
9 chr6:119815200-119817400 Enhancers Fetal Intestine Large intestine
10 chr6:119815600-119816800 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr6:119815600-119817000 Enhancers Gastric stomach
12 chr6:119815600-119817200 Enhancers Rectal Mucosa Donor 29 rectum
13 chr6:119815600-119817400 Enhancers Duodenum Mucosa Duodenum
14 chr6:119815600-119818800 Weak transcription Primary hematopoietic stem cells blood
15 chr6:119815800-119817400 Enhancers Left Ventricle heart
16 chr6:119815800-119819000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
17 chr6:119816000-119816600 Weak transcription Fetal Thymus thymus
18 chr6:119816000-119816800 Weak transcription Spleen Spleen
19 chr6:119816200-119817400 Enhancers Liver Liver
20 chr6:119816200-119818000 Enhancers Fetal Heart heart

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