Variant report

Variant rs371793196
Chromosome Location chr2:86620051-86620052
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:86615000-86620200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr2:86615800-86620200 Weak transcription Fetal Adrenal Gland Adrenal Gland
3 chr2:86619600-86620800 Enhancers Left Ventricle heart
4 chr2:86619600-86621200 Enhancers Fetal Muscle Leg muscle
5 chr2:86619600-86621600 Enhancers Fetal Intestine Large intestine
6 chr2:86619600-86622000 Enhancers Fetal Intestine Small intestine
7 chr2:86619800-86620400 Enhancers Fetal Heart heart
8 chr2:86619800-86621800 Enhancers HSMMtube muscle
9 chr2:86619800-86622800 Enhancers Psoas Muscle Psoas
10 chr2:86620000-86621000 Enhancers Duodenum Mucosa Duodenum
11 chr2:86620000-86621000 Enhancers Rectal Mucosa Donor 31 rectum
12 chr2:86620000-86621600 Enhancers Primary hematopoietic stem cells short term culture blood
13 chr2:86620000-86621600 Enhancers Primary T helper naive cells from peripheral blood blood
14 chr2:86620000-86621600 Enhancers Primary T helper naive cells fromperipheralblood blood
15 chr2:86620000-86621600 Enhancers Cortex derived primary cultured neurospheres brain
16 chr2:86620000-86621600 Enhancers Colonic Mucosa Colon
17 chr2:86620000-86621600 Enhancers HSMM muscle

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