Variant report

Variant rs6759989
Chromosome Location chr2:86179591-86179592
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:86175000-86183600 Weak transcription ES-I3 Cell Line embryonic stem cell
2 chr2:86175800-86180600 Enhancers Liver Liver
3 chr2:86176200-86180400 Enhancers Fetal Adrenal Gland Adrenal Gland
4 chr2:86177000-86180800 Weak transcription Adipose Nuclei Adipose
5 chr2:86177200-86180000 Weak transcription Fetal Lung lung
6 chr2:86177800-86179600 Weak transcription Fetal Thymus thymus
7 chr2:86178000-86181000 Enhancers K562 blood
8 chr2:86178800-86180400 Enhancers Primary neutrophils fromperipheralblood blood
9 chr2:86178800-86181800 Enhancers A549 lung
10 chr2:86178800-86188200 Enhancers Fetal Muscle Leg muscle
11 chr2:86179000-86180000 Weak transcription Gastric stomach
12 chr2:86179200-86180800 Enhancers Primary hematopoietic stem cells short term culture blood
13 chr2:86179200-86182200 Weak transcription Esophagus oesophagus
14 chr2:86179200-86183600 Enhancers Pancreas Pancrea
15 chr2:86179200-86183800 Enhancers Stomach Mucosa stomach
16 chr2:86179400-86179600 Flanking Active TSS HepG2 liver
17 chr2:86179400-86179800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
18 chr2:86179400-86180400 Enhancers Fetal Intestine Small intestine

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