Variant report

Variant rs35797130
Chromosome Location chr1:223372677-223372678
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:223349800-223375400 Weak transcription Right Atrium heart
2 chr1:223369000-223373600 Weak transcription Primary T helper cells PMA-I stimulated --
3 chr1:223369400-223373800 Weak transcription Fetal Thymus thymus
4 chr1:223370600-223375000 Enhancers Primary monocytes fromperipheralblood blood
5 chr1:223371200-223389800 Weak transcription Gastric stomach
6 chr1:223371400-223375200 Weak transcription Esophagus oesophagus
7 chr1:223371600-223372800 Flanking Active TSS Monocytes-CD14+_RO01746 blood
8 chr1:223371800-223372800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr1:223371800-223372800 Enhancers HMEC breast
10 chr1:223371800-223372800 Enhancers NHEK skin
11 chr1:223371800-223373400 Enhancers Primary neutrophils fromperipheralblood blood
12 chr1:223372400-223372800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr1:223372600-223372800 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
14 chr1:223372600-223372800 Enhancers Pancreas Pancrea

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