Variant report

Variant rs62438173
Chromosome Location chr7:4136562-4136563
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:4119400-4153000 Weak transcription Gastric stomach
2 chr7:4129400-4150000 Weak transcription Pancreas Pancrea
3 chr7:4130800-4136600 Weak transcription Pancreatic Islets Pancreatic Islet
4 chr7:4131800-4143400 Weak transcription Fetal Intestine Small intestine
5 chr7:4132200-4141600 Weak transcription Fetal Stomach stomach
6 chr7:4132400-4180200 Weak transcription Colon Smooth Muscle Colon
7 chr7:4134400-4139200 Weak transcription Spleen Spleen
8 chr7:4135800-4136600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
9 chr7:4135800-4138200 Enhancers Primary T helper naive cells fromperipheralblood blood
10 chr7:4136200-4137400 Enhancers Fetal Thymus thymus
11 chr7:4136400-4136600 Flanking Active TSS Primary T cells from cord blood blood
12 chr7:4136400-4136800 Genic enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
13 chr7:4136400-4137200 Strong transcription Aorta Aorta
14 chr7:4136400-4137200 Enhancers Fetal Muscle Leg muscle
15 chr7:4136400-4137600 Weak transcription Primary T helper cells PMA-I stimulated --

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