Variant report

Variant rs10277830
Chromosome Location chr7:4136245-4136246
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 chr7:4130600-4136400 Weak transcription Aorta Aorta
4 chr7:4130800-4136600 Weak transcription Pancreatic Islets Pancreatic Islet
5 chr7:4131800-4143400 Weak transcription Fetal Intestine Small intestine
6 chr7:4132200-4141600 Weak transcription Fetal Stomach stomach
7 chr7:4132400-4180200 Weak transcription Colon Smooth Muscle Colon
8 chr7:4134400-4136400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr7:4134400-4139200 Weak transcription Spleen Spleen
10 chr7:4135800-4136400 Enhancers Primary T helper cells PMA-I stimulated --
11 chr7:4135800-4136400 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
12 chr7:4135800-4136600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
13 chr7:4135800-4138200 Enhancers Primary T helper naive cells fromperipheralblood blood
14 chr7:4136200-4136400 Active TSS Primary T cells from cord blood blood
15 chr7:4136200-4137400 Enhancers Fetal Thymus thymus

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