Variant report

Variant rs7791238
Chromosome Location chr7:4137183-4137184
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 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 chr7:4131800-4143400 Weak transcription Fetal Intestine Small intestine
4 chr7:4132200-4141600 Weak transcription Fetal Stomach stomach
5 chr7:4132400-4180200 Weak transcription Colon Smooth Muscle Colon
6 chr7:4134400-4139200 Weak transcription Spleen Spleen
7 chr7:4135800-4138200 Enhancers Primary T helper naive cells fromperipheralblood blood
8 chr7:4136200-4137400 Enhancers Fetal Thymus thymus
9 chr7:4136400-4137200 Strong transcription Aorta Aorta
10 chr7:4136400-4137200 Enhancers Fetal Muscle Leg muscle
11 chr7:4136400-4137600 Weak transcription Primary T helper cells PMA-I stimulated --
12 chr7:4136600-4137600 Enhancers Primary T helper naive cells from peripheral blood blood
13 chr7:4136600-4139200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
14 chr7:4136600-4139400 Enhancers Primary T cells from cord blood blood
15 chr7:4136800-4140000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
16 chr7:4136800-4141200 Weak transcription Lung lung
17 chr7:4137000-4137600 Enhancers Primary T helper 17 cells PMA-I stimulated --
18 chr7:4137000-4137600 Enhancers Primary T killer naive cells fromperipheralblood blood
19 chr7:4137000-4138200 Enhancers Primary T helper cells fromperipheralblood blood

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