Variant report

Variant rs7375552
Chromosome Location chr4:174075465-174075466
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:174047000-174079000 Weak transcription Fetal Thymus thymus
2 chr4:174055000-174086000 Weak transcription Thymus Thymus
3 chr4:174065200-174087200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr4:174065400-174083600 Weak transcription Primary hematopoietic stem cells short term culture blood
5 chr4:174066800-174089000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
6 chr4:174066800-174089000 Weak transcription HSMM muscle
7 chr4:174069200-174088800 Weak transcription HMEC breast
8 chr4:174071800-174080800 Weak transcription Primary B cells from cord blood blood
9 chr4:174072000-174077000 Weak transcription Primary hematopoietic stem cells blood
10 chr4:174072000-174081000 Weak transcription Monocytes-CD14+_RO01746 blood
11 chr4:174072200-174089000 Weak transcription Fetal Stomach stomach
12 chr4:174073000-174085400 Weak transcription Fetal Muscle Leg muscle
13 chr4:174073600-174089000 Weak transcription Pancreas Pancrea
14 chr4:174073600-174089200 Weak transcription Aorta Aorta
15 chr4:174073800-174089000 Weak transcription NHLF lung
16 chr4:174074200-174083600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
17 chr4:174074600-174088800 Weak transcription Fetal Intestine Small intestine
18 chr4:174075200-174075600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
19 chr4:174075400-174088600 Weak transcription Fetal Intestine Large intestine

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