Variant report

Variant rs7548952
Chromosome Location chr1:211797358-211797359
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:211790400-211798400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
2 chr1:211790400-211803600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr1:211793400-211803000 Weak transcription Fetal Intestine Small intestine
4 chr1:211795200-211798200 Weak transcription Hela-S3 cervix
5 chr1:211795200-211800000 Weak transcription Left Ventricle heart
6 chr1:211795200-211802400 Weak transcription Right Atrium heart
7 chr1:211795200-211803400 Weak transcription HUES6 Cell Line embryonic stem cell
8 chr1:211795400-211798200 Weak transcription HepG2 liver
9 chr1:211795400-211800200 Weak transcription Fetal Muscle Trunk muscle
10 chr1:211796400-211797800 Enhancers Primary hematopoietic stem cells blood
11 chr1:211796400-211797800 Enhancers K562 blood
12 chr1:211796400-211798400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
13 chr1:211796400-211798600 Enhancers Primary hematopoietic stem cells short term culture blood
14 chr1:211796600-211797400 Enhancers Primary T helper cells PMA-I stimulated --
15 chr1:211796600-211798400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
16 chr1:211796600-211803600 Weak transcription Spleen Spleen
17 chr1:211796800-211797400 Enhancers Primary T helper memory cells from peripheral blood 2 blood
18 chr1:211796800-211797400 Enhancers Primary T helper naive cells from peripheral blood blood
19 chr1:211797000-211797600 Weak transcription Fetal Intestine Large intestine
20 chr1:211797000-211800000 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
21 chr1:211797200-211800400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived

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