Variant report

Variant rs164980
Chromosome Location chr1:180180669-180180670
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:180159200-180182800 Weak transcription HSMMtube muscle
2 chr1:180164800-180187800 Weak transcription Right Atrium heart
3 chr1:180166600-180182800 Weak transcription Brain Substantia Nigra brain
4 chr1:180168400-180180800 Weak transcription Esophagus oesophagus
5 chr1:180168800-180182800 Weak transcription Brain Germinal Matrix brain
6 chr1:180169600-180182600 Weak transcription Muscle Satellite Cultured Cells --
7 chr1:180176000-180182600 Weak transcription Spleen Spleen
8 chr1:180176800-180182600 Weak transcription Primary T helper 17 cells PMA-I stimulated --
9 chr1:180177600-180182600 Weak transcription Fetal Thymus thymus
10 chr1:180177600-180182800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
11 chr1:180178000-180182400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr1:180178000-180182600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
13 chr1:180179200-180180800 Bivalent Enhancer Fetal Muscle Trunk muscle
14 chr1:180179600-180181000 Weak transcription NHEK skin
15 chr1:180179800-180181000 Weak transcription HMEC breast
16 chr1:180180400-180181200 Enhancers Primary hematopoietic stem cells short term culture blood
17 chr1:180180400-180181200 Enhancers K562 blood
18 chr1:180180400-180181400 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin

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