Variant report

Variant rs187777979
Chromosome Location chr7:103256039-103256040
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:4 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:103245000-103259600 Weak transcription HepG2 liver
2 chr7:103255400-103256200 Enhancers K562 blood
3 chr7:103255800-103256800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
4 chr7:103256000-103256800 Enhancers Ganglion Eminence derived primary cultured neurospheres brain

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