Variant report

Variant rs4667104
Chromosome Location chr2:187405115-187405116
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:187363000-187408800 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
2 chr2:187367200-187405800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr2:187371000-187407800 Weak transcription Placenta Amnion Placenta Amnion
4 chr2:187381800-187406600 Weak transcription NHEK skin
5 chr2:187386200-187405200 Weak transcription HSMM muscle
6 chr2:187386200-187408000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr2:187399400-187405200 Weak transcription A549 lung
8 chr2:187399400-187408200 Weak transcription Cortex derived primary cultured neurospheres brain
9 chr2:187400000-187405200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr2:187400600-187405200 Weak transcription HepG2 liver
11 chr2:187404200-187405600 Weak transcription HUES64 Cell Line embryonic stem cell
12 chr2:187404200-187406400 Weak transcription HUVEC blood vessel
13 chr2:187404400-187405400 Weak transcription HUES48 Cell Line embryonic stem cell
14 chr2:187404400-187405400 Weak transcription iPS-18 Cell Line embryonic stem cell
15 chr2:187405000-187405200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
16 chr2:187405000-187405600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin

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