Variant report

Variant rs6671629
Chromosome Location chr1:220095113-220095114
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:220085400-220100000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
2 chr1:220086200-220097400 Genic enhancers Liver Liver
3 chr1:220086600-220097400 Weak transcription Fetal Brain Female brain
4 chr1:220087200-220097800 Weak transcription Brain Anterior Caudate brain
5 chr1:220087200-220099600 Weak transcription Brain Hippocampus Middle brain
6 chr1:220087400-220099600 Weak transcription Brain Angular Gyrus brain
7 chr1:220088800-220095800 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
8 chr1:220089000-220101000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr1:220089200-220100000 Weak transcription Brain Germinal Matrix brain
10 chr1:220089400-220097600 Weak transcription Brain Cingulate Gyrus brain
11 chr1:220092200-220095200 Weak transcription Fetal Intestine Small intestine
12 chr1:220092200-220096200 Weak transcription Fetal Adrenal Gland Adrenal Gland
13 chr1:220092200-220096400 Weak transcription Duodenum Mucosa Duodenum
14 chr1:220094200-220096600 Strong transcription Fetal Intestine Large intestine
15 chr1:220094600-220095400 Weak transcription HepG2 liver
16 chr1:220094800-220095600 Weak transcription K562 blood
17 chr1:220095000-220096200 Weak transcription Brain Substantia Nigra brain

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