Variant report

Variant	rs876694
Chromosome Location	chr1:159146308-159146309
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:159143000-159156800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr1:159143200-159155600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr1:159143400-159150200	Weak transcription	Brain Substantia Nigra	brain
4	chr1:159143400-159151600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr1:159143600-159155800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr1:159143600-159157600	Weak transcription	Placenta	Placenta
7	chr1:159144000-159154200	Weak transcription	Brain Germinal Matrix	brain
8	chr1:159144400-159146600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr1:159144800-159146600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr1:159145000-159150600	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr1:159145000-159157400	Weak transcription	Brain Cingulate Gyrus	brain
12	chr1:159145200-159148800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr1:159145600-159146400	Weak transcription	Fetal Brain Female	brain
14	chr1:159145800-159148600	Weak transcription	Brain Angular Gyrus	brain
15	chr1:159145800-159154800	Weak transcription	Brain Anterior Caudate	brain
16	chr1:159146000-159147000	Weak transcription	Fetal Brain Male	brain
17	chr1:159146200-159146400	Enhancers	Brain Hippocampus Middle	brain

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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