Variant report

Variant	rs17098938
Chromosome Location	chr14:32850835-32850836
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:32845200-32851000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr14:32846800-32851800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr14:32847000-32854000	Weak transcription	Fetal Brain Female	brain
4	chr14:32847600-32852800	Weak transcription	Brain Anterior Caudate	brain
5	chr14:32849000-32851200	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr14:32849000-32867400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr14:32849200-32851200	Weak transcription	Brain Hippocampus Middle	brain
8	chr14:32849200-32853000	Weak transcription	Psoas Muscle	Psoas
9	chr14:32849600-32851800	Weak transcription	Brain Cingulate Gyrus	brain
10	chr14:32849800-32851000	Weak transcription	HMEC	breast
11	chr14:32849800-32851200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr14:32850000-32851000	Weak transcription	Brain Angular Gyrus	brain
13	chr14:32850200-32851200	Weak transcription	Brain Substantia Nigra	brain
14	chr14:32850800-32851000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr14:32850800-32854200	Enhancers	NHEK	skin
16	chr14:32850800-32854400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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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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