Variant report

Variant	rs59462187
Chromosome Location	chr8:125054581-125054582
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Variant related genes	Relation type
FER1L6-AS1	TF binding region
ENSG00000254249	TF binding region
ENSG00000164983	Chromatin interaction
ENSG00000254249	Chromatin interaction

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:125050600-125054800	Enhancers	Fetal Intestine Small	intestine
2	chr8:125051200-125054800	Enhancers	Fetal Intestine Large	intestine
3	chr8:125052200-125054600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr8:125052600-125083600	Weak transcription	Gastric	stomach
5	chr8:125053000-125060400	Weak transcription	Left Ventricle	heart
6	chr8:125053600-125054600	Enhancers	Brain Germinal Matrix	brain
7	chr8:125053600-125058600	Enhancers	Fetal Heart	heart
8	chr8:125053800-125056200	Weak transcription	Duodenum Mucosa	Duodenum
9	chr8:125053800-125059800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr8:125053800-125062400	Weak transcription	Stomach Mucosa	stomach
11	chr8:125054000-125055400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr8:125054200-125056400	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr8:125054200-125056400	Weak transcription	A549	lung
14	chr8:125054200-125061000	Weak transcription	Fetal Stomach	stomach
15	chr8:125054400-125056600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr8:125054400-125056800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

Quick Search:

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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