Variant report

Variant	rs9483424
Chromosome Location	chr6:132596138-132596139
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:132592600-132596400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr6:132594200-132599200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:132595400-132596200	Enhancers	Aorta	Aorta
4	chr6:132595400-132596200	Enhancers	Fetal Intestine Large	intestine
5	chr6:132595400-132596200	Enhancers	Fetal Intestine Small	intestine
6	chr6:132595800-132596600	Enhancers	Fetal Muscle Trunk	muscle
7	chr6:132595800-132596600	Enhancers	Osteobl	bone
8	chr6:132595800-132596800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr6:132595800-132596800	Enhancers	Fetal Muscle Leg	muscle
10	chr6:132595800-132597000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr6:132595800-132597000	Enhancers	Gastric	stomach
12	chr6:132596000-132596200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr6:132596000-132596200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr6:132596000-132596200	Flanking Active TSS	Duodenum Mucosa	Duodenum
15	chr6:132596000-132596200	Enhancers	Fetal Kidney	kidney
16	chr6:132596000-132596200	Flanking Active TSS	NHEK	skin
17	chr6:132596000-132596800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr6:132596000-132596800	Flanking Active TSS	Stomach Mucosa	stomach
19	chr6:132596000-132597000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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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