Variant report

Variant	rs73250398
Chromosome Location	chr4:20435188-20435189
allele	A/G
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	chr4:20431200-20435400	Enhancers	Fetal Intestine Small	intestine
2	chr4:20432400-20436000	Enhancers	Fetal Intestine Large	intestine
3	chr4:20433000-20435400	Enhancers	Fetal Lung	lung
4	chr4:20433200-20435200	Active TSS	Colon Smooth Muscle	Colon
5	chr4:20433800-20435400	Enhancers	Small Intestine	intestine
6	chr4:20434000-20435200	Enhancers	HUVEC	blood vessel
7	chr4:20434000-20435400	Enhancers	Duodenum Mucosa	Duodenum
8	chr4:20434200-20435200	Enhancers	Rectal Smooth Muscle	rectum
9	chr4:20434600-20435400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr4:20434800-20435200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr4:20434800-20435800	Enhancers	Duodenum Smooth Muscle	Duodenum
12	chr4:20434800-20446000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr4:20435000-20435200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr4:20435000-20435200	Enhancers	Fetal Stomach	stomach
15	chr4:20435000-20435200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
16	chr4:20435000-20435400	Active TSS	Stomach Smooth Muscle	stomach
17	chr4:20435000-20444200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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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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