Variant report

Variant	rs12317246
Chromosome Location	chr12:57048179-57048180
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:57039800-57055800	Weak transcription	Gastric	stomach
2	chr12:57039800-57059200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr12:57040400-57056200	Weak transcription	Fetal Muscle Trunk	muscle
4	chr12:57040400-57059200	Weak transcription	Aorta	Aorta
5	chr12:57040400-57059400	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr12:57040400-57069400	Weak transcription	Right Atrium	heart
7	chr12:57040600-57054600	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr12:57040600-57056400	Weak transcription	Brain Substantia Nigra	brain
9	chr12:57040600-57056400	Weak transcription	Colonic Mucosa	Colon
10	chr12:57040600-57056400	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr12:57040600-57056800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr12:57040600-57058200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr12:57040600-57058200	Weak transcription	Colon Smooth Muscle	Colon
14	chr12:57040600-57058800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr12:57046200-57051800	Weak transcription	Spleen	Spleen
16	chr12:57046200-57059400	Weak transcription	Lung	lung
17	chr12:57047000-57055600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr12:57048000-57055600	Weak transcription	Stomach Smooth Muscle	stomach

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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