Variant report

Variant	rs17128156
Chromosome Location	chr14:55553220-55553221
allele	A/G
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	chr14:55530000-55554000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr14:55541600-55556800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr14:55544200-55556800	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr14:55544400-55556200	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr14:55544800-55557000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr14:55544800-55558600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr14:55545000-55561400	Weak transcription	HMEC	breast
8	chr14:55547000-55557200	Weak transcription	Hela-S3	cervix
9	chr14:55549200-55559800	Weak transcription	Ovary	ovary
10	chr14:55551400-55560800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr14:55551400-55564800	Weak transcription	Right Atrium	heart
12	chr14:55551600-55556200	Weak transcription	GM12878-XiMat	blood
13	chr14:55552000-55557400	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr14:55552200-55557000	Weak transcription	Monocytes-CD14+_RO01746	blood
15	chr14:55552200-55558400	Weak transcription	Duodenum Mucosa	Duodenum
16	chr14:55552400-55558600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr14:55552400-55559800	Weak transcription	Stomach Mucosa	stomach
18	chr14:55553200-55554000	Strong transcription	Fetal Intestine Small	intestine

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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