Variant report

Variant	rs2464170
Chromosome Location	chr12:116898535-116898536
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:116894600-116900600	Weak transcription	Right Atrium	heart
2	chr12:116895000-116900000	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr12:116896400-116899400	Enhancers	Fetal Brain Male	brain
4	chr12:116896800-116898600	Enhancers	Fetal Muscle Leg	muscle
5	chr12:116897200-116898600	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr12:116897200-116903800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr12:116897800-116898600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr12:116897800-116898600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr12:116898000-116898600	Enhancers	Colon Smooth Muscle	Colon
10	chr12:116898200-116898600	Enhancers	Fetal Brain Female	brain
11	chr12:116898200-116900000	Weak transcription	A549	lung
12	chr12:116898400-116903400	Weak 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

what's new

Quick links