Variant report

Variant	rs2803813
Chromosome Location	chr10:119023190-119023191
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs2429506	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2490630	1.00[AMR][1000 genomes]
rs2532790	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2532837	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2794417	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2794420	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2803798	1.00[AMR][1000 genomes]
rs2803800	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2803806	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2803812	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs363266	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs363378	1.00[AMR][1000 genomes]
rs74159202	1.00[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:119017400-119034000	Weak transcription	Gastric	stomach
2	chr10:119018400-119023800	Enhancers	Fetal Thymus	thymus
3	chr10:119019800-119023200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr10:119019800-119031200	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr10:119020000-119034000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr10:119020000-119042600	Weak transcription	Primary hematopoietic stem cells	blood
7	chr10:119020600-119024000	Weak transcription	Primary T cells from cord blood	blood
8	chr10:119020600-119024200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr10:119020600-119028000	Weak transcription	Thymus	Thymus
10	chr10:119020600-119035000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr10:119020600-119043200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr10:119020600-119045400	Weak transcription	Fetal Heart	heart
13	chr10:119021400-119043200	Weak transcription	Fetal Intestine Small	intestine
14	chr10:119021800-119023600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr10:119022000-119024600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr10:119022200-119023200	Enhancers	K562	blood
17	chr10:119022600-119026200	Enhancers	Pancreas	Pancrea
18	chr10:119022600-119042000	Weak transcription	Fetal Intestine Large	intestine
19	chr10:119023000-119031800	Weak transcription	Ovary	ovary

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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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