Variant report

Variant	rs2104369
Chromosome Location	chr10:95580793-95580794
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:95579387..95581432-chr10:96050777..96053319,2	MCF-7	breast:
2	chr10:95580280..95581845-chr10:95611763..95614711,2	MCF-7	breast:

rs_ID	r²[population]
rs10430654	0.93[ASN][1000 genomes]
rs10430655	0.93[ASN][1000 genomes]
rs10748617	0.93[ASN][1000 genomes]
rs10786140	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10786141	0.93[ASN][1000 genomes]
rs10786143	0.93[ASN][1000 genomes]
rs10786148	0.89[ASN][1000 genomes]
rs10882345	0.93[ASN][1000 genomes]
rs10882346	0.93[ASN][1000 genomes]
rs10882347	0.93[ASN][1000 genomes]
rs10882348	0.93[ASN][1000 genomes]
rs10882349	0.88[ASN][1000 genomes]
rs10882352	0.84[ASN][1000 genomes]
rs10882353	0.84[ASN][1000 genomes]
rs10882354	0.93[ASN][1000 genomes]
rs10882360	0.91[ASN][1000 genomes]
rs10882361	0.90[ASN][1000 genomes]
rs10882363	0.89[ASN][1000 genomes]
rs10882364	0.89[ASN][1000 genomes]
rs11187684	0.90[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs11187692	0.93[ASN][1000 genomes]
rs11187693	0.81[ASN][1000 genomes]
rs11187695	0.93[ASN][1000 genomes]
rs11187697	0.93[ASN][1000 genomes]
rs11187698	0.93[ASN][1000 genomes]
rs11187700	0.93[ASN][1000 genomes]
rs11187710	0.91[ASN][1000 genomes]
rs11187718	0.90[ASN][1000 genomes]
rs11187724	0.89[ASN][1000 genomes]
rs11187725	0.89[ASN][1000 genomes]
rs11187729	0.89[ASN][1000 genomes]
rs12098741	0.90[ASN][1000 genomes]
rs1364823	0.90[ASN][1000 genomes]
rs17412233	0.93[ASN][1000 genomes]
rs17412253	0.93[ASN][1000 genomes]
rs1986401	0.93[ASN][1000 genomes]
rs2113956	0.89[ASN][1000 genomes]
rs2422330	0.91[ASN][1000 genomes]
rs2422331	0.89[ASN][1000 genomes]
rs2901715	0.82[ASN][1000 genomes]
rs3088126	0.89[ASN][1000 genomes]
rs35298830	0.93[ASN][1000 genomes]
rs35640487	0.90[ASN][1000 genomes]
rs4917955	0.91[ASN][1000 genomes]
rs4917956	0.91[ASN][1000 genomes]
rs4917958	0.90[ASN][1000 genomes]
rs4919555	0.93[ASN][1000 genomes]
rs4919557	0.93[ASN][1000 genomes]
rs4919558	0.93[ASN][1000 genomes]
rs4919560	0.93[ASN][1000 genomes]
rs4919568	0.93[ASN][1000 genomes]
rs58055107	0.93[ASN][1000 genomes]
rs60994317	0.93[ASN][1000 genomes]
rs7076661	0.93[ASN][1000 genomes]
rs7086303	0.91[ASN][1000 genomes]
rs7088236	0.89[ASN][1000 genomes]
rs7090399	0.93[ASN][1000 genomes]
rs7092643	0.93[ASN][1000 genomes]
rs7092830	0.91[ASN][1000 genomes]
rs7092839	0.91[ASN][1000 genomes]
rs7092860	0.91[ASN][1000 genomes]
rs7093763	0.93[ASN][1000 genomes]
rs7094460	0.93[ASN][1000 genomes]
rs7094548	0.93[ASN][1000 genomes]
rs7094662	0.93[ASN][1000 genomes]
rs7094961	0.93[ASN][1000 genomes]
rs7097533	0.93[ASN][1000 genomes]
rs7100676	0.91[ASN][1000 genomes]
rs7898970	0.89[ASN][1000 genomes]
rs7899974	0.82[ASN][1000 genomes]
rs7900260	0.93[ASN][1000 genomes]
rs7904095	0.93[ASN][1000 genomes]
rs7905161	0.90[ASN][1000 genomes]
rs7906044	0.90[ASN][1000 genomes]
rs7906262	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7913113	0.93[ASN][1000 genomes]
rs7913175	0.93[ASN][1000 genomes]
rs7913189	0.93[ASN][1000 genomes]
rs7913238	0.89[ASN][1000 genomes]
rs7913342	0.89[ASN][1000 genomes]
rs7917744	0.89[ASN][1000 genomes]
rs7921176	0.93[ASN][1000 genomes]
rs7921454	0.93[ASN][1000 genomes]
rs7922581	0.93[ASN][1000 genomes]
rs7924240	0.91[ASN][1000 genomes]
rs919003	0.93[ASN][1000 genomes]
rs919004	0.91[ASN][1000 genomes]
rs950085	0.93[ASN][1000 genomes]
rs950086	0.93[ASN][1000 genomes]
rs9787520	0.93[ASN][1000 genomes]

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:95578200-95585400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr10:95579400-95581200	Enhancers	Fetal Intestine Small	intestine
3	chr10:95579600-95581600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr10:95580000-95581000	Enhancers	Duodenum Mucosa	Duodenum
5	chr10:95580000-95581200	Enhancers	Fetal Intestine Large	intestine
6	chr10:95580600-95581000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr10:95580600-95581000	Enhancers	Rectal Mucosa Donor 31	rectum
8	chr10:95580600-95581000	Enhancers	HUVEC	blood vessel

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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