Variant report

Variant	rs9425332
Chromosome Location	chr1:172448251-172448252
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:172444678..172448407-chr1:172449595..172452783,4	MCF-7	breast:
2	chr1:172442117..172444152-chr1:172447245..172449151,2	MCF-7	breast:
3	chr1:172446186..172449465-chr1:172453290..172456468,4	MCF-7	breast:
4	chr1:172446479..172448732-chr1:172458386..172460620,2	MCF-7	breast:
5	chr1:172446019..172448737-chr1:172490304..172491873,2	MCF-7	breast:
6	chr1:172443532..172455037-chr1:172498094..172506505,15	MCF-7	breast:
7	chr1:172418092..172419733-chr1:172445872..172448682,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000094975	Chromatin interaction

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs1009802	0.93[EUR][1000 genomes]
rs1041911	0.91[EUR][1000 genomes]
rs6656400	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs71485882	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7551242	0.83[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs9425333	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9425623	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9425625	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:172438200-172449200	Weak transcription	Fetal Muscle Leg	muscle
2	chr1:172443000-172448400	Weak transcription	K562	blood
3	chr1:172444200-172448400	Enhancers	HMEC	breast
4	chr1:172444200-172456200	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr1:172445000-172449400	Weak transcription	Primary T cells from cord blood	blood
6	chr1:172445000-172452400	Weak transcription	Primary neutrophils fromperipheralblood	blood
7	chr1:172445600-172448600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr1:172445600-172449800	Weak transcription	HepG2	liver
9	chr1:172445800-172448600	Enhancers	NHEK	skin
10	chr1:172445800-172449200	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr1:172445800-172450800	Weak transcription	Fetal Intestine Large	intestine
12	chr1:172445800-172451000	Weak transcription	Fetal Intestine Small	intestine
13	chr1:172445800-172451600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr1:172446800-172449200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr1:172446800-172449200	Weak transcription	Pancreas	Pancrea
16	chr1:172446800-172451000	Weak transcription	A549	lung
17	chr1:172447600-172452800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr1:172447800-172449800	Enhancers	Placenta	Placenta
19	chr1:172447800-172449800	Enhancers	Placenta Amnion	Placenta Amnion
20	chr1:172448000-172448600	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr1:172448000-172449200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr1:172448200-172452600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr1:172448200-172452800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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