Variant report

Variant	rs56167327
Chromosome Location	chr14:69187275-69187276
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:69186666..69188197-chr14:69195401..69198346,2	K562	blood:
2	chr14:69185841..69187521-chr14:69260406..69261940,2	K562	blood:
3	chr14:69185847..69187659-chr14:69204580..69206147,2	K562	blood:
4	chr14:69186631..69190079-chr14:69260120..69263014,4	K562	blood:
5	chr14:69183888..69188009-chr14:69213725..69217312,4	K562	blood:
6	chr14:69185412..69187789-chr14:69192194..69193757,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000185650	Chromatin interaction

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10138752	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10483821	0.90[AFR][1000 genomes]
rs11622758	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11623906	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11625565	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11626345	0.90[AFR][1000 genomes]
rs11626392	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17106198	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17106203	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55687730	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55867915	0.97[EUR][1000 genomes]
rs55929214	0.97[EUR][1000 genomes]
rs61985011	0.80[EUR][1000 genomes]
rs7152463	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8015093	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8015388	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8015998	0.89[AFR][1000 genomes]
rs8016115	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8019389	0.98[EUR][1000 genomes]

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:69173600-69194200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr14:69173600-69196400	Weak transcription	Right Ventricle	heart
3	chr14:69176600-69189400	Weak transcription	Pancreas	Pancrea
4	chr14:69181000-69191400	Weak transcription	Fetal Muscle Trunk	muscle
5	chr14:69181000-69195200	Weak transcription	Spleen	Spleen
6	chr14:69182000-69202600	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr14:69182200-69191200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr14:69184200-69188600	Weak transcription	Placenta	Placenta
9	chr14:69184400-69187600	Weak transcription	Fetal Intestine Small	intestine
10	chr14:69184400-69188400	Weak transcription	Fetal Intestine Large	intestine
11	chr14:69184800-69188800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr14:69185200-69187400	Enhancers	Primary T killer memory cells from peripheral blood	blood
13	chr14:69185800-69188400	Weak transcription	HepG2	liver
14	chr14:69186200-69187400	Enhancers	Primary T helper cells fromperipheralblood	blood
15	chr14:69187000-69187400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
16	chr14:69187000-69187800	Weak transcription	Ovary	ovary
17	chr14:69187000-69194200	Weak transcription	HUVEC	blood vessel
18	chr14:69187200-69187400	Enhancers	Small Intestine	intestine
19	chr14:69187200-69187800	Enhancers	Primary T cells fromperipheralblood	blood
20	chr14:69187200-69187800	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
21	chr14:69187200-69187800	Enhancers	K562	blood

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