Variant report

Variant	rs11623724
Chromosome Location	chr14:71654539-71654540
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:71647368..71649559-chr14:71652567..71655238,2	MCF-7	breast:
2	chr14:71653618..71655729-chr14:71657519..71659044,2	MCF-7	breast:
3	chr14:71652746..71656489-chr14:71786272..71789220,3	MCF-7	breast:
4	chr14:71652798..71655797-chr14:71786372..71789241,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000259146	Chromatin interaction
ENSG00000259907	Chromatin interaction
ENSG00000197555	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10133704	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10139738	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10139748	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1079823	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11158896	0.97[ASN][1000 genomes]
rs11621135	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11623455	0.94[ASN][1000 genomes]
rs11623722	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11626311	0.97[ASN][1000 genomes]
rs11628388	0.97[ASN][1000 genomes]
rs11628426	0.97[ASN][1000 genomes]
rs11850268	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12893350	0.97[ASN][1000 genomes]
rs2057829	0.97[ASN][1000 genomes]
rs2057830	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2189799	0.97[ASN][1000 genomes]
rs2332537	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2332538	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4899389	0.97[ASN][1000 genomes]
rs4902914	0.97[ASN][1000 genomes]
rs4902919	0.97[ASN][1000 genomes]
rs4902920	0.97[ASN][1000 genomes]
rs66549050	0.97[ASN][1000 genomes]
rs724839	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1041980	chr14:71196358-71767339	Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv542125	chr14:71196358-71767339	Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
3	nsv1038007	chr14:71269747-71667680	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
4	nsv1036929	chr14:71469148-71683412	Strong transcription Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv1044090	chr14:71496198-71780026	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:71638600-71654600	Weak transcription	Pancreas	Pancrea
2	chr14:71648600-71654600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr14:71650000-71654600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr14:71650000-71654800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr14:71651000-71654600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr14:71653800-71655200	Enhancers	HUVEC	blood vessel
7	chr14:71654000-71655000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr14:71654000-71655000	Enhancers	HSMM	muscle
9	chr14:71654000-71655400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr14:71654200-71655400	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr14:71654200-71655400	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr14:71654200-71655400	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr14:71654200-71655400	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr14:71654200-71655400	Enhancers	Fetal Heart	heart
15	chr14:71654200-71655600	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr14:71654400-71654600	Enhancers	Fetal Muscle Leg	muscle
17	chr14:71654400-71654800	Enhancers	HSMMtube	muscle
18	chr14:71654400-71655000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr14:71654400-71655000	Enhancers	Hela-S3	cervix
20	chr14:71654400-71655200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
21	chr14:71654400-71655200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr14:71654400-71655400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr14:71654400-71655600	Enhancers	H9 Cell Line	embryonic stem cell
24	chr14:71654400-71655600	Enhancers	HUES6 Cell Line	embryonic stem cell

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