Variant report

Variant	rs61174376
Chromosome Location	chr14:71654869-71654870
allele	C/T
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
ENSG00000197555	Chromatin interaction
ENSG00000259907	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10130213	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11844320	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11850267	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11851589	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17109116	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17177822	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17767266	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17767296	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1990035	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4899390	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4902916	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4902917	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4902918	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4902922	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55737377	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59985720	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60526802	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60536344	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61989206	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61989207	1.00[ASN][1000 genomes]
rs61989208	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6574006	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6574007	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7146169	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7150921	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7153194	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72726657	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72726677	1.00[ASN][1000 genomes]
rs8005089	0.80[AMR][1000 genomes]
rs8005615	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8005925	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8010203	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8017895	0.81[EUR][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:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:71653800-71655200	Enhancers	HUVEC	blood vessel
2	chr14:71654000-71655000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr14:71654000-71655000	Enhancers	HSMM	muscle
4	chr14:71654000-71655400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr14:71654200-71655400	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr14:71654200-71655400	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr14:71654200-71655400	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr14:71654200-71655400	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr14:71654200-71655400	Enhancers	Fetal Heart	heart
10	chr14:71654200-71655600	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr14:71654400-71655000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr14:71654400-71655000	Enhancers	Hela-S3	cervix
13	chr14:71654400-71655200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
14	chr14:71654400-71655200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr14:71654400-71655400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr14:71654400-71655600	Enhancers	H9 Cell Line	embryonic stem cell
17	chr14:71654400-71655600	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr14:71654600-71655200	Enhancers	Stomach Mucosa	stomach
19	chr14:71654600-71655400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr14:71654600-71655400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr14:71654600-71655400	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr14:71654600-71655400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr14:71654600-71655600	Enhancers	H1 Cell Line	embryonic stem cell
24	chr14:71654600-71655600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr14:71654600-71655600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr14:71654600-71655600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr14:71654600-71655600	Enhancers	Pancreas	Pancrea
28	chr14:71654800-71655000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr14:71654800-71655000	Bivalent Enhancer	Fetal Intestine Small	intestine
30	chr14:71654800-71655200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr14:71654800-71655400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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