Variant report

Variant	rs61989175
Chromosome Location	chr14:71631671-71631672
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:71631309..71633976-chr14:71786806..71788570,3	MCF-7	breast:
2	chr14:71630664..71636301-chr14:71785635..71788811,7	MCF-7	breast:
3	chr14:71536680..71538584-chr14:71630559..71632306,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000197555	Chromatin interaction
ENSG00000259146	Chromatin interaction

Extended variants
information (count: 80 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:75)

rs_ID	r²[population]
rs10140218	1.00[ASN][1000 genomes]
rs11623477	1.00[ASN][1000 genomes]
rs11844339	1.00[ASN][1000 genomes]
rs17766986	1.00[ASN][1000 genomes]
rs28706321	0.82[AFR][1000 genomes]
rs45498105	1.00[ASN][1000 genomes]
rs45517434	1.00[ASN][1000 genomes]
rs4902905	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4902908	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55896578	1.00[ASN][1000 genomes]
rs56150143	0.82[AFR][1000 genomes]
rs57204407	1.00[ASN][1000 genomes]
rs57723945	1.00[ASN][1000 genomes]
rs58952176	1.00[ASN][1000 genomes]
rs59060154	1.00[ASN][1000 genomes]
rs59081846	0.82[AFR][1000 genomes]
rs59400895	0.84[AFR][1000 genomes]
rs61988735	1.00[ASN][1000 genomes]
rs61988736	1.00[ASN][1000 genomes]
rs61988737	1.00[ASN][1000 genomes]
rs61988738	1.00[ASN][1000 genomes]
rs61988740	1.00[ASN][1000 genomes]
rs61989174	0.98[AFR][1000 genomes];0.90[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs61989177	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61989179	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61989180	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61989234	1.00[ASN][1000 genomes]
rs61989239	1.00[ASN][1000 genomes]
rs61989240	1.00[ASN][1000 genomes]
rs61990375	1.00[ASN][1000 genomes]
rs61990382	1.00[ASN][1000 genomes]
rs61990383	1.00[ASN][1000 genomes]
rs61990384	1.00[ASN][1000 genomes]
rs61990385	1.00[ASN][1000 genomes]
rs61990404	1.00[ASN][1000 genomes]
rs61990406	1.00[ASN][1000 genomes]
rs61990407	1.00[ASN][1000 genomes]
rs61990408	1.00[ASN][1000 genomes]
rs61990409	1.00[ASN][1000 genomes]
rs61990410	1.00[ASN][1000 genomes]
rs61990411	1.00[ASN][1000 genomes]
rs61990412	1.00[ASN][1000 genomes]
rs61990414	1.00[ASN][1000 genomes]
rs61990416	1.00[ASN][1000 genomes]
rs61990417	1.00[ASN][1000 genomes]
rs61990418	1.00[ASN][1000 genomes]
rs61990420	1.00[ASN][1000 genomes]
rs61990451	1.00[ASN][1000 genomes]
rs61990452	1.00[ASN][1000 genomes]
rs61990453	1.00[ASN][1000 genomes]
rs61990458	1.00[ASN][1000 genomes]
rs61992061	1.00[ASN][1000 genomes]
rs61992066	1.00[ASN][1000 genomes]
rs61992068	1.00[ASN][1000 genomes]
rs61992069	1.00[ASN][1000 genomes]
rs61992070	1.00[ASN][1000 genomes]
rs61992080	1.00[ASN][1000 genomes]
rs61992081	1.00[ASN][1000 genomes]
rs61992086	1.00[ASN][1000 genomes]
rs61992088	1.00[ASN][1000 genomes]
rs61992090	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61992091	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7155259	1.00[ASN][1000 genomes]
rs7156194	1.00[ASN][1000 genomes]
rs7159252	1.00[ASN][1000 genomes]
rs7160587	1.00[ASN][1000 genomes]
rs7161431	0.98[AFR][1000 genomes]
rs73297564	0.84[AFR][1000 genomes]
rs73297566	0.84[AFR][1000 genomes]
rs73297572	0.84[AFR][1000 genomes]
rs73297577	0.84[AFR][1000 genomes]
rs73297587	0.84[AFR][1000 genomes]
rs73297594	0.84[AFR][1000 genomes]
rs73299437	0.98[AFR][1000 genomes]
rs7492426	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:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:71629400-71632800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr14:71629400-71633400	Enhancers	Fetal Intestine Small	intestine
3	chr14:71629400-71633800	Enhancers	Liver	Liver
4	chr14:71629600-71632600	Enhancers	Rectal Mucosa Donor 31	rectum
5	chr14:71629600-71633600	Enhancers	Fetal Intestine Large	intestine
6	chr14:71630200-71632200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr14:71630200-71633000	Enhancers	Colonic Mucosa	Colon
8	chr14:71630400-71631800	Weak transcription	Duodenum Mucosa	Duodenum
9	chr14:71630400-71632200	Enhancers	Brain Anterior Caudate	brain
10	chr14:71630400-71633000	Enhancers	Pancreas	Pancrea
11	chr14:71630400-71633200	Enhancers	Sigmoid Colon	Sigmoid Colon
12	chr14:71630400-71633800	Enhancers	Fetal Kidney	kidney
13	chr14:71630600-71631800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr14:71630600-71633400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr14:71630600-71633600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr14:71631000-71633400	Enhancers	Placenta	Placenta
17	chr14:71631200-71633000	Enhancers	Fetal Muscle Leg	muscle
18	chr14:71631400-71632000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr14:71631400-71632600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr14:71631400-71632600	Enhancers	Fetal Heart	heart
21	chr14:71631400-71633200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr14:71631400-71633400	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr14:71631600-71631800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
24	chr14:71631600-71631800	Bivalent Enhancer	HepG2	liver
25	chr14:71631600-71632400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr14:71631600-71632400	Enhancers	Fetal Muscle Trunk	muscle
27	chr14:71631600-71632600	Enhancers	HMEC	breast
28	chr14:71631600-71632600	Enhancers	HSMM	muscle
29	chr14:71631600-71632600	Enhancers	HSMMtube	muscle
30	chr14:71631600-71633000	Enhancers	Fetal Lung	lung
31	chr14:71631600-71633200	Enhancers	NHEK	skin
32	chr14:71631600-71633400	Enhancers	Primary monocytes fromperipheralblood	blood
33	chr14:71631600-71636600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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