Variant report

Variant	rs72711566
Chromosome Location	chr14:105768490-105768491
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2)
CpG islands
(count:0)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr14:105766625-105768562	K562	blood:	n/a	n/a
2	ZNF384	chr14:105767876-105768632	K562	blood:	n/a	n/a

No data

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:105766350..105771356-chr14:105955110..105959126,6	MCF-7	breast:
2	chr14:105765282..105769482-chr14:105778355..105784135,18	K562	blood:
3	chr14:105768384..105770510-chr14:105839259..105840826,2	MCF-7	breast:
4	chr14:105265110..105267765-chr14:105766806..105769681,2	K562	blood:
5	chr14:105765307..105769571-chr14:105774220..105784135,13	K562	blood:
6	chr14:105713379..105716522-chr14:105764463..105769159,4	MCF-7	breast:

No data

Variant related genes	Relation type
BRF1	TF binding region
ENSG00000179627	Chromatin interaction
ENSG00000179364	Chromatin interaction
ENSG00000185024	Chromatin interaction
ENSG00000185347	Chromatin interaction
ENSG00000184887	Chromatin interaction

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs1008629	0.95[EUR][1000 genomes]
rs4270098	0.89[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs45527637	0.95[EUR][1000 genomes]
rs4572314	0.89[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs56776600	0.95[EUR][1000 genomes]
rs58705971	0.95[EUR][1000 genomes]
rs67308076	0.95[EUR][1000 genomes]
rs67426629	0.81[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs67502922	0.95[EUR][1000 genomes]
rs67579680	0.95[EUR][1000 genomes]
rs67936859	0.95[EUR][1000 genomes]
rs7149185	0.80[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs72709737	0.95[EUR][1000 genomes]
rs72711555	0.95[EUR][1000 genomes]
rs72711562	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72711563	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72711565	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72711567	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72711569	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73353763	0.95[EUR][1000 genomes]
rs8015997	0.95[EUR][1000 genomes]
rs8016364	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1828345	chr14:105100787-105803170	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
2	nsv542225	chr14:105133688-105803170	Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
3	nsv542227	chr14:105157572-105803170	Enhancers Flanking Active TSS Genic enhancers Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	147 gene(s)	inside rSNPs	diseases
4	nsv917106	chr14:105339195-105803170	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
5	nsv902422	chr14:105420215-105803170	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
6	nsv902423	chr14:105430890-105803170	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
7	nsv902424	chr14:105436222-105803170	Genic enhancers Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	86 gene(s)	inside rSNPs	diseases
8	esv2758369	chr14:105513346-105803170	Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
9	esv2760014	chr14:105513346-105803170	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
10	nsv902441	chr14:105602619-105803170	Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
11	nsv902442	chr14:105602619-105803170	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
12	esv1817919	chr14:105605199-105803170	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
13	nsv530813	chr14:105607701-106453697	Strong transcription Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	149 gene(s)	inside rSNPs	diseases
14	nsv566186	chr14:105675701-105779305	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
15	nsv902466	chr14:105704465-105803170	Active TSS Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
16	esv29986	chr14:105707292-105803170	Flanking Active TSS Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
17	nsv832887	chr14:105717339-105803170	Strong transcription Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
18	nsv832888	chr14:105717339-105803170	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
19	nsv1049929	chr14:105718240-105772037	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases
20	nsv1052355	chr14:105718240-105789157	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	17 gene(s)	inside rSNPs	diseases
21	nsv566187	chr14:105756485-105780704	Weak transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases
22	esv3420807	chr14:105764707-105769605	Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	13 gene(s)	inside rSNPs	diseases
23	esv3380677	chr14:105766332-105769080	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105766400-105768600	Active TSS	K562	blood
2	chr14:105766600-105768600	Active TSS	HUES64 Cell Line	embryonic stem cell
3	chr14:105766600-105768600	Active TSS	iPS-15b Cell Line	embryonic stem cell
4	chr14:105768200-105768600	Enhancers	Primary B cells from cord blood	blood
5	chr14:105768200-105768600	Enhancers	Primary T cells fromperipheralblood	blood
6	chr14:105768200-105768600	Enhancers	Primary T helper cells fromperipheralblood	blood
7	chr14:105768200-105768600	Enhancers	Fetal Muscle Trunk	muscle
8	chr14:105768200-105768800	Enhancers	Fetal Thymus	thymus
9	chr14:105768200-105769000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr14:105768200-105769000	Weak transcription	HSMM	muscle
11	chr14:105768200-105769200	Enhancers	Hela-S3	cervix
12	chr14:105768200-105769400	Enhancers	Primary monocytes fromperipheralblood	blood
13	chr14:105768200-105770000	Weak transcription	Left Ventricle	heart
14	chr14:105768200-105770000	Weak transcription	Stomach Mucosa	stomach
15	chr14:105768200-105770200	Weak transcription	Esophagus	oesophagus
16	chr14:105768200-105770200	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr14:105768200-105770200	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr14:105768200-105771200	Weak transcription	Primary T cells from cord blood	blood
19	chr14:105768200-105771200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr14:105768200-105771200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr14:105768200-105771400	Weak transcription	Primary T helper cells PMA-I stimulated	--
22	chr14:105768200-105771400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr14:105768200-105771600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr14:105768200-105771600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr14:105768200-105771800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr14:105768200-105771800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr14:105768200-105771800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr14:105768200-105771800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr14:105768200-105775200	Weak transcription	HMEC	breast
30	chr14:105768200-105775400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr14:105768200-105775600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr14:105768200-105775600	Weak transcription	NHEK	skin
33	chr14:105768200-105777600	Weak transcription	Brain Cingulate Gyrus	brain
34	chr14:105768200-105778000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr14:105768200-105778000	Weak transcription	Brain Anterior Caudate	brain
36	chr14:105768200-105778000	Weak transcription	Brain Substantia Nigra	brain
37	chr14:105768200-105778000	Weak transcription	Fetal Stomach	stomach
38	chr14:105768200-105778000	Weak transcription	Right Ventricle	heart
39	chr14:105768200-105778000	Weak transcription	Stomach Smooth Muscle	stomach
40	chr14:105768200-105778800	Weak transcription	Fetal Lung	lung
41	chr14:105768200-105779400	Weak transcription	Colonic Mucosa	Colon
42	chr14:105768200-105779400	Weak transcription	Thymus	Thymus
43	chr14:105768200-105779600	Weak transcription	GM12878-XiMat	blood
44	chr14:105768200-105779800	Weak transcription	NHLF	lung
45	chr14:105768200-105780000	Weak transcription	NHDF-Ad	bronchial
46	chr14:105768200-105780200	Weak transcription	Gastric	stomach
47	chr14:105768200-105780200	Weak transcription	Right Atrium	heart
48	chr14:105768400-105768600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
49	chr14:105768400-105769000	Enhancers	HepG2	liver
50	chr14:105768400-105769400	Enhancers	Monocytes-CD14+_RO01746	blood

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