Variant report

Variant	rs11628787
Chromosome Location	chr14:104323984-104323985
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:104321542..104325039-chr14:104354434..104358481,6	MCF-7	breast:
2	chr14:104319613..104324063-chr14:104346589..104349290,5	MCF-7	breast:
3	chr14:104320208..104324271-chr14:104346660..104350133,4	MCF-7	breast:
4	chr14:104284106..104288227-chr14:104321092..104325164,4	MCF-7	breast:
5	chr14:104322796..104324811-chr14:104333710..104335450,2	K562	blood:
6	chr14:104321329..104324090-chr14:104325687..104328665,2	K562	blood:
7	chr14:104320014..104324951-chr14:104331915..104336985,8	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTD-2134A5.2.1-1	chr14:104322461-104324386	XLOC_010944

No data

Extended variants
information (count: 47 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1040813	0.81[EUR][1000 genomes]
rs10873539	0.81[EUR][1000 genomes]
rs11160766	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11627258	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1187416	0.81[EUR][1000 genomes]
rs12434686	0.81[EUR][1000 genomes]
rs12437066	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12587013	0.86[AFR][1000 genomes]
rs12897150	0.81[EUR][1000 genomes]
rs1547604	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1955660	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2006281	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2024669	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2144079	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2144080	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2295140	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2368558	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2368559	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs28698555	0.81[EUR][1000 genomes]
rs4906368	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs58948234	0.84[ASN][1000 genomes]
rs6575998	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6576003	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6576005	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs67478160	0.90[ASN][1000 genomes]
rs7141473	0.81[EUR][1000 genomes]
rs7141928	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7159810	0.80[EUR][1000 genomes]
rs8009868	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs8011137	0.81[EUR][1000 genomes]
rs8014294	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8018363	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs941475	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3332028	chr14:103581471-104328811	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	162 gene(s)	inside rSNPs	diseases
2	nsv1045162	chr14:104140525-104594841	Flanking Active TSS Strong transcription Bivalent Enhancer Enhancers Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
3	nsv542204	chr14:104140525-104594841	Active TSS Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
4	esv2758368	chr14:104147525-104412813	Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
5	esv2760013	chr14:104147525-104412813	Enhancers Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
6	nsv902313	chr14:104162263-104378087	Bivalent Enhancer Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
7	nsv902318	chr14:104255083-104464809	Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
8	nsv902319	chr14:104255083-104620077	Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	64 gene(s)	inside rSNPs	diseases
9	esv1838047	chr14:104283104-104359121	Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
10	nsv902321	chr14:104283104-104378087	Strong transcription Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
11	esv1818596	chr14:104312697-104359121	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
12	esv1836134	chr14:104312697-104359121	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
13	esv1837236	chr14:104313426-104332759	Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
14	nsv566028	chr14:104314023-104332759	Weak transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104315200-104327600	Weak transcription	Ovary	ovary
2	chr14:104320000-104325400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr14:104320200-104325200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr14:104321800-104325200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr14:104321800-104325800	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr14:104321800-104326200	Weak transcription	Right Atrium	heart
7	chr14:104322400-104326000	Weak transcription	Adipose Nuclei	Adipose
8	chr14:104322600-104324800	Enhancers	HepG2	liver
9	chr14:104322600-104327800	Weak transcription	Fetal Heart	heart
10	chr14:104322800-104327800	Weak transcription	Duodenum Mucosa	Duodenum
11	chr14:104322800-104327800	Weak transcription	Gastric	stomach
12	chr14:104323000-104324600	Weak transcription	Esophagus	oesophagus
13	chr14:104323000-104324800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr14:104323000-104326000	Weak transcription	Lung	lung
15	chr14:104323200-104324600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr14:104323200-104324600	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr14:104323400-104324000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
18	chr14:104323400-104324800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr14:104323400-104326000	Weak transcription	Right Ventricle	heart
20	chr14:104323400-104326000	Weak transcription	HUVEC	blood vessel
21	chr14:104323600-104324800	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr14:104323600-104326000	Weak transcription	Left Ventricle	heart
23	chr14:104323600-104327800	Weak transcription	Pancreas	Pancrea
24	chr14:104323600-104336000	Weak transcription	Placenta Amnion	Placenta Amnion
25	chr14:104323600-104337600	Weak transcription	Fetal Intestine Small	intestine
26	chr14:104323800-104324200	Weak transcription	Spleen	Spleen
27	chr14:104323800-104324600	Weak transcription	Fetal Muscle Leg	muscle

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