Variant report

Variant	rs10145063
Chromosome Location	chr14:104370420-104370421
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:104366173..104368914-chr14:104369657..104372808,3	MCF-7	breast:
2	chr14:104364346..104365968-chr14:104369278..104370785,2	MCF-7	breast:
3	chr14:104320527..104323273-chr14:104369468..104371736,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TDRD9-2	chr14:104369722-104370458	NONHSAT040228

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10145840	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17095273	1.00[AMR][1000 genomes]
rs17101877	1.00[AMR][1000 genomes]
rs28644378	1.00[AMR][1000 genomes]
rs28721938	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35169220	1.00[AMR][1000 genomes]
rs57648252	1.00[AMR][1000 genomes]
rs59515472	1.00[AMR][1000 genomes]
rs59855870	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	nsv1053305	chr14:104326137-104372608	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
10	nsv542205	chr14:104326137-104372608	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
11	nsv542206	chr14:104326137-104377507	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
12	nsv1042792	chr14:104326137-104384260	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
13	nsv542207	chr14:104326137-104384260	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
14	nsv1048353	chr14:104361402-104483286	Flanking Active TSS Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
15	nsv902322	chr14:104365310-104464809	Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104363200-104376400	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr14:104363200-104387000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr14:104363600-104375800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr14:104364800-104375800	Weak transcription	Right Ventricle	heart
5	chr14:104365000-104377400	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr14:104365400-104375800	Weak transcription	Gastric	stomach
7	chr14:104366000-104370800	Weak transcription	Stomach Mucosa	stomach
8	chr14:104366200-104376400	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr14:104366400-104375800	Weak transcription	Spleen	Spleen
10	chr14:104366600-104377400	Weak transcription	Esophagus	oesophagus
11	chr14:104367600-104372200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr14:104367600-104372400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr14:104367600-104376400	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr14:104367600-104376600	Weak transcription	NHLF	lung
15	chr14:104367800-104372200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr14:104367800-104372200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr14:104367800-104372200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr14:104367800-104372200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr14:104367800-104372200	Weak transcription	HepG2	liver
20	chr14:104367800-104372200	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr14:104367800-104372400	Weak transcription	Primary T helper cells fromperipheralblood	blood
22	chr14:104367800-104374600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
23	chr14:104367800-104374600	Weak transcription	Fetal Intestine Small	intestine
24	chr14:104367800-104375800	Weak transcription	Duodenum Mucosa	Duodenum
25	chr14:104367800-104375800	Weak transcription	Dnd41	blood
26	chr14:104367800-104376000	Weak transcription	Liver	Liver
27	chr14:104367800-104376200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
28	chr14:104367800-104376200	Weak transcription	Fetal Thymus	thymus
29	chr14:104367800-104376200	Weak transcription	Rectal Mucosa Donor 29	rectum
30	chr14:104367800-104376400	Weak transcription	Primary B cells from peripheral blood	blood
31	chr14:104367800-104376400	Weak transcription	Adipose Nuclei	Adipose
32	chr14:104367800-104376400	Weak transcription	Colonic Mucosa	Colon
33	chr14:104367800-104376400	Weak transcription	Placenta	Placenta
34	chr14:104367800-104376400	Weak transcription	Lung	lung
35	chr14:104367800-104376600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr14:104367800-104378000	Weak transcription	K562	blood
37	chr14:104368800-104376400	Weak transcription	Fetal Stomach	stomach
38	chr14:104369600-104372200	Weak transcription	Primary monocytes fromperipheralblood	blood
39	chr14:104370000-104378600	Weak transcription	Aorta	Aorta

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