Variant report

Variant	rs10141944
Chromosome Location	chr14:31117979-31117980
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:31026939..31029879-chr14:31115213..31118106,2	K562	blood:

Variant related genes	Relation type
ENSG00000092140	Chromatin interaction

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10131166	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10136727	0.80[ASN][1000 genomes]
rs10146357	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10147257	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10149966	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11156637	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1123860	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11622076	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11623154	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11627421	0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11628700	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11846293	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11846408	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11851205	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12586678	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12882048	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12882931	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12888568	0.81[EUR][1000 genomes]
rs12894186	0.88[EUR][1000 genomes]
rs17096941	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17097023	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2038451	0.81[EUR][1000 genomes]
rs2057284	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2070340	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2273520	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2273521	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2273522	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs229164	0.83[EUR][1000 genomes]
rs229244	0.83[AMR][1000 genomes]
rs2378780	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs28567474	0.95[ASN][1000 genomes]
rs34935871	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35069045	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35389182	0.82[EUR][1000 genomes]
rs3736773	0.81[EUR][1000 genomes]
rs4430662	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61976741	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6571356	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6571357	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7141333	0.89[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs7141624	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7149113	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7493549	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs761956	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs8008094	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8012325	0.80[EUR][1000 genomes]
rs8013017	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8018993	0.93[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs8019637	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9322864	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv564169	chr14:30819087-31541494	Strong transcription Genic enhancers ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv1036419	chr14:30969616-31224226	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv901581	chr14:30978745-31585289	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
4	nsv564171	chr14:31068090-31149630	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:31092200-31121000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr14:31092200-31133200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr14:31092200-31133200	Weak transcription	Esophagus	oesophagus
4	chr14:31092400-31122800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr14:31093600-31127200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr14:31093800-31159600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr14:31094000-31122000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr14:31094200-31121000	Weak transcription	Spleen	Spleen
9	chr14:31094200-31145200	Weak transcription	Small Intestine	intestine
10	chr14:31095200-31119200	Weak transcription	Colonic Mucosa	Colon
11	chr14:31095800-31121000	Weak transcription	Ovary	ovary
12	chr14:31095800-31121000	Weak transcription	Thymus	Thymus
13	chr14:31096000-31121000	Weak transcription	Pancreas	Pancrea
14	chr14:31096000-31167400	Weak transcription	Gastric	stomach
15	chr14:31097200-31133800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr14:31099600-31133800	Strong transcription	Primary T helper cells fromperipheralblood	blood
17	chr14:31099600-31134000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr14:31100600-31123600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr14:31102000-31123600	Strong transcription	NHDF-Ad	bronchial
20	chr14:31102400-31121000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr14:31102800-31128800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr14:31104000-31121200	Weak transcription	NHEK	skin
23	chr14:31104200-31121200	Weak transcription	Brain Cingulate Gyrus	brain
24	chr14:31104200-31133200	Weak transcription	Aorta	Aorta
25	chr14:31104800-31121200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
26	chr14:31105200-31118000	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr14:31109400-31120600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr14:31109400-31125200	Strong transcription	Primary monocytes fromperipheralblood	blood
29	chr14:31109400-31125800	Strong transcription	Monocytes-CD14+_RO01746	blood
30	chr14:31109600-31118400	Weak transcription	HMEC	breast
31	chr14:31109800-31118600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
32	chr14:31110600-31141800	Weak transcription	Stomach Mucosa	stomach
33	chr14:31111200-31120600	Weak transcription	NH-A	brain
34	chr14:31111600-31121000	Weak transcription	Sigmoid Colon	Sigmoid Colon
35	chr14:31112600-31121200	Weak transcription	Fetal Stomach	stomach
36	chr14:31113600-31118800	Weak transcription	Colon Smooth Muscle	Colon
37	chr14:31113600-31118800	Weak transcription	HSMM	muscle
38	chr14:31113600-31121000	Weak transcription	Brain Angular Gyrus	brain
39	chr14:31113800-31121000	Weak transcription	K562	blood
40	chr14:31113800-31205400	Weak transcription	Fetal Brain Male	brain
41	chr14:31114000-31119000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr14:31114400-31134000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr14:31114600-31119200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
44	chr14:31114600-31121200	Weak transcription	Hela-S3	cervix
45	chr14:31114800-31121200	Weak transcription	A549	lung
46	chr14:31115000-31121000	Weak transcription	Fetal Thymus	thymus
47	chr14:31115000-31121000	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr14:31115000-31122200	Weak transcription	Psoas Muscle	Psoas
49	chr14:31115000-31124000	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr14:31115000-31124800	Strong transcription	Primary B cells from peripheral blood	blood

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