Variant report

Variant	rs10099929
Chromosome Location	chr8:10694671-10694672
allele	C/T
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:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:10683525..10686850-chr8:10694502..10697878,5	K562	blood:
2	chr8:10683547..10686608-chr8:10694341..10697878,5	K562	blood:
3	chr8:10674954..10678350-chr8:10693952..10697087,3	K562	blood:
4	chr8:10694381..10696683-chr8:10699083..10701009,2	K562	blood:
5	chr8:10687156..10690707-chr8:10693616..10698468,7	K562	blood:
6	chr8:10692044..10695028-chr8:10695086..10697405,2	MCF-7	breast:
7	chr8:10450511..10453354-chr8:10693058..10695560,2	K562	blood:
8	chr8:10405123..10407146-chr8:10694080..10697115,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000254093	Chromatin interaction
ENSG00000258724	Chromatin interaction

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs10046628	0.93[ASN][1000 genomes]
rs10088888	0.81[ASN][1000 genomes]
rs10091386	0.97[ASN][1000 genomes]
rs10093774	0.92[ASN][1000 genomes]
rs10098699	0.85[ASN][1000 genomes]
rs10109416	0.93[ASN][1000 genomes]
rs11250081	0.98[ASN][1000 genomes]
rs11250083	0.88[ASN][1000 genomes]
rs11776674	0.93[ASN][1000 genomes]
rs11776767	0.92[ASN][1000 genomes]
rs11986845	0.92[ASN][1000 genomes]
rs11986935	0.97[ASN][1000 genomes]
rs11996727	0.97[ASN][1000 genomes]
rs12541110	0.99[ASN][1000 genomes]
rs13254059	0.87[ASN][1000 genomes]
rs13254592	0.87[ASN][1000 genomes]
rs13274017	0.90[ASN][1000 genomes]
rs1469556	0.87[ASN][1000 genomes]
rs1549796	0.97[ASN][1000 genomes]
rs17152576	0.93[ASN][1000 genomes]
rs1991649	0.88[ASN][1000 genomes]
rs1991650	0.88[ASN][1000 genomes]
rs1991651	0.88[ASN][1000 genomes]
rs2271357	0.92[ASN][1000 genomes]
rs2277130	0.84[ASN][1000 genomes]
rs2278335	0.92[ASN][1000 genomes]
rs2292370	0.93[ASN][1000 genomes]
rs2292371	0.93[ASN][1000 genomes]
rs2409649	0.93[ASN][1000 genomes]
rs2409650	0.93[ASN][1000 genomes]
rs28613656	0.99[ASN][1000 genomes]
rs34653170	0.85[ASN][1000 genomes]
rs35091929	0.98[ASN][1000 genomes]
rs3808603	0.95[ASN][1000 genomes]
rs4840519	0.98[ASN][1000 genomes]
rs4841452	0.93[ASN][1000 genomes]
rs6601533	0.92[ASN][1000 genomes]
rs6601534	0.97[ASN][1000 genomes]
rs6601535	0.99[ASN][1000 genomes]
rs6601536	0.98[ASN][1000 genomes]
rs66844016	0.93[ASN][1000 genomes]
rs67211633	0.90[ASN][1000 genomes]
rs6980805	0.83[ASN][1000 genomes]
rs6982769	0.93[ASN][1000 genomes]
rs6984388	0.93[ASN][1000 genomes]
rs6987200	0.93[ASN][1000 genomes]
rs6988598	0.93[ASN][1000 genomes]
rs6990055	0.93[ASN][1000 genomes]
rs6991499	0.93[ASN][1000 genomes]
rs6991526	0.93[ASN][1000 genomes]
rs6992366	0.93[ASN][1000 genomes]
rs6993121	0.93[ASN][1000 genomes]
rs7000939	0.93[ASN][1000 genomes]
rs7001887	0.98[ASN][1000 genomes]
rs7004998	0.90[ASN][1000 genomes]
rs7010680	0.93[ASN][1000 genomes]
rs7012206	0.97[ASN][1000 genomes]
rs7013032	0.89[ASN][1000 genomes]
rs7818181	0.98[ASN][1000 genomes]
rs7825100	0.81[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs7829089	0.92[ASN][1000 genomes]
rs7829201	0.92[ASN][1000 genomes]
rs7830317	0.95[ASN][1000 genomes]
rs7830431	0.95[ASN][1000 genomes]
rs7833128	0.92[ASN][1000 genomes]
rs7833945	0.95[ASN][1000 genomes]
rs7846449	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917085	chr8:10237508-10828204	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
2	nsv1026802	chr8:10576444-10754489	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
3	nsv539469	chr8:10576444-10754489	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
4	nsv1017836	chr8:10591801-10803617	Enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
5	nsv1034988	chr8:10591801-10804243	Genic enhancers Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
6	nsv831232	chr8:10606053-10774948	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
7	nsv1019754	chr8:10617908-10700140	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
8	nsv539471	chr8:10617908-10700140	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
9	nsv1031726	chr8:10627742-10749369	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
10	nsv508497	chr8:10680621-10750255	Genic enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10663000-10696200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr8:10666400-10695200	Strong transcription	Primary T cells from cord blood	blood
3	chr8:10668400-10696200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr8:10674800-10696200	Weak transcription	Stomach Mucosa	stomach
5	chr8:10676200-10696200	Weak transcription	Fetal Heart	heart
6	chr8:10683200-10696000	Weak transcription	NHLF	lung
7	chr8:10683600-10696200	Weak transcription	Fetal Kidney	kidney
8	chr8:10684400-10696200	Weak transcription	NHDF-Ad	bronchial
9	chr8:10686200-10696600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr8:10686400-10696400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr8:10688000-10696000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr8:10688000-10696200	Weak transcription	Fetal Brain Male	brain
13	chr8:10688400-10694800	Strong transcription	NHEK	skin
14	chr8:10688800-10696200	Weak transcription	Rectal Smooth Muscle	rectum
15	chr8:10688800-10696400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr8:10689800-10696200	Weak transcription	Primary hematopoietic stem cells	blood
17	chr8:10690600-10696000	Weak transcription	HUVEC	blood vessel
18	chr8:10690600-10696200	Weak transcription	NH-A	brain
19	chr8:10690800-10696000	Weak transcription	HSMM	muscle
20	chr8:10690800-10696200	Weak transcription	Primary neutrophils fromperipheralblood	blood
21	chr8:10691000-10695400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
22	chr8:10691000-10696000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr8:10691000-10696000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
24	chr8:10691000-10696000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr8:10691000-10696000	Weak transcription	HSMMtube	muscle
26	chr8:10691000-10696000	Weak transcription	Osteobl	bone
27	chr8:10691000-10696200	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr8:10691000-10696200	Weak transcription	Brain Angular Gyrus	brain
29	chr8:10691200-10695400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr8:10691400-10696000	Weak transcription	Brain Substantia Nigra	brain
31	chr8:10691400-10696000	Weak transcription	Colon Smooth Muscle	Colon
32	chr8:10691400-10696200	Weak transcription	Fetal Intestine Small	intestine
33	chr8:10691400-10696600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr8:10691400-10696600	Weak transcription	Small Intestine	intestine
35	chr8:10691600-10696200	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr8:10691600-10696600	Weak transcription	Aorta	Aorta
37	chr8:10691800-10695200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr8:10691800-10696000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
39	chr8:10691800-10696000	Weak transcription	Fetal Stomach	stomach
40	chr8:10691800-10696200	Weak transcription	Placenta	Placenta
41	chr8:10691800-10696600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr8:10691800-10696600	Weak transcription	Lung	lung
43	chr8:10691800-10696600	Weak transcription	Ovary	ovary
44	chr8:10692000-10694800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
45	chr8:10692000-10695800	Weak transcription	Pancreatic Islets	Pancreatic Islet
46	chr8:10692000-10696000	Weak transcription	Primary B cells from peripheral blood	blood
47	chr8:10692000-10696000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr8:10692000-10696000	Weak transcription	Muscle Satellite Cultured Cells	--
49	chr8:10692000-10696000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr8:10692000-10696000	Weak transcription	Brain Cingulate Gyrus	brain

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