Variant report

Variant	rs8177745
Chromosome Location	chr10:5994833-5994834
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:3)
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	chr10:5990354..5995622-chr10:5995920..5999201,5	K562	blood:
2	chr10:5991870..5998426-chr10:6018061..6021300,7	MCF-7	breast:
3	chr10:5993851..5996017-chr10:6018079..6020858,3	MCF-7	breast:
4	chr10:5989579..5992507-chr10:5992737..5995204,2	MCF-7	breast:
5	chr10:5993943..5996022-chr10:5999962..6001752,2	K562	blood:
6	chr10:5993943..5996506-chr10:5999317..6001462,2	K562	blood:
7	chr10:5993229..5995375-chr10:6003228..6005603,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IL15RA-2	chr10:5994334-5995169	NONHSAT011197
2	lnc-IL15RA-2	chr10:5994356-5995169	NONHSAT011198
3	lnc-IL15RA-2	chr10:5994356-5995169	NONHSAT011199

No data

Variant related genes	Relation type
ENSG00000134470	Chromatin interaction

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs10508299	1.00[YRI][hapmap]
rs3136622	1.00[YRI][hapmap]
rs7087996	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34147	chr10:5726821-6105717	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Bivalent Enhancer 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 target site	42 gene(s)	inside rSNPs	diseases
2	esv34061	chr10:5726821-6225187	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv1042286	chr10:5795129-6578445	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer 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	76 gene(s)	inside rSNPs	diseases
4	nsv831775	chr10:5804335-6000849	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats 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 target site	34 gene(s)	inside rSNPs	diseases
5	nsv1041261	chr10:5962635-6052196	Weak transcription Active TSS Genic enhancers Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv1050983	chr10:5963921-6052196	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:71 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5969600-6012000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr10:5971400-6013200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr10:5980000-6013200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr10:5980800-6017800	Weak transcription	Thymus	Thymus
5	chr10:5981000-6003600	Weak transcription	Primary T cells from cord blood	blood
6	chr10:5982800-5995000	Weak transcription	GM12878-XiMat	blood
7	chr10:5986200-6018600	Weak transcription	Aorta	Aorta
8	chr10:5986800-5995600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr10:5987600-6018000	Weak transcription	Psoas Muscle	Psoas
10	chr10:5987800-6017800	Weak transcription	Fetal Thymus	thymus
11	chr10:5988000-5995000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr10:5988000-6000800	Weak transcription	Colonic Mucosa	Colon
13	chr10:5988000-6001400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr10:5988200-5998600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr10:5988200-6001800	Weak transcription	Primary T helper cells PMA-I stimulated	--
16	chr10:5988400-6001200	Weak transcription	Ovary	ovary
17	chr10:5988400-6001600	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr10:5988600-6011800	Weak transcription	Colon Smooth Muscle	Colon
19	chr10:5989200-6001600	Weak transcription	Rectal Smooth Muscle	rectum
20	chr10:5989400-6001200	Weak transcription	Primary hematopoietic stem cells	blood
21	chr10:5991400-5999000	Weak transcription	Brain Hippocampus Middle	brain
22	chr10:5991400-6000800	Weak transcription	K562	blood
23	chr10:5991400-6004800	Weak transcription	Brain Anterior Caudate	brain
24	chr10:5992800-5995000	Weak transcription	Fetal Muscle Trunk	muscle
25	chr10:5992800-5997800	Weak transcription	Left Ventricle	heart
26	chr10:5993000-5999800	Weak transcription	HUVEC	blood vessel
27	chr10:5993200-5996400	Strong transcription	Fetal Intestine Small	intestine
28	chr10:5993200-6001600	Weak transcription	Stomach Smooth Muscle	stomach
29	chr10:5993400-6000400	Weak transcription	NHLF	lung
30	chr10:5993600-5995800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr10:5993600-5996800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr10:5993600-6013200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr10:5993800-5996000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr10:5993800-5996000	Strong transcription	Liver	Liver
35	chr10:5993800-5996000	Strong transcription	Skeletal Muscle Female	skeletal muscle
36	chr10:5993800-5996200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr10:5994000-5995400	Strong transcription	Esophagus	oesophagus
38	chr10:5994000-5995600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
39	chr10:5994000-5995600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr10:5994000-5996000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
41	chr10:5994000-5996000	Strong transcription	Primary T helper cells fromperipheralblood	blood
42	chr10:5994000-5996000	Strong transcription	Adipose Nuclei	Adipose
43	chr10:5994000-5996200	Strong transcription	Primary T cells fromperipheralblood	blood
44	chr10:5994000-5998200	Weak transcription	Placenta	Placenta
45	chr10:5994000-5998800	Strong transcription	Duodenum Mucosa	Duodenum
46	chr10:5994000-6011000	Strong transcription	Monocytes-CD14+_RO01746	blood
47	chr10:5994000-6012800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr10:5994200-5995400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr10:5994200-5996000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr10:5994200-5998400	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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