Variant report

Variant	rs919951
Chromosome Location	chr8:103553703-103553704
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:5)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:103552930..103556301-chr8:103557588..103560805,4	K562	blood:
2	chr8:103553403..103555856-chr8:103556123..103559694,3	MCF-7	breast:
3	chr8:103552849..103555582-chr8:103602690..103604723,2	K562	blood:
4	chr8:103423499..103426368-chr8:103552580..103554247,2	K562	blood:
5	chr8:103549075..103551753-chr8:103552917..103555861,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLF10-5	chr8:103553392-103553821	NONHSAT128100

No data

Variant related genes	Relation type
ENSG00000104517	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10088534	0.84[ASN][1000 genomes]
rs10103471	0.91[ASN][1000 genomes]
rs10104124	0.91[CHB][hapmap];0.95[JPT][hapmap]
rs13250010	0.84[ASN][1000 genomes]
rs13251724	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13258245	0.91[JPT][hapmap];1.00[YRI][hapmap]
rs1347319	0.84[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs1347320	0.84[ASN][1000 genomes]
rs1347321	0.84[ASN][1000 genomes]
rs2033561	0.91[CHB][hapmap];0.85[GIH][hapmap];0.95[JPT][hapmap]
rs2033562	0.84[ASN][1000 genomes]
rs2436910	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs28372594	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4734059	0.89[ASN][1000 genomes]
rs4734636	0.91[CHB][hapmap];0.85[GIH][hapmap];0.95[JPT][hapmap]
rs4734637	0.92[YRI][hapmap];0.87[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs4734638	0.95[CHB][hapmap];0.98[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.91[ASN][1000 genomes]
rs7823812	0.91[ASN][1000 genomes]
rs7836143	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs919950	1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv33118	chr8:103358567-104068172	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	145 gene(s)	inside rSNPs	diseases
2	nsv1031769	chr8:103460754-103620283	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv539703	chr8:103460754-103620283	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh 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	17 gene(s)	inside rSNPs	diseases
4	esv2762761	chr8:103492356-103625244	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	esv1831575	chr8:103498317-103585093	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	esv1838972	chr8:103498317-103585093	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv1024876	chr8:103512785-103576658	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	esv3419415	chr8:103525141-103575507	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs919951	UBR5	cis	lymphoblastoid	seeQTL
rs919951	LOC730429///UBR5	Cis_1M	lymphoblastoid	RTeQTL
rs919951	COX6C	cis	parietal	SCAN
rs919951	UBR5	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:103547000-103556800	Weak transcription	Spleen	Spleen
2	chr8:103550200-103553800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr8:103550400-103554800	Weak transcription	HSMM	muscle
4	chr8:103550600-103554000	Weak transcription	Fetal Thymus	thymus
5	chr8:103550800-103553800	Weak transcription	NH-A	brain
6	chr8:103550800-103589000	Weak transcription	Right Atrium	heart
7	chr8:103551000-103556000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr8:103551200-103556400	Weak transcription	Brain Germinal Matrix	brain
9	chr8:103551400-103553800	Enhancers	Skeletal Muscle Female	skeletal muscle
10	chr8:103551600-103554000	Weak transcription	Fetal Brain Male	brain
11	chr8:103551600-103556600	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr8:103552000-103556400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr8:103552400-103553800	Enhancers	Left Ventricle	heart
14	chr8:103553000-103554600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr8:103553200-103553800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr8:103553200-103553800	Enhancers	Duodenum Smooth Muscle	Duodenum
17	chr8:103553200-103553800	Enhancers	Fetal Intestine Large	intestine
18	chr8:103553200-103553800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
19	chr8:103553200-103553800	Enhancers	Stomach Smooth Muscle	stomach
20	chr8:103553200-103554000	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr8:103553200-103554200	Enhancers	A549	lung
22	chr8:103553200-103554400	Enhancers	Fetal Intestine Small	intestine
23	chr8:103553200-103554400	Enhancers	Gastric	stomach
24	chr8:103553200-103554400	Enhancers	GM12878-XiMat	blood
25	chr8:103553200-103554800	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr8:103553200-103555000	Enhancers	Hela-S3	cervix
27	chr8:103553400-103553800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr8:103553400-103553800	Enhancers	Adipose Nuclei	Adipose
29	chr8:103553400-103553800	Enhancers	Fetal Brain Female	brain
30	chr8:103553400-103553800	Enhancers	Rectal Smooth Muscle	rectum
31	chr8:103553400-103554000	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr8:103553400-103554000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
33	chr8:103553400-103554000	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr8:103553400-103554000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr8:103553400-103554200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr8:103553400-103554400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr8:103553400-103554400	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr8:103553400-103554600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr8:103553400-103554600	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr8:103553400-103554600	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr8:103553600-103553800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr8:103553600-103554200	Enhancers	Fetal Heart	heart
43	chr8:103553600-103554400	Enhancers	H9 Cell Line	embryonic stem cell
44	chr8:103553600-103554400	Flanking Active TSS	K562	blood
45	chr8:103553600-103554400	Enhancers	Osteobl	bone
46	chr8:103553600-103558800	Weak transcription	Psoas Muscle	Psoas

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