Variant report

Variant	rs1362
Chromosome Location	chr7:112117861-112117862
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:7)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:7 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr7:112116592-112118819	IMR90	lung:	n/a	n/a
2	POLR2A	chr7:112117753-112117871	HepG2	liver:	n/a	n/a
3	POLR2A	chr7:112117852-112118261	SK-N-SH	brain:	n/a	n/a
4	POLR2A	chr7:112116027-112120055	A549	lung:	n/a	n/a
5	POLR2A	chr7:112115869-112121327	K562	blood:	n/a	n/a
6	POLR2A	chr7:112115373-112119161	HepG2	liver:	n/a	n/a
7	POLR2A	chr7:112116155-112118266	Hela-S3	cervix:	n/a	n/a

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:112088943..112098465-chr7:112111106..112127214,31	K562	blood:
2	chr7:112117720..112119517-chr7:112121271..112122829,2	K562	blood:
3	chr7:112116935..112118572-chr7:112119944..112122258,2	MCF-7	breast:
4	chr7:112108291..112109853-chr7:112116761..112118478,2	MCF-7	breast:
5	chr7:112113016..112114522-chr7:112116589..112118218,2	K562	blood:
6	chr7:112114725..112118373-chr7:112118548..112121134,7	K562	blood:
7	chr7:112109911..112112772-chr7:112114561..112118551,4	K562	blood:

No data

Variant related genes	Relation type
LSMEM1	TF binding region
ENSG00000006652	Chromatin interaction
ENSG00000181016	Chromatin interaction

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs1024571	0.82[LWK][hapmap]
rs11763010	1.00[ASW][hapmap];0.92[CEU][hapmap];0.94[GIH][hapmap];1.00[LWK][hapmap];0.98[MKK][hapmap];0.95[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12154282	0.92[CEU][hapmap];1.00[GIH][hapmap];0.86[MKK][hapmap];0.98[TSI][hapmap];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12155248	0.95[CEU][hapmap];0.82[YRI][hapmap];0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs67523617	0.82[AMR][1000 genomes]
rs6944024	0.81[AMR][1000 genomes]
rs6963813	0.87[CEU][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9649354	0.93[ASW][hapmap];0.92[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];0.89[MKK][hapmap];0.98[TSI][hapmap];0.91[YRI][hapmap];0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531436	chr7:111856171-112585407	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	105 gene(s)	inside rSNPs	diseases
2	nsv1030033	chr7:112092709-112140430	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:112092600-112121800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:112094000-112118200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr7:112094000-112121400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr7:112094400-112118200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
5	chr7:112095600-112118800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr7:112095800-112118000	Strong transcription	Placenta	Placenta
7	chr7:112095800-112118200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr7:112095800-112118200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr7:112096400-112121600	Strong transcription	Liver	Liver
10	chr7:112096400-112121800	Weak transcription	Stomach Mucosa	stomach
11	chr7:112100600-112135000	Weak transcription	Esophagus	oesophagus
12	chr7:112101000-112118000	Strong transcription	Rectal Mucosa Donor 29	rectum
13	chr7:112102800-112119800	Strong transcription	Monocytes-CD14+_RO01746	blood
14	chr7:112103000-112118200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr7:112103000-112118200	Strong transcription	Hela-S3	cervix
16	chr7:112103000-112119600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr7:112103200-112118200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr7:112103200-112118200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr7:112103200-112118600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr7:112103600-112121200	Strong transcription	Primary neutrophils fromperipheralblood	blood
21	chr7:112103600-112121800	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr7:112104600-112118000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr7:112105600-112121800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
24	chr7:112107600-112118200	Strong transcription	Duodenum Smooth Muscle	Duodenum
25	chr7:112107800-112120800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
26	chr7:112109800-112118000	Strong transcription	NHLF	lung
27	chr7:112110600-112120400	Weak transcription	Fetal Heart	heart
28	chr7:112110600-112124600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr7:112111200-112127200	Weak transcription	Fetal Brain Male	brain
30	chr7:112111600-112122200	Weak transcription	Fetal Kidney	kidney
31	chr7:112112000-112120400	Weak transcription	Gastric	stomach
32	chr7:112112400-112119400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
33	chr7:112112400-112121800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr7:112112400-112122200	Weak transcription	Pancreatic Islets	Pancreatic Islet
35	chr7:112112600-112129000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr7:112112800-112120600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr7:112112800-112120600	Weak transcription	Brain Angular Gyrus	brain
38	chr7:112113200-112120200	Weak transcription	Psoas Muscle	Psoas
39	chr7:112113200-112122600	Weak transcription	Colonic Mucosa	Colon
40	chr7:112113200-112124600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr7:112113200-112124800	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr7:112113200-112125000	Weak transcription	Right Ventricle	heart
43	chr7:112113400-112118600	Weak transcription	Fetal Brain Female	brain
44	chr7:112113400-112127600	Weak transcription	Spleen	Spleen
45	chr7:112114200-112120600	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr7:112114400-112118000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
47	chr7:112114400-112120200	Weak transcription	Rectal Smooth Muscle	rectum
48	chr7:112114400-112120800	Weak transcription	Brain Hippocampus Middle	brain
49	chr7:112114400-112132000	Weak transcription	HepG2	liver
50	chr7:112114600-112119200	Weak transcription	Brain Germinal Matrix	brain

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