Variant report

Variant	rs2108254
Chromosome Location	chr7:108202114-108202115
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:0)
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	chr7:108175296..108178679-chr7:108201125..108203447,3	K562	blood:
2	chr7:108168430..108172542-chr7:108200740..108204398,3	K562	blood:
3	chr7:108193337..108196664-chr7:108198034..108202692,4	K562	blood:
4	chr7:108191362..108206184-chr7:108206645..108216261,27	K562	blood:
5	chr7:108200654..108204288-chr7:108205009..108207830,4	MCF-7	breast:
6	chr7:108159403..108171484-chr7:108200740..108214365,45	K562	blood:
7	chr7:108165059..108167985-chr7:108201651..108203639,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000177683	Chromatin interaction
ENSG00000135241	Chromatin interaction
ENSG00000128590	Chromatin interaction

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10215124	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10258344	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2041002	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2190403	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2190404	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2214911	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2227272	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2240449	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28667688	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][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	esv3348839	chr7:107377311-108286538	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
2	nsv817371	chr7:108199882-108649799	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:80 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:108191400-108204600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr7:108195600-108208400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr7:108197600-108208600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr7:108197800-108208600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr7:108198000-108204200	Weak transcription	Fetal Thymus	thymus
6	chr7:108198000-108208400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr7:108198400-108207800	Weak transcription	Brain Hippocampus Middle	brain
8	chr7:108198400-108208400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr7:108198600-108203000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr7:108198600-108204200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr7:108198600-108204200	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr7:108198600-108204600	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr7:108198600-108204800	Weak transcription	Dnd41	blood
14	chr7:108198600-108207400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr7:108198600-108208600	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr7:108198600-108208600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr7:108198600-108208600	Weak transcription	Fetal Brain Male	brain
18	chr7:108198600-108208600	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr7:108198600-108208600	Weak transcription	Thymus	Thymus
20	chr7:108198800-108202400	Weak transcription	Primary hematopoietic stem cells	blood
21	chr7:108198800-108204200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr7:108198800-108204200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr7:108198800-108204400	Weak transcription	Primary neutrophils fromperipheralblood	blood
24	chr7:108198800-108204400	Weak transcription	Primary B cells from peripheral blood	blood
25	chr7:108198800-108205800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr7:108198800-108206000	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr7:108199000-108202200	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr7:108199000-108207600	Weak transcription	Duodenum Mucosa	Duodenum
29	chr7:108199400-108202200	Strong transcription	A549	lung
30	chr7:108199400-108207400	Weak transcription	Stomach Smooth Muscle	stomach
31	chr7:108199400-108208200	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr7:108199600-108204200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr7:108199600-108204600	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr7:108199600-108204600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr7:108199800-108204200	Weak transcription	K562	blood
36	chr7:108199800-108204800	Weak transcription	Adipose Nuclei	Adipose
37	chr7:108199800-108204800	Weak transcription	GM12878-XiMat	blood
38	chr7:108200000-108204000	Weak transcription	Fetal Lung	lung
39	chr7:108200000-108204200	Weak transcription	Liver	Liver
40	chr7:108200000-108207000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr7:108200000-108207800	Weak transcription	HepG2	liver
42	chr7:108200200-108204600	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr7:108200200-108206000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr7:108200200-108208000	Weak transcription	Brain Angular Gyrus	brain
45	chr7:108200400-108209400	Weak transcription	Spleen	Spleen
46	chr7:108200600-108208400	Weak transcription	NHLF	lung
47	chr7:108200800-108202200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
48	chr7:108200800-108202600	Strong transcription	Ovary	ovary
49	chr7:108201000-108202200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr7:108201200-108202600	Strong transcription	Placenta	Placenta

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