Variant report

Variant	rs1115274
Chromosome Location	chr2:20181381-20181382
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:20175190..20177737-chr2:20179339..20181997,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RHOB-15	chr2:20181061-20181389	l_1786_chr2:20178128-20181389_testes

Variant related genes	Relation type
ENSG00000118965	Chromatin interaction

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10153717	0.85[AFR][1000 genomes]
rs10165128	0.87[ASN][1000 genomes]
rs10178256	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10187524	0.81[ASN][1000 genomes]
rs10190308	0.87[ASN][1000 genomes]
rs10191437	0.84[ASN][1000 genomes]
rs10197369	0.89[ASN][1000 genomes]
rs10495700	0.89[ASN][1000 genomes]
rs12477955	0.84[ASN][1000 genomes]
rs12478934	0.82[ASN][1000 genomes]
rs12612708	0.89[ASN][1000 genomes]
rs12616917	0.89[ASN][1000 genomes]
rs1437859	0.87[ASN][1000 genomes]
rs1595414	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1595415	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1824661	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1947730	0.90[ASN][1000 genomes]
rs2028207	0.84[AFR][1000 genomes]
rs2045779	0.89[ASN][1000 genomes]
rs2118444	0.86[AFR][1000 genomes]
rs28401180	0.84[ASN][1000 genomes]
rs28598872	0.84[ASN][1000 genomes]
rs3731663	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3820949	0.84[ASN][1000 genomes]
rs6736663	0.84[ASN][1000 genomes]
rs6741091	0.84[ASN][1000 genomes]
rs7569975	0.84[ASN][1000 genomes]
rs7572536	0.89[ASN][1000 genomes]
rs7575732	0.89[ASN][1000 genomes]
rs7604699	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1006404	chr2:20167688-20216509	Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv1005431	chr2:20174676-20210163	Enhancers Flanking Active TSS Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv1011244	chr2:20174676-20216204	Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:20117600-20188400	Weak transcription	Brain Angular Gyrus	brain
2	chr2:20128400-20188400	Weak transcription	Colon Smooth Muscle	Colon
3	chr2:20128400-20189200	Weak transcription	Small Intestine	intestine
4	chr2:20129400-20184800	Weak transcription	Esophagus	oesophagus
5	chr2:20129600-20189000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr2:20130200-20189000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr2:20130400-20188800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr2:20130600-20188800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr2:20131800-20189000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr2:20133600-20184800	Weak transcription	Psoas Muscle	Psoas
11	chr2:20136800-20188800	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr2:20136800-20189000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr2:20138200-20188800	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr2:20138600-20184800	Weak transcription	Aorta	Aorta
15	chr2:20145200-20188000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr2:20153200-20184400	Weak transcription	Brain Hippocampus Middle	brain
17	chr2:20157800-20187200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr2:20162400-20188200	Weak transcription	Brain Substantia Nigra	brain
19	chr2:20163200-20188800	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr2:20164200-20187800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr2:20164600-20187000	Strong transcription	HUES64 Cell Line	embryonic stem cell
22	chr2:20164600-20189000	Weak transcription	Placenta	Placenta
23	chr2:20164800-20189000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
24	chr2:20165000-20181600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
25	chr2:20165000-20187000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr2:20165000-20188400	Weak transcription	K562	blood
27	chr2:20165400-20187600	Weak transcription	Primary B cells from peripheral blood	blood
28	chr2:20165600-20184600	Weak transcription	Gastric	stomach
29	chr2:20165800-20184600	Weak transcription	Lung	lung
30	chr2:20165800-20188200	Weak transcription	Brain Cingulate Gyrus	brain
31	chr2:20169000-20184800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr2:20169000-20188800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr2:20169000-20189000	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr2:20169200-20188800	Weak transcription	Right Ventricle	heart
35	chr2:20171000-20181800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
36	chr2:20171000-20182200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr2:20171800-20187800	Weak transcription	Primary monocytes fromperipheralblood	blood
38	chr2:20172000-20188800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
39	chr2:20172800-20181600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr2:20173000-20182000	Strong transcription	H1 Cell Line	embryonic stem cell
41	chr2:20173000-20182000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr2:20173200-20181400	Strong transcription	HepG2	liver
43	chr2:20173200-20182000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr2:20173200-20182200	Strong transcription	HUES6 Cell Line	embryonic stem cell
45	chr2:20173200-20182200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr2:20173600-20181800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr2:20174000-20184800	Strong transcription	HUES48 Cell Line	embryonic stem cell
48	chr2:20174000-20188800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr2:20174000-20189000	Weak transcription	Fetal Intestine Small	intestine
50	chr2:20174200-20189400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood

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