Variant report

Variant	rs11651510
Chromosome Location	chr17:59768890-59768891
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr17:59767717..59769593-chr21:41754353..41755861,2	MCF-7	breast:
2	chr17:59484501..59486450-chr17:59767839..59770288,2	MCF-7	breast:
3	chr17:59768178..59770991-chr17:59939868..59941400,2	MCF-7	breast:
4	chr17:59746953..59749677-chr17:59767586..59769308,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000235123	Chromatin interaction
ENSG00000121068	Chromatin interaction
ENSG00000136492	Chromatin interaction

Extended variants
information (count: 101 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:99)

rs_ID	r²[population]
rs1015771	0.86[EUR][1000 genomes]
rs10221278	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10438771	0.87[EUR][1000 genomes]
rs10468558	0.87[EUR][1000 genomes]
rs10515206	0.86[EUR][1000 genomes]
rs10515207	0.85[EUR][1000 genomes]
rs10853038	0.87[EUR][1000 genomes]
rs10853039	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11079445	0.87[EUR][1000 genomes]
rs11079446	0.87[EUR][1000 genomes]
rs11079448	0.87[EUR][1000 genomes]
rs11650471	0.87[EUR][1000 genomes]
rs11871753	0.86[EUR][1000 genomes]
rs12449319	0.87[EUR][1000 genomes]
rs12450027	0.86[EUR][1000 genomes]
rs12451862	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12453293	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12453801	0.87[EUR][1000 genomes]
rs12453966	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12603485	0.86[EUR][1000 genomes]
rs12603617	0.89[EUR][1000 genomes]
rs12937232	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12950438	0.86[EUR][1000 genomes]
rs1541346	0.86[EUR][1000 genomes]
rs16945500	0.87[EUR][1000 genomes]
rs17532528	0.87[EUR][1000 genomes]
rs2024188	0.86[EUR][1000 genomes]
rs2040608	0.86[EUR][1000 genomes]
rs2109252	0.85[EUR][1000 genomes]
rs2109254	0.85[EUR][1000 genomes]
rs2109255	0.85[EUR][1000 genomes]
rs2158006	0.85[EUR][1000 genomes]
rs2159450	0.85[EUR][1000 genomes]
rs2188731	0.86[EUR][1000 genomes]
rs2191247	0.85[EUR][1000 genomes]
rs2191249	0.86[EUR][1000 genomes]
rs2214184	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2378874	0.86[EUR][1000 genomes]
rs2378875	0.86[EUR][1000 genomes]
rs2378884	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2378902	0.85[EUR][1000 genomes]
rs28571892	0.86[EUR][1000 genomes]
rs2890012	0.87[EUR][1000 genomes]
rs2890013	0.89[EUR][1000 genomes]
rs2890021	0.86[EUR][1000 genomes]
rs36031690	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4309463	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4343344	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4580256	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4968444	0.89[EUR][1000 genomes]
rs4968447	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4968577	0.86[EUR][1000 genomes]
rs4968579	0.87[EUR][1000 genomes]
rs4968580	0.87[EUR][1000 genomes]
rs4968582	0.87[EUR][1000 genomes]
rs4968584	0.87[EUR][1000 genomes]
rs4968585	0.87[EUR][1000 genomes]
rs4968588	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs55797010	0.87[EUR][1000 genomes]
rs56284136	0.87[EUR][1000 genomes]
rs57099937	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs57393813	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61599541	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs62070615	0.87[EUR][1000 genomes]
rs62070616	0.87[EUR][1000 genomes]
rs62070617	0.87[EUR][1000 genomes]
rs62070624	0.83[EUR][1000 genomes]
rs6504068	0.86[EUR][1000 genomes]
rs6504070	0.81[EUR][1000 genomes]
rs67273191	0.86[EUR][1000 genomes]
rs67938055	0.87[EUR][1000 genomes]
rs717961	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs717962	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7207074	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7207881	0.86[EUR][1000 genomes]
rs7212423	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7213470	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7213587	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7213759	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7217292	0.85[EUR][1000 genomes]
rs7220688	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7220719	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72841508	0.87[EUR][1000 genomes]
rs8074949	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs8075370	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs8075397	0.87[EUR][1000 genomes]
rs8078977	0.83[EUR][1000 genomes]
rs8182296	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9303449	0.87[EUR][1000 genomes]
rs9807012	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9896013	0.86[EUR][1000 genomes]
rs9897450	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9897928	0.86[EUR][1000 genomes]
rs9901428	0.87[EUR][1000 genomes]
rs9902995	0.86[EUR][1000 genomes]
rs9903041	0.87[EUR][1000 genomes]
rs9904294	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9905870	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9906313	0.86[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	esv3378293	chr17:59744117-60124899	ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	175 gene(s)	inside rSNPs	diseases
2	nsv908673	chr17:59767501-59926645	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	94 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:48 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:59751000-59777200	Weak transcription	HepG2	liver
2	chr17:59755600-59778000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr17:59756600-59772600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr17:59756600-59777000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr17:59757000-59772000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr17:59757400-59775600	Weak transcription	A549	lung
7	chr17:59758400-59772400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr17:59759400-59772000	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr17:59759400-59772400	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr17:59759600-59771200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr17:59759800-59769200	Weak transcription	Thymus	Thymus
12	chr17:59759800-59775400	Weak transcription	Primary hematopoietic stem cells	blood
13	chr17:59759800-59776600	Weak transcription	GM12878-XiMat	blood
14	chr17:59760200-59774000	Weak transcription	Hela-S3	cervix
15	chr17:59761200-59772800	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr17:59761400-59771600	Weak transcription	NHDF-Ad	bronchial
17	chr17:59761400-59776000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr17:59761600-59776200	Weak transcription	HUVEC	blood vessel
19	chr17:59762400-59772200	Weak transcription	NHLF	lung
20	chr17:59762600-59777400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr17:59763000-59772000	Weak transcription	Fetal Intestine Large	intestine
22	chr17:59763400-59792800	Weak transcription	NH-A	brain
23	chr17:59763600-59771400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr17:59763800-59772800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr17:59764400-59769000	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr17:59764400-59777000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr17:59764800-59771600	Weak transcription	Brain Germinal Matrix	brain
28	chr17:59765800-59771400	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr17:59765800-59771600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr17:59765800-59771600	Weak transcription	Fetal Stomach	stomach
31	chr17:59766000-59769200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr17:59766000-59819000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr17:59767000-59772600	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr17:59767200-59769200	Weak transcription	Fetal Thymus	thymus
35	chr17:59767200-59771400	Weak transcription	Osteobl	bone
36	chr17:59767400-59771600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr17:59767400-59772400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr17:59767400-59773400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr17:59767600-59769200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr17:59767600-59769200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr17:59767600-59769200	Weak transcription	Dnd41	blood
42	chr17:59767600-59771600	Weak transcription	Primary neutrophils fromperipheralblood	blood
43	chr17:59767600-59773200	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr17:59767600-59792800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr17:59767600-59793200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr17:59767800-59777000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr17:59768600-59770800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr17:59768600-59771200	Weak transcription	K562	blood

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