Variant report

Variant	rs1869737
Chromosome Location	chr18:9611497-9611498
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr18:9610312..9611854-chr18:9611926..9614343,2	MCF-7	breast:
2	chr18:9598014..9601741-chr18:9607589..9612497,6	MCF-7	breast:
3	chr18:9611182..9615699-chr18:9705314..9711194,13	MCF-7	breast:
4	chr18:9610247..9612763-chr18:9683592..9685519,2	K562	blood:

Variant related genes	Relation type
ENSG00000168461	Chromatin interaction
ENSG00000154845	Chromatin interaction

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs1036930	0.92[AFR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11081487	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12327541	0.80[AFR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16955297	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1869738	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1869739	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2028657	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2277709	1.00[JPT][hapmap]
rs2840354	0.92[ASW][hapmap];1.00[CHB][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.86[ASN][1000 genomes]
rs55841197	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs56883068	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57539299	0.86[ASN][1000 genomes]
rs58800301	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58982927	0.86[ASN][1000 genomes]
rs60290408	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61275183	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62087427	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62087456	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62088860	0.92[AFR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62088870	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62088872	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62088873	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62088875	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62088876	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62088880	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62088881	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62088884	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62088885	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62088904	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62088906	0.82[AFR][1000 genomes];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62088908	0.94[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6506677	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];0.96[GIH][hapmap];0.85[JPT][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7228280	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7231531	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7233308	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7233649	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7234355	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7235935	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7236274	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7237018	0.92[ASW][hapmap];0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[LWK][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];0.84[TSI][hapmap];0.96[YRI][hapmap];0.86[ASN][1000 genomes]
rs7238137	0.85[CEU][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7239083	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[MKK][hapmap];0.84[TSI][hapmap];0.82[AFR][1000 genomes];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7244365	0.82[CHD][hapmap]
rs72945737	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs732698	0.82[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8096551	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3693417	chr18:9512985-9693638	Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv458024	chr18:9558240-9828448	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
3	nsv576448	chr18:9558240-9828448	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
4	nsv543644	chr18:9576145-9612516	Strong transcription Enhancers Genic enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	esv1836290	chr18:9611497-9614851	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:9551000-9612200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr18:9553800-9613600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr18:9588600-9612400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr18:9594200-9613600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr18:9595200-9612000	Weak transcription	Esophagus	oesophagus
6	chr18:9597400-9613200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr18:9598000-9612600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr18:9601800-9612200	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr18:9604800-9612200	Weak transcription	Primary B cells from peripheral blood	blood
10	chr18:9604800-9612400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr18:9605600-9611600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr18:9607200-9613400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr18:9608000-9611600	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr18:9608200-9613600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
15	chr18:9609000-9612200	Weak transcription	Fetal Kidney	kidney
16	chr18:9609000-9612400	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr18:9609200-9612200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
18	chr18:9609400-9612000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr18:9609400-9612000	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr18:9609400-9612400	Weak transcription	Aorta	Aorta
21	chr18:9609400-9612600	Weak transcription	Brain Angular Gyrus	brain
22	chr18:9609400-9612800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr18:9609400-9613600	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr18:9609600-9612000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr18:9609600-9612200	Weak transcription	Primary T helper cells fromperipheralblood	blood
26	chr18:9609600-9612200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr18:9609600-9612200	Weak transcription	Brain Substantia Nigra	brain
28	chr18:9609600-9612200	Weak transcription	Left Ventricle	heart
29	chr18:9609600-9612200	Weak transcription	Small Intestine	intestine
30	chr18:9609600-9612200	Strong transcription	HSMM	muscle
31	chr18:9609600-9612400	Weak transcription	Ovary	ovary
32	chr18:9609600-9612400	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr18:9609600-9612400	Weak transcription	Right Atrium	heart
34	chr18:9609600-9612400	Weak transcription	Right Ventricle	heart
35	chr18:9609600-9612600	Weak transcription	Primary T cells from cord blood	blood
36	chr18:9609600-9613000	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr18:9609600-9613200	Weak transcription	Thymus	Thymus
38	chr18:9609600-9613400	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr18:9609800-9612200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr18:9609800-9612200	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr18:9609800-9613000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr18:9610000-9612400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr18:9610200-9612200	Genic enhancers	K562	blood
44	chr18:9610400-9611600	Strong transcription	Fetal Intestine Small	intestine
45	chr18:9610400-9611600	Genic enhancers	Fetal Muscle Leg	muscle
46	chr18:9610400-9612000	Genic enhancers	HUVEC	blood vessel
47	chr18:9610400-9612200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
48	chr18:9610400-9612200	Genic enhancers	A549	lung
49	chr18:9610400-9612400	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr18:9610600-9611600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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