Variant report

Variant	rs11857155
Chromosome Location	chr15:33424198-33424199
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:33358789..33361787-chr15:33421659..33424986,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000248905	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs11072237	0.91[EUR][1000 genomes]
rs11072238	0.91[EUR][1000 genomes]
rs12906147	0.87[CEU][hapmap];0.94[EUR][1000 genomes]
rs12909746	0.94[EUR][1000 genomes]
rs12910096	0.85[CEU][hapmap];0.94[EUR][1000 genomes]
rs12911944	0.87[CEU][hapmap];0.91[EUR][1000 genomes]
rs12916976	0.91[EUR][1000 genomes]
rs17816808	0.91[EUR][1000 genomes]
rs2444955	0.86[ASN][1000 genomes]
rs2468736	0.94[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs2468737	0.87[ASN][1000 genomes]
rs2468761	0.85[ASN][1000 genomes]
rs34830403	0.94[EUR][1000 genomes]
rs3861197	0.80[CHB][hapmap]
rs3861198	0.87[CEU][hapmap];0.90[EUR][1000 genomes]
rs3861199	0.87[CEU][hapmap];0.94[EUR][1000 genomes]
rs6494893	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8023846	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8024139	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8041426	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs815481	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv903979	chr15:33144202-33550256	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv1052966	chr15:33149753-33541951	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv542340	chr15:33149753-33541951	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv903981	chr15:33207082-33550256	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv568918	chr15:33244672-33446971	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv903982	chr15:33282844-33616150	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
7	nsv903983	chr15:33388030-33550256	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:33419200-33424200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr15:33419200-33427600	Weak transcription	Brain Cingulate Gyrus	brain
3	chr15:33419200-33427600	Weak transcription	Lung	lung
4	chr15:33419200-33428600	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr15:33419200-33430000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr15:33419200-33430400	Weak transcription	Psoas Muscle	Psoas
7	chr15:33420000-33425200	Weak transcription	Adipose Nuclei	Adipose
8	chr15:33420000-33425200	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr15:33420000-33427200	Weak transcription	Colon Smooth Muscle	Colon
10	chr15:33420400-33424200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr15:33420400-33426200	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr15:33420600-33434800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr15:33423200-33425400	Enhancers	Fetal Thymus	thymus
14	chr15:33423600-33424200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr15:33423600-33424400	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr15:33423600-33424400	Enhancers	Fetal Lung	lung
17	chr15:33423600-33424400	Enhancers	Sigmoid Colon	Sigmoid Colon
18	chr15:33423600-33424600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr15:33423600-33424600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr15:33423600-33424600	Enhancers	Rectal Mucosa Donor 29	rectum
21	chr15:33423600-33424600	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr15:33423600-33425000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
23	chr15:33423600-33425000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr15:33423600-33425200	Enhancers	Primary T helper cells PMA-I stimulated	--
25	chr15:33423600-33425200	Enhancers	Thymus	Thymus
26	chr15:33423600-33425400	Enhancers	Muscle Satellite Cultured Cells	--
27	chr15:33423600-33425400	Enhancers	Hela-S3	cervix
28	chr15:33423600-33425400	Enhancers	NHEK	skin
29	chr15:33423600-33425600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr15:33423600-33425600	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr15:33423600-33425600	Enhancers	HSMM	muscle
32	chr15:33423600-33425600	Enhancers	NHLF	lung
33	chr15:33423600-33428400	Enhancers	Skeletal Muscle Male	skeletal muscle
34	chr15:33423600-33428800	Enhancers	Skeletal Muscle Female	skeletal muscle
35	chr15:33423800-33424400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr15:33423800-33424400	Enhancers	Rectal Smooth Muscle	rectum
37	chr15:33423800-33424400	Enhancers	HMEC	breast
38	chr15:33423800-33424600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr15:33423800-33424600	Enhancers	Brain Angular Gyrus	brain
40	chr15:33423800-33424600	Enhancers	Duodenum Mucosa	Duodenum
41	chr15:33423800-33424800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr15:33423800-33424800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr15:33423800-33425000	Enhancers	HUVEC	blood vessel
44	chr15:33423800-33425000	Enhancers	NH-A	brain
45	chr15:33423800-33425400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr15:33423800-33425400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr15:33423800-33425400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr15:33423800-33425400	Enhancers	Fetal Kidney	kidney
49	chr15:33423800-33425400	Enhancers	NHDF-Ad	bronchial
50	chr15:33423800-33425600	Enhancers	Fetal Muscle Leg	muscle

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