Variant report

Variant	rs2555376
Chromosome Location	chr15:44450991-44450992
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:44450623..44452763-chr15:44479639..44481622,2	MCF-7	breast:
2	chr15:44448968..44451672-chr15:65596750..65598435,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000200156	Chromatin interaction

Extended variants
information (count: 141 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:127)

rs_ID	r²[population]
rs10459588	1.00[CEU][hapmap]
rs10518994	1.00[CEU][hapmap]
rs10851415	1.00[CEU][hapmap]
rs10851416	1.00[CEU][hapmap]
rs11070419	1.00[CEU][hapmap]
rs1115870	1.00[CEU][hapmap]
rs1160066	1.00[CEU][hapmap]
rs11631340	1.00[CEU][hapmap]
rs11635948	1.00[CEU][hapmap]
rs11854312	1.00[CEU][hapmap]
rs11857696	1.00[CEU][hapmap]
rs12324261	1.00[CEU][hapmap]
rs12437804	1.00[CEU][hapmap];0.82[TSI][hapmap]
rs12591537	1.00[CEU][hapmap]
rs12900237	1.00[CEU][hapmap]
rs12900880	1.00[CEU][hapmap]
rs1426657	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs1426658	1.00[CEU][hapmap];0.85[GIH][hapmap];0.82[TSI][hapmap]
rs1808509	1.00[CEU][hapmap]
rs1813196	0.84[AMR][1000 genomes]
rs1820482	1.00[CEU][hapmap];0.82[TSI][hapmap]
rs1820484	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1820485	0.86[EUR][1000 genomes]
rs1834641	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2012384	0.93[AFR][1000 genomes]
rs2015277	1.00[CEU][hapmap]
rs2042738	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs2042739	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs2042741	1.00[CEU][hapmap]
rs2114416	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2114421	1.00[CEU][hapmap]
rs2114422	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs2162365	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2162366	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2217108	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2256928	0.95[LWK][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs2412845	1.00[CEU][hapmap]
rs2412846	1.00[CEU][hapmap]
rs2412849	1.00[CEU][hapmap]
rs2412850	1.00[CEU][hapmap]
rs2412851	1.00[CEU][hapmap]
rs2412853	0.86[GIH][hapmap];0.82[TSI][hapmap]
rs2412854	1.00[CEU][hapmap];0.86[GIH][hapmap];0.82[TSI][hapmap]
rs2447333	0.83[YRI][hapmap]
rs2447334	0.83[ASW][hapmap];0.93[GIH][hapmap];0.92[LWK][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs2463448	0.84[AFR][1000 genomes]
rs2464692	0.84[AFR][1000 genomes]
rs2555366	0.82[EUR][1000 genomes]
rs2555368	0.86[EUR][1000 genomes]
rs2555375	1.00[CEU][hapmap]
rs2555380	1.00[CEU][hapmap]
rs2555382	0.86[EUR][1000 genomes]
rs2555384	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs2555387	1.00[CEU][hapmap];0.98[EUR][1000 genomes]
rs2555389	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2615269	0.86[EUR][1000 genomes]
rs2615277	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2615278	1.00[CEU][hapmap];1.00[TSI][hapmap];0.98[EUR][1000 genomes]
rs2615280	0.86[EUR][1000 genomes]
rs2615281	1.00[CEU][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs2615285	1.00[CEU][hapmap]
rs2615286	0.86[EUR][1000 genomes]
rs2615287	1.00[CEU][hapmap]
rs2615288	1.00[CEU][hapmap]
rs2615293	1.00[CEU][hapmap]
rs2615294	1.00[CEU][hapmap]
rs2615295	1.00[CEU][hapmap]
rs2615297	1.00[CEU][hapmap];0.93[GIH][hapmap];0.88[TSI][hapmap]
rs2615299	1.00[CEU][hapmap];0.83[YRI][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2615300	0.83[ASW][hapmap];0.93[GIH][hapmap];0.83[LWK][hapmap];0.83[YRI][hapmap]
rs2615303	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2623019	1.00[CEU][hapmap]
rs2663990	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2696072	1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs2696073	0.84[AFR][1000 genomes]
rs2696074	0.83[ASW][hapmap];0.93[GIH][hapmap];0.95[LWK][hapmap];0.92[MKK][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes]
rs2696075	0.84[AFR][1000 genomes]
rs2696078	0.83[YRI][hapmap]
rs2696094	1.00[CEU][hapmap]
rs2696098	1.00[CEU][hapmap];0.87[GIH][hapmap];0.81[MKK][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs2706461	0.80[YRI][hapmap];0.84[AFR][1000 genomes]
rs2706472	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs2706473	1.00[CEU][hapmap]
rs2706477	1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs2706478	0.96[YRI][hapmap];0.84[AFR][1000 genomes]
rs2706481	1.00[CEU][hapmap]
rs2706484	0.96[AFR][1000 genomes]
rs2706486	1.00[CEU][hapmap];0.94[TSI][hapmap];0.86[EUR][1000 genomes]
rs2706487	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2706488	1.00[CEU][hapmap];0.88[TSI][hapmap]
rs2706490	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs2706492	0.86[EUR][1000 genomes]
rs2706495	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2733203	1.00[CEU][hapmap]
rs2733204	1.00[CEU][hapmap]
rs2733208	1.00[CEU][hapmap];0.94[TSI][hapmap];0.86[EUR][1000 genomes]
rs2733209	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2733213	1.00[CEU][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2733221	1.00[CEU][hapmap];0.92[GIH][hapmap];0.88[TSI][hapmap]
rs2733226	1.00[CEU][hapmap]
rs2733234	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2899103	1.00[CEU][hapmap]
rs2929281	1.00[CEU][hapmap]
rs2930528	1.00[CEU][hapmap]
rs2957581	1.00[CEU][hapmap];0.88[TSI][hapmap]
rs2957583	1.00[CEU][hapmap]
rs4923976	1.00[CEU][hapmap];0.96[YRI][hapmap];0.95[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs4924727	1.00[CEU][hapmap]
rs4924728	1.00[CEU][hapmap]
rs4924729	1.00[CEU][hapmap];0.86[GIH][hapmap]
rs4924734	1.00[CEU][hapmap]
rs4924737	1.00[CEU][hapmap]
rs6493092	1.00[CEU][hapmap]
rs6493093	1.00[CEU][hapmap]
rs6493094	1.00[CEU][hapmap];0.86[GIH][hapmap];0.82[TSI][hapmap]
rs7166715	1.00[CEU][hapmap];0.88[TSI][hapmap]
rs7174819	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs8033233	1.00[CEU][hapmap];0.86[GIH][hapmap];0.82[TSI][hapmap]
rs8035212	1.00[CEU][hapmap]
rs8036541	1.00[CEU][hapmap]
rs8037596	1.00[CEU][hapmap]
rs8038096	1.00[CEU][hapmap];0.82[TSI][hapmap]
rs8041487	1.00[CEU][hapmap]
rs8042697	0.86[EUR][1000 genomes]
rs890465	1.00[CEU][hapmap]
rs958485	1.00[CEU][hapmap]
rs9920249	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv431387	chr15:43929378-44862930	Weak transcription Strong transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	158 gene(s)	inside rSNPs	diseases
2	nsv931051	chr15:43988761-44833518	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	154 gene(s)	inside rSNPs	diseases
3	nsv1044435	chr15:44176103-44507403	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
4	nsv1052511	chr15:44266441-44719023	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
5	nsv542371	chr15:44266441-44719023	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
6	nsv832989	chr15:44306469-44461710	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	esv3351630	chr15:44334624-44547841	Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
8	nsv904173	chr15:44391572-44522214	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	nsv904174	chr15:44391572-44538660	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	nsv569298	chr15:44401266-44513090	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
11	nsv904175	chr15:44403988-44538660	Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
12	nsv904176	chr15:44403988-44579854	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
13	esv1843598	chr15:44417606-44526813	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
14	esv3410956	chr15:44425145-44823647	Strong transcription Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:44437400-44451000	Weak transcription	Brain Cingulate Gyrus	brain
2	chr15:44447800-44451600	Enhancers	NHEK	skin
3	chr15:44448000-44452000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr15:44448200-44451400	Enhancers	HMEC	breast
5	chr15:44448800-44451800	Enhancers	Osteobl	bone
6	chr15:44448800-44452200	Enhancers	NHLF	lung
7	chr15:44449000-44451400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr15:44449000-44452200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr15:44449400-44451000	Enhancers	GM12878-XiMat	blood
10	chr15:44449400-44451400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr15:44449400-44451600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr15:44449600-44451200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr15:44449600-44451400	Enhancers	HSMMtube	muscle
14	chr15:44449800-44451000	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr15:44450000-44451000	Enhancers	Fetal Heart	heart
16	chr15:44450000-44452000	Enhancers	A549	lung
17	chr15:44450000-44452000	Enhancers	HUVEC	blood vessel
18	chr15:44450000-44452200	Enhancers	Brain Hippocampus Middle	brain
19	chr15:44450200-44451200	Enhancers	Placenta Amnion	Placenta Amnion
20	chr15:44450200-44451600	Enhancers	NHDF-Ad	bronchial
21	chr15:44450200-44452000	Enhancers	Brain Substantia Nigra	brain
22	chr15:44450400-44451400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr15:44450400-44452000	Enhancers	Brain Angular Gyrus	brain
24	chr15:44450400-44452200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr15:44450600-44451400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr15:44450600-44452200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr15:44450800-44451000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
28	chr15:44450800-44451000	Flanking Active TSS	HSMM	muscle
29	chr15:44450800-44451200	Flanking Active TSS	NH-A	brain
30	chr15:44450800-44451400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr15:44450800-44452200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin

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