Variant report

Variant	rs2412849
Chromosome Location	chr15:44276555-44276556
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 111 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:104)

rs_ID	r²[population]
rs10459588	1.00[CEU][hapmap]
rs10518994	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes]
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];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap]
rs11631340	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes]
rs11635948	1.00[CEU][hapmap]
rs11854312	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes]
rs11857696	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.97[YRI][hapmap]
rs12324261	1.00[CEU][hapmap]
rs12437804	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs12591537	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs12900237	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs12900880	1.00[CEU][hapmap]
rs13379739	0.80[CHB][hapmap];1.00[JPT][hapmap]
rs1365457	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs1426657	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap]
rs1426658	1.00[CEU][hapmap]
rs16959032	0.91[JPT][hapmap]
rs16959345	0.90[JPT][hapmap]
rs1808509	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap]
rs1820482	1.00[CEU][hapmap]
rs1834641	1.00[CEU][hapmap]
rs2015277	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap]
rs2042738	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap]
rs2042739	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap]
rs2042741	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap]
rs2114420	0.90[CHB][hapmap];0.91[JPT][hapmap];0.89[AFR][1000 genomes]
rs2114421	1.00[CEU][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.82[AFR][1000 genomes]
rs2114422	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap]
rs2162366	1.00[CEU][hapmap]
rs2217108	1.00[CEU][hapmap]
rs2412845	1.00[CEU][hapmap]
rs2412846	1.00[CEU][hapmap]
rs2412850	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes]
rs2412851	1.00[CEU][hapmap]
rs2412852	0.86[AFR][1000 genomes]
rs2412854	1.00[CEU][hapmap]
rs2555375	1.00[CEU][hapmap]
rs2555376	1.00[CEU][hapmap]
rs2555380	1.00[CEU][hapmap]
rs2555384	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap]
rs2555387	1.00[CEU][hapmap];0.80[CHB][hapmap];1.00[JPT][hapmap]
rs2555389	1.00[CEU][hapmap]
rs2615278	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs2615281	1.00[CEU][hapmap];0.89[CHB][hapmap];0.90[JPT][hapmap]
rs2615285	1.00[CEU][hapmap]
rs2615287	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap]
rs2615288	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap]
rs2615293	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap]
rs2615294	1.00[CEU][hapmap]
rs2615295	1.00[CEU][hapmap];0.88[CHB][hapmap];0.83[YRI][hapmap]
rs2615297	1.00[CEU][hapmap]
rs2623019	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap]
rs2696094	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap]
rs2696098	1.00[CEU][hapmap]
rs2706472	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap]
rs2706473	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap]
rs2706481	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap]
rs2706486	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap]
rs2706487	1.00[CEU][hapmap]
rs2706488	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap]
rs2706490	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap]
rs2706495	1.00[CEU][hapmap]
rs2733203	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap]
rs2733204	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap]
rs2733208	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap]
rs2733209	1.00[CEU][hapmap]
rs2733210	0.80[CHB][hapmap];1.00[JPT][hapmap]
rs2733213	1.00[CEU][hapmap]
rs2733221	1.00[CEU][hapmap]
rs2733226	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap]
rs2899103	1.00[CEU][hapmap]
rs2929281	1.00[CEU][hapmap]
rs2930528	1.00[CEU][hapmap]
rs2957581	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap]
rs2957583	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[YRI][hapmap];0.93[AFR][1000 genomes]
rs4419034	0.90[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap];0.82[AFR][1000 genomes]
rs4597286	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs4923976	1.00[CEU][hapmap]
rs4924727	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes]
rs4924728	1.00[CEU][hapmap]
rs4924729	1.00[CEU][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]
rs7166715	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap]
rs7168522	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs8030309	0.80[CHB][hapmap];1.00[JPT][hapmap]
rs8033233	1.00[CEU][hapmap]
rs8035212	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.85[AFR][1000 genomes]
rs8035946	0.91[JPT][hapmap]
rs8036541	1.00[CEU][hapmap]
rs8037596	1.00[CEU][hapmap]
rs8038096	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs8039970	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs8041487	1.00[CEU][hapmap]
rs890465	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs958485	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[YRI][hapmap];0.87[AFR][1000 genomes]
rs9920249	1.00[CEU][hapmap]

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	nsv1037786	chr15:43888926-44318587	Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
2	nsv542370	chr15:43888926-44318587	Weak transcription Genic enhancers Flanking Active TSS Active TSS Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
3	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
4	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
5	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
6	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
7	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

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:44257400-44281000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr15:44259200-44285600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr15:44263000-44295600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr15:44267400-44276600	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr15:44267400-44290600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr15:44268800-44290400	Weak transcription	Fetal Heart	heart
7	chr15:44269400-44278000	Weak transcription	Brain Anterior Caudate	brain
8	chr15:44269600-44278000	Weak transcription	Brain Substantia Nigra	brain
9	chr15:44269600-44283600	Weak transcription	Brain Angular Gyrus	brain
10	chr15:44269800-44291800	Weak transcription	NH-A	brain
11	chr15:44269800-44292200	Weak transcription	HMEC	breast
12	chr15:44270800-44278000	Weak transcription	GM12878-XiMat	blood
13	chr15:44274600-44281200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr15:44275600-44276600	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr15:44275600-44276600	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr15:44275600-44276600	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr15:44275600-44276800	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr15:44275800-44276600	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr15:44275800-44276800	Enhancers	H1 Cell Line	embryonic stem cell
20	chr15:44275800-44276800	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr15:44276200-44278600	Enhancers	Brain Hippocampus Middle	brain
22	chr15:44276200-44281800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr15:44276400-44287200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr15:44276400-44287800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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