Variant report

Variant	rs61678411
Chromosome Location	chr15:59035579-59035580
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:58841936..58843699-chr15:59035411..59037859,2	MCF-7	breast:
2	chr15:59030373..59033312-chr15:59035023..59037730,3	MCF-7	breast:
3	chr15:59033587..59035480-chr15:59035555..59037744,3	K562	blood:
4	chr15:59030650..59032606-chr15:59033863..59036396,2	K562	blood:
5	chr15:59021059..59023749-chr15:59034779..59037397,2	K562	blood:

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs16940570	1.00[EUR][1000 genomes]
rs16940574	1.00[EUR][1000 genomes]
rs16940584	1.00[EUR][1000 genomes]
rs16940586	1.00[EUR][1000 genomes]
rs16940602	1.00[EUR][1000 genomes]
rs16940614	1.00[EUR][1000 genomes]
rs16940638	1.00[EUR][1000 genomes]
rs16940723	1.00[EUR][1000 genomes]
rs16940751	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16940766	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs16940768	1.00[EUR][1000 genomes]
rs16940771	1.00[EUR][1000 genomes]
rs2414609	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs4277293	1.00[EUR][1000 genomes]
rs55939313	1.00[EUR][1000 genomes]
rs56039925	1.00[EUR][1000 genomes]
rs56357958	1.00[EUR][1000 genomes]
rs56935364	1.00[EUR][1000 genomes]
rs56942476	1.00[EUR][1000 genomes]
rs57083702	1.00[EUR][1000 genomes]
rs57845422	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58937576	1.00[EUR][1000 genomes]
rs6494024	1.00[EUR][1000 genomes]
rs7163948	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7164104	1.00[EUR][1000 genomes]
rs7166901	1.00[EUR][1000 genomes]
rs7167240	1.00[EUR][1000 genomes]
rs7168066	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7172673	1.00[EUR][1000 genomes]
rs7173048	1.00[EUR][1000 genomes]
rs7174279	1.00[EUR][1000 genomes]
rs7175610	1.00[EUR][1000 genomes]
rs7176715	1.00[EUR][1000 genomes]
rs74016920	1.00[EUR][1000 genomes]
rs74016943	1.00[EUR][1000 genomes]
rs74016946	1.00[EUR][1000 genomes]
rs74016947	1.00[EUR][1000 genomes]
rs74017259	1.00[EUR][1000 genomes]
rs74017261	1.00[EUR][1000 genomes]
rs74017264	1.00[EUR][1000 genomes]
rs74017265	1.00[EUR][1000 genomes]
rs74017270	1.00[EUR][1000 genomes]
rs74017281	1.00[EUR][1000 genomes]
rs74017286	1.00[EUR][1000 genomes]
rs74017293	1.00[EUR][1000 genomes]
rs74017296	1.00[EUR][1000 genomes]
rs74017297	1.00[EUR][1000 genomes]
rs74017298	1.00[EUR][1000 genomes]
rs74017300	1.00[EUR][1000 genomes]
rs74017301	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74018920	1.00[EUR][1000 genomes]
rs8025475	1.00[EUR][1000 genomes]
rs8027618	1.00[EUR][1000 genomes]
rs8028872	1.00[EUR][1000 genomes]
rs8029869	0.82[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs8031250	1.00[EUR][1000 genomes]
rs8031412	1.00[EUR][1000 genomes]
rs8032451	1.00[EUR][1000 genomes]
rs8033613	1.00[EUR][1000 genomes]
rs8043275	1.00[EUR][1000 genomes]
rs881117	1.00[EUR][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	nsv1051058	chr15:58519922-59092530	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv542401	chr15:58519922-59092530	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers 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 target site	50 gene(s)	inside rSNPs	diseases
3	esv34110	chr15:58949991-59381634	Weak transcription Bivalent Enhancer Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
4	esv1843037	chr15:59005922-59115159	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
5	esv1826703	chr15:59005922-59213678	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
6	esv1798487	chr15:59027139-59213678	Strong transcription Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
7	nsv428638	chr15:59032300-59126567	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:111 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:58977200-59039200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr15:59022200-59040200	Weak transcription	Fetal Muscle Trunk	muscle
3	chr15:59022600-59038600	Weak transcription	Fetal Brain Female	brain
4	chr15:59023600-59040000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
5	chr15:59024000-59038200	Weak transcription	Fetal Stomach	stomach
6	chr15:59025600-59038200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr15:59025600-59038200	Weak transcription	Gastric	stomach
8	chr15:59025600-59040000	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr15:59026800-59039600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
10	chr15:59027000-59039800	Enhancers	Primary T helper cells fromperipheralblood	blood
11	chr15:59027600-59037800	Weak transcription	Fetal Intestine Small	intestine
12	chr15:59027600-59038000	Weak transcription	Fetal Intestine Large	intestine
13	chr15:59027600-59040200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr15:59030600-59037800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr15:59030800-59037800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr15:59030800-59038200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr15:59030800-59038400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr15:59030800-59039400	Enhancers	Primary T helper cells PMA-I stimulated	--
19	chr15:59031000-59039200	Weak transcription	Duodenum Mucosa	Duodenum
20	chr15:59031200-59037800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr15:59031200-59037800	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr15:59031400-59035800	Enhancers	Monocytes-CD14+_RO01746	blood
23	chr15:59031400-59037800	Weak transcription	Hela-S3	cervix
24	chr15:59031400-59037800	Weak transcription	NHEK	skin
25	chr15:59032000-59036000	Weak transcription	Dnd41	blood
26	chr15:59032200-59036800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
27	chr15:59032200-59038400	Weak transcription	Aorta	Aorta
28	chr15:59032400-59036800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
29	chr15:59032600-59037800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr15:59032600-59038000	Weak transcription	Brain Cingulate Gyrus	brain
31	chr15:59032600-59038400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr15:59033000-59038800	Weak transcription	Primary B cells from cord blood	blood
33	chr15:59033200-59037000	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr15:59033400-59037200	Enhancers	Brain Substantia Nigra	brain
35	chr15:59033400-59038200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr15:59033400-59039000	Enhancers	Brain Hippocampus Middle	brain
37	chr15:59033600-59035600	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr15:59033600-59036400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr15:59033600-59036600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
40	chr15:59033600-59036800	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr15:59033600-59040000	Enhancers	Primary T helper naive cells from peripheral blood	blood
42	chr15:59033600-59040400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
43	chr15:59033800-59038200	Weak transcription	Pancreatic Islets	Pancreatic Islet
44	chr15:59034000-59035600	Enhancers	Ovary	ovary
45	chr15:59034000-59035600	Enhancers	Right Ventricle	heart
46	chr15:59034000-59035600	Enhancers	NH-A	brain
47	chr15:59034000-59035800	Enhancers	Placenta Amnion	Placenta Amnion
48	chr15:59034000-59035800	Enhancers	HUVEC	blood vessel
49	chr15:59034000-59036200	Enhancers	Liver	Liver
50	chr15:59034000-59036200	Enhancers	NHLF	lung

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