Variant report

Variant	rs9358050
Chromosome Location	chr6:15089607-15089608
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:15085986..15094450-chr6:15243173..15249347,32	MCF-7	breast:
2	chr6:15088454..15091086-chr6:32937354..32938883,2	MCF-7	breast:
3	chr6:15088518..15090840-chr6:15243708..15248817,8	MCF-7	breast:
4	chr6:15060990..15063217-chr6:15088088..15090210,2	MCF-7	breast:
5	chr6:15087697..15090095-chr6:15243505..15246959,6	K562	blood:
6	chr6:15087697..15092455-chr6:15243972..15249952,11	K562	blood:
7	chr6:14725985..14728380-chr6:15088035..15090181,2	K562	blood:
8	chr6:15087836..15090279-chr6:15247303..15249952,4	K562	blood:
9	chr10:5507144..5509626-chr6:15088279..15090071,2	MCF-7	breast:
10	chr6:15088011..15090050-chr6:15218799..15221115,2	MCF-7	breast:
11	chr6:15088400..15090087-chr6:15163313..15165658,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000271888	Chromatin interaction
ENSG00000235488	Chromatin interaction
ENSG00000204256	Chromatin interaction
ENSG00000223837	Chromatin interaction
ENSG00000008083	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs13191059	0.90[ASN][1000 genomes]
rs13210483	0.91[ASN][1000 genomes]
rs16876061	0.91[CEU][hapmap];0.94[CHB][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35957683	0.86[ASN][1000 genomes]
rs4715965	0.91[ASN][1000 genomes]
rs6906466	0.93[CHB][hapmap];0.94[JPT][hapmap];0.96[ASN][1000 genomes]
rs6928159	0.91[CEU][hapmap];0.94[CHB][hapmap];0.94[JPT][hapmap];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6928936	0.91[CEU][hapmap];0.94[CHB][hapmap];0.94[JPT][hapmap];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6936729	0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72832873	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72832876	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72832881	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72832884	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72832887	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72832890	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72832892	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7756288	0.91[ASN][1000 genomes]
rs7767571	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9349965	0.91[CEU][hapmap];0.94[CHB][hapmap];0.91[CHD][hapmap];0.94[JPT][hapmap];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9367859	0.95[ASN][1000 genomes]
rs9367860	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9370791	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9383017	0.92[EUR][1000 genomes]
rs9383020	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9383022	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9383023	0.82[CHB][hapmap];0.82[CHD][hapmap];0.88[JPT][hapmap];0.85[ASN][1000 genomes]
rs9383024	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9383025	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9396553	0.91[CEU][hapmap];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9396554	0.91[CEU][hapmap];0.92[EUR][1000 genomes]
rs9396555	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9396556	0.90[CEU][hapmap];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9396557	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9396558	0.89[ASN][1000 genomes]
rs9800553	0.91[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830593	chr6:15049636-15244190	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15077000-15090000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr6:15083800-15093000	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr6:15087200-15091600	Enhancers	Placenta	Placenta
4	chr6:15087400-15090000	Weak transcription	Primary B cells from cord blood	blood
5	chr6:15087400-15117600	Weak transcription	Right Atrium	heart
6	chr6:15087600-15090200	Weak transcription	Fetal Thymus	thymus
7	chr6:15087800-15090000	Weak transcription	Primary hematopoietic stem cells	blood
8	chr6:15087800-15090000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr6:15088200-15089800	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr6:15088400-15089800	Active TSS	K562	blood
11	chr6:15088800-15090000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr6:15089000-15091800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr6:15089200-15090000	Enhancers	Fetal Stomach	stomach
14	chr6:15089200-15091000	Enhancers	NHEK	skin
15	chr6:15089400-15089800	Flanking Active TSS	Fetal Kidney	kidney
16	chr6:15089400-15090400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr6:15089400-15090800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr6:15089400-15090800	Enhancers	Placenta Amnion	Placenta Amnion
19	chr6:15089400-15091000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr6:15089400-15091000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr6:15089400-15091000	Enhancers	Stomach Mucosa	stomach
22	chr6:15089400-15091200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr6:15089400-15091400	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr6:15089600-15090000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr6:15089600-15090000	Enhancers	Duodenum Mucosa	Duodenum
26	chr6:15089600-15090200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
27	chr6:15089600-15090200	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr6:15089600-15090200	Enhancers	Esophagus	oesophagus
29	chr6:15089600-15090200	Enhancers	Gastric	stomach
30	chr6:15089600-15090400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr6:15089600-15091000	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr6:15089600-15091800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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