Variant report

Variant	rs7818155
Chromosome Location	chr8:92033167-92033168
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:92017586..92020319-chr8:92031030..92033233,2	K562	blood:
2	chr8:92032234..92033819-chr8:92034186..92035851,2	K562	blood:
3	chr8:92025815..92029280-chr8:92031287..92035096,5	K562	blood:
4	chr8:92031862..92034841-chr8:92087690..92089532,2	K562	blood:
5	chr8:92026033..92029085-chr8:92032219..92035096,5	K562	blood:
6	chr8:92030935..92034138-chr8:92080148..92083540,3	K562	blood:
7	chr8:92029069..92031274-chr8:92031690..92034648,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000253738	Chromatin interaction
ENSG00000155100	Chromatin interaction
ENSG00000253358	Chromatin interaction

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs1003996	0.89[CEU][hapmap];0.82[EUR][1000 genomes]
rs10106570	0.83[AMR][1000 genomes]
rs10108486	0.89[CEU][hapmap];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10112439	0.89[CEU][hapmap];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1011254	0.83[CEU][hapmap]
rs13265644	0.88[CEU][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13276591	1.00[CEU][hapmap];0.94[CHB][hapmap];0.95[JPT][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1386112	0.89[CEU][hapmap]
rs1463921	0.81[CHB][hapmap]
rs1471847	0.81[AMR][1000 genomes]
rs1486465	0.83[CEU][hapmap]
rs1504791	0.81[CHB][hapmap]
rs1504792	0.81[CHB][hapmap]
rs1542666	0.89[CEU][hapmap];0.82[EUR][1000 genomes]
rs16905571	0.94[CEU][hapmap]
rs2054805	1.00[CEU][hapmap];0.88[CHB][hapmap];0.95[JPT][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2129261	0.85[EUR][1000 genomes]
rs2255173	0.85[EUR][1000 genomes]
rs2339289	0.89[CEU][hapmap];0.81[EUR][1000 genomes]
rs2339291	0.89[CEU][hapmap];0.82[EUR][1000 genomes]
rs2631014	0.89[CEU][hapmap]
rs2631017	0.85[EUR][1000 genomes]
rs2631023	0.81[AMR][1000 genomes]
rs2631024	0.86[EUR][1000 genomes]
rs2631025	0.81[AMR][1000 genomes]
rs2677573	0.89[CEU][hapmap];0.83[EUR][1000 genomes]
rs2677580	0.83[EUR][1000 genomes]
rs2740772	0.81[AMR][1000 genomes]
rs2740773	0.81[AMR][1000 genomes]
rs2740774	0.81[AMR][1000 genomes]
rs2740776	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2740784	0.81[AMR][1000 genomes]
rs2740788	0.80[JPT][hapmap]
rs2740792	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2740799	0.83[CEU][hapmap]
rs28404401	0.84[AMR][1000 genomes]
rs28618232	0.84[AMR][1000 genomes]
rs28675099	0.85[AMR][1000 genomes]
rs35972814	0.84[AMR][1000 genomes]
rs4448231	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4529427	0.86[AMR][1000 genomes]
rs4634599	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7005565	0.89[CEU][hapmap];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7018395	0.83[CEU][hapmap];0.83[EUR][1000 genomes]
rs72664410	0.88[AMR][1000 genomes]
rs7818187	0.86[AMR][1000 genomes]
rs7825360	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7828122	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7831333	0.85[AMR][1000 genomes]
rs7832881	0.86[AMR][1000 genomes]
rs7837376	0.86[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1028628	chr8:91680968-92418954	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv539672	chr8:91680968-92418954	Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
3	nsv891185	chr8:91923776-92056288	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	esv2758623	chr8:91974499-92273724	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS 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 miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
5	esv2759629	chr8:91974499-92273724	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
6	esv1851089	chr8:92006663-92038304	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:92003800-92040200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr8:92015800-92052200	Weak transcription	Pancreas	Pancrea
3	chr8:92023600-92045600	Weak transcription	Right Ventricle	heart
4	chr8:92026000-92038400	Weak transcription	Esophagus	oesophagus
5	chr8:92027800-92033400	Strong transcription	Primary neutrophils fromperipheralblood	blood
6	chr8:92028000-92034400	Weak transcription	Small Intestine	intestine
7	chr8:92028000-92035200	Strong transcription	Primary monocytes fromperipheralblood	blood
8	chr8:92028000-92036200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr8:92028000-92038000	Weak transcription	Brain Germinal Matrix	brain
10	chr8:92028000-92038000	Weak transcription	Psoas Muscle	Psoas
11	chr8:92028200-92049200	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr8:92028400-92033600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr8:92029000-92033200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr8:92029000-92033400	Strong transcription	Primary T helper cells PMA-I stimulated	--
15	chr8:92029000-92033400	Strong transcription	NHDF-Ad	bronchial
16	chr8:92029000-92033800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr8:92029000-92034800	Strong transcription	Primary T helper cells fromperipheralblood	blood
18	chr8:92029200-92033400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr8:92029200-92033600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
20	chr8:92029200-92033800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
21	chr8:92029400-92033200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
22	chr8:92029400-92033600	Strong transcription	HUES48 Cell Line	embryonic stem cell
23	chr8:92029400-92034200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr8:92029400-92035000	Strong transcription	Monocytes-CD14+_RO01746	blood
25	chr8:92029400-92049400	Weak transcription	Fetal Brain Male	brain
26	chr8:92029600-92033400	Strong transcription	HUES64 Cell Line	embryonic stem cell
27	chr8:92029600-92033600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr8:92029600-92051000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
29	chr8:92030400-92037800	Weak transcription	Aorta	Aorta
30	chr8:92030800-92033400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr8:92030800-92033800	Weak transcription	NHLF	lung
32	chr8:92030800-92034400	Weak transcription	Rectal Smooth Muscle	rectum
33	chr8:92030800-92035200	Weak transcription	Brain Substantia Nigra	brain
34	chr8:92030800-92035400	Weak transcription	Fetal Kidney	kidney
35	chr8:92030800-92037400	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chr8:92030800-92038000	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr8:92030800-92038200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr8:92030800-92039000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr8:92030800-92039000	Weak transcription	HMEC	breast
40	chr8:92030800-92039200	Weak transcription	HUVEC	blood vessel
41	chr8:92030800-92039400	Weak transcription	HSMMtube	muscle
42	chr8:92030800-92039400	Weak transcription	NHEK	skin
43	chr8:92030800-92040000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr8:92030800-92049400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
45	chr8:92030800-92052400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr8:92030800-92052400	Weak transcription	Lung	lung
47	chr8:92031000-92033600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
48	chr8:92031000-92037600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr8:92031000-92038200	Weak transcription	Duodenum Mucosa	Duodenum
50	chr8:92031000-92038400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood

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