Variant report

Variant	rs905162
Chromosome Location	chr5:75878994-75878995
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:75878372..75880301-chr5:75883948..75885454,2	K562	blood:
2	chr5:75633485..75634409-chr5:75878986..75879511,2	K562	blood:
3	chr5:75699529..75700200-chr5:75878922..75879530,2	K562	blood:

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10041515	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10044688	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10051729	0.83[AMR][1000 genomes]
rs10065424	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10073592	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10080190	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10474482	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10942784	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13355881	0.81[AMR][1000 genomes]
rs1501690	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2134190	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2173926	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2202114	0.80[EUR][1000 genomes]
rs2840106	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs3776768	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3797380	0.85[ASN][1000 genomes]
rs4704326	0.81[AMR][1000 genomes]
rs4704330	0.84[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs4704332	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4704333	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4704336	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6453231	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6453232	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6869692	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6889411	0.86[ASN][1000 genomes]
rs7735600	0.80[EUR][1000 genomes]
rs905163	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs905164	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9293687	0.83[EUR][1000 genomes]
rs9654416	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022032	chr5:75785106-75914003	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv598679	chr5:75823965-75914729	Flanking Active TSS Weak transcription Genic enhancers Enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1023953	chr5:75831037-75913784	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1026257	chr5:75831037-75914003	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1016823	chr5:75831037-75915905	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1019669	chr5:75836365-76477788	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
7	nsv598680	chr5:75839165-75914729	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv598681	chr5:75863987-75902533	Enhancers Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:64 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:75843800-75884400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr5:75846800-75902600	Weak transcription	Rectal Smooth Muscle	rectum
3	chr5:75851800-75892000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr5:75853200-75896400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr5:75861200-75889600	Weak transcription	Fetal Stomach	stomach
6	chr5:75862200-75885400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr5:75862800-75880200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr5:75865400-75885800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr5:75867800-75886000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr5:75868000-75884400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr5:75868000-75885200	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr5:75868000-75885400	Weak transcription	Primary T cells from cord blood	blood
13	chr5:75873600-75903600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr5:75874000-75892400	Weak transcription	Spleen	Spleen
15	chr5:75874200-75882000	Weak transcription	Esophagus	oesophagus
16	chr5:75875000-75879200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr5:75875200-75884000	Weak transcription	Primary T helper cells fromperipheralblood	blood
18	chr5:75876400-75879400	Enhancers	Liver	Liver
19	chr5:75876600-75879200	Enhancers	Primary T helper cells PMA-I stimulated	--
20	chr5:75876600-75879200	Enhancers	Fetal Intestine Large	intestine
21	chr5:75876600-75879200	Enhancers	Fetal Intestine Small	intestine
22	chr5:75876600-75879200	Enhancers	Rectal Mucosa Donor 31	rectum
23	chr5:75876600-75879600	Enhancers	Duodenum Mucosa	Duodenum
24	chr5:75877000-75879200	Genic enhancers	Primary hematopoietic stem cells	blood
25	chr5:75877000-75879200	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr5:75877000-75879200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
27	chr5:75877000-75880200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
28	chr5:75877000-75885200	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr5:75877000-75902800	Weak transcription	Adipose Nuclei	Adipose
30	chr5:75877200-75879400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr5:75877200-75880200	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr5:75877400-75880200	Weak transcription	Gastric	stomach
33	chr5:75877400-75902800	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr5:75877600-75879200	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr5:75877800-75879000	Flanking Active TSS	GM12878-XiMat	blood
36	chr5:75877800-75879000	Enhancers	NH-A	brain
37	chr5:75877800-75879200	Enhancers	Primary B cells from peripheral blood	blood
38	chr5:75877800-75879400	Enhancers	K562	blood
39	chr5:75878000-75879200	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr5:75878200-75879000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr5:75878200-75879200	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr5:75878200-75879200	Enhancers	Primary B cells from cord blood	blood
43	chr5:75878200-75879400	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr5:75878200-75879400	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr5:75878200-75879600	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr5:75878400-75879000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr5:75878400-75879000	Enhancers	Small Intestine	intestine
48	chr5:75878400-75879200	Enhancers	H9 Cell Line	embryonic stem cell
49	chr5:75878400-75879200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
50	chr5:75878400-75879200	Enhancers	Fetal Lung	lung

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