Variant report

Variant	rs4869626
Chromosome Location	chr5:36205998-36205999
allele	A/C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:36203656..36205206-chr5:36205240..36207135,2	MCF-7	breast:
2	chr5:36202913..36206774-chr5:36238619..36242174,4	K562	blood:
3	chr5:36205557..36207840-chr5:36241465..36243259,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000152620	Chromatin interaction

Extended variants
information (count: 75 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs10051604	0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10079844	0.91[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs10079850	0.91[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs10080095	0.88[ASN][1000 genomes]
rs10214173	0.88[ASN][1000 genomes]
rs10223062	0.88[ASN][1000 genomes]
rs1035480	0.88[ASN][1000 genomes]
rs10473001	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10473002	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10512643	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10737962	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10805609	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10805610	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10805611	0.88[ASN][1000 genomes]
rs10805612	0.88[ASN][1000 genomes]
rs11747169	0.88[ASN][1000 genomes]
rs13360059	0.88[ASN][1000 genomes]
rs1345776	0.88[ASN][1000 genomes]
rs1363843	0.88[ASN][1000 genomes]
rs1363844	0.88[ASN][1000 genomes]
rs1364017	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1423223	0.88[ASN][1000 genomes]
rs1423226	0.88[ASN][1000 genomes]
rs152365	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs152366	0.88[AFR][1000 genomes];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1816101	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1862543	0.88[ASN][1000 genomes]
rs1862544	0.88[ASN][1000 genomes]
rs2303163	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2362978	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2362980	0.88[ASN][1000 genomes]
rs27733	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs33663	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34888491	0.88[ASN][1000 genomes]
rs3761974	0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3849786	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3860801	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3906394	0.91[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs41445147	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs430421	0.90[ASN][1000 genomes]
rs4869473	0.88[ASN][1000 genomes]
rs4869474	0.88[ASN][1000 genomes]
rs4869634	0.88[ASN][1000 genomes]
rs4869635	0.87[ASN][1000 genomes]
rs4869636	0.88[ASN][1000 genomes]
rs6451262	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6451263	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6451265	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6451269	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6451270	0.88[ASN][1000 genomes]
rs6863707	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6866745	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6869599	0.88[ASN][1000 genomes]
rs6870255	0.96[ASN][1000 genomes]
rs6873176	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6874389	0.88[ASN][1000 genomes]
rs6881086	0.88[ASN][1000 genomes]
rs6886098	0.88[ASN][1000 genomes]
rs6891120	0.91[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs6892199	0.88[ASN][1000 genomes]
rs6893107	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6895423	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6898215	0.87[ASN][1000 genomes]
rs7705209	0.88[ASN][1000 genomes]
rs7705396	0.91[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7705858	0.88[ASN][1000 genomes]
rs7705985	0.88[ASN][1000 genomes]
rs7715317	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7720779	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7722251	0.88[ASN][1000 genomes]
rs7724057	0.88[ASN][1000 genomes]
rs878607	0.88[ASN][1000 genomes]
rs991032	0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830262	chr5:36074311-36293872	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers 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 miRNA	63 gene(s)	inside rSNPs	diseases
2	nsv1015638	chr5:36203646-36312576	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:36154400-36210800	Weak transcription	Small Intestine	intestine
2	chr5:36164800-36220800	Weak transcription	Gastric	stomach
3	chr5:36171800-36220600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr5:36172000-36229200	Weak transcription	Colonic Mucosa	Colon
5	chr5:36175200-36220800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr5:36175600-36222400	Weak transcription	Rectal Smooth Muscle	rectum
7	chr5:36179000-36222800	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr5:36179000-36230000	Weak transcription	Psoas Muscle	Psoas
9	chr5:36179200-36210400	Weak transcription	Fetal Kidney	kidney
10	chr5:36179200-36212600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr5:36181400-36212800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr5:36182200-36214800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr5:36182800-36220400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr5:36182800-36220600	Weak transcription	Brain Angular Gyrus	brain
15	chr5:36190000-36220800	Weak transcription	Spleen	Spleen
16	chr5:36190200-36207400	Strong transcription	Dnd41	blood
17	chr5:36190200-36220800	Weak transcription	Esophagus	oesophagus
18	chr5:36190400-36220800	Weak transcription	Lung	lung
19	chr5:36190600-36211000	Weak transcription	Fetal Stomach	stomach
20	chr5:36190600-36227400	Weak transcription	Thymus	Thymus
21	chr5:36190800-36206200	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr5:36190800-36211000	Weak transcription	Fetal Intestine Small	intestine
23	chr5:36191800-36220600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr5:36191800-36230000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr5:36192000-36206000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr5:36192000-36224200	Weak transcription	Aorta	Aorta
27	chr5:36192600-36227800	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr5:36193600-36220800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr5:36193600-36220800	Weak transcription	Pancreas	Pancrea
30	chr5:36194000-36207400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
31	chr5:36194200-36207800	Weak transcription	Stomach Mucosa	stomach
32	chr5:36196600-36210000	Weak transcription	HSMMtube	muscle
33	chr5:36196600-36236600	Weak transcription	GM12878-XiMat	blood
34	chr5:36197000-36212400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr5:36197800-36220800	Weak transcription	Placenta Amnion	Placenta Amnion
36	chr5:36197800-36224800	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr5:36198000-36238400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
38	chr5:36198200-36214800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr5:36199600-36207400	Strong transcription	Primary T cells from cord blood	blood
40	chr5:36200000-36229600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
41	chr5:36200200-36220800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr5:36200200-36239400	Weak transcription	Fetal Brain Male	brain
43	chr5:36200400-36214800	Weak transcription	Skeletal Muscle Male	skeletal muscle
44	chr5:36201000-36214600	Weak transcription	HMEC	breast
45	chr5:36201200-36209000	Weak transcription	Duodenum Smooth Muscle	Duodenum
46	chr5:36201200-36210000	Weak transcription	NHEK	skin
47	chr5:36201200-36210200	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr5:36201200-36212400	Weak transcription	K562	blood
49	chr5:36201200-36212800	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr5:36201200-36214800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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