Variant report

Variant	rs38014
Chromosome Location	chr7:8044268-8044269
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:8006704..8009086-chr7:8043010..8045321,2	MCF-7	breast:
2	chr7:8043881..8046196-chr7:8058398..8061346,2	MCF-7	breast:
3	chr7:8009265..8011101-chr7:8042338..8044850,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000233108	Chromatin interaction
ENSG00000106415	Chromatin interaction

Extended variants
information (count: 72 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs10215645	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10226050	1.00[CEU][hapmap];0.81[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10228900	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10229643	1.00[CEU][hapmap];0.95[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10231036	0.96[CEU][hapmap];0.95[CHB][hapmap];0.93[JPT][hapmap];0.88[AMR][1000 genomes]
rs10241457	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10243846	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10246564	0.82[CEU][hapmap]
rs10247928	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10248588	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10258788	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10273241	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10486205	1.00[CEU][hapmap];0.86[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11976862	0.83[YRI][hapmap]
rs11984078	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12702692	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12702693	0.91[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17568389	0.90[CHB][hapmap];0.93[JPT][hapmap];0.97[YRI][hapmap];0.85[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs2079853	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2109382	0.93[CEU][hapmap];0.90[YRI][hapmap];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2191321	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2348774	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs258853	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28488572	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs28670736	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3735457	0.82[CEU][hapmap];0.87[YRI][hapmap]
rs37974	0.90[YRI][hapmap]
rs37975	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs37977	1.00[CEU][hapmap];0.90[YRI][hapmap];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs37978	0.87[EUR][1000 genomes]
rs37981	1.00[CEU][hapmap];0.92[JPT][hapmap];0.86[YRI][hapmap];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs37983	0.88[EUR][1000 genomes]
rs37988	1.00[CEU][hapmap];0.81[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.98[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs37992	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs37994	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs37995	1.00[CEU][hapmap];0.85[CHB][hapmap];0.92[JPT][hapmap];0.96[YRI][hapmap];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs37997	0.86[YRI][hapmap]
rs37998	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs37999	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs38001	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs38002	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs38003	0.92[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs38004	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs38006	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs38010	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs38011	1.00[CEU][hapmap];0.95[CHB][hapmap];0.93[JPT][hapmap];0.93[YRI][hapmap];0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs38012	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs38013	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs38016	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs38017	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs38018	1.00[CEU][hapmap];0.90[CHB][hapmap];0.92[JPT][hapmap];0.96[YRI][hapmap];0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs38019	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs38021	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs38022	1.00[CEU][hapmap];0.95[CHB][hapmap];0.93[JPT][hapmap];0.97[YRI][hapmap];0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs38023	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4140809	0.83[YRI][hapmap]
rs4236406	0.93[YRI][hapmap];0.81[AMR][1000 genomes]
rs4720761	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4725057	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4725060	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4725065	1.00[JPT][hapmap]
rs4725068	0.86[YRI][hapmap]
rs62433404	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7785493	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9692283	0.93[CEU][hapmap];0.85[CHB][hapmap];0.93[JPT][hapmap];0.88[YRI][hapmap];0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][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	nsv1026758	chr7:7187491-8075259	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
2	esv2752177	chr7:7729247-8177689	Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv917172	chr7:7854632-8807385	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
4	nsv1030180	chr7:7860424-8059221	Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
5	esv3346837	chr7:7915187-8068557	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
6	nsv1020161	chr7:7929384-8047553	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
7	esv1796855	chr7:8042555-8047169	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs38014	GLCCI1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:8015000-8045000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr7:8029800-8046400	Weak transcription	Brain Cingulate Gyrus	brain
3	chr7:8029800-8049000	Weak transcription	Fetal Heart	heart
4	chr7:8035200-8045000	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr7:8036400-8044400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr7:8036400-8044400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr7:8036400-8045000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr7:8036400-8046600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr7:8036400-8077400	Weak transcription	Right Ventricle	heart
10	chr7:8036600-8044600	Weak transcription	Osteobl	bone
11	chr7:8036600-8045600	Weak transcription	Liver	Liver
12	chr7:8036600-8045600	Weak transcription	Stomach Smooth Muscle	stomach
13	chr7:8036600-8045800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr7:8036600-8045800	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr7:8036600-8053800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
16	chr7:8036600-8057200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr7:8036600-8064400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr7:8036600-8064400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr7:8036600-8074600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr7:8036800-8046400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr7:8038000-8066000	Weak transcription	Pancreas	Pancrea
22	chr7:8038200-8045800	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr7:8038400-8046400	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr7:8038400-8066000	Weak transcription	Spleen	Spleen
25	chr7:8039200-8044400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
26	chr7:8039400-8045200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr7:8039400-8046400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr7:8039400-8046400	Weak transcription	Left Ventricle	heart
29	chr7:8039400-8046400	Weak transcription	Ovary	ovary
30	chr7:8040000-8046400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr7:8041000-8045400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr7:8041000-8045800	Weak transcription	Fetal Kidney	kidney
33	chr7:8041200-8046400	Weak transcription	Duodenum Mucosa	Duodenum
34	chr7:8041400-8044400	Weak transcription	Placenta	Placenta
35	chr7:8041600-8044400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr7:8041600-8044400	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr7:8041600-8046400	Weak transcription	Rectal Smooth Muscle	rectum
38	chr7:8041600-8053800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
39	chr7:8041600-8064400	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr7:8041600-8095000	Weak transcription	Gastric	stomach
41	chr7:8041800-8044400	Weak transcription	Fetal Intestine Large	intestine
42	chr7:8041800-8075400	Weak transcription	Brain Hippocampus Middle	brain
43	chr7:8042200-8045600	Weak transcription	Brain Germinal Matrix	brain
44	chr7:8042200-8045800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr7:8042400-8046400	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr7:8042600-8045600	Weak transcription	Primary T cells from cord blood	blood
47	chr7:8042600-8045600	Weak transcription	Fetal Muscle Trunk	muscle
48	chr7:8042800-8044400	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr7:8042800-8046800	Strong transcription	Primary hematopoietic stem cells	blood
50	chr7:8042800-8047200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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