Variant report

Variant	rs10952045
Chromosome Location	chr7:7230388-7230389
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:7227526..7230413-chr7:7241533..7244202,2	K562	blood:
2	chr7:7227727..7230614-chr7:7280890..7283240,2	K562	blood:
3	chr7:7228949..7231828-chr7:7247534..7249931,2	K562	blood:
4	chr7:7220661..7223527-chr7:7229219..7232233,3	MCF-7	breast:
5	chr7:7229626..7232056-chr7:7343354..7345777,2	K562	blood:

Variant related genes	Relation type
ENSG00000106392	Chromatin interaction

Extended variants
information (count: 48 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs1008897	0.86[ASN][1000 genomes]
rs10246303	0.86[ASN][1000 genomes]
rs10246435	0.86[ASN][1000 genomes]
rs10251492	0.86[ASN][1000 genomes]
rs10251505	0.93[ASN][1000 genomes]
rs10253167	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10257662	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10279324	0.86[ASN][1000 genomes]
rs10279376	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10279432	0.86[ASN][1000 genomes]
rs10281784	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1432192	0.82[AMR][1000 genomes]
rs2024122	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2108780	0.86[ASN][1000 genomes]
rs2108790	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2347893	0.86[ASN][1000 genomes]
rs3807862	0.86[ASN][1000 genomes]
rs4141100	0.86[ASN][1000 genomes]
rs4318980	0.89[ASN][1000 genomes]
rs4720727	0.96[ASN][1000 genomes]
rs5010183	0.86[ASN][1000 genomes]
rs6463652	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6463656	0.93[ASN][1000 genomes]
rs6463657	0.93[ASN][1000 genomes]
rs767298	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7788032	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7790219	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs971481	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1015277	chr7:6705439-7303195	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv1023133	chr7:6854098-7516700	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
3	nsv869091	chr7:6927461-7567820	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
4	nsv1020929	chr7:6954959-7232920	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	39 gene(s)	inside rSNPs	diseases
5	nsv949293	chr7:6990891-7711883	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
6	nsv464300	chr7:7040176-7368699	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
7	nsv606033	chr7:7040176-7368699	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
8	nsv1016369	chr7:7053923-7375567	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
9	nsv1023788	chr7:7053923-7407783	Weak transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
10	nsv538720	chr7:7053923-7407783	Enhancers Weak transcription Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
11	nsv1032813	chr7:7053923-7497484	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
12	nsv1030246	chr7:7053923-7569633	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
13	nsv1019498	chr7:7053923-7668373	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
14	nsv538721	chr7:7053923-7668373	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
15	nsv1032974	chr7:7145831-7393218	Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
16	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
17	nsv508445	chr7:7190518-7261098	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
18	esv2758102	chr7:7209911-7493901	Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription 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 target site	33 gene(s)	inside rSNPs	diseases
19	esv2759505	chr7:7209911-7493901	Flanking Active TSS Active TSS Enhancers Strong transcription ZNF genes & repeats Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
20	nsv8041	chr7:7228104-7230462	Weak transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10952045	C1GALT1	cis	Thyroid	GTEx

Chromatin state (count:77 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:7223200-7234000	Weak transcription	Small Intestine	intestine
2	chr7:7223400-7240800	Weak transcription	Esophagus	oesophagus
3	chr7:7223400-7241400	Weak transcription	Pancreas	Pancrea
4	chr7:7223800-7234800	Weak transcription	Right Ventricle	heart
5	chr7:7223800-7240800	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr7:7223800-7241000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr7:7223800-7279600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr7:7224000-7230400	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr7:7224600-7232800	Weak transcription	HUVEC	blood vessel
10	chr7:7225000-7231000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr7:7225000-7243200	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr7:7225200-7233000	Weak transcription	Thymus	Thymus
13	chr7:7225200-7233200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr7:7225200-7241000	Weak transcription	HMEC	breast
15	chr7:7225200-7241200	Weak transcription	Hela-S3	cervix
16	chr7:7225400-7230800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr7:7225400-7233600	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr7:7225600-7232000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr7:7225800-7233000	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr7:7225800-7233000	Weak transcription	Psoas Muscle	Psoas
21	chr7:7226000-7240800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr7:7226200-7230600	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr7:7226200-7235200	Weak transcription	Brain Substantia Nigra	brain
24	chr7:7226400-7231800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr7:7226400-7232600	Weak transcription	Primary hematopoietic stem cells	blood
26	chr7:7226600-7231600	Weak transcription	Fetal Brain Male	brain
27	chr7:7226600-7232000	Weak transcription	Dnd41	blood
28	chr7:7226800-7232800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
29	chr7:7226800-7233800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr7:7227400-7241000	Weak transcription	Fetal Thymus	thymus
31	chr7:7227600-7230600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr7:7227800-7231000	Weak transcription	NHEK	skin
33	chr7:7228000-7232600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr7:7228000-7233600	Weak transcription	Primary B cells from cord blood	blood
35	chr7:7228000-7240800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr7:7228000-7241200	Weak transcription	Duodenum Mucosa	Duodenum
37	chr7:7228800-7233200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr7:7229200-7233600	Weak transcription	Stomach Mucosa	stomach
39	chr7:7229600-7232200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
40	chr7:7229800-7231000	Enhancers	Primary neutrophils fromperipheralblood	blood
41	chr7:7229800-7231200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr7:7229800-7231800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
43	chr7:7230000-7230400	Weak transcription	K562	blood
44	chr7:7230000-7230600	Weak transcription	Primary B cells from peripheral blood	blood
45	chr7:7230000-7230800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr7:7230000-7230800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
47	chr7:7230000-7231000	Weak transcription	Primary T cells fromperipheralblood	blood
48	chr7:7230000-7231200	Weak transcription	Primary T helper cells PMA-I stimulated	--
49	chr7:7230000-7232200	Weak transcription	Primary T helper cells fromperipheralblood	blood
50	chr7:7230000-7232200	Weak transcription	Brain Cingulate Gyrus	brain

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