Variant report

Variant	rs4428582
Chromosome Location	chr7:7196424-7196425
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	FOXA1	chr7:7196240-7196748	HepG2	liver:	n/a	n/a
2	FOXA1	chr7:7196215-7196911	HepG2	liver:	n/a	n/a
3	FOXA1	chr7:7196223-7196709	HepG2	liver:	n/a	n/a
4	FOXA1	chr7:7196312-7196713	HepG2	liver:	n/a	n/a
5	NR2F2	chr7:7196167-7196835	HepG2	liver:	n/a	n/a
6	USF1	chr7:7196369-7196584	HepG2	liver:	n/a	chr7:7196501-7196512
7	USF1	chr7:7196373-7196593	HepG2	liver:	n/a	chr7:7196501-7196512
8	FOXA2	chr7:7196310-7196705	HepG2	liver:	n/a	n/a
9	EP300	chr7:7196213-7196782	HepG2	liver:	n/a	n/a

Variant related genes	Relation type
C1GALT1	TF binding region

Extended variants
information (count: 56 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs12530890	0.89[ASN][1000 genomes]
rs12531397	0.88[ASN][1000 genomes]
rs12539981	0.85[ASN][1000 genomes]
rs13238772	0.85[EUR][1000 genomes]
rs17164011	0.87[EUR][1000 genomes]
rs17249770	0.93[EUR][1000 genomes]
rs17250084	0.94[EUR][1000 genomes]
rs17309555	0.87[EUR][1000 genomes]
rs2116533	0.94[EUR][1000 genomes]
rs2116534	0.93[EUR][1000 genomes]
rs2116535	0.94[EUR][1000 genomes]
rs2163638	0.94[EUR][1000 genomes]
rs2163639	0.87[EUR][1000 genomes]
rs34419200	0.85[EUR][1000 genomes]
rs34491888	0.85[EUR][1000 genomes]
rs34705126	0.85[EUR][1000 genomes]
rs4324853	0.93[EUR][1000 genomes]
rs4582461	0.92[EUR][1000 genomes]
rs57285757	0.87[ASN][1000 genomes]
rs58312319	0.87[EUR][1000 genomes]
rs58843310	0.87[EUR][1000 genomes]
rs62449960	0.86[EUR][1000 genomes]
rs62449964	0.85[EUR][1000 genomes]
rs62449965	0.85[EUR][1000 genomes]
rs62453491	0.93[EUR][1000 genomes]
rs62453504	0.87[EUR][1000 genomes]
rs62453505	0.87[EUR][1000 genomes]
rs62453506	0.87[EUR][1000 genomes]
rs62453507	0.94[EUR][1000 genomes]
rs62453510	0.87[EUR][1000 genomes]
rs62453511	0.87[EUR][1000 genomes]
rs62453512	0.84[EUR][1000 genomes]
rs62453513	0.87[EUR][1000 genomes]
rs9648103	0.85[EUR][1000 genomes]
rs980405	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 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	nsv428160	chr7:6936949-7219553	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
5	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
6	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
7	nsv887469	chr7:7036939-7205749	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
8	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
9	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
10	nsv1015553	chr7:7053923-7201291	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
11	nsv538719	chr7:7053923-7201291	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4428582	C1GALT1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:7189000-7196800	Weak transcription	Duodenum Mucosa	Duodenum
2	chr7:7189200-7199600	Weak transcription	K562	blood
3	chr7:7195200-7196600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
4	chr7:7195200-7196800	Enhancers	Primary T cells fromperipheralblood	blood
5	chr7:7195400-7196800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
6	chr7:7195600-7196600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr7:7195600-7196600	Enhancers	Primary B cells from cord blood	blood
8	chr7:7195600-7196600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr7:7195600-7196600	Enhancers	Muscle Satellite Cultured Cells	--
10	chr7:7195600-7196800	Enhancers	Primary B cells from peripheral blood	blood
11	chr7:7195600-7196800	Enhancers	Primary T helper cells fromperipheralblood	blood
12	chr7:7195600-7196800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
13	chr7:7195600-7196800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr7:7195800-7196800	Enhancers	HMEC	breast
15	chr7:7195800-7197000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr7:7195800-7197000	Enhancers	GM12878-XiMat	blood
17	chr7:7196000-7196800	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr7:7196200-7196600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr7:7196200-7196800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
20	chr7:7196200-7196800	Flanking Active TSS	Dnd41	blood
21	chr7:7196200-7196800	Enhancers	NHDF-Ad	bronchial
22	chr7:7196200-7198200	Flanking Active TSS	Osteobl	bone
23	chr7:7196200-7200200	Flanking Active TSS	Primary T cells from cord blood	blood
24	chr7:7196400-7196600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr7:7196400-7196600	Flanking Active TSS	HSMM	muscle
26	chr7:7196400-7196800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr7:7196400-7196800	Enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr7:7196400-7196800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr7:7196400-7196800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
30	chr7:7196400-7196800	Enhancers	Fetal Thymus	thymus
31	chr7:7196400-7196800	Flanking Active TSS	HSMMtube	muscle
32	chr7:7196400-7196800	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr7:7196400-7196800	Enhancers	NH-A	brain
34	chr7:7196400-7196800	Enhancers	NHLF	lung
35	chr7:7196400-7197000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr7:7196400-7197000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr7:7196400-7197000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
38	chr7:7196400-7197000	Enhancers	Thymus	Thymus
39	chr7:7196400-7197000	Enhancers	NHEK	skin
40	chr7:7196400-7197600	Enhancers	Stomach Mucosa	stomach
41	chr7:7196400-7197800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
42	chr7:7196400-7197800	Flanking Active TSS	HepG2	liver
43	chr7:7196400-7198000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
44	chr7:7196400-7198000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
45	chr7:7196400-7198000	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
46	chr7:7196400-7198000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
47	chr7:7196400-7198000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr7:7196400-7198000	Enhancers	Placenta Amnion	Placenta Amnion
49	chr7:7196400-7198000	Enhancers	Small Intestine	intestine
50	chr7:7196400-7198400	Enhancers	Primary hematopoietic stem cells	blood

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