Variant report

Variant	rs536650013
Chromosome Location	chr10:978610-978611
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:12)
CpG islands
(count:0)
Chromatin interactive
region (count:13)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:12 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr10:976657-978728	A549	lung:	n/a	n/a
2	HEY1	chr10:977885-978648	HepG2	liver:	n/a	chr10:977945-977960
3	POLR2A	chr10:977299-979229	K562	blood:	n/a	n/a
4	POLR2A	chr10:978594-978638	H1-hESC	embryonic stem cell:	n/a	n/a
5	ZBTB7A	chr10:978585-978699	K562	blood:	n/a	n/a
6	POLR2A	chr10:977222-978687	A549	lung:	n/a	n/a
7	POLR2A	chr10:978608-978619	MCF-7	breast:	n/a	n/a
8	POLR2A	chr10:978476-979217	HepG2	liver:	n/a	n/a
9	POLR2A	chr10:978128-978663	A549	lung:	n/a	n/a
10	POLR2A	chr10:976659-978611	GM12878	blood:	n/a	n/a
11	POLR2A	chr10:978314-978685	A549	lung:	n/a	n/a
12	POLR2A	chr10:976451-978680	GM12878	blood:	n/a	n/a

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:975330..979257-chr10:1093215..1097529,5	K562	blood:
2	chr10:976566..978917-chr20:33411823..33413821,2	MCF-7	breast:
3	chr10:977031..978658-chr10:1101205..1103073,2	K562	blood:
4	chr10:976344..979673-chr10:1032747..1036349,14	K562	blood:
5	chr10:975309..980832-chr10:1031626..1035973,12	K562	blood:
6	chr10:975582..978698-chr10:1119494..1122267,3	MCF-7	breast:
7	chr10:974439..980732-chr10:1030011..1038533,28	MCF-7	breast:
8	chr10:976647..980794-chr10:1093154..1097319,8	MCF-7	breast:
9	chr10:976200..979208-chr10:1093606..1097726,5	MCF-7	breast:
10	chr10:975330..979545-chr10:1093428..1097529,6	K562	blood:
11	chr10:976553..979064-chr17:56707717..56709888,2	MCF-7	breast:
12	chr10:976152..979108-chr10:1085303..1088696,4	MCF-7	breast:
13	chr10:974636..980819-chr10:1029938..1037009,15	MCF-7	breast:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GTPBP4-3	chr10:978420-978683	NONHSAT010879

No data

Variant related genes	Relation type
ENSG00000229869	TF binding region
LARP4B	TF binding region
ENSG00000067064	Chromatin interaction
ENSG00000047056	Chromatin interaction
ENSG00000212195	Chromatin interaction
ENSG00000238924	Chromatin interaction
ENSG00000198646	Chromatin interaction
ENSG00000107937	Chromatin interaction
ENSG00000205740	Chromatin interaction

Extended variants
information (count: 22 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916591	chr10:224406-1088734	Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv540386	chr10:224406-1197416	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats 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	51 gene(s)	inside rSNPs	diseases
3	nsv1054659	chr10:611444-1133578	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
4	nsv466697	chr10:734229-1129527	ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
5	nsv549765	chr10:734229-1129527	Genic enhancers Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription 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	39 gene(s)	inside rSNPs	diseases
6	nsv1043812	chr10:776547-981126	Strong transcription Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
7	nsv540406	chr10:776547-981126	Bivalent Enhancer Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
8	nsv530116	chr10:776548-1401075	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS 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 miRNA target site	41 gene(s)	inside rSNPs	diseases
9	nsv948978	chr10:813426-1019115	Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
10	nsv1052540	chr10:887562-1300134	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS 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	34 gene(s)	inside rSNPs	diseases
11	nsv540407	chr10:887562-1300134	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers 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 target site	34 gene(s)	inside rSNPs	diseases
12	nsv533861	chr10:945438-1382068	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
13	nsv530117	chr10:945438-1729634	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
14	nsv540408	chr10:955835-1260680	Enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
15	nsv825207	chr10:957020-1005451	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
16	nsv817532	chr10:964660-1885945	Bivalent/Poised TSS Enhancers Strong transcription Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
17	nsv825208	chr10:965883-1004836	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
18	esv3381643	chr10:975752-979950	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
19	esv3394984	chr10:976102-979400	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
20	esv3422999	chr10:976377-979825	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
21	esv3370662	chr10:976702-979450	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
22	esv3386200	chr10:978542-978793	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:975200-979200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr10:975600-978800	Active TSS	Psoas Muscle	Psoas
3	chr10:975600-979000	Active TSS	HUES6 Cell Line	embryonic stem cell
4	chr10:976200-978800	Active TSS	Right Ventricle	heart
5	chr10:976200-978800	Active TSS	A549	lung
6	chr10:976200-979000	Active TSS	ES-I3 Cell Line	embryonic stem cell
7	chr10:976200-979000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr10:976200-979000	Active TSS	HSMM	muscle
9	chr10:976400-978800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr10:976400-979000	Active TSS	Muscle Satellite Cultured Cells	--
11	chr10:976400-979200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr10:976600-978800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr10:976600-979000	Active TSS	Skeletal Muscle Female	skeletal muscle
14	chr10:976600-979200	Active TSS	HMEC	breast
15	chr10:976800-978800	Active TSS	Thymus	Thymus
16	chr10:976800-978800	Active TSS	HepG2	liver
17	chr10:977200-978800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr10:977200-978800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr10:978200-978800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr10:978200-978800	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr10:978200-978800	Weak transcription	Colon Smooth Muscle	Colon
22	chr10:978200-978800	Weak transcription	Gastric	stomach
23	chr10:978200-978800	Weak transcription	NHDF-Ad	bronchial
24	chr10:978200-979000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr10:978200-979000	Weak transcription	Adipose Nuclei	Adipose
26	chr10:978200-979000	Weak transcription	Fetal Lung	lung
27	chr10:978200-979000	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr10:978200-979000	Weak transcription	HSMMtube	muscle
29	chr10:978200-979400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr10:978200-980200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr10:978200-980600	Weak transcription	Fetal Kidney	kidney
32	chr10:978200-985000	Weak transcription	Spleen	Spleen
33	chr10:978200-985400	Weak transcription	Brain Angular Gyrus	brain
34	chr10:978400-978800	Enhancers	Primary B cells from cord blood	blood
35	chr10:978400-978800	Enhancers	Primary T cells fromperipheralblood	blood
36	chr10:978400-978800	Weak transcription	Brain Anterior Caudate	brain
37	chr10:978400-978800	Enhancers	Fetal Brain Male	brain
38	chr10:978400-978800	Weak transcription	Fetal Muscle Trunk	muscle
39	chr10:978400-979000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr10:978400-979000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr10:978400-979000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr10:978400-979000	Weak transcription	Skeletal Muscle Male	skeletal muscle
43	chr10:978400-979000	Enhancers	Small Intestine	intestine
44	chr10:978400-979000	Weak transcription	Stomach Smooth Muscle	stomach
45	chr10:978400-979000	Weak transcription	NHEK	skin
46	chr10:978400-979400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr10:978400-979400	Enhancers	Fetal Muscle Leg	muscle
48	chr10:978400-980800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
49	chr10:978400-982200	Weak transcription	Lung	lung
50	chr10:978400-982200	Weak transcription	GM12878-XiMat	blood

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