Variant report

Variant	rs7802552
Chromosome Location	chr7:39614390-39614391
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3)
CpG islands
(count:0)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr7:39614357-39614775	SK-N-SH	brain:	n/a	n/a
2	POLR2A	chr7:39612877-39615191	K562	blood:	n/a	n/a
3	ZNF384	chr7:39614315-39614461	K562	blood:	n/a	n/a

No data

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:39613001..39614812-chr7:39768164..39770870,2	K562	blood:
2	chr7:39604590..39607851-chr7:39609967..39614867,7	K562	blood:
3	chr7:39612446..39614989-chr7:39616627..39618783,2	MCF-7	breast:
4	chr7:39610504..39612853-chr7:39613535..39615540,2	K562	blood:
5	chr7:39609139..39613691-chr7:39613860..39617111,6	K562	blood:

No data

Variant related genes	Relation type
ENSG00000236015	TF binding region
ENSG00000227172	Chromatin interaction
ENSG00000236015	Chromatin interaction
ENSG00000241127	Chromatin interaction

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs17171603	0.80[AFR][1000 genomes]
rs58299139	0.80[AFR][1000 genomes]
rs59071947	0.97[AFR][1000 genomes]
rs6462933	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6948276	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6980317	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73375670	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73375695	0.83[AFR][1000 genomes]
rs73377370	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs73377373	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs7777434	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7785964	0.80[AFR][1000 genomes]
rs7786253	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9768664	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9770659	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1021180	chr7:39424988-39642261	Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv1026951	chr7:39429036-39642261	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv1018430	chr7:39455497-39643569	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv887970	chr7:39587912-39688152	Bivalent Enhancer Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
5	nsv970467	chr7:39605971-39615006	Strong transcription Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:39606600-39616200	Weak transcription	Spleen	Spleen
2	chr7:39606600-39616600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr7:39606600-39616800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr7:39606600-39618600	Weak transcription	Gastric	stomach
5	chr7:39606600-39619800	Weak transcription	Lung	lung
6	chr7:39607000-39616800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr7:39607000-39618800	Weak transcription	Right Ventricle	heart
8	chr7:39607000-39619800	Weak transcription	Ovary	ovary
9	chr7:39607000-39623800	Weak transcription	Pancreas	Pancrea
10	chr7:39607000-39631400	Weak transcription	Aorta	Aorta
11	chr7:39607200-39615600	Weak transcription	Psoas Muscle	Psoas
12	chr7:39607200-39616000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr7:39607200-39617200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr7:39607200-39619200	Weak transcription	Colonic Mucosa	Colon
15	chr7:39607200-39620000	Weak transcription	Rectal Smooth Muscle	rectum
16	chr7:39607200-39620200	Weak transcription	Small Intestine	intestine
17	chr7:39607200-39620200	Weak transcription	Stomach Mucosa	stomach
18	chr7:39607200-39620200	Weak transcription	Thymus	Thymus
19	chr7:39607200-39621000	Weak transcription	Right Atrium	heart
20	chr7:39607200-39623200	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr7:39607200-39628800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
22	chr7:39607200-39629000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr7:39607400-39614600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr7:39607400-39616000	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr7:39607600-39615400	Weak transcription	Fetal Brain Male	brain
26	chr7:39607600-39615600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr7:39607600-39615800	Weak transcription	HSMMtube	muscle
28	chr7:39607600-39618000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
29	chr7:39607600-39618000	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr7:39607600-39619000	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr7:39607600-39620200	Weak transcription	Brain Substantia Nigra	brain
32	chr7:39607600-39620200	Weak transcription	Fetal Heart	heart
33	chr7:39607600-39628600	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr7:39607600-39629400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr7:39607800-39616000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr7:39607800-39623400	Weak transcription	NHEK	skin
37	chr7:39608600-39619000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr7:39608800-39615400	Strong transcription	HUES64 Cell Line	embryonic stem cell
39	chr7:39609000-39614800	Strong transcription	Fetal Intestine Large	intestine
40	chr7:39609000-39616200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr7:39609000-39618400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr7:39609200-39614800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr7:39609200-39615800	Strong transcription	Primary B cells from cord blood	blood
44	chr7:39609200-39616400	Strong transcription	Adipose Nuclei	Adipose
45	chr7:39609400-39619000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
46	chr7:39609600-39620000	Weak transcription	K562	blood
47	chr7:39609800-39620000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
48	chr7:39609800-39622200	Weak transcription	Esophagus	oesophagus
49	chr7:39610000-39614800	Strong transcription	Primary B cells from peripheral blood	blood
50	chr7:39610000-39617000	Strong transcription	Fetal Lung	lung

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