Variant report

Variant	rs9784938
Chromosome Location	chr7:104706922-104706923
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:104705262..104710596-chr7:104710916..104715928,6	K562	blood:
2	chr7:104706055..104708042-chr7:104708063..104710703,2	K562	blood:
3	chr7:104702912..104705436-chr7:104706409..104709574,3	K562	blood:
4	chr7:104619886..104621956-chr7:104705400..104707760,2	K562	blood:
5	chr7:104650546..104656206-chr7:104695535..104706992,23	K562	blood:
6	chr7:104621807..104625592-chr7:104704805..104708118,3	K562	blood:
7	chr7:104651595..104655365-chr7:104705718..104710034,4	MCF-7	breast:
8	chr7:104647926..104656528-chr7:104691112..104706949,31	K562	blood:
9	chr7:104699830..104702178-chr7:104704805..104707713,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000239569	Chromatin interaction
ENSG00000228393	Chromatin interaction
ENSG00000005483	Chromatin interaction

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs2299302	1.00[AMR][1000 genomes]
rs55931372	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60766560	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73717957	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73717959	1.00[AMR][1000 genomes]
rs73717961	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73717963	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029283	chr7:104571741-104729168	Strong transcription Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	132 gene(s)	inside rSNPs	diseases
2	nsv888927	chr7:104614664-104781644	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
3	nsv608068	chr7:104622402-104757483	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
4	esv1801863	chr7:104699637-104713419	Genic enhancers Enhancers Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:104677800-104758200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr7:104678000-104812200	Strong transcription	Dnd41	blood
3	chr7:104680600-104727000	Strong transcription	Fetal Thymus	thymus
4	chr7:104681200-104758400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr7:104681200-104760400	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr7:104681400-104727000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr7:104685400-104708000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr7:104685600-104708200	Weak transcription	Esophagus	oesophagus
9	chr7:104685600-104709000	Weak transcription	Lung	lung
10	chr7:104685600-104720400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr7:104685600-104759000	Strong transcription	Primary B cells from peripheral blood	blood
12	chr7:104687800-104721200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr7:104688200-104707600	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr7:104688800-104707400	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr7:104689400-104708200	Weak transcription	NHLF	lung
16	chr7:104689800-104708200	Weak transcription	Pancreas	Pancrea
17	chr7:104694000-104711200	Strong transcription	Primary B cells from cord blood	blood
18	chr7:104694400-104708200	Weak transcription	Gastric	stomach
19	chr7:104694600-104708200	Weak transcription	Right Atrium	heart
20	chr7:104694600-104708200	Weak transcription	Spleen	Spleen
21	chr7:104695200-104708800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr7:104697000-104726600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr7:104697400-104708200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr7:104697600-104726600	Strong transcription	HUES64 Cell Line	embryonic stem cell
25	chr7:104699800-104738400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr7:104700800-104726800	Strong transcription	Primary monocytes fromperipheralblood	blood
27	chr7:104701200-104707000	Strong transcription	HSMM	muscle
28	chr7:104701200-104711400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
29	chr7:104701200-104727000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr7:104701400-104758800	Strong transcription	Rectal Mucosa Donor 29	rectum
31	chr7:104701600-104708600	Weak transcription	Ovary	ovary
32	chr7:104701600-104726800	Strong transcription	Rectal Mucosa Donor 31	rectum
33	chr7:104701600-104727000	Strong transcription	Primary T cells fromperipheralblood	blood
34	chr7:104701800-104710200	Strong transcription	NHDF-Ad	bronchial
35	chr7:104702000-104707600	Weak transcription	Fetal Heart	heart
36	chr7:104702000-104708000	Weak transcription	HSMMtube	muscle
37	chr7:104702000-104708200	Weak transcription	Right Ventricle	heart
38	chr7:104702000-104709800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr7:104702200-104707000	Weak transcription	Brain Substantia Nigra	brain
40	chr7:104702200-104710600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr7:104702200-104727000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
42	chr7:104702200-104738200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr7:104702200-104747800	Weak transcription	Stomach Mucosa	stomach
44	chr7:104702600-104709000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
45	chr7:104702600-104716400	Weak transcription	Pancreatic Islets	Pancreatic Islet
46	chr7:104702800-104722600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr7:104702800-104758800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr7:104703200-104710800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr7:104703200-104710800	Strong transcription	Adipose Nuclei	Adipose
50	chr7:104703200-104725400	Strong transcription	Muscle Satellite Cultured Cells	--

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