Variant report

Variant	rs3792666
Chromosome Location	chr4:95457089-95457090
allele	C/T
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:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:95456523..95459012-chr4:95469903..95471763,2	MCF-7	breast:
2	chr4:95373908..95375518-chr4:95456117..95457720,2	K562	blood:
3	chr4:95455418..95457640-chr4:95458337..95460219,4	K562	blood:
4	chr4:95373570..95375959-chr4:95453474..95457865,4	K562	blood:
5	chr4:95455231..95457643-chr4:95461903..95464194,2	K562	blood:
6	chr4:95449221..95452678-chr4:95455541..95457733,4	K562	blood:
7	chr4:95455791..95459041-chr4:95471671..95474537,3	K562	blood:
8	chr4:95371767..95374402-chr4:95456594..95458553,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000163110	Chromatin interaction
ENSG00000203436	Chromatin interaction

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10034824	0.86[CHB][hapmap]
rs1032420	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12645971	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13110115	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13122786	0.80[CHB][hapmap]
rs13143502	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13146878	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17394213	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs1972011	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2452008	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2452010	0.92[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2452563	0.84[CEU][hapmap]
rs2452569	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2452570	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2452571	0.96[CEU][hapmap];0.95[CHB][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2452572	0.89[ASN][1000 genomes]
rs2452574	0.92[CEU][hapmap];1.00[CHB][hapmap];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2452575	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2452576	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2452577	0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs2452580	0.96[CEU][hapmap];0.89[CHB][hapmap];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2452582	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2452584	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2452585	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2452586	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2452589	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2510768	0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2510769	0.81[CEU][hapmap];0.84[CHB][hapmap];0.85[JPT][hapmap];0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2510772	0.84[CEU][hapmap];0.89[CHB][hapmap];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2510774	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2510775	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2510776	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2510777	0.96[CEU][hapmap];0.95[CHB][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2510779	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2510780	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2510781	0.92[CEU][hapmap];1.00[CHB][hapmap];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2510793	0.84[CEU][hapmap]
rs3805285	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4699505	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs766520	0.80[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv993495	chr4:94992315-95482578	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv594901	chr4:95254730-95493246	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv1003743	chr4:95255957-95469831	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:95422400-95482800	Weak transcription	Fetal Muscle Trunk	muscle
2	chr4:95442000-95469600	Weak transcription	Primary T cells from cord blood	blood
3	chr4:95447800-95457200	Weak transcription	NHLF	lung
4	chr4:95449200-95470200	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr4:95449400-95457200	Enhancers	Fetal Heart	heart
6	chr4:95449800-95460400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr4:95450400-95465800	Weak transcription	Lung	lung
8	chr4:95450600-95459600	Weak transcription	Brain Angular Gyrus	brain
9	chr4:95452400-95457600	Genic enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr4:95452600-95458000	Enhancers	HUVEC	blood vessel
11	chr4:95453800-95459400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr4:95453800-95459600	Weak transcription	NHDF-Ad	bronchial
13	chr4:95453800-95460400	Enhancers	Skeletal Muscle Male	skeletal muscle
14	chr4:95453800-95465400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr4:95454000-95457200	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr4:95454200-95458400	Enhancers	Fetal Intestine Large	intestine
17	chr4:95454400-95458200	Enhancers	Fetal Intestine Small	intestine
18	chr4:95454400-95458400	Enhancers	Placenta Amnion	Placenta Amnion
19	chr4:95454400-95459000	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr4:95454600-95457200	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr4:95454600-95457400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr4:95454600-95457400	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr4:95454600-95457400	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr4:95454600-95458400	Enhancers	Liver	Liver
25	chr4:95454600-95458400	Enhancers	Rectal Smooth Muscle	rectum
26	chr4:95454600-95460200	Enhancers	Colon Smooth Muscle	Colon
27	chr4:95454600-95462600	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr4:95454800-95457600	Enhancers	Primary hematopoietic stem cells	blood
29	chr4:95454800-95458200	Enhancers	Placenta	Placenta
30	chr4:95455000-95457800	Enhancers	Rectal Mucosa Donor 29	rectum
31	chr4:95455000-95458000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr4:95455000-95459000	Enhancers	Adipose Nuclei	Adipose
33	chr4:95455200-95457200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
34	chr4:95455400-95457200	Weak transcription	Fetal Kidney	kidney
35	chr4:95455400-95458800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr4:95455600-95457400	Enhancers	Fetal Muscle Leg	muscle
37	chr4:95455600-95460000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr4:95455800-95457400	Enhancers	Psoas Muscle	Psoas
39	chr4:95455800-95457600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr4:95455800-95458000	Enhancers	Brain Hippocampus Middle	brain
41	chr4:95455800-95458000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr4:95455800-95460200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr4:95456000-95457400	Enhancers	Aorta	Aorta
44	chr4:95456000-95457400	Enhancers	Pancreas	Pancrea
45	chr4:95456000-95458000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr4:95456000-95459600	Enhancers	H1 Cell Line	embryonic stem cell
47	chr4:95456200-95457400	Enhancers	H9 Cell Line	embryonic stem cell
48	chr4:95456200-95457400	Enhancers	Brain Anterior Caudate	brain
49	chr4:95456200-95457400	Enhancers	Right Atrium	heart
50	chr4:95456200-95457800	Enhancers	Brain Substantia Nigra	brain

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