Variant report

Variant	rs3823652
Chromosome Location	chr7:16805971-16805972
allele	A/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	chr7:16805819..16808162-chr7:16843228..16844918,2	MCF-7	breast:
2	chr7:16791492..16793805-chr7:16805072..16808217,3	K562	blood:
3	chr7:16794915..16798218-chr7:16804001..16806170,3	MCF-7	breast:
4	chr7:16805955..16808414-chr7:16808769..16810759,2	K562	blood:
5	chr7:16685200..16687861-chr7:16804946..16807324,2	K562	blood:
6	chr7:16794764..16798120-chr7:16805812..16808493,3	MCF-7	breast:
7	chr7:16655192..16657272-chr7:16805854..16808580,2	MCF-7	breast:
8	chr7:16800951..16805401-chr7:16805504..16810552,5	K562	blood:

No data

Variant related genes	Relation type
ENSG00000136261	Chromatin interaction
ENSG00000106537	Chromatin interaction
ENSG00000106541	Chromatin interaction
ENSG00000106524	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10233465	0.87[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10238328	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1149519	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs1149522	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1149524	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.80[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1149526	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12530923	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12535558	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12540544	0.87[CEU][hapmap]
rs13232235	0.89[ASN][1000 genomes]
rs13244013	0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1997114	0.83[ASN][1000 genomes]
rs1997115	0.86[ASN][1000 genomes]
rs2085706	0.87[ASN][1000 genomes]
rs2290836	0.91[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2290837	0.91[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34614062	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3779051	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs3807490	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs3807492	0.91[CEU][hapmap];0.89[CHB][hapmap];0.91[JPT][hapmap];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3807493	0.82[CEU][hapmap]
rs3807509	0.84[CHB][hapmap];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4400279	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4721535	0.86[ASN][1000 genomes]
rs4721536	0.85[ASN][1000 genomes]
rs4721538	0.83[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4721539	0.85[CEU][hapmap];0.90[CHB][hapmap];0.91[JPT][hapmap];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs55802535	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62441050	0.99[ASN][1000 genomes]
rs6951449	0.95[CEU][hapmap];0.85[CHB][hapmap];0.91[JPT][hapmap];0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6962578	0.94[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs6975847	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs6980298	0.85[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs706055	0.86[ASN][1000 genomes]
rs73299615	0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs747347	0.87[CEU][hapmap]
rs7781646	0.86[CHB][hapmap];0.91[JPT][hapmap];0.85[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs7808455	0.83[CEU][hapmap]
rs7809197	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs818803	0.85[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs818804	0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1028125	chr7:16529160-16847225	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv1024059	chr7:16639432-16836425	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	35 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:16795000-16806000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:16795000-16810200	Weak transcription	HMEC	breast
3	chr7:16795000-16810400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr7:16795000-16828400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr7:16795200-16810000	Weak transcription	NHEK	skin
6	chr7:16795200-16810600	Weak transcription	Fetal Muscle Leg	muscle
7	chr7:16795400-16813000	Weak transcription	Right Ventricle	heart
8	chr7:16796200-16806400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr7:16796400-16810200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr7:16796600-16810400	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr7:16796600-16816200	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr7:16799000-16807800	Weak transcription	Primary hematopoietic stem cells	blood
13	chr7:16799000-16810400	Weak transcription	K562	blood
14	chr7:16799600-16810000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr7:16799600-16813000	Weak transcription	Stomach Mucosa	stomach
16	chr7:16800600-16825600	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr7:16801400-16810600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr7:16801600-16811200	Weak transcription	Spleen	Spleen
19	chr7:16802200-16810800	Weak transcription	Fetal Heart	heart
20	chr7:16802800-16817800	Weak transcription	Duodenum Mucosa	Duodenum
21	chr7:16803400-16806000	Weak transcription	Gastric	stomach
22	chr7:16803400-16810200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr7:16803600-16818000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr7:16803800-16825600	Weak transcription	Fetal Intestine Small	intestine
25	chr7:16804800-16806000	Weak transcription	Psoas Muscle	Psoas
26	chr7:16805000-16832400	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr7:16805200-16806000	Genic enhancers	Primary B cells from cord blood	blood
28	chr7:16805200-16806000	Weak transcription	Pancreas	Pancrea
29	chr7:16805200-16807200	Weak transcription	Esophagus	oesophagus
30	chr7:16805200-16808000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr7:16805200-16810600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr7:16805200-16813600	Weak transcription	Left Ventricle	heart
33	chr7:16805200-16815600	Weak transcription	Fetal Brain Female	brain
34	chr7:16805200-16815800	Weak transcription	Fetal Intestine Large	intestine
35	chr7:16805400-16806200	Enhancers	HUVEC	blood vessel
36	chr7:16805800-16806200	Enhancers	Fetal Brain Male	brain
37	chr7:16805800-16806200	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr7:16805800-16806400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr7:16805800-16806800	Enhancers	Primary B cells from peripheral blood	blood

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