Variant report

Variant	rs8073229
Chromosome Location	chr17:45358844-45358845
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr17:45342094..45343983-chr17:45358070..45360151,2	K562	blood:
2	chr17:45358149..45359670-chr17:45360367..45361975,2	K562	blood:
3	chr17:45352188..45358928-chr17:45361878..45368448,10	K562	blood:

Variant related genes	Relation type
ENSG00000259207	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs11079771	0.87[CHB][hapmap]
rs11867192	0.95[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11867253	0.82[CEU][hapmap];0.81[CHB][hapmap];0.81[TSI][hapmap];0.95[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11868344	0.95[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11868912	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11869835	0.82[CEU][hapmap];0.81[CHB][hapmap];0.81[TSI][hapmap];0.95[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11870252	0.95[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11870781	0.95[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12051795	1.00[JPT][hapmap]
rs13306485	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16941751	0.81[CHB][hapmap]
rs16941771	0.81[CHB][hapmap]
rs16941855	0.82[CEU][hapmap];0.81[CHB][hapmap];0.97[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs16941861	0.82[CEU][hapmap];0.81[CHB][hapmap];0.95[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1878067	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2292700	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.95[MKK][hapmap];0.90[TSI][hapmap];0.94[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2317676	0.82[CEU][hapmap];0.81[CHB][hapmap];0.81[TSI][hapmap];0.95[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs3785870	0.87[CHB][hapmap]
rs3785873	0.82[CEU][hapmap];0.81[CHB][hapmap];0.95[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs55706706	0.95[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs56722403	0.95[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs5919	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.81[TSI][hapmap];0.81[YRI][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73322309	0.95[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs8064871	0.93[ASN][1000 genomes]
rs8073179	0.86[ASN][1000 genomes]
rs8077238	0.90[ASN][1000 genomes]
rs8077375	0.88[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1062983	chr17:45030095-45789543	Strong transcription Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45350600-45359400	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr17:45351600-45359000	Enhancers	Skeletal Muscle Male	skeletal muscle
3	chr17:45351800-45359200	Enhancers	Primary B cells from peripheral blood	blood
4	chr17:45352400-45359200	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr17:45354600-45359000	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr17:45354600-45372000	Weak transcription	Esophagus	oesophagus
7	chr17:45355600-45359200	Enhancers	Placenta	Placenta
8	chr17:45356000-45359200	Enhancers	HMEC	breast
9	chr17:45356200-45362000	Weak transcription	Liver	Liver
10	chr17:45356800-45359000	Enhancers	K562	blood
11	chr17:45356800-45359800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr17:45356800-45377200	Weak transcription	Fetal Intestine Large	intestine
13	chr17:45357200-45359000	Enhancers	Muscle Satellite Cultured Cells	--
14	chr17:45357200-45359800	Weak transcription	HUVEC	blood vessel
15	chr17:45357200-45363800	Weak transcription	Fetal Heart	heart
16	chr17:45357200-45371600	Weak transcription	Right Ventricle	heart
17	chr17:45357200-45398000	Weak transcription	Psoas Muscle	Psoas
18	chr17:45357400-45359000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr17:45357600-45359000	Enhancers	Osteobl	bone
20	chr17:45357600-45359200	Enhancers	GM12878-XiMat	blood
21	chr17:45357600-45360600	Weak transcription	Fetal Stomach	stomach
22	chr17:45357800-45359000	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr17:45357800-45359200	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr17:45357800-45360400	Weak transcription	Aorta	Aorta
25	chr17:45357800-45365800	Weak transcription	Ovary	ovary
26	chr17:45357800-45365800	Weak transcription	HSMMtube	muscle
27	chr17:45357800-45369400	Weak transcription	Fetal Intestine Small	intestine
28	chr17:45358000-45359000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr17:45358000-45359800	Weak transcription	Fetal Muscle Trunk	muscle
30	chr17:45358000-45361400	Weak transcription	Stomach Smooth Muscle	stomach
31	chr17:45358200-45359000	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr17:45358200-45360800	Weak transcription	Fetal Muscle Leg	muscle
33	chr17:45358200-45362000	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr17:45358200-45363600	Weak transcription	Spleen	Spleen
35	chr17:45358200-45363800	Weak transcription	Skeletal Muscle Female	skeletal muscle
36	chr17:45358200-45364000	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr17:45358200-45365000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr17:45358200-45366000	Weak transcription	Right Atrium	heart
39	chr17:45358200-45367600	Weak transcription	Adipose Nuclei	Adipose
40	chr17:45358200-45371800	Weak transcription	Colonic Mucosa	Colon
41	chr17:45358200-45377200	Weak transcription	Rectal Mucosa Donor 29	rectum
42	chr17:45358400-45362400	Weak transcription	Rectal Smooth Muscle	rectum
43	chr17:45358400-45363600	Weak transcription	HSMM	muscle
44	chr17:45358400-45365800	Weak transcription	NH-A	brain
45	chr17:45358400-45366000	Weak transcription	Duodenum Mucosa	Duodenum
46	chr17:45358600-45360400	Weak transcription	Colon Smooth Muscle	Colon
47	chr17:45358600-45364000	Weak transcription	Cortex derived primary cultured neurospheres	brain
48	chr17:45358600-45371000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr17:45358800-45359000	Enhancers	Left Ventricle	heart
50	chr17:45358800-45359000	Enhancers	Rectal Mucosa Donor 31	rectum

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