Variant report

Variant	rs17073596
Chromosome Location	chr6:144621908-144621909
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:144619381..144622236-chr6:144622938..144625711,2	K562	blood:

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs11962764	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12662696	0.87[JPT][hapmap]
rs12662872	0.93[JPT][hapmap];0.81[ASN][1000 genomes]
rs12662914	0.93[JPT][hapmap];0.81[ASN][1000 genomes]
rs12664304	0.87[JPT][hapmap]
rs1322447	0.81[MEX][hapmap]
rs1474630	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.92[TSI][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17073571	0.93[JPT][hapmap]
rs17073578	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.92[TSI][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17073580	0.93[JPT][hapmap]
rs17073598	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs17073602	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs17073610	0.87[JPT][hapmap]
rs17073623	0.87[JPT][hapmap]
rs17073629	0.93[CHB][hapmap];0.93[JPT][hapmap];0.86[ASN][1000 genomes]
rs17073631	0.80[CHB][hapmap];0.93[JPT][hapmap];0.83[ASN][1000 genomes]
rs17073678	0.87[JPT][hapmap]
rs2143009	1.00[CEU][hapmap];0.84[GIH][hapmap];0.87[EUR][1000 genomes]
rs2473133	0.81[MEX][hapmap]
rs2473134	0.81[MEX][hapmap]
rs2473151	0.81[CHB][hapmap]
rs59718967	0.81[ASN][1000 genomes]
rs59803839	0.91[ASN][1000 genomes]
rs60661533	0.88[ASN][1000 genomes]
rs60857439	0.86[ASN][1000 genomes]
rs60859726	1.00[ASN][1000 genomes]
rs6903169	0.87[JPT][hapmap];0.83[ASN][1000 genomes]
rs6911171	0.81[ASN][1000 genomes]
rs6916795	0.93[JPT][hapmap]
rs6919115	0.93[JPT][hapmap]
rs6924797	0.93[JPT][hapmap]
rs6927798	0.87[JPT][hapmap]
rs6941296	0.93[JPT][hapmap];0.82[ASN][1000 genomes]
rs73588920	0.82[ASN][1000 genomes]
rs73589002	0.81[ASN][1000 genomes]
rs73591113	0.81[ASN][1000 genomes]
rs73778598	0.90[EUR][1000 genomes]
rs73780508	0.98[ASN][1000 genomes]
rs73780509	0.95[EUR][1000 genomes]
rs7741466	0.93[CHB][hapmap];0.93[JPT][hapmap];0.91[ASN][1000 genomes]
rs7745998	0.93[JPT][hapmap]
rs7750916	1.00[CEU][hapmap];0.84[GIH][hapmap];1.00[TSI][hapmap];0.97[EUR][1000 genomes]
rs7768531	0.87[JPT][hapmap]
rs9321968	0.80[CHB][hapmap];0.93[JPT][hapmap];0.82[ASN][1000 genomes]
rs9321969	0.80[CHB][hapmap];0.93[JPT][hapmap];0.82[ASN][1000 genomes]
rs9496922	0.98[EUR][1000 genomes]
rs9496925	0.80[CHB][hapmap];0.93[JPT][hapmap];0.82[ASN][1000 genomes]
rs9496928	0.81[ASN][1000 genomes]
rs9496930	0.93[JPT][hapmap]

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	nsv830831	chr6:144501371-144649509	Bivalent/Poised TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv830832	chr6:144572378-144759023	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv2422260	chr6:144574591-144731630	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1031253	chr6:144599055-144883013	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv538461	chr6:144599055-144883013	Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:144608400-144626600	Weak transcription	Spleen	Spleen
2	chr6:144608600-144626800	Weak transcription	Esophagus	oesophagus
3	chr6:144608600-144629800	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr6:144608600-144631400	Weak transcription	Colonic Mucosa	Colon
5	chr6:144609200-144623800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr6:144609200-144623800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr6:144609200-144626800	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr6:144609200-144641600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr6:144609600-144628800	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr6:144609600-144629000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr6:144609600-144629800	Weak transcription	Stomach Smooth Muscle	stomach
12	chr6:144611400-144626800	Weak transcription	Fetal Thymus	thymus
13	chr6:144612400-144624000	Weak transcription	Ovary	ovary
14	chr6:144613800-144626800	Weak transcription	Thymus	Thymus
15	chr6:144615400-144630200	Weak transcription	Hela-S3	cervix
16	chr6:144615800-144623800	Weak transcription	HMEC	breast
17	chr6:144616400-144648000	Weak transcription	NHEK	skin
18	chr6:144617000-144623800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr6:144617200-144629400	Weak transcription	Placenta	Placenta
20	chr6:144617200-144636400	Weak transcription	A549	lung
21	chr6:144617400-144623800	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr6:144617400-144625600	Weak transcription	Fetal Kidney	kidney
23	chr6:144617400-144626800	Weak transcription	Aorta	Aorta
24	chr6:144617400-144628600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr6:144617400-144628800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr6:144617400-144629000	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr6:144617400-144630200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr6:144617400-144632800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr6:144617600-144623800	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr6:144617600-144629000	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr6:144617600-144629800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr6:144617800-144622800	Weak transcription	Fetal Stomach	stomach
33	chr6:144617800-144629800	Weak transcription	Primary neutrophils fromperipheralblood	blood
34	chr6:144618000-144623800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr6:144618000-144626800	Weak transcription	Gastric	stomach
36	chr6:144618000-144626800	Weak transcription	Right Ventricle	heart
37	chr6:144618000-144626800	Weak transcription	NH-A	brain
38	chr6:144618200-144623200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr6:144618200-144628600	Weak transcription	Primary hematopoietic stem cells	blood
40	chr6:144618200-144629400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr6:144618200-144629800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr6:144618200-144630200	Weak transcription	Rectal Smooth Muscle	rectum
43	chr6:144618200-144630200	Weak transcription	HUVEC	blood vessel
44	chr6:144618400-144622400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr6:144618400-144622400	Weak transcription	Fetal Muscle Leg	muscle
46	chr6:144618400-144622800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr6:144618400-144622800	Weak transcription	Left Ventricle	heart
48	chr6:144618400-144622800	Weak transcription	Lung	lung
49	chr6:144618400-144623000	Weak transcription	Fetal Muscle Trunk	muscle
50	chr6:144618400-144623600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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