Variant report

Variant	rs73039135
Chromosome Location	chr6:167489806-167489807
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:167487932..167489942-chr6:167492963..167495055,2	K562	blood:

Extended variants
information (count: 140 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:119)

rs_ID	r²[population]
rs16899770	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs16899771	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs16899777	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs16899781	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs16899788	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs16899799	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs16899801	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs16899811	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs16899812	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs16899821	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs16899825	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs16899828	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs16899831	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs16899833	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs16899835	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs16899837	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17856382	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs34585172	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs3752519	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs3798308	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs3798309	1.00[AMR][1000 genomes]
rs3798310	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs3798311	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs3798312	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs3798313	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs3822914	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs41269603	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs41269605	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs41269607	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs56028052	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs56266102	1.00[AMR][1000 genomes]
rs61751042	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs6922071	0.81[ASN][1000 genomes]
rs6941099	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73023509	1.00[AMR][1000 genomes]
rs73023517	1.00[AMR][1000 genomes]
rs73024229	1.00[AMR][1000 genomes]
rs73024302	1.00[AMR][1000 genomes]
rs73026203	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73026206	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73026210	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73026212	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73026214	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73026216	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73026224	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73026225	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73026226	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73026230	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73026236	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73026238	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73026240	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73026241	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73026247	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73026249	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73026251	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73028276	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73028277	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73028278	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73028283	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73028285	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73028286	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73028287	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73028288	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73028290	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73028292	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73028293	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73028295	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73028297	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73028298	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73028301	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73030105	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73030106	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73030108	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73030112	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73030117	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73030122	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73030125	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73030128	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73030129	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73031587	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73031588	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73031589	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73031596	1.00[AMR][1000 genomes]
rs73033003	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73033006	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73033009	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73033012	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73033013	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73033017	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73033024	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73033025	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73033027	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73033031	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73033033	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73033036	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73033038	1.00[AMR][1000 genomes]
rs73035055	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73035056	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73035058	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73035071	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73035084	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73035085	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73035091	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73037103	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73039146	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73039162	0.90[ASN][1000 genomes]
rs73039163	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73039164	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73039174	1.00[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs73039179	1.00[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs73039184	0.87[ASN][1000 genomes]
rs73041151	1.00[AMR][1000 genomes]
rs73041158	1.00[AMR][1000 genomes]
rs73043118	1.00[AMR][1000 genomes]
rs73043122	1.00[AMR][1000 genomes]
rs73043135	1.00[AMR][1000 genomes]
rs73043163	1.00[AMR][1000 genomes]
rs7775261	1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs7775430	1.00[AMR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019381	chr6:167090236-167558598	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
2	nsv538541	chr6:167090236-167558598	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
3	nsv948634	chr6:167200671-167838993	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
4	nsv532074	chr6:167320656-167781977	Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
5	nsv1031039	chr6:167324021-167741439	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	21 gene(s)	inside rSNPs	diseases
6	nsv538543	chr6:167324021-167741439	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	21 gene(s)	inside rSNPs	diseases
7	nsv1026972	chr6:167335031-167671042	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	19 gene(s)	inside rSNPs	diseases
8	nsv464140	chr6:167426681-167492552	Active TSS Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
9	nsv886943	chr6:167440244-167502638	Strong transcription Flanking Active TSS Genic enhancers Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	esv2752099	chr6:167448181-167579102	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
11	esv3471970	chr6:167486262-167491260	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv3486518	chr6:167486912-167490660	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
13	esv3471975	chr6:167486987-167490835	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv3486516	chr6:167487362-167490560	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
15	esv2459172	chr6:167487650-167490333	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
16	esv6026	chr6:167487874-167489832	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
17	esv3486517	chr6:167487993-167489818	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
18	esv3471972	chr6:167487999-167489840	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
19	esv1838869	chr6:167488211-167492552	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
20	esv1841284	chr6:167488211-167492552	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
21	esv1842395	chr6:167488211-167492552	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167487000-167494400	Enhancers	Primary B cells from peripheral blood	blood
2	chr6:167487400-167492600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr6:167487600-167492400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr6:167488400-167491000	Weak transcription	Primary B cells from cord blood	blood
5	chr6:167489200-167492200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr6:167489800-167490200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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