Variant report

Variant	rs1633298
Chromosome Location	chr1:158946086-158946087
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:158944012..158946277-chr1:158956964..158958723,2	K562	blood:
2	chr1:158647173..158649566-chr1:158944147..158946933,2	K562	blood:
3	chr1:158934253..158936901-chr1:158944231..158946210,2	K562	blood:

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs10489847	1.00[EUR][1000 genomes]
rs1101999	1.00[EUR][1000 genomes]
rs1102000	1.00[EUR][1000 genomes]
rs1102017	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1104171	1.00[EUR][1000 genomes]
rs12057331	1.00[EUR][1000 genomes]
rs12059838	1.00[EUR][1000 genomes]
rs12060241	1.00[EUR][1000 genomes]
rs12061139	1.00[EUR][1000 genomes]
rs12062789	1.00[EUR][1000 genomes]
rs12063682	1.00[EUR][1000 genomes]
rs12063973	1.00[EUR][1000 genomes]
rs12064129	1.00[EUR][1000 genomes]
rs12068030	1.00[EUR][1000 genomes]
rs1341409	1.00[EUR][1000 genomes]
rs1612810	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1612844	1.00[EUR][1000 genomes]
rs1615480	0.81[ASW][hapmap]
rs1616270	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1626284	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1629682	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1629702	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1631448	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1633293	1.00[EUR][1000 genomes]
rs1633296	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs1633297	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16841729	1.00[EUR][1000 genomes]
rs16841784	1.00[EUR][1000 genomes]
rs16841789	1.00[EUR][1000 genomes]
rs1772398	1.00[EUR][1000 genomes]
rs1772439	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1772441	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1772442	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1772444	1.00[EUR][1000 genomes]
rs3026930	1.00[AMR][1000 genomes]
rs3026944	1.00[EUR][1000 genomes]
rs3026947	1.00[EUR][1000 genomes]
rs3026970	1.00[EUR][1000 genomes]
rs34870435	1.00[EUR][1000 genomes]
rs35122728	1.00[EUR][1000 genomes]
rs36103299	1.00[EUR][1000 genomes]
rs73023773	1.00[EUR][1000 genomes]
rs73023775	1.00[EUR][1000 genomes]
rs74122265	1.00[EUR][1000 genomes]
rs856059	1.00[EUR][1000 genomes]
rs856060	1.00[EUR][1000 genomes]
rs856061	1.00[EUR][1000 genomes]
rs856062	1.00[EUR][1000 genomes]
rs856063	1.00[EUR][1000 genomes]
rs856065	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs856069	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs856075	0.93[LWK][hapmap];0.89[MKK][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs856076	0.93[LWK][hapmap];0.89[MKK][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs856078	1.00[EUR][1000 genomes]
rs856082	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs856087	1.00[EUR][1000 genomes]
rs856128	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs856129	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs856130	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs856137	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs856138	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs856139	1.00[EUR][1000 genomes]
rs856144	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs856145	1.00[EUR][1000 genomes]
rs856147	1.00[EUR][1000 genomes]
rs856148	1.00[EUR][1000 genomes]
rs864439	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002401	chr1:158712627-158972031	Flanking Active TSS Strong transcription Active TSS Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	esv3376764	chr1:158761947-158998617	Enhancers Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	esv3369957	chr1:158915589-159003393	Strong transcription Genic enhancers Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
4	nsv947329	chr1:158944939-158948344	Enhancers Weak transcription Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:158920600-158950600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr1:158923000-158949600	Weak transcription	Primary B cells from cord blood	blood
3	chr1:158933400-158949400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr1:158940600-158953000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr1:158941200-158952200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr1:158941400-158948400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr1:158942400-158948600	Strong transcription	Primary T helper cells fromperipheralblood	blood
8	chr1:158942800-158947400	Strong transcription	Primary T cells fromperipheralblood	blood
9	chr1:158943000-158949200	Strong transcription	Primary T helper cells PMA-I stimulated	--
10	chr1:158944000-158947400	Strong transcription	Primary T cells from cord blood	blood
11	chr1:158945400-158946400	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr1:158945800-158946200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr1:158945800-158946400	Enhancers	H9 Cell Line	embryonic stem cell
14	chr1:158945800-158946400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr1:158945800-158947800	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr1:158946000-158946200	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr1:158946000-158946400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr1:158946000-158946400	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr1:158946000-158947800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--

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