Variant report

Variant	rs62390313
Chromosome Location	chr6:14862107-14862108
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	chr6:14853802..14857029-chr6:14858944..14862650,3	K562	blood:
2	chr6:14861978..14864557-chr6:14877421..14879911,2	MCF-7	breast:

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

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10949261	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12190539	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12374664	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1258993	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs16875778	0.80[EUR][1000 genomes]
rs16875782	0.83[EUR][1000 genomes]
rs16875788	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs16875810	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2124291	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2168315	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs373633	0.92[EUR][1000 genomes]
rs387877	0.97[EUR][1000 genomes]
rs389438	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs394849	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs403392	0.96[EUR][1000 genomes]
rs410494	0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs423468	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs425233	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs443427	0.94[EUR][1000 genomes]
rs52875	0.92[EUR][1000 genomes]
rs62390307	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62390308	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62390309	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62390310	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62390312	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62390314	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62390316	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62390318	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62390319	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62390320	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62390321	0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6912084	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6912613	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72826859	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72826868	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72826874	0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72826878	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9476670	0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9476671	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9476672	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1031668	chr6:14774036-15044308	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv538138	chr6:14774036-15044308	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1017572	chr6:14830510-14906933	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Strong transcription	Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:14850400-14866200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:14855600-14864400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr6:14855800-14864200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr6:14858000-14864400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr6:14858000-14864400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr6:14858400-14864600	Weak transcription	Primary B cells from cord blood	blood
7	chr6:14858400-14865600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr6:14858400-14865800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr6:14858400-14866000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr6:14858600-14864200	Weak transcription	Primary B cells from peripheral blood	blood
11	chr6:14860000-14865800	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr6:14860600-14862200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr6:14861400-14862200	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr6:14861400-14862200	Enhancers	Fetal Thymus	thymus
15	chr6:14861400-14862200	Enhancers	Stomach Mucosa	stomach
16	chr6:14861400-14862200	Enhancers	K562	blood
17	chr6:14861400-14862400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr6:14861600-14862200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr6:14861800-14862200	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr6:14861800-14862200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr6:14861800-14862200	Enhancers	Primary neutrophils fromperipheralblood	blood
22	chr6:14861800-14864400	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr6:14862000-14862200	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr6:14862000-14863600	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr6:14862000-14864000	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr6:14862000-14864000	Weak transcription	Monocytes-CD14+_RO01746	blood
27	chr6:14862000-14864200	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr6:14862000-14864200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr6:14862000-14864200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr6:14862000-14864400	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr6:14862000-14864600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr6:14862000-14865400	Weak transcription	Primary hematopoietic stem cells	blood
33	chr6:14862000-14865800	Weak transcription	Primary T cells fromperipheralblood	blood
34	chr6:14862000-14865800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
35	chr6:14862000-14865800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
36	chr6:14862000-14865800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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