Variant report

Variant	rs631019
Chromosome Location	chr8:104009172-104009173
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:103996495..103999134-chr8:104007444..104009301,2	MCF-7	breast:

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs16869976	0.83[ASN][1000 genomes]
rs16869978	0.83[ASN][1000 genomes]
rs2513873	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2513874	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2646307	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs28372883	0.83[ASN][1000 genomes]
rs3018948	0.91[ASN][1000 genomes]
rs3824225	0.83[ASN][1000 genomes]
rs3824228	0.83[ASN][1000 genomes]
rs473142	0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs473152	0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs486506	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs488420	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs492701	0.95[ASN][1000 genomes]
rs548291	0.80[EUR][1000 genomes]
rs613121	0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs615348	0.93[AFR][1000 genomes];0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62525309	0.83[ASN][1000 genomes]
rs628793	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs630236	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs642994	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs644305	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs677398	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs677415	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs681859	0.92[EUR][1000 genomes];0.95[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	esv33118	chr8:103358567-104068172	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	145 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:103990400-104011400	Weak transcription	Placenta	Placenta
2	chr8:103993400-104012400	Weak transcription	Spleen	Spleen
3	chr8:104001600-104011400	Weak transcription	Fetal Brain Male	brain
4	chr8:104004000-104010200	Weak transcription	Primary hematopoietic stem cells	blood
5	chr8:104006600-104009200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr8:104006800-104009200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr8:104006800-104012400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr8:104007200-104014400	Weak transcription	Primary B cells from peripheral blood	blood
9	chr8:104007600-104010600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr8:104007600-104010600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr8:104007600-104011400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr8:104007600-104011800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr8:104007600-104014200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr8:104008000-104012200	Weak transcription	Monocytes-CD14+_RO01746	blood
15	chr8:104008600-104010600	Weak transcription	Primary B cells from cord blood	blood
16	chr8:104008600-104012400	Weak transcription	Primary monocytes fromperipheralblood	blood
17	chr8:104009000-104010800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr8:104009000-104011800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr8:104009000-104012400	Weak transcription	Primary neutrophils fromperipheralblood	blood

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