Variant report

Variant	rs4902383
Chromosome Location	chr14:65764573-65764574
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:65763315..65764947-chr14:65767837..65770740,2	MCF-7	breast:
2	chr14:65763015..65765090-chr14:65776527..65778731,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000258760	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10134589	0.89[JPT][hapmap];0.84[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs10137464	0.84[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs10138662	0.89[JPT][hapmap];0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs10142617	0.89[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs10144975	0.88[JPT][hapmap];0.89[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs11158587	0.89[JPT][hapmap];0.84[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs17102587	0.89[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs17102598	0.84[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs4902385	0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs4902386	0.89[JPT][hapmap];0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs57071950	0.84[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs6573598	0.89[JPT][hapmap];0.84[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs6573599	0.89[JPT][hapmap];0.84[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs6573600	0.80[AMR][1000 genomes]
rs6573602	0.84[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs6573604	0.88[JPT][hapmap];0.84[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs7151212	0.89[JPT][hapmap];0.84[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs7151301	0.84[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs7156013	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs8004239	0.84[AMR][1000 genomes]
rs8006316	0.84[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs8012054	0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs8013568	0.89[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs8017974	0.89[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs8019473	0.89[JPT][hapmap];0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs8019767	0.89[JPT][hapmap];0.84[AMR][1000 genomes];0.80[ASN][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	nsv832817	chr14:65637069-65810406	Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
2	nsv832818	chr14:65706859-65882320	Enhancers Strong transcription Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
3	nsv1036403	chr14:65724229-66208114	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
4	nsv515522	chr14:65746566-65771110	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:65754600-65768600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr14:65758800-65770000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr14:65758800-65773400	Weak transcription	Spleen	Spleen
4	chr14:65759000-65764600	Weak transcription	Colonic Mucosa	Colon
5	chr14:65759000-65766000	Weak transcription	Fetal Thymus	thymus
6	chr14:65759000-65766000	Weak transcription	Thymus	Thymus
7	chr14:65759800-65766000	Weak transcription	Primary T cells from cord blood	blood
8	chr14:65759800-65766200	Weak transcription	Primary hematopoietic stem cells	blood
9	chr14:65760000-65781000	Weak transcription	Primary B cells from cord blood	blood
10	chr14:65763200-65764600	Enhancers	HepG2	liver
11	chr14:65763200-65774200	Enhancers	Primary B cells from peripheral blood	blood
12	chr14:65763600-65765600	Enhancers	Stomach Mucosa	stomach
13	chr14:65763800-65765200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr14:65763800-65765600	Flanking Active TSS	GM12878-XiMat	blood
15	chr14:65763800-65766200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr14:65763800-65771200	Enhancers	Fetal Intestine Small	intestine
17	chr14:65764200-65764600	Weak transcription	Pancreas	Pancrea
18	chr14:65764200-65765600	Enhancers	Fetal Intestine Large	intestine
19	chr14:65764400-65764600	Enhancers	A549	lung
20	chr14:65764400-65765000	Enhancers	Rectal Mucosa Donor 31	rectum
21	chr14:65764400-65765400	Enhancers	Rectal Mucosa Donor 29	rectum
22	chr14:65764400-65767200	Enhancers	Duodenum Mucosa	Duodenum

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