Variant report

Variant	rs4702029
Chromosome Location	chr5:14346413-14346414
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	chr5:14346102..14348503-chr5:14664203..14665893,2	MCF-7	breast:
2	chr5:14342477..14345158-chr5:14346178..14348281,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000261360	Chromatin interaction
ENSG00000154124	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs11955578	0.94[CEU][hapmap];0.86[EUR][1000 genomes]
rs11957060	0.85[CEU][hapmap]
rs13172149	0.81[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs13172877	0.92[EUR][1000 genomes]
rs13189406	0.92[EUR][1000 genomes]
rs154151	0.87[EUR][1000 genomes]
rs17304403	0.81[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs185355	0.87[EUR][1000 genomes]
rs187667	0.85[EUR][1000 genomes]
rs247137	0.87[EUR][1000 genomes]
rs256412	0.85[EUR][1000 genomes]
rs28343	0.85[EUR][1000 genomes]
rs30766	0.87[EUR][1000 genomes]
rs30767	0.87[EUR][1000 genomes]
rs30768	0.87[EUR][1000 genomes]
rs30772	0.86[EUR][1000 genomes]
rs30773	0.90[CEU][hapmap];0.87[TSI][hapmap];0.85[EUR][1000 genomes]
rs30785	0.87[EUR][1000 genomes]
rs30786	0.90[CEU][hapmap];0.87[EUR][1000 genomes]
rs30787	0.90[CEU][hapmap];0.86[EUR][1000 genomes]
rs30788	0.90[CEU][hapmap];0.87[EUR][1000 genomes]
rs30789	0.90[CEU][hapmap];0.87[EUR][1000 genomes]
rs30790	0.90[CEU][hapmap];0.86[EUR][1000 genomes]
rs30791	0.90[CEU][hapmap];0.87[TSI][hapmap];0.87[EUR][1000 genomes]
rs30793	0.82[EUR][1000 genomes]
rs30799	0.86[EUR][1000 genomes]
rs30800	0.85[EUR][1000 genomes]
rs30801	0.85[EUR][1000 genomes]
rs35860741	0.81[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs36077682	0.81[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs378369	0.89[CEU][hapmap];0.85[EUR][1000 genomes]
rs382403	0.90[CEU][hapmap];0.85[YRI][hapmap]
rs389729	0.85[CEU][hapmap];0.84[TSI][hapmap]
rs397319	0.89[CEU][hapmap]
rs40278	0.85[EUR][1000 genomes]
rs40572	0.90[CEU][hapmap];0.85[EUR][1000 genomes]
rs42555	0.90[CEU][hapmap];0.85[EUR][1000 genomes]
rs42556	0.90[CEU][hapmap];0.85[EUR][1000 genomes]
rs434279	0.87[EUR][1000 genomes]
rs4702028	0.82[YRI][hapmap]
rs71614085	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs923616	0.84[ASW][hapmap];0.81[MEX][hapmap];0.82[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948355	chr5:14160447-14395478	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
2	nsv1026914	chr5:14237782-14751588	Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
3	nsv830210	chr5:14255039-14431552	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv3329343	chr5:14346052-14348550	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	esv3366769	chr5:14346079-14348744	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4702029	FAM105B	cis	cerebellum	SCAN

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:14319200-14349400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr5:14331000-14348000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr5:14331400-14350000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr5:14334000-14349400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
5	chr5:14335000-14360600	Weak transcription	Psoas Muscle	Psoas
6	chr5:14335200-14348600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr5:14336400-14349400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr5:14337800-14346600	Weak transcription	Fetal Heart	heart
9	chr5:14338000-14357200	Weak transcription	Colonic Mucosa	Colon
10	chr5:14338400-14358000	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr5:14338600-14348000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr5:14338800-14347000	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr5:14338800-14357600	Weak transcription	Esophagus	oesophagus
14	chr5:14339200-14357600	Weak transcription	Gastric	stomach
15	chr5:14339200-14358000	Weak transcription	Thymus	Thymus
16	chr5:14339200-14358200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr5:14339400-14358400	Weak transcription	Fetal Thymus	thymus
18	chr5:14339800-14348800	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr5:14340000-14347000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr5:14340400-14353800	Strong transcription	Muscle Satellite Cultured Cells	--
21	chr5:14340800-14353600	Strong transcription	HSMM	muscle
22	chr5:14341200-14350400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr5:14341400-14355000	Weak transcription	Ovary	ovary
24	chr5:14341400-14359400	Weak transcription	Primary T cells from cord blood	blood
25	chr5:14341600-14347400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr5:14341600-14348600	Weak transcription	Aorta	Aorta
27	chr5:14341600-14357400	Weak transcription	Brain Cingulate Gyrus	brain
28	chr5:14342400-14347600	Weak transcription	Colon Smooth Muscle	Colon
29	chr5:14342600-14357200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
30	chr5:14342600-14358200	Weak transcription	Pancreas	Pancrea
31	chr5:14342800-14346600	Weak transcription	Fetal Intestine Small	intestine
32	chr5:14342800-14347600	Weak transcription	Stomach Mucosa	stomach
33	chr5:14342800-14348400	Weak transcription	Primary hematopoietic stem cells	blood
34	chr5:14342800-14348600	Weak transcription	Spleen	Spleen
35	chr5:14342800-14350000	Weak transcription	Brain Germinal Matrix	brain
36	chr5:14342800-14351000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr5:14342800-14351600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr5:14342800-14352000	Strong transcription	Osteobl	bone
39	chr5:14342800-14352200	Strong transcription	NH-A	brain
40	chr5:14342800-14354000	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr5:14342800-14355000	Weak transcription	Right Ventricle	heart
42	chr5:14342800-14357200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr5:14342800-14357200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr5:14342800-14365200	Weak transcription	Small Intestine	intestine
45	chr5:14343000-14347200	Strong transcription	HepG2	liver
46	chr5:14343000-14347400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr5:14343000-14347600	Strong transcription	NHLF	lung
48	chr5:14343000-14349400	Strong transcription	HSMMtube	muscle
49	chr5:14343000-14351200	Strong transcription	Fetal Intestine Large	intestine
50	chr5:14343200-14347200	Strong transcription	HUVEC	blood vessel

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