Variant report

Variant	rs326155
Chromosome Location	chr5:7816645-7816646
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:7815132..7817938-chr5:7825115..7826911,2	K562	blood:
2	chr5:7775938..7777683-chr5:7815092..7817097,2	MCF-7	breast:
3	chr5:7816149..7817026-chr5:7856829..7857627,3	MCF-7	breast:
4	chr5:7392850..7393487-chr5:7816258..7816812,2	MCF-7	breast:
5	chr5:6820753..6821547-chr5:7816144..7817013,2	MCF-7	breast:
6	chr5:7755134..7755770-chr5:7816100..7816964,3	MCF-7	breast:
7	chr5:7762082..7763082-chr5:7816072..7817044,6	MCF-7	breast:
8	chr5:7816093..7817014-chr5:7850949..7851566,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000124275	Chromatin interaction
ENSG00000215217	Chromatin interaction

Extended variants
information (count: 20 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs11134255	1.00[EUR][1000 genomes]
rs11960468	1.00[EUR][1000 genomes]
rs16879182	1.00[EUR][1000 genomes]
rs16879196	1.00[EUR][1000 genomes]
rs16879215	1.00[EUR][1000 genomes]
rs326154	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs326158	1.00[ASW][hapmap];1.00[EUR][1000 genomes]
rs326161	1.00[EUR][1000 genomes]
rs326163	1.00[EUR][1000 genomes]
rs326165	1.00[EUR][1000 genomes]
rs35209447	1.00[EUR][1000 genomes]
rs6885060	1.00[EUR][1000 genomes]
rs7714729	1.00[EUR][1000 genomes]
rs9313202	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916892	chr5:7634377-8158890	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv949492	chr5:7682909-7953909	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv533983	chr5:7701457-8275379	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
4	nsv1024268	chr5:7707047-7821303	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv461927	chr5:7757812-7854289	Active TSS Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv597004	chr5:7757812-7854289	Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

Variant related diseases (count:1)

Disease	PMID	Source
Visceral fat	22589738	GWAS catalog

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:7795800-7819800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr5:7803800-7824800	Weak transcription	Aorta	Aorta
3	chr5:7806000-7823600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr5:7808400-7827000	Weak transcription	Brain Substantia Nigra	brain
5	chr5:7809000-7816800	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr5:7814600-7816800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr5:7814800-7816800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
8	chr5:7814800-7817000	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr5:7814800-7817400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr5:7815000-7817200	Enhancers	H1 Cell Line	embryonic stem cell
11	chr5:7815000-7817400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr5:7815200-7816800	Enhancers	Primary hematopoietic stem cells	blood
13	chr5:7815200-7817400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr5:7815800-7816800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
15	chr5:7815800-7817000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr5:7816000-7816800	Enhancers	Brain Anterior Caudate	brain
17	chr5:7816000-7816800	Bivalent Enhancer	Fetal Muscle Leg	muscle
18	chr5:7816000-7817000	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr5:7816000-7817000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr5:7816000-7817800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr5:7816000-7819200	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr5:7816000-7819200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr5:7816200-7816800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
24	chr5:7816200-7816800	Enhancers	Primary B cells from peripheral blood	blood
25	chr5:7816200-7816800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr5:7816200-7816800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr5:7816200-7816800	Enhancers	Adipose Nuclei	Adipose
28	chr5:7816200-7816800	Enhancers	Brain Hippocampus Middle	brain
29	chr5:7816200-7816800	Enhancers	Brain Inferior Temporal Lobe	brain
30	chr5:7816200-7816800	Enhancers	Rectal Smooth Muscle	rectum
31	chr5:7816200-7817000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr5:7816400-7816800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr5:7816400-7816800	Active TSS	iPS-20b Cell Line	embryonic stem cell
34	chr5:7816400-7816800	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr5:7816400-7816800	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
36	chr5:7816400-7816800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
37	chr5:7816400-7816800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr5:7816400-7816800	Weak transcription	Brain Angular Gyrus	brain
39	chr5:7816400-7816800	Enhancers	Esophagus	oesophagus
40	chr5:7816400-7816800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
41	chr5:7816400-7817000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr5:7816400-7817000	Enhancers	Brain Cingulate Gyrus	brain
43	chr5:7816400-7817000	Enhancers	Lung	lung
44	chr5:7816400-7817200	ZNF genes & repeats	Right Atrium	heart
45	chr5:7816400-7819400	Weak transcription	Skeletal Muscle Male	skeletal muscle
46	chr5:7816400-7820400	Weak transcription	Colon Smooth Muscle	Colon
47	chr5:7816400-7825200	Weak transcription	Fetal Intestine Small	intestine
48	chr5:7816600-7816800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
49	chr5:7816600-7816800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
50	chr5:7816600-7816800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell

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