Variant report

Variant	rs34414425
Chromosome Location	chr7:6426318-6426319
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:6421413..6423710-chr7:6424469..6426937,2	MCF-7	breast:
2	chr7:6425587..6427672-chr7:6434203..6435980,2	K562	blood:
3	chr7:6415178..6416975-chr7:6426266..6428182,2	MCF-7	breast:
4	chr7:6421014..6427961-chr7:6430347..6436546,11	K562	blood:
5	chr7:6425290..6426951-chr7:6443487..6445552,2	MCF-7	breast:
6	chr7:6424186..6426386-chr7:6428771..6430313,2	K562	blood:
7	chr7:6425039..6427961-chr7:6431283..6434070,6	K562	blood:
8	chr7:6408313..6409948-chr7:6425652..6428069,2	MCF-7	breast:
9	chr7:6423770..6428087-chr7:6429749..6432812,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000136238	Chromatin interaction

Extended variants
information (count: 68 )
Associated
traits (count: 7 )

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10261256	0.83[ASN][1000 genomes]
rs10266716	0.82[ASN][1000 genomes]
rs1055428	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10951982	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10951983	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1123675	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11514801	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11514802	0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11514804	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11760556	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11760562	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11763354	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11767078	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11772942	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12532493	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12535659	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12537483	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12537894	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12538142	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs12539027	0.82[ASN][1000 genomes]
rs13221129	0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs17196595	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1880118	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2272157	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2303361	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2347339	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs33986000	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs33986648	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs33999234	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34106847	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34884077	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35277609	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs35444732	0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs35733871	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35745599	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs3729790	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3750038	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs3828944	0.86[AMR][1000 genomes]
rs4724800	0.83[ASN][1000 genomes]
rs4724801	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4724802	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4724803	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4724804	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4724806	0.85[AMR][1000 genomes]
rs58072643	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs71524068	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs71531381	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs71531384	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs71531392	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7455288	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7456834	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7797644	0.86[AMR][1000 genomes]
rs836470	0.80[EUR][1000 genomes]
rs836545	0.83[AMR][1000 genomes]
rs9374	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948912	chr7:5803903-6623553	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	123 gene(s)	inside rSNPs	diseases
2	nsv1034060	chr7:5814823-6745710	Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	138 gene(s)	inside rSNPs	diseases
3	nsv538711	chr7:5814823-6745710	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	138 gene(s)	inside rSNPs	diseases
4	nsv1028242	chr7:5819084-6645024	Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	127 gene(s)	inside rSNPs	diseases
5	nsv538712	chr7:5819084-6645024	Weak transcription Active TSS Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	127 gene(s)	inside rSNPs	diseases
6	nsv949531	chr7:5949371-6753694	Strong transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	129 gene(s)	inside rSNPs	diseases
7	nsv1021037	chr7:6070792-6426966	Strong transcription Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
8	nsv538713	chr7:6070792-6426966	Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
9	nsv530989	chr7:6176729-6438197	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
10	nsv1020236	chr7:6248930-6690377	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
11	nsv497874	chr7:6296768-6614902	Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
12	nsv605999	chr7:6396719-6472881	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
13	nsv967451	chr7:6417630-6427589	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs34414425	DAGLB	cis	Skin Sun Exposed Lower leg	GTEx
rs34414425	DAGLB	cis	Adipose Subcutaneous	GTEx
rs34414425	DAGLB	cis	Artery Tibial	GTEx
rs34414425	DAGLB	cis	Thyroid	GTEx
rs34414425	DAGLB	cis	Whole Blood	GTEx
rs34414425	DAGLB	cis	Nerve Tibial	GTEx
rs34414425	RAC1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6415800-6427400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr7:6417000-6427400	Weak transcription	Thymus	Thymus
3	chr7:6417200-6426400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr7:6417200-6435400	Weak transcription	Fetal Brain Male	brain
5	chr7:6419000-6427000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr7:6419400-6426400	Enhancers	Primary T cells fromperipheralblood	blood
7	chr7:6419600-6426600	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr7:6421400-6427400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr7:6421800-6426400	Enhancers	Pancreas	Pancrea
10	chr7:6422600-6427000	Enhancers	HMEC	breast
11	chr7:6423000-6432400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr7:6423200-6426800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr7:6423600-6426400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr7:6423600-6426400	Enhancers	Psoas Muscle	Psoas
15	chr7:6423600-6426800	Enhancers	Duodenum Smooth Muscle	Duodenum
16	chr7:6423800-6427800	Enhancers	Placenta Amnion	Placenta Amnion
17	chr7:6424000-6426400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr7:6424000-6432400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr7:6424000-6432400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr7:6424200-6426800	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr7:6424200-6426800	Weak transcription	Dnd41	blood
22	chr7:6424600-6431400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr7:6424800-6427000	Weak transcription	Fetal Muscle Trunk	muscle
24	chr7:6425200-6426600	Enhancers	HUVEC	blood vessel
25	chr7:6425200-6427000	Weak transcription	Primary T helper cells fromperipheralblood	blood
26	chr7:6425400-6432600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr7:6425600-6426400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr7:6425600-6426400	Enhancers	NHDF-Ad	bronchial
29	chr7:6425600-6426600	Enhancers	Rectal Smooth Muscle	rectum
30	chr7:6425600-6426600	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr7:6425600-6426800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr7:6425600-6426800	Enhancers	Osteobl	bone
33	chr7:6425600-6427000	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr7:6425600-6427200	Weak transcription	Brain Germinal Matrix	brain
35	chr7:6425600-6427400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr7:6425600-6427400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr7:6425600-6427600	Enhancers	Stomach Mucosa	stomach
38	chr7:6425600-6427800	Weak transcription	Colonic Mucosa	Colon
39	chr7:6425600-6432200	Weak transcription	Fetal Heart	heart
40	chr7:6425800-6426400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr7:6425800-6426400	Enhancers	Esophagus	oesophagus
42	chr7:6425800-6426400	Enhancers	Sigmoid Colon	Sigmoid Colon
43	chr7:6425800-6426600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr7:6425800-6426600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr7:6425800-6426600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr7:6425800-6426800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr7:6425800-6426800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr7:6425800-6426800	Weak transcription	Fetal Kidney	kidney
49	chr7:6425800-6427000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr7:6425800-6427000	Enhancers	NH-A	brain

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