Variant report

Variant	rs40944
Chromosome Location	chr7:108205800-108205801
allele	A/C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1)
CpG islands
(count:0)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr7:108199426-108221976	K562	blood:	n/a	n/a

No data

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:108204810..108207831-chr7:108207857..108211042,6	MCF-7	breast:
2	chr7:108200654..108204288-chr7:108205009..108207830,4	MCF-7	breast:
3	chr7:108166428..108168148-chr7:108205249..108207059,2	K562	blood:
4	chr7:108191362..108206184-chr7:108206645..108216261,27	K562	blood:
5	chr7:108159403..108171484-chr7:108200740..108214365,45	K562	blood:

No data

Variant related genes	Relation type
DNAJB9	TF binding region
ENSG00000135241	Chromatin interaction
ENSG00000128590	Chromatin interaction
ENSG00000177683	Chromatin interaction

Extended variants
information (count: 63 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs10487859	0.81[ASN][1000 genomes]
rs11974559	0.86[ASN][1000 genomes]
rs11981670	0.81[ASN][1000 genomes]
rs12666562	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13229488	0.81[ASN][1000 genomes]
rs17155828	0.81[ASN][1000 genomes]
rs17424206	0.81[ASN][1000 genomes]
rs194587	0.81[ASN][1000 genomes]
rs3202837	0.81[ASN][1000 genomes]
rs34814097	0.81[ASN][1000 genomes]
rs34887057	0.81[ASN][1000 genomes]
rs35372181	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35880371	0.81[ASN][1000 genomes]
rs3763457	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs40843	0.81[ASN][1000 genomes]
rs40845	0.81[ASN][1000 genomes]
rs40850	0.81[ASN][1000 genomes]
rs40854	0.81[ASN][1000 genomes]
rs40872	0.86[ASN][1000 genomes]
rs40875	0.86[ASN][1000 genomes]
rs40878	0.86[ASN][1000 genomes]
rs40880	0.86[ASN][1000 genomes]
rs40882	0.81[ASN][1000 genomes]
rs40885	0.86[ASN][1000 genomes]
rs40886	0.86[ASN][1000 genomes]
rs40895	0.86[ASN][1000 genomes]
rs40899	0.86[ASN][1000 genomes]
rs40900	0.86[ASN][1000 genomes]
rs40901	0.86[ASN][1000 genomes]
rs40902	0.86[ASN][1000 genomes]
rs40908	0.86[ASN][1000 genomes]
rs40910	0.86[ASN][1000 genomes]
rs40912	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs40914	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs40915	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs40919	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs40921	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs40923	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs40924	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs40925	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs40926	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs40928	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs40931	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs40932	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs40934	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs40936	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs40938	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs40939	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs40940	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs40941	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs40942	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs40945	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs40946	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs40947	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs40948	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs60426977	0.81[ASN][1000 genomes]
rs6466238	0.81[ASN][1000 genomes]
rs67694466	0.81[ASN][1000 genomes]
rs6947492	0.81[ASN][1000 genomes]
rs6955152	0.81[ASN][1000 genomes]
rs71568528	0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3348839	chr7:107377311-108286538	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised 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	91 gene(s)	inside rSNPs	diseases
2	nsv817371	chr7:108199882-108649799	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs40944	THAP5	Cis_1M	lymphoblastoid	RTeQTL
rs40944	THAP5	cis	Esophagus Muscularis	GTEx
rs40944	THAP5	cis	Muscle Skeletal	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:108195600-108208400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr7:108197600-108208600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr7:108197800-108208600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr7:108198000-108208400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr7:108198400-108207800	Weak transcription	Brain Hippocampus Middle	brain
6	chr7:108198400-108208400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr7:108198600-108207400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr7:108198600-108208600	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr7:108198600-108208600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr7:108198600-108208600	Weak transcription	Fetal Brain Male	brain
11	chr7:108198600-108208600	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr7:108198600-108208600	Weak transcription	Thymus	Thymus
13	chr7:108198800-108205800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr7:108198800-108206000	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr7:108199000-108207600	Weak transcription	Duodenum Mucosa	Duodenum
16	chr7:108199400-108207400	Weak transcription	Stomach Smooth Muscle	stomach
17	chr7:108199400-108208200	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr7:108200000-108207000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
19	chr7:108200000-108207800	Weak transcription	HepG2	liver
20	chr7:108200200-108206000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr7:108200200-108208000	Weak transcription	Brain Angular Gyrus	brain
22	chr7:108200400-108209400	Weak transcription	Spleen	Spleen
23	chr7:108200600-108208400	Weak transcription	NHLF	lung
24	chr7:108201200-108208600	Weak transcription	Pancreas	Pancrea
25	chr7:108201600-108207200	Weak transcription	HUVEC	blood vessel
26	chr7:108201600-108208600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr7:108201600-108208600	Weak transcription	Left Ventricle	heart
28	chr7:108201600-108208600	Weak transcription	Right Ventricle	heart
29	chr7:108201800-108207400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr7:108201800-108208400	Weak transcription	Brain Germinal Matrix	brain
31	chr7:108202000-108207000	Strong transcription	Primary B cells from cord blood	blood
32	chr7:108202000-108207600	Weak transcription	Hela-S3	cervix
33	chr7:108202000-108207800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr7:108202000-108208400	Weak transcription	Fetal Intestine Small	intestine
35	chr7:108202200-108206200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr7:108202200-108207200	Weak transcription	Fetal Heart	heart
37	chr7:108202200-108207600	Strong transcription	HUES64 Cell Line	embryonic stem cell
38	chr7:108202200-108208600	Weak transcription	Fetal Stomach	stomach
39	chr7:108202200-108209200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr7:108202400-108206600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
41	chr7:108202400-108208000	Weak transcription	Fetal Brain Female	brain
42	chr7:108202400-108208400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr7:108202400-108208400	Weak transcription	HSMMtube	muscle
44	chr7:108202600-108205800	Weak transcription	Ovary	ovary
45	chr7:108202800-108208400	Weak transcription	NH-A	brain
46	chr7:108202800-108208400	Weak transcription	NHDF-Ad	bronchial
47	chr7:108203000-108208200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr7:108203600-108206200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr7:108203600-108206800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr7:108203600-108207000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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