Variant report

Variant	rs7699102
Chromosome Location	chr4:76429217-76429218
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	chr4:76425741..76429884-chr4:76437670..76440920,5	MCF-7	breast:
2	chr4:76423980..76426785-chr4:76427353..76430216,3	K562	blood:

Variant related genes	Relation type
ENSG00000174796	Chromatin interaction
ENSG00000163743	Chromatin interaction

Extended variants
information (count: 33 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10009558	0.88[CEU][hapmap];0.94[GIH][hapmap];0.87[EUR][1000 genomes]
rs10018377	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap];0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10020976	0.87[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];0.95[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10022673	0.87[EUR][1000 genomes]
rs10026125	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10032148	0.83[CHB][hapmap]
rs10518139	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13103482	0.88[CEU][hapmap];0.97[GIH][hapmap];0.87[EUR][1000 genomes]
rs13134862	0.85[CEU][hapmap];0.86[EUR][1000 genomes]
rs13137105	0.88[CEU][hapmap];0.94[GIH][hapmap];0.86[EUR][1000 genomes]
rs1841933	0.87[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2126852	0.83[CHB][hapmap];0.86[MKK][hapmap];0.82[TSI][hapmap]
rs28504656	0.81[EUR][1000 genomes]
rs28609645	0.86[EUR][1000 genomes]
rs2867917	0.92[CEU][hapmap]
rs28871288	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28877578	0.86[EUR][1000 genomes]
rs34402235	0.87[EUR][1000 genomes]
rs35362134	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35931543	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62318629	0.80[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62318632	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6835573	0.83[CEU][hapmap];0.87[EUR][1000 genomes]
rs6838603	0.84[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7657576	0.81[CEU][hapmap];0.87[EUR][1000 genomes]
rs7662152	0.92[CEU][hapmap]
rs7681108	0.88[ASN][1000 genomes]
rs7685936	0.95[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9307834	0.88[CEU][hapmap];0.87[EUR][1000 genomes]
rs9994735	0.92[CEU][hapmap];0.82[GIH][hapmap]
rs9998576	0.88[AMR][1000 genomes];0.80[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	nsv594687	chr4:76154064-76502748	Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv534570	chr4:76214619-76498362	ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Bivalent Enhancer 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	27 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs7699102	THAP6	cis	multi-tissue	Pritchard
rs7699102	RCHY1	cis	multi-tissue	Pritchard

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:76392600-76434800	Weak transcription	Gastric	stomach
2	chr4:76395800-76437000	Weak transcription	Aorta	Aorta
3	chr4:76395800-76437000	Weak transcription	Lung	lung
4	chr4:76395800-76437000	Weak transcription	Pancreas	Pancrea
5	chr4:76396200-76437000	Weak transcription	Esophagus	oesophagus
6	chr4:76397800-76437000	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr4:76398200-76434200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr4:76398800-76437200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr4:76399400-76434400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr4:76400600-76437000	Weak transcription	Spleen	Spleen
11	chr4:76401000-76436200	Weak transcription	Brain Angular Gyrus	brain
12	chr4:76403800-76433600	Strong transcription	Primary B cells from peripheral blood	blood
13	chr4:76405600-76434400	Weak transcription	Fetal Heart	heart
14	chr4:76406000-76436600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr4:76406600-76438800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr4:76408000-76436600	Weak transcription	Hela-S3	cervix
17	chr4:76410000-76437200	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr4:76411400-76435400	Weak transcription	Small Intestine	intestine
19	chr4:76414600-76429400	Weak transcription	HSMMtube	muscle
20	chr4:76415400-76430200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr4:76415400-76435600	Weak transcription	Brain Substantia Nigra	brain
22	chr4:76415400-76436400	Weak transcription	Brain Cingulate Gyrus	brain
23	chr4:76415800-76430200	Weak transcription	Colonic Mucosa	Colon
24	chr4:76416000-76429400	Weak transcription	Left Ventricle	heart
25	chr4:76416600-76436200	Weak transcription	Brain Anterior Caudate	brain
26	chr4:76416600-76437000	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chr4:76417600-76436800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
28	chr4:76419600-76429400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
29	chr4:76421200-76433600	Strong transcription	Primary neutrophils fromperipheralblood	blood
30	chr4:76421400-76437000	Weak transcription	Stomach Mucosa	stomach
31	chr4:76422400-76433800	Strong transcription	Primary monocytes fromperipheralblood	blood
32	chr4:76422400-76434800	Strong transcription	Monocytes-CD14+_RO01746	blood
33	chr4:76422600-76432600	Weak transcription	Colon Smooth Muscle	Colon
34	chr4:76423000-76431400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr4:76423000-76434400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
36	chr4:76423800-76430200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
37	chr4:76423800-76434400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
38	chr4:76423800-76434400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr4:76424000-76430600	Strong transcription	Rectal Mucosa Donor 31	rectum
40	chr4:76424200-76432800	Strong transcription	Primary T helper cells PMA-I stimulated	--
41	chr4:76424200-76434400	Strong transcription	HUES48 Cell Line	embryonic stem cell
42	chr4:76424400-76431400	Strong transcription	Duodenum Smooth Muscle	Duodenum
43	chr4:76424600-76433800	Strong transcription	Primary T helper cells fromperipheralblood	blood
44	chr4:76424800-76436200	Weak transcription	Rectal Smooth Muscle	rectum
45	chr4:76424800-76437000	Weak transcription	Psoas Muscle	Psoas
46	chr4:76424800-76437000	Weak transcription	NHLF	lung
47	chr4:76425000-76429400	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr4:76425000-76430200	Weak transcription	Muscle Satellite Cultured Cells	--
49	chr4:76425000-76434800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr4:76425000-76435000	Strong transcription	HSMM	muscle

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