Variant report

Variant	rs7774713
Chromosome Location	chr6:71536606-71536607
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs16869506	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16869513	0.81[AFR][1000 genomes]
rs4605842	0.86[AFR][1000 genomes]
rs6455379	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6908248	0.88[AFR][1000 genomes]
rs6916698	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7753170	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv932111	chr6:70736835-71633094	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv1027049	chr6:70961610-71561488	Strong transcription Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv524328	chr6:70961833-71558805	Flanking Bivalent TSS/Enh Active TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	nsv917312	chr6:70961903-71601688	Enhancers Genic enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS 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	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:71474600-71568800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr6:71492400-71563600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr6:71506800-71570600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr6:71508400-71543800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr6:71511600-71554600	Weak transcription	Dnd41	blood
6	chr6:71514800-71548400	Weak transcription	Ovary	ovary
7	chr6:71516200-71538400	Weak transcription	Esophagus	oesophagus
8	chr6:71516200-71538600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr6:71516200-71546200	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr6:71516400-71562200	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr6:71516400-71567600	Weak transcription	Pancreas	Pancrea
12	chr6:71516600-71543400	Weak transcription	Adipose Nuclei	Adipose
13	chr6:71516600-71567600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr6:71518400-71552400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr6:71520600-71538400	Weak transcription	Fetal Intestine Small	intestine
16	chr6:71522000-71558200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr6:71524600-71548200	Weak transcription	Psoas Muscle	Psoas
18	chr6:71531200-71543600	Weak transcription	Liver	Liver
19	chr6:71531200-71571000	Weak transcription	Stomach Mucosa	stomach
20	chr6:71532000-71543400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr6:71532400-71557200	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr6:71533000-71567600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr6:71533200-71541200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr6:71533200-71545600	Weak transcription	Primary T cells from cord blood	blood
25	chr6:71533200-71547600	Weak transcription	Primary T helper cells fromperipheralblood	blood
26	chr6:71533200-71548000	Weak transcription	Primary T cells fromperipheralblood	blood
27	chr6:71533200-71557000	Weak transcription	Primary hematopoietic stem cells	blood
28	chr6:71534000-71550200	Weak transcription	Primary B cells from cord blood	blood
29	chr6:71534000-71563200	Weak transcription	Primary B cells from peripheral blood	blood
30	chr6:71534600-71543600	Weak transcription	NHDF-Ad	bronchial
31	chr6:71534800-71541200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr6:71534800-71546800	Weak transcription	Monocytes-CD14+_RO01746	blood
33	chr6:71534800-71567600	Weak transcription	Aorta	Aorta
34	chr6:71535600-71548200	Weak transcription	Left Ventricle	heart

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