Variant report

Variant	rs41464647
Chromosome Location	chr7:127539867-127539868
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:127539859..127542368-chr7:127543054..127544559,2	K562	blood:
2	chr7:127535349..127538608-chr7:127539437..127541786,4	MCF-7	breast:
3	chr7:127539496..127544017-chr7:127546415..127549727,4	MCF-7	breast:
4	chr7:127539523..127541289-chr7:127544674..127547671,2	K562	blood:

Variant related genes	Relation type
ENSG00000197157	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs12154492	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs12537331	0.85[GIH][hapmap];1.00[MEX][hapmap]
rs12706821	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];0.85[MEX][hapmap];0.97[TSI][hapmap]
rs13236338	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs13236900	0.81[ASW][hapmap]
rs13238924	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs13246200	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs13246286	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs1419970	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs17151466	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.83[YRI][hapmap]
rs17151488	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs17151507	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs17151639	0.89[CEU][hapmap]
rs17151668	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.89[TSI][hapmap]
rs17151707	1.00[GIH][hapmap];1.00[MEX][hapmap];0.80[TSI][hapmap]
rs17151739	0.85[GIH][hapmap];0.92[MEX][hapmap]
rs6467157	1.00[CHB][hapmap];0.85[GIH][hapmap];0.92[MEX][hapmap]
rs6953231	1.00[CHB][hapmap];0.85[MEX][hapmap];0.89[TSI][hapmap]
rs6962635	1.00[GIH][hapmap];1.00[MEX][hapmap];0.89[TSI][hapmap]
rs741094	0.90[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap]
rs7805021	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];0.88[TSI][hapmap]
rs7809182	1.00[CEU][hapmap];0.85[GIH][hapmap];0.92[TSI][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022385	chr7:127246656-127971194	Weak transcription Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
2	nsv539120	chr7:127246656-127971194	Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
3	nsv1016143	chr7:127251359-127726762	Strong transcription Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Active TSS 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 miRNA target site	27 gene(s)	inside rSNPs	diseases
4	nsv526535	chr7:127445594-127623840	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1024743	chr7:127498695-127670004	Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs41464647	SND1	cis	Artery Tibial	GTEx

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:127505800-127542000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr7:127515400-127540600	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr7:127516400-127540200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr7:127524800-127540400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr7:127526200-127544600	Weak transcription	Stomach Smooth Muscle	stomach
6	chr7:127526600-127540600	Weak transcription	Fetal Brain Female	brain
7	chr7:127526600-127540600	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr7:127527200-127540400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr7:127528800-127540400	Weak transcription	Colonic Mucosa	Colon
10	chr7:127528800-127569200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr7:127529000-127540200	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr7:127529000-127557200	Weak transcription	Esophagus	oesophagus
13	chr7:127529200-127540400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr7:127529200-127540400	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr7:127529200-127540800	Weak transcription	Spleen	Spleen
16	chr7:127529200-127544600	Weak transcription	Thymus	Thymus
17	chr7:127529200-127545600	Weak transcription	Fetal Stomach	stomach
18	chr7:127529200-127546200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr7:127529200-127548400	Weak transcription	Right Ventricle	heart
20	chr7:127529200-127569400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr7:127529400-127542200	Weak transcription	Fetal Heart	heart
22	chr7:127529400-127551000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
23	chr7:127530800-127540400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr7:127531200-127540400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr7:127531600-127540400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr7:127531800-127542000	Weak transcription	Fetal Kidney	kidney
27	chr7:127532200-127540000	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr7:127532200-127569200	Weak transcription	Hela-S3	cervix
29	chr7:127532400-127540600	Weak transcription	Fetal Muscle Leg	muscle
30	chr7:127532400-127540600	Weak transcription	Gastric	stomach
31	chr7:127532400-127547400	Weak transcription	A549	lung
32	chr7:127532400-127569200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr7:127532600-127540000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr7:127532600-127541000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr7:127532600-127541200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr7:127532600-127546000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr7:127532800-127540400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr7:127532800-127540400	Weak transcription	Placenta	Placenta
39	chr7:127532800-127540800	Weak transcription	Primary hematopoietic stem cells	blood
40	chr7:127532800-127541000	Weak transcription	Primary T cells fromperipheralblood	blood
41	chr7:127532800-127541600	Weak transcription	Dnd41	blood
42	chr7:127532800-127544800	Weak transcription	Primary T helper cells fromperipheralblood	blood
43	chr7:127532800-127545600	Weak transcription	Fetal Muscle Trunk	muscle
44	chr7:127533000-127540600	Weak transcription	Liver	Liver
45	chr7:127533000-127540800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr7:127533000-127541000	Weak transcription	Lung	lung
47	chr7:127533800-127541400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr7:127534000-127540400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr7:127534000-127542200	Weak transcription	Adipose Nuclei	Adipose
50	chr7:127534400-127544400	Weak transcription	Fetal Brain Male	brain

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