Variant report

Variant	rs73815373
Chromosome Location	chr4:48853772-48853773
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	FOS	chr4:48853674-48854044	MCF10A-Er-Src	breast:	n/a	chr4:48853782-48853790 chr4:48853782-48853789 chr4:48853781-48853790 chr4:48853782-48853791
2	FOS	chr4:48853635-48854075	MCF10A-Er-Src	breast:	n/a	chr4:48853782-48853790 chr4:48853782-48853789 chr4:48853781-48853790 chr4:48853782-48853791
3	STAT3	chr4:48853672-48854012	MCF10A-Er-Src	breast:	n/a	chr4:48853782-48853791 chr4:48853781-48853790 chr4:48853728-48853735
4	JUND	chr4:48853748-48853951	K562	blood:	n/a	chr4:48853782-48853790 chr4:48853782-48853789 chr4:48853781-48853790 chr4:48853782-48853791
5	FOS	chr4:48853586-48854041	HUVEC	blood vessel:	n/a	chr4:48853782-48853790 chr4:48853782-48853789 chr4:48853781-48853790 chr4:48853782-48853791
6	STAT3	chr4:48853616-48854034	MCF10A-Er-Src	breast:	n/a	chr4:48853782-48853791 chr4:48853781-48853790 chr4:48853728-48853735
7	STAT3	chr4:48853634-48854021	MCF10A-Er-Src	breast:	n/a	chr4:48853782-48853791 chr4:48853781-48853790 chr4:48853728-48853735
8	STAT3	chr4:48853639-48854012	MCF10A-Er-Src	breast:	n/a	chr4:48853782-48853791 chr4:48853781-48853790 chr4:48853728-48853735
9	FOS	chr4:48853662-48854046	MCF10A-Er-Src	breast:	n/a	chr4:48853782-48853790 chr4:48853782-48853789 chr4:48853781-48853790 chr4:48853782-48853791
10	PBX3	chr4:48853601-48854134	SK-N-SH	brain:	n/a	n/a
11	POLR2A	chr4:48853003-48854899	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:48853235..48855592-chr4:48860236..48864497,3	MCF-7	breast:

Variant related genes	Relation type
OCIAD1	TF binding region
ENSG00000248256	Chromatin interaction

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs55909053	1.00[AFR][1000 genomes]
rs55948409	1.00[AFR][1000 genomes]
rs56013049	1.00[AFR][1000 genomes]
rs56077860	1.00[AFR][1000 genomes]
rs56196120	1.00[AFR][1000 genomes]
rs56229581	1.00[AFR][1000 genomes]
rs56393041	1.00[AFR][1000 genomes]
rs56784253	1.00[AFR][1000 genomes]
rs58706281	1.00[AFR][1000 genomes]
rs59582819	1.00[AFR][1000 genomes]
rs61152134	1.00[AFR][1000 genomes]
rs6447671	1.00[AFR][1000 genomes]
rs6447672	1.00[AFR][1000 genomes]
rs6447673	1.00[AFR][1000 genomes]
rs6815745	1.00[AFR][1000 genomes]
rs6829709	1.00[AFR][1000 genomes]
rs6842198	1.00[AFR][1000 genomes]
rs6842954	1.00[AFR][1000 genomes]
rs6844156	1.00[AFR][1000 genomes]
rs6849135	1.00[AFR][1000 genomes]
rs6850227	1.00[AFR][1000 genomes]
rs6850983	1.00[AFR][1000 genomes]
rs6857526	1.00[AFR][1000 genomes]
rs6857571	1.00[AFR][1000 genomes]
rs73815328	1.00[AFR][1000 genomes]
rs73815329	1.00[AFR][1000 genomes]
rs73815333	1.00[AFR][1000 genomes]
rs73815337	1.00[AFR][1000 genomes]
rs73815371	1.00[AFR][1000 genomes]
rs73815393	1.00[AFR][1000 genomes]
rs73815397	1.00[AFR][1000 genomes]
rs73815399	1.00[AFR][1000 genomes]
rs73817712	1.00[AFR][1000 genomes]
rs73817713	1.00[AFR][1000 genomes]
rs73817714	1.00[AFR][1000 genomes]
rs73817715	0.83[AFR][1000 genomes]
rs73817717	1.00[AFR][1000 genomes]
rs73817719	1.00[AFR][1000 genomes]
rs73817721	1.00[AFR][1000 genomes]
rs73817723	1.00[AFR][1000 genomes]
rs73817726	1.00[AFR][1000 genomes]
rs73817729	1.00[AFR][1000 genomes]
rs73817741	1.00[AFR][1000 genomes]
rs73817742	1.00[AFR][1000 genomes]
rs7658876	1.00[AFR][1000 genomes]
rs7674901	1.00[AFR][1000 genomes]
rs7676916	1.00[AFR][1000 genomes]
rs7682222	1.00[AFR][1000 genomes]
rs7684655	1.00[AFR][1000 genomes]
rs7695125	1.00[AFR][1000 genomes]
rs7700082	1.00[AFR][1000 genomes]
rs7700186	1.00[AFR][1000 genomes]
rs9685193	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002674	chr4:48507608-49032909	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv537087	chr4:48507608-49032909	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv1010923	chr4:48575156-49083089	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv537088	chr4:48575156-49083089	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
5	nsv1013762	chr4:48580484-49032909	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv537089	chr4:48580484-49032909	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
7	esv1793455	chr4:48686817-48859142	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
8	nsv1010381	chr4:48701525-49309842	Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
9	nsv1003718	chr4:48771947-49083089	Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
10	nsv916809	chr4:48784318-49083302	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
11	nsv1011910	chr4:48784332-49154757	ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
12	nsv879010	chr4:48794403-49061141	Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
13	nsv1008733	chr4:48827603-48971172	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
14	nsv427680	chr4:48829607-49660117	ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:48834000-48859800	Weak transcription	Aorta	Aorta
2	chr4:48834000-48864600	Weak transcription	Stomach Mucosa	stomach
3	chr4:48834800-48856600	Strong transcription	Primary monocytes fromperipheralblood	blood
4	chr4:48835000-48858000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr4:48835000-48859800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr4:48835000-48861400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr4:48835000-48862400	Strong transcription	Fetal Thymus	thymus
8	chr4:48835000-48863000	Strong transcription	HUES6 Cell Line	embryonic stem cell
9	chr4:48835000-48864400	Strong transcription	HSMM	muscle
10	chr4:48835200-48863200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
11	chr4:48835200-48863800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr4:48835200-48864200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr4:48835400-48857400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr4:48835400-48863200	Strong transcription	Monocytes-CD14+_RO01746	blood
15	chr4:48835400-48863400	Strong transcription	HUES48 Cell Line	embryonic stem cell
16	chr4:48835600-48856200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr4:48835600-48864000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr4:48835800-48856200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
19	chr4:48835800-48857000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr4:48835800-48857000	Strong transcription	Primary T helper cells fromperipheralblood	blood
21	chr4:48835800-48863200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr4:48836000-48858000	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr4:48836000-48863600	Strong transcription	HUES64 Cell Line	embryonic stem cell
24	chr4:48836200-48854800	Strong transcription	Primary B cells from cord blood	blood
25	chr4:48836200-48863600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr4:48836400-48857200	Strong transcription	Primary B cells from peripheral blood	blood
27	chr4:48836600-48854400	Strong transcription	Primary T cells from cord blood	blood
28	chr4:48836800-48856000	Weak transcription	Psoas Muscle	Psoas
29	chr4:48836800-48863200	Strong transcription	Dnd41	blood
30	chr4:48837000-48856000	Weak transcription	HepG2	liver
31	chr4:48837200-48861400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr4:48838000-48855800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr4:48838000-48859600	Weak transcription	Gastric	stomach
34	chr4:48838000-48859600	Weak transcription	Spleen	Spleen
35	chr4:48838000-48859800	Weak transcription	Pancreas	Pancrea
36	chr4:48838000-48859800	Weak transcription	Right Ventricle	heart
37	chr4:48838000-48864400	Weak transcription	Esophagus	oesophagus
38	chr4:48838200-48866800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr4:48838400-48863400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr4:48839400-48859600	Weak transcription	Colonic Mucosa	Colon
41	chr4:48839600-48854000	Weak transcription	Brain Cingulate Gyrus	brain
42	chr4:48840200-48860000	Weak transcription	Small Intestine	intestine
43	chr4:48841000-48865400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
44	chr4:48843800-48854000	Weak transcription	NHLF	lung
45	chr4:48844000-48856600	Strong transcription	NHDF-Ad	bronchial
46	chr4:48844200-48854800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr4:48844200-48857400	Strong transcription	H1 Cell Line	embryonic stem cell
48	chr4:48844800-48858000	Strong transcription	Liver	Liver
49	chr4:48845400-48863800	Weak transcription	Hela-S3	cervix
50	chr4:48846400-48856000	Weak transcription	Ovary	ovary

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