Variant report

Variant	rs6871212
Chromosome Location	chr5:107142894-107142895
allele	C/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	FOSL2	chr5:107142331-107142910	MCF-7	breast:	n/a	chr5:107142508-107142519
2	JUND	chr5:107142325-107142931	HCT-116	colon:	n/a	chr5:107142508-107142519 chr5:107142610-107142621
3	FOSL1	chr5:107142269-107142905	HCT-116	colon:	n/a	chr5:107142508-107142519
4	MAX	chr5:107142335-107142897	A549	lung:	n/a	n/a
5	FOS	chr5:107142337-107142925	MCF10A-Er-Src	breast:	n/a	chr5:107142610-107142621 chr5:107142508-107142519
6	JUND	chr5:107142358-107142911	SK-N-SH	brain:	n/a	chr5:107142508-107142519 chr5:107142610-107142621
7	STAT3	chr5:107142461-107142897	MCF10A-Er-Src	breast:	n/a	n/a
8	FOS	chr5:107142390-107143005	HUVEC	blood vessel:	n/a	chr5:107142610-107142621 chr5:107142508-107142519

No.	Distal block	Cell Line	Cell type
1	chr5:107141836..107143424-chr5:107150743..107153310,2	MCF-7	breast:
2	chr5:107135763..107138365-chr5:107141825..107143430,2	K562	blood:
3	chr5:107139921..107141469-chr5:107142790..107144472,2	K562	blood:
4	chr1:69106008..69107508-chr5:107141802..107143595,2	MCF-7	breast:

Variant related genes	Relation type
RN7SKP122	TF binding region

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10066422	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11742684	0.81[ASN][1000 genomes]
rs11747409	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11748620	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2410957	1.00[CEU][hapmap];0.92[CHB][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2410958	1.00[CEU][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2410959	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2898606	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3843493	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs3846692	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3846693	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3909359	0.88[ASN][1000 genomes]
rs3909360	0.88[ASN][1000 genomes]
rs3909362	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3910210	0.83[ASN][1000 genomes]
rs3931059	0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3931060	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3931725	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4099186	1.00[CEU][hapmap];0.85[CHB][hapmap];0.82[JPT][hapmap];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4099187	1.00[CEU][hapmap];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4099188	0.96[CEU][hapmap];0.85[CHB][hapmap];0.82[JPT][hapmap];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4099189	1.00[CEU][hapmap];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4100173	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4957541	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4957721	0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4957722	0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs55976515	0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6596749	1.00[CEU][hapmap];0.92[CHB][hapmap];0.96[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6596750	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6596751	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6596755	0.92[ASN][1000 genomes]
rs6860214	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6860370	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6860400	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6860649	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6861427	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6866321	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6867170	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6867698	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6868088	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6870561	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6871231	1.00[CEU][hapmap];0.92[CHB][hapmap];0.96[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6875432	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6876427	0.94[EUR][1000 genomes]
rs6879536	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6879852	0.95[EUR][1000 genomes]
rs6880537	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6882183	1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6885982	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6888461	0.95[EUR][1000 genomes]
rs6889417	0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6892119	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6892137	1.00[CEU][hapmap];0.92[CHB][hapmap];0.96[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6893393	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6895001	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7702274	0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7704143	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830440	chr5:107074116-107278905	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv969928	chr5:107132237-107143800	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1022155	chr5:107138981-107149604	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:107135400-107143000	Weak transcription	Right Atrium	heart
2	chr5:107138400-107144800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr5:107140200-107144200	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr5:107140200-107144400	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr5:107140400-107144000	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr5:107140400-107144000	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr5:107140400-107144200	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr5:107140400-107148800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr5:107140600-107144000	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr5:107140800-107144400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr5:107140800-107145000	Enhancers	H1 Cell Line	embryonic stem cell
12	chr5:107140800-107146600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr5:107141000-107143800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr5:107141200-107144400	Weak transcription	Dnd41	blood
15	chr5:107141400-107144200	Weak transcription	Fetal Intestine Large	intestine
16	chr5:107141400-107146000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr5:107141400-107146600	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr5:107141600-107143600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr5:107141600-107143600	Enhancers	Fetal Muscle Leg	muscle
20	chr5:107141800-107143000	Enhancers	HSMM	muscle
21	chr5:107142000-107143000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr5:107142000-107143200	Enhancers	HMEC	breast
23	chr5:107142000-107143400	Enhancers	NHDF-Ad	bronchial
24	chr5:107142000-107143600	Enhancers	HSMMtube	muscle
25	chr5:107142200-107143200	Enhancers	NH-A	brain
26	chr5:107142200-107144200	Weak transcription	Fetal Stomach	stomach
27	chr5:107142200-107144600	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr5:107142400-107143000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr5:107142400-107144000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr5:107142400-107144400	Weak transcription	Brain Germinal Matrix	brain
31	chr5:107142400-107144800	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr5:107142400-107145200	Weak transcription	Hela-S3	cervix
33	chr5:107142600-107144400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr5:107142600-107145400	Enhancers	Fetal Kidney	kidney
35	chr5:107142800-107143200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr5:107142800-107143400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr5:107142800-107144000	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr5:107142800-107144000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr5:107142800-107144200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr5:107142800-107145000	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr5:107142800-107145000	Weak transcription	NHLF	lung

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