Variant report

Variant	rs7872124
Chromosome Location	chr9:16488167-16488168
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10810570	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs16934624	1.00[TSI][hapmap]
rs16934678	1.00[TSI][hapmap]
rs6475057	0.83[LWK][hapmap];0.91[MKK][hapmap]
rs7021318	1.00[TSI][hapmap]
rs7022640	1.00[TSI][hapmap]
rs7846746	1.00[TSI][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530933	chr9:16251206-16830845	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv530934	chr9:16281246-16779432	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv1032856	chr9:16465330-16773471	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv540073	chr9:16465330-16773471	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv892646	chr9:16476144-16514375	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS	lncRNA	n/a	inside rSNPs	diseases
6	nsv892647	chr9:16476144-16521534	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv466265	chr9:16484731-16516941	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS	n/a	n/a	inside rSNPs	diseases
8	nsv613670	chr9:16484731-16516941	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:16457800-16493400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr9:16459600-16499800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr9:16459600-16500000	Weak transcription	NHLF	lung
4	chr9:16471000-16504600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr9:16482400-16488600	Enhancers	Colon Smooth Muscle	Colon
6	chr9:16483200-16513600	Weak transcription	Psoas Muscle	Psoas
7	chr9:16483600-16491400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr9:16483800-16490400	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr9:16484000-16490000	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr9:16484200-16488200	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr9:16484400-16489400	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr9:16485000-16499800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr9:16485000-16500000	Weak transcription	HSMM	muscle
14	chr9:16485000-16504800	Weak transcription	Stomach Smooth Muscle	stomach
15	chr9:16485200-16488600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr9:16485200-16491800	Weak transcription	Fetal Lung	lung
17	chr9:16485400-16499800	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr9:16485400-16505000	Weak transcription	HSMMtube	muscle
19	chr9:16485800-16489400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr9:16485800-16490800	Weak transcription	Ovary	ovary
21	chr9:16485800-16505800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr9:16486200-16488200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
23	chr9:16486200-16489000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr9:16486200-16500000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr9:16486400-16488200	Enhancers	H9 Cell Line	embryonic stem cell
26	chr9:16486400-16488800	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr9:16486400-16489600	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr9:16486600-16489800	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr9:16486600-16500000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr9:16487000-16488800	Enhancers	Rectal Smooth Muscle	rectum
31	chr9:16487400-16488800	Enhancers	H1 Cell Line	embryonic stem cell
32	chr9:16487400-16500000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr9:16487600-16488200	Enhancers	Fetal Stomach	stomach
34	chr9:16487600-16489400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr9:16488000-16489000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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