Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:119824290..119825948-chr12:119827954..119830665,2	MCF-7	breast:

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

rs_ID	r²[population]
rs10774492	0.85[ASN][1000 genomes]
rs10849647	1.00[CHB][hapmap];0.95[CHD][hapmap];0.94[JPT][hapmap];0.95[ASN][1000 genomes]
rs10849651	0.83[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.88[LWK][hapmap];0.90[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10849652	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs10849653	0.97[ASN][1000 genomes]
rs10849654	0.83[ASN][1000 genomes]
rs10849656	1.00[CHB][hapmap];0.94[JPT][hapmap];0.80[ASN][1000 genomes]
rs10849657	0.93[CHB][hapmap];0.94[JPT][hapmap];0.81[ASN][1000 genomes]
rs10849658	0.81[ASN][1000 genomes]
rs10849659	0.93[CHB][hapmap];1.00[CHD][hapmap];0.94[JPT][hapmap];0.81[ASN][1000 genomes]
rs11064761	0.82[CHB][hapmap];0.80[JPT][hapmap];0.87[ASN][1000 genomes]
rs11064763	1.00[CHB][hapmap];0.94[JPT][hapmap];0.93[ASN][1000 genomes]
rs11064764	1.00[CHB][hapmap];0.94[JPT][hapmap];0.82[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs12370130	0.80[CHB][hapmap];0.92[CHD][hapmap];0.80[JPT][hapmap];0.85[ASN][1000 genomes]
rs4300442	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs4465416	0.93[CHB][hapmap];0.97[CHD][hapmap];0.94[JPT][hapmap]
rs4991185	1.00[CHB][hapmap];0.94[JPT][hapmap];0.82[ASN][1000 genomes]
rs56686166	0.96[ASN][1000 genomes]
rs7298161	0.93[CHB][hapmap];0.89[JPT][hapmap]
rs7301599	0.93[CHB][hapmap];0.97[CHD][hapmap];0.90[JPT][hapmap]
rs7313792	0.93[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs73404383	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1047036	chr12:119477583-119992640	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv916688	chr12:119801814-120044407	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10774496	TMEM120B	cis	cerebellum	SCAN

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:119819400-119830800	Weak transcription	Right Atrium	heart
2	chr12:119825200-119829400	Weak transcription	Fetal Heart	heart
3	chr12:119825400-119830000	Weak transcription	Fetal Lung	lung
4	chr12:119827000-119828800	Weak transcription	Left Ventricle	heart
5	chr12:119827000-119829200	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr12:119827400-119829000	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr12:119827400-119829600	Enhancers	H1 Cell Line	embryonic stem cell
8	chr12:119827400-119829600	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr12:119827600-119829200	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr12:119827800-119828800	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr12:119827800-119829200	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr12:119828000-119829400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr12:119828200-119829200	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr12:119828400-119829200	Enhancers	ES-I3 Cell Line	embryonic stem cell

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