Variant report

Variant	rs6906716
Chromosome Location	chr6:150967987-150967988
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:150966591..150968646-chr6:150981306..150983343,2	MCF-7	breast:
2	chr6:150960489..150962367-chr6:150966319..150968724,2	MCF-7	breast:

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

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs12198116	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs275344	0.83[JPT][hapmap]
rs275345	0.83[JPT][hapmap]
rs6557549	1.00[CEU][hapmap];0.99[EUR][1000 genomes]
rs6936123	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs931488	0.91[CHB][hapmap]
rs9372083	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9384570	0.84[JPT][hapmap];0.81[ASN][1000 genomes]
rs9384571	0.83[JPT][hapmap];0.81[ASN][1000 genomes]
rs9384572	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9397340	0.81[CHB][hapmap]
rs981392	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[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	nsv886772	chr6:150743364-151024280	Enhancers Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv886774	chr6:150931131-150983318	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1030326	chr6:150967665-151641372	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS 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 miRNA target site	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150955800-150972400	Weak transcription	Fetal Stomach	stomach
2	chr6:150958200-150971200	Weak transcription	Left Ventricle	heart
3	chr6:150959800-150987400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:150960400-150980600	Weak transcription	Stomach Mucosa	stomach
5	chr6:150961600-150975200	Weak transcription	Fetal Muscle Trunk	muscle
6	chr6:150961600-150980200	Weak transcription	Lung	lung
7	chr6:150961800-150972600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr6:150963000-150979200	Weak transcription	Fetal Lung	lung
9	chr6:150963800-150974200	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr6:150964000-150974000	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr6:150964200-150975200	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr6:150964600-150971200	Weak transcription	Brain Substantia Nigra	brain
13	chr6:150964600-150977400	Weak transcription	Small Intestine	intestine
14	chr6:150964600-150979200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr6:150964600-150980000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr6:150964800-150975400	Weak transcription	Fetal Kidney	kidney
17	chr6:150964800-150987400	Weak transcription	Brain Cingulate Gyrus	brain
18	chr6:150965000-150971400	Weak transcription	Fetal Thymus	thymus
19	chr6:150965000-150971600	Weak transcription	Primary B cells from peripheral blood	blood
20	chr6:150965000-150974600	Weak transcription	Thymus	Thymus
21	chr6:150967000-150968000	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr6:150967000-150968800	Enhancers	Brain Germinal Matrix	brain
23	chr6:150967400-150975400	Weak transcription	Esophagus	oesophagus
24	chr6:150967800-150968200	Weak transcription	Primary B cells from cord blood	blood
25	chr6:150967800-150968400	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr6:150967800-150968800	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr6:150967800-150974400	Weak transcription	Spleen	Spleen
28	chr6:150967800-150980200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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