Variant report

Variant	rs67045330
Chromosome Location	chr7:20070576-20070577
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:20069778..20072332-chr7:20074470..20077366,2	MCF-7	breast:
2	chr7:20070077..20071655-chr7:20071816..20074085,2	MCF-7	breast:
3	chr7:20069192..20071216-chr7:20076408..20079057,2	K562	blood:

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10247632	0.88[ASN][1000 genomes]
rs10263340	0.84[ASN][1000 genomes]
rs10268448	0.86[ASN][1000 genomes]
rs17142321	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2160025	0.86[EUR][1000 genomes]
rs2190416	0.91[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs38129	0.90[ASN][1000 genomes]
rs38136	0.86[ASN][1000 genomes]
rs38137	0.86[ASN][1000 genomes]
rs38138	0.82[ASN][1000 genomes]
rs56104985	0.90[ASN][1000 genomes]
rs59439583	0.96[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs66662580	0.89[ASN][1000 genomes]
rs66926140	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs68109726	0.89[ASN][1000 genomes]
rs6953051	0.87[ASN][1000 genomes]
rs73076650	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7796210	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1033223	chr7:19682192-20461375	Enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv538795	chr7:19682192-20461375	Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
3	nsv1027445	chr7:19947297-20211733	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	nsv887830	chr7:19970584-20114589	Enhancers Strong transcription Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1027849	chr7:20003094-20084998	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	esv2762658	chr7:20023224-20127561	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv1023992	chr7:20053816-20104675	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:20060400-20075000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr7:20061400-20072800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr7:20067000-20092800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr7:20067600-20072800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr7:20067800-20073000	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr7:20068200-20077200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr7:20068400-20073000	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr7:20069200-20071000	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr7:20069400-20072800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr7:20069600-20071400	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr7:20070000-20070800	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr7:20070000-20070800	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr7:20070000-20070800	Enhancers	Rectal Smooth Muscle	rectum
14	chr7:20070000-20071000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr7:20070000-20071400	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr7:20070000-20071400	Enhancers	Primary B cells from peripheral blood	blood
17	chr7:20070000-20071400	Flanking Active TSS	GM12878-XiMat	blood
18	chr7:20070000-20071600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr7:20070000-20071600	Enhancers	Primary B cells from cord blood	blood
20	chr7:20070000-20072800	Enhancers	Osteobl	bone
21	chr7:20070000-20073000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr7:20070000-20073400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr7:20070000-20074000	Enhancers	NHDF-Ad	bronchial
24	chr7:20070200-20070600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr7:20070200-20070600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr7:20070200-20071200	Enhancers	HSMMtube	muscle
27	chr7:20070200-20071200	Enhancers	NH-A	brain
28	chr7:20070200-20072000	Enhancers	Colon Smooth Muscle	Colon
29	chr7:20070400-20071200	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr7:20070400-20074800	Weak transcription	H1 Cell Line	embryonic stem cell

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