Variant report

Variant	rs73728117
Chromosome Location	chr7:150023090-150023091
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4)
CpG islands
(count:0)
Chromatin interactive
region (count:14)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr7:150023045-150023114	GM12878	blood:	n/a	n/a
2	FOXA2	chr7:150022942-150023239	HepG2	liver:	n/a	n/a
3	CEBPB	chr7:150023055-150023129	K562	blood:	n/a	chr7:150023081-150023092
4	CEBPB	chr7:150022991-150023196	HepG2	liver:	n/a	chr7:150023081-150023092

No data

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

No.	Distal block	Cell Line	Cell type
1	chr7:150019150..150025305-chr7:150035524..150043799,10	MCF-7	breast:
2	chr7:150018389..150025798-chr7:150030734..150040389,17	MCF-7	breast:
3	chr7:150022933..150025401-chr7:150110012..150111550,2	K562	blood:
4	chr7:150021516..150023885-chr7:150100772..150104958,4	K562	blood:
5	chr7:150017660..150019696-chr7:150021703..150024720,3	MCF-7	breast:
6	chr7:150017073..150026383-chr7:150074145..150079980,13	MCF-7	breast:
7	chr7:150022690..150024481-chr7:150024522..150026288,2	MCF-7	breast:
8	chr7:150021836..150024611-chr7:150100772..150103819,4	K562	blood:
9	chr7:150018539..150023441-chr7:150073756..150077036,7	MCF-7	breast:
10	chr7:150021038..150023907-chr7:150765022..150767583,2	MCF-7	breast:
11	chr7:150022840..150024821-chr7:150064135..150066417,2	MCF-7	breast:
12	chr7:150015754..150018552-chr7:150022043..150024814,2	MCF-7	breast:
13	chr7:150018458..150023402-chr7:150064103..150067772,7	MCF-7	breast:
14	chr7:150020266..150021791-chr7:150021831..150023826,2	MCF-7	breast:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRC61-3	chr7:150022930-150023099	NONHSAT124103

No data

Variant related genes	Relation type
ZBED6CL	TF binding region
ACTR3C	TF binding region
ENSG00000106526	Chromatin interaction
ENSG00000261305	Chromatin interaction
ENSG00000127399	Chromatin interaction
ENSG00000106538	Chromatin interaction
ENSG00000164889	Chromatin interaction
ENSG00000196456	Chromatin interaction
ENSG00000214022	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs55732298	1.00[AMR][1000 genomes]
rs57637449	1.00[AMR][1000 genomes]
rs58431502	1.00[AMR][1000 genomes]
rs59330319	1.00[AMR][1000 genomes]
rs61322575	1.00[AMR][1000 genomes]
rs6953531	1.00[AMR][1000 genomes]
rs73728108	1.00[AMR][1000 genomes]
rs73728111	1.00[AMR][1000 genomes]
rs73728113	1.00[AMR][1000 genomes]
rs73728114	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7788084	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034409	chr7:149844639-150447071	Flanking Active TSS Active TSS Genic enhancers Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
2	nsv608990	chr7:149961274-150707488	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
3	nsv1015582	chr7:149967986-150285104	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
4	nsv508490	chr7:150006068-150051241	Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
5	nsv889453	chr7:150009838-150104410	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
6	nsv889454	chr7:150009838-150115183	Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
7	nsv889455	chr7:150013393-150104410	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
8	nsv889456	chr7:150013393-150115183	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
9	nsv1017368	chr7:150016952-150655773	Bivalent Enhancer ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
10	nsv539195	chr7:150016952-150655773	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
11	nsv516052	chr7:150020295-150034184	Genic enhancers Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
12	nsv518774	chr7:150020295-150036664	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
13	nsv889457	chr7:150020295-150104410	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
14	nsv889458	chr7:150020295-150115183	Enhancers Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
15	nsv521407	chr7:150020295-150118590	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:100 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150020400-150030000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:150020600-150023600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
3	chr7:150021200-150023400	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr7:150021400-150026600	Weak transcription	Brain Cingulate Gyrus	brain
5	chr7:150021400-150029400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr7:150021400-150037000	Weak transcription	Brain Substantia Nigra	brain
7	chr7:150021600-150025600	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr7:150021600-150026400	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr7:150021600-150026600	Weak transcription	Brain Hippocampus Middle	brain
10	chr7:150021600-150026600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr7:150021600-150028800	Weak transcription	NHEK	skin
12	chr7:150021800-150023600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr7:150021800-150024000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr7:150021800-150025600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr7:150021800-150026600	Weak transcription	Brain Anterior Caudate	brain
16	chr7:150021800-150030800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
17	chr7:150021800-150032600	Weak transcription	Brain Angular Gyrus	brain
18	chr7:150021800-150033600	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr7:150021800-150037200	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr7:150022000-150023400	Enhancers	Adipose Nuclei	Adipose
21	chr7:150022000-150023800	Weak transcription	Rectal Smooth Muscle	rectum
22	chr7:150022000-150025600	Weak transcription	Rectal Mucosa Donor 29	rectum
23	chr7:150022000-150026400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
24	chr7:150022000-150032200	Weak transcription	Colon Smooth Muscle	Colon
25	chr7:150022000-150032200	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr7:150022000-150036400	Weak transcription	Fetal Kidney	kidney
27	chr7:150022200-150025000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
28	chr7:150022200-150025400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr7:150022200-150025800	Strong transcription	HUES6 Cell Line	embryonic stem cell
30	chr7:150022200-150026600	Weak transcription	Colonic Mucosa	Colon
31	chr7:150022200-150031400	Strong transcription	Thymus	Thymus
32	chr7:150022200-150031600	Strong transcription	Fetal Stomach	stomach
33	chr7:150022200-150037200	Weak transcription	Small Intestine	intestine
34	chr7:150022400-150023200	Weak transcription	Primary T cells fromperipheralblood	blood
35	chr7:150022400-150023400	Transcr. at gene 5' and 3'	Hela-S3	cervix
36	chr7:150022400-150023800	Weak transcription	Gastric	stomach
37	chr7:150022400-150024000	Genic enhancers	K562	blood
38	chr7:150022400-150024200	Strong transcription	iPS-15b Cell Line	embryonic stem cell
39	chr7:150022400-150025000	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr7:150022400-150025600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
41	chr7:150022400-150026000	Strong transcription	HUES64 Cell Line	embryonic stem cell
42	chr7:150022400-150026400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr7:150022400-150026400	Weak transcription	HSMMtube	muscle
44	chr7:150022400-150027400	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr7:150022400-150029200	Weak transcription	Right Atrium	heart
46	chr7:150022400-150031200	Strong transcription	Primary T cells from cord blood	blood
47	chr7:150022400-150032200	Strong transcription	Fetal Intestine Small	intestine
48	chr7:150022400-150035600	Weak transcription	Fetal Heart	heart
49	chr7:150022400-150037400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
50	chr7:150022600-150023200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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