Variant report

Variant	rs2177784
Chromosome Location	chr7:16887232-16887233
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:16885940..16887633-chr7:16888107..16889643,2	MCF-7	breast:
2	chr7:16880852..16883494-chr7:16885535..16888915,3	MCF-7	breast:
3	chr7:16886651..16887248-chr7:16961321..16961836,2	MCF-7	breast:
4	chr7:16852860..16855364-chr7:16884704..16887275,2	MCF-7	breast:
5	chr7:16847748..16852819-chr7:16884544..16888713,8	MCF-7	breast:
6	chr7:16883300..16885078-chr7:16885250..16887314,2	K562	blood:
7	chr7:16885425..16887633-chr7:16956037..16959031,2	MCF-7	breast:
8	chr7:16840256..16845659-chr7:16882127..16888432,10	MCF-7	breast:
9	chr7:16842139..16846678-chr7:16885089..16889372,16	MCF-7	breast:
10	chr7:16882638..16888125-chr7:16917806..16922749,7	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000106541	Chromatin interaction
ENSG00000173467	Chromatin interaction

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10227514	1.00[CEU][hapmap]
rs10228088	1.00[CEU][hapmap]
rs10228338	1.00[CEU][hapmap]
rs10237800	1.00[CEU][hapmap]
rs10260136	1.00[CEU][hapmap]
rs10273406	1.00[CEU][hapmap]
rs10275921	1.00[CEU][hapmap]
rs10280750	1.00[CEU][hapmap]
rs10282680	1.00[CEU][hapmap]
rs1149516	1.00[EUR][1000 genomes]
rs1149517	1.00[EUR][1000 genomes]
rs1149518	1.00[EUR][1000 genomes]
rs1149520	1.00[EUR][1000 genomes]
rs1149521	1.00[EUR][1000 genomes]
rs1149523	1.00[EUR][1000 genomes]
rs1149525	1.00[EUR][1000 genomes]
rs11976539	1.00[CEU][hapmap]
rs55722030	1.00[EUR][1000 genomes]
rs56302012	1.00[EUR][1000 genomes]
rs57776102	1.00[EUR][1000 genomes]
rs6968207	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs706054	1.00[EUR][1000 genomes]
rs706056	1.00[EUR][1000 genomes]
rs706058	1.00[EUR][1000 genomes]
rs706060	1.00[EUR][1000 genomes]
rs706066	1.00[EUR][1000 genomes]
rs706067	1.00[EUR][1000 genomes]
rs706068	1.00[EUR][1000 genomes]
rs706069	1.00[EUR][1000 genomes]
rs73067698	1.00[EUR][1000 genomes]
rs73069705	1.00[EUR][1000 genomes]
rs73069707	1.00[EUR][1000 genomes]
rs73069710	1.00[EUR][1000 genomes]
rs73069712	1.00[EUR][1000 genomes]
rs73069719	1.00[EUR][1000 genomes]
rs73069720	1.00[EUR][1000 genomes]
rs73069724	1.00[EUR][1000 genomes]
rs73069745	1.00[EUR][1000 genomes]
rs73069748	1.00[EUR][1000 genomes]
rs73069757	1.00[EUR][1000 genomes]
rs7777674	1.00[CEU][hapmap]
rs7802611	1.00[CEU][hapmap]
rs818492	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs818582	1.00[CEU][hapmap]
rs818584	1.00[CEU][hapmap]
rs818807	1.00[EUR][1000 genomes]
rs818808	1.00[EUR][1000 genomes]
rs819003	1.00[EUR][1000 genomes]
rs866565	1.00[EUR][1000 genomes]
rs9690166	1.00[CEU][hapmap]
rs9791491	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv887761	chr7:16834361-17732490	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	nsv887762	chr7:16834361-17746628	Enhancers Genic enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
3	nsv887763	chr7:16834361-17750811	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
4	nsv887764	chr7:16839835-17218800	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv887765	chr7:16839835-17750811	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
6	nsv1027284	chr7:16849986-17008167	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
7	nsv606339	chr7:16852808-17004301	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
8	nsv1016695	chr7:16854300-16991627	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
9	nsv1017413	chr7:16854300-17125005	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
10	nsv538749	chr7:16854300-17125005	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
11	nsv1015831	chr7:16854300-17732227	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
12	nsv538750	chr7:16854300-17732227	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
13	esv2752152	chr7:16863727-16946225	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
14	nsv870171	chr7:16872876-17188633	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
15	nsv529874	chr7:16877677-17703617	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
16	nsv532093	chr7:16877677-17712291	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
17	nsv887766	chr7:16883936-16991565	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:16880400-16889600	Weak transcription	Gastric	stomach
2	chr7:16885800-16892600	Enhancers	Primary hematopoietic stem cells	blood
3	chr7:16886000-16889600	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr7:16886000-16900000	Weak transcription	Small Intestine	intestine
5	chr7:16886200-16887400	Enhancers	Fetal Lung	lung
6	chr7:16886200-16887600	Flanking Active TSS	Hela-S3	cervix
7	chr7:16886200-16890400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr7:16886400-16887400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr7:16886400-16887600	Enhancers	NHEK	skin
10	chr7:16886400-16887800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr7:16886400-16889600	Weak transcription	Duodenum Mucosa	Duodenum
12	chr7:16886600-16887400	Enhancers	Muscle Satellite Cultured Cells	--
13	chr7:16886600-16887400	Enhancers	Fetal Kidney	kidney
14	chr7:16886600-16887400	Enhancers	HepG2	liver
15	chr7:16886600-16887600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr7:16886600-16890400	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr7:16886800-16887400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr7:16886800-16887400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr7:16886800-16887400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr7:16886800-16887400	Flanking Active TSS	Fetal Intestine Small	intestine
21	chr7:16886800-16887400	Active TSS	A549	lung
22	chr7:16886800-16887400	Enhancers	HSMMtube	muscle
23	chr7:16886800-16887600	Enhancers	Fetal Heart	heart
24	chr7:16886800-16887600	Flanking Active TSS	Fetal Intestine Large	intestine
25	chr7:16886800-16888200	Enhancers	Placenta	Placenta
26	chr7:16887000-16887400	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr7:16887000-16887400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr7:16887000-16887400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr7:16887000-16887400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr7:16887000-16887400	Enhancers	Fetal Muscle Leg	muscle
31	chr7:16887000-16887400	Enhancers	Pancreas	Pancrea
32	chr7:16887000-16887400	Enhancers	HSMM	muscle
33	chr7:16887000-16887400	Enhancers	Osteobl	bone
34	chr7:16887000-16887600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr7:16887200-16887400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
36	chr7:16887200-16887400	Flanking Active TSS	Stomach Mucosa	stomach
37	chr7:16887200-16887400	Enhancers	K562	blood
38	chr7:16887200-16887600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
39	chr7:16887200-16888200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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