Variant report

Variant	rs7140781
Chromosome Location	chr14:65211458-65211459
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:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:65197276..65199503-chr14:65210432..65212746,2	MCF-7	breast:
2	chr14:65211034..65213398-chr14:65224947..65227987,3	MCF-7	breast:
3	chr14:65170123..65171910-chr14:65210680..65212434,2	MCF-7	breast:
4	chr14:65181414..65183805-chr14:65210426..65213903,3	MCF-7	breast:
5	chr14:65170433..65175465-chr14:65207632..65214317,8	MCF-7	breast:
6	chr14:65210793..65213211-chr14:65239512..65241809,2	MCF-7	breast:
7	chr14:65206432..65210320-chr14:65210807..65215364,7	MCF-7	breast:
8	chr14:65203723..65205643-chr14:65211160..65213335,2	K562	blood:
9	chr14:65138592..65140467-chr14:65210995..65212825,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000126822	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10138034	0.88[EUR][1000 genomes]
rs11621159	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11621379	0.81[EUR][1000 genomes]
rs11622754	0.88[EUR][1000 genomes]
rs11625500	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11628301	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12883289	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12884903	0.88[EUR][1000 genomes]
rs12892852	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12895353	0.82[CEU][hapmap];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1553163	0.88[EUR][1000 genomes]
rs170683	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs170685	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs229622	0.82[CEU][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs229645	0.90[EUR][1000 genomes]
rs229648	1.00[ASN][1000 genomes]
rs229649	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs229653	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs229656	1.00[CEU][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34340219	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71420472	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs732311	0.82[CEU][hapmap];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9943995	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1818582	chr14:65172898-65256685	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA	11 gene(s)	inside rSNPs	diseases
2	nsv1035833	chr14:65176371-65246181	Enhancers Strong transcription Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
3	esv1801406	chr14:65193725-65264416	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA	11 gene(s)	inside rSNPs	diseases
4	nsv902023	chr14:65200821-65243885	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
5	nsv902024	chr14:65200821-65244950	Strong transcription Enhancers Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:65193200-65212200	Weak transcription	Fetal Heart	heart
2	chr14:65193400-65212400	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr14:65193400-65212400	Weak transcription	HSMMtube	muscle
4	chr14:65193600-65212800	Weak transcription	HUVEC	blood vessel
5	chr14:65193800-65212200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr14:65193800-65214400	Strong transcription	Primary monocytes fromperipheralblood	blood
7	chr14:65194200-65216200	Strong transcription	Cortex derived primary cultured neurospheres	brain
8	chr14:65196600-65212200	Weak transcription	NHLF	lung
9	chr14:65198000-65214800	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr14:65201000-65221800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr14:65201400-65212600	Strong transcription	Primary neutrophils fromperipheralblood	blood
12	chr14:65202200-65217400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr14:65202400-65212000	Strong transcription	Stomach Smooth Muscle	stomach
14	chr14:65202800-65211800	Strong transcription	Placenta Amnion	Placenta Amnion
15	chr14:65202800-65212200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr14:65202800-65213000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr14:65202800-65215200	Strong transcription	H9 Cell Line	embryonic stem cell
18	chr14:65203000-65211800	Weak transcription	Primary T cells from cord blood	blood
19	chr14:65203000-65214400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr14:65203200-65211800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr14:65203200-65212000	Weak transcription	Primary T helper cells PMA-I stimulated	--
22	chr14:65203400-65212000	Strong transcription	Colon Smooth Muscle	Colon
23	chr14:65203600-65212000	Strong transcription	Placenta	Placenta
24	chr14:65203600-65212400	Strong transcription	Brain Inferior Temporal Lobe	brain
25	chr14:65203600-65215000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
26	chr14:65203800-65212200	Strong transcription	HUES6 Cell Line	embryonic stem cell
27	chr14:65203800-65212400	Strong transcription	HUES64 Cell Line	embryonic stem cell
28	chr14:65203800-65212600	Strong transcription	HUES48 Cell Line	embryonic stem cell
29	chr14:65203800-65214400	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr14:65203800-65216800	Strong transcription	H1 Cell Line	embryonic stem cell
31	chr14:65204000-65212200	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr14:65204000-65212800	Strong transcription	Fetal Stomach	stomach
33	chr14:65204000-65213000	Strong transcription	Rectal Mucosa Donor 29	rectum
34	chr14:65204000-65215200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
35	chr14:65204000-65217200	Strong transcription	NHEK	skin
36	chr14:65204200-65211600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
37	chr14:65204200-65211600	Strong transcription	Sigmoid Colon	Sigmoid Colon
38	chr14:65204200-65212000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr14:65204200-65212400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr14:65204200-65212600	Strong transcription	Fetal Muscle Trunk	muscle
41	chr14:65204200-65216800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
42	chr14:65204200-65217400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr14:65204400-65211800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
44	chr14:65204400-65211800	Strong transcription	Brain Cingulate Gyrus	brain
45	chr14:65204400-65211800	Strong transcription	A549	lung
46	chr14:65204400-65212000	Strong transcription	Brain Hippocampus Middle	brain
47	chr14:65204400-65212400	Strong transcription	Rectal Mucosa Donor 31	rectum
48	chr14:65204400-65217000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr14:65204600-65212200	Strong transcription	HMEC	breast
50	chr14:65204600-65212400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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