Variant report

Variant	rs7141082
Chromosome Location	chr14:69281215-69281216
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:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:68851706..68853897-chr14:69281039..69283463,3	MCF-7	breast:
2	chr14:69086694..69088416-chr14:69280164..69284434,3	K562	blood:
3	chr14:68934022..68936494-chr14:69279866..69281612,2	K562	blood:
4	chr14:68671642..68674353-chr14:69280864..69282712,2	MCF-7	breast:
5	chr14:68409426..68412262-chr14:69280020..69282868,2	MCF-7	breast:
6	chr14:68552453..68555171-chr14:69280931..69283453,2	MCF-7	breast:
7	chr14:68658060..68659603-chr14:69279653..69281747,2	MCF-7	breast:
8	chr14:68712832..68721681-chr14:69280637..69286048,12	MCF-7	breast:
9	chr14:69281086..69282985-chr14:69289138..69291882,2	K562	blood:
10	chr14:68609991..68612093-chr14:69279827..69282795,2	MCF-7	breast:
11	chr14:69125254..69128271-chr14:69281181..69284141,4	MCF-7	breast:
12	chr14:69270505..69278428-chr14:69279681..69285729,13	K562	blood:
13	chr14:68676342..68679181-chr14:69280243..69283048,2	MCF-7	breast:
14	chr14:68710192..68712093-chr14:69280950..69283017,2	MCF-7	breast:
15	chr14:68734764..68737197-chr14:69278376..69281274,2	MCF-7	breast:
16	chr14:68406192..68411564-chr14:69279428..69286293,11	MCF-7	breast:
17	chr14:68429695..68431817-chr14:69281066..69283231,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000182185	Chromatin interaction

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11847206	0.84[AMR][1000 genomes]
rs11848561	0.93[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs55753128	0.84[AMR][1000 genomes]
rs56944540	0.93[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs57487210	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57544284	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59647223	0.84[AMR][1000 genomes]
rs73279154	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs73279175	1.00[EUR][1000 genomes]
rs74060189	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8008250	0.91[AMR][1000 genomes]
rs8011424	0.95[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs9743642	0.84[AMR][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	nsv1035267	chr14:69230254-69348126	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
2	nsv542123	chr14:69230254-69348126	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
3	nsv902070	chr14:69244214-69308182	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	78 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:69276600-69286200	Weak transcription	Ovary	ovary
2	chr14:69279200-69282800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr14:69279200-69283000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr14:69279400-69281800	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr14:69279600-69281800	Enhancers	Brain Anterior Caudate	brain
6	chr14:69279800-69281800	Enhancers	H1 Cell Line	embryonic stem cell
7	chr14:69279800-69282800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr14:69279800-69282800	Enhancers	Spleen	Spleen
9	chr14:69279800-69283000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr14:69279800-69283000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
11	chr14:69279800-69284000	Enhancers	Placenta	Placenta
12	chr14:69280000-69281400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr14:69280000-69281400	Flanking Active TSS	Primary B cells from cord blood	blood
14	chr14:69280000-69281800	Enhancers	Primary hematopoietic stem cells	blood
15	chr14:69280000-69281800	Enhancers	Pancreas	Pancrea
16	chr14:69280000-69282000	Enhancers	Stomach Mucosa	stomach
17	chr14:69280000-69282200	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr14:69280000-69282200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
19	chr14:69280000-69282600	Enhancers	Esophagus	oesophagus
20	chr14:69280000-69282800	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr14:69280000-69282800	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr14:69280000-69282800	Enhancers	Left Ventricle	heart
23	chr14:69280000-69282800	Enhancers	Psoas Muscle	Psoas
24	chr14:69280000-69283000	Flanking Active TSS	Colon Smooth Muscle	Colon
25	chr14:69280000-69283000	Enhancers	Lung	lung
26	chr14:69280000-69283000	Flanking Active TSS	GM12878-XiMat	blood
27	chr14:69280000-69283800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr14:69280200-69281400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
29	chr14:69280200-69281600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
30	chr14:69280200-69282600	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr14:69280200-69282600	Flanking Active TSS	Primary T cells from cord blood	blood
32	chr14:69280200-69282600	Enhancers	Sigmoid Colon	Sigmoid Colon
33	chr14:69280200-69283000	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr14:69280200-69284400	Flanking Active TSS	Stomach Smooth Muscle	stomach
35	chr14:69280400-69281400	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
36	chr14:69280400-69282800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr14:69280400-69282800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr14:69280400-69283200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr14:69280600-69281400	Enhancers	HUVEC	blood vessel
40	chr14:69280600-69281600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr14:69280600-69282400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr14:69280600-69283000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
43	chr14:69280600-69283000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
44	chr14:69280600-69283000	Flanking Active TSS	Duodenum Mucosa	Duodenum
45	chr14:69280600-69283000	Flanking Active TSS	Rectal Smooth Muscle	rectum
46	chr14:69280600-69283200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
47	chr14:69280600-69283200	Flanking Active TSS	Brain Hippocampus Middle	brain
48	chr14:69280800-69281400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr14:69280800-69281400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
50	chr14:69280800-69281400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--

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