Variant report

Variant	rs74060260
Chromosome Location	chr14:70131250-70131251
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:70129166..70132900-chr14:70155782..70158446,3	K562	blood:
2	chr14:70130032..70132900-chr14:70156054..70158446,2	K562	blood:
3	chr14:70123757..70125764-chr14:70130188..70132000,2	K562	blood:
4	chr14:70129521..70131459-chr14:70177879..70180104,2	MCF-7	breast:
5	chr14:70126205..70128384-chr14:70129571..70131836,3	K562	blood:

Variant related genes	Relation type
ENSG00000100647	Chromatin interaction

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs17107167	0.84[AFR][1000 genomes]
rs55634075	1.00[AFR][1000 genomes]
rs56762756	0.83[AFR][1000 genomes]
rs58658815	0.84[AFR][1000 genomes]
rs61389585	1.00[AFR][1000 genomes]
rs61710255	1.00[AFR][1000 genomes]
rs74060254	0.84[AFR][1000 genomes]
rs74060255	0.84[AFR][1000 genomes]
rs74060265	0.83[AFR][1000 genomes]
rs74060266	1.00[AFR][1000 genomes]
rs74060268	1.00[AFR][1000 genomes]
rs74060273	1.00[AFR][1000 genomes]
rs74060275	0.83[AFR][1000 genomes]
rs74060276	1.00[AFR][1000 genomes]
rs74060279	1.00[AFR][1000 genomes]
rs74060287	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049280	chr14:70036804-70172630	Weak transcription Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv542124	chr14:70036804-70172630	Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv456336	chr14:70081956-70574149	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
4	nsv565007	chr14:70081956-70574149	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:70123200-70143800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
2	chr14:70123800-70137600	Weak transcription	Dnd41	blood
3	chr14:70125200-70131400	Genic enhancers	GM12878-XiMat	blood
4	chr14:70125600-70132600	Weak transcription	HSMMtube	muscle
5	chr14:70125800-70131600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr14:70125800-70132200	Enhancers	Stomach Mucosa	stomach
7	chr14:70125800-70133400	Weak transcription	HSMM	muscle
8	chr14:70125800-70133600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr14:70127200-70131600	Genic enhancers	Primary T helper cells fromperipheralblood	blood
10	chr14:70127200-70133200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr14:70127200-70139200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr14:70127400-70133400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr14:70127400-70133800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr14:70127400-70134200	Enhancers	Colon Smooth Muscle	Colon
15	chr14:70127400-70134200	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr14:70127400-70137200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr14:70127600-70134800	Enhancers	Skeletal Muscle Female	skeletal muscle
18	chr14:70127600-70135000	Enhancers	Adipose Nuclei	Adipose
19	chr14:70127600-70135000	Enhancers	Psoas Muscle	Psoas
20	chr14:70127800-70133000	Enhancers	HepG2	liver
21	chr14:70127800-70133600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
22	chr14:70127800-70134000	Enhancers	Fetal Intestine Large	intestine
23	chr14:70128000-70132600	Enhancers	Right Ventricle	heart
24	chr14:70128000-70133000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr14:70128200-70133600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr14:70128200-70140200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr14:70128400-70131600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr14:70128400-70132800	Weak transcription	HUVEC	blood vessel
29	chr14:70128400-70133800	Enhancers	Primary T helper cells PMA-I stimulated	--
30	chr14:70128400-70136200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr14:70128400-70138000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr14:70128400-70138000	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr14:70128600-70131400	Weak transcription	Ovary	ovary
34	chr14:70128600-70133600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr14:70128600-70137800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr14:70129000-70132400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr14:70129000-70132800	Weak transcription	Esophagus	oesophagus
38	chr14:70129000-70134000	Enhancers	Liver	Liver
39	chr14:70129000-70137000	Enhancers	Small Intestine	intestine
40	chr14:70129200-70132000	Enhancers	Rectal Mucosa Donor 31	rectum
41	chr14:70129200-70133000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr14:70129200-70133800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
43	chr14:70129200-70135000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
44	chr14:70129400-70133200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr14:70129400-70134200	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr14:70129400-70134800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr14:70129600-70131400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr14:70129600-70134200	Enhancers	Fetal Heart	heart
49	chr14:70129800-70131800	Genic enhancers	Monocytes-CD14+_RO01746	blood
50	chr14:70129800-70134000	Enhancers	K562	blood

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