Variant report

Variant	rs11976682
Chromosome Location	chr7:150972140-150972141
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:150971574..150973333-chr7:151038730..151040359,2	K562	blood:
2	chr7:150971574..150974411-chr7:151038667..151040359,3	K562	blood:
3	chr7:150941689..150943266-chr7:150971664..150974365,2	K562	blood:
4	chr7:150922541..150925891-chr7:150969834..150974111,4	K562	blood:
5	chr7:150809552..150813512-chr7:150971172..150974114,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000082014	Chromatin interaction
ENSG00000133612	Chromatin interaction
ENSG00000013374	Chromatin interaction
ENSG00000033050	Chromatin interaction

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10236491	1.00[AMR][1000 genomes]
rs10238747	1.00[AMR][1000 genomes]
rs10268063	1.00[AMR][1000 genomes]
rs11972504	1.00[AMR][1000 genomes]
rs11973593	1.00[AMR][1000 genomes]
rs11976868	1.00[AMR][1000 genomes]
rs61453037	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1821419	chr7:150593315-150974269	Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	128 gene(s)	inside rSNPs	diseases
2	nsv889487	chr7:150922952-150988172	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
3	nsv465216	chr7:150951819-150991795	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
4	nsv609036	chr7:150951819-150991795	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
5	nsv1023436	chr7:150967147-150997692	Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
6	nsv1022782	chr7:150970748-150992935	Weak transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150950400-150973400	Weak transcription	Brain Substantia Nigra	brain
2	chr7:150959600-150972800	Weak transcription	Ovary	ovary
3	chr7:150960200-150973200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr7:150967400-150973000	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr7:150967800-150972800	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr7:150968000-150972600	Weak transcription	Brain Hippocampus Middle	brain
7	chr7:150968000-150974000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr7:150968200-150973800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
9	chr7:150968400-150973200	Weak transcription	Brain Angular Gyrus	brain
10	chr7:150969000-150972800	Weak transcription	Colonic Mucosa	Colon
11	chr7:150969000-150973000	Enhancers	Fetal Brain Male	brain
12	chr7:150969000-150973400	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr7:150969200-150973200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
14	chr7:150969400-150972200	Enhancers	Fetal Brain Female	brain
15	chr7:150969400-150972200	Weak transcription	Fetal Intestine Small	intestine
16	chr7:150969600-150972600	Weak transcription	Liver	Liver
17	chr7:150969600-150972800	Weak transcription	Primary T helper cells fromperipheralblood	blood
18	chr7:150969600-150972800	Weak transcription	Colon Smooth Muscle	Colon
19	chr7:150969600-150973000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr7:150969600-150973000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr7:150969600-150973200	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr7:150969600-150973200	Weak transcription	Hela-S3	cervix
23	chr7:150969800-150972600	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr7:150969800-150972800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
25	chr7:150969800-150972800	Weak transcription	Primary T helper cells PMA-I stimulated	--
26	chr7:150969800-150972800	Weak transcription	Esophagus	oesophagus
27	chr7:150969800-150973000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
28	chr7:150970000-150972400	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr7:150970000-150972600	Strong transcription	Fetal Stomach	stomach
30	chr7:150970000-150972800	Weak transcription	Fetal Lung	lung
31	chr7:150970000-150973000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
32	chr7:150970000-150973200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr7:150970000-150973400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr7:150970000-150974200	Weak transcription	Primary T cells from cord blood	blood
35	chr7:150970200-150973000	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr7:150970200-150973400	Weak transcription	Primary hematopoietic stem cells	blood
37	chr7:150970400-150973400	Weak transcription	Adipose Nuclei	Adipose
38	chr7:150970600-150972400	Weak transcription	Right Ventricle	heart
39	chr7:150970600-150974000	Weak transcription	Left Ventricle	heart
40	chr7:150970800-150972400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr7:150970800-150972600	Strong transcription	Cortex derived primary cultured neurospheres	brain
42	chr7:150970800-150972800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr7:150970800-150975000	Enhancers	Spleen	Spleen
44	chr7:150971200-150972600	Enhancers	Fetal Muscle Trunk	muscle
45	chr7:150971400-150972200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr7:150971400-150972800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr7:150971400-150973200	Weak transcription	Fetal Heart	heart
48	chr7:150971600-150972400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr7:150971600-150973000	Weak transcription	Lung	lung
50	chr7:150971600-150973200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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