Variant report

Variant	rs60763897
Chromosome Location	chr7:40137549-40137550
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:40135569..40137778-chr7:40140510..40143010,2	MCF-7	breast:
2	chr7:40132356..40134649-chr7:40137450..40139023,2	K562	blood:
3	chr7:40131598..40134106-chr7:40137449..40139937,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000065883	Chromatin interaction

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs10232700	1.00[AFR][1000 genomes]
rs10237243	1.00[AFR][1000 genomes]
rs10268069	1.00[AFR][1000 genomes]
rs28367148	1.00[AFR][1000 genomes]
rs28681038	1.00[AFR][1000 genomes]
rs57920895	0.81[AFR][1000 genomes]

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	nsv1015322	chr7:40006195-40141195	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
2	esv2761319	chr7:40006195-40142139	Strong transcription Enhancers Weak transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv606708	chr7:40021044-40157040	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
4	nsv429748	chr7:40054760-40140660	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
5	esv2756801	chr7:40060180-40269583	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers 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	17 gene(s)	inside rSNPs	diseases
6	esv2759525	chr7:40060180-40269583	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
7	nsv887979	chr7:40067021-40193535	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
8	nsv887980	chr7:40067021-40203356	Strong transcription Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
9	nsv887981	chr7:40075461-40203356	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
10	nsv971193	chr7:40075881-40197955	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
11	esv34547	chr7:40077032-40230965	Strong transcription Enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
12	nsv824080	chr7:40077089-40198644	Weak transcription Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
13	nsv464437	chr7:40094641-40197168	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
14	nsv606709	chr7:40094641-40197168	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
15	nsv1032278	chr7:40097371-40396300	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
16	nsv887982	chr7:40098787-40193535	Weak transcription Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
17	esv3324215	chr7:40135127-40141025	Enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:40117600-40138000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr7:40122800-40137600	Strong transcription	Dnd41	blood
3	chr7:40124000-40137600	Strong transcription	Duodenum Mucosa	Duodenum
4	chr7:40124000-40137800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr7:40124000-40138400	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr7:40124400-40137800	Strong transcription	Primary T cells from cord blood	blood
7	chr7:40125000-40137600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
8	chr7:40125800-40137600	Strong transcription	Rectal Mucosa Donor 31	rectum
9	chr7:40125800-40137800	Strong transcription	Primary T helper cells PMA-I stimulated	--
10	chr7:40126000-40142400	Weak transcription	Fetal Heart	heart
11	chr7:40127400-40137600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr7:40131000-40137800	Strong transcription	HSMM	muscle
13	chr7:40131200-40137600	Strong transcription	Hela-S3	cervix
14	chr7:40131400-40137800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr7:40131400-40141400	Weak transcription	Stomach Mucosa	stomach
16	chr7:40131600-40137600	Strong transcription	Rectal Mucosa Donor 29	rectum
17	chr7:40132400-40137600	Strong transcription	NH-A	brain
18	chr7:40134200-40137600	Weak transcription	Colon Smooth Muscle	Colon
19	chr7:40134600-40138200	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr7:40134600-40140800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr7:40134600-40141000	Weak transcription	Ovary	ovary
22	chr7:40134600-40141200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr7:40134600-40141200	Weak transcription	Brain Cingulate Gyrus	brain
24	chr7:40134600-40141200	Weak transcription	Colonic Mucosa	Colon
25	chr7:40134600-40141200	Weak transcription	Esophagus	oesophagus
26	chr7:40134600-40145200	Weak transcription	Aorta	Aorta
27	chr7:40134600-40148200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr7:40134600-40151400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr7:40134600-40151600	Weak transcription	Gastric	stomach
30	chr7:40134600-40159600	Weak transcription	Left Ventricle	heart
31	chr7:40134600-40161800	Weak transcription	Pancreas	Pancrea
32	chr7:40134600-40171800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr7:40134600-40173200	Weak transcription	Lung	lung
34	chr7:40134800-40141000	Weak transcription	Psoas Muscle	Psoas
35	chr7:40134800-40143400	Weak transcription	Brain Substantia Nigra	brain
36	chr7:40134800-40148200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
37	chr7:40134800-40155800	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr7:40134800-40166800	Weak transcription	Fetal Stomach	stomach
39	chr7:40135000-40137600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr7:40135000-40138600	Weak transcription	Brain Angular Gyrus	brain
41	chr7:40135000-40149000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
42	chr7:40135000-40152400	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr7:40135000-40157000	Weak transcription	HSMMtube	muscle
44	chr7:40135000-40166800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr7:40135000-40172800	Weak transcription	Fetal Kidney	kidney
46	chr7:40135200-40147400	Weak transcription	Brain Germinal Matrix	brain
47	chr7:40135200-40153200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr7:40135200-40153800	Weak transcription	Stomach Smooth Muscle	stomach
49	chr7:40135200-40171000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr7:40135200-40171400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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