Variant report

Variant	rs2003506
Chromosome Location	chr7:104761741-104761742
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:104760924..104763369-chr7:104766253..104769218,2	MCF-7	breast:
2	chr7:104755441..104758675-chr7:104758800..104762280,3	K562	blood:
3	chr7:104651567..104655647-chr7:104761359..104764221,4	K562	blood:
4	chr7:104752347..104754991-chr7:104761307..104763859,2	K562	blood:
5	chr7:104652845..104655647-chr7:104761359..104763517,2	K562	blood:

Variant related genes	Relation type
ENSG00000239569	Chromatin interaction
ENSG00000005483	Chromatin interaction
ENSG00000135250	Chromatin interaction
ENSG00000228393	Chromatin interaction

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs1019040	0.81[ASN][1000 genomes]
rs10238507	0.88[EUR][1000 genomes]
rs10487150	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10953468	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1142	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1143	0.81[ASN][1000 genomes]
rs1144	0.91[EUR][1000 genomes]
rs11760317	0.91[EUR][1000 genomes]
rs2192932	0.81[EUR][1000 genomes]
rs2299304	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs3823752	0.81[EUR][1000 genomes]
rs6948885	0.82[EUR][1000 genomes]
rs6950620	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6967587	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7797912	0.95[EUR][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	nsv888927	chr7:104614664-104781644	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
2	esv34588	chr7:104737612-105153242	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	esv2757233	chr7:104758250-105208492	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
4	esv2759549	chr7:104758250-105208492	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:104678000-104812200	Strong transcription	Dnd41	blood
2	chr7:104740400-104787400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr7:104750200-104777000	Weak transcription	Right Atrium	heart
4	chr7:104752800-104763200	Weak transcription	Fetal Heart	heart
5	chr7:104752800-104807400	Weak transcription	Fetal Brain Male	brain
6	chr7:104753600-104768000	Weak transcription	Psoas Muscle	Psoas
7	chr7:104753800-104762000	Weak transcription	NHEK	skin
8	chr7:104753800-104763800	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr7:104753800-104764400	Weak transcription	Esophagus	oesophagus
10	chr7:104753800-104764400	Weak transcription	Fetal Stomach	stomach
11	chr7:104753800-104764400	Weak transcription	Pancreas	Pancrea
12	chr7:104753800-104764400	Weak transcription	Spleen	Spleen
13	chr7:104753800-104764600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr7:104753800-104765800	Weak transcription	Right Ventricle	heart
15	chr7:104753800-104766200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr7:104753800-104766200	Weak transcription	Gastric	stomach
17	chr7:104753800-104768400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr7:104753800-104772200	Weak transcription	Aorta	Aorta
19	chr7:104753800-104772800	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr7:104753800-104776600	Weak transcription	Stomach Mucosa	stomach
21	chr7:104753800-104822000	Weak transcription	Small Intestine	intestine
22	chr7:104754400-104776800	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr7:104754400-104850400	Weak transcription	Fetal Kidney	kidney
24	chr7:104754800-104764400	Weak transcription	Brain Germinal Matrix	brain
25	chr7:104754800-104765800	Weak transcription	Rectal Smooth Muscle	rectum
26	chr7:104755000-104772600	Weak transcription	Fetal Brain Female	brain
27	chr7:104755200-104767000	Weak transcription	Skeletal Muscle Male	skeletal muscle
28	chr7:104755200-104782000	Weak transcription	Colonic Mucosa	Colon
29	chr7:104755600-104776600	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr7:104755600-104778200	Weak transcription	Hela-S3	cervix
31	chr7:104755600-104790400	Weak transcription	NH-A	brain
32	chr7:104756000-104764200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr7:104756000-104765600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr7:104756200-104765800	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr7:104756400-104779400	Weak transcription	A549	lung
36	chr7:104756400-104806600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
37	chr7:104756800-104764000	Weak transcription	K562	blood
38	chr7:104757400-104764400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr7:104757800-104763800	Weak transcription	Adipose Nuclei	Adipose
40	chr7:104757800-104764400	Weak transcription	HSMM	muscle
41	chr7:104757800-104765600	Weak transcription	HUVEC	blood vessel
42	chr7:104758400-104762000	Weak transcription	Fetal Lung	lung
43	chr7:104758400-104763000	Weak transcription	Primary monocytes fromperipheralblood	blood
44	chr7:104758400-104763800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr7:104758400-104764200	Weak transcription	NHDF-Ad	bronchial
46	chr7:104758400-104764400	Weak transcription	Colon Smooth Muscle	Colon
47	chr7:104758400-104764400	Weak transcription	Duodenum Mucosa	Duodenum
48	chr7:104758600-104762000	Weak transcription	Fetal Muscle Leg	muscle
49	chr7:104758600-104762600	Weak transcription	Brain Cingulate Gyrus	brain
50	chr7:104758600-104765800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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