Variant report

Variant	rs2635042
Chromosome Location	chr18:44680214-44680215
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr18:44680213-44680682	HepG2	liver:	n/a	n/a
2	POLR2A	chr18:44678500-44681193	HepG2	liver:	n/a	n/a

Variant related genes	Relation type
HDHD2	TF binding region

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs11663321	0.96[ASN][1000 genomes]
rs12960378	0.83[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12963648	0.82[ASN][1000 genomes]
rs2251948	0.85[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2277717	0.96[ASN][1000 genomes]
rs2461247	0.85[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2571001	1.00[ASN][1000 genomes]
rs2571009	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs2571016	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs2576030	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs2576031	1.00[ASN][1000 genomes]
rs2576056	0.85[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2576060	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs2635040	0.85[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2635041	0.82[ASN][1000 genomes]
rs2635043	1.00[ASN][1000 genomes]
rs2635045	0.82[ASN][1000 genomes]
rs2635046	1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs2635049	0.85[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2635050	0.98[ASN][1000 genomes]
rs2668779	0.89[ASN][1000 genomes]
rs2684818	1.00[JPT][hapmap]
rs2684820	1.00[ASN][1000 genomes]
rs2684822	0.82[ASN][1000 genomes]
rs2684825	1.00[ASN][1000 genomes]
rs2684826	1.00[ASN][1000 genomes]
rs28693565	0.96[ASN][1000 genomes]
rs2932126	1.00[JPT][hapmap]
rs3816125	0.90[JPT][hapmap];0.87[ASN][1000 genomes]
rs7242978	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs7504798	0.85[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs9304341	0.82[ASN][1000 genomes]
rs9960264	0.90[JPT][hapmap];0.87[ASN][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	nsv9629	chr18:44264693-44757511	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv833640	chr18:44552276-44714872	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv909612	chr18:44560875-44681485	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	nsv909613	chr18:44644530-44690107	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44677600-44685400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr18:44677600-44700200	Weak transcription	Aorta	Aorta
3	chr18:44677800-44680400	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr18:44677800-44680400	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr18:44677800-44680400	Weak transcription	Fetal Thymus	thymus
6	chr18:44677800-44680400	Weak transcription	Ovary	ovary
7	chr18:44677800-44680400	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr18:44677800-44680400	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr18:44677800-44680600	Weak transcription	HMEC	breast
10	chr18:44677800-44680800	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr18:44677800-44681000	Weak transcription	Brain Germinal Matrix	brain
12	chr18:44677800-44682800	Weak transcription	Colonic Mucosa	Colon
13	chr18:44677800-44684800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr18:44677800-44685600	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr18:44677800-44686400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr18:44677800-44686600	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr18:44677800-44686600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr18:44677800-44689800	Weak transcription	Rectal Smooth Muscle	rectum
19	chr18:44677800-44693400	Weak transcription	Gastric	stomach
20	chr18:44677800-44698200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr18:44677800-44699000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr18:44677800-44700400	Weak transcription	Spleen	Spleen
23	chr18:44677800-44701000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr18:44677800-44701000	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr18:44677800-44701000	Weak transcription	A549	lung
26	chr18:44677800-44701800	Weak transcription	Esophagus	oesophagus
27	chr18:44678000-44680400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr18:44678000-44680400	Weak transcription	Primary B cells from cord blood	blood
29	chr18:44678000-44680400	Weak transcription	Brain Anterior Caudate	brain
30	chr18:44678000-44680400	Weak transcription	Duodenum Mucosa	Duodenum
31	chr18:44678000-44680600	Weak transcription	Placenta Amnion	Placenta Amnion
32	chr18:44678000-44681600	Weak transcription	Brain Hippocampus Middle	brain
33	chr18:44678000-44682200	Weak transcription	Fetal Brain Female	brain
34	chr18:44678000-44682800	Weak transcription	Brain Substantia Nigra	brain
35	chr18:44678000-44683400	Weak transcription	Brain Cingulate Gyrus	brain
36	chr18:44678000-44684400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr18:44678000-44687000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr18:44678000-44689200	Weak transcription	GM12878-XiMat	blood
39	chr18:44678000-44699600	Weak transcription	Colon Smooth Muscle	Colon
40	chr18:44678000-44700400	Weak transcription	Small Intestine	intestine
41	chr18:44678000-44700800	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr18:44678000-44701000	Weak transcription	Fetal Stomach	stomach
43	chr18:44678200-44680400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
44	chr18:44678200-44680400	Weak transcription	Primary B cells from peripheral blood	blood
45	chr18:44678200-44680400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr18:44678200-44680400	Weak transcription	Adipose Nuclei	Adipose
47	chr18:44678200-44683400	Weak transcription	Stomach Smooth Muscle	stomach
48	chr18:44678200-44684200	Weak transcription	Fetal Brain Male	brain
49	chr18:44678200-44685400	Weak transcription	Hela-S3	cervix
50	chr18:44678200-44685600	Weak transcription	Pancreatic Islets	Pancreatic Islet

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