Variant report

Variant	rs34035404
Chromosome Location	chr12:57569466-57569467
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:57517758..57518605-chr12:57568901..57570114,3	MCF-7	breast:
2	chr12:57401619..57402252-chr12:57569148..57569899,2	K562	blood:
3	chr12:57449683..57452110-chr12:57569238..57570942,2	K562	blood:
4	chr12:57568829..57570904-chr12:57589670..57592502,2	MCF-7	breast:
5	chr12:57517341..57518789-chr12:57568484..57570374,10	K562	blood:
6	chr12:57567624..57569926-chr12:57631899..57633807,2	K562	blood:
7	chr12:57518245..57520223-chr12:57568924..57570929,2	K562	blood:
8	chr12:57516403..57523563-chr12:57569385..57572660,8	MCF-7	breast:
9	chr12:57569385..57570138-chr12:57632553..57633485,3	K562	blood:
10	chr12:57568118..57572450-chr12:57574080..57578347,5	MCF-7	breast:
11	chr12:57567688..57569393-chr12:57569418..57572218,2	K562	blood:
12	chr12:57555965..57558204-chr12:57567969..57569560,2	MCF-7	breast:
13	chr12:57520537..57522971-chr12:57567650..57571522,4	MCF-7	breast:
14	chr12:57558276..57561076-chr12:57569172..57570958,2	MCF-7	breast:
15	chr12:57567760..57571658-chr12:57632861..57635535,3	K562	blood:
16	chr12:57569226..57571527-chr12:57578285..57580181,2	K562	blood:
17	chr12:57567893..57570087-chr12:57570718..57572481,2	K562	blood:
18	chr12:57480591..57482592-chr12:57568508..57571251,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000123384	Chromatin interaction
ENSG00000166881	Chromatin interaction
ENSG00000166888	Chromatin interaction
ENSG00000185633	Chromatin interaction

Extended variants
information (count: 25 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11172083	1.00[AMR][1000 genomes]
rs11172087	1.00[AMR][1000 genomes]
rs2229281	1.00[AMR][1000 genomes]
rs34241718	1.00[AMR][1000 genomes]
rs57244425	1.00[AMR][1000 genomes]
rs60301769	1.00[AMR][1000 genomes]
rs60957079	1.00[AMR][1000 genomes]
rs61609471	1.00[AMR][1000 genomes]
rs73330570	1.00[AMR][1000 genomes]
rs73330571	1.00[AMR][1000 genomes]
rs73332659	1.00[AMR][1000 genomes]
rs73332662	1.00[AMR][1000 genomes]
rs73332664	1.00[AMR][1000 genomes]
rs73332676	1.00[AMR][1000 genomes]
rs73332678	1.00[AMR][1000 genomes]
rs73332681	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1040850	chr12:57055011-57679209	Strong transcription Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	181 gene(s)	inside rSNPs	diseases
2	nsv559023	chr12:57530670-57616061	Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
3	nsv518980	chr12:57532982-57637593	Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
4	nsv899112	chr12:57535266-57601388	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
5	nsv525873	chr12:57535266-57616013	Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
6	nsv899113	chr12:57543572-57601388	Genic enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	12 gene(s)	inside rSNPs	diseases
7	nsv899114	chr12:57556768-57587839	Strong transcription Enhancers Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
8	esv1810281	chr12:57558657-57641094	Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
9	esv1827238	chr12:57561918-57641094	Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:97 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:57531800-57576000	Strong transcription	Fetal Brain Female	brain
2	chr12:57541600-57606600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr12:57541800-57607400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr12:57547000-57575600	Strong transcription	H1 Cell Line	embryonic stem cell
5	chr12:57547000-57575600	Strong transcription	HUES64 Cell Line	embryonic stem cell
6	chr12:57547000-57606400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
7	chr12:57547400-57575400	Strong transcription	HUES6 Cell Line	embryonic stem cell
8	chr12:57547600-57575400	Strong transcription	Cortex derived primary cultured neurospheres	brain
9	chr12:57547600-57575600	Strong transcription	iPS-15b Cell Line	embryonic stem cell
10	chr12:57549000-57575200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr12:57552800-57575200	Strong transcription	Duodenum Mucosa	Duodenum
12	chr12:57552800-57606800	Strong transcription	Fetal Intestine Large	intestine
13	chr12:57552800-57607000	Strong transcription	Liver	Liver
14	chr12:57553200-57607400	Strong transcription	Fetal Intestine Small	intestine
15	chr12:57555400-57583200	Weak transcription	Fetal Heart	heart
16	chr12:57557400-57606800	Strong transcription	Primary monocytes fromperipheralblood	blood
17	chr12:57558000-57575800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr12:57558400-57575600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr12:57558800-57575600	Strong transcription	Sigmoid Colon	Sigmoid Colon
20	chr12:57560800-57606200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr12:57560800-57606600	Strong transcription	Monocytes-CD14+_RO01746	blood
22	chr12:57562000-57570800	Weak transcription	Pancreas	Pancrea
23	chr12:57563600-57573800	Weak transcription	Small Intestine	intestine
24	chr12:57564000-57572200	Weak transcription	Left Ventricle	heart
25	chr12:57564600-57570000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr12:57565400-57570000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr12:57565400-57574400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr12:57565400-57575600	Strong transcription	Lung	lung
29	chr12:57565600-57573800	Strong transcription	Adipose Nuclei	Adipose
30	chr12:57565600-57576200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr12:57565800-57575200	Strong transcription	Fetal Lung	lung
32	chr12:57565800-57606600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr12:57566000-57570200	Strong transcription	Osteobl	bone
34	chr12:57566000-57604200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr12:57566200-57574800	Strong transcription	Placenta Amnion	Placenta Amnion
36	chr12:57566200-57576000	Strong transcription	HSMMtube	muscle
37	chr12:57566400-57571400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr12:57566400-57583600	Strong transcription	Colon Smooth Muscle	Colon
39	chr12:57566600-57575800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
40	chr12:57566600-57575800	Strong transcription	Right Ventricle	heart
41	chr12:57566600-57606200	Strong transcription	HUES48 Cell Line	embryonic stem cell
42	chr12:57566800-57575200	Strong transcription	H9 Cell Line	embryonic stem cell
43	chr12:57566800-57575600	Strong transcription	Aorta	Aorta
44	chr12:57567000-57576000	Strong transcription	HepG2	liver
45	chr12:57567000-57576400	Strong transcription	Duodenum Smooth Muscle	Duodenum
46	chr12:57567200-57571400	Genic enhancers	Stomach Mucosa	stomach
47	chr12:57567200-57572200	Strong transcription	Spleen	Spleen
48	chr12:57567200-57583600	Weak transcription	Right Atrium	heart
49	chr12:57567400-57569800	Weak transcription	Fetal Kidney	kidney
50	chr12:57567400-57584200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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