Variant report

Variant	rs551725404
Chromosome Location	chr12:104530485-104530486
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:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:104322684..104325586-chr12:104530441..104532019,2	K562	blood:
2	chr12:104529689..104531446-chr12:104719514..104721289,2	K562	blood:
3	chr12:104456193..104459744-chr12:104529847..104533076,6	K562	blood:
4	chr12:104348297..104351124-chr12:104530392..104533056,3	MCF-7	breast:
5	chr12:104529986..104533486-chr12:104678703..104682517,5	MCF-7	breast:
6	chr12:104510515..104519727-chr12:104525085..104533754,15	MCF-7	breast:
7	chr12:104528672..104531458-chr12:104545242..104548166,2	K562	blood:
8	chr12:104528672..104531458-chr12:104545242..104548166,3	K562	blood:
9	chr12:104528011..104530810-chr12:104621683..104623795,2	K562	blood:
10	chr12:104456335..104459744-chr12:104529847..104533076,5	K562	blood:
11	chr12:104481200..104483346-chr12:104529918..104531545,2	K562	blood:
12	chr12:104356409..104362053-chr12:104528975..104533138,7	MCF-7	breast:
13	chr12:104530438..104533662-chr12:104564030..104567253,5	K562	blood:
14	chr12:104528832..104532197-chr12:105351511..105353407,3	MCF-7	breast:
15	chr12:104487179..104490226-chr12:104527814..104531447,3	K562	blood:
16	chr12:104530239..104532383-chr12:105499797..105502736,2	MCF-7	breast:
17	chr12:104529888..104531745-chr12:104641591..104644080,2	MCF-7	breast:
18	chr12:104530429..104534144-chr12:104679811..104684673,6	MCF-7	breast:
19	chr12:104455182..104458865-chr12:104529769..104532559,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000199415	Chromatin interaction
ENSG00000265072	Chromatin interaction
ENSG00000139372	Chromatin interaction
ENSG00000166598	Chromatin interaction
ENSG00000111727	Chromatin interaction
ENSG00000120820	Chromatin interaction
ENSG00000198431	Chromatin interaction
ENSG00000257193	Chromatin interaction
ENSG00000257999	Chromatin interaction
ENSG00000136051	Chromatin interaction
ENSG00000204954	Chromatin interaction
ENSG00000214198	Chromatin interaction
ENSG00000136052	Chromatin interaction

Extended variants
information (count: 9 )
Associated
traits (count: 0)

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	esv1823607	chr12:104506318-104549541	Genic enhancers Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	n/a
2	esv1816017	chr12:104510676-104531860	Flanking Active TSS Genic enhancers Enhancers Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	n/a
3	nsv1045725	chr12:104524153-104614108	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	n/a
4	nsv541586	chr12:104524153-104614108	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	n/a
5	nsv560047	chr12:104529349-104531705	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	29 gene(s)	inside rSNPs	n/a
6	esv1795002	chr12:104529349-104532159	Active TSS Flanking Active TSS Weak transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	n/a
7	esv1837667	chr12:104529349-104532159	Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	n/a
8	esv1841869	chr12:104529349-104532159	Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	n/a
9	esv3378083	chr12:104530222-104533220	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:104493800-104530600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr12:104495600-104530800	Weak transcription	Esophagus	oesophagus
3	chr12:104523600-104530600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr12:104523800-104530600	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr12:104526600-104530600	Weak transcription	Psoas Muscle	Psoas
6	chr12:104526600-104531000	Weak transcription	Lung	lung
7	chr12:104526800-104530800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr12:104526800-104530800	Weak transcription	Gastric	stomach
9	chr12:104526800-104531000	Weak transcription	Spleen	Spleen
10	chr12:104527800-104530600	Weak transcription	Colonic Mucosa	Colon
11	chr12:104528000-104530600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr12:104528000-104530600	Weak transcription	Placenta	Placenta
13	chr12:104528600-104530600	Enhancers	Primary T helper naive cells from peripheral blood	blood
14	chr12:104528600-104530800	Enhancers	Primary T killer memory cells from peripheral blood	blood
15	chr12:104528800-104530600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
16	chr12:104528800-104530600	Enhancers	Colon Smooth Muscle	Colon
17	chr12:104529000-104530600	Enhancers	Primary T helper cells fromperipheralblood	blood
18	chr12:104529000-104530800	Weak transcription	Ovary	ovary
19	chr12:104529000-104531000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr12:104529200-104530600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr12:104529200-104530800	Weak transcription	Pancreas	Pancrea
22	chr12:104529200-104532400	Active TSS	iPS-20b Cell Line	embryonic stem cell
23	chr12:104529400-104530600	Enhancers	Primary hematopoietic stem cells	blood
24	chr12:104529400-104530600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
25	chr12:104529400-104530600	Enhancers	Liver	Liver
26	chr12:104529400-104530800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr12:104529600-104530600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
28	chr12:104529600-104530600	Enhancers	Rectal Smooth Muscle	rectum
29	chr12:104529600-104530800	Flanking Active TSS	Osteobl	bone
30	chr12:104529600-104531000	Flanking Active TSS	Dnd41	blood
31	chr12:104529600-104532400	Active TSS	NHLF	lung
32	chr12:104529800-104530600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr12:104529800-104530600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
34	chr12:104529800-104530600	Enhancers	Brain Hippocampus Middle	brain
35	chr12:104529800-104530600	Enhancers	Fetal Intestine Large	intestine
36	chr12:104529800-104530600	Enhancers	Fetal Intestine Small	intestine
37	chr12:104529800-104530600	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr12:104529800-104530600	Enhancers	Skeletal Muscle Male	skeletal muscle
39	chr12:104529800-104530800	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr12:104529800-104530800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
41	chr12:104529800-104531000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr12:104529800-104531000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr12:104529800-104531000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
44	chr12:104529800-104531000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
45	chr12:104529800-104531000	Flanking Active TSS	A549	lung
46	chr12:104529800-104532200	Active TSS	Right Atrium	heart
47	chr12:104530000-104530600	Enhancers	Primary monocytes fromperipheralblood	blood
48	chr12:104530000-104530600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
49	chr12:104530000-104530600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr12:104530000-104530600	Enhancers	Brain Substantia Nigra	brain

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