Variant report

Variant	rs201819884
Chromosome Location	chr12:123435953-123435954
allele	C/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	FOS	chr12:123435916-123436235	MCF10A-Er-Src	breast:	n/a	chr12:123436052-123436063
2	PRDM1	chr12:123435927-123436262	Hela-S3	cervix:	n/a	chr12:123436072-123436087
3	FOS	chr12:123435909-123436284	MCF10A-Er-Src	breast:	n/a	chr12:123436052-123436063
4	MAX	chr12:123435813-123436524	A549	lung:	n/a	chr12:123436104-123436114
5	FOSL2	chr12:123435764-123436426	A549	lung:	n/a	n/a
6	RAD21	chr12:123435803-123437497	HCT-116	colon:	n/a	chr12:123437031-123437050 chr12:123437049-123437068 chr12:123437033-123437045 chr12:123437034-123437047
7	MAX	chr12:123435925-123436309	K562	blood:	n/a	chr12:123436104-123436114
8	SIN3AK20	chr12:123435907-123436277	SK-N-SH	brain:	n/a	n/a
9	JUN	chr12:123435795-123436416	K562	blood:	n/a	n/a
10	MAX	chr12:123435805-123436467	HCT-116	colon:	n/a	chr12:123436104-123436114
11	JUND	chr12:123435943-123436167	K562	blood:	n/a	chr12:123436052-123436063
12	MAX	chr12:123435939-123436258	NB4	blood:	n/a	chr12:123436104-123436114
13	MAX	chr12:123435840-123436363	SK-N-SH	brain:	n/a	chr12:123436104-123436114
14	MAX	chr12:123435868-123436465	A549	lung:	n/a	chr12:123436104-123436114
15	FOS	chr12:123435856-123436309	HUVEC	blood vessel:	n/a	chr12:123436052-123436063
16	MYC	chr12:123435905-123436240	HUVEC	blood vessel:	n/a	chr12:123436104-123436114
17	MAX	chr12:123435948-123436310	Hela-S3	cervix:	n/a	chr12:123436104-123436114
18	FOS	chr12:123435929-123436235	MCF10A-Er-Src	breast:	n/a	chr12:123436052-123436063
19	MAX	chr12:123435802-123437585	HCT-116	colon:	n/a	chr12:123436104-123436114
20	FOSL2	chr12:123435915-123436259	A549	lung:	n/a	n/a
21	MYC	chr12:123435937-123436329	MCF10A-Er-Src	breast:	n/a	chr12:123436104-123436114
22	POLR2A	chr12:123435923-123436123	HUVEC	blood vessel:	n/a	n/a
23	PBX3	chr12:123435824-123436379	SK-N-SH	brain:	n/a	n/a
24	RUNX3	chr12:123435931-123436345	GM12878	blood:	n/a	n/a
25	FOSL2	chr12:123435817-123436385	SK-N-SH	brain:	n/a	n/a
26	JUND	chr12:123435756-123436523	SK-N-SH	brain:	n/a	chr12:123436052-123436063
27	BATF	chr12:123435931-123436247	GM12878	blood:	n/a	n/a
28	FOS	chr12:123435888-123436288	MCF10A-Er-Src	breast:	n/a	chr12:123436052-123436063
29	MYC	chr12:123435929-123436288	MCF10A-Er-Src	breast:	n/a	chr12:123436104-123436114
30	PBX3	chr12:123435843-123436442	SK-N-SH	brain:	n/a	n/a
31	MAX	chr12:123435889-123436275	SK-N-SH	brain:	n/a	chr12:123436104-123436114
32	EBF1	chr12:123435924-123436309	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:123345450..123347445-chr12:123435441..123437142,2	K562	blood:
2	chr12:123426745..123429433-chr12:123432536..123436941,4	K562	blood:
3	chr12:123341218..123343418-chr12:123435392..123437282,2	MCF-7	breast:
4	chr12:123433587..123436454-chr12:123458977..123461529,2	K562	blood:

Variant related genes	Relation type
ABCB9	TF binding region
ENSG00000111325	Chromatin interaction
ENSG00000150967	Chromatin interaction
ENSG00000256028	Chromatin interaction
ENSG00000130787	Chromatin interaction

Extended variants
information (count: 12 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3388790	chr12:123275902-123655103	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
2	nsv899572	chr12:123292503-123477311	Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	nsv899573	chr12:123312051-123528405	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
4	nsv517200	chr12:123312051-123654498	Strong transcription Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
5	nsv899576	chr12:123335527-123528405	Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
6	nsv832532	chr12:123395927-123573137	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
7	nsv832533	chr12:123395927-123589290	Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
8	nsv427924	chr12:123412172-123722059	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	78 gene(s)	inside rSNPs	diseases
9	nsv560491	chr12:123425575-123444422	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
10	nsv455732	chr12:123427573-123574838	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
11	nsv560492	chr12:123427573-123574838	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
12	nsv899577	chr12:123435248-123484474	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:92 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:123403000-123444200	Weak transcription	Aorta	Aorta
2	chr12:123412800-123449200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr12:123413400-123449600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr12:123413600-123450000	Weak transcription	Primary T cells from cord blood	blood
5	chr12:123417400-123441800	Weak transcription	Ovary	ovary
6	chr12:123417600-123446200	Weak transcription	Fetal Lung	lung
7	chr12:123429600-123444000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr12:123429800-123436400	Strong transcription	Fetal Stomach	stomach
9	chr12:123429800-123444000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr12:123430000-123441800	Weak transcription	Fetal Brain Male	brain
11	chr12:123431800-123439600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr12:123432000-123436000	Weak transcription	HepG2	liver
13	chr12:123432000-123439800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr12:123432000-123444000	Weak transcription	Thymus	Thymus
15	chr12:123432200-123436400	Weak transcription	HSMMtube	muscle
16	chr12:123432200-123439600	Weak transcription	Fetal Muscle Trunk	muscle
17	chr12:123432200-123441800	Weak transcription	Right Ventricle	heart
18	chr12:123432200-123444200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr12:123432200-123446000	Weak transcription	Right Atrium	heart
20	chr12:123432200-123446000	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr12:123432200-123446000	Weak transcription	K562	blood
22	chr12:123432200-123450000	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr12:123432200-123450200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr12:123432400-123436000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr12:123432400-123436000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr12:123432400-123436000	Weak transcription	NH-A	brain
27	chr12:123432400-123436000	Weak transcription	NHLF	lung
28	chr12:123432400-123436200	Weak transcription	NHDF-Ad	bronchial
29	chr12:123432400-123436400	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr12:123432400-123436600	Weak transcription	Fetal Thymus	thymus
31	chr12:123432400-123436800	Weak transcription	Primary T helper cells PMA-I stimulated	--
32	chr12:123432400-123439600	Weak transcription	Fetal Muscle Leg	muscle
33	chr12:123432400-123444200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr12:123432400-123444200	Weak transcription	Pancreas	Pancrea
35	chr12:123432400-123448200	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr12:123432400-123449600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
37	chr12:123432400-123450000	Weak transcription	Primary T helper cells fromperipheralblood	blood
38	chr12:123432600-123436000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr12:123432600-123436000	Weak transcription	GM12878-XiMat	blood
40	chr12:123432600-123436200	Weak transcription	Primary B cells from peripheral blood	blood
41	chr12:123432600-123436600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
42	chr12:123432600-123441600	Weak transcription	Lung	lung
43	chr12:123432600-123444200	Weak transcription	Esophagus	oesophagus
44	chr12:123432600-123444200	Weak transcription	Spleen	Spleen
45	chr12:123432600-123444400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr12:123432600-123448200	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr12:123432600-123450000	Weak transcription	Primary hematopoietic stem cells	blood
48	chr12:123433000-123436000	Weak transcription	Hela-S3	cervix
49	chr12:123433000-123441800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr12:123433200-123436800	Weak transcription	Primary T cells fromperipheralblood	blood

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