Variant report

Variant	rs570674842
Chromosome Location	chr5:179219800-179219801
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:23)
CpG islands
(count:0)
Chromatin interactive
region (count:5)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:23 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr5:179219673-179219895	GM12878	blood:	n/a	n/a
2	SPI1	chr5:179219708-179220149	HL-60	blood:	n/a	n/a
3	SPI1	chr5:179219506-179220249	GM12878	blood:	n/a	n/a
4	MAX	chr5:179219679-179220028	HepG2	liver:	n/a	n/a
5	HNF4A	chr5:179219710-179220015	HepG2	liver:	n/a	chr5:179219862-179219877
6	MYC	chr5:179219717-179219810	HepG2	liver:	n/a	n/a
7	POLR2A	chr5:179218996-179221960	HL-60	blood:	n/a	n/a
8	MYC	chr5:179219630-179220084	NB4	blood:	n/a	n/a
9	EBF1	chr5:179219709-179220059	GM12878	blood:	n/a	n/a
10	MAX	chr5:179219723-179219889	HepG2	liver:	n/a	n/a
11	MAX	chr5:179219615-179221657	NB4	blood:	n/a	n/a
12	SPI1	chr5:179219771-179220032	GM12878	blood:	n/a	n/a
13	SPI1	chr5:179219697-179220050	GM12891	blood:	n/a	n/a
14	SPI1	chr5:179219725-179219999	K562	blood:	n/a	n/a
15	SPI1	chr5:179219573-179220274	HL-60	blood:	n/a	n/a
16	POLR2A	chr5:179219707-179219906	GM12878	blood:	n/a	n/a
17	SPI1	chr5:179219711-179220098	GM12891	blood:	n/a	n/a
18	MAX	chr5:179219567-179220123	HepG2	liver:	n/a	n/a
19	RUNX3	chr5:179219689-179219984	GM12878	blood:	n/a	n/a
20	SPI1	chr5:179219723-179220034	K562	blood:	n/a	n/a
21	HNF4A	chr5:179219778-179220216	HepG2	liver:	n/a	chr5:179219862-179219877
22	PML	chr5:179219585-179219968	GM12878	blood:	n/a	n/a
23	POLR2A	chr5:179219447-179224493	HepG2	liver:	n/a	n/a

No data

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:179205387..179207447-chr5:179218747..179220491,2	K562	blood:
2	chr5:179157523..179162988-chr5:179219694..179224698,13	MCF-7	breast:
3	chr5:179213701..179215933-chr5:179218776..179220680,2	K562	blood:
4	chr5:179205957..179207615-chr5:179218348..179219920,2	MCF-7	breast:
5	chr5:179192680..179196164-chr5:179217971..179221244,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LTC4S-1	chr5:179218765-179220536	NONHSAT105621

No data

Variant related genes	Relation type
LTC4S	TF binding region
ENSG00000161021	Chromatin interaction

Extended variants
information (count: 15 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949554	chr5:178832325-179309513	Transcr. at gene 5' and 3' Weak transcription Strong transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	312 gene(s)	inside rSNPs	diseases
2	nsv883270	chr5:178951106-179350387	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	312 gene(s)	inside rSNPs	diseases
3	nsv531997	chr5:179107599-179588082	Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	339 gene(s)	inside rSNPs	diseases
4	nsv469579	chr5:179184831-179360191	Genic enhancers Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	182 gene(s)	inside rSNPs	diseases
5	nsv883274	chr5:179186397-179310330	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
6	nsv518964	chr5:179193598-179227286	Strong transcription Enhancers Active TSS Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	151 gene(s)	inside rSNPs	diseases
7	nsv883275	chr5:179193598-179267783	Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Enhancers Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
8	nsv883276	chr5:179193598-179310330	Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
9	nsv883277	chr5:179193598-179350387	Genic enhancers Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	182 gene(s)	inside rSNPs	diseases
10	nsv823361	chr5:179213324-179251243	Genic enhancers Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	173 gene(s)	inside rSNPs	diseases
11	nsv600659	chr5:179214251-179225594	Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	147 gene(s)	inside rSNPs	diseases
12	nsv600660	chr5:179214251-179231248	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	149 gene(s)	inside rSNPs	diseases
13	nsv883278	chr5:179214818-179238794	Active TSS Genic enhancers Strong transcription Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	154 gene(s)	inside rSNPs	diseases
14	nsv883279	chr5:179214818-179248774	Enhancers Strong transcription Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	173 gene(s)	inside rSNPs	diseases
15	nsv870188	chr5:179218824-179235424	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	154 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:179202000-179221800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr5:179203400-179221600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr5:179203600-179220400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr5:179203600-179222000	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr5:179204000-179221200	Weak transcription	Small Intestine	intestine
6	chr5:179205200-179220600	Weak transcription	Rectal Smooth Muscle	rectum
7	chr5:179205200-179221800	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr5:179206000-179220200	Weak transcription	Ovary	ovary
9	chr5:179207000-179220200	Weak transcription	GM12878-XiMat	blood
10	chr5:179207200-179220600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr5:179207400-179221000	Weak transcription	Brain Substantia Nigra	brain
12	chr5:179207600-179220000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr5:179207600-179220200	Weak transcription	Brain Cingulate Gyrus	brain
14	chr5:179207600-179220200	Weak transcription	Duodenum Mucosa	Duodenum
15	chr5:179207600-179220200	Weak transcription	Pancreas	Pancrea
16	chr5:179207600-179220600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr5:179207600-179220800	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr5:179207600-179221200	Weak transcription	Fetal Intestine Large	intestine
19	chr5:179207600-179222200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr5:179207600-179222600	Weak transcription	Aorta	Aorta
21	chr5:179207800-179220200	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr5:179207800-179220200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr5:179207800-179220400	Weak transcription	Primary T helper cells PMA-I stimulated	--
24	chr5:179207800-179220400	Weak transcription	Brain Angular Gyrus	brain
25	chr5:179207800-179220400	Weak transcription	HSMM	muscle
26	chr5:179207800-179220600	Weak transcription	Primary T helper cells fromperipheralblood	blood
27	chr5:179207800-179222200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr5:179208000-179220200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr5:179208000-179220200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
30	chr5:179208000-179220400	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr5:179208000-179220600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
32	chr5:179209000-179220400	Weak transcription	Brain Anterior Caudate	brain
33	chr5:179209000-179220800	Weak transcription	Dnd41	blood
34	chr5:179209200-179220000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr5:179209400-179222200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr5:179209600-179220400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr5:179209600-179221600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr5:179209800-179220200	Weak transcription	Primary T cells from cord blood	blood
39	chr5:179215600-179220000	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr5:179215600-179221200	Weak transcription	Thymus	Thymus
41	chr5:179215600-179223200	Weak transcription	HSMMtube	muscle
42	chr5:179218200-179220000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr5:179218200-179220200	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr5:179218200-179220400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr5:179218200-179220600	Enhancers	Primary hematopoietic stem cells	blood
46	chr5:179218400-179220200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr5:179218600-179221000	Enhancers	Fetal Muscle Leg	muscle
48	chr5:179218600-179221600	Enhancers	Placenta	Placenta
49	chr5:179218600-179222800	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr5:179218800-179219800	Strong transcription	Fetal Brain Female	brain

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