Variant report

Variant	rs568242702
Chromosome Location	chr1:113496852-113496853
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:15)
CpG islands
(count:0)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:15 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ZNF384	chr1:113496766-113496854	GM12878	blood:	n/a	n/a
2	IRF1	chr1:113496710-113499275	K562	blood:	n/a	chr1:113498874-113498888
3	RCOR1	chr1:113496237-113497046	K562	blood:	n/a	n/a
4	GATA2	chr1:113496612-113497021	SH-SY5Y	brain:	n/a	n/a
5	GATA2	chr1:113496408-113497124	HUVEC	blood vessel:	n/a	n/a
6	GATA3	chr1:113496636-113497006	SH-SY5Y	brain:	n/a	n/a
7	TEAD4	chr1:113495977-113497191	K562	blood:	n/a	n/a
8	MXI1	chr1:113496452-113500651	SK-N-SH	brain:	n/a	n/a
9	POLR2A	chr1:113496614-113501021	MCF10A-Er-Src	breast:	n/a	n/a
10	TAL1	chr1:113496385-113499187	K562	blood:	n/a	n/a
11	SIN3A	chr1:113496700-113500418	H1-hESC	embryonic stem cell:	n/a	chr1:113498030-113498043
12	GATA3	chr1:113496581-113496960	T-47D	breast:	n/a	n/a
13	MXI1	chr1:113496819-113499323	K562	blood:	n/a	n/a
14	GATA3	chr1:113496378-113497377	SK-N-SH	brain:	n/a	n/a
15	GATA3	chr1:113496440-113497160	SK-N-SH	brain:	n/a	n/a

No data

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:113470982..113473508-chr1:113495282..113498149,2	K562	blood:
2	chr1:113459369..113469193-chr1:113493855..113500263,12	K562	blood:
3	chr1:113255626..113260544-chr1:113496476..113500122,4	K562	blood:
4	chr1:113495044..113497639-chr1:113562401..113565157,2	K562	blood:
5	chr1:113423471..113424047-chr1:113496482..113497380,2	MCF-7	breast:
6	chr1:113467781..113469713-chr1:113495884..113497441,2	K562	blood:
7	chr1:113476476..113482692-chr1:113494893..113501777,18	K562	blood:
8	chr1:113496138..113497721-chr1:113563292..113564960,2	MCF-7	breast:
9	chr1:113417890..113419473-chr1:113495009..113497982,2	K562	blood:
10	chr1:113240296..113243095-chr1:113496225..113498995,2	K562	blood:
11	chr1:113495059..113500488-chr1:113613593..113618010,11	K562	blood:
12	chr1:113493791..113500715-chr1:113613796..113618010,15	K562	blood:
13	chr1:113495708..113498262-chr1:114506476..114508244,2	K562	blood:
14	chr1:113495642..113498034-chr1:114469610..114473117,3	K562	blood:
15	chr1:113496225..113498697-chr7:153107803..153110252,2	K562	blood:

No data

Variant related genes	Relation type
SLC16A1-AS1	TF binding region
ENSG00000163349	Chromatin interaction
ENSG00000234722	Chromatin interaction
ENSG00000229020	Chromatin interaction
ENSG00000155367	Chromatin interaction
ENSG00000155380	Chromatin interaction
ENSG00000238198	Chromatin interaction
ENSG00000235527	Chromatin interaction
ENSG00000155363	Chromatin interaction
ENSG00000261595	Chromatin interaction
ENSG00000198799	Chromatin interaction

Extended variants
information (count: 14 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002971	chr1:112924725-113740584	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	166 gene(s)	inside rSNPs	diseases
2	nsv535059	chr1:112924725-113740584	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	166 gene(s)	inside rSNPs	diseases
3	nsv1010276	chr1:113123932-113740584	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	158 gene(s)	inside rSNPs	diseases
4	nsv533295	chr1:113167645-113589588	Flanking Active TSS Active TSS Strong transcription Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
5	nsv1012119	chr1:113214869-113759081	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
6	nsv535060	chr1:113214869-113759081	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
7	nsv529238	chr1:113229946-113759080	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	100 gene(s)	inside rSNPs	diseases
8	nsv997426	chr1:113288282-113639507	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
9	nsv1004102	chr1:113295805-113551210	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
10	esv3399982	chr1:113358580-113542255	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
11	nsv999915	chr1:113360145-113684833	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
12	esv18293	chr1:113375437-113852815	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
13	nsv1007045	chr1:113425222-113839910	Genic enhancers Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
14	esv1827123	chr1:113496841-113531848	Strong transcription Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:113467000-113497400	Weak transcription	Fetal Muscle Trunk	muscle
2	chr1:113469800-113497000	Weak transcription	Fetal Stomach	stomach
3	chr1:113481400-113497000	Weak transcription	Osteobl	bone
4	chr1:113492600-113498000	Weak transcription	Pancreas	Pancrea
5	chr1:113493400-113497800	Weak transcription	Esophagus	oesophagus
6	chr1:113493800-113497000	Transcr. at gene 5' and 3'	HUES6 Cell Line	embryonic stem cell
7	chr1:113494000-113497000	Transcr. at gene 5' and 3'	K562	blood
8	chr1:113494000-113497600	Transcr. at gene 5' and 3'	iPS-18 Cell Line	embryonic stem cell
9	chr1:113494000-113497800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr1:113494000-113497800	Weak transcription	Small Intestine	intestine
11	chr1:113494200-113497800	Transcr. at gene 5' and 3'	iPS-20b Cell Line	embryonic stem cell
12	chr1:113494600-113497200	Transcr. at gene 5' and 3'	HUES48 Cell Line	embryonic stem cell
13	chr1:113495000-113497200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr1:113495000-113497800	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr1:113495200-113501400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr1:113495400-113497000	Enhancers	Liver	Liver
17	chr1:113495400-113497000	Flanking Active TSS	Hela-S3	cervix
18	chr1:113495400-113497200	Transcr. at gene 5' and 3'	NHEK	skin
19	chr1:113495600-113497600	Weak transcription	Primary hematopoietic stem cells	blood
20	chr1:113495800-113497000	Weak transcription	Ovary	ovary
21	chr1:113495800-113497200	Active TSS	Colon Smooth Muscle	Colon
22	chr1:113495800-113500200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr1:113495800-113500600	Active TSS	H9 Cell Line	embryonic stem cell
24	chr1:113495800-113500600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr1:113495800-113500800	Active TSS	ES-I3 Cell Line	embryonic stem cell
26	chr1:113495800-113501400	Active TSS	iPS-15b Cell Line	embryonic stem cell
27	chr1:113496000-113497000	Enhancers	Stomach Mucosa	stomach
28	chr1:113496000-113497200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr1:113496000-113497800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr1:113496000-113497800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr1:113496000-113497800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr1:113496000-113501000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr1:113496200-113497200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
34	chr1:113496200-113497400	Enhancers	Brain Substantia Nigra	brain
35	chr1:113496200-113497400	Enhancers	Rectal Mucosa Donor 31	rectum
36	chr1:113496200-113497400	Flanking Active TSS	HUVEC	blood vessel
37	chr1:113496200-113497600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
38	chr1:113496200-113497600	Enhancers	Primary T helper cells fromperipheralblood	blood
39	chr1:113496200-113497600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr1:113496200-113497600	Flanking Active TSS	Fetal Heart	heart
41	chr1:113496200-113497800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr1:113496200-113497800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr1:113496200-113497800	Flanking Active TSS	Brain Cingulate Gyrus	brain
44	chr1:113496200-113497800	Flanking Active TSS	Dnd41	blood
45	chr1:113496200-113498000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr1:113496200-113500400	Active TSS	Stomach Smooth Muscle	stomach
47	chr1:113496200-113501800	Active TSS	Right Ventricle	heart
48	chr1:113496400-113497000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr1:113496400-113497000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr1:113496400-113497000	Flanking Active TSS	Brain Anterior Caudate	brain

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